连续流改进A~2/O反应器去污效果及分相培养研究

以生活污水为原水,在常温(25~33℃)条件下采用连续流改进A2/O反应器进行脱氮除磷实验研究。系统内COD降解,TN与TP去除主要在活性污泥段完成,而NH4+-N去除基本在生物接触氧化区完成。从中沉池出水硝态氮影响因素分析可知,选用较高的有机负荷有利于实现系统内分相培养。泥龄对实现系统内微生物异养菌和自养菌的分相培养具有关键影响。当泥龄10 d,可实现系统内异养菌与自养菌的分相培养。     

A method of detecting carbonyl compounds in tree leaves in China

Background, aim, and scope  

Carbonyl compounds have been paid more and more attention because some carbonyl species have been proven to be carcinogenic or a risk for human health. Plant leaves are both an important emission source and an important sink of carbonyl compounds. But the research on carbonyl compounds from plant leaves is very scarce. In order to make an approach to the emission mechanism of plant leaves, a new method was established to extract carbonyl compounds from fresh plant leaves.     

Reducing ammonia emissions from laying-hen houses through dietary manipulation

Feed additives can change the microbiological environment of the animal digestive track, nutrient composition of feces, and its gaseous emissions. This 2-yr field study involving commercial laying-hen houses in central Iowa was conducted to assess the effects of feeding diets containing EcoCal and corn-dried distillers grain with solubles (DDGS) on ammonia (NH3), hydrogen sulfide (H2S), and greenhouse gas (CO2, CH4, and N2O) emissions. Three high-rise layer houses (256,600 W-36 hens per house) received standard industry diet (Control), a diet containing 7% EcoCal (EcoCal) or a diet containing 10% DDGS (DDGS). Gaseous emissions were continuously monitored during the period of December 2007 to December 2009, covering the full production cycle. The 24-month test results revealed that mean NH3 emission rates were 0.58 +/- 0.05, 0.82 +/- 0.04, and 0.96 +/- 0.05 g/hen/day for the EcoCal, DDGS, and Control diet, respectively. Namely, compared to the Control diet, the EcoCal and DDGS diets reduced NH3 emission by an average of 39.2% and 14.3%, respectively. The concurrent H2S emission rates were 5.39 +/- 0.46, 1.91 +/- 0.13, and 1.79 +/- 0.16 mg/ hen/day for the EcoCal, DDGS, and Control diet, respectively. CO2 emission rates were similar for the three diets, 87.3 +/- 1.37, 87.4 +/- 1.26, and 89.6 +/- 1.6 g/hen/day for EcoCal, DDGS, and Control, respectively (P = 0.45). The DDGS and EcoCal houses tended to emit less CH4 than the Control house (0.16 and 0.12 vs. 0.20 g/hen/day) during the monitored summer season. The efficacy of NH3 emission reduction by the EcoCal diet decreased with increasing outside temperature, varying from 72.2% in February 2009 to -7.10% in September 2008. Manure of the EcoCal diet contained 68% higher ammonia nitrogen (NH3-N) and 4.7 times higher sulfur content than that of the Control diet. Manure pH values were 8.0, 8.9, and 9.3 for EcoCal, DDGS, and Control diets, respectively. This extensive field study verifies that dietary manipulation provides a viable means to reduce NH3 emissions from modern laying-hen houses.     

Nationwide monitoring of atmospheric PCDD/Fs and dioxin-like PCBs in South Korea

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) were measured in ambient air samples collected from different parts of South Korea in 2008, and the measured levels were used for assessing the spatial and temporal distribution of atmospheric PCDDFs and DL-PCBs in South Korea. The average concentrations of atmospheric PCDD/Fs and DL-PCBs among the 37 sites were 28 fg I-TEQ m⁻³ (ND ∼ 617) and 1 fg WHO-TEQ m⁻³ (ND ∼ 0.016). Elevated atmospheric levels of PCDD/Fs and DL-PCBs observed at residential/industrial sites and in the north-west of Korea, indicated a potential contribution and impacts of anthropogenic sources of PCDD/Fs and DL-PCBs. These levels were similar or lower than those previously reported in other ambient air surveys. Average concentrations of PCDD/Fs showed small seasonal variations (ANOVA analysis, p = 0.144). The highest concentrations of PCDD/Fs were observed during winter, followed by spring, autumn and summer. Atmospheric PCDD/Fs and DL-PCBs in South Korea rapidly decreased during the last 10 years (1998-2008), demonstrating the efficiency of stricter regulations and the application of best available technologies/best environmental practices at emission sources. Comparison of the congener profiles and principal component analysis showed that current atmospheric PCDD/Fs are mostly influenced by industrial sources and PCBs from old commercial PCB uses. Nationwide POPs monitoring will continue and allows an effective evaluation of the implementation of the Stockholm Convention on POPs.     

