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1.
This paper presents the compressive strength of fly‐ash‐based geopolymer concretes at elevated temperatures of 200, 400, 600 and 800 °C. The source material used in the geopolymer concrete in this study is low‐calcium fly ash according to ASTM C618 class F classification and is activated by sodium silicate (Na2SiO3) and sodium hydroxide (NaOH) solutions. The effects of molarities of NaOH, coarse aggregate sizes, duration of steam curing and extra added water on the compressive strength of geopolymer concrete at elevated temperatures are also presented. The results show that the fly‐ash‐based geopolymer concretes exhibited steady loss of its original compressive strength at all elevated temperatures up to 400 °C regardless of molarities and coarse aggregate sizes. At 600 °C, all geopolymer concretes exhibited increase of compressive strength relative to 400 °C. However, it is lower than that measured at ambient temperature. Similar behaviour is also observed at 800 °C, where the compressive strength of all geopolymer concretes are lower than that at ambient temperature, with only exception of geopolymer concrete containing 10 m NaOH. The compressive strength in the latter increased at 600 and 800 °C. The geopolymer concretes containing higher molarity of NaOH solution (e.g. 13 and 16 m ) exhibit greater loss of compressive strength at 800 °C than that of 10 m NaOH. The geopolymer concrete containing smaller size coarse aggregate retains most of the original compressive strength of geopolymer concrete at elevated temperatures. The addition of extra water adversely affects the compressive strength of geopolymer concretes at all elevated temperatures. However, the extended steam curing improves the compressive strength at elevated temperatures. The Eurocode EN1994:2005 to predict the compressive strength of fly‐ash‐based geopolymer concretes at elevated temperatures agrees well with the measured values up to 400 °C. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

2.
Compressive behavior of three-dimensionally reinforced carbon/carbon composite (3D-C/C) was examined from room temperature to elevated temperatures up to about 3000 K. Three-dimensionally reinforced C/C was found to have an inclination to induce kinks at the ends of specimens due to extremely low shear strength. In order to avoid this type of premature fracture and to conduct high-temperature tests, discussion was made on specimen geometry and testing procedure, and the combination of a dumbbell-shape specimen and test configuration without a supporting jig were found to be suitable for the present study. Using this set-up, the compressive strength of a 3D-C/C was evaluated as a function of temperature up to about 3000 K. The compressive strength of the 3D-C/C monotonically increased with the increase in temperature up to 2300 K, but decreased above this temperature. The strength enhancement was suggested to be caused by improvement in the fiber/matrix interfacial bonding, and the degradation over 2300 K was by softening of the matrix at high temperatures.  相似文献   

3.
Geopolymerisation of mechanically activated fly ash was studied at ambient (27 °C) and elevated (60 °C) temperatures by isothermal conduction calorimeter. Under both the conditions, mechanical activation enhanced the rate and decreased time of reaction. It was interesting to observe that in the samples milled for 45 min (median size ∼5 μm), a broad peak corresponding to geopolymerisation initiated at 27 °C after 32 h. The rate maxima at 60 °C, a measure of fly ash reactivity, showed a non-linear dependence on particle size and increased rapidly when the median size was reduced to less than 5-7 μm. Improvement in strength properties is correlated with median particle size, and reactivity of fly ash. The characterisation of the geopolymer samples by SEM-EDS, XRD and FTIR revealed that mechanical activation leads to microstructure and structural variations which can be invoked to explain the variation in the properties.  相似文献   

4.
This paper presents the effect of elevated temperatures up to 700 °C on compressive strength and water absorption of two alkali‐activated aluminosilicate composites (one of them is river sand aggregate geopolymer concrete; the other one is crushed sand aggregate geopolymer concrete) and ordinary Portland cement based concretes. To obtain binding geopolymer material, Elaz?? ferrochrome slag was ground as fine as cement, and then it was alkali activated with chemical (NaOH and Na2SiO3). Geopolymer concrete samples were produced by mixing this binding geopolymer material with aggregates. At each target temperature, concrete samples were exposed to fire for the duration of 1 h. Fire resistance and water absorption of geopolymer and ordinary Portland cement concrete samples were determined experimentally. Experimental results indicated that compressive strength of geopolymer concrete samples increased at 100 °C and 300 °C temperatures when compared with unexposed samples. In geopolymer concrete samples, the highest compressive strength was obtained from river aggregates ones at 300 °C with 37.06 MPa. Water absorption of geopolymer concrete samples increased at 700 °C temperature when compared with unexposed samples. However, a slight decrease in water absorption of concrete samples was observed up to 300 °C when compared with unexposed samples. SEM and X‐ray diffraction tests were also carried out to investigate microstructure and mineralogical changes during thermal exposure. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

