Rate coefficients are reported for the gas-phase reaction of the hydroxyl radical (OH) with C2HCl3 (k(1)) and C2Cl4 (k2) over an extended temperature range at 740+/-10 Torr in a He bath gas. These absolute rate measurements were accomplished using a laser photolysis/laser-induced fluorescence (LP/LIF) technique under slow flow conditions. The simple Arrhenius equation adequately describes the low temperature data for k1 (<650 K) and the entire data set for k2 and is given by (in units of cm3 molecule(-1) s(-1)): k1(291 - 650 K) = (9.73+/-1.15) x 10(-13) exp (158.7+/-44.0)/T, k2(293 - 720 K ) = (1.53+/-0.14) x 10(-12) exp (-688.2+/-67.5)/T. Error limits are 2sigma values. The room temperature values for k1 and k2 are within +/-2sigma of previous data using different techniques. The Arrhenius activation energies for k1 and k2 are a factor of 2-3 lower than previously reported values. The experimental measurements for both k1 and k2 in conjunction with transition state and variation transition state theory calculations infer an OH addition mechanism. The lack of a measurable kinetic isotope effect for k1 is consistent with this mechanism. Insight into the subsequent reactions of the chemically activated intermediate are presented in the form of potential energy diagrams derived from ab initio calculations. 相似文献
Journal of Polymers and the Environment - Due to extensive concerns of tremendous environment pollutions, particularly microplastic as an emerging pollutant, the development and investigate on... 相似文献
Journal of Polymers and the Environment - In this study, carboxymethyl chitosan with gum Arabic (CG) based novel functional films containing Cinnamomum camphora seeds extract (CCSE) at varying... 相似文献
Water contamination by emerging organic pollutants is calling for advanced methods of remediation such as iron-activated sulfite-based advanced oxidation. Sulfate radical, SO4??, and hydroxyl radical, ?OH, are the primary reactive intermediates formed in the Fe(III)/sulfite system, yet the possible involvement of Fe(IV) produced from Fe(II) and persulfates is unclear. Here we explored the role of Fe(IV) in the Fe(III)/sulfite system by methyl phenyl sulfoxide (PMSO) probe assay, electron paramagnetic resonance spectra analysis, alcohol scavenging experiment, and kinetic simulation. Results show that PMSO is partially transformed into methyl phenyl sulfone (PMSO2), thus evidencing Fe(IV) formation. The remaining degradation of PMSO is due to SO4?? and ?OH. The contribution of Fe(IV) versus free radicals is progressively promoted when the Fe(III)-sulfite reaction proceeds, with an upper limit of 80–90%. The contribution of Fe(IV) versus free radicals increases with Fe(III) and sulfite dosages, and decreases with increasing pH. Overall, our findings demonstrate the involvement of Fe(IV) in the Fe-catalyzed sulfite auto-oxidation process.
• Municipal solid waste (MSW) was fermented, screened, gasified, then co-processed.• Co-processing MSW in cement kilns could cause excessive pollutant emissions.• Bypass flue gas can be disposed of through the main flue system.• Popular MSW co-processing methods do not affect cement quality. Cement kiln co-processing techniques have been developed in the past 20 years in China, and more than 60 factories now use fermentation, screening, and gasification pre-treatment techniques to co-process municipal solid waste (MSW). There three complete MSW pre-treatment techniques, co-processing procedures, and environmental risk assessments have been described in few publications. In this study, we assessed the effectiveness of each technique. The results suggested that the pollutant content released by each pre-treatment technology was lower than the emission standard. To reveal the mechanisms of pollutant migration and enrichment, the substances in the kiln and kiln products are investigated. The input of co-processing materials (Co-M) produced by fermentation caused formation of polychlorinated dibenzo-p-dioxins and dibenzofuran (PCDD/Fs) in the bypass flue gas (By-gas) in excess of the regulatory standard. The Co-M input produced by the screening and gasifier technologies caused the total organic carbon (TOC) concentration to exceed the standard. In addition, the NOx, TOC, and PCDD/Fs in the By-gas exceeded the regulatory standard. Raw meal was the primary chlorine and heavy metals input stream, and clinker (CK) and cement kiln dust (CKD) accounted for>90% of the total chlorine output stream. Flue gas and CKD were the primary volatile heavy metal (Hg) output streams. Greater than 70% of the semi-volatile heavy metals (Cd, Pb, Tl and Se) distributed in hot raw meal and bypass cement kiln dust. The low-volatility heavy metals were concentrated in the CK. These results indicated that co-processing techniques used in China still require improvement. 相似文献
• The synthesis and physicochemical properties of various CNMs are reviewed.• Sb removal using carbon-based nano-adsorbents and membranes are summarized.• Details on adsorption behavior and mechanisms of Sb uptake by CNMs are discussed.• Challenges and future prospects for rational design of advanced CNMs are provided. Recently, special attention has been deserved to environmental risks of antimony (Sb) element that is of highly physiologic toxicity to human. Conventional coagulation and ion exchange methods for Sb removal are faced with challenges of low efficiency, high cost and secondary pollution. Adsorption based on carbon nanomaterials (CNMs; e.g., carbon nanotubes, graphene, graphene oxide, reduced graphene oxide and their derivatives) may provide effective alternative because the CNMs have high surface area, rich surface chemistry and high stability. In particular, good conductivity makes it possible to create linkage between adsorption and electrochemistry, thereby the synergistic interaction will be expected for enhanced Sb removal. This review article summarizes the state of art on Sb removal using CNMs with the form of nano-adsorbents and/or filtration membranes. In details, procedures of synthesis and functionalization of different forms of CNMs were reviewed. Next, adsorption behavior and the underlying mechanisms toward Sb removal using various CNMs were presented as resulting from a retrospective analysis of literatures. Last, we prospect the needs for mass production and regeneration of CNMs adsorbents using more affordable precursors and objective assessment of environmental impacts in future studies. 相似文献
Environmental Science and Pollution Research - In an effort to control dust pollution in open-air environments such as pit coal mines and coal transportation systems, a new dust suppressant with a... 相似文献