共查询到18条相似文献,搜索用时 125 毫秒
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采用NaOH溶液对腈纶进行水解,表面接枝蛋白质制得改性腈纶。讨论了NaOH浓度、水解温度、水解时间对腈纶接枝效果的影响。结果表明:在水解反应温度80~90℃、NaOH溶液质量分数14%、水解时间15 m in时,改性腈纶接枝率较高。力学性能分析和电镜表面观察表明:在腈纶表面接枝大豆蛋白质,不仅可以赋予纤维表面完整的蛋白质覆盖层,而且还可以较好的弥补纤维因水解而产生的表面损伤和力学性能下降等缺陷。 相似文献
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研究了腈纶表面接枝蛋白质水解工艺条件对吸水率和接枝率的影响关系。通过红外光谱分析结果证实了腈纶纤维已接枝上大豆蛋白。实验结果还表明,水解时间、水解温度及NaOH浓度都对腈纶纤维的吸水率和接枝率有很大的影响。在一定的水解强度范围内,腈纶的吸水率及接枝率均随水解强度的增加而不断提高;当水解强度过高时,接枝率反而会下降。腈纶表面接枝蛋白质的最佳水解工艺条件为:水解时间15 min、水解温度为90℃、NaOH浓度为10%。X-射线衍射分析表明,腈纶经过水解、接枝后,纤维的聚集态结构没有明显变化。 相似文献
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采用自组装技术制备了一系列在金表面不同摩尔比的PEG硫醇混合自组装膜,并将蛋白质共价固定在膜表面。通过AFM、接触角测试仪和XPS技术对混合自组装膜和蛋白质接枝反应后表面的物理和化学性质进行了分析表征。通过抗原-抗体反应实验检验了蛋白质膜表面生物活性的相对大小。结果表明:自组装膜表面的比例组成与溶液中的组成并不完全一致。接枝后蛋白质的形貌及蛋白质膜表面粘附力分布与自组装膜的表面组分有关并会影响其与抗体的反应活性。当反应溶液中SH-PEG-OCH3/SH-PEG-COOH摩尔比为1∶6时,所形成的自组装膜的表面羧基含量最大,同时粘附力也达到最高值,蛋白质活性也最大。 相似文献
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结合膜色谱分离蛋白质的应用背景,采用钴源辐射接枝法和紫外辐射接枝法对聚乙烯膜进行了膜孔表面接枝改性的初步研究与探讨。 相似文献
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蚕丝蛋白改性腈纶的研制(英文) 总被引:4,自引:1,他引:4
先用丙烯腈对蚕丝蛋白进行接枝改性 ,然后将其与常规腈纶纺丝原液共混纺丝 ,制备了蚕丝蛋白改性腈纶。结果表明 :随着蛋白含量的增加 ,蚕丝蛋白改性腈纶的断裂强度会逐渐下降 ,断裂伸长则变化不大 ,当纤维中蚕丝蛋白的含量小于 15 %时 ,其机械性能基本上能满足后纺加工的要求 ;随着蛋白含量的增加和改性比的增大 ,蚕丝蛋白改性腈纶的保水率增加 ;改性比的变化对蚕丝蛋白改性腈纶的机械性能基本没有影响 ;蚕丝蛋白改性腈纶织物的导湿性能较常规腈纶织物有显著提高 相似文献
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蛋白质在载体表面的吸附行为,如其吸附速率、吸附量以及取向和构象的变化,在很大程度上依赖于载体材料的表面化学组成。调控载体材料的表面化学组成已成为控制蛋白质吸附行为的重要手段。本文主要对载体材料表面不同组成对蛋白质吸附行为的影响进行了归纳。介绍了材料表面的功能基团包括疏水基团(甲基和含氟基团)和亲水基团(羟基、氨基和羧基)对蛋白质吸附行为的影响。另外,在载体材料表面接枝聚合物链是一种常用的有效调控表面化学组成的方法。重点介绍了材料表面接枝不同聚合物链时,聚合物链的种类、长度、密度和链的结构对蛋白质吸附行为的影响。 相似文献
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Summary A novel method of modifying polyacrylonitrile (PAN) fibers by grafting of soybean protein (SP) onto it was studied. The reactant
of PAN-g-SP fiber was prepared based on chlorination of the hydrolyzed PAN fiber. The effects of chlorination and grafting
conditions on the grafting efficiency were investigated. The grafting efficiency first increases with the increase of the
addition of thionyl chloride (SOCl2), chlorination time and temperature and then levels off. In grafting reaction, grafting efficiency increases at first and
then declines significantly with increasing addition of sodium hydroxide (NaOH), grafting temperature and time. The grafted
polymer was characterized by FT-IR spectroscopy, X-ray diffraction and SEM images. The results indicated that SP was grafted
onto the PAN fiber. PAN-g-SP also exhibits good hygroscopicty and proper mechanical properties. 相似文献
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Yufang Liu Chen Xu Binbin Xie Wenhan Hu Yi Li Chen Yao 《Journal of Coatings Technology and Research》2018,15(2):403-414
In this report, antifouling polyacrylonitrile (PAN) ultrafiltration membranes were prepared from blends of PAN/polyglycidyl methacrylate (PGMA) via phase inversion method followed by the grafting of natural amino acids through epoxy ring-opening reaction. The grafted PAN membranes possessed highly stable hydrophilic surfaces as a result of the grafting of amino acids, which was adequately demonstrated in attenuated total reflectance–Fourier transform infrared spectroscopy (ATR/FTIR), X-ray photoelectron spectroscopy (XPS), and contact angle measurements. The results of tensile strength and scanning electron microscopy (SEM) images further proved that the surface modification had little effect on their mechanical properties, surface, and cross-sectional morphologies. Meanwhile, remarkable resistance against bovine serum albumin (BSA) and lysozyme (Lyz) fouling was observed for the neutral amino acid-based PAN membranes due to the formation of zwitterionic hydration layer on the membrane surface, while PAN membranes grafted with charged amino acids were able to prohibit the approach of like charged proteins with reduced deposition and provide the driving force for oppositely charged protein adsorption. Furthermore, the ultrafiltration and antifouling performance of PAN membranes were investigated by BSA filtration experiments. Compared with the pristine PAN membrane, all the modified PAN membranes exhibited higher pure water flux, better flux recovery ratio, lower rejection, less total permeation resistance, and preferable stability, having potential applications in protein separation and purification. 相似文献