5.
This paper attempted to isolate variables that govern concrete spalling when exposed to a hydrocarbon fire. The influence of specimen size was investigated by studying 4 specimen sizes consisting of cylinders, columns, and panels. Three aggregate sizes, 7 mm, 14 mm, and 20 mm were used in the concrete mixes to determine their effect on concrete spalling. Influence of aggregate type on concrete spalling was also investigated. Forty‐two different specimens were considered in this investigation. Concrete spalling was quantified as nominal spalling depth, which has been presented as a new way of quantifying the degree of concrete spalling. The results indicated that specimen size did have an effect on the spalling of concrete under hydrocarbon fire exposure and that nominal spalling depth of concrete increases as the specimen size increases. Aggregate size effect was evident when the maximum aggregate size increased from 7 mm to 20 mm, and explosive spalling was more severe for specimens with small size aggregates. Specimens with 14‐mm aggregate size showed inconsistent results and the spalling behavior witnessed was more random and sporadic. The type of aggregate used has no clear bearing on concrete spalling given both aggregates had similar linear expansion profiles.  相似文献   

6.
Expansions due to alkali-silica reaction (ASR) in the accelerated concrete prism test (ACPT-60 °C) show a significant reduction at 13 weeks compared to 52 week testing in the standard concrete prism test (CPT-38 °C). Previous work indicated that increased leaching, higher mass loss and a reduction in the pH were observed when temperature was increased from 38 to 60 °C. After further investigation the authors have revealed that non-reactive fine aggregate from certain sources combined with the same reactive coarse aggregate exhibited further reduction in expansion in the ACPT. Expansion data for a wide range of reactive coarse aggregates in 38 and 60 °C testing regimes is shown. Data investigating the Spratt reactive coarse aggregate combined with seven different non-reactive sands will be shown to demonstrate the dramatic effect of the non-reactive sand. Selected pore solution analyses will be given to further elucidate this issue.  相似文献   

7.
The research was carried out to develop geopolymers mortars and concrete from fly ash and bottom ash and compare the characteristics deriving from either of these products. The mortars were produced by mixing the ashes with sodium silicate and sodium hydroxide as activator solution. After curing and drying, the bulk density, apparent density and porosity, of geopolymer samples were evaluated. The microstructure, phase composition and thermal behavior of geopolymer samples were characterized by scanning electron microscopy, XRD and TGA-DTA analysis respectively. FTIR analysis revealed higher degree of reaction in bottom ash based geopolymer. Mechanical characterization shows, geopolymer processed from fly ash having a compressive strength 61.4 MPa and Young's modulus of 2.9 GPa, whereas bottom ash geopolymer shows a compressive strength up to 55.2 MPa and Young's modulus of 2.8 GPa. The mechanical characterization depicts that bottom ash geopolymers are almost equally viable as fly ash geopolymer. Thermal conductivity analysis reveals that fly ash geopolymer shows lower thermal conductivity of 0.58 W/mK compared to bottom ash geopolymer 0.85 W/mK.  相似文献   

8.
Solid particle erosion tests have been conducted on three different alumina-based refractories at elevated temperatures up to 1400 °C, using sharp SiC particles between 325 and 830 μm in diameter. The impact speed is 50 m/s and the impact angle is varied between 30° and 90°. The objective of this study is to ascertain the effects of temperature and impact angle on the erosion resistance of alumina refractories. The experimental results reveal that the alumina-based refractories, in general, exhibit increasing erosion resistance with increasing temperature and decreasing impact angle, with the minimum erosion rate at 1200 °C and 30° impact angle. Chrome corundum refractory brick is the most resistant to vertical erosion, due to its highest alumina content, and associated hardness and density, as well as strongly bonded aggregate and binder phase. The primary material removal mechanisms are fracture and chipping of binder phase and aggregate, as well as aggregate pull-out.  相似文献   

