Evaluation of the performance of rural wastewater treatment plants using chemical measurements in combination with statistical techniques: a case study

The performance of a wastewater treatment plant was assessed statistically using multivariate cluster and principle component analysis. This was after measuring some physico-chemical properties in the influent, effluent, downstream, and upstream waters over a 4-month period. The cluster analysis grouped the sampling sites into three clusters: relatively non-polluted (upstream), medium polluted (downstream), and polluted (influent and effluent). The polluted water was further subdivided into very highly (influent) and highly (effluent) polluted. The grouping of influent and effluent into one cluster was due to some water quality parameters such as amount of copper, lead, and phosphates that are not efficiently removed by the plant. Using principal component analysis, samples from the same site taken over a period of 4 months were scattered, indicating inconsistencies in the performance of the plant. This was more pronounced during the rainy season, suggesting that increased water volumes from open sewers make the already poorly performing plant worse. The major loading factors found by principle component analysis were phosphate, lead, iron, zinc, copper, pH, and conductivity. Generally, the wastewater treatment system was found to be efficient in removing heavy metals and these were found in the sludge, but not anions. The mean percentage metal removal could be arranged in the following decreasing order: iron (85%)?>?zinc (57%)?>?copper (40%) and lead (38%) following the concentrations (mg?kg^?1) found in the sludge: iron (11,300)?>?zinc (820)?>?copper (180)?>?lead (20)?>?cadmium (3). Phosphate and iron concentrations in the effluent were found to be above the South African Bureau of Standards (SABS) recommendations. The major cause of poor performance is the high volume of the wastewater, exceeding the capacity of the plant 10 times.     

Dispersive liquid–liquid microextraction of cadmium(II) for preconcentration prior to flame atomic absorption spectrometric detection in water

A dispersive liquid–liquid microextraction procedure for cadmium(II) as its 2-(5-bromo-2-pyridylazo)-5-diethylamino-phenol chelate is presented. Carbon tetrachloride and methanol were used as extraction and dispersive solvents, respectively. After phase separation, the preconcentrated-separated cadmium(II) is determined by flame atomic absorption spectrometry with a microinjection technique. The factors which affected the extraction efficiency, i.e. the pH of the sample solution and the volumes of reagent and sample were investigated. The effects of some alkali, alkali earth, and transition metal ions, and of some anions on the recovery of cadmium were also studied. A preconcentration factor of 250 was obtained for a sample volume of 50?mL under optimum conditions. The method was validated by analysis of certified reference materials and applied to some water samples from Turkey.     

Cobalt speciation assay for human serum,Part II. Method validation in a study of human volunteers ingesting cobalt(II) chloride dietary supplement for 90 days

A new analytical method for determining cobalt (Co) species in human serum by size exclusion chromatography with inductively coupled plasma mass spectrometry (SEC-ICP-MS) was applied to serum samples collected from 12 human volunteers who participated in a Co(II) chloride supplement study involving ingestion of 1 mg Co/day for up to 90 consecutive days. The study protocol included determination of serum total Co by acid digestion followed by ICP-MS. Co speciation assay measurements were conducted for up to 13 time points per individual spanning from one to two weeks before dosing began to two weeks after dosing ceased. The Co speciation assay showed good recovery >91% relative to total Co measurements. Undiluted serum demonstrated uniform fractions of large molecular Co defined as Co bound to albumin and other proteins >50 kDa at 96% and the residual as small molecular Co defined as free Co(II) and <1 kDa Co-complexes for individual serum Co concentrations up to 146 μg/L. There were no dose-related changes in Co distribution. Analysis of the same serum samples with tenfold dilution in 0.1 M acetic acid led to a lower fraction of large molecular Co at 87%, with the difference between diluted and undiluted measurements being 8.4%. The difference noted between undiluted and diluted large molecular Co may be attributed to Co release from albumin. Data demonstrated that large molecular Co was the predominant Co species in both undiluted and diluted human serum over a broad range of in vivo Co concentrations, reflecting high albumin–Co binding capacity. These data validate the Co speciation assay and may be employed in understanding further the toxicokinetics and dose-response relationships for Co species.     

