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This work describes a novel approach to improve the dispersion of a nanoparticle MgCr2O4 additive in the matrix of magnesia-chrome refractories by functionalizing the nanoparticle surfaces with silanol groups. The effect of the silanol groups on the nanoparticles within the refractory matrix was shown by FTIR spectroscopy, zeta potential measurements, UV–visible spectroscopy, Dynamic Light Scattering (DLS) and TEM to result in a decrease of the average particle size of the MgCr2O4 additive by about 50% due to de-agglomeration of the nano particles by the silanol groups. Silanol functionalization of the nano-additives in the magnesia-chrome refractories fired at 1600 °C resulted in a 65 Kgf/cm2 increase in their compressive strength, while the hot modulus of rupture and corrosion resistance values of these refractories fired at 1400 °C were similar to those containing unfunctionalized nano-additives fired at 1600 °C. XRD and SEM results suggest the improvement in corrosion resistance is related to the formation of spinel phases in the refractories containing silanol-modified nano-additives.

Semiconducting nanocomposites were formed from layers of reduced graphene oxide (RGO) and ZnO and nanoparticle or mesoporous forms of TiO2 by dip-coating on fluorine-doped tin oxide (FTO) substrates. The effect of nanoparticle or mesoporous TiO2 on the electrical conductivity was compared. The crystalline phases and microstructures of the nanocomposites were investigated by XRD, DRS-UV, FTIR and FE-SEM, showing the layers to be homogeneous and of consistent thickness, with the TiO2 in the anatase form. The bandgaps and electrical conductivities of the nanocomposites, determined by Tauc plots and electrochemical impedance spectroscopy (EIS), show that under UV irradiation, the nanocomposites containing nanoparticle TiO2 have higher electrical conductivities than those containing mesoporous TiO2. A mechanism is suggested involving the formation of nano-capacitors on the surface of the ZnO layer, the pores in the mesoporous TiO2 acting as the dielectric and the conducting electrodes formed by UV irradiation of the TiO2.

Silicon carbide synthesis by a magnesiothermal method was investigated using MCM-48 as the silica source mechanically mixed with carbon nanotubes (CNTs) as the carbon source, and nanocomposites of MCM-48/functionalized CNTs (CNTF). SiC syntheses were carried out with different molar ratios of MCM-48, carbon and magnesium at 700 °C in argon. The MCM-48 and carbon nanotube starting materials and the SiC products were characterized by BET, XRD, FESEM, EDX and TEM. The effect of the carbon content and the type of CNTs (either functionalized or unfunctionalized) on the SiC synthesis was studied. The results show that an improved yield of SiC is obtained when the carbon nanotubes are functionalized, producing a better contact with the MCM-48. This improved contact between the reactants ensures a good degree of reaction in a stoichiometric mixture of silicon and carbon, with no improvement in product formation being achieved by the use of additional carbon. These findings suggest that the degree of contact between reactants is an important factor in the magnesiothermal synthesis of SiC. The SiC products from magnesiothermal synthesis of the functionalized nanocomposite precursors were shown by TEM and FESEM to have unusual nanofiber morphologies mimicking the morphology of the CNTF nanotubes.

Geopolymers are ceramic-like materials prepared at low temperatures by reacting natural aluminosilicates (clays) or aluminosilicate wastes (fly ash and blast furnace slag) with alkalis or acids. Like ceramics, they fracture in brittle mode, but graceful failure can be induced by fiber reinforcement. Since geopolymers are processed at low temperatures, organic reinforcing fibers can be used without thermal degradation. This chapter provides a brief description of the synthesis, structure, and properties of the aluminosilicate geopolymer matrix, and reviews the effect on the physical and mechanical properties of plant-based (cellulose) reinforcing fibers and protein-based fibers (wool). The possible degradation of the fibers by the highly alkaline geopolymer matrix is discussed, as well as the comparative benefits benefits associated with the mechanical properties of long and short fibers and woven cloth reinforcement. The literature reviewed here suggests that geopolymers produced at low temperatures (

A microstructural study of Coode Island Silt (CIS), a soft silty clay from the Melbourne area of Australia, stabilised with slag lime is reported. Slag lime is a blend of 80–85 wt% slag, 15 wt% hydrated lime, Ca(OH)2 and 3–8 wt% gypsum CaSO4.2H2O, and is typically used for soil stabilisation in roading applications. The morphologies of several homogeneous mixtures of slag lime and CIS were studied by Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD), which indicated the formation of the cementitious phases calcium carbonate, calcium silicate hydrate, calcium aluminium silicate hydrate, and calcium aluminium silicate carbonate. The progress of the CIS-slag lime reactions was also investigated by pH measurements. Slag lime was found to very actively promote pozzolanic reactions with CIS, shown by SEM to form crystalline reticular calcium silicate hydrate and other cementitious products. The most effective pozzolanic reactions occurred in a composite containing 12.5 wt% slag lime with CIS and contained the cement mineral ettringite, contributing to its high strength. These composites constitute a new class of materials with excellent potential for construction applications.

