The concentrations, distribution and sources of PAHs in agricultural soils and vegetables from Shunde, Guangdong, China

The concentrations, distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) were determined in 30 agricultural soil and 16 vegetable samples collected from subtropical Shunde area, an important manufacturing center in China. The total PAHs ranged from 33.7 to 350 μg/kg in soils, and 82 to 1,258 μg/kg in vegetables. The most abundant individual PAHs are phenanthrene, fluoranthene, chrysene, pyrene and benzo(b)fluoranthene for soil samples, and anthracene, naphthalene, phenanthrene, pyrene and chrysene for vegetable samples. Average vegetable–soil ratios of total PAHs were 2.20 for leafy vegetables and 1.27 for fruity vegetables. Total PAHs in vegetable samples are not significantly correlated to those in corresponding soil samples. Principal component analyses were conducted to distinguish samples on basis of their distribution in each town, soil type and vegetable specie. Relatively abundant soil PAHs were found in town Jun’an, Beijiao, Chencun, Lecong and Ronggui, while abundant vegetable PAHs were observed in town Jun’an, Lecong, Xingtan, Daliang and Chenchun. The highest level of total PAHs were found in vegetable soil, followed by pond sediment and “stacked soil” on pond banks. The PAHs contents in leafy vegetables are higher than those in fruity vegetables. Some PAH compound ratios suggest the PAHs derived from incomplete combustion of petroleum, coal and refuse from power generation and ceramic manufacturing, and paint spraying on furniture, as well as sewage irrigation from textile industries. Soil PAHs contents have significant logarithmic correlation with total organic carbon, which demonstrates the importance of soil organic matter as sorbent to prevent losses of PAHs.     

Distribution of heavy metals in sediments of the Pearl River Estuary, Southern China: Implications for sources and historical changes

The distribution of heavy metals (Pb, Zn, Cd and As) in sediments of the Pearl River Estuary was investigated. The spatial distribution of heavy metals displayed a decreasing pattern from the turbidity maxima to both upstream and downstream of the estuary, which suggested that suspended sediments played an important role in the trace metal distribution in the Pearl River Estuary. In addition, metal concentrations were higher in the west part of the estuary which received most of the pollutants from the Pearl River. In the sediment cores, fluxes of heavy metals were consistent with a predominant anthropogenic input in the period 1970-1990. From the mid-1990s to the 2000s, there was a significant decline in heavy metal pollution. The observed decline has shown the result of pollution control in the Pearl River Delta. However, it is noteworthy that the metal concentrations in the most recent sediment still remained considerably high. Taken together, the enrichment of heavy metals in sediments was largely controlled by anthropogenic pollution.     

Ammonia volatilization and availability of Cu, Zn induced by applications of urea with and without coating in soils

Ammonia volatilization and the distribution of Cu and Zn were investigated in two types of soil treated with coated and uncoated urea. The rate of ammonia volatilization in two weeks after fertilizing with coated urea was 8% in soil 1 (soil derived from river alluvial deposits in Dongting Lake Plain) and 5.15% in soil 2 (red soil derived from quaternary red clay), about half the rates observed when fertilizing with common urea, implying that the hydrolysis speed of the coated urea was lower than for common urea, and that the coated urea can increase nitrogen use efficacy. As for the availability of Cu and Zn, their concentrations decreased in the first week after fertilization, and then increased, which was contrary to the effect of treatment on soil pH. For example, when the pH was 7.99, there was 0.79 mg/kg exchangeable Cu and 0.85 mg/kg exchangeable Zn in the soil derived from river alluvial deposits in Dongting Lake Plain. However, the concentrations of exchangeable Cu and Zn were generally lower for the common urea treatments than those with the coated urea because the peak pH for the common urea treatment was greater. The concentrations of these elements correlated well with pH in the range 4-8 in second order polynomial fits.     

