电子束深度氧化烟气净化技术

介绍电子束烟气净化技术的特点，对传统电子束法与深度氧化法的反应原理、工艺流程进行了比较及分析，实验结果表明，电子束深度氧化烟气净化技术能耗低、可靠性高，是一种具有广阔工业应用前景的环保新技术。     

电子束半干法烟气净化技术

电子束烟气净化技术由于能够同时脱除烟气中的SO2 和NOx 而得到世界各国环保界的重视。传统的电子束烟气净化技术在工业应用中存在能耗高、副产品黏结严重、工作可靠性低等问题。新型电子束半干法烟气净化技术解决了传统工艺在工业化应用中存在的问题 ,可以在较小的辐照剂量下获得更为理想的烟气净化效果 ,提高了系统的工作可靠性 ,是一项工业应用前景十分广阔的环保技术。     

电子束半干法烟气净化技术

电子束烟气净化技术由于能够同时脱除烟气中的SO2和NOx而得到世界各国环保界的重视,传统的电子束烟气净化技术在工业应用中存在能耗高,副产品黏结严重,工作可靠性低等问题,新型电子束半干法烟气净化技术解决了传统工艺在工业化应用中存在的问题,可以在较小的辐射剂量下获得更为理想的烟气净化效果,提高了系统的工作可靠性,是一项工业应用前景十分广阔的环保技术.     

面向废水深度净化的氧化石墨烯膜过滤技术

膜过滤技术作为一种高效、低能耗、二次污染少的技术,已广泛用于工业废水的深度净化与再生中。传统有机膜在工业废水深度净化处理中存在着耐氧化性不足、使用条件苛刻、膜污染控制困难等问题。同时,膜过滤过程中产生的有机物/无机盐混合浓水也阻碍了浓水的资源化利用。氧化石墨烯膜作为下一代的膜材料具有更好的耐氧化性、亲水性,且制备成本低廉,对有机物与无机盐的分离性能优异,有望在工业废水的深度净化与回用中得到广泛应用。在阅读文献资料的基础上,梳理了氧化石墨烯膜的制备、性能特点,采用氧化石墨烯膜过滤技术进行工业废水深度净化的研究现状及尚待解决的问题,如材料的稳定性能及膜污染控制等。最后指出氧化石墨烯膜过滤技术在未来应逐步实现应用放大,并在工业废水深度净化、实现水与资源回用,达到近"零排放"的水处理过程中发挥重要作用。     

烟气中多种污染物协同脱除的研究

烟气中多种污染物协同脱除是烟气净化领域的研究热点.在现有烟气脱硫技术研究的基础上,对活性焦干法、多级增湿半干法、氧化性添加剂湿法以及等离子体湿法这4种烟气污染物协同脱除技术进行了系统的研究.研究发现,以活性焦为载体添加适当的催化剂能够实现在高效脱硫基础上的同时脱硝;多级增湿半干法技术提高了脱硫剂颗粒在吸收塔内反应全过程的含湿均匀性,通过添加复合促进剂可以提高反应速率,强化烟气中SO_2、NO_X等污染物协同脱除;在传统的湿法烟气脱硫技术中,向脱硫剂中加入KMnO_4和NaClO_2等强氧化剂或者采用等离子体前置氧化,能够有效的将难吸收的NO氧化成NO_2、HNO_2和HNO_3,最终实现同时脱硫脱硝.     

中国燃煤锅炉烟气脱硫技术的发展前景

本文在综述我国燃煤中小型锅炉和电站锅炉烟气脱硫技术现状的基础上，分析了我国燃煤锅炉烟气脱硫技术的发展前景．分析结果指出：我国中小型燃煤锅炉烟气脱硫技术近期是以完善湿法脱硫技术为主，远期将大力发展干法脱硫技术；在电站锅炉烟气脱硫方面，规模较小的电站锅炉将以喷雾干燥法为主要发展方向，大型电站锅炉近期仍以湿式石灰石－石膏法为主，远期将大力发展电子束辐照氨法脱硫脱硝技术。     

