Electrochemical formation of AlN in molten LiCl-KCl-Li3N systems

Electrochemical formation of aluminum nitride was investigated in molten LiCl-KCl-Li₃N systems at 723 K. When Al was anodically polarized at 1.0 V (versus Li⁺/Li), oxidation of nitride ions proceeded to form adsorbed nitrogen atoms, which reacted with the surface to form AlN film. The obtained nitrided film had a thickness of sub-micron order. The obtained nitrided layer consisted of two regions; the outer layer involving AlN and aluminum oxynitride and the inner layer involving metallic Al and AlN. When Al electrode was anodically polarized at 2.0 V, anodic dissolution of Al electrode occurred to give aluminum ions, which reacted with nitride ions in the melt to produce AlN particles (1-5 μm of diameter) of wurtzite structure.     

岩盐溶解速率的研究

在岩盐溶解速率及其影响因素的实验研究基础上,建立了岩盐溶解速率的计算公式。研究的结果可为岩盐开采和其他水溶法矿物开采提供参考。     

中国铬盐生产现状与发展建议

较全面地回顾了中国铬盐生产历史和现状，系统总结了铬盐行业发展过程中的经验教训，提出了中国铬盐生产发展的建议，即中国铬盐工业在大型化的同时，应推广采用新工艺、新技术；应开发新品种，进行深加工；应密切注意最新技术动向，并及时跟进。     

合成方法对NH_4MPO_4·H_2O(M=Mn,Fe,Co,Ni,Cu)颗粒形貌的影响

采用低温固相法与常规液相法合成系列磷酸铵复盐NH4MPO4.H2O(M=Mn,Fe,Co,Ni,Cu),用XRD,FT-IR和SEM对产物进行表征,比较两种合成工艺及产物的颗粒形貌和大小。结果表明,除铜盐为斜方晶系外,其余都为正交晶系。与常规液相法相比,低温固相法不需要使用溶剂,能在低温短时间内合成磷酸铵复盐类化合物,但是需要晶化才能得到良好结晶体,合成的条件较为苛刻,容易有副反应发生,所得产品是片状结构,厚度为纳米尺寸的二维纳米材料,液相反应得到的产物颗粒是层状结构的微米级产品。     

芘四硫酸四钠盐／甲基紫精复合物光物理性质的研究

本文通过吸收光谱滴定和时间分辨瞬态吸收光谱对芘四硫酸四钠盐（ｐｙｒｅｎｅｔｅｔｒａｓｕｌｆｏｎｉｃａｃｉｄｔｅｔｒａｓｏｄｉｕｍｓａｌｔ，ＰｙＴＳ）／甲基紫精（ｍｅｔｈｙｌｖｉｏｌｏｇｅｎ，ＭＶ２＋）复合物在水溶液中的光物理性质进行研究．用甲基紫精滴定芘四硫酸四钠盐时，得到该复合物的组成成份是１∶１，反之，用芘四硫酸四钠盐滴定甲基紫精时，同样得到１∶１组成成份的复合物．该复合物的形成常数是２．４×１０６ｍｏｌ－１·Ｌ，当用光激发该复合物时，发现其中存在芘四硫酸四钠盐到甲基紫精的电子转移过程，并得到该过程的动力学模型．     

Polyimide foams with ultralow dielectric constants

To explore ultralow dielectric constant polyimide, the crosslinked polyimide foams (PIFs) were prepared from 3,3′,4,4′‐benzophenonetetracarboxylic dianhydride (BTDA), 4,4′‐oxydianiline (ODA), and 2,4,6‐triaminopyrimidine (TAP) via a poly(ester–amine salt) (PEAS) process. FTIR measurements indicated that TAP did not yield a negative effect on imidization of PEAS precursors. SEM measurement revealed the homogeneous cell structure. Through using TAP as a crosslinking monomer, the mechanical properties of PIFs could be improved in comparison with uncrosslinked BTDA/ODA based PIF. The crosslinked PIFs still exhibited excellent thermal stability with 5% weight loss temperatures higher than 520°C. In the field with frequency higher than 100 Hz, the dielectric constants of the obtained PIFs ranged from 1.77 to 2.4, and the dielectric losses were smaller than 3 × 10^?2 at 25–150°C. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1734–1740, 2006     

