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微波助离子液体中氮掺杂TiO2催化剂的制备及其微波强化光催化活性
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作者 孙婧 蒋文建 +1 位作者 贺锋 毕先钧 《中国化工贸易》 2013年第6期276-278,共3页
在室温离子液体介质中,采用溶胶-凝胶法以及微波干燥的方法制备了氯掺杂的光催化剂TiO2-N。在室温条件下,以甲基橙为模拟污染物,在微波超声波组合催化合成仪中,分别利用微波辐射(MW)、紫外光照(UV)和微波辐射一紫外光照(MW—U... 在室温离子液体介质中,采用溶胶-凝胶法以及微波干燥的方法制备了氯掺杂的光催化剂TiO2-N。在室温条件下,以甲基橙为模拟污染物,在微波超声波组合催化合成仪中,分别利用微波辐射(MW)、紫外光照(UV)和微波辐射一紫外光照(MW—UV)三种降解方式,主要考察了N掺杂量、微波干燥功率、微波干燥时间、煅烧温度和煅烧时间等因素对TiO2-N光催化活性的影响。结果表明,在离子液体用量为5.6mL、N掺杂量n(N)/n(Ti)=3:1、微波干燥功率210W、微波干燥时间20min、煅烧温度600℃、煅烧时间2h的条件下所制得的TiO2-N光催化剂具有较高的光催化活性;TiO2-N光催化剂在三种降解方式下对甲基橙的降解效果为:MW—UV〉UV〉MW,这表明微波与紫外光照有较好的协同作用,即微波一紫外光照具有强化TiO2-N催化剂降解甲基橙的效果。 展开更多
关键词 催化化学微波 离子液体掺杂二氧化钛光催化降解
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利用NO_2^-对对硝基苯胺的褪色作用光度法测定污水中NO_2 被引量:1
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作者 李雅枫 田亚赛 《干旱环境监测》 北大核心 1999年第3期129-131,共3页
在006 m ol/ L 的盐酸介质中, N O2- 与对硝基苯胺(10×10- 4 m ol/ L)反应生成无色的重氮盐使对硝基苯胺溶液褪色,于382 nm 处测量吸光度的变化。 N O2- 在006~40 m g/ L ... 在006 m ol/ L 的盐酸介质中, N O2- 与对硝基苯胺(10×10- 4 m ol/ L)反应生成无色的重氮盐使对硝基苯胺溶液褪色,于382 nm 处测量吸光度的变化。 N O2- 在006~40 m g/ L 内服从比耳定律,回收率为95% ~104% 。本法选择性好,操作简便,适用于污水中 N O2- 的测定。 展开更多
关键词 对硝基苯胺 褪色 污水监测 二氧化氮离子
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介质阻挡放电分解O_2/N_2的试验及机理分析 被引量:1
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作者 王军 蔡忆昔 +2 位作者 赵卫东 李小华 王攀 《江苏大学学报(自然科学版)》 EI CAS 北大核心 2011年第3期301-304,共4页
通过建立介质阻挡放电型低温等离子体反应器实验系统,利用Q-VLissajous图形法对反应器电学参量进行测试,研究了该反应器分解O2/N2混合气时,激励峰值电压、放电功率、电场强度对生成的臭氧及二氧化氮体积分数的影响.结果表明:反应器放电... 通过建立介质阻挡放电型低温等离子体反应器实验系统,利用Q-VLissajous图形法对反应器电学参量进行测试,研究了该反应器分解O2/N2混合气时,激励峰值电压、放电功率、电场强度对生成的臭氧及二氧化氮体积分数的影响.结果表明:反应器放电功率、电场强度随激励峰值电压和放电频率的升高而增大,放电频率对电场强度的影响较小;反应器产生的高能电子可断裂O2,N2的分子键,生成O3及NO2,其体积分数均随激励峰值电压的增大先升高后降低;随着O2/N2混合气中O2初始体积分数的增大,产生的O3及NO2体积分数也相应增大,其中O3体积分数增加更为明显. 展开更多
关键词 低温等离子体:臭氧:二氧化:介质阻挡放电:体积分数
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High-Resolution Experimental Study on Photodissocaition of N2O
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作者 俞盛锐 袁道福 +4 位作者 陈文韬 谢婷 王思雯 杨学明 王兴安 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2016年第1期135-139,I0002,I0003,共7页
We study the photodissociation dynamics of nitrous oxide using the time-sliced ion veloc- ity imaging technique at three photolysis wavelengths of 134.20, 135.30, and 136.43 nm. The O(^1Sj=0)+N2(XI∑g+) product ... We study the photodissociation dynamics of nitrous oxide using the time-sliced ion veloc- ity imaging technique at three photolysis wavelengths of 134.20, 135.30, and 136.43 nm. The O(^1Sj=0)+N2(XI∑g+) product channels were investigated by measuring images of the O(iSj=0) products. Vibrational states of N2(XI∑g+) products were fully resolved in the images. Product total kinetic energy releases (TKER) and the branching ratios of vibrational states of N2 products were determined. It is found that the most populated vibrational states of N2 products are v--2 and v--3. The angular anisotropy parameters (8 values) were also derived. The β values are very close to 2 at low vibrational states of the correlated N2 (X1 ∑g+) products at all three photolysis wavelengths, and gradually decrease to about 1.4 at v--7. This indicates the dissociation is mainly through a parallel transition state to form products at lower vibrational states, and the highly vibrational exited products are from a more bent configuration. This is consistent with the observed shift of the most intense rotational structure in the TKER as the vibrational quantum number increases. 展开更多
