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首页> 外文期刊>Journal of Applied Polymer Science >Mild synthesis of benzylated bamboo in LiCl/DMSO solution
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Mild synthesis of benzylated bamboo in LiCl/DMSO solution

机译:在LiCl / DMSO溶液中轻度合成苄基竹

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摘要

Benzylated bamboo was mildly synthesized in nonaqueous medium without mercerization pretreatment. The ball-milled bamboo was firstly preswelled in lithium chloride/dimethyl sulfoxide (LiCl/DMSO) solution and then reacted with benzyl chloride in the presence of solid NaOH with varying molar ratios of benzyl chloride to OH groups of bamboo (1-4), reaction times (1-8 h), and temperatures (60-90°C). Benzylated bamboo products with yields from 51.1 to 106.9% and with degrees of substitution [DS, apparent value evaluated by Fourier transform infrared (FTIR) spectra] between 0.2 and 1.2 were synthesized. FTIR and ~(13)C cross polarization/magic angle spinning nuclear magnetic resonance (CP/MAS NMR) spectroscopy confirmed the incorporation of benzyl groups into bamboo; SEM observations of the highly benzylated bamboo showed porous surface with small irregular slices ascribed to the disruption of intermolecular and intramolecular hydrogen bonds between cellulose. Because of the degradation of amorphous components, the crystallinity decreased negligibly after modification and the thermal stability increased slightly but was lower than that of cellulose.
机译:苯甲酰化的竹子是在非水介质中温和合成的,无需进行丝光预处理。首先将球磨过的竹子在氯化锂/二甲基亚砜(LiCl / DMSO)溶液中预溶胀,然后在固体NaOH的存在下与苄基氯反应,而NaOH的苄基氯与竹基的OH基的摩尔比不同,反应时间(1-8小时)和温度(60-90°C)。合成了收率为51.1%至106.9%且取代度为[DS,通过傅里叶变换红外(FTIR)光谱评估的表观值]在0.2至1.2之间的苯甲酰化竹制品。 FTIR和〜(13)C交叉极化/魔角旋转核磁共振(CP / MAS NMR)光谱证实了苄基已掺入竹子中。 SEM观察到高度苄基化的竹子显示出多孔表面,带有小的不规则切片,这归因于纤维素之间的分子间和分子内氢键的破坏。由于无定形组分的降解,改性后的结晶度可忽略不计,热稳定性略有提高,但低于纤维素。

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