The solubility of ettringite at 25°C

Available solubility constants indicate that ettringite should be the stable form of calcium aluminate sulfate hydrate with respect to monosulfate in cement porewater. However, monosulfate is generally present in mature cement pastes, usually in the absence of ettringite. The objectives of this study were to determine the solubility product of ettringite under equilibrium conditions and to examine the solubility data used in predictive thermodynamic models. Solubility products were calculated for ettringite prepared from both supersaturated and undersaturated solutions with a pH range between 10.4 and 13.7. The mean solubility product for ettringite dissolution: Ca₆Al₂O₆(SO₄)₃ · 32H₂O → 6Ca²⁺ + 2Al(OH)₄⁻ + 3SO₄²⁻ + 4OH⁻ + 26H₂O was 10^−44.91, i.e. Log K_sp = -44.91 ± 1.06 (2 S.D.). Activity coefficients were calculated using the specific ion interaction approach. The mean solubility product was close to other values calculated from concentrations reported elsewhere for the solubility of ettringite. As is the case for all solubility products, this value cannot be inserted directly into the databases of other thermodynamic models because of differences in the methods used to calculate activity coefficients and the manner in which ion-pairing is handled by different models. However, raw solubility data are provided for recalculation of the solubility product for use in other models.     

Medium effects in hydrochloric acid solutions containing phosphoric acid at 25°C

The emf of the cell Pt, H₂ | HCl(m), phosphoric acid (M) | AgCl, Ag was measured at 25°C at various concentrations of HCl and phosphoric acid. The standard potential of the cell decreases with increase in phosphoric acid concentration. Values of the activity coefficient of HCl and medium effects are calculated. A comparison with the previously studied succinic, maleic and tartaric acid systems is given. The results are interpreted on the basis of the effect of the solutes on the structure of liquid water.     

Miscibility of chitosan–hydroxyethylcellulose blends in aqueous acetic acid solutions at 35°C

The miscibility of blends of chitosan and hydroxyethylcellulose in a 2% acetic acid solution was studied by viscometry, densitometry, and refractometry at 35°C. The data suggest that the blends were completely miscible in all proportions. Further, the membranes were fabricated from concentrated blend solutions. The solid‐state compatibility of the blends was confirmed by scanning electron microscopy. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1996–1998, 2005     

Thermal stability of ettringite in alkaline solutions at 80 °C

The thermal stability of synthetic ettringite was examined in NaOH solutions up to 1 M after 12 h of heat treatment at 80 °C, with or without the coexistence of C₃S in the system. Ettringite was found to convert to the U phase, a sodium-substituted AFm phase, over the heat treatment in the absence of C₃S. The presence of C₃S, leading to C-S-H formation, prevents the U phase formation and results in the conversion of ettringite to monosulfate. Sulfate ions generated from ettringite decomposition mostly remain in the solution, but some is incorporated into C-S-H. During subsequent storage at room temperature, the majority of monosulfate slowly converts back to secondary ettringite under moist conditions, using the supply of sulfate ions from the solution and C-S-H. The observations support the current mechanism of delayed ettringite formation (DEF).     

Liquid-liquid equilibrium data for the ternary system water-isopropyl alcohol-ethylbenzene at 25°

Liquid-liquid equilibrium data at 25° for the system water-isopropyl alcohol-ethyl benzene together with refractive index and density data for mixtures on the binodal curve, are presented. A number of correlation methods were found to represent satisfactorily the equilibrium data and comparison is made with known water-isopropyl alcohol-benzene and water-isopropyl alcohol-toluene systems.     

Sorption and transport of aqueous salt solution in polyurethane membrane at 25, 44, and 60°C

Sorption and transport of aqueous salt solutions in polyurethane elastomer has been investigated over the temperature interval of 25–60°C by using an immersion/weight gain method. The size of the ions has no significant effect on the penetrant transport coefficients. The sorption data have been explained in terms of the simple Fickian model. Attempts have also been made to estimate the transport parameters by applying corrections to include the spatial diffusivity of the liquids within the polymer sample. Temperature dependence of the transport coefficients has been used to estimate the activation parameters from the Arrhenius plots.     

Suppressed Reactivity of AlN Powder in Water at 5°C

The hydrolysis behavior of AlN powder suspensions (5–25 wt%) at 5°C has been investigated to explore the impact of low temperatures on the hydrolysis behavior. Throughout the 312‐h long experiment, the pH value of the suspensions was below 9, where the hydrolysis remained in the induction period and was eventually suppressed due to the formation of a few‐nanometers‐thick film of amorphous aluminum hydroxide gel around the AlN particles, acting as a passivation layer. Moreover, the aqueous part of the suspension possessed a remarkably high value of dissolved [Al(III)]_aq, being an order of magnitude higher at a given pH value than the aqueous AlCl₃ solution.     

