Let's start a new assignment project together, Get Exclusive Free Assistance Now!

Need Help? Call Us :

Place Order

EMS5ARA Advanced Research Learning Literature Review

Mar 13,23

Question:

Background:

Department of Engineering

EMS5ARA Advanced Research Learning Literature Review

Grades and Assessment Comments

Student Name ID Number
Grades given by
Please indicate Supervisor Co-Supervisor Additional Marker
Evaluation
Presentation (written) Quality and Student’s Professional Approach Technical Content

(Student’s) Knowledge/Understanding

Please provide a letter grade only: i.e. NS, N, D-, D, D+, C-, C, C+, B-, B, B+, A-, A, A+, AA-, AA, AA+ or AAA for each of the above categories (using Rubric in the next page). Although if you provide a fail grade then please also indicate an indicative mark e.g. N (35).

Please provide below summary assessment review comments roughly 100-200 words. These will be provided to the student along with the letter grades above.

Please give your summary here and indicate the marks out of 100.

Assessment task: Literature Review
POOR (1-4) AVERAGE (4-6) GOOD (6-8) EXEMPLARY (8-10)
OVERALL PRESENTATION & FORMAT

(0.75%)

Has not used appropriate format; or has used standard but not included all required components. Poor formatting and inconsistencies in text throughout the report. Has used appropriate format and included all required components; but formatting of headings and spacing within text has significant inconsistencies Has used appropriate format, has all required components; formatting of headings and spacing within the text may have some minor inconsistencies Has used appropriate format and included all required components. Formatting is consistent throughout the document
LITERATURE REVIEW No evidence of Evidence of relevant Evidence of relevant Evidence of relevant
BODY (6%) relevant literature literature review however literature review with literature review with
review, no critical no critical analysis and critical analysis and critical analysis and
discussion and discussion. discussion. discussion, and outcome
analysis. of proper conclusions.
LANGUAGE (1%) Poor sentence structure, punctuation and inappropriate vocabulary. Language lacks professional conventions. Dot points used instead of paragraph structure. Ideas are expressed in a professional style, although there may be minor sentence structure, punctuation and spelling errors. Ideas are clearly expressed in a professional manner, using appropriate vocabulary. There are very few grammar, punctuation and spelling errors. Ideas are eloquently expressed in a professional manner, using appropriate vocabulary. There are no grammar, punctuation and spelling errors.
TABLES AND FIGURES (0.25%) Tables and figures are not referred to in the text. Tables and figures are not numbered sequentially. Figures and tables are unclear or unreferenced. Tables and figures are numbered sequentially. There is some reference to them in the text. Most figures are clear and the tables appropriate. Tables and figures are numbered sequentially and integrated into the text. Tables and figures are clear and appropriate. Tables and figures are referred to sequentially and integrated to add value to the text. Figures and tables are clear and appropriate and correctly formatted.
CITATIONS (1%) References are either poorly cited or not cited in the text at all. They are not all in the reference list. They not formatted correctly in APA system format in either citation or reference list. References are mostly correctly cited in text and most are formatted correctly in reference list References are all correctly cited, but may have a few errors in the format of the reference list. References are all correctly formatted in citations and reference list.
QUALITY OF REFERENCES (1%) References are of poor quality, generic in nature and show no evidence of wide research. References are not relevant. References are of adequate quality and show some evidence of relevant research/reading. References are of good quality and show evidence of relevant wide research/reading. References are of excellent quality, showing strong evidence of relevant reading/research.

The performance of fly ash as an alkali-activated binder in geopolymer concrete and development of guidelines for mix design of cast-in-situ geopolymer concrete

Authored by Bradley Connolly – 17697347

Under the supervision of Dr D. Ionescu and Dr V. Patel

This document has been developed and submitted in partial fulfilment of EMS4EMP in the Bachelor of Civil Engineering (Honours) Degree at La Trobe University,

Bendigo

June 2017

Abstract

Geopolymer concrete has a number of environmental advantages when compared to Ordinary Portland Cement (OPC) concrete, yet its adoption is delayed by gaps-in-knowledge, particularly for concrete cured in ambient conditions [1]. Fly ash, a waste material, has shown promise to replace OPC as a concrete binder in some circumstances. This yields benefits including the reducing the carbon footprint of infrastructure development. Recent research has found that chemical composition of fly ash reagents is a poor indictor of the performance of geopolymer concrete, instead Zhang et al (2016) have proposed a ‘reactivity index’ to assess the suitability of fly ashes. In this discourse the mechanical properties of fly ash based geopolymer concrete has been examined from available literature. Fly ash based geopolymer concrete is seen to behave in a similar manner to OPC concrete, with differences in magnitude in some parameters and effectively identical in others. The largest gap-in-knowledge is the performance of geopolymer concrete in in-situ applications.

Table of Contents

Abstract……………………………………………………………………………………………………………………………….. 2

Table of Contents…………………………………………………………………………………………………………………… 3

List of Figures………………………………………………………………………………………………………………………… 4

List of Equations…………………………………………………………………………………………………………………….. 5

List of Tables…………………………………………………………………………………………………………………………. 6

Literature Review…………………………………………………………………………………………………………………… 7

Environmental Impact of Ordinary Portland Cement…………………………………………………………………. 8

Chemistry of Aluminosilicate Gel…………………………………………………………………………………………… 9

Fly Ash…………………………………………………………………………………………………………………………… 10

Stress-Strain Relationship…………………………………………………………………………………………………… 13

Suitability as Flexural Members…………………………………………………………………………………………… 15

Beams…………………………………………………………………………………………………………………………. 15

Columns………………………………………………………………………………………………………………………. 16

Water content and Workability…………………………………………………………………………………………… 18

Mixing and Placement Requirements……………………………………………………………………………………. 19

Tensile Strength………………………………………………………………………………………………………………. 20

Fire Resistance………………………………………………………………………………………………………………… 21

Drying Shrinkage……………………………………………………………………………………………………………… 22

Creep…………………………………………………………………………………………………………………………….. 24

Conclusion……………………………………………………………………………………………………………………… 25

References………………………………………………………………………………………………………………………….. 26

List of Figures

Figure 1: Greenhouse Gas Emissions of Constituent Materials [1]……………………………………………………… 8

Figure 2: Structure of Sodium-polysialate as proposed by Barbosa, MacKenzie and Thaumaturgo [16]………. 9

Figure 3: Particle size distribution of 5 Australian fly ashes [2]………………………………………………………… 10

Figure 4: SEM images of 5 Australian fly ashes [2]………………………………………………………………………… 12

Figure 5a, 5b and 5c : Stress strain comparison of equation 4 and sample specimens of different composition[24]………………………………………………………………………………………………………………………………………… 14

Figure 6: Failure of Geopolymer composite beams in single curvature [27]……………………………………….. 15

Figure 7: Failure of geopolymer columns [27]…………………………………………………………………………….. 17

Figure 8: Concrete slump versus excess water [24]………………………………………………………………………. 18

Figure 9: 7-day f’c versus Water/Geopolymer ratio of specimens cured at different temperatures [24]……. 18

Figure 10: Compressive strength versus mixing time [24]………………………………………………………………. 19

Figure 11: Compressive Strength vs temperature exposure for a Fly Ash Based Geopolymer [32]…………… 21

Figure 12: Thermal Shrinkage versus exposed temperature of a Fly Ash Based Geopolymer [32]……………. 21

Figure 13: Drying Shrinkage Strain [17]……………………………………………………………………………………… 22

Figure 14: Drying Shrinkage of Heat Cured Geopolymer Concrete compared to predictions as per AS3600-2009 [17], [26]……………………………………………………………………………………………………………………………. 23

Figure 15: Drying Shrinkage of Ambient Cured Geopolymer Concrete compared to predictions as per AS3600-2009 [17], [26]…………………………………………………………………………………………………………………….. 23

Figure 16: Creep of a Heat Cured Geopolymer Concrete [17]…………………………………………………………. 24

List of Equations

Equation 1: Reactivity Index (RI) as proposed by Zhang et al [2]………………………………………………………. 11

Equation 2: SSA [2]……………………………………………………………………………………………………………….. 11

Equation 3: Sauter Mean Diameter [23]…………………………………………………………………………………….. 11

Equation 4: Stress Strain Curve of OPC concrete as proposed by Collins et. al (1993) [3] [24]…………………. 13

Equation 5: Modulus of elasticity (in Megapascals) as per AS3600-2009 [26]……………………………………… 13

Equation 6: Muo as per AS3600-2009 [26]…………………………………………………………………………………… 15

Equation 7: Characteristic Flexural Tensile Strength of Concrete [26]……………………………………………….. 20

Equation 8: Characteristic Uniaxial Tensile Strength of Concrete [26]……………………………………………….. 20

Equation 9: Uniaxial Tensile Strength of Concrete from Indirect Tensile Testing as per AS1012.10-2000 [26]20Equation 10: Characteristic Tensile Strength of Concrete as proposed by Neville (2000) [24]…………………. 20

List of Tables

Table 1: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]………………. 16

Table 2: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]………………. 17

Table 3: Tensile Strengths of Fly Ah Based Geopolymer Concrete [24], [26]……………………………………….. 20

Literature Review

Concrete is the most widely used construction material in the world, with the production of the Ordinary Portland Cement (OPC) binder accounting for an estimated 5% of global carbon dioxide pollution [4]. In 1978 the French researcher, Joseph Davidovits, proposed an alternative concrete binders, ‘geopolymers’ [5]. Such geopolymers involve the formation of an inorganic SOL-gel polymer from the alkalisation of materials rich in silicon oxides and aluminium oxides, that solidifies to form a cement comparable with OPC [6][6], [7]. Fly ash has been proposed as a source material for geopolymerisation, with the mechanical behaviours assessed and a mix design methodologies proposed by numerous researchers [6], [8], [9], [10].

Recent research has assessed the mechanical performance of various fly ashes, proposing chemical composition is a poor indicator of performance [2]. This suggests parameters in previous studies, such as the silica to alkaline ratio or the fly ash to alkaline ratio, are ill founded. It is logical therefore to draw on this new knowledge to propose an alternate mix design methodology considering an empirical ‘reactivity index’ as proposed by Zhang et al (2016). A standard methodology for fly ash based geopolymer formulation which considers the heterogeneous nature of fly ash would be beneficial in enabling full adoption by industry [2], [3].

Environmental Impact of Ordinary Portland Cement

Globally, the production of OPC accounts for between 5 and 7% of CO2 emissions [1]. Australia’s cement industry, accounts for approximately 1.3% of total national emissions [1]. McLellan et al. (2011) suggests adopting geopolymer concrete as a substitute for OPC concretes has the potential to halve the atmospheric pollution of the cement industry in some circumstances. It is important however to look at localised areas on a case-by-case basis for geopolymer concrete adoption, since silica and alumina sources can be significant distances away, resulting in vast transportation distances which may be more detrimental environmentally when compared to OPC concretes [1].

Given geopolymer concretes can utilize fly ash as a source of alumina and silicate, the adoption of geopolymer concrete has added environmental benefits. Fly ash is the residue extracted from coal fired power-plant exhaust gasses [11]. It is mostly landfilled with some being utilized in pavement stabilization or in OPC concretes as a pozzolan [4], [12]. One tonne of OPC emits nearly one tonne of CO2, the reduction in CO2 emissions noted with fly ash based geopolymer concrete is due to the minimal processing of the material required, with the main pollutants been attributed to the transportation of the fly ash and the production of the alkaline activators [1], [4] .

Portland cement is a synthetic product comprised mostly of lime [13]. The process of lime manufacture includes the quarrying of appropriate material, generally limestone, and superheating it in a process known as calcination with the resulting product being ground to a fine powder [7]. An additional benefit of geopolymer adoption is the reduced required mining of feedstock materials for OPC formulation.

Geopolymer concrete had shown promise as a means of industrial waste product removal. Waste materials such as Ground Granulated Blast Furnace Slag, Fly Ash and Bottom Ash are all possible sources of the alumino-silicate reagent [3]. The average equivalent CO2 emissions for common constituent materials in geopolymer concrete is shown in Figure 1, with Sodium Hydroxide being the most carbon intensive [1]. A proposition has been suggested by Van Riessen et al (2013) that alkaline waste materials obtained from industrial alumina synthesis can be employed in geopolymer manufacture [14].

Figure 1: Greenhouse Gas Emissions of Constituent Materials [1]

Chemistry of Aluminosilicate Gel

‘Geopolymer’ is a general term proposed by Davidovits, used to describe an inorganic polymer consisting of an alumina-silicate SOL-gel matrix [3], [7]. Under acidic or basic conditions, alkoxides such as silicon oxides and aluminium oxides are interchanged with hydroxyl groups [7]. Such groups are mobilised in the solution and interlink with oxygen, while the cation from the hydroxyl activator, which is also mobile, acts as a charge balancer [7], [15]. At a molecular level three main basic structures can be identified, these are sialate units [– Si–O–Al–O–], sialate siloxo units [–Si–O–Al–I–Si–O–], and sialate disiloxo units [–Si–O–Al–O–Si–I–Si–O–] [15], [16]. These monomer units interconnect throughout the solution to form a gel comprised of liquid and solid phases, this is shown in Figure 2 with a solid polysialate network entrapping the liquid [7], [16]. When larger portions of the network are examined however, less order can be appreciated due to a far greater complexity of the reaction.

