换流站联锁防误与微机防误系统实现方式比较

为确保安全生产过程中不发生人为误操作责任事故,分析了银川东换流站联锁防误闭锁软、硬件实现方式,并与综自站微机防误系统实现方式进行了比较,阐述了换流站联锁实现方式的优点及换流站引入微机防误系统的弊端。分析结果表明:换流站联锁防误系统软、硬件实现方式与综自站“五防”闭锁实现方式相比存在实时性好、可靠性高、人为干扰因素少、利于实现顺序控制和集中监控且使用便捷等优点。可考虑在部分综自站推广使用。     

非离子表面活性剂对土壤中甲基对硫磷的增溶、洗脱及其在土壤中的吸附

探讨了3种非离子表面活性剂Brij30、Brij35和Tween80溶液对水溶液中甲基对硫磷的增溶作用,对土壤中甲基对硫磷的洗脱作用以及土壤对3种非离子表面活性剂的吸附作用.增溶实验结果表明,3种非离子表面活性剂在水溶液中均对甲基对硫磷有较好的增溶作用,而且无论在临界胶束浓度前或后,表面活性剂对甲基对硫磷的增溶顺序均为:Tween80,Brij30和Brij35.淋洗实验结果表明,3种非离子表面活性剂对土壤中甲基对硫磷的去除效果不如蒸馏水好,而且实验土壤对3种非离子表面活性剂均有较强的吸附作用.这种吸附作用对土壤中甲基对硫磷的去除有严重不利影响.     

Characteristics of chemical components in PM<Subscript>2.5</Subscript> at a plateau city,South-west China

A sampling campaign including summer, autumn and winter of 2014 and spring of 2015 was accomplished to obtain the characteristic of chemical components in PM_2.5 at three sites of Kunming, a plateau city in South-west China. Nine kinds of water-soluble inorganic ions (WSI), organic and element carbon (OC and EC) in PM_2.5 were analyzed by ion chromatography and thermal optical reflectance method, respectively. Results showed that the average concentrations of total WSI, OC and EC were 22.85±10.95 µg·m^-3, 17.83±9.57 µg·m^-3 and 5.11±4.29 µg·m^-3, respectively. They totally accounted for 53.0% of PM_2.5. Secondary organic and inorganic aerosols (SOA and SIA) were also assessed by the minimum ratio of OC/EC, nitrogen and sulfur oxidation ratios. The annual average concentrations of SOA and SIA totally accounted for 28.3% of the PM_2.5 concentration. The low proportion suggested the primary emission was the main source of PM_2.5 in Kunming. However, secondary pollution in the plateau city should also not be ignorable, due to the appropriate temperature and strong solar radiation, which can promote the atmospheric photochemical reactions.

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Removing carbonyl sulfide with metal-modified activated carbon

A Cu-Co-K/activated carbon (AC) adsorbent has been developed for the removal of carbonyl sulfide (COS). The effects of COS concentration, reaction temperature and relative humidity were closely examined. A breakthrough of 33.23 mg COS·g⁻¹ adsorbent at 60°C, under 30% relative humidity and in presence of 1.0% oxygen was exhibited in the Cu-Co-K/AC adsorbent prepared. Competitive adsorption studies for COS in the presence of CS₂, and H₂S were also conducted. TPD analysis was used to identify sulfur-containing products on the carbon surface, and the results indicated that H₂S, COS and SO₂ were all evident in the effluent gas generated from the exhausted Cu-Co-K/AC. Structure of the activated carbon samples has been characterized using nitrogen adsorption, and their surface chemical structures were also determined with X-ray photoelectron spectroscopy (XPS). It turns out that the modification with Cu(OH)₂CO₃-CoPcS-KOH can significantly improve the COS removal capacity, forming SO42− species simultaneously. Regeneration of the spent activated carbon sorbents by thermal desorption has also been explored.     

渤海湾表层沉积物各形态重金属的分布特征与生态风险评价

根据2008年春对渤海湾的调查,通过分级萃取的实验方法以及总量和分形态风险评价的手段,重点研究了渤海湾表层沉积物各形态重金属的分布特征、影响因素和潜在生态风险.结果表明,重金属在渤海湾中央的泥质区富集,自然来源是控制V、Ni、Cu、Pb、Co和Cd分布的主要因素,而Zn和Cr较易受环境变化或人为输入等影响,其中Pb作为大气沉降和陆源输入都存在的重金属,其受控因素与其他重金属有一定差异.形态分析表明,V、Zn和Cr以残渣态为主,Co、Ni和Cu则是可浸取态占优势.其中Co的可浸取态质量分数在A断面先增加后降低,Ni的可浸取态质量分数在海河口附近A3站达最大值(98.86%),Cu和Pb的可浸取态高值区出现在A断面的中央区域,优势形态是铁锰氧化物结合态,Cu在湾口的A10站降到最小值(43.83%),在黄河口的D1站达最大值(73.89%).风险评价表明,重金属总量富集因子由大到小:Pb>Cd>Zn>Cr>V>Co>Cu>Ni,其中Pb、Cd和Zn的富集因子均大于1,但渤海湾沉积物总体质量良好,潜在生态风险较低.从形态角度评价,V和Cr基本无污染,Zn局部轻微污染,Co大部分轻度污染,Cu由无污染到中度污染,Ni由轻度污染到重度污染,Pb则属重度污染,其中Pb在渤海湾口A11站的P%(次生相与原生相分布比值)达1 329%.综合评价得出,Pb是渤海湾沉积物污染最严重的重金属,Cu和Zn有潜在污染,V、Cr和Co基本清洁.     

