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Microwave-enabled rapid,continuous,and substrate-free synthesis of few-layer graphdiyne nanosheets for enhanced potassium metal battery performance 被引量:1
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作者 KONG Ya ZHANG Shi-peng +6 位作者 YIN Yu-ling ZHANG Zi-xuan FENG Xue-ting DING Feng ZHANG Jin TONG Lian-ming GAO Xin 《新型炭材料(中英文)》 北大核心 2025年第3期642-650,共9页
Graphdiyne(GDY)is a two-dimensional carbon allotrope with exceptional physical and chemical properties that is gaining increasing attention.However,its efficient and scalable synthesis remains a significant challenge.... Graphdiyne(GDY)is a two-dimensional carbon allotrope with exceptional physical and chemical properties that is gaining increasing attention.However,its efficient and scalable synthesis remains a significant challenge.We present a microwave-assisted approach for its continuous,large-scale production which enables synthesis at a rate of 0.6 g/h,with a yield of up to 90%.The synthesized GDY nanosheets have an average diameter of 246 nm and a thickness of 4 nm.We used GDY as a stable coating for potassium(K)metal anodes(K@GDY),taking advantage of its unique molecular structure to provide favorable paths for K-ion transport.This modification significantly inhibited dendrite formation and improved the cycling stability of K metal batteries.Full-cells with perylene-3,4,9,10-tetracarboxylic dianhydride(PTCDA)cathodes showed the clear superiority of the K@GDY anodes over bare K anodes in terms of performance,stability,and cycle life.The K@GDY maintained a stable voltage plateau and gave an excellent capacity retention after 600 cycles with nearly 100%Coulombic efficiency.This work not only provides a scalable and efficient way for GDY synthesis but also opens new possibilities for its use in energy storage and other advanced technologies. 展开更多
关键词 Graphdiyne Microwave-assisted synthesis Few-layer Potassium metal battery Dendrite-free
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Mechanism for Hydrothermal-carbothermal Synthesis of AlN Nanopowders
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作者 FENG Guanzheng YANG Jian +3 位作者 ZHOU Du CHEN Qiming XU Wentao ZHOU Youfu 《无机材料学报》 北大核心 2025年第1期104-110,I0009-I0011,共10页
Currently,the carbothermal reduction-nitridation(CRN)process is the predominant method for preparing aluminum nitride(AlN)powder.Although AlN powder prepared by CRN process exhibits high purity and excellent sintering... Currently,the carbothermal reduction-nitridation(CRN)process is the predominant method for preparing aluminum nitride(AlN)powder.Although AlN powder prepared by CRN process exhibits high purity and excellent sintering activity,it also presents challenges such as the necessity for high reaction temperatures and difficulties in achieving uniform mixing of its raw materials.This study presents a comprehensive investigation into preparation process of AlN nanopowders using a combination of hydrothermal synthesis and CRN.In the hydrothermal reaction,a homogeneous composite precursor consisting of carbon and boehmite(γ-AlOOH)is synthesized at 200℃using aluminum nitrate as the aluminum source,sucrose as the carbon source,and urea as the precipitant.During the hydrothermal process,the precursor develops a core-shell structure,with boehmite tightly coated with carbon(γ-AlOOH@C)due to electrostatic attraction.Compared with conventional precursor,the hydrothermal hybrid offers many advantages,such as ultrafine particles,uniform particle size distribution,good dispersion,high reactivity,and environmental friendliness.The carbon shell enhances thermodynamic stability of γ-Al_(2)O_(3) compared to the corundum phase(α-Al_(2)O_(3))by preventing the loss of the surface area in alumina.This stability enables γ-Al_(2)O_(3) to maintain high reactivity during CRN process,which initiates at 1300℃,and concludes at 1400℃.The underlying mechanisms are substantiated through experiments and thermodynamic calculations.This research provides a robust theoretical and experimental foundation for the hydrothermal combined carbothermal preparation of non-oxide ceramic nanopowders. 展开更多
