<?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[ -->木质纤维基凝胶材料的设计策略]]></title>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation of Lignin Nanoparticles and Their Application in the Hydrogel Materials]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303009&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Lignin as a renewable natural aromatic polymer and a biomass resource is receiving more and more attention， and the research on the high value utilization of lignin is in progress. The preparation and application of lignin nanoparticles （LNP） are an effective way to realize the high-value utilization of lignin. Lignin has the advantages of being good environmental and biocompatibility， low price and abundant ， but its inherent problems of heterogeneity， large particle size and poor dispersion hinder its high value application. Lignin nanosizing can control particle size and morphology， and increase the specific surface area and surface functional sites of LNP， and further enhance the antioxidant and UV resistance compared with the original lignin. Lignin nanosizing has a wide application prospect. In this paper， the preparation of LNP and its application in hydrogel materials were reviewed and the future development was anticipated.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[WANG Zhongshan,XIAO Tianyuan,LIU Xiaodi,CAO Xinyu,JIA Wenchao,SHI Haiqiang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Zhongshan,XIAO Tianyuan,LIU Xiaodi,CAO Xinyu,JIA Wenchao,SHI Haiqiang</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303009&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[Design Strategy and Application Progress of Lignin-based Hydrogel Materials]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303010&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Lignin is the second most abundant natural polymer in nature and one of the rare renewable resources among aromatic compounds. As the main by-product of pulp and paper industry， lignin is cheap and easy to obtain. Due to its three-dimensional network structure and abundant active functional groups such as alcohol hydroxyl group， phenol hydroxyl group and double bond， lignin has many advantages such as antibacterial， anti-inflammatory and adsorption， and is an ideal material for preparing hydrogels. Unfortunately， due to the complex structure， high spatial resistance and insufficient reactivity of lignin， it is difficult to purify. The high value and industrial utilization of lignin are low. Using lignin and its derivatives to prepare hydrogels not only broadens its application range， but also solves the problems such as poor biocompatibility problems existing in the synthetic polymer hydrogels. Based on this， starting from the structure and properties of lignin， this paper summarized the main preparation methods， advantages and disadvantages of lignin-based hydrogel materials， and summarized its application status in biomedicine， sewage treatment， agriculture， electronic devices and other aspects. The limitations of the current research on lignin-based hydrogels and the possible future research prospects were also proposed.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[XU Tingting,GU Xunhong,GAO Huanli,DAI Hongqi]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XU Tingting,GU Xunhong,GAO Huanli,DAI Hongqi</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303010&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 Cellulose/Polyacrylamide Double-network Hydrogels Based on AlCl<sub>3</sub>/ZnCl<sub>2 </sub>Aqueous System Construction]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303011&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In recent years， ionic conductive hydrogels with good mechanical properties and freezing-tolerant have attracted great attention in the fields of artificial intelligence， biomedicine， and flexible sensor. In this work， AlCl<sub>3</sub>/ZnCl<sub>2</sub> aqueous system was used as the mild solvent of cellulose raw material to dissolve cellulose. The intrinsic metal ions in the solvent system were effectively utilized to catalyze the polymerization of acrylamide （AM） monomer， resulting in a tight link between the polyacrylamide （PAM） network and the cellulose network. The multifunctional hydrogel with cellulose/polyacrylamide double-network was prepared. The mechanical and electrochemical properties of hydrogels were regulated by controlling the mass ratio of acrylamide to cellulose. The results showed that the metal ions in AlCl<sub>3</sub>/ZnCl<sub>2</sub> aqueous system endowed the hydrogels with excellent freezing-tolerant ability （it can work normally at -45 ℃） and ionic conductivity （2.04 S/m）. The second polymerization network constructed by polyacrylamide was strategic， and effectively improved the mechanical properties of the hydrogels. Besides， the double-network hydrogels exhibited good elastic properties in 10 compression cycles， and showed strong adhesion to different material interfaces.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[WANG Youlong,LI Xin,TIAN Yahui,MA Jinxia]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Youlong,LI Xin,TIAN Yahui,MA Jinxia</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303011&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[Study on Copper Salt Assisted Fast Preparation of Lignin-based Carbon Aerogel and Its Electrochemical Properties]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303012&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[A fast synthesis method of lignin nanoparticles （LNP）-based aerogel was proposed to prepare three-dimensional （3D） interconnected carbon aerogel with a typical micropores structure. Green and low-cost deep eutectic solvent （DES） used as the reaction solvent， three copper salts added <i>in-situ</i> as the catalyst， and LNP-based cryogel（LRF） as a precursor can be rapidly synthesized for lignin-based carbon aerogel （LRFC）. The study results showed that <i>in-situ</i> doped copper salt can accelerate the gelation rate of gel formation and decrease the gelation time of LRF. Herein， the gel formation of Cu（NO<sub>3</sub>）<sub>2</sub> assisted LRF can be shortened to 2.5 h， and the resultant carbon aerogel （N-LRFC） had the highest microporous rate of 94.44% and pore size of 1 nm， high graphitization， and excellent electrochemical performances. At current density of 0.5 A/g， N-LRFC demonstrated exceptional electrochemical performance with a specific capacitance of up to 347.6 F/g. and the diffusion control dominated the electrochemical process.