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671.
Understanding the commonalities among previous chemical process incidents can help mitigate recurring incidents in the chemical process industry and will be useful background knowledge for designers intending to foster inherent safety. The U.S. Chemical Safety and Hazard Investigation Board (CSB) reports provide detailed and vital incident information that can be used to identify possible commonalities. This study aims to develop a systematic approach for extracting data from the CSB reports with the objective of establishing these commonalities. Data were extracted based on three categories: attributed incident causes, scenarios, and consequences. Seventeen causal factors were classified as chemical indicators or process indicators. Twelve chemical indicators are associated with the hazards of the chemicals involved in the incidents, whereas five process indicators account for the hazards presented by process conditions at the time of the incident. Seven scenario factors represent incident sequences, equipment types, operating modes, process units, domino effects, detonation likelihood for explosion incidents, and population densities. Finally, three consequence factors were selected based on types of chemical incidents, casualties, population densities, and economic losses. Data from 87 CSB reports covering 94 incidents were extracted and analyzed according to the proposed approach. Based on these findings, the study proposes guidelines for future collection of information to provide valuable resources for prediction and risk reduction of future incidents. 相似文献
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673.
Wajih Ur Rehman Minhan Park Jihyo Chong Kwangyul Lee Jiho Jang 《Environmental Forensics》2020,21(1):48-58
AbstractTo determine the sources of particulate matter less than 2.5?μm (PM2.5 in different ambient atmospheres (urban, roadside, industrial, and rural sites), the chemical components of PM2.5 such as ions (Cl-, NO3-, SO42-, NH4+, Na+, K+, Ca2+, and Mg2+), carbonaceous species, and elements (Al, As, Ba, Cd, Cu, Fe, Mn, Ni, Pb, Se, V, and Zn) were measured. The average mass concentrations of PM2.5 at the urban, roadside, industrial, and rural sites were 31.5?±?14.8, 31.6?±?22.3, 31.4?±?16.0, and 25.8?±?12.4?μg/m3, respectively. Except for secondary ammonium sulfate and ammonium nitrate, the model results showed that the traffic source (i.e., the sum of gasoline and diesel vehicle sources) was the most dominant source of PM2.5 (17.1%) followed by biomass burning (13.8%) at the urban site. The major primary sources of PM2.5 were consistent with the site characteristics (diesel vehicle source at the roadside site, coal-fired plants at the industrial site, and biomass burning at the rural site). Seasonal data from the urban site suggested that ammonium sulfate and ammonium nitrate were the most dominant sources of PM2.5 during all seasons. Further, the contribution of road dust source to PM2.5 increased during spring and fall seasons. We conclude that the determination of the major PM2.5 sources is useful for establishing efficient control strategies for PM2.5 in different regions and seasons. 相似文献
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676.
根据生产数据和实测参数,通过工程分析和物料平衡,计算确定生产过程中物料微和污染源强,为清洁生产审计,污染防治对策提供依据。 相似文献
677.
农用化学物资对土壤的污染状况与控制措施 总被引:5,自引:0,他引:5
随着现代化学农业的兴起与发展,不可避免地给环境造成污染。结合目前研究进展,主要从化肥、农药、地膜三方面入手,论述现代农业生产实践中,农用化学物资对重要的自然资源—土壤的污染状况及控制措施 相似文献
678.
水热条件下绿矾稳定垃圾焚烧飞灰的研究 总被引:1,自引:1,他引:0
研究了饱和温度为200 ℃的水热条件下绿矾对垃圾焚烧飞灰中重金属的稳定效果,并与常温常压下的稳定效果进行了对比.研究结果表明,高温水热条件有利于Pb特别是Cr(Ⅵ)的稳定,对Cd的稳定无明显影响,同时绿矾的用量大为降低,降低了药剂的成本. 相似文献
679.
