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1.
The adsorption of some heavy metals onto the walls of harvested, washed, and dried non-living biomass cells of different Pseudomonas strains was studied at optimum experimental conditions using a simplified single component system. The Langmuir adsorption model was found to be a suitable approach to describe the system via multi-step processes. Isotherms measured at 30.0°C and pH 5.5 with [M]total?=?10–100 mM for tight, reversible Cr6+(aq), Ni2+(aq), Cu2+(aq) and Cd2+(aq) binding by the cell walls of the investigated biomass fit the Langmuir model and give the pH-independent stoichiometric site capacities ν i and equilibrium constants K i for metal binding at specific biomass sites i?=?A, B, C, and D. Tight binding sites A, B, and D of the non-living biomass are occupied by CrVI, sites A and C by NiII, sites A and D by CdII, and only site B by CuII. It is concluded that ν i is a stoichiometric parameter that is independent of the magnitude of K i for binding site i and that the studied heavy metals selectively and tightly bind at different biomass sites. 相似文献
2.
Jantanee Jamsangtong Preeda Parkpian R. D. Delaune Aroon Jugsujinda 《Chemistry and Ecology》2004,20(4):241-256
Adsorption and desorption of 137Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha-1) on 137Cs adsorption-desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of 137Cs were nonlinear. A large portion (98.26-99.97%) of added 137Cs (3.7 × 103-7.03 × 105 Bq l-1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of 137Cs as compared with soil with no lime, which was supported by higher Kads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of 137Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high 137Cs adsorption capacity. Competing cations such as NH4+, K+, Na+, Ca2+, and Mg2+ had little influence on 137Cs adsorption as compared with liming, where a significant positive correlation between Kads and soil pH was observed. The 137Cs adsorption-desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09-0.58%) of 137Cs adsorbed at the highest added initial 137Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high 137Cs adsorption capacity, which limits the 137Cs bioavailability. 相似文献
3.
Mingxing GAO Yingying LI Hong YANG Yucheng GU 《Frontiers of Environmental Science & Engineering》2016,10(1):1-10
Pymetrozine is a selective insecticide with a unique chemical structure and mode to control hemipteran and homopteran. While pymetrozine has brought great benefits to crop production by killing insects, its residues in soil may have a detrimental effect on environment. Therefore, it is of great importance to investigate its behaviors in soil. In this study, the sorption and desorption of pymetrozine on six Chinese soils were investigated using a batch equilibrium approach to understand its mobile behavior in the soils. Both sorption and desorption isotherms of pymetrozine were in good agreement with the Freundlich model. The sorption coefficient KF varied between 3.37 and 58.32 mL∙g−1 and the sorption isotherms were nonlinear, with 1/n ranging from 0.57 to 0.91. A regression equation was proposed to predict the sorption of pymetrozine on six different soil samples: log KF = 4.3708 − 4.5709 × log (pH in 0.01mol·L−1 CaCl2) + 0.4700 × log OC% + 0.0057 × sand (%) + 0.0022 × CEC(clay), with R2 = 0.9982. The organic carbon content of soil positively affected the sorption of pymetrozine, but soil pH had a negative effect on the sorption. Additionally, effects of CaCl2 concentration, soil to solution ratio and pesticide form were investigated. The sorption was promoted with an increase in soil to solution ratio and a decrease in CaCl2 concentration. The possible variation of the five formulated products of pymetrozine was also investigated. 相似文献
4.
