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1.
有机-无机杂化膜的研究进展   总被引:4,自引:0,他引:4  
有机-无机杂化膜结合了传统有机膜与无机膜的优良性能,已成为膜领域的研究热点之一。本文综述了有机-无机杂化膜的研究现状,归纳了有机-无机杂化膜的分类、制备技术、应用及其优越性,并针对现存的问题及今后的研究发展提出了一些建议。  相似文献   

2.
有机无机杂化膜材料的制备技术   总被引:18,自引:1,他引:17  
有机无机杂化膜兼有机膜韧性和无机膜耐高温性能,具有优良的气体渗透选择性,成为高分子化学和材料科学等领域的研究热点.本文综述了近年来有机无机杂化膜材料的制备技术进展,着重探讨了溶胶-凝胶法制备聚酰亚胺类杂化膜材料的研究状况,并作了简要述评。  相似文献   

3.
有机-无机杂化分离膜研究进展   总被引:1,自引:0,他引:1  
有机-无机杂化膜材料结合了有机膜材料和无机膜材料的优良性能,已成为分离膜材料研究的一个热点。本文以有机、无机组分间相互作用类型对其进行分类,着重介绍组分间以化学键相结合的有机-无机杂化膜的优良特性,总结了影响此类杂化膜结构和性能的主要因素,概括了它在膜分离中的应用,提出了目前研究工作中存在的不足,并做出了简要的述评。  相似文献   

4.
采用溶胶-凝胶法,将钛酸酯和硅烷偶联剂(KH-560)进行共水解,经涂膜、固化,制备了一系列含有无机二氧化钛纳米相的无机/有机杂化膜层材料,通过不同方法对杂化膜层的微结构、光学、机械和热性质进行了表征.结果表明,所得到的有机/无机纳米复合膜层,在可见光范围内的透过率均在90%以上,同时具有较好的耐热性和较高的折射率(nd=1.47~1.73),并且膜层与基材的附着性好,铅笔硬度达到4~5H.  相似文献   

5.
阴离子交换膜的制备和改性研究进展   总被引:3,自引:0,他引:3  
离子膜交换有广泛的应用,本文介绍了有机阴离子交换膜的修饰和改性以及新兴的有机-无机杂化阴离子交换膜的制备方法和发展现状,特别是介绍了近年来开发的一些不需要使用氯甲醚的阴离子膜制备新路线。  相似文献   

6.
利用手性阴离子酸表面活性剂, 采用软模板法制备了具有不对称孔道结构的小介孔二氧化硅(SiO2)粒子. 将小介孔SiO2粒子引入聚偏四氟乙烯(PVDF)和聚酰亚胺(PI)中构建了两种有机/无机杂化膜. 利用傅里叶变换红外光谱(FTIR)、 透射电子显微镜(TEM)、 扫描电子显微镜(SEM)和比表面积分析等表征了小介孔SiO2粒子和有机/无机杂化膜的微结构, 并通过超滤实验和气体渗透实验分别考察两种杂化膜的性能. 研究结果表明, 表面含有大量亲水基团的小介孔SiO2粒子具有规则有序排列的孔道结构, 该孔道结构呈现螺旋扭曲和不对称性. 构建的两种有机/无机杂化膜的极性显著提升, 进而有效增强了PVDF杂化膜的膜通量和抗污染性能及PI杂化膜对CO2气体的分离性能, 克服了高分子膜的博弈效应(Trade-off效应). 另外, SiO2的小介孔孔道还可以在PI杂化膜中引入优先通过CO2分子的限域传质通道, 加速了CO2气体在杂化膜中扩散. 但过多小介孔SiO2粒子的加入导致其在高分子基质中团聚, 削弱杂化膜的极性和亲水性, 从而降低了两种杂化膜的分离性能.  相似文献   

7.
本文通过含溴聚芳醚砜合成可溶性含(4-磷酸)苯侧基聚芳醚砜, 并通过与磺酸功能化聚倍半硅氧烷杂化的方法, 制备了磷酸聚合物为基体的有机-无机杂化高性能质子交换膜材料.  相似文献   

