Waste-bearing foamed ceramic from granite scrap and red mud

Using granite scrap and red mud as raw materials, SiC as foaming agent, powder sintering method was used to prepare closed-pore foamed ceramic. The effects of the ratio of red mud and granite scrap, foaming agent content, sintering temperature and holding time on the crystalline phase, pore structure, and performance of foamed ceramic were systematically studied. The results showed that, when the content of red mud was 10 wt%, together with 1.0 wt% SiC addition, the heating rate was 5°C/min, the foamed ceramic sintered at 1130°C for 30 min exhibited optimal properties, including bulk density of 483.11 kg/m³, porosity of 77.27%, compressive strength of 1.62 MPa and water absorption of .49%. Based on these properties, it possessed broad potential application prospects in the fields of sound and thermal insulation, lightweight construction materials. In this study, the utilization ratio of industrial solid waste was 100%, realized the comprehensive utilization of granite scrap and red mud, and provided a new idea to realize their low-cost utilization by preparing foamed ceramic with associated economic and environmental benefits.     

Spark plasma sintering of TiN ceramics codoped with SiC and CNT

In this research, we investigated the effects of SiC and multi-walled carbon nanotube (MWCNTs) addition on the densification and microstructure of titanium nitride (TiN) ceramics. Four samples including monolithic TiN, TiN-5?wt% MWCNTs, TiN-20?vol% SiC and TiN-20?vol% SiC-5?wt% MWCNTs were prepared by spark plasma sintering at 1900?°C for 7?min under 40?MPa pressure. X-ray powder diffraction patterns and scanning electron microscope (SEM) micrographs of the prepared ceramics showed that no new phase was formed during the sintering process. The highest calculated relative density was related to the TiN ceramic doped with 20?vol% SiC, while the sample doped with 5?wt% MWCNTs presented the lowest density. In addition, the SEM investigations revealed that the addition of sintering aids e.g. SiC and MWCNTs leads to a finer microstructure ceramic. These additives generally remain within the spaces among the TiN particles and prohibit extensive grain growth in the fabricated ceramics.     

Preparation of ultra-light ceramic foams from waste glass and fly ash

Ultra-light ceramic foams were successfully prepared by a green spheres technique, which used waste glass powder and fly ash as the main material. Besides, borax and SiC were introduced as fluxing agent and foaming agent, respectively. The effects of fly ash content, borax content and sintering temperature on the microstructures and properties of ceramic foams were systematically investigated. The optimum composition is 30?wt-% fly ash, 70?wt-% waste glass, 15?wt-% borax and 0.5?wt-% SiC. Ultra-light ceramic foams sintered at 680–780°C possess bulk density of 0.14–0.41?g?cm^?3, porosity of 82.9–94.1%, compressive strength of 0.91–6.37?MPa and thermal conductivity of 0.070–0.121?W?m^?1?K^?1, respectively. This method is convenient, low-cost and environment friendly, which makes it a promising way for recycling solid wastes.     

Synthesis and characterization of porous ceramics from spodumene tailings and waste glass wool

Glass wool waste remains a challenging waste fraction with relatively little utilization prospects. The present study investigated the development of porous ceramic materials from glass wool waste and spodumene tailings mainly made of quartz feldspar sand (QFS), with 0.05–0.5% silica carbide (SiC) as a pore-forming agent. The formulated compositions were sintered at 950 °C and analyzed in terms of mechanical properties, phase composition, and microstructure using X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray micro-computed tomography. The results showed that a synergetic effect of glass wool and SiC started to be significant from 15 wt% glass wool and 0.05 wt% SiC, the strength reducing and the porosity increasing with the increase of SiC. The porous ceramics were largely amorphous, with compressive strength ranging from 5 to 30 MPa while the water absorption and apparent density ranged from 2 to 10% and 0.7–1.2 g/cm³, respectively. The total porosity varied between 20 and 75%, and the wall thickness between 62 and 68 μm; besides, most of the prepared materials floated in water. These results are of interest for the repurposing of glass wool waste in the development of non-flammable lightweight materials for potential filtering or high-rise building applications.     