Comparing the adsorption behaviors of Cd,Cu and Pb from water onto Fe-Mn binary oxide,MnO2 and FeOOH
Wei XU Huachun LAN Hongjie WANG Hongming LIU Jiuhui QU 《Frontiers of Environmental Science & Engineering》2015,9(3):385
The adsorption potential of FMBO, FeOOH, MnO2 for the removal of Cd2+, Cu2+ and Pb2+ in aqueous systems was investigated in this study. Comparing to FMBO and FeOOH, MnO2 offered a much higher removal capacity towards the three metal ions. The maximal adsorption capacity of MnO2 for Cd2+, Cu2+ and Pb2+ were 1.23, 2.25 and 2.60 mmol·g-1, respectively. And that for FMBO were 0.37, 1.13, and 1.18 mmol·g-1 and for FeOOH were 0.11, 0.86 and 0.48 mmol·g-1, respectively. The adsorption behaviors of the three metal ions on the three adsorbents were all significantly affected by pH values and heavy metal removal efficiency increased with pH increased. The Langmuir and Freundlich adsorption models were used to describe the adsorption equilibrium of the three metal ions onto the three adsorbents. Results showed that the adsorption equilibrium data fitted well to Langmuir isotherm and this indicated that adsorption of metal ions occurred on the three metal oxides adsorbents limited to the formation of a monolayer. More negative charged of MnO2 surface than that of FMBO and FeOOH could be ascribed by lower pHiep of MnO2 than that of FMBO and FeOOH and this could contribute to more binding sites on MnO2 surface than that of FMBO and FeOOH. The higher metal ions uptake by MnO2 than FMBO and FeOOH could be well explained by the surface charge mechanism. 相似文献
5.
Xiang Zhang Yue Xuan Bin Wang Chuan Gao Shengli Niu Gaiju Zhao Dong Wang Junhua Li Chunmei Lu John C. Crittenden 《Frontiers of Environmental Science & Engineering》2022,16(7):88
6.
Chen Zhou Ermias Gebrekrstos Tesfamariam Youneng Tang Ang Li 《Frontiers of Environmental Science & Engineering》2023,17(9):107
7.
Xinyu Wang Ye Jin Weirui Chen Ruini Zou Jinxin Xie Yiming Tang Xukai Li Laisheng Li 《Frontiers of Environmental Science & Engineering》2021,15(6):122
8.
Excess nitrate in Mississippi River water entering offshore areas is reported to contribute to low oxygen (hypoxia) conditions in the Gulf of Mexico. Excessive algal growth driven by the excess nitrogen results in a decrease in dissolved oxygen in bottom water. Reintroduction of Mississippi River waters into a Louisiana coastal wetland has the potential to reduce the amount of nitrate reaching offshore waters. In this study, reduction in the concentration of added NO3- was determined in sediment-water-columns collected from a wetland site in Breton Sound estuary receiving nutrient inputs from the Mississippi River. The capacity of a wetland to process nitrate in floodwater was determined in the laboratory. The rates of NO3- removal (determined from change in nitrate concentration in the floodwater) averaged 97 mg N m-2 d-1 over 16 d for a 1750-mg NO3-N m-2 addition, and 170 mg N m-2 d-1 over 16 d for a 3500-mg NO3-N m-2 addition. The total N2O-N emissions from the 1750- and 3500-mg NO3-N m-2 additions were 19 and 54 mg N m-2 accounting for 1.1% and 1.5% of the applied NO3-N, respectively. Using the acetylene-inhibition technique, the average denitrification rate was determined to be 57 and 87 mg N m-2 d-1 (21 and 32 g N m-2 yr-1) during the most active denitrification period of 5 d after incubation for 1750 and 3500 mg NO3--N m-2 of added nitrate in floodwater, respectively. The total N evolved over 11 d as N2O + N2 was equivalent to 436 and 921 mg N m-2 (24.9% and 26.3%, respectively, of added N). Increasing the amount of NO3- applied to the overlying water increased the rate of NO3- loss and N2O emission significantly. The thickness of the oxidized surface sediment layer was also influenced by the NO3- application to the floodwater with a significant linear correlation between nitrate addition and thickness of the oxidized layer (r = 0.9998, p = 0.01). This study indicates that wetlands receiving diverted Mississippi River water have the potential to process and remove NO3- in the river water, reducing the amount of NO3- reaching to offshore areas. 相似文献
9.
Noshan Bhattarai Shuxiao Wang Yuepeng Pan Qingcheng Xu Yanlin Zhang Yunhua Chang Yunting Fang 《Frontiers of Environmental Science & Engineering》2021,15(6):126
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11.
