用于评价水污染的生物指数

对各国学者所建立的应用较广泛的生物指数作了综述 ,通过分析各种生物指数的优点与缺陷 ,指出了目前建立生物指数方法上的不足 ,并提出了建立生物指数应该采用的更合理的方法。     

Conserving water by optimizing production schedules in the dyeing industry

Industrial dyeing processes generate a huge amount of wastewater, because the production lines have to be washed out each time when the dye changes. We propose an algorithm for the optimization of production schedule. It aims to reduce the production time and the amount of freshwater consumption by optimization the groups orders according to color. Furthermore, we develop software based on the genetic algorithm and implement it in a Chinese company. We optimize the schedules in three months of the case company and compare its output to actual data. The results show that compared to the original manual schedules, the optimized schedules cut production time by 10–15%, reduce freshwater consumption by 20–30%, and reduce wastewater generation by about 20%.     

含汞气田污水脱汞新技术

国内气田含汞污水处理主要采用硫化物沉淀法,辅以水处理絮凝剂增加沉淀效果。国外研究了一些含汞污水脱汞新工艺:沉淀一絮凝法、活性炭吸附法、离子交换法等,组合使用效果更佳,可脱除单质汞、离子汞和有机汞,脱汞深度可达1.0×10~(-9)mg/L级。借鉴国外含汞气田污水处理工艺,研究经济高效的脱汞工艺,减少汞污染,对我国含汞气田的合理开发具有重要的现实意义。     

基于余震序列分布信息的地震极灾区快速判断方法研究

利用震级加权标准差椭圆法研究了基于震后短期内(24 h)余震序列判定地震极灾区的方法,研究结果表明:1利用该方法判断宏观震中是一种比较可行的方法,不同震源破裂方式的震例利用该方法判断宏观震中的精度不同,倾滑-近倾滑型破裂方式的震例利用余震序列判定宏观震中的精度最高;2整体上看,利用该方法判断极灾区长轴方向的准确性低于利用距震中最近活动断裂判断的准确性,但对于倾滑-近倾滑型破裂方式的震例,利用该方法的准确性高于利用断层数据判定的准确性。     

Phosphorus recovery from biogas fermentation liquid by Ca–Mg loaded biochar

Shortage in phosphorus (P) resources and P wastewater pollution is considered as a serious problem worldwide. The application of modified biochar for P recovery from wastewater and reuse of recovered P as agricultural fertilizer is a preferred process. This work aims to develop a calcium and magnesium loaded biochar (Ca–Mg/biochar) application for P recovery from biogas fermentation liquid. The physico-chemical characterization, adsorption efficiency, adsorption selectivity, and postsorption availability of Ca-Mg/biochar were investigated. The synthesized Ca–Mg/biochar was rich in organic functional groups and in CaO and MgO nanoparticles. With the increase in synthesis temperature, the yield decreased, C content increased, H content decreased, N content remained the same basically, and BET surface area increased. The P adsorption of Ca–Mg/biochar could be accelerated by nano-CaO and nano-MgO particles and reached equilibrium after 360 min. The process was endothermic, spontaneous, and showed an increase in the disorder of the solid–liquid interface. Moreover, it could be fitted by the Freundlich model. The maximum P adsorption amounts were 294.22, 315.33, and 326.63 mg/g. The P adsorption selectivity of Ca–Mg/biochar could not be significantly influenced by the typical pH level of biogas fermentation liquid. The nano-CaO and nano-MgO particles of Ca–Mg/biochar could reduce the negative interaction effects of coexisting ions. The P releasing amounts of postsorption Ca–Mg/biochar were in the order of Ca–Mg/B600 > Ca–Mg/B450 > Ca–Mg/B300. Results revealed that postsorption Ca–Mg/biochar can continually release P and is more suitable for an acid environment.     

Adsorption of three pharmaceuticals on two magnetic ion-exchange resins

The presence of pharmaceuticals in aquatic environments poses potential risks to the ecology and human health. This study investigated the removal of three widely detected and abundant pharmaceuticals, namely, ibuprofen (IBU), diclofenac (DC), and sulfadiazine (SDZ), by two magnetic ion-exchange resins. The adsorption kinetics of the three adsorbates onto both resins was relatively fast and followed pseudo-second-order kinetics. Despite the different pore structures of the two resins, similar adsorption patterns of DC and SDZ were observed, implying the existence of an ion-exchange mechanism. IBU demonstrated a combination of interactions during the adsorption process. These interactionswere dependent on the specific surface area and functional groups of the resin. The adsorption isothermfittings verified the differences in the behavior of the three pharmaceuticals on the two magnetic ion-exchange resins. The presence of Cl^- and SO₄^2- suppressed the adsorption amount, butwith different inhibition levels for different adsorbates. This work facilitates the understanding of the adsorption behavior andmechanismof pharmaceuticals onmagnetic ion-exchange resins. The results will expand the application of magnetic ion-exchange resins to the removal of pharmaceuticals in waters.     

Can arbuscular mycorrhiza and fertilizer management reduce phosphorus runoff from paddy fields?

Our study sought to assess how much phosphorus (P) runoff from paddy fields could be cut down by fertilizer management and inoculation with arbuscular mycorrhizal fungi. A field experiment was conducted in Lalin River basin, in the northeast China: six nitrogen–phosphorus–potassium fertilizer levels were provided (0, 20%, 40%, 60%, 80%, and 100% of the recommended fertilizer supply), with or without inoculation with Glomus mosseae. The volume and concentrations of particle P (PP) and dissolved P (DP) were measured for each runoff during the rice growing season. It was found that the seasonal P runoff, including DP and PP, under the local fertilization was 3.7 kg/ha, with PP, rather than DP, being the main form of P in runoff water. Additionally, the seasonal P runoff dropped only by 8.9% when fertilization decreased by 20%; rice yields decreased with declining fertilization. We also found that inoculation increased rice yields and decreased P runoff at each fertilizer level and these effects were lower under higher fertilization. Conclusively, while rice yields were guaranteed arbuscular mycorrhizal inoculation and fertilizer management would play a key role in reducing P runoff from paddy fields.     

Water chemistry controlled aggregation and photo-transformation of silver nanoparticles in environmental waters

The inevitable release of engineered silver nanoparticles (AgNPs) into aquatic environments has drawn great concerns about its environmental toxicity and safety. Although aggregation and transformation play crucial roles in the transport and toxicity of AgNPs, how the water chemistry of environmental waters influences the aggregation and transformation of engineered AgNPs is still not well understood. In this study, the aggregation of polyvinylpyrrolidone (PVP) coated AgNPs was investigated in eight typical environmental water samples (with different ionic strengths, hardness, and dissolved organic matter (DOM) concentrations) by using UV–visible spectroscopy and dynamic light scattering. Raman spectroscopy was applied to probe the interaction of DOM with the surface of AgNPs. Further, the photo-transformation and morphology changes of AgNPs in environmental waters were studied by UV–visible spectroscopy, inductively coupled plasma mass spectrometry, and transmission electron microscopy. The results suggested that both electrolytes (especially Ca^2 + and Mg^2 +) and DOM in the surface waters are key parameters for AgNP aggregation, and sunlight could accelerate the morphology change, aggregation, and further sedimentation of AgNPs. This water chemistry controlled aggregation and photo-transformation should have significant environmental impacts on the transport and toxicity of AgNPs in the aquatic environments.