LLDPE料仓燃爆原因分析及防静电措施

论述了LLDPE料仓粉尘爆炸的原因,提出了避免料仓静电燃爆的对策措施以及采取相关防静电措施后的运行效果.     

世界三大黑土区水土流失与防治比较分析

论文首先明晰了黑土及黑土区的概念与范围界定,将中国东北黑土区分为典型黑土区与黑土区两个层次。在此基础上对世界三大黑土区在成土条件,开发利用过程、水土流失及水土流失防治模式方面进行了对比分析。通过比较分析认为:在自然条件上虽然三大黑土区具有一定的相似性,但我国东北黑土区由于地势起伏相对较大,更易遭受水土流失的危害;国外两大黑土区大规模的开发利用比我国黑土区相对早一些,大规模的农业开垦与不合理的耕作方式是世界三大黑土区水土流失与土地退化的主要原因;国外两大黑土区主要以风蚀为主,我国东北黑土区则是以水蚀为主,但风蚀面积也较大;国外两大黑土区在耕作制度、土地使用政策、水土保持资金投入、水土保持宣传教育及科学试验等方面已经采取了相对有效的措施,我国在这些方面还相对滞后。通过对国外黑土区水土流失治理的借鉴与思考,提出了我国东北黑土区在水土流失防治方面亟待解决的几个问题。     

电子受体类型对聚磷污泥胞外聚合物的影响研究

采用3种电子受体(硝氮、亚硝氮、氧),在SBR反应器中分别驯化了具有稳定除磷能力的聚磷污泥。对比研究了不同聚磷污泥胞外聚合物(EPS)的组分与含量,结合三维荧光光谱对EPS中有机物质进行分析。研究表明,以硝氮、亚硝氮为电子受体的聚磷污泥EPS平均浓度较为接近,分别为115.6mg/gVSS、133.5 mg/gVSS,由厌氧段至缺氧段,EPS总浓度有所下降。以氧为电子受体聚磷污泥的EPS平均浓度相对较高,为194.5 mg/gVSS,由厌氧段至好氧段,EPS总浓度略有升高。不同聚磷污泥的EPS组分均以胞外蛋白为主,占EPS总量的53%~65%,多糖与核酸占EPS总量28%~34%、5%~7%。三维荧光光谱显示3种聚磷污泥EPS均具有芳香结构蛋白质、可溶性代谢物的荧光峰,另外,以硝氮为电子受体的聚磷污泥还具有明显的腐殖酸类物质的荧光峰。研究结果表明电子受体对聚磷污泥EPS的组分、浓度、有机质类别有一定的影响。     

大型河流大面积死鱼应急监测案例分析研究

以湖南湘江干流大面积死鱼突发环境事件为例,详细阐述了该事件开展应急监测的全过程,并就河流大面积死鱼突发环境事件应急监测方案、监测指标确定、原因分析等内容进行探讨。溶解氧低是死鱼的主要原因,而大体量低溶解氧污染团的形成与持续高温干旱天气、暴雨以及特殊的开闸放水方式有关。所分析的案例为死鱼事件应急监测工作提供借鉴和参考。     

Characterization of submicron particles during autumn in Beijing, China

In this study, we performed a highly time-resolved chemical characterization of nonrefractory submicron particles(NR-PM_1) in Beijing by using an Aerodyne high-resolution time-of-flight aerosol mass spectrometer(HR-ToF-AMS). The results showed the average NR-PM_1 mass concentration to be 56.4 ± 58.0 μg/m~3, with a peak at 307.4 μg/m~3. Due to the high frequency of biomass burning in autumn, submicron particles significantly increased in organic content, which accounted for 51% of NR-PM_1 on average. Secondary inorganic aerosols(sulfate + nitrate + ammonium) accounted for 46% of NR-PM_1, of which sulfate,nitrate, and ammonium contributed 15%, 20%, and 11%, respectively. To determine the intrinsic relationships between the organic and inorganic species, we used the positive matrix factorization(PMF) model to merge the high-resolution mass spectra of the organic species and NO+and NO_2~+ions. The PMF analysis separated the mixed organic and nitrate(NO+and NO_2~+) spectra into four organic factors, including hydrocarbon-like organic aerosol(HOA), oxygenated organic aerosol(OOA), cooking organic aerosol(COA), and biomass burning organic aerosol(BBOA), as well as one nitrate inorganic aerosol(NIA) factor. COA(33%) and OOA(30%) contributed the most to the total organic aerosol(OA) mass, followed by BBOA(20%) and HOA(17%). We successfully quantified the mass concentrations of the organic and inorganic nitrates by the NO+and NO2+ions signal in the organic and NIA factors. The organic nitrate mass varied from 0.01-6.8 μg/m~3, with an average of 1.0 ±1.1 μg/m~3, and organic nitrate components accounted for 10% of the total nitrate mass in this observation.     

