好氧+物化组合工艺处理甲醇废水的工程应用研究

通过邳州某二甲醚生产企业的工程实例,介绍了好氧＋物化组合工艺在处理甲醇废水中的应用。该工艺具有处理设施运行稳定、处理效果好的优点,系统出水水质能够达到国家循环冷却水系统补充水水质标准的排放要求,可对二甲醚生产行业的废水处理有一定参考价值。     

生态补偿机制要素、系统结构与概念模型的研究

在系统解析生态补偿机制概念的基础上,深入探讨了生态补偿机制的主体、对象、方式、标准、法律与政策等基本要素和系统结构,构建了包括补偿主体子系统、补偿对象子系统、补偿操作子系统和补偿保障子系统的生态补偿机制概念模型,该模型描述了生态补偿机制的自身运行方式和各个子系统之间的作用关系,最后指出科学构建和成功实践生态补偿机制亟待解决的若干核心问题和难点问题.     

Theoretical versus observed gas-particle partitioning of carbonyl emissions from motor vehicles

A state-of-the-science thermodynamic model describing gas-particle absorption processes was used to predict the gas-particle partitioning of mixtures of approximately 60 carbonyl compounds emitted from low-emission gasoline-powered vehicles, three-way catalyst gasoline-powered vehicles, heavy-duty diesel vehicles under the idle-creep condition (HDDV idle), and heavy-duty diesel vehicles under the five-mode test (HDDV 5-mode). Exhaust was diluted by a factor of 120-580 with a residence time of approximately 43 sec. The predicted equilibrium absorption partitioning coefficients differed from the measured partitioning coefficients by several orders of magnitude. Time scales to reach equilibrium in the dilution sampling system were close to the actual residence time during the HDDV 5-mode test and much longer than the actual residence time during the other vehicle tests. It appears that insufficient residence time in the sampling system cannot uniformly explain the failure of the absorption mechanism to explain the measured partitioning. Other gas-particle partitioning mechanisms (e.g., heterogeneous reactions, capillary adsorption) beyond the simple absorption theory are needed to explain the discrepancy between calculated carbonyl partitioning coefficients and observed partitioning. Both of these alternative partitioning mechanisms imply great challenges for the measurement and modeling of semi-volatile primary organic aerosol (POA) species from motor vehicles. Furthermore, as emitted particle concentrations from newer vehicles approach atmospheric background levels, dilution sampling systems must fundamentally change their approach so that they use realistic particle concentrations in the dilution air to approximately represent real-world conditions. Samples collected with particle-free dilution air yielding total particulate matter concentrations below typical ambient concentrations will not provide a realistic picture of partitioning for semi-volatile compounds.     

Source apportionment of wintertime secondary organic aerosol during the California regional PM10/PM2.5 air quality study

The UCD/CIT air quality model with the Caltech Atmospheric Chemistry Mechanism (CACM) was used to predict source contributions to secondary organic aerosol (SOA) formation in the San Joaquin Valley (SJV) from December 15, 2000 to January 7, 2001. The predicted 24-day average SOA concentration had a maximum value of 4.26 μg m^?3 50 km southwest of Fresno. Predicted SOA concentrations at Fresno, Angiola, and Bakersfield were 2.46 μg m^?3, 1.68 μg m^?3, and 2.28 μg m^?3, respectively, accounting for 6%, 37%, and 4% of the total predicted organic aerosol. The average SOA concentration across the entire SJV was 1.35 μg m^?3, which accounts for approximately 20% of the total predicted organic aerosol. Averaged over the entire SJV, the major SOA sources were solvent use (28% of SOA), catalyst gasoline engines (25% of SOA), wood smoke (16% of SOA), non-catalyst gasoline engines (13% of SOA), and other anthropogenic sources (11% of SOA). Diesel engines were predicted to only account for approximately 2% of the total SOA formation in the SJV because they emit a small amount of volatile organic compounds relative to other sources. In terms of SOA precursors within the SJV, long-chain alkanes were predicted to be the largest SOA contributor, followed by aromatic compounds. The current study identifies the major known contributors to the SOA burden during a winter pollution episode in the SJV, with further enhancements possible as additional formation pathways are discovered.     

Carbon dioxide and methane fluxes in the littoral zones of two lakes,east Antarctica

During the summertime of 2007/2008, carbon dioxide (CO₂) and methane (CH₄) fluxes across air–water interface were investigated in the littoral zones of Lake Mochou and Lake Tuanjie, east Antarctica, using a static chamber technique. The mean fluxes of CO₂ and CH₄ were ?70.8 mgCO₂ m^?2 h^?1 and 144.6 μgCH₄ m^?2 h^?1, respectively, in the littoral zone of Lake Mochou; The mean fluxes were ?36.9 mgCO₂ m^?2 h^?1 and 109.8 μgCH₄ m^?2 h^?1, respectively, in the littoral zone of Lake Tuanjie. Their fluxes showed large temporal and spatial dynamics. The CO₂ fluxes showed a significantly negative correlation with daily total radiation (DTR) and a weakly negative correlation with air temperature and water temperature, indicating that sunlight intensity controlled the magnitude of CO₂ fluxes from the open lakes. The CH₄ fluxes significantly correlated with local air temperature, water table and total dissolved solids (TDS), indicating that they were the predominant factors influencing CH₄ fluxes. Summertime CO₂ budgets in the littoral zones of Lake Mochou and Lake Tuanjie were estimated to be ?152.9 gCO₂ m^?2 and ?79.7 gCO₂ m^?2, respectively, and net CH₄ emissions were estimated to be 312.3 mgCH₄ m^?2 and 237.2 mgCH₄ m^?2, respectively. Our results show that shallow, open, alga-rich lakes might be strong summertime CO₂ absorbers and small CH₄ emitters during the open water in coastal Antarctica.     

