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硝化体系及精制棉干燥处理对硝化棉含氮量均匀性的影响 被引量:3
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作者 张云华 邵自强 +2 位作者 王文俊 王飞俊 吕少一 《火炸药学报》 EI CAS CSCD 北大核心 2013年第1期68-72,共5页
将不同预处理方法得到的精制棉在普通硝硫混酸体系和绿色无硫硝化体系(HNO3/CH2Cl2)中进行硝化,采用偏光显微镜研究了产物硝化的均匀性。结果表明,改变原料棉纤维素处理方法,产物硝化的均匀性有较明显的变化,对原料棉纤维素进行干燥处理... 将不同预处理方法得到的精制棉在普通硝硫混酸体系和绿色无硫硝化体系(HNO3/CH2Cl2)中进行硝化,采用偏光显微镜研究了产物硝化的均匀性。结果表明,改变原料棉纤维素处理方法,产物硝化的均匀性有较明显的变化,对原料棉纤维素进行干燥处理后,硝化产物性能有较明显的变化,适当含有水分的棉纤维素干燥处理后,由于角质化作用,制得的硝化棉(NC)含氮量和硝化均匀性比干燥处理前均有所降低;含氮量不同,产品的硝化均匀性有规律性变化,在中含氮量(如12%)时,NC的均匀性比含氮量为13%或11%的硝化棉好。 展开更多
关键词 应用化学硝化 硝化体系 绿色硝化 含氮量 分布均匀性
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利用新型硝化体系制备硝化纤维素的工艺研究 被引量:1
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作者 刘洪波 冯才敏 张永雄 《广东化工》 CAS 2009年第5期38-40,共3页
研究了N2O5-N2O4-HNO3新型硝化体系对纤维素硝化反应中各组分和反应条件对硝化纤维素含氮量及其质量的影响,探讨了硝化组分及反应条件影响硝化纤维素含氮量和分布的规律和内在原因,达到通过调节硝化剂组分含量和反应条件的变化控制硝化... 研究了N2O5-N2O4-HNO3新型硝化体系对纤维素硝化反应中各组分和反应条件对硝化纤维素含氮量及其质量的影响,探讨了硝化组分及反应条件影响硝化纤维素含氮量和分布的规律和内在原因,达到通过调节硝化剂组分含量和反应条件的变化控制硝化纤维素含氮量的目的。 展开更多
关键词 硝化体系 N2O5 N2O4 硝化 硝化纤维素
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亚硝化模拟体系中油脂对N-亚硝胺形成的影响 被引量:6
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作者 熊凤娇 马俪珍 +3 位作者 王洋 梁丽雅 杨华 李双燕 《食品科学》 EI CAS CSCD 北大核心 2018年第18期21-28,共8页
为了解油脂对N-亚硝胺形成的影响,采用体外模拟亚硝化反应体系,研究油脂种类(花生油、亚麻籽油和葵花籽油)和比例(0%、10%、20%、30%、40%)对N-二甲基亚硝胺(N-nitrosodimethylamine,NDMA)、N-二乙基亚硝胺(N-nitrosodiethylamine,NDEA... 为了解油脂对N-亚硝胺形成的影响,采用体外模拟亚硝化反应体系,研究油脂种类(花生油、亚麻籽油和葵花籽油)和比例(0%、10%、20%、30%、40%)对N-二甲基亚硝胺(N-nitrosodimethylamine,NDMA)、N-二乙基亚硝胺(N-nitrosodiethylamine,NDEA)生成量的影响;同时,在油脂参与条件下(20%花生油),以不含油脂的水相体系为对照,考察亚硝化反应条件(底物浓度比、p H值、反应温度及反应时间)对NDMA、NDEA、N-亚硝基吡咯烷(N-nitrosopyrrolidine,NPYR)生成量的影响。结果表明:3种油脂对NDMA和NDEA的形成均有一定的促进作用,相比于葵花籽油,花生油和亚麻籽油的添加更易促进N-亚硝胺的形成,且随添加比例升高有增加的趋势。亚硝酸盐浓度对NDMA和NDEA形成的影响大于对NPYR形成的影响;在p H值为5.4~7.0范围内随着p H值的升高,NDMA和NDEA生成量有下降趋势,p H值对NPYR形成影响较小;当反应温度高于80℃时,N-亚硝胺生成量随着温度上升有明显增加的趋势;NDMA和NDEA的生成量随着反应时间的延长呈现出先增加后略下降的趋势,NPYR的生成量随着反应时间的延长变化不大;含有油脂的乳化体系中NDMA、NDEA和NPYR的生成量均显著高于对照组水相体系,且在相同反应条件下,3种N-亚硝胺的生成量依次为NDMA>NDEA>NPYR。结果表明,较高的温度、较低的p H值、较高的亚硝酸盐浓度以及一定量的油脂存在条件下,可以明显促进NDMA和NDEA的形成,而对NPYR形成影响最大的因素是反应温度,因此在肉制品实际生产中可以通过控制这些因素从而降低N-亚硝胺的生成。 展开更多
关键词 N-亚硝胺 油脂 硝化反应体系 影响因素
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2,6-二氨基(4-氨基)吡啶的二硝化反应 被引量:3
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作者 成健 刘祖亮 +2 位作者 姚其正 周新利 杜扬 《火炸药学报》 EI CAS CSCD 北大核心 2009年第3期9-11,共3页
为考察氨基吡啶硝化反应产物收率和硝化副产物的影响因素,研究了4-氨基吡啶和2,6-二氨基吡啶在混酸和超酸硝化体系中的二硝化反应。结果表明,采用超酸硝化体系可以降低副产物比例并显著提高硝化产物收率。在混酸硝化体系中,硝化产... 为考察氨基吡啶硝化反应产物收率和硝化副产物的影响因素,研究了4-氨基吡啶和2,6-二氨基吡啶在混酸和超酸硝化体系中的二硝化反应。结果表明,采用超酸硝化体系可以降低副产物比例并显著提高硝化产物收率。在混酸硝化体系中,硝化产物4-氨基-3,5-二硝基吡啶和2,6-二氨基-3,5-二硝基吡啶的收率分别为55%和66.4%,副产物的含量为5%~8%;在超酸硝化体系中,目标化合物的收率分别可达到85.5%和92%,而副产物的含量降到0.5%以下。采用核磁共振光谱、红外光谱、质谱对目标化合物及副产物的结构进行了表征。 展开更多
关键词 有机合成 4-氨基吡啶 2 6-二氨基吡啶 硝化反应 混酸 超酸硝化体系
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NH_3 selective catalytic reduction of NO: A large surface TiO_2 support and its promotion of V_2O_5 dispersion on the prepared catalyst 被引量:3
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作者 刘欣 李俊华 +4 位作者 李想 彭悦 王虎 江晓明 王兰武 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第6期878-887,共10页