Although complex and mostly indeterminable, this is not dissimilar to OPC and other hydraulic binders [7]. Hardened OPC is comprised of mostly interlinked calcium-silicate hydrate as well as crystalline calcium hydroxide [7]. This too is of equivalent complexity and can only be examined at the basic constituent level, thus leaving technical investigation as the most reliable means of assessment into mechanical properties.

The rate of reaction for geopolymers is analogous to OPC concrete with a characteristic compressive strength being reached at 28 days, this is a statistical determination since the strength of geopolymer concrete can been observed to increase with time [6], [17]. Temperature also is an important consideration in the chemistry of the SOL-gel matrix , with heat cured specimens of identical proportioning reaching greater characteristic strengths [17].

Figure 2: Structure of Sodium-polysialate as proposed by Barbosa, MacKenzie and Thaumaturgo [16].

Fly Ash

Fly ash is defined by AS3582.1-2016 as the “solid material extracted from the flue gasses of a boiler fired with pulverized coal” [18]. This standard also specifies grades of fly ash as one of three: Special Grade, Grade

1 and Grade 2. This can be seen as supplementary grading to the often quoted ASTM C618-2005 classification, which classes fly ash as either class F or class C [11]. By comparing these two referencing tools, it can be seen that AS3582.1-2016 is a further categorisation of ASTM class F fly ashes, allowing for greater distinction between fly ashes. AS3582.1-2016 largely disregards all fly ashes that would otherwise be categorised as ASTM class C, this is of little concern since these ashes have been found to be unsuited to geopolymer concrete due to noted durability issues as well as unpractical setting times owing to their relatively high calcium oxide content [3], [9], [17].

AS3582.1-2016 refers to a number of additional standards which specify methods for testing of various properties, one such property is ‘strength index’ which is to be undertaken as per AS3583.6-1995 (reconfirmed 2016). This stipulates a direct comparison between the compressive strength of a binder with and without the supplementary fly ash. Such a strength index, although a similar concept, should not be confused with the reactivity index as proposed by Zhang et. al. (2016) since the performance of fly ash may be vastly different under different binding mechanisms, as an alkalised inorganic polymer or a pozzolan [12].

Fly ash is of small particle size, with a particle size distribution of 5 Australian fly ashes displayed in Figure 3. AS3582.1-2016 stipulates Special Grade, Grade 1 and Grade 2 fly ashes to have a minimum of 85, 75 and 55 percent by mass passing a 45μm sieve, respectively. Based solely on the particle size and neglecting the other properties as specified in AS3582.1-2016, fly ash A in Figure 3 could be classed as Special Grade, with fly ashes B and C being Grade 1 whereas fly ashes D and E could only make Grade 2 limits.

Figure 3: Particle size distribution of 5 Australian fly ashes [2]

It has been shown that fly ash generally has a spherical shape, with a Scanning Electron Microscope (SEM) image presented in Figure 4 [2], [12], [19], [20]. Considering this as well as additional parameters discussed below, Zhang et. at (2016) propose a reactivity index for fly ashes, as the inconsistencies in the fly ash properties leads to variation in performance [2]. This novel approach proposes a formula for reactivity index, see Equation 1.

Network Formers (NF) are identified as available Si, Al, Fe and Ti and Network Modifiers (NM) are Na, Al, K, Ca, Mg and Fe [2], [21]. These ions can have complex functions in geopolymerisation, for example Al and Fe can behave as both a NF and as a NM; varying weighting coefficients may apply for each elemental parameter [2], [22]. There is little available information however that permits the enumeration of network modifiers and network formers interacting; due to the complexity of their interaction with some behaving as either, under different conditions [2]. A method of Empirical Potential Structure Refinement (EPSR) modelling should be undertaken on fly ashes to further understand the influence of such ions, Zhang et. al (2016) was able to confirm the applicability of their model by fitting results of a EPSR study of silicate network glasses [2]. This is an area needing significant research that could allow the performance of fly ashes to be assessed without the need for in depth mechanical testing.

Where;

IPV is the inter-particle volume, which can be found by using the Archimedes method of comparing the density of the fly ash with the particle density, thus to determine the volume of voids which defines the IPV [2]

SSA is the geometric specific surface area; this is given by Equation 2. This however relies on the Sauter Mean Diameter (SMD), given in Equation 3. The SMD is the diameter of a theoretical sphere that has the same surface area to volume ratio as the actual particle [23]

Figure 4: SEM images of 5 Australian fly ashes [2]

Stress-Strain Relationship

The stress-strain relationship of geopolymer concrete was investigated by Hardjito and Rangan (2005), confirming that it is comparable to that of OPC concretes [3], [6], [24]. This study noted that the gradual loading of 100x200mm compression cylinders resulted in a reduced compressive strength when compared to more brisk loading, this is a similar phenomenon as what is observed with OPC concretes [24]. Equation 4 was proposed by Collins et. al (1993) for OPC concretes, and has been found to simulate geopolymer concretes well also, graphs comparing the applied formula to test specimens are presented in

Figure 5 [24], [25]. Due to the similar stress-strain relationship of geopolymer concrete when compared to OPC concrete, the current provisions in AS3600-2009 for the modulus of elasticity given in Equation 5canbe considered applicable [24],[26].

Figure 5a, 5b and 5c : Stress strain comparison of equation 4 and sample specimens of different composition [24]

Suitability as Flexural Members

Beams

Investigations of the applicability of geopolymer concretes to current design standards has been undertaken to the degree which the Concrete Institute of Australia has published its recommended practice guidelines for in geopolymer concrete, informing the members of the institute that AS3600-2009 can be used to design geopolymer concrete members [3]. Testing of beams in single curvature has been investigated and compared AS3600-2009 by Sumajouw & Rangan (2006), Table 1 tabulates the measured properties of the test specimens of this study and their anticipated performance determined as per AS3600-2009 [26], [27]. Such testing yielded identical failure modes to under-reinforced concrete beams with tensile crack precipitation occurring at the bottom of the beams before compression failure of the concrete at the top of the beam, this can be seen in Figure 6 [27]. The bending moment induced where compression failure of the concrete occurs is indicative of the ultimate moment capacity of the beam, this is referred to as Muo in AS3600-2009 [26], [28]. Compressive failure of concrete is considered brittle as no warning is given, however since the beams tested were under-reinforced the tensile reinforcement has already yielded before compressive failure and the beam had shown sufficient sign of strain through deflection and large tensile cracks [27], [28]. It is worth noting however the specimens tested in the study were head cured and confirmation that some of the conclusions drawn in this study apply for ambient cured geopolymers is yet to be provided.

Table 1: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]

Beam Tensile Reinforce

-ment

Ratio (%)

Nominal Ast (mm) F’c

(MPa)

α₂ fsy (MPa) Mid span deflection

(mm)

Muo from testing

(kNm)

Muo as per Equatio

n 6

Muo Ratio

Test/calc

GBI-1 0.55 330 37 0.85 550 56.63 56.30 51.83 1.09
GBI-2 1.00 600 42 0.85 560 46.01 87.65 92.89 0.94
GBI-3 1.55 930 42 0.85 560 27.87 116.85 137.25 0.85
GBI-4 2.25 1350 37 0.85 557 29.22 160.50 180.64 0.89
GBII-1 0.55 330 46 0.85 550 54.27 58.35 52.34 1.11
GBII-2 1.00 600 53 0.84 560 47.2 90.55 94.47 0.96
GBII-3 1.55 930 53 0.84 560 30.01 119.00 141.03 0.84
GBII-4 2.25 1350 46 0.85 557 27.47 168.70 189.43 0.89
GBIII-1 0.55 330 76 0.77 550 69.75 64.90 53.05 1.22
GBIII-2 1.00 600 72 0.78 560 40.69 92.90 95.80 0.97
GBIII-3 1.55 930 72 0.78 560 34.02 126.80 144.23 0.88
GBIII-4 2.25 1350 76 0.77 557 35.85 170.59 201.49 0.85
Average 0.96
Std Dev. 0.12

Columns

As with beams, the Concrete Institute of Australia has publicised that geopolymer concrete complies to AS3600-2009 for concrete structural members, this includes columns also [3]. Columns can be subjected to flexural loading, but are subjected to axial loading also [28]. Such members were also tested extensively by Sumajouw and Rangan (2006) with induced moment and axial loading, these specimens were found to behave analogous to OPC concrete columns [27]. The failure of such members, presented in Figure 7, can be seen to fail with compression failure of the concrete and buckling of the steel reinforcement, tensile cracking can also be observed due to the induced moment in the column [27]. It can be seen in Table 2 that AS3600- 2009 can be confidently used to design slender columns using geopolymer concrete [3], [26], [27].

Figure 7: Failure of geopolymer columns [27]

Table 2: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]

Column f’c (Mpa) e (mm) p (%) N* (kN) Nᵤₒ ratio

N*/Nᵤₒ

GCI-1 42 15 1.47 940 962 0.98
GCI-2 42 35 1.47 674 719 0.94
GCI-3 42 50 1.47 555 573 0.97
GCII-1 43 15 2.95 1237 1120 1.10
GCII-2 43 35 2.95 852 832 1.02
GCII-3 43 50 2.95 666 665 1.00
GCIII-1 66 15 1.47 1455 1352 1.08
GCIII-2 66 35 1.47 1030 1010 1.02
GCIII-3 66 50 1.47 827 760 1.09
GCIV-1 59 15 2.95 1559 1372 1.14
GCIV-2 59 35 2.95 1057 1021 1.04
GCIV-3 59 50 2.95 810 800 1.01
average 1.03
std dev 0.06

Water content and Workability

Being an important physical restraint in concrete placement, workability is important to be specified for a given application [3]. It has been found that like OPC concrete, the addition of water increases workability but too reduces the quality of the concrete, the increase in slump with water is presented in Figure 8 [3], [10], [24]. Figure 9 shows the results of a study in mixing proportions of heat cured fly ash concrete displaying that an increase in excess water, that is water surplus to the absorption capacity of the aggregates, is detrimental to the mechanical strength of the geopolymer concrete [10], [24]. Certain admixtures can be used to modify the properties of plastic of geopolymer concrete, for example a naphthalene based superplasticiser has been employed in previous studies; admixtures however have been developed specifically for OPC concrete and mostly not required or are not effective for geopolymer concrete [3], [13], [24], [29]. It is appropriate to note however that water is an integral part of the system, performing the role of the medium in which allows the polymerisation process to occur, this has been discussed previously [6], [7].

Figure 9: 7-day f’c versus Water/Geopolymer ratio of specimens cured at different temperatures [24]

Mixing and Placement Requirements

When mixing geopolymer concrete it is preferable to use high shear folding mixers, although conventional mixer are acceptable [3]. The Concrete Institute of Australia has identified that an area in need of development is measuring the viscosity of geopolymer concrete as mixing times increase and as it undergoes polymerisation, this will allow for better manufacture of geopolymer concrete as well as assurance it can be placed after a delay between batching and placement [3]. It has been observed that as mixing times increase, the slump of the concrete increases, this is obviously up to a point as when the SOL-gel develops the viscosity increases until it is rigid structure [3]. It too has been noted that as mixing times increase the mechanical performance of the concrete is improved as shown in Figure 10.

Figure 10: Compressive strength versus mixing time [24]

It has been observed that geopolymer concrete is more adhesive than regular concrete [3], [30]. This has been noted as being a significant issues since additional cleaning of handling equipment may generally be required [3], [30]. Due to the different chemical nature when compared to OPC concrete, geopolymer concrete tends to breakdown conventional formwork release agents, as such different products need to be identified overcome this [30].

The recommended practice for geopolymer concrete in Australia suggests that, like for OPC concretes, air voids can be of concern and low amplitude internal vibration is the preferred compaction technique, with conventional methods of compaction for no-slump concretes applicable to geopolymers [3].

Tensile Strength

The characteristic tensile strength of geopolymer concrete has been assessed by Hardjito and Rangan (2005) as specified in AS1012.10-2000 (reconfirmed 2014) and compared it to AS3600-2009, this is presented in Table 3 [26], [31]. AS3600-2009 deems the characteristic flexural and uniaxial tensile strengths of concrete shall be determined from their characteristic 28-day compressive strength, presenting Equation 7 and Equation 8 [26]. Equation 10 perhaps is the best method of determining the tensile strength of geopolymer concrete, more economic that the current provisions in AS3600-2009 yet meeting an important factor of safety of AS3600-2009 presented in Equation 9 [26]. These equations suggest the characteristic uniaxial tensile strength and the characteristic flexural tensile strength are considered similar, with a factor of difference of 0.04 (0.40-0.36=0.04). The existing provisions in AS3600-2009 are suitable for geopolymer concretes, with the characteristic uniaxial tensile strength determined from the characteristic 28-day compressive strength being around 1.8 times the uniaxial tensile strength as determined from the indirect tensile splitting test. As such the current provisions can be considered conservative, for full realisation of the environmental and technical benefits of geopolymer concrete, adaptations for geopolymer concrete’s superior tensile strength should be made [3], [6], [24].

