碱渣对锌(Ⅱ)离子吸附特性的研究

研究了锌在碱渣表面的吸附特征.结果表明,碱渣总吸附量随体系温度的升高而降低;随体系 pH 值的升高而增加;随吸附质初始浓度的增加而增大.在 pH<5.51 时其等温吸附能较好地符合 Freudlich 等温吸附规律,而在 pH5.51 时,能较好地符合 Langmuir 等温吸附规律,吸附热随 pH 的增大而升高.当pH≤5.51时,碱渣的吸附力以范德华力平和疏水键力的作用为主,而当 pH6.17 时,以化学键力为主.在 pH 为 5.05、6.07和7.03时,碱渣对 Zn26 的吸附动力学方程都以 Langmuir 方程的拟合效果最优.     

Elevation of biochar application as regulator on denitrification/NH3 volatilization in saline soils

Environmental Science and Pollution Research - Denitrification and NH3 volatilization are the main removal processes of nitrogen in coastal saline soils. In this incubation study, the effects of...     

锰铜铈氧化物催化剂氧化NO性能及动力学研究

实验以TiO2为载体采用浸渍法制备CuOx/TiO2、CeOx/TiO2、CuCeOx/TiO2和MnCuCeOx/TiO2催化剂,考察这些催化剂氧化NO活性,探究Cu、Ce摩尔比和添加Mn元素对CuCeOx/TiO2催化剂氧化NO活性的影响,使用扫描电镜观察催化剂表面结构.研究发现,Cu、Ce元素配合后的CuCeOx/TiO2催化剂氧化活性明显好于单独含Cu、Ce的催化剂,当Cu、Ce摩尔比为Cu:Ce=1:2时,CuCeOx/TiO2催化剂氧化活性最好,在NO浓度500×10-6,O2 10%,空速为24 000 h-1,350℃时,NO氧化度为0.62;添加Mn元素可以提高CuCeOx/TiO2催化剂低温氧化活性, 250℃时,MnCuCe/Ti-3和MnCuCe/Ti-5催化剂氧化度为0.53和0.69,300℃时,MnCuCe/Ti-3和MnCuCe/Ti-5催化剂氧化度均为0.76;此外,实验还研究了NO在MnCuCe/Ti-3催化剂上反应的动力学方程.     

废水中2,6-二硝基酚厌氧毒性和降解动力学研究

在中温(35℃±1℃)厌氧条件下,以葡萄糖为共基质,采用间歇实验方法,研究了2,6-二硝基酚(2,6-DNP)的厌氧产甲烷毒性和厌氧降解动力学.厌氧毒性试验(ATA)以累计产甲烷量和相对活性(RA)为指标,评价了不同浓度2,6-DNP对产甲烷菌的抑制程度;结果表明,2,6-DNP浓度＜20 mg/L时,对产甲烷菌没有抑制作用,浓度为40 mg/L时产生轻度抑制,浓度为80～120 mg/L时产生重度抑制;24 h 2,6-DNP的75%、50%、25%相对抑制浓度分别为30、70和＞120 mg/L.2,6-DNP降解动力学可用Haldane方程来描述,利用非线性拟合求得动力学参数Ks、Rm、Ki分别为179.7 mg/L、4.84 mg/g VSS·h、206.5 mg/L,方差R2=0.94,拟合效果很好.     

Characteristics of single atmospheric particles in a heavily polluted urban area of China: size distributions and mixing states

To investigate the chemical composition, size distribution, and mixing state of aerosol particles on heavy pollution days, single-particle aerosol mass spectrometry was conducted during 9–26 October 2015 in Xi’an, China. The measured particles were classified into six major categories: biomass burning (BB) particles, K-secondary particles, elemental carbon (EC)–related particles, metal-containing particles, dust, and organic carbon (OC) particles. BB and EC-related particles were the dominant types during the study period and mainly originated from biomass burning, vehicle emissions, and coal combustion. According to the ambient air quality index, two typical episodes were defined: clean days (CDs) and polluted days (PDs). Accumulation of BB particles and EC-related particles was the main reason for the pollution in Xi’an. Most types of particle size were larger on PDs than CDs. Each particle type was mixed with secondary species to different degrees on CDs and PDs, indicating that atmospheric aging occurred. The mixing state results demonstrated that the primary tracers were oxidized or vanished and that the amount of secondary species was increased on PDs. This study provides valuable information and a dataset to help control air pollution in the urban areas of Xi’an.