Nanocomposites of MCM-48 mesoporous silica and hydroxyapatite (HA) are investigated as possible alternatives for the commonly used Mineral Trioxide Aggregate (MTA) dental cement, and the effect of their Ca/P ratio on their structure, properties and setting times is reported. XRD, FTIR and EDS/SEM analysis of the nanocomposites indicate that crystalline HA is formed within the mesoporous silica structure. High Ca/P ratios lead to the formation of free CaO within the nanocomposite, decreasing its setting time; the shortest setting time (~ 40 min), which occurs in the MCM-48/HA nanocomposite with a Ca/P ratio of 5, in physiological saline solution, is considerably shorter than the setting time of MTA (~ 140 min under identical conditions). Thus, the shorter setting time of the MCM-48/HA nanocomposites, coupled with their lack of toxicity, high degree of bioactivity and their stability in tissue fluids, suggest that they could serve as a useful replacement for MTA.

Inorganic polymers (geopolymers) were synthesized by alkali activation of water treatment residue, a waste material containing aluminosilicates and a significant concentration of iron in the form of a ferric nanoparticle oxide gel. The effect on the structures of these geopolymers of incorporating the heavy metals chromium, zinc and iron, as occur in industrial wastewaters, was studied by their addition at the geopolymer synthesis stage, both as the pre-prepared hydroxides and as 1 M nitrate solutions. The heavy metals form several new crystalline phases, but the geopolymers display typical solid-state 27Al and 29Si MAS NMR characteristics. The 28-day strengths of the geopolymers without the metals (up to 11.2 MPa) were significantly degraded by the presence of the heavy metals, particularly 1 M zinc nitrate solution. The deleterious effect of the heavy metals on the strength may arise from their presence as the hydroxides rather than their incorporation as charge-balancing cations in the geopolymer structure. Leaching tests in simulated acid rain indicate that the geopolymers with molar ratios of SiO2/Al2O3 = 1.78 are capable of immobilizing all three metals to within safe leachate levels. The geopolymers are sufficiently strong to withstand handling and transportation and are capable of immobilizing wastes containing these heavy metals for storage or disposal.

New photoactive composites to efficiently remove organic dyes from water are reported. These consist of Cu2O/TiO2 nanoparticles in a novel inorganic geopolymer matrix modified by a large tertiary ammonium species (cetyltrimethylammonium bromide, CTAB) whose presence in the matrix is demonstrated by FTIR spectroscopy. The CTAB does not disrupt the tetrahedral geopolymer structural silica and alumina units as demonstrated by (29)Si and (27)Al MAS NMR spectroscopy. SEM/EDS, TEM and BET measurements suggest that the Cu2O/TiO2 nanoparticles are homogenously distributed on the surface and within the geopolymer pores. The mechanism of removal of methylene blue (MB) dye from solution consists of a combination of adsorption (under dark conditions) and photodegradation (under UV radiation). MB adsorption in the dark follows pseudo second-order kinetics and is described by Freundlich-Langmuir type isotherms. The performance of the CTAB-modified geopolymer based composites is superior to composites based on unmodified geopolymer hosts, the most effective composite containing 5wt% Cu2O/TiO2 in a CTAB-modified geopolymer host. These composites constitute a new class of materials with excellent potential in environmental protection applications.

The photocatalytic activity of mesoporous TiO 2 modified by the addition of carbon nanotubes (CNTs) and Cu is reported. Nanocomposites of carbon nanotubes (CNTs) containing varying amounts of Cu were formed by treatment with Cu 2+ then reduced to Cu 0 using NaBH 4 as the reducing agent. The mesoporous TiO 2 , synthesized by a sol-gel method from titanium isopropoxide, was combined with the CNT/Cu nanocomposites to form the photocatalysts which were characterized by XRD, SEM, TEM, FTIR, XPS and BET surface area analysis. The photocatalytic properties of the mesoporous TiO 2 composites were studied by measuring the degradation of methyl orange (MO) which was optimal in the sample containing 20 wt% of the Cu-CNT nanocomposite. The degradation efficiency for MO was a synergistic effect of photo-degradation of TiO 2 and may be due to improvement of the electrical conductivity of the system by the presence of the CNT/Cu networks, since the photodegradation of MO and the photocatalytic activity of the photoactive systems increased with increasing copper content.

A new synthesis of β-Sialon/TiN composites by reaction bonding of aluminium powder coated with nanosized titania is reported. A sol–gel method was used to coat the aluminium particles with titania and the resulting powder was calcined in an inert atmosphere to produce a Ti x Al y –Al 2 O 3 composite which was heat-treated in nitrogen to form an AlN–Al 2 O 3 –TiN composite. After addition of a suitable silicon phase and yttrium oxide as a nitridation and sintering aid, a β-Sialon/TiN composite was formed by reaction bonding under nitrogen. Young׳s modulus, hardness, fracture toughness, tensile strength and thermal shock resistance of the new composites were measured and compared with a standard β-Sialon fabricated by reaction bonding of Al 2 O 3 , AlN and Si under similar conditions.

The synthesis of novel composites of spherical Cu2O nanoparticles and P25 TiO2 with aluminosilicate inorganic polymers (geopolymers) is described and the morphology of the homogeneous oxide nanoparticle dispersion within the geopolymer matrix demonstrated by SEM/EDS and TEM. XRD and FTIR confirmed the formation of a well-reacted geopolymer matrix that was unaffected by the insertion of the Cu2O/TiO2 nanoparticles. Experiments in dark conditions and under UV irradiation showed that these materials efficiently remove a model organic pollutant (methylene blue dye) from solution by a dual process of adsorption on the geopolymer matrix, and photodecomposition of the dye without destroying the geopolymer structure. The adsorption kinetics are described by a pseudo-first-order model and Freundlich-type isotherms. Incorporation of 10 wt% Cu2O/TiO2 nanoparticles into the geopolymer composites decreases their adsorption ability by blocking the active adsorption, sites, but at higher Cu2O/TiO2 concentrations, dye adsorption is facilitated, probably by expanding the geopolymer matrix structure. Under UV irradiation, the composites remove the MB dye by a combination of adsorption and photodegradation without destroying the geopolymer structure. The combination of nanosized Cu2O particles and photoreactive P25 titania in an aluminosilicate inorganic polymer matrix is a more efficient photocatalyst under UV irradiation than geopolymer composites containing either of the individual oxides alone. These new geopolymer composites show promise as ecologically-friendly materials which can efficiently remove organic pollutants from water or the atmosphere.