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A new kind of functionalized polypropylene(PP)-acrylate grafted fiber were prepared by radiation-induced graft polymerization
of methyl acrylate (MA), ethyl acrylate(EA) and butyl acrylate (BA) monomer onto the PP fiber matrix, as a recovery adsorbent
for insoluble organic chemicals. The grafting conditions of monomer concentration and irradiation time on the grafting degree
were optimized. The obtained grafted fiber sample was identified by Fourier transform infrared (FT-IR) spectrometer and scanning
electron microscopy (SEM) to characterize the chemical and morphological changes of the polypropylene fiber surface. The adsorption
results indicated that the grafted fiber could be used to remove organic chemicals from water surface. The adsorption capacity
of grafted fiber with different acrylate monomer was obviously different for the same chemicals, therefore, investigations
with respect to organic removal, dynamic oil retention, and reusability, the effect of monomer polarity on the adsorption
capacity of grafted fiber was especially highlighted in this study. 相似文献
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The cellophane films were grafted with PAN for various time durations in magnetron enhanced air plasma. A magnetron-coupled plasma system was developed for the purpose. The rates of polymer deposition and etching were studied. The changes occurring in the angle of contact of water were studied. The attenuated total reflection—infrared spectroscopic studies confirmed the grafting of cellophane surface by polyacrylonitrile (PAN). The water vapor transmission rates through the grafted samples were also studied. 相似文献
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Vandana Singh Ashutosh Tiwari Devendra Narayan Tripathi Rashmi Sanghi 《应用聚合物科学杂志》2004,92(3):1569-1575
Using microwave (MW) irradiation grafting of polyacrylonitrile (PAN) onto guar gum in water was done without using any radical initiator or catalyst within a very short reaction time. The extent of grafting could be adjusted by controlling the reaction conditions and maximum percentage grafting (%G) of about 188% was obtained under optimum conditions in 1.66 min. The average molecular weight of the grafted PAN chains and water‐retention power of the alkali hydrolyzed MW‐grafted gums were also determined and compared with those of the conventionally synthesized (cs) graft copolymer. A representative MW‐grafted copolymer, guar‐g‐polyacrylonitrile was characterized by IR, NMR, XRD, TGA, and elemental analysis. A plausible mechanism for the grafting under MW was proposed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1569–1575, 2004 相似文献
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Surface modification of membranes of an acrylonitrile copolymer (PAN) containing 5.5% methyl methacrylate (MMA) and 4.0% sodium methylpropylenesulfonate by grafting acrylamide (AAm) with cetric ammonium nitrate as initiator in the aqueous medium has been studied. Results showed that the extent of grafting was varied with some parameters, such as dimethyl formamide and Tween-20 amount in the reaction solution, concentration of AAm, and reaction time. The grafted copolymer was verified by infrared spectra and X-ray photoelectron spectroscopy. Both of these methods also showed that the ester group of MMA unit on the surface of PAN membranes may be partially hydrolyzed into carboxyl group in the copolymerization condition. Surface and pore structures of PAN membranes after grafting were viewed under a scanning electron microscope (SEM). From SEM photos we know that AAm homopolymer branches were grafted onto the surface of the membrane and the morphology of membrane did not change. Results of contact angle of isooctane on the membrane under water showed that the wettability of the modified membrane was improved. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1521–1529, 1997 相似文献