Chemical characteristics of fine particles and their impact on visibility impairment in Shanghai based on a 1-year period observation

In this work, a one-year observation focusing on high time resolution characteristics of components in fine particles was conducted at an urban site in Shanghai. Contributions of different components on visibility impairment were also studied. Our research indicates that the major components of PM_2.5 in Shanghai are water-soluble inorganic ions and carbonaceous aerosol, accounting for about 60% and 30% respectively. Higher concentrations of sulfate (SO₄²⁻) and organic carbon (OC) in PM_2.5 occurred in fall and summer, while higher concentrations of nitrate (NO₃⁻) were observed in winter and spring. The mass concentrations of Cl⁻ and K⁺ were higher in winter. Moreover, NO₃⁻ increased significantly during PM_2.5 pollution episodes. The high values observed for the sulfate oxidizing rate (SOR), nitrate oxidizing rate (NOR) and secondary organic carbon (SOC) in OC indicate that photochemical reactions were quite active in Shanghai. The IMPROVE (Interagency Monitoring of Protected Visual Environments) formula was used in this study to investigate the contributions of individual PM_2.5 chemical components to the light extinction efficient in Shanghai. Both NH₄NO₃ and (NH₄)₂SO₄ had close relationships with visibility impairment in Shanghai. Our results show that the reduction of anthropogenic SO₂, NO_x and NH₃ would have a significant effect on the improvement of air quality and visibility in Shanghai.     

固定床活性炭干法烟气脱硫过程的模拟研究

采用流程模拟软件对固定床活性炭干法烟气脱硫过程进行模拟,并用已公开发表的文献实验数据进行了模型验证。模型验证结果与文献值吻合较好。利用该模型对活性炭干法烟气脱硫过程进行模拟研究,探讨了脱硫过程中床层高度、进口烟气中SO_2质量浓度、吸附温度等工艺参数对SO_2脱除率的影响。模拟结果表明:随床层高度增加,SO_2脱除率提高;随进口烟气中SO_2质量浓度增加,SO_2脱除率提高;在吸附温度为100~160℃的范围内,随吸附温度升高,SO_2脱除率逐渐下降。     

石油开采区域生态环境质量综合评价研究

石油开采在规模不断扩张的同时,也造成了大面积的采区环境污染,严重降低了生态环境质量.为探索石油开采区域生态环境质量综合评价的有效方法,通过对石油开采区域生态环境质量及综合评价现状的分析,精选指标构建了石油开采区域生态环境质量的综合评价指标体系,利用专家调查法确定了各评价指标的相对权值,并构建了石油开采区域生态环境质量模糊综合评价模型,选择胜利油田某采区进行了综合评价的应用研究,对模糊综合评价模型的有效性进行了验证.     

基于GMM模型的山东省能源消费主要驱动因素分析研究

山东省是中国的经济大省和人口大省,更是能源消费最大的省份.本文运用广义矩阵模型(GMM)对2000-2014年间山东省能源消费的驱动因素进行分析,结果表明:山东省能源消费总量呈不断上升趋势,各驱动因素中人口规模影响最大,其次为城市化水平和第二产业比重,对外贸易与GDP增长影响较小且都为负效应.因此,依靠相关法律法规合理控制人口增长和城市化进程有利于减少能源消费水平.本文根据最新统计数据深入研究山东省能源消费的主要驱动.     

火电厂烟气脱硫设施工况监控系统研究与应用

本文介绍了火电厂烟气脱硫设施工况监控系统,研究了系统关键技术。通过建立数学模型,对火电厂烟气脱硫设施主要参数进行数据有效性范围校验、关联度判断、逻辑判断,实现对脱硫设施运行异常状态的报警,最后通过实例说明了工况监控系统在环境监管中的应用。     

基于高原环境的保障装备适应性技术研究

目的寻找和发现现役保障装备在高原保障过程中存在的问题,评估装备的高原工作性能,全面提升保障装备高原环境适应能力。方法依据高原环境特点,全面、准确定量掌握现役保障保障装备在高原环境下的实际性能,找出存在的突出问题,并在此基础上有针对性地开展高原环境保障装备适应性技术研究。结果从技术措施、调试工艺、各分系统间的匹配这三个方面提出提高保障装备高原环境适应性技术。结论通过适应性技术高原型保障装备可达到功能完备、性能可靠、适应高原环境现役主战装备的保障需求。     

连续型超临界水氧化系统出水酸碱性分流试验研究

在用连续型超临界水氧化设备处理废水时,经常发现系统的净化出水pH值变小、排盐出水pH值变大。为了深入研究并揭示其机理,选择原碱性废水中和水、原酸性废水中和水、弱碱性废水、NaCl水溶液、纯自来水和纯NaOH水溶液6种典型水样进行定量试验。结果表明,连续型超临界水氧化系统存在净化出水和排盐出水pH值变化的现象,即使废水在进入系统前调整为中性(pH=7),反应后依然是净化出水pH7,排盐出水pH7。该现象很可能是由于在超临界状态下原水中无机酸根离子和金属阳离子的结晶盐离解生成了H~+、OH~-,随后各自缔合成酸性和碱性物质。缔合的酸性物质留在超临界水中,并随之从净化水出口排出,降低了出水的pH值;缔合的碱性物质混入盐结晶析出物中,随之在亚临界区溶解并经过排盐口流出,而重新溶解的金属氢氧化物增加了排水的pH值。另外,在超临界水氧化反应器复杂的氧化腐蚀环境下也生成了一定量的OH~-和酸缔合物,它们对改变出水pH值有一定作用。酸根离子极难从超临界水氧化系统中分离,因此对碱性废水要慎重中和,特别要慎重选择酸根离子,最好不要用盐酸中和,这是因为其带入的Cl~-会引起超临界系统内的氯腐和系统净化出水口的酸腐。研究表明,因为存在出水pH值的变化,对超临界水氧化系统出水的纯净程度必须予以重新考虑。     

