超临界锅炉中T23管内氧化皮的生成及剥落机理研究

通过对超临界锅炉中T23管内氧化皮检查和剥落物取样，利用能量色散谱仪和X射线衍射仪对其进行试验研究。分析了T23管内氧化皮的成分和结构特征，阐述了氧化皮生成和剥落机理及其影响因素，并提出了防治氧化皮大面积脱落的措施，为减轻超临界锅炉高温受热面管内氧化皮的生成，避免超温爆管等提供了一定的基础。     

超临界锅炉受热面管内氧化皮的防治措施研究

目前，超临界锅炉受热面管内氧化皮生成、脱落的防治一直是国内外安全生产的技术难题。针对锅炉受热面管内氧化皮的生成、脱落的成因及其造成的安全隐患进行了详细分析，并结合多年的生产实践经验，配合实例介绍了相应的防治措施，对同类电厂超临界锅炉受热面管内氧化皮的处理提供了一定参考。     

关于进口氧化皮分级管理的可行性探讨

结合进口氧化皮的检验结果、实际作用和监管情况等,论述了对进口氧化皮进行分级管理的必要性和可行性.     

用铁泥制氧化铁红

研究了以染化厂废料铁泥和工业废硫酸为原料,采用高温干法制取氧化铁红的工艺,简要介绍了该法生产氧化铁红的反应机理,探讨了氧化剂,氧化时间,氧化温度等对产品质量的影响,确定了适宜工艺条件,提出了工业生产流程和尾气治理方案。     

不锈钢酸洗过程中NOx的产生机制及控制

为降低奥氏体不锈钢混酸(HNO_3+HF)酸洗过程中产生的NO_x量,利用自制的酸洗-吸收装置研究了HNO_3和HF质量浓度及抑制剂和促进剂加入量对NO_x生成量的影响,探讨了NO_x的产生机制。结果表明,奥氏体不锈钢酸洗的优化工艺条件为:酸洗温度20～50℃,HNO_3质量浓度90～110 g/L,HF质量浓度40 g/L,抑制剂加入量30 g/L,促进剂加入量1～2 g/L。抑制剂的加入降低了NO_x的生成量,促进剂的加入减少了氧化皮酸洗时间,提高了酸洗效率。酸洗产生的NO_x来源于两部分:一是氧化皮与酸洗液反应,约占NO_x生成量的70%,二是裸露基体与酸洗液反应,约占NO_x生成量的30%。     

TiO_2纳米管阵列的制备及光催化性能的研究进展

阐述了阳极氧化法制备TiO2纳米管阵列的机理,分析了制备过程中电解液组成、电解液pH、阳极氧化电压、氧化时间、热处理温度及其他操作条件对所制备的TiO2纳米管阵列结构的影响,介绍了能够提高TiO2纳米管阵列催化降解污染物效果的各种手段,并针对目前存在的问题对今后的研究发展提出展望。     

用电化学氧泵调节氧含量测定TOD的方法

采用高温催化氧化、电化学氧泵供氧、半导体致冷、高温固体电解质检测器等新技术测定 TOD,具有氧化效率高、氧量稳定可调、除湿效果好、检测范周广、灵敏度高等特点。该法可为废水处理工艺控制及环境水质监测提供综合性的分析数据。     

高级氧化法处理抗生素废水研究进展

针对抗生素废水的处理,详细阐述了芬顿氧化法、光催化氧化法、电化学氧化法、电催化氧化法、低温等离子体法等各种高级氧化法的机理及效果,对比分析了各种处理方法的优缺点,指出了目前抗生素废水处理方法存在的问题,并对抗生素废水处理技术的未来发展进行了展望。     

高级氧化技术再生吸附剂的研究进展

对高级氧化技术再生吸附剂的研究现状进行了综述,重点介绍了光催化氧化技术、Fenton氧化技术、活化过硫酸盐氧化技术和臭氧氧化技术4种方法再生吸附剂的应用,分析了4种氧化技术用于吸附剂再生的机理,指出了各种再生方法存在的不足,并对后续的研究方向进行了展望。     

