Effect of outside air ventilation rate on volatile organic compound concentrations in a call center

A study of the relationship between outside air ventilation rate and concentrations of volatile organic compounds (VOCs) generated indoors was conducted in a call center office building. The building, with two floors and a total floor area of 4600 m², is located in the San Francisco Bay Area, CA. Ventilation rates were manipulated with the building's four air handling units (AHUs). VOC and CO₂ concentrations in the AHU returns were measured on 7 days during a 13-week period. VOC emission factors were determined for individual zones on days when they were operating at near steady-state conditions. The emission factor data were subjected to principal component (PC) analysis to identify groups of co-varying compounds. Potential sources of the PC vectors were ascribed based on information from the literature. The per occupant CO₂ generation rates were 0.0068–0.0092 l s⁻¹. The per occupant isoprene generation rates of 0.2–0.3 mg h⁻¹ were consistent with the value predicted by mass balance from breath concentration and exhalation rate. The relationships between indoor minus outdoor VOC concentrations and ventilation rate were qualitatively examined for eight VOCs. Of these, acetaldehyde and hexanal, which likely were associated with material sources, and decamethylcyclopentasiloxane, associated with personal care products, exhibited general trends of higher concentrations at lower ventilation rates. For other compounds, a clear inverse relationship between VOC concentrations and ventilation was not observed. The net concentration of 2,2,4-trimethyl-1,3-pentanediol monoisobutyrate isomers, examples of low-volatility compounds, changed very little with ventilation likely due to sorption and re-emission effects. These results illustrate that the efficacy of ventilation for controlling VOC concentrations can vary considerably depending upon the operation of the building, the pollutant sources and the physical and chemical processes affecting the pollutants. Thus, source control measures, in addition to adequate ventilation, are required to limit concentrations of VOCs in office buildings.     

用锥面砧镦粗减小镦偏的分析

由于剪切坯料端面偏斜,拍扁时压成椭圆形,此文称此现象为镦偏。此文分析了用锥形砧镦粗减小镦偏的作用,建立了分步压缩的主应力法计算模型模拟减小镦偏过程,描述了锥砧的斜角、接触面摩擦系数、压下量等参量对减小镦偏的作用,给出了具有参考价值的计算结果。     

Heavy metals contamination of soils under oak ecosystems in the Sofia region

We studied the contamination of Cu, Zn, Pb, and Cd in soils under oak ecosystems of urban (U), suburban (SU), and rural (R) regions in Sofia, Bulgaria. The urban sampling sites are located in the large forest parks of Sofia under oak ecosystems, while the others are located between the centre of the town and the surrounding mountains and are also from oak ecosystems. The concentrations of Cu, Zn, Pb, and Cd in soils were measured for identifying the sources and degree of contamination, and calculating the concentration coefficients (Hc) and enrichment factors (EF). The result of applying principal component analysis (PCA), showed that Cd and Pb accounted for the anthropogenic pollution and could be inferred as its tracers, whereas Cu is located mainly in the parent material. The Zn concentration levels were controlled both by its original content in the parent material as well as by anthropogenic pollution. The results obtained for the city forest parks allow for their successful use for recreation purposes.     

Organic carbon and environmental quality of riverine and off-shore sediments from the Gulf of Cádiz,Spain

Here we show that heavy metal geoaccumulation is apparent in the Tinto and Odiel estuary and, at a lower magnitude, in off-shore sediments. Values above probable effects level (PEL) are recorded for As, Cu, Hg, Pb and Zn in the Tinto and Odiel estuary, for As and Hg in the associated off-shore sediments and for As in the Guadiana River. Significant correlations were found between total organic carbon (TOC) and Cr, Cu, Ni and Zn in the Tinto and Odiel estuary, and Cr, Cu, Ni, Pb, Hg and As in the Guadiana River. PCA analysis differentiated the three studied locations.     

海平面上升对珠江口水位影响的分析

珠江三角洲水位变化存在着大量不确定性、不精确性,这些特性既具有模糊特征,也具有灰色特征。在分析珠江三角洲灯笼山站年平均水位的变化特征和闸坡站海平面变化趋势的基础上,利用灰关联法分析代表站灯笼山站年平均水位与流量、海平面、潮差等8个因素的关系,年平均水位与影响因素之间的灰关联度均大于0.7,说明各因子对年平均水位均产生显著影响,其中海平面变化与年平均水位的灰关联度为0.736,说明海平面变化是年平均水位的重要影响因素。选取灰关联度较大的（马＋三）流量、闸坡站海平面、灯笼山站的年最高水位、年最低水位、年平均低潮、年平均潮差这6个指标进行主成分分析。结果表明：第一主成分为径流潮汐作用,第二主成分的代表因素为海平面上升,第三主成分的代表因素为年最高水位;其中海平面上升为代表的第二主成分对年平均水位的贡献率为20.1%。因此,海平面上升对灯笼山站年平均水位的影响虽然弱于径流潮汐作用,但其影响也是显著的。     

