共查询到19条相似文献,搜索用时 78 毫秒
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研究了乙腈-水两相中Pt电极上1,4-二氯苯的降解途径和氧化特性。实验结果表明,1,4-二氯苯在乙腈-水两相中的氧化电位区间约为2.0~2.3 V(vs SCE),且氧化反应是受扩散控制的不可逆过程。液相色谱、液相色谱-质谱联用、离子色谱等的分析结果表明,乙腈-水两相中1,4-二氯苯氧化中间产物包括对氯苯酚、对苯醌、2,5-二氯对苯醌、草酸根离子、乙酸根离子、甲酸根离子、顺丁烯二酸根离子和氯离子,最终产物为H_2O和CO_2。得出了1,4-二氯苯主要的降解途径有两种。 相似文献
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引言2,4-二氯苯氧乙酸(2,4-D,又名2,4-滴)是一种广泛使用的除草剂[1],应用历史较长,是我国主要的除草剂品种之一,用量也比较大。2,4-D属于苯氧羧酸类除草剂的一种,可有效去除阔叶杂草,目前仍广泛用于农作物除草和草坪养护[2]。2,4-D的水溶性较高,挥发性较低,在自然界中难以生物 相似文献
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3,4—二氯苯腈及其衍生物广泛应用于农药、医药、颜料、染料等行业[1~ 5 ] 。文献报道 3,4—二氯苯腈的合成方法主要有 :1 .由α,α,α,3,4—五氯甲苯与 NH4Cl反应合成 [6 ] ;2 .由 3,4—二氯苯甲酰胺在 H2 SO4中脱水成腈 [7] ;3.由 3,4—二氯苯甲醛肟脱水制备 [8] ;4 .由 3,4—二氯甲苯在催化剂作用下经氨氧化反应制得 [9]。前 3种方法存在原料昂贵、污染严重等缺点 ,难以实现工业化 ;第4种方法是目前制备芳腈类化合物的最佳方法 ,关键是找到高活性、高选择性的催化剂。文献 [9] 报道用 ( NH4) 2 [( VO) 3( P2 O7) 2 ]作为氨氧化催化… 相似文献
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以正己烷为溶剂,Cr6 /Cr3 为氧化介质,间接电氧化2-甲基萘得到2-甲基-1,4-萘醌(2-MNQ)和6-甲基-1,4-萘醌(6-MNQ)的混合物,分离出水相后,用亚硫酸氢钠水溶液处理有机相, 6-MNQ与亚硫酸氢钠优先反应,生成加成产物溶解在水相,溶解在有机相中的2-MNQ经结晶和精制,得到2-MNQ产品.通过优化工艺条件和采用改进的分离提纯方法,2-MNQ的收率可达72.5%以上,质量分数大于99.5%,回收得到的6-MNQ可以转化为相应的蒽醌加以利用. 相似文献
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环氧化反式- 1,4-聚异戊二烯的合成 总被引:1,自引:0,他引:1
以负载钛催化异戊二烯本体沉淀聚合所合成的粉状反式-1,4-聚异戊二烯(TPI)为原料,过氧乙酸水溶液为介质,研究了水相悬浮法合成环氧化TPI(ETPI)的合成条件及动力学特性,并考察了ETPI的环氧度测定方法和反应残液的回收利用问题.结果表明,用该法合成ETPI适宜的反应条件为体系pH值等于4.5,且于约20℃反应1~3 h,可获得环氧度小于50%的ETPI;聚合动力学特性为过氧乙酸参与了环氧化反应,过氧乙酸的生成反应可忽略不计,反应的活化能为(72±5)KJ/mol,ETPI的环氧度可由反应前后过氧乙酸浓度的变化求得,与核磁共振法测得的环氧度相比,误差为±10%,有利于环氧度的控制. 相似文献
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用循环伏安法研究了含二甘醇的1.0mol·L^-1H2SO4溶液在铂电极上的电氧化行为,证明它是一个不可逆的复杂的氧化还原过程,并考察了温度和浓度对该过程的影响。 相似文献
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The electrochemical oxidation of aniline at boron-doped diamond (BDD) electrodes was investigated by cyclic voltammetry, steady-state polarization measurements and bulk electrolysis under potentiostatic control. It was found that acidic media is suitable for efficient electrochemical oxidation of aniline, because at low pH, the potential required for avoiding electrode fouling is lower than in neutral and alkaline media. The results of the longtime polarization measurements suggested that more anodic potentials ensure slightly higher efficiency for the conversion of aniline to CO2, while the direct oxidation process does not play a prominent part in the overall electrochemical incineration of aniline. The current efficiencies (44%) and the efficiency of aniline conversion to CO2 (80%) favourably compare with those reported for other electrochemical methods for aniline destruction. The results demonstrate the possibility of using BDD as an electrode material for electrochemical wastewater treatment, mainly when very high anodic potentials are required. 相似文献
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P. Cañizares J. García-Gómez C. Sáez M.A. Rodrigo 《Journal of Applied Electrochemistry》2003,33(10):917-927
The electrochemical oxidation of 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol aqueous wastes using boron-doped diamond electrodes was studied. This treatment led to complete mineralization of the wastes regardless of the operating conditions. A simple mechanistic model is consistent with the voltammetric and electrolysis results. According to this model, the electrochemical treatment of chlorophenol aqueous wastes involves the anodic and cathodic release of chlorine followed by the formation of non-chlorinated aromatic intermediates. Subsequent cleavage of the aromatic ring gives rise to non-chlorinated carboxylic acids. Chlorine atoms arising from the hydrodehalogenation of the chlorophenols are converted into more oxidized molecules at the anode. These molecules react with unsaturated C4 carboxylic acid to finally yield trichloroacetic acid through a haloform reaction. The non-chlorinated organic acids are ultimately oxidized to carbon dioxide and the trichloroacetic acid into carbon dioxide and volatile organo-chlorinated molecules. Both direct and mediated electrochemical oxidation processes are involved in the electrochemical treatment of chlorophenols. 相似文献
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Electrochemical oxidation of 2-methylnaphthalene-1,4-diacetate 总被引:1,自引:0,他引:1
Cyclic-voltammetric measurements show that 2-methylnaphthalene-1,4-diacetate is electrochemically oxidized on glassy-carbon electrode in glacial acetic acid at +1.45V vs SCE. The process is irreversible and diffusion controlled. Preparative controlled-potential electrolysis indicates that 2-methyl-1,4-naphthoquinone is a sole product. The material and current yields of the process are 94 and 99%, respectively. 相似文献