Solid phase extraction of trace metals from environmental samples using Amberlite XAD-7 loaded with 2-hydroxy-propiophenone-4-phenyl-3-thiosemicarbazone and determination by inductively coupled plasma–atomic emission spectrometry

A method for the solid phase extraction of trace metals, namely Co, Cu, Pb, Ni and Zn, from environmental and biological samples using column Amberlite XAD-7 loaded with 2-hydroxy-propiophenone-4-phenyl-3-thiosemicarbazone (HPPPTSC) and determination by inductively coupled spectrometry (ICP–AES) has been developed. The reagent has the capacity to form chelate complexes with the metals because of three binding sites in the reagent molecule. The optimum experimental conditions for the quantitative sorption of five metals, pH, effect of flow rate, concentration of eluent, sorption capacity and the effect of diverse ions on the preconcentration of analytes have been investigated. The sorption capacity of the resin has 83, 127, 35, 88 and 85?µmol?g^?1 for Co²⁺, Cu²⁺, Pb²⁺, Ni²⁺ and Zn²⁺, respectively. The preconcentration factors for Co²⁺, Cu²⁺, Pb²⁺, Ni²⁺ and Zn²⁺ were 100, 110, 120, 140 and 150, respectively. The accuracy of the proposed procedure was evaluated by standard reference materials. The achieved results were in good agreement with certified values. The proposed method was applied for the determination of trace metals in river water and plant leaves.     

异质结型光催化剂CuO/SnO2的制备及产氢性能

光催化降解有机废水可以实现在降解污染物同时回收清洁能源.本研究采用简单沉淀法制备了CuO/SnO2系列复合光催化剂,并用XRD、TEM对其结构进行表征.分别考察了氧化铜含量和乙醇浓度对复合材料光催化产氢性能的影响.实验结果表明,通过氧化铜与二氧化锡适当比例复合能显著提高复合材料的光催化产氢性能.复合材料48.51%CuO/SnO2的产氢性能比纯二氧化锡提高了近5倍.乙醇的浓度也对复合材料的产氢性能有较大影响,最佳的乙醇浓度为2.00 mol.L-1左右.长时间光催化产氢结果表明,每降解废水中1 kg的COD可产生氢气3724 mL.另外,对复合材料光催化分解乙醇的产氢机理也进行了分析.     

焙烧条件对Ru/AC催化剂去除溴酸盐的影响

考察了以RuCl₃·3H₂O为前驱物,以AC(颗粒活性炭)为载体制备Ru/AC时,焙烧氛围、焙烧温度、焙烧时间对Ru/AC催化活性的影响,并利用XPS(X-ray photoelectron spectra,X射线光电子能谱分析)、BET(brunner-emmet-teller method,比表面积测定)和SEM(scanning electronic microscopy,扫描电镜)等手段对样品进行了表征. 结果表明,不同焙烧氛围中制备的Ru/AC活性有较大差异:在N₂焙烧氛围中,容易形成去除BrO₃-的有效活性组分(RuO₂);而在真空焙烧氛围中,几乎没有活性组分的产生;在H₂-N₂〔φ(H₂)为1.5%,φ(N₂)为98.5%〕氛围中焙烧,负载在AC上的活性组分有Ru₀(单质钌)和RuO₂. 焙烧温度对Ru/AC去除BrO₃-的性能有着较为显著的影响,高温有利于AC的石墨化进程,载体性能得到优化;但焙烧温度过高(1 000 ℃)时,会产生金属颗粒团聚现象;最适宜的焙烧温度为900 ℃. Ru/AC的活性随着焙烧时间的延长呈先增后降的趋势;焙烧时间为3 h时,载体的比表面积和孔容积得到提高且有效活性组分能够均匀地分散在AC载体上. 综上,Ru/AC催化剂的最优焙烧条件:焙烧氛围为N₂,焙烧温度为900 ℃,焙烧时间为3 h. 在该条件下制备的Ru/AC利于形成去除BrO₃-的活性物质RuO₂,并且其能够均匀地分布在AC载体上,使催化反应进行得更为彻底,可在2 h内将BrO₃-全部去除.      