Shellac-coated iron oxide nanoparticles for removal of cadmium(II) ions from aqueous solution

This study describes a new effective adsorbent for cadmium removal from aqueous solution synthesized by coating a shellac layer, a natural biodegradable and renewable resin with abundant hydroxyl and carboxylic groups, on the surface of iron oxide magnetic nanoparticles. Transmission Electron Microscopy (TEM) imaging showed shellac-coated magnetic nanoparticle (SCMN) adsorbents had a core-shell structure with a core of 20 nm and shell of 5 nm. Fourier Transform Infrared Spectroscopic analysis suggested the occurrence of reaction between carboxyl groups on the SCMN adsorbent surface and cadmium ions in aqueous solution. Kinetic data were well described by pseudo second-order model and adsorption isotherms were fitted with both Langmuir and Freundlich models with maximum adsorption capacity of 18.80 mg/g. SCMN adsorbents provided a favorable adsorption capacity under high salinity conditions, and cadmium could easily be desorbed using mild organic acid solutions at low concentration.     

Photodegradation of amoxicillin by catalyzed Fe3+/H2O2 process

Three oxidation processes of UV-Fe³⁺(EDTA)/H₂O₂ (UV: ultraviolet light; EDTA: ethylenediaminetetraacetic acid), UV-Fe³⁺/H₂O₂ and Fe³⁺/H₂O₂ were simultaneously investigated for the degradation of amoxicillin at pH 7.0. The results indicated that, 100% amoxicillin degradation and 81.9% chemical oxygen demand (COD_Cr) removal could be achieved in the UV-Fe³⁺ (EDTA)/H₂O₂ process. The treatment efficiency of amoxicillin and COD_Cr removal were found to decrease to 59.0% and 43.0% in the UV-Fe³⁺/H₂O₂ process; 39.6% and 31.3% in the Fe³⁺/H₂O₂ process. Moreover, the results of biodegradability (biological oxygen demand (BOD₅)/COD_Cr ratio) revealed that the UV-Fe³⁺ (EDTA)/H₂O₂ process was a promising strategy to degrade amoxicillin as the biodegradability of the effluent was improved to 0.45, compared with the cases of UV-Fe³⁺/H₂O₂ (0.25) and Fe³⁺/H₂O₂ (0.10) processes. Therefore, it could be deduced that EDTA and UV light performed synergetic catalytic effect on the Fe³⁺/H₂O₂ process, enhancing the treatment efficiency. The degradation mechanisms were also investigated via UV-Vis spectra, and high performance liquid chromatography-mass spectra. The degradation pathway of amoxicillin was further proposed.     

非枝晶半固态金属成形技术的发展概况

此文叙述了非枝晶半固态金属成形技术的发展概况。主要介绍了压铸成形、模锻成形、连续流变铸造成形、注射成形以及半固态金属锭料制造等技术的特点和应用现状。     

锅炉监控仪表的改进与实践

在原有"锅炉高低水位报警器"的基础上,研制出锅炉智能监控仪表.该仪表系统实现了自动操作、失误防护、报警及连锁保护等功能,对锅炉各类事故有积极的预防作用.     

Anthropogenic nitrogen sources and exports in a village-scale catchment in Southeast China

An experimental village-scale catchment was selected for investigation of nitrogen (N) sources and exports. The mean N application rate over the catchment was 350.2 kg N ha⁻¹, but this rate varied spatially and temporally. The N leaching loss rate varied from 8.1 to 52.7 kg N ha⁻¹ under different land use regimes. The average N leaching loss rate was 13.4 kg N ha⁻¹ over the whole catchment, representing about 3.8% of the total N inputs. The N export rate through stormflows was 28.8 kg N ha⁻¹, about 8.2% of the total N inputs. Seasonal patterns showed that 95% of N exports through stormflows occurred during July to September in 2002. Overall, the maximum riverine N exports were 12.1% of total N inputs and 15.5% of the inorganic fertilizer N applied. Understanding N sources and exports in a village-scale catchment can provide a knowledge base for amelioration of diffuse agricultural pollution.