铝电解烟气净化工程通过技术鉴定

中国有色金属工业总公司于1988年11月16日在山东铝厂召开了技术鉴定会,对山东铝厂电解槽烟气净化工程进行技术鉴定。来自院所、厂矿从事环保工作的38名学者、专家参加了鉴定会。山东铝厂电解铝分厂年产金属铝2.7万吨,设有180台60KA旁插自焙电解槽,含氟烟气排放量7000～9000米~3/台·时,电解槽卷帘密闭,上部集气送入烟气净化工程。所采用的湿碱法净化技术有     

电子束净化烟气机理探讨

探讨了电子束法净化电厂烟道气过程中自由粒子的产生以及SO2与NOx的脱除机理。结果表明:SO2的脱除有两条途径——热化学和辐射化学,在当量氨的存在下,热化学起主导作用;脱除NOx的过程则纯粹是辐射诱发的氧化-还原反应。     

高级氧化污泥深度脱水技术研究进展

污泥脱水是污泥处理中的一个重要环节,可以减少污泥容量,削减污泥运输和最终处置费用。基于目前污泥处理中污泥脱水的现状,综述了几种高级氧化法对污泥深度脱水的研究进展,包括臭氧氧化法,Fenton、类Fenton氧化法和过硫酸盐氧化法;并展望了污泥脱水技术的发展与应用前景,以期为高级氧化技术在污泥深度脱水理论研究及工程应用提供技术参考。     

电子束净化烟气机理探讨

探讨了电子束法净化电厂烟道气过程中自由粒子的产生以及SO2与NOx的脱除机理，结果表明：SO2的脱除有两条途径-热化学和辐射化学，在当量氨的存在下，热化学起主导作用，脱除NOx的过程则纯粹是辐射诱发的氧化-还原反应。     

Microwave pretreatment for enhancement of phosphorus release from dairy manure

Both the advanced oxidation process (AOP) using a combination of hydrogen peroxide addition and microwave heating (H2O2/microwave), and the microwave heating process were used for solubilization of phosphorus from liquid dairy manure. About 80% of total phosphate was released into the solution at a microwave heating time of 5 min at 170 degrees C. With an addition of H2O2, more than 81% of total phosphate could be released over a reaction period of 49 h at ambient temperature. The AOP process could achieve up to 85% of total phosphate release at 120 degrees C. The results indicated that both the microwave, and the AOP processes could effectively release phosphate from liquid dairy manure. These processes could serve as pretreatments for phosphorus recovery from animal wastes, and could be combined with the struvite crystallization process to provide a new approach in treating animal wastes.     

Degradation of chelating agents in aqueous solution using advanced oxidation process (AOP)

This article presents an overview with critical analysis of technical applicability of advanced oxidation process (AOP) in removing chelating agents from aqueous solution. Apart from the effect of metals for chelating agents as a major influencing factor, selected information such as pH, oxidant’s dose, concentrations of pollutants and treatment performance is presented. The performance of individual AOP is compared. It is evident from our literature survey that photocatalysis with UV irradiation alone or coupled with TiO₂, ozonation and Fenton’s oxidation are frequently applied to mineralize target pollutants. Overall, the selection of the most suitable AOP depends on the characteristics of effluents, technical applicability, discharge standard, regulatory requirements and environmental impacts.     

Biological assessment of bisphenol A degradation in water following direct photolysis and UV advanced oxidation

