{"title":"Silylation of phosphorylated cellulosic fibers with an aminosilane","authors":"","doi":"10.1016/j.carbpol.2024.122500","DOIUrl":null,"url":null,"abstract":"<div><p>In this work, phosphorylated cellulosic fibers were functionalized with an aminosilane ((3-aminopropyl)triethoxysilane, APTES) using a simple and economical method. Several characterization were performed to determine the types of bonds between phosphorylated fibers and grafted APTES. The thermal behavior, hydrophobicity and surface charge variation as a function of pH of the multifunctional cellulose fibers were determined.</p><p>Results demonstrate that APTES should proceed through Si-O-C, and possibly Si-O-P, covalent bonds with cellulose although the dimerization of silane through Si-O-Si bonds has also been observed. The terminal amino groups are expected to be partially involved in hydrogen bonds with phosphate hydroxyl groups found at phosphorylated cellulose fiber surface, causing a pulling in the configuration of the grafted APTES. The two chemical modifications proposed in this work do not significantly modify the morphology of cellulose fibers. XRD analysis also shows that the crystal structure of the phosphorylated fibers did not change after functionalization with APTES. The silylated phosphorylated fibers show potential flame-retardant properties with improved hydrophobicity. Furthermore, the functionalization of phosphorylated fibers with APTES changes the pH of zero charge point from 3.2 to 9.4 and providing a zwitterionic structure suitable for the simultaneous adsorption of both cationic and anionic species.</p></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":null,"pages":null},"PeriodicalIF":10.7000,"publicationDate":"2024-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0144861724007264/pdfft?md5=840ec87b25e1d08abb67654cc33a48e6&pid=1-s2.0-S0144861724007264-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbohydrate Polymers","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0144861724007264","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
In this work, phosphorylated cellulosic fibers were functionalized with an aminosilane ((3-aminopropyl)triethoxysilane, APTES) using a simple and economical method. Several characterization were performed to determine the types of bonds between phosphorylated fibers and grafted APTES. The thermal behavior, hydrophobicity and surface charge variation as a function of pH of the multifunctional cellulose fibers were determined.
Results demonstrate that APTES should proceed through Si-O-C, and possibly Si-O-P, covalent bonds with cellulose although the dimerization of silane through Si-O-Si bonds has also been observed. The terminal amino groups are expected to be partially involved in hydrogen bonds with phosphate hydroxyl groups found at phosphorylated cellulose fiber surface, causing a pulling in the configuration of the grafted APTES. The two chemical modifications proposed in this work do not significantly modify the morphology of cellulose fibers. XRD analysis also shows that the crystal structure of the phosphorylated fibers did not change after functionalization with APTES. The silylated phosphorylated fibers show potential flame-retardant properties with improved hydrophobicity. Furthermore, the functionalization of phosphorylated fibers with APTES changes the pH of zero charge point from 3.2 to 9.4 and providing a zwitterionic structure suitable for the simultaneous adsorption of both cationic and anionic species.
期刊介绍:
Carbohydrate Polymers stands as a prominent journal in the glycoscience field, dedicated to exploring and harnessing the potential of polysaccharides with applications spanning bioenergy, bioplastics, biomaterials, biorefining, chemistry, drug delivery, food, health, nanotechnology, packaging, paper, pharmaceuticals, medicine, oil recovery, textiles, tissue engineering, wood, and various aspects of glycoscience.
The journal emphasizes the central role of well-characterized carbohydrate polymers, highlighting their significance as the primary focus rather than a peripheral topic. Each paper must prominently feature at least one named carbohydrate polymer, evident in both citation and title, with a commitment to innovative research that advances scientific knowledge.