Source Profiles of Particulate Matter Emissions from a Pilot-Scale Boiler Burning North American Coal Blends

ABSTRACT

Recent awareness of suspected adverse health effects from ambient particulate matter (PM) emission has prompted publication of new standards for fine PM with aerodynamic diameter less than 2.5 μm (PM_2.5). However, scientific data on fine PM emissions from various point sources and their characteristics are very limited. Source apportionment methods are applied to identify contributions of individual regional sources to tropospheric particulate concentrations. The existing industrial database developed using traditional source measurement techniques provides total emission rates only, with no details on chemical nature or size characteristics of particulates. This database is inadequate, in current form, to address source-receptor relationships.

A source dilution system was developed for sampling and characterization of total PM, PM_2.5, and PM₁₀ (i.e., PM with aerodynamic diameter less than 10 μm) from residual oil and coal combustion. This new system has automatic control capabilities for key parameters, such as relative humidity (RH), temperature, and sample dilution. During optimization of the prototype equipment, three North American coal blends were burned using a 0.7-megawatt thermal (MW_t) pulverized coal-fired, pilot-scale boiler. Characteristic emission profiles, including PM_2.5 and total PM soluble acids, and elemental and carbon concentrations for three coal blends are presented.     

Determination of pentachlorophenol (PCP) in waste wood--method comparison by a collaborative trial

Two independently developed and validated procedures for the determination of pentachlorophenol (PCP) in waste wood were compared by means of a collaborative trial. Both methods foresee quantification of PCP by gas chromatography (GC-ECD) after acetylation and differ with regard to the use of methanol or toluene/sulphuric acid, respectively, as solvent in the sonication extraction step. Test samples with established analyte homogeneity were prepared from a ground "real life" starting material. A total of 23 participating laboratories with experience in wood preservative analysis were instructed to apply both methods to three levels of content in the range of 0.5-20 mg PCP/kg. In case of the toluene/sulphuric acid extraction, lower recoveries and higher interlaboratory dispersion of results at the higher PCP contents were observed. Seen against the background of the Horwitz equation a reproducibility standard deviation of approximately 19% for the methanol extraction at the 4.5 mg/kg level meets the requirement for a sound analytical method. Thus, the sonication extraction procedure with methanol has been annexed as a reference method to the German waste wood regulation.     

农业源头流域景观异质性与溪流水质耦合关系

以丹江口库区胡家山流域为研究区域,分析了溪流枯、丰水期的水质变化特征,结合流域和河岸缓冲带景观类型及其格局,运用Spearman秩相关分析筛选了影响溪流水质的景观指数,利用逐步回归和冗余排序法定量描述景观格局与溪流水质的耦合关系.结果表明：溪流水质指标中氨氮和总磷浓度时空变化较大,其标准变异系数范围分别为69.8%~207.6%和52.0%~146.1%.景观类型中耕地和居民地是溪流水体污染的重要来源,两者在100m河岸缓冲带尺度上对氨氮的解释程度为58.6%,高于流域尺度;景观格局指数中蔓延度、林地和居民地斑块密度、林地和居民地最大斑块指数以及林地和耕地聚集度指数等显著影响溪流水质（P<0.05）,流域尺度上各景观类型的景观指数对总氮和总磷的解释程度分别介于71.1%~81.6%和74.5%~83.8%,均高于100m河岸缓冲带尺度,其中蔓延度对总氮和总磷均有显著影响（P<0.05）.无显著因子进入高锰酸盐指数模型中,其浓度变化是各景观指数共同作用的结果.此外,景观格局季节变化也显著影响溪流水质.枯水期景观指数能够更好的解释总氮和总磷变化,而丰水期对氨氮的解释程度要好于枯水期.     

Enhancement of photocatalytic performance in sonochemical synthesized ZnO–rGO nanocomposites owing to effective interfacial interaction

