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Chinese chemical Letters 2024年第7期35卷 173-177页

作者： Xin Li Xuan Ding junkun Zhou Hui Shi Zhenxi dai Jiayi Liu Yongcun Ma Penghui Shao Liming Yang Xubiao Luo Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle Nanchang Hangkong UniversityNanchang 330063China School of Life Science Jinggangshan UniversityJi’an 343009China

The preparation of hydrogel adsorbents with admirable performance for efficient selective remove Pb(Ⅱ)in complex wastewater still remains a great ***,a novel bifunctional modified polymer hydrogel PAM-PAMPS was prepared by crosslinking acrylamide(AM)and 2-acrylamido-2-methylpropanesulfonic acid(AMPS).Compared with PEg,PAA and PAMPS,PAM-PAMPS exhibited both the maximum adsorption capacity of Pb(Ⅱ)(541.90 mg/g)and satisfactory selectivity for Pb(Ⅱ)in multiple heavy metal ions coexistence *** characterizations indicated that–SO3H and–NH2as active sites on PAM-PAMPS occur the synergistic effects of ion-exchange and coordination with Pb(Ⅱ)during the adsorption process,*** adsorption energy Ead(PAM-PAMPS)obtained from density functional theory(DFT)calculations was lower than the other three hydrogels,manifesting that PAMPAMPS formed the most stable complex with Pb(Ⅱ),which further demonstrated that Pb(Ⅱ)preferred to combine with PAM-PAMPS to selective capture of Pb(Ⅱ).The practice utilization of PAM-PAMPS was assessed by wastewater of electroplate containing Pb(Ⅱ).Meanwhile,the removal ratio of PAM-PAMPS was maintained at about 89%after 4 adsorption-desorption *** study establishes a new and effective idea for the design and fabrication of bifunctionalized modified polymer hydrogels.

关键词： Synergistic effects Bifunctional Polymer hydrogel Selective capture Pb(Ⅱ)

Polymer engineering for electrodes of aqueous zinc ion batteries

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Journal of Energy chemistry 2024年第4期91卷 345-369页

作者： Zhi Peng Zemin Feng Xuelian Zhou Siwen Li Xuejing Yin Zekun Zhang Ningning Zhao Zhangxing He Lei dai Ling Wang Chao Lu School of chemical Engineering North China University of Science and TechnologyTangshan 063210HebeiChina State Key Laboratory of chemical Resource Engineering Beijing University of Chemical TechnologyBeijing 100029China

With the increasing demand for scalable and cost-effective electrochemical energy storage,aqueous zinc ion batteries(AZIBs)have a broad application prospect as an inexpensive,efficient,and naturally secure energy storage ***,the limitations suffered by AZIBs,including volume expansion and active materials dissolution of the cathode,electrochemical corrosion,irreversible side reactions,zinc dendrites of the anode,have seriously decelerated the civilianization process of ***,polymers have tremendous superiority for application in AZIBs attributed to their exceptional chemical stability,tunable structure,high energy density and outstanding mechanical *** the expanding applications of AZIBs and the superiority of polymers,this comprehensive paper meticulously reviews the benefits of utilizing polymeric applied to cathodes and anodes,*** begin with,with adjustable structure as an entry point,the correlation between polymer structure and the function of energy storage as well as optimization is deeply investigated in respect to the ***,depending on the diversity of properties and structures,the development of polymers in AZIBs is summarized,including conductive polymers,redox polymers as well as carbon composite polymers for cathode and polyvinylidene fluoride-,carbonyl-,amino-,nitrile-based polymers for anode,and a comprehensive evaluation of the shortcomings of these strategies is ***,an outlook highlights some of the challenges posed by the application of polymers and offers insights into the potential future direction of polymers in *** is designed to provide a thorough reference for researchers and developers working on polymer for AZIBs.