9.
Highly porous geopolymers, with homogeneous microstructure, open cells and porosity up to 80 vol%, were fabricated by gel-casting, a process commonly used to produce ceramic foams. Geopolymer foams were prepared by stirring an activated blend of metakaolin and fly ash with a mixture of potassium hydroxide and potassium silicate with Si/K=1.66. The cell size and size distribution of the geopolymer foams could be efficiently adjusted by the control of some parameters such as solid content, surfactant type and content and mixing speed. The influence of each parameter on the porosity and other characteristics of the geopolymer foams were investigated. The foams were evaluated only after heat treatment at 80 °C, which was conducted in order to complete the geopolymerization reactions. The produced components could be heat treated up to 1200 °C in air without melting, if desired.The characteristics (morphology, strength, chemical and thermal resistance) of the geopolymer foams suggest that they could be employed as low cost replacement for highly porous ceramics in applications such as catalysis supports, adsorption and separation, filtration of hot gases and refractory insulation of furnaces. In addition, these components could be considered sustainable, because they reach their final properties after processing at temperatures not exceeding 100 °C and part of the raw materials employed are industrial waste.  相似文献   

10.
Recently, AAR was identified in submerged piles of some bridges in tidal waters. Microstructural examination detected chloroaluminate salts in some cracks. To clarify whether seawater had influenced the deterioration an experimental program was planned to examine the effects of sodium chloride on AAR under various curing conditions.Concrete prisms containing either of highly-reactive, slowly-reactive or nonreactive aggregate, and either low or high alkali contents, were stored in saltwater (representing seawater) or at 100% RH, at temperatures of 38, 60 and 80 °C, for expansion measurement over 600 days, after which the temperature for those stored in saltwater was lowered to 23 °C, to check its effect on further expansion, which could be attributed to precipitation of ettringite and/or Ca-chloroaluminate.The results indicate that the type of aggregate and concrete alkali content had the greatest effect on AAR expansion. Exposure to saltwater did not have any significant effect on the AAR expansion.  相似文献   

11.
The volcanic ash occurring as an abundant and readily accessible natural resource in the Central African country of Cameroon was used to synthesize aluminosilicate geopolymers using sodium hydroxide as the sole alkaline activator. Both the curing conditions and the Na2O/SiO2 molar ratio were found to influence the development of compressive strength of the geopolymer cement paste, which achieved a maximum strength of 55 MPa at Na2O/SiO2 = 0.3. The formation of a mortar by the addition of 40 wt% sand to the optimized geopolymer cement composition reduced the compressive strength to 30 MPa, still within the useful range for construction applications. The geopolymers consist largely of X-ray amorphous material with a small content of crystalline phases. Scanning electron microscopy showed a homogenously distributed mixture of lath-shaped and agglomerated morphologies, with a homogeneous distribution of Si, Al and O in the geopolymer matrix. The geopolymers are relatively stable to heat, shrinking only slowly and retaining about 60% of their as synthesized compressive strength on heating to 900 °C. The FTIR spectra of both the as synthesized and heated geopolymers show two broad absorbance bands, between 820-1250 cm−1 and 450-730 cm−1 assigned to the internal vibrations of Si-O-Si, and Si-O-Al respectively. The compressive strengths and the thermal stability of these materials suggest their suitability for building applications and low-grade refractories.  相似文献   

12.
Unidirectional carbon fiber reinforced geopolymer composite (Cuf/geopolymer) is prepared by a simple ultrasonic-assisted slurry infiltration method, and then heat treated at elevated temperatures. Effects of high-temperature heat treatment on the microstructure and mechanical properties of the composites are studied. Mechanical properties and fracture behavior are correlated with their microstructure evolution including fiber/matrix interface change. When the composites are heat treated in a temperature range from 1100 to 1300 °C, it is found that mechanical properties can be greatly improved. For the composite heat treated at 1100 °C, flexural strength, work of fracture and Young's modulus reach their highest values increasing by 76%, 15% and 75%, respectively, relative to their original state before heat treatment. The property improvement can be attributed to the densified and crystallized matrix, and the enhanced fiber/matrix interface bonding based on the fine-integrity of carbon fibers. In contrast, for composite heat treated at 1400 °C, the mechanical properties lower substantially and it tends to fracture in a very brittle manner owing to the seriously degraded carbon fibers together with matrix melting and crystal phases dissolve.  相似文献   