Solubility of potassium ferrate in 12 M alkaline solutions between 20°C and 60°C

The solubility of potassium ferrate (K₂FeO₄) was measured in aqueous solutions of NaOH and KOH of total concentration 12 M containing various molar ratios of KOH:NaOH in the range 12:0 to 3:9. Several analytical methods were tested for the determination of ferrate concentration. The final method chosen consisted of potentiometric titration of the ferrate sample with an alkaline solution of As₂O₃. The assumption was made that ferrate dissociates in concentrated KOH solutions predominantly to KFeO₄⁻. The solubility constant, S, defined as the product of the molar concentration of the potassium ion, K⁺, and the ferrate anion, KFeO₄⁻, was found to be 0·044 ± 0·006 mol² dm⁻⁶ for 20°C, 0·093 ± 0·004 mol² dm⁻⁶ for 40°C and 0·15 ± 0·09 mol² dm⁻⁶ for 60°C. From these results the heat of dissolution of K₂FeO₄ was calculated as −14·3 kJ mol⁻¹. At 60°C the enhanced decomposition of the ferrate at the higher temperature led to a greater deviation in solubility values compared with data for either 20°C or 40°C.     

Sulphide inhibition of methanogenic activity at various pH levels at 55°C

The purpose of this study was to evaluate the toxic effect of sulphide on thermophilic methanogenic bacteria, pre-cultivated in UASB-reactors fed with and without sulphate, at 55°C and different pH levels. For granular sludge, precultivated in the presence of sulphate, the inhibition caused by hydrogen sulphide was dependent on the pH imposed. At alkaline pH the inhibitory effect of hydrogen sulphide was higher than at neutral or acidic pH. The effect of sulphide could not be described in terms of free hydrogen sulphide level only. For dispersed sludge, pre-cultivated in the absence of sulphate, the inhibition caused by free hydrogen sulphide was independent of the pH, and the toxic effect of sulphide could be described in terms of free hydrogen sulphide.     

Measurement and prediction of the density of aqueous ternary mixtures of methyldiethanolamine and diethanolamine at temperatures from 25°c to 80°c

Densities have been measured for mixed aqueous solutions of N-methyldiethanolamine (MDEA) and diethanolamine (DEA) at 25, 30,40,50, 60,70, and 80°C. The compositions of the ternary solutions are near 30 mass% solute, because of industrial applications for the absorption of acid gases. The isopycnotic (same density) method, for predicting densities of multicomponent aqueous systems at 25°C has been used to predict the densities of the present non-electrolyte mixed solutions at other temperatures. Predicted and observed density values are in good agreement (<0.06% error). The method has also been used to predict densities of some aqueous sea salt mixtures at temperatures ranging from 5 to 95°C. Again the predicted and observed values are in good agreement (generally <0.1% error).     

Thermal degradation of poly(methyl methacrylate) at 50°C to 125°C

Small but significant numbers of chain scissions occur in a commercial poly(methyl methacrylate) sheet exposed to temperatures between 50 and 125°C. The scission rate is initially high and then levels off to a constant rate. The short-time rate of chain scissions is temperature dependent, while the long-time rate of chain scissions appears to be temperature independent. Four possible sources of random chain scission initiation were considered: (1) the presence of unreacted initiators of polymerization, (2) free radicals generated from additives in the commercial film, (3) weak links in the polymer chain, and (4) free radicals generated from the thermal decomposition of an oxidation product of methyl methacrylate (MMA) monomer. The source most consistent with our results is the one involving free radicals generated from the oxidation product of MMA monomer.     

C–(N)–S–H and N–A–S–H gels: Compositions and solubility data at 25°C and 50°C

Calcium silicate hydrates containing sodium [C–(N)–S–H], and sodium aluminosilicate hydrates [N–A–S–H] are the dominant reaction products that are formed following reaction between a solid aluminosilicate precursor (eg, slags, fly ash, metakaolin) and an alkaline activation agent (eg NaOH) in the presence of water. To gain insights into the thermochemical properties of such compounds, C–(N)–S–H and N–A–S–H gels were synthesized with compositions: 0.8≤Ca/Si≤1.2 for the former, and 0.25≤Al/Si≤0.50 (atomic units) for the latter. The gels were characterized using thermogravimetric analysis (TGA), scanning electron microscopy with energy‐dispersive X‐ray microanalysis (SEM‐EDS), and X‐ray diffraction (XRD). The solubility products (K_S0) of the gels were established at 25°C and 50°C. Self‐consistent solubility data of this nature are key inputs required for calculation of mass and volume balances in alkali‐activated binders (AABs), and to determine the impacts of the precursor chemistry on the hydrated phase distributions; in which, C–(N)–S–H and N–A–S–H compounds dominate the hydrated phase assemblages.     

Wear of zirconia-dispersed alumina at ambient temperature, 140 °C and 250 °C

Commercial grade alumina along with 5, 10, 15 and 20 wt.% zirconia-dispersed aluminas were tested for their wear resistance at ambient temperature, 140 °C and 250 °C using a pin on disk tribotester fitted with a hot stage. The sample suite was investigated for physical characteristics including hardness, fracture toughness, bulk density, alumina grain size and zirconia grain size. The wear track and wear debris were investigated using profilometry, SEM as well as TEM.

