硫酸铝催化乙酸异戊酯的合成研究

以冰醋酸和异戊醇为原料,利用硫酸铝(A12(SO4)3.18H2O)作催化剂合成乙酸异戊酯取得了阶段性成果。重点采用对比实验的方法探讨了投料比、催化剂用量、反应温度及反应时间对产率的影响。最佳工艺条件为:M冰醋酸∶M异戊醇=3∶2,催化剂用量为1 g;反应时间2 h;反应温度93~107℃。该合成方法具有操作安全简便、催化剂可回收使用等优点。     

硫酸铀酰印迹离子交换树脂的合成及识别特性研究

为进行稀溶液中铀的浓缩,以硫酸铀酰为模板、二乙基烯丙基胺为功能单体,在水中采用自组装分子印迹技术制备了硫酸铀酰印迹离子交换树脂.对树脂合成条件进行了优化,研究了pH值对吸附量的影响、分子印迹聚合物MIPs-4的等温吸附与吸附动力学、柱内吸附与淋洗曲线等树脂识别性能.结果表明:印迹树脂对硫酸铀酰的吸附性能比非印迹树脂好,可以在pH=1～6范围内应用,并在pH为2左右时吸附能力最强.MIPs-4树脂的吸附等温线为"优吸"型,吸附在约3h达到平衡.当C0=0.125mg·mL-1时,Kd=0.249L·g-1.吸附液ρ(U)=1.0 mg·mL-1、接触时间4min进行的柱内试验得出MIPs-4的穿透体积、穿透容量和饱和容量分别为柱内树脂的床体积(BV)的22倍、21.6 mg·mL-1和36.2 mg·mL-1.以0.05 mol·L-1 H2SO4 1.0 mol·L-1 NaCl为淋洗液时,淋洗体积仅4BV,流出液中最大铀浓度达到17.6 mg·mL-1.印迹树脂的吸附和解吸性能好,可应用于低浓度铀的浓缩及含铀废水的处理.     

钢纤维自应力混凝土力学性能试验研究

研究了在三维乱向分布钢纤维的限制下,掺有钢纤维的硫铝盐酸自应力混凝土（SFRSC）的直接拉伸、抗压、 劈拉、抗折强度特性,由于钢纤维和基体间的摩阻限制所引入的自应力和钢纤维的三向限制作用,使得钢纤维对于自应力混凝土的增强效应要比对于普通混凝土的高,另外,在现有钢纤维混凝土强度计算模式的基础上,通过优化方法得出了对于不同目标自应力等级的自应力混凝土的钢纤维增强效应系数。     

钛白副产硫酸亚铁制备超细透明氧化铁黄研究

以钛白粉厂副产物硫酸亚铁为原料,以氨水为沉淀剂,采用空气氧化法制备超细透明氧化铁黄.分别研究了影响晶种形成和晶体生长的主要影响因素.通过优化实验,得出了最佳工艺条件.晶种制备阶段：温度为30℃,空气流量为2L/min,溶液的pH为4～6,搅拌速度为400r/min,Fe2＋浓度为1mol/L.晶体生长阶段：温度为85℃,空气流量为2L/min,溶液pH为4～6.     

Optimization of pH value and aluminium sulphate quantity in the chemical treatment of molasses

The aim of this investigation was to find the optimal working conditions for the chemical treatment of molasses that guarantee coagulation and precipitation of undesired macromolecules. Twenty experiments were performed, within the limits: 3.5pH8.5 and 0.1 mol Al/lc0.5 mol Al/l, on samples of molasses treated with Al₂(SO₄)₃ as a precipitant. The efficiency of the treatment was controlled through measuring both the zeta potential and solution absorbance at 560 nm. By analysing the experimental results, it was concluded that the optimum lies within reduced limits of: 4pH7 and 0.2 mol Al/lc0.4 mol Al/l, which covers nine experimental points. Based on these measurements, a mathematical model of absorbance changes was defined, in terms of pH and Al₂(SO₄)₃ quantity. The model was taken as the objective function, and the optimal calculated values were obtained: pH=5.3 and c=0.34 mol Al/l. They guarantee a minimal absorbance value of: 0.124 at 560 nm.     

