A series of alditol derivatives were designed and synthesized with relatively high yield. On the basis of reaction between sorbitol and a series of substituted benzaldehyde in the presence of an acid catalyst, a serie...A series of alditol derivatives were designed and synthesized with relatively high yield. On the basis of reaction between sorbitol and a series of substituted benzaldehyde in the presence of an acid catalyst, a series of acetal derivatives were synthesized through free hydroxyl esterification. D-sorbitol acetal amido derivatives were prepared by reduction of nitryl and acylation of amino. D-sorbitol acetal carboxyl esterification derivatives were prepared through esterification and hydrolysis. By high performance liquid chromatography-mass spectra (HPLC-MS) and 1H nuclear magnetic resonance spectra (1H-NMR), 36 compounds prepared were identified. Among these derivatives prepared, 26 compounds have not been reported in the previous literatures.展开更多
Based on the principle of biomimetic catalysis, β-cyclodextrin was applied to the acetalation reaction as a facile and efficient catalyst, and the synthesis was environmentally friendly with atomic economy. The influ...Based on the principle of biomimetic catalysis, β-cyclodextrin was applied to the acetalation reaction as a facile and efficient catalyst, and the synthesis was environmentally friendly with atomic economy. The influencing factors of the acetalation reaction e.g. the reaction time, the volume of water-carrying agent,the molar ratio of catalyst to benzaldehyde and the molar ratio of glycol to benzaldehyde had been studied.The yield of benzaldehyde glycol acetal would reach a maximum of 81.3% under the conditions approached.Six of other acetals were also synthesized. Moreover, a plausible reaction mechanism for the formation of acetal had been proposed.展开更多
Pjridine has been generally synthesized by aldehydes and ammonia in a turbulent fluidized-bed reactor. In this paper, a novel riser reactor was proposed for pyridine synthesis. Experiment result showed that the yield ...Pjridine has been generally synthesized by aldehydes and ammonia in a turbulent fluidized-bed reactor. In this paper, a novel riser reactor was proposed for pyridine synthesis. Experiment result showed that the yield of pyridine and 3-picoline decreased, but the selectivity of pyridine over 3-picoline increased compared to turbulent fluidized-bed reactor. Based on experimental data, a modified kinetic model was used for the determination of optimal operating condition for riser reactor. The optimal operating condition of riser reactor given by this modified model was as follows： The reaction temperature of 755 K, catalyst to feedstock ratio （CTFR） of 87, residence timeof3.8sandinitialacetaldehydesconcentrationof0.0029mol.L-1 （acetaldehydes to formaldehydes ratio by mole （ATFR） of 0.65 and ammonia to aldehydes ratio by mole （ATAR） of 0.9, water contention of 63wt% （formaldehyde solution））.展开更多
The mesoporous Ti O2 has been synthesized by evaporation induced self assembly(EISA) method. The thermogravimetric/differential scanning calorimetric(TG/DSC), X-ray diffraction(XRD), high-resolution transmission elect...The mesoporous Ti O2 has been synthesized by evaporation induced self assembly(EISA) method. The thermogravimetric/differential scanning calorimetric(TG/DSC), X-ray diffraction(XRD), high-resolution transmission electron microscopy(HR-TEM) and N2 adsorption desorption and adsorption are used to study the effects of the synthesized process condition on the microstructure of the as-synthesized mesoporous Ti O2. The photocatalytic performances of as-synthesized samples are evaluated by the degradation of the formaldehyde under ultraviolet light irradiations. The results demonstrate that the as-synthesized mesoporous Ti O2 are anatase with the uniform size about 20-40 nm. The sample is prepared using cetyltrimethyl ammonium bromide(CTAB) as the template with average pore size distribution of 8.12 nm, specific surface area of 68.47 m2/g and pore volume of 0.213 m L/g. The samples show decomposition of formaldehyde 95.8% under ultraviolet light irradiations for 90 min. These results provide a basic experimental process for preparation mesoporous Ti O2, which will posses a broad prospect in terms of the applications in improving indoor air quality.展开更多
