Synthesis and characterization of cellulose acetate from cellophane industry residues. Application as acetaminophen controlled-release membranes

被引:0
|
作者
Sabrina Dias Ribeiro
Andréia Bagliotti Meneguin
Hernane da Silva Barud
Jhonatan Miguel Silva
Rafael L. Oliveira
Rosana Maria Nascimento de Asunção
Thiago Faria Tormin
Rodrigo Alejandro Abarza Muñoz
Guimes Rodrigues Filho
Clovis Augusto Ribeiro
机构
[1] Federal Institute of Education,School of Pharmaceutical Science
[2] Science,Department of Biotechnology
[3] and Technology of the Triangulo Mineiro (IFTM),Pontal Institute of Exact and Natural Science
[4] São Paulo State University,Institute of Chemistry
[5] Araraquara University (UNIARA),undefined
[6] Federal University of Uberlandia (UFU),undefined
[7] Federal University of Uberlândia (UFU),undefined
[8] São Paulo State University (UNESP),undefined
[9] Institute of Chemistry,undefined
关键词
Cellulose acetate; Homogeneous reaction; Cellophane; Industrial waste; Thermal behavior; Controlled release;
D O I
暂无
中图分类号
学科分类号
摘要
Cellophane film production generates cellulosic residues from scraps, edges, and low-quality films. In this work, cellophane was used as a raw material to produce cellulose acetate (CA). CA was produced through the homogeneous route for 6 to 24 hours producing materials with a degree of substitution (DS) between 2.6 and 2.9. The CA materials were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and viscosity-average molecular weight. DS values (DS > 2.6) indicate the preferential formation of cellulose triacetate, and the reaction time leads to materials with different molecular weight from 32,000 to 121,000 g mol-1\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$^{-1}$$\end{document} The TGA and DSC curves allowed obtaining information that, together with other techniques, confirm the formation of cellulose triacetate and the production of a material with a heterogeneous structure. The CA membrane was prepared with CA produced with 14 hours of the reaction intended to control the release rates of acetaminophen (ACP). A dense, seemingly pore-free membrane has been produced, as seen by SEM images, which allows the release of small amounts of ACP. The results were promising in the development of CA membranes for the controlled release of drugs from the chemical modification of cellophane residues.
引用
收藏
页码:7265 / 7275
页数:10
相关论文
共 24 条
  • [21] Synthesis, characterization, and anti-fouling properties of cellulose acetate/polyethylene glycol-grafted nanodiamond nanocomposite membranes for humic acid removal from contaminated water
    Habib Etemadi
    Reza Yegani
    Mahdi Seyfollahi
    Mahyar Rabiee
    Iranian Polymer Journal, 2018, 27 : 381 - 393
  • [22] Synthesis, characterization, and anti-fouling properties of cellulose acetate/polyethylene glycol-grafted nanodiamond nanocomposite membranes for humic acid removal from contaminated water
    Etemadi, Habib
    Yegani, Reza
    Seyfollahi, Mahdi
    Rabiee, Mahyar
    IRANIAN POLYMER JOURNAL, 2018, 27 (06) : 381 - 393
  • [23] Synthesis and Characterization of Zero Valent Iron/Cellulose Acetate (Fe0-x/CA) Membranes for the Catalytic Degradation of Methylene Blue from Aqueous Media by Activating Peroxymonosulfate
    Zohaib, Muhammad
    Sayed, Murtaza
    Rehman, Faiza
    Gul, Saman
    Noreen, Saima
    Sohni, Saima
    Gul, Ikhtiar
    Ali, Adnan
    CATALYSIS SURVEYS FROM ASIA, 2024, 28 (03) : 283 - 297
  • [24] Synthesis, characterization and application of poly [(1-vinyl-2-pyrrolidone)-co-(2-hydroxyethyl methacrylate)] as controlled-release polymeric system for 2,4-dichlorophenoxyacetic chloride using an ultrafiltration technique
    Pizarro, Guadalupe del C.
    Marambio, Oscar G.
    Jeria-Orell, Manuel
    Avellan, Miguel C.
    Rivas, Bernabe L.
    POLYMER INTERNATIONAL, 2008, 57 (07) : 897 - 904