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<title cf:type="text"><![CDATA[ -->· Lignocellulose-based Composite Materials ·]]></title>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Study on Antibacterial Paper Prepared by Starch-based Coating Solution Based on Orange Peel Essential Oil Emulsified with Cellulose Nanocrystalline]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404012&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Using mung bean starch （MBS） as the substrate and citric acid as the crosslinking agent， TEMPO oxidized cellulose nanocrystalline （TOCN） was used to emulsify orange peel essential oil （OPO）， and to prepare TOCN-OPO Pickering emulsion as the antibacterial agent， so as to further prepare starch-based coating solution MBS/TOCN-OPO. Then the antibacterial paper was prepared by coating MBS/TOCN-OPO on the original paper. The effect of MBS/TOCN-OPO coating amount on the strength and antibacterial properties of antibacterial paper was discussed. The results showed that compared with original paper， when the MBS/TOCN-OPO coating amount was 9 g/m<sup>2</sup>， the folding strength of antibacterial paper was increased from 9 to 60 times， the tensile index and burst index were increased by 35.0% and 42.1%， respectively， the water vapor transmission rate was decreased by 38.6%， and the water contact angle was increased to 65.42°. The antibacterial paper had the best antibacterial effect on penicillium. MBS/TOCN-OPO antibacterial paper had a good antibacterial fresh-keeping application effect when applied to packaging tomato.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[CHEN Qijie,LUO Chengyu,ZHENG Xueming,JIN Xingming,YOU Na,LIU Tao,WAN Jinming]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CHEN Qijie,LUO Chengyu,ZHENG Xueming,JIN Xingming,YOU Na,LIU Tao,WAN Jinming</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404012&flag=1]]></guid><cfi:id>10</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Protein Imprinted Materials Based on MOFs Composite Wood Sponges for Efficient and Selective Separation of Glycoproteins]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404013&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The efficient enrichment and identification of glycoproteins hold significant relevance to proteomics-related medical and biological research. However， constructing high-performance glycoprotein imprinted materials remains challenging. In this study， the wood sponge@ UIO-66 composite （WCS@UIO-66） was employed as a carrier， and 4-vinylphenylboronic acid was taken as a covalent functional monomer to design and synthesize horseradish peroxidase-imprinted materials （WCS@UIO-66@MIPs）. Utilizing the porous structure and abundant functional groups of the wood sponge and metal-organic framework， the immobilization of template proteins was facilitated while reducing the mass transfer resistance. Consequently， WCS@UIO-66@MIPs not only demonstrated exceptionally high adsorption capacity （182.0 mg/g） and excellent selectivity （Imprinting Factor=2.68） towards horseradish peroxidase， but also achieved adsorption equilibrium within 60 min. Moreover， it could specifically capture target proteins in mixed protein solutions， demonstrating its promising potential applications for glycoprotein enrichment and identification.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[ZHANG Yuhao,YANG Miaoxiu,LIU Zhenhua,YANG Yuxuan,GUO Chun,YANG Menghao,HUANG Ju,ZHANG Jingwei,CHEN Liqing,QIAN Liwei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Yuhao,YANG Miaoxiu,LIU Zhenhua,YANG Yuxuan,GUO Chun,YANG Menghao,HUANG Ju,ZHANG Jingwei,CHEN Liqing,QIAN Liwei</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404013&flag=1]]></guid><cfi:id>9</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress on Waterborne Oxygen and Moisture Barrier Coatings for Packaging Materials]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404014&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[As the increasingly demands for barrier performance and green environmental sustainability of coatings in the packaging industry， using waterborne barrier coatings to give packaging materials high barrier performance has become one of the research hotspots in the industry. This paper reviewed the recent research progress in waterborne barrier coating to improve the oxygen and moisture barrier performance of packaging materials. The bio-based waterborne barrier coatings of polysaccharides and proteins with controllable rheological properties and excellent film-forming properties were introduced. The non-biological based waterborne barrier coatings of polyvinyl alcohol， polyacrylic acid emulsion and polyvinylidene chloride emulsion were also summarized. Waterborne barrier coatings have the advantages of environment， safety and no solvent residue， in line with the green concept of sustainable development. Waterborne barrier coatings have great application potential in barrier packaging materials.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[XIAO Guihua,SU Yanqun,LI Hongcai,JIN Xinming,ZHANG Ruijuan,LIU Jingang,YANG Xiaobo,FU Xianling,LI Hong,CHEN Liqing,ZHANG Jingwen]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XIAO Guihua,SU Yanqun,LI Hongcai,JIN Xinming,ZHANG Ruijuan,LIU Jingang,YANG Xiaobo,FU Xianling,LI Hong,CHEN Liqing,ZHANG Jingwen</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404014&flag=1]]></guid><cfi:id>8</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation of Intelligent Colorimetric Paper Strip Based on SKN@TOCN/CGG and Its Application in Freshness Detection of Chicken Breast]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404015&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The intelligent colorimetric paper strip was prepared with shikonin （SKN） as the sensing component and TEMPO-oxidized cellulose nanoﬁbrils （TOCN）/cationic guar gum （CGG） hydrogel