序列间歇式好氧活性污泥法处理生物制药废水研究

本研究采用好氧ＳＢＲ法处理生物制药废水。试验结果表明，废水中不需另加氮磷营养物质，当进水ＣＯＤＣｒ为９１１～３２８０ｍｇ／Ｌ时，在曝气１６ｈ条件下，出水ＣＯＤＣｒ在３５０ｍｇ／Ｌ以下，ＢＯＤ５在８０ｍｇ／Ｌ以下，ＳＳ在１５０ｍｇ／Ｌ以下，皆达到生物制药工业废水二级排放标准。本文还对好氧ＳＢＲ法的有机物降解动力学过程进行了研究。     

Effect of catalyzed diesel particulate filter and its catalyst loading on emission characteristics of a non-road diesel engine

In this study, the effects of a diesel oxidation catalyst (DOC) coupled with a catalyzed diesel particulate filter (CDPF) with different catalyst loadings on the power, fuel consumption, gaseous and particulate emissions from a non-road diesel engine were investigated. Results showed that the after-treatment had a negligible effect on the power and fuel consumption. The reduction effect of the DOC on the CO and hydrocarbon (HC) increased with the engine load. Further reductions occurred coupling with the CDPF. Increasing the catalyst loading resulted in a more significant reduction in the HC emissions than CO emissions. The DOC could increase the NO₂ proportion to 37.9%, and more NO₂ was produced when coupled with the CDPF below 250°C; above 250°C, more NO₂ was consumed. The after-treatment could reduce more than 99% of the particle number (PN) and 98% of the particle mass (PM). Further reductions in the PN and PM occurred with a higher CDPF catalyst loading. The DOC had a better reduction effect on the nucleation particles than the accumulation ones, but the trend reversed with the CDPF. The DOC shifted the particle size distribution (PSD) to larger particles with an accumulation particle proportion increasing from 13% to 20%, and the geometric mean diameter (GMD) increased from 18.2 to 26.0 nm. The trend reversed with the CDPF and the accumulation particle proportion declined to less than 10%. A lower catalyst loading on the CDPF led to a higher proportion of nucleation particles and a smaller GMD.     

Comparison of UV-based advanced oxidation processes for the removal of different fractions of NOM from drinking water

This study examined the effectiveness for degradation of hydrophobic (HPO), transphilic (TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H₂O₂, UV/TiO₂ and UV/K₂S₂O₈ (UV/PS) advanced oxidation processes (AOPs). The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC), the specific UV absorbance (SUVA), trihalomethanes formation potential (THMFP), organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs). In the three UV-based AOPs, HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI, and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction. In terms of the specific THMFP of HPO, TPI and HPI, a reduction was achieved in the UV/H₂O₂ process, and the higest removal rate even reached to 83%. UV/TiO₂ and UV/PS processes can only decrease the specific THMFP of HPI. The specific AOXFP of HPO, TPI and HPI fractions were all able to be degraded by the three UV-based AOPs, and HPO content is more susceptible to decompose than TPI and HPI content. UV/H₂O₂ was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions. C1 (microbial or marine derived humic-like substances), C2 (terrestrially derived humic-like substances) and C3 (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment. C3 of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs. Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.     

非溶解态胡敏酸对土壤中硬碳有机质解吸多环芳烃的影响

土壤有机碳是控制土壤中多环芳烃的吸附解吸及其生物有效性的主要因素之一,土壤中硬碳类吸附剂是土壤有机碳中的重要部分,土壤中软碳类物质和硬碳类物质的相互作用对研究土壤中多环芳烃的解吸行为和生物有效性有重要影响。研究将溶解有机质胡敏酸,通过条件的变化使其转变为非溶解态,研究其对土壤碳质吸附剂(胡敏素和黑碳)吸附多环芳烃的解吸行为的影响。研究结果表明:非溶解态胡敏酸会显著降低土壤硬碳类物质中多环芳烃的解吸能力,解吸滞后性增加,作者认为非溶解态胡敏酸的添加会覆盖土壤硬碳类物质的表面吸附位点和填充吸附多环芳烃的孔隙,造成硬碳类有机质中的多环芳烃解吸能力下降,滞后性增强。研究还发现硬碳类有机质的比表面积和孔隙度和解吸能力的变化强度呈正相关关系。     

