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Studies on fluorescence of cellulosics

机译:纤维素荧光研究

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Steady-state fluorescence emission spectra of various celluloses were measured at an excitation wavelength of 320 nm. Various spectra recorded in the solid state were compared: (1) ECF bleached papers made of hardwood, the anhydroglucose units of which were chemically modified at C_1 and C_6 or C_2 and C_3 positions with carboxylic groups; (2) microcrystalline cellulose; (3) cotton linters; and (4) delignified sisal fibers (mercerized or not). Fluorescence emission was quite independent of the carboxylic acid content and average molecular weight (determined by viscosimetry) of the cellulose polymers. Microcrystalline cellulose (Avicel), cotton linters, and mercerized delignified sisal cellulose were acetylated in homogeneous medium (DMAc/LiCI as solvent system) to obtain soluble polymers in dichloromethane for comparison of spectra recorded in the solid and liquid states. Fluorescence of cellulose acetates in solution (CH_2Cl_2) and in the solid state was compared under similar experimental conditions to non-esterified celluloses in the solid state. The importance of the solid state for fluorescence emission could be demonstrated. Fluorophores are present in minute amounts in the polymer and their favorable energy transfer for excitation in the solid state likely enhances fluorescence emission. Among numerous fluorophores, dityrosine appeared to be a good candidate for fluorescence because it displayed emission in the fluorescence range of cellulose. Dityrosine is an amino acid involved in the lignification of non-woody plants. Mercerized sisal impregnated with tyrosine in the presence of peroxidase and hydrogen peroxide did not show enhanced emission, in contrast to para-hydroxycinnamic acid (coumaric acid), which is also involved in the lignification process at least for non-woody plants. The origin of cellulose fluorescence remains uncertain and appears to have several origins. This study clearly underlines thernimportance of the solid state for enhancing fluorophore emission.
机译:在320nm的激发波长下测量了各种纤维素的稳态荧光发射光谱。比较了固态记录的各种光谱:(1)ECF漂白纸由硬木制成,其脱水葡萄糖单元在C_1和C_6或C_2和C_3位置被羧基化学修饰; (2)微晶纤维素; (3)棉短绒; (4)剑麻纤维脱木质素(丝光或不丝光)。荧光发射与纤维素聚合物的羧酸含量和平均分子量(由粘度测定法确定)完全无关。将微晶纤维素(Avicel),棉短绒和丝光化脱木质素的剑麻纤维素在均相介质(DMAc / LiCl作为溶剂体系)中乙酰化,得到可溶于二氯甲烷的聚合物,用于比较固态和液态记录的光谱。在相似的实验条件下,将溶液中(CH_2Cl_2)和固态的醋酸纤维素的荧光与固态的未酯化纤维素进行了比较。可以证明固态对于荧光发射的重要性。荧光团以极少量存在于聚合物中,它们在固态激发时有利的能量转移可能会增强荧光发射。在许多荧光团中,二氢异丁胺似乎是荧光的良好候选者,因为它在纤维素的荧光范围内显示出发射。二酪氨酸是涉及非木本植物木质化的氨基酸。与过羟基肉桂酸(香豆酸)相比,在过氧化物酶和过氧化氢存在下用酪氨酸浸渍的丝光剑麻并没有显示出增强的发射,对羟基肉桂酸(香豆酸)至少在非木本植物中也参与木质化过程。纤维素荧光的起源仍然不确定,并且似乎有多个起源。该研究清楚地强调了固态对于增强荧光团发射的重要性。

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