Rongfang YUAN Beihai ZHOU Duo HUA Chunhong SHI 《Frontiers of Environmental Science & Engineering》2015,9(5):850
The effect of ion-doping on TiO2 nanotubes were investigated to obtain the optimal TiO2 nanotubes for the effective decomposition of humic acids (HA) through O3/UV/ion-doped TiO2 process. The experimental results show that changing the calcination temperature, which changed the weight fractions of the anatase phase, the average crystallite sizes, the Brunauer-Emmett-Teller surface area, and the energy band gap of the catalyst, affected the photocatalytic activity of the catalyst. The ionic radius, valence state, and configuration of the dopant also affected the photocatalytic activity. The photocatalytic activities of the catalysts on HA removal increased when Ag+, Al3+, Cu2+, Fe3+, V5+, and Zn2+ were doped into the TiO2 nanotubes, whereas such activities decreased as a result of Mn2+- and Ni2+-doping. In the presence of 1.0 at.% Fe3+-doped TiO2 nanotubes calcined at 550°C, the removal efficiency of HA was 80% with a pseudo-first-order rate constant of 0.158 min−1. Fe3+ in TiO2 could increase the generation of ·OH, which could remove HA. However, Fe3+ in water cannot function as a shallow trapping site for electrons or holes. 相似文献
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13.
Lina GAN Shan LEI Jian YU Hongtao MA Yo YAMAMOTO Yoshizo SUZUKI Guangwen XU Zhanguo ZHANG 《Frontiers of Environmental Science & Engineering》2015,9(6):979-987
Monolith SCR catalysts coated with V2O5-WO3/TiO2 were prepared by varying binder and coating thickness. Comparing with a monolith extruded with 100% V2O5-WO3/TiO2 powder, a coated monolith with a catalyst-coating layer of 260 μm in thickness exhibited the similar initial NOx reduction activity at 250°C. After 4 h abrasion (attrition) in an air stream containing 300 g·m−3 fine sands (50–100 μm) at a superficial gas velocity of 10 m·s−1, the catalyst still has the activity as a 100% molded monolith does in a 24-h activity test and it retains about 92% of its initial activity at 250°C. Estimation of the equivalent durable hours at a fly ash concentration of 1.0 g·m−3 in flue gas and a gas velocity of 5 m·s−1 demonstrated that this coated monolith catalyst is capable of resisting abrasion for 13 months without losing more than 8% of its initial activity. The result suggests the great potential of the coated monolith for application to de-NOx of flue gases with low fly ash concentrations from, such as glass and ceramics manufacturing processes. 相似文献
14.
Qiuzhun Chen Xiang Zhang Bing Li Shengli Niu Gaiju Zhao Dong Wang Yue Peng Junhua Li Chunmei Lu John Crittenden 《Frontiers of Environmental Science & Engineering》2021,15(5):92
15.
Ning Wang Jiangtao Feng Wei Yan Luohong Zhang Yonghong Liu Ruihua Mu 《Frontiers of Environmental Science & Engineering》2022,16(8):105
16.
Lijing DONG Zhiliang ZHU Yanling QIU Jianfu ZHAO 《Frontiers of Environmental Science & Engineering》2016,10(1):28-36
A novel composite adsorbent, hydroxyapatite/manganese dioxide (HAp/MnO2), has been developed for the purpose of removing lead ions from aqueous solutions. The combination of HAp with MnO2 is meant to increase its adsorption capacity. Various factors that may affect the adsorption efficiency, including solution pH, coexistent substances such as humic acid and competing cations (Ca2+, Mg2+), initial solute concentration, and the duration of the reaction, have been investigated. Using this composite adsorbent, solution pH and coexistent calcium or magnesium cations were found to have no significant influence on the removal of lead ions under the experimental conditions. The adsorption equilibrium was described well by the Langmuir isotherm model, and the calculated maximum adsorption capacity was 769 mg·g−1. The sorption processes obeyed the pseudo-second-order kinetics model. The experimental results indicate that HAp/MnO2 composite may be an effective adsorbent for the removal of lead ions from aqueous solutions. 相似文献
17.
Yaobin Lu Songli He Dantong Wang Siyuan Luo Aiping Liu Haiping Luo Guangli Liu Renduo Zhang 《Frontiers of Environmental Science & Engineering》2018,12(5):9
18.
