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321.
本研究采用O3/UV工艺降解喹啉溶液,系统地探讨了喹啉初始浓度、反应后置时间、初始p H、HCO-3浓度等因素对降解过程的影响.通过测定降解过程中的中间产物,分析了喹啉的降解机制及途径.结果表明随着喹啉初始浓度增加,反应表观速率常数和去除率都降低;p H(7~9)碱性条件时降解效果最好;HCO-3的存在明显降低了喹啉的去除率,加入100 mg·L-1HCO-3喹啉去除率降低了42.01%;反应后置时间对喹啉的去除率及矿化率基本没有影响.喹啉的降解中间产物主要为8-羟基喹啉、5-羟基喹啉、2(1H)-喹啉酮、2-吡啶甲醛等,喹啉在O3/UV体系中的降解途径主要由羟基自由基(·OH)、O3氧化剂发生的加成反应、取代反应、亲电反应等. 相似文献
322.
郑州市多站点大气VOCs变化特征及源解析 总被引:1,自引:1,他引:0
于2020年7月至2021年6月,在郑州市3个城市站点和1个郊区站点开展逐月大气VOCs离线样品采样及实验室分析,探讨郑州市大气VOCs体积分数水平、组成特征、反应活性和来源贡献.结果表明,观测期间,郑州市大气φ(VOCs)为(37.50±14.30)×10-9,组分占比为:烷烃(33%)>OVOCs(24%)>卤代烃(23%)>芳香烃(8%)>烯烃(7%)>炔烃(4%)>硫化物(1%).季节变化表现为:冬季>秋季>夏季>春季,VOCs月均值在1月出现最高值,5月出现最低值,空间变化则表现为:郑州大学>市监测站>经开区管委>岗李水库.采样周期·OH消耗速率(L·OH)均值为4.24 s-1,臭氧生成潜势(OFP)均值为172.27μg·m-3,各站点和各季节L·OH和OFP贡献率前10位物种均以烯烃、 OVOCs和芳香烃为主.正交矩阵因子分解模型(PMF)结果显示,VOCs主要来源为机动车排放(28%)、溶... 相似文献
323.
氰化钠溶液的电子束辐照降解 总被引:1,自引:1,他引:0
研究了利用电子束辐照降解氰化钠水溶液的效果.分别考察了CN-初始浓度、溶解氧浓度、辐照剂量率对 CN-降解效果的影响.采用总有机碳(TOC)分析仪、离子色谱仪(IC)、紫外分光光度计等分析了 CN-在不同实验条件下的辐照降解产物.实验结果表明,电子束能有效降解水溶液中的 CN-,较低的 CN-初始浓度,较高的辐照剂量,较高的溶解氧浓度以及较低的辐照剂量率能够提高CN-降解效率.CN-辐照后转化为 NH3、NO3-、NO2-、碳酸盐和有机物. 相似文献
324.
Lei Zhao Jun Ma Zhizhong Sun Zhengqian Liu Yixin Yang 《Frontiers of Environmental Science & Engineering in China》2008,2(1):44-50
The ozonation of nitrobenzene in aqueous solution was carried out in a semi-batch reactor to investigate the degradation efficiency,
the effect factors, and the reaction mechanism, where honeycomb ceramic was used as a catalyst. The presence of honeycomb
ceramic could improve the degradation rate of nitrobenzene by 15.46% compared to the results of ozonation alone. Under the
conditions of this experiment, the degradation rate of honeycomb ceramic-catalyzed ozonation increased by 12.94% with the
increase of the amount of catalyst from 1 to 5 blocks. The degradation rates all increased greatly with the increase of temperature
and pH of the solution in the processes of honeycomb ceramiccatalyzed ozonation and ozonation alone. But, when the pH of the
solution increased to 9.50, the advantage of the honeycomb ceramic-catalyzed ozonation process would be lost. The experimental
findings indicated that in the processes of ozonation alone and honeycomb ceramic-catalyzed ozonation, nitrobenzene was primarily
oxidized by ·OH free radical in aqueous solution. The adsorption of nitrobenzene was too limited to have an important influence
on the degradation rate of nitrobenzene. With the same total dosage of applied ozone, the multiple step addition of ozone
showed much higher removal efficiency than that obtained by one step in the two processes. 相似文献
325.
Shuangyang Zhao Chengxin Chen Jie Ding Shanshan Yang Yani Zang Nanqi Ren 《Frontiers of Environmental Science & Engineering》2022,16(3):36
326.
2019年对沈阳市大气挥发性有机物(VOCs)开展了为期l a的观测,并对得到的53种物种进行浓度特征以及反应活性的研究.结果表明,观测期间沈阳市VOCs平均浓度为65.33 μg·m-3,烷烃、烯烃和芳香烃质量分数分别为62.44%、16.52%和19.32%.浓度排名前10的物种主要是C3~C5的烷烃、烯烃和部分芳香烃,累计占VOCs总浓度的64.13%.大气中烷烃、烯烃和芳香烃浓度均表现为双峰型的日变化特征,峰值分别出现在06:00~08:00和19:00~20:00,最低点出现在14:00~15:00;月变化上,该地ρ(VOCs)分别在12月和5月达到最高值(136.44μg.m-3)和最低值(35.61 μg·m-3);VOCs表现出明显的季节变化特征,即冬季>秋季>夏季>春季,且烷烃、烯烃和芳香烃均随季节表现出增加趋势.通过特征值甲苯/苯(T/B)研究发现,沈阳春季VOCs主要来源于交通源和采暖源,夏季主要来源机动车尾气以及溶剂挥发,秋冬季主要受生物质燃烧和煤燃烧等排放源的影响.通过对反应活性分析,燃烧源是沈阳市控制臭氧污染的关键,丙烯、乙烯和1-己烯是沈阳市大气VOCs中反应活性最高的物种. 相似文献
327.
328.
Formation mechanisms of nitrous acid (HONO) during the haze and non-haze periods in Beijing, China
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Deng Lin Shengrui Tong Wenqian Zhang Weiran Li Fangjie Li Chenhui Ji Gen Zhang Meifang Chen Xinran Zhang Zhen Wang Maofa Ge Xiang He 《环境科学学报(英文版)》2022,34(4):343-353
As an important precursor of hydroxyl radical (OH), nitrous acid (HONO) plays a significant role in atmospheric chemistry. Here, an observation of HONO and relevant air pollutants in an urban site of Beijing from 14 to 28 April, 2017 was performed. Two distinct peaks of HONO concentrations occurred during the observation. In contrast, the concentration of particulate matter in the first period (period Ⅰ) was significantly higher than that in the second period (period Ⅱ). Comparing to HONO sources in the two periods, we found that the direct vehicle emission was an essential source of the ambient HONO during both periods at night, especially in period Ⅱ. The heterogeneous reaction of NO2 was the dominant source in period Ⅰ, while the homogeneous reaction of NO with OH was more critical source at night in period Ⅱ. In the daytime, the heterogeneous reaction of NO2 was a significant source and was confirmed by the good correlation coefficients (R2) between the unknown sources (Punknown) with NO2, PM2.5, NO2 × PM2.5 in period Ⅰ. Moreover, when solar radiation and OH radicals were considered to explore unknown sources in the daytime, the enhanced correlation of Punknown with photolysis rate of NO2 and OH ( × OH) were 0.93 in period Ⅰ, 0.95 in period Ⅱ. These excellent correlation coefficients suggested that the unknown sources released HONO highly related to the solar radiation and the variation of OH radicals. 相似文献