modified filter paper as the substrate. The effects of different drying treatments on the surface morphology， mechanical properties， water contact angle， hydrolysis rate， dissolution rate， and the shikonin stability of the paper strip were analyzed. The results showed that the paper strip prepared by freeze-drying had a porous structure with the lowest hydrolysis rate. SKN could be reserved stably in the paper strip. The paper strip was used to determine the freshness of chicken breast， and the results demonstrated the total volatile base nitrogen （TVB-N） reached 17.354 mg/100 g when the chicken breast was stored for 5 days at 4 ℃， indicating that the chicken breast was not fresh. Meanwhile， the paper strip changed its color from light pink to dark pink， and even to purplish-red after 8 days， showing that the paper strip prepared in this work could reflect the freshness of chicken breast in the real time.]]></description>
<pubDate>2024/12/25 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[TIAN Sihan,LUO Qing,HE Ping,LI Yan,HUA Feiguo,DAI Lei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>TIAN Sihan,LUO Qing,HE Ping,LI Yan,HUA Feiguo,DAI Lei</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404015&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[Construction of Polymeric Ionic Liquid Crosslinked Structures on Porous Cellulose and Study on Adsorption Performance]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403001&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[This study developed a novel polymeric imidazolium ionic liquid-modified porous cellulose （PC@PCIL） for the removal of azo dyes from water with high efficiency. Porous cellulose substrates （PC） were prepared from cotton pulp through an alkali/urea solvent system， following by the introduction of 3，3-（［1，1-biphenyl］-4，4-diylbis（methylene））bis（1-vinyl-1H-imidazol-3-ium） chloride and 3-butyl-1-vinyl-1H-imidazol-3-ium chloride as co-monomers. Controlled living polymerization technique was employed to construct polymeric ionic liquid interlinked structures on the surface of PC to prepare adsorbent PC@PCIL. This adsorbent exhibited an adsorption capacity of up to 544 mg/g for congo red in water， and the adsorption process was primarily governed by a synergistic chemical adsorption mechanism involving electrostatic interactions， π-π stacking， and hydrophobic effects， following the pseudo-second-order kinetic model and Freundlich isotherm model.]]></description>
<pubDate>2024/9/18 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[SONG Wenqi,FU Zepeng,WANG Zi,REN Zhihua,WANG Siyu,YANG Chenglin,ZHU Xueyao,PENG Qin,YANG Miaoxiu]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SONG Wenqi,FU Zepeng,WANG Zi,REN Zhihua,WANG Siyu,YANG Chenglin,ZHU Xueyao,PENG Qin,YANG Miaoxiu</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403001&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[Progress in Hydrophobic Modification of Bio-based Polysaccharides and Their Application in Paper-based Materials]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403002&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Paper-based materials have great application properties， but their strong water absorption seriously restricts their application in many fields. The hydrophobic treatment for petroleum-based products disrupts the original degradability of paper-based materials. Therefore， in recent years， researchers have become more concerned about using polysaccharides with good biocompatibility as raw materials for hydrophobic modification. This article reviewed the research progress of bio-based polysaccharides in improving the hydrophobicity of paper-based materials in recent years， with a focus on the hydrophobic modification of cellulose， starch， chitosan， alginate， and other bio-based polysaccharides， as well as their application status in the hydrophobicity treatment of paper-based materials. It also summarized and prospected the future development trends.]]></description>
<pubDate>2024/9/18 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[WANG Feng,ZHANG Yazeng,DENG Songlin,JIN Xingming,LUAN Pengcheng,CHEN Qijie]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Feng,ZHANG Yazeng,DENG Songlin,JIN Xingming,LUAN Pengcheng,CHEN Qijie</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403002&flag=1]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[CNF/PMIA/PPTA Lithium-ion Battery Separator Prepared by Paper-making Process]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403003&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[CNF/PMIA/PPTA lithium-ion battery separators were prepared by wet forming of paper-making method using water-soluble polyimide （PI） as reinforcing agent， and mixing cellulose nanofiber （CNF） and poly（ethylene oxide）‍-modified poly（aramid fiber） （PMIA/PPTA） suspension. After characterization and analysis of separator performance， the effects of dispersion and stability of CNF and PMIA/PPTA suspensions and the mass fraction of each component on the mechanical and electrochemical properties of the separator were investigated. The results showed that the composition and dosage for the optimum properties of separator was： CNF （mass fraction of 0.5%， relative to the mixed total pulp mass， the same below）， PMIA/PPTA fibers （mass fraction of 0.5%， mass ratio of 5：5）， diatomaceous earth （mass fraction of 0.05%）； and PI aqueous solution was sprayed （spraying quantity of 1.5%， relative to the absolate dry mass of the separator）. At this time， the tensile strength of the lithium-ion battery separator was 23.74 MPa， the elongation at break was 3.41%， the liquid absorption， liquid retention， and porosity were 237.16%， 152.88%， and 69.34%， respectively， and the thermal shrinkage was only 0.31%， with an ionic conductivity of up to 1.041 mS/cm； the first discharge capacity of the lithium-ion battery assembled by separator was 158.2 mAh/g. The CNF/PMIA/PPTA lithium-ion battery separator not only had excellent thermal stability， but also higher ionic conductivity， wider electrochemical stabilization window， excellent multiplicity and cycling performance， which met the technical safety requirements of lithium-ion battery separator.]]></description>
