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国家自然科学基金(21176145)

作品数:21 被引量:34H指数:4
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21 条 记 录,以下是 1-10
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Enhancement of the Hydrogen Storage Properties of Mg/C Nanocomposites Prepared by Reactive Milling with Molybdenum被引量:1
2017年
The effect of Mo on the morphology, crystal structure and hydrogen sorption properties of Mg/C composites prepared by reactive milling was studied. Transmission electron microscopic(TEM) observation shows that Mg/C composites prepared with the addition of Mo are of nanoscale with particle size about 20-120 nm after 3 h of milling under 1 MPaH2. MgH2 of tetrahedral crystal structure predominates in the materials with the geometric shape of oblique hexagonal prism. From X-ray diffraction(XRD) and hydrogen content studies, Mo and crystallitic carbon have a synergistic effect on promoting the hydrogenation rate in the reactive milling process. From differential scanning calorimetric(DSC) studies, the dehydrogenation peak temperature of the Mg/C materials with Mo is lowered to 299-340 ℃.
韩宗盈周仕学CHEN HaipengNIU HailiWANG Naifei
TiO_2对镁碳复合纳米材料吸放氢性能的影响研究被引量:2
2013年
将TiO2引入镁碳复合材料中反应球磨,在快速纳米化的过程中,TiO2纳米颗粒较容易镶嵌到金属Mg和碳的基体中,对复合材料的吸放氢性能具有良好的催化作用。DSC分析表明,(70Mg30C)2TiO2材料的初始放氢温度比MgH2降低了95℃,高峰放氢温度也降低了80℃。当TiO2的添加量为2%(质量分数,下同)时,(70Mg30C)2TiO2反应球磨储氢密度达到最大值4.78%,300℃放氢量达到3.75%。
卢国俭辛春雨周仕学
关键词:镁粉TIO2纳米晶吸放氢性能
不同温度下噻吩与氢化镁反应路径分析
2017年
以球磨法制备镁基储氢材料,并作为供氢体对噻吩进行加氢脱硫研究。程序升温脱附(TPD)和差示扫描量热(DSC)测试表明,材料放氢峰温为320℃,可与噻吩加氢温度匹配。噻吩加氢脱硫实验表明,当反应温度为350℃时,噻吩加氢反应转化率最高;反应温度继续升高,转化率则随之下降。加氢脱硫反应产物分析表明,由于温度升高,储氢材料中的活性氢将直接结合生成氢气分子,从而使加氢反应较难进行,噻吩转化率下降。第一性原理计算结果表明,MgH_2直接对噻吩加氢的能量位垒为62.65kJ/mol,而由MgH_2所放出的氢气对噻吩加氢的2个位垒为275.36kJ/mol和365.36kJ/mol。MgH_2与噻吩直接反应更有利于加氢脱硫反应的进行。
刘博古张莉华李淑芳蒋瑞乾刘晓静李辛元周仕学
关键词:噻吩加氢脱硫第一性原理
氢氧化钠碱浸钴钼废催化剂综合回收研究被引量:7
2014年
采用氢氧化钠碱浸、硫酸酸化分步沉淀法从废催化剂中回收Mo,Al,Bi,Co,Ni等有色金属。首先对废催化剂进行氢氧化钠一、二次碱浸,使氧化钼和氧化铝生成可溶性的盐与氧化铋、氧化钴、氧化镍分离,然后通过分段沉淀使钼和铝分离,制备钼酸铵和硫酸铝。其次对碱浸富集氧化铋、氧化钴和氧化镍渣,利用氢氧化物溶度积不同,采用分步沉淀―酸溶萃取法使钴、铋、镍得到有效分离。试验结果表明:球磨时间30 min、催化剂粒度小于74μm、氢氧化钠的加量为金属Mo和Al理论耗量的1.2倍、液固比选取4∶1、浸出温度90℃时,一次碱浸钼的浸出率可达96.25%,一次碱浸渣再次碱浸率可达99.50%。碱浸富集金属混合渣采用加热酸浸、氧化除铁,将滤液的pH控制在2左右使铋以氢氧化铋沉淀分离,控制pH为9.5,使镍、钴以氢氧化物形式沉淀,然后酸溶、萃取使钴镍分离。整个回收工艺中,钼和铝的总回收率分别为94.56%和96.89%。
卢国俭欧阳春冉维娴张倩倩辛春雨
关键词:氢氧化钠废催化剂回收
Preferential adsorption behaviour of CH_4 and CO_2 on high-rank coal from Qinshui Basin,China被引量:4
2014年
In order to better understand the prevailing mechanism of CO2 storage in coal and estimate CO2 sequestration capacity of a coal seam and enhanced coalbed methane recovery (ECBM) with CO2 injection into coal, we investigated the preferential adsorption of CH4 and CO2 on coals. Adsorption of pure CO2, CH4 and their binary mixtures on high-rank coals from Qinshui Basin in China were employed to study the preferential adsorption behaviour. Multiple regression equations were presented to predict CH4 equi- librium concentration from equilibrium pressure and its initial-composition in feed gas. The results show that preferential adsorption of CO2 on coals over the entire pressure range under competitive sorption conditions was observed, however, preferential adsorption of CH4 over CO2 on low-volatile bituminous coal from higher CH4-compostion in source gas was found at up to 1O MPa pressure. Preferential adsorp- tion of CO2 increases with increase of CH4 concentration in source gas, and decreases with increasing pressure. Although there was no systematic investigation of the effect of coal rank on preferential adsorp- tion, there are obvious differences in preferential adsorption of gas between low-volatile bituminous coal and anthracite. The obtained preferential adsorption gives rise to the assumption that CO2 sequestration in coal beds with subsequent CO2-ECBM might be an ootion in Qinshui Basins, China.