微囊藻毒素-LR对鸡肝脏的氧化损伤影响

蓝藻虽然能产生有毒的生物毒素,但是也含有较高的蛋白质。为探索蓝藻饲料化利用的可能性,本文通过腹腔注射的方式研究了微囊藻毒素-LR(MC-LR)对崇仁麻鸡的半数致死剂量(LD_(50))及其对肝脏的氧化损伤。实验设计了4个剂量组(对照组、5、10和20μg·kg~(-1)MC-LR),并在1、3、12、24和48 h检测了谷胱甘肽(GSH)含量以及谷胱甘肽S-转移酶(GST)、谷胱甘肽过氧化物酶(GPX)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性变化。结果表明,MC-LR对崇仁麻鸡的LD_(50)值为34.67μg·kg~(-1)体重(bw),95%的置信限为33.51～35.83μg·kg~(-1)bw。在MC-LR的作用下,鸡肝出现了氧化应激现象。3个染毒组鸡肝中GSH含量呈现先下降而后上升恢复至正常水平的趋势,GST酶活力表现为先上升而后下降至正常值的趋势,这说明GSH和GST共同参与了鸡肝中MC-LR的解毒;鸡肝中GPX酶活性在前3小时先保持不变(除了1 h的高剂量组),随即显著上升,这说明GPX和GSH共同参与了鸡肝中过量活性氧自由基(ROS)的清除,GPX可以作为监测MC-LR引起鸡毒性作用的生物标志物。CAT酶活力表现为先显著下降(P<0.05)而后快速上升至正常值的趋势,SOD酶在整个实验期间几乎保持稳定,这可能与SOD酶活性较高所致。     

冲击负荷对厌氧序批式反应器的影响及其恢复重建过程

研究了在厌氧条件下以葡萄糖为基质的厌氧序批式反应器(ASBR)中冲击负荷对基质吸收和储存的影响及其恢复重建过程.结果表明,正常状态下,反应器在进水COD为5 000.0 mg/L,出水COD为188.6 mg/L,当进水负荷提高至正常状态2倍后,反应器中COD大量累积,其中51.13％为挥发性有机酸(VFA),48.87％则被转化为糖原储存在细胞体内,出水COD最高为2 368.9 mg/L,污泥糖原储存量最高为273.55 mg/g(以挥发性固体计),是正常状态的4.2倍.在冲击负荷条件下,反应器的产甲烷能力恢复较快,胞内糖原储存恢复较慢,出水COD和胞内糖原分别经过20、41 d后恢复冲击负荷前水平.     

PbO_2复合电极预处理甲苯二胺废水

通过涂覆—热分解法与电沉积法制备了β-PbO_2/α-PbO_2/SnO_2-Sb2O3/Ti复合电极(PbO_2复合电极),采用X射线衍射(XRD)、扫描电子显微镜(SEM)、循环伏安法(CV)、线性极化法(LSV)和加速寿命试验对电极进行表征。将PbO_2复合电极用于处理甲苯二胺(TDA)废水,考察了电解质浓度、电流密度对TDA降解效果的影响。实验结果表明:α-PbO_2呈梭状,β-PbO_2呈花菜状,多层结构的PbO_2电极利于提高电极的稳定性和活性;PbO_2复合电极的析氧电位(1.9 V)明显高于TDA的氧化电位(1.28 V),其使用寿命长达486 d;在电流密度为60 m A/cm2、Na2SO4质量浓度为10 g/L、电解时间为240 min的条件下,对COD为4 791.74 mg/L、TDA质量浓度为486.4mg/L的废水进行处理,TDA去除率高达97.3%,COD去除率可达88.1%。     

天池风景资源开发过程中的环境预警评价

在天池风景名胜区专家咨询和环境质量综合分析的基础上,对天池风景名胜区旅游资源的开发活动进行了预警评价,提出了天池风景名胜区风景资源开发的保护对策,为天池景区的环境管理工作提供了依据。     

华北高产粮区桓台县农民地下水污染防治意愿的调查分析

桓台县是华北平原的具有代表性的高产粮区,长期集约化的农业耕作模式,导致地下水硝态氮含量的大幅上升,威胁当地居民的身体健康。为更好地保护地下水,降低农业生产对地下水的污染,在2007年春季对桓台县323位农民进行了地下水保护意愿调查,分别对农民农业生产环保意识、改善地下水污染的意愿和农民的环境保护责任意识进行了分析,结果显示多数农民担心地下水污染会对人体造成伤害,但是仅少数的农民了解不合理的农业耕作会导致地下水的污染;大多数农民乐意接受新型环保肥料,但是接近一半的农民表示当地缺乏农技人员的指导;多数农民表示愿意加入农业生产协会以改善农业生产方式,但是农民对于农业所造成的地下水污染责任意识不强;受教育程度和收入状况越高的农民地下水保护意识越强,越容易接受改善农业生产模式,责任心相对也较强。建议在桓台县加大对地下水污染防治的宣传和投入力度的同时,加强农业技术推广体系建设和健全地下水水质监控与监管体系等措施。