关键词 aluminum nitride carbothermal reduction-nitridation MECHANISM hydrothermal synthesis PRECURSOR
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Real-Time Smart Meter Abnormality Detection Framework via End-to-End Self-Supervised Time-Series Contrastive Learning with Anomaly Synthesis
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作者 WANG Yixin LIANG Gaoqi +1 位作者 BI Jichao ZHAO Junhua 《南方电网技术》 北大核心 2025年第7期62-71,89,共11页
The rapid integration of Internet of Things(IoT)technologies is reshaping the global energy landscape by deploying smart meters that enable high-resolution consumption monitoring,two-way communication,and advanced met... The rapid integration of Internet of Things(IoT)technologies is reshaping the global energy landscape by deploying smart meters that enable high-resolution consumption monitoring,two-way communication,and advanced metering infrastructure services.However,this digital transformation also exposes power system to evolving threats,ranging from cyber intrusions and electricity theft to device malfunctions,and the unpredictable nature of these anomalies,coupled with the scarcity of labeled fault data,makes realtime detection exceptionally challenging.To address these difficulties,a real-time decision support framework is presented for smart meter anomality detection that leverages rolling time windows and two self-supervised contrastive learning modules.The first module synthesizes diverse negative samples to overcome the lack of labeled anomalies,while the second captures intrinsic temporal patterns for enhanced contextual discrimination.The end-to-end framework continuously updates its model with rolling updated meter data to deliver timely identification of emerging abnormal behaviors in evolving grids.Extensive evaluations on eight publicly available smart meter datasets over seven diverse abnormal patterns testing demonstrate the effectiveness of the proposed full framework,achieving average recall and F1 score of more than 0.85. 展开更多
关键词 abnormality detection cyber-physical security anomaly synthesis contrastive learning time-series
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Ethanol-assisted direct synthesis of wafer-scale nitrogen-doped graphene for III-nitride epitaxial growth
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作者 WEI Wen-ze GAO Xiang +4 位作者 YU Chao-jie SUN Xiao-li WEI Tong-bo JIA Li SUN Jing-yu 《新型炭材料(中英文)》 北大核心 2025年第3期678-687,共10页
Among the synthesis techniques for graphene,chemical vapor deposition(CVD)enables the direct growth of graphene films on insulating substrates.Its advantages include uniform coverage,high quality,scalability,and compa... Among the synthesis techniques for graphene,chemical vapor deposition(CVD)enables the direct growth of graphene films on insulating substrates.Its advantages include uniform coverage,high quality,scalability,and compatibility with industrial processes.Graphene is chemically inert and has a zero-bandgap which poses a problem for its use as a functional layer,and nitrogen doping has become an important way to overcome this.Post-plasma treatment has been explored for the synthesis of nitrogen-doped graphene,but the procedures are intricate and not suitable for large-scale production.We report the direct synthesis of nitrogen-doped graphene on a 4-inch sapphire wafer by ethanol-assisted CVD employing pyridine as the carbon feedstock,where the nitrogen comes from the pyridine and the hydroxyl group in ethanol improves the quality of the graphene produced.Additionally,the types of nitrogen dopant produced and their effects on III-nitride epitaxy were also investigated,resulting in the successful illumination of LED devices.This work presents an effective synthesis strategy for the preparation of nitrogen-doped graphene,and provides a foundation for designing graphene functional layers in optoelectronic devices. 展开更多
关键词 III-nitride epitaxy Direct synthesis Ethanol-assisted CVD LED devices Nitrogen-doped graphene
