Nitroaromatics are usually prepared using a mixed acid of nitric acid with strong acids. However, the use of strong acids caused dangerous work-up and the disposal of large amounts of acid-waste. Therefore, much effor...Nitroaromatics are usually prepared using a mixed acid of nitric acid with strong acids. However, the use of strong acids caused dangerous work-up and the disposal of large amounts of acid-waste. Therefore, much effort has been made on the improvement of nitration process without strong acids. We examined solid-phase aromatic nitration with Mg(NO3)2 on silica gel in order to establish the nitration process without strong acids. The nitration of 1,2- and 1,3-, 1,4-dimethoxybenzenes and 4-methylanisole with Mg(NO3)2 proceeded by heating on silica gel at 150°C for 4 - 5 h to produce the nitroaromatics. The nitration of 1,3,5-trimethoxybenzene produced the nitrated dimer, 2,4,6,2’, 4’,6’-hexamethoxy-3-nitrobiphenyl, which was not isolated in other solid-phase nitration. In the cases of naphthalene derivatives, the α-nitrated compounds were obtained. In the cases of p-cresol and 2-naphthol, the esterification occurred at the hydroxyl group to give 4-tolyl nitrate and 2-naphthyl nitrate, respectively. It is synthetic interest to note that nitrate esters were isolated in solid phase. Thus Mg(NO3)2-SiO2 composite was mild reagent for solid-phase nitration. Acidity of Mg(NO3)2-SiO2 composite was determined to be pH 0.96 by the measurement of absorption spectra on a micro spectrophotometer using meso-tetra(p-cyanophenyl)porphyrin as a pH-indicator. Mg(NO3)2-SiO2 composite made acidic conditions. Therefore, it was suggested that Mg(NO3)2 reacted with proton on silica gel to form the NO+2. Thus, electron-rich aromatic hydrocarbons led the efficient nitration through electrophilic attack of NO+2. After the nitration, acidic Mg(NO3)2-SiO2 composite could be turned into neutrality by exposing wet conditions and disposed safely since the composite did not involve harmful elements. Thus the solid-phase nitration using Mg(NO3)2-SiO2 composite will provide safety and environmentally conscious chemical process.展开更多
Thiophene (C4H4S) and 3-methylthiophene(3-MC4H4S) are typical thiophenenic sulfur compounds that exist in fluid catalytic cracking (FCC) gasoline. Oxidation of C4H4S and 3-MC4H4S were conducted in hydrogen peroxide (H...Thiophene (C4H4S) and 3-methylthiophene(3-MC4H4S) are typical thiophenenic sulfur compounds that exist in fluid catalytic cracking (FCC) gasoline. Oxidation of C4H4S and 3-MC4H4S were conducted in hydrogen peroxide (H2O2) and formic acid system over a series of silica gel loaded with metal oxide. The silica gel loaded with copper and cobalt (1:1) oxide was found very active for the model compound oxidation using H2O2/formic acid, while the silica gel unloaded with metal oxide was less active. The sulfur removal rate of thiophenes was different as solvent was changed. And the conversation of C4H4S and 3-MC4H4S was improved at higher temperature,but reduced when olefin was added. The sulfur removal rate of model sulfur compounds was enhanced when the phase transfer catalyst emulsifier polyethylene glycol octyl phenyl ether or tetrabutylammonium bromide(TBAB)in a H2O2 and formic acid system with the addition of TBAB, a bromine substitution trend appeared in the oxidation of thiophenes, suggesting the influence of TBAB.展开更多
Under different annealing temperatures, Eu 3+ doped SiO 2 gel and glass were prepared by sol gel method, and the structure and luminescent properties were studied with excitation spectra, emission spectra, IR ...Under different annealing temperatures, Eu 3+ doped SiO 2 gel and glass were prepared by sol gel method, and the structure and luminescent properties were studied with excitation spectra, emission spectra, IR and DTA TG. The results show that the fluorescent intensity tends to get stable when concentration of Eu 3+ doped is above 1 86 % (mass fraction) most water absorbed by the gel was removed at 300 ℃, and that the emission spectrum of Eu 3+ , with peaks at 614, 588, 577 nm, is due to 5D 0→ 7F 2, 5D 0→ 7F 1, 5D 0→ 7F 0 transitions, and the excitation peaks at 318, 362, 380, 393, 412 and 462 nm were observed. These results illustrate that the temperature range of 300～500 ℃ is critical for the structure conversion from gel to glass, and the fluorescence is strongly quenched by water.展开更多
