The Sanjiang Plain, the largest inland freshwater marshland in China, was extensive reclaimed into agricultural land. To assess the effects of marshland reclamation on Collembola, we investigated collembolan communities in a chronosequence of soybean plantations (2, 15, and 25 years) in Sanjiang marshland, Northeastern China. We found that: 1) the densities and species richness of Collembola were promoted after short-term (2 years) cultivation of soybean, but significantly decreased after medium-term cultivation (15 years); 2) the densities of epi-edaphic Collembola increased while the densities of hemi-edaphic Collembola decreased as the elongation of soybean cultivation; 3) compared with S0, two species of Collembola appeared while five species disappeared in S25. The changes of plant communities and the soil traits were supposed to be the key factors affecting the composition of soil Collembola. We thus suggest that original marshland should be saved for preserving high diversity and densities of Collembola in the Sanjiang Plain.
China is the country with the largest coal mining production and consumption in the world, but due to a large amount of coal burning, air pollution and climate change are exasperating related problems. The previous literature mainly has discussed coal mine production and environmental pollution, but failed to take into account external factors such as climate change and seldom discussed the relationship between coal mine land use and land restoration. Therefore, this study uses the meta-Epsilon-Based Measure two-stage Data Envelopment Analysis under the exogenous model and incorporates coal mine land use and land restoration use into the model to explore the relationship between the two under climate change. The research results are as follows. (1) If the external climate factors are not considered, then the phenomenon of overestimation or underestimation of the technology gap arises. (2) The efficiency value of the coal mining stage in most provinces is generally higher than the land restoration efficiency value. 相似文献
Environmental Chemistry Letters - Branched allylic sulfones are scaffolds widely distributed in bioactive molecules and organic functional materials. The synthesis of allylic sulfones has been... 相似文献
• UV/O3 process had higher TAIC mineralization rate than O3 process.• Four possible degradation pathways were proposed during TAIC degradation.• pH impacted oxidation processes with pH of 9 achieving maximum efficiency.• CO32– negatively impacted TAIC degradation while HCO3– not.• Cl– can be radicals scavenger only at high concentration (over 500 mg/L Cl–). Triallyl isocyanurate (TAIC, C12H15N3O3) has featured in wastewater treatment as a refractory organic compound due to the significant production capability and negative environmental impact. TAIC degradation was enhanced when an ozone(O3)/ultraviolet(UV) process was applied compared with the application of an independent O3 process. Although 99% of TAIC could be degraded in 5 min during both processes, the O3/UV process had a 70%mineralization rate that was much higher than that of the independent O3 process (9%) in 30 min. Four possible degradation pathways were proposed based on the organic compounds of intermediate products identified during TAIC degradation through the application of independent O3 and O3/UV processes. pH impacted both the direct and indirect oxidation processes. Acidic and alkaline conditions preferred direct and indirect reactions respectively, with a pH of 9 achieving maximum Total Organic Carbon (TOC) removal. Both CO32– and HCO3– decreased TOC removal, however only CO32– negatively impacted TAIC degradation. Effects of Cl– as a radical scavenger became more marked only at high concentrations (over 500 mg/L Cl–). Particulate and suspended matter could hinder the transmission of ultraviolet light and reduce the production of HO· accordingly. 相似文献
The effects of three compounded curing agents on the properties and performance of the urea-formaldehyde (UF) resin were investigated in this study. The compounded curing agents were prepared by mixing ammonium chloride with hexamethylenetetramine, citric acid, and oxalic acid respectively at a ratio of 1:1, named N-H, N–CA, and N–OA, respectively. The curing process, crystallinity, and physical properties were measured, and the three-ply plywood was fabricated to measure its prepress strength, wet shear strength, and formaldehyde emission. Results showed that the compounded curing agents N–CA and N–OA enhanced the initial viscosity, crosslinking density and thermal stability of UF resin. Additionally, the prepress strength of the plywood bonded by UF resin with N–CA and N–OA increased by 82 and 111% respectively compared to the UF resin with NH4Cl, and the wet shear strength increased by 14 and 16%, the formaldehyde emission decreased by 19 and 42% respectively. However, owing to the short pot-life of these curing agent limited their storage time, the curing agents N–CA and N–OA should be applied to fabricate plywood in winter for obtaining a better bond strength and a lower formaldehyde emission. While the UF resin with N–HT showed a suitable pot-life, so it could be applied to fabricate plywood in summer for long time storage and avoiding procuring problem. 相似文献
• Strong metal-support interaction exists on Pt/Fe3O4 catalysts.• Pt metal particles facilitate the formation of oxygen vacancies on Fe3O4.• Fe3O4 supports enhance the strength of CO adsorption on Pt metal particles. The self-inhibition behavior due to CO poisoning on Pt metal particles strongly impairs the performance of CO oxidation. It is an effective method to use reducible metal oxides for supporting Pt metal particles to avoid self-inhibition and to improve catalytic performance. In this work, we used in situ reductions of chloroplatinic acid on commercial Fe3O4 powder to prepare heterogeneous-structured Pt/Fe3O4 catalysts in the solution of ethylene glycol. The heterogeneous Pt/Fe3O4 catalysts achieved a better catalytic performance of CO oxidation compared with the Fe3O4 powder. The temperatures of 50% and 90% CO conversion were achieved above 260°C and 290°C at Pt/Fe3O4, respectively. However, they are accomplished on Fe3O4 at temperatures higher than 310°C. XRD, XPS, and H2-TPR results confirmed that the metallic Pt atoms have a strong synergistic interaction with the Fe3O4 supports. TGA results and transient DRIFTS results proved that the Pt metal particles facilitate the release of lattice oxygen and the formation of oxygen vacancies on Fe3O4. The combined results of O2-TPD and DRIFTS indicated that the activation step of oxygen molecules at surface oxygen vacancies could potentially be the rate-determining step of the catalytic CO oxidation at Pt/Fe3O4 catalysts. The reaction pathway involves a Pt-assisted Mars-van Krevelen (MvK) mechanism. 相似文献
Environmental Science and Pollution Research - This study aims at investigating the electrocatalytic oxidation of sodium pentachlorophenate (PCP-Na) using a novel nano-PbO2 powder anode. The... 相似文献