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Synthesis and crystal structure characterization of yttrium imido complex:The reactivity of 2-substituted-1-amino-o-carborane with yttrium dialkyl complex
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作者 GUO Liping 《无机化学学报》 北大核心 2025年第7期1409-1415,共7页
2-substituted-1-amino-o-carboranes 2-R-1-NH_(2)-o-C_(2)B_(10)H_(10)(R=CH_(3),1a;R=Ph,1b)were synthesized and the reactions of these compounds with the yttrium dialkyl complex[Y(L)(CH_(2)SiMe3)_(2)](L=[2-(2,5-Me_(2)C_(... 2-substituted-1-amino-o-carboranes 2-R-1-NH_(2)-o-C_(2)B_(10)H_(10)(R=CH_(3),1a;R=Ph,1b)were synthesized and the reactions of these compounds with the yttrium dialkyl complex[Y(L)(CH_(2)SiMe3)_(2)](L=[2-(2,5-Me_(2)C_(4)H_(2)N)C_(6)H4NC(Ph)=NDipp]-,Dipp=2,6-iPr_(2)C_(6)H_(3))were investigated.The 1H NMR spectroscopy indicate that the reaction of ytrrium dialkyl complex with one equivalent of 2-R-1-NH_(2)-o-C_(2)B_(10)H_(10) produce the mixture of ytrrium alkyl-amido complex[Y(L)(2-R-1-NH-o-C_(2)B_(10)H_(10))(CH_(2)SiMe3)](R=CH_(3),2a;R=Ph,2b)and bis(amido)complex[Y(L)(2-R-1-NH-o-C_(2)B_(10)H_(10))_(2)](R=CH_(3),3a;R=Ph,3b).The yttrium bridging imido complex[Y(L)(2-CH_(3)-1-N-o-C_(2)B_(10)H_(10))]_(2)(4a)was obtained by heating the mixture at 55℃for 12 h.Complex 3a was isolated and characterized by treating the yttrium dialkyl complex with two equivalents of 1a.The structures of complexes 3a and 4a were verified by single-crystal Xray diffraction.CCDC:2424136,3a;2424137,4a. 展开更多
关键词 yttrium imide O-CARBORANE synthesis structure characterization
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Water-promoted green synthesis of heterocyclicβ-ketosulfides
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作者 GU Wen ZHANG Shu-ting +2 位作者 YANG Fei ZUO Yi-wei ZHAO Zhi-gang 《化学研究与应用》 北大核心 2025年第5期1274-1287,共14页
A strategy for the green synthesis of heterocyclicβ-ketosulfides via nucleophilic substitution ofα-halogenated ketone with het-eroaryl thiols in water media is presented.Compared with the available literature report... A strategy for the green synthesis of heterocyclicβ-ketosulfides via nucleophilic substitution ofα-halogenated ketone with het-eroaryl thiols in water media is presented.Compared with the available literature reports,this new method had the advantages of base-free,additives-free,simple operation,mild condition,greenness,high efficiency,tolerance of a broad scope of substrates.Furth-more,the reaction could easily be scaled up in gram scale and the products also could easily transformed to other useful organic compounds.Mechanism investigation indicated that the tautomerism of pyrimidine-2-thiol to pyrimidine-2(1H)-thione and the hy-drogen bonds played important roles in the reaction. 展开更多
关键词 green synthesis water media heterocyclicβ-ketosulfides base-free
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Synthesis of energetic materials by microfluidics
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作者 Shuo Liu Chuanyu Zhang +1 位作者 Yanlan Wang Xueyong Wei 《Defence Technology(防务技术)》 2025年第2期306-319,共14页
Energetic materials,characterized by their capacity to store and release substantial energy,hold pivotal significance in some fields,particularly in defense applications.Microfluidics,with its ability to manipulate fl... Energetic materials,characterized by their capacity to store and release substantial energy,hold pivotal significance in some fields,particularly in defense applications.Microfluidics,with its ability to manipulate fluids and facilitate droplet formation at the microscale,enables precise control of chemical reactions.Recent scholarly endeavors have increasingly harnessed microfluidic reactors in the realm of energetic materials,yielding morphologically controllable particles with enhanced uniformity and explosive efficacy.However,crucial insights into microfluidic-based methodologies are dispersed across various publications,necessitating a systematic compilation.Accordingly,this review addresses this