The 5 wt.% zirconia-dispersed aluminas had the lowest wear volume loss over the temperature range. The alumina sample exhibited a wear dependence with relative humidity which is attributed to the formation of a tribochemical layer. Investigation of the tribochemical layer using SEM/EDS and TEM electron diffraction showed the tribochemical layer to be aluminium hydroxide. The major wear mechanism for all samples was brittle fracture.     

Electrolyte—solvent interaction in the dipolar aprotic solvent dimethyl sulphoxide at 25°C

Conductance measurements are reported for s-alkylisothiouronium bromide, iodide and picrate salts in the dipolar aprotic solvent DMSO at 25°C. The data were analysed by Fuoss's equation (1975–1980) for 1:1 electrolytes, from which the values of Λ₀, the Gurney's cosphere diameter R and K_A are obtained. The results are discussed in the light of the recorded values of the constants K_R and K_S and the free energy term G_s.     

The start‐up of anaerobic sequencing batch reactors at 20 °C and 25 °C for the treatment of slaughterhouse wastewater

The objective of this research was to evaluate the feasibility, the stability and the efficiency of a start‐up at 20 °C and 25 °C of anaerobic sequencing batch reactors (ASBRs) treating slaughterhouse wastewater. Influent chemical oxygen demand (COD) and suspended solids concentrations averaged 7500 and 1700 mg dm^?3, respectively. Reactor start‐up was completed in 168 and 136 days at 20 °C, and 25 °C, respectively. The start‐up process was stable at both temperatures, except for a short period at 20 °C, when effluent volatile fatty acid (VFA) concentrations increased from an average of 40 to 400 mg dm^?3. Effluent quality varied throughout start‐up, but in the last 25 days of the experiment, as the ASBRs were operated under organic loading rates of 2.25 ± 0.21 and 2.86 ± 0.24 kg m^?3 d^?1 at 20 °C and 25 °C, respectively, total COD was reduced by 90.3% ± 1.3%. Methanogenesis was not a limiting factor during start‐up. At 20 °C, the limiting factor was the acidification of the soluble organics and, to a smaller extent, the reduction of propionic, isobutyric and isovaleric acids into lower VFAs. At 25 °C, the limiting factor was the hydrolysis of particulate organics. To minimize biomass loss during the start‐up period, the organic loading rate should be increased only when 75 –80% of the COD fed has been transformed into methane within the design hydraulic retention time. © 2001 Society of Chemical Industry     

Stability of ferrous hydroxide in aqueous suspension at 300°c

The decomposition of ferrous hydroxide in aqueous suspension at 300° and in PTFE containers has been studied. The reaction rate is slow but is catalysed by nickel and platinum. This explains the results of earlier workers who have found the decomposition of ferrous hydroxide supported in metallic containers to be rapid.     

The thermal degradation of an amine-cured epoxide resin at temperatures between 200°C. and 310°C.

This paper describes the nonoxidative thermal degradation of an epoxide resin based on the diglycidyl ether of bisphenol A crosslinked with p,p′-diaminodiphenyl methane. Temperatures of degradation lay between 200 and 310°C. and the process was followed concurrently by three means: changes in dielectric properties, changes in infrared spectra, and weight loss. Dielectric properties support the contention that there is a dehydration step during degradation. It is proposed that vacuum curing at high temperature can produce optimum crosslinking. Evidence of phenol and N-methyl aniline as degradation products is advanced, and possible degradation mechanisms are discussed.     

Specific refractive index increments of ethylene–vinyl acetate copolymers in trichlorobenzene solutions at 145°C

Specific refractive index increments of ethylene/vinyl acetate copolymers have been masured in trichlorobenzene at 145°C. A relationship between these values and copolymer composition has been determined for use in light scattering measurements of weight-average molecular weights of these materials. The data are also required for analysis of molecular weight distributions by size exclusion chromatography with light scattering detection.     

Reactivity of heat-treated coals in air at 500 °C

Twenty one US coals, of widely ranging rank, have been carbonized under controlled conditions to 1000 °C, and the reactivity in air at 500 °C of the resulting chars or cokes has been measured by a gravimetric method. The reactivities lie within a well-defined band when plotted against rank of the parent coal. The lower-rank coal chars are more reactive than those prepared from high-rank coals. In extreme cases, the reactivity found for a Montana lignite char is some 100 times as great as that obtained for a char produced from a Pennsylvania low-volatile coal. Variation of reactivity with heat-treatment temperature (600 to 1000 °C) has been studied for three coals. As heat-treatment temperature increases, there is a decrease in reactivity. Some results are reported on the effects which mineral matter and pore structure have on the reactivity parameter. Chars containing high concentrations of magnesium and calcium impurities are most reactive. The amount of macro and transitional porosity in a char has a marked influence on reactivity.