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141.
研究了导电聚合物聚(3-丁基噻吩)(PBT)在大气环境下的导电热稳定性。在室温至220℃范围内,测试电导率随时间及温度的变化。TGA分析以及化学分析的结果表明:掺杂态的PBT大约在140℃附近有一转化温度,低于或高于这一转化温度,电导率下降的决定因素各不相同。高于转化温度时,电导率下降的主要原因是反离子和高分子主链的解离,进而发生化学反应,影响了高分子主链的结构。XPS测试结果表明:经热处理后的P 相似文献
142.
Highly ordered mesoporous bioactive glasses with superior in vitro bone-forming bioactivities 总被引:3,自引:0,他引:3
143.
毛细管电泳质谱联用技术及其应用 总被引:9,自引:0,他引:9
本文介绍了用于毛细管电泳质谱联用仪器的多种接口技术,描述了CZE,CIEF,CGE,MEKC和CITP等毛细管电泳技术和四极质谱,离子阱质谱,傅 叶变换离子回旋共振质谱,飞行时间质谱,磁质谱,解吸质谱等联用的现状及发展前景,对近年来CE-MS在酶解产物。蛋白质和肽,核苷酸,药物及代谢产物等领域中的应用作了详细述评。 相似文献
144.
145.
Alcohol dehydrogenase (ADH) has been immobilized on a nickel hexacyanoferrate modified microband gold electrode surface by a glutaraldehyde/bovine serum albumin (BSA) cross-linking procedure to provide a new amperometric sensor for the assay of ethanol. The resulting enzyme electrode exhibits excellent electrocatalysis for the oxidation of reduced nicotinamide-adenine dinucleotide (NADH). The amperometric determination is based on the electrochemical detection of NADH which is generated in the enzymatic reaction of ethanol with NAD(+) under catalysis of ADH. The influence of various experimental conditions was examined for the determination of the optimum analytical performance. The sensor responds rapidly to ethanol with a detection limit of (5.0 +/- 0.3) x 10(-7) mol 1(-1). The response current increases linearly with ethanol concentration up to 5 mmol 1(-1). The sensor remains relatively stable for about 1 week. 相似文献
146.
Junfeng Zhou Xiaochen Dong Tao Chen Qiang Yang Qiaohua Tan Jianjun Wang 《European Polymer Journal》2007,43(5):2088-2095
A series of well-defined two-armed polymers containing a crown ether core, poly(stearyl methacrylate)-crown ether-poly(stearyl methacrylate) (PSMA-crown-PSMA), with different molecular weight were synthesized via atom transfer radical polymerization (ATRP). The resultant polymers were characterized by 1H NMR and GPC. The self-assembly behaviors of this kind of polymer in selective solvents were studied by TEM, and it was found that polymers with different molecular weight can directly self-assemble into hollow spheres, solid spheres and a monolayer film with regular pores by varying molecular weight and water content. The possible molecular packing motels for their self-assembly behaviors were proposed. 相似文献
147.
148.
[structure: see text] Two sequential transition states are calculated at the B3LYP/6-31G(d,p) level for the deazetization of 3b. The intrinsic reaction coordinate for loss of nitrogen passes through a transition state and then a valley-ridge inflection point and ultimately leads to the transition state for the Cope rearrangement of semibullvalene 4b. The energetic and geometrical consequences are discussed. 相似文献
149.
三(2-苯并咪唑亚甲基)胺硝酸镍(Ⅱ)配合物的合成及结构 总被引:5,自引:0,他引:5
三(2-苯并咪唑亚甲基)胺简称NTB与Ni(Ⅱ)的硝酸盐形成配合物C28H35N9O9S2Ni。本文报道其合成,红外光谱及晶体结构。该化合物为三斜晶系,空间P1↑-,a=9.650(3),b=12.716(2),c=14.436A,α=11.46(2),β=91.66(3),γ=97.55(2)°,V=1718(2)A^3,Z=2,F(000)=793,Dc=1.48g/cm^3,Mr=764.1 相似文献
150.
A series of P[N-isopropylacrylamide (NIPAM)] latexes with different contents of cyano groups were successfully prepared by either seeded
or shot-growth polymerizations of an aqueous solution containing acrylonitrile (AN) onto a seed P[NIPAM] latex, respectively, and further characterized by FT-IR, 1H-NMR, elemental analysis, as well as by quasielastic light scattering (QELS) and scanning electron microscopy (SEM). All
prepared surface-cyanofunctionalized P[NIPAM] latexes exhibited the same range of lower critical solution temperature (LCST) as a pure P[NIPAM] latex. The shot polymerization process proved more efficient at yielding cyano derivatized latexes than the seeded
polymerization technique. The amount of incorporated cyano groups onto the particles was determined with a good correlation
both by 1H-NMR and elemental analysis. The higher the amount of initially introduced AN monomer in the reaction mixture, the more cyano
groups were incorporated onto the particles. The surface of the particles with high content of cyano groups appeared quite
rough by SEM in comparison with that of the pure P[NIPAM] particles.
Received: 25 February 1998 Accepted: 23 June 1998 相似文献