Yu HongguanJing RenxiaWang PanpanChen LihuiYang Yongjie
焦煤用于镁基储氢粉体造粒的研究
2013年
用无烟煤作助磨剂(球磨减小镁的粒度),用焦煤作热成型的粘结剂,制得了具有一定粒度和机械强度的储氢材料.扫描电镜观测结果表明,储氢材料中的镁和无烟煤颗粒被受热时发生熔融的焦煤粘结了起来.X射线衍射测试结果表明,镁吸氢后成为四方晶系MgH2.当焦煤添加量为15%~25%、热处理温度为500~600℃时,制得耐磨强度较高的块状储氢材料.
丁超贺柄慧楚慧超沈怡君李爱峰冉维娴
关键词:储氢材料焦煤造粒
Mg/C/Al储氢材料制备及其吸放氢性能研究被引量:1
2014年
将镁粉、微晶碳、铝粉反应球磨制备70Mg30CxAl系列储氢材料,XRD测试表明,复合材料主相为MgH2、Mg和Al,纳米晶粒在16.5 ~73.4 nm之间.随着Al质量分数的增加,材料的活化能降低显著,放氢速率增加明显,但储氢密度有所降低.在低温区放氢,Al质量分数越高,放氢量越大,放氢时间越短.
卢国俭周仕学
关键词:活化能
Characterization of calcium deposition induced by Synechocystis sp. PCC6803 in BG11 culture medium被引量:7
2014年
Calcium carbonate (CaCO3) crystals in their preferred orientation were obtained in BG11 culture media inoculated with Synechocystis sp. PCC6803 (inoculated BG11). In this study, the features of calcium carbonate deposition were investigated. Inoculated BGll in different calcium ion concentrations was used for the experimental group, while the BGll culture medium was used for the control group. The surface morphologies of the calcium carbonate deposits in the experimental and control groups were determined by scanning and transmission electron microscopy. The deposits were analyzed by electronic probe micro-analysis, Fourier transform infrared spectrum, X-ray diffraction, thermal gravimetric analysis and differential scanning calorimetry. The results show that the surfaces of the crystals in the experimental group were hexahedral in a scaly pattern. The particle sizes were micrometer-sized and larger than those in the control group. The deposits of the control group contained calcium (Ca), carbon (C), oxygen (O), phosphorus (P), iron (Fe), copper (Cu), zinc (Zn), and other elements. The deposits in the experimental group contained Ca, C, and O only. The deposits of both groups contained calcite. The thermal decomposition temperature of the deposits in the control group was lower than those in the experimental group. It showed that the CaCO3 deposits of the experimental group had higher thermal stability than those of the control group. This may be due to the secondary metabolites produced by the algae cells, which affect the carbonate crystal structure and result in a close-packed structure. The algae cells that remained after thermal weight loss were heavier in higher calcium concentrations in BGll culture media. There may be more calcium- containing crystals inside and outside of these cells. These results shall be beneficial for understanding the formation mechanism of carbonate minerals.
闫华晓韩作振赵辉周仕学迟乃杰韩梅寇小燕张艳徐琳琳田晨晨秦松
关键词:BIOMINERALIZATION
Genetic Diversity Analysis on Rep-PCR Genomic Fingerprinting and 16S rDNA Sequences of Desulfurization Bacteria
2016年
In order to reduce deleterious effect on environment,human health and facilities caused by original sulfides, more attention should be paid to biodesulfurization studying for fossil fuels. In this work, eight isolates were characterized by several DNA-based methods such as BOX element polymerase chain reaction( BOX-PCR), enterobacterial repetitive intergenic consensus( ERIC)-PCR and random amplification of polymorphic DNA( RAPD)-PCR. The desulfurization performance was determined by micro-coulometric method,Gibb's assay and barium sulfate test. It was found out that ERIC-PCR displays a much higher inter-strain heterogeneity compared with using BOX. The length of the primer didnot play the most important role in bacterial classification. The combination of the analysis of repetitive-sequence-based polymerase chain reaction ngerprinting and 16 S r DNA was able to provide more effective way in the separation and identification of bacteria.According to the analysis of 16 S r DNA,the more efficient desulfurization strain should belong to Klebsiella variicola.
吕英海祝加伟张雨晴蔡晓青郭凯周仕学
关键词:DESULFURIZATION
Crystal Structure and Hydrogen Storage Behaviors of Mg/MoS2 Composites from Ball Milling被引量:2
2016年
The Mg/MoS2 composites were prepared by ball milling under argon atmosphere,and the effect of MoS2 on the crystal structure and hydrogen storage properties of Mg was investigated.It is found that 10 wt% of MoS2 is sufficient to prevent particle aggregation and cold welding during the milling process.The crystallite size of Mg will remain constant at slightly less than 38.8 nm with the milling process due to the size confinement effect of MoS2.The dehydrogenation temperature of MgH2 is reduced to 390.4-429.4 ℃ due to the crystallite size reduction.Through fitting by Johnson-Mehl-Avrami model,it is found that Mg crystal grows by three dimension controlled by interface transformation during the process of MgH2 decomposition.MoS2 has a weak catalyst effect on the decomposition of MgH2 and activation energy of 148.9 k J/mol is needed for the dehydrogenation process calculated by the Arrhenius equation.
韩宗盈周仕学WANG NaifeiZHANG QianqianZHANG TonghuanRAN Weixian
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