In this present, a new series of Schiffbases from 2,5-di（p-aminophenyl）-3,6-diphenyl pyrazine in the presence of the benzil, 4-bromo benzaldehyde, 4-chlor benzaldehyde, 4-hydroxy benzaldehyde, 4-nitro benzaldehyde a...In this present, a new series of Schiffbases from 2,5-di（p-aminophenyl）-3,6-diphenyl pyrazine in the presence of the benzil, 4-bromo benzaldehyde, 4-chlor benzaldehyde, 4-hydroxy benzaldehyde, 4-nitro benzaldehyde and 4-methyl benzaldehyde were studied. The structures of the synthesized compounds were determined on the basis of their Infra-red spectra, H-nuclear magnetic resonase and analysis elemental analysis spectral data. The purity of the synthesized compounds was checked by performing thin layer chromatography. The antibacterial activity was evaluated by paper disc diffusion method.展开更多
The solubility of C.I. reactive blue 19 in aqueous alkali is poor, so it isn't used to dye cellulosic fiber in cold pad-batch dyeing. In order to improve the solubility of this dyestuff in alkali liquor, the right...The solubility of C.I. reactive blue 19 in aqueous alkali is poor, so it isn't used to dye cellulosic fiber in cold pad-batch dyeing. In order to improve the solubility of this dyestuff in alkali liquor, the right dispersants will be needed. A series of condensates are synthesized by changing the synthesis conditions such as the ratio of naphthalenesulfonic (N) to formaldehyde (F), acidity, and their compositions are confirmed by MS spectrum. It is found that in acidity scope of 20%-24% and the ratio of N to F 1∶0.33, the synthesized condensates can efficiently improve the solubility of C.I. reactive blue 19 in alkali liquor. In addition, the influences of the condensates on the exhaust dyeing and the cold pad-batch dyeing are tested.展开更多
A rapid and simple procedure for synthesis of 2,6-di（naphthalene thioureido carbamino）pyridine fluorescine anion acceptor by the reaction between pyridine-2,6-dicarbohydrazide obtained from 2,6-dimethylpyridine afte...A rapid and simple procedure for synthesis of 2,6-di（naphthalene thioureido carbamino）pyridine fluorescine anion acceptor by the reaction between pyridine-2,6-dicarbohydrazide obtained from 2,6-dimethylpyridine after three-step reaction and 1-napbthyl isothiocyanate is described, and all reactions could be carried out under microwave heating condition.展开更多
基金National Natural Science Foundation of China (No 20306022)
文摘A series of alditol derivatives were designed and synthesized with relatively high yield. On the basis of reaction between sorbitol and a series of substituted benzaldehyde in the presence of an acid catalyst, a series of acetal derivatives were synthesized through free hydroxyl esterification. D-sorbitol acetal amido derivatives were prepared by reduction of nitryl and acylation of amino. D-sorbitol acetal carboxyl esterification derivatives were prepared through esterification and hydrolysis. By high performance liquid chromatography-mass spectra (HPLC-MS) and 1H nuclear magnetic resonance spectra (1H-NMR), 36 compounds prepared were identified. Among these derivatives prepared, 26 compounds have not been reported in the previous literatures.
基金Supported by the National Natural Science Foundation of China(21376265)
文摘Based on the principle of biomimetic catalysis, β-cyclodextrin was applied to the acetalation reaction as a facile and efficient catalyst, and the synthesis was environmentally friendly with atomic economy. The influencing factors of the acetalation reaction e.g. the reaction time, the volume of water-carrying agent,the molar ratio of catalyst to benzaldehyde and the molar ratio of glycol to benzaldehyde had been studied.The yield of benzaldehyde glycol acetal would reach a maximum of 81.3% under the conditions approached.Six of other acetals were also synthesized. Moreover, a plausible reaction mechanism for the formation of acetal had been proposed.
