二元联合作用藻红外测试方法——以重金属为例

为检验二元联合作用藻红外测试方法的可行性,用Cu~(2+)、Fe3+、Mn~(2+)、Al3+、Cr3+、Hg~(2+)、Cd~(2+)、Pb~(2+)、Zn~(2+)进行了二元联合作用测试实验。结果显示:联合药液的参照浓度与单药液的参照浓度比为0.5:0.25的有15组二元组合,为2.0:1.0的有10组二元组合,为1.0:0.5的有11组二元组合;在9种重金属的36组二元联合作用测试结果中出现拮抗作用、相加作用、协同作用,表明联合作用类型表现出多样性;14组拮抗作用中单组的再现性为50%~100%、多组的再现性的出现率为93%、单组的重现性为67%~100%、多组的重现性的出现率为100%,21组相加作用中单组的再现性为50%~100%、多组的再现性的出现率为86%、单组的重现性为67%~100%、多组的重现性的出现率为100%,1组协同作用重现性67%;36组联合作用测试结果的再现性为50%~100%、再现性的出现率为86%,重现性为67%~100%、重现性的出现率为100%。上述分析可知,9种重金属的36种二元联合作用测试结果具有较好的多样性、再现性、重现性,表明测试条件、藻温测试方法、三指标评价法能够保证藻响应温差和藻响应药品评价结果的质量,参照浓度分析方法、联合作用评价方法能够控制联合作用分析结果的质量;藻响应的有毒有害物都存在敏感浓度,用参照浓度分析方法可分析出藻响应有毒有害物的参照浓度。因此,藻红外测试技术可以用于测试重金属、农药、有机药品、抗生素等的二元联合作用。     

Tetra-detector size exclusion chromatography characterization of molecular and solution properties of soluble microbial polysaccharides from an anaerobic membrane bioreactor

Characterization of the molecular properties of soluble microbial products (SMP) is critical for understanding the membrane filtration and fouling mechanisms in anaerobic and aerobic membrane bioreactors (AnMBR & MBR). In this study, the distributions of the absolute molecular weight and intrinsic viscosity of SMP polysaccharides from an AnMBR were effectively determined by a high performance size exclusion chromatography (HPSEC) that was coupled with the refractive index (RI), diode array UV (DAUV), right and low angle light scattering (LS), and viscometer (Vis) detectors. Based on the tetra-detector HPSEC determined absolute molecular weights and intrinsic viscosity, a universal calibration relationship for the SMP polysaccharides was developed and the molecular conformations, average molecular weights, and hydrodynamic sizes of the SMP polysaccharides were also explored. Two factors which can be derived from the tetra-detector HPSEC analysis were proposed for the characterization of the viscous and osmotic pressure properties of the SMP polysaccharides. In addition, it was also extrapolated how to analyze the resistance characteristics of the concentration polarization layers formed in membrane filtration based on the molecular properties determined by the tetra-detector HPSEC analysis.

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Urinary metabolomic profiling in rats exposed to dietary di(2-ethylhexyl) phthalate (DEHP) using ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS)

Di(2-ethylhexyl) phthalate (DEHP) is an omnipresent environmental chemical with widespread nonoccupational human exposure through multiple ways. Although considerable efforts have been invested to investigate mechanisms of DEHP toxicity, the key metabolic biomarkers of DEHP toxicity remain to be identified. The aim of this study was to assess the urinary metabonomics of dietary DEHP in rats using the technique of ultra-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC/Q-TOF-MS). Fourteen female Wistar rats were divided into two groups and given increasing dietary doses of DEHP for 30 consecutive days. The urinary metabolite profile was studied using ultra-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. Principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) enabled clusters to be clearly separated. Eleven principal urinary metabolites were identified as contributing to the clusters. The clusters in the positive electrospray ionization (ESI) mode were xanthurenic acid, kynurenic acid, nonate, N6-methyladenosine, and L-isoleucyl-L-proline. The clusters in the negative ESI mode were hippuric acid, tetrahydrocortisol, citric acid, phenylpropionylglycine, cPA(18:2(9Z, 12Z)/0:0), and LysoPC(14:1(9Z)). The urinary metabonomic changes indicated that exposure to dietary DEHP can affect energy-related metabolism, liver and renal function, fatty acid metabolism, and cause DNA damage in rats. The findings of this study on the urinary metabolites and metabolic pathways of DEHP may form the basis for future studies on the mechanisms of toxicity of this commonly found environmental chemical.     

