新型复合预氧化技术控制副产物的试验研究

臭氧被广泛应用于饮用水预氧化工艺中,但是成本较高,而且会生成臭氧化副产物,如可同化有机碳(AOC)、溴酸盐和甲醛.因此,提出臭氧/高锰酸钾复合预氧化技术,并对照预臭氧化技术,进行了消毒副产物前质及臭氧化副产物控制的小试试验研究.结果表明,与预臭氧化(1.5 mg/L臭氧)相比,复合预氧化(0.6 mg/L臭氧 0.4 mg/L高锰酸钾)能促进混凝沉淀对消毒副产物前质的去除,总去除率与单独预臭氧化的去除率相当.而且又能降低AOC生成量,并促进混凝沉淀对AOC的去除,合计AOC去除率达43%左右.此外,对溴酸盐和甲醛生成量也有明显去除效果,比单独预臭氧化降低了78.4%和21.2%.     

一种高效的圆盘板式臭氧发生器

本文介绍臭氧的应用领域及其作用机理 ,对一种新型臭氧发生器的结构、原理及其技术参数进行了系统分析     

绿色洗衣机

科研人员不断研究，推陈出新，研制出一些不用洗涤剂的绿色洗衣机。美国佛罗里达的臭氧技术公司发明了一种用臭氧代替洗涤剂的新型洗衣机，它用一台电动臭氧发生器将臭氧泵入水中，臭氧分子使衣服上的尘埃和污垢中的有机物分子裂解并溶入水中，使衣服很快就洗净。这种洗衣机无噪声、无震动，且不用洗涤剂，避免了对环境的污染，是理想的绿色洗衣机。     

氧化铈/活性炭催化臭氧氧化技术去除水中邻苯二甲酸二甲酯

用浸渍法在活性炭(AC)上负载氧化铈(CeO2)制备催化刺CeO2/AC催化臭氧氧化去除邻苯二甲酸二甲酯(DMP),考察了臭氧投加量,DMP初始浓度和溶液初始pH的影响.结果表明,CeO2/AC催化臭氧氧化去除DMP的最佳臭氧投加量为50mg/h,DMP初始浓度和溶液初始pH对CeO2/AC催化臭氧氧化DMP过程都有一定的影响.在DMP初始质量浓度为30 mg/L、溶液初始pH为5、臭氧投加量为50 mg/h、反应60 min时,CeO2/AC的加入(1.5g/L)有利于催化臭氧氧化DMP过程中总有机碳(TOC)的去除,TOC去除率由AC催化臭氧氧化的48%提高到68%.而单独臭氧氧化过程中的TOC去除率仅22%;且单独臭氧氧化与AC、CeO2/AC催化臭氧氧化DMP的矿化过程均符合二级反应动力学方程,CeO2/AC催化臭氧氧化DMP时TOC降解的二级反应动力学常数为0.0015L/(mg·min),分别是AC催化臭氧氧化的2.5倍和单独臭氧氧化的7.5倍.     

一种高效的圆盘板式臭氧发生器

本文介绍臭氧的应用领域及其作用机理，对一种新型臭氧发生器的结构、原理及其技术参数进行了系统分析。     

臭氧/ 生物活性炭深度处理循环养殖废水

随着工厂化循环水养殖的不断发展,高浓度循环养殖废水对环境污染日益严重.为实现环境友好和资源节约,采用臭氧/生物活性炭对循环养殖废水进行深度处理中试研究.实验结果表明,臭氧化臭氧最佳投加量为4 mg/L,显著增强水体的可生化性,使TOC(总有机碳)/UV254(在波长为254 nm处的单位比色皿光程下的紫外吸光度)提高80%.臭氧/生物活性炭对循环养殖废水中的有机物和氨氮具有良好的去除效果.臭氧/生物活性炭对TOC、高锰酸盐指数和UV254的最终去除率比生物活性炭分别高11.9%、13.4%和6.5%.臭氧/生物活性炭和生物活性炭对氨氮的最终去除率分别为96.0%、90.7%.     