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[ZHANG Yiyi,LOU Rui,CAO Qihang,NIU Taoyuan,ZHANG Bin,WEI Guodong,CHEN Haifeng]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Yiyi,LOU Rui,CAO Qihang,NIU Taoyuan,ZHANG Bin,WEI Guodong,CHEN Haifeng</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303012&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[Construction of Nanocellulose Aerogel and Its Filtration Properties for Polystyrene Microplastics]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303013&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Bleached eucalyptus pulp was chemically modified by 2，2，6，6-tetramethylpiperidine-1-oxyl （TEMPO） and 2，3-epoxypropyltrimethylammonium chloride （EPTMAC）， respectively， to produce modified cellulose nanofibrils （CNF） by high pressure homogenization. Then， modified CNF aerogels were prepared by freeze-drying process. The effects of types and concentrations of polystyrene microplastics （PSMPs） on the filtration properties of modified CNF aerogels were studied. Results showed that the filtration efficiency of EPTMAC modified aerogel （QCNF） for carboxylated polystyrene （PS-COOH） was 99%， while the filtration efficiency of TEMPO-oxidized CNF aerogel （TCNF） for aminated polystyrene （PS-NH<sub>2</sub>） was 75%. The excellent filtration performance of modified aerogels mainly relied on the super hydrophilicity， unique three-dimensional porous structure and abundant surface active binding sites of the material. In addition， the filtration efficiency and flux of the modified CNF aerogels were over 99% and 20.2 L/（m<sup>2</sup>·h） after 8 cycles of filtration， showing good stability and reusability.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[WANG Jie,WANG Xiaotong,ZHU Gaojian,LIU Chao,WU Weibing,DAI Hongqi,BIAN Huiyang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Jie,WANG Xiaotong,ZHU Gaojian,LIU Chao,WU Weibing,DAI Hongqi,BIAN Huiyang</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303013&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[Research Progress of Woody Biomass-based Adhesive Hydrogels]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303014&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[As the most abundant biomass resource， woody biomass has the characteristics of renewability， good biocompatibility and biodegradability， and has attracted much attention in many research fields. In addition to the above properties， adhesive hydrogels constructed by modification of woody biomass are endowed with special functions such as high strength， high toughness， antibacterial or anti-ultraviolet， etc. so that it has a wide range of application prospects in biomedicine， sensor and other fields. In this paper， around the structural construction methods of adhesive hydrogels based on wood biomass， the characteristics and formation mechanisms of different adhesive hydrogels based on wood biomass were introduced from the three aspects of covalent bond， non-covalent bond and dynamic reversible bond， and the latest progress of their applications in wound repair， smart wearable devices and food were reviewed. Finally， the challenges faced by lignocellulosic bio-based adhesive hydrogels were prospected.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[DU Xiaoyun,XIU Huijuan,LIANG Yanbo,LI Na,WU Minzhe,LI Jinbao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>DU Xiaoyun,XIU Huijuan,LIANG Yanbo,LI Na,WU Minzhe,LI Jinbao</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303014&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[Effect of Attapulgite on the Structure and Properties of Cellulose Nanofibrils Composite Aerogel]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303015&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Using cellulose nanofibers （CNF） as raw material and attapulgite （ATP） as reinforcing material， CNF-ATP suspension with different ratios were prepared， and then CNF-ATP composite aerogels prepared by liquid nitrogen gradient freezing and freeze-drying. The effect of different amount of ATP on the structure of CNF-ATP aerogel was analyzed by means of infrared spectroscopy （FT-IR）， X-ray diffraction （XRD） and thermogravimetric analysis （TG）. The results showed that the Zeta potential of the precursor suspension of CNF-ATP was -31.20 mV， and the particle size distribution was mainly above 1000 nm. As the amount of ATP added increasing， the humidity and heat stability and strain resistance of the CNF-ATP composite aerogel were also significantly improved. The thermal decomposition temperature exceeded 305 ℃， and the humidity stability was maintained after 72 h of immersion in the solution. At the same time， the study found that when the mass ratio of CNF and ATP was 2∶1， the CNF-ATP composite aerogel had the best strain resistance and flexibility balance， and the deformation tolerance could be as high as 45%. The humidity and heat stability of the CNF-ATP composite aerogel at this ratio has also been improved to the greatest extent， and the distribution of ATP on the pore wall of the aerogel showed its good dispersion.]]></description>
<pubDate>2023/9/20 0:00:00</pubDate>
<category><![CDATA[木质纤维基凝胶材料的设计策略]]></category>
<author><![CDATA[LIN Jiacheng,LIN Tao,WEI Xiaoyao,LU Lulu,LIU Feiya,YIN Xuefeng]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIN Jiacheng,LIN Tao,WEI Xiaoyao,LU Lulu,LIU Feiya,YIN Xuefeng</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202303015&flag=1]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
</channel>
</rss>