<pubDate>2024/9/18 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[SUN Zhonghua,LI Jian,WANG Xiaodi,LIU Xin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SUN Zhonghua,LI Jian,WANG Xiaodi,LIU Xin</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403003&flag=1]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress of Hydrogels Crosslinked by Borate Ester Bonds]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403004&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Borate ester bond is a special type of dynamic covalent bond that can undergo bonding within seconds at room temperature， with faster reaction rate than most dynamic covalent bonds， and has significant self-healing ability. Using appropriate physical or chemical crosslinking strategy to design hydrogels based on borate ester bonds can give materials excellent physicochemical properties. In this paper， the hydrogels with excellent biocompatibility prepared by polysaccharide like cellulose and polyhydroxy polymers like polyvinyl alcohol based on borate ester bonds in recent years were summarized， and the outstanding properties were introduced. The research progress in the biomedical field and flexible electronic devices were reviewed， which provided an idea for achieving multi-functional applications of hydrogels.]]></description>
<pubDate>2024/9/18 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[SHEN Zhenpeng,ZHOU Tongxin,WANG Yannan,LIU Wenxia,WANG Huili]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SHEN Zhenpeng,ZHOU Tongxin,WANG Yannan,LIU Wenxia,WANG Huili</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403004&flag=1]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation and Application of Manganese<bold>-</bold>loaded Activated Carbon<bold>-</bold>Cellulose Composite Adsorbent for Enhancing Laccase Enzyme Activity]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403005&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[A novel manganese-loaded activated carbon-cellulose composite adsorbent that could immobilize laccase and increase the enzyme activity was prepared by solvent regeneration method， using waste manganese-loaded activated carbon and cellulose， and further prepared the laccase-carrier material after immobilizing laccase. The results showed that the content of Mn<sup>2+</sup> had a certain effect on the enzyme activity of the laccase-carrier material， and the enzyme activity of the laccase-carrier material was the highest when the content of Mn<sup>2+</sup> in the composite adsorbent was 1.5 mg/g. The optimum process conditions for the immobilization of laccase were the immobilization temperature of 45 ℃， the pH value of 4， and the initial enzyme concentration of 6.5 g/L. The immobilization ratio of the laccase-carrier material was the highest to 48.24% under the optimum conditions of immobilization； the thermal and pH stabilities of the laccase-carrier material were significantly enhanced； the degradation rate of bisphenol A using the laccase-carrier material reached 68%， and the relative degradation rate of bisphenol A was still up to 51% after 5 times of reuse.]]></description>
<pubDate>2024/9/18 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[LI Na,MENG Xiangrui,PENG Chuanbo,YU Fangrui,ZHANG Jian,SHENG Xueru,PING Qingwei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Na,MENG Xiangrui,PENG Chuanbo,YU Fangrui,ZHANG Jian,SHENG Xueru,PING Qingwei</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403005&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[Preparation of Lithium Battery Separator by Non-solvent-induced Phase Separation of Cellulose]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403006&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In this study， regenerated cellulose lithium battery separator was prepared by NaOH/urea/thiourea dissolution system and non-solvent-induced phase separation method， and the electrochemical properties of regenerated cellulose lithium battery separator and commercial polyolefin Celgard 2400 separators and cellulose separators were compared. The results showed that the regenerated cellulose lithium battery separator had a porosity of 56.1%， an average pore size of 305 nm， an electrolyte absorption rate of 339%， a liquid retention rate of 68.9%， and an ionic conductivity of 1.88 mS/cm； the specific capacity reached 156.55 mAh/g， and the Coulombic efficiency was higher than 96% after 100 charge/discharge cycles at a rate of 0.5 C. The Celgard 2400 separator had an ionic conductivity of 0.43 mS/cm， and the specific capacity was only 74.26 mAh/g after 100 charge/discharge cycles at a rate of 0.5 C， and the Coulomb efficiency was lower than 88%. Compared with Celgard 2400 separator， the regenerated cellulose lithium battery separator had higher porosity， better electrolyte wettability， lower internal resistance， faster ion transport speed， as well as the advantages of renewability and environmental friendliness， which made the regenerated cellulose lithium battery separator to be a broad application prospect in the field of lithium batteries.]]></description>
<pubDate>2024/9/18 0:00:00</pubDate>
<category><![CDATA[· Lignocellulose-based Composite Materials ·]]></category>
<author><![CDATA[XU Shuoyuan,Yang Liuqing,LIU Quanxin,HU Zhijun,CHEN Huanghuang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XU Shuoyuan,Yang Liuqing,LIU Quanxin,HU Zhijun,CHEN Huanghuang</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202403006&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
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