Influence of the inherent properties of drinking water treatment residuals on their phosphorus adsorption capacities

Batch experiments were conducted to investigate the phosphorus（P） adsorption and desorption on five drinking water treatment residuals（WTRs） collected from different regions in China. The physical and chemical characteristics of the five WTRs were determined. Combined with rotated principal component analysis, multiple regression analysis was used to analyze the relationship between the inherent properties of the WTRs and their P adsorption capacities. The results showed that the maximum P adsorption capacities of the five WTRs calculated using the Langmuir isotherm ranged from 4.17 to8.20 mg/g at a p H of 7 and further increased with a decrease in p H. The statistical analysis revealed that a factor related to Al and 200 mmol/L oxalate-extractable Al（Alox） accounted for 36.5% of the variations in the P adsorption. A similar portion（28.5%） was attributed to an integrated factor related to the p H, Fe, 200 mmol/L oxalate-extractable Fe（Feox）, surface area and organic matter（OM） of the WTRs. However, factors related to other properties（Ca,P and 5 mmol/L oxalate-extractable Fe and Al） were rejected. In addition, the quantity of P desorption was limited and had a significant negative correlation with the（Feox＋ Alox） of the WTRs（p 〈 0.05）. Overall, WTRs with high contents of Alox, Feoxand OM as well as large surface areas were proposed to be the best choice for P adsorption in practical applications.     

太湖东部水域浮游硅藻群落特征及其与环境因子关系

对太湖东部水域9个点位浮游硅藻的群落结构进行了分析。结果表明,9个点位的生物多样性处于一般到较丰富状态,其水质为中污染到轻污染;硅藻群落的物种丰富度、生物量和密度因水域地形特点、换水周期等因素出现差异,在半封闭水体中的物种丰富度较差,生物量和藻密度较高,优势种所指示的水质处于中等偏下水平。硅藻相对多度和各项环境因子冗余分析显示,总磷(TP)对群落的组成和分布影响显著。东北部水域浮游硅藻群落主要受到TP和浊度(NTU)的影响,东南部水域浮游硅藻群落受到TP和NTU的影响则很小。     

长江重庆段溶解性有机物的荧光特性分析

利用三维荧光光谱(EEMs),并结合平行因子分析(PARAFAC)及主成分分析(PCA),研究了长江重庆段溶解有机物(DOM)的荧光组分特征及其污染来源,并探讨了荧光强度同溶解性有机碳(DOC)及溶解氧(DO)的相关性.结果表明,PARAFAC模型识别出长江重庆段DOM由2类6个荧光组分组成,即类腐殖质荧光组分C1(350/422 nm)、C4(245,305/395 nm)、C5(260,340/420 nm)、C6(260/480 nm)及类蛋白荧光组分C2(275/300 nm)、C3(227,278/329 nm).在DOM来源组成中,陆源的类腐殖质含量占62.56%,类蛋白物质含量占31.31%.类腐殖质组分的荧光强度同DOC的含量存在明显的线性正相关(r=0.73),类蛋白组分的荧光强度同DO的含量呈明显的线性负相关(r=0.80).EEMs-PARAFAC不仅可以表征长江重庆段DOM的光谱特征,示踪长江重庆段的有机污染程度,还可以为三峡库区水体保护提供依据.     

铅锌矿区农田土壤重金属的统计分析及空间分布研究

对广西某铅锌矿区周边农田表层进行了采样分析,测定了土壤中Zn、Pb、Cd、Hg、Cu、As、Ni、Cr的含量,依据土壤环境质量标准,分析了研究区域内表层土壤重金属污染程度,并通过主要成分分析和半变异函数分析,对重金属的空间分布特征进行了研究.结果表明,调查区域不同程度地受到Zn、Pb、Cd、Hg.Cu.As、Ni、Cr的污染.其中污染最重的是Cd,100%超标,超标倍数在0.67～311.93之间;其次是Zn、Hg、Pb,超标率分别为97%、84%、36%,平均超标倍数分别为10.94、3.03、1.09;污染较轻的是As、Ni、Cu、Cr.主成分分析结果将8种重金属元素分为第一主成分(Zn、Pb、Cd、Hg)和第二主成分(As、Ni、Cu、Cr),第一和第二主成分的贡献率分别为54.36%和31.19%.第一主成分在离矿区较近的西北偏西面有着较高的分布,说明第一主成分主要受铅锌矿厂污染的影响;而第二主成分在离矿区较近的西北偏西面和离矿区较远的东南偏南面都有着较高的分布,说明第二主成分不仅与铅锌矿厂的污染有关,而且与土壤母质也有很大的关系.