Assessment of China's economic loss resulting from the degradation of agricultural land in the end of 20th century

Land degradation is a consequence stemming from both natural processes and social economic activities. On the bases of analyzing general situation of agricultural land degradation in China, the monetary estimating methods such as market value method and shadow engineering method were used to quantitatively assess the economic loss resulting from land deterioration. Results showed that the economic loss in 1999 was 326.8l billion RMB Yuan, which accounted for 4.1% of GDP in the same year of China. If taking five items namely farmland conversion, soil erosion, salinization, decline in reservoir functions, and siltation in waterways and, comparing with that in 1992, the percentage of economic loss to GDP has increased by 1.5 in the only 7 years.     

Influence of coal particles on methane/air mixture ignition in a heated environment

The temperature at which coal dust glows is normally much lower than the auto-ignition temperature (AIT) of methane/air mixtures, and thus a better understanding is needed regarding methane/air ignition in a heated environment in the presence of coal particles. A horizontal tube apparatus was used to test the effect of brown coal and two kinds of bituminous and anthracite on methane/air combustibility. For the four coal samples tested, the presence of coal particles significantly reduced the minimum temperature for ignition of methane/air mixtures in a heated environment. No. 1 bituminous coal with 12 mm diameter decreased the ignition temperature value from 595 to 500 °C. It is thought that pre-ignition of low-AIT volatiles emitted from the heated coal particles ignited the methane/air mixtures. Volatiles, sulfur content, and large porosity of piled coal particles all enhanced ignition of methane/air mixtures in a hot environment, while water content and small particle size reduced ignition. For anthracite, no ignition occurred when temperatures of the heated environment were lower than the AIT of methane (595 °C), except for the 12-mm-diameter sample. Anthracite did not readily ignite methane/air mixtures and the ignition mechanism was somewhat similar to that of a burning cigarette.     

2002年我国事故与灾害状况综述

本对我国2002年的安全生产事故及自然灾害情况进行了总结和评述。包括火灾(城乡火灾、森林火灾、草原火灾)、天气气候特征、农业自然灾害(干旱、洪涝、风雹、低温冻害)、海洋灾害(风暴潮、赤潮、海浪)、地质灾害(地震、泥石流、水土流失)等。     

氯甲烷与偶氮染料混合废水的超声脱色

使用40 kHz超声（US）脱色氯甲烷（包括CCl4、CHCl3和CH2Cl2）与偶氮染料（包括甲基橙与铬黑T）混合模拟废水,考察了氯甲烷初始浓度对偶氮染料超声脱色和TOC去除的影响。结果表明：偶氮染料的单独超声脱色速率很慢;而在CCl4与CHCl3存在时超声能使偶氮染料短时间内脱色至无色,但对其TOC的超声去除促进作用较差;CH2Cl2对偶氮染料的超声脱色促进作用很小。使用0.392 W/cm2的超声处理24 mg/L铬黑T水溶液,当CCl4和CHCl3初始浓度分别为6.22 mmol/L和8.30 mmol/L时,20 min脱色率均达到90.86%,但相应的TOC去除率只有22.72%和17.76%。同样条件下,甲基橙处理效果比铬黑T稍优。     

Incidence of polybrominated diphenyl ethers in central air conditioner filter dust from a new office building

This study examined polybrominated diphenyl ethers (PBDEs) in central air conditioner filter (CACF) dust from a new office building in Shenzhen, China. Human exposure to PBDE via dust inhalation and ingestion were also estimated. PBDEs level in CACF dust was lower than those in the other countries and regions. Approximately 0.671 pg/kg bw/day PM_2.5 (Particulate Matter up to 2.5 μm in size) bounded Σ₁₅PBDEs can be inhaled deep into the lungs and 4.123 pg/kg bw/day PM₁₀ (Particulate Matter up to 10 μm in size) bounded Σ₁₅PBDEs tend to be deposited in the upper parts of the respiratory system. The average total intake of Σ₁₅PBDEs via dust inhalation and ingestion for adults reached ∼141 pg/kg bw/day in this building. This value was far below the reference dose (RfD) recommended by United States Environmental Protection Agency. Human exposure to PBDEs via dust inhalation and ingestion in the new building is less than the old ones.     

Removal of 2-chlorophenol from water using rice-straw derived ash

Removal of 2-chlorophenol from water using rice-straw derived ash (RSDA) was evaluated in this study to compare with commercial activated carbon. RSDA was obtained by burning rice-straw at 400 °C and 700 °C for 1 h. This ash can provide a better adsorbent for 2-chlorophenol. The adsorption capacities of RSDA at 400 °C and 700 °C are 37 and 52 mg g?1 at pH 4, respectively, and decrease to 9.0 and 40 mg g?1 at pH 10. Adsorption of either neutral or anionic 2-cholorphenol by the RSDA are shown as L-shaped nonlinear isotherms, suggesting surface adsorption rather than partitioning is occurring. At higher-burning temperatures, the surface area, porosity, point of zero charge and aromaticity of the resultant RSDA increase, but the oxygen content and surface acidity decrease. The combined effects result in a higher 2-chlorophenol adsorption of RSDA at 700 °C, which shows a slight pH effect on the adsorption of 2-chlorophenol, due to the lower content of oxygen-containing functional groups. Oxygen-containing functional groups contribute to surface acidity and H-bonding sites for adsorbed water, which compromises the interaction between 2-chlorophenol and the adsorbents. Thus, it suggests that rice-straw derived carbon (RSDC) can be used as an effective low-cost substitute material for activated carbon for removal of chlorophenols from wastewater.     

Atmospheric bulk deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in the vicinity of an iron and steel making plant

An IRA-743 resin bulk sampler was validated to monitor long-term bulk deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). Six consecutive sampling campaigns (2008-2009) were conducted at four sites around steel complexes in Pohang, South Korea to investigate spatial and seasonal variations of PCDD/F bulk deposition. The bulk deposition within the steel complex showed the highest ∑_4-8PCDD/F (Tetra-Octa) fluxes, ranging from 204 to 608 (mean: 352) pg m⁻² d⁻¹, indicating steel complexes were major sources of PCDD/Fs. The homologue profiles were dominated with lower chlorinated PCDFs. Furthermore, the prevailing winds were confirmed to influence the spatial distribution of PCDD/F deposition. There were apparent seasonal variations of the bulk deposition at each site, and seasonal homologue patterns of PCDD/Fs were clearly observed. According to the passive air sampling, however, no significant seasonal change of ambient air concentrations of PCDD/Fs was observed. Therefore, it was concluded that the seasonal variations of deposition fluxes of PCDD/Fs probably resulted from temperature-dependent gas/particle partitioning.