关键词： Aqueous zinc ion batteries Polymer Multi-function Anode protection Energy storage

Hypoxia inducible factor-1α related mechanism and TCM intervention in process of early fracture healing

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Chinese Herbal Medicines 2024年第1期16卷 56-69页

作者： Wenxian Zhang Fusen Yang Qikai Yan Jiahui Li Xiaogang Zhang Yiwei Jiang Jianye dai Affiliated Hospital of gansu University of Traditional Chinese Medicine Lanzhou 730000China School of Pharmacy Lanzhou UniversityLanzhou 730000China Xi’an Hospital of Traditional Chinese Medicine Xi’an 710021China

As a common clinical disease, fracture is often accompanied by pain, swelling, bleeding as well as other symptoms and has a high disability rate, even threatening life, seriously endangering patients’ physical and psychological health and quality of life. Medical practitioners take many strategies for the treatment of fracture healing, including Traditional Chinese Medicine(TCM). In the early stage of fracture healing,the local fracture is often in a state of hypoxia, accompanied by the expression of hypoxia inducible factor-1α(HIF-1α), which is beneficial to wound healing. Through literature mining, we thought that hypoxia, HIF-1α and downstream factors affected the mechanism of fracture healing, as well as dominated this process. Therefore, we reviewed the local characteristics and related signaling pathways involved in the fracture healing process and summarized the intervention of TCM on these mechanisms,in order to inspirit the new strategy for fracture healing, as well as elaborate on the possible principles of TCM in treating fractures based on the HIF molecular mechanism.

关键词： fracture healing hypoxia hypoxia inducible factor-1α traditional chinese medicine molecular mechanism

微波等离子体飞行时间质谱仪研制及元素检测应用研究

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质谱学报 2024年第3期45卷 343-353,I0002页

作者：左凯代渐雄赵忠俊郭星段忆翔四川大学机械工程学院四川成都610065 成都艾立本科技有限公司四川成都611930

微波等离子体炬(microwave plasma torch,MPT)具有功耗低、操作方便、结构简单等优点,与质谱仪联用可快速分析元素。本文报道了一套自制的低功耗微波等离子体炬飞行时间质谱仪(MPT-TOF MS)及进样装置,并考察了维持气流速、载气流速、超... 详细信息

微波等离子体炬(microwave plasma torch,MPT)具有功耗低、操作方便、结构简单等优点,与质谱仪联用可快速分析元素。本文报道了一套自制的低功耗微波等离子体炬飞行时间质谱仪(MPT-TOF MS)及进样装置,并考察了维持气流速、载气流速、超截取锥电压、MPT炬焰位置及微波功率对元素检测的影响,系统地研究了该仪器的性能。结果表明,MPT-TOF MS具有耗气量少(氩维持气流速800 mL/min、氩载气流速400 mL/min、氮干燥气流速2000 mL/min)、离子源功耗低(100 W)的优势,且线性范围覆盖5个数量级,分辨率高,锂、钠、钾、铷和铯元素的检出限分别为0.49、3.05、1.31、0.74、0.34μg/L。该仪器可用于盐湖中锂、钠、钾、铷及铯碱金属元素的快速检测,是电感耦合等离子体质谱(ICP-MS)元素检测方法的补充。

关键词：微波等离子体炬(MPT) 飞行时间质谱(TOF MS) 元素检测

Flexible interdigitated layered framework with multiple accessible active sites for high-performance CH_(3)I capture

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Science China chemistry 2024年第5期67卷 1569-1577页

作者： Bo Tai Baoyu Li Linwei He Zhonglin Ma Shujing Lin Mingxing Zhang junchang chen Fuqi Wu Long chen Xing dai Fuyin Ma Zhifang Chai Shuao Wang State Key Laboratory of Radiation Medicine and Protection School for Radiological and interdisciplinary Sciences(RAD-X)and Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education InstitutionsSoochow UniversitySuzhou 215123China

The development of adsorbent materials for effective capture of radioactive iodomethane(CH_(3)I) from the off-gas of used nuclear fuel reprocessing, remains a significant and challenging line of research because currently state-of-art adsorbents still suffer from low binding affinity with CH_(3)I. Here, we proposed a brand-new adsorption topological structure by developing a 2D interdigitated layered framework, named SCU-20, featuring slide-like channel with multiple active sites for CH_(3)I capture. The responsive rotating-adaptive aperture of SCU-20 enables the optimal utilization of all active sites within the pore for highly selective recognition and capture of CH_(3)I. A record-breaking CH_(3)I uptake capacity of 1.84 g/g was achieved under static sorption conditions with saturated CH_(3)I vapor. Both experimental and theoretical findings demonstrated that the exceptional uptake of SCU-20 towards CH_(3)I can be attributed to the confined physical electrostatic adsorption of F sites, coupled with the chemical nitrogen methylation reaction with uncoordinated N atoms of pyrazine. Moreover, dynamic CH_(3)I uptake capacity potentially allows for the capture of CH_(3)I in simulated real-world off gas reprocessing conditions. This study highlights the potential of SCU-20 as a promising candidate for efficient capture of iodine species and contributes to the development of effective solutions for radioactive iodine remediation.

