کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7790762 | 1500644 | 2014 | 27 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Surface esterification of cellulose nanofibers by a simple organocatalytic methodology
ترجمه فارسی عنوان
استرینگ سطحی نانو فیبرهای سلولز با استفاده از متدولوژی الکتروکاتالیستی ساده
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کلمات کلیدی
سلولز باکتریایی، استرینگ سطحی، سلول های بنیادی، تعیین مشخصات،
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
چکیده انگلیسی
Bacterial cellulose nanofibers were esterified with two short carboxylic acids by means of a simple and novel organic acid-catalyzed route. The methodology proposed relayed on the use of a non-toxic biobased α-hydroxycarboxylic acid as catalyst, and proceeded under moderate reaction conditions in solventless medium. By varying the esterification interval, acetylated and propionized bacterial cellulose nanofibers with degree of substitution (DS) in the 0.02-0.45 range could be obtained. Esterified bacterial cellulose samples were characterized by means of Solid-State CP/MAS 13C Nuclear Magnetic Resonance spectroscopy (CP/MAS 13C NMR), Fourier Transform Infrared spectroscopy (FTIR), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and chosen hydrophobicity test assays. TGA results showed that the esterified nanofibers had increased thermal stability, whereas XRD data evidenced that the organocatalytic esterification protocol did not alter their crystallinity. The analysis of the ensuing modified nanofibers by NMR, FTIR, XRD and TGA demonstrated that esterification occurred essentially at the surface of bacterial cellulose microfibrils, something highly desirable for changing their surface hydrophilicity while not affecting their ultrastructure.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Carbohydrate Polymers - Volume 114, 19 December 2014, Pages 416-423
Journal: Carbohydrate Polymers - Volume 114, 19 December 2014, Pages 416-423
نویسندگان
Jhon Alejandro Ávila RamÃrez, Camila Juan Suriano, Patricia Cerrutti, MarÃa Laura Foresti,