Concurrent catalytic removal of typical volatile organic compound mixtures over Au-Pd/α-MnO2 nanotubes

α-MnO_2 nanotubes and their supported Au-Pd alloy nanocatalysts were prepared using hydrothermal and polyvinyl alcohol-protected reduction methods, respectively. Their catalytic activity for the oxidation of toluene/m-xylene, acetone/ethyl acetate, acetone/m-xylene and ethyl acetate/m-xylene mixtures was evaluated. It was found that the interaction between Au-Pd alloy nanoparticles and α-MnO_2 nanotubes significantly improved the reactivity of lattice oxygen, and the 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst outperformed the α-MnO_2 nanotube catalyst in the oxidation of toluene, m-xylene, ethyl acetate and acetone. Over the0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst,(i) toluene oxidation was greatly inhibited in the toluene/m-xylene mixture, while m-xylene oxidation was not influenced;(ii) acetone and ethyl acetate oxidation suffered a minor impact in the acetone/ethyl acetate mixture; and(iii) m-xylene oxidation was enhanced whereas the oxidation of the oxygenated VOCs(volatile organic compounds) was suppressed in the acetone/m-xylene or ethyl acetate/m-xylene mixtures. The competitive adsorption of these typical VOCs on the catalyst surface induced an inhibitive effect on their oxidation, and increasing the temperature favored the oxidation of the VOCs. The mixed VOCs could be completely oxidized into CO_2 and H_2 O below 320°C at a space velocity of 40,000 m L/(g·hr). The 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst exhibited high catalytic stability as well as good tolerance to water vapor and CO_2 in the oxidation of the VOC mixtures. Thus, the α-MnO_2 nanotube-supported noble metal alloy catalysts hold promise for the efficient elimination of VOC mixtures.     

石油化工装置开停工及检维修挥发性有机物排放的控制

对石油化工装置开停工及检维修过程中挥发性有机物(VOCs)的排放进行了系统分析,对典型设备——储罐在清洗过程中的VOCs排放量进行了核算。介绍了国内外石油化工装置开停工及检维修过程中VOCs排放的现状及控制措施,针对国内的实际情况,提出了现阶段有效的控制措施。阐述了移动式VOCs控制技术及在石油化工装置开停工及检维修过程中的应用前景。     

过敏与非过敏儿童室内PM2.5的细胞毒性比较研究

流行病学研究表明,空气细颗粒污染物(PM_(2.5))的暴露与过敏性疾病有一定的联系;然而,PM_(2.5)暴露与过敏性疾病之间的关系尚未完全阐明,特别是室内环境中PM_(2.5)涉及到过敏或非过敏的作用不详.为了比较研究过敏与非过敏儿童室内PM_(2.5)的细胞毒性,在武汉市洪山区10户家庭室内进行了为期3个月的采样,分别收集过敏与非过敏儿童的室内PM_(2.5).采用有机/元素碳测定仪对二者PM_(2.5)成分中的含碳组分进行了分析,并通过检测昆明小鼠巨噬细胞的形态及吞噬功能影响、细胞活力、乳酸脱氢酶(LDH)漏出率等指标,来检测PM_(2.5)暴露所致的细胞毒性.结果表明,高剂量(200μg·mL~(-1))PM_(2.5)暴露对小鼠巨噬细胞的形态及吞噬功能会产生不利的影响;与非过敏儿童的室内PM_(2.5)暴露组相比,过敏儿童的室内PM_(2.5)暴露组诱导巨噬细胞产生的毒性作用更明显.细胞体外测试结果提示:在相同PM_(2.5)暴露剂量下,引起儿童过敏症的室内PM_(2.5)成分具有重要影响.