林产化学与工业
林產化學與工業
림산화학여공업
CHEMISTRY AND INDUSTRY OF FOREST PRODUCTS
2014年
2期
91-96
,共6页
郑怀玉%卢泽湘%范立维%黄彪%廖益强%胡阳
鄭懷玉%盧澤湘%範立維%黃彪%廖益彊%鬍暘
정부옥%로택상%범립유%황표%료익강%호양
离子液体%杉木屑%催化%液化
離子液體%杉木屑%催化%液化
리자액체%삼목설%최화%액화
ionic liquid%fir sawdust%catalyst%liquefaction
合成了1-磺酸丙基-3-甲基咪唑硫酸氢盐离子液体([ Psmim] HSO4),对其结构进行了傅里叶红外光谱( FT-IR)和核磁共振(13C NMR)表征。以正辛醇为溶剂,初步考察了该离子液体对杉木屑液化的催化性能,并对残渣、重油和轻油液化产物进行了FT-IR、X射线粉末衍射( XRD)、热重分析( TG)、气质联用( GC-MS)表征。 FT-IR和13C NMR分析结果证实了合成产物与目标离子液体结构一致。液化实验结果表明该离子液体具有较好的催化液化性能,10 g杉木屑、60 g正辛醇在催化剂用量8.6 mmol、150℃、60 min条件下,木屑的液化率达66.5%。液化残渣表面的木质素衍生物含量高;轻油主要由纤维素和半纤维素的液化产物组成,重油主要由木质素的液化产物组成。
閤成瞭1-磺痠丙基-3-甲基咪唑硫痠氫鹽離子液體([ Psmim] HSO4),對其結構進行瞭傅裏葉紅外光譜( FT-IR)和覈磁共振(13C NMR)錶徵。以正辛醇為溶劑,初步攷察瞭該離子液體對杉木屑液化的催化性能,併對殘渣、重油和輕油液化產物進行瞭FT-IR、X射線粉末衍射( XRD)、熱重分析( TG)、氣質聯用( GC-MS)錶徵。 FT-IR和13C NMR分析結果證實瞭閤成產物與目標離子液體結構一緻。液化實驗結果錶明該離子液體具有較好的催化液化性能,10 g杉木屑、60 g正辛醇在催化劑用量8.6 mmol、150℃、60 min條件下,木屑的液化率達66.5%。液化殘渣錶麵的木質素衍生物含量高;輕油主要由纖維素和半纖維素的液化產物組成,重油主要由木質素的液化產物組成。
합성료1-광산병기-3-갑기미서류산경염리자액체([ Psmim] HSO4),대기결구진행료부리협홍외광보( FT-IR)화핵자공진(13C NMR)표정。이정신순위용제,초보고찰료해리자액체대삼목설액화적최화성능,병대잔사、중유화경유액화산물진행료FT-IR、X사선분말연사( XRD)、열중분석( TG)、기질련용( GC-MS)표정。 FT-IR화13C NMR분석결과증실료합성산물여목표리자액체결구일치。액화실험결과표명해리자액체구유교호적최화액화성능,10 g삼목설、60 g정신순재최화제용량8.6 mmol、150℃、60 min조건하,목설적액화솔체66.5%。액화잔사표면적목질소연생물함량고;경유주요유섬유소화반섬유소적액화산물조성,중유주요유목질소적액화산물조성。
1-( 4-sulfopropyl )-3-methylimidazolium hydrosulfate ( [ Psmim ] HSO4 ) was synthesized and its structure was characterized by FT-IR and 13C NMR . The catalytic performance of [ Psmim ] HSO4 in liquefaction of fir sawdust was preliminarily investigated using 1-octanol as solvent. The liquefaction products were characterized by FT-IR, XRD, TG, GC-MS. The structure of the synthesized ionic liquid was confirmed by the analysis of FT-IR and 13C NMR characterization. The liquefaction experimental results showed that the ionic liquid exhibited a good catalytic performance for the liquefaction of sawdust. The conversion of 66. 5% was achieved when 8. 6 mmol of catalyst was used with application of 10 g fir sawdust and 60 g 1-octanol at the temperature of 150 ℃ for 60 min. The surface of the solid residue was covered with lignin derivatives. The light oil mainly contained the liquefied products originated from cellulose and hemicellulose, and the heavy oil consisted mainly of the degradation products from lignin.