关于超细玻璃纤维隔板吸酸值测定方法及指标的探讨

通过对几种隔板用不同方法测定吸酸值进行比较分析，并选择了一种较为合适的吸酸值测定方法及在某压力下的吸酸值指标。

Sorption of Pyruvic Acid with Weakly Basic Polymer Sorbents

Uptakes of pyruvic acid for two types of commercially available weakly basic polymer sorbents, D301G and D301R, have been measured over a wide pH range and at various salinities of MgSO4. The results show that the overloading adsorption of pyruvic acid occurs on both weakly basic polymer sorbents, and the overloading models can predict the experimental data of uptake very well. The overloading value for D301G is larger than that for D301R. The adsorption isotherm of pyruvic acid for both polymeric sorbents is greatly affected by the solution pH and MgSO4 concentration in the aqueous phase, and a high recovery efficiency of pyruvic acid from aqueous solution can be obtained at the solution pH around 2.

Soil Components Affecting Phosphate Sorption Parameters of Acid Paddy Soils in Guangdong Province

Soil components affecting phosphate sorption parameters were studied using acid paddy soils derived from basalt, granite, sand-shale and the Pearl River Delta sediments, respectively, in Guangdong Province. For each soil, seven 2.50 g subsamples were equilibrated with 50 mL 0.02 mol L-1 (pH=7.0) of KCI containing 0, 5, 10, 15, 25, 50 and 100 mg P kg-1, respectively, in order to derive P sorption parameters (P sorption maximum, P sorption intensity factor and maximum buffer capacity) by Langmuir isotherm equation. It was shown that the main soil components influencing phosphate sorption maximum (Xm) included soil clay, PH, amorphous iron oxide (Feo) and amorphous aluminum oxide (Alo), with their effects in the order of Alo > Feo > pH > clay. Among these components, pH had a negative effect, and the others had a positive effect. Organic matter (OM) was the only soil component influencing P sorption intensity factor (K). The main components influencing maximum phosphate buffer capacity (MBC) consisted of soil clay, OM,pH, Feo and Alo, with their effects in the order of Alo > OM > pH > Feo > clay. Path analysis indicated that among the components with positive effects on maximum phosphate buffer capacity (MBC), the effect was in the order of Alo > Feo > Clay, while among the components with negative effects, OM > pH. OM played an important role in mobilizing phosphate in acid paddy soils mainly through decreasing the sorption immensity of phosphate by soil particles.

Phosphate Adsorption and Surface Charge Characteristics and Their Relations to Mineralogy of Some Soils from Southern China

The phosphate adsorption and surface charge characteristics of the tropical and subtropical soils derived from different parent materials in China were determined, and their relations to soil mineralogy were analysed.The results showed that all soil phosphate adsorption curves were well fitted by Freundlich equation and Langmuir equation. The maximum buffering capacity of P ranged from 66 to 9880 mg kg-1, with an increasing order of purple soil, skeletal soil, red soil, lateritic red soil, yellow soil and latosol; and the highest value was 149 times the lowest value, which indicated great differences among these soils in phosphate adsorption and supplying characteristics. The pHo (zero point of charge) values obtained by salt titrationpotential titration varied from 3.03 to 5.49, and the highest value was found in the latosol derived from basalt whereas the lowest value was found in the purple soil. The correlation analysis indicated that the main minerals responsible for phosphate adsorption in the soils were gibbsite, amorphous iron oxide and kaolinite; and the pHo was mainly controlled by kaolinite, gibbsite and oxides.

Preparation of nitric humic acid by catalytic oxidation from Guizhou coal with catalysts

Nitric humic acid was prepared by catalytic oxidation between nitric acid and Guizhou coal, with added catalysts. We investigated catalytic oxidation processes and the factors that affect the reactions. The effects of different catalysts, including NiSO4 support on active carbon （AC-NiS04）, NiS04 support on sil- icon dioxide （SiO2-NiSO4）, composites of SO42-1Fe203, Zr-iron and vanadium-iron composite were stud- ied. As well, we investigated nitric humic acid yields and the chemical structure of products by element analysis, FT-IR and E4/E6 （an absorbance ratio at wavelengths of 465 and 665 nm of humic acid alkaline extraction solutions）. The results show that the catalytic oxidation reaction with added catalysts can increase humic acid yields by 18.7%, 16.36% 12.94%, 5.61% and 8.59%, respectively. The highest yield of humic acid, i.e., 36.0%, was obtained with AC-NiSO4 as the catalyst. The amounts of C and H decreased with the amount of nitrogen. The increase in the E4/E6 ratio in catalytic oxidation of （Guizhou） coal shows that small molecular weights and high yields of nitric humic acid can be obtained by catalytic oxidation reactions.

Adsorption Characteristics of Remazol Black B on Anoxic Sludge

The adsorption characteristics of Remazol Black B on anoxic sludge were investigated.The parameters,such as initial pH,sulphate concentration,and temperature,affecting the dye adsorption were studied.The adsorption data were analyzed with three adsorption isotherm models,namely Langmuir,Freudlich,and linear partition.The results showed that adsorption of Remazol Black B on the sterilized sludge reached equilibrium in 4 h.It also indicated that pH had significant effect on anoxic sludge adsorption behavior.The adsorption capacity of anoxic sludge decreased with the increase of pH value and the maximum adsorption capacity of dyes occurred at pH=3.The adsorptive capacities increased with the decrease of temperature and increase of sulphate concentration.Results also indicated that the adsorption equilibrium of Remazol Black B on anoxic sludge could be well fitted by Freundlich model.

Influence of Inorganic Salts during the Photooxidative Process of Nitrobenzene

Into the photooxidation process, several factors such as pH, time of irradiation, dose of UV light, lamp power, contaminant concentration, turbidity of the solution and the presence of salts can interfere with the photodegradation of pollutants. This research aims to evaluate the influence of salts： NaCl, MgCl2, CaCI2, BaC12, CuCl2, Na2SO4, MgSO4, MnSO4, FeSO4, CuSO4, Na3PO4, K2CrO4 and K2Cr207 in concentrations of 0.0005 M, 0.005 M and 0.05 M during photodegradation of aqueous solution of 59.5 mg/L of nitrobenzene at a pH of 2.5. It was observed that the presence of salts such as CuCI2, CuSO4, FeSO4, K2CrO4 and K2Cr207 interfere negatively in the system UV/H202 applied for degradation of nitrobenzene; possibly by oxidation of Fe2＋ to Fe3＋ and Cu＋ to Cu2＋ in the Cr case, due to the difficulty of transforming the Cr6＋ to Cr3＋ or because these solutions have color and act as radiation absorbing filter.