The electrochemical study of a chromium plating bath. II. Chromium metal and surface film formation

The investigation of the electrode reactions occurring at metal and vitreous carbon cathodes in the standard chromium electroplating solution, 200 g dm^?3 CrO₃ and 2 g dm^?3 H₂SO₄, has been continued and this paper considers the mechanism of deposition of metallic chromium and the role of surface films in this process. It is confirmed that chromium deposition occurs at potentials negative to ?1.6 V versus Hg/Hg₂SO₄ and under galvanostatic or potentiostatic conditions, the current efficiency is 30–45%. Moreover at a vitreous carbon electrode, potential step experiments lead to risingI-t transients characteristic of instantaneous nucleation and three dimensional phase growth. At potentials just prior to metal deposition the potential sweep and step experiments show clear evidence for the formation of a strongly passivating film (this may be in addition to an existing less passivating layer). The important of the film varies with H₂SO₄ concentration and at intermediate concentrations, potential step experiments lead to unusual oscillatingI-t transients.     

采用HR型离心机处理烧碱回收盐的工艺改造

介绍了在烧碱蒸发处理回收盐时,采用HR型离心机后进行的工艺改造.确定了保证正常运行的操作关键和主要因素.     

水力循环澄清池的技术改造

张掖沙湾水厂的水力循环澄清池是上世纪70年代初建造。由于池深，各部分功能不匹配，动能有效利用率低，排泥不畅,对水量、水质变化适应性差，限制了产水量的提高。经强化絮凝、增设斜管、折板等综合性改造后．单池产水量由原来80m^3／d增加到140m^3／d，药耗降低了15％～20％。改造后仅1年多时间．即可从增产水的效益和节省药耗中收回投资。     

南极假丝酵母脂肪酶发酵条件优化及酶学性质

分别用摇瓶和15L发酵罐,对南极假丝酵母产胞外脂肪酶的培养基成分和操作条件进行了实验研究。得到最优的培养基组成为:豆粉40g／L,淀粉15g／L,豆油5mL／L,K2HPO4g／L,MgsO4·7H2O1g／L,Tween-800.1％,酵母膏5g／L;操作条件为:温度24℃,初始pH值为6.0,通气量为10.0L／min。在此培养条件下,发酵周期缩短至54h。由15L发酵罐生产的酶液酶活达到19.2U／mL。酶液在pH值为4.0～6.0和7.5～9.0范围内较稳定,其最适宜pH值范围为6～8.5;70℃时酶的催化活性最大.在40～70℃的温度范围内保持1h后残留酶活为60％。     

显像管屏玻璃池炉耐火材料侵蚀机理

显像管玻璃池炉耐火材料侵蚀是引发其缺陷的主要原因之一,本文主要论述了彩色显像管屏玻璃池炉耐火材料侵蚀机理,并简要讨论了它们所形成的玻璃缺陷.     

Phase Assemblages of Pr α-sialon Derived from SHS-ed Powders and TEM Study on the Nucleation of Pr α-sialon

The Pr α-sialon powders prepared by self-propagating high-temperature synthesis (SHS), consisting of 55 wt% Pr α-sialon and 45 wt% of β-sialon (abbreviated as α' and β'), were hot-pressed at 1800°C for 1 h. The results showed that Pr α' phase would transfer to β' with the appearance of JEM phase (Pr(Si_{6− z} Al _z )(N_{10− z} O _z )) after sintering, thus resulting in the increase of β' phase to 86 wt%. The addition of Y₂O₃ into SHS-ed Pr α' powders as the starting materials restrains the transformation of α' to β' and prevents the formation of JEM phase as well. The nucleation mechanism of Pr α' grain during hot-pressing was investigated in terms of transmission electron microscope and energy-dispersive spectrometer analysis. Two nucleation modes of Pr α' grains were found, i.e., nucleating on the undissolved Pr α' grains and on the nuclei of (Pr, Y) α' grains precipitated from liquid phase.     

建筑卫生陶瓷行业发展战略选择

通过对佛山、东莞等地的陶瓷产区相关企业的调查研究,在SWOT分析的基础上,研究了相关的竞争战略,归纳总结出现阶段适合建筑卫生陶瓷企业的战略:即以低成本为竞争生存方式,差异性为竞争发展动力,国际化为发展长期最终目标。     

季戊四醇的超分子化学

介绍季戊四醇的超分子化学,包括超分子网状结构、螺环冠醚、非常规液晶、富勒烯衍生物、固相光催化反应、Janus树枝状分子等等。     

Preparation,characterization, and prominent thermal stability of phase‐change microcapsules with phenolic resin shell and n‐hexadecane core

Microcapsules with phenolic resin (PFR) shell and n‐hexadecane (HD) core were prepared by controlled precipitation of the polymer from droplets of oil‐in‐water emulsion, followed by a heat‐curing process. The droplets of the oil phase are composed of a polymer (PFR), a good solvent (ethyl acetate), and a poor solvent (HD) for the polymer. Removal of the good solvent from the droplets leads to the formation of microcapsules with the poor solvent encapsulated by the polymer. The microstructure, morphology, and phase‐change property as well as thermal stability of the microcapsules were systematically characterized by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimety (DSC), and thermogravimetric analysis (TGA). The phase‐change microcapsules exhibit smooth and perfect structure, and the shell thickness is a constant fraction of the capsule radius. The initial weight loss temperature of the microcapsules was determined to be 330°C in N₂ and 255°C in air, respectively, while that of the bulk HD is only about 120°C both in air and N₂ atmospheres. The weight loss mechanism of the microcapsules in different atmosphere is not the same, changing from the pyrolysis temperature of the core material in N₂ to the evaporation of core material caused by the fracture of shell material in air. The melting point of HD in microcapsules is slightly lower than that of bulk HD, and a supercooling was observed upon crystallization. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007