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| 1 | Zinc Isotope Characteristics in the Biogeochemical Cycle as Revealed by Analysis of Suspended Particulate Matter(SPM) in Aha Lake and Hongfeng Lake, Guizhou, China显示文摘Zn isotope is a useful tool for tracing biogeochemical processes as zinc plays important roles in the biogeochemistry of natural systems. However, the Zn isotope composition in the lake ecosystems has not been well characterized. In order to resolve this problem, we investigate the Zn isotope compositions of suspended particulate matter(SPM) and biological samples collected from the Aha Lake and Hongfeng Lake, and their tributaries in summer and winter, aiming to explore the potential of this novel isotope system as a proxy for biogeochemical processes in aqueous environments. Concentration of dissolved Zn ranges from 0.65 to 5.06 μg/L and 0.74 to 12.04 μg/L for Aha Lake and Hongfeng Lake, respectively, while Zn(SPM) ranges from 0.18 to 0.70 mg/g and 0.24 to 0.75 mg/g for Aha Lake and Hongfeng Lake, respectively. The Zn isotope composition in SPM from Aha Lake and its main tributaries ranges from -0.18‰ to 0.27‰ and -0.17‰ to 0.46‰, respectively, and it varies from -0.29‰ to 0.26‰ and -0.04‰ to 0.48‰, respectively in Hongfeng Lake and its main tributaries, displaying a wider range in tributaries than lakes. These results imply that Zn isotope compositions are mainly affected by tributaries inputting into Aha Lake, while adsorption process by algae is the major factor for the Zn isotope composition in Hongfeng Lake, and ZnS precipitation leads to the light Zn isotope composition of SPM in summer. These data and results provide the basic information of the Zn isotope for the lake ecosystem, and promote the application of Zn isotope in biogeochemistry. | Lili Liang Cong-Qiang Liu Xiangkun Zhu Bryne TNgwenya Zhongliang Wang Liuting Song Jin Li | 2020 | Journal of Earth Science2020，31，1： | 4 |
| 2 | Significantly improved hydrogen storage behaviors in MgH_(2) with Nb nanocatalyst显示文摘The study explores the excellent modification effect of Nb nanocatalyst prepared via surfactant assisted ball milling technique(SABM)on the hydrogen storage properties of MgH_(2).Optimal catalyst doping concentration was determined by comparing onset decomposition temperature,released hydrogen capacity,and reaction rate for different MgH_(2)-ywt%Nb(y=0,3,5,7,9)composites.The MgH_(2)-5wt%Nb composite started releasing hydrogen at 186.7℃ and a total of 7.0wt%hydrogen was released in the dehydrogenation process.In addition,5wt%Nb doped MgH_(2) also managed to release 4.2wt%H_(2) within 14 min at 250℃ and had the ability to absorb 4.0wt%hydrogen in 30 min at 100℃.Cycling tests revealed that MgH_(2)-5wt%Nb could retain 6.3wt%H_(2) storage capacity(89.2%)after 20 cycles.Dehydrogenation and hydrogenation activation energy values were decreased from 140.51±4.74 and 70.67±2.07 kJ·mol^(−1) to 90.04±2.83 and 53.46±3.33 kJ·mol^(−1) after doping MgH_(2) with Nb,respectively.Microstructure analysis proved that homogeneously distributed NbH acted as active catalytic unit for improving the hydrogen storage performance of MgH_(2).These results indicate SABM can be considered as an option to develop other nanocatalysts for energy related areas. | Farai Michael Nyahuma Liuting Zhang Mengchen Song Xiong Lu Beibei Xiao Jiaguang Zheng Fuying Wu | 2022 | International Journal of Minerals,Metallurgy and Materials2022，29，9： | 3 |
