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用于集成到丙烯酸酯纳米复合薄膜中的ZrO₂纳米微晶的表面功能化。

Surface functionalization of ZrO2 nanocrystallites for the integration into acrylate nanocomposite films.

作者信息

Scholz S, Kaskel S

机构信息

Department of Inorganic Chemistry, Technical University of Dresden, Mommsenstr. 6, 01069 Dresden, Germany.

出版信息

J Colloid Interface Sci. 2008 Jul 1;323(1):84-91. doi: 10.1016/j.jcis.2008.03.051. Epub 2008 Apr 16.

Abstract

Surface functionalized zirconia nanoparticles were prepared by covalent grafting of a methacrylate functionalized silane (methacryloxypropyltrimethoxysilane, MPTS) onto the surface of the zirconia nanoparticles (tetragonal and mixed monoclinic/tetragonal phase) obtained by hydrothermal treatment of zirconyl chloride octahydrate. The particles are 70 nm aggregates of nanometric primary grains (4-12 nm) with inter particle porosity. BET measurements show that the specific surface area of the particles after activation at 100 degrees C is between 85 and 204 m2/g depending on the mineralizer used (Sr2+, Ca2+, Mg2+). IR-measurements show that the surface of the particles can be covered with functional groups bound through a variable number of ZrOSi bonds to render them organocompatible. The surface modified particles were dispersed in monomer solution (butanediol monoacrylate, BDMA) and polymerized to form films by adding a cross linking agent (trimethylolpropane triacrylate, Laromer TMPTA) and an UV initiator (2,4,6-trimethylbenzoyldiphenylphosphine oxide, Lucirin TPO). The received films were characterized with thermogravimetry and UV-vis spectroscopy.

摘要

通过将甲基丙烯酸酯官能化硅烷(甲基丙烯酰氧基丙基三甲氧基硅烷,MPTS)共价接枝到通过水热法处理八水合氧氯化锆制得的氧化锆纳米颗粒(四方相以及单斜相/四方相混合)表面,制备了表面功能化的氧化锆纳米颗粒。这些颗粒是由纳米级原生晶粒(4 - 12纳米)组成的70纳米聚集体,颗粒间存在孔隙。BET测量表明,根据所使用的矿化剂(Sr2 +、Ca2 +、Mg2 +)不同,在100℃活化后颗粒的比表面积在85至204平方米/克之间。红外测量表明,颗粒表面可被通过可变数量的Zr - O - Si键结合的官能团覆盖,从而使其具有有机相容性。将表面改性颗粒分散在单体溶液(丁二醇单丙烯酸酯,BDMA)中,并通过添加交联剂(三羟甲基丙烷三丙烯酸酯,Laromer TMPTA)和紫外线引发剂(2,4,6 - 三甲基苯甲酰基二苯基氧化膦,Lucirin TPO)聚合形成薄膜。通过热重分析和紫外 - 可见光谱对所得薄膜进行表征。

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