Inorganic polymers (geopolymers) containing carbon are shown to be viable precursors for CRN synthesis of SiAlONs at 1400 °C in nitrogen. The reaction mechanism and rate depends on the form and fineness of the carbon, the formation of β-SiAlON being faster and more complete with fine carbon black. The presence of the charge-compensating alkali cations in the geopolymer leads to the formation of a mixture of β-SiAlONs of low and high z -value, the former being formed via O-SiAlON resulting from the presence of silica-rich eutectics, and the latter forming by CRN reaction from an alumina-rich amorphous component. In ammonium-exchanged geopolymers lacking the alkali, SiAlON formation occurs primarily by conventional CRN of crystalline mullite and cristobalite intermediates. The potential advantages of geopolymer CRN precursors include their ability to be tailored to specific SiAlON compositions and their formation and curing at ambient temperatures to required shapes prior to the CRN reaction.

Magnesiothermal synthesis of nanosized SiC has been successfully achieved from a mixture of the natural zeolite clinoptilolite and a high-surface area mesoporous carbon CMK-1, synthesized by impregnating a mesoporous silica template MCM-48 with sucrose, followed by carbonization in argon and removal of the silica template. Magnesium powder was used to initiate the self-combustion reaction. Removal of the alkaline and alkaline earth exchangeable cations from the clinoptilolite by ion exchange with NH 4 + was essential for a good yield of product, which is also dependent on the use of excess of carbon. TEM confirmed the nanostructure and size of the 15–25 nm SiC product crystallites.

Novel photoactive composites of cubic Cu2O nanoparticles with aluminosilicate geopolymers were prepared and their structure was shown by SEM/EDS and TEM. XRD, FTIR, 27Al and 29Si MAS NMR to consist of a well-reacted geopolymer matrix containing homogeneously dispersed Cu2O nanoparticles. Under dark conditions, both the geopolymer matrix and the composites were shown to adsorb a model organic compound (methylene blue, chosen for its colour stability at high pH) by a process which follows pseudo-first-order kinetics and can be described by Langmuir-type isotherms. At concentrations >20 wt%, the oxide decreases the adsorption rate by blocking the active adsorption sites of the geopolymer. Under UV radiation, the composites remove the methylene blue by a combination of adsorption and photodegradation, without deterioration of the geopolymer structure or the photoactive Cu2O component, as evidenced by 63Cu NQR spectroscopy, suggesting that these geopolymer composites should function as useful new materials for the removal of organic pollutants from water or the atmosphere.

This paper reports the synthesis and characterization of a microporous geopolymer body based on metakaolin. Two kaolinites were used as the starting materials in conjunction with sodium silicate and sodium hydroxide and three sizes of polylactic acid (PLA) fibers (12, 20 and 29 mm diameter) were used as the pore-forming media. The microporous bodies were formed from geopolymer pastes of optimized composition by extrusion, which yielded bodies with reasonably well-aligned pore-forming fibers which were decomposed by the alkaline conditions during curing and drying of the bodies. XRD, FTIR, 27 Al MAS NMR, and SEM were used to characterize the chemistry and microstructure of the porous products and their compressive strengths were also measured. The molar composition SiO2/Al2O3¼4 was found to give the best geopolymer characteristics, while the optimal ratio Na2O/Al2O3 which affected the leachability of the PLA fibers and thus the size of the resulting pores, was optimized in the range 1.5–1.75 depending on the kaolinite. Water permeability measurements indicate that the use of PLA fibers as pore-formers significantly increases the permeability of the samples, while the maximum pore size of the porous bodies, determined by bubble point measurements, is related to the size of the particulate matter that could be retained, and indicates that their performance could be tailored for particular filtering applications by adjusting their synthesis parameters. & 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.

Nanostructured SiC was synthesized by magnesiothermal reduction of silica derived from zeolite ZSM-5 with a Si/Al ratio of about 80 and four carbons from different sources. The carbons were carbon black and three carbons synthesized by impregnating furfuryl alcohol or sucrose into three porous templates (ZSM-5, clinoptilolite and MCM-48). Magnesiothermal reduction was carried out by reacting mixtures of silica, carbon and magnesium powder at 600–800 °C in a flowing argon atmosphere. The starting materials and final products were characterized by X-Ray diffraction, thermogravimetric analysis, scanning electron microscopy and BET analysis. The results indicated that the synthesis of nanostructured SiC is influenced by the chemical nature of the carbon and its surface area.

