The migration and transformation of dissolved organic matter during the freezing processes of water

This study investigated the partitioning behavior of dissolved organic matter(DOM) in liquid and ice phases, as well as the changes in the optical properties and chlorine reactivity of DOM during the freezing processes of water. DOM was rejected from the ice phase and accumulated in the remaining liquid phase during water freezing. Moreover, the decrease in freezing temperature, as well as the increase in dissolved organic carbon(DOC)concentration of feed water, caused an increase in DOM captured in the ice phase. The ultraviolet-absorbing compounds, trihalomethane precursors, as well as fulvic acid- and humic acid-like fluorescent materials, were more liable to be to be rejected from the ice phase and were more easily retained in the unfrozen liquid phase during water freezing, as compared with organics(on average) that comprise DOC. In addition, it was also found a higher accumulation of these organics in the unfrozen liquid phase during water freezing at higher temperature. The freeze/thaw processes altered the quantity, optical properties, and chlorine reactivity of DOM. The decrease in ultraviolet light at 254 nm as well as the production of aromatic protein- and soluble microbial byproduct-like fluorescent materials in DOM due to freeze/thaw were consistently observed. On the other hand, the changes in DOC, trihalomethane formation potential, and fulvic acid- and humic acid-like fluorescence caused by freeze/thaw varied significantly between samples.     

Study on the migration mechanisms of water-soluble agents in high-pressure rotary jetting remediation

Environmental Science and Pollution Research - High-pressure rotary jetting (HPRJ) remediation is a recent-applied technology for in situ remediation of contaminated soils. The effectiveness of...     

Measuring the integrated risk of China’s carbon financial market based on the copula model

Measuring the risks of the carbon financial market is of great significance for investment decision-making, risk supervision, and the healthy development of the carbon trading market. Different from previous studies based on traditional VaR (value at risk), this study measures the integrated risk of China’s carbon market based on the Copula-EVT (Extreme Value Theory) -VaR model which can explore the unique strength of the copula and EVT-VaR models, of which the copula model is applied to capture the dependence between the different risk factors of carbon price volatility and macroeconomic fluctuation, while the EVT-VaR is used to explore the risk value. The empirical results show that the traditional VaR that only considers a single risk factor from carbon price volatility is likely to overestimate the risk. In addition, compared with other methods that do not consider the interdependence between risk factors, using the copula function to measure the carbon market integration risk is more effective, and backtesting also confirms this conclusion. This paper provides a specific reference for carbon emission companies to participate in the carbon market. It provides a theoretical basis for the supervision of the risk management of the carbon market.

     

Particle size effects in microbial characteristics in thermophilic anaerobic digestion of cattle manure containing copper oxide

Environmental Science and Pollution Research - Roles of bulk-, micron-, and nano-copper oxide (CuO) on methane production, microbial diversity, functions during thermophilic anaerobic digestion...     

Spectroscopic characterization and photochemistry of the Criegee intermediate CF3C(H)OO

Criegee intermediates (CIs), also known as carbonyl oxide, are reactive intermediates that play an important role in the atmospheric chemistry. Investigation on the structures and reactivity of CIs is of fundamental importance in understanding the underlying mechanism of their atmospheric reactions. In sharp contrast to the intensively studied parent molecule (CH₂OO) and the alkyl-substituted derivatives, the knowledge about the fluorinated analogue CF₃C(H)OO is scarce. By carefully heating the triplet carbene CF₃CH in an O₂-doped Ar-matrix to 35 K, the elusive carbonyl oxide CF₃C(H)OO in syn- and anti-conformations has been generated and characterized with infrared (IR) and ultraviolet-visible (UV-vis) spectroscopy. The spectroscopic identification is supported by ¹⁸O-labeling experiments and quantum chemical calculations at the B3LYP/6-311++G(3df,3pd) and MP2/6-311++G(2d,2p) levels. Upon the long-wavelength irradiation (λ > 680 nm), both conformers of CF₃C(H)OO decompose to give trifluoroacetaldehyde CF₃C(H)O and simultaneously rearrange to the isomeric dioxirane, cyclic-CF₃CH(OO), which undergoes isomerization to the lowest-energy carboxylic acid CF₃C(O)OH upon UV-light excitation at 365 nm. The O₂-oxidation of CF₃CH via the intermediacy of CF₃C(H)OO and cyclic-CF₃CH(OO) might provide new insight into the mechanism for the degradation of hydro-chlorofluorocarbon CF₃CHCl₂ (HCFC-123) in the atmosphere.