Multiple copper adsorption and regeneration by zeolite 4A synthesized from bauxite tailings

Copper ions were first adsorbed by zeolite 4A synthesized from bauxite tailings, the desorption of Cu(II) using Na₂EDTA solutions was performed, and the recycling of zeolite 4A in adsorption and desorption was systematically investigated. It was observed that the Cu(II) removal efficiency was directly dependent on the initial pH value. The maximum removal efficiency of Cu(II) was 96.2% with zeolite 4A when the initial pH value was 5.0. Cu(II) was completely absorbed in the first 30 min. It was also observed that the desorption efficiency and zeolite recovery were highly dependent on the initial pH and concentration of Na₂EDTA in the solution. The desorption efficiency and percent of zeolite recovered were 73.6 and 85.9%, respectively, when the Na₂EDTA solution concentration was 0.05 mol L^?1 and the pH value was 8. The recovered zeolites were pure single phase and highly crystalline. After 3 cycles, the removal efficiency of Cu(II) was as high as 78.9%, and the zeolite recovery was 46.9%, indicating that the recovered zeolites have good adsorption capacity and can repeatedly absorb Cu(II).

     

Individual and combined inhibition of phenol and thiocyanate on microbial activity of partial nitritation

This study evaluated the individual and interactive effect of phenol and thiocyanate (SCN⁻) on partial nitritation (PN) activity using batch test and response surface methodology. The IC₅₀ of phenol and SCN⁻ on PN sludge were 5.6 and 351 mg L⁻¹, respectively. The PN sludge was insensitive to phenol and SCN⁻ at levels lower than 1.77 and 43.3 mg L⁻¹, respectively. A regression model equation was developed and validated to predict the relative specific respiration rate (RSRR) of PN sludge exposed to different phenol and SCN⁻ concentrations. In the range of independent variables, the most severe inhibition was observed with a valley value (17%) for RSRR, when the phenol and SCN⁻ concentrations were 4.08 and 198 mg L⁻¹, respectively. An isobole plot was used to judge the combined toxicity of phenol and SCN⁻, and the joint inhibitory effect was variable depending on the composition and concentration of the toxic components. Furthermore, the toxic compounds showed independent effects, which is the most common type of combined toxicity.

     

Distribution and controls of heavy metals and organic matter in the surface sediments of the Southern Yellow Sea,China

Environmental Science and Pollution Research - Accurate and effective determination of the source of heavy metals is essential for the treatment of marine ecological environments. This article...     

Characteristics of PM<Subscript>2.5</Subscript>, CO<Subscript>2</Subscript> and particle-number concentration in mass transit railway carriages in Hong Kong

Fine particulate matter (PM_2.5) levels, carbon dioxide (CO₂) levels and particle-number concentrations (PNC) were monitored in train carriages on seven routes of the mass transit railway in Hong Kong between March and May 2014, using real-time monitoring instruments. The 8-h average PM_2.5 levels in carriages on the seven routes ranged from 24.1 to 49.8 µg/m³, higher than levels in Finland and similar to those in New York, and in most cases exceeding the standard set by the World Health Organisation (25 µg/m³). The CO₂ concentration ranged from 714 to 1801 ppm on four of the routes, generally exceeding indoor air quality guidelines (1000 ppm over 8 h) and reaching levels as high as those in Beijing. PNC ranged from 1506 to 11,570 particles/cm³, lower than readings in Sydney and higher than readings in Taipei. Correlation analysis indicated that the number of passengers in a given carriage did not affect the PM_2.5 concentration or PNC in the carriage. However, a significant positive correlation (p < 0.001, R ² = 0.834) was observed between passenger numbers and CO₂ levels, with each passenger contributing approximately 7.7–9.8 ppm of CO₂. The real-time measurements of PM_2.5 and PNC varied considerably, rising when carriage doors opened on arrival at a station and when passengers inside the carriage were more active. This suggests that air pollutants outside the train and passenger movements may contribute to PM_2.5 levels and PNC. Assessment of the risk associated with PM_2.5 exposure revealed that children are most severely affected by PM_2.5 pollution, followed in order by juveniles, adults and the elderly. In addition, females were found to be more vulnerable to PM_2.5 pollution than males (p < 0.001), and different subway lines were associated with different levels of risk.     

