The levels of lead, cadmium, copper, zinc, aluminum, chromium, and iron in street dust, soil, and plants in the Jordanian petroleum refinery were determined using flame and graphite-furnace atomic absorption spectrophotometry. Major cations (Li+, Na+, NH4+, K+, Mg2+, and Ca2+) and anions (F-, Cl-, NO3-, SO4(2-), and Br-) were also determined using suppression mode ion chromatography. Generally, higher levels of the heavy metals studied were found in street dust samples than in soil samples. On the other hand, except Cl-, and Li+ ions, other anions and cations showed higher concentrations in soil than in street dust samples. For plant samples, unwashed samples showed higher levels of heavy metals than their washed counterparts, indicating that dust fall is a source of heavy metal contamination. 相似文献
Airborne particulate matter (PM) concentrations were measured in Iksan, a suburban area in South Korea during April, 2003.
PM2.5 (particles with an aerodynamic diameter less than 2.5 μm) and PM10 (particles with an aerodynamic diameter less than 10 μm) samples were collected, and the chemical characteristics of particles
were examined for diurnal patterns, yellow dust/rainfall influences, and scavenging effects. Average concentrations of PM2.5 and PM10 mass measured were 37.3 ± 16.2 μg m−3 and 60.8 ± 29.5 μg m−3, respectively. The sum of ionic chemical species concentrations for PM2.5 and PM10 was 16.9 ± 7.3 and 23.1 ± 10.1 μg/m3, respectively. A significant reduction in PM mass concentrations during rainfall days was observed for coarse mode (PM2.5 − 10) particles, but less reduction was found for fine (PM2.5) mass concentration. SO42−, NH4+, and K+ predominated in fine particulate mode, NO3− and Cl− predominated in fine particle mode and coarse particle mode, but Na+, Mg2+, and Ca2+ mostly existed in coarse mode. The high concentration of ammonium due to local emissions and long-range transport neutralized
sulfate and nitrate to ammonium sulfate and ammonium nitrate, which were major forms of airborne PM in Iksan. Average mass
concentrations of PM10 in daytime and at night were 57.6 and 70.0 μg m−3, and those of PM2.5 were 35.4 and 42.5 μg m−3, respectively. NO3− and Cl− in both PM2.5 and PM10 were about double at night than in the daytime, while the rest of the chemical species were equal or a little higher at night
than in the daytime. The results suggest the formation of ammonium nitrate and chloride when high ammonia concentration and
low air temperature are allowed. Backward air trajectory analyses showed that air masses arriving at the site during yellow
dust period were transported from arid Chinese regions, which resulted in high concentrations of airborne PM mass concentrations.
In the meantime, air mass trajectories during a rainfall period were mostly from the Pacific Ocean or the East China Sea,
along with a relatively low PM concentration. 相似文献
Knowledge of water movement in the plant-xylem system and contaminant bioavailability in the soil environment is crucial to evaluate the success of phytoremediation practices. This study investigated the removal of 2,4,6-trinitrotoluene (TNT) from a contaminated sandy soil by a single poplar (Populus fastigiata) tree through the examinations of temporal variations of xylem water potential, root water uptake, and soil TNT bioavailability. A mathematical model, CTSPAC (Coupled Transport of water, heat, and solutes in the Soil-Plant-Atmosphere Continuum), was modified for the purpose of this study. The model was calibrated using laboratory measurements before its application. Our simulations show that the xylem water potential was high in the roots and low in the leaves with a potential head difference of 3.55 cm H2O, which created a driving force for water flow and chemical transport upward from the roots through the stem to the leaves. The daily average root water uptake rate was 25 cm3 h(-1) when an equilibrium condition was reached after 24 h. Our simulations further reveal that no TNT was found in the stem and leaves and only about 1% of total TNT mass was observed in the roots due to the rapid biodegradation and transformation of TNT into its daughter products. About 13% of the soil TNT was removed by the poplar tree, resulting mainly from root uptake since TNT is a recalcitrant compound. In general, the soil TNT bioavailability decreased with time due to the depletion of soil solution TNT by the poplar tree. A constant bioavailability (i.e., 3.1 x 10(-6)) was obtained in 14 d in which the soil TNT concentration was about 10 mg L(-1). Our study suggests that CTSPAC is a useful model to simulate phytoremediation of TNT-contaminated sites. 相似文献
