游离亚硝酸抑制硝化杆菌属(Nitrobacter)活性动力学研究

为探究游离亚硝酸（FNA）对亚硝酸盐氧化细菌中硝化杆菌属（Nitrobacter）活性抑制动力学影响,采用序批式活性污泥（SBR）反应器,在通过改变系统进水FNA浓度达到富集Nitrobacter基础上,以富含Nitrobacter污泥为对象（宏基因组物种注释和丰度分析显示上Nitrobacter占细菌总数40.3%）,基于批次试验,考察不同FNA浓度梯度下亚硝酸盐氧化过程比亚硝态氮氧化速率（SNiOR）变化规律,进而拟合FNA抑制Nitrobacter活性抑制动力学模型,并进行统计学分析.结果表明,当FNA≤0.1mg/L时,随着FNA浓度升高,SNiOR迅速升高.当FNA>0.1mg/L时,SNiOR随着FNA浓度升高而降低.尤其当FNA浓度高于0.7mg/L时,SNiOR始终维持在0gN/（gVSS·d）,表明Nitrobacter活性统被完全抑制.统计学分析结果显示相对于Haldane、Aiba、Edwards-1#、Edwards-2#、Luong抑制动力学模型,Han-Levenspiel模型最适合描述FNA对Nitrobacter活性的抑制影响.其统计学常数：残差平方和（RSS）为0.02、可决系数（R²）为0.90、拟合方程的方差检验统计量F值为78.1、可信度P值为3.29×10^-12,其动力学常数值分别为：最大比亚硝态氮氧化速率（r_max）为1.57gN/（gVSS·d）;半饱和常数（K_S）为0.01mg/L;临界抑制常数（S_m）为0.66mg/L.     

中试SAD-ASBR系统处理含盐废水的启动与工艺特性

采用ASBR(530 L)接种A~2/O厌氧污泥,考察了厌氧氨氧化(ANAMMOX)的启动及其与反硝化耦合处理含盐废水的脱氮特性,并对菌群结构进行了分析.结果表明,温度35℃±1℃、反应时间为14 h,160 d可实现ANAMMOX的成功启动.稳定运行阶段,ANAMMOX与反硝化耦合(SAD)使得总氮(TN)去除率和去除负荷分别达91.1%和0.45 kg·(m~3·d)~(-1);污泥呈浅红色颗粒状,厌氧氨氧化菌为优势菌,且主要菌属为Candidatus Brocadia(10.6%).此外,采用按梯度逐步提高盐度的驯化方式,可实现SAD对高盐(Cl-浓度8 000 mg·L-1)模拟火电厂废水的高效脱氮除碳,COD和TN去除率分别达93.2%和90.0%.推测SAD中反硝化主要为NO_3~--N→N_2,部分反硝化(NO_3~--N→NO_2~--N)仅占30.3%.     

Watershed characteristics and climate factors effect on the temporal variability of mercury in the southern Baltic Sea rivers

Mercury(Hg) is a neurotoxic metal which can enter into the human organism mainly by fish consumption, skin and transpiration. In the coastal zone of the southern Baltic Sea, rivers are the main source of Hg. The Polish region represents the largest proportion of the Baltic Sea catchment and this research included four rivers of the Baltic watershed: the Reda,Zagórska Struga, Kacza and Gizdepka. The samples were collected in the years 2011–2013.Total and particulate Hg concentration in these rivers were measured. Due to intensive rain,deposited mercury on the catchment area was washed out into the riverines water and introduced into the Baltic Sea. Consequently, the load of Hg increased three times.Additionally, the intensive dry atmospheric deposition during heating season caused the increase of the concentration of particulate Hg in the river water even by 85%. The research confirmed the role of the river flow magnitude in the load of mercury introduced into the sea by rivers. Moreover, a high variability of mercury concentration was connected to the additional sources such as the chemicals containing Hg and no municipal sewage system.The analysis of stable isotopes indicated that the SPM contained terrestrial organic matter;however, there was no clear correlation between Hgtot, Corgand Ntotconcentrations and δ~(13)C, δ~(15)N, C/N in particulate matter.     

