Electrochemical determination of anaerobic microbial decay coefficients

The biokinetics of attached and suspended bacteria are an essential component of activated sludge models, anaerobic digestion models and biofilm models. These parameters are often assumed or “confirmed” based on the goodness-of-fit of the bioprocess models. Using a microbial fuel cell with a baffled reactor chamber, the attached- and mixed-growth microbial decay coefficients were evaluated under anaerobic conditions. The capability for real-time voltage recording allows easy and accurate measurement of the anaerobic microbial decay coefficients (b_L, lysis-regrowth approach), which were determined to be 0.11 ± 0.01 and 0.15 ± 0.01 d⁻¹ for attached (to anode) and mixed (present in the anode chamber) growth microorganisms, respectively. The corresponding half-saturation constants using glucose as a substrate were 204 ± 10 and 123 ± 1 mg COD l⁻¹. Hence, like an oxygen uptake rate-based approach to measure the microbial kinetics under aerobic conditions, the electrochemical recording provides an attractive method to measure anaerobic microbial decay coefficients.     

Solubility of toluene, benzene and TCE in high-microbial concentration systems

We report measurements of solubility limits for benzene, toluene, and TCE in systems that contain varying levels of biomass up to 0.13 g mL⁻¹ for TCE and 0.25 g mL⁻¹ for benzene and toluene. The solubility limit increased from 21 to 48 mM when biomass (in the form of yeast) was added to aqueous batch systems containing benzene. The toluene solubility limit increased from 4.9 to greater than 20 mM. For TCE, the solubility increased from 8 mM to more than 1000 mM. Solubility for TCE (trichloroethylene) was most heavily impacted by biomass levels, changing by two orders of magnitude as the microbial concentrations approach those in biofilms.     

Laboratory longitudinal diffusion tests: 2. Parameter estimation by inverse analysis

This study focuses on the verification of test interpretations for different state analyses of diffusion experiments. Part 1 of this study identified that steady, quasi-steady and equilibrium state analyses for the through- and in-diffusion tests with solution reservoirs are generally feasible where the tracer is not highly sorptive. In Part 2 we investigate parameter identifiability in transient-state analysis of reservoir concentration variation using a numerical approach. For increased generality, the analytical models, objective functions and Jacobian matrix necessary for inverse analysis of transient-state data are reformulated using unified dimensionless parameters. In these dimensionless forms, the number of unknown parameters is reduced and a single dimensionless parameter represents the sorption property. The dimensionless objective functions are evaluated for individual test methods and parameter identifiability is discussed in relation to the sorption property. The effects of multiple minima and measurement error on parameter identifiability are also investigated. The main findings are that inverse problems for inlet and outlet reservoir concentration analyses are generally unstable and well-posed, respectively. Where the tracer is sorptive, the inverse problem for the inlet reservoir concentration analysis may have multiple minima. When insufficient measurement data is collected, multiple solutions may result and this should be taken into consideration when inversely analyzing data including that of inlet reservoir concentration. Verification of test interpretation by cross-checking different state analyses is feasible where the tracer is not highly sorptive. In an actual experiment, test interpretation validity is demonstrated through consistency between theory and practice for different state analyses.     

海南省几种草本植物微量元素的组成

海南省位于我国热带地区,草本植物微量元素组成可反映热带区域生物地球化学特点。海南植物微量元素含量属正常范围值,仅个别植物Ｃｄ、Ｈｇ含量偏高。植物Ｚｎ、Ｃｕ、Ｍｏ含量大多在５ｍｇ／ｋｇ以上,Ｐｂ、Ｃｕ、Ｃｄ含量一般低于２ｍｇ／ｋｇ,Ｈｇ、Ａｓ、Ｎｉ通常不足１ｍｇ／ｋｇ。雀稗（Ｐａｓｐａｌｕｍｃｏｍｍｅｒｓｏｎｉ）、地胆草（Ｅｌｅｐｈａｎｔｏｐｕｓｓｃａｂｅｒ）等微量元素含量普遍较高。红裂稃草（Ｓｃｈｉｚａｃｈｙｒｉｕｍｓａｎｇｕｉｎｅｕｍ）、白茅（Ｉｍｐｅｒａｔａｃｙｌｉｎｄｒｉｃａ）等微量元素含量一般较低。植物微量元素组成与植物种类及其生境条件有关。生物吸收系数反映植物摄取元素的强度,Ｍｏ、Ｃｄ、Ｈｇ、Ｚｎ、Ｃｕ的生物吸收系数通常大于１．０,属强积聚元素,Ｐｂ、Ｃｒ、Ｎｉ、Ａｓ的生物吸收系数大多低于０．３,是弱摄取元素。     