Developed fungal–bacterial biofilms as a novel tool for bioremoval of hexavelant chromium from wastewater

Remediation measures for hexavalent chromium [Cr(VI)] are required for a safe environment. As a recent development in microbiology, bacterial biofilms are being studied as effective bioremediation agents. When bacteria are in fungal surface-attached biofilm mode, they are called fungal–bacterial biofilms (FBBs). They have not been tested for bioremediation so far. Hence, this study was conducted to develop FBBs and glass-wool-attached bacterial biofilms (BBs), and to evaluate Cr(VI) tolerability and removal of bacterial monocultures, BBs and FBBs. FBBs showed a significantly high level of Cr(VI) tolerance and resistance compared with its BBs or monocultures. After 10 days, up to 90% of Cr(VI) had been removed, which was significantly higher than that of BBs or its monocultures. Thus, it is clear that FBBs can be used as a novel tool to decontaminate Cr(VI) both in situ and ex situ.     

A multispecies assessment of wildlife impacts on local community livelihoods

Conflicts between the interests of agriculture and wildlife conservation are a major threat to biodiversity and human well-being globally. Addressing such conflicts requires a thorough understanding of the impacts associated with living alongside protected wildlife. Despite this, most studies reporting on human–wildlife impacts and the strategies used to mitigate them focus on a single species, thus oversimplifying often complex systems of human–wildlife interactions. We sought to characterize the spatiotemporal patterns of impacts by multiple co-occurring species on agricultural livelihoods in the eastern Okavango Delta Panhandle in northern Botswana through the use of a database of 3264 wildlife-incident reports recorded from 2009 to 2015 by the Department of Wildlife and National Parks. Eight species (African elephants [Loxodonta africana], hippopotamuses [Hippopotamus amphibious], lions [Panthera leo], cheetah [Acinonyx jubatus], African wild dogs [Lycaon pictus], hyenas [Crocuta crocuta], leopards [Panthera pardus], and crocodiles [Crocodylus niloticus]) appeared on incident reports, of which 56.5% were attributed to elephants. Most species were associated with only 1 type of damage (i.e., either crop damage or livestock loss). Carnivores were primarily implicated in incident reports related to livestock loss, particularly toward the end of the dry season (May–October). In contrast, herbivores were associated with crop-loss incidents during the wet season (November–April). Our results illustrate how local communities can face distinct livelihood challenges from different species at different times of the year. Such a multispecies assessment has important implications for the design of conservation interventions aimed at addressing the costs of living with wildlife and thereby mitigation of the underlying conservation conflict. Our spatiotemporal, multispecies approach is widely applicable to other regions where sustainable and long-term solutions to conservation conflicts are needed for local communities and biodiversity.     

Home composting as an alternative treatment option for organic household waste in Denmark: An environmental assessment using life cycle assessment-modelling

An environmental assessment of the management of organic household waste (OHW) was performed from a life cycle perspective by means of the waste-life cycle assessment (LCA) model EASEWASTE. The focus was on home composting of OHW in Denmark and six different home composting units (with different input and different mixing frequencies) were modelled. In addition, incineration and landfilling was modelled as alternatives to home composting. The most important processes contributing to the environmental impact of home composting were identified as greenhouse gas (GHG) emissions (load) and the avoided emissions in relation to the substitution of fertiliser and peat when compost was used in hobby gardening (saving). The replacement of fertiliser and peat was also identified as one of the most sensible parameters, which could potentially have a significant environmental benefit. Many of the impact categories (especially human toxicity via water (HTw) and soil (HTs)) were affected by the heavy metal contents of the incoming OHW. The concentrations of heavy metals in the compost were below the threshold values for compost used on land and were thus not considered to constitute a problem. The GHG emissions were, on the other hand, dependent on the management of the composting units. The frequently mixed composting units had the highest GHG emissions. The environmental profiles of the home composting scenarios were in the order of −2 to 16 milli person equivalents (mPE) Mg⁻¹ wet waste (ww) for the non-toxic categories and −0.9 to 28 mPE Mg⁻¹ ww for the toxic categories. Home composting performed better than or as good as incineration and landfilling in several of the potential impact categories. One exception was the global warming (GW) category, in which incineration performed better due to the substitution of heat and electricity based on fossil fuels.