Fire Resistance

The development of geopolymer concrete was originally developed as a heat resistant building material after a number of fires in France in the early 1970’s [29]. Fly ash based geopolymers have been investigated for their fire resistance and found to increase in mechanical strength when temperatures exceed about 600⁰C as shown in in Figure 11, this strength increases is due to a sintering liquid phase [32]. This sintering however also responsible for an increase in the thermal shrinkage, this is presented in Figure 12 [32]. In the circumstance that thermal shrinkage reaches a threshold value, usually in the range of 1 to 2% the material may fail despite the increase in its mechanical strength, this is due to cracking and changes in the material volume [32]. When compared to OPC concrete however it is a vast improvement with OPC concretes deteriorating in strength at around 300⁰C, characterised by explosive failure as the water molecules inside the concrete vaporise [6], [13]. The failure mode for geopolymers however is not explosive but results by melting of the inorganic polymer [32]. Certain geopolymers have been investigated and are in use in ultra- high temperature applications, however these systems perform differently to geopolymer binders used in concrete due to variation in the monomers that make up the geopolymer network [6], [33].

Drying Shrinkage

Shrinkage is a phenomenon observed with OPC concretes, as the OPC hydrates into a crystalline matrix it reduces in volume, this makes sense since crystalline structures are much denser than the overall concrete so the remaining volume is made up of millions of small air voids [7]. Additional shrinkage is due to aggregates in the concrete absorbing water that would otherwise contribute to the volume of the concrete [34]. It has been observed that drying shrinkage of geopolymer concretes is less than that of OPC concretes [3], [17], [35]. Since geopolymer concrete undergoes polymerisation not hydration into a crystalline matrix it makes sense that the shrinkage of geopolymer concretes is less than OPC concrete [7]. As drying shrinkage occurs it, creates strain within the concrete structure [34]. Since most of the studies of geopolymer concrete have been on heat cured specimens it is interesting for Wallah and Rangan (2006) to report that shrinkage of ambient cured geopolymer concrete is far greater than that of heat cured geopolymer concrete as can be seen in Figure 13. This cause for concern since the Recommended Practice for Geopolymer Concrete in Australia suggests that the shrinkage joints or saw-cuts may not be required [3]. It can be seen in Figure 14 that provisions AS3600-2009 are conservative, yet are inadequate for ambient cured geopolymer concrete as presented in Figure 15. An experimental footpath was constructed at Curtin University of Technology in Perth, Australia, with no shrinkage cracks observable in 1.5x12m slabs, yet cracking at 3m centres for an OPC concrete reference footpath [3]. This is obviously contradictory to the findings of Wallah and Rangan (2006), and with lack of research on ambient cured geopolymer concrete this is an area requiring further research.

Figure 15: Drying Shrinkage of Ambient Cured Geopolymer Concrete compared to predictions as per AS3600- 2009 [17], [26]

Creep

Creep is a phenomenon that can be defined as the increase in strain under a sustained stress [34]. It can also be seen as the relaxation of stress with time for concrete subject to constant stress [34]. For the design of concrete members, AS3600-2009 employs a creep coefficient which is defined as the “mean value of the ratio of creep strain to elastic strain under conditions of constant stress” [26]. The creep strain of heat cured geopolymer concrete was investigated by Wallah and Rangan (2006) noting that creep can reduce the strength of geopolymer concrete [17]. The current provisions in AS3600-2009 however are conservative for heat cured geopolymer concrete [6], [17].

Figure 16Figure 16 presents a predicted creep strain curve calculated as per AS3600-2009 and an actual test specimen [17], [26]. Like for drying shrinkage, little research has been undertaken for geopolymer concrete cured at ambient temperatures.

Conclusion

By reviewing the properties of fly ash based geopolymers it is clear there is a substantial lack of knowledge on the effect of curing conditions on the various mechanical parameters of geopolymer concrete. Although heat cured specimens have largely been presented in in this discourse, a mix design methodology and an assessment of the applicability of Australian design codes for in-situ geopolymer concrete is the objective of this associated research project. Since recognition of geopolymer concrete by some professional institutions and governmental authorities is based on heat cured concrete, there have been assumptions made that are yet to be confirmed for in-situ concretes [3], [36]. As research progresses it is likely that these gaps-in- knowledge will be addressed since the behaviour of geopolymer concrete is similar to that of OPC concretes, but with differences in magnitude. Future research lies in investigating the in-situ performance of geopolymer concretes and subsequent commercial realisation by the adaptations of existing standards to economically realise the mechanical performance of geopolymer concretes.

References

  • C. McLellan, R. P. Williams, J. Lay, A. Van Riessen, and G. D. Corder, “Costs and carbon emissions for geopolymer pastes in comparison to ordinary portland cement,” J. Clean. Prod., vol. 19, no. 9–10, pp. 1080–1090, 2011.
  • Zhang, J. L. Provis, J. Zou, A. Reid, and H. Wang, “Toward an indexing approach to evaluate fly ashes for geopolymer manufacture,” Cem. Concr. Res., vol. 85, pp. 163–173, 2016.
  • Concrete Institute of Australia, Z16: Recommended Practice for Geopolymer Concrete. North Sydney, Australia: Concrete Insitute of Australia,
  • Muttashar, W. Lokuge, and W. Karunasena, “Geopolymer Concrete : the Green Alternative With Suitable Structural Properties,” in 23rd Australasian Conference on the Mechanics of Structures and Materials (ACMSM23), 2014, December, pp. 101–106.
  • Xu and J. S. J. Van Deventer, “the Geopolymerisation of Natural Alumino-Silicates,” Int. J. Miner. Process., vol. 59, pp. 247–266, 2000.
  • Davidovits, Geopolymer Chemistry and Applications 4e. 2015.
  • E. Carraher Jr., Intrduction to Polymer Chemistry. Boca Raton, Florida, USA: CRC Press, 2007.
  • Pavithra, M. Srinivasula Reddy, P. Dinakar, B. Hanumantha Rao, B. K. Satpathy, and A. N. Mohanty, “A mix design procedure for geopolymer concrete with fly ash,” J. Clean. Prod., vol. 133, pp. 117–125, 2016.
  • T. Junaid, O. Kayali, A. Khennane, and J. Black, “A mix design procedure for low calcium alkali

activated fly ash-based concretes,” Constr. Build. Mater., vol. 79, pp. 301–310, 2015.

  • Ferdous, A. Manalo, A. Khennane, and O. Kayali, “Geopolymer concrete-filled pultruded composite beams – Concrete mix design and application,” Cem. Concr. Compos., vol. 58, pp. 1–13, 2015.
  • ASTM, Standard Specification for Coal Fly Ash and Raw or Calcined Natural Pozzolan for Use in Concrete. West Conshohocken, PA, USA: ASTM International,
  • D. A. Thomas, “Optimizing the Use of Fly Ash in Concrete,” New Brunswick, NJ, USA, 2007.
  • S. J. Van Deventer, J. L. Provis, and P. Duxson, “Technical and commercial progress in the adoption

of geopolymer cement,” Miner. Eng., vol. 29, pp. 89–104, 2012.

  • Van Riessen, E. Jamieson, C. S. Kealley, R. D. Hart, and R. P. Williams, “Bayer-geopolymers: An exploration of synergy between the alumina and geopolymer industries,” Cem. Concr. Compos., vol. 41, pp. 29–33, 2013.
  • Davidovits, Geopolymer Chemistry and Applications 4th edition. Saint-Quentin, France: Geopolymer Institute, 2015.
  • F. F. Barbosa, K. J. D. MacKenzie, and C. Thaumaturgo, “Synthesis and characterisation of materials based on inorganic polymers of alumina and silica: Sodium polysialate polymers,” Int. J. Inorg. Mater., vol. 2, no. 4, pp. 309–317, 2000.
  • E. Wallah and B. V. Rangan, “Low-Calcium Fly Ash-Based Geopolymer Concrete: Long-Term

Properties,” Research Report, Curtin University of Technology, Perth, Australia, 2006.

  • Standards Australia, 1 Supplementary cementitious material – Fly Ash. 2016.
  • Yunsheng, S. Wei, Z. Li, and Z. Xiangming, “Geopolymer extruded composites with incorporated fly

ash and polyvinyl alcohol short fiber,” ACI Mater. J., vol. 106, no. 1, pp. 3–10, 2009.

  • Concrete Institute of Australia, Z7/04. Good practice through design, concrete supply and construction. Rhodes Australia: Concrete Insitute of Australia,
  • Wang, Z. Zhang, J. L. Provis, and J. Zou, “Specifying fly ash for use in geopolymer : A conception of reactivity index.”
  • Duxson and J. L. Provis, “Designing Precursors for Geopolymer Cements.”
  • S. Patience, Experimental Methods and Instrumentation for Chemical Engineers. Amsterdam, The Netherlands: Elsevier, 2013.
  • Hardjito and B. V. Rangan, “Development and properties of low-calcium fly ash-based geopolymer

concrete,” Research Report, Curtin University of Technology, Perth, Australia, 2005.

  • P. Collins, D. Mitchell, and J. G. MacGregor, “Structural Design Considerations for High Stregth Concrete,” ACI Concr. Int., vol. 15, no. 5, pp. 27–34, 1993.
  • Standards Australia, AS3600-2009 Concrete structures.
  • D. J. Sumajouw and B. V. Rangan, “Low-calcium fly ash-based geopolymer concrete: reinforced

beams and columns,” Curtin Univ. Technol. Perth, Aust., pp. 1–120, 2006.

  • S. Gupta, Principals of Sturctural Design. Boca Raton, Florida, USA: CRC Press, 2011.
  • Davidovits, “Properties of Geopolymer Cements,” in First International Conference of Alkaline Cements and Concretes, 1994, pp. 131–149.
  • Mukhin, R. Khatri, I. Dumitru, and F. Ash, Some Limitations of Geopolymer Concrete. Adelaide, Australia, 2007.
  • Standards Australia, AS 10-2000 ( R2014 ) Methods of testing concrete – Determination of

indirect tensile strength of concrete cylinders (’Brasil’ or splitting test ). 2014.

  • L. Provis and J. S. J. Van Deventer, Geopolymers: Structure, processing, propertes and industrial applications. Boca Ranton, Florida, USA: CRC Press, 2009.
  • Davidovits and M. Davidovics, “Geopolymer: Ultra-High temperature Tooling Material for the Manufacture of Advanced composites,” SAMPE, vol. 36, no. 2, pp. 1939–1949, 1991.
  • M. Neville, Properties of Concrete, 4th ed. Harlow, England: Pearson Eduaction Limited, 2006.
  • Duxson, A. Fernández-Jiménez, J. L. Provis, G. C. Lukey, A. Palomo, and J. S. J. Van Deventer,

“Geopolymer technology: The current state of the art,” J. Mater. Sci., vol. 42, pp. 2917–2933, 2007.

  • VicRoads, Section 703 – General Concrete Paving. VicRoads,

The performance of fly ash as an alkali-activated binder in geopolymer concrete and development of guidelines for mix design of cast-in-situ geopolymer concrete

Authored by Bradley Connolly – 17697347

Under the supervision of Dr D. Ionescu and Dr V. Patel

This document has been developed and submitted in partial fulfilment of EMS4EMP in the Bachelor of Civil Engineering (Honours) Degree at La Trobe University,

Bendigo

June 2017

Abstract

Geopolymer concrete has a number of environmental advantages when compared to Ordinary Portland Cement (OPC) concrete, yet its adoption is delayed by gaps-in-knowledge, particularly for concrete cured in ambient conditions [1]. Fly ash, a waste material, has shown promise to replace OPC as a concrete binder in some circumstances. This yields benefits including the reducing the carbon footprint of infrastructure development. Recent research has found that chemical composition of fly ash reagents is a poor indictor of the performance of geopolymer concrete, instead Zhang et al (2016) have proposed a ‘reactivity index’ to assess the suitability of fly ashes. In this discourse the mechanical properties of fly ash based geopolymer concrete has been examined from available literature. Fly ash based geopolymer concrete is seen to behave in a similar manner to OPC concrete, with differences in magnitude in some parameters and effectively identical in others. The largest gap-in-knowledge is the performance of geopolymer concrete in in-situ applications.

