The Adsorption of Lead and Copper from Aqueous Solution on Modified Peat–Resin Particles

Raw peat was modified with sulfuric acid, then mixed modified with resin to prepare the modified peat–resin particles. Using the batch experimental systems, the removal of heavy metals (copper and lead) on the modified peat–resin particles was investigated. The data of the adsorption isotherm could be fitted by the Langmuir equation well. The adsorption rate of heavy metals on modified peat–resin particles was very swift. The removal processes of heavy metals on modified peat–resin particles could be well described by pseudo-second order model. The adsorption rate of lead was affected by the initial heavy metal concentration, initial pH, particle size, agitation speed and particle mass. In the adsorption of heavy metals (lead and copper) on the modified peat–resin particles, ion exchange was the major reaction mechanism. Desorption data showed that the lead adsorbed by modified peat–resin particle could be desorbed by 0.5 N or 1.0 N HNO₃. The desorption rate was swift. The experiments indicated that the modified peat–resin particles have great potential for the removal of heavy metals from wastewater.     

Optimum Nitrogen Use and Reduced Nitrogen Loss for Production of Rice and Wheat in the Yangtse Delta Region

A long-term field and lysimeter experiment under different amount of fertilizer-N application was conducted to explore the optimal N application rates for a high productive rice–wheat system and less N leaching loss in the Yangtse Delta region. In this region excessive applications of N fertilizer for the rice–wheat production has resulted in reduced N recovery rates and environment pollution. Initial results of the field experiments showed that the optimal N application rate increased with the yield. On the two major paddy soils (Hydromorphic paddy soil and Gleyed paddy soil) of the region, the optimal N application rate was 225–270 kg N hm^–2 for rice and 180–225 kg N hm^–2 for wheat, separately. This has resulted in the highest number of effective ears and Spikelets per unit area, and hence high yield. Nitrogen leaching in the form of NO ₃ ^– -N occurs mainly in the wheat-growing season and in the ponding and seedling periods of the paddy field. Its concentration in the leachate increased with the N application rate in the lysimeter experiment. When the application rate reached 225 kg N hm^–2, the concentration rose to 5.4–21.3 mgN l^–1 in the leachate during the wheat-growing season. About 60% of the leachate samples determined contained NO ₃ ^– -N beyond the criterion (NO ₃ ^– -N 10 mg l^–1) for N pollution. In the field experiment, when the N application rate was in the range of 270–315 kg hm^–2, the NO ₃ ^– -N concentration in the leachate during the wheat-growing season ranged from 1.9 to 11.0 mg l^–1. About 20% of the leachate samples reached close to, and 10% exceeded, the criterion for N pollution. Long-term accumulation of NO ₃ ^– -N from leaching will no doubt constitute a potential risk of N contamination of the groundwater in the Yangtse Delta Region.     

湖南种子植物重要科属地理分布研究(二)——五味子科

湖南五味子科植物有2属11种2变种,分布于31个县,多生长在海拔600—1200m的山地灌丛或林中。本文依据湖南五味子科植物的地理分布,结合系统分类,植物区系和土壤资料,经分析和推论得知:1.湖南五味子科植物种质资源丰富,以中国特有种为主,它们与毗邻省区的关系密切。2.湖南五味子科植物区系表现为多种区系成分的过渡与汇集,即华南、华东、华中和滇黔桂4个区系成分的交汇、混杂和过渡。3.湖南五味子科植物的多数种类是从湖南以西地区迁移扩散而来,有的种类是从本省西北或西南以外地区而来,极少数植物在本省西南地区及其周边省区分化形成。4.湘西北至湘西南地区是湖南五味子科植物的现代分布中心,现代分化中心是湘西南地区。     

Interactions between nitrate and ammonium uptake: variation with growth rate,nitrogen source and species

