广东化工
廣東化工
엄동화공
GUANGDONG CHEMICAL INDUSTRY
2012年
11期
3-4
,共2页
谢成%刘志明%王海英%孟围
謝成%劉誌明%王海英%孟圍
사성%류지명%왕해영%맹위
纳米纤维素%溶胶-凝胶法%热稳定性%粒度分布
納米纖維素%溶膠-凝膠法%熱穩定性%粒度分佈
납미섬유소%용효-응효법%열은정성%립도분포
nano-cellulose%sol-gel method%thermal stability%particle size distribution
通过傅里叶变换红外光谱、X射线衍射、热重、透射电子显微镜分析及激光粒度分析对基于溶胶-凝胶技术制备的纳米纤维素进行表征,结果表明原料微晶纤维素超分子结构为纤维素Ⅰ型,制备的纳米纤维素为纤维素Ⅱ型;微晶纤维素的结晶度为87.54%,纳米纤维素的结晶度为73.49%,纳米纤维素结晶度较微晶纤维素有所下降;制备的纳米纤维素热稳定性低于微晶纤维素;纳米纤维素平均粒度425 nm,粒度分布呈现正态分布;纳米纤维素长径比为5∶1~40∶1。
通過傅裏葉變換紅外光譜、X射線衍射、熱重、透射電子顯微鏡分析及激光粒度分析對基于溶膠-凝膠技術製備的納米纖維素進行錶徵,結果錶明原料微晶纖維素超分子結構為纖維素Ⅰ型,製備的納米纖維素為纖維素Ⅱ型;微晶纖維素的結晶度為87.54%,納米纖維素的結晶度為73.49%,納米纖維素結晶度較微晶纖維素有所下降;製備的納米纖維素熱穩定性低于微晶纖維素;納米纖維素平均粒度425 nm,粒度分佈呈現正態分佈;納米纖維素長徑比為5∶1~40∶1。
통과부리협변환홍외광보、X사선연사、열중、투사전자현미경분석급격광립도분석대기우용효-응효기술제비적납미섬유소진행표정,결과표명원료미정섬유소초분자결구위섬유소Ⅰ형,제비적납미섬유소위섬유소Ⅱ형;미정섬유소적결정도위87.54%,납미섬유소적결정도위73.49%,납미섬유소결정도교미정섬유소유소하강;제비적납미섬유소열은정성저우미정섬유소;납미섬유소평균립도425 nm,립도분포정현정태분포;납미섬유소장경비위5∶1~40∶1。
Nano-cellulose prepared by sol-gel method was characterized by using Fourier transform infrared(FTIR) spectroscopy,X-ray diffraction(XRD),thermal gravimetric analysis(TGA),transmission electron microscopy(TEM) and laser particle size test.The results showed that supramolecular structure of microcrystalline cellulose(MCC) as raw material was cellulose I,while the prepared nano-cellulose was cellulose Ⅱ.The crystallinity of MCC was calculated as 87.54 %,for nano-cellulose,the crystallinity was 73.49 %.The crystallinity of nano-cellulose decreased slightly compared with that of MCC.The thermal stability of nano-cellulose was less than that of MCC.The mean size of nano-cellulose was 425 nm,its particle size distribution appeared normal distribution.Aspect ratio of nano-cellulose was 5∶1 to 40∶1.