微量臭氧催化氧化深度处理煤气化废水

采取固定床连续式水处理方式,实验研究了在固体催化剂作用下微量臭氧催化氧化深度处理地下煤气化废水的效果.结果表明,当处理COD为300 mg,/L左右的该类型废水时,加入微量臭氧,水处理装置COD去除率提高了45％,平均1 mg的臭氧处理了2.4 mg有机物;当废水COD为200 mg/L左右,进水速度为1 L/h时,最佳臭氧投加量为每升废水20 mg左右的臭氧,此时气水比为15:1左右;同时实验发现,不同COD的废水色度均可以被有效去除.通过与其他类似的实验研究比较发现,微量臭氧催化氧化技术具有成本优势.     

污泥基活性炭催化臭氧氧化对氯苯甲酸效能

以城市污水处理厂剩余污泥和玉米芯为原料,用氯化锌活化法制备出污泥基活性炭(SCAC),研究了其催化臭氧氧化去除水中对氯苯甲酸(p-CBA)的效能和机理,同时,考察了臭氧浓度、SCAC投量、p-CBA初始浓度以及自由基抑制剂叔丁醇的加入对SCAC催化活性的影响。实验结果表明,SCAC的加入可以显著提高臭氧对p-CBA的氧化去除效果,在反应初期尤为明显,反应1.0 min时p-CBA的去除率由单独臭氧氧化的26.1%提高到SCAC催化臭氧氧化的60.2%。SCAC催化臭氧氧化对p-CBA的去除率随臭氧浓度的增加和p-CBA初始浓度的减小而增加。此外,在一定范围内增加催化剂的投量可以增加p-CBA的去除率。叔丁醇的加入显著减弱了SCAC催化臭氧氧化降解p-CBA的效能,表明SCAC催化臭氧氧化反应的主要活性物种为羟基自由基(·OH)。     

硫化氢硫醇废气的臭氧氧化试验

介绍了臭氧氧化法去除工业废气中的硫化氢、硫醇的试验情况,考察了臭氧浓度、停留时间和催化作用等不同因素对去除率的影响.试验结果表明能达到较好的去除效果,硫化氢、硫醇的最终氧化产物不是二氧化硫,不会增加二氧化硫的污染.     

金属氧化物催化剂消除臭氧的初步探索

初步研究了多种催化剂在不同条件下对臭氧的去除效果 ,发现金属氧化物催化剂对臭氧的去除能力顺序为Pt-Pd/ Al2 O3=Ag/ Al2 O3=Ni/ Al2 O3>Co/ Al2 O3>Fe/ Al2 O3>Mn/ Al2 O3>Cu/ Al2 O3>Cr/ Al2 O3,且负载量越多 ,臭氧的去除效果越好 ,用 γ-Al2 O3作载体效果较好 ,成本较低。     

Background ozone levels of air entering the west coast of the US and assessment of longer-term changes

An analysis of surface ozone measurements at a west coast site in northern California (Trinidad Head) demonstrates that this location is well situated to sample air entering the west coast of the US from the Pacific Ocean. During the seasonal maximum in the spring, this location regularly observes hourly average ozone mixing ratios 50 ppbv in air that is uninfluenced by the North American continent. Mean daytime values in the spring exceed 40 ppbv. A location in southern California (Channel Islands National Park) demonstrates many of the characteristics during the spring as Trinidad Head in terms of air flow patterns and ozone amounts suggesting that background levels of ozone entering southern California from the Pacific Ocean are similar to those in northern California. Two inland locations (Yreka and Lassen Volcanic National Park) in northern California with surface ozone data records of 20 years or more are more difficult to interpret because of possible influences of local or regional changes. They show differing results for the long-term trend during the spring. The 10-year ozone vertical profile measurements obtained with weekly ozonesondes at Trinidad Head show no significant longer-term change in tropospheric ozone.     

