Impact of carbon,oxygen and sulfur content of microscale zerovalent iron particles on its reactivity towards chlorinated aliphatic hydrocarbons

Zerovalent iron (ZVI) abiotically degrades several chlorinated aliphatic hydrocarbons (CAHs) via reductive dechlorination, which offers perspectives for in situ groundwater remediation applications. The difference in reactivity between ZVI particles is often linked with their specific surface area. However, other parameters may influence the reactivity as well. Earlier, we reported for a set of microscale zerovalent iron (mZVI) particles the disappearance kinetic of different CAHs which were collected under consistent experimental conditions. In the present study, these kinetic data were correlated with the carbon, oxygen and sulfur content of mZVI particles. It was confirmed that not only the specific surface area affects the disappearance kinetic of CAHs, but also the chemical composition of the mZVI particles. The chemical composition, in addition, influences CAHs removal mechanism inducing sorption onto mZVI particles instead of dechlorination. Generally, high disappearance kinetic of CAHs was observed for particles containing less oxygen. A high carbon content, on the other hand, induced nonreactive sorption of the contaminants on the mZVI particles. To obtain efficient remediation of CAHs by mZVI particles, this study suggested that the carbon and oxygen content should not exceed 0.5% and 1% respectively. Finally, the efficiency of the mZVI particles may be improved to some extent by enriching them with sulfur. However, the impact of sulfur content on the reactivity of mZVI particles is less pronounced than that of the carbon and oxygen content.     

脱硫石膏粒径分布与脱水性能实验研究

脱硫石膏粒径分布是影响脱硫石膏浆液脱水性能的重要因素之一,以干法、湿法筛分和研磨破碎获得不同粒径分布的脱硫石膏,在相同的过滤条件下,对不同粒径分布脱硫石膏浆液脱水性能进行了研究,实验结果表明,当脱硫石膏粒径d50大于50μm且（d90-d10）小于100μm,真空过滤最大真空度不低于0．098MPa,过滤时间不少于2．5min,滤饼厚度不超过20mm时,石膏滤饼含水率可以降低到12％以下（最低可达10％）;d50在17μm为脱硫石膏在相同的过滤条件下能够实现真空脱水干燥的转折点;d50和（d90-d10）共同影响石膏脱水性能,d50小于20μm时,仅表现为d50的影响。     

机械清洗法对MBR膜泥饼层的影响

膜污染是制约MBR发展的瓶颈。考察投加ABS颗粒对MBR膜组件上膜泥饼层的影响,并设对照实验。结果表明,对照MBR膜通量下降速度快,膜污染严重,膜表面上累积厚厚的泥饼层,而在ABS MBR中膜通量下降速度则缓慢的多,且膜上泥饼层积累量则明显少于对照MBR;曝气量越大,颗粒运行的速度也越快,泥饼层被撞落量也越多;颗粒以碰撞角度为45°冲刷膜的情况下,泥饼层掉落效果明显增加;泥饼层包裹的膜丝根数越多,泥饼层的静摩擦力和保持泥饼层不被破坏的力也越大,泥饼层就越难被冲刷掉。SEM照片显示,ABS MBR的膜孔堵塞要严重于对照MBR,表面的褶皱要较对照MBR多。     

改性蚁酸木质素的制备与应用

采用加拿大一枝黄花茎杆为原料提取蚁酸木质素,通过氧化或接枝复合的方法对蚁酸木质素进行改性,对改性产物进行了FTIR和SEM表征。实验结果表明：接枝复合改性产物中存在-CONH的接枝复合链,氧化改性产物基本保持了蚁酸木质素原来的吸收峰;采用接枝复合改性产物处理初始质量浓度为50 mg/L的亚甲基蓝废水,在废水pH 7、吸附时间4 h、改性产物加入量22 mg/mL的条件下,亚甲基蓝去除率为90.94%;采用氧化改性产物处理相同亚甲基蓝废水,在废水pH 10、吸附时间12 h、改性产物加入量22 mg/mL的条件下,亚甲基蓝去除率为81.93%。     