A titania support with a large surface area was developed, which has a BET surface area of 380.5 m^2/g, four times that of a traditional titania support. The support was ultrasonically impregnated with 5 wt% vanadia. ... A titania support with a large surface area was developed, which has a BET surface area of 380.5 m^2/g, four times that of a traditional titania support. The support was ultrasonically impregnated with 5 wt% vanadia. A special heat treatment was used in the calcination to maintain the large surface area and high dispersion of vanadium species. This catalyst was compared to a common V2O5-TiO2 catalyst with the same vanadia loading prepared by a traditional method. The new catalyst has a surface area of 117.7 m^2/g, which was 38% higher than the traditional V2O5-TiO2 catalyst. The selective catalytic reduction(SCR) performance demonstrated that the new catalyst had a wider temperature window and better N2 selectivity compared to the traditional one. The NO conversion was 80% from 200 to 450 °C. The temperature window was 100 °C wider than the traditional catalyst. Raman spectra indicated that the vanadium species formed more V-O-V linkages on the catalyst prepared by the traditional method. The amount of V-O-Ti and V=O was larger for the new catalyst. Temperature programmed desorption of NH3, temperature programmed reduction by H2 and X-ray photoelectron spectroscopy results showed that its redox ability and total acidity were enhanced. The results are helpful for developing a more efficient SCR catalyst for the removal of NOx in flue gases. 展开更多
关键词 V2O5-TiO2 catalyst DENITRIFICATION TITANIA Surface area DISPERSIBILITY
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Chlorine inclusion mechanism in high purity copper electrorefining from nitric acid system 被引量:2
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作者 Hua-zhen CAO Wen-yu FENG +1 位作者 Hui-bin ZHANG Guo-qu ZHENG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2020年第5期1387-1396,共10页
A practical approach was introduced to study the inclusion mechanism of chlorine in high purity copper electrorefining from nitric acid system via cyclic voltammetry(CV) combined with electrodeposition experiments. Th... A practical approach was introduced to study the inclusion mechanism of chlorine in high purity copper electrorefining from nitric acid system via cyclic voltammetry(CV) combined with electrodeposition experiments. The CV curves display an obvious reduction peak of Cu Cl intermediate, which can provide an insight into the electrochemical behavior of this inclusion. Experimental results show that the increase of HNO3 concentration is favorable to reducing the quantity of chlorine inclusion although there is a slight decline in cathodic current efficiency. The optimum conditions for copper electrorefining in nitric acid system are HNO3 concentration in solution of 1-2 mol/L, moderate temperature of ~35 ℃ with current density not exceeding 25 m A/cm2. Based on the theoretical studies, an optimized copper electrorefining experiment was designed to simulate the industrial electrolysis, by which high purity copper can be obtained with chlorine inclusion less than 10 μg/g and current efficiency higher than 90%. 展开更多
关键词 copper electrorefining nitric acid system cuprous chlorine inclusion mechanism