Thiophene C4H4S and 3-methylthiophene3-MC4H4S are typical thiophenenic sulfur compounds that exist in fluid catalytic cracking FCC gasoline. Oxidation of C4H4S and 3-MC4H4S were conducted in hydrogen peroxide H2O2 and...Thiophene C4H4S and 3-methylthiophene3-MC4H4S are typical thiophenenic sulfur compounds that exist in fluid catalytic cracking FCC gasoline. Oxidation of C4H4S and 3-MC4H4S were conducted in hydrogen peroxide H2O2 and formic acid system over a series of silica gel loaded with metal oxide. The silica gel loaded with copper and cobalt 1:1 oxide was found very active for the model compound oxidation using H2O2formic acid, while the silica gel unloaded with metal oxide was less active. The sulfur removal rate of thiophenes was dif- ferent as solvent was changed. And the conversation of C4H4S and 3-MC4H4S was improved at higher temperature, but reduced when olefin was added. The sulfur removal rate of model sulfur compounds was enhanced when the phase transfer catalyst emulsifier polyethylene glycol octyl phenyl ether or tetrabutylammonium bromideTBAB was added. The sulfur removal rate of simulated gasoline containing 524μg·ml-1 sulfur reached 90%. Interestingly, in a H2O2 and formic acid system with the addition of TBAB, a bromine substitution trend appeared in the oxidation of thiophenes, suggesting the influence of TBAB.展开更多
以实验室自制1,3-二油酸甘油二酯粗品(含量76.41%)为原料,采用硅胶柱色谱法制备高纯1,3-二油酸甘油二酯。通过硅胶薄层色谱对4种混合溶剂洗脱剂进行筛选,确定硅胶柱色谱最佳洗脱剂为D(正己烷-乙酸乙酯-乙醚-乙酸的混合液)。以1,3-二油...以实验室自制1,3-二油酸甘油二酯粗品(含量76.41%)为原料,采用硅胶柱色谱法制备高纯1,3-二油酸甘油二酯。通过硅胶薄层色谱对4种混合溶剂洗脱剂进行筛选,确定硅胶柱色谱最佳洗脱剂为D(正己烷-乙酸乙酯-乙醚-乙酸的混合液)。以1,3-二油酸甘油二酯的回收率和纯度为指标,系统考察了硅胶柱色谱的洗脱流速、上样质量浓度、硅胶量对纯化效果的影响,确定最佳硅胶柱色谱纯化条件为:洗脱流速1.5 m L/min,上样质量浓度75 mg/m L(上样体积10 m L),硅胶量30 g。该条件下制得的1,3-二油酸甘油二酯样品纯度达98.03%,回收率为69.90%。展开更多
文摘Nitroaromatics are usually prepared using a mixed acid of nitric acid with strong acids. However, the use of strong acids caused dangerous work-up and the disposal of large amounts of acid-waste. Therefore, much effort has been made on the improvement of nitration process without strong acids. We examined solid-phase aromatic nitration with Mg(NO3)2 on silica gel in order to establish the nitration process without strong acids. The nitration of 1,2- and 1,3-, 1,4-dimethoxybenzenes and 4-methylanisole with Mg(NO3)2 proceeded by heating on silica gel at 150°C for 4 - 5 h to produce the nitroaromatics. The nitration of 1,3,5-trimethoxybenzene produced the nitrated dimer, 2,4,6,2’, 4’,6’-hexamethoxy-3-nitrobiphenyl, which was not isolated in other solid-phase nitration. In the cases of naphthalene derivatives, the α-nitrated compounds were obtained. In the cases of p-cresol and 2-naphthol, the esterification occurred at the hydroxyl group to give 4-tolyl nitrate and 2-naphthyl nitrate, respectively. It is synthetic interest to note that nitrate esters were isolated in solid phase. Thus Mg(NO3)2-SiO2 composite was mild reagent for solid-phase nitration. Acidity of Mg(NO3)2-SiO2 composite was determined to be pH 0.96 by the measurement of absorption spectra on a micro spectrophotometer using meso-tetra(p-cyanophenyl)porphyrin as a pH-indicator. Mg(NO3)2-SiO2 composite made acidic conditions. Therefore, it was suggested that Mg(NO3)2 reacted with proton on silica gel to form the NO+2. Thus, electron-rich aromatic hydrocarbons led the efficient nitration through electrophilic attack of NO+2. After the nitration, acidic Mg(NO3)2-SiO2 composite could be turned into neutrality by exposing wet conditions and disposed safely since the composite did not involve harmful elements. Thus the solid-phase nitration using Mg(NO3)2-SiO2 composite will provide safety and environmentally conscious chemical process.