有机氯废料的回收利用和净化处理方法

介绍了有机氯废料回收利用和净化处理的几种方法,着重介绍了低温等离子流法、氢化法、高温氯化法、火焰氧化法的工艺原理和工艺过程。     

Technology review and evaluation of different chemical oxidation conditions on treatability of PFAS

Per‐ and polyfluoroalkyl substances (PFAS) are a class of stable compounds widely used in diverse applications. These emerging contaminants have unique properties due to carbon–fluorine (C–F) bonds, which are some of the strongest bonds in chemistry. High energy is required to break C–F bonds, which results in this class of compounds being recalcitrant to many degradation processes. Many technologies studied that have shown treatment effectiveness for PFAS cannot be implemented in situ. Chemical oxidation is a demonstrated remediation technology for in situ treatment of a wide range of organic environmental contaminants. An overview of relevant literature is presented, summarizing the use of single or combined reagent chemical oxidation processes that offer insight into oxidation–reduction chemistries potentially capable of PFAS degradation. Based on the observations and results of these studies, bench‐scale treatability tests were designed and performed to establish optimal conditions for the formation of specific free radical species, including superoxide and sulfate radicals, via various combinations of oxidants, catalysts, pH buffers, and heat to assess PFAS treatment by chemical oxidants. The study also suggests the possible abiotic transformations of some PFAS when chemical oxidation is or was used for treatment of primary organic contaminants (e.g., petroleum or chlorinated organic compounds) at a site. The bench‐scale tests utilized field‐collected samples from a firefighter training area. Much of the available data related to chemical oxidation of PFAS has only been reported for one or both of the two more commonly discussed PFAS (perfluorooctane sulfonic acid and/or perfluorooctanoic acid). In contrast, this treatability study evaluates oxidation of a diverse list of PFAS analytes. The results of this study and published literature conclude that heat‐activated persulfate is the oxidation method with the best degradation of PFAS. Limited reduction of reported PFAS concentrations in this study was observed in many oxidation reactors; however, unknown mass of PFAS (such as precursors of perfluoroalkyl acids) that cannot be identified in a field collected sample complicated quantification of how much oxidative destruction of PFAS actually occurred.     

Aerobic in situ stabilization of Landfill Konstanz Dorfweiher: Leachate quality after 1 year of operation

Modern landfill understanding points out controlled operation of landfills. Emissions from landfills are caused mainly by anaerobic biodegradation processes which continue for very long time periods after landfill closure. In situ landfill stabilization aims controlled reduction of emissions towards reduced expenditures as well as aftercare measures. Since April 2010, a new in situ stabilization technique is being applied at a pilot scale landfill (BAIV) within Landfill Konstanz Dorfweiher. This new method utilizes intermittent aeration and leachate recirculation for waste stabilization. In this study, influence of this technique on leachate quality is investigated. Among many other parameters, leachate analyses were conducted for COD, BOD₅, NH₄–N, NO₂–N, NO₃–N, TKN and chloride besides continuously on site recorded pH, electrical conductivity and oxidation–reduction potential (ORP). Results from leachate quality analyses showed that biological activity in the landfill was accelerated resulting in initial higher leachate strength and reduced emission potential of landfill. During full scale in situ aeration, ambient conditions differ from optimized laboratory scale conditions which mainly concern temperature increase and deficient aeration of some landfill parts (Ritzkowski and Stegmann, 2005). Thus, as a field application results of this study have major importance on further process optimization and application.     

Investigations on enhanced in situ bioxidation of methane from landfill gas (LFG) in a lab-scale model

The performance of an exogenous bacterium, Methylobacterium extorquens, in inducing bioxidation of methane from landfill gas (LFG) was assessed in a laboratory scale bioreactor. The study show that enhanced oxidation of methane is attained when the bacteria are introduced into the landfill soil. The maximum percentage reduction of methane fraction from LFG when the bioreactor was inoculated with the methanotrophic bacteria was 94.24 % in aerobic treatment process and 99.97 % in anaerobic process. In the experiments with only the indigenous microorganisms present in the landfill soil, the maximum percentage reduction of methane for the same flow rate of LFG was 59.67 % in aerobic treatment and 45 % in anaerobic treatment. The methane oxidation efficiency of this exogenous methanotrophic bacterium can be considered to be the optimum in anaerobic condition and at a flow rate of 0.6 L/m²/min when the removal percentage is 99.95 %. The results substantiate the use of exogenous microorganisms as potential remediation agents of methane in LFG.     