Fly ash from the 4th thermal power station of Ulaanbaatar city has two drawbacks to its use as a raw material for producing geopolymers suitable for construction applications; these are its high radium equivalent radioactivity resulting from the radioactive Mongolian coal burnt in this power station (314–343 Bq/kg), and its high CaO content (14–30 wt%). Two fly ashes, from the Baganuur and Shivee Ovoo coal deposits were activated either by sodium hydroxide solution or mixtures of sodium hydroxide and sodium silicate solutions and cured at 70 °C for 22 h. Flash setting of these high-calcium fly ash systems occurs where the activating solutions contain sodium silicate in addition to NaOH, but the fly ashes can be activated by 8 M NaOH solution alone, producing pastes with usefully long setting times (up to 10 h) and good 7-day compressive strengths (up to 32 MPa in the Baganuur ash and 23 MPa in the Shivee Ovoo fly ash). The addition of 1–5 mm river gravels produced geopolymer concretes with 7-day compressive strengths of 26 MPa and good freeze-thaw resistance. The radioactivity of the concretes prepared from these fly ashes was 130–152 Bq/kg, well within the standard safe limits for construction of dwellings. The durability of the concrete is influenced by the mineralogy of the calcium component of the fly ash; the presence of crystalline calcium components such as lime, anhydrite and amorphous calcium compounds in the higher-Ca Shivee Ovoo fly ash negatively influencing the freeze-thaw resistance. By contrast, Baganuur fly ash, which contains less calcium in the form of crystalline components, produces a geopolymer concrete with high durability.

A novel in situ synthesis is presented of a hydroxyapatite composite with the mesoporous silicate MCM-48 with potential applications as a drug delivery agent. The structure and properties of this nanocomposite, investigated by a number of techniques including XRD, SEM and TEM, show the intergrowth of the hydroxyapatite particles with the silica structure. The bioactivity of the new material was determined by measuring the decrease in the calcium ion concentration of simulated body fluid (SBF) after soaking the nanocomposite, while the uptake of ibuprofen on MCM-48 and MCM-48/HAp composite from ethanol was monitored by UV spectroscopy at 222 nm which was also used to monitor the release of ibuprofen into SBF, MTT assay was used to assess effect of the sample on MG68 cell live proliferation. The results confirm the successful synthesis of a MCM-48/hydroxyapatite nanocomposite and its potential biomedical applications as a bioactive ceramic and as a drug delivery agent with a higher rate of ibuprofen release compared to MCM-48.

The aim of this paper was to improve the magnetic properties of magnetoplumbite-type (M-type) strontium hexaferrite substituted with Co 2+ –La 3+ produced by conventional ceramic forming techniques. The effect on the magnetic properties of varying the composition of the target compound Sr 1− x La x Fe 12− y Co y O 19 and the primary and secondary firing temperatures was investigated. Microstructure studies and XRD phase analysis indicated that optimum values of the remanent magnetization B r and coercive field H cj were obtained with a primary firing temperature of 1240 °C and a final firing temperature of 1180 °C, where ( x = y ) th 1 =0.15, ( y / x ) exp 2 =0.75 and the molar ratio of ferric oxide to strontium oxide=5.8. The optimized magnetic properties obtained under these conditions were B r =4070 Gs, H cj =4710 Oe, ( H k / H cj )=82.

The formation of an X-sialon/mullite nanocomposite by a combination of mechanical activation and silicothermal reduction and nitridation is reported. The starting materials (andalusite, Si and various aluminium sources) were activated in a planetary mill and fired in N2 at 1450 °C. Microstructure and phase analysis was carried out on fired and unfired samples using X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Taguchi statistical experiments were carried out to optimize the formation and crystallinity of the X-sialon component of the sialon–mullite composite. The milling time is the factor of greatest influence on the formation and crystallite size of X-sialon; milling for 15 h increases the amount of X-sialon formed but longer milling times decrease the crystallinity of the products and the sialon/mullite ratio. High-energy milling of an andalusite/Si/alumina mixture produces a mullite-sialon nanocomposite powder. TiO2 additive stabilises the mullite component whereas Y2O3 enhances the formation of X-sialon and Al(OH)3 increases the crystallinity. The optimized conditions for the production of X-sialon/mullite nanocomposite powders are the use of Al2O3 as the Al source, milling time 15 h, avoiding the use of TiO2 as an additive.

Nanocomposites of Al–SBA-15 with the organic polymers poly-4-vinyl pyridine (P4VP) and polyacrylamide (PAM) were synthesized to produce SiAlON precursors containing various carbon contents. These CRN precursors, and their products after firing under N 2 at 1450 °C for 3 h were investigated by XRD, SEM/EDS and surface area analysis (BET) to compare the influence of the organic polymer carbon source. The results were also compared with those from precursors containing carbon black as the carbon source. XRD and SEM/EDS analysis of the Al–SBA-15 confirmed the formation of mesoporous structures, while BET and pore size distribution measurements indicated that the entry of P4VP into the Al–SBA-15 nanocomposite precursor is significantly more efficient than that of PAM. Firing these precursors in nitrogen produced β-SiAlON and β-cristobalite. At all carbon concentrations the P4VP nanocomposite precursors formed significantly more SiAlON than those of the PAM and carbon black precursors, due to the proximity of a greater amount of the organic carbon source to the silica template in the P4VP composite, and possibly also to the lack of oxygen in the P4VP monomer, in contrast with PAM. At least twice the stoichiometric amount of carbon was required in all cases, with optimal SiAlON formation occurring in the P4VP precursor containing 6 times the stoichiometric amount of carbon. Increasing the carbon content further suppresses SiAlON formation, possibly due to the build-up of back pressure of CO by-products in the pores of the nanocomposite.