gap by concentrating on the synthesis of energetic materials through microfluidics.Specifically,the methods based on micro-mixing and droplets in the previous papers are summarized and the strategies to control the critical parameters within chemical reactions are discussed in detail.Then,the comparison in terms of advantages and disadvantages is attempted.As demonstrated in the last section regarding perspectives,challenges such as clogging,dead zones,and suboptimal production yields are non-ignoble in the promising fields and they might be addressed by integrating sound,optics,or electrical energy to meet heightened requirements.This comprehensive overview aims to consolidate and analyze the diverse array of microfluidic approaches in energetic material synthesis,offering valuable insights for future research directions. 展开更多
关键词 Microfluidic technology Energetic materials synthesis MICRO-MIXING Micro-droplets
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Self-interference cancellation and pattern synthesis for in-band full-duplex phased array systems
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作者 LIU Ao SHENG Weixing RIIHONEN Taneli 《Journal of Systems Engineering and Electronics》 2025年第4期914-921,共8页
This paper considers the short-range sensing imple-mentation in continuous-wave(CW)phased array systems.We specifically address this CW short-range sensing challenges stemming from the self-interference cancellation(S... This paper considers the short-range sensing imple-mentation in continuous-wave(CW)phased array systems.We specifically address this CW short-range sensing challenges stemming from the self-interference cancellation(SIC)operation and synthesis requirement of arbitrary beampatterns for the sensing purpose,which has rarely been researched before.In this paper,unlike the only existed work that exploits the heuris-tic method and shares no analytical solution,an SIC pattern syn-thesis design is presented with a closed-form solution.By utiliz-ing the null-space projection(NSP)method,the proposed method effectively mitigates the self-interference to enable the in-band full-duplex operation of the array system.Subsequently,the NSP design will be innovatively embedded in a singular value decomposition(SVD)based weighted alternating reserve projec-tion(WARP)approach to efficiently synthesize an arbitrary desired pattern by solving a unique rank-deficient weighted least mean square problem.Numerical results validate the effective-ness of the proposed method in terms of beampattern,SIC per-formance,and sensing performance. 展开更多
关键词 in-band full-duplex pattern synthesis self-interfe-rence cancellation(SIC).
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Synthesis and Crystal Structure of t he Complex of Antimony Trichloride and Dioxane 被引量:1
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作者 臧祥生 陈娅如 +2 位作者 栾绍嵘 钟国清 郭应臣 《无机化学学报》 SCIE CAS CSCD 北大核心 2001年第6期901-904,共4页
New solid complex of the antimony trichloride and dioxane was obtained th rough a reaction of the dioxane and the absolute methanol solution of the antimony trichloride.The formula of the complex is[SbCl_(3)·{(CH... New solid complex of the antimony trichloride and dioxane was obtained th rough a reaction of the dioxane and the absolute methanol solution of the antimony trichloride.The formula of the complex is[SbCl_(3)·{(CH_(2))_(4)O_(2)}_(1.5)].The crystal structure of the comple x belongs to cubic system,space group I-43d,a=17.1417(5)?,Z=16.The trivalent antimony ion not only bonds directly to three chlorine anions,but also is co ordinated by three oxygen atoms of th e dioxane molecules.Two oxygen atoms in a dioxane molecule wi ll coordinate to different antimony ions,respectively. 展开更多
关键词 dioxane complex of antimony trichloride synthesis crystal structure
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Synthesis前兆群体异常信息提取与地震短期预测研究 被引量:1
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作者 曹刻 石绍先 《地震研究》 CSCD 北大核心 2003年第1期20-25,共6页
