Effect of alkyl-chain-modified lignin in the PLA matrix
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  • 作者:Sunghoon Kim (1)
    Seungtaek Oh (1)
    Jungmin Lee (1)
    Narang Ahn (1)
    Hyungyu Roh (1)
    Jaewhan Cho (2)
    Byoungchul Chun (3)
    Jongshin Park (1)

    1. Department of Biosystems & Biomaterials Science and Engineering
    ; Research Institute for Agriculture and Life Sciences ; Seoul National University ; Seoul ; 151-742 ; Korea
    2. Department of Textile Engineering
    ; Konkuk University ; Seoul ; 143-701 ; Korea
    3. Department of Nano Engineering
    ; Inje University ; Gimhae ; 621-749 ; Korea
  • 关键词:Alkyl ; chain ; modified lignin ; Ligno ; cellulose complex ; Bio ; mimic ; Modified lignin/PLA blends ; Mechanical properties ; Thermal properties
  • 刊名:Fibers and Polymers
  • 出版年:2014
  • 出版时间:December 2014
  • 年:2014
  • 卷:15
  • 期:12
  • 页码:2458-2465
  • 全文大小:598 KB
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  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Polymer Sciences
  • 出版者:The Korean Fiber Society
  • ISSN:1875-0052
文摘
Lignin has enormous potential for use as a raw material in the polymer industry. However, lignin has not been utilized as a raw material despite its many advantages because of its brittleness and difficulty of processing. Chemical modification of lignin is an important area of lignin research. In this study, two types of alkyl-chain-based modification agents were used. In the case of the polymeric materials blend, polymers are blended well so that the polymer solubility parameter (SP) values are close to each other. This is similar to the well-mixed combination of water and alcohol. If the SP value is very different, phase separation occurs, as in the relationship between water and oil. The two alkyl chain derivatives block the hydroxyl groups of lignin and replace them with glycoside. Moreover, they can alter the SP value of the modified lignin to make it similar to that of a synthetic polymer to enable blending. Cellulose is compatible with hemicellulose, which is coupled to lignin by ether, glycoside, and ester bonds in plant fibers. To mimic this structure, in this study, lignin was combined with an alkyl chain with a similar SP value and was used as a matrix polymer to form glycoside bonds. This relationship between lignin and the alkyl chain is similar to that between the cellulose and lignin-carbohydrate-complex (LCC). PLA-modified lignin (PLAL) and tetrahydrofuran-modified lignin (THFL) exhibited remarkable changes in the presence of an alcohol functional group. The results of 1H-NMR analysis confirm those obtained by FT-IR analysis. The results of the DSC analyses indicate that lignin and modified lignin exhibit different thermal properties. The results of the thermal and mechanical analyses of the modified lignin/PLA blends demonstrate that the characteristics of the alkyl chains used to modify lignin were well reflected in the final blends. Alkyl-chain-modified lignin that mimics LCC was observed to enhance the compatibility between the matrix polymers used in this study and modified lignin.

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