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壳聚糖-聚乙烯基聚吡咯烷酮(PVPP)复合材料的合成及染料吸附动力学

Synthesis and Dye Adsorption Dynamics of Chitosan-Polyvinylpolypyrrolidone (PVPP) Composite.

作者信息

Kyomuhimbo Hilda Dinah, McHunu Wandile, Arnold Marco, Feleni Usisipho, Haneklaus Nils H, Brink Hendrik Gideon

机构信息

Department of Chemical Engineering, University of Pretoria, Pretoria 0028, South Africa.

Institute for Nanotechnology and Water Sustainability (iNanoWS), College of Science, Engineering and Technology, University of South Africa, Johannesburg 1709, South Africa.

出版信息

Polymers (Basel). 2024 Sep 10;16(18):2555. doi: 10.3390/polym16182555.

DOI:10.3390/polym16182555
PMID:39339020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11434811/
Abstract

One major environmental issue responsible for water pollution is the presence of dyes in the aquatic environment as a result of human activity, particularly the textile industry. Chitosan-Polyvinylpolypyrrolidone (PVPP) polymer composite beads were synthesized and explored for the adsorption of dyes (Bismarck brown (BB), orange G (OG), brilliant blue G (BBG), and indigo carmine (IC)) from dye solution. The CS-PVPP beads demonstrated high removal efficiency of BB (87%), OG (58%), BBG (42%), and IC (49%). The beads demonstrated a reasonable surface area of 2.203 m/g and were negatively charged in the applicable operating pH ranges. TGA analysis showed that the polymer composite can withstand decomposition up to 400 °C, proving high stability in harsh conditions. FTIR analysis highlighted the presence of N-H amine, O-H alcohol, and S=O sulfo groups responsible for electrostatic interaction and hydrogen bonding with the dye molecules. A shift in the FTIR bands was observed on N-H and C-N stretching for the beads after dye adsorption, implying that adsorption was facilitated by hydrogen bonding and Van der Waals forces of attraction between the hydroxyl, amine, and carbonyl groups on the surface of the beads and the dye molecules. An increase in pH increased the adsorption capacity of the beads for BB while decreasing OG, BBG, and IC due to their cationic and anionic nature, respectively. While an increase in temperature did not affect the adsorption capacity of OG and BBG, it significantly improved the removal of BB and IC from the dye solution and the adsorption was thermodynamically favoured, as demonstrated by the negative Gibbs free energy at all temperatures. Adsorption of dye mixtures followed the characteristic adsorption nature of the individual dyes. The beads show great potential for applications in the treatment of dye wastewater.

摘要

人类活动,尤其是纺织工业,导致水生环境中存在染料,这是造成水污染的一个主要环境问题。合成了壳聚糖-聚乙烯基聚吡咯烷酮(PVPP)聚合物复合珠,并研究了其对染料溶液中染料(俾斯麦棕(BB)、橙G(OG)、亮蓝G(BBG)和靛蓝胭脂红(IC))的吸附性能。CS-PVPP珠对BB(87%)、OG(58%)、BBG(42%)和IC(49%)表现出较高的去除效率。这些珠子的比表面积为2.203 m/g,在适用的操作pH范围内带负电荷。热重分析表明,该聚合物复合材料在高达400℃时仍能抵抗分解,证明了其在苛刻条件下的高稳定性。傅里叶变换红外光谱(FTIR)分析突出了N-H胺、O-H醇和S=O磺基的存在,这些基团负责与染料分子的静电相互作用和氢键作用。染料吸附后,珠子的FTIR谱带在N-H和C-N伸缩振动处发生了位移,这意味着珠子表面的羟基、胺基和羰基与染料分子之间的氢键作用和范德华吸引力促进了吸附。由于BB、OG、BBG和IC分别具有阳离子和阴离子性质,pH值的升高增加了珠子对BB的吸附容量,同时降低了对OG、BBG和IC的吸附容量。虽然温度升高对OG和BBG的吸附容量没有影响,但显著提高了染料溶液中BB和IC的去除率,且吸附在热力学上是有利的,所有温度下的吉布斯自由能均为负值。染料混合物的吸附遵循各单一染料的特征吸附性质。这些珠子在染料废水处理中具有很大的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/ffabe705d204/polymers-16-02555-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/77ab22209e17/polymers-16-02555-g0A1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/678216c21e0d/polymers-16-02555-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/065901d45e4c/polymers-16-02555-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/7fa07928a019/polymers-16-02555-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/ffabe705d204/polymers-16-02555-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/77ab22209e17/polymers-16-02555-g0A1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/28e6e7a6dba6/polymers-16-02555-g0A4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/4252be2e5cbd/polymers-16-02555-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/c2fed2312c1b/polymers-16-02555-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/a2bf7b203fae/polymers-16-02555-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/678216c21e0d/polymers-16-02555-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/065901d45e4c/polymers-16-02555-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/7fa07928a019/polymers-16-02555-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/5c36c31c7ade/polymers-16-02555-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/9de83f8043d8/polymers-16-02555-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/4a63cfd07708/polymers-16-02555-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6579/11434811/ffabe705d204/polymers-16-02555-g010.jpg

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