Table of Contents

Abstract……………………………………………………………………………………………………………………………….. 2

Table of Contents…………………………………………………………………………………………………………………… 3

List of Figures………………………………………………………………………………………………………………………… 4

List of Equations…………………………………………………………………………………………………………………….. 5

List of Tables…………………………………………………………………………………………………………………………. 6

Literature Review…………………………………………………………………………………………………………………… 7

Environmental Impact of Ordinary Portland Cement…………………………………………………………………. 8

Chemistry of Aluminosilicate Gel…………………………………………………………………………………………… 9

Fly Ash…………………………………………………………………………………………………………………………… 10

Stress-Strain Relationship…………………………………………………………………………………………………… 13

Suitability as Flexural Members…………………………………………………………………………………………… 15

Beams…………………………………………………………………………………………………………………………. 15

Columns………………………………………………………………………………………………………………………. 16

Water content and Workability…………………………………………………………………………………………… 18

Mixing and Placement Requirements……………………………………………………………………………………. 19

Tensile Strength………………………………………………………………………………………………………………. 20

Fire Resistance………………………………………………………………………………………………………………… 21

Drying Shrinkage……………………………………………………………………………………………………………… 22

Creep…………………………………………………………………………………………………………………………….. 24

Conclusion……………………………………………………………………………………………………………………… 25

References………………………………………………………………………………………………………………………….. 26

List of Figures

Figure 1: Greenhouse Gas Emissions of Constituent Materials [1]……………………………………………………… 8

Figure 2: Structure of Sodium-polysialate as proposed by Barbosa, MacKenzie and Thaumaturgo [16]………. 9

Figure 3: Particle size distribution of 5 Australian fly ashes [2]………………………………………………………… 10

Figure 4: SEM images of 5 Australian fly ashes [2]………………………………………………………………………… 12

Figure 5a, 5b and 5c : Stress strain comparison of equation 4 and sample specimens of different composition[24]………………………………………………………………………………………………………………………………………… 14

Figure 6: Failure of Geopolymer composite beams in single curvature [27]……………………………………….. 15

Figure 7: Failure of geopolymer columns [27]…………………………………………………………………………….. 17

Figure 8: Concrete slump versus excess water [24]………………………………………………………………………. 18

Figure 9: 7-day f’c versus Water/Geopolymer ratio of specimens cured at different temperatures [24]……. 18

Figure 10: Compressive strength versus mixing time [24]………………………………………………………………. 19

Figure 11: Compressive Strength vs temperature exposure for a Fly Ash Based Geopolymer [32]…………… 21

Figure 12: Thermal Shrinkage versus exposed temperature of a Fly Ash Based Geopolymer [32]……………. 21

Figure 13: Drying Shrinkage Strain [17]……………………………………………………………………………………… 22

Figure 14: Drying Shrinkage of Heat Cured Geopolymer Concrete compared to predictions as per AS3600-2009 [17], [26]……………………………………………………………………………………………………………………………. 23

Figure 15: Drying Shrinkage of Ambient Cured Geopolymer Concrete compared to predictions as per AS3600-2009 [17], [26]…………………………………………………………………………………………………………………….. 23

Figure 16: Creep of a Heat Cured Geopolymer Concrete [17]…………………………………………………………. 24

List of Equations

Equation 1: Reactivity Index (RI) as proposed by Zhang et al [2]………………………………………………………. 11

Equation 2: SSA [2]……………………………………………………………………………………………………………….. 11

Equation 3: Sauter Mean Diameter [23]…………………………………………………………………………………….. 11

Equation 4: Stress Strain Curve of OPC concrete as proposed by Collins et. al (1993) [3] [24]…………………. 13

Equation 5: Modulus of elasticity (in Megapascals) as per AS3600-2009 [26]……………………………………… 13

Equation 6: Muo as per AS3600-2009 [26]…………………………………………………………………………………… 15

Equation 7: Characteristic Flexural Tensile Strength of Concrete [26]……………………………………………….. 20

Equation 8: Characteristic Uniaxial Tensile Strength of Concrete [26]……………………………………………….. 20

Equation 9: Uniaxial Tensile Strength of Concrete from Indirect Tensile Testing as per AS1012.10-2000 [26]20Equation 10: Characteristic Tensile Strength of Concrete as proposed by Neville (2000) [24]…………………. 20

List of Tables

Table 1: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]………………. 16

Table 2: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]………………. 17

Table 3: Tensile Strengths of Fly Ah Based Geopolymer Concrete [24], [26]……………………………………….. 20

Literature Review

Concrete is the most widely used construction material in the world, with the production of the Ordinary Portland Cement (OPC) binder accounting for an estimated 5% of global carbon dioxide pollution [4]. In 1978 the French researcher, Joseph Davidovits, proposed an alternative concrete binders, ‘geopolymers’ [5]. Such geopolymers involve the formation of an inorganic SOL-gel polymer from the alkalisation of materials rich in silicon oxides and aluminium oxides, that solidifies to form a cement comparable with OPC [6][6], [7]. Fly ash has been proposed as a source material for geopolymerisation, with the mechanical behaviours assessed and a mix design methodologies proposed by numerous researchers [6], [8], [9], [10].

Recent research has assessed the mechanical performance of various fly ashes, proposing chemical composition is a poor indicator of performance [2]. This suggests parameters in previous studies, such as the silica to alkaline ratio or the fly ash to alkaline ratio, are ill founded. It is logical therefore to draw on this new knowledge to propose an alternate mix design methodology considering an empirical ‘reactivity index’ as proposed by Zhang et al (2016). A standard methodology for fly ash based geopolymer formulation which considers the heterogeneous nature of fly ash would be beneficial in enabling full adoption by industry [2], [3].

Environmental Impact of Ordinary Portland Cement

Globally, the production of OPC accounts for between 5 and 7% of CO2 emissions [1]. Australia’s cement industry, accounts for approximately 1.3% of total national emissions [1]. McLellan et al. (2011) suggests adopting geopolymer concrete as a substitute for OPC concretes has the potential to halve the atmospheric pollution of the cement industry in some circumstances. It is important however to look at localised areas on a case-by-case basis for geopolymer concrete adoption, since silica and alumina sources can be significant distances away, resulting in vast transportation distances which may be more detrimental environmentally when compared to OPC concretes [1].

Given geopolymer concretes can utilize fly ash as a source of alumina and silicate, the adoption of geopolymer concrete has added environmental benefits. Fly ash is the residue extracted from coal fired power-plant exhaust gasses [11]. It is mostly landfilled with some being utilized in pavement stabilization or in OPC concretes as a pozzolan [4], [12]. One tonne of OPC emits nearly one tonne of CO2, the reduction in CO2 emissions noted with fly ash based geopolymer concrete is due to the minimal processing of the material required, with the main pollutants been attributed to the transportation of the fly ash and the production of the alkaline activators [1], [4] .

Portland cement is a synthetic product comprised mostly of lime [13]. The process of lime manufacture includes the quarrying of appropriate material, generally limestone, and superheating it in a process known as calcination with the resulting product being ground to a fine powder [7]. An additional benefit of geopolymer adoption is the reduced required mining of feedstock materials for OPC formulation.

Geopolymer concrete had shown promise as a means of industrial waste product removal. Waste materials such as Ground Granulated Blast Furnace Slag, Fly Ash and Bottom Ash are all possible sources of the alumino-silicate reagent [3]. The average equivalent CO2 emissions for common constituent materials in geopolymer concrete is shown in Figure 1, with Sodium Hydroxide being the most carbon intensive [1]. A proposition has been suggested by Van Riessen et al (2013) that alkaline waste materials obtained from industrial alumina synthesis can be employed in geopolymer manufacture [14].

Figure 1: Greenhouse Gas Emissions of Constituent Materials [1]

Chemistry of Aluminosilicate Gel

‘Geopolymer’ is a general term proposed by Davidovits, used to describe an inorganic polymer consisting of an alumina-silicate SOL-gel matrix [3], [7]. Under acidic or basic conditions, alkoxides such as silicon oxides and aluminium oxides are interchanged with hydroxyl groups [7]. Such groups are mobilised in the solution and interlink with oxygen, while the cation from the hydroxyl activator, which is also mobile, acts as a charge balancer [7], [15]. At a molecular level three main basic structures can be identified, these are sialate units [– Si–O–Al–O–], sialate siloxo units [–Si–O–Al–I–Si–O–], and sialate disiloxo units [–Si–O–Al–O–Si–I–Si–O–] [15], [16]. These monomer units interconnect throughout the solution to form a gel comprised of liquid and solid phases, this is shown in Figure 2 with a solid polysialate network entrapping the liquid [7], [16]. When larger portions of the network are examined however, less order can be appreciated due to a far greater complexity of the reaction.

Although complex and mostly indeterminable, this is not dissimilar to OPC and other hydraulic binders [7]. Hardened OPC is comprised of mostly interlinked calcium-silicate hydrate as well as crystalline calcium hydroxide [7]. This too is of equivalent complexity and can only be examined at the basic constituent level, thus leaving technical investigation as the most reliable means of assessment into mechanical properties.

The rate of reaction for geopolymers is analogous to OPC concrete with a characteristic compressive strength being reached at 28 days, this is a statistical determination since the strength of geopolymer concrete can been observed to increase with time [6], [17]. Temperature also is an important consideration in the chemistry of the SOL-gel matrix , with heat cured specimens of identical proportioning reaching greater characteristic strengths [17].

Figure 2: Structure of Sodium-polysialate as proposed by Barbosa, MacKenzie and Thaumaturgo [16].

Fly Ash

Fly ash is defined by AS3582.1-2016 as the “solid material extracted from the flue gasses of a boiler fired with pulverized coal” [18]. This standard also specifies grades of fly ash as one of three: Special Grade, Grade

1 and Grade 2. This can be seen as supplementary grading to the often quoted ASTM C618-2005 classification, which classes fly ash as either class F or class C [11]. By comparing these two referencing tools, it can be seen that AS3582.1-2016 is a further categorisation of ASTM class F fly ashes, allowing for greater distinction between fly ashes. AS3582.1-2016 largely disregards all fly ashes that would otherwise be categorised as ASTM class C, this is of little concern since these ashes have been found to be unsuited to geopolymer concrete due to noted durability issues as well as unpractical setting times owing to their relatively high calcium oxide content [3], [9], [17].

AS3582.1-2016 refers to a number of additional standards which specify methods for testing of various properties, one such property is ‘strength index’ which is to be undertaken as per AS3583.6-1995 (reconfirmed 2016). This stipulates a direct comparison between the compressive strength of a binder with and without the supplementary fly ash. Such a strength index, although a similar concept, should not be confused with the reactivity index as proposed by Zhang et. al. (2016) since the performance of fly ash may be vastly different under different binding mechanisms, as an alkalised inorganic polymer or a pozzolan [12].

Fly ash is of small particle size, with a particle size distribution of 5 Australian fly ashes displayed in Figure 3. AS3582.1-2016 stipulates Special Grade, Grade 1 and Grade 2 fly ashes to have a minimum of 85, 75 and 55 percent by mass passing a 45μm sieve, respectively. Based solely on the particle size and neglecting the other properties as specified in AS3582.1-2016, fly ash A in Figure 3 could be classed as Special Grade, with fly ashes B and C being Grade 1 whereas fly ashes D and E could only make Grade 2 limits.

Figure 3: Particle size distribution of 5 Australian fly ashes [2]

It has been shown that fly ash generally has a spherical shape, with a Scanning Electron Microscope (SEM) image presented in Figure 4 [2], [12], [19], [20]. Considering this as well as additional parameters discussed below, Zhang et. at (2016) propose a reactivity index for fly ashes, as the inconsistencies in the fly ash properties leads to variation in performance [2]. This novel approach proposes a formula for reactivity index, see Equation 1.

Network Formers (NF) are identified as available Si, Al, Fe and Ti and Network Modifiers (NM) are Na, Al, K, Ca, Mg and Fe [2], [21]. These ions can have complex functions in geopolymerisation, for example Al and Fe can behave as both a NF and as a NM; varying weighting coefficients may apply for each elemental parameter [2], [22]. There is little available information however that permits the enumeration of network modifiers and network formers interacting; due to the complexity of their interaction with some behaving as either, under different conditions [2]. A method of Empirical Potential Structure Refinement (EPSR) modelling should be undertaken on fly ashes to further understand the influence of such ions, Zhang et. al (2016) was able to confirm the applicability of their model by fitting results of a EPSR study of silicate network glasses [2]. This is an area needing significant research that could allow the performance of fly ashes to be assessed without the need for in depth mechanical testing.

Equation 1: Reactivity Index (RI) as proposed by Zhang et al [2]

= × ℎ ( )

( )

Where;

IPV is the inter-particle volume, which can be found by using the Archimedes method of comparing the density of the fly ash with the particle density, thus to determine the volume of voids which defines the IPV [2]

SSA is the geometric specific surface area; this is given by Equation 2. This however relies on the Sauter Mean Diameter (SMD), given in Equation 3. The SMD is the diameter of a theoretical sphere that has the same surface area to volume ratio as the actual particle [23]

Equation 2: SSA [2]

0.60⁄

=

Equation 3: Sauter Mean Diameter [23]

= ∑

,

Figure 4: SEM images of 5 Australian fly ashes [2]

Stress-Strain Relationship

The stress-strain relationship of geopolymer concrete was investigated by Hardjito and Rangan (2005), confirming that it is comparable to that of OPC concretes [3], [6], [24]. This study noted that the gradual loading of 100x200mm compression cylinders resulted in a reduced compressive strength when compared to more brisk loading, this is a similar phenomenon as what is observed with OPC concretes [24]. Equation 4 was proposed by Collins et. al (1993) for OPC concretes, and has been found to simulate geopolymer concretes well also, graphs comparing the applied formula to test specimens are presented in

Figure 5 [24], [25]. Due to the similar stress-strain relationship of geopolymer concrete when compared to OPC concrete, the current provisions in AS3600-2009 for the modulus of elasticity given in Equation 5canbe considered applicable [24],[26].