Li-geopolymer precursors containing silicon were fabricated by a solid-state method and fired in nitrogen at 1100°C–1400°C to produce lithium aluminosilicate (LAS), the amount and crystallinity of which was independent of the silicon used, as shown by X-ray diffraction and solid-state magic angle spinning nuclear magnetic resonance (MAS NMR). LAS/Al2O3 composites were formed by adding ρ-Al2O3 to the Li-geopolymer precursor and firing under nitrogen at 1400°C. Although no nitride phases were formed under these reaction conditions, scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) showed a small amount of unreacted silicon in the fired samples, suggesting that it may be possible to adapt this procedure to produce LAS-nitride composites.

Aluminosilicate nanotubes and Cu(II)-grafted TiO2 composites were prepared, and the acetaldehyde degradation activity of the composites was evaluated at various relative humidities. The aluminosilicate nanotubes were synthesized hydrothermally and characterized by TEM, XRD, 27Al and 29Si NMR, FT-IR, N2 and water vapor isotherms. Their morphology was nanotubular with 3–5 nm outer diameter, and the specific surface area was 245 m2/g. The aluminosilicate had a strong affinity for water molecules, and the structure was determined to be an imogolite by 27Al and 29Si NMR. TiO2 and imogolite composites exhibited higher activity for the photodegradation of acetaldehyde under UV irradiation than TiO2, but was dependent on the relative humidity. Cu(II)-grafted TiO2 and imogolite composites exhibited higher activity for the photodegradation of acetaldehyde under visible light irradiation than Cu(II)-grafted TiO2, and were less affected by the relative humidity. These results show that Cu(II)-grafted TiO2 - imogolite composites exhibit very efficient absorption and photodecomposition of acetaldehyde in a variety of environments.

Highly charged swelling sodium micas (Na-2-, Na-3-, and Na-4-micas) with different layer charge densities were synthesized and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and solid-state 29Si and 27Al magic-angle spinning nuclear magnetic resonance (MASNMR) spectroscopy. Their ion exchange properties were examined for Sr2+ and Ba2+ ions using isotherms and Kielland plots. XRD patterns after 2Na+ → Sr2+ or Ba2+ exchange were investigated to check for change in ‘d’ values of 0 0 1 reflections of Na-micas. The ‘d’ values of 0 0 1 reflections were shifted from two-layer hydrate to one-layer hydrate depending on layer charge density and the extent of ion exchange by divalent cations. A comparison of shifting in ‘d’ values of 0 0 1 reflections indicates that there are two different hydration states of Sr2+ and Ba2+ in the interlayer space of Na-micas. Na-2-mica showed the highest selectivity for Sr2+ and Ba2+ among Na-micas because of easier expansibility of its interlayers and thus accessibility to exchanging sites. Therefore, Na-2-mica is a good candidate for decontamination of Sr2+ and Ba2+ from drinking water and contaminated soils or nuclear waste solutions.

Nano-silicas extracted from a pure rice husk ash calcined in the laboratory (RHA) and ash from an impure industrial rice husk waste (BRHA), were used to form belite cement by firing with two different calcium sources (calcium carbonate and calcium nitrate). The nano-silica extracted from RHA was highly reactive due to its high pore volume and low activation energy of dehydration. The formation of belite cement from both nano-silicas was studied by firing with two different calcium sources, Ca(NO 3 ) 2 and CaCO 3 at 800–1100 °C. Both nano-silicas formed the principal phase in belite cement (larnite or β-C 2 S) at temperatures as low as 800 °C, especially with calcium nitrate as the calcium source. Thus, highly impure BRHA is shown to be very suitable as a starting material for the low-temperature production of belite cement, especially in conjunction with calcium nitrate as the calcium source.

Attempts to synthesise magnesium-containing analogues of aluminosilicate geopolymers from the 1:1 and 2:1 layer magnesiosilicate minerals chrysotile and talc, as well as the magnesium mineral sepiolite are reported. The effect of pre-treating these starting minerals by grinding and/or dehydroxylation was also investigated by XRD, 29Si and natural-abundance 25Mg solid-state magic angle spinning (MAS) NMR spectroscopy. The products from sepiolite most closely resembled an aluminosilicate geopolymer, setting at 40 °C to an X-ray amorphous product containing a broad characteristic 29Si MAS NMR resonance at −90 ppm. The 25Mg MAS NMR spectrum of this product also showed evidence that some of the Mg was located in tetrahedral sites, as expected for a conventional geopolymer. A similar 25Mg MAS NMR result was obtained for chrysotile, but talc proved to be extremely resistant to geopolymer synthesis, requiring treatment at 120 °C for 3 days to set to a friable material retaining the XRD and NMR characteristics of the original talc or its crystalline dehydroxylation products. This lack of reactivity may be related to the 2:1 layer-lattice talc structure, or to the fact that a suitably reactive amorphous product is not formed upon dehydroxylation.