Endocrine disrupting compounds (EDCs) are exogenous environmental chemicals that can interfere with normal hormone function and present a potential threat to both environmental and human health. The fate, distribution and degradation of EDCs is a subject of considerable investigation. To date, several studies have demonstrated that conventional water treatment processes are ineffective for removal of most EDCs and in some instances produce multiple unknown transformation products. In this study we have investigated the use of direct photolysis with low-pressure (LP) Hg UV lamps and UV+hydrogen peroxide (H(2)O(2)) advanced oxidation process (AOP) for the degradation of a prototypic endocrine disrupter, bisphenol A (BPA), in laboratory water. Removal rates of BPA and formation of degradation products were determined by high performance liquid chromatography (HPLC) analysis. Changes in estrogenic activity were evaluated using both in vitro yeast estrogen screen (YES) and in vivo vitellogenin (VTG) assays with Japanese medaka fish (Oryzias latipes). Our results demonstrate that UV alone did not effectively degrade BPA. However, UV in combination with H(2)O(2) significantly removed BPA parent compound and aqueous estrogenic activity in vitro and in vivo. Removal rates of in vivo estrogenic activity were significantly lower than those observed in vitro, demonstrating differential sensitivities of these bioassays and that certain UV/AOP metabolites may retain estrogenic activity. Furthermore, the UV/H(2)O(2) AOP was effective for reducing larval lethality in treated BPA solutions, suggesting BPA degradation occurred and that the degradation process did not result in the production of acutely toxic intermediates.     

Microwave Pretreatment for Enhancement of Phosphorus Release from Dairy Manure

Both the advanced oxidation process (AOP) using a combination of hydrogen peroxide addition and microwave heating (H₂O₂/microwave), and the microwave heating process were used for solubilization of phosphorus from liquid dairy manure. About 80% of total phosphate was released into the solution at a microwave heating time of 5 min at 170°C. With an addition of H₂O₂, more than 81% of total phosphate could be released over a reaction period of 49 h at ambient temperature. The AOP process could achieve up to 85% of total phosphate release at 120°C. The results indicated that both the microwave, and the AOP processes could effectively release phosphate from liquid dairy manure. These processes could serve as pretreatments for phosphorus recovery from animal wastes, and could be combined with the struvite crystallization process to provide a new approach in treating animal wastes.     

SARS-CoV-2 pharmaceutical drugs: a critical review on the environmental impacts,chemical characteristics,and behavior of advanced oxidation processes in water

This review summarizes research data on the pharmaceutical drugs used to treat the novel SARS-CoV-2 virus, their characteristics, environmental impacts, and the advanced oxidation processes (AOP) applied to remove them. A literature survey was conducted using the electronic databases Science Direct, Scopus, Taylor & Francis, Google Scholar, PubMed, and Springer. This complete research includes and discusses relevant studies that involve the introduction, pharmaceutical drugs used in the SARS-CoV-2 pandemic: chemical characteristics and environmental impact, advanced oxidation process (AOP), future trends and discussion, and conclusions. The results show a full approach in the versatility of AOPs as a promising solution to minimize the environmental impact associated with these compounds by the fact that they offer different ways for hydroxyl radical production. Moreover, this article focuses on introducing the fundamentals of each AOP, the main parameters involved, and the concomitance with other sources and modifications over the years. Photocatalysis, sonochemical technologies, electro-oxidation, photolysis, Fenton reaction, ozone, and sulfate radical AOP have been used to mineralize SARS-CoV-2 pharmaceutical compounds, and the efficiencies are greater than 65%. According to the results, photocatalysis is the main technology currently applied to remove these pharmaceuticals. This process has garnered attention because solar energy can be directly utilized; however, low photocatalytic efficiencies and high costs in large-scale practical applications limit its use. Furthermore, pharmaceuticals in the environment are diverse and complex. Finally, the review also provides ideas for further research needs and major concerns.

Graphical abstract

     

The degradation of dissolved organic nitrogen associated with melanoidin using a UV/H2O2 AOP