Equation 4: Stress Strain Curve of OPC concrete as proposed by Collins et. al (1993) [3] [24]

=

 

∙ − 1 + ( ⁄

)

Where;

=

=

= 0.8 +

17

= {

0.67 +

62

, ⁄ > 1

 

 

1 , ⁄ ≤ 1

Equation 5: Modulus of elasticity (in Megapascals) as per AS3600-2009 [26]

1.5 ∙ 0.043 ∙ √ , ≤ 40

 

= { 1.5 ∙ 0.024 ∙ √ + 0.12 , ≤ 40

Where is 90% of the average test cylinder compressive strength

Figure 5a, 5b and 5c : Stress strain comparison of equation 4 and sample specimens of different composition [24]

Suitability as Flexural Members

Beams

Investigations of the applicability of geopolymer concretes to current design standards has been undertaken to the degree which the Concrete Institute of Australia has published its recommended practice guidelines for in geopolymer concrete, informing the members of the institute that AS3600-2009 can be used to design geopolymer concrete members [3]. Testing of beams in single curvature has been investigated and compared AS3600-2009 by Sumajouw & Rangan (2006), Table 1 tabulates the measured properties of the test specimens of this study and their anticipated performance determined as per AS3600-2009 [26], [27]. Such testing yielded identical failure modes to under-reinforced concrete beams with tensile crack precipitation occurring at the bottom of the beams before compression failure of the concrete at the top of the beam, this can be seen in Figure 6 [27]. The bending moment induced where compression failure of the concrete occurs is indicative of the ultimate moment capacity of the beam, this is referred to as Muo in AS3600-2009 [26], [28]. Compressive failure of concrete is considered brittle as no warning is given, however since the beams tested were under-reinforced the tensile reinforcement has already yielded before compressive failure and the beam had shown sufficient sign of strain through deflection and large tensile cracks [27], [28]. It is worth noting however the specimens tested in the study were head cured and confirmation that some of the conclusions drawn in this study apply for ambient cured geopolymers is yet to be provided.

Equation 6: Muo as per AS3600-2009 [26]

0.5 ∙ ∙

2

 

= ∙ ∙ (1 −

)

∙ ∙ ∙

Figure 6: Failure of Geopolymer composite beams in single curvature [27]

Table 1: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]

Beam Tensile Reinforce

-ment

Ratio (%)

Nominal Ast (mm) F’c

(MPa)

α₂ fsy (MPa) Mid span deflection

(mm)

Muo from testing

(kNm)

Muo as per Equatio

n 6

Muo Ratio

Test/calc

GBI-1 0.55 330 37 0.85 550 56.63 56.30 51.83 1.09
GBI-2 1.00 600 42 0.85 560 46.01 87.65 92.89 0.94
GBI-3 1.55 930 42 0.85 560 27.87 116.85 137.25 0.85
GBI-4 2.25 1350 37 0.85 557 29.22 160.50 180.64 0.89
GBII-1 0.55 330 46 0.85 550 54.27 58.35 52.34 1.11
GBII-2 1.00 600 53 0.84 560 47.2 90.55 94.47 0.96
GBII-3 1.55 930 53 0.84 560 30.01 119.00 141.03 0.84
GBII-4 2.25 1350 46 0.85 557 27.47 168.70 189.43 0.89
GBIII-1 0.55 330 76 0.77 550 69.75 64.90 53.05 1.22
GBIII-2 1.00 600 72 0.78 560 40.69 92.90 95.80 0.97
GBIII-3 1.55 930 72 0.78 560 34.02 126.80 144.23 0.88
GBIII-4 2.25 1350 76 0.77 557 35.85 170.59 201.49 0.85
Average 0.96
Std Dev. 0.12

Columns

As with beams, the Concrete Institute of Australia has publicised that geopolymer concrete complies to AS3600-2009 for concrete structural members, this includes columns also [3]. Columns can be subjected to flexural loading, but are subjected to axial loading also [28]. Such members were also tested extensively by Sumajouw and Rangan (2006) with induced moment and axial loading, these specimens were found to behave analogous to OPC concrete columns [27]. The failure of such members, presented in Figure 7, can be seen to fail with compression failure of the concrete and buckling of the steel reinforcement, tensile cracking can also be observed due to the induced moment in the column [27]. It can be seen in Table 2 that AS3600- 2009 can be confidently used to design slender columns using geopolymer concrete [3], [26], [27].

Figure 7: Failure of geopolymer columns [27]

Table 2: Comparison of geopolymer concrete beam performance and AS3600-2009 [26], [27]

Column f’c (Mpa) e (mm) p (%) N* (kN) Nᵤₒ ratio

N*/Nᵤₒ

GCI-1 42 15 1.47 940 962 0.98
GCI-2 42 35 1.47 674 719 0.94
GCI-3 42 50 1.47 555 573 0.97
GCII-1 43 15 2.95 1237 1120 1.10
GCII-2 43 35 2.95 852 832 1.02
GCII-3 43 50 2.95 666 665 1.00
GCIII-1 66 15 1.47 1455 1352 1.08
GCIII-2 66 35 1.47 1030 1010 1.02
GCIII-3 66 50 1.47 827 760 1.09
GCIV-1 59 15 2.95 1559 1372 1.14
GCIV-2 59 35 2.95 1057 1021 1.04
GCIV-3 59 50 2.95 810 800 1.01
average 1.03
std dev 0.06

Water content and Workability

Being an important physical restraint in concrete placement, workability is important to be specified for a given application [3]. It has been found that like OPC concrete, the addition of water increases workability but too reduces the quality of the concrete, the increase in slump with water is presented in Figure 8 [3], [10], [24]. Figure 9 shows the results of a study in mixing proportions of heat cured fly ash concrete displaying that an increase in excess water, that is water surplus to the absorption capacity of the aggregates, is detrimental to the mechanical strength of the geopolymer concrete [10], [24]. Certain admixtures can be used to modify the properties of plastic of geopolymer concrete, for example a naphthalene based superplasticiser has been employed in previous studies; admixtures however have been developed specifically for OPC concrete and mostly not required or are not effective for geopolymer concrete [3], [13], [24], [29]. It is appropriate to note however that water is an integral part of the system, performing the role of the medium in which allows the polymerisation process to occur, this has been discussed previously [6], [7].

Figure 8: Concrete slump versus excess water [24]

Figure 9: 7-day f’c versus Water/Geopolymer ratio of specimens cured at different temperatures [24]

Mixing and Placement Requirements

When mixing geopolymer concrete it is preferable to use high shear folding mixers, although conventional mixer are acceptable [3]. The Concrete Institute of Australia has identified that an area in need of development is measuring the viscosity of geopolymer concrete as mixing times increase and as it undergoes polymerisation, this will allow for better manufacture of geopolymer concrete as well as assurance it can be placed after a delay between batching and placement [3]. It has been observed that as mixing times increase, the slump of the concrete increases, this is obviously up to a point as when the SOL-gel develops the viscosity increases until it is rigid structure [3]. It too has been noted that as mixing times increase the mechanical performance of the concrete is improved as shown in Figure 10.

Figure 10: Compressive strength versus mixing time [24]

It has been observed that geopolymer concrete is more adhesive than regular concrete [3], [30]. This has been noted as being a significant issues since additional cleaning of handling equipment may generally be required [3], [30]. Due to the different chemical nature when compared to OPC concrete, geopolymer concrete tends to breakdown conventional formwork release agents, as such different products need to be identified overcome this [30].

The recommended practice for geopolymer concrete in Australia suggests that, like for OPC concretes, air voids can be of concern and low amplitude internal vibration is the preferred compaction technique, with conventional methods of compaction for no-slump concretes applicable to geopolymers [3].

Tensile Strength

The characteristic tensile strength of geopolymer concrete has been assessed by Hardjito and Rangan (2005) as specified in AS1012.10-2000 (reconfirmed 2014) and compared it to AS3600-2009, this is presented in Table 3 [26], [31]. AS3600-2009 deems the characteristic flexural and uniaxial tensile strengths of concrete shall be determined from their characteristic 28-day compressive strength, presenting Equation 7 and Equation 8 [26]. Equation 10 perhaps is the best method of determining the tensile strength of geopolymer concrete, more economic that the current provisions in AS3600-2009 yet meeting an important factor of safety of AS3600-2009 presented in Equation 9 [26]. These equations suggest the characteristic uniaxial tensile strength and the characteristic flexural tensile strength are considered similar, with a factor of difference of 0.04 (0.40-0.36=0.04). The existing provisions in AS3600-2009 are suitable for geopolymer concretes, with the characteristic uniaxial tensile strength determined from the characteristic 28-day compressive strength being around 1.8 times the uniaxial tensile strength as determined from the indirect tensile splitting test. As such the current provisions can be considered conservative, for full realisation of the environmental and technical benefits of geopolymer concrete, adaptations for geopolymer concrete’s superior tensile strength should be made [3], [6], [24].

Equation 7: Characteristic Flexural Tensile Strength of Concrete [26]

′ . = 0.4 ∙ √ ′

Equation 8: Characteristic Uniaxial Tensile Strength of Concrete [26]

′ = 0.36 ∙ √ ′

Equation 9: Uniaxial Tensile Strength of Concrete from Indirect Tensile Testing as per AS1012.10-2000 [26]

= 0.9 ∙ .

Equation 10: Characteristic Tensile Strength of Concrete as proposed by Neville (2000) [24]

 

′ = 0.3 ∙ ′ 2⁄3

Table 3: Tensile Strengths of Fly Ah Based Geopolymer Concrete [24], [26]

Fire Resistance

The development of geopolymer concrete was originally developed as a heat resistant building material after a number of fires in France in the early 1970’s [29]. Fly ash based geopolymers have been investigated for their fire resistance and found to increase in mechanical strength when temperatures exceed about 600⁰C as shown in in Figure 11, this strength increases is due to a sintering liquid phase [32]. This sintering however also responsible for an increase in the thermal shrinkage, this is presented in Figure 12 [32]. In the circumstance that thermal shrinkage reaches a threshold value, usually in the range of 1 to 2% the material may fail despite the increase in its mechanical strength, this is due to cracking and changes in the material volume [32]. When compared to OPC concrete however it is a vast improvement with OPC concretes deteriorating in strength at around 300⁰C, characterised by explosive failure as the water molecules inside the concrete vaporise [6], [13]. The failure mode for geopolymers however is not explosive but results by melting of the inorganic polymer [32]. Certain geopolymers have been investigated and are in use in ultra- high temperature applications, however these systems perform differently to geopolymer binders used in concrete due to variation in the monomers that make up the geopolymer network [6], [33].

Figure 11: Compressive Strength vs temperature exposure for a Fly Ash Based Geopolymer [32]

Figure 12: Thermal Shrinkage versus exposed temperature of a Fly Ash Based Geopolymer [32]

Drying Shrinkage

Shrinkage is a phenomenon observed with OPC concretes, as the OPC hydrates into a crystalline matrix it reduces in volume, this makes sense since crystalline structures are much denser than the overall concrete so the remaining volume is made up of millions of small air voids [7]. Additional shrinkage is due to aggregates in the concrete absorbing water that would otherwise contribute to the volume of the concrete [34]. It has been observed that drying shrinkage of geopolymer concretes is less than that of OPC concretes [3], [17], [35]. Since geopolymer concrete undergoes polymerisation not hydration into a crystalline matrix it makes sense that the shrinkage of geopolymer concretes is less than OPC concrete [7]. As drying shrinkage occurs it, creates strain within the concrete structure [34]. Since most of the studies of geopolymer concrete have been on heat cured specimens it is interesting for Wallah and Rangan (2006) to report that shrinkage of ambient cured geopolymer concrete is far greater than that of heat cured geopolymer concrete as can be seen in Figure 13. This cause for concern since the Recommended Practice for Geopolymer Concrete in Australia suggests that the shrinkage joints or saw-cuts may not be required [3]. It can be seen in Figure 14 that provisions AS3600-2009 are conservative, yet are inadequate for ambient cured geopolymer concrete as presented in Figure 15. An experimental footpath was constructed at Curtin University of Technology in Perth, Australia, with no shrinkage cracks observable in 1.5x12m slabs, yet cracking at 3m centres for an OPC concrete reference footpath [3]. This is obviously contradictory to the findings of Wallah and Rangan (2006), and with lack of research on ambient cured geopolymer concrete this is an area requiring further research.

Figure 13: Drying Shrinkage Strain [17]

Figure 14: Drying Shrinkage of Heat Cured Geopolymer Concrete compared to predictions as per AS3600- 2009 [17], [26]

Figure 15: Drying Shrinkage of Ambient Cured Geopolymer Concrete compared to predictions as per AS3600- 2009 [17], [26]

Creep

Creep is a phenomenon that can be defined as the increase in strain under a sustained stress [34]. It can also be seen as the relaxation of stress with time for concrete subject to constant stress [34]. For the design of concrete members, AS3600-2009 employs a creep coefficient which is defined as the “mean value of the ratio of creep strain to elastic strain under conditions of constant stress” [26]. The creep strain of heat cured geopolymer concrete was investigated by Wallah and Rangan (2006) noting that creep can reduce the strength of geopolymer concrete [17]. The current provisions in AS3600-2009 however are conservative for heat cured geopolymer concrete [6], [17].

