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《国际聚合物材料杂志》2012,61(3):140-144
An amperometric cholesterol biosensor was fabricated using polyaniline-coated polyester films. Polyaniline was dissolved in chloroform with camphorsulfonic acid, and polystyrene was added to this solution. Using this mixed solution, the coating was placed onto polyester films. Cholesterol oxidase was immobilized onto these films using an electrostatic layer-by-layer adsorption technique. Poly(diallyldimethylammonium chloride) was used as the counter ion source. The level of adsorption was examined and evidence of layer-by-layer adsorption was investigated using a quartz crystal microbalance (QCM). A cholesterol biosensor was fabricated from these films as a working electrode, and it was used to measure the cholesterol concentration. 相似文献
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新型聚苯胺纳米复合材料研究进展 总被引:4,自引:0,他引:4
系统综述了聚苯胺纳米复合材料的制备方法,结合典型实例详细论述了近年来研制的新型聚苯胺纳米复合材料的制备及性能,指出了聚苯胺纳米复合材料的研究方向。 相似文献
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Raju Khan Pratima R. Solanki Ajeet Kaushik S. P. Singh Sharif Ahmad B. D. Malhotra 《Journal of Polymer Research》2009,16(4):363-373
Cholesterol biosensor has been fabricated by covalently coupling cholesterol oxidase (ChOx) via glutaraldehyde onto electrochemically
prepared polyaniline film in presence of TritonX-100 [4-(1,1,3,3-tetramethylbutyl) phenyl polyethylene glycol], a non-ionic
surfactant onto indium-tin-oxide (ITO) glass substrate. These ChOx/PANI-TX-100/ITO bioelectrodes have been characterized using
Fourier transform infrared (FTIR) spectroscopy, cyclic voltammetry (CV) and scanning electron microscopy (SEM) techniques.
The results of response measurements carried out on ChOx/PANI-TX-100/ITO bioelectrodes using amperometric and photometric
techniques, reveal detection limit as 5 mg/dl, linearity from 5 to 400 mg/dl of cholesterol and sensitivity as 131 μA/(mg/dl
cm−2). These biosensing electrodes are thermally stable up to 65 °C, can be used about 20 times and have a shelf-life of about
10 weeks when stored at 4 °C. Attempts have also been made to utilize the ChOx/PANI-TX-100/ITO bioelectrodes for estimation
of free cholesterol concentration in serum samples. 相似文献
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《国际聚合物材料杂志》2012,61(11):549-556
The nanocomposite film was obtained by electrochemical co-polymerization of the corresponding monomers in the presence of functionalized carbon nanotubes and different additives. By immobilizing urease on a modified electrode of type nanocomposite film/platinum substrate a novel amperometric biosensor for the detection of urea was prepared. The polymeric and nanocomposite films were utilized as conducting films for amperometric urea sensing after covalent immobilization of urease onto film-coated electrode. The electrochemical performance of the modified electrode was studied by cyclic voltammetry, chronoamperometry, and scanning electron microscopy. The immobilized urease on the nanocomposite film surface exhibited an excellent electrocatalytic response toward reduction urea. Amperometric response was measured as a function of urea concentration at a fixed potential, in this case the open circuit potential. The obtained sensor showed rapid response and good reversibility. The response time was less than 10 s, while the reversible time was about 5–15 s. The enzymatic nanostructured electrode exhibited high sensitivity, a wide linear range, and low detection limit for electrochemical detection of urea. 相似文献
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《国际聚合物材料杂志》2012,61(7):730-744
In the present work, a simple technique is described for constructing a poly(o-anisidine) (POA)-dodecylbenzene sulphonic acid (DBS)-glucose oxidase (GOx) (POA-DBS-GOx) electrode. The enzyme glucose oxidase (GOx) was immobilized by crosslinking via glutaraldehyde on the POA-DBS film. The POA-DBS films were synthesized electrochemically on platinum substrate. The synthesized films were characterized by using electrochemical technique, conductivity measurement, UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The conductivity of the polymer films was found to be about 7.61 × 10?2 S/cm. The crosslinking of enzyme and the porous morphology of the polymer film lead to good stability and good response time of the enzyme electrode. The stability and lifetime of the POA-DBS-GOx electrode have been studied. It shows very good stability and response for 3–4 weeks at 4°C. The results of this study reveal that a phosphate buffer gives better response than acetate buffer in amperometric measurements. 相似文献
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采用3种不同制备方法获得了聚氢酯/蒙脱土(PU/MMT)纳米复合材料。通过对材料力学性能测试,发现制备方法对纳米复合材料的拉伸强度杀Ⅱ断裂伸长率有明显影响。蒙脱土和三羟基聚氧化丙烯醚(GP03)预研磨混合制备法所得的纳米复合材料呈现出较好的力学性能。当有机蒙脱土质量分数为2%时,其拉伸强度和断裂伸长率分别比纯聚氨酯材料提高丁30%-68%。 相似文献
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尼龙6/粘土纳米复合材料的性能研究进展 总被引:1,自引:1,他引:0
粘土是一种层状硅酸盐,以纳米尺寸分布在聚合物中能提高聚合物的各种性能,本文综述了尼龙6/粘土纳米复合材料在机械性能、热稳定性、阻隔性能、结晶性能和流变行为等与纯尼龙6性能相比的优越性,同时详细地论述了性能得到改善的机理。 相似文献
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首先以甲基丙烯酸二甲氨基乙酯(DMAEMA)为分散助剂得到石墨烯/MMA分散液,然后采用乳液聚合法制备了PMMA/石墨烯纳米复合材料。通过傅里叶变换红外光谱仪、拉曼光谱仪、扫描电子显微镜、透射电子显微镜、差示扫描量热仪、热重分析仪以及电子万能试验机、冲击试验机、高阻计等仪器设备对PMMA/石墨烯纳米复合材料的结构与性能进行分析和测试。结果表明,通过DMAEMA的助分散作用,实现了PMMA对石墨烯的完全包覆,并且DMAEMA的胺基与石墨烯表层官能团间存在强相互作用;石墨烯的引入提高了PMMA/石墨烯纳米复合材料的热稳定性,玻璃化转变温度(Tg)增加约6.4 ℃、初始热分解温度增加约38.3 ℃;石墨烯的引入改善了PMMA/石墨烯纳米复合材料的抗静电性能及拉伸性能,但冲击性能略有下降。 相似文献