制取高浓度臭氧水的实验研究

采用介质阻挡强电离放电技术制取高浓度臭氧 ,使用射流器和气液溶解分离器溶解臭氧制取高浓度臭氧水。讨论了应用臭氧量、气液比、系统压力和气液溶解方式对臭氧水浓度和臭氧有效溶解效率的影响     

柴油机微粒捕集器臭氧再生法离线再生

由R175型柴油机、微粒捕集器(Φ90 mm×150 mm)、CF-G10型臭氧发生器组成实验系统,进行了臭氧再生法离线再生研究。研究表明,在190℃温度下,再生气从DPF上游侧进气再生时,臭氧可以有效再生DPF,再生效率可达90%以上,再生效率达到65%左右时发生臭氧穿透,臭氧利用率下降;穿透时间点随微粒捕集时的柴油机载荷增大而提前,随微粒捕集时间增加而提前;臭氧供给量不变,再生气流量越大,再生效果越明显;再生气从DPF下游侧进气再生时,臭氧穿透时间点较上游侧进气再生滞后,但发生穿透后DPF几乎不再再生,总再生效率低于70%。结果表明,微粒捕集器臭氧再生法是可行的,对于如何提高臭氧利用率需进一步研究。     

Mediterranean rural ozone characteristics around the urban area of Athens

A systematic analysis of surface ozone observations in rural areas surrounding Athens is presented. The analysis is based on ozone data for the rural station Aliartos about 80 km NW of Athens center and for two stations on the northern periphery of the Athens basin: Demokritos, located 10 km NE of Athens center and Liossia, 12 km to the north. The data for these two stations are screened for cases of strong air flow from rural areas. Average hourly summer afternoon ozone mixing ratios are similar for all three stations about 60 ppb and thus exceed for the hours 12:00–20:00 LST the 55 ppb WHO guideline for human health for 8 h ozone exposure. The corresponding winter afternoon mixing ratios are at 35 ppb. However, due to the large diurnal variation, mean monthly ozone mixing ratios at Aliartos, for the months April–September vary from 32 to 40 ppb, which is comparable to the higher average ozone levels at rural stations in south-central Europe. In cases of southerly air flow in the summer in the Athens basin, afternoon ozone levels at Demokritos and Liossia are generally the highest of any in the monitoring network. Hourly average concentrations, however, are only 40% greater than rural values. A background ozone level of such magnitude will have a significant impact on estimates for the effectiveness of pollution control measures for Athens.     

Ozone patterns for three metropolitan statistical areas in North Carolina, USA

As part of an effort by the state of North Carolina to develop a State Implementation Plan (SIP) for 1-h peak ozone control, a network of ozone stations was established to monitor surface ozone concentrations across the state. Between 19 and 23 ozone stations made continuous surface measurements between 1993 and 1995 surrounding three major metropolitan statistical areas (MSAs): Raleigh/Durham (RDU), Charlotte/Mecklenburg (CLT), and Greensboro/High Point/Winston-Salem (GSO). Statistical averages of the meteorological and ozone data were performed at each Metropolitan Statistical Area (MSA) to study trends and/or relationships on high ozone days (days in which one of the MSA sites measured an hourly ozone concentration90.0 ppbv). County emission maps of precursor gases, wind roses, total area averages of ozone, total downwind averages of ozone deviations, upwind averages of ozone, and a modified delta ozone analysis were all obtained and analyzed. The results of this study show a reduction in the delta ozone relative to an earlier study at RDU, but no average significant change at CLT (no comparison can be made for GSO). The statistical data analyses in this study are used to quantify the importance of local contributions and regional transport, to ozone air pollution in the MSAs.     