Microstructure and properties of a graphene platelets toughened boron carbide composite ceramic by spark plasma sintering

A kind of B₄C/SiC composite ceramic toughened by graphene platelets and Al was fabricated by spark plasma sintering. The effects of graphene platelets and Al on densification, microstructure and mechanical properties were studied. The sintering temperature was decreased about 125–300?°C with the addition of 3–10?wt% Al. Al can also improve fracture toughness but decrease hardness. The B₄C/SiC composite ceramic with 3?wt%Al and 1.5?wt% graphene platelets sintered at 1825?°C for 5?min had the optimal performances. It was fully densified, and the Vickers hardness and fracture toughness were 30.09?±?0.39?GPa and 5.88?±?0.49?MPa?m^1/2, respectively. The fracture toughness was 25.6% higher than that of the composite without graphene platelets. The toughening mechanism of graphene platelets was also studied. Pulling-out of graphene platelets, crack deflection, bridging and branching contributed to the toughness enhancement of the B₄C-based ceramic.     

Fine grained Al2O3/SiC composite ceramic tool material prepared by two-step microwave sintering

Fine-grained Al₂O₃/SiC composite ceramic tool materials were synthesized by two-step microwave sintering. The effects of first-step sintering temperature (T1), content and particle size of SiC on the microstructure and mechanical properties were studied. It was found that the sample with higher content of SiC was achieved with finer grains, and the incorporation of SiC particles could bridge, branch and deflect the cracks, thus improving the fracture toughness. Higher T1 was required for the densification of the samples with higher content of SiC (>5?wt%). The sample containing 3?wt% SiC particles with the mean particle size of 100?nm, which was sintered at 1600?°C (T1) and 1100?°C (T2) for 5?min had the fine microstructure and optimal properties. Its relative density, grain size, Vickers hardness and fracture toughness obtained were 98.37%, 0.78?±?0.31?μm, 18.40?±?0.24?GPa and 4.97?±?0.30?MPa?m^1/2, respectively. Compared to the sample prepared by single-step microwave sintering, although near full densification can be achieved in both two methods, the grain size was reduced by 36% and the fracture toughness was improved by 28% in two-step microwave sintering.     

Microstructural development during spark plasma sintering of ZrB2–SiC–Ti composite

The present study investigates the effect of Ti addition on the microstructure development and phase evolution during spark plasma sintering of ZrB₂–SiC ceramic composite. A ZrB₂–20?vol% SiC sample with 15?wt% Ti was prepared by high-energy milling and spark plasma sintering at 2000?°C for 7?min under 50?MPa. The X-ray diffraction test, microstructural studies and thermodynamic assessments indicated the in-situ formation of several compounds due to the chemical reactions of Ti with ZrB₂ and SiC. The Ti additive was completely consumed during the sintering process and converted to the ceramic compounds of TiC, TiB and TiSi₂. In addition, another refractory phase of ZrC was also formed as a result of sidelong reaction of ZrB₂ and SiC with the Ti additive.     

Effect of carbon content on electrical,thermal, and mechanical properties of porous SiC ceramics with B4C and C additives

The electrical, thermal, and mechanical properties of porous SiC ceramics with B₄C-C additives were investigated as functions of C content and sintering temperature. The electrical resistivity of porous SiC ceramics decreased with increases in C content and sintering temperature. A minimal electrical resistivity of 4.6 × 10^?2 Ω·cm was obtained in porous SiC ceramics with 1 wt% B₄C and 10 wt% C. The thermal conductivity and flexural strength increased with increasing sintering temperature and showed maxima at 4 wt% C addition when sintered at 2000 °C and 2100 °C. The thermal conductivity and flexural strength of porous SiC ceramics can be tuned independently from the porosity by controlling C content and sintering temperature. Typical electrical resistivity, thermal conductivity, and flexural strength of porous SiC ceramics with 1 wt% B₄C-4 wt% C sintered at 2100 °C were 1.3 × 10^?1 Ω·cm, 76.0 W/(m·K), and 110.3 MPa, respectively.     