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Isolation and Characterization of Heterotrophic Nitrifying Strain W1 被引量:5
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作者 吕永康 王荀 +2 位作者 刘博凯 刘玉香 杨晓华 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2012年第5期995-1002,共8页
In a high concentration substrate medium, a heterotrophic bacterium with high removal efficiency of ammonium, named W1, was isolated from activated sludge of coking wastewater treatment facility. The bacterium was Gra... In a high concentration substrate medium, a heterotrophic bacterium with high removal efficiency of ammonium, named W1, was isolated from activated sludge of coking wastewater treatment facility. The bacterium was Gram-negative, rod-shaped, and identified preliminarily as Alcaligenes sp. according to its morphological and physiological properties and its 16S rRNA gene sequence analysis. In the high concentration ammonium medium (400 mg·L 1 4 NH -N), the effects of C source, N source, C/N ratio and initial pH of medium on ammonium removal were investigated in order to determine the optimal condition for strain W1. The maximum ammonium removal was around 95% in 4 days in an improved medium. The production of N 2 gas was examined in a closed system that was full of pure oxygen at the beginning. N 2 gas was detected in the system after 4 days of cultivation, which further testified that strain W1 has heterotrophic nitrification and aerobic denitrification abilities simultaneously. 展开更多
关键词 heterotrophic nitrification aerobic de-nitrification high concentration ammonium Alcaligenes sp.
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Liquid-solid Equilibria in Quinary System Na^+,K^+,Mg^2+//Cl^-,NO3^--H2O at 25°C 被引量:4
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作者 黄雪莉 李松菀 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2011年第1期101-107,共7页
The solubilities of the quinary system Na^+ ,K^+ ,Mg^2+ //Cl ,NO 3 ^-H2O and its two quaternary subsystems, Na^+ ,K^+ ,Mg^2+ //NO 3 -H2O and K^ + ,Mg ^2+ //Cl ,NO 3 ^-H2O,were studied by isothermal method at 2... The solubilities of the quinary system Na^+ ,K^+ ,Mg^2+ //Cl ,NO 3 ^-H2O and its two quaternary subsystems, Na^+ ,K^+ ,Mg^2+ //NO 3 -H2O and K^ + ,Mg ^2+ //Cl ,NO 3 ^-H2O,were studied by isothermal method at 25°C and their phase diagrams were plotted.In the equilibrium phase diagram of quaternary system Na^ + ,K^ + ,Mg ^2+ //NO 3 ^-H2O, there are one invariant point,three univariant curves and three regions of crystallization with one salt:NaNO3, KNO3 and Mg(NO3)2·6H2O.In the equilibrium phase diagram of quaternary system K ^+ ,Mg ^2+ //Cl ,NO 3 ^-H2O,there are three invariant points,seven univariant curves and five regions of crystallization with one salt:KNO3,KCl, Mg(NO3)2·6H2O,MgCl2·6H2O and KCl·MgCl2·6H2O.In the equilibrium phase diagram of the quinary system Na ^+ , K^ + ,Mg ^2+ //Cl ,NO 3^ -H2O,there are four invariant points,and seven regions of crystallization with one salt:NaCl, KCl,NaNO3,KCl·MgCl2·6H2O,KNO3,MgCl2·6H2O and Mg(NO3)2·6H2O. 展开更多
关键词 quinary system phase equilibrium NITRATE SOLUBILITY
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Synthesis of 2-Methyl-4-methoxyaniline from o-Nitrotoluene Using Pt/C and Acidic Ionic Liquid as Catalyst System