Polar organic tracers in PM2.5 aerosols from an inland background area in Southwest China: Correlations between secondary organic aerosol tracers and source apportionment

PM_(2.5) aerosol samples were collected over 12 hr and 24 hr intervals in an inland background area, Gongga Mountain National Nature Reserve(hereafter shortened to Gongga), during the summer of 2011. Polar organic tracers, inorganic ions and meteorological data were measured. The purpose of this work was to investigate the variation patterns, formation and sources of the secondary organic aerosol tracers in the studied atmosphere. The average concentrations of isoprene oxidation products, α-pinene oxidation products, β-caryophyllinic acid, sugars, sugar alcohols and anhydrosugars were 88.6 ± 106.1, 3.6 ± 5.7,0.13 ± 0.30, 13.6 ± 13.1, 31.9 ± 31.4 and 14.8 ± 10.7 ng/m3 respectively in all aerosol samples.The aged α-pinene second organic aerosol(SOA) tracers(i.e., 3-hydroxyglutraric acid(3 HGA), 3-hydroxy-2,2-dimethylglutaric acid(HDMGA), 3-acetylpentandioic acid(APDA) and 3-methyl-1,2,3-butanetricarboxylic acid(MBTCA)) correlated significantly with each other in the 24 hr PM2.5 aerosol samples, indicating that OH· is the major factor controlling the formation of these α-pinene SOA tracers. Using the positive matrix factorization(PMF) model and the tracer-based source apportionment method, we calculated that isoprene oxidation products, α-pinene oxidation products, sesquiterpene oxidation products, biomass burning, fungi spores and anthropogenic SOA accounted for 21.9% ± 5.5%, 8.4% ± 2.1%, 3.0% ± 0.7%, 5.2% ± 5.3%, 5.0% ± 6.2% and 31.4% ± 7.8% of organic carbon respectively during the sampling period.     

吸水性还原性材料对煤自燃影响的实验研究

为了解决吸水性盐和还原性材料仅依靠其单一特性抑制煤自燃而抑制效果并不理想的问题,提出了利用羟甲基磺酸钠的吸水性和还原性来抑制煤自燃。将原煤-20%羟甲基磺酸钠通过对比原煤、原煤-20%MgCl2和原煤-20%VC,利用程序升温实验和FTIR测试来研究其抑制煤自燃的效果。研究结果表明:3种溶液处理煤均在一定程度上抑制了煤自燃,其中,20%羟甲基磺酸钠溶液对抑制煤低温氧化的效果最好,经过其处理的煤样表观活化能最大,同时,依靠其还原性很好地保护了煤中的亚甲基和羟基不被破坏,抑制煤自燃效果明显优于20%MgCl2溶液和20%VC溶液。     

煤自燃特性及自然发火预测预报指标体系研究

以梁宝寺矿3号煤层为背景,采用色谱吸氧法和氧化动力法对其自燃倾向性进行了对比分析。同时,通过煤氧化升温热解实验对其升温过程中各气体随温度的变化规律进行了分析,以实验所得和灰色关联分析所得定性和定量相结合的方式,优选出了不同温度阶段煤自然发火预测预报所对应的第一、第二和第三预测指标,建立了煤自然发火预测预报体系,为有效抑制该矿及同类矿井火灾的发生具有重要意义。     

