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Mengmeng Zheng Hua Zheng Yingxia Wu Yi Xiao Yihua Du Weihua Xu Fei Lu Xiaoke Wang Zhiyun Ouyang 《环境科学学报(英文版)》2015
The nitrogen balance can serve as an indicator of the risk to the environment of nitrogen loss from agricultural land. To investigate the temporal and spatial changes in agricultural nitrogen application and its potential threat to the environment of the Haihe Basin in China, we used a database of county-level agricultural statistics to calculate agricultural nitrogen input, output, surplus intensity, and use efficiency. Chemical fertilizer nitrogen input increased by 51.7% from 1990 to 2000 and by 37.2% from 2000 to 2010, concomitant with increasing crop yields. Simultaneously, the nitrogen surplus intensity increased by 53.5% from 1990 to 2000 and by 16.5% from 2000 to 2010, presenting a continuously increased environmental risk. Nitrogen use efficiency decreased from 0.46 in 1990 to 0.42 in 2000 and remained constant at 0.42 in 2010, partly due to fertilizer composition and type improvement. This level indicates that more than half of nitrogen inputs are lost in agroecosystems. Our results suggest that although the improvement in fertilizer composition and types has partially offset the decrease in nitrogen use efficiency, the environmental risk has still increased gradually over the past 20 years, along with the increase in crop yields and nitrogen application. It is important to achieve a better nitrogen balance through more effective management to significantly reduce the environmental risk, decrease nitrogen surplus intensity, and increase nitrogen use efficiency without sacrificing crop yields. 相似文献
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Shuidi He Minjuan Huang Lianming Zheng Ming Chang Weihua Chen Qianqian Xie Xuemei Wang 《环境科学学报(英文版)》2022,34(4):444-453
This study attempts to identify the dominant transport pathways, potential source areas, and their seasonal variation at sites with high inorganic nitrogen (IN) wet deposition flux in southern China. This is a long-term study (2010–2017) based on continuous deposition measurements at the Guangzhou urban site (GZ) and the Dinghushan Natural Reserve site (DHS) located in the Pearl River Delta (PRD) region. A dataset on monthly IN concentration in precipitation and wet deposition flux were provided. The average annual fluxes measured at both sites (GZ: 33.04±9.52, DHS: 20.52±10.22 kg N/(ha∙year)) were higher, while the ratios of reduced to oxidized N (GZ: 1.19±0.77, DHS: 1.25±0.84) were lower compared with the national mean level and the previous reported level throughout the PRD region. The dominant pathways were not always consistent with the highest proportional trajectory clusters. The transport pathways contributing most of deposition were identified in the north and north-northeast in the dry season and in the east-southeast, east, and south-southwest in the wet season. A weighted potential source contribution function (WPSCF) value >0.3 was determined reasonably to define the potential source area. Emission within the PRD region contributed the majority (≥95% at both sites) of the IN deposition in the wet season, while the contribution outside the region increased significantly in the dry season (GZ: 27.86%, DHS: 95.26%). Our results could help create more effective policy to control precursor emissions for IN fluxes, enabling reduction of the ecological risks due to excessive nitrogen. 相似文献
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悬浮填料生物膜反应器处理黑水的启动挂膜 总被引:1,自引:0,他引:1
采用自然挂膜法在低碳氮比的黑水中启动悬浮填料生物膜反应器,探讨了进水有机物和氨氮负荷率对挂膜启动的影响,分析了挂膜过程中溶解性化学需氧量(SCOD)、氨氮(NH4+-N)和总氮(TN)的去除转化规律及填料上附着生物量和填料生物相的变化规律。研究结果表明,在DO为1.5~2.5 mg/L、温度为(21±2) ℃等条件下可快速(43 d)启动生物硝化挂膜,SCOD、NH4+-N和TN去除率分别可达到84%、62%和46%,单个填料上的生物膜量达到0.49 g/个。进水SCOD、NH4+-N负荷率明显影响硝化细菌在填料上的成膜和生物硝化效率。研究认为,进水SCOD、NH4+-N 负荷率分别保持5.34 g/(m2·d)、1.44 g/(m2·d)左右,能够促快速挂膜并获得良好的短程硝化和同步硝化反硝化效果。 相似文献
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脉冲放电等离子体烟气脱硫脱硝工业试验研究 总被引:8,自引:0,他引:8
40000~50000Nm^3/h工业试验结果表明,烟气温度75~80℃,脱硫效率〉90%,脱硝效率〉40%,烟气温度90~95℃,脱硫效率>80%,脱硝效率>50%;脉冲能耗<3Wh/Nm^3;随着温度升高,SO2热化学反应效率逐渐降低;随着氨硫化学计量比增大,氨泄漏逐渐增加,烟气温度90~95℃,氨泄漏增加更为迅速。并分析了副产物的成分,阐述了脱硫脱硝的机理,并探讨了烟气排放的温度。 相似文献
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城市污泥中富含具有内分泌干扰活性的壬基酚(NP)和短链壬基酚聚氧乙烯醚(NP2EO、NP1EO)。污泥堆肥土地利用是国内外城市污泥最重要的处置方式。通过在污泥中添加促腐剂后堆肥发酵,进行了壬基酚类物质的变化研究,研究发现:从壬基酚二氧乙烯醚(NP2EO)、壬基酚单氧乙烯醚(NP1EO)和NP这3种物质总量的降解效果来看,好氧发酵优于厌氧发酵;好氧发酵过程中添加促腐剂对消除壬基酚和壬基酚聚氧乙烯醚(长链NPnEO,短链NP2EO、NP1EO)类物质是有利的。对污泥中壬基酚类物质的污染控制具有一定的指导意义。 相似文献
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Enhancement of phenanthrene adsorption on a clayey soil and clay minerals by coexisting lead or cadmium 总被引:1,自引:0,他引:1
Phenanthrene is commonly present together with heavy metals at many contaminated sites. This study investigated the influence of coexisting lead (Pb2+) or cadmium (Cd2+) on phenanthrene adsorption on soils. Batch experiments were conducted under different geochemical conditions including pH, mineral structure, organic matter content, and varying amounts of heavy metals. The results showed that the presence of heavy metals in solution at a fixed pH of 5.8 ± 0.1 enhanced phenanthrene adsorption, the extent of which was closely related to the concentrations and the electro-negativity of the metals. The enhancement on phenanthrene adsorption was positively correlated to the amount of adsorbed metals. Although Cd2+ is a softer Lewis acid, Pb2+ displayed a more significant effect as it was adsorbed to a greater extent on the soil surfaces. Thus, density of cation accumulation appears to be more influential than metal softness in enhancing phenanthrene adsorption. Moreover, with a portion of organic matter removed by heating at 550 °C, there was a stronger enhancement of phenanthrene adsorption by coexisting Pb2+, indicating an increasingly dominant mechanisms associated with Pb2+ at a lower organic matter content. Similar enhancement phenomenon was observed on bentonite and kaolinite, probably resulting from the cation-π bonding between the adsorbed soft metal cations and the aromatic ring of phenanthrene in solution. The desorption experiments further suggested that the bonding of phenanthrene adsorption was strengthened in the presence of Pb2+ and that a larger proportion of adsorbed phenanthrene remained on the soils (residual fraction) even after sequential methanol extractions. Further spectroscopic analyses and surface characterization are required to provide direct evidence of the formation and relative significance of cation-π bond for phenanthrene adsorption. 相似文献
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