Figure 16Figure 16 presents a predicted creep strain curve calculated as per AS3600-2009 and an actual test specimen [17], [26]. Like for drying shrinkage, little research has been undertaken for geopolymer concrete cured at ambient temperatures.

Figure 16: Creep of a Heat Cured Geopolymer Concrete [17]

Conclusion

By reviewing the properties of fly ash based geopolymers it is clear there is a substantial lack of knowledge on the effect of curing conditions on the various mechanical parameters of geopolymer concrete. Although heat cured specimens have largely been presented in in this discourse, a mix design methodology and an assessment of the applicability of Australian design codes for in-situ geopolymer concrete is the objective of this associated research project. Since recognition of geopolymer concrete by some professional institutions and governmental authorities is based on heat cured concrete, there have been assumptions made that are yet to be confirmed for in-situ concretes [3], [36]. As research progresses it is likely that these gaps-in- knowledge will be addressed since the behaviour of geopolymer concrete is similar to that of OPC concretes, but with differences in magnitude. Future research lies in investigating the in-situ performance of geopolymer concretes and subsequent commercial realisation by the adaptations of existing standards to economically realise the mechanical performance of geopolymer concretes.

References

  • C. McLellan, R. P. Williams, J. Lay, A. Van Riessen, and G. D. Corder, “Costs and carbon emissions for geopolymer pastes in comparison to ordinary portland cement,” J. Clean. Prod., vol. 19, no. 9–10, pp. 1080–1090, 2011.
  • Zhang, J. L. Provis, J. Zou, A. Reid, and H. Wang, “Toward an indexing approach to evaluate fly ashes for geopolymer manufacture,” Cem. Concr. Res., vol. 85, pp. 163–173, 2016.
  • Concrete Institute of Australia, Z16: Recommended Practice for Geopolymer Concrete. North Sydney, Australia: Concrete Insitute of Australia,
  • Muttashar, W. Lokuge, and W. Karunasena, “Geopolymer Concrete : the Green Alternative With Suitable Structural Properties,” in 23rd Australasian Conference on the Mechanics of Structures and Materials (ACMSM23), 2014, December, pp. 101–106.
  • Xu and J. S. J. Van Deventer, “the Geopolymerisation of Natural Alumino-Silicates,” Int. J. Miner. Process., vol. 59, pp. 247–266, 2000.
  • Davidovits, Geopolymer Chemistry and Applications 4e. 2015.
  • E. Carraher Jr., Intrduction to Polymer Chemistry. Boca Raton, Florida, USA: CRC Press, 2007.
  • Pavithra, M. Srinivasula Reddy, P. Dinakar, B. Hanumantha Rao, B. K. Satpathy, and A. N. Mohanty, “A mix design procedure for geopolymer concrete with fly ash,” J. Clean. Prod., vol. 133, pp. 117–125, 2016.
  • T. Junaid, O. Kayali, A. Khennane, and J. Black, “A mix design procedure for low calcium alkali

activated fly ash-based concretes,” Constr. Build. Mater., vol. 79, pp. 301–310, 2015.

  • Ferdous, A. Manalo, A. Khennane, and O. Kayali, “Geopolymer concrete-filled pultruded composite beams – Concrete mix design and application,” Cem. Concr. Compos., vol. 58, pp. 1–13, 2015.
  • ASTM, Standard Specification for Coal Fly Ash and Raw or Calcined Natural Pozzolan for Use in Concrete. West Conshohocken, PA, USA: ASTM International,
  • D. A. Thomas, “Optimizing the Use of Fly Ash in Concrete,” New Brunswick, NJ, USA, 2007.
  • S. J. Van Deventer, J. L. Provis, and P. Duxson, “Technical and commercial progress in the adoption

of geopolymer cement,” Miner. Eng., vol. 29, pp. 89–104, 2012.

  • Van Riessen, E. Jamieson, C. S. Kealley, R. D. Hart, and R. P. Williams, “Bayer-geopolymers: An exploration of synergy between the alumina and geopolymer industries,” Cem. Concr. Compos., vol. 41, pp. 29–33, 2013.
  • Davidovits, Geopolymer Chemistry and Applications 4th edition. Saint-Quentin, France: Geopolymer Institute, 2015.
  • F. F. Barbosa, K. J. D. MacKenzie, and C. Thaumaturgo, “Synthesis and characterisation of materials based on inorganic polymers of alumina and silica: Sodium polysialate polymers,” Int. J. Inorg. Mater., vol. 2, no. 4, pp. 309–317, 2000.
  • E. Wallah and B. V. Rangan, “Low-Calcium Fly Ash-Based Geopolymer Concrete: Long-Term

Properties,” Research Report, Curtin University of Technology, Perth, Australia, 2006.

  • Standards Australia, 1 Supplementary cementitious material – Fly Ash. 2016.
  • Yunsheng, S. Wei, Z. Li, and Z. Xiangming, “Geopolymer extruded composites with incorporated fly

ash and polyvinyl alcohol short fiber,” ACI Mater. J., vol. 106, no. 1, pp. 3–10, 2009.

  • Concrete Institute of Australia, Z7/04. Good practice through design, concrete supply and construction. Rhodes Australia: Concrete Insitute of Australia,
  • Wang, Z. Zhang, J. L. Provis, and J. Zou, “Specifying fly ash for use in geopolymer : A conception of reactivity index.”
  • Duxson and J. L. Provis, “Designing Precursors for Geopolymer Cements.”
  • S. Patience, Experimental Methods and Instrumentation for Chemical Engineers. Amsterdam, The Netherlands: Elsevier, 2013.
  • Hardjito and B. V. Rangan, “Development and properties of low-calcium fly ash-based geopolymer

concrete,” Research Report, Curtin University of Technology, Perth, Australia, 2005.

  • P. Collins, D. Mitchell, and J. G. MacGregor, “Structural Design Considerations for High Stregth Concrete,” ACI Concr. Int., vol. 15, no. 5, pp. 27–34, 1993.
  • Standards Australia, AS3600-2009 Concrete structures.
  • D. J. Sumajouw and B. V. Rangan, “Low-calcium fly ash-based geopolymer concrete: reinforced

beams and columns,” Curtin Univ. Technol. Perth, Aust., pp. 1–120, 2006.

  • S. Gupta, Principals of Sturctural Design. Boca Raton, Florida, USA: CRC Press, 2011.
  • Davidovits, “Properties of Geopolymer Cements,” in First International Conference of Alkaline Cements and Concretes, 1994, pp. 131–149.
  • Mukhin, R. Khatri, I. Dumitru, and F. Ash, Some Limitations of Geopolymer Concrete. Adelaide, Australia, 2007.
  • Standards Australia, AS 10-2000 ( R2014 ) Methods of testing concrete – Determination of

indirect tensile strength of concrete cylinders (’Brasil’ or splitting test ). 2014.

  • L. Provis and J. S. J. Van Deventer, Geopolymers: Structure, processing, propertes and industrial applications. Boca Ranton, Florida, USA: CRC Press, 2009.
  • Davidovits and M. Davidovics, “Geopolymer: Ultra-High temperature Tooling Material for the Manufacture of Advanced composites,” SAMPE, vol. 36, no. 2, pp. 1939–1949, 1991.
  • M. Neville, Properties of Concrete, 4th ed. Harlow, England: Pearson Eduaction Limited, 2006.
  • Duxson, A. Fernández-Jiménez, J. L. Provis, G. C. Lukey, A. Palomo, and J. S. J. Van Deventer,

“Geopolymer technology: The current state of the art,” J. Mater. Sci., vol. 42, pp. 2917–2933, 2007.

  • VicRoads, Section 703 – General Concrete Paving. VicRoads,

Analysis of Ultra-High Strength Concrete Filled Steel Tubular Short Columns

Mitchell Edwards – 17686220 Supervisor – Dr. Vipul Patel Co-supervisor – Dr. Tai Thai

Abstract

In the field of civil engineering, practitioners of the science strive to maximise efficiency in order to reduce construction and design costs. However, the tools available to civil engineers are limited to the number and relevance of designs freely available to them. By expanding the pool of knowledge available to civil engineers through increasing the variety of designs at their disposal, their work is made easier, cheaper and safer for use by the public. In order to provide a wider array of tools available to engineers, more methods and types of construction elements need to be designed. The main objective of this literature review is to collect and summarise the relevant background information behind the title topic – the development of a finite element model of an ultra-high strength concrete filled steel tubular short column. The physics behind construction elements in regards to civil engineering and the methods of construction element analysis will be reviewed, as well as how to output the results of this analysis into a form relevant for use in the greater field of civil engineering and construction.

Introduction

In the field of civil engineering, columns provide the backbone of standing structures – taking the weight of the building and floor slabs and transferring them down into the foundation.

Extremely large structures which require strong columns to support their weight are known as high-demand structures, and include buildings such as skyscrapers and hospitals.

Contemporary civil engineering design uses a type of column design known as the steel reinforced concrete column, wherein a concrete column is supported on the inside with a steel rebar core to increase ductility and compression strength. These columns can be further reinforced with steel stirrups or internal steel frames. However, high-demand structures can require the steel reinforced columns to be designed extremely large in order to accommodate the incredible load, resulting in either increased size of the building or decreased floorspace available. In today’s increasingly centralised economical climate, space within cities is becoming extremely thin and real-estate is at an all-time premium. Differences in design, such as with the thickness of the supporting column, of up to a mere few square meters can

mean a difference in cost of tens or even hundreds of thousands of dollars in real estate costs and lost floorspace. In order to counteract this, engineers need to be given the tools to be able to reduce the size of the supporting columns to maximise the economicalabilty of their design. This can be achieved through the research of superior construction materials or construction techniques. Another option of achieving this goal however is through the research of additional types of support column types – columns with superior loading capability, so that engineers may design them thinner to carry the same weight. One such column design under development is the circular concrete-filled steel tubular (CFST) column– a column reinforced by steel on the outside, rather than the inside [2]. Figure 1 shows the cross section of one such column [4].

Figure 1: CFST Column Under Shear Compression [4]

CFST Columns

CFST columns have shown considerable promise in the field of civil engineering. Showing prominence early in its developmental lifespan in the mid 1980s, wherein a number of high- rise buildings in Seattle first started using CFST columns based on small-scale test design [4]. Since then, they have seen scattered use across the globe, including Europe, Singapore and Japan [3]. Despite promising results, their relative infrequency compared to the less efficient steel reinforced column is due to the lack of research done for CFST columns [5]. One such reason behind this is the relative difficulty in quantifying the various effects the steel tube has on the concrete core and the relative strength of the column as a whole. For example, neither the effect of compression from the steel tube [1] nor the effect of the L/D steel thickness ratio

[6] have been fully quantified. However, there has been a wide array of promising research done in this area and this problem is soon to be rectified.

Experimental Studies

The initial theory behind the invention of the CFST column was the positive effect the confining steel tube would have on the inner concrete. In regular steel reinforced columns, the steel rebar reinforcement protects well against cracking in the concrete due to shear and tensile loads by taking on those stresses itself, as steel is strong in tension stresses and concrete is weak. However, in axial loading scenarios such as in supporting columns, the downward stress on the concrete causes it to squash and expand outwards, weakening the concrete through the development of microcracks, as there is no lateral reinforcement to prevent it from doing so. The net effect of this is the reduction of ultimate axial strength in the column [9]. However, it was theorised that by reinforcing the concrete column on the outside with a steel tube would increase the ultimate axial strength through the compressive forces on the concrete preventing this squashing effect and the damaging of the concrete [5].

Experimental studies have confirmed this theory, with CFST columns performing superior to steel reinforced columns in regards to axial loading [6]. However, the confined column is made less ductile due to the rigidity of the composite design. Speculation has also made it clear that the column would perform poorly in regards to a fire event, as CFST columns lack the thermal insulation effect of the concrete compared to regular steel reinforced columns.

In the creation of the CFST columns for these experiments, it was noted that CFST columns could be made more quickly and cheaply than steel reinforced columns due to the subtraction of time and labour in casting the concrete around the steel reinforcing bars. Another effect of this is that CFST columns require less formwork to create on-site and can therefore drastically reduce the project length in regards to the installation of columns [9].

Experiments showed that, between the circular steel tube design and the rectangular steel tube design in CFST columns, the circular design preformed better in all fields [4][8].

Ultra-high Strength Concrete

Ultra-high strength (UHS) concrete is a composite concrete of design optimised to maximise performance strength. UHS concrete has seen increasing prominence in high-demand infrastructure. UHS concrete was initially developed as a means of constructing stronger and more durable transport infrastructure, such as in high-demand bridges, in order to minimise the requirement of steel reinforcement. The net effect of this design results in lighter, cheaper and longer-lasting bridges which require less formwork and design to construct [10].