周年磷肥旱季集中底施对玉-稻轮作磷肥效应的影响

春玉米-晚稻水旱轮作是近年来南方稻区种植制度变化下出现的新型两熟制模式。明确两季作物间磷肥的合理分配对玉-稻轮作作物产量与磷素利用效率的影响,对玉-稻轮作养分高效与高产协同实现,及丰富对水旱轮作前后季作物养分利用关系的认识具有理论意义。采用春玉米-水稻周年轮作田间试验,根据晚稻季磷肥前移至玉米季做底肥施用的比例及周年施磷量,设置7个磷肥施用处理,分别为两季作物均不施磷(P_0)、两季作物均按常规方法施磷(P_1)、1/3晚稻季磷肥前移(P_2)、2/3晚稻季磷肥前移(P_3)、全部晚稻季磷肥前移(P_4)、全部晚稻季磷肥前移且周年总施磷量减少15%(P_5)、全部晚稻季磷肥前移且周年总施磷量减少30%(P_6),分析了不同施磷处理作物产量、磷素吸收量及磷素利用效率的变化。与P_1相比,P_3与P_4处理显著提高了晚稻花后干物质的分配比例及晚稻产量,且其周年产量分别提高了4.87%和6.74%;P_5处理晚稻产量与P_1处理差异不显著,但P_6显著降低了晚稻产量。晚稻季磷肥前移施用明显促进了玉米及晚稻对磷素的吸收,显著降低了磷素的表观盈余量。与P_1处理相比,P_2、P_3、P_4处理两季作物周年土壤磷素依存率分别减少了11.63%、26.47%与22.08%。从磷肥利用效率看,P_4处理的磷肥周年累积回收效率、农学利用效率、偏生产力及磷肥产量贡献率均显著高于P_1处理,分别提高了102.46%、194.83%、6.73%与176.16%。与P_1处理相比,P_5处理周年磷肥产量贡献率及农学利用效率差异不显著,但分别提高了其磷肥回收效率与偏生产力32.56%和58.05%。玉米季施用的磷肥对晚稻有明显的后效作用,且比晚稻季施用磷肥具有更高的磷肥利用效率。所以在春玉米免耕复种晚稻时,可将晚稻季的磷肥全部前移至玉米季施用,并可减少15%周年施磷量。     

原铝生产流程温室气体排放主要影响因素的关联度分析

铝是国民经济建设和发展的关键基础材料,然而由其生产过程所产生的大量温室气体排放也逐渐成为政府关注的焦点。本研究计算了我国原铝生产不同年度的生命周期能耗和温室气体排放量,并分析了资源消耗和生产工序能耗等影响因素与温室气体排放的关联性。结果表明,在各年原铝生产的温室气体排放总量中,电力和阳极效应导致的排放所占比重分别为68.5%和7.9%,其他影响因素所占比重均低于6%;与温室气体排放关联度最高的3个影响因素依次是电耗、煤气燃烧和石灰石煅烧,其值分别为0.937、0.899和0.893;在目前铝电耗和阳极效应控制水平提升空间有限的情况下,降低煤气的消耗,提高石灰石的使用效率,是实现原铝生产温室气体减排的有效途径。     

DO浓度对间歇曝气单级自养脱氮系统N2O排放的影响

以单级自养脱氮系统为研究对象,采用有效容积为15 L的SBBR反应器,系统进水NH+4-N浓度约为360 mg/L,控制温度为(30±2)℃,采用间歇曝气方式运行,曝气段DO浓度从2.4~2.6 mg/L逐渐下降到0.9~1.1 mg/L,研究了单级自养脱氮系统的脱氮性能与N2O排放情况。结果表明,反应器曝气段DO浓度从2.4~2.6 mg/L下降到0.9~1.1mg/L,系统TN去除率均达到80%,但在相同运行时间内的TN去除率依次降低,NH+4-N平均反应速率从0.19 mg/(L·min)降低至0.05 mg/(L·min),NO-3-N累计产生量稳定于14.9~16.5 mg/L,NO-2-N浓度在反应器内未产生明显的积累。随着曝气段DO浓度的下降,最大N2O释放速率逐渐降低,N2O累计释放量从73.8 mg下降到61.0 mg,N2O转化率介于2.4%~2.9%。