Pierre-Franois Biard Annabelle Couvert Christophe Renner Jean-Pierre Levasseur 《Chemosphere》2009,77(2):182-187
Dimethyl disulphide (DMDS) removal was investigated in a compact scrubber (hydraulic residence time ≈20 ms), composed of a wire mesh packing structure where liquid and gas flow at co-current and high gas superficial velocity (>12 m s−1). In order to regenerate the scrubbing liquid and to maintain a driving force in the scrubber, ozone and hydrogen peroxide were added to water since they allow the generation of nonselective and highly reactive species, hydroxyl radicals HO. Three ways of reagent distribution were tested. The influence of several parameters (liquid flow rate(s), ozone flow rate, pH and reagent concentrations) was investigated. The best configuration was obtained when ozone is transferred in the scrubbing liquid before introduction at the top of the scrubber simultaneously with the hydrogen peroxide solution, allowing to generate hydroxyl radical in the scrubber. With this configuration, DMDS removal could be increased from 16% with water to 34% at the same gas and liquid flow rates in the scrubber showing the potentiality of advanced oxidation process. 相似文献
680.
Background, aim, and scope The pulp and paper industry is the sixth largest polluter discharging a variety of gaseous, liquid, and solid wastes into
the environment. Effluents from bleached Kraft mill effluents (BKME) are polluting waters to a great extent These effluents
cause considerable damage to the receiving waters if discharged untreated since they have high levels of biological oxygen
demand (BOD), chemical oxygen demand (COD), chlorinated compounds (measured as AOX), suspended solids (mainly fibers), fatty
acids, tannins, resin acids, lignin and its derivatives, sulfur and sulfur compounds, etc. This study aimed to remove adsorbed
organic halogen (AOX), total nitrogen, and lignin-degrading products in the wastewater (4,500 m3/h) from the paper mill in the pulp and paper industry, which is discharged to sea from a plant located in western Turkey.
Materials and methods The photocatalytic degradation of AOX, total nitrogen, and chlorinated lignin in BKME have been investigated in different
parameters, such as time, H2O2 and TiO2 concentration. In addition, for investigating the effect of chlorine on the removal of lignin, pure lignin solution was prepared
in equal amounts to chlorinated lignin degradation products found in BKME. The same experiments were conducted for this solution.
Experiments were carried out in photocatalytic reactor made of Pyrex glass. The mercury lamp was used as a radiation source.
All irradiation was carried out under constant stirring. The existence of dissolved O2 is an important factor which increases the photocatalytic degradation. Hence, we used an air pump for the aeration of the
wastewater solutions. The temperature of the wastewater was controlled and adjusted to 25°C by thermostat pump in conjunction
with a cooler. At the end of all experiments, AOX, total nitrogen and lignin concentrations were analyzed according to standard
methods. All experiments were performed in duplicate and average values were used.
Results and discussion When the effect of H2O2 and time were investigated, it was observed that the AOX concentration increased from 3.0 to 11.0 mg/L by only UV. However,
when H2O2 was added, AOX concentration decreased from approximately 3.0 to 0.0 mg/L. The optimal conditions for the removal of AOX
appear to be an initial H2O2 concentration of 20.0 mL/L and reaction time of 50 min. In addition, at the same experiment conditions, it was seen that
the total nitrogen concentration decreased from 23.0 to 15.0 mg/L by only UV and by increasing H2O2 concentration, the concentration of 20.0 mL/L H2O2 appears to be optimal (9.0 mg/L). The AOX, total nitrogen and lignin degradation products and pure lignin go through a minimum
when the concentration of H2O2 and TiO2 increases at constant pH and UV intensity. The kinetics for the degradation of AOX, total nitrogen and lignin degradation
products followed a pseudo-first order law with respect to the products, and the degradation rates (min−1) for the UV/TiO2/H2O2 system were higher than that of the corresponding values for the UV/H2O2 system.
Conclusions The AOX, total nitrogen and lignin concentration go through a minimum when the concentration of H2O2 and TiO2 increases at constant pH and UV intensity. It was found that the UV/TiO2/H2O2 system has proved capable of the degradation of total nitrogen as well as chlorinated and degraded lignin in BKME.
Recommendations and perspectives The photocatalytic process can be considered a suitable alternative for the remove of some compounds from the BKME. Nevertheless,
further studies should be carried out to confirm the practical feasibility of BKME. Another result obtained from the study
is that pre-purification carried out with UV/TiO2/H2O2 photocatalytic process may constitute an important step for further purification processes such as adsorption, membrane processes,
etc. 相似文献