关键词： 2D interdigitated layered framework iodomethane dual-sites electrostatic interaction physisorption and chemisorption

Building stabilized Cu_(0.17)Mn_(0.03)V_(2)O_(5−□)·2.16H_(2)O cathode enables an outstanding room‐/low‐temperature aqueous Zn‐ion batteries

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Carbon Energy 2024年第8期6卷 25-35页

作者： Ao Wang dai‐Huo Liu Lin Yang Fang Xu Dan Luo Haozhen Dou Mengqin Song Chunyan Xu Beinuo Zhang Jialin Zheng Zhongwei chen Zhengyu Bai Key Laboratory of green chemical Media and Reactions Ministry of EducationCollaborative Innovation Center of Henan Province for Green Manufacturing of Fine ChemicalsSchool of Chemistry and Chemical EngineeringHenan Normal UniversityXinxiangHenanChina The State Key Laboratory of Catalysis(SKLC) Power Battery and System Research CenterDalian Institute of Chemical PhysicsChinese Academy of SciencesDalianChina

Vanadium oxide cathode materials with stable crystal structure and fast Zn^(2+)storage capabilities are extremely important to achieving outstanding electrochemical performance in aqueous zinc‐ion *** this work,a one‐step hydrothermal method was used to manipulate the bimetallic ion intercalation into the interlayer of vanadium *** pre‐intercalated Cu ions act as pillars to pin the vanadium oxide(V‐O)layers,establishing stabilized two‐dimensional channels for fast Zn^(2+)*** occupation of Mn ions between V‐O interlayer further expands the layer spacing and increases the concentration of oxygen defects(Od),which boosts the Zn^(2+)diffusion *** a result,as‐prepared Cu_(0.17)Mn_(0.03)V_(2)O_(5−□)·2.16H_(2)O cathode shows outstanding Zn‐storage capabilities under room‐and lowtemperature environments(e.g.,440.3 mAh g^(−1)at room temperature and 294.3 mAh g^(−1)at−60°C).Importantly,it shows a long cycling life and high capacity retention of 93.4%over 2500 cycles at 2 A g^(−1)at−60°***,the reversible intercalation chemistry mechanisms during discharging/charging processes were revealed via operando X‐ray powder diffraction and ex situ Raman *** strategy of a couple of 3d transition metal doping provides a solution for the development of superior room‐/lowtemperature vanadium‐based cathode materials.

关键词： aqueous zinc‐ion batteries Cu_(0.17)Mn_(0.03)V_(2)O_(5−□)·2.16H_(2)O oxygen defects room‐/lowtemperature performance stabilized nanostructure

Cooperative structure of Li/Ni mixing and stacking faults for achieving high-capacity Co-free Li-rich oxides

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Journal of Energy chemistry 2024年第8期95卷 315-324,I0007页

作者： Zhen Wu Yu-Han Zhang Hao Wang Zewen Liu Xudong Zhang Xin dai Kunyang Zou Xiaoming Lou Xuechen Hu Lijing Ma Yan Liu Yongning Liu State Key Laboratory for Mechanical Behavior of Materials Xi’an Jiaotong UniversityXi’an 710049ShaanxiChina Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess TechnologyChinese Academy of SciencesQingdao 266101ShandongChina Hefei Advanced Computing Center Operation Management Corp Ltd Hefei 230088AnhuiChina Center for High Performance Computing Network Information CenterXi’an Jiaotong UniversityXi’an 710049ShaanxiChina Wuhan Dongfeng Motor Corporation Ltd Wuhan 430056HubeiChina School of Materials Science and Intelligent Engineering Nanjing UniversitySuzhou 215163JiangsuChina Key Laboratory of MEMS of the Ministry of Education Southeast UniversityNanjing 210096JiangsuChina International Research Center for Renewable Energy State Key Laboratory of Multiphase Flow in Power Engineering Xi’an Jiaotong UniversityXi’an 710049ShaanxiChina

