Impact of Reaction Conditions on MnO2 Genesis during Permanganate Oxidation

To enhance the understanding of the behavior and effects of the precipitation of MnO2 particles in the subsurface generated during in situ chemical oxidation (ISCO) using permanganate, laboratory batch experiments were completed to examine the influence that varied reaction matrix conditions have on the generation and properties of manganese oxides. The conditions examined include organic material type and concentration, permanganate concentration, pH, and the presence of calcium (as a representative divalent cation) in solution. Experimental studies included: (1) spectrophotometric examination of permanganate depletion and manganese oxides generation over time during reactions with trichloroethene; (2) scanning electron microscopy analyses of manganese particle morphology; (3) particle size distribution (filtration) characterization studies; and (4) optical particle sizing and numeration studies. Bench-scale, batch experiments were conducted to focus on fundamental chemical properties affecting particle development under varied potential environmental conditions. The amount of manganese oxides particles that develop, grow, and potentially settle as a result of permanganate ISCO of organic contaminants is a function of the particle size and concentration, the time allowed for particle development, and the impact of matrix conditions on the ability of particles to agglomerate.     

Characterization and modification of fillers for paints and coatings

This paper highlights the possibility of inverse gas chromatography for the surface characterization of common fillers (CaCO₃, talc, SiO₂,) for paints and coatings. Divided solids are described, on the one hand, by the dispersive component of their surface energy and, on the other, by a specific parameter indicating their acid-base interaction potential. The role of the surface morphology at a molecular level is also examined. It is demonstrated that steric effects play an important role in the adsorption of probes on lamellar solids like talc. The consequences of surface treatments as well as examples of practical applications are also reported.     

降低氧化铝生产中熟料折合比的探讨

在氧化铝生产过程中，熟料折合比是烧结法一项重要的综合性指标，本文通过对熟料折合比的定义、计算公式的剖析，分析了生产过程中影响熟料折合比的主要因素，对有效降低熟料折合比的措施进行了探讨。     

Effect of Organic Additives on Electrochemical Surface Precipitation and Polymorphism of CaCO3

The inhibition effect of three organic additives on the precipitation and polymorphism of CaCO₃ deposited on gold surfaces was investigated using electrochemical and microscopic techniques. Additives, two polyacrylic acid (PAA) polymers with different molecular weights (Mw 2100, Mw 30,000), and 1,2,4,5‐benzenetetracarboxylic acid (BTCA), were either added to the solution before or during deposition. In the presence of 100 ppm of one of the three additives in solution, almost no scale was observed on the surface for at least 24 hours. In the presence of lower concentrations of PAA Mw 2100, only distorted calcite crystals were obtained while with PAA Mw 30,000 the polymorph was spherical vaterite. A mixture of calcite and vaterite was observed with the BTCA additive. Addition of the polymers inhibits further nucleation and growth even if added after partial deposition of CaCO₃ while BTCA has no effect once nucleation has started. The results indicate that the inhibit ion effect of the PAA polymers is due to adsorption on the electrode surface while the effect of BTCA is related to chelation of calcium ions in solution.     

饲料级磷酸氢钙中氟的几种分析方法比较

本文采用茜素络合酮比色法和氟离子选择电极法对饲料磷酸氢钙进行氟的测定实验对比,得出常用的氟离子选择电极法完全可以代替经典的蒸馏比色法的结论。     

六铝酸钙材料的合成及其显微结构研究

分别采用轻质碳酸钙和活性氧化铝 ,或纯铝酸钙水泥和活性氧化铝为初始原料 ,反应烧结合成了六铝酸钙 (CA6)材料 ,研究了原料和成型压力对合成材料的烧结性能和显微结构的影响 ,同时借助于XRD、TG -DSC、SEM和EDAX等测试手段对其反应过程、物相变化和显微结构进行了分析和观察。研究结果表明 :(1) 130 0℃时 ,合成材料的主晶相为刚玉相和CA2 ,并开始有CA6形成 ;温度升至14 0 0℃ ,CA6大量生成 ;15 0 0℃时反应完成 ,产物全部为CA6相。 130 0～ 15 0 0℃时 ,上述反应表现为体积膨胀过程 ,试样的体积密度和径向线收缩率随温度的变化不大 ;而高于 15 0 0℃时 ,试样明显趋向烧结 ,体积密度升高 ,线收缩率加大。采用纯铝酸钙水泥和活性氧化铝合成的试样的体积密度均高于采用轻质CaCO3 和活性氧化铝的 ,尤其在烧成温度高于 15 0 0℃时。坯体的成型压力对这两种合成试样的烧结性能均没有显著影响。 (2 )合成六铝酸钙材料的晶粒形貌与合成工艺有关 ,制备片状晶粒的六铝酸钙材料需满足两个条件 :一是晶核有足够的发育空间 ,二是从晶核生长形成片状结构需足够的物质扩散。采用纯铝酸钙水泥和活性氧化铝为原料的试样 ,其CA6晶核很容易发育成片状晶形 ,且随着坯体成型压力的增加 ,片状CA6有向等轴状发展的趋势 ;采用     

