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甲基丙烯酸3-(三甲氧基硅基)丙酯与三羟甲基丙烷三甲基丙烯酸酯的多孔共聚物制备:结构表征与热降解

Porous Copolymers of 3-(Trimethoxysilyl)propyl Methacrylate with Trimethylpropane Trimethacrylate Preparation: Structural Characterization and Thermal Degradation.

作者信息

Maciejewska Małgorzata, Rogulska Magdalena

机构信息

Department of Polymer Chemistry, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Skłodowska University in Lublin, Gliniana 33, 20-614 Lublin, Poland.

出版信息

Materials (Basel). 2024 Sep 29;17(19):4796. doi: 10.3390/ma17194796.

DOI:10.3390/ma17194796
PMID:39410367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11477589/
Abstract

Porous polymeric microspheres are among the most effective adsorbents. They can be synthesized from numerous monomers using different kinds of polymerization techniques with a broad selection of synthesis factors. The main goal of this study was to prepare copolymeric microspheres and establish the relationship between copolymerization parameters and the porosity and thermal stability of the newly synthesized materials. Porous microspheres were obtained via heterogenous radical copolymerization using 3-(trimethoxysilyl)propyl methacrylate (TMPSM) as functional monomers and trimethylolpropane trimethacrylate (TRIM) as the crosslinker. In the course of the copolymerization, toluene or chlorobenzene was used as the pore-forming diluent. Consequently, highly porous microspheres were produced. Their specific surface area was established by a nitrogen adsorption/desorption method and it was in the range of 382 m/g to 457 m/g for toluene and 357-500 m/g in the case of chlorobenzene. The thermal degradation process was monitored by thermogravimetry and differential scanning calorimetry methods in inert and oxidative conditions. The copolymers were stable up to 269-283 °C in a helium atmosphere, whereas in synthetic air the range was 266-298 °C, as determined by the temperature of 5% mass loss. Thermal stability of the investigated copolymers increased along with an increasing TMPSM amount in the copolymerization mixture. In addition, the poly(TMSPM--TRIM) copolymers were effectively used as the stationary phase in GC analyses.

摘要

多孔聚合物微球是最有效的吸附剂之一。它们可以由多种单体通过不同的聚合技术合成,合成因素的选择范围很广。本研究的主要目标是制备共聚微球,并建立共聚参数与新合成材料的孔隙率和热稳定性之间的关系。通过以甲基丙烯酸3-(三甲氧基硅基)丙酯(TMPSM)为功能单体、三羟甲基丙烷三甲基丙烯酸酯(TRIM)为交联剂的非均相自由基共聚反应获得多孔微球。在共聚过程中,使用甲苯或氯苯作为致孔稀释剂。因此,制备出了高度多孔的微球。通过氮气吸附/脱附法测定其比表面积,甲苯体系下比表面积在382 m²/g至457 m²/g范围内,氯苯体系下为357 - 500 m²/g。在惰性和氧化条件下,通过热重分析和差示扫描量热法监测热降解过程。根据5%质量损失温度确定,在氦气气氛中,共聚物在269 - 283℃以下稳定,而在合成空气中,该范围为266 - 298℃。所研究共聚物的热稳定性随着共聚混合物中TMPSM含量的增加而提高。此外,聚(TMSPM - TRIM)共聚物在气相色谱分析中有效地用作固定相。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/419873681d2d/materials-17-04796-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/63e489452137/materials-17-04796-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/788a7e791c8a/materials-17-04796-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/69487a4c897e/materials-17-04796-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/6914c9a53f17/materials-17-04796-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/e809ab28d5b5/materials-17-04796-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/419873681d2d/materials-17-04796-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/63e489452137/materials-17-04796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/33f971c4d193/materials-17-04796-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/9eb8a25913c2/materials-17-04796-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/e6bdf6005e3c/materials-17-04796-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/dc2afb2528d2/materials-17-04796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/788a7e791c8a/materials-17-04796-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/69487a4c897e/materials-17-04796-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/6914c9a53f17/materials-17-04796-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/e809ab28d5b5/materials-17-04796-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ffb/11477589/419873681d2d/materials-17-04796-g010.jpg

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