Higher CO2 absorption using a new class of calcium hydroxide (Ca(OH)2) nanoparticles

Environmental Chemistry Letters - With rising atmospheric carbon dioxide (CO2) concentrations globally, there is an urgent need for highly efficient CO2 capture technologies. This report introduces...     

Response of indigenous Cd-tolerant electrochemically active bacteria in MECs toward exotic Cr(VI) based on the sensing of fluorescence probes

Electrochemically active bacteria (EAB) on the cathodes of microbial electrolysis cells (MECs) can remove metals from the catholyte, but the response of these indigenous EAB toward exotic metals has not been examined, particularly from the perspective of the co-presence of Cd(II) and Cr(VI) in a wastewater. Four known indigenous Cd-tolerant EAB of Ochrobactrum sp X1, Pseudomonas sp X3, Pseudomonas delhiensis X5, and Ochrobactrum anthropi X7 removed more Cd(II) and less Cr(VI) in the simultaneous presence of Cd(II) and Cr(VI), compared to the controls with individual Cd(II) or single Cr(VI). Response of these EAB toward exotic Cr(VI) was related to the associated subcellular metal distribution based on the sensing of fluorescence probes. EAB cell membrane harbored more cadmium than chromium and cytoplasm located more chromium than cadmium, among which the imaging of intracelluler Cr(III) ions increased over time, contrary to the decreased trend for Cd(II) ions. Compared to the controls with single Cd(II), exotic Cr(VI) decreased the imaging of Cd(II) ions in the EAB at an initial 2 h and negligibly affected thereafter. However, Cd(II) diminished the imaging of Cr (III) ions in the EAB over time, compared to the controls with individual Cr(VI). Current accelerated the harboring of cadmium at an initial 2 h and directed the accumulation of chromium in EAB over time. This study provides a viable approach for simultaneously quantitatively imaging Cd(II) and Cr (III) ions in EAB and thus gives valuable insights into the response of indigenous Cd-tolerant EAB toward exotic Cr(VI) in MECs.

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A Cu-modified active carbon fiber significantly promoted H2S and PH3 simultaneous removal at a low reaction temperature

• Cu_0.15-ACF performs the best for H₂S and PH₃ simultaneous removal. • 550°C and 90°C are separately calcination and reaction temperatures. • The reason why Cu_0.15/ACF shows better performance was found. • The accumulation of H₂PO₄⁻ and SO₄²⁻(H₂O)₆ is the deactivation cause of Cu_0.15/ACF. Poisonous gases, such as H₂S and PH₃, produced by industrial production harm humans and damage the environment. In this study, H₂S and PH₃ were simultaneously removed at low temperature by modified activated carbon fiber (ACF) catalysts. We have considered the active metal type, content, precursor, calcination, and reaction temperature. Experimental results exhibited that ACF could best perform by loading 15% Cu from nitrate. The optimized calcination temperature and reaction temperature separately were 550°C and 90°C. Under these conditions, the most removal capacity could reach 69.7 mg/g and 132.1 mg/g, respectively. Characterization results showed that moderate calcination temperature (550°C) is suitable for the formation of the copper element on the surface of ACF, lower or higher temperature will generate more cuprous oxide. Although both can exhibit catalytic activity, the role of the copper element is significantly greater. Due to the exceptional dispersibility of copper (oxide), the ACF can still maintain the advantages of larger specific surface area and pore volume after loading copper, which is the main reason for better performance of related catalysts. Finally, increasing the copper loading amount can significantly increase the crystallinity and particle size of copper (oxide) on the ACF, thereby improving its catalytic performance. In situ IR found that the reason for the deactivation of the catalyst should be the accumulation of generated H₂PO₄⁻ and SO₄²⁻(H₂O)₆ which could poison the catalyst.     

生态环境重大工程项目全过程管理体系评价与对策

生态环境重大工程是实施国家中长期规划、具有中国特色的一项制度安排。本研究通过梳理我国重大生态环境工程项目管理现状,包括制度建设、工程标准体系建设、绩效管理体系建设等,结合“十四五”生态环境保护形势和任务要求,分析当前我国在生态环境工程项目管理体系建设上存在的主要问题。在此基础上,构建出我国重大生态环境项目组织管理的框架和路线图,提出“十四五”加强和提升我国重大生态环境保护项目全过程管理的对策与建议。     

被动采样-UV法测定环境空气中的臭氧浓度

研究被动采样-UV法测定臭氧浓度.以NaNO2作为诱捕试剂,用被动采样器吸收O3,然后在紫外分光光度计上进行测定.通过测定所生成的NO-3浓度,间接计算出臭氧浓度.结果表明,测得臭氧浓度范围在20～100 μg/m3,NO-3浓度线性范围在0～0.6 mmol/L.在测定NO-3浓度时,NO-2会造成很大的干扰,但在实验中,NO-2浓度在0～0.8 mmol/L,氨基磺酸都能有效地去除其干扰.该方法是简单、灵敏、可靠的测定环境空气中臭氧浓度的良好方法.