Bench‐ and pilot‐scale applications of electrochemical peroxidation: A new remedial concept

Electrochemical peroxidation (ECP) is a proprietary process that utilizes sacrificial iron electrodes and stochiometrically balanced applications of hydrogen peroxide to efficiently destroy aqueous phase contaminants. In laboratory trials it has been successful in reducing, often to non‐detectable levels, BTEX, fuel additives, chlorinated solvents, and polychlorinated biphenyls in ground waters. The process has also been found effective in reducing the chemical and biological oxygen demand of industrial waste water. Agency‐approved pilot tests will be conducted at two gasoline spill sites during 2000 where traditional pump and treat methods have proven ineffectual because of ground water chemistry or subsurface hydrologic conditions. The ECP process utilizes a tripartite treatment strategy consisting of 1) ex situ chemical oxidation; 2) in situ oxidation by reinjection of treated water with residual oxidants at the head of the plume; and 3) reestablishment of aerobic biodegradation by alteration of subsurface redox conditions. In contrast to other in situ oxidation treatment methods, dissolved iron is derived electrochemically, negating the need for ferrous salt addition. Dilute hydrogen peroxide (3 percent) is incrementally added to maximize oxidation efficiency and eliminate safety and environmental concerns accompanying the use of highly concentrated solutions. Results of laboratory trials and the geological and geochemical considerations of upcoming pilot‐scale applications are presented. Other potential applications currently under investigation include combination with other remedial processes (e.g. permeable barriers and hydrogen release compounds) to insure complete and rapid contaminant mineralization.     

Temporal variability of soil gas composition in landfill covers

In order to assess the temporal variability of the conditions for the microbial oxidation of methane in landfill cover soils and their driving variables, gas composition at non-emissive and strongly emissive locations (hotspots) was monitored on a seasonal, daily and hourly time scale on an old, unlined landfill in northern Germany. Our study showed that the impact of the various environmental factors varied with the mode of gas transport and with the time scale considered. At non-emissive sites, governed by diffusive gas transport, soil gas composition was subject to a pronounced seasonal variation. A high extent of aeration, low methane concentrations and a high ratio of CO₂ to CH₄ were found across the entire depth of the soil cover during the warm and dry period, whereas in the cool and moist period aeration was less and landfill gas migrated further upward. Statistically, variation in soil gas composition was best explained by the variation in soil temperature. At locations dominated by advective gas transport and showing considerable emissions of methane, this pattern was far less pronounced with only little increase in the extent of aeration during drier periods. Here, the change of barometric pressure was found to impact soil gas composition. On a daily scale under constant conditions of temperature, gas transport at both types of locations was strongly impacted by the change in soil moisture. On an hourly scale, under constant conditions of temperature and moisture, gas migration was impacted most by the change in barometric pressure. It was shown that at diffusion-dominated sites complete methane oxidation was achieved even under adverse wintry conditions, whereas at hotspots, even under favorable dry and warm conditions, aerobic biological activity can be limited to the upper crust of the soil.     

Use of Oxidation Onset Temperature Measurements for Evaluating the Oxidative Degradation of Isotatic Polypropylene

The widespread use of polymeric materials in many applications requires polymers that are weather resistant. The aim of this study is to examine the usefulness of oxidation onset temperature measurements as a tool for evaluating oxidative degradation of isotatic polypropylene. Differential scanning calorimetry was used to measure the oxidation onset temperature in formulations of isotatic polypropylene containing different concentrations of light and thermal stabilizers after aging in a Weather-Ometer. Oxidation onset temperature gave better results than oxidation induction time for evaluating the degradation of isotatic polypropylene during aging in a Weather-Ometer. However, both tests showed a poor correlation with the appearance of cracks seen by optical microscopy.     

