Based on the analysis of the properties of oily sludge samples,the effect of modification parameters,such as liquid to solid (L/S) ratio,agitation temperature,agitation intensity,agitation time and pH on the modificat...Based on the analysis of the properties of oily sludge samples,the effect of modification parameters,such as liquid to solid (L/S) ratio,agitation temperature,agitation intensity,agitation time and pH on the modification of oily sludge was investigated with the content of oil remnants in dry sludge as a reference index. Remixing experiments were carried out according to a simplex-lattice design,where Sx4056 was used as the demulsifier,petroleum sulfonate as the surfactant and sodium silicate (Na2SiO3) as the dispersant. The surface modification reagent formulation was optimized by a regression equation on the modified effect and based on the amounts of surface modification reagents. The results show that the content of the oil remaining in dry oily sludge is 0.28% of 10.15% oily sludge,when the reagent concentration rises to 3.5 g/L under the optimum experimental conditions.展开更多
Nickel and cobalt were extracted from low-grade nickeliferous laterite ore using a reduction roasting-ammonia leaching method.The reduction roasting-ammonia leaching experimental tests were chiefly introduced,by which...Nickel and cobalt were extracted from low-grade nickeliferous laterite ore using a reduction roasting-ammonia leaching method.The reduction roasting-ammonia leaching experimental tests were chiefly introduced,by which fine coal was used as a reductant.The results show that the optimum process conditions are confirmed as follows:in reduction roasting process,the mass fraction of reductant in the ore is 10%,roasting time is 120 min,roasting temperature is 1 023-1 073 K;in ammonia leaching process,the liquid-to-solid ratio is 4:1(mL/g),leaching temperature is 313 K,leaching time is 120 min,and concentration ratio of NH3 to CO2 is 90 g/L:60 g/L.Under the optimum conditions,leaching efficiencies of nickel and cobalt are 86.25% and 60.84%,respectively.Therefore,nickel and cobalt can be effectively reclaimed,and the leaching agent can be also recycled at room temperature and normal pressure.展开更多
Micaceous iron oxide （MIO） with a hexagonal flaky shape was prepared by hydrothermal method. The ferric hydroxide used as precursor was obtained by an acidic leaching solution of pyrite cinders reacting with ammonia...Micaceous iron oxide （MIO） with a hexagonal flaky shape was prepared by hydrothermal method. The ferric hydroxide used as precursor was obtained by an acidic leaching solution of pyrite cinders reacting with ammonia solution. The optimal experimental conditions for preparing micaceous iron oxide were investigated by orthogonal experiments. Micaceous iron oxide can be successfully prepared when optimal parameters of total iron concentration of 2.0 mol/L, pH value of 8, n（Fe2＋）/n（Fe3＋） of 0.1, mass of seed crystal of 1 g, reaction temperature of 260 ℃ and reaction time of 30 min are applied. X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and selected area electron diffractometry （SAEM） were adopted to characterize the hydrothermal products prepared under optimal conditions. The results indicate that highly crystallized α-Fe2O3 hexagonal flakes, about 1.0-1.5 μm in diameter and 0.1 μm in thickness, are prepared. Furthermore, the quality of micaceous iron oxide prepared can meet the required characteristics of micaceous iron oxide pigments for paints （ISO 10601--2007）.展开更多
Based on the existing form of Zn2 Si O4 in willemite, the chemical precipitation method was used to synthesize Zn2 Si O4.Through the orthogonal experimentation, the reaction conditions of melten Na OH decomposing Zn2 ...Based on the existing form of Zn2 Si O4 in willemite, the chemical precipitation method was used to synthesize Zn2 Si O4.Through the orthogonal experimentation, the reaction conditions of melten Na OH decomposing Zn2 Si O4 were optimized, and the optimal experimental conditions include reaction temperature of 400 °C, reaction time of 4 h, and alkaline-to-ore molar ratio of 20:1.Based on the optimized experiment, on-line detection for the alkali leaching was made by using Raman spectroscopy; XRD was used to analyze the structure of water leaching residue, to explore the reaction mechanism of Na OH decomposing Zn2 Si O4. The results show that during the reaction process, the Si — O bond in Si O4 is destroyed, and the Na OH inserts itself into the silicate lattice,producing an immediate Na2 Zn Si O4 product. After the alkali leaching process, Zn2+ can be separated from the Si O4 array, which can be released out of the silicate in the form of ZnO.展开更多
One-pot synthesis of cyclic aldol tetramer and α, β-unsaturated aldol from C3-C8 linear aldehydes using phase-transfer catalyst（PTC）, quaternary ammonium, combined with sodium hydroxide as catalysts was investigat...One-pot synthesis of cyclic aldol tetramer and α, β-unsaturated aldol from C3-C8 linear aldehydes using phase-transfer catalyst（PTC）, quaternary ammonium, combined with sodium hydroxide as catalysts was investigated. Butanal was subjected for detail investigations to study the effect of parameters. It was found that the selectivity of cyclic aldol tetramer depends greatly on the operating conditions of the reaction, especially the PTC/butanal molar ratio. The average selectivity of 2-hydroxy-6-propyl-l, 3, 5-triethyl-3-cyclohexene-1-carboxaldehyde（HPTECHCA） was 54.41% using tetrabutylammonium chloride combined with 14%（mass fraction） Na OH as catalysts at 60 ℃for 2 h with a PTC-to-butanal molar ratio of 0.09：1. Pentanal was more likely to generate cyclic aldol tetramer compared with other aldehydes under the optimum experimental conditions. Recovery of the PTC through water washing followed by adding enough sodium hydroxide from the washings was also demonstrated.展开更多
基金Project(50974119) supported by the National Natural Science Foundation of ChinaProject(2006A019) supported by the Science and Technology Fund of China University of Mining and Technology
文摘Based on the analysis of the properties of oily sludge samples,the effect of modification parameters,such as liquid to solid (L/S) ratio,agitation temperature,agitation intensity,agitation time and pH on the modification of oily sludge was investigated with the content of oil remnants in dry sludge as a reference index. Remixing experiments were carried out according to a simplex-lattice design,where Sx4056 was used as the demulsifier,petroleum sulfonate as the surfactant and sodium silicate (Na2SiO3) as the dispersant. The surface modification reagent formulation was optimized by a regression equation on the modified effect and based on the amounts of surface modification reagents. The results show that the content of the oil remaining in dry oily sludge is 0.28% of 10.15% oily sludge,when the reagent concentration rises to 3.5 g/L under the optimum experimental conditions.
