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<title cf:type="text"><![CDATA[ -->The Youth Talent Support Program of China Association for Science and Technology]]></title>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress on Lignocellulosic-based Solar-driven Interface Evaporators]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404001&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Solar-driven desalination technology is an effective way to address global fresh water scarcity and water pollution. The solar-driven interface evaporator has attracted great attention due to its unique advantages， including the green use of solar energy， low pollution and high efficiency. Among the photothermal materials for solar-driven interfacial evaporators， lignocellulose has gradually become a research hotspot of solar-driven interface evaporators due to its wide sources， low price， and environmental protection. In this paper， the photothermal materials formed by combining lignocellulose and carbon materials， semiconductors， metal nanoparticles or organic polymers were introduced. Their research progress in solar-driven interfacial evaporation was reviewed， and the application of lignocellulose-based solar-driven interface evaporator was summarized and prospected， in order to provide reference for the development of high-value utilization of lignocellulose and its practical application in the field of seawater desalination.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[The Youth Talent Support Program of China Association for Science and Technology]]></category>
<author><![CDATA[DENG Boyan,LI Wei,XU Ting,SI Chuanling]]></author>
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<atom:name>DENG Boyan,LI Wei,XU Ting,SI Chuanling</atom:name>
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<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404001&flag=1]]></guid><cfi:id>6</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[Study on PAM/PU Compression-resistant Hydrogels]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404002&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[This study introduced the preparation process of polyacrylamide （PAM）/polyurethane （PU） compression-resistant hydrogels. Firstly， a systematic study was conducted on the effects of addition amounts of water-based PU and acrylamide （AM）. Furtherly， the preformance of compression and swelling resistance of different PAM/PU hydrogels were investigated， and the potential of its application in articular cartilage substitutes was discussed. The results indicated that the prepared PAM/PU hydrogels exhibited excellent compressive strength， resilience， and toughness. When the mass fraction of AM aqueous solution was 35%， and the amount of PU （calculated by the volume of PU emulsion， solid content of 30%） added was 4 mL， the prepared AM65PU4 gel showed the most excellent compression-resistant performance， with the maximum compression rate up to 69%， and the compression strength of 2.1 MPa. In addition， the hydrogel showed good swelling resistance. The equilibrium swelling rate of AM65PU4 gel in deionized water was 15%， in alkaline condition was 212%， and in acid condition was 9%， which was suitable for use as articular cartilage， and could function stably for a long period of time.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[The Youth Talent Support Program of China Association for Science and Technology]]></category>
<author><![CDATA[TONG Yuhang,LI Kun,LONG Zhu,ZHANG Dan,SI Pengxiang]]></author>
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<atom:name>TONG Yuhang,LI Kun,LONG Zhu,ZHANG Dan,SI Pengxiang</atom:name>
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<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404002&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[Preparation and Properties of High-efficiency Luminescent Perovskite Quantum Dots/Nanocellulose Composite Reinforced Films]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404003&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In this study， the inorganic CsPbBr<sub>3</sub> quantum dots （BVA-CsPbBr<sub>3</sub> PQDs） with uniform size， controllable morphology， and high fluorescence quantum yield （PLQY=58.1%） were synthesized by adopting the thermal injection method， and the 5-bromovaleric acid （BVA） was used to replace the oleic acid （OA） as the surface ligand in the synergic action with oleylamine （OLA）. Based on that， the excellent mechanical properties and abundant porous structure of cellulose nanofibers （CNF） were combined to prepare the PQDs@CNF composite reinforced films， which enabled the BVA-CsPbBr<sub>3</sub> PQDs to be uniformly dispersed and firmly anchored in the CNF fiber network， effectively avoiding the agglomeration of the PQDs and enhancing the mechanical strength of the PQDs@CNF composite reinforced films. The results showed that the PQDs@CNF composite reinforced films had excellent luminescence and mechanical properties， which not only retained the original high photoluminescence intensity of BVA-CsPbBr<sub>3</sub> PQDs， but also had the environmental adaptability and stability due to the combination with CNF.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[The Youth Talent Support Program of China Association for Science and Technology]]></category>