Nanocomposites composed of two or more components with desirable performance have attracted tremendous attention, mainly due to the synergic effect between the components. The effective combination of ZnO and reduced graphene oxide would lead to ameliorate the photocatalytic performance. To enhance applicability of semiconductor photocatalytic, the composites used should be good interfacial contact governed by suitable particle size distribution. Herein we aim to fabricate the different crystallize size of ZnO nanoparticles (NPs) in ZnO–reduced graphene oxide (ZnO–rGO) nanocomposites by sonochemical synthesis and subsequent facile drying treatment method. The Zn precursor, Zn(Ac)₂, with a plenty of functional groups, was used as a starting source for both reduction of graphene oxide and formation of ZnO on rGO sheets through chemical bonds without the addition of hazardous reducing agents. LiOH was chosen as an assistive reagent to enhance the complete reaction between Zn(Ac)₂ and GO in the formation of ZnO–rGO nanocomposites. More remarkably, drying condition has the great influence on the crystallize size of ZnO NPs in as-prepared ZnO–rGO nanocomposites. It is found that ZnO–rGO nanocomposites dried at ?50 °C (freeze drying) show the highest photocatalytic efficiency in the degradation of rhodamine B (RhB) as compared to ZnO–rGO nanocomposites by other drying conditions under visible-light irradiation. Correlating the crystallize size obtained by different drying temperatures with the photocatalytic activity, it is probed that the smaller crystallize size in ZnO–rGO nanocomposites enhances the interfacial contact and a chemical bonding between rGO and ZnO NPs leading to the effective separation of electrons and holes. In addition, the O ₂ ^·? anion was determined to be the main active oxidant by free radicals trapping experiment and a photodegradation mechanism of ZnO–rGO nanocomposites over rhodamine B (RhB) was proposed based on our observations.     

Atmospheric HULIS and its ability to mediate the reactive oxygen species (ROS): A review

Atmospheric humic-like substances(HULIS) are not only an unresolved mixture of macroorganic compounds but also powerful chelating agents in atmospheric particulate matters(PMs); impacting on both the properties of aerosol particles and health effects by generating reactive oxygen species(ROS). Currently, the interests of HULIS are intensively shifting to the investigations of HULIS-metal synergic effects and kinetics modeling studies, as well as the development of HULIS quantification, findings of possible HULIS sources and generation of ROS from HULIS. In light of HULIS studies, we comprehensively review the current knowledge of isolation and physicochemical characterization of HULIS from atmospheric samples as well as HULIS properties(hygroscopic, surface activity, and colloidal) and possible sources of HULIS.This review mainly highlights the generation of reactive oxygen species(ROS) from PMs, HULIS and transition metals, especially iron. This review also summarized the mechanism of ironorganic complexation and recent findings of OH formation from HULIS-metal complexes. This review will be helpful to carry out the modeling studies that concern with HULIS-transition metals and for further studies in the generation of ROS from HULIS-metal complexes.     

Political transition and emergent forest‐conservation issues in Myanmar

Political and economic transitions have had substantial impacts on forest conservation. Where transitions are underway or anticipated, historical precedent and methods for systematically assessing future trends should be used to anticipate likely threats to forest conservation and design appropriate and prescient policy measures to counteract them. Myanmar is transitioning from an authoritarian, centralized state with a highly regulated economy to a more decentralized and economically liberal democracy and is working to end a long‐running civil war. With these transitions in mind, we used a horizon‐scanning approach to assess the 40 emerging issues most affecting Myanmar's forests, including internal conflict, land‐tenure insecurity, large‐scale agricultural development, demise of state timber enterprises, shortfalls in government revenue and capacity, and opening of new deforestation frontiers with new roads, mines, and hydroelectric dams. Averting these threats will require, for example, overhauling governance models, building capacity, improving infrastructure‐ and energy‐project planning, and reforming land‐tenure and environmental‐protection laws. Although challenges to conservation in Myanmar are daunting, the political transition offers an opportunity for conservationists and researchers to help shape a future that enhances Myanmar's social, economic, and environmental potential while learning and applying lessons from other countries. Our approach and results are relevant to other countries undergoing similar transitions.     

Analytik von Mineralölkohlenwasserstoffen: Die Problematik der Probenaufbereitung

For the determination of mineral oil hydrocarbons in water and soil, IR-as well as GC/FID-methods (DEV H-18, ISO/TR 11046, NEN 5733) are used. Independent of the measurement method, different clean-up procedures are prescribed in these standard methods. Aluminium oxide, silica gel and magnesium silicate (Florisil^®) are used as adsorbents. This article describes the problems of clean-up occurring in mineral oil analysis using selected substances. Tests concerning the type of adsorbent, extract medium, clean-up-technique and extract/adsorbent-ratio are presented. It will be shown that the clean-up procedure has to be counted as a significant factor of influence in the determination of mineral oil hydrocarbons. The sources of errors resulting from clean-up as well as the possibilities to avoid them are presented. An extraction solvent for soils which is simple to handle and optimally adjustable to the requirements of the clean-up procedure is presented.