壳聚糖对沸石表面的吸附改性

IF 0.3 Q4 CHEMISTRY, MULTIDISCIPLINARY
Zhadra Tattibayeva, Mirzhan T. Tursynbetov, S. Tazhibayeva, W. Kujawski, K. Musabekov
{"title":"壳聚糖对沸石表面的吸附改性","authors":"Zhadra Tattibayeva, Mirzhan T. Tursynbetov, S. Tazhibayeva, W. Kujawski, K. Musabekov","doi":"10.15328/cb1073","DOIUrl":null,"url":null,"abstract":"1Al-Farabi Kazakh National University, Almaty, Kazakhstan 2Nicolaus Copernicus University in Torun, Faculty of Chemistry, Torun, Poland *E-mail: jani-1989@mail.ru In order to modify the surface, thermal acid activation of the zeolite of the Chankanai deposit was conducted. It was found that the treatment of the mineral with acid at high temperature leads to a decrease in the content of Ca, Al and Sr in its composition. Adsorption of chitosan on the surface of thermoacid-activated zeolite was also studied. Processing of the adsorption isotherms according to Langmuir and Freundlich models showed that the maximum adsorption of chitosan on the zeolite surface is 30.1 mg/g and the Freundlich constant 1/n is 0.75. On the IR-spectra of chitosan-modified zeolite, a certain shift to the higher frequencies of the peak was found at the oscillation frequency of 1638 cm-1, which can be explained by the contribution of amino groups adsorbed on the surface of the mineral. The shift to the left of the peak at 581 cm-1, typical for aluminosilicate groups, is also an evidence of their interactions with chitosan. When studying the effect of chitosan concentration on the wetting of the modified zeolite powder, it was found that at concentration of 2.10-3 base mol/L, an increase in the wetting angle from 10° to 47° occurs due to surface overcharging. According to the data of adsorption, IR spectroscopy and wetting of the surface, the main mechanism for binding chitosan to the zeolite surface was due to the electrostatic interaction of polymer amino groups with silicate and aluminosilicate groups of the mineral, stabilized by hydrogen bonds between the OH-groups of the polymer and ≡Si-O-groups of the solid phase.","PeriodicalId":9860,"journal":{"name":"Chemical Bulletin of Kazakh National University","volume":"1 1","pages":"20-26"},"PeriodicalIF":0.3000,"publicationDate":"2019-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Adsorption modification of the zeolite surface with chitosan\",\"authors\":\"Zhadra Tattibayeva, Mirzhan T. Tursynbetov, S. Tazhibayeva, W. Kujawski, K. Musabekov\",\"doi\":\"10.15328/cb1073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"1Al-Farabi Kazakh National University, Almaty, Kazakhstan 2Nicolaus Copernicus University in Torun, Faculty of Chemistry, Torun, Poland *E-mail: jani-1989@mail.ru In order to modify the surface, thermal acid activation of the zeolite of the Chankanai deposit was conducted. It was found that the treatment of the mineral with acid at high temperature leads to a decrease in the content of Ca, Al and Sr in its composition. Adsorption of chitosan on the surface of thermoacid-activated zeolite was also studied. Processing of the adsorption isotherms according to Langmuir and Freundlich models showed that the maximum adsorption of chitosan on the zeolite surface is 30.1 mg/g and the Freundlich constant 1/n is 0.75. On the IR-spectra of chitosan-modified zeolite, a certain shift to the higher frequencies of the peak was found at the oscillation frequency of 1638 cm-1, which can be explained by the contribution of amino groups adsorbed on the surface of the mineral. The shift to the left of the peak at 581 cm-1, typical for aluminosilicate groups, is also an evidence of their interactions with chitosan. When studying the effect of chitosan concentration on the wetting of the modified zeolite powder, it was found that at concentration of 2.10-3 base mol/L, an increase in the wetting angle from 10° to 47° occurs due to surface overcharging. According to the data of adsorption, IR spectroscopy and wetting of the surface, the main mechanism for binding chitosan to the zeolite surface was due to the electrostatic interaction of polymer amino groups with silicate and aluminosilicate groups of the mineral, stabilized by hydrogen bonds between the OH-groups of the polymer and ≡Si-O-groups of the solid phase.\",\"PeriodicalId\":9860,\"journal\":{\"name\":\"Chemical Bulletin of Kazakh National University\",\"volume\":\"1 1\",\"pages\":\"20-26\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2019-12-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Bulletin of Kazakh National University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15328/cb1073\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Bulletin of Kazakh National University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15328/cb1073","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 1

摘要

1Al-Farabi哈萨克斯坦国立大学,阿拉木图2Nicolaus哥白尼大学,化学系,托伦,波兰*E-mail: jani-1989@mail.ru为了修饰表面,对Chankanai矿床的沸石进行了热酸活化。结果表明,在高温下用酸处理后,其组成中Ca、Al和Sr的含量降低。研究了壳聚糖在热酸活化沸石表面的吸附性能。根据Langmuir和Freundlich模型对吸附等温线进行处理表明,壳聚糖在沸石表面的最大吸附量为30.1 mg/g, Freundlich常数1/n为0.75。在壳聚糖修饰的沸石红外光谱上,在1638 cm-1的振荡频率处发现了一定的高频偏移,这可以解释为矿物表面吸附的氨基的贡献。铝硅酸盐基团在581 cm-1处的典型峰左移,也是它们与壳聚糖相互作用的证据。在研究壳聚糖浓度对改性沸石粉体润湿性能的影响时,发现在浓度为2.10-3碱mol/L时,由于表面过充,润湿角由10°增加到47°。根据吸附、红外光谱和表面润湿数据,壳聚糖与沸石表面结合的主要机制是由于聚合物氨基与矿物的硅酸盐和铝硅酸盐基团的静电相互作用,聚合物的oh基团和固相的≡si - o基团之间的氢键稳定了壳聚糖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adsorption modification of the zeolite surface with chitosan
1Al-Farabi Kazakh National University, Almaty, Kazakhstan 2Nicolaus Copernicus University in Torun, Faculty of Chemistry, Torun, Poland *E-mail: jani-1989@mail.ru In order to modify the surface, thermal acid activation of the zeolite of the Chankanai deposit was conducted. It was found that the treatment of the mineral with acid at high temperature leads to a decrease in the content of Ca, Al and Sr in its composition. Adsorption of chitosan on the surface of thermoacid-activated zeolite was also studied. Processing of the adsorption isotherms according to Langmuir and Freundlich models showed that the maximum adsorption of chitosan on the zeolite surface is 30.1 mg/g and the Freundlich constant 1/n is 0.75. On the IR-spectra of chitosan-modified zeolite, a certain shift to the higher frequencies of the peak was found at the oscillation frequency of 1638 cm-1, which can be explained by the contribution of amino groups adsorbed on the surface of the mineral. The shift to the left of the peak at 581 cm-1, typical for aluminosilicate groups, is also an evidence of their interactions with chitosan. When studying the effect of chitosan concentration on the wetting of the modified zeolite powder, it was found that at concentration of 2.10-3 base mol/L, an increase in the wetting angle from 10° to 47° occurs due to surface overcharging. According to the data of adsorption, IR spectroscopy and wetting of the surface, the main mechanism for binding chitosan to the zeolite surface was due to the electrostatic interaction of polymer amino groups with silicate and aluminosilicate groups of the mineral, stabilized by hydrogen bonds between the OH-groups of the polymer and ≡Si-O-groups of the solid phase.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
17
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信