<author><![CDATA[XING Jialong,MA Cong,ZHANG Jingru,ZHANG Meiyun]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XING Jialong,MA Cong,ZHANG Jingru,ZHANG Meiyun</atom:name>
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<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404003&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[Catalytic Hydrogenation of Lignin Using CeO<sub>2</sub> Supported Ni Single Atom Catalyst]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404004&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Converting lignin into high-value chemicals is one of the important ways for sustainable development. In this study， a CeO<sub>2</sub>-loaded Ni single atom catalyst Ni<sub>1</sub>/CeO<sub>2</sub> that can be used to catalysis the hydrogenolysis of lignin was prepared by an impregnation-pyrolysis-reduction strategy. It was found that the abundant oxygen vacancies in the CeO<sub>2</sub> supporter facilitated the high dispersion of Ni single atoms on the CeO<sub>2</sub> surface， and synchrotron radiation demonstrated that the Ni atoms could be linked with four O atoms to form the NiO<sub>4</sub> catalytic activity centre. The catalyst Ni<sub>1</sub>/CeO<sub>2</sub> not only exhibited excellent activity in catalyzing the hydrogenolysis of lignin model compounds diphenyl ether （4-O-5）， benzyl phenyl ether （<i>α</i>-O-4）， and 2-phenoxy-1-phenylethanol （<i>β</i>-O-4）， but also showed good performance in catalyzing lignin depolymerization， giving the hydrogenolysis products of lignin a good prospect for application.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[The Youth Talent Support Program of China Association for Science and Technology]]></category>
<author><![CDATA[LI Fuhua,LIU Yunzhuo,LU Tingjie,SUN Jiancheng,YU Xinyu,WEN Zhengtang,ZHOU Yaosen,XIA Xuelian,GUO Ming,SHI Changbo,HE Qian]]></author>
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<atom:name>LI Fuhua,LIU Yunzhuo,LU Tingjie,SUN Jiancheng,YU Xinyu,WEN Zhengtang,ZHOU Yaosen,XIA Xuelian,GUO Ming,SHI Changbo,HE Qian</atom:name>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Preparation of <i>Miscanthus</i>-based Lignocellulosic Nanofibrils Aerogel and Its Adsorption Property Towards Rhodamine B]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404005&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Lignocellulosic nanofibrils （LCNF） was prepared from <i>Miscanthus</i> using citric acid pretreatment combined with high-pressure homogenization， and LCNF aerogel was obtained after freeze-drying. The adsorption performance and mechanism of the aerogel towards cationic dye Rhodamine B （RB） was investigated. The results showed that the adsorption capacity towards RB by LCNF aerogel was the best under neutral conditions， and the equilibrium adsorption capacity increased to 40.0 mg/g at 55 ℃. The adsorption kinetics and thermodynamics studies showed that the adsorption towards RB by LCNF aerogel conformed to the pseudo-second-order kinetic model， which was mainly dominated by chemical adsorption and spontaneous. There were some interactions such as hydrogen bonding and electrostatic attraction between LCNF and RB during the adsorption process. In addition， LCNF aerogel showed good reusability and the removal rate of RB remained above 83% after four cycles.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[The Youth Talent Support Program of China Association for Science and Technology]]></category>
<author><![CDATA[CHEN Lidong,DUAN Sheng,WU Jin,LIU Chao,YAO Shuangquan,XU Tingting,DAI Hongqi,BIAN Huiyang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CHEN Lidong,DUAN Sheng,WU Jin,LIU Chao,YAO Shuangquan,XU Tingting,DAI Hongqi,BIAN Huiyang</atom:name>
</atom:author>
<guid><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404005&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 and Characterization of Novel Biodegradable Nanofiber Films in Seawater]]></title>
<link><![CDATA[http://zgzzxb.ijournals.cn/zzxben/ch/reader/view_abstract.aspx?file_no=202404006&flag=1]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Cellulose acetate （CA） and polylactic acid （PLA） were used as raw materials to prepare CA/PLA nanofiber films with different proportions by salivary membrane method， and the biodegradability was tested in simulated seawater. The effect of mass ratio of CA and PLA on physicochemical structure and thermal properties of the CA/PLA nanofiber films were studied by scanning electron microscopy， Fourier transform infrared spectroscopy， thermogravimetric analysis and other techniques. In addition， the degradability of CA/PLA nanofiber films in simulated seawater was conducted by a 15-day simulated seawater degradation experiment. The results showed that the degradation rate of the CA/PLA nanofiber films was better than that of a pure CA film， and the degradation rate of the CA/PLA nanofiber film with a mass ratio of 8：2 of CA and PLA was up to 86.80%.]]></description>
<pubDate>2024/12/23 0:00:00</pubDate>
<category><![CDATA[The Youth Talent Support Program of China Association for Science and Technology]]></category>
<author><![CDATA[ZHANG Juntao,XIE Yuxin,ZHAO Mingwei,ZHAO Yurong,LIAO Guangfu]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Juntao,XIE Yuxin,ZHAO Mingwei,ZHAO Yurong,LIAO Guangfu</atom:name>
</atom:author>
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