| 3 | Constructing graphene nanosheet-supported FeOOH nanodots for hydrogen storage of MgH2显示文摘Novel graphene-supported FeOOH nanodots(FeOOH NDs@G)were successfully prepared by a facile hydrothermal method and doped into MgH_(2)through mechanical ball-milling.MgH_(2)with 10wt%FeOOH NDs@G began to release hydrogen at 229.8℃,which is106.8℃ lower than that of pure MgH_(2).The MgH_(2)-10wt%FeOOH NDs@G composite could reversibly absorb 6.0wt%hydrogen at 200℃ under a 3.2 MPa hydrogen pressure within 60 min.With the addition of FeOOH NDs@G,the dehydrogenation and hydrogenation activation energy of MgH_(2)was decreased to 125.03 and 58.20 kJ·mol^(-1)(156.05 and 82.80 kJ·mol^(-1)for pure MgH_(2)),respectively.Furthermore,the hydrogen capacity of the FeOOH NDs@G composite retained 98.5%of the initial capacity after 20 cycles,showing good cyclic stability.The catalytic action of FeOOH NDs@G towards MgH_(2)could be attributed to the synergistic effect between graphene nanosheets and in-situ formed Fe,which prevented the aggregation of Mg/MgH2 particles and accelerated the hydrogen diffusion during cycling,thus enabling the Mg H_(2)-10wt%FeOOH NDs@G composite to exhibit excellent hydrogen storage performance. | Mengchen Song Liuting Zhang Jiaguang Zheng Zidong Yu Shengnan Wang | 2022 | International Journal of Minerals,Metallurgy and Materials2022，29，7： | 3 |
| 4 | Boosting the hydrogen storage performance of magnesium hydride with metal organic framework-derived Cobalt@Nickel oxide bimetallic catalyst显示文摘In this study,a MOF-derived bimetallic Co@NiO catalyst was synthesized and doped into MgH_(2)to improve the hydrogen desorption and resorption kinetics.The Co@NiO catalyst decreased the onset dehydrogenation temperature of MgH_(2)by 160℃,compared with un-doped MgH_(2).The MgH^(2+)9%(mass)Co@NiO composite released 6.6%(mass)hydrogen in 350 s at 315℃and uptook 5.4%(mass)hydrogen in500 s at 165℃,showing greatly accelerated de/rehydrogenation rates.Besides,the desorption activation energy of MgH^(2+)9%(mass)Co@NiO was decreased to(93.8±8.4)kJ·mol^(-1).Noteworthy,symbiotic Mg_(2)NiH_(4)/Mg_(2)CoH_(5)clusters were in-situ formed from bimetallic precursors and inlaid on MgH_(2)surface,which are considered as'multi-step hydrogen pumps',and provides surface pathways for hydrogen absorption.Meanwhile,the introduced Mg_(2)NiH_(4)/Mg_(2)CoH_(5)interfaces could provide numerous low energy barrier H diffusion channels,therefore accelerating the hydrogen release and uptake.This research proposes new insights to design high-efficiency bimetallic catalyst for MgH_(2)hydrogen storage. | Yan Zhang Jiaguang Zheng Zhiyu Lu Mengchen Song Jiahuan He Fuying Wu Liuting Zhang | 2022 | Chinese Journal of Chemical Engineering2022，，12： | 2 |
| 5 | Seasonal variations in sulfur isotopic composition of dissolved SO_4^(2-) in the Aha Lake, Guiyang and their implications显示文摘The Aha Lake is a seasonal anoxic water system in the southwest of Guiyang City, Guizhou Province, China. Seasonal variations in SO42- concentrations and their isotopic compositions in lake water as well as in the tributaries were investigated in this study. The results showed that sulfate concentrations in river water range from 0.94 to 6.52 mmol/L and their δ34S values range from -14.9‰ and 0.9‰, while lake water has sulfate concentrations ranging from 1.91 to 2.79 mmol/L, and δ34S values from -9.8‰ to -5.9‰. It is suggested that coal mining drainage is the major source of SO42- in the Aha Lake. Rainfall, sewage discharge, sulfide oxidation and gypsum dissolution have made only limited contributions. Different depth-dependent distributions of dissolved SO42- and δ34S were de-veloped for both DB and LJK in summer and winter. Due to water overturn, δ34S values display homogenous vertical distributions in winter and spring. While in summer and autumn, significant positive shifts of δ34S were clearly ob-served in epilimnion and bottom strata as a result of water stratification. High δ34S values in epilimnion may result from the retention of rainwater during water stratification. Dissimilatory sulfate reduction by bacteria was thought to be responsible for the increase of δ34S value in hypolimnion. | SONG Liuting LIU Congqiang WANG Zhongliang TENGYanguo WANG Jinsheng LIANG Lili BAI Li | 2011 | Chinese Journal Of Geochemistry2011，30，4： | 2 |
