Modelling Phosphorus Retention in Lakes and Reservoirs

Steady-state models for the prediction of P retention coefficient (R) in lakes were evaluated using data from 93 natural lakes and 119 reservoirs situated in the temperate zone. Most of the already existing models predicted R relatively successfully in lakes while it was seriously under-estimated in reservoirs. A statistical analysis indicated the main causes of differences in R between lakes and reservoirs: (a) distinct relationships between P sedimentation coefficient, depth, and water residence time; (b) existence of significant inflow–outflow P concentration gradients in reservoirs. Two new models of different complexity were developed for estimating R in reservoirs: , where τ is water residence time (year), was derived from the Vollenweider/Larsen and Mercier model by adding a calibrated parameter accounting for spatial P non-homogeneity in the water body, and is applicable for reservoirs but not lakes, and , where [P_in] is volume-weighted P concentration in all inputs to the water body (μg l⁻¹), was obtained by re-calibrating the OECD general equation, and is generally applicable for both lakes and reservoirs. These optimised models yield unbiased estimates over a large range of reservoir types.     

运用QSPR预测有机磷农药的色谱保留值

通过计算43种有机磷农药的各种结构参数,运用多元线性回归分析方法比较了适用于有机磷农药色谱保留值的定量关系表达式,建立了有机磷农药结构参数对色谱保留值的QSPR模型.模型分析表明:磷酸酯与硫逐磷酸酯两类有机磷农药的模型非交叉验证相关系数R2分别为0.991和0.998,标准误差SE分别为0.0539和0.2874,交叉验证相关系数Q2分别为0.976和0.990,标准偏差Scv分别为0.086和0.610.在已知磷酸酯与硫逐磷酸酯两类有机磷农药结构参数的情况下,此模型可有助于有机磷农药的色谱分析.     

河口近岸水体中颗粒态重金属的潮周期变化

对长江口崇明东滩近岸水体中颗粒态重金属的潮周期变化特征及其影响机制进行了研究.结果表明,受粒度影响,底层水体中颗粒态Cu、Pb、Fe、Mn、Zn、Cr、Al的总量分别高出表层沉积物的184%、99%、56%、62%、147%、50%和45%,其中Cu、Pb、Fe、Mn、Zn、Al可还原态部分在底层水体悬浮颗粒物中的含量也明显高出表层沉积物的2～3倍,但与重金属总量相比,上述元素的可还原态部分所占比例与表层沉积物相差不大.在5次潮汐循环过程中,颗粒态重金属均在涨潮初期、高平潮前后及落潮末期出现较高含量.这种变化主要与水动力条件有关,当水体流速增大时,从底部沉积物再悬浮起来的颗粒态重金属对水体中的永久性悬浮颗粒起了很大的稀释效应.水体中的盐度、DO及pH等环境因子对潮周期内颗粒态重金属的变化影响不大.     

固定源稀释通道的设计和外场测试研究

为研究固定源产生的颗粒物的污染情况,自行设计了固定源稀释通道采样装置以便模拟颗粒物在大气中的稀释扩散过程.该装置采用不同尺寸的采样嘴,以保证对烟道内的颗粒物等速采样,采样烟气与洁净空气在稀释腔内混合,腔内雷诺数典型值可以达到10000,保证了采样烟气和洁净空气能够稀释混合均匀.颗粒物在停留室中的停留时间达到90s,保证了颗粒物有足够的时间长大成核.将该装置应用于国内的9个燃煤、燃油固定源,取得了颗粒物的质量浓度、OC、EC组成、排放因子等数据.     

纳米级铁粉脱氯降解四氯化碳

四氯化碳的生产和使用,给人类带来了较大危害.为此,采用纳米铁粉这一新方法对其进行脱氯处理.试验以纳米级铁粉对四氯化碳的脱氯率为考察指标,选用L25(56)正交试验方案,考察了降解介质的初始pH值、纳米铁粉的质量、降解温度、摇床转速和脱氯时间5个影响因素.结果表明,pH值这一因素有极显著影响;在得出的纳米铁粉对四氯化碳脱氯的最佳工艺条件下,获得了99.5%的脱氯率,为有机氯化物脱氯开辟了一条新途径.     