8.
近年来 ,用 L B技术组装有机 -多酸超分子光、电和磁功能杂化材料进展迅速 ,已引起研究者的广泛兴趣与关注 [1~ 4 ] . Clemente- Leon等 [5] 首次用 Keggin结构钨系杂多酸 ( XW12 On- 40 ,X=H2 ,P,Si,B,Co)与类脂作用制备了一系列有机 /无机超晶格 LB膜 ,并研究了它们的磁学性能 .为了设计出新型功能性有机 /无机杂化材料 ,本文报道了氧化能力更强的 1 2 -钨钼磷混配杂多阴离子与二甲基双十八烷基铵杂化 L B膜的制备、结构与成膜性能 .1 实验部分1 . 1 试剂与仪器  N ,N -二甲基双十八烷基氯化铵 (日本株式会社 ,简称 DODA ) …  相似文献   

9.
将天然聚合物褐藻酸钠添加到无机硅溶胶-凝胶膜,获得一种新型的无机/有机杂化膜。用此杂化膜包埋酪氨酸酶,制备电化学苯酚传感器。研究表明:硅溶胶-凝胶/褐藻酸钠复合膜能有效克服纯无机溶胶-凝胶膜的脆性;避免膜的裂开;提供生物酶所适宜的微环境;有效保持所固定酶的生物活性。所制备的传感器测定苯酚的线性响应范围为3.4-93.1μmol/L,其线性回归方程i(μA)=0.0774C(μmol/L) 0.1616,r=0.9980。检出限为1.33μmol/L。  相似文献   

10.
溶胶-凝胶法制备硅系有机-无机杂化分离膜   总被引:3,自引:0,他引:3  
以α-Al2O3多孔陶瓷片为载体,用溶胶-凝胶法制备有机-无机杂化分离膜.通过考察前驱物的组成及杂化溶胶的合成条件对制膜工艺过程的影响,得到了制备有机-无机杂化分离膜的各种适宜性参数.红外光谱(FTIR)分析结果表明,杂化溶胶的性能不仅决定分离膜的性能,而且对膜热处理过程中的龟裂有很大影响.膜层的厚度为1~2μm;在膜两侧压差为0.10MPa、n(PTMOS)/n(TEOS)=1.16时,膜对O2/N2,CO2/N2和CO2/O2的分离因子分别为2.30,4.31和1.17,渗透系数为75.81×10-17,75.28×10-17和72.78×10-17m3(STP)·m/(m2·s·Pa).  相似文献   

11.
This critical review presents a discussion on the major advances in the field of organic-inorganic hybrid membranes for fuel cells application. The hybrid organic-inorganic approach, when the organic part is not conductive, reproduces to some extent the behavior of Nafion where discrete hydrophilic and hydrophilic domains are homogeneously distributed. A large variety of proton conducting or non conducting polymers can be combined with various functionalized, inorganic mesostructured particles or an inorganic network in order to achieve high proton conductivity, and good mechanical and chemical properties. The tuning of the interface between these two components and the control over chemical and processing conditions are the key parameters in fabricating these hybrid organic-inorganic membranes with a high degree of reproducibility. This dynamic coupling between chemistry and processing requires the extensive use and development of complementary ex situ measurements with in situ characterization techniques, following in real time the molecular precursor solutions to the formation of the final hybrid organic-inorganic membranes. These membranes combine the intrinsic physical and chemical properties of both the inorganic and organic components. The development of the sol-gel chemistry allows a fine tuning of the inorganic network, which exhibits acid-based functionalized pores (-SO(3)H, -PO(3)H(2), -COOH), tunable pore size and connectivity, high surface area and accessibility. As such, these hybrid membranes containing inorganic materials are a promising family for controlling conductivity, mechanical and chemical properties (349 references).  相似文献   