External mass transfer during the adsorption of various pollutants onto activated carbon

A wide range of experimental studies are reported for the adsorption of phenol and p-chlorophenol onto activated carbon—Type Filtrasorb 400—in an agitated batch adsorber. A model has been used to determine the external mass transfer coefficient for the systems and the effect of several experimental variables have been investigated: these include agitation, initial pollutant concentration, carbon mass, carbon particle size and solution temperature. The mass transfer coefficient has been correlated in terms of the dimensionless Sh/Sc^0.33 against each variable. The Sherwood number, Sh = k_fR/D_mol, relates the external mass transfer coefficient k_f to particle radius, R, and molecular diffusivity, D_mol. The Schmidt number, Sc, is the ratio of kinematic viscosity, v, to molecular diffusivity. A few results are also reported for the adsorption of sodium dodecyl sulphate and mercuric ions onto activated carbon.     

Neriifolin S, a dimeric serine protease from Euphorbia neriifolia Linn.: Purification and biochemical characterisation

A dimeric serine protease Neriifolin S of molecular mass 94 kDa with milk clotting activity has been purified from the latex of Euphorbia neriifolia by anion exchange and size-exclusion chromatography. It hydrolyses peptidyl substrates l-Ala-pNA with highest affinity (K_m of 0.195 mM) and physiological efficiency (K_cat/K_m of 144.5 mM s). Enzyme belongs to the class of neutral proteases with pI value of 6.8, optimal proteolytic activity displayed at pH 9.5 and temperature 45 °C. Its proteolytic activity is strongly stimulated in the presence of Ca⁺² ions and exclusively inhibited by serine protease inhibitors. Enzyme is fairly stable toward chemical denaturants, pH and temperature. The apparent T_m, was found to be 65 °C. Thermal inactivation follow first order kinetics with activation energy (Ea), activation enthalpy (ΔH∗), free energy change (ΔG∗) and entropy (ΔS∗) of 27.54 kJ mol⁻¹, 24.89 kJ mol⁻¹, −82.34 kJ mol⁻¹ and 337.20 J mol⁻¹ K⁻¹.     

聚硅硫酸铝处理长江水的生产性应用研究

用聚硅硫酸铝处理长江水进行生产性应用研究,研究结果表明:与硫酸铝相比,聚硅硫酸铝可降低混凝剂投加量20%~30%;在混凝剂投加量相近时,浊度平均值降低20%～50%;可以增大澄清池处理量15%;投加聚硅硫酸铝,滤池的主要运行参数及效能没有受到不利的影响.     

Performance of plate heat exchangers during calcium sulphate fouling — investigation with an in-line filter

The uncertainty about the fouling behaviour is one of the main reasons why plate and frame heat exchangers are not more widely installed in the chemical process industry and in power generating facilities. In the present investigation, the deposition of calcium sulphate in two different plate heat exchanger geometries was investigated. The deposition process was deliberately focused on crystallisation fouling through the installation of an in-line filter and the mode of preparation of the test solution. The investigated operating parameters were solution concentration, flow velocity, and bulk and surface temperatures. The heat exchangers were opened after each experiment to record the appearance and distribution of the deposits. The key result of this investigation is the strong correlation between the plate design and the tendency for deposit formation.     

Effect of hydrogen sulphide on nitric oxide adsorption and decomposition on Cu-containing molecular sieves

NO adsorption and decomposition were studied on sulphided and sulphated copper-exchanged ZSM-5, AlMCM-41 and NbMCM-41 molecular sieves. FTIR, temperature-programmed reduction (H₂-TPR) techniques, adsorption, and catalytic measurements were applied. H₂S adsorption drastically decreases the activity of copper-containing micro- and mesoporous materials studied in NO decomposition due to their sulphidation. This decrease is higher than that observed after SO₂ treatment and is assigned to the formation of sulphide species. H₂S is strongly chemisorbed on all copper active sites. Oxidation of sulphide species leading to the formation of sulphates does not increase the activity in the decomposition of NO, suggesting that some sulphided species are not oxidised.