排污权交易基准价定价机制探讨

构建科学合理的基准价定价机制是推动排污权交易的基础性工作,本文以政策、管理、技术三个方面作为立足点,探讨了基准价定价机制,构建了工作框架。研究认为现阶段基准价定价采取成本定价法是合适的,并对基准价定价技术难点进行了剖析,提出了建议。     

Applicability of a continuous-flow system inner-coated with S-doped titania for the photocatalysis of dimethyl sulfide at low concentrations

The present study investigated the photocatalytic activity of an S-doped TiO₂ photocatalyst with regards to dimethyl sulfide degradation under visible-light irradiation, along with its deactivation and reactivation. The dimethyl sulfide conversion was between 85% and 93% for the lowest relative humidity range (10–20%) and close to 100% for the two higher relative humidity ranges (45–55% and 80–90%). The conversion was also close to 100% for the two lowest input concentrations (0.039 and 0.195 ppm), while it was between 91% and 96% at 3.9 ppm and between 85% and 90% at 7.9 ppm. In contrast to the input concentration dependences on conversion, the calculated degradation rates increased as input concentrations increased. The dimethyl sulfide conversion at low concentrations (≤0.39 ppm), which are associated with non-occupational inn occurring. However, catalyst deactivations were observed during the photocatalytic process whdoor air quality issues, was up to nearly 100% for long time periods (at least 603 h), without any significant catalyst deactivatioen higher concentrations (3.9 and 7.8 ppm) were used. The photocatalyst, reactivated by using two types of air (dried and humidified) under visible-light irradiation, did not regain all of its initial activities. Sulfate groups were qualitatively identified as the reaction products on the photocatalyst surface. In addition, gaseous byproducts, quantitatively determined, included dimethyl disulfide, methanol, and SO₂. It is noteworthy that the peak concentration of dimethyl disulfide (0.79 ppm = 790 ppb), generated over the photocatalytic process with the highest dimethyl sulfide input concentration, exceeded the odor threshold value of 0.1–3.6 ppb for dimethyl disulfide.     

The stability of dieldrin,aldrin, lindane,chlorpyrifos and prothiofos in stored roof water

Abstract

The stability of dieldrin, aldrin, lindane, chlorpyrifos and prothiofos was determined in distilled water and in roof water from either galvanised or concrete tanks. Samples were stored in the dark at 23°C. Dieldrin and lindane were stable for the 36 week period. Aldrin dissipated rapidly with a half‐life of 4–5 weeks, with no dieldrin being formed. Chlorpyrifos and prothiofos also broke down, with half‐lives ranging 12–18 weeks and 11–14 weeks respectively. No significant effect of water type was found. For the purpose of domestic usage, an activated carbon filter would be essential otherwise all contaminated water would have to be disposed of safely.     

Synthesis of a highly recoverable 3D MnO2/rGO hybrid aerogel for efficient adsorptive separation of pharmaceutical residue

Water contamination by non-steroidal anti-inflammatory drugs, such as acetaminophen, is an emerging ecological concern. In this study, a new three-dimensional manganese dioxide-engrafted reduced graphene oxide (3D MnO₂/rGO) hybrid aerogel was developed for acetaminophen sequestration. The synthesis involved firstly the self-assembly of GO aerogel, followed by thermal reduction and in-situ MnO₂ growth by redox-reaction. The aerogel demonstrated interlinked planes with smooth surfaces deposited with MnO₂ nanospheres and pores of 138.4 – 235.3 µm width. The influences of adsorbent dosage, initial pH, acetaminophen concentration, temperature and contact time were investigated. It was determined that the adsorption of acetaminophen occurred on uniform sorption sites in the aerogel, as suggested by the best fit of data to the Langmuir isotherm, yielding a maximum adsorption capacity of 252.87 mg/g. This highest adsorption performance of the 3D MnO₂/rGO aerogel was attained at a dosage of 0.6 g/L, initial pH of 6.2 and temperature of 40°C. The process kinetics were in-line with the pseudo-first-order and pseudo-second-order kinetics at 10 and 20 – 500 mg/L concentrations, respectively. Thermodynamic assay showed the spontaneity and endothermicity features of the 3D MnO₂/rGO-acetaminophen system. The acetaminophen adsorption mechanisms were mainly hydrogen bonding and pore entrapment. Moreover, the as-synthesised aerogel was effectively regenerated using acetone and re-utilised in four adsorption-desorption cycles. Overall, the results highly recommend the implementation of the 3D MnO₂/rGO hybrid aerogel for purification of wastewater polluted by acetaminophen residue.     