强电离放电产生臭氧等离子体过程及其应用研究

电子从强电场 (>30 0Td)放电过程中取得的平均能量大于 8.4eV ;促使氧分子分解、分解电离成高浓度的氧原子、氧原子离子 ,从而产生高浓度 (>2 0 0 g/Nm3 )臭氧 ,实现了用电离放电电场的物理量控制臭氧产生浓度、产生效率及臭氧分解速率 ,并实现臭氧产生装置小型化。极大地拓宽了臭氧在环境工程领域上的应用     

炼油厂含油冷却水处理回用技术研究

开展了O3 氧化和强碱性阴离子交换组合工艺用于炼油厂含油冷却水回用处理的实验研究。结果表明 ,O3 氧化过程中的最佳pH值约为 10 .5 ,O3 氧化的除油效率为 86 .7% (紫外法测定 ) ,去除 1mg石油类约需消耗 5 .7mgO3 ,O3 氧化后产物以乙酸和丙酸等挥发性脂肪酸为主。离子交换处理后油的含量达到未检出的水平。研究结果表明 ,O3 氧化和离子交换组合处理技术能使炼油厂含油冷却水达到回用水水质标准。     

Modelling critical levels of ozone for the forested area of austria modifications of the aot40 concept

GOAL, SCOPE AND BACKGROUND: Ozone is the most important air pollutant in Europe for forest ecosystems and the increase in the last decades is significant. The ozone impact on forests can be calculated and mapped based on the provisional European Critical Level (AOT40 = accumulated exposure over a threshold of 40 ppb, 10,000 ppb x h for 6 months of one growing season calculated for 24 h day(-1)). For Norway spruce, the Austrian main tree species, the ozone risk was assessed in a basis approach and because the calculations do not reflect the health status of forests in Austria, the AOT40 concept was developed. METHODS: Three approaches were outlined and maps were generated for Norway spruce forests covering the entire area of Austria. The 1st approach modifies the AOT40 due to the assumption that forests have adapted to the pre-industrial levels of ozone, which increase with altitude (AOTalt). The 2nd approach modifies the AOT40 according to the ozone concentration in the sub-stomata cavity. This approach is based on such factors as light intensity and water vapour saturation deficit, which affect stomatal uptake (AOTsto). The 3rd approach combines both approaches and includes the hemeroby. The pre-industrial ozone level approach was applied for autochthonous ('natural') forest areas, the ozone-uptake approach for non-autochthonous ('altered') forest areas. RESULTS AND DISCUSSION: The provisional Critical Level (AOT40) was established to allow a uniform assessment of the ozone risk for forested areas in Europe. In Austria, where ozone risk is assessed with utmost accuracy due to the dense grid of monitoring plots of the Forest Inventory and because the continuously collected data from more than 100 air quality measuring stations, an exceedance up to the five fold of the Critical Level was found. The result could lead to a yield loss of up to 30-40% and to a severe deterioration in the forest health status. However, the data of the Austrian Forest Inventory and the Austrian Forest Damage Monitoring System do not reflect such an ozone impact. Therefore, various approaches were outlined including the tolerance and avoidance mechanisms of Norway spruce against ozone impact. Taking into consideration the adaptation of forests to the pre-industrial background level of ozone, the AOT40 exceedances are markedly reduced (1st approach). Taking into account the stomatal uptake of ozone, unrealistic high amounts of exceedances up to 10,000 ppb x h were found. The modelled risk does not correspond with the health status and the wood increment of the Austrian forests (2nd approach). Consolidating the forgoing two approaches, a final map including the hemeroby was generated. It became clear that the less natural ('altered') forested regions are highly polluted. This means, that more than half of the spruce forests are endangered by ozone impact and AOT40 values of up to 30,000 ppb x h occur (3rd approach). CONCLUSIONS: The approaches revealed that a plausible result concerning the ozone impact on spruce forests in Austria could only be reached by combining pre-industrial ozone levels, ozone flux into the spruce needles and the hemeroby of forests.