Mitigation of methane emission from Fakse landfill using a biowindow system

Landfills are significant sources of atmospheric methane (CH₄) that contributes to climate change, and therefore there is a need to reduce CH₄ emissions from landfills. A promising cost efficient technology is to integrate compost into landfill covers (so-called “biocovers”) to enhance biological oxidation of CH₄. A full scale biocover system to reduce CH₄ emissions was installed at Fakse landfill, Denmark using composted yard waste as active material supporting CH₄ oxidation. Ten biowindows with a total area of 5000 m² were integrated into the existing cover at the 12 ha site. To increase CH₄ load to the biowindows, leachate wells were capped, and clay was added to slopes at the site. Point measurements using flux chambers suggested in most cases that almost all CH₄ was oxidized, but more detailed studies on emissions from the site after installation of the biocover as well as measurements of total CH₄ emissions showed that a significant portion of the emission quantified in the baseline study continued unabated from the site. Total emission measurements suggested a reduction in CH₄ emission of approximately 28% at the end of the one year monitoring period. This was supported by analysis of stable carbon isotopes which showed an increase in oxidation efficiency from 16% to 41%. The project documented that integrating approaches such a whole landfill emission measurements using tracer techniques or stable carbon isotope measurements of ambient air samples are needed to document CH₄ mitigation efficiencies of biocover systems. The study also revealed that there still exist several challenges to better optimize the functionality. The most important challenges are to control gas flow and evenly distribute the gas into the biocovers.     

Scrutinizing compost properties and their impact on methane oxidation efficiency

Methane emissions from active or closed landfills can be reduced by means of microbial methane oxidation enhanced by properly designed landfill covers and engineered biocovers. Composts produced using different waste materials have already been proven to support methane oxidation, and may represent a low-cost alternative to other suitable substrates such as sandy or humic-rich soils, which are frequently not available in sufficient amounts or are too costly. In the present study a data set of 30 different compost materials (different age and input materials) and mixtures, as well as seven soils and mineral substrates were tested to assess methane oxidation rate under similar conditions in a laboratory column set-up. Multivariate data analysis (discriminant analysis) was applied to predict the influence of 21 different parameters (chemical, maturation and physical) on methane oxidation rate in a PLS-DA model. The results show that bulk density, total nutrient content (nitrogen and phosphorus), as well as the quantity and quality (with respect to maturity) of organic matter determined methane oxidation rate in this data set. The model explained 50% of the data variation, indicating how characterisation of oxidation rate by single, even diverse conventional parameters was limited. Thus for the first time, Fourier Transform Infrared (FTIR) spectroscopy was applied to a series of samples to better determine the characteristics of methane-oxidising materials. The initial data obtained in this study appear to be most promising. The prediction of specific methane oxidation rate of a potential biocover material from FTIR spectra and multivariate data analyses is a target to be focused on in the future.     

强化二氧化钛光催化氧化技术的研究进展

光催化氧化技术被认为是在环境保护领域内一项有前途的新型高级氧化技术,其他污染治理技术强化光催化氧化成为污水处理和废气净化的一个研究热点。介绍了国内外其他污染治理技术——化学法、物理化学法、生物法强化二氧化钛光催化氧化技术的研究和应用现状,分析了这些技术的强化光催化氧化机理,并对其今后的发展前景进行了展望。     

高级氧化技术降解环烷酸的研究进展

针对原油及油砂洗脱废水中的环烷酸所具有的酸性、毒性、腐蚀性等特点，介绍了多种降解环烷酸的高级氧化技术，包括Fenton氧化法、臭氧氧化法、光催化氧化法、超临界氧化法、微波辐照法等。评述了高级氧化技术降解环烷酸的最新进展和发现，分析了各种技术的处理效果，并总结了各种技术的优缺点。最后，提出了处理石油行业环烷酸废水的一些思路，为现阶段石油行业环烷酸废水的处理提供了参考。