The interaction between nitrate and ammonium uptake was examined as a function of preconditioning growth rate and nitrogen source by adding nitrate, ammonium, or both to nitrogen-sufficient,-deficient, and-starvedSkeletonema costatum (Grev.) Cleve and nitrogen-deficientChaetoceros debilis Cleve. By simultaneously measuring the internal accumulation of intermediates of nitrogen assimilation and the rates of nitrogen assimilation, the metabolic control of nitrogen uptake could be assessed. After the simultaneous addition of nitrate and ammonium to culture, both nitrate and ammonium uptake rates were decreased in comparison with the rates observed when each was added alone, although nitrate uptake was usually decreased more than ammonium uptake. Since both nitrate and ammonium uptake rates vary with time, preconditioning growth conditions, nitrogen sources present, and species, it was necessary to use several different indices to quantify inhibition. In general, ammonium inhibition of nitrate uptake inS. costatum was greatest in cultures preconditioned to ammonium and those at low growth rates, whereas ammonium uptake was inhibited most in cultures preconditioned to nitrate. In nitrogen-deficientC. debilis, nitrate uptake was more inhibited by ammonium, but uptake returned to normal rates more quickly than inS. costatum, whereas inhibition of ammonium uptake was similar. These results explain why the interaction between nitrate and ammonium uptake in the field can be so variable. Inhibition of uptake is not controlled by internal ammonium or total amino acids, nor is it related to the inability to reduce nitrate. Instead, inhibition must be determined in part by the external concentration of nitrogen compounds and in part by some intermediate(s) of nitrogen assimilation present inside the cell.Bigelow Laboratory Contribution No. 82022     

Biodegradation of quinoline by gel immobilized Burkholderia sp

Burkholderia sp, a gram-negative, rod-shaped, aerobe, capable of degrading quinoline was immobilized in calcium alginate gel beads and used for degradation of quinoline in aqueous solution in the reactor. The optimal conditions for immobilization of the microorganism, such as alginate concentration, calcium ion concentration, initial cell loading, hardening time and bead size, were determined with a view to improving the quinoline degradation rate. The characteristics of quinoline degradation by immobilized microbial cells were investigated. The repeated use of immobilized cells for quinoline degradation was performed and the results revealed that the bioactivity of immobilized cells was stable over 100 h in the repeated batch cultivation for quinoline degradation.     

Thermochemical studies of the toxic actions of heavy metal ions on Rhizopus nigricans

By using a LKB2277 BioActivity Monitor (heat conduction microcalorimeter), stopped-flow method, the thermogenetic curves of Rhizopus nigricans growth at 25 degrees C inhibited by four kinds of heavy metal ions are determined, parameters such as growth rate constants k, inhibitory ratio I, half inhibitory concentration IC50 et al. are obtained. The experimental results show that heavy metal ions can inhibit Rhizopus nigricans growth obviously, low concentration of Cu2+ has promoting action. The inhibitory sequence is Cd2+ > Hg2+ > Pb2+ > Cu2+, half inhibitory concentration of them are Cd+ 0.8 micro g x ml(-1), Hg2+ 1.7 micro g x ml(-1), Pb2+ 48.0 micro g x ml(-1), Cu2+ 110 micro g x ml(-1). This microclorimetric bioassay for acute cellular toxicity is based on metabolic heat evolution from cultured cells. The assay is quantitative, inexpensive, and versatile; moreover, toxicological information can be obtained with cell from other species of interest.     

Electrochemical degradation of bromopyrogallol red in presence of cobalt ions

This paper summarizes the results of a degradation test of bromopyrogallol red (BPR) and textile dye wastewater (TDW) with a conventional three-electrode potentiostatic system in the presence of cobalt ions (electro Co(2+)-H2O2 system). H2O2, produced by the two-electron reduction of O2 at the cathode, would react with Co2+ ions, leading to the generation of hydroxyl radicals (*OH), which caused the degradation of the organic pollutants. With BPR degradation process as the reference point, the optimal conditions (pH=4.0 and the concentration of Co2+ is 0.1 mM) and the treating capacity of the system were both studied and compared with electro-Fenton's reagent. Many benefits were shown by the electro Co(2+)-H2O2 system, such as less metal ions consumption, more moderate conditions and faster reaction process. Treated with the system for 0.5 h, chemical oxygen demand and biological oxygen demand of TDW (pH=5.2), without pH adjustment, were reduced by 95.7% and 92.7%, respectively. These characteristics make the method another appropriate solution for wastewater treatment, especially for those contaminated by organic pollutants.     

