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上海臭氧及前体物变化特征与相关性研究 总被引:19,自引:15,他引:4
于2010年1~12月期间,在上海城区内采用在线连续观测,分析该地区近地臭氧与其前体物的季节变化规律及相关性,探讨了臭氧浓度与OX和NO2光解速率之间的关系。结果表明,观测期间,上海地区O3总超标天数为13天,超标率为3.56%。O3浓度变化呈现明显的秋冬低、春夏高的季节变化。O3浓度日变化规律呈典型单峰变化,O3各前体物呈双峰形分布,冬季O3与NOX的相关性最强。对OX的贡献中,秋冬以NO2为主,春夏以O3为主;夜间以NO2为主,白天以O3为主。臭氧浓度与OX和NO2光解速率变化规律基本一致。 相似文献
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《Environmental engineering science》2011,28(12):891-896
Abstract In this study, iron oxides immobilized onto silica and alumina granular carriers in a fluidized-bed reactor were applied as silica granule (SG) and alumina granule (AG) catalysts, respectively; the SG and AG catalysts were used to explore the catalytic decomposition of H2O2. Effects of H2O2 concentration and temperature on the oxidation of aniline were determined to compare the reactive efficiencies of the SG and AG catalysts. Results showed that H2O2 decomposition could be efficiently catalyzed by the SG and AG catalysts. Degradation rates of aniline increased with increasing H2O2 concentration and temperature in both catalyst systems. The AG catalyst (smaller particle size) had more surface sites for precipitation of iron oxide than the SG catalyst (larger particle size). Consequently, in the initial stages of the reaction, hydroxyl radicals (?OH) were generated more rapidly with the AG catalyst than with the SG catalyst and the degradation of aniline by the AG catalyst was faster than that by ... 相似文献
396.
As an important precursor of hydroxyl radical, nitrous acid (HONO) plays a key role in the chemistry of the lower atmosphere. Recent atmospheric measurements and model calculations show strong enhancement for HONO formation during daytime, while they are inconsistent with the known sources in the atmosphere, suggesting that current models are lacking important sources for HONO. In this article, heterogeneous photochemical reactions of nitric acid/nitrate anion and nitrogen oxide on various aerosols were reviewed and their potential contribution to HONO formation was also discussed. It is demonstrated that HONO can be formed by photochemical reaction on surfaces with deposited HNO3 , by photocatalytic reaction of NO2 on TiO2 or TiO2 -containing materials, and by photochemical reaction of NO2 on soot, humic acids or other photosensitized organic surfaces. Although significant uncertainties still exist in the exact mechanisms and the yield of HONO, these additional sources might explain daytime observations in the atmosphere. 相似文献
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活性炭催化臭氧氧化处理染料废水生化出水研究 总被引:3,自引:1,他引:2
采用饱和活性炭作为臭氧氧化催化剂,对染料废水生化出水进行深度处理.以废水COD、DOC去除率为指标,考察饱和活性炭对臭氧的催化效果.使用6种不同的活性炭作为催化剂(编号1#~6#),并将6#活性炭采用KMnO4、NaOH、ZnCl2、H2SO4、H3PO4进行表面处理,在活性炭的孔体积、酸碱基团等表面性质测定的基础上,探讨活性炭性质与催化臭氧化效率的关系.结果显示,活性炭催化效果与大孔体积密切相关;另一方面,使用微孔膜片减小臭氧气泡尺寸,增大臭氧的传质面积,提高臭氧利用率,可以改善臭氧/活性炭催化氧化处理效果. 相似文献
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利用水热法成功制备了Fe3O4/FeS2催化剂,并将其用于构建非均相芬顿体系降解典型的苯胂酸类污染物(洛克沙胂,ROX).XRD、SEM、XPS和磁学测量系统(VSM)等表征结果表明,Fe3O4/FeS2呈明显的颗粒状且具有良好的磁性.降解实验结果显示,在最优条件下(初始pH值为4.5、ROX起始浓度为20mg/L、Fe3O4/FeS2投加量为0.15g/L和H2O2浓度为0.034g/L,Fe3O4/FeS2介导的非均相芬顿体系可以超快速降解ROX,1min后的降解效率达到96.74%,明显优于单独的Fe3O4或FeS2体系.此外,Fe3O4/FeS2可以通过磁铁进行快速回收利用,同时也具有良好的重复利用性能,使用3次后,ROX的降解效率仍超过80%.机理分析表明,Fe3O4/FeS2能够快速地催化H2O2产生具有强氧化性的羟基自由基(·OH).在·OH的作-用下,ROX分子结构中C-As、C-N和C-C等化学键发生断裂,发生脱砷、脱硝和开环等反应,进而生成一系列的有机产物(如酚类、醌类、小分子有机酸等)和无机产物(As (V)和NO3-).之后,无机砷能够被吸附在催化剂表面,而有机产物则进一步被矿化. 相似文献
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Caicai Wang Shengwang Gao Jianchao Zhu Xunfeng Xi Mingxin Wang Yanna Xiong 《环境科学学报(英文版)》2021,33(1):249-259
A series of Sr-doped BiFeO3 perovskites (Bi1-xSrxFeO3, BSFO) fabricated via sol-gel method was applied as peroxydisulfate (PDS) activator for ciprofloxacin (CIP) degradation. Various technologies were used to characterize the morphology and physicochemical features of prepared BSFO samples and the results indicated that Sr was successfully inserted into the perovskites lattice. The catalytic performance of BiFeO3 was significantly boosted by strontium doping. Specifically, Bi0.9Sr0.1FeO3 (0.1BSFO) exhibited the highest catalytic performance for PDS activation to remove CIP, where 95% of CIP (10 mg/L) could be degraded with the addition of 1 g/L 0.1BSFO and 1 mmol/L PDS within 60 min. Moreover, 0.1BSFO displayed high reusability and stability with lower metal leaching. Weak acidic condition was preferred to neutral and alkaline conditions in 0.1BSFO/PDS system. The boosted catalytic performance can be interpreted as the lower oxidation state of Fe and the existence of affluent oxygen vacancies generated by Sr doping, that induced the formation of singlet oxygen (1O2) which was confirmed as the dominant reactive species by radical scavenging studies and electron spin resonance (ESR) tests. The catalytic oxidation mechanism related to major 1O2 and minor free radicals was proposed. Current study opens a new avenue to develop effective A-site modified perovskite and expands their application for PDS activation in wastewater remediation. 相似文献
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