化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2015年
6期
2295-2302
,共8页
赵旭红%石海强%张健%李娜%牛梅红%平清伟
趙旭紅%石海彊%張健%李娜%牛梅紅%平清偉
조욱홍%석해강%장건%리나%우매홍%평청위
紫外光谱%生物质%水解%木素%降解%糠醛
紫外光譜%生物質%水解%木素%降解%糠醛
자외광보%생물질%수해%목소%강해%강철
UV spectral%biomass%hydrolysis%lignin%degradation%furfural
采用紫外光谱探讨了低分子有机酸、糠醛和木质纤维高温预水解液(PHL)的紫外吸收谱图特征。甲酸和乙酸在近205 nm处有显著吸收,而糠醛在近280 nm处有显著吸收,以205 nm或280 nm为木素特征吸收位置的传统木素测定方法不适于高温预水解液的溶解性木素测定。研究提出碱性硼氢化钠还原处理预水解液,消除糠醛的紫外吸收,进而定量测定溶解性木素含量的方法。结果表明,硼氢化钠可显著降低近280 nm 处吸收值,预水解条件越高,还原前后吸收差值降低越多,说明糠醛类物质含量高。以提取相思木和芦苇木素为标样,280 nm处吸光度与浓度线性相关系数均达到0.999,满足定量测定的需要。充分还原前后280 nm吸收差值可用于糠醛的定量,糠醛标样280 nm处吸光度与浓度线性相关性为0.998,糠醛测定回收率为98.14%~99.88%,相对标准偏差为0.17%~0.35%。
採用紫外光譜探討瞭低分子有機痠、糠醛和木質纖維高溫預水解液(PHL)的紫外吸收譜圖特徵。甲痠和乙痠在近205 nm處有顯著吸收,而糠醛在近280 nm處有顯著吸收,以205 nm或280 nm為木素特徵吸收位置的傳統木素測定方法不適于高溫預水解液的溶解性木素測定。研究提齣堿性硼氫化鈉還原處理預水解液,消除糠醛的紫外吸收,進而定量測定溶解性木素含量的方法。結果錶明,硼氫化鈉可顯著降低近280 nm 處吸收值,預水解條件越高,還原前後吸收差值降低越多,說明糠醛類物質含量高。以提取相思木和蘆葦木素為標樣,280 nm處吸光度與濃度線性相關繫數均達到0.999,滿足定量測定的需要。充分還原前後280 nm吸收差值可用于糠醛的定量,糠醛標樣280 nm處吸光度與濃度線性相關性為0.998,糠醛測定迴收率為98.14%~99.88%,相對標準偏差為0.17%~0.35%。
채용자외광보탐토료저분자유궤산、강철화목질섬유고온예수해액(PHL)적자외흡수보도특정。갑산화을산재근205 nm처유현저흡수,이강철재근280 nm처유현저흡수,이205 nm혹280 nm위목소특정흡수위치적전통목소측정방법불괄우고온예수해액적용해성목소측정。연구제출감성붕경화납환원처리예수해액,소제강철적자외흡수,진이정량측정용해성목소함량적방법。결과표명,붕경화납가현저강저근280 nm 처흡수치,예수해조건월고,환원전후흡수차치강저월다,설명강철류물질함량고。이제취상사목화호위목소위표양,280 nm처흡광도여농도선성상관계수균체도0.999,만족정량측정적수요。충분환원전후280 nm흡수차치가용우강철적정량,강철표양280 nm처흡광도여농도선성상관성위0.998,강철측정회수솔위98.14%~99.88%,상대표준편차위0.17%~0.35%。
A method to measure the contents of soluble lignin and furfural in the lingocellulosic pre-hydrolysis liquid was developed based on UV spectroscopy in the present work. The UV spectrograms of the low molecular organic acids, furfural and the pre-hydrolysis liquid were discussed. Formic acid and acetic acid had significant absorption at 205 nm, and furfural had absorption maxima close to 280 nm. The traditional methods for quantification of lignin based on lignin characteristic peak location of 205 nm and 280 nm was not suitable for the determination of soluble lignin in the pre-hydrolysis liquid. The study presented elimination of the interference of furanic compounds by reduction with alkaline sodium borohydride. The results showed that sodium borohydride significantly decreased absorbance close to 280 nm, and the higher the pre-hydrolysis conditions, the more decreased the absorbance after reduction, indicating high level of furfural. With lignin extracted from Acacia wood and reeds as standard sample, the relationship between absorbance at 280 nm and concentration of lignin was linear and pertinent coefficient reached 0.999, which met the needs of quantitative determination. The difference of absorbance between the samples before and after full reduction could be used for quantification of furfural. The pertinent coefficient of absorbance at 280 nm and concentration of furfural reached 0.998. The results of reproductive experiment showed that recovery was 98.14%—99.88%and relative standard deviation was 0.17%—0.35%.