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Electrochemical oxidation of phenolic compounds using a flow-through electrolyser with porous solid electrodes 总被引:1,自引:0,他引:1
Organic compounds such as phenol and cresols may be found in industrial wastewater along with other organics and are difficult to be economically removed down to concentrations below environmentally permissible limits. By circulating a wastewater through an electrolytic reactor with a stack of porous solid anodes and cathodes, it has been demonstrated that it is feasible to electrochemically oxidize phenolic compounds in the presence of other organic molecules. A porous solid DSA®-type titanium anode coated with several mixed oxide layers was used as the active material. At low applied current densities, phenol and cresol concentrations were reduced from 5000 ppb to below 20 ppb. The influence of the flow rate and electrodes number was also studied and it was demonstrated that the current density was the main factor to be considered. This work confirms the hypotheses of other authors on the reaction mechanisms involved during the electrochemical oxidation of cresol and phenol. 相似文献
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Methanol oxidation on Pt electrodes is studied by ac voltammetry. Data from voltammograms at frequencies from 0.5 Hz to 20 kHz are assembled into electrochemical impedance spectra and analysed using equivalent circuits. Inductive behavior and negative relaxation times are attributed to nucleation and growth behavior. The rate-determining step is proposed to be the reaction of adsorbed CO and OH at the edge of islands of OH, with competition between OH and CO adsorption for the released reaction sites. 相似文献
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J. Sanabria-Chinchilla M.P. Soriaga R. Bussar H. Baltruschat 《Journal of Applied Electrochemistry》2006,36(11):1253-1260
The electrochemical hydrogenation and oxidation of p-dihydroxybenzene (hydroquinone) chemisorbed at polycrystalline Pt, well-ordered Pt(111) and disordered Pt(111) electrodes were studied by differential electrochemical mass spectrometry (DEMS). For comparative purposes, benzene was investigated at polycrystalline Pt. Anodic oxidation yielded only CO2 as the volatile (DEMS-detectable) product. However, at least three oxidation cycles were necessary for exhaustive oxidation; this indicates that: (i) non-volatile products were generated in the first cycle, (ii) these products either stayed adsorbed or, in part, were re-adsorbed during a cathodic scan into the double-layer potential region, and (iii) these species were further oxidized on subsequent anodic scans. Electrocatalytic hydrogenation of hydroquinone at polycrystalline Pt followed two parallel (not sequential) paths to generate benzene and cyclohexane: the “branching ratio” was heavily in favor of the latter product. The adsorbate can be displaced by CO at potentials in the double layer region. Since no volatile species was observed during this process, the adsorbate is not already reduced; e.g., to benzene. On well-ordered Pt(111), no cyclohexane was produced and only a minuscule fraction of benzene was observed; however, quantitative desorption of (unidentified) non-volatile organic material took place at the negative potential. The disordered Pt(111) surface behaved more like the polycrystalline rather than the monocrystalline surface. The H2Q-hydrogenation reaction proceeds more readily on Pt with surface steps and kinks. 相似文献
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H2 oxidation on Pt electrodes, a comparatively simple electrocatalytic reaction, has been known for a long time to exhibit a variety of complex temporal oscillations, depending on the composition of the supporting electrolyte. We report, on the one hand, recent observations of spatial instabilities in the bistable and oscillatory region in this system. The studies indicate that the spatio-temporal dynamic is by far richer than has been assumed so far. On the other hand, aperiodic responses of the system in cyclic voltammetric experiments are described. This behavior is similar to the one observed in potentiodynamic measurements during the electro-oxidation of small organic molecules. A possible common origin of all these complex, current–voltage responses is discussed. 相似文献