厌氧污泥处理含铬废物的研究

利用城市污水处理厂的厌氧污泥对含铬废物进行解毒研究,结果表明,在厌氧条件下,厌氧污泥对重铬酸钾溶液和铬渣进行解毒后,滤液中的Cr6+质量浓度极低,大大低于《污水综合排放标准》的0.5 mg/L。厌氧污泥的解毒效果与含铬物料的量、解毒时间等因素有关。     

高效防腐中温磷化液LC-1的制备及性能

制备了一种含Zn2+、Mn2+、N i2+三系离子的LC-1磷化液,通过硫酸铜点滴、氯化钠浸蚀、SEM等手段对磷化膜进行了测试,测定了磷化温度、磷化时间对膜层耐蚀性的影响。结果表明,在磷化温度大于65℃,磷化时间大于10 m in的条件下,所形成的磷化膜结晶均匀、致密、黑褐色,耐蚀性良好。LC-1三系磷化液可适用于大批量钢铁工件的磷化生产。     

Electrochemical behaviour of copper/LDPE composites in the simulated uterine solution

Two metal/insulator composites, copper/low-density polyethylene (LDPE) microcomposites and copper/LDPE nanocomposites, were prepared in a uniform metal mass fraction. The corrosion characteristics of the two composites in the simulated uterine solution have been studied by cyclic voltammetry, potentiodynamic polarization measurement and electrochemical impedance spectroscopy. Results obtained during this study show that there are obvious differences on the corrosive rates and mechanisms between the two materials. The nanocomposites have stable corrosive reaction, hardly passivation, low corrosion rate and high transformation ratio of copper to soluble cupric ions compared with microcomposites, which indicate that the nanocomposites are perfect to be the novel material for intrauterine device. The corrosion behaviour of the microcomposites was controlled by both the processes of the pervasion of Cu²⁺ and the transfer of the charge, while that of the nanocomposites was only controlled by the transfer of the charge. This paper also compared the corrosion behaviours of the composites and bulk copper in the simulated uterine solution, there were more insoluble subproducts in the corrosion process of bulk copper than the composites. Further, the electrochemical method in this study is proved to be useful to characterize the corrosion behaviour of high electrical resistivity materials.     

1H NMR方法研究以DMSD6为溶剂高醇Formalin溶液

用^1HNMR Formalin方法研究了工业高醇formalin溶液体系，发现以DMSD6（氘代二甲基亚砜）为溶剂的^1HNMR Formalin谱图中，溶剂与样品的不同配比，使谱图发生明显变异，这与通常NMR能得到确定的试样谱图不同。通过对formalin溶液体系的分析，对此反常现象进行了令人满意的解释。     

溶液共混法制备高强度淀粉基完全生物降解塑料薄膜

利用一步溶液共混法，将预糊化的淀粉糊与PvA溶液共混，用乙二醛进行交联，制备淀粉／聚乙烯醇（PVA）完全生物降解塑料薄膜。研究不同乙二醛和甘油的用量对薄膜性能的影响。薄膜的力学性能、热性能和微观形态表征表明，淀粉／PvA体系具有较好的相容性和较高的力学性能，薄膜的拉伸强度和断裂伸长率分别可达到28．52MPa和307．5％。     

Influences of zinc oxide and an organic additive on the electrochemical behavior of pure aluminum in an alkaline solution

The corrosion behavior of pure aluminum in inhibited and uninhibited 4 MKOH was investigated by means of hydrogen collection, polarization curve measurement and electrochemical impedance spectroscopy (EIS). The results showed that the corrosion of pure aluminum was greatly inhibited by the addition of ZnO and dimethyl amine epoxy propane (designated as DE). EIS and EDAX analyses revealed that ZnO produces its effect by depositing on the aluminum surface, which increases the overpotential of hydrogen evolution. It was also found that the addition of DE could greatly improve the deposition of zinc layers.     

酸性镀锡液的新进展

从近几年美国发明专利的角度扼要综述酸性镀锡液的新进展。说明酸性镀锡液由氟硼酸盐型发展为烷基磺酸盐型的改进过程。列出参考文献９篇。     

膜内介质传递现象

论述了组分在膜分离过程中的传递行为。简要论述了介质通过膜的途径，对膜传递过程中所产生的理论体系进行归纳和解释，并对其内在联系进行总结；最后根据介质与膜的相互关系，把组分在均质膜中的传递过程分为理想扩散过程、弱相互作用扩散过程、强相互作用扩散过程，并分别进行探讨。     

Physical agglomeration behavior in preparation of cellulose‐N‐methyl morpholine N‐oxide hydrate solutions by simple mixing

The different melting temperatures of N‐methyl morpholine N‐oxide (NMMO) hydrates in the cellulose–NMMO hydrate solution may be explained by the rather different crystal structures of NMMO hydrates, which are determined by the amount of the hydrates. The preparative process of cellulose–NMMO hydrate solution may result in cellulose structural change from cellulose I to cellulose II, depending on the amount of the hydrate. Mixtures of cellulose and NMMO hydrate in a blender was changed from the granules to slurry with increasing mixing time at 60–70°C, which is below the melting point of the NMMO hydrate. In the case of 15 wt % cellulose–NMMO hydrate granules, which were made by mixing for 20 min, the melting points of various NMMO hydrates were obtained as 77.8°C (n = 0.83), 70.2°C (n = 0.97), and 69.7°C (n = 1.23), respectively, depending on the hydrate number. However, the melting points of cellulose–NMMO hydrate slurry and solution were shifted lower than those of cellulose granules, while the mixing time of slurry and solution are 25 and 35 min, respectively. These melting behaviors indicate instantaneous liquefaction of the NMMO hydrate and the diffusion of the NMMO hydrate into cellulose during mixing in a blender. When cellulose was completely dissolved in NMMO hydrate, the crystal structure of cellulose showed only cellulose II structure. In the cellulose–NMMO products of granules or slurry obtained by high‐speed mixing, which is a new preparation method, they still retained the original cellulose I structure. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1687–1697, 2004