Sintering behaviour and characterisation of low-cost ceramic foams from coal gangue and waste quartz sand

New ceramic foams have been successfully synthesised with coal gangue and waste quartz sand, which supply a feasible way to recycle these hazardous solid wastes. An objective of this research was to investigate the sintering behaviour and effects of sintering conditions on the crystalline phase change, microstructure and main properties of final ceramic foams. Good correlations among porosity, thermal conductivity, water absorption, bulk density, mechanical properties were studied. Results indicated that increasing sintering temperature or time had similar effects on the physical–mechanical properties. Samples sintering at 1140°C for 1 hour exhibited the highest porosity (87.5%), lowest bulk density (0.39?×?10^?3?kg?m^?3), lowest thermal conductivity (0.085?W·(m?K)^?1), moderate water absorption (9.38%) and adequate flexible strength (2.4?MPa). Combined with excellent properties and low-cost characteristics, the new development for ceramic foams preparation will be widely used in building insulation materials for no-load bearing walls.     

High-porosity mullite ceramic foams prepared by selective laser sintering using fly ash hollow spheres as raw materials

A novel method to prepare high-porosity mullite ceramic foams by selective laser sintering (SLS) using fly ash hollow spheres (FAHSs) as raw materials was reported. The complex-shaped FAHS green bodies and ceramic foams without delamination or cracks were prepared by SLS. The influence of sintering temperatures on linear shrinkage, phase composition, porosity and mechanical properties was investigated. With the increase of sintering temperature from 1250?°C to 1400?°C, the compressive strength of ceramic foams increased from 0.2?MPa to 6.7?MPa causing the fracture mechanism change from fracturing along FAHSs to across FAHSs, while the porosity of ceramic foams decreased from 88.7% to 79.9% which was higher than those of ceramic foams prepared by the conventional methods. The relatively high porosity of ceramic foams was resulted from the inner hollow structure of FAHSs, the interspaces between stacking FAHSs, and the gaps between FAHSs directly related to SLS. The results above indicated that the fabrication of high-porosity FAHS ceramic foams by SLS could achieve the advanced utilization of FAHS solid waste.     

Recycling of extracted titanium slag and gold tailings for preparation of self-glazed ceramic foams

Self-glazed ceramic foams were successfully synthesized via powder sintering method, using extracted titanium slag (ETS) and gold tailings (GT) as raw materials without adding any sintering aids and foaming agents. Influence of ETS addition and sintering temperature on crystal phase evolution, physical–mechanical properties, and micro-morphology of ceramic foams was systematically studied. Results indicated that products sintered at 1180 °C with 30 wt% ETS and 70 wt% GT showed the best performance, i.e., bulk density of 1.66 g cm^?3, flexural strength of 20.4 MPa, water absorption of 0.14%, open porosity of 0.23%, and glaze Vickers hardness of 6.5 GPa. Moreover, it was observed that there existed strong correlation between bulk density and bending strength. Self-glazed ceramic foams developed in this study are expected to be used as building envelope materials and provide new ideas for effective reuse of other similar solid wastes.     

Elaboration and characterization of tubular macroporous ceramic support for membranes from kaolin and dolomite

A low cost macroporous support for ceramic membranes was prepared by in situ reaction sintering from local natural mineral kaolin with dolomite as sintering inhibitor. The characterization focused on the phase evolution, microstructure, pore structure, mechanical strength and water permeability at various compositions and sintering temperatures. The sintering of kaolin was improved with 5 wt% dolomite, but clearly inhibited with ≥10 wt% dolomite. For the 20 wt% dolomite samples, the crystalline phases were mainly composed of mullite, cordierite and anorthite after sintering between 1,150 and 1,300 °C. Moreover, both mean pore size and mechanical strength increased with increasing sintering temperature from 1,100 to 1,300 °C, but the water permeability and porosity decreased. The 1,250 °C sintered macroporous support with 20 wt% dolomite exhibited good performances such as porosity 44.6%, mean pore size 4.7 μm, bending strength 47.6 MPa, water permeability 10.76 m³ m⁻² h⁻¹ bar⁻¹, as well as good chemical resistance. This work provides opportunities to develop cost-effective ceramic supports with controllable pore size, porosity, and high strength for high performance membranes.     

Low-temperature preparation of porous SiC ceramics using phosphoric acid as a pore-forming agent and a binder

Porous SiC ceramics combine the properties of both SiC ceramics and porous materials. Herein, we design a facile method via pressureless sintering at relatively low temperatures for the synthesis of porous SiC ceramics. In the synthesis process, phosphoric acid was used as the sintering additive that reacted with SiO₂ on the surface of SiC to form phosphates. The formed phosphates acted as a binder to connect the SiC particles. At a fixed temperature, the phosphates were partially decomposed and released a large amount of gas. This changed the pore structure of the ceramics and greatly improved their porosity. Finally, we obtained the porous SiC ceramics with high porosity and high strength. We investigate the effects of H₃PO₄ content on the phase composition, microstructure, porosity, mechanical properties and thermal expansion coefficient of the prepared porous SiC ceramics. It was shown that at the sintering temperature of 1200 °C, the highest porosity of the samples can reach 70.42% when the H₃PO₄ content is 25 wt%, and their bending strength reaches 36.11 MPa at room temperature when the H₃PO₄ content is 15 wt%. In addition, the porous SiC ceramics show good high-temperature stability with a bending strength of 42.05 MPa at 1000 °C and the thermal expansion coefficient of 3.966 × 10⁻⁶/°C.     

Influence of additive contents on the properties of SiC ceramic membranes and their performance in oil-water separation

The high processing cost is the key challenge for the economic industrial use of SiC membrane The aim of this research was to fabricate mullite bonded porous SiC ceramic membrane at low temperature from novel combinations of fly ash and alumina (FA) in weight ratio 44.5:55.5 as sintering additives. The influences of FA and pore former content on the porosity, morphology, crystalline phase composition, mechanical performance, permeability properties were investigated. The membrane prepared at 1300°C using 20 wt% FA showed pure water permeability 3690 Lm⁻²h⁻¹bar⁻¹ and exhibited high oil removal efficiency of ∼ 98% from the synthetic oil-water emulsion having oil concentration of 1000 mg/L. The corrosion behaviour of silicon carbide membrane in the strong acid and alkali solution and its mechanism were investigated. The utilization of fly ash successfully reduced the raw material cost and sintering temperature and the use of alumina reduced the amount of oxidation of SiC as well as increased the amount of mullite bond phase which resulted excellent mechanical strength to the final ceramics.     

Fabrication of low cost,green silica based ceramic hollow fibre membrane prepared from waste rice husk for water filtration application

In order to develop low cost ceramic membranes and effectively utilize abundantly and dumped waste agriculture, fabrication of green silica based ceramic hollow fibre membranes from waste rice husk was evaluated. Rice husk was converted into amorphous and crystalline silica based rice husk ash (ARHA and CRHA) by burning process at 600?°C and 1000?°C, respectively. The properties of silica based rice husk ashes were studied by transmission electron microscopy (TEM), x-ray powder diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), BET analysis, thermogravimetry and differential thermal analysis (TG/DTA) and x-ray fluorescence (XRF). Effect of silica content and sintering temperature towards membrane fabrication were investigated and characterized in term of morphological properties, mechanical strength, surface roughness, pore size distribution, porosity and pure water flux (PWF). The ceramic hollow fibre membrane (CHFM) prepared at 37.5?wt% CRHA content and sintered at 1200?°C achieved a good mechanical strength (71.2?MPa) and excellent porosity (50.2%). As a result, high PWF with value ~ 300?L/m² h and stable at 20?min was obtained. Due to the excellent pure water flux, the prepared ceramic membrane from waste rice husk hold promise for water treatment application.     

Effects of porosity on electrical and thermal conductivities of porous SiC ceramics

The effects of porosity on the electrical and thermal conductivities of porous SiC ceramics, containing Y₂O₃–AlN additives, were investigated. The porosity of the porous SiC ceramic could be controlled in the range of 28–64 % by adjusting the sacrificial template (polymer microbead) content (0–30 wt%) and sintering temperature (1800–2000 °C). Both electrical and thermal conductivities of the porous SiC ceramics decreased, from 7.7 to 1.7 Ω⁻¹ cm⁻¹ and from 37.9 to 5.8 W/(m·K), respectively, with the increase in porosity from 30 to 63 %. The porous SiC ceramic with a coarser microstructure exhibited higher electrical and thermal conductivities than those of the ceramic with a finer microstructure at the equivalent porosity because of the smaller number of grain boundaries per unit volume. The decoupling of the electrical conductivity from the thermal conductivity was possible to some extent by adjusting the sintering temperature, i.e., microstructure, of the porous SiC ceramic.     

Electrically conductive SiC ceramics processed by pressureless sintering

Polycrystalline SiC ceramics with 10 vol% Y₂O₃-AlN additives were sintered without any applied pressure at temperatures of 1900-2050°C in nitrogen. The electrical resistivity of the resulting SiC ceramics decreased from 6.5 × 10¹ to 1.9 × 10⁻² Ω·cm as the sintering temperature increased from 1900 to 2050°C. The average grain size increased from 0.68 to 2.34 μm with increase in sintering temperature. A decrease in the electrical resistivity with increasing sintering temperature was attributed to the grain-growth-induced N-doping in the SiC grains, which is supported by the enhanced carrier density. The electrical conductivity of the SiC ceramic sintered at 2050°C was ~53 Ω⁻¹·cm⁻¹ at room temperature. This ceramic achieved the highest electrical conductivity among pressureless liquid-phase sintered SiC ceramics.     

Fabrication and properties of SiC porous ceramics using a polyurethane preparation process

SiC porous ceramics can be prepared by introducing the polyurethane preparation method into the production process of ceramic biscuits, followed by sintering at 1300?°C for 2?h under N₂ flux after the cross-linking of polycarbosilane at 220?°C for 4?h in air. The microstructures, mechanical properties and infiltrations of the SiC porous ceramics are investigated in detail. The best dispersal effect comes from the SiC slurry with xylene as the solvent and a mixture of Silok®7096 (1?wt%) and Anjeka®6041 (4?wt%) as the dispersant. The compressive strength of SiC porous ceramics with high porosity (69.53%) reaches 16.9?MPa. The heat treatment can increase infiltration, the rate of which (4.296?×?10^?7 mm²) after the heat treatment at 750?°C in air is approximately two times faster than that before the heat treatment. The SiC porous ceramics fabricated in this study will have potential application in active thermal protection systems.     

Alkali-bonded SiC based foams

Silicon carbide (SiC) foams were developed by using a low temperature process such as chemical consolidation that is suitable to replace the sintering step. An alkali aluminosilicates binder, also known as geopolymer, was used. It was prepared from metakaolin, as aluminosilicatic raw powder, and KOH/K₂SiO₃ aqueous solution. The foaming agent was the metallic silicon present as impurity in SiC powders. Different grades of SiC were used as the main component (90 wt%) of the foams and the micro and macrostructures varied with the morphologies of the SiC raw powders. The surface of SiC grains participates to the geopolymeric process because of the dissolution of the silica layer into the alkaline solution. SiC foams were tested and characterized under oxidative atmospheres up to 1200 °C.     

Preparation and properties of anorthite-based ceramics by using metallurgical solid waste and fly ash

A large amount of metallurgical solid waste accumulation poses a serious threat to the environment. Study on synergistic reinforcement of synthetic process of metallurgical solid waste-based ceramics with fly ash is of great significance in reducing environmental pollution and resource utilization. A metallurgical solid waste-based ceramic used as building ceramic was developed with the erosion part of used MgO–C bricks and fly ash as main raw materials, and the amount of solid waste added to the prepared ceramics was at least 60 wt% and up to 90 wt%. The effects of fly ash content and sintering temperature on the crystalline phase transitions, morphologies, and the main physical and mechanical properties of ceramics were investigated by X-ray diffraction, scanning electron microscopy, and mechanical testing. The results show that the obtained ceramics presented maximum bending strength and minimum water absorption, 80.14 MPa and 5.04%, respectively, when the raw material proportions were the erosion part of used refractories accounted for 60 wt%, fly ash 20 wt%, pyrophyllite 10 wt%, and quartz sands 10 wt%, and the process parameters were the sintering temperature 1150°C, sintering time 120 min, and molding pressure 15 MPa.