Transfer station, incineration plant, and landfill site made up the major parts of municipal solid waste disposal system of S city in Eastern China. Characteristics of volatile compounds (VCs) and odor pollution of each facility were investigated from a systematic perspective. Also major index related to odor pollution, i.e., species and concentration of VCs, olfactory odor concentration, and theoretic odor concentration, was quantified. Oxygenated compounds and hydrocarbons were the most abundant VCs in the three facilities. Different chemical species were quantified, and the following average concentrations were obtained: transfer station, 54 VCs, 2472.47 μg/m3; incineration plant, 75 VCs, 33,129.25 μg/m3; and landfill site, 71 VCs, 1694.33 μg/m3. Furthermore, the average olfactory odor concentrations were 20,388.80; 50,677.50; and 4951.17, respectively. The highest odor nuisance was detected in the waste tipping port of the incineration plant. A positive correlation between the olfactory and chemical odor concentrations was found with R2 = 0.918 (n = 15, P < 0.01). The result shows odor pollution risk transfer from landfill to incineration plant when adopting thermal technology to deal with the non-source-separated waste. Strong attention thus needs to be paid on the enclosed systems in incineration plant to avoid any accidental odor emission.
The objective of this study was to examine the effects of vegetation change from a native broadleaf forest to a coniferous plantation on selected soil properties, including soil texture, pH, organic matter, total nitrogen (N), total phosphorus (P), exchangeable cations (Ca2+, K+, Na+), and cation exchange capacity (CEC). Results showed that the amount of clay particles, Ca2+, and K+ values significantly increased, whereas Na+, total N, and organic matter and soil pH values decreased on the treatment plot after vegetation change. Soil acidity also increased and soil textural group changed from moderately fine-textured soils (clay loam) to medium-textured soils (loam) under both control and treatment plots. Organic matter, total N, and Na+ values increased, whereas Ca2+ concentration decreased through time on the control plot. Soil pH, total P, K+, and CEC did not show significant changes through time on the control plot. 相似文献
In this study, exergy, exergoeconomic, exergoenvironmental analyses, and exergoeconomic environmental optimization are applied to a four-cylinder, spark ignition, naturally aspirated and air-cooled piston-prop aircraft engine in the cruise phase of flight for the first time to the best of the authors` knowledge. Here, three piston-prop aircraft engine parameters (altitude, air–fuel ratio (AF), and rated power setting (PS)) are selected for optimization purposes. All exergy, exergoeconomic, and exergoenvironmental values are calculated first. These values are then optimized to find the best results of all analyses. The best altitude, AF ratio, and PS values are finally found while the maximum exergy efficiency, the minimum product specific environmental impact, and the minimum average unit fuel exergy cost are obtained. The best results of optimization indicated that the maximum exergy efficiency varied between 19.54% and 19.80%, the minimum unit fuel exergy cost ranged from 126.30 $/GJ to 127.23 $/GJ, and the minimum specific environmental impact of production was in the range of 8.70–9.59 mPts/MJ. Based on the results obtained, for ensuring the optimum conditions, the low AF ratios and the low-altitude flight at high rated power settings have to be selected. 相似文献
Cadmium is perhaps environmentally the most significant heavy metal in soils. Bioavailability, remobilization and fate of Cd entering in soils are usually controlled by adsorption-desorption reactions on Fe oxides. Adsorption of Cd on soil colloids including Fe oxides has been extensively studied but Cd desorption from such soil minerals has received relatively little attention. Some factors that affect Cd adsorption on goethite include pH, temperature, aging, type of index cations, Cd concentrations, solution ionic strength and presence of organic and inorganic ions. This research was conducted to study the influence of pH, temperature and aging on Cd desorption from goethite. Batch experiments were conducted to evaluate Cd desorption from goethite with 0.01 M Ca(NO3)2. In these experiments Cd desorption was observed at 20, 40 and 70 degrees C in combination with aging for 16 h, 30, 90 and 180 d from goethite that adsorbed Cd from solutions containing initial Cd concentrations of 20, 80 and 180 