The aim of this study was to examine the simultaneous degradation of dissolved organic nitrogen (DON) and associated colour from wastewater containing melanoidins by an advanced oxidation process (AOP). UV irradiation of H2O2 was used as the mechanism to create the hydroxyl radical for oxidation. Melanoidins are large nitrogenous organic compounds that are refractory during biological wastewater treatment processes. The simultaneous degradation of DON and colour, present as a result of these compounds, was investigated using an AOP. The oxidation process was much more capable of removing colour (99% degradation), dissolved organic carbon (DOC) (50% degradation) and DON (25% degradation) at the optimal applied dose of hydrogen peroxide for the system (3300 mg l(-1)). This indicated that colour and DON removal were decoupled problems for the purpose of treating melanoidin by an AOP and thus colour removal can not be used as an indication of DON removal Colour was caused by organic molecules with molecular weight greater than 10 kDa. Oxidation caused a partial reduction of the DON (41-15% of the total dissolved nitrogen) and DOC (29-14% of the DOC) associated with the large molecular weight fraction (>10 kDa) and almost complete colour removal (87-3% of the total colour). The degraded DON was mostly accounted for by the formation of ammonia (31% of the nitrogen removed from the large fraction) and small molecular weight compounds (66% of the nitrogen removed from the large fraction). The degraded DOC appeared to be mostly mineralised (to CO2) with only 20% of the degraded compounds appearing as small molecular weight DOC.     

Elucidation of the behavior of tannery wastewater under advanced oxidation conditions

Diverse advanced oxidation process (AOP) techniques applying UV, TiO2/UV, O3 and O3/UV were used to degrade pollutants contained in tannery wastewater. The total mineralization of these pollutants is desirable, but it is quite energy consuming and sometimes impossible. Therefore the objective was to achieve an enhancement of biodegradability, preferentially with a decrease in toxicity in parallel. This work demonstrates that the dominant pollutants were chemically degraded by oxidation, while changes in carbon content were only marginal. These results were obtained monitoring the total organic carbon content (TOC), chemical and biochemical oxygen demand (COD and BOD), and substance-specific pollutant content by application of gas chromatography/mass spectrometry (GC-MS) and liquid chromatography/mass spectrometry (LC-MS). Daphnia magna toxicity testing performed in parallel proved a decrease in toxicity after AOP treatment of the tannery wastewater.     

UV-H2O2 based AOP and its integration with biological activated carbon treatment for DBP reduction in drinking water

The presence of disinfection byproducts (DBPs) such as trihalomethanes (THMs) and haloacetic acids (HAAs) in drinking water is of great concern due to their adverse effects on human health. Emerging regulation limiting the concentration of DBPs in drinking water has increased demands for technologies and processes which reduce the formation of DBPs in drinking water. In this study, UV-H₂O₂ based advance oxidation process (AOP) was used to treat raw surface water. Experiments were conducted using low pressure mercury vapor UV lamps in collimated beam and flow-through annular photoreactors. The effect of UV fluence (0–3500 mJ cm⁻²) and hydrogen peroxide concentration (0–23 mg l⁻¹) in reducing the concentration of THMs and HAAs was examined. The UV-H₂O₂ AOP was then coupled with a downstream biological activated carbon (BAC) treatment to assess the synergetic benefits of combining the two treatments. It was observed that UV-H₂O₂ AOP was only effective at reducing DBPs at UV fluences of more than 1000 mJ cm⁻²and initial H₂O₂ concentrations of about or greater than 23 mg l⁻¹. However, the combined AOP–BAC treatment showed significant reductions of 43%, 52%, and 59% relative to untreated raw water for DBPs, TOC, and UV₂₅₄, respectively.     

Computer estimation of the Atmospheric gas-phase reaction rate of organic compounds with hydroxyl radicals and ozone

The Atmospheric Oxidation Program (AOP) is a computer program that estimates the rate constant for the atmospheric, gas-phase reaction between photochemically produced hydroxyl radicals (OH) and organic chemicals. It also estimates the rate constant for the gas-phase reaction between ozone and olefinic/acetylenic compounds. AOP, which uses estimation methods developed by Atkinson and co-workers, estimates more accurate rate constants than the PCFAP (Fate of Atmospheric Pollutants) program that was part of the U.S. EPA's Graphical Exposure Modeling System (GEMS). Due to its superior predictive ability, the EPA is currently using AOP to evaluate the atmospheric fate of compounds defined under Sections 4, 5 and 6 of the Toxic Substances Control Act (TSCA).