Journal of Liaoning Petrochemical University
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Catalytic Synthesis of 2⁃Phenylthioethanol under Mild Conditions
Chen Shuai, Wang Rui, Gong Hong, Wei Yushi, Wang Jiale, Zhang Chi, Min Jiachen
Abstract301)   HTML    PDF (759KB)(145)      
2⁃Phenylthioethanol was synthesized from thiophenol and ethylene carbonate using 1,5⁃diazabicyclo[4.3.0]non⁃5⁃ene (DBN) as a catalyst. The effects of catalyst type and amount, reaction time and temperature on the reaction were studied. The results showed that, the conversion of 2⁃phenylthioethanol can reach more than 90% when the reaction temperature is 50 ℃ and 100% conversion can be obtained when the reaction temperature is 90 ℃ using DBN as the catalyst, n(thiophenol)/n(DBN)=100, the reaction time 10 min. The selectivity of the catalyst of the synthetic route is 100% The paper discusses the reaction mechanism according to the theory of soft and hard acid and alkali.
2021, 41 (2): 17-20. DOI: 10.3969/j.issn.1672-6952.2021.02.004
Synthesis of Supported Al(OH) 3/SiO 2 and Its Adsorption Properties for Uranyl
Wang Peisong,Yu Fang,Jin Yu,Zhang Xi,Zhang Qingchen,Li Yingxue,Wang Rui
Abstract526)      PDF (3966KB)(459)      
The preparation of supported adsorbent Al(OH) 3/SiO 2 and its adsorption behavior on uranyl ions were studied.The effects of adsorbent quality,solution pH,initial solution concentration,temperature and contact time on adsorption performance were investigated.The adsorption mechanism was preliminarily studied based on adsorption isotherm,thermodynamics,and kinetics.The effects of coexisting ions and fulvic acid on the adsorption properties were also investigated.The results showed that when the adsorbent mass was 0.03 g,pH=5,initial concentration of uranyl ions was 1 mmol/L,temperature was 303 K and contact time was 60 min,the maximum adsorption capacity was 110.4 mg/g,which could be reused four times.The adsorption process of uranyl ion on Al(OH) 3/SiO 2 is endothermic and spontaneous.The adsorption of monolayers is dominant,the adsorption behavior conforms to the quasisecondary kinetic model,and the chemical adsorption is the rate control step.
2018, 38 (06): 10-16. DOI: 10.3969/j.issn.1672-6952.2018.06.002
The Effect of Initial Concentration and pH Value of the Uranyl Nitrate Solution on the Its Hydrolysis Reaction
Wu Xiaomeng, Liu Hongxue, Wang Rui, Jiang Heng
Abstract675)      PDF (2419KB)(556)      
The effect of initial concentration and pH value of the uranyl nitrate solution on the uranyl ion (UO2+2) hydrolysis reaction was studied by spectrophotometry. The maximum absorption wavelength of the obtained complexes in the reaction of UO2+2 ions with arsenazo (Ⅲ) at different pH values was also investigated. The results show that the absorption wavelength is 652 nm in the range of pH 3.0~7.0. It is easier for the uranyl nitrate solution to hydrolysis at higher pH value than the lower in the range of pH 4.0~6.0 at the same UO2+2 concentration. The uranyl solution at high concentration is prior to occurring hydrolysis reaction in the same pH value. Lowest pH values of various uranyl solutions were obtained for hydrolysis reaction. The results indicate that the concentration of uranyl solution should not exceed 1.000×10-3 mol/L at pH 5.0.
2015, 35 (5): 18-21. DOI: 10.3969/j.issn.1672-6952.2015.05.005
Preparation and Adsorption Performance of q-CS/TEOS Hybrid Membranes
WANG Rui, FENG Rui-jiang, WANG Ji-lin, AO Min
Abstract430)      PDF (2298KB)(301)      
 
A series of hybrid membranes composed of quaternized chitosan (q-CS) and tetraethoxysilane (TEOS) were prepared by sol-gel method,taking q-CS and the TEOS as organic and inorganic component respectively. The structure of the hybrid membranes was investigated by FT-IR. The adsorption performance of the membranes for Cr(Ⅵ) ions from aqueous solution was also studied. The effect of adsorption time, the pH value of solution and temperature of the adsorption on adsorption results were studied and show that the suitable membrane is composed of 38wt% TEOS, and the optimum adsorption conditions were carried out at 35 ℃ for 180 minutes with pH value of 5.0~8.0.
2011, 31 (1): 13-16. DOI: 10.3696/j.issn.1672-6952.2011.01.004
Synthesis and Characterization of Nickel(Ⅱ) Complex of 2-Hydroxy-4-Methoxybenzophenone
WANG Rui, YANG Xiao-na, GONG Hong
Abstract346)      PDF (211KB)(226)      
A new Nickel(Ⅱ) complex was sythesized with 2-hydroxy-4-methoxybenzophenone and NiCl2 used as raw materials, and characterized through IR, TG, UV. The results show that the complex ratio of 2-hydroxy-4-methoxybenzophenone to Nickel(Ⅱ) is 1∶2; the metal ion coordinates with oxygen atoms of -C=O and next to -OH group. Meanwhile, its thermal decomposition process is divided into three weightless stages during 120~630 ℃, of which 120~258 ℃ is the process of a coordinated water lost, and 258~630 ℃ has two thermal decomposition stages. Finally, the complex is decomposed into NiO. UV analysis indicates that thermal stability of the complex is better than that of 2-hydroxy-4-methoxybenzophenone. The complex remains the quality of absorbing ultraviolet radiation.
2009, 29 (3): 23-25.
Synthesis and Characterization of Transitional Metal Complexes of Pyromellitic Acid
WANG Rui
Abstract366)      PDF (207KB)(326)      
        Transitional metal complexes of pyromellitic acid were synthesized by homogeneous precipitation method , and characterized by TG, element analysis and FTIR.The results of TG and element analysis show their general formula .TG and DTG curves show that the the rmalstability of four anhydrous transitional metal complexes decrease in the order :Zn 2(C 10H 2O 8)>Cd 2 (C 10 H 2O 8)>Mn 2(C 10 H 2O 8)>Cu 2 (C 10 H 2O 8).The IR spectrum of prepared complexes suggests that carboxylate groups in the complexes of M(Ⅱ)acted as bidentate chelating with the exception o f the complex of Zn(Ⅱ) as bidentate bridging .
2007, 27 (4): 24-26.
Synthesis and Characterization of Cerium(Ⅲ)Complex With Cyclohexane Carboxylic Acid
WANG Rui
Abstract376)      PDF (282KB)(273)      
        Cerium(Ⅲ)complex was synthesized in water solution by reaction of cerium pro to chloride with cyclohexane carboxylic acid (C6H11COOH)as ligand and using ammonia to adjust its pH value to 5.5.The complex was characterized by thermog ravimetric analysis, element analysis and IR spectra .The results of TG and element analysis show that the formula of the cerium (Ⅲ)complex is Ce(C7H11O2)3.The IR spectrum o f the prepared complex suggests that the coordination of cerium (Ⅲ)complex is chelating .The influence of different post treatment technics on the purity of complex was discussed .And then a better post treatment technics  was obtained.The product obtained is respectively w ashed with hot water and hot alcohol thrice during the process of filtration .After that , the product is dried in vacuum at 120 ℃ for 3 hours.Finally , the pure cerium (Ⅲ)complex with cyclohexane carboxylic acidis obtained.
2005, 25 (3): 36-38.