Novel decomposition of polycarbonate and effect for marine ecosystem.

Analysis of pollution of the ocean plastics is presently being extensively carried out but special attention should be direct to matters. It is widely believed that plastic dose not decompose in the ocean. Certain contaminants, bisphenol-A (BPA) that serves the material for polycarbonate (PC) and epoxy resin (EPX) both of which may possibly be elute or degrade from commercial products, have often been detected in rivers, lakes and oceans.

Aquatic toxicity and fate of styrene oligomers in the environment.

Styrene oligomers (SOs) are ubiquitous contaminants that appear in the environment, sometimes to significant extent (see section 3.1). Despite the ongoing international debate on the human health risks posed by SOs, to the best of my knowledge, there are no studies on the aquatic toxicity and environmental fates (biodegradation and atmospheric degradation) of SOs in the environment.

Sandy beaches as hotspots of bisphenol A.

Bisphenol A (BPA) poses a serious environmental threat and health concern. This study presents the global monitoring of BPA on oceanic sandy beaches. According to monitoring results, many beach sands contain a harmful concentrations of BPA.

Physicochemical properties of styrene oligomers in the environment.

Currently, styrene oligomers (SOs) are persistent contaminants that are present in the environment globally. SOs are artificial substances originating from styrene-based polymer materials, mainly including PS plastic, resin, and rubber. However, the behavior of SOs in the environment is not well-understood yet due to the scarcity of experimental data.

Evidence of transport of styrene oligomers originated from polystyrene plastic to oceans by runoff.

This study demonstrates for the first time that styrene oligomers (SOs), which are indicators of polystyrene (PS) plastic contamination in the environment, are transported from land to the ocean. Samples of sand and seawater were taken from the coastline of the Tokyo Bay over the past four years, and all samples of both sand and seawater were found to contain SOs such as styrene monomer (SM), styrene dimers (SD), and styrene trimers (ST), with the concentration distributions of these being in the order of ST > SD > SM. The concentrations of these SOs are linearly proportional to monthly precipitation.

Qualitative assessment to determine internal and external factors influencing the origin of styrene oligomers pollution by polystyrene plastic in coastal marine environments.

The objective of this study is to investigate the qualitative contribution of internal and external factors of the area contaminated by polystyrene (PS) in coastal marine environments. This study is based on the extensive results of monitoring the styrene oligomers (SOs) present in sand and seawater samples along various coastlines of the Pacific Ocean. Here, anthropogenic SOs is derived from PS during manufacture and use, and can provide clues about the origin of SOs by PS pollution.

Monitoring of styrene oligomers as indicators of polystyrene plastic pollution in the North-West Pacific Ocean.

Styrene oligomers (SOs) as global contaminants are an environmental concern. However, little is known on the distribution of SOs in the ocean. Here, we show the distribution of anthropogenic SOs generated from discarded polystyrene (PS) plastic monitored from the coastal ocean surface waters (horizontal distribution) and deep seawaters (vertical distribution) in the North-West Pacific Ocean.

Global styrene oligomers monitoring as new chemical contamination from polystyrene plastic marine pollution.

Polystyrene (PS) plastic marine pollution is an environmental concern. However, a reliable and objective assessment of the scope of this problem, which can lead to persistent organic contaminants, has yet to be performed. Here, we show that anthropogenic styrene oligomers (SOs), a possible indicator of PS pollution in the ocean, are found globally at concentrations that are higher than those expected based on the stability of PS.

Biodegradation of perfluorooctanesulfonate (PFOS) as an emerging contaminant.

Perfluorooctanesulfonate (PFOS) is a compound of global concern because of its persistence and bioaccumulation in the environment. Nevertheless, little is known of the potential for PFOS biodegradation, even though the importance of characterizing the function and activity of microbial populations detected in the environment has been discussed. This study focused on the biodegradation of PFOS by a specific microorganism.

Regional distribution of styrene analogues generated from polystyrene degradation along the coastlines of the North-East Pacific Ocean and Hawaii.

Beach sand and seawater taken from the coastlines of the North-East Pacific Ocean and Hawaii State were investigated to determine the causes of global chemical contamination from polystyrene (PS). All samples were found to contain styrene monomer (SM), styrene dimers (SD), and styrene trimers (ST) with a concentration distribution of styrene analogues in the order of ST > SD > SM. The contamination by styrene analogues along the West Coast proved more severe than in Alaska and other regions.

New analytical method for the determination of styrene oligomers formed from polystyrene decomposition and its application at the coastlines of the North-West Pacific ocean.

The pollution caused by plastic debris is an environmental problem with increasing concern in the oceans. Among the plastic polymers, polystyrene (PS) is one of the most problematic plastics due to the direct public health risk associated with their dispersion, as well as the numerous adverse environmental impacts which arise both directly from the plastics and from their degradation products. Little is known about their potential distribution characteristics throughout the oceans.

The formation of reactive species having hydroxyl radical-like reactivity from UV photolysis of N-nitrosodimethylamine (NDMA): kinetics and mechanism.

This study focuses on the detailed mechanism by which N-nitrosodimethylamine (NDMA) is photolyzed to form oxidized products, i.e., NO(2)(-) and NO(3)(-), and reveals a key reactive species produced during the photolysis of NDMA.

Pentachlorophenol decomposition by electron beam process enhanced in the presence of Fe(III)-EDTA.

This study focuses on the enhanced decomposition of pentachlorophenol (PCP) in an electron beam (E-beam) process. To attain this objective, we investigated a synergistic effect of