Lead contamination in tea garden soils and factors affecting its bioavailability

The consumption of heavy metals is detrimental to human health and most countries restrict the concentration of metals such as lead (Pb) in food and beverages. Recent tests have detected high Pb concentrations in certain commercial brands of tea leaves and this finding has raised concerns for both producers and consumers. To investigate what factors may be contributing to the increase in Pb accumulation in the tea leaves we collected tea leaves and soils from tea producing areas and analyzed them for Pb concentration, pH and organic matter content. The result showed the Pb concentration of 47% investigated tea leaves samples was beyond 2 mg kg(-1), the permissible levels given by China. The total Pb concentration in the surface and subsurface soil layers averaged 36.4 and 32.2 mg kg(-1), respectively which fall below of the 60 mg kg(-1) limit provided for organic tea gardens in China. The pH of the tea garden soils was severely acidic with the lowest pH of 3.37. Soils under older tea gardens tended to have a lower pH and a higher Pb bioavailability which was defined as the amount of lead extracted by CaCl2 solution than those under younger tea gardens. We found that the concentration of bioavailable Pb and the percentage of bioavailable Pb (bioavailable Pb relative to total Pb concentration) were positively correlated with soil H+ activity and soil organic matter content, and the organic matter accumulation contribute more effects on Pb bioavailability in these two factors. We conclude that soil acidification and organic matter accumulation could contribute to increasing Pb bioavailability in soil and that these could increase Pb uptake and accumulation in the tea leaves.     

Removal of arsenic(V) from aqueous solutions using iron-oxide-coated modified activated carbon.

Removal of arsenic(V) from aqueous solutions was evaluated with the following three different sorption materials: coal-based activated carbon 12 x 40 (activated carbon), iron(II) oxide (FeO)/activated carbon-H, and iron oxide. The apparent characteristics and physical chemistry performances of these adsorbents were investigated by X-ray diffraction, nitrogen adsorption, and scanning electronic microscope. Also, batch experiments for arsenic removal were performed, and the effects of pH value on arsenic(V) removal were studied. The results suggest that the main phases of the iron oxide surface are magnetite, maghemite, hematite, and goethite; fine and uniform iron oxide particles can cover activated carbon surfaces and affect the surface area or pore structures of activated carbon; adsorption kinetics obey a pseudo-first-order rate equation; and adsorption capacities of adsorbents are affected by the values of pH. The optimum value of pH for iron oxide lies in a narrow range between 4.0 and 5.5, and arsenic(V) removal by FeO/activated carbon-H is ideal and stable in the pH range 3 to 7, while activated carbon has the lowest adsorption capacity in the entire pH range. Also, the adsorption characteristics of FeO/activated carbon-H composites and virgin activated carbon match well the Langmuir adsorption model, while those of iron oxide fit well the Freundlich adsorption model.     

Arsenic species and leachability in the fronds of the hyperaccumulator Chinese brake (Pteris vittata L.)

Arsenic speciation is important not only for understanding the mechanisms of arsenic accumulation and detoxification by hyperaccumulators, but also for designing disposal options of arsenic-rich biomass. The primary objective of this research was to understand the speciation and leachability of arsenic in the fronds of Chinese brake (Pteris vittata L.), an arsenic hyperaccumulator, with an emphasis on the implications for arsenic-rich biomass disposal. Chinese brake was grown for 18 weeks in a soil spiked with 50 mg As kg(-1) as arsenate (AsO4(3-)), arsenite (AsO3(3-)), dimethylarsinic acid (DMA), or methylarsonic acid (MMA). Plant samples were extracted with methanol/water (1:1) and arsenic speciation was performed using high performance liquid chromatography coupled with atomic fluorescence spectrometry. The impacts of air-drying on arsenic species and leachability in the fronds were examined in the laboratory. After 18 weeks, water-soluble arsenic in soil was mainly present as arsenate with little detectable organic species or arsenite regardless of arsenic species added to the soil. However, arsenic in the fronds was primarily present as inorganic arsenite with an average of 94%. Arsenite re-oxidation occurred in the old fronds and the excised dried tissues. Arsenic species in the fronds were slightly influenced by arsenic forms added to the soil. Air-drying of the fronds resulted in leaching of substantial amounts of arsenic. These findings can be of significance when looking at disposal options of arsenic-rich biomass from the point of view of secondary contamination.