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作者 LIU Yingxin LI Xiying FANG Yanyan ZHANG Lin 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2013年第6期701-704,共4页
2-Methyl-4-methoxyaniline (MMA) was synthesized by one-pot method through the hydrogenation and Bamberger rearrangement of o-nitrotoluene in methanol using acidic ionic liquid and 3% Pt/C as catalyst system. The eff... 2-Methyl-4-methoxyaniline (MMA) was synthesized by one-pot method through the hydrogenation and Bamberger rearrangement of o-nitrotoluene in methanol using acidic ionic liquid and 3% Pt/C as catalyst system. The effects of ionic liquid type, dosage of ionic liquid and 3% Pt/C, reaction temperature and reaction pressure on o-nitrotoluene conversion and MMA selectivity were investigated. The results indicated that the imidazolium-based acidic ionic liquid which contains SO3H-functionalized cation showed higher selectivity to MMA than other acidic ionic liquids used in this work. Using 1-(propyl-3-sulfonate)-3-methylimidazolium hydrosulfate ([HSO3-pmim][HSO4]) as the acid catalyst, the selectivity to MMA was as high as 67.6% at 97.8% of o-nitrotoluene conversion. As 3% Pt/C increased from 0.01 g to 0.025 g, the selectivity to MMA decreased from 73.4% to 62.5%, because of the hydrogenation of intermediate o-methyl-phenylhydroxylamine to o-toluidine becoming more dominant. An increase in hydrogen pressure also had obviously dramatic effect in lowering the MMA selectivity. After easy separation from the products, the catalyst system could be reused at least 3 times. 展开更多
关键词 acidic ionic liquid Bamberger rearrangement 2-methyl-4-methoxyaniline O-NITROTOLUENE hydrogenation
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A Highly Efficient and Selective Water-Soluble Bimetallic Catalyst for Hydrogenation of Chloronitrobenzene to Chloroaniline 被引量:1
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作者 Zhou Yafen Yang Wenjuan +2 位作者 Zhou Limei Wang Manman Ma Xiaoyan 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2015年第2期26-31,共6页
Selective hydrogenation of chloronitrobenzene(CNB) to chloroaniline(CAN) catalyzed by water-soluble Ru/Pt bimetallic catalyst in an aqueous-organic biphasic system was studied. It was found that the catalytic activity... Selective hydrogenation of chloronitrobenzene(CNB) to chloroaniline(CAN) catalyzed by water-soluble Ru/Pt bimetallic catalyst in an aqueous-organic biphasic system was studied. It was found that the catalytic activity increased obviously due to the addition of platinum. Ru/Pt bimetallic catalysts exhibited a strong synergistic effect when the molar ratio of Pt was in the range of 5%—80%. Under the mild conditions including a temperature of 25 ℃, a hydrogen pressure of 1.0 MPa and a Pt molar ratio of 20%, the conversion of p-chloronitrobenzene(p-CNB) reached 99.9%, with the selectivity to p-chloroaniline(p-CAN) equating to 99.4%. The Ru/Pt catalyst also showed high activity and selectivity for the hydrogenation of other chloro- and dichloro-nitrobenzenes with different substituted positions. In addition, the catalyst can be recycled five times without significant loss of activity. 展开更多
关键词 water-soluble bimetallic catalyst HYDROGENATION CHLORONITROBENZENE CHLOROANILINE
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