| 6 | Bullet-like vanadium-based MOFs as a highly active catalyst for promoting the hydrogen storage property in MgH_(2)显示文摘The practical application of magnesium hydride(MgH_(2))was seriously limited by its high desorption temperature and slow desorp-tion kinetics.In this study,a bullet-like catalyst based on vanadium related MOFs(MOFs-V)was successfully synthesized and doped with MgH_(2) by ball milling to improve its hydrogen storage performance.Microstructure analysis demonstrated that the as-synthesized MOFs was consisted of V_(2)O_(3) with a bullet-like structure.After adding 7wt%MOFs-V,the initial desorption temperature of MgH_(2) was reduced from 340.0 to 190.6℃.Besides,the MgH_(2)+7wt%MOFs-V composite released 6.4wt%H_(2) within 5 min at 300℃.Hydrogen uptake was started at 60℃under 3200 kPa hydrogen pressure for the 7wt%MOFs-V containing sample.The desorption and absorption apparent activity energies of the MgH_(2)+7wt%MOFs-V composite were calculated to be(98.4±2.9)and(30.3±2.1)kJ·mol^(-1),much lower than(157.5±3.3)and(78.2±3.4)kJ·mol^(−1) for the as-prepared MgH_(2).The MgH_(2)+7wt%MOFs-V composite exhibited superior cyclic property.During the 20 cycles isothermal dehydrogenation and hydrogenation experiments,the hydrogen storage capacity stayed almost unchanged.X-ray diffraction(XRD)and X-ray photoelectron spectrometer(XPS)measurements confirmed the presence of metallic vanadium in the MgH_(2)+7wt%MOFs-V composite,which served as catalytic unit to markedly improve the hydrogen storage properties of Mg/MgH_(2) system. | Zhiyu Lu Jiahuan He Mengchen Song Yan Zhang Fuying Wu Jiaguang Zheng Liuting Zhang Lixin Chen | 2023 | International Journal of Minerals,Metallurgy and Materials2023，30，1： | 1 |
| 7 | Soil and soil environmental quality monitoring in China: A review显示文摘 | Yanguo Teng Jin Wu Sijin Lu Yeyao Wang Xudong Jiao Liuting Song | 2014 | Environment International2014，，： | 1 |
| 8 | Iron isotope fractionation during biogeochemical cycle: information from suspended particulate matter (SPM) in Aha Lake and its tributaries, Guizhou, China显示文摘 | SONG Liuting LIU Congqiang WANG Zhongliang | 2011 | Chemical Geology2011，280，12： | 1 |
| 9 | Adipose-derived stem cell: a better stem cell than BMSC 显示文摘 | ZHU Y LIUT SONG K | 2008 | Cell Biochem Funct2008，26，6： | 1 |
| 10 | Recent advances of magnesium hydride as an energy storage material显示文摘Energy storage is the key for large-scale application of renewable energy,however,massive efficient en-ergy storage is very challenging.Magnesium hydride(MgH_(2))offers a wide range of potential applications as an energy carrier due to its advantages of low cost,abundant supplies,and high energy storage capac-ity.However,the practical application of MgH_(2) for energy storage is still impeded by its sluggish kinetics,poor cycling stability,etc.Herein,we provide an overview of recent advances of MgH_(2) for enhancing the hydrogen storage,lithium-ion storage,and heat storage performances.For hydrogen storage,a particular emphasis was put on altering the kinetics and thermodynamics of MgH_(2) via catalyzing,alloying,nano-sizing,and compositing.Modifications to MgH_(2) as a battery anode material mainly focus on the effect of additives,electrolytes,and structure configurations.Prototype heat storage apparatus was proposed based on MgH_(2) and coupled with other materials or systems to improve the heat storage and economic efficiency.Besides,prospects of MgH_(2) in these fields are discussed.This review would stimulate more insightful and pioneering research for the design and preparation of MgH_(2) with excellent energy storage performances. | Mengchen Song Liuting Zhang Fuying Wu Haoyu Zhang Hu Zhao Lixin Chen Hong Li | 2023 | Journal of Materials Science & Technology2023，，18： | 0 |
