<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005">
<channel xmlns:cfi="http://www.microsoft.com/schemas/rss/core/2005/internal" cfi:lastdownloaderror="None">
<title cf:type="text"><![CDATA[ -->Clean Separation & High-value Utilization of Fiber Components]]></title>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation of Lignin-based High Efficiency Dye Adsorption Materials and Their Performance]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407010&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The industrial alkali lignin was subjected to co-activation treatment with ZnCl<sub>2</sub>， KOH， urea， and lignin-based adsorption material with high adsorption capacity （Zn-LB）was prepared by high temperature carbonization（700 ℃）. The prepared material was used in adsorption experiments with methylene blue and methyl orange dyes to explore the effects of dye type， adsorption temperature， and a multi-component dye system on the adsorption capacity of Zn-LB. The results showed that the specific surface area of the prepared Zn-LB samples reached 2 190.3 m<sup>2</sup>/g. The maximum equilibrium adsorption capacities of Zn-LB for methylene blue and methyl orange， as fitted through the Langmuir adsorption isotherm model， were 1 345.9 and 1 732.4 mg/g， respectively. Additionally， the adsorption capacity for methylene blue increased with increasing temperature， indicating that the adsorption of methylene blue was an endothermic process. Conversely， the adsorption capacity for methyl orange decreased with rising temperature， suggesting an exothermic process.]]></description>
<pubDate>2024/7/22 18:25:50</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[WEN Mohan,XU Xin,LI Lijun,HUANG Jianbo,ZHANG Xueming]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WEN Mohan,XU Xin,LI Lijun,HUANG Jianbo,ZHANG Xueming</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407010&flag=1]]></guid><cfi:id>7</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Investigation on the Dispersion Properties of Carboxylated Cellulose Nanofibrils for Monolayer Montmorillonite]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407011&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In this study， colloidally stable monolayer montmorillonite （MMT） dispersions were prepared using cellulose nanofibrils （CNF） as dispersant， and the effects of carboxyl content and aspect ratio of CNF on the dispersion stability， average particle size， viscosity， and yield of monolayer MMT dispersions were explored. The results showed that 2,2,6,6-tetramethylpiperidine nitride oxide （TEMPO） oxidized CNF （TOCNF） was more effective than carboxymethylated CNF （CMCNF） in dispersing monolayer MMT dispersions. Specifically， TOCNF with a carboxyl content of 1.24 mmol/g presented the best dispersion capability and the as-prepared monolayer MMT had an average particle size of 317 nm. Additionally， when the concentration of TOCNF （1.24 mmol/g） dispersion was 0.1%， the maximum initial concentration of the dispersed MMT was 1.5%， the yield and concentration of the monolayer MMT after ultrasonication and centrifugation were 52% and 0.78%， respectively.]]></description>
<pubDate>2024/7/22 18:25:51</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[PENG Liyuan,FANG Zhiqiang,LI Guanhui,LIN Xiaoqi]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>PENG Liyuan,FANG Zhiqiang,LI Guanhui,LIN Xiaoqi</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407011&flag=1]]></guid><cfi:id>6</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation and Properties of Self-healing Lignin-based Flame Retardant Polyurethane Elastomers Based on Coordination Reaction]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407012&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[By controlling the ratio of star structure lignin （L-TA） sealed with triazole group and polyurethane prepolymer （P-TA）， lignin-based self-healing elastomers were prepared under the coordination reactions with different metal ions， and the flame retardant properties of the elastomers were improved by adding flame retardant DT containing triazole group. The tensile strength of 70P-TA/20L-TA/10DT with DT instead of 10% L-TA was 88.4% higher than that of pure P-TA under the coordination reaction with Fe<sup>3+</sup>， and the LOI value of the sample 70P-TA/20L-TA/10DT reached 29.5%， and the UL-94 reached V-0 level. However， the addition of L-TA and DT further increased the steric hindrance inside the sample and decreased the molecular chain mobility， so that the self-healing efficiency of 70P-TA/20L-TA/10DT decreased to 81.3% from 91.1% of 100P-TA. In addition， compared with other metal ions， the lower coordination bond strength of Zn<sup>2+</sup>—N decreased the glass transition temperature （<i>T</i><sub>g</sub>） of the elastomer 70P-TA/20L-TA/10DT：Zn<sup>2+</sup>， which improved the fluidity of the polymer chain and entitled it a higher self-healing efficiency （87.7%）.]]></description>
