Wu Xiaoxiao, Yuan Xushuo, Zhao Jiaxin, Ji Decai, Guo Haiyang, Yao Wentao, Li Xiaoping, Zhang Lianpeng
Yunnan Provincial Key Laboratory of Wood Adhesives and Glued Products, Southwest Forestry University Kunming 650224 Yunnan China
College of Biological, Chemical Sciences and Engineering, Jiaxing University Jiaxing 314001 Zhejiang China
RSC Adv. 2023 Feb 9;13(8):5149-5157. doi: 10.1039/d2ra08172e. eCollection 2023 Feb 6.
With the development of science and technology, efficient, fast and green methods are increasingly being pursued. The production of nanocellulose by green methods, such as bio-enzymes-assisted ultrasound treatment, has been the focus of many studies. However, the yield of cellulose nanocrystals prepared by this method is very low. In this paper, by pretreatment of microcrystalline cellulose (MCC), nanocellulose was prepared by heating and stirring + pectinase/cellulase + ultrasonic treatment (HSt - P/C - Ultr). The effects of the ratios of pectinase and cellulase and the hydrolysis time on the yield of nanocellulose were studied. FTIR, XRD, SEM, TEM and TG were used to determine the structure, crystallinity, morphology and thermal stability of nanocellulose. The results showed that optimal hydrolysis conditions were determined as a pectinase : cellulase ratio of 1 : 1, 90 min and 50 °C. The yield of nanocellulose was about 32.0%. The yield of pectinase cellulase = 1 : 1 was higher than that of microcrystalline cellulose (MCC) treated by a single bio-enzyme. This indicated that the synergistic effects of pectinase and cellulase have a certain effect on the formation of nanocellulose. During the preparation, the crystalline form of cellulose did not change. It was still cellulose I with a crystallinity of 73.5%, which is 9.50% higher than that of microcrystalline cellulose (MCC), a width of 20-50 nm, a high aspect ratio and a winding network structure. Therefore, nanocellulose prepared by this method is an ideal toughening material for manufacturing composite materials.
随着科学技术的发展,人们越来越追求高效、快速和绿色的方法。通过生物酶辅助超声处理等绿色方法生产纳米纤维素一直是许多研究的重点。然而,用这种方法制备的纤维素纳米晶体的产率非常低。本文通过对微晶纤维素(MCC)进行预处理,采用加热搅拌+果胶酶/纤维素酶+超声处理(HSt - P/C - Ultr)制备纳米纤维素。研究了果胶酶与纤维素酶的比例以及水解时间对纳米纤维素产率的影响。利用傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和热重分析(TG)来确定纳米纤维素的结构、结晶度、形态和热稳定性。结果表明,最佳水解条件确定为果胶酶∶纤维素酶比例为1∶1、水解90分钟和50℃。纳米纤维素的产率约为32.0%。果胶酶纤维素酶 = 1∶1时的产率高于用单一生物酶处理的微晶纤维素(MCC)。这表明果胶酶和纤维素酶的协同作用对纳米纤维素的形成有一定影响。在制备过程中,纤维素的晶型没有改变。它仍然是纤维素I,结晶度为73.5%,比微晶纤维素(MCC)高9.50%,宽度为20 - 50纳米,长径比高且具有缠绕网络结构。因此,用这种方法制备的纳米纤维素是制造复合材料的理想增韧材料。