白腐菌Panus conchatus降解稻草木素机理研究──(一)低分子木素降解产物各组分的分离及特征

经白腐菌Panusconchatuss发酵15天的稻草用乙酸乙酯进行抽提可有效分离出生物作用后的低分子量木煮降解产物。利用这些低分子降解产物在酸碱度不同的介质以及不同的有机溶剂中的溶解度不同进一步分离、分级和提纯，获得酚类（LP），芳香酸类（LA1—4）以及中性物质三个组份。我们发现LP与LA是降解产物中的主要组份，它们的得率分别为51．1％和34．4％。如此高的LP得率是白腐菌P．conchatus降解稻草木素的重要特征。本文还利用红外光谱和核磁共振技术对LP和LA中最多的一个组份LA—1的可能化学结构特征进行剖析。     

双轴向载荷Ⅰ－Ⅱ复合型裂纹J积分断裂准则探讨

通过理论分析和双轴向断裂试验，对我国压力容器常用钢１６ＭｎＲ所制成的含中心穿透Ⅰ－Ⅱ复合型裂纹十字形试样的断裂规律进行了试验研究，探讨了Ⅰ－Ⅱ复合型裂纹Ｊ积分断裂准则。结果表明，不同的载荷比和裂纹倾角下Ⅰ－Ⅱ复合型裂纹的启裂Ｊｉ值接近，复合型Ｊ积分断裂准则预测的启裂载荷与试验结果相吻合     

机压成型高效节能格子砖

机压成型高效节能格子砖丘必云，黄渊鳞，林剑成（中国轻工总会玻璃搪瓷研究所２０００５２）ＰｒｅｓｓｅｄＨｉｇｈＥｆｆｉｃｉｅｎｔＣｈｅｃｋｅｒｓ￥ＱｉｕＢｉｙｕｎ；ＨｕａｎｇＹｕａｎｌｉｎ；ＬｉｎＪｉａｎｃｈｅｎｇ（Ｇｌａｓｓ＆ＥｎａｍｅｌＲｅｓｅａｒ...     

Novel fluorescent polynorbornenes with multi-functional armed structure by using highly stable block macroinitiators via a combination of living ring-opening metathesis polymerization and atom transfer radical polymerization

Novel organosoluble fluorescent polynorbornenes with multi-functional armed structure were designed and prepared by using highly stable block macroinitiators via a combination of living ring-opening metathesis polymerization (ROMP) and atom transfer radical polymerization (ATRP). A bromo-containing functional norbornene (NBMBr) was prepared from the Diels-Alder reaction of cyclopentadiene and allyl bromide. The diblock copolymer of 5-(N-carbazolyl methyl)bicycle[2.2.1]hept-2-ene (CbzNB) and NBMBr was successfully prepared using living ROMP and used as a novel macroinitiator [poly(CbzNB-b-NBMBr)] for ATRP. Carbazoyl-containing multi-functional armed copolymer with poly(methyl methacrylate) (PMMA) was prepared by using poly(CbzNB-b-NBMBr) as a macroinitiator for ATRP. Strong fluorescence emissions (370-450 nm) were observed in the low excimer-forming multi-functional armed fluorescent polynorbornenes. The fact is that low excimer-forming carbazole-containing polymeric compound would apparently be favorable in photoconductive materials. The multi-functional armed structure make this compound an attractive candidate for applications as multi-modified hole transport materials in molecular electronic devices. Multi-modification could be further considered to be carried out by using such a functional bromo group at the end of multi-arms.     