光纤光栅传感器及其应用

综述了几种典型光纤光栅传感器及在传感领域的应用。首先介绍了光纤光栅传感的基本原理,然后对布拉格光栅、长周期光栅、倾斜光栅和啁啾光栅的结构、光学特性进行了说明。最后阐述了光纤光栅传感器在温度传感、结构健康监测、腐蚀研究等方面的应用,以及在应用上的不足和今后的发展方向。     

云南省滑坡泥石流与强降水的相关性和多时间尺度特征研究

以云南省1961-2011年的滑坡泥石流灾害和逐日降水观测数据为基础,采用相关分析和小波变换分析方法,研究了云南滑坡泥石流与强降水变化的相关性特征和多时间尺度特征。结论为:近51年来云南滑坡泥石流活动频次呈现出逐步增长的趋势,云南滑坡泥石流与强降水的变化具有显著的相关关系,与暴雨的相关性最高,其次为大暴雨和大雨。云南滑坡泥石流与强降水变化表现出十分明显的多时间尺度变化特征。滑坡泥石流与强降水的变化均存在有6年的特征时间尺度变化,在6年的特征时间尺度上,云南滑坡泥石流的变化一般是相同或滞后于强降水的变化。     

Triazine and metolachlor herbicide residues in farm areas of the Lower Fraser valley, British Columbia, Canada

Crop soils, ditch sediments and water flowing from several Lower Fraser River (LFR) farm areas of British Columbia, Canada, to salmon tributary streams of that river were sampled in 2004-2005 to quantify for residues of triazine [atrazine, desethylatrazine (a transformation product of atrazine), propazine, and simazine] and metolachlor (a chloroacetamide) herbicides. Average concentrations [microg kg-1 dry weight (d.w.)] of triazine (10,110) and metolachlor (8,910) herbicides detected in crop soils at the start (May 2004, 2005) of the growing season were about 17 and 6 times, respectively, higher than those found for both herbicide groups during (June-Sept, 2004, 2005) the growing season. In contrast, mean concentrations (microg L-1) of triazines (0.092) and metolachlor (0.014) in permanent ditches adjacent to farms were about 7 and 28 times, respectively, lower at the start than during the growing season. Both herbicide groups in ditch sediments were detected only during the growing season at concentrations averaging about 315 microg kg-1 d.w. The risk potential of these herbicides for non-target aquatic organisms inhabiting permanent farm ditches contiguous to tributary streams of the LFR during the growing season is evaluated and discussed.     

Ecological risk of pesticide residues in the British Columbia environment: 1973–2012

An updated ecological risk assessment was conducted to re-evaluate and review the overall risk of pesticide residues to certain aquatic life. The focus was the impact on offsite non-target, freshwater organisms of pesticide operational sprays in British Columbia from 1973 until 2012. The values of risk quotients for pesticides of selected indicator organisms were determined to measure the effect. When compared with organophosphorus, carbamate, and other miscellaneous pesticides, this risk assessment analysis suggests that the historical use of persistent and highly toxic organochlorine pesticides posed, and continue to pose, a deleterious ecological risk. The risk is both short-term acute and long-term sub-acute, chronic toxicity to offsite, non-target aquatic invertebrates and juvenile salmonid fish. Data indicated that these organisms were, and remain, subjected to harmful effects of pesticide residues to varying degrees. Most vulnerable were, and also are, benthic organisms inhabiting bottom sediments. This substrate is the natural sink for persistent pesticide residues, predominantly organochlorine pesticides from historical use, as well as dioxins, furans, and polycyclic aromatic hydrocarbons from wood preservatives, and other sources. Environment Canada's main aquatic protection strategy was a 10 metre no-treatment buffer zone, augmented with an additional appropriate setback along shorelines of fishery and wildlife resource-sensitive water bodies. This study discusses why this guideline was necessary, useful and effective, but was only partially successful. The physical-chemical properties of pesticide residues, from either an individual compound or different compounds in combination, also influence the nature of biological impacts on non-target, aquatic organisms. Few studies have been conducted in British Columbia aquatic environments to investigate the significance of this aspect.     

热修复过程中重质非水相液体(DNAPL)共沸实验

本研究开展单组分和多组分DNAPL加热实验,旨在建立热处理过程中温度与DNAPL去除之间的联系.结果表明,单组分DNAPL实验中可以观察到明显的共沸温度平台,而多组分DNAPL实验则是一段温度逐渐上升的共沸区域,两组实验中共沸时间均与初始DNAPL饱和度呈正相关.仅根据局部温度数据判断热修复进程可能会导致错误的结论,当温度结果显示共沸结束后,体系内仍残留有饱和度0.94%~1.60%的DNAPL.温度数据会受到DNAPL组成和温度监测点位置影响,它通常仅能反映局部加热情况,修复时可结合气体和土壤样品中污染物组分变化情况辅助判断修复进程.