垂直面绿化植物遮阳系数与叶面积指数研究

比较、分析了农业研究中提出的叶面积指数LAI与用于建筑节能领域的垂直面绿化植物叶片遮阳系数SCPVW两个概念的异同和各自的应用范围。指出城市绿化采用水平或垂直绿化方式时,由于下垫面差异,植物叶片的遮阳系数应当分别采用LAI和SCPVW进行计算。     

Spectral tests of randomness for spatial point patterns

We develop a spectral framework for testing the hypothesis of complete spatial randomness (CSR) for a spatial point pattern. Five formal tests based on the periodogram (sample spectrum) proposed in Mugglestone (1990) are considered. A simulation study is used to evaluate and compare the power of the tests against clustered, regular and inhomogeneous alternatives to CSR. A subset of the tests is shown to be uniformly more powerful than the others against the alternatives considered. The spectral tests are also compared with three widely used space-domain tests that are based on the mean nearest-neighbor distance, the reduced second-order moment function (K-function), and a bivariate Cramér-von Mises statistic. The test based on the scaled cumulative R-spectrum is more powerful than the space-domain tests for detecting clustered alternatives to CSR, especially when the number of events is small.     

燃煤电厂在线监测系统颗粒物浓度排放系数影响因素的探讨

选取上海市7家未安装气-气换热器的国控燃煤电厂作为研究对象,从煤质、除尘器、脱硫协同脱除作用以及锅炉工况负荷等方面探讨对颗粒物浓度排放系数 K值产生的影响,得出上述因素通过改变脱硫进口颗粒物浓度值影响 K值,当脱硫进口颗粒物浓度较低、波动范围较小时,其 K值也维持相对稳定的状态;当脱硫进口颗粒物浓度较高、波动范围较大时,其 K值也会发生较大的变化等结论。     

污泥掺烧对燃煤电厂痕量元素排放特性影响

采用EPAMethod29方法、冷原子吸收光谱法和电感耦合等离子体质谱法采集和分析一台超低排放燃煤机组污泥掺烧前后的原燃料、烟气和副产物样品中各痕量元素浓度,研究污泥掺烧对燃煤电厂痕量元素排放特性的影响.结果表明:污泥中富含Zn、Cu元素,浓度分别是煤样中的18.81倍和17.64倍.污泥掺烧使掺配后入炉煤中痕量元素含量普遍升高.污泥掺烧前后整个系统、锅炉系统和全流程大气污染控制设施的痕量元素质量平衡率均在可接受范围内.污泥掺烧对痕量元素的分布特征无明显影响,随粉煤灰排放是痕量元素的主要排放去向.通过烟囱排放到大气环境的痕量元素排放量占比很小,不超过0.43%.污泥掺烧前后SCR入口烟气中痕量元素除Hg外主要以颗粒态形式存在.污泥掺烧后各痕量元素在粉煤灰和底渣中的相对富集系数未显著改变.经过全流程大气污染控制设施协同控制后,污泥掺烧前后烟囱总排口痕量元素排放浓度分别为0～12.76,0～14.97μg/m³.污泥掺烧后痕量元素排放浓度均满足美国燃煤发电机组有害大气污染物排放标准、上海市燃煤耦合污泥电厂大气污染排放标准和生态环境部生活垃圾焚烧污染控制标准的限值要求....     

Plant/soil concentration ratios for paired field and garden crops, with emphasis on iodine and the role of soil adhesion

In the effort to predict the risks associated with contaminated soils, considerable reliance is placed on plant/soil concentration ratio (CR) values measured at sites other than the contaminated site. This inevitably results in the need to extrapolate among the many soil and plant types. There are few studies that compare CR among plant types that encompass both field and garden crops. Here, CRs for 40 elements were measured for 25 crops from farm and garden sites chosen so the grain crops were in close proximity to the gardens. Special emphasis was placed on iodine (I) because data for this element are sparse. For many elements, there were consistent trends among CRs for the various crop types, with leafy crops > root crops ≥ fruit crops ≈ seed crops. Exceptions included CR values for As, K, Se and Zn which were highest in the seed crops. The correlation of CRs from one plant type to another was evident only when there was a wide range in soil concentrations. In comparing CRs between crop types, it became apparent that the relationships differed for the rare earth elements (REE), which also had very low CR values. The CRs for root and leafy crops of REE converged to a minimum value. This was attributed to soil adhesion, despite the samples being washed, and the average soil adhesion for root crops was 500 mg soil kg⁻¹ dry plant and for leafy crops was 5 g kg⁻¹. Across elements, the log CR was negatively correlated with log Kd (the soil solid/liquid partition coefficient), as expected. Although, this correlation is expected, measures of correlation coefficients suitable for stochastic risk assessment are not frequently reported. The results suggest that r ≈ −0.7 would be appropriate for risk assessment.