<pubDate>2024/7/22 18:25:53</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[YUE Xiaopeng,GUAN Lixiang,ZHANG Siqian,CAO Panpan,WANG Zhiwei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YUE Xiaopeng,GUAN Lixiang,ZHANG Siqian,CAO Panpan,WANG Zhiwei</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407012&flag=1]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress of Novel Fractionation Methods of Lignocellulosic Biomass Components]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407013&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Lignocellulosic biomass is the most abundant renewable resource on the earth， which is widely considered to be the most promising alternative to fossil resources. How to effectively convert lignocellulosic materials into products such as biomaterials， chemicals and biofuels has always been a hot topic for scientific and technological workers. Exploring efficient separation technology to breek down lignocellulosic biomass into cellulose， hemicellulose， and lignin which are easy to convert is the key for achieving high-value and diversified utilization of lignocellulosic resources. The purpose of this paper was to introduce the research progress of the whole component separation of lignocellulosic biomass components， focusing on four kinds of novel component separation methods， including organic solvent method， ionic liquid method， deep eutectic solvent method and catalytic separation method under the “lignin priority” strategy. The development status of these new separation methods and the challenges faced in the industrialization process were discussed， and the future development prospects were prospected.]]></description>
<pubDate>2024/7/22 18:25:54</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[BU Qi,FU Yingjuan,QIN Menghua,ZHANG Yongchao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>BU Qi,FU Yingjuan,QIN Menghua,ZHANG Yongchao</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407013&flag=1]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress on Preparation of Lignin Nanoparticles and Their Application in Photothermal Conversion]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407014&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Photothermal conversion is the most direct way to utilize solar energy. With the comprehensive utilization of sustainable biomass resources and the continuous development of nanotechnology， nano-biomass materials have received more and more attention in the field of photothermal conversion as a renewable resource. Lignin， as a natural polymer second only to cellulose in nature， has excellent ultraviolet absorption and photothermal conversion ability. At present， the utilization degree of lignin is still low， and the preparation and application of lignin nanoparticle （LNP） is an effective way to achieve high-value lignin utilization. Compared with the original lignin， the high specific surface area and tunable morphology and size of LNP further enhance its antioxidant and UV resistance properties. In view of this， this paper summarized preparation methods of LNP， and focused on the application status of LNP in the field of photothermal conversion. Finally， the main challenges and prospects in the field of photothermal conversion were discussed.]]></description>
<pubDate>2024/7/22 18:25:55</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[GAI Xiaoqian,YU Zhaochuan,LI Yu,LEI Tong,WANG Yuting,BIAN Huiyang,XIAO Huining,LIU Chao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>GAI Xiaoqian,YU Zhaochuan,LI Yu,LEI Tong,WANG Yuting,BIAN Huiyang,XIAO Huining,LIU Chao</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407014&flag=1]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[A Review on the Application of Lignin in Sunscreen]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407015&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In this paper， the structure， species and properties of lignin， as well as its research progress in the field of sunscreen were reviewed. Combined with our research in describing the preparation of different lignin-based sunscreens， the anti-ultraviolet radiation performance and color presentation mechanism of lignin were highlighted， and strategies of protecting anti-ultraviolet radiation performance while reducing color of lignin were explored. Furthermore， the development and utilization of lignin were prospected. In order to provide a significant reference for the resource utilization of lignin in the field of cosmetics.]]></description>
<pubDate>2024/7/22 18:25:58</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[HU Dongbin,LI Yarong,ZHOU Xiaohan,PANG Jingdong,SONG Xueping,LI Kai]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HU Dongbin,LI Yarong,ZHOU Xiaohan,PANG Jingdong,SONG Xueping,LI Kai</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407015&flag=1]]></guid><cfi:id>2</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress on Chiral Materials of Cellulose Nanocrystals]]></title>
<link><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407016&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Cellulose nanocrystals （CNC） are nanofibers extracted from natural fibers. It not only has the characteristics of nanoparticles， but also shows the advantages of renewability， biodegradability， and biocompatibility. Colloidal stable CNC particles have a tendency to self-assemble into cholesteric liquid crystals in water， which can be modified according to their periodicity， structure， and morphology， therefore the CNC has been widely studied and has broad application prospects. CNC can form an iridescent film with chiral nematic liquid crystal phase by evaporation-induced self-assembly （EISA）. The chiral nematic liquid crystal behavior， environmental response， and application of CNC in electronic， medical and food industries were reviewed in this paper. The futural research highlights and development of CNC-based chiral nematic materials were proposed as well， which in order to provide reference for the future application of chiral materials.]]></description>
<pubDate>2024/7/22 18:25:59</pubDate>
<category><![CDATA[Clean Separation & High-value Utilization of Fiber Components]]></category>
<author><![CDATA[PING Xinxin,XU Huawei,DONG Hanqi,YAN Mengxing,LING Zhe]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>PING Xinxin,XU Huawei,DONG Hanqi,YAN Mengxing,LING Zhe</atom:name>
</atom:author>
<guid><![CDATA[http://zgzz.ijournals.cn/zgzzen/ch/reader/view_abstract.aspx?file_no=202407016&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
</channel>
</rss>