绿色润滑剂的生物降解性及特点

阐述了绿色友好润滑剂的生物降解性和摩擦化学特点，提出了绿色润滑剂在发展过程中存在的主要问题，并对未来的发展趋势进行了预测。     

丙烯酸酯类助剂ACR的生产简况及市场分析

概述了ACR的功能、生产简况及市场趋势。     

The Structure of the Irreversibly Bound Adhesion Promoter-Substrate Interfacial Layer of γ-Aminopropylsilanetriol on Crystalline Si, as Measured by XPS and FTIR

The irreversibly bound interfacial layer deposited by the γ-aminopropysilanetriol adhesion promoter onto a crystalline silicon substrate, which remains even after profuse washing, was found by XPS to have resulted from the fragmentation and rearrangement of the original γ-aminopropylsilanetriol molecule. A mechanism is proposed, involving the homolytic scission of the terminal N-C bond. One of the subsequent reactions is believed to involve hydrogen loss by abstraction and the formation of a terminal vinyl group, which bonds to the substrate. Support for this mechanism is found in IR spectroscopy of this layer.     

由二氧化碳出发合成有机碳酸酯

对以二氧化碳为原料合成有机碳酸酯的环氧路线、酯交换和直接合成方法作了综合评述 ,认为直接合成是最佳的合成路线。碳酸酯的直接合成可在均相及多相催化体系中进行 ,负载金属、金属甲氧基化合物及碱均可作为催化剂。直接法研究的关键在于高性能催化剂的开发、由二氧化碳对金属 -氧键插入反应导致的催化循环的构筑及耦合反应的应用。     

Direct ethoxylation of fatty methyl ester over Al-Mg composite oxide catalyst

For the purpose of estimating the reaction mechanism of the direct ethoxylation of a fatty ester in the presence of an Al-Mg composite oxide catalyst, a labeled fatty methyl ester C₁₁H₂₃CO¹⁸OCH₃ containing ¹⁸O isotope was synthesized and directly ethoxylated. The product was evaluated by gas chromatography-mass spectrometry (GC-MS). The GC-MS spectra showed that the ¹⁸O isotope label was present only in the methoxy group at the molecular end of the ethoxylated fatty methyl ester. This supports the reaction mechanism of coordination anionic polymerization where the bond between the acyl and methoxy groups of the fatty methyl ester molecule was broken, caused by the bifunctional effect of the acid-base active sites; an intermediate chemisorption species was formed; and then ethylene oxide was addition-polymerized sequentially, in parallel.     

Surface modification of a biomedical poly(ester)urethane by several low‐powered gas plasmas

Several low‐powered gas plasmas were employed to treat a biomedical poly(ester)urethane using the treatment gases of CO₂, O₂, NH₃, and SO₂ with different treatment time (2, 5, 10, and 15 min). The changes of the physical and chemical characteristics of the biopolymer surface were studied. Surface morphology was evaluated by scanning probe microscopy, which showed increased roughness of the surface after plasma treatment. The wettability of the surface was examined by static water contact angle (SCA) measurements, which presented that there was a decrease of SCA in all plasma treatments compared with the untreated surface and that each gas plasma had an optimum treatment time accompanied by a minimum contact angle. X‐ray photoelectron spectroscopy indicated the changes of the surface functional groups. The data demonstrated that CO₂ and O₂ plasmas resulted in the incorporation of oxygen‐containing groups, while NH₃ plasma resulted in the combination of nitrogen‐containing groups, and SO₂ plasma resulted in the formation of sulfur‐containing groups. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1273–1282, 2006     

Solvent and oxygen effects on the free radical polymerization of 6-O-vinyladipoyl-d-glucopyranose

The vinyl ester-type glycomonomer 6-O-vinyladipoyl-d-glucopyranose was polymerized in water and alcohol solutions. In all cases, long polymerization times were necessary to achieve reasonable conversions. Depending on the nature of the solvent, polydisperse glycopolymers were obtained possessing a molecular weight ranging between 10,000 and 122,000 Da (PS equivalent). Higher alcohols appeared to act as chain transfer agents and oligomers with DP_n between 2 and 6 were indeed obtained when 2-propanol was the solvent. Also, thorough oxygen removal from the reaction mixture proved to be essential for the success of the experiment, plain nitrogen sparging being ineffective in most cases.     

乙酰柠檬酸三丁酯的合成

用柠檬酸、正丁醇、乙酸酐为原料，经酯化和酰化两步反应合成乙酰柠檬酸三丁酯。考察了催化剂、原料配比、反应温度和反应时间等因素对合成反应的影响，确定了最佳反应条件。     

尿素醇解法合成氨基甲酸乙酯的研究

对尿素醇解法合成氨基甲酸乙酯工艺进行了系统地研究,全面考察了反应温度、原料配比、反应时间及搅拌速度等因素对反应性能的影响。研究发现在反应温度为140℃,乙醇与尿素的摩尔比为4∶1,反应3.5 h,氨基甲酸乙酯最高收率为79.2%。     

含水混酸的酯化分离试验

基于中国石化扬子石化公司化工厂醋酸装置产生大量的含水甲酸、乙酸副产品,通过试验将含水混酸进行酯化、分离,得到符合工业品规格的甲酸乙酯、乙酸乙脂。试验确定酯化塔回流比为3∶1,乙醇分批次加入,乙醇实际投入量与理论量的比为1.2。酯化分离结果:甲酸乙酯的单程收率89.5%,纯度大于97%,乙酸乙酯的单程收率80.1%,纯度大于97%。