A novel, simple and sensitive resonance scattering spectral method for the determination of chlorite in water by means of rhodamine B

A new resonance scattering method was proposed for the determination of chlorite, basing on the resonance scattering effect of rhodamine dye. In HCl-sodium acetate buffer solution, chlorite oxidizes 1- into 12 and the reaction of 12 and excess 1- results in If. It is respectively combined with rhodaminc dyes, including rhodamine B （RhB）, butyl rhodamine B （b-RhB）, rhodamine G （RhG） and rhodamine S （RhS）, to form association complex particles, which exhibit stronger resonance scattering （RS） effect at 400 nm. The chlorite concentration of ClO2 in the range of 0.00726-0.218 μg/ml, 0.0102-0.292 μg/ml, 0.00726-0.145 μg/ml and 0.0290- 0.174 μg/ml is respectively linear to the RS intensity of association complex particle systems at 400 nm for the RhB, b-RhB, RhG and RhS. The detection limits of the four systems were respectively 0.00436, 0.00652, 0.00580 and 0.01450μg/ml ClO2^-. In the four systems, the RhB system possesses good stability and high sensitivity. It has been applied to the analysis of chlorite in wastewater with satisfactory results.     

厌氧折流板式微生物燃料电池堆影响因素研究

微生物燃料电池(MFC)中输出电压/电流的提升,以及反应器体积的扩展放大是其工程化应用的关键。本文构建了一个总体积为6.4 L的新型厌氧折流板式微生物燃料电池堆(ABSMFC)。以葡萄糖作为底物,探讨了阳极材料、液面高程差和水力停留时间(HRT)等因素对ABSMFC性能的影响。结果表明,碳纤维毡作为阳极时,电池单体外电路平均分压(R_(ex)=1 000Ω)为210 mV,填充石墨颗粒后增加到319.8 mV。格室间存在液面高程差时,电池单体、串联和并联的功率密度分别为207.1、181.1和215.7 mW/m~2,当无液面高程差(即水力相连)时为205.8、69.5和151.5 mW/m~2。4个电池单体串联和并联连接时,HRT对ABSMFC的产电稳定性无影响,溶解性COD的去除率和库仑效率均随HRT的增加而升高,且并联效果优于串联。     

HRT对固定床厌氧反应器运行效果的影响

为了考察水力停留时间(HRT)对炭纤维载体固定床厌氧反应器运行效果的影响,在进水COD分别为20 000~25 000 mg/L和40 000~45 000 mg/L2个浓度范围下,研究了不同HRT对反应器运行效果的影响。结果表明,通过HRT的调整,在达到相同有机负荷(OLR)下,进水COD为20 000~25 000 mg/L的COD去除率和产气量,明显比进水COD为40 000~45 000 mg/L的运行效果好;进水COD为20 000~25 000 mg/L,HRT为14 h,相应的OLR为41.09 kgCOD/(m3.d)时,COD去除率仍然维持在68%以上,沼气容积产气率达到14.55 m3/(m3.d)。炭纤维载体固定床厌氧反应器具有较高的COD去除率、产气效率以及抵抗低pH、高负荷冲击的能力,运行过程中没有发生反应器堵塞的现象。     

Potential effects of particulate matter from combustion during services on human health and on works of art in medieval churches in Cyprus

Indoor and outdoor particulate matter (PM_0.3-10) number concentrations were established in two medieval churches in Cyprus. In both churches incense was burnt occasionally during Mass. The highest indoor PM_0.5-1 concentrations compared with outdoors (10.7 times higher) were observed in the church that burning of candles indoors was allowed. Peak indoor black carbon concentration was 6.8 μg m⁻³ in the instances that incense was burning and 13.4 μg m⁻³ in the instances that the candles were burning (outdoor levels ranged between 0.6 and 1.3 μg m⁻³). From the water soluble inorganic components determined in PM₁₀, calcium prevailed in all samples indoors or outdoors, whilst high potassium concentration indoors were a clear marker of combustion. Indoor sources of PM were clearly identified and their emission strengths were estimated via modeling of the results. Indoor estimated PM_0.3-10 mass concentrations exceeded air quality standards for human health protection and for the preservation of works of art.     

Appraisal of measurement methods, chemical composition and sources of fine atmospheric particles over six different areas of Northern Belgium

Daily and seasonal variation in the total elemental, organic carbon (OC) and elemental carbon (EC) content and mass of PM_2.5 were studied at industrial, urban, suburban and agricultural/rural areas. Continuous (optical Dustscan, standard tapered element oscillating micro-balance (TEOM), TEOM with filter dynamics measurement system), semi-continuous (Partisol filter-sampling) and non-continuous (Dekati-impactor sampling and gravimetry) methods of PM_2.5 mass monitoring were critically evaluated. The average elemental fraction accounted for 2-6% of the PM_2.5 mass measured by gravimetry. Metals, like K, Mn, Fe, Cu, Zn and Pb were strongly inter-correlated, also frequently with non-metallic elements (P, S, Cl and/or Br) and EC/OC. A high OC/EC ratio (2-9) was generally observed. The total carbon content of PM_2.5 ranged between 3 and 77% (averages: 12-32%), peaking near industrial/heavy trafficked sites. Principal component analysis identified heavy oil burning, ferrous/non-ferrous industry and vehicular emissions as the main sources of metal pollution.