电动力学-过硫酸钠氧化联用修复二氯苯污染土壤的研究

为解决氯苯污染场地的修复问题,尤其是受污染的低渗透介质的原位修复问题,以1,2-二氯苯、1,3-二氯苯、1,4-二氯苯为研究对象,采用电动力学-过硫酸钠氧化联用技术,并在阳极室添加Na2CO3/Na HCO3缓冲液来控制阳极p H,探讨了土壤中3种二氯苯的迁移和去除效果。实验结果表明:在外加1.5 V/cm恒定电压,以铁为阴阳电极,以5 mmol/L Na2S2O8溶液作阴阳电极液,阳极液含0.025 mol/L Na2CO3/Na HCO3缓冲液,运行5 d后,该联用技术对污染壤土中3种二氯苯的总去除效果较好且较为均匀,去除率均在75%以上。该方法对于原位修复受污染的低渗透介质具备可行性。     

Oxidation state specific analysis of arsenic species in tissues of wild-type and arsenic (+ 3 oxidation state) methyltransferase-knockout mice

Arsenic methyltransferase(As3mt) catalyzes the conversion of inorganic arsenic(i As) to its methylated metabolites, including toxic methylarsonite(MAs~Ⅲ) and dimethylarsinite(DMAs~Ⅲ). Knockout(KO) of As3 mt was shown to reduce the capacity to methylate i As in mice. However, no data are available on the oxidation states of As species in tissues of these mice. Here, we compare the oxidation states of As species in tissues of male C57BL/6 As3mt-KO and wild-type(WT) mice exposed to arsenite(iA s~Ⅲ) in drinking water. WT mice were exposed to50 mg/L As and As3mt-KO mice that cannot tolerate 50 mg/L As were exposed to 0, 15, 20, 25 or30 mg/L As. iA s~Ⅲaccounted for 53% to 74% of total As in liver, pancreas, adipose, lung, heart, and kidney of As3mt-KO mice; tri- and pentavalent methylated arsenicals did not exceed 10% of total As. Tissues of WT mice retained iA s and methylated arsenicals: iA s~Ⅲ, MAs~Ⅲand DMAs~Ⅲ represented 55%‐68% of the total As in the liver, pancreas, and brain. High levels of methylated species, particularly MAs~Ⅲ, were found in the intestine of WT, but not As3mt-KO mice,suggesting that intestinal bacteria are not a major source of methylated As. Blood of WT mice contained significantly higher levels of As than blood of As3mt-KO mice. This study is the first to determine oxidation states of As species in tissues of As3mt-KO mice. Results will help to design studies using WT and As3mt-KO mice to examine the role of iA s methylation in adverse effects of iA s exposure.     

A preliminary analysis of the surface chemistry of atmospheric aerosol particles in a typical urban area of Beijing

Atmospheric aerosol particle samples were collected using an Ambient Eight Stage(Non-Viable) Cascade Impactor Sampler in a typical urban area of Beijing from 27 th Sep.to 5th Oct.,2009.The surface chemistry of these aerosol particles was analyzed using Static Time of Flight-Secondary Ion Mass Spectrometry(Static TOF-SIMS).The factors influencing surface compositions were evaluated in conjunction with the air pollution levels,meteorological factors,and air mass transport for the sampling period.The results show that a variety of organic ion groups and inorganic ions/ion groups were accumulated on the surfaces of aerosol particles in urban areas of Beijing;and hydrophobic organic compounds with short-or middle-chain alkyl as well as hydrophilic secondary inorganic compounds were observed.All these compounds have the potential to affect the atmospheric behavior of urban aerosol particles.PM1.1–2.1and PM3.3–4.7had similar elements on their surfaces,but some molecules and ionic groups demonstrated differences in Time of Flight-Secondary Ion Mass Spectrometry spectra.This suggests that the quantities of elements varied between PM1.1–2.1and PM3.3–4.7.In particular,more intense research efforts into fluoride pollution are required,because the fluorides on aerosol surfaces have the potential to harm human health.The levels of air pollution had the most significant influence on the surface compositions of aerosol particles in our study.Hence,heavier air pollution was associated with more complex surface compositions on aerosol particles.In addition,wind,rainfall,and air masses from the south also greatly influenced the surface compositions of these urban aerosol particles.