关键词 N2O Ion imaging Vacuum ultraviolet PHOTODISSOCIATION
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Effect of Carbon and Nitrogen Availability on Metabolism of Amino Acids in Germinating Spores of Arbuscular Mycorrhizal Fungi 被引量:4
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作者 JIN Hai-Ru JIANG Dong-Hua ZHANG Ping-Hua 《Pedosphere》 SCIE CAS CSCD 2011年第4期432-442,共11页
The effects of carbon (C) and nitrogen (N) sources on N utilization and biosynthesis of amino acids were examined in the germinating spores of the arbuscular mycorrhizal (AM) fungus Glomus intraradices Schenck ... The effects of carbon (C) and nitrogen (N) sources on N utilization and biosynthesis of amino acids were examined in the germinating spores of the arbuscular mycorrhizal (AM) fungus Glomus intraradices Schenck & Smith after exposure to various N substrates, CO2, glucose, and/or root exudates. The N uptake and de novo biosynthesis of amino acids were analyzed using stable isotopic labeling with mass spectrometric detection. High-performance liquid chromatography-based analysis was used to measure amino acid levels. In the absence of exogenous N sources and in the presence of 25 mL L^-1 CO2, the germinating AM fungal spores utilized internal N storage as well as C skeletons derived from the degradation of storage lipids to biosynthesize the free amino acids, in which serine and glycine were produced predominantly. The concentrations of internal amino acids increased gradually as the germination time increased from 0 to 1 or 2 weeks. However, asparagine and glutamine declined to the low levels; both degraded to provide the biosynthesis of other amino acids with C and N donors. The availability of exogenous inorganic N (ammonium and nitrate) and organic N (urea, arginine, and glutamine) to the AM fungal spores using only CO2 for germination generated more than 5 times more internal free amino acids than those in the absence of exogenous N. A supply of exogenous nitrate to the AM fungal spores with only CO2 gave rise to more than 10 times more asparagine than that without exogenous N. In contrast, the extra supply of exogenous glucose to the AM fungal spores generated a significant enhancement in the uptake of exogenous N sources, with more than 3 times more free amino acids being produced than those supplied with only exogenous CO2. Meanwhile, arginine was the most abundant free amino acid produced and it was incorporated into the proteins of AM funsal spores to serve as an N storage compound. 展开更多
关键词 BIOSYNTHESIS exogenous C and N sources isotopic labeling N uptake N storage compound
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