有广阔市场前景的化工产品—过氧化钙

本文叙述过氧化钙的性质,并以实例说明过氧比钙在水产养殖、食品加上、果蔬保鲜。环境保护、农作物栽培、橡胶及化工等奋方面的应用。     

用预分解技术改造Φ4×60m预热器窑的又一成功实例

介绍南京水泥工业设计研究院用预分解生产技术对山东水泥厂Φ4×60m预热器窑烧成系统进行的成功技术改造。技改设计指标为：熟料产量保证指标1500t／d，争取指标1700t／d，熟料热耗＜3762kJ／kg，熟料28d抗压强度＞60MPa。整个工程停产施工耗时仅用48d，烧成系统技改共耗资约3000万元。技改后一次点火投料成功，且点火当月即实现72h达标考核，所有设计指标均达标。     

Effect of particle size on quality of crab meatballs using enzymatically deproteinized crab by-products

The production of crab meatballs generates large amount of crab shell waste, it is therefore necessary to develop a green, economical and environmentally friendly process to vaporize the waste. This study was aimed at investigating the applicability of microwave heating combined with ultrasonic field-assisted alkaline protease (MUSED) (50 ℃, pH = 9.0, 14025.67 U/g, 4.21 h and liquid/material = 14.41:1) for pretreatment of ball-milled crab shells. The ball milling efficiency of the crab shell powder pretreated by MUSED was observed to increase by 50 % compared to the control group, with the final average particle size of D₄ = 4.88 ± 0.20 um. High calcium solubility and low energy consumption of the ball-milled powder increased dietary calcium bioavailability and reduced the potential for high calorie intake. The addition of 6 % (w/w) crab shell powder treated by MUSED improved the texture of the crab meatballs (CM-D₄) and gave the product enhanced crab flavor relative to the control group. Moreover, the lower cooking loss of CM-D₄ resulted in significant retention of nutrients (p < 0.05). The crab shell powder treated by MUSED method was more efficient in ball milling, which improved the quality of crab meatballs while relieving environmental pressure.     

Phase change materials in the ternary system NH4Cl+CaCl2+H2O

Solubility isotherms of the ternary system (NH₄Cl+CaCl₂+H₂O) were elaborately determined at T= (273.15 and 298.15) K by using the isothermal method. In the equilibrium phase diagram, there are two solubility branches corresponding to the solid phases CaCl₂⋅6H₂O and NH₄Cl. Invariant point compositions are 36.32 wt% CaCl₂ and 3.4 wt% NH₄Cl at 273.15 K, and 45.86 wt% CaCl₂ and 5.22 wt% NH₄Cl at 298.15 K. A Pitzer-Simonson-Clegg thermodynamic model was applied to represent the thermodynamic properties of this ternary system and to construct a partial phase diagram of the ternary system at temperatures between (273.15 and 323.15) K. It was found in the predicted solubility phase diagram that the double salt 2NH₄Cl⋅CaCl₂⋅3H₂O, found by other authors at (323.1 and 348.1) K, will disappear at temperatures below 298.15 K. Besides, it was found that there are two peritectic points in the ternary system with peritectic temperatures at 299.65 K and 298.15 K, and the former peritectic point falls just on the line between the composition points of NH₄Cl and CaCl₂⋅6H₂O. According to phase rule, a solution made of this point will begin to crystallize at 299.65 K and end at 298 K and therefore can be acted as a “pseudo eutectic” phase change material (PCM). A heat storing and releasing experiment of 50 grams of the PCM was carried out, obtaining a satisfying result.