Co-free Li-rich layered oxides(LLOs)are emerging as promising cathode materials for Li-ion batteries due to their low cost and high ***,they commonly face severe structural instability and poor electrochemical activity,leading to diminished capacity and voltage ***,we introduce a Co-free LLO,Li_(1.167)Ni_(0.222)Mn_(0.611)O_(2)(Cf-L1),which features a cooperative structure of Li/Ni mixing and stacking *** structure regulates the crystal and electronic structures,resulting in a higher discharge capacity of 300.6 mA h g^(-1)and enhanced rate capability compared to the typical Co-free LLO,Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)(Cf-Ls).Density functional theory(DFT)indicates that Li/Ni mixing in LLOs leads to increased Li-O-Li configurations and higher anionic redox activities,while stacking faults further optimize the electronic interactions of transition metal(TM)3d and non-bonding O 2p ***,stacking faults accommodate lattice strain,improving electrochemical reversibility during charge/discharge cycles,as demonstrated by the in situ XRD of Cf-L1 showing less lattice evolution than *** study offers a structured approach to developing Co-free LLOs with enhanced capacity,voltage,rate capability,and cyclability,significantly impacting the advancement of the next-generation Li-ion batteries.

关键词： Co-free Li-rich oxides Li/Ni mixing Stacking faults Electronic structure

ρ-meson longitudinal leading-twist distribution amplitude revisited and the D→ρsemileptonic decay

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Chinese Physics C 2024年第6期48卷 82-91页

作者：钟涛代亚红付海冰 Department of Physics Guizhou Minzu UniversityGuiyang 550025China

Motivated by our previous study[***.D 104(1),016021(2021)]on the pionic leading-twist distribution amplitude(DA),we revisit theρ-me son leading-twist longitudinal DAφ_(2;ρ)^(‖)(x,μ)in this study.A model proposed by Chang based on the DYyson-Schwinger equations is adopted to describe the behavior ofφ_(2;ρ)^(‖)(x,μ).However,theξ-moments ofφ_(2;ρ)^(‖)(x,μ)are calculated with the QCD sum rules in the framework of the background field *** sum rule formulas for these moments are *** accurate values for the first five nonzeroξ-moments at the typical scaleμ=(1.0,1.4,2.0,3.0)geV are given,e.g.,atμ=1 geV,(ξ^(2))>_(2;ρ)^(‖)=0.220(6),(ξ^(4))>_(2;ρ)^(‖)=0.103(4),(ξ^(6))>_(2;ρ)^(‖)=0.066(5),(ξ^(8))>_(2;ρ)^(‖)=0.046(4),and(ξ^(10))>_(2;ρ)^(‖)=0.035(3).By fitting these values with the least squares method,the DSE model forφ_(2;ρ)(x,μ)is *** taking the left-handed current light-cone sum rule approach,we obtain the transition form factor in the large recoil region,i.e.,A_(1)(0)=0.498_(-0.012)^(+0.014),A_(2)(0)=0.460_(-0.047)^(+0.055),and V(0)=0.800_(-0.014)^(+0.015),and the ratio r_(2)=0.923_(-0.119)^(+0.133),rV=1.607_(-0.071)^(+0.071).After extrapolating with a rapidly converging series based on z(t)-expansion,we present the|V_(cd)|-independent decay width for the semileptonic decays D→ρ^(l+)v_(l).Finally,the branching fractions are B(D^(0)→ρ^(-)e+v_(e))=1.825_(-0.162)^(+0.170)±0.004,B(D^(+)→ρ^(0)e+v_(e))=2.299_(-0.204)^(+0.214)±0.011,B(D^(0)→ρ^(-)μ^(+)v_(μ))=1.816_(-0.160)^(+0.168)±0.004,and B(D^(+)→ρ^(0)μ+v_(μ))=2.288_(-0.201)^(+0.212)±0.011.

关键词： QCD sum rule charmed meson semileptonic decay Rho meson light-cone distribution amplitude

Enhancing green Ammonia Electrosynthesis Through Tuning Sn Vacancies in Sn‑Based MXene/ MAX Hybrids

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Nano-Micro Letters 2024年第5期16卷 154-168页

作者： Xinyu dai Zhen‑Yi Du Ying Sun Ping chen Xiaoguang Duan junjun Zhang Hui Li Yang Fu Baohua Jia Lei Zhang Wenhui Fang Jieshan Qiu Tianyi Ma Key Laboratory for green Synthesis and Preparative chemistry of Advanced Materials of Liaoning Province College of ChemistryInstitute of Clean Energy ChemistryLiaoning UniversityShenyang 110036People’s Republic of China State Key Laboratory of Clean and Efficient Coal Utilization Taiyuan University of TechnologyTaiyuan 030024People’s Republic of China School of chemistry and chemical Engineering Anhui UniversityHefei 230601People’s Republic of China School of chemical Engineering The University of AdelaideAdelaideSA 5005Australia State Key Laboratory of High‑Efficiency Utilization of Coal and green chemical Engineering College of Chemistry and Chemical EngineeringNingxia UniversityYinchuan 750021NingxiaPeople’s Republic of China School of Science RMIT UniversityMelbourneVIC 3000Australia guangdong Provincial Key Laboratory of Advanced Energy Storage Materials School of Chemistry and Chemical EngineeringSouth China University of TechnologyGuangzhou 510640People’s Republic of China College of chemical Engineering State Key Laboratory of Chemical Resource EngineeringBeijing University of Chemical TechnologyBeijing 100029People’s Republic of China