Biosorption of colours is an important technology for treatment of different types of industrial wastewaters containing dyes. The objective of this study was to convert green alga Ulva lactuca to dye adsorbents for wastewater treatment. The importance of commonly available green alga Ulva lactuca was investigated as viable biomaterials for the biological treatment of synthetic basic blue 9 (5-ch1oro-N,N,N',N'-tetramethyl-5λ4-phenothiazine-3,7-diamine) effluents. The results obtained from the batch experiments revealed the ability of the green algae to remove the basic blue 9, and this was dependent on the dye concentration, pH, and algal biomass. We investigated the equilibrium and kinetics of adsorption, and the Langmuir and Freundlich equations were used to fit the equilibrium isotherm. The adsorption isotherm of basic blue 9 followed both the Langmuir and Freundlich models with a correlation coefficient of ∼0.96-0.99, and the adsorption kinetics followed the pseudo-second-order model (R2=1.0). The maximum adsorption capacity was about 40.2 mg of dye per gram of dry green algae at pH 10, 25 g l-1 dye and 2.5 g l-1 alga concentrations. This study demonstrated that the green algae could be used as an effective biosorbent for the treatment of dye-containing wastewater streams. 相似文献
19.
The chromium(VI) biosorption onto guava seeds, as an alternative method for Cr6+ removal from aqueous solutions, was investigated. The parameters affecting kinetics and equilibrium of Cr6+ adsorption onto guava seeds were studied. An external mass-transfer diffusion coefficient k and intra-particle diffusion coefficient ki were determined to measure the rate-limiting step of adsorption. A single external mass-transfer diffusion model and intra-particle diffusion models were used. The effects of initial pH, sorbent mass, and initial Cr6+ concentrations on mass-transfer coefficients were investigated. The external mass-transfer coefficient has an average value of 7.2×10-3 cm s-1, while the intra-particle mass-transfer diffusion coefficient was 0.34 mg g-1 min-0.5. This indicates that external diffusion to the guava seeds surface and intra-particle diffusion are both involved in the sorption process. The isotherm equilibrium data were well fitted by the Langmuir and Freundlich models with an average correlation coefficient R2=0.98. The maximum removal of Cr6+ was obtained at pH 1 (about 100% for adsorbent dose of 15 g l-1 and 25 mg l-1 initial concentration of Cr6+). The results indicated that the guava seeds exhibit acceptable sorption capacity. 相似文献
20.
Origin and Distribution of Suspended Organic Matter As Inferred From Carbon Isotope Composition in A Mediterranean Semi-Enclosed Marine System 总被引:2,自引:0,他引:2
A. Mazzola G. Sar F. Venezia M. Caruso D. Catalano S. Hauser 《Chemistry and Ecology》1999,16(2):215-238
The origin and distribution of suspended organic matter, the trophic features and the stable carbon isotopic composition of particulate organic carbon (POC) were studied monthly in a Western Mediterranean semi-enclosed basin. Sampling stations were selected as a function of wind-exposure and the degree of vegetation cover and then compared with an adjacent unvegetated site. the predominant vegetation was seagrass (Posidonia oceanica and Cymodocea nodosa) and Caulerpa prolifera. Water samples were analyzed for total suspended matter (inorganic and organic fractions), photosynthetic pigments (chlorophyll-a and phaeopigments), dissolved organic carbon, particulate organic carbon and their isotopic composition. Temperature and salinity were also measured at the same sampling sites within range of Mediterranean limits. the suspended organic matter concentration was 1.77 ± 1.55 mg l-1; the chlorophyll-a concentration was low (0.35 ± 0.24 μg l-1); the disolved organic carbon concentration was 2,140 ± 2,010 μg l-1; the particulate organic carbon concentration was 212 ± 106 μg l-1 and the isotopic composition was 18.77 ± 2.51%°. There were significant temporal differences except for phaeopigments, POC and its POC isotopic composition, and there were no spatial differences other than for δ13C. This picture highlighted a general seasonal trend and trophical features similar to adjacent sea.
Spatial differences in δ13C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In 相似文献
Spatial differences in δ13C showed that the source of suspended organic matter was different between stations as that between sources and wind-hydrodynamic constraints. In 相似文献