Novel method for preparation of quaternary ammonium ionomer from epoxidized styrene–butadiene–styrene triblock copolymer and its use as compatibilizer for blending of styrene–butadiene–styrene and chlorosulfonated polyethylene

A novel method for the preparation of a quaternary ammonium ionomer of styrene–butadiene–styrene triblock copolymer (SBS) was developed by a ring‐opening reaction of epoxidized SBS with triethylamine hydrochloride in the presence of a phase transfer catalyst. The optimum conditions were studied. The ionomer was characterized by quantitative analysis, IR spectroscopy, and ¹H‐NMR spectroscopy. Its water absorbency, oil absorbency, dilute solution viscosity, and use as a compatibilizer for the blending of SBS and chlorosulfonated polyethylene (CSPE) were investigated. The results showed that, under optimum conditions, the epoxy groups can be completely converted to the quaternary ammonium groups. The IR spectrum did not exhibit the absorption peak for quaternary ammonium groups, whereas the ¹H‐NMR spectrum and titration method demonstrated it. With increasing ionic group content, the water absorbency of the ionomer increased whereas its oil absorbency decreased. These indicated the amphiphilic character of the SBS ionomer. The dilute solution viscosity of the ionomer in toluene/methanol (9/1) solvent increased with increasing quaternary ammonium group content. The ionomer was used as a compatibilizer for the blends of SBS and CSPE. The addition of a small amount of the ionomer to the blend enhanced the mechanical properties of the blends: 2 wt % ionomer based on the blend increased the tensile strength and ultimate elongation of the blend nearly 2 times. The blends of equal parts SBS and CSPE behaved as oil‐resistant thermoplastic elastomers. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1975–1980, 2006     

发酵液的组成对纳滤分离谷氨酰胺的影响

研究了谷氨酰胺发酵液中盐离子对纳滤分离提取谷氨酰铵的作用，系统地考察了操作温度和发酵液组成对纳滤分离透过特性的影响，确定了纳滤分离时发酵液最佳稀释倍数和操作温度. 结果表明，二价阳离子通过改变膜面电荷密度对谷氨酸的透过特性产生很大影响，使其截留率降低了8%. 发酵液中较高浓度的(NH4)2SO4使谷氨酸和谷氨酰胺的截留率和透过通量明显降低，但较高浓度的NH4Cl影响较小，这体现了纳滤膜对不同离子排斥力的差异. 当发酵液稀释至谷氨酰胺浓度为1%，pH调至7时，发酵液中的其它盐离子和残糖因浓度较低而对纳滤分离影响不显著.     

十二烷基苯磺酸钠水溶液聚集性质的研究

用滴体积法测出十二烷基苯磺酸钠（ＳＤＢＳ）稀水溶液的表面张力；然后求出其临界胶束浓度（ＣＭＣ）。同时通过溶液的电导率、吸收光谱以及荧光光谱测定求出其ＣＭＣ。这样测出的ＣＭＣ值为１．２～１．６×１０－３ｍｏｌ／Ｌ，与文献值相符。也研究了部分水解的聚丙烯酰胺（ＰＨＰＡＭ）对ＳＤＢＳ聚集性质的影响；发现ＳＤＢＳ的ＣＭＣ值随ＰＨＰＡＭ的加人而减少并且ＰＨＰＡＭ水溶液的粘度随ＳＤＢＳ的存在而急剧降低（类似盐效应）。这些方法与性质对强化采油（ＥＯＲ）是重要的。     

烧碱蒸发装置的改进

通过改进工艺流程，科学确定加热面积的配比，合理选择采盐泵等技术改进措施，提高了生产强度，满足了高气压的生产条件，延长了洗效周期，减少了设备的腐蚀，提高了成品碱的质量，满足了生产联二脲的要求并降低了汽耗和电耗，年可节约ll0万元。