改性活性炭纤维吸附炸药废水中TNT实验研究

本文研究了改性活性炭纤维对炸药废水中TNT的吸附行为。研究表明:1 mol/L HNO3改性的活性炭纤维吸附效果最好,其对炸药废水中TNT的最佳吸附条件为:吸附剂用量为0.6 g/25 m L,吸附平衡时间为60 min,升温有利于吸附进行。Langmuir和Freundlich吸附等温线均能较好地描述活性炭纤维对TNT的吸附,吸附动力学分析表明,吸附过程遵循准二级动力学规律。     

铁碳微电解法预处理垃圾渗滤液膜滤浓缩液

对垃圾渗滤液膜滤浓缩液采用铁碳微电解法进行预处理,探讨了p H值、反应时间及气液比对COD去除效率的影响。结果表明,当p H值为3、反应时间120 min、气液比10∶1时,COD、TN的去除率分别为79.6%,56.4%;NH3-N由进水的70.9 mg/L上升为77.0 mg/L;预处理效果较好。但是由于铁碳微电解对盐度没有去除效果,影响后续反应进行。如何经济有效地降低含盐量成为今后研究重点。     

活性炭纤维对于离子的电吸附选择性能研究

通过循环伏安测试、交流阻抗测试、电吸附实验等方法研究了单组分和多组分溶液中不同离子在活性炭纤维电极表面的选择性电吸附性能。结果表明,电吸附选择性能与离子的水合半径、离子价态、离子浓度有关;增大初始浓度可以提高电吸附容量;并且,由于强烈的选择吸附作用,Ca2+离子可以吸附取代其它已经被吸附的离子。     

铁碳微电解法预处理猪场沼液中氨氮的研究

铁碳微电解是新型的污水处理技术,为了研究猪场沼液中氨氮的去除,将铁碳微电解技术应用于预处理难降解的厌氧沼液中的氨氮。经预先浸泡处理后的铁碳已达到吸附饱和,以此铁碳材料,分别采用了单因素实验和正交试验,用可见光分光光度法测试氨氮的浓度。单因素实验确定了铁碳微电解法影响氨氮去除的因素,选取pH值、反应时间、铁碳比为正交试验因素,通过正交试验得到,当温度为(20±1)℃,铁碳比为1∶1,pH值为3,反应时间为60 min时去除氨氮的效果最好,去除率为34.01%。铁碳微电解法预处理猪场沼液有一定的应用前景。     

二氧化碳灭火系统扑灭风电机组舱内火灾试验研究

为有效遏制全国多地风力发电机组火灾事故的势头,基于灭火系统在风电机组防火设计中的重要性,提出采用二氧化碳灭火系统对风电机舱进行灭火保护的解决方案。在建造国内首台风电机组火灾模拟试验装置的基础上,通过试验研究二氧化碳灭火系统在常温状态和低温状态下对风电机组火灾的灭火能力。结果表明,该灭火系统能够对风力发电机组进行全淹没灭火保护,适用于空间狭小且结构复杂的风电机舱;在低温条件下,其喷放时间和灭火时间虽比常温状态下长,但灭火效能并未降低。     

基于生命周期的轨道交通能耗与碳排放分析

轨道交通的高效低污染特征备受关注,以广佛二期地铁为研究对象,测算广佛二期地铁的能源消费量,以及CO2、CH4、N2O等温室气体(Greenhouse Gases,GHGs)排放量;再基于生命周期理论,采用量化方法对比广佛二期地铁与出租车、私人载客汽车、公交车、私人摩托车4种客运交通工具的能源利用效率、能源强度、碳排放强度;最后,分析广佛二期地铁对佛山市交通行业能耗和GHGs排放的影响.结果表明,广佛二期地铁近期能源消费量为4 562.95 t标准煤,CO2排放量为12 651.57 t,CH4排放量为0.152 t,N2O排放量为0.201 t.与燃油机动车相比,广佛二期地铁具有更高的能源利用效率,同时具有较高的节能减排潜力.研究表明,广佛二期地铁的开通不但是缓解佛山市机动车辆增长的重要方式,而且对城市交通节能减排具有重要意义.     