13.
Abstract

Aluminosilicate type materials can be activated in alkaline environment and can produce geopolymer cements with low environmental impacts. Geopolymers are believed to provide good fire resistance so the effects of elevated temperatures on mechanical and microstructural properties of pumice based geopolymer were investigated in this study. Pumice based geopolymer was exposed to elevated temperatures of 100, 200, 300, 400, 500, 600, 700 and 800°C for 3?h. The residual strength of these specimens were determined after cooling at room temperature as well as ultrasonic pulse velocity, and the density of pumice based geopolymer pastes before and after exposing to high temperature was determined. Microstructures of these samples were investigated by Fourier transform infrared for all temperatures and SEM analyses for samples that were exposed to 200, 400, 600 and 800°C. Specimens, which were initially grey, turned whitish accompanied by the appearance of cracks as temperatures increased to 600 and 800°C. Consequently, compressive strength losses in geopolymer paste were increased with increasing temperature level. On the other hand, compressive strength of geopolymer paste was less affected by high temperature in comparison with the ordinary Portland cement. As a result of this study, it is concluded that pumice based geopolymer is useful in compressive strength losses exposed to elevated temperatures.  相似文献   

14.
The mechanical and microstructural properties of geopolymer concretes were assessed before, during and after high temperature exposure in order to better understand the engineering properties of the material. Fly ash based geopolymer concretes with either quartz aggregate or expanded clay aggregate were exposed to various temperatures up to 750 °C using a thermo-mechanical testing apparatus. Microstructural investigations were also undertaken to better understand the measured changes in the mechanical properties. It was found that dehydration of capillary water caused cracking and strength losses at temperatures ≤ 300 °C, an effect that was more severe in the quartz aggregate geopolymer due to its lower permeability. At higher temperatures (T  500 °C) sintering promoted strength increases which enabled both concrete types to yield significant strength advantages over conventional materials. Stress–mechanical strain curves, which form the basis of the fire design of concrete structures, are reported.  相似文献   

15.
We propose the distillation method to synthesize Ni–Cu–Zn ferrite powder and to recover nitric acid, using scrap iron and the waste solution of electroplating as the starting materials. It was found that the Ni–Cu–Zn ferrite powder prepared from industry wastes also showed the formation of cubic ferrite with a saturation magnetization (Ms) of 55,825 A m2 g−1 and an intrinsic coercive force (Hci) of 579 A m−1. For sintered Ni–Cu–Zn ferrite specimen, the toroidal specimen sintered at 950 °C for 2 h presented an maximum initial permeability (μi) of 176 at 28.3 MHz, a maximum quality factor (Q) of 32 at 3 MHz. The AC impedance measurements were performed by using impedance analyzer Solartron 1260. The semicircles in the impedance spectra shift to higher frequencies with increasing temperatures. The values of resistance (grain interior, grain boundary, and total) decreased with increasing temperatures. The semicircles of grain boundary and electrode are observed clearly. These data can be used to analyze typical the grain interior and the grain boundary resistance of Ni–Cu–Zn ferrite.  相似文献   

16.
An experimental research is performed on the complete compressive stress-strain relationship for concrete after heating to temperatures of 100-800 °C. All concrete specimens are ?15 cm × 30 cm standard cylinders, made with siliceous aggregate. The heated specimens are tested at 1 month after they are cooled to room temperature. From the results of 108 specimens with two original unheated strengths, a single equation for the complete stress-strain curves of heated concrete is developed to consider the shape varying with temperature. Through the regression analysis, the relationships of the mechanical properties with temperature are proposed to fit the test results, including the residual compressive strength, peak strain and elastic modulus. Compared with the experimental curves, the proposed equation is shown to be applicable to unheated and heated concrete for different temperatures. In addition, the split-cylinder tests of 54 specimens are also carried out to study the relationship of splitting tensile strength with temperature.  相似文献   