基金Supported by the National Natural Science Foundation of China (No.20276015) and the Natural Science Foundation of Hebei Province (No.203364).
文摘Thiophene (C4H4S) and 3-methylthiophene(3-MC4H4S) are typical thiophenenic sulfur compounds that exist in fluid catalytic cracking (FCC) gasoline. Oxidation of C4H4S and 3-MC4H4S were conducted in hydrogen peroxide (H2O2) and formic acid system over a series of silica gel loaded with metal oxide. The silica gel loaded with copper and cobalt (1:1) oxide was found very active for the model compound oxidation using H2O2/formic acid, while the silica gel unloaded with metal oxide was less active. The sulfur removal rate of thiophenes was different as solvent was changed. And the conversation of C4H4S and 3-MC4H4S was improved at higher temperature,but reduced when olefin was added. The sulfur removal rate of model sulfur compounds was enhanced when the phase transfer catalyst emulsifier polyethylene glycol octyl phenyl ether or tetrabutylammonium bromide(TBAB)in a H2O2 and formic acid system with the addition of TBAB, a bromine substitution trend appeared in the oxidation of thiophenes, suggesting the influence of TBAB.
文摘Under different annealing temperatures, Eu 3+ doped SiO 2 gel and glass were prepared by sol gel method, and the structure and luminescent properties were studied with excitation spectra, emission spectra, IR and DTA TG. The results show that the fluorescent intensity tends to get stable when concentration of Eu 3+ doped is above 1 86 % (mass fraction) most water absorbed by the gel was removed at 300 ℃, and that the emission spectrum of Eu 3+ , with peaks at 614, 588, 577 nm, is due to 5D 0→ 7F 2, 5D 0→ 7F 1, 5D 0→ 7F 0 transitions, and the excitation peaks at 318, 362, 380, 393, 412 and 462 nm were observed. These results illustrate that the temperature range of 300～500 ℃ is critical for the structure conversion from gel to glass, and the fluorescence is strongly quenched by water.
基金the National Natural Science Foundation of China (No.20276015) the Natural Science Foundation of HebeiProvince (No.203364)
文摘Thiophene C4H4S and 3-methylthiophene3-MC4H4S are typical thiophenenic sulfur compounds that exist in fluid catalytic cracking FCC gasoline. Oxidation of C4H4S and 3-MC4H4S were conducted in hydrogen peroxide H2O2 and formic acid system over a series of silica gel loaded with metal oxide. The silica gel loaded with copper and cobalt 1:1 oxide was found very active for the model compound oxidation using H2O2formic acid, while the silica gel unloaded with metal oxide was less active. The sulfur removal rate of thiophenes was dif- ferent as solvent was changed. And the conversation of C4H4S and 3-MC4H4S was improved at higher temperature, but reduced when olefin was added. The sulfur removal rate of model sulfur compounds was enhanced when the phase transfer catalyst emulsifier polyethylene glycol octyl phenyl ether or tetrabutylammonium bromideTBAB was added. The sulfur removal rate of simulated gasoline containing 524μg·ml-1 sulfur reached 90%. Interestingly, in a H2O2 and formic acid system with the addition of TBAB, a bromine substitution trend appeared in the oxidation of thiophenes, suggesting the influence of TBAB.
文摘以实验室自制1,3-二油酸甘油二酯粗品(含量76.41%)为原料,采用硅胶柱色谱法制备高纯1,3-二油酸甘油二酯。通过硅胶薄层色谱对4种混合溶剂洗脱剂进行筛选,确定硅胶柱色谱最佳洗脱剂为D(正己烷-乙酸乙酯-乙醚-乙酸的混合液)。以1,3-二油酸甘油二酯的回收率和纯度为指标,系统考察了硅胶柱色谱的洗脱流速、上样质量浓度、硅胶量对纯化效果的影响,确定最佳硅胶柱色谱纯化条件为:洗脱流速1.5 m L/min,上样质量浓度75 mg/m L(上样体积10 m L),硅胶量30 g。该条件下制得的1,3-二油酸甘油二酯样品纯度达98.03%,回收率为69.90%。
