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RISS 인기검색어
- 검색키워드
- 저자 : Jinjuan Xue (검색결과 4 건)
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Oxidation of cyclopentene catalyzed by phosphotungstic quaternary ammonium salt catalysts
Jinjuan Xue,Aili Wang,Jingbo Wang,Dongzhi Zhang,Weiguang Chen,Longbao Yu,Tingshun Jiang,Hengbo Yin 한국공업화학회 2010 Journal of Industrial and Engineering Chemistry Vol.16 No.2
A series of phosphotungstic quaternary ammonium salts, Q3 (PW12O40) and Q3(PW4O16) [Q = (C5H5)N+(C16H33), (C16H33)N+(CH3)3, (C4H9)4N+, and (CH3)4N+], were used as the catalysts in oxidation of cyclopentene. The catalysts [(C5H5)N(C16H33)]3(PW4O16) and [(C16H33)N(CH3)3]3(PW4O16) showed high catalytic activity in the selective oxidation of cyclopentene while using H2O2 (50%) as an oxidant and 2-propanol as a solvent. The oxidation products mainly consisted of glutaraldehyde, cis-1,2-cyclopentanediol and trans-1,2-cyclopentanediol. The above-mentioned two catalysts were dissolved completely in the reaction medium during the catalysis process and precipitated themselves from the reaction system after reaction, showing the characteristics of reaction-controlled phase-transfer catalysis. The types of quaternary ammonium cations and the phosphotungstic anions in phosphotungstic quaternary ammonium salts affected catalytic activity.
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Oxidation of cyclopentene catalyzed by tungsten-substituted molybdophosphoric acids
Jinjuan Xue,Haixia Li,Dongzhi Zhang,Tingshun Jiang,Longbao Yu,Yutang Shen,Hengbo Yin 한국화학공학회 2009 Korean Journal of Chemical Engineering Vol.26 No.3
A series of Keggin type tungsten-substituted molybdophosphoric acids (H3PMo12−nWnO40·XH2O) were synthesized and characterized by ICP-AES, FT-IR, TG-DSC, and XRD. The tungsten substitution extent significantly affected their catalytic activity in the oxidation of cyclopentene and the selectivity of the resultant products. The tungsten-substituted molybdophosphoric acids with tungsten substitution numbers in a range of 3-6.8 exhibited high catalytic activity in the oxidation of cyclopentene. After reaction for 8 h, the conversion of cyclopentene was up to 97%; the oxidation products mainly consisted of glutaraldehyde, cis-1,2-cyclopentanediol and trans-1,2-cyclopentanediol with the yields of ca. 23%, 27%, and 45%, respectively.
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Xinyao Li,Jinjuan Xue,Shuaishuai Ma,Peng Xu 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2019 NANO Vol.14 No.6
A novel heterojunction photocatalyst consisting of three-dimensional (3D) flower-like MgAl LDH and acidified g-C3N4 (CN-H) was first developed by a simple facile coating method. The obtained MgAl LDH/CN-H samples were thoroughly characterized by powder X-ray diffraction (XRD), UV–Vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS) and Brunauer–Emmett–Teller (BET) analyzer. The detailed results demonstrated that g-C3N4 could transform from a generally two-dimensional layered structure into special cavity-like structure after acid treatment. CN-H increased specific surface to expose more active reaction sites in comparison to pristine g-C3N4. MgAl LDH and CN-H with matched band gaps were tightly bonded to form heterojunction structure by strong electrostatic intercalation. The combination could obviously boost the separation of photogenerated carriers. The as-prepared MgAl LDH/CN-H exhibited high photocatalytic performance in the degrading on typical antibiotic tetracycline hydrochloride (TC · HCl), of which degradation rate was 6.5 and even 22 times higher than that of MgAl LDH and pristine g-C3N4, respectively. The synthesis of MgAl LDH/CN-H heterojunction photocatalyst could have some positive suggestions for the rational construction of new photocatalysts and also has great application prospect in the degradation of environmental pollutants.
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Dongzhi Zhang,Chen Ge,Jinjuan Xue,Tingshun Jiang,Longbao Yu,Yutang Shen,Hengbo Yin 한국공업화학회 2009 Journal of Industrial and Engineering Chemistry Vol.15 No.4
A series of Cu–Zn–Zr catalysts were prepared by a coprecipitation method and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, temperature programmed reduction, and N2 adsorption. The catalytic activity of the Cu–Zn–Zr catalyst in the hydrogenation of maleic anhydride using ethanol as a solvent was studied at 220–280℃ and 1 MPa. Maleic anhydride was mainly hydrogenated to gbutyrolactone and tetrahydrofuran while ethanol dehydrogenated to ethyl acetate. After reduction, CuO species present in the calcined Cu–Zn–Zr catalysts were converted to metallic copper (Cu0). The presence of ZrO2 favored the deep hydrogenation of g-butyrolactone to tetrahydrofuranwhile the presence of ZnO was beneficial to the formation of the intermediate product g-butyrolactone. The molar ratios of the hydrogen produced in ethanol dehydrogenation to the hydrogen consumed in maleic anhydride hydrogenation increased with the increase of the reaction temperature.
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