Renewable energy driven N_(2) electroreduction with air as nitrogen source holds great promise for realizing scalable green ammonia ***,relevant out-lab research is still in its ***,a novel Sn-based MXene/MAX hybrid with abundant Sn vacancies,Sn@Ti_(2)CTX/Ti_(2)SnC–V,was synthesized by controlled etching Sn@Ti_(2)SnC MAX phase and demonstrated as an efficient electrocatalyst for electrocatalytic N2 *** to the synergistic effect of MXene/MAX heterostructure,the existence of Sn vacancies and the highly dispersed Sn active sites,the obtained Sn@Ti2CTX/Ti_(2)SnC–V exhibits an optimal NH_(3) yield of 28.4μg h^(−1) mg_(cat)^(−1) with an excellent FE of 15.57% at−0.4 V versus reversible hydrogen electrode in 0.1 M Na_(2)SO_(4),as well as an ultra-long ***,this catalyst represents a satisfactory NH3 yield rate of 10.53μg h^(−1) mg^(−1) in the home-made simulation device,where commercial electrochemical photovoltaic cell was employed as power source,air and ultrapure water as feed *** as-proposed strategy represents great potential toward ammonia production in terms of financial cost according to the systematic technical economic *** work is of significance for large-scale green ammonia production.

关键词： green ammonia synthesis N2 electroreduction Renewable energy Sn MXene/MAX hybrid

Syntheses and properties of associative acrylamide copolymers containing short hydrophobic chains used in a friction reducer for slick-water fracturing

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Petroleum Science 2024年第3期21卷 1889-1901页

作者： Ya-Xing dai Xian-Li Zhang Si-Yuan Liu Feng-Run-Ze Zhang Yi-Xi Zhang Yu-Tong Sang Jing-Xi Zheng Zhao-Sheng Liu Peng Zhang College of chemistry and chemical Engineering Chongqing University of Science and TechnologyChongqing401331China College of Ecology and Environment Chongqing Resources and Environmental Protection of UniversityChongqing401331China China China Property Project Department of Dezhou Mining Property Service CenterShengli Oilfield Company of SinopecDezhou253000ShandongChina

Two allyldimethylalkyl quaternary ammonium salt(AQAS)monomers,N,N-dimethylallylphenylpropylammonium bromide(AQAS1)and N,N-dimethylallylnonylammonium bromide(AQAS2),were synthesized and used to prepare modified polyacrylamide *** new drag reducers were synthesized from acrylamide(AM),sodium acrylate(Na AA)and a cationic modified monomer(AQAS1 or AQAS2)via aqueous solution polymerization,and the copolymers were named P(AM/Na AA/AQAS1)and P(AM/Na AA/AQAS2),*** structures of the drag reduction agents were confirmed by IR and1H NMR *** molecular weight(Mw)of P(AM/Na AA/AQAS1)was 1.79×10^(6)g/*** the copolymer concentration was 1000 mg/L and the flow rate was 45 L/min,in fresh water the highest drag reduction rate was 75.8%,in 10,000 mg/L Na Cl solution the drag reduction rate decreased to 72.9%.The molecular weight of P(AM/Na AA/AQAS2)was 3.17×10^(6)g/*** the copolymer concentration was500 mg/L and the flow rate was 45 L/min,the drag reduction rate reached 75.2%,and in 10,000 mg/L Na Cl solution the drag reduction rate was 73.3%,decreased by approximately 1.9%.The drag reduction rate for partially hydrolyzed polyacrylamide(HPAM)was also investigated,and the results showed that the drag reduction rates for 500 and 1000 mg/L HPAM solutions were merely 43.2%and 49.0%in brine,*** with HPAM,both of the above copolymers presented better drag reduction capacities.

关键词： Shale gas Slick water Drag reducer Modified monomer Copolymerization