This design philosophy for UHS concrete has been applied in the field of standing structures too, with many urban and inner-city civil engineers using it in the same fashion to develop structures with thinner and fewer support columns in order to maximise floorspace. In this sense, the application of UHS concrete shares similar functions to that of CFST column design. These shared strengths mean that the two work well in tandem together where their strengths can be applied, such as in the construction of high-demand infrastructure support columns.

Development

UHS concrete, compared to high-strength concrete, exhibits superior compressive strength and resistance to weathering and damage [10]. UHS concrete can reach compressive strengths of up to 150MPa, where as regular high-strength concrete reaches only up to 100MPa. However, the downsides to UHS concrete compared to its contemporaries are a reduction in flexibility and ductility, and a more thorough and involved mixing period.

UHS concrete is developed in similar fashion to regular high-strength concrete – the addition of silica and other admixtures to a Portland mix in order to minimise porosity and weakness in the concrete. However, UHS concrete also applies the addition of steel fibers as an admixture in order to increase the overall strength of the concrete. A more empirically efficient mix of aggregates are used as well.

Finite Element Modelling

Finite element modelling is a technique used by engineers to create true-to-reality models of construction elements for virtual testing. This method of element design has been rapidly developed alongside the modernisation of computers, becoming used widespread in the profession of engineering. These engineering modelling softwares, such as ABAQUS, simulate real-world physics to allow designers to create and test models without having to actually build them for each individual test. This significantly cuts down the time, cost and resources spent on element design and has allowed the field of design research to flourish.

In order to create these models, engineers need to design and tweak their work so as to fit real life conditions to the utmost highest degree. However, simply creating the models is not the end of the work – the models need to be verified against real-world results. By applying the same test conditions as a real-world specimen, differences in results can be extrapolated and explored so as to find out how the model is made different from that which is real. Changes and tweaks can be made to the model so that it eventually becomes an accurate representation of reality. In doing so, engineers are able to take the verified accurate model and apply it under different test conditions, tests which could otherwise require the construction of additional specimens or advanced testing equipment. Parameters within the model can also be modified, such as the exchanging of materials or a change in design properties. For example – creating a model of a construction element true to reality, and then changing the properties of the inner concrete to see how it fares under the same conditions, so as to test the nature of that concrete. Figure 2 shows an example of ABAQUS modelling software in action, used to model and analyse a potentially dangerous gusset plate [11].

Figure 2: Stress Analysis of Cleveland Inner Belt I‐90 Bridge element [11]

Concluding remarks

This literature review was conducted in relation to the thesis ‘Analysis of Ultra-High Strength Concrete Filled Steel Tubular Short Columns’ and covers the topics relevant to the subject.

The nature and history of CFST columns, the properties of ultra-high strength concrete and the methods for which these two elements can be modelled and analysed were investigated, to provide a solid pool of knowledge to draw from for the project. As can be drawn from the survey, the composite design of CFST columns with ultra-high strength concrete can utilise the combined strengths of both in order to solve what is a very relevant problem in an increasingly centralised modern society. The need for space and the downturn of the boom economy has driven engineers to continuously develop taller and thinner buildings, requiring stronger and more efficient tools. With the continued development and analysis of new construction elements, the field of civil engineering can be expanded so as to find increasingly better solutions to these problems.

References

  • Richard-Liew, JY, Xiong, MX & Xiong, DX 2017, Axial performance of short concrete filled steel tubes with high- and ultra-high- strength materials, Elsevier
  • Richard-Liew, JY & Xiong, DX 2012, Ultra-high Strength Concrete Filled Composite Columns for Multi-Storey Building Construction, Department of Civil Engineering, National University of Singapore, Singapore
  • Tao, Z, W, ZB & Yu, Q 2013, Finite element modelling of concrete-filled steel stub columns under axial compression, Elsevier
  • Roeder, C, Lehman, D, Maki, T & Heid, A 2016, Shear Strength of Circular Concrete- Filled Steel Tubes: Experiments and Analysis, Department of Structural Engineering,

University of Washington, USA

  • Quan Liang, Q 2009, Performance-based analysis of concrete-filled steel tubular beam– columns, Part I: Theory and algorithms, School of Architectural, Civil and Mechanical Engineering, Victoria University, Australia
  • Quan Liang, Q 2009, Performance-based analysis of concrete-filled steel tubular beam– columns, Part II: Verification & Applications, School of Architectural, Civil and Mechanical Engineering, Victoria University, Australia
  • Patel, V, Quan Liang, Q & Hadi, M 2012, High strength thin-walled rectangular concrete-filled steel tubular slender beam-columns, Part I: Modelling, School of Architectural, Civil and Mechanical Engineering, Victoria University, Australia
  • Patel, V, Quan Liang, Q & Hadi, M 2012, High strength thin-walled rectangular concrete-filled steel tubular slender beam-columns, Part II: Behaviour, School of Architectural, Civil and Mechanical Engineering, Victoria University, Australia
  • Morino, S & Tsuda, K 2003, Design and Construction of Concrete-Filled Steel Tube Column System in Japan, Department of Architecture, Faculty of Engineering, Mie University, Japan
  • Graybeal, B 2011, Ultra-High Performance Concrete, Federal Highway Administration,

McLean, USA

  • Farkas, K 2009, ‘FEA Imaging Sounds Warning about Freeway Bridge’, Design World, 8 October, viewed 29 March 2017, <http://www.designworldonline.com/fea-imaging-sounds- warning-about-freeway-bridge/>

Answer:

Introduction

INTRODUCTION

Boron nitride, the inorganic chemical compound, is basically composed of two elements of the periodic table, namely Boron and Nitrogen. The chemical formula for this compound is simply given as BN. However, the polymorph of this compound is also present, the formula of which is usually written as (BN)x, where x stands for the degree of polymorph. A number of lattice crystal structures of this compound are there. However, the most stable form among all other crystal structures is the hexagonal graphite like structure. Because of this hexagonal graphite-like structure, the boron nitride polymorph has the stability as well as the lubricating property. On the other hand, another crystal structure of this compound is there, which belong to the cubic crystal class of the classification, and this is alike the diamond structure. However, the softness of this diamond-like crystal structure is comparatively softer than the diamond structure. One of the important property for which the wide application of boron nitride is found is its advanced ceramic properties. Not to mention under the given context, the ceramics are the compounds made up of non-metallic inorganic elements, which has the property of hardness, rigidity, brittleness, and the corrosion resistance. In addition to this, the ceramics are flexible enough to convert themselves into the desired size and shape, just like clay. For this, the high temperature treatment and processing is needed. As for example, the shape determination of the clay materials, porcelain, bricks, etc. depends on the desired of one’s to provide size. Like these soft and flexible materials, boron nitride also can be used to make certain size and shapes depending on the desire of one’s under certain condition. This is why it is increasingly found that this boron nitride is being used for the purpose of the advanced ceramics. Certain properties, including physical and chemical and some of the specifications along with the manufacturing and the material genomics are being provided in the subsequent section of the report.

Literature review

The development

The hexagonal crystal form of the boron nitride is superior over the other crystal form of the boron nitride. This crystal structure is made up of graphite-like hexagonal layers, which makes it exceptionally stable as well as lubricant in nature. Because of the exceptional stability in the hexagonal form of the crystal structure, the stability is extended up to certain elevated level of temperature, where the high temperature provides the flexibility to the composite to provide the desired shape and size (Wang et al., 2015). Because of this property, it has been recently used as an excellent ceramic material. In the crystal structure, it has been reported that the boron atoms are connected to the nitrogen atom via the formation of sp2 hybrid bond, which are mostly covalent in nature along with the formation of hexagonal layers. A number of such hexagonal layers are there which formed due to the covalent bonding between boron and nitrogen. These hexagonal layers are further connected via the van-der walls force of attraction. These structural and crystal status off the compound in this hexagonal state introduces certain property to the material, because of which it has got extra attention over other materials currently is being used as ceramics.

A number of important mechanical properties of this compound have been provided in the Table 1. The important point in terms of the properties is that this compound has lower value of dielectric constant and extremely high sublimation temperature. The presence of these two properties is extremely important to determine the advanced ceramic properties of boron nitride. First of all, extreme lower value of the dielectric constant makes it as an excellent insulating material. On the other hand, higher value of the sublimation temperature makes it exceptional stable. Because of these two properties of exceptional stability and the insulation property, this compound is superior to act as an advanced ceramic material. In addition to this, the thermal shock resistance property of boron nitride is also appreciably high and the desirable level of the machinability is also exceptionally good. Under the given context it is worth of mentioning the transmission electron microscopy (TEM) image of a piece of boron nitride under the high resolution of the microscope with the operating electronic voltage of around 200 kV, as mentioned in the below Figure 1 (Xiaoming et al., 2016).

In terms of the characterisation of the c

On the other hand, certain limitation of the direct use of boron nitride as the advanced ceramic is there, which on the case to case basis limits the use of this material alone as an excellent ceramic material of advanced type. This is because of the fact that the covalence bond between the boron ad nitrogen is extremely strong in nature, which indicates a lower value of the self-diffusion of the corresponding bond between boron and nitrogen in the compound (Eichler et al., 2008). Because of the lower value of the diffusion-coefficient of the covalent bond between boron and nitrogen, it becomes sometimes difficult to obtain the dense material under the condition when the temperature is appreciably high, as high as more than 2000 degree Celsius (Cai et al., 2016). To cope up with this problem, some of the sintering materials are known to add with the boron nitride. One class of such sintering materials belong to the oxide family, like silicon oxide or the boron oxide (Wen et al., 2011). The powders of the boron nitride along with the powders of the silicon or the boron oxides are then mixed in absence of application of pressure. However, the properties which improve due to the sintering of these oxide classes of the sintering materials are not exceptionally good. This reflects in the lower value of relative density of the composite of boron nitride with the oxide sintering materials. The development hence urges the manufacturing of such advanced sintering materials which upon addition with the boron nitride further elevates the physical as well as chemical properties compared to the composite obtained due to the coupling of boron nitride with the oxide class of sintering materials (Jia et al., 2011). This ultramodern development and the introduction of the latest class of sintering materials are mulite, Yttrium aluminium garnet (YAG), Aluminium nitride (AlN), silicon nitride (Si3N), etc. The composite provides excellent and better mechanical properties when coupled with the boron nitride powder of the hexagonal class of crystal (hBN) (Yongli et al., 2002). The mechanicals, thermal as well as the electrical properties of such composite materials of boron nitride are now of enough quality grade after the sintering with these nitride class of sintering materials, and therefore becomes excellent category advanced ceramics. This is why this composite ceramics of boron nitride coupled with the sintering materials have seen its extensive use in recent times in the field of chemical engineering, in the manufacturing of lubricating materials as well as in the use of the high temperature furnaces.

Experimental manufacturing protocol

The sintering protocol of the preparation of the boron nitride ceramics is extremely challenging because of the very strong covalent bond between the boron and nitrogen. This puts a challenge in terms of the experimental success of the sintering of this material with the common sintering materials. This is why the pressure assisted protocol must have to apply to overcome this problem. The vigorous condition, like, high temperature and high pressure must be applied for the successful composition formation of the composite ceramics of boron nitride and the sintering materials. A number of pressure assisted experimental protocol are there, which are worth of describing under the given context of the experimental protocol for the formation of the boron nitride ceramics.

One of the widely used experimental protocols for the pressure-assisted preparation of the boron nitride composite is the execution of the sintering protocol with the help of the spark plasma (Omori, 2000). This spark plasma sintering method is a very efficient method of sintering, where the sintering materials quickly couple with the powder of the boron nitride, and the required temperature for such coupling between the boron nitride powder and the sintering materials are relatively low. Very soon after the initiation of this process, high density of the materials obtained. In this method, the application of the pulse current helps to introduce the electrical discharge on the surface of the materials, where the materials are being subjected to promoting the sintering (Guo, 2009). In addition to this, the sintering time is also short enough; where the homogeneity of the composite might be achieved within small period of time. This is the major advantage of this protocol over the hot pressing method of the preparation of the composites. However, one of the major challenge of using this techniques is that this plasma based protocol is costly compared to the other protocol for the preparation of the composites of the boron nitride with the added sintering materials.

Another pressure based manufacturing protocol is termed as the hot isostatic method of the composite preparation (Helle et al., 1985). In this hot isostatic method of the composite preparation, first the pre-sintering materials are being subjected to the formation of the powders, which them are subjected to introduce in tot vigorous condition of high temperature and high pressure. This simultaneous application of high temperature and high pressure makes the composite with very dense properties. The efficiency of this protocol is majorly due to the application of pressure in the range of 150 to 250 MPa, which is extremely high compared to the either simple hot pressing method, or the plasma sintering method (Yucheng Lei et al., 2005). The high pressure applied in this protocol helps to remove the pores as well as defects, if any, and hence the homogeneity of the composite becomes exceptionally good with relatively high value of the density. In fact an appreciably high density value of more than 95% can be achieved due to the application of this protocol. In fact, in terms of achieving the good degree of the density after this protocol, the earlier literature report based on the experimental evidence proves that the post treatment of this protocol to the composite of the boron nitride and the sintering material elevates the value of density from 1.81 g/cc to the value of 2.32 g/cc. This has been reported to the achievement of the density close to the value of full density of the composite. The TEM image of a composite obtained after such treatment is being provided in the below figure 2, which is basically the ceramic made up of the composite of boron nitride with MAS.