Oil/Suspended Particulate Material Interactions and Sedimentation

The interactions of physically dispersed oil droplets with suspended particulate material (SPM) can be important for the transport of bulk quantities of spilled crude oil and polycyclic aromatic hydrocarbons (PAH) to subtidal sediments. The literature regarding oil/SPM interactions is reviewed, and results from whole-oil droplet/SPM interaction kinetics and pure-component (Prudhoe Bay crude oil distillate cut) equilibrium partitioning experiments are presented. The effects of oil type, SPM characteristics, and salinity on the interaction rates are examined, and the importance of whole-oil droplet/SPM interactions on particle agglomeration and settling behavior are discussed. Whole-oil droplet/SPM interactions are retarded as oil droplet dispersion into the water column is inhibited by oil viscosity increases due to evaporation weathering and water-in-oil emulsification. Compared to whole oil droplet/SPM interactions, dissolved-component/SPM adsorption is not as significant for transport of individual components to sediments. The information presented in this paper can be used to augment computer-based models designed to predict oil-spill trajectories, oil-weathering behavior, and spilled oil impacts to the marine environment.     

铁合金电炉烟尘治理技术分析

本文在分析了半封闭铁合金电炉产生的烟气、烟尘的特性和各种除尘设备性能的基础上，提出了净化铁合金电炉烟尘的三种技术：袋式除尘、强化湿式除尘和文丘里除尘器。并对袋式除尘工艺和Calvert洗涤器除尘工艺作了介绍，分析了它们的经济技术指标。半封闭铁合金电炉烟尘只能采用布袋除尘器净化，只有那些建在环境空气质量三类区的铁合金电炉，当资金非常紧缺时，才可采用Cavlert洗涤器除尘。     

多目标灰色关联度决策模型分析

本文针对多目标决策的复杂性,运用灰色系统分析方法和物元分析理论,建立了决策方案的评价体系并对评价指标进行规范化处理。以决策方案的灰色关联度作为评判准则,建立了一种目标灰色关联度决策模型。     

物元分析法在大气环境质量评价中的应用

应用物元分析方法构建大气环境质量的综合评价模型，并将该方法用于唐山市大气环境质量评价中，获得了与实际情况基本符合的评价结果。     

除湿机的冷凝水化学成分与空气环境质量的关系

本文采用家用除湿机作为空气水溶性物质采样器方法，并验证了该方法作为空气水溶性物质采样嚣的可行性。本文通过空气冷凝水化学成分与空气总悬浮微粒(TSP)可溶性化学成分的对比，得到水汽中大部分阴阳离子的含量只比TSP低1个数量级，而水汽中的微量元素含量与各种碳的浓度不都比TSP低，TSP中一般检测不出亚硝酸根，而水汽中则检出大量亚硝酸根。     

CO2-free paper?

Black liquor gasification–combined cycle (BLGCC) is a new technology that has the potential to increase electricity production of a chemical pulping mill. Increased electricity generation in combination with the potential to use biomass (e.g. bark, hog fuel) more efficiently can result in increased power output compared to the conventional Tomlinson-boiler. Because the BLGCC enables an integrated pulp and paper mill to produce excess power, it can offset electricity produced by power plants. This may lead to reduction of the net-CO₂ emissions. The impact of BLGCC to offset CO₂ emissions from the pulp and paper industry is studied. We focus on two different plant designs and compare the situation in Sweden and the US. The CO₂ emissions are studied as function of the share of recycled fibre used to make the paper. The study shows that under specific conditions the production of “CO₂-free paper” is possible. First, energy efficiency in pulp and paper mills needs to be improved to allow the export of sufficient power to offset emissions from fossil fuels used in boilers and other equipment. Secondly, the net-CO₂ emission per ton of paper depends strongly on the emission reduction credits for electricity export, and hence on the country or grid to which the paper mill is connected. Thirdly, supplemental use of biomass to replace fossil fuel inputs is important to reduce the overall emissions of the pulp and paper industry.