microM. Following the adsorption step Cd desorption was measured by 15 successive desorptions after aging at various temperatures. At the lowest amount of initially adsorbed Cd and equilibrium pH 5.5, cumulative Cd desorption decreased from 71% to 17% with aging from 16 h to 180 d and the corresponding decrease at equilibrium pH 6.0 was from 32% to 3%. There was a substantial decrease in Cd desorption with increasing equilibration temperature. For example, in goethite with the lowest amount of initial adsorption at equilibrium pH 5.5, cumulative Cd desorption decreased from 71% to 31% with increase in temperature from 20 to 70 degrees C, even after 16 h. Dissolution of Cd adsorbed goethite in 1M HCl, after 15 successive desorptions with 0.01 M Ca(NO3)2, indicated that approximately 60% of the Cd was surface adsorbed. Overall, dissolution kinetics data revealed that 23% to 88% Cd could not be desorbed, which could possibly be diffused into the cracks and got entrapped in goethite crystals. At elevated temperature increased equilibrium solution pH favoured the formation of CaCO3 and CdCO3 which reasonably decreased Cd desorption. Cadmium speciation showed the formation of calcite and otavite minerals at 40 and 70 degrees C due to increase in pH (>9.5) during aging. X-ray diffraction analysis (XRD) of these samples also revealed the formation of CaCO3 at elevated temperatures with aging. While mechanisms such as Cd diffusion and/or entrapment into fissures and cracks in goethite structure with increase in temperature and aging are possible. 相似文献
Turkey, due to its location in the Alpine-Himalayan belt, has numerous marble deposits. More than 250 marble types with different colours and patterns have been produced from these deposits and one hundred of these are well known around the world. One such well-known marble type is Afyon-Iscehisar. Afyon-Iscehisar is Palaeozoic in age and has been quarried since the era of the Roman empire. The Afyon region is known as one of the most important marble production and processing centres in Turkey. The Afyon province, which possesses 3.5% of exploitable marble reserves (3,872,000,000 tonne) in Turkey, yields 9% of the total marble block production. The 409 marble processing plants in Afyon produce 19% of the total slab in Turkey. As a result of marble production activities, approximately 340,000 tonne of marble waste has accumulated in the area. While some of these unshaped marble blocks are re-used and returned to the economy, the majority are discarded. There are two waste marble storage fields located in the Afyon-Iscehisar region. All of the solid and fine-grained marble waste is stored in waste marble storage fields in Susuz Bo?az? and in the nearby Iscehisar marble quarries. The ecological effects of the marble waste, which were once discharged everywhere and exhibited visual pollution, has now been reduced to a minimal level. 相似文献
FeSO4·xH2O is generated in large amounts in galvanizing workshops. It can be reutilized by conversion to Fe2O3. In this study, the recovery of Fe2O3 from FeSO4·xH2O formed in the galvanizing process has been examined. The experimental work was carried out at various temperatures and times in the oxidizing medium. The reaction temperatures and times were selected as 450, 500, 550, 600, 650, 700, 800 and 900°C, and 15, 30, 45, 60, 90 and 120 minutes, respectively. In order to determine the amount of Fe2O3, a titrimetric method was applied. The reaction products were characterized by means of IR and XRD techniques.The extent of conversion is low at temperatures below 650°C. Almost all of the iron (II) sulfate in the original sample was converted to iron(III) oxide at 650°C (120 min), 700°C (90 min), 800°C (60 min) and 900°C (45 min). 相似文献
A solid phase extraction method for the determination of gold(III) at trace levels by flame atomic absorption spectrometer
(FAAS) was developed. The method was based on retention of gold as chloro complexes through the Amberlite XAD-2000. The effect
of some analytical parameters including hydrochloric acid concentration, sample volume, sample and eluent flow rates, eluent
volume, eluent concentration and interfering ions on the recovery of gold(III) was investigated. The retention of gold(III)
from 1.5 mol l−1 HCl solution and the recovery of gold with 0.07 mol l−1 NH3 solution were quantitative (≥95%). The relative standard deviation (RSD) was calculated as 3.2% (n = 10). The detection limit for gold was 2 μg l−1. The accuracy was checked with the determination of gold spiked an artificial seawater and a pure copper samples. 相似文献