建立了Synthesis法前兆群体异常信息提取的数学模型。选取滇东地区 1995~ 2 0 0 0年 9月间常用的 2 0项前兆资料 ,研究中强地震前后Synthesis法前兆群体异常的变化特征。研究结果表明 ,在研究时段内 ,Synthesis法前兆群体异常占时率为 ... 建立了Synthesis法前兆群体异常信息提取的数学模型。选取滇东地区 1995~ 2 0 0 0年 9月间常用的 2 0项前兆资料 ,研究中强地震前后Synthesis法前兆群体异常的变化特征。研究结果表明 ,在研究时段内 ,Synthesis法前兆群体异常占时率为 0 15 8,为小概率事件。地震对应率为 5 / 6 =0 83 ,虚报率为 1/ 6 =0 17,地震均是在异常结束后 3个月之内发生 ,是对应概率很高的短期预报指标。成组异常出现均有成组地震对应 ,群体前兆“组异常”特征显著。处于计算前兆观测点中心的澄江地震前 ,异常幅度突出 ,预示了Synthesis值计算有利于提取近源短期异常。实际检验了Synthesis法在地震短期预报中的预报意义 ,获得了满意的效果。 展开更多
关键词 地震前兆 synthesis 信息提取 短期预报
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Simultaneous anti-windup synthesis for linear systems subject to actuator saturation 被引量:1
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作者 Maopeng Ran Qing Wang +1 位作者 Chaoyang Dong Maolin Ni 《Journal of Systems Engineering and Electronics》 SCIE EI CSCD 2015年第1期119-126,共8页
A synthesis method for global stability and performance of input constrained linear systems, which uses a linear outputfeedback controller and a static anti-windup compensator is investigated. Different from the tradi... A synthesis method for global stability and performance of input constrained linear systems, which uses a linear outputfeedback controller and a static anti-windup compensator is investigated. Different from the traditional two-step anti-windup design procedure, the proposed method synthesizes all controller parameters simultaneously. Sufficient conditions for global stability and minimizing the induced L2 gain are formulated and solved as a linear matrix inequalities(LMIs) optimization problem, which also provides an opportunity to search for a better performance tradeoff between the linear controller and the anti-windup compensator.The well-posedness of the close-loop system is also guaranteed.Simulation results show the effectiveness of the proposed method. 展开更多
关键词 actuator saturation ANTI-WINDUP simultaneous synthesis L2 synthesis linear matrix inequalities(LMIs)
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SYNTHESIS OF (+)-CAMPHOR-BASED SULFINIMINES AND THEIR UTILITY IN ASYMMETRIC SYNTHESIS OF AMINE DERIVATIVES
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《厦门大学学报(自然科学版)》 CAS CSCD 北大核心 1999年第S1期229-229,共1页
关键词 Chen CAMPHOR-BASED SULFINIMINES AND THEIR UTILITY IN ASYMMETRIC synthesis OF AMINE DERIVATIVES synthesis OF
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基于Catapult C Synthesis的图像校正算法设计 被引量:3
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作者 李杨 《电子测量技术》 2016年第7期92-95,共4页
为解决遥感相机在运动过程中的抖动造成的图像位置偏移问题,提出了一种实时图像校正算法。由于在FPGA中采用HDL进行算法设计难度大、开发周期长,故设计中采用了C语言进行算法设计,然后借助Calypto公司的Catapult C Synthesis工具将抽象... 为解决遥感相机在运动过程中的抖动造成的图像位置偏移问题,提出了一种实时图像校正算法。由于在FPGA中采用HDL进行算法设计难度大、开发周期长,故设计中采用了C语言进行算法设计,然后借助Calypto公司的Catapult C Synthesis工具将抽象的C设计转换成硬件RTL代码。在Catapult C Synthesis中对设计的算法进行了C/C++、RLT协同仿真测试,并在Xilinx XC5VLX110T型FPGA上进行了验证。仿真测试及硬件验证结果表明,采用Catapult C Synthesis设计的算法在时序、性能方面均满足设计要求,能够对偏移的图像进行实时校正。 展开更多
关键词 实时图像校正 FPGA Catapult C synthesis RTL
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CATALYSTS FOR SYNTHESIS OF N-VINYLPYRROLIDONE 被引量:15
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作者 崔英德 易国斌 +1 位作者 廖列文 康正 《化工学报》 EI CAS CSCD 北大核心 2000年第4期443-445,共3页
关键词 N-VINYLPYRROLIDONE CATALYST synthesis
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Synthesis of pure powder of La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(2.825) by microwave-induced solution combustion method
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作者 翟玉玲 叶畅 肖建中 《电池》 CAS CSCD 北大核心 2006年第5期377-379,共3页
关键词 SOFC synthesis microwave sr and Mg doped LaGaO3(LSGM) combustion method
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Synthesis and properties of acrylate latex modified by vinyl alkoxy siloxane 被引量:9
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作者 张心亚 孙志娟 +3 位作者 黄洪 黎永津 蓝仁华 陈焕钦 《Journal of Central South University of Technology》 EI 2007年第5期666-672,共7页