Figure 2. The ceramic made up of the composite of boron nitride with MAS.

In terms of the characterisation of the ceramic made up of the composite of boron nitride with MAS, a number of experimental protocols were followed, like the x-ray diffraction pattern to find the lattice crystal faces and the surfaces (Figure 3a1, a2). On the other hand, energy dispersive x-ray spectroscopy was also applied on the given composite, as mentioned in the Figure 3a3, a4.

Figure 3. The x-ray diffraction pattern to find the lattice crystal faces and the surfaces (Figure a1, a2); Energy dispersive x-ray spectroscopy (EDS) was also applied on the given composite, as mentioned in the figure a3, a4.

The properties of the ceramics

In terms of the exploration of the typical mechanical properties, a number of experiments were performed, based on which important parameters regarding the mechanical properties were estimated, as mentioned din the Table 2.

As it is already established that the sole ceramic made up of only boron nitride possesses poor property of the ceramics, the use of the additive as the sintering materials were added to the boron nitride, which elevates the mechanical properties of the boron nitride ceramics. In this context, Cai et al earlier reported the preparation of the boron nitride ceramics with the sintering with MS (Magnesium aluminium silicate), which is able to show improved properties of stiffness, rigidity, hardness and other superior exterior and interior properties of the composite material made up of boron nitride and the MAS (Cai et al., 2015). This was achieved through the execution of the co-enhanced effect, where the presence of two phases was there simultaneously. This leads to the formation of the ceramics having no cracks either in the exterior or the interior surface of the ceramic body. In fact, it has been proved that the 50% addition of the sintering material (MAS) to the boron nitride, the value of toughness as well as the bending strength elevates to the value of 2.49 MPa, and 213 MPa, respectively.

Various important properties of the boron nitride ceramics

Under the given context of the composite preparation between the boron nitride and the sintering material, it is of utmost important to measure and explain the properties of the only boron nitride ceramics. Since the origin of the colloidal properties of either the single boron nitride ceramic or the boron nitride ceramic composite largely depends on the individual properties of the basic structure, therefore, the documentation of the properties of the boron nitride ceramic itself is important prior to the description of the colloidal properties of the ceramic conjugate. In terms of the density, the boron nitride ceramic has a value of 3.092 gm/cc with the crystal size of around 6 microns. The value of the water absorption as well as the value of the porosity of the boron nitride ceramics is almost close to zero. The value of the gas permeability is also nil and the colour of the composite is ivory in nature. The summary of these properties have been depicted below in Table 3.

Table 3. The summary of properties of boron nitride ceramics

Density g.cm3 3.9
Size of crystal Microns 6
Porosity value % 0
Gas permeability % 0
The colour ¯ Ivory

On the other hand, in terms of the thermal properties, the boron nitride ceramics was subjected to a number of experimental tests. This indicates the value corresponding to the coefficient of the thermal expansion as 7.5 per degree Celsius. On the other hand, the values for the thermal conductivity at 25 degree Celsius were found to be 25 W/m K. The value of the specific heat capacity for this ceramics was found to be 850 J/Kg-K. The recommended maximum use of this ceramic is approximately 1800 degree Celsius. These properties have been summarised under the Table 4 below.

Table 4. The thermal properties of the boron nitride ceramic

Thermal Conductivity 20°C 25 W/m K
Coefficient of Thermal Expansion 25-1000°C 7.5/°C
Specific Heat 100°C 850 J/kg*K
Maximum Use Temperature 1800 °C

In terms of the mechanical properties, the elastic modulus of the boron nitride ceramics has been found to be around 370 MPa. On the other hand, the Poisson ratio value for this compound is 0.19. This ceramic has a very high value of the compressive strength, the value of which is roughly 2500 MPa. In addition to this, the advance use as a ceramic for boron nitride over other is due to its rigidity, the value of which is 13.5 GPa. The associated estimation of the tensile strength was also found to be 35 MPa. These properties have been summarised under the Table 5.

Table 5. Mechanical properties of boron nitride ceramics, when measured at 25 degree Celsius.

Flexural Strength (MOR) 20°C 370 MPa (psi x 103)
Modulus of elasticityElastic Modulus 20°C 365 GPa (psi x 106)
Value for the Poisson’s Ratio 20°C 0.19
Compressive Strength 20°C 2500 MPa (psi x 103)
Hardness 13 GPa (kg/mm2)

In terms of the electrical properties of the boron nitride ceramic, it has been concluded based on the experimental result that the value of the strength corresponding to the dielectric at 6.5 mm is 8.5 ac-kv/mm (Munir et al., 2006). On the other hand, the value obtained for the dielectric constant for the boron nitride ceramic was found to be 9.0, when measured at 25 degree Celsius. In addition to this, the value of the tan delta was proved to be approximately less than the value of 0.0001. The resistivity of the volume for this boron nitride ceramic was found to be greater than 10 ohm-cm, and this values has been reported to be strongly dependent on the type and quantity of the sintering and doping material added. All of these electrical properties of the boron nitride ceramics have been tabulated under the Table 6.

Table 6. Electrical properties of the boron nitride ceramics

Dielectric Strength 6.35mm 8.5 ac-kV/mm (ac V/mil)
Dielectric Constant 1 MHz 9.0 at 25°C
Dielectric Loss (tan delta) 1 MHz <0.0001 at 25°C
Volume Resistivity 25°C Greater than 10 ohm-cm

In terms of the measurement of the colloidal properties of the ceramics of the composite of the boron nitride in presence of some of the sintering materials, like SiO2, first their synthesis was performed followed by the zeta potential measurement. In the synthetic protocol, first the aqueous suspension of the silicon oxide was prepared in the water with the concentration of 0.05 weight percent of the boron nitride. This was followed by the addition of this solution to the previously prepared solution of the boron nitride in the concentration range of 10-3 M. Strong acid, like nitric acid, or strong base, like sodium hydroxide was added to maintain the desired level of the pH of the resulting solution. Once the composite of the boron nitride and the silicon oxide is prepared, they were subjected to the examination of some of the colloidal properties. First of all, the composite mixture was placed in the rotational viscometer in order to get an idea about the rheological properties of the ceramic composite (Topper, 2008). Further, the Malvern zeta potential instrument was used to measure the colloidal zeta potential value of the ceramic composite. In order to obtain the data about the rheological property, the suspension of the composite mixture was allowed to stirring for around 60 minutes, followed by the study of the sedimentation behaviour of the composite ceramics made up f boron nitride with the silicon oxide (Zhou et al., 2007). The regime of pH over which the study was performed lies in the range of 2 to 10. The height of the sedimentation of the corresponding phases was obtained based on the height, as observed from the bottom of the tube after the experiment was finished. The data obtained from the zeta potential measurement was fitted and proved in the below image in Figure 4.

Figure 4. Zeta potential behaviour of the boron nitride ceramic and the composite of the ceramic made up of boron nitride with the silicon oxide sintering

From the data as obtained from the zeta potential study, it has been concluded that the both of the SiO2 as well as boron nitride (BN) provides a like value of the electrophoretic behaviour in presence of the doping material (A-1). In absence of the doping material, the point of the isoelectric pH was very close to the value of pH in between 2 to 3. However, on increasing the value of the Ph of the media in the range from 2 to 12, the magnitude of the negative zeta Potential was found to increase. The value increases as high as -73.8 mV in cased of the Sio2 powder, and it increases up to -66 mV for the BN only. On the other hand, addition of the doping material increased the isoelectric value of the pH, and the zeta potential becomes more and more negative. The increment of the negative zeta potential indicates the more stability of the suspension of the composite in presence of the doping material.

On the other hand, in terms of the experimental result based on the sedimentation part, the height of sedimentation for SiO2/BN composite in absence and presence of doping material (A-1) was determined, as provided in the Figure 5.

Figure 5. The height of sedimentation for SiO2/BN composite in absence and presence of doping material (A-1)

It has been observed that the addition of doping to the ceramics decreases the height of the sedimentation. On the other hand, the rheological properties were determined with the estimation of the viscosity as a function of the shear rate, as shown in figure 6 below.

Figure 6. Estimation of the viscosity as a function of the shear rate for the ceramic composite made up of BN and SiO2

In the presence of the sintering material with a concentration of 0.2 to 0.6 weight percent of the boron nitride, the value of the viscosity was found to decrease gradually. On the other hand, addition of the dispersant in the composite which was previously formed increases the viscosity. This indicates the formation of more structures with the consolidated microstructures within it, where the small elevation in the viscosity the underlying reason for this.

Furthermore, in terms of the shaping of the boron nitride ceramic, the protocols, like slip casting and tape casting are usually used. The protocol through which these are made is being provided below in Figure 7.

Conclusion:

The literature review for the advance use of the boron nitride as a ceramic in modern time seems to contain high volume. The extensive research on the sole boton nitride ceramic was first introduced. However, due to some of the additional requirement and the limitation of the boron nitride ceramics, the development of the additional addition of the sintering materials was designed and added for the specific elevation of certain ceramic properties as well as the mechanical properties. The sintering and doping increase the thermal, electrical;, as well as the mechanical properties of the boron nitride ceramics, and hence the practical use of this material becomes extensive. The lab-based and the industrial testing and the corresponding mutually inclusive conclusions for those testing therefore prove this material as an advanced ceramic one.

References

Cai, D.L., Yang, Z.H., Duan, X.M., & Zhou, Y. (2015). A novel BN-MASsystem composite ceramics with greatly improved mechanical propertiesprepared by low temperature hot-pressing, Mater. Sci. Eng. A-Struct. Mater.Prop. Microstruct. Process., 633. 194-199.

Eichler, C. (2008). Lesniak, Boron nitride (BN) and BN composites forhigh-temperature applications, J. Eur. Ceram. Soc., 28(5), 1105–1109

Cai, D.L., Yang, Z.H., Duan, X., & Zhou, Y. (2016). Inhibitingcrystallization mechanism of h-BN on cordierite in BN-MAS composites. J.Eur. Ceram. Soc.,36 (3), 905–909.

Wen, G., Wu, G.L., Lei, T.Q., Zhou, Y., Guo, Z.X. (2011). Co-enhanced SiO2-BN ceramicsfor high-temperature dielectric applications. J. Eur. Ceram. Soc. 20(12), 1923–1928.

Jia, D.C., Zhou, L.Z., Yang, Z.H., Duan, X.M., & Zhou, Y. (2011). Effect of preforming processand starting fused SiO2 particle size on microstructure and mechanicalproperties of pressurelessly sintered BNp/SiO2Ceramic composites. J. Am.Ceram. Soc., 94(10), 3552–3560.

Yongli, L., Guanjun, Q., & Zhihao, J. (2002). Machinable Al2O3/BN composite ceramicswith strong mechanical properties. Mater. Res. Bull. 37 (8), 1401–1409.

Xiaoming, D., Zhihua, Y., Lei, C., Zhuo, T., Zhou, Y. (2016). Review on the properties of hexagonal boron nitride matrixcomposite ceramics. J Eur Ceram Soc., 12, 1-12.

Zhou , L., & Dechang, J. (2007). Rheological Properties of Boron Nitride-Silica Composite Suspensions. Key Engineering Material, (336), 988-990.

Topper, C. (2008). Preliminary results of low energy sputter yields of boron nitride due to xenon ion bombardment, 44th AIAA Joint Propulsion Conference.

Wang, Z., Zhou, P., & Wu, W.Z. (2015). Effect of surface oxidation on thermal shockresistance of ZrB2-SiC-ZrC ceramic at temperature difference from 800to1900 degrees C. Corros. Sci., 98, 233–239.

Omori, M. (2000). Sintering, consolidation, reaction and crystal growth by the sparkplasma system (SPS). Mater. Sci. Eng. A-Struct. Mater. Prop. Microstruct.Process. 287 (2), 183–188.

Guo, S.Q. (2009). Densification of ZrB2-based composites and their mechanical andphysical properties: a review. J. Eur. Ceram. Soc., 29 (6), 995–1011.

Munir, Z. A., Anselmi-Tamburini, U., & Ohyanagi, M. (2006). The effect of electric field andpressure on the synthesis and consolidation of materials: a review of the spark plasma sintering method. J. Mater. Sci. 41 (3), 763–777.

Helle, A.S., Easterling, K.E., & Ashby, M.F. (1985). Hot-isostatic pressing diagrams—newdevelopments. Acta Metall., 33 (12), 2163–2174.

Yucheng Lei, X.B., Liu, J., & Zhang, Y. (2005). Research on pressureless sintering of hexagonal boron nitride. Ordnance Mat. Sci. Eng. 28 (4), 20–23.

0 responses on "EMS5ARA Advanced Research Learning Literature Review"

Leave a Message

Your email address will not be published. Required fields are marked *