O3氧化结合化学吸收同时脱硫脱硝的动力学及热力学研究

构建了O3氧化多种污染物的反应机制,并对O3氧化SOx、NOx过程进行动力学模拟,然后利用热力学原理计算出Ca(OH)2和CaCO3湿法烟气同时脱硫脱硝吸收反应达到平衡时SOx和NOx的分压力.结果表明,Ca(OH)2作吸收剂湿法烟气同时脱硫脱硝比CaCO3作吸收剂效果好,而且两者几乎100％地去除烟气中的SOx和NO...     

厌氧膨胀床处理低浓度污水的污泥颗粒和生物活性变化

污泥的聚集形态和活性，是影响厌氧反应器处理效率的关键因素。通过对厌氧膨胀床反应器（anaerobicex—pandedblanketreactor，AEBR）处理低浓度城镇污水在启动和稳定运行期的污泥活性研究，AEBR在启动运行期内，接种颗粒污泥为适应低浓度基质条件，污泥粒径经历从大变小，再重新颗粒化粒径变大的过程。在运行期第103天，粒径小于1000μm污泥的体积比达到44．7％，平均粒径为952μm，到运行期第173天，粒径小于1000μm污泥的体积比降为28％，平均粒径达1179μm，污泥重新颗粒化完成。颗粒污泥适应新的环境后，单位重量污泥的最大比产甲烷活性（specificmetha．nogensisactivity，SMA）值和胞外聚合物含量增加，分别达到112mLCH4／（gVSS·d）和215mg／gVSS。在处理实际城镇污水的AEBR反应器内，辅酶F420含量可以有效指示污泥样品的产甲烷活性，AEBR反应器不同高度位置的污泥活性不一样，反应器底部污泥活性低于中上部区域污泥的活性。     

电渗析在丙烯酸丁酯废水预处理中的应用

采用电渗析法预处理丙烯酸丁酯生产废水,可将废水中的有机酸盐浓缩回收,同时大大降低废水的污染物浓度.重点研究了淡水浓水初始体积比的影响,同时考察了电渗析过程中水的迁移.实验确定了淡水浓水的最佳初始体积比为5∶1,此时对COD为61 650 mg/L的废水,COD去除率可达99.5%,脱盐率在99.5%以上,同时可将废水的...     

Inverse modeling of Asian Rn flux using surface air Rn concentration

When used with an atmospheric transport model, the ²²²Rn flux distribution estimated in our previous study using soil transport theory caused underestimation of atmospheric ²²²Rn concentrations as compared with measurements in East Asia. In this study, we applied a Bayesian synthesis inverse method to produce revised estimates of the annual ²²²Rn flux density in Asia by using atmospheric ²²²Rn concentrations measured at seven sites in East Asia. The Bayesian synthesis inverse method requires a prior estimate of the flux distribution and its uncertainties. The atmospheric transport model MM5/HIRAT and our previous estimate of the ²²²Rn flux distribution as the prior value were used to generate new flux estimates for the eastern half of the Eurasian continent dividing into 10 regions.The ²²²Rn flux densities estimated using the Bayesian inversion technique were generally higher than the prior flux densities. The area-weighted average ²²²Rn flux density for Asia was estimated to be 33.0 mBq m⁻² s⁻¹, which is substantially higher than the prior value (16.7 mBq m⁻² s⁻¹). The estimated ²²²Rn flux densities decrease with increasing latitude as follows: Southeast Asia (36.7 mBq m⁻² s⁻¹); East Asia (28.6 mBq m⁻² s⁻¹) including China, Korean Peninsula and Japan; and Siberia (14.1 mBq m⁻² s⁻¹). Increase of the newly estimated fluxes in Southeast Asia, China, Japan, and the southern part of Eastern Siberia from the prior ones contributed most significantly to improved agreement of the model-calculated concentrations with the atmospheric measurements. The sensitivity analysis of prior flux errors and effects of locally exhaled ²²²Rn showed that the estimated fluxes in Northern and Central China, Korea, Japan, and the southern part of Eastern Siberia were robust, but that in Central Asia had a large uncertainty.     