基金Project(50674014) supported by the National Natural Science Foundation of China
文摘Nickel and cobalt were extracted from low-grade nickeliferous laterite ore using a reduction roasting-ammonia leaching method.The reduction roasting-ammonia leaching experimental tests were chiefly introduced,by which fine coal was used as a reductant.The results show that the optimum process conditions are confirmed as follows:in reduction roasting process,the mass fraction of reductant in the ore is 10%,roasting time is 120 min,roasting temperature is 1 023-1 073 K;in ammonia leaching process,the liquid-to-solid ratio is 4:1(mL/g),leaching temperature is 313 K,leaching time is 120 min,and concentration ratio of NH3 to CO2 is 90 g/L:60 g/L.Under the optimum conditions,leaching efficiencies of nickel and cobalt are 86.25% and 60.84%,respectively.Therefore,nickel and cobalt can be effectively reclaimed,and the leaching agent can be also recycled at room temperature and normal pressure.
基金Project(2008A090300016) supported by Major Science & Technology Special Program of Guangdong Province,China
文摘Micaceous iron oxide （MIO） with a hexagonal flaky shape was prepared by hydrothermal method. The ferric hydroxide used as precursor was obtained by an acidic leaching solution of pyrite cinders reacting with ammonia solution. The optimal experimental conditions for preparing micaceous iron oxide were investigated by orthogonal experiments. Micaceous iron oxide can be successfully prepared when optimal parameters of total iron concentration of 2.0 mol/L, pH value of 8, n（Fe2＋）/n（Fe3＋） of 0.1, mass of seed crystal of 1 g, reaction temperature of 260 ℃ and reaction time of 30 min are applied. X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and selected area electron diffractometry （SAEM） were adopted to characterize the hydrothermal products prepared under optimal conditions. The results indicate that highly crystallized α-Fe2O3 hexagonal flakes, about 1.0-1.5 μm in diameter and 0.1 μm in thickness, are prepared. Furthermore, the quality of micaceous iron oxide prepared can meet the required characteristics of micaceous iron oxide pigments for paints （ISO 10601--2007）.
基金Project(2007CB613603)supported by the National Basic Research Program of ChinaProject(51204037)supported by the National Natural Science Foundation of China
文摘Based on the existing form of Zn2 Si O4 in willemite, the chemical precipitation method was used to synthesize Zn2 Si O4.Through the orthogonal experimentation, the reaction conditions of melten Na OH decomposing Zn2 Si O4 were optimized, and the optimal experimental conditions include reaction temperature of 400 °C, reaction time of 4 h, and alkaline-to-ore molar ratio of 20:1.Based on the optimized experiment, on-line detection for the alkali leaching was made by using Raman spectroscopy; XRD was used to analyze the structure of water leaching residue, to explore the reaction mechanism of Na OH decomposing Zn2 Si O4. The results show that during the reaction process, the Si — O bond in Si O4 is destroyed, and the Na OH inserts itself into the silicate lattice,producing an immediate Na2 Zn Si O4 product. After the alkali leaching process, Zn2+ can be separated from the Si O4 array, which can be released out of the silicate in the form of ZnO.
基金Project(2013AA064102)supported by the National High-Tech Research Program of ChinaProject(11JJ6014)supported by the Hunan Provincial Natural Science Foundation of China
文摘One-pot synthesis of cyclic aldol tetramer and α, β-unsaturated aldol from C3-C8 linear aldehydes using phase-transfer catalyst（PTC）, quaternary ammonium, combined with sodium hydroxide as catalysts was investigated. Butanal was subjected for detail investigations to study the effect of parameters. It was found that the selectivity of cyclic aldol tetramer depends greatly on the operating conditions of the reaction, especially the PTC/butanal molar ratio. The average selectivity of 2-hydroxy-6-propyl-l, 3, 5-triethyl-3-cyclohexene-1-carboxaldehyde（HPTECHCA） was 54.41% using tetrabutylammonium chloride combined with 14%（mass fraction） Na OH as catalysts at 60 ℃for 2 h with a PTC-to-butanal molar ratio of 0.09：1. Pentanal was more likely to generate cyclic aldol tetramer compared with other aldehydes under the optimum experimental conditions. Recovery of the PTC through water washing followed by adding enough sodium hydroxide from the washings was also demonstrated.