Effects of poly(methyl methacrylate)‐based low‐profile additives on the properties of cured unsaturated polyester resins. II. Volume shrinkage characteristics and internal pigmentability

The effects of three series of self‐synthesized poly(methyl methacrylate) (PMMA)‐based low‐profile additives (LPAs), including PMMA, poly(methyl methacrylate‐co‐butyl acrylate), and poly(methyl methacrylate‐co‐butyl acrylate‐co‐maleic anhydride) with different chemical structures and MWs on the volume shrinkage characteristics and internal pigmentability for low‐shrink unsaturated polyester (UP) resins during curing were investigated by an integrated approach of static phase characteristics of the ternary styrene (ST)/UP/LPA system, reaction kinetics, cured‐sample morphology, microvoid formation, and property measurements. The relative volume fraction of microvoids generated during the cure was controlled by the stiffness of the UP resin used, the compatibility of the uncured ST/UP/LPA systems, and the glass‐transition temperature of the LPAs used. On the basis of the Takayanagi mechanical model, the LPA mechanism on volume shrinkage control, which accounted for phase separation and microvoid formation, and factors leading to both a good volume shrinkage control and acceptable internal pigmentability for the molded parts are discussed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3388–3397, 2004     

反应性乳化剂应用于丙烯酸酯类乳液压敏胶的研制

使用正交试验法设计压敏胶配方,得到用反应性乳化剂参与的AA、HEA、BA和EA、M AA等多元共聚物乳液,研究该聚合物应用于压敏胶的初粘、持粘、剥离强度等力学性能。结果表明,在该体系下引发剂用量、反应温度、AA、反应性乳化剂用量对压敏胶乳液综合性能关系密切,其它各因素影响不明显。得到的优化配方为BA(83%)、AA(1%)、HEA(1%)、MM A和EA的混合单体(15%)。     

Gel polymer electrolyte based on poly(acrylonitrile-co-styrene) and a novel organic iodide salt for quasi-solid state dye-sensitized solar cell

A gel polymer electrolyte based on poly(acrylonitrile-co-styrene) as polymer matrix and N-methyl pyridine iodide salt as I⁻ source was prepared. Controlling the concentration of polymer matrix of poly(acrylonitrile-co-styrene) at 17.5 wt.%, mixing the binary organic solvents mixture ethylene carbonate and propylene carbonate with 6:4 (w/w), and the concentration of N-methyl pyridine iodide and iodine with 0.5 and 0.05 M, respectively, the gel polymer electrolyte attains the maximum ionic conductivity (at 30 °C) of 4.63 mS cm⁻¹. Based on the gel polymer electrolyte, a quasi-solid state dye-sensitized solar cell was fabricated and its overall energy conversion efficiency of light-to-electricity of 3.10% was achieved under irradiation of 100 mW cm⁻².     

Controllable fabrication of SnO2-coated multiwalled carbon nanotubes by chemical vapor deposition

A simple and efficient approach for coating multiwalled carbon nanotubes (MWCNTs) with size-controllable SnO₂ nanoparticles by chemical vapor deposition has been developed using tin hydride (SnH₄) gas as the source of SnO₂ at 550 °C. The size and coverage of SnO₂ nanoparticles can be adjusted by simply controlling the deposition time and the flow rate of the SnH₄/N₂ mixture gas during the CVD procedure. In addition, by using the MWCNTs as a sacrificial template, a kind of one-dimensional chain-like SnO₂ nanostructure has been synthesized by increasing the deposition temperature to 730 °C. This technique may provide a good way to produce tunable SnO₂-MWCNT composites.     

Curing of unsaturated polyester resins: Effects of comonomer composition. II. High-temperature reactions

The effects of comonomer composition of the curing kinetics of unsaturated polyester (UP) resins at 100–120°C were investigated by differential scanning calorimetry (DSC) and infrared spectroscopy (IR) over the entire conversion range. One commercial UP resin, UP2821, with 6.82 unsaturated C?C bonds per polyester molecule, was used. For styrene/UP2821 reactions, experimental results of the initial and maximum reaction rates by DSC at 100–120°C revealed that the styrene content, as well as the reaction temperature, would affect the formation of microgel structures. As the initial molar ratio of styrene to polyester C?C bonds increased, the styrene swelling effect could enhance the intramicrogel crosslinking reactions, while the styrene dilution effect could diminish the intermicrogel crosslinking reactions. The competition between the two reactions would depend on the reaction temperatures. Finally, a microgel-based reaction mechanism was proposed for the high temperature reactions. © 1993 John Wiley & Sons, Inc.