17.
Densification of nanocrystalline cubic yttria (nc-Y2O3) powder, with 18 nm crystal size and 1 wt% LiF as a sintering additive was investigated. Specimens were fabricated by spark plasma sintering at 100 MPa, within the temperature range of 700-1500 °C. Sintering at 700 °C for 5 and 20 min resulted in 95% and 99.7% dense specimens, with an average grain size of 84 and 130 nm, respectively. nc-Y2O3 without additive was only 65% dense at 700 °C for 5 min. The presence of LiF at low sintering temperatures facilitated rapid densification by particle sliding and jamming release. Sintering at high temperatures resulted in segregation of LiF to the grain boundaries and its entrapment as globular phase within the fast growing Y2O3 grains. The sintering enhancement advantage of LiF was lost at high SPS temperatures.  相似文献   

18.
Nickel oxide nanoparticles were synthesized via a simple and inexpensive microwave-assisted synthesis method within a fast reaction time of less than 20 min. The calcination of as-prepared precursor at 600 °C produces single phase nickel oxide. The lattice structure and morphology of the sample were investigated by X-ray diffraction, field-emission scanning electron microscopy and field-emission transmission electron microscopy. The particle size range of the nickel oxide nanoparticles varied from 50 to 60 nm. Nickel oxide nanoparticles exhibited good electrochemical performances as an anode material for lithium-ion batteries. The prepared nickel oxide anode revealed a large initial discharge capacity of 1111.08 mAh g−1 at 0.03 C rate and retained 80% of initial capacity (884.30 mAh g−1) after 20 cycles. Furthermore, at elevated rate of 3.7 C, the charge capacity of the nickel oxide electrode was as high as 253.1 mAh g−1, which was 35% greater than that of commercial bulk nickel oxide (188 mAh g−1). The enhancement of the electrochemical performance was attributed to the high specific surface area, good electric contact among the particles and easier lithium ion diffusion.  相似文献   

19.
杨鹏辉  姚远 《硅酸盐通报》2023,42(1):239-247
为探究橡胶再生集料在地聚物混凝土中的增韧作用,采用不同比例的橡胶再生集料(粒径为0.15~0.3 mm和1~4 mm)代替地聚物混凝土中的普通集料。首先,采用工业废渣中粒化高炉矿渣粉为原料,水玻璃溶液和NaOH为激发剂制备地聚物胶凝材料,并与普通集料、橡胶再生集料混合制备地聚物橡胶混凝土;然后对地聚物橡胶混凝土的力学性能、抗冲击性能和强度机理进行探究。结果表明:添加适量比例的橡胶再生集料可提高地聚物混凝土的抗压强度,增幅为5%左右,这与橡胶再生集料表面在NaOH碱环境中的氧化和降解作用有关;但地聚物橡胶混凝土在劈裂荷载和弯曲荷载下易断裂,劈裂抗拉强度和抗折强度降低20%~30%,这是地聚物橡胶混凝土的典型特点。通过落锤冲击试验和弯拉冲击试验可知,橡胶再生集料能大幅提高地聚物混凝土的抗冲击性能,最高增幅超过200%。这是由于橡胶再生集料具有的柔性和弹性特征吸收了部分冲击能量,同时延缓了冲击荷载下混凝土初始开裂到失效破坏过程,减少了裂缝开裂应力集中,提高了地聚物混凝土的延性。在地聚物碱性条件下,橡胶颗粒表面发生氧化和降解作用,表面变得粗糙,与地聚物基体结合紧密;橡胶表面在NaOH作用下,产生羟基、羧基等亲水基团,有利于水化产物在橡胶再生集料表面附着。  相似文献   

20.
In order to apply carbon/carbon composites (C/Cs) to various hot structures, secondary bonding techniques effective at elevated temperatures are frequently required. In the present study, carbon bonding between lamination type C/Cs was formed by the carbonation of polymer adhesive, and the strength of the bonding was evaluated at temperatures up to 2273 K in a vacuum using the double-notched shear method. The results revealed that bonding strength increased with increasing temperature and became higher than the inter-laminar shear strength of the substrate C/C when the bonding layer was thin. The enhancement of carbon bonding strength with increasing temperature was shown to be caused mainly by the evaporation of absorbed gases, probably water, up to temperatures of 1800 K with a slight additional contribution of thermal residual stress. It was also shown that heat treatment at higher temperatures made the bonding stronger.  相似文献   

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