北京和上海典型复合包装废物处置环境影响比较

采用生命周期评价法研究比较了北京和上海两地纸塑铝复合包装处置阶段的环境影响。通过现场和资料调研的方式获得此阶段的能量物质的输入输出和环境外排数据。结果表明:北京和上海两地纸塑铝复合包装处置阶段的环境影响潜值分别为-0.428 Pt和9.776 Pt,其主要集中在气候变化、土地占用和无机物对健康的损害三方面;每提高10%的回收率,其环境影响潜值北京和上海可分别降低5.446 Pt和5.799 Pt;上海地区纸塑铝复合包装处置阶段对环境的影响在任何同回收率的情况都要高于北京地区,其主要原因是上海地区填埋产生的温室气体释放量过大和再生企业距离打包点较远。     

剩余污泥对活性黑KN-B的吸附性能

用剩余污泥对活性黑KN-B进行吸附研究,考察了pH、吸附时间、温度、盐类和污泥量等对活性黑KN-B吸附的影响.结果表明,剩余污泥对活性黑KN-B的吸附是一个快速过程,吸附时间可控制在30 min；其吸附过程可以用准二级动力学模型进行描述和预测；温度对污泥吸附活性黑KN-B产生的影响较小；其吸附等温线,25℃、35℃时与Freundlich方程拟合良好,45℃时则可以由Langmuir方程更好地描述.未调pH的剩余污泥,对pH≤2的废水中活性黑KN-B吸附性能良好；剩余污泥pH为1时,对pH＜12的废水中活性黑KN-B均可有效吸附；氯化钠浓度低于500 mg/L或氯化钠和硫酸钠的混合盐浓度低于100 mg/L时,有利于吸附；氯化钠浓度高于500 mg/L、混合盐浓度高于100 mg/L或单独加入硫酸钠后,随盐浓度的增加,吸附量呈下降趋势.     

厌氧氨氧化菌活性恢复及富集培养研究

为了防止微生物流失,向厌氧序批式反应器(ASBR)中投加纤维膜(无纺布)作为厌氧氨氧化菌的载体,而使ASBR改为厌氧序批式生物膜反应器(ASBBR),研究了厌氧氨氧化菌活性恢复及富集培养过程中氮负荷提高对ASBBR的影响。经过23d的培养,厌氧氨氧化菌的活性恢复到原有的水平,然后提高TN容积负荷培养厌氧氨氧化菌。至132d时,反应器TN容积去除负荷达到了2.060kg/(m3·d)。整个过程中NH4+-N和NO2--N去除率一直保持在98%以上。当厌氧氨氧化菌活性恢复后,NH4+-N、NO2--N消耗量与NO3--N生成量之比最终趋于一定值(1.00∶1.30∶0.25)。在培养过程中,污泥颜色逐渐由灰色变为红棕色,最终变为浅红色。结果表明,反应器运行很稳定,NH4+-N、NO2--N出水浓度非常低,在短时间内能提高到较高的容积去除负荷。可见,ASBBR很适合厌氧氨氧化菌的富集培养。     

Harvesting of Chlorella sp. using hollow fiber ultrafiltration

Introduction

The suitability of the application of ultrafiltration (UF) to harvest Chlorella sp. from the culture medium was examined. We investigated the effects of two improved UF system, forward air?Cwater flushing and backwash with permeate, on the concentration process.

Materials and methods

Backwash with permeate was selected as an optimization of the improved UF system, which was more effective for permeate flux recovery. Moreover, the hollow fiber UF system by adding periodical backwash with permeate was examined for Chlorella sp. harvesting.

Results and discussion

It was found that Chlorella sp. could be concentrated with high recovery in a lab-scale experiment. An overall algal biomass recovery of above 90% was achieved when the volume concentration factor was 10. For an original biomass of 1.3?±?0.05?g/L, 1?min backwash followed by 20?min forward concentrating was more effective, which resulted in a recovery of 94% and a high average flux of 30.3?L/m²/h. In addition, the algal recovery was highly correlated to the volume concentration factor and the initial biomass. A high concentration factor or a high initial biomass resulted in a low biomass recovery.     

Effects of compositional heterogeneity and nanoporosity of raw and treated biomass-generated soot on adsorption and absorption of organic contaminants

A biomass-generated soot was sequentially treated by HCl-HF solution, organic solvent, and oxidative acid to remove ash, extractable native organic matter (EOM), and amorphous carbon. The compositional heterogeneity and nano-structure of the untreated and treated soot samples were characterized by elemental analysis, thermal gravimetric analysis, BET-N₂ surface area, and electron microscopic analysis. Sorption properties of polar and nonpolar organic pollutants onto the soot samples were compared, and individual contributions of adsorption and absorption were quantified. The sorption isotherms for raw sample were practically linear, while were nonlinear for the pretreated-soot. The removal of EOM enhanced adsorption and reduced absorption, indicating that EOM served as a partitioning phase and simultaneously masked the adsorptive sites. By drastic-oxidation, the outer amorphous carbon and the inner disordered core of the soot particles were completely removed, and a fullerene-like nanoporous structure (aromatic shell) was created, which promoted additional π-π interaction between phenanthrene and the soot.     

Climate change mitigation policy paradigms—national objectives and alignments

The aim of this paper is to assess how policy goals in relation to the promotion of green growth, energy security, pollution control and greenhouse gas (GHG) emissions reductions have been aligned in policies that have been implemented in selected countries during the last decades as a basis for discussing how a multi objective policy paradigm can contribute to future climate change mitigation. The paper includes country case studies from Brazil, Canada, China, the European Union (EU), India, Japan, Mexico, Nigeria, South Africa, South Korea and the United States covering renewable energy options, industry, transportation, the residential sector and cross-sectoral policies. These countries and regions together contribute more than two thirds of global GHG emissions. The paper finds that policies that are nationally driven and that have multiple objectives, including climate-change mitigation, have been widely applied for decades in both developing countries and industrialised countries. Many of these policies have a long history, and adjustments have taken place based on experience and cost effectiveness concerns. Various energy and climate-change policy goals have worked together in these countries, and in practice a mix of policies reflecting specific priorities and contexts have been pursued. In this way, climate-change mitigation has been aligned with other policy objectives and integrated into broader policy packages, though in many cases specific attention has not been given to the achievement of large GHG emission reductions. Based on these experiences with policy implementation, the paper highlights a number of key coordination and design issues that are pertinent to the successful joint implementation of several energy and climate-change policy goals.