12.
13.
The design, preparation, and properties of organic-inorganic hybrid compounds are described and discussed with respect to their potential uses as intelligent and bioinspired materials. Several synthesis strategies based on intercalation in 2D solids, the grafting of organic groups onto silica and silicates, and the self-assembly of organo-silica materials are presented, focusing on the soft procedures that are used to modify the functionality of the inorganic substrates. The combination of both organic and inorganic moieties at the nanometer level forms the basis for preparing multifunctional solids that are provided with specific functions in response to different types of stimuli. In some cases these resemble materials that are found in biological systems. Examples include organic-inorganic membranes that are based on intercalated macrocyclic compounds and bi-layer vesicles that consist of alkyl long-chains arranged either in the confined region of layered silicates or as self-organized organo-silica micelles. The role of certain hybrid materials such as membranes provides a different approach to the development of artificial liposomes and other mimetic systems that have an organic-inorganic composition and nanostructural organization. Their potential uses for DDS or DNA-dense phases are also discussed and novel alternatives to bioinspired systems development are proposed.  相似文献   

14.
A series of novel organic-inorganic hybrid proton-conducting electrolyte membranes with silane-crosslinked sulfonated poly(aryl ether ketone)(SC-SPAEK) networks was prepared via a simple procedure that includes solution casting and acid treatment. The organosilicon pendants of the silane-grafted SPAEK, which were expected to serve as coupling and crosslinking agents, were found to play a key role in the homogenous dispersion of inorganic particles and improved the performance of hybrid membranes. The hybrid membranes exhibited enhanced proton conductivity, and SC-SPAEK/TiO2-4 showed an extremely high proton conductivity of 0.1472 S/cm at 100℃. The crosslinked hybrid membranes also demonstrated good chemical resistance, oxidative stability, and mechanical properties. The crosslinked hybrid membranes with excellent comprehensive performance may be a promising material for proton exchange membrane fuel cells.  相似文献   

15.
Unprecedented hydrothermal stability in functional membranes has been obtained with hybrid organic-inorganic nanoporous materials, enabling long-term application in energy-efficient molecular separation, including dehydration up to at least 150 degrees C.  相似文献   

16.
Novel organic–inorganic hybrid membranes were prepared through sol–gel reaction of poly(vinyl alcohol) (PVA) with γ-aminopropyl-triethoxysilane (APTEOS) for pervaporation (PV) separation of ethanol/water mixtures. The membranes were characterized by FTIR, EDX, WXRD and PALS. The amorphous region of the hybrid membranes increased with increasing APTEOS content, and both the free volume and the hydrophilicity of the hybrid membranes increased when APTEOS content was less than 5 wt%. The swelling degree of the hybrid membranes has been restrained in an aqueous solution owing to the formation of hydrogen and covalent bonds in the membrane matrix. Permeation flux increased remarkably with APTEOS content increasing, and water permselectivity increased at the same time, the trade-off between the permeation flux and water permselectivity of the hybrid membranes was broken. The sorption selectivity increased with increasing temperature, and decreased with increasing water content. In addition, the diffusion selectivity and diffusion coefficient of the permeants through the hybrid membranes were investigated. The hybrid membrane containing 5 wt% APTEOS has highest separation factor of 536.7 at 50 °C and permeation flux of 0.0355 kg m−2 h−1 in PV separation of 5 wt% water in the feed.  相似文献   

17.
One important application of hybrid organic-inorganic materials with nano-sized interfaces is the preparation of membranes for Proton Exchange Membrane Fuel Cells (PEMFC) operating at high temperature. Poly (styrene-co-methacrylate)--silica covalent hybrid membranes have been synthesised by copolymerization of monomers (styrene and 2-hydroxyethyl methacrylate), with formation of covalent bonds between hydroxyl group of HEMA and pre-hydrolysed tetraethoxysilane (TEOS). Sulfonation of benzyl groups was applied to endow the membranes of proton conductivity. The incorporation of an inorganic component to a polymeric one modifies properties like thermal, chemical and mechanical stability, and proton conductivity. A compromise between these properties has to be achieved to produce adequate proton conducting membranes with application in PEMFC. The hybrid membrane with 25% SiO2 combines these properties being a promising candidate for application in PEMFC.  相似文献   

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