Acrylate latex modified by vinyl triisopropoxy silane (C-1706) was synthesized by seeded emulsion polymerization with anionic emulsifier sodium dodecyl sulphonate(SDS) and nonionic emulsifier OP-10 as the multiple emu... Acrylate latex modified by vinyl triisopropoxy silane (C-1706) was synthesized by seeded emulsion polymerization with anionic emulsifier sodium dodecyl sulphonate(SDS) and nonionic emulsifier OP-10 as the multiple emulsifiers at (78±2) ℃. The effects of different factors, such as the emulsifier, C-1706 monomer and its feeding manner on the properties of acrylate latex modified by C-1706 were investigated. The particle size distribution and the structure, the configuration, the weather durability and stain resistance of copolymer latex were characterized by particle size analyzer, Fourier transform infrared spectroscopy (FT-IR), transmission electron microscope(TEM), scanning electron microscope(SEM) and ultraviolet aging instrument respectively. The results show that SDS to OP-10 as multiple emulsifiers can lead to coordinated efficiency, the optimal emulsifier dosage is 2.4%?3.2%(mass fraction), and the mass ratio of SDS to OP-10 is 1?1? 1?2. The seeded emulsion polymerization can effectively introduce a organic-siloxane bonding in a macromolecule inter polymer, and the obtained acrylate latex modified by organic-siloxane possesses narrow distribution of particle size with mean diameter of 51.8?76.6 nm and has the excellent properties in weather durability and stain-resistance especially. 展开更多
关键词 vinyl alkoxy siloxane acrylate latex emulsion polymerization synthesis characterization
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Synthesis of γ-alkoxy-propylamines and their collecting properties on aluminosilicate minerals 被引量:12
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作者 曹学锋 胡岳华 徐兢 《Journal of Central South University of Technology》 EI 2004年第3期280-285,共6页
alkoxy-propylamines, C12H25O(CH2)3NH2, C14H29O(CH2)3NH2, C16H33O(CH2)3NH2, C18H37O-(CH2)3NH2 were synthesized from aliphatic alcohol and acrylonitrile. The flotation tests of kaolinite, pyrophyllite and illite... alkoxy-propylamines, C12H25O(CH2)3NH2, C14H29O(CH2)3NH2, C16H33O(CH2)3NH2, C18H37O-(CH2)3NH2 were synthesized from aliphatic alcohol and acrylonitrile. The flotation tests of kaolinite, pyrophyllite and illite were conducted. The flotation mechanisms were explained in view of the structures of reagents and aluminium silicate minerals, zeta potential and Fourier transform infrared spectrum measurements. The results show that the synthesized r-alkoxy-propylamines are more effective than dodecyl amine for flotation of kaolinite, pyrophyllite and illite. For flotation kaolinite and illite, the collecting ability is in the order of C18H37O(CH2)3NH2>C16H33O-(CH2)3NH2>C14H29O(CH2)3NH2>C12H25O(CH2)3NH2, but the r-alkoxy-propylamines types of collectors have almost the same collecting ability on pyrophyllite, which demonstrating that γ-alkoxy-propylamines are new selective collectors for reverse floatation to remove aluminium silicate minerals from bauxite. 展开更多
关键词 alkoxy-propylamine synthesis ALUMINOSILICATE reverse floatation structure-reactivity
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Single-step synthesis of magnetic chitosan composites and application for chromate(Cr(Ⅵ))removal 被引量:6
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作者 杨卫春 唐琼芝 +2 位作者 董舒宇 柴立元 王海鹰 《Journal of Central South University》 SCIE EI CAS CSCD 2016年第2期317-323,共7页
Magnetic chitosan composites(Fe3O4@chitosan) were synthesized in one single-step, characterized and applied in Cr(VI) removal from water. With the increase of loading proportion of chitosan, Cr(Ⅵ) adsorption capacity... Magnetic chitosan composites(Fe3O4@chitosan) were synthesized in one single-step, characterized and applied in Cr(VI) removal from water. With the increase of loading proportion of chitosan, Cr(Ⅵ) adsorption capacity of Fe3O4@chitosan composites increased from 10.771 to 21.040 mg/g. The optimum adsorption capacities of Cr(VI) on Fe3O4@chitosan-3 were found in a pH range of 3.0-5.0. Kinetic study results show that the adsorption process follows pseudo-second-order model, indicating that the rate-limiting step in the adsorption of Cr(Ⅵ) involves chemisorptions. Moreover, FT-IR spectra analysis confirms that the amine and hydroxyl groups of chitosan are predominantly responsible for binding. Results from this work demonstrate that the prepared Fe3O4@chitosan composites possess great potential in Cr(Ⅵ) removal from contaminated water. 展开更多