Environmental Science and Pollution Research - The effects of different biotransformation temperatures (250, 550, and 850 °C) and different dose (0–1%) of biochar on the physiological... 相似文献
The interprovincial trade embodied carbon emissions plays an important role in the national emission reduction target among China’s provinces. Furthermore, it will affect the smooth start-up of the national carbon trade market as well as the implementation of targets in 2030 for dealing with the climate change. Based on constructed MRIO model, this paper analyzes the embodied carbon emission trade flows among Beijing, Tianjin, Hebei and surrounding regions such as Shanxi, Shaanxi, and Inner Mongolia. The results indicate that six provinces have formed different patterns of carbon trade balance, where Beijing, Tianjin, and Hebei provinces are in a deficit position, while the other three provinces are in a surplus position. Beijing, Tianjin, and Hebei have transferred part of the carbon emissions to the other three provinces, which shows greater heterogeneity among various provinces and provincial different sectors. On basis of the conclusions, this paper puts forward some suggestions on provincial decomposition, responsibility distribution, and provincial collaborative reduction for national emission reduction targets. 相似文献
The Ti-modified sepiolite (Ti-Sep)-supported Mn-Cu mixed oxide (yMn5Cu/Ti-Sep) catalysts were synthesized using the co-precipitation method. The materials were characterized by the X-ray diffraction scanning electron microscope, N2 adsorption-desorption, H2-TPR, O2-TPD, and XPS techniques, and their catalytic activities for CO oxidation were evaluated. It was found that the catalytic activities of yMn5Cu/Ti-Sep were higher than those of 5Cu/Ti-Sep and 30Mn/Ti-Sep, and the Mn/Cu molar ratio had a distinct influence on catalytic activity of the sample. Among the yMn5Cu/Ti- Sep samples, the 30Mn5Cu/Ti-Sep catalyst showed the best activity (which also outperformed the 30Mn5Cu/Sep catalyst), giving the highest reaction rate of 0.875 × 10–3 mmol·g–1·s–1 and the lowest T50% and T100% of 56°C and 86°C, respectively. Moreover, the 30Mn5Cu/Ti-Sep possessed the best low-temperature reducibility, the lowest O2 desorption temperature, and the highest surface Mn3+/Mn4+ atomic ratio. It is concluded that factors, such as the strong interaction between the copper or manganese oxides and the Ti-Sep support, good low-temperature reducibility, and good mobility of chemisorbed oxygen species, were responsible for the excellent catalytic activity of 30Mn5Cu/Ti-Sep.
Zero-valent iron (Fe0) has been widely used for Cr(VI) removal; however, the removal mechanisms of Cr(VI) from aqueous solution under complex hydrogeochemical conditions were poorly understood. In this research, the mixed materials containing cast iron and activated carbon were packed in columns for the treatment of aqueous Cr(VI)-Cr(III) in groundwater with high concentration of Ca2+, Mg2+, HCO3−, NO3−, and SO42−. We investigate the influences of those ions on Cr(VI) removal, especially emphasizing on the reaction mechanisms and associated precipitations which may lead to porosity loss by using X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) techniques. The results show that the precipitations accumulated on the material surface were (Fe/Cr) (oxy)hydroxide, mixed Fe(III)-Cr(III) (oxy)hydroxides, Fe2O3, CaCO3, and MgCO3. During these reactions, the Cr(VI) was reduced to Cr(III) coupled with the oxidated Fe0 to Fe(II) through the galvanic corrosion formed by the Fe0-C and/or the direct electron transfer between Fe0 and Cr(VI). In addition, Cr(VI) could be reduced by aqueous Fe(II), which dominated the whole removal efficiency. The primary aqueous Cr(III) was completely removed together with Cr(III) reduced from Cr(VI) even when Cr(VI) was detected in the effluent, which meant that the aqueous Cr(III) could occupy the adsorption sites. In general, the combined system was useful for the Cr(VI)-Cr(III) treatment based on galvanic corrosion, and the hardness ions had a negative effect on Cr(VI) removal by forming the carbonates which might promote the passivation of materials and decrease the removal capacity of the system.
Environmental Science and Pollution Research - Brown carbon (BrC) has recently received much attention because of its light absorption features. The chemical compositions, optical properties, and... 相似文献