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Structural coarsening of aspen wood by hydrothermal pretreatment monitored by small- and wide-angle scattering of X-rays and neutrons on oriented specimens

机译:通过水热预处理对白杨木进行结构粗化,并通过定向样品上的X射线和中子的小角度和广角散射进行监测

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摘要

Structural changes across multiple length scales associated with hydrothermal pretreatments of biomass were investigated by using small- and wideangle X-ray and neutron scattering on oriented specimens. Isotropic and anisotropic scattering components were numerically separated and then interpreted as contributions from matrix and cellulose components, respectively. Equatorial diffraction peaks present in the isotropic component became sharper after hydrothermal treatments or ammonia treatment. Before pretreatment the wet cell wall was found to be homogeneous in the 10–100 nm range and scattering below Q = 0.5 (nm~(-1)) was dominated by surface scattering from the lumen. After pretreatment with acid or steam at 160 or 180 ℃, density fluctuation developed in the cell wall at length scales above 10 nm, most likely due to lateral coalescence of microfibrils that partially co-crystallize to give larger apparent crystal sizes. A density fluctuation up to about 100 nm appeared in the isotropic component after acid and steam pretreatments due to morphological changes in the hemicellulose and lignin matrix.
机译:通过使用小角度和广角X射线以及中子在定向标本上的散射,研究了与生物质水热预处理相关的多个长度尺度上的结构变化。将各向同性和各向异性的散射成分进行数值分离,然后分别解释为基质和纤维素成分的贡献。在水热处理或氨处理后,各向同性组分中存在的赤道衍射峰变得更尖锐。在进行预处理之前,发现湿细胞壁在10–100 nm范围内是均匀的,低于Q = 0.5(nm〜(-1))的散射主要来自管腔的表面散射。用160或180℃的酸或蒸汽进行预处理后,细胞壁上的长度尺度在10 nm以上时会出现密度波动,这很可能是由于部分共结晶以产生更大的表观晶体尺寸的微纤维的横向聚结。由于半纤维素和木质素基质的形态变化,在酸和蒸汽预处理后,各向同性组分中出现了高达约100 nm的密度波动。

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