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镧元素钼钒杂多配合物的合成与表征 被引量:2
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作者 赵儒铭 龚大春 +2 位作者 黄沛力 周宏立 单永奎 《稀土》 EI CAS CSCD 北大核心 1999年第2期12-15,共4页
报道了两种镧元素钼钒杂多配合物的合成方法,元素及热重分析确定其结构式分别为K11H14La(Mo4V8O39)2·39H2O和K11H18La(Mo2V10O39)2·38H2O。利用IR、UV和XRD对其进... 报道了两种镧元素钼钒杂多配合物的合成方法,元素及热重分析确定其结构式分别为K11H14La(Mo4V8O39)2·39H2O和K11H18La(Mo2V10O39)2·38H2O。利用IR、UV和XRD对其进行了表征,确定了它们的分解温度范围。 展开更多
关键词 钼钒杂多酸 镧元素 杂多酸合物
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钼钒体系中稀土草酸盐溶解时的pH值及溶解度的测定 被引量:1
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作者 赵儒铭 周佰斌 刘宗绪 《稀土》 EI CAS CSCD 1994年第1期22-24,共3页
本文根据投料比,分别合成出稀土、钼、钒不同比例的杂多配合物,利用氨水破坏稀土钼钒杂多配合物,并在一定温度下,加入草酸溶液沉淀稀土,继续滴加草酸,稀土草酸盐溶解,当其溶解完全后,测定溶液的pH值,再向溶液中加入稀土硝酸... 本文根据投料比,分别合成出稀土、钼、钒不同比例的杂多配合物,利用氨水破坏稀土钼钒杂多配合物,并在一定温度下,加入草酸溶液沉淀稀土,继续滴加草酸,稀土草酸盐溶解,当其溶解完全后,测定溶液的pH值,再向溶液中加入稀土硝酸盐,测其最大溶解度。利用此方法,测定了不同比例的钼钒杂多配合物中稀土草酸盐溶解时的pH值和溶解最大稀土量。研究结果表明:钼钒杂多配合物中,Mo:V比例不同,则该配合物稀土草酸盐溶解的pH值亦不相同,稀土草酸盐的溶解度也不相同。 展开更多
关键词 溶解度 杂多酸 稀土族
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磷的一种间接测定方法
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作者 刘成亮 江丽 王继强 《浙江化工》 CAS 2004年第4期28-29,共2页
研究了醋酸丁酯萃取磷钼杂多酸铬合物的最佳条件,选用乙醇的稀硫酸溶液洗涤进入有机相中的钼酸盐,用氨水反萃有机相中与磷结合的钼,以硫氰酸钾为显色剂,吐温-20进行胶束增溶测定钼,从而间接测定磷含量。
关键词 醋酸丁酯 萃取 磷钼杂多酸 磷含量 测定
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Synthesis of Bisphenols Carrying Long Hydrocarbon Side Chains 被引量:1
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作者 XUJing-zhe JIANGNan-zhe ZHANGJian JIANGRi-shan 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2005年第1期65-68,共4页
Bisphenols containing long aliphatic hydrocarbon side chains were synthesized by the condensation of phenol with aldehyde or ketone in the presence of heteropolyacid. Their structures were characterized by IR, 1H NMR,... Bisphenols containing long aliphatic hydrocarbon side chains were synthesized by the condensation of phenol with aldehyde or ketone in the presence of heteropolyacid. Their structures were characterized by IR, 1H NMR, 13C NMR and element analysis. The experiment results show that when heteropolyacid was used as a catalyst, these bisphenols were obtained in high selectivity and high yields. 展开更多
关键词 BISPHENOLS HETEROPOLYACID PHENOL CONDENSATION
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Synthesis and characterization of PMoV/Fe_3O_4/g-C_3N_4 from melamine:An industrial green nanocatalyst for deep oxidative desulfurization 被引量:2
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作者 Ezzat Rafiee Maryam Khodayari 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2017年第3期458-468,共11页
A facile approach to the preparation of a novel magnetically separable H_5PMo_(10)V_2O_(40)/Fe_3O_4/g-C_3N_4(PMoV/Fe_3O_4/g-C_3N_4) nanocomposite by chemical impregnation is demonstrated.The prepared nanocomposi... A facile approach to the preparation of a novel magnetically separable H_5PMo_(10)V_2O_(40)/Fe_3O_4/g-C_3N_4(PMoV/Fe_3O_4/g-C_3N_4) nanocomposite by chemical impregnation is demonstrated.The prepared nanocomposite was characterized and its acidity was measured by potentiometric titration.PMoV/Fe_3O_4/g-C_3N_4 showed high catalytic activity in the selective oxidative desulfurization of sulfides to their corresponding sulfoxides or sulfones.The catalytic oxidation of a dibenzothiophene(DBT)-containing model oil and that of real oil were also studied under optimized conditions.In addition,the effects of various nitrogen compounds,as well as the use of one- and two-ring aromatic hydrocarbons as co-solvents,on the catalytic removal of sulfur from DBT were investigated.The catalyst was easily separated and could be recovered from the reaction mixture by using an external magnetic field.Additionally,the remaining reactants could be separated from the products by simple decantation if an appropriate solvent was chosen for the extraction.The advantages of this nanocatalyst are its high catalytic activity and reusability;it can be used at least four times without considerable loss of activity. 展开更多
关键词 Graphitic carbon nitride NANOCOMPOSITE MELAMINE Heteropoly acid Oxidative desulfurization OIL
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Hydrothermal Synthesis and Structure of a Novel Molybdenum Phosphate: Na_4(H_3O) [Na(HPO_4)_2(PO_4)_4Mo_(18)O_(49)]·16H_2O
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作者 林郑忠 张汉辉 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2001年第6期447-450,共4页
The title compound Na5H37P6Mo18O90 1 (Mr=1658) was synthesized under hydrothermal condition and its crystal structure was determined by X-ray diffraction. It crystallized in the monoclinic system, space group P21 with... The title compound Na5H37P6Mo18O90 1 (Mr=1658) was synthesized under hydrothermal condition and its crystal structure was determined by X-ray diffraction. It crystallized in the monoclinic system, space group P21 with a =14.957(1), b =16.535(1), c = 16.159(1)?β=108.586(2)°, V=3787.85?, Dc =3.040g/cm3, Z=2,μ(MoK)=3.17mm-1, F(000)=3242. The final R and wR are 0.0500 and 0.1535 for 6643 observable reflections with I≥2?I), respectively. The result of structure analysis indicates that [Na(HPO4)2(PO4)4-Mo18 O49]5-anions 2 in 1 has the symmetry of C2V, in which each MoVIO6 octahedron is connected to adjacent PO4 tetrahedra through corner-sharing and to adjacent octahedra through edge-sharing or corner-sharing. 展开更多
关键词 HYDROTHERMAL molybdenum phosphate crystal structure
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