牡蛎壳生物滤池处理含盐污水中的硝化特性

采用牡蛎壳为曝气生物滤池填料,以含NaCl的生活污水为处理对象,在SBR操作条件下,系统考察进水NaCl浓度、曝气时间及进水pH值等对硝化性能的影响。结果表明,进水NaCl浓度为10~15 g/L时,平均氨氮去除率可稳定在97%以上;较高浓度NaCl对亚硝酸化菌活性影响较弱,对硝酸化菌活性影响较强,特别是在日曝气时间少于12 h时,其出水中亚硝氮的含率大于50%;当进水pH值在6~9变化时,反应器内pH值可稳定在6.5~7.5,硝化性能良好,表明牡蛎壳填料可为硝化反应提供碱度。     

UV/Fenton技术处理某工厂高浓度乳化油废水

研究了UV/Fenton技术对高浓度金属清洗乳化油废水的处理效果,考察了亚铁与双氧水浓度、pH、反应时间和搅拌对COD去除效果的影响。实验结果表明,UV/Fenton技术对高浓度乳化油废水(COD平均浓度为35 000 mg/L)具有较高的去除效果,最佳工艺条件为:亚铁与双氧水浓度分别为2 400 mg/L和6 000 mg/L,pH为3,经过2 h反应,COD可降低至1 050 mg/L,去除率为97%。搅拌会降低COD的去除率。研究表明,UV/Fenton技术对高浓度乳化油废水具有很好的降解效果,且药品消耗较低,为目前此类高浓度有机废水的处理提供了技术参考。     

MBR在橡胶废水处理中的应用

橡胶废水具有含盐量高、色度高、有机污染成分含量高且难于生化降解等特点。膜生物反应器(MBR)技术的核心是生化处理加微滤膜过滤,通过将MBR技术应用于橡胶废水处理的实践表明,该技术对COD、氨氮、磷酸盐的平均去除率都达到了85%以上,再辅之以药剂处理后,降低了色度和难降解有机物含量,出水水质完全符合排放标准的要求,是一种解决橡胶污水处理难题的有效途径。     

臭氧同时脱硫脱硝技术研究进展

对利用臭氧同时脱硫脱硝技术进行了综述，分析了臭氧对NOx的脱除机理。臭氧同时脱硫脱硝技术具有明显的一体化脱除特性，但臭氧的发生费用却制约了它的应用。介绍了目前国外在工程上应用的低温氧化技术（LOTOX），分析了其脱除效果及优缺点。     

The effect of alkyl chain length on the degradation of alkylimidazolium- and pyridinium-type ionic liquids in a Fenton-like system

Background, aim, and scope  Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them, the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride. Materials and methods  The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide. All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with the aid of ¹H NMR. Results  Degradation of ionic liquids in this system was quite effective. Increasing the H₂O₂ concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance to degradation was weaker, the shorter the alkyl chain. Discussion  The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Conclusions  The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium chloride when the resistance of imidazolium ionic liquids decreases with increasing H₂O₂ concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Recommendations and perspectives  Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the future structural design as well as tailor the technological process of these chemicals     

沿面放电氧化液相亚硫酸铵

为了解决湿式氨法烟气脱硫生成不稳定亚硫酸铵（（NH4）2SO3）副产物的问题,设计了以不锈钢弹簧和溶液分别作为高压和低压电极的沿面放电系统,对液相（NH4）2SO3的氧化进行了研究。空气从反应器上方进入后经放电区域形成活性物质,再由底部的曝气头鼓入溶液并与（NH4）2SO3发生反应。比较了沿面放电处理与传统曝气处理的氧化效率,考察了放电电压、载气气量和初始浓度等因素对（NH4）2SO3氧化的影响。结果表明,沿面放电对（NH4）2SO3有显著的氧化效果;优化条件下的（NH4）2SO3氧化率接近100%;溶液中（NH4）2SO4与（NH4）2SO3的浓度比小于1时有利于（NH4）2SO3的氧化。