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离子液体和低共熔溶剂中再生纤维素在磺化碳催化剂上的水解反应

Hydrolysis of regenerated cellulose from ionic liquids and deep eutectic solvent over sulfonated carbon catalysts.

作者信息

Kim Han Ung, Kim Jong Wha, Seo Sumin, Jae Jungho

机构信息

School of Chemical Engineering, Pusan National University Busan 46241 Republic of Korea

出版信息

RSC Adv. 2023 Mar 13;13(12):8153-8162. doi: 10.1039/d2ra08224a. eCollection 2023 Mar 8.

DOI:10.1039/d2ra08224a
PMID:36922947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10009878/
Abstract

The efficient hydrolysis of cellulose into its monomer unit such as glucose or valuable cello-oligosaccharides is the critical step for the cost-effective production of biofuels and biochemicals. However, the current cellulose hydrolysis process involves high energy-demanding pretreatment (, ball-milling) and long reaction times (>24 h). Herein, we investigated the feasibility of the dissolution/regeneration (DR) of cellulose in ionic liquids (ILs) and deep eutectic solvent (DES) as an alternative to ball-milling pretreatment for the effective hydrolysis of cellulose. Because chlorine-based solvents were reported to be the most active for cellulose pretreatment, [EMIM]Cl and [DMIM]DMP were selected as the IL molecules, and choline chloride-lactic acid and choline chloride-imidazole were selected as the DES molecules. The level of the crystallinity reduction of the regenerated cellulose were analyzed using XRD and SEM measurements. The hydrolysis kinetics of the regenerated cellulose from ILs and DES were examined at 150 °C using sulfonated carbon catalysts and compared with those of the ball-milled cellulose. Overall, the cellulose pretreatment using the ILs and the DES had superior kinetics for cellulose hydrolysis to the conventional ball milling treatment, suggesting a possibility to replace the current high energy-demanding ball-milling process with the energy-saving DR process. In addition, the utilization of supercritical carbon dioxide-induced carbonic acid as an acid catalyst for the enhanced hydrolysis of cellulose was presented for the first time.

摘要

将纤维素高效水解为其单体单元(如葡萄糖)或有价值的低聚纤维素是具有成本效益地生产生物燃料和生物化学品的关键步骤。然而,当前的纤维素水解过程涉及高能量需求的预处理(如球磨)和较长的反应时间(>24小时)。在此,我们研究了纤维素在离子液体(ILs)和深共熔溶剂(DES)中的溶解/再生(DR)作为球磨预处理的替代方法用于纤维素有效水解的可行性。由于据报道氯基溶剂对纤维素预处理最具活性,因此选择[EMIM]Cl和[DMIM]DMP作为离子液体分子,选择氯化胆碱 - 乳酸和氯化胆碱 - 咪唑作为深共熔溶剂分子。使用XRD和SEM测量分析再生纤维素的结晶度降低水平。在150°C下使用磺化碳催化剂研究了由离子液体和深共熔溶剂得到的再生纤维素的水解动力学,并与球磨纤维素的水解动力学进行了比较。总体而言,使用离子液体和深共熔溶剂进行纤维素预处理在纤维素水解动力学方面优于传统的球磨处理,这表明有可能用节能的溶解/再生过程取代当前高能量需求的球磨过程。此外,首次提出利用超临界二氧化碳诱导的碳酸作为酸催化剂来增强纤维素的水解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/3f76bf6f9dfb/d2ra08224a-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/8d33106cbf83/d2ra08224a-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/0d984b33f985/d2ra08224a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/7fc4c86e7a22/d2ra08224a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/031c03e207a1/d2ra08224a-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/0947185cd22f/d2ra08224a-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/3f76bf6f9dfb/d2ra08224a-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/8d33106cbf83/d2ra08224a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/27a673d2168b/d2ra08224a-f2.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/b3bc4f77def7/d2ra08224a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/0d984b33f985/d2ra08224a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/7fc4c86e7a22/d2ra08224a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/031c03e207a1/d2ra08224a-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/0947185cd22f/d2ra08224a-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f52/10009878/3f76bf6f9dfb/d2ra08224a-f9.jpg

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