Graphical abstract

     

硫酸钙垢层清洗方法研究

从化学热力学角度和沉淀转化角度,理论上分析了碳酸钠、氢氧化钠分别与硫酸钙发生化学反应的可能性和反应进行的限度。并结合动力学规律,提出影响化学反应的条件,通过实验进行检验。最后提出,在实际工作中,达到良好清洗目的可采取的措施。     

某钢厂烧结烟气脱硫系统滤袋失效原因分析

分析了聚苯硫醚自身特性,从而了解目前烧结烟气脱硫系统袋式除尘器中选择其作为滤料的原因。并就目前某钢厂烧结烟气脱硫系统实际发生的滤袋失效问题,通过扫描电镜、EDS能谱分析及烧失量实验对滤袋进行分析,发现材料中混入的玻璃纤维是造成其失效的主要原因,为今后实际工程中滤袋的选择提供依据,从而尽量减少不必要的损失,确保烟气脱硫项目的正常运行。     

Contamination status and potential release of trace metals in a mangrove forest sediment in Ho Chi Minh City,Vietnam

Can Gio district is located in the coastal area of Ho Chi Minh City, southern Vietnam. Discharge of wastewater from Ho Chi Minh City and neighboring provinces to the rivers of Can Gio has led to concerns about the accumulation of trace metals (As, Cu, Cr, Ni, Pb, and Zn) in the coastal sediments. The main objective of this study was to assess the distribution of As, Cu, Cr, Ni, Pb, and Zn in surface and core sediments and to evaluate the contamination status in relation to local background values, as well as the potential release of these selected trace metals from sediments to the water environment. Sediment characteristization, including determination of fine fraction, pH, organic matter, and major elements (Al, Fe, Ca, K, Mg, and S), was carried out to investigate which parameters affect the trace metal enrichment. Fine fraction and Al contents were found to be the controlling proxies affecting the distribution of trace metals while other sediment characteristics did not show any clear influence on trace metals’ distribution. Although As concentrations in the sediments were much higher compared to its reference value in other areas, the enrichment factor based on local background values suggests minor contamination of this element as well as for Cr, Cu, and Pb. Risk assessment suggested a medium to very high risk of Mn, Zn, and Ni under acidification. Of importance is also that trace metals in sediments were not easily mobilized by organic complexation based on their low extractabilities by ammonium-EDTA extraction.

     

Electrogeneration of H(2) for Pd-catalytic hydrodechlorination of 2,4-dichlorophenol in groundwater

A novel electrolytic groundwater remediation process, which used the H₂ continuously generated at cathode to achieve in situ catalytic hydrodechlorination, was developed for the treatment of 2,4-dichlorophenol (2,4-DCP) in groundwater. Catalytic hydrodechlorination using Pd supported on bamboo charcoal and external H₂ showed that 2,4-DCP was completely dechlorinated to phenol within 30 min at pH ? 5.5. In a divided electrolytic system, the catalytic hydrodechlorination of 2,4-DCP in cathodic compartment by H₂ generated at the cathode under 20 and 50 mA reached 100% at 120 and 60 min, respectively. Two column experiments with influent pHs of 5.5 (unconditioned) and 2 were conducted to evaluate the feasibility of this process. The 2,4-DCP removal efficiencies were about 63% and nearly 100% at influent pHs of 5.5 and 2, respectively. Phenol was solely produced by 2,4-DCP hydrodechlorination, and was subsequently degraded at the anode. A low pH could enhance the hydrodechlorination, but was not necessarily required. This study provides the preliminary results of a novel effective electrolytic process for the remediation of groundwater contaminated by chlorinated aromatics.