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41.
L. Sauguet B. Ameduri B. Boutevin 《Journal of polymer science. Part A, Polymer chemistry》2006,44(15):4566-4578
The radical terpolymerization of 8‐bromo‐1H,1H,2H‐perfluorooct‐1‐ene with vinylidene fluoride (VDF) and perfluoro(4‐methyl‐3,6‐dioxaoct‐7‐ene) sulfonyl fluoride is presented. Changing the feed compositions of these three fluorinated comonomers enabled us to obtain different random‐type poly[vinylidene fluoride‐ter‐perfluoro(4‐methyl‐3,6‐dioxaoct‐7‐ene) sulfonyl fluoride‐ter‐8‐bromo‐1H,1H,2H‐perfluorooct‐1‐ene] terpolymers containing various sulfonyl fluoride and brominated side groups. Yields higher than 70% were reached in all cases. The hydrolysis of the sulfonyl fluoride group into the ? SO3Li function in the presence of lithium carbonate was quantitatively achieved without the content of VDF being affected, and so dehydrofluorination of the VDF base unit was avoided. These original terpolymers were then crosslinked via dangling bromine atoms in the presence of a peroxide/triallyl isocyanurate system, which produced films insoluble in organic solvents such as acetone and dimethylformamide (which totally dissolved uncured terpolymers). The acidification of ? SO3Li into the ? SO3H function enabled protonic membranes to be obtained. The thermal stabilities of the crosslinked materials were higher than those of the uncured terpolymers, and their electrochemical performances were investigated. According to the contents of the sulfonic acid side functions, the ion‐exchange capacities ranged from 0.6 to 1.5 mequiv of H+/g, whereas the water uptake and conductivities ranged from 5–26% (±11%) and from 0.5 to 6.0 mS/cm, respectively. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4566–4578, 2006 相似文献
42.
Marc Visseaux Mickael Terrier Andr Mortreux Pascal Roussel 《Comptes Rendus Chimie》2007,10(12):1195-1199
The reaction of one equivalent of Nd(BH4)3(THF)3 with an half equivalent of dialkylmagnesium in the presence of a stoichiometric amount of pentamethylcyclopentadiene cleanly affords a new kind of half-sandwich of neodymium that is stable toward comproportionation. This strategy can be advantageously applied to generate in situ catalysts allowing the controlled polymerisation of isoprene. 相似文献
43.
Carlo Carlini Valentina De Luise Anna Maria Raspolli Galletti Glauco Sbrana 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):200-206
Novel catalytic systems, prepared in situ by the oxidative addition of 8‐hydroxyquinoline ligands to bis(1,5‐cyclooctadiene)nickel(0) and activated by methylaluminoxane, were studied in ethylene polymerization. When 8‐hydroxyquinoline was employed, only oligomeric products were obtained. On the contrary, 5,7‐dinitro‐8‐hydroxyquinoline gave linear polyethylene (PE), but with a modest activity. For the catalyst based on 5‐nitro‐8‐hydroxyquinoline, the productivity was largely dependent on the content of free trimethylaluminum (TMA) present in the commercial aluminoxane. The progressive optimization of the TMA/oligomeric methylaluminoxane ratio increased the productivity, which reached 700 kg of PE/(mol of Ni × h), by an order of magnitude. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 200–206, 2006 相似文献
44.
对于均值K IRCHHOFF板非线性边界镇定问题给出几点注记.首先应用G reen公式对具有非线性边界反馈控制的均值K IRCHHOFF板所决定的非线性系统的能量衰减速度进行了重新推导,从而修正了前人的结果.然后应用极大单调函数的定义和分部积分技巧,对均值K IRCHHOFF板非线性边界镇定问题所决定的非线性算子A的极大单调性给出了重新证明,进而更正了已有文献中相应证明的欠妥之处. 相似文献
45.
46.
以2-萘甲酸为原料,经硝化,酯化,重氮化,选择性催化氢化,BOC酸酐保护等六步反应,完成了N-BOC-8氨甲基-2-萘甲酸(1a)的合成,为化合物1的合成提供了新的合成途径。 相似文献
47.
Two greener procedures for flow-injection spectrophotometric determination of nitrite in natural waters were developed and critically compared. Replacement of toxic reagents, waste minimization and treatment were exploited to attend the standards of clean chemistry. The flow system was designed with solenoid micro-pumps in order to minimize reagent consumption and waste generation. The first procedure is based on the Griess diazo-coupling reaction with sulfanilamide and N-(1-naphthyl)ethylenediamine (NED) yielding an azo dye, followed by photodegradation of the low amount of waste generated based on the photo-Fenton reaction. The second procedure is based on the formation of iodine from nitrite and iodide in acid medium in order to avoid the use of toxic reagents. For Griess method, linear response was achieved up to 1.0 mg L− 1, described by the equation A = − 0.007 + 0.460C (mg L− 1), r = 0.999. The detection limit was estimated as 8 μg L− 1 at the 99.7% confidence level and the coefficient of variation was 0.8% (n = 20). The sampling rate was estimated as 108 determinations per hour. The consumption of the most toxic reagent (NED) is reduced 55-fold and 20-fold in comparison to batch method and flow injection with continuous reagent addition, respectively. A colorless residue was obtained by in-line photodegradation with reduction of 87% of the total organic carbon content. The results obtained for natural water samples were in agreement with those achieved by the reference method at the 95% confidence level. For the nitrite–iodide method, linear response was observed up to 2.0 mg L− 1, described by the equation A = − 0.024 + 0.148C (mg L− 1), r = 0.999. The detection limit was estimated as 25 μg L− 1 at the 99.7% confidence level and the coefficient of variation was 0.6% (n = 20). The sampling rate was estimated as 44 determinations per hour. Despite avoiding the use of toxic reagents, the nitrite–iodide method presented worst performance in terms of selectivity and sensitivity. 相似文献
48.
新试剂3,5—二溴—4—偶氮8—羟基喹啉苯基荧光酮光度法测定微量铝 总被引:9,自引:0,他引:9
在溴化十六烷基三甲胺(CTMAB)存在下,PH6,0的HAc-NaAc缓冲介质中,铝与新试剂3,5-二溴-4-偶氮8-羟基喹啉苯基荧光酮形成红色三元胶束配合物,最大吸收波长位于564nm,表观摩尔吸光系数ε为1.35×10^5.mol^-1.cm^-1,铝浓度在0~5μg/25mL范围内符合比耳定律,拟定的方法用于铝铁黄铜中微量铝的测定,结果满意。 相似文献
49.
50.
冠醚型电极对局部麻醉药响应功能的研究 总被引:3,自引:0,他引:3
用二苯并24-冠-8作为活性物质、邻苯二甲酸二(2-乙基)己酯为增塑剂制得PVC膜电极。电极对局麻药丁卡因、普鲁卡因和利多卡因具有能斯特响应,用于局麻药针剂的测定取得满意的结果。 相似文献