关键词 Cr(VI) magnetic chitosan one single-step synthesis ADSORPTION
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Synthesis of glycerine-xanthate and its depressing mechanism in separation of marmatite from arsenopyrite 被引量:6
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作者 熊道陵 胡岳华 +1 位作者 覃文庆 何名飞 《Journal of Central South University of Technology》 EI 2006年第6期678-682,共5页
A small molecular organic depressor glycerine-xanthate was synthesized. The effect of glycerine-xanthate on the flotation of sulfide minerals was investigated based on a function of pH value and concentration of glyce... A small molecular organic depressor glycerine-xanthate was synthesized. The effect of glycerine-xanthate on the flotation of sulfide minerals was investigated based on a function of pH value and concentration of glycerine-xanthate through flotation experiments in the presence and absence of Cu^2+. The results show that glycerinee-xanthate has a strong dressing effect on marmatite at pH〉6 and on arsenopyrite in weak acid and base conditions with butyl-xanthate as collector. In the presence of glycerine -xanthate, marmatite is activated by addition of Cu^2+, but arsenopyrite cannot be activated and remains unfloatable. So the selective separation can be achieved for two minerals. The depression of glycerine-xanthate on sulfide minerals was discussed based on the radical electronegative calculation and the theory of HSAB. Infrared spectrum shows that there are some -OH and-CSS-in glycedne-xanthate molecule, which competes with butyl-xanthate on the mineral surface. As a result of many hydrophilic groups in glycerine-xanthate, the surfaces of marmatite and arsenopyrite become hydrophilic, thus the flotation of marmatite and arsenopyrite is depressed. The collector is adsorbed preferentially on the surface of marmatite and it shows a better floatability in the presence of Cu^2+, whereas, the surface of arsenopyrite absorbs glycerine-xanthate and the flotation of arsenopyrite is depressed by glycerine-xanthate. 展开更多
关键词 organic depressant synthesis glycerine-xanthate MARMATITE ARSENOPYRITE FLOTATION
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A review on the high energy oxidizer ammonium dinitramide:Its synthesis,thermal decomposition,hygroscopicity,and application in energetic materials 被引量:5
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作者 Fu-yao Chen Chun-lei Xuan +8 位作者 Qiang-qiang Lu Lei Xiao Jun-qing Yang Yu-bing Hu Guang-Pu Zhang Ying-lei Wang Feng-qi Zhao Ga-zi Hao Wei Jiang 《Defence Technology(防务技术)》 SCIE EI CAS CSCD 2023年第1期163-195,共33页
Ammonium dinitramide(ADN)is considered as a potential substitute for ammonium perchlorate in energetic materials due to its high density,positive oxygen balance,and halogen-free characteristics.However,its application... Ammonium dinitramide(ADN)is considered as a potential substitute for ammonium perchlorate in energetic materials due to its high density,positive oxygen balance,and halogen-free characteristics.However,its application has been severely limited because of its strong hygroscopicity,difficult storage,and incompatibility with isocyanate curing agents.In order to better bloom the advantages of the highly energetic and environment-friendly ADN in the fields of energetic materials,an in-depth analysis of the current situation and discussion of key research points are particularly important.In this paper,a detailed overview on the synthesis,thermal decomposition,hygroscopic mechanism,and antihygroscopicity of ADN has been discussed,its application in powdes and explosives are also presented,and its future research directions are proposed. 展开更多
关键词 Ammonium dinitramide High energy oxidizer synthesis PROPERTIES APPLICATIONS
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