基金Supported by the National Basic Research Program of China(973 Program,2012CB215000)
文摘Pjridine has been generally synthesized by aldehydes and ammonia in a turbulent fluidized-bed reactor. In this paper, a novel riser reactor was proposed for pyridine synthesis. Experiment result showed that the yield of pyridine and 3-picoline decreased, but the selectivity of pyridine over 3-picoline increased compared to turbulent fluidized-bed reactor. Based on experimental data, a modified kinetic model was used for the determination of optimal operating condition for riser reactor. The optimal operating condition of riser reactor given by this modified model was as follows： The reaction temperature of 755 K, catalyst to feedstock ratio （CTFR） of 87, residence timeof3.8sandinitialacetaldehydesconcentrationof0.0029mol.L-1 （acetaldehydes to formaldehydes ratio by mole （ATFR） of 0.65 and ammonia to aldehydes ratio by mole （ATAR） of 0.9, water contention of 63wt% （formaldehyde solution））.
基金Projects(51102026,51272032) supported by the Program for the National Natural Science Foundation of ChinaProject(11A014) supported by the Scientific Research Fund of Hunan Provincial Education DepartmentProject supported by the Aid Program for Science and Technology Innovative Research Team in Higher Educational Instituions of Hunan Province,China
文摘The mesoporous Ti O2 has been synthesized by evaporation induced self assembly(EISA) method. The thermogravimetric/differential scanning calorimetric(TG/DSC), X-ray diffraction(XRD), high-resolution transmission electron microscopy(HR-TEM) and N2 adsorption desorption and adsorption are used to study the effects of the synthesized process condition on the microstructure of the as-synthesized mesoporous Ti O2. The photocatalytic performances of as-synthesized samples are evaluated by the degradation of the formaldehyde under ultraviolet light irradiations. The results demonstrate that the as-synthesized mesoporous Ti O2 are anatase with the uniform size about 20-40 nm. The sample is prepared using cetyltrimethyl ammonium bromide(CTAB) as the template with average pore size distribution of 8.12 nm, specific surface area of 68.47 m2/g and pore volume of 0.213 m L/g. The samples show decomposition of formaldehyde 95.8% under ultraviolet light irradiations for 90 min. These results provide a basic experimental process for preparation mesoporous Ti O2, which will posses a broad prospect in terms of the applications in improving indoor air quality.
文摘In this present, a new series of Schiffbases from 2,5-di（p-aminophenyl）-3,6-diphenyl pyrazine in the presence of the benzil, 4-bromo benzaldehyde, 4-chlor benzaldehyde, 4-hydroxy benzaldehyde, 4-nitro benzaldehyde and 4-methyl benzaldehyde were studied. The structures of the synthesized compounds were determined on the basis of their Infra-red spectra, H-nuclear magnetic resonase and analysis elemental analysis spectral data. The purity of the synthesized compounds was checked by performing thin layer chromatography. The antibacterial activity was evaluated by paper disc diffusion method.
文摘The solubility of C.I. reactive blue 19 in aqueous alkali is poor, so it isn't used to dye cellulosic fiber in cold pad-batch dyeing. In order to improve the solubility of this dyestuff in alkali liquor, the right dispersants will be needed. A series of condensates are synthesized by changing the synthesis conditions such as the ratio of naphthalenesulfonic (N) to formaldehyde (F), acidity, and their compositions are confirmed by MS spectrum. It is found that in acidity scope of 20%-24% and the ratio of N to F 1∶0.33, the synthesized condensates can efficiently improve the solubility of C.I. reactive blue 19 in alkali liquor. In addition, the influences of the condensates on the exhaust dyeing and the cold pad-batch dyeing are tested.
文摘A rapid and simple procedure for synthesis of 2,6-di（naphthalene thioureido carbamino）pyridine fluorescine anion acceptor by the reaction between pyridine-2,6-dicarbohydrazide obtained from 2,6-dimethylpyridine after three-step reaction and 1-napbthyl isothiocyanate is described, and all reactions could be carried out under microwave heating condition.