| 11 | Combined “Gateway” and “Spillover” effects originated from a CeNi_(5) alloy catalyst for hydrogen storage of MgH_(2)显示文摘Efficient catalysts enable MgH2 with superior hydrogen storage performance.Herein,we successfully synthesized a catalyst composed of Ce and Ni (i.e.CeNi_(5) alloy) with splendid catalytic action for boosting the hydrogen storage property of magnesium hydride (MgH_(2))The MgH2–5wt%CeNi_(5) composite’s initial hydrogen release temperature was reduced to 174℃ and approximately 6.4wt%H_(2) was released at 275℃ within 10 min.Besides,the dehydrogenation enthalpy of MgH_(2) was slightly decreased by adding CeNi_(5).For hydrogenation,the fully dehydrogenated sample absorbed 4.8wt%H_(2) at a low temperature of 175℃.The hydrogenation apparent activation energy was decreased from(73.60±1.79) to (46.12±7.33) kJ/mol.Microstructure analysis revealed that Mg_(2)Ni/Mg_(2)NiH_(4) and CeH_(2.73) were formed during the process of hydrogen absorption and desorption,exerted combined“Gateway”and“Spillover”effects to reduce the operating temperature and improve the hydrogen storage kinetics of MgH_(2).Our work provides an example of merging“Gateway”and“Spillover”effects in one catalyst and may shed light on designing novel highly-effective catalysts for MgH_(2) in near future. | Mengchen Song Runkai Xie Liuting Zhang Xuan Wang Zhendong Yao Tao Wei Danhong Shang | 2023 | International Journal of Minerals,Metallurgy and Materials2023，30，5： | 0 |
| 12 | FeCoNiCrMo high entropy alloy nanosheets catalyzed magnesium hydride for solid-state hydrogen storage显示文摘The catalytic effect of FeCoNiCrMo high entropy alloy nanosheets on the hydrogen storage performance of magnesium hydride(MgH_(2))was investigated for the first time in this paper.Experimental results demonstrated that 9wt%FeCoNiCrMo doped MgH_(2)started to dehydrogenate at 200℃and discharged up to 5.89wt%hydrogen within 60 min at 325℃.The fully dehydrogenated composite could absorb3.23wt%hydrogen in 50 min at a temperature as low as 100℃.The calculated de/hydrogenation activation energy values decreased by44.21%/55.22%compared with MgH_(2),respectively.Moreover,the composite’s hydrogen capacity dropped only 0.28wt%after 20 cycles,demonstrating remarkable cycling stability.The microstructure analysis verified that the five elements,Fe,Co,Ni,Cr,and Mo,remained stable in the form of high entropy alloy during the cycling process,and synergistically serving as a catalytic union to boost the de/hydrogenation reactions of MgH_(2).Besides,the FeCoNiCrMo nanosheets had close contact with MgH_(2),providing numerous non-homogeneous activation sites and diffusion channels for the rapid transfer of hydrogen,thus obtaining a superior catalytic effect. | Tao Zhong Haoyu Zhang Mengchen Song Yiqun Jiang Danhong Shang Fuying Wu Liuting Zhang | 2023 | International Journal of Minerals,Metallurgy and Materials2023，30，11： | 0 |
| 13 | Iron Isotope Compositions of Natural River and Lake Samples in the Karst Area,Guizhou Province,Southwest China显示文摘为了更好理解天赋的 Fe 同位素特征,在石灰岩地区常见的地形区域取样,河流的推迟的微粒的 Fe 同位素作文,湖推迟了微粒,湖沉积, porewaters ,浮游植物,并且在湖啊哈(一个使矿物化的水系统)和洪芬湖(一个 mesotrophic 水系统)的分水岭的喷雾器,位于石灰岩地区常见的地形区域,西南中国,被调查。学习样品显示了在 56Fe=2.03 之间的一个可变范围并且 0.36。喷雾器和浮游植物相对火的岩石的一般水准有类似或稍微更重的 Fe 同位素作文。河流的推迟的微粒物质(SPM ) 的 Fe 同位素作文被支流的类型主要影响。从严重与煤矿排水污染的支流收集的推迟的微粒在夏天期间显示了否定 56Fe 价值(0.89 ~ 0.31 ) ,并且有在冬季的 56Fe 价值的重要增加,它与两煤矿排水和污水自河被弄脏,除了 AR2。湖的特征在推迟的微粒,湖沉积,和 porewaters 的 Fe 同位素作文上有重要影响。当更轻的 Fe 同位素作文从湖啊哈为微粒 Fe 被测量时,洪芬湖的 epilimnetic 微粒 Fe 有 56Fe=0.04 到 0.13,从 0.42 ~ 0.09 。从洪芬湖的吴厚(HW ) 车站收集的沉积有 0.09 的平均 56Fe 价值,从 0.57 ~ 0.31 并且他们的相应 porewaters 有更轻的 Fe 同位素作文;没有重要变化被观察了。为湖啊哈的梁·强·考(LJK ) 车站,反应 Fe 的内容和硫酸盐的集中都高。由于再循环的反应 Fe,包括 dissimilatory Fe 减小,吸附,和 Fesulfide 形成, porewaters 近取样了沉积表面被发现了有象 2.03 一样低的 56Fe 价值和增加直到 0.12,与 10 厘米的埋葬深度。相反,一个相反的变化趋势被作出对有利的裁决 LJK 沉积。在 1 厘米的深度取样的沉积有 56Fe=0.59 和与埋葬深度象 1.75 一样低的减少的价值。这调查证明重要 Fe 同位素分别发生在表面环境。微粒 Fe 的 Fe 同位素作文被 Fe 来源严重影响,并且再循环的 Fe biogeochemical 在湖沉积在 Fe 同位素分别上有重要影响,特别当有反应 Fe 和硫酸盐的重要数量时。 | SONG Liuting LIU Congqiang WANG Zhongliang ZHU Xiangkun TENG Yanguo WANG Jinsheng TANG Suohan LI Jin LIANG Lili | 2011 | Acta Geologica Sinica(English Edition)2011，85，3： | 0 |
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