离子液体对CO2吸收性能的研究进展

CO2引起的气候变暖已成为全球最关注的环境问题之一,利用离子液体固定CO2引起了众多学者的关注。介绍了近年来离子液体吸收CO2的研究进展,包括常规离子液体和含氨基离子液体、氨基酸离子液体、聚离子液体及其他离子液体等4种功能化离子液体,并简要分析了吸收机理。综合分析了每种离子液体的吸收性能,离子液体对CO2的吸收能力均随温度上升而减小,随压力升高而增加。烷基链的增长以及含氟基团的增加有利于对CO2的吸收。功能化离子液体由于引入了功能化基团,相同条件下,其对CO2的吸收力几乎是常规离子液体的两倍。此外,将离子液体与有机溶液(特别是醇胺溶液)混合能提高离子液体对CO2的吸收能力,且能降低生产费用。最后指出了高吸收性能、低黏度、低毒以及低成本是未来离子液体的研究方向。     

Are we counting what counts? A closer look at environmental concern,pro-environmental behaviour,and carbon footprint

Three parallel lines of inquiry regarding individuals' support for the environment have developed within the environmental social sciences. These include individuals' concern for the environment, research on private sphere pro-environmental behaviour (PEB), i.e. household actions seeking to improve the environment (e.g. buying better light bulbs), and more recently, ecological and carbon footprints. Researchers have noted that the correlates of this third form of support for the environment are not necessarily the same as the predictors of the first two forms. Using Canadian survey data, this study examines the relationships among, and predictors of, all three forms. Evidence that there is not a link between private sphere PEB and household carbon footprints, and that measures of socio-economic status (education and income) have different effects on different types of support for the environment, invites a discussion of whether environmental social scientists are really counting what counts.     

Heterogeneous oxidation of SO2 by O3-aged black carbon and its dithiothreitol oxidative potential

Ozone (O₃) is an important atmospheric oxidant. Black carbon (BC) particles released into the atmosphere undergo an aging process via O₃ oxidation. O₃-aged BC particles may change their uptake ability toward trace reducing gases such as SO₂ in the atmosphere, leading to different environmental and health effects. In this paper, the heterogeneous reaction process between O₃-aged BC and SO₂ was explored via in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Combined with ion chromatography (IC), DRIFTS was used to qualitatively and quantitatively analyze the sulfate product. The results showed that O₃-aged BC had stronger SO₂ oxidation ability than fresh BC, and the reactive species/sites generated on the surface had an important role in the oxidation of SO₂. Relative humidity or 254 nm UV (ultraviolet) light illumination enhanced the oxidation uptake of SO₂ on O₃-aged BC. The oxidation potentials of the BC particles were detected via dithiothreitol (DTT) assay. The DTT activity over BC was decreased in the process of SO₂ reduction, with the consumption of oxidative active sites.     

Activated carbon coated palygorskite as adsorbent by activation and its adsorption for methylene blue

An activation process for developing the surface and porous structure of palygorskite/carbon(PG/C) nanocomposite using ZnC l2 as activating agent was investigated. The obtained activated PG/C was characterized by X-ray diffraction(XRD), Fourier transform infrared spectroscopy(FTIR), field-emission scanning electron microscopy(SEM), and Brunauer–Emmett–Teller analysis(BET) techniques. The effects of activation conditions were examined,including activation temperature and impregnation ratio. With increased temperature and impregnation ratio, the collapse of the palygorskite crystal structure was found to accelerate and the carbon coated on the surface underwent further carbonization. XRD and SEM data confirmed that the palygorskite structure was destroyed and the carbon structure was developed during activation. The presence of the characteristic absorption peaks of C_C and C–H vibrations in the FTIR spectra suggested the occurrence of aromatization. The BET surface area improved by more than 11-fold(1201 m2/g for activated PG/C vs. 106 m2/g for PG/C) after activation, and the material appeared to be mainly microporous. The maximum adsorption capacity of methylene blue onto the activated PG/C reached 351 mg/g. The activated PG/C demonstrated better compressive strength than activated carbon without palygorskite clay.