Polychlorinated dibenzo-p-dioxin and dibenzofuran in urban air of an Andean city

Particle-bound polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) in ambient air were monitored together with particulate matter less than 10 μm (PM₁₀) at three sampling sites of the Andean city of Manizales, Colombia; during September 2009 and July 2010. PCDD/Fs ambient air emissions ranged from 1 fg WHO-TEQ m⁻³ to 52 fg WHO-TEQ m⁻³ in particulate fraction. The PM₁₀ concentrations ranged from 23 μg m⁻³ to 54 μg m⁻³. Concentrations of PM₁₀ and PCDD/Fs in ambient air observed for Manizales - a medium sized city with a population of 380 000 - were comparable to concentrations in larger cities. The highest concentrations of PCDD/Fs and PM₁₀ found in this study were determined at the central zone of the city, characterized by public transportation density, where diesel as principal fuel is used. In addition, hypothetical gas fractions of PCDD/Fs were calculated from theoretical K_p data. Congener profiles of PCDD/Fs exhibited ratios associated with different combustion sources at the different sampling locations, ranging from steel recycling to gasoline and diesel engines. Taking into account particle and gas hypothetical fraction of PCDD/Fs, Manizales exhibited values of PCDD/Fs equivalent to rural and urban-industrial sites in the southeast and center of the city respectively. Poor correlation of PCDDs with PM₁₀ (r = −0.55 and r = 0.52) suggests ambient air PCDDs were derived from various combustion sources. Stronger correlation was observed of PCDFs with PM₁₀. Poor correlation between precipitation and reduced PM₁₀ concentration in ambient air (r = −0.45) suggested low PM₁₀ removal by rainfall.     

Variability of dust iron solubility in atmospheric waters: Investigation of the role of oxalate organic complexation

Atmospheric dust deposition is a major external iron source for remote surface ocean waters. Organic complexation is known to play a role in the dissolution of iron-containing minerals. In this paper, we present our study on the effect of oxalate on dust iron solubility in simulated rainwater. Our results reveal that the solubility of iron carried by analogs of different African dusts varies with the dust source. Our experiments indicate a positive linear correlation between iron solubility and oxalate concentration. Soluble iron (SFe) increases from 0.0025(±0.0005)% to 0.26(±0.01)% of total iron, considering all dust sources and with oxalate concentrations ranging from 0 to 8 μM. These results show that the observed variability of iron solubility in aerosols collected over the Atlantic Ocean is, at least partly, due to an increase in dust iron solubility, with the presence of oxalate complexation, rather than to the presence of more soluble anthropogenic iron. Considering the mineralogical composition of those particles, experiments with pure minerals (hematite, goethite and illite) were performed to study the dissolution process. We found that oxalate promotes the solubility of iron contained in clay and hence confirmed that more than 95% of SFe from soil dust is provided by clay (illite). This experimental work enables us to establish a parameterization of iron solubility in dust as a function of oxalate concentration and based on the individual iron solubility of pure iron-bearing minerals usually present in dust particles. Finally, our results emphasize that oxalate contributes to iron solubility on the same order of magnitude as the acid processes. Organic complexation appears to be a process that increases iron solubility and likely enhances the bioavailability of iron from dust.     

300MW燃煤锅炉机组超细颗粒聚并器的实验研究

为了解决燃煤锅炉烟气中超细颗粒难以脱除的问题,基于流体动力学原理设计了一种超细颗粒聚并器,并在300 MW燃煤锅炉机组电除尘器的前置烟道中进行了实验研究。结果表明,聚并器内部存在超细颗粒之间以及超细颗粒与大颗粒之间的相互聚集行为,从而使超细颗粒数量显著减少。例如,对于粒径在2.65和10.48μm以下的颗粒,其体积比例在聚并器出口分别减少了56.7%和62.3%,在电除尘器出口的粉尘浓度减少了26.34 mg/Nm3,这表明,基于流体动力学原理的聚并器对超细颗粒的聚并作用明显,具有良好的应用前景。     

火电厂烟气排放对广州大气环境的影响

广州市是酸雨、可吸入颗粒物污染严重的地区之一,这与其能源结构以煤为主有关.广州发电厂以燃煤为主,其周围大气采样数据分析显示燃煤电厂可对周围大气环境造成较大影响,是酸雨前体物、可吸入颗粒物的主要排放源.酸雨破坏了生态环境,也阻碍了经济的发展;燃煤排放的烟尘细颗粒物属于可吸入颗粒物,其上附着的As、Cr等微量元素多为致癌物质和致基因毒性诱变物质,对周围居民的健康危害极大.最后, 对当前的环境保护工作及存在的问题进行了阐述.     

锚喷粉尘受力及产尘机理分析

通过对锚喷粉尘的受力分析,基于粉尘颗粒的基本性质,运用牛顿运动规律、流体力学的紊流射流、两相流等相关理论,对锚喷产尘原因及运动规律研究,认为锚喷尘源产生的4种方式: 粉尘颗粒自身的特性及二次风流的影响,高速喷射气流带动周围的空气运动所产生的剪切作用,锚喷高速射流内部中团粒间的相互作用以及物料与受喷面的碰撞是影响锚喷产生粉尘的主要原因.     

北京地区PM10与秸秆燃烧排放单颗粒对比分析

采用场发射带能谱扫描电镜(FESEM/EDS)法分析北京怀柔地区PM10与秸秆燃烧排放颗粒的形貌特征和成分差异.结果显示:秸秆燃烧后排放颗粒物多为大粒径颗粒,成分上都含S、Cl和K元素.含有生物质燃烧标志元素K的PM10颗粒物多为含Si、Al和Na元素的燃煤飞灰和矿物颗粒,与秸秆燃烧排放颗粒组成化学元素差异明显.据此推...