投加FeSO4对序批式生物膜反应器中DHA、EPS和处理效果的影响

针对化学协同生物除磷过程,研究了序批式生物膜反应器(SBBR)中FeSO_4对悬浮相活性污泥脱氢酶活性(DHA)、胞外聚合物(EPS)及系统处理效果的影响.结果表明,少量FeSO_4对DHA和EPS的分泌具有促进作用,但最佳投加量不一致,分别为0.10 mmol·L-1和0.20 mmol·L-1;大量的FeSO_4则会引发抑制.FeSO_4投加量少于0.30 mmol·L-1时会使污泥MLVSS、MLVSS/MLSS增加,超过0.30 mmol·L-1时则使MLVSS、MLVSS/MLSS下降,但MLSS和SVI随着FeSO_4投加量的增加分别持续增加和下降.FeSO_4对COD和TN的去除具有抑制作用,但并不显著,去除率分别在77%和72%左右;TP的去除效果明显改善,在投加量为0.30 mmol·L-1时效果最好.投加FeSO_4协同生物除磷时建议最佳投加量为0.30 mmol·L-1,此时污泥DHA被轻微抑制,但污泥浓度、EPS、TP去除率均已达到最大,出水水质满足一级A排放标准.     

Application of polyacrylamide to reduce phosphorus losses from a Chinese purple soil: A laboratory and field investigation

Use of anionic polyacrylamide (PAM) to control phosphorus (P) losses from a Chinese purple soil was studied in both a laboratory soil column experiment and a field plot experiment on a steep slope (27%). Treatments in the column study were a control, and PAM mixed uniformly into the soil at rates of 0.02, 0.05, 0.08, 0.10, and 0.20%. We found that PAM had an important inhibitory effect on vertical P transport in the soil columns, with the 0.20% PAM treatment having the greatest significant reduction in leachate soluble P concentrations and losses resulting from nine leaching periods. Field experiments were conducted on 5 m wide by 21 m long natural rainfall plots, that allowed collection of both surface runoff and subsurface drainage water. Wheat was planted and grown on all plots with typical fertilizer applied. Treatments included a control, dry PAM at 3.9 kg ha^?1, dry PAM at 3.9 kg ha^?1 applied together with lime (CaCO₃ at 4.9 t ha^?1), and dry PAM at 3.9 kg ha^?1 applied together with gypsum (CaSO₄·2H₂O at 4 t ha^?1). Results from the field plot experiment in which 5 rainfall events resulted in measurable runoff and leachate showed that all PAM treatments significantly reduced runoff volume and total P losses in surface runoff compared to the control. The PAM treatments also all significantly reduced water volume leached to the tile drain. However, total P losses in the leachate water were not significantly different due to the treatments, perhaps due to the low PAM soil surface application rate and/or high experimental variability. The PAM alone treatment resulted in the greatest wheat growth as indicated by the plant growth indexes of wheat plant height, leaf length, leaf width, grain number per head, and dried grain mass. Growth indexes of the PAM with Calcium treatments were significantly lesser. These results indicate that the selection and use of soil amendments need to be carefully determined based upon the most important management goal at a particular site (runoff/nutrient loss control, enhanced plant growth, or a combination).     

g-C3N4制备及其协同PDS可见光催化降解布洛芬的研究

以尿素为主要原料,采用热聚合法在不同条件下制备了光催化剂g-C3N4(石墨相碳化氮),通过改变尿素在马弗炉中加热的温度(350℃、400℃、450℃、500℃)和时间(0.5 h、1 h、1.5 h),得到不同烧结温度和时间的光催化剂,并对其进行X射线衍射(XRD)、扫描电子显微镜(SEM)、傅立叶红外光谱分析仪(FT-IR)、紫外可见漫反射光(UV-Vis)表征,并通过可见光光催化降解布洛芬试验,探究了制备温度、时间对g-C3N4光催化性能的影响;并在溶液中加入PDS(过硫酸钾),联合g-C3N4在可见光下光催化降解布洛芬。结果表明,当烧结温度为500℃、烧结时间为1.5 h时,制备的g-C3N4在可见光区有较强吸收且具有较大的比表面积,以致其表现出最佳的光催化性能;PDS的存在对布洛芬的降解有促进作用,且加快了g-C3N4对布洛芬的光催化降解,相比于纯g-C3N4,4 h内布洛芬的降解率由63%提升为90.5%。以异丙醇、甲醇、对苯醌、草酸钠、重铬酸钾、甲醇分别为羟基自由基(·OH)、·OH和硫酸根自由基(SO4^-·)、超氧自由基(·O2-)、空穴(h+)、电子(e^-)的捕获剂。通过对反应过程的活性物种鉴定,·OH、SO4^-·、h+、e^-均参与了布洛芬的光催化降解,其中h+在反应中的贡献率达到了82.9%,在降解布洛芬过程中起主导作用;在反应体系中添加PDS后,催化剂g-C3N4的荧光强度变小,即加入PDS能够有效降低g-C3N4的光生空穴与电子的复合率,提高g-C3N4的光催化性能。