Two different microporous Na-titanosilicates with high cation exchange capacities were synthesized and characterized by X-ray diffraction, scanning electron microscopy (SEM) and solid-state 29 Si and 27 Al magic-angle spinning nuclear magnetic resonance (MASNMR) spectroscopy. The ion exchange properties of Na-ETS-4 (ETS = Engelhard TitanoSilicate) and Na-titanosilicate were investigated for Sr 2+ and Ba 2+ using isotherms and Kielland plots in order to check the potential for the decontamination of 90 Sr and 133 Ba from nuclear waste solutions. Na-ETS-4 and Na-titanosilicate show high affinity for Sr 2+ to high equivalent fraction of Sr 2+ on solid phase. In case of Ba 2+ the selectivity coefficient of both titanosilicate exchangers rapidly decreased due to the steric hindrance at exchange sites at X ¯ Ba > ∼0.5. However, Na-ETS-4 was still selective for Ba 2+ even after the above rapid decrease in selectivity, unlike Na-titanosilicate. Therefore, Na-ETS-4 is one of the best candidates for the removal of both Sr 2+ and Ba 2+ from nuclear waste solutions.

The nanocomposite precursor (P4VP/Al-SBA-15) was synthesized and then fired under N2 atmosphere at 1450°C with 10°C/min heating rate and soaking time of 0 and 6 h in order to form β-SiAlON by using the carbothermal reduction and nitridation process (CRN). The nanocomposites was characterized by small-angle XRD (SXRD), microstructure studies (TEM/DSC) and 27Al-NMR (MAS-NMR). Results, from the sample fired under N2 atmosphere, showed that not only the carbon amount, type of carbon and the surface area of the precursor was important, but that a higher than stochiometric amount of carbon was unavoidable.

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 Na 2 O/SiO 2 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 Na 2 O/SiO 2 = 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.

This paper reports the use of a nanocomposite precursor of mesoporous silica–alumina (Al-SBA-15) with poly 4-vinyl pyridine (P4VP) to synthesise β-SiAlON by carbothermal reduction and nitridation under N2 at 1,450 °C. Small-angle XRD, SEM/TEM, 29Si and 27Al MAS-NMR and BET specific surface area measurements of the Al-SBA-15 and P4VP/Al-SBA-15 composite confirmed the mesoporous structure and the presence of Al in the precursors, while surface polymerization of the Al-SBA-15 was indicated by 29Si-NMR. Firing the nanocomposite in a N2 atmosphere forms the nitride phase, depending on the amount and type of carbon present, on the surface area of the precursor. Even with these precursors of high surface area, the present result was obtained using approximately twice the stochiometric amount of carbon.

Strontium hexaferrite (SrFe12O19) which crystallizes in the hexagonal system and has a uniaxial magnetoplumbite structure, displays distinctive magnetic characteristics, good chemical stability, good tribological properties and a weak temperature dependent coercivity at about room temperature. In the present work the synthesis conditions for the solid-state preparation of the chromium-doped hexaferrite SrCr0.3Fe11.7O19 were optimised and the effect on the magnetic properties of this compound of additions of nanosized SrFe12O19 was studied. The nanosized SrFe12O19 additive, synthesized by the citrate–nitrate reaction, was substituted in varying amounts for a commercial calcium silicate borate sintering additive mixture. A combination of 0.75 wt% of nano-sized SrFe12O19 with 0.75 wt% of the commercial additive increases the intrinsic coercivity, remanence magnetization and rectangularity ratio and results in superior magnetic properties than obtained with 1.5 wt% of nanosized SrFe12O19 or the commercial sintering additive alone.

Lithium aluminosilicate inorganic polymers were synthesised from dehydroxylated kaolin-type clay (halloysite) by the conventional method under highly alkaline conditions with lithium hydroxide or lithium silicate solutions of two different Li2O/SiO2 molar ratios. Variants were also developed of a solid-state synthesis method involving the thermal reaction of dehydroxylated halloysite with LiOH followed by hydration of the product. The molar compositions of the materials prepared by all three methods (SiO2/Al2O3 = 2.41–3.27, Li2O/SiO2 = 0.30–0.61, and H2O/Li2O = 9.33–10.40) fall within the range of compositions previously reported to produce viable geopolymers. Curing at 40 °C produces solid samples of varying viability depending on the amount of synthesis water. The cured materials are not characteristically X-ray amorphous, but contain the lithium zeolites Li-ABW and fibrous Li-EDI, the latter in the materials synthesised by solid-state reaction. The 27Al and 29Si MAS NMR spectra of the cured materials contain narrow resonances more characteristic of zeolites than of inorganic polymers. Heating the synthesised products at

A new synthesis method is described to produce aluminosilicate inorganic polymers by direct reaction of aluminium hydroxide with amorphous silica under alkaline conditions. XRD and 27Al and 29Si MAS NMR spectroscopy suggest that the reaction mechanism involves the dissolution of the aluminium hydroxide in the alkali. The best results are obtained with more reactive gibbsite of small particle size and X-ray amorphous ρ-alumina containing 5-fold coordinated Al, and with compositions in the previously reported optimum range (SiO2: Al2O3 = 3.0, M2O: SiO2 = 0.34, H2O: M2O = 9.4). Unreacted aluminium hydroxide occurs where there is insufficient silica for complete inorganic polymer formation but the reaction is less sensitive to variations in the K2O: Al2O3 and K2O: SiO2 ratios. Zeolite formation was not observed in any of the present samples. More complex alumina sources such as thermally activated hydrotalcite can also be used to form an inorganic polymer, but under the alkaline synthesis conditions the unused alumina reacts with the poorly crystalline MgO present to re-form hydrotalcite, presumably containing atmospheric carbonate as the interlayer anion. This synthesis method can also potentially be extended to hydroxides other than those of aluminium.

In vitro studies are reported of the behaviour of potassium aluminosilicate inorganic polymers containing 10 wt% Ca(OH)2, nanostructured calcium silicate and Ca3(PO4)2 exposed to simulated body fluid (SBF). Heating to 600 °C lowers the alkalinity of Ca3(PO4)2-containing samples, but their X-ray powder diffraction characteristics, 27Al, 29Si and 43Ca MAS NMR spectra are unchanged by heating. Exposure of the heated compounds to SBF usually results in the formation of the crystalline biomineral phases hydroxylapatite and hydroxycarbonate apatite in the samples containing Ca(OH)2 and Ca3(PO4)2, but scanning electron microscopy/energy dispersive spectroscopy suggests that all the samples in the present study form calcium phosphates on exposure to SBF. This conclusion is also consistent with the removal of P from the SBF by all the samples. The concentrations of Al leached from the samples containing nanostructured calcium silicate and Ca3(PO4)2 (0.05 and 0.47 ppm, respectively) are acceptable for biomaterials use, but apart from the Ca3(PO4)2-containing sample, which takes up Ca from the SBF, the levels of Ca released into the SBF by the other samples are well in excess of the published optimum amount for stimulation of new bone growth by gene transcription in osteoblasts. Only the calcium silicate-containing samples release Si into the SBF, but in a concentration that falls short of the optimum amount. The strength of all the present compounds after heating is probably adequate for applications as biomaterials, but the Ca3(PO4)2-containing compound shows slightly greater strength. Thus, on balance, the Ca3(PO4)2-containing compound appears to be the most promising as a bioactive material.

The DC electrical conductance of potassium aluminosilicate inorganic polymers (geopolymers) containing up to 6 wt% single-wall carbon nanotubes has been determined as a function of temperature up to 340 °C. After removal of the processing water during the first heating cycle, the conductance in subsequent heating cycles increases as a function of carbon nanotube content and temperature from 9.75 × 10−4 to 1.87 × 10−3 S m−1 in the composites containing 0 and 0.2 wt% carbon nanotubes, respectively, at 290 °C. By comparison, the electrical conductance of potassium inorganic polymer composites containing graphite was generally lower. The conductance activation energies of the carbon nanotube and graphite composites were similar, and decreased from about 55 to 5 kJ mole−1 with increasing carbon content. The tensile strengths of carbon nanotube and graphite-containing potassium geopolymer composites, determined by the Brazil method on 10–12 replicates, were about 2 MPa, and showed little change with increasing carbon nanotube content up to 0.3 wt%. By contrast, the tensile strengths of an analogous set of sodium composites were up to four times greater, possibly reflecting the necessity for less processing water in the synthesis of the sodium samples.

Ceramics based on Bi 3 NbTiO 9 (BNT) were investigated for their high-temperature pyroelectric properties. Doping BNT with 0.05 atoms of W 6+ donor ions decreased its DC conductivity, enhanced its dielectric strength and remnant polarization. Thick films of BNT produced by airflow deposition show preferential grain orientation and enhanced sinterability, giving improved polarizability and higher dielectric strength than the comparable ceramic. Further improvements in grain orientation and enhanced remnant polarization are derived by sintering under an applied electric field. Airflow deposition was also used to prepare graded films of Ba (1− x ) Sr x TiO 3 (BST), showing temperature dependent hysteresis offsets that originate from asymmetric leakage currents and are not related to the pyroelectric properties. These graded films show an enhanced conventional pyroelectric coefficient over a wide temperature range. These results predict that a graded structure of BaBi 2 Ta 2 O 9 and Bi 3 NbTi 0.95 W 0.05 O 9 should show enhanced high-temperature pyroelectric properties.

Bismuth forms double oxides with the oxides of aluminium, gallium, iron and manganese, all of which have the mullite structure. Since other bismuth-based complex oxides show useful functional properties including high-temperature pyroelectricity and piezoelectricity, the electronic and magnetic properties of the mullite-structured bismuth compounds are of potential interest. In the present study, all the above compounds were synthesised in pure form by solid-state reaction, and their thermal behaviour and structures characterised by thermal analysis, powder X-ray diffraction, solid-state MAS NMR and Mőssbauer spectroscopy as appropriate. The thermal analysis information allowed highly sintered polycrystalline samples to be produced. After the application of silver electrodes, the electronic properties of the pellet samples were determined as a function of frequency and temperature up to 900 °C. Frequency-dependent inflexions in the relative permittivity and loss angle curves of the ferrate and gallate may be due to losses due to dielectric relaxation, but the most notable and consistent electronic phenomenon in all samples is a steep rise in the dc conductivity at higher temperatures. The P – E hysteresis loops for the ferrate and manganate indicate that these are very poor ferroelectric materials, consistent with the centrosymmetric crystal structure of all these compounds.

Al-27 magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectra were acquired at 8.45, 14.1 and 16.45 T for a series of aluminium borates with the mullite structure (Al6-x B (x) O-9, where x has nominal values of 1 to 4) augmented with Al-27 multiple-quantum MAS NMR spectra at 8.45 T. Even though the Al-27 NMR spectra are complex, simulation of the combined set of data produced a relatively well-defined set of parameters (e.g., quadrupolar interaction, isotropic chemical shift, etc.) for each site. The B-11 MAS NMR spectra of the same compounds were also acquired at 14.1 T. Linear changes in the X-ray a-, b- and c-cell parameters with composition suggest that these compounds constitute a continuous series. Based on a Rietveld structural refinement of the compound synthesized as Al4B2O9, the resulting site occupancies and relative site distortions allow the identification of particular sites with specific NM resonances. Changes in the Al-27 and B-11 MAS NMR spectra of the related compounds with x = 1-4 show at the lowest Al contents a greater degree of asymmetry in the Al sites of the octahedral chains. A fairly distorted cross-linking tetrahedral site, which persists throughout the composition range, is accompanied in the lower Al compositions by two 5-fold coordinated Al-O units which are replaced by two more-regular tetrahedral Al-O sites as the Al content increases. In the compounds of lowest Al composition (i.e., highest B content) both the tetrahedral and trigonal cross-linking sites are distinguishable, but as the Al content increases, the BO4 units progressively disappear.

Al-containing mesoporous silicas were synthesized by hydrothermal treatment of microporous silica prepared by selectively acid leached metakaolinites with Si/Al = 3.9–92.5 mixed with a surfactant of cetyltrimethylammonium bromide (CTABr). The specific surface area of the products increased with higher surfactant/microporous silica (surf/Si) ratio and Si/Al ratio of the microporous silica, reaching about 1400 m2/g at CTABr/Si ⩾ 0.1 and Si/Al ⩾ 40. The XRD patterns of these products show a hexagonal (100) peak with the lattice parameter a0=4.2–4.3nm and the N2 adsorption isotherms show steep increase of adsorption between relative pressure of 0.3 and 0.4. Hexagonal mesoporous microstructure is observed by high resolution TEM. The pore size distributions of the products show a sharp peak at 2.8 nm by the BJH method. The high specific surface area of the present mesoporous samples is attributed to the lower matrix density and surface roughness of mesopore wall. The highest specific surface area of the products reached up to 1420 m2/g and this value is apparently higher than those reported in hexagonal mesoporous silicas. A unique microporous structure of the starting material is thought to be related to achieve such a high specific surface area of the products.

Aluminosilicate geopolymers with SiO2/Al2O3 ratios ranging from 0.5 to 300 have been prepared from mixtures of dehydroxylated kaolinite with either ρ-Al2O3 or fine Aerosil SiO2, with the ratios Na2O/SiO2 and H2O/SiO2 kept constant throughout the series. All the compositions hardened at ambient temperature, but the high-alumina compositions were of low strength and did not display typical XRD and NMR geopolymer characteristics, by contrast with the compositions of S/A between 2 and 300 which showed typical amorphous geopolymer XRD traces and 27Al, 29Si and 23Na NMR spectra. The samples with increasing SiO2 content (S/A > 24) showed increasingly elastic behaviour, deforming rather than crushing in brittle fashion, and upon heating at 100–250 °C, their hydration water was expelled as bubbles, forming stable foamed materials at about 300 °C.

Scanning electron micrographs of a well-cured polysialate siloxo geopolymer (silica:alumina ratio 2:1) prepared from metakaolinite reveal a microstructure consisting of a glass-like matrix containing metakaolinite relicts and impurity quartz grains. This inhomogeneity probably results from viscosity increases during preparation militating against efficient mixing of the components, but does not appear to seriously degrade the physical properties of the product. The matrix composition, determined by EDAX, conforms closely to the expected molar ratio and is unchanged by heating at 1200 ° C, which however, brings about the crystallization of mullite needles in areas of the geopolymer matrix, the dissolution of the quartz impurities and the depletion of silica from the metakaolinite relicts, leaving behind fine alumina grains. These previously unsuspected thermal reactions help to explain the exceptional stability of the geopolymer matrix. Transmission electron micrographs confirm the essentially amorphous nature of both the as-prepared and heated geopolymer samples, but unexpectedly reveal in the latter nanometre-sized features resembling spinodal decomposition structures in glass.

Traditionally, X-ray powder diffraction has been a favoured method for studying chemical reactions in the solid state, but the increasing importance of energy-efficient synthesis methods for solids (e.g. sol–gel synthesis, mechanochemical synthesis) has led to the need for an analytical method not dependent on long-range structural periodicity. Multinuclear solid state nuclear magnetic resonance (NMR) represents a technique which is equally applicable to amorphous or crystalline solids, and is now used in increasing numbers of solid state studies. This paper briefly outlines the principles and practical details of this powerful technique and gives examples of its use in solid-state chemistry, particularly in very recent studies of mechanochemical synthesis of advanced sialon ceramics. The temperature at which these technically important silicon aluminium oxynitride compounds are formed can be significantly lowered by high-energy grinding of their components to produce X-ray amorphous precursors. Solid-state NMR has been used to provide detailed information which could not have been obtained by any other means about the chemical environment of the Si and Al atoms in these amorphous precursors, and the various atomic movements undergone as they crystallise to the final product.

The characteristics of an acid-leached montmorillonite-containing clay from Tuulant (Mongolia) were studied by XRD, DTA-TG, FTIR and N 2 adsorption techniques. Sample aliquots (2 g) were treated with 50 ml 2 M hydrochloric acid at 80 °C for various times. Leaching caused the surface area of the clay to increase 3-fold to 93.9 m 2 /g reflecting the formation in the porous silica product of 3–5 nm micropores and 6–10 nm mesopores, the latter resulting from a delaminated card-house structure rather than from the condensation of the micropores. Differences between the surface area of the present leached samples and those reported for other montmorillonite clays reflect the mineralogical composition of the clay, particularly the presence of non-clay constituents.