Removal of fluorescence and ultraviolet absorbance of dissolved organic matter in reclaimed water by solar light

Storing reclaimed water in lakes is a widely used method of accommodating changes in the consumption of reclaimed water during wastewater reclamation and reuse. Solar light serves as an important function in degrading pollutants during storage, and its effect on dissolved organic matter（DOM） was investigated in this study. Solar light significantly decreased the UV_（254） absorbance and fluorescence（FLU） intensity of reclaimed water.However, its effect on the dissolved organic carbon（DOC） value of reclaimed water was very limited. The decrease in the UV_（254） absorbance intensity and FLU excitation–emission matrix regional integration volume（FLU volume） of reclaimed water during solar light irradiation was fit with pseudo-first order reaction kinetics. The decrease of UV_（254） absorbance was much slower than that of the FLU volume. Ultraviolet light in solar light had a key role in decreasing the UV_（254） absorbance and FLU intensity during solar light irradiation. The light fluence-based removal kinetic constants of the UV_（254） and FLU intensity were independent of light intensity. The peaks of the UV_（254） absorbance and FLU intensity with an apparent molecular weight（AMW） of 100 Da to 2000 Da decreased after solar irradiation, whereas the DOC value of the major peaks did not significantly change.

Promising Ultraviolet Absorbers——Novel Guanine Analogs Having Significantly Improved Ultraviolet Absorption Capacity and Dissipating the Energy of Absorbed Photons by Nonradiative Decay Mechanism

Structural properties of nucleobase underlie their ultrafast excited-state dynamics and low fluorescence quantum yields, which cause effectively nonradiative decay process and render them like sunscreens. Thus, eight guanine analogs[N-2-（2＇-nitrobenzoyl）-guanine, N-2-（3＇-nitrohenzoyl）-guanine, N-2-（4＇-nitrobenzoyl）-guanine, N-2-（2＇-hydroxybenzoyl）-guanine, N-2-（4＇-methoxylbenzoyl）-guanine, N-2-（4＇-chloricbenzoyl）-guanine, N-2-（4＇- me- thylicbenzoyl）-guanine and N-2-（3＇,5＇-dinitrobenzoyl）-guanine] with different substituted benzoyls, except N-2-（4＇-chloricbenzoyl）-guanine, were newly synthesized. In contrast with guanine, they exhibit wider ultraviolet absorbent range, higher molar extinction coefficient and lower fluorescence intensity.

Cloud Point Extraction of Polycyclic Aromatic Hydrocarbons in Aqueous Solution with Silicone Surfactants

Cloud point extraction （CPE） processes with two silicone surfactants, Dow Coming DC-190 and DC-193, were studied as preconcentration and treatment for the water polluted by three trace polycyclic aromatic hydrocarbons （PAHs）： anthracene, phenanthrene and pyrene. For all cases, the volumes of surfactant-rich phase obtained by two silicone surfactants were very small, i.e. a lower water content in the surfactant-rich phase was obtained. For example, less than 3% of the initial solution was obtained in a 1% （by mass） surfactant solution, which was much smaller than that of TX-114 in the same surfactant concentration. And TX-114 is known as a high compact surfactant-rich phase among most nonionic surfactants, thus the comparison showed that an excellent enrichment was ensured in the analysis application by the CPE process with the silicone surfactants, and the lower water content obtained in the surfactant-rich phase is also important in the large scale water treatment. The influences of additives and phase separation methodology on the recovery of PAHs were discussed. Comparing with DC-193, DC-190 has a lower cloud point and a higher recovery （near 100%） of all the three PAHs in same surfactant concentration, which was required for application as a preconcentration process prior to HPLC system. However the DC-190 solution is hard to be phase separated only by heating, whereas DC-193 has a relative higher phase separating speed by heating, but a high cloud point （around 360K） limits its application. Due to the phase separation by heating is the only method of CPE suitable to the large scale water treatment, the mixtures of two silicone surfacrants solutions were investigated in this study. A solution containing 1% of mixed DC-190 and DC-193 （in the ratio of 90 ： 10） removed anthracene, phenanthrene and pyrene near 100% with a relative low cloud point and quick phase separating speed.

An Influencing Factor - Water-Filter Ratio on Heat Resistance of Condensate Polishing Filter Material in Water

In air-cooled condenser, high temperature condensing water m summer which approaching and exceed 60＊ C, which may result in filter materials degradation and release impurities. This paper discusses an influencing factor, water-filter ratio （soaking solution and filter quality ratio）, on leachable dissolution rate and filter material degradation rate m high temperature water. The UV absorption at 254nm （A254） and the exchange capacity ware measured after heat test as composite indicators. In addition, the Wends of A254 variation with heating time were measured in different water-filter ratio. The stability is probably due to the effect of water-filter ratio. This has been further borne out that, water-filter ratio increases, leachable concentration decreases exponentially and tends to a fLxed value.

Effect of Photostablizers on Surface Color and Mechanical Property of Wood-flour/HDPE Composites after Weathering

The effects of photostabilizers of ultraviolet absorbers （UVA）, hindered amine light stabilizer （HALS） and pigment on surface color change and mechanical properties of weathered wood-flour/ polyethylene （HDPE） composites were investigated. After being added UVA with high UV absorbance, the WPC exhibites better ability to resist color fading and mechanical property loss. High molecular weight HALS is found to be the most effective in controlling long term fading and yellowing changes. Pigments cover the composites for remaining the original color after weathering regardless of less contribution to mechanical property. Addition of photostabilizer and pigment together show great synergism in decreasing color fading and flexural property loss.

Percutaneous Penetration and Dermal Exposure Risk Assessment of UV Absorbents in Sunscreens and Isolation Cosmetics

Ultraviolet absorbents(UVs)make up a group of industrial chemicals that is used in various consumer products and industrial applications.Due to their extensive production and usage,UVs have been detected in multiple environmental matrixes.Recently,UVs have garnered significant attention because of their probable adverse impacts on human health and the environment.This study examines UVs levels in sunscreens and isolation cosmetics and further assesses human exposure to UVs through the application of cosmetics.The total concentrations of nine UVs in 87 sunscreen and isolation cosmetic products ranged from 75.5 to 4.25×10^(4) ng/g.Among them,2-(2-hydroxy-5-methyl-phenyl)benzotriazole(UV-P)and 2-hydroxy-4-(octoxy)benzophenone(UV-531)had the highest concentrations.Use of the EpiSkin model indicated rapid absorption and strong dermal penetration by UV-328 following 36 h of exposure with a cumulative absorption rate of 41.8%±2.82%.Other congeners are expected to be distributed in the dermal tissue and donor fluid.Furthermore,this study explored potential mechanisms implicating skin biochemical barriers in the metabolism and transport of UVs.The potential of UVs to act as substrates and inhibitors of P450 enzymes was assessed,and their metabolites were predicted.Molecular docking simulations demonstrated that UVs can significantly interact and bind with three transport proteins in skin:MDR1,OATP2B1,and OATP3A1.Daily UVs exposure through the skin was assessed,revealing that dermal absorption levels of UV-P in sunscreen sprays(4.66×10^(3) ng/(kg bw day))and sunscreens(6.01×10^(3) ng/(kg bw day))were close to or exceeded the reference dose(RfD)and therefore require more attention.

Genotoxicity removal of reclaimed water during ozonation

Genotoxicity in wastewater and reclaimed water now is gaining increased attention because of genotoxins＇ potential damage to the ecosystem and human health. The effect of ozonation on genotoxicity in reclaimed water was investigated. It was found that ozonation decreased the genotoxicy dramatically in three tertiary treatment plants. In the further batch ozonation experiment in laboratory, secondary effluent sample used exhibited the genotoxicity of （41.1 ± 4.1） μg 4NQO/L. Ozonation with a dose of 10 mg O3/L completely removed the genotoxicity in secondary effluent. However, after ozonation, the dissolved organic carbonvalue of the sample didn＇t change much but the specific ultraviolet absorbance （SUVA） value dropped sharply. With the help of Fourier transform infrared spectroscopy, ozonation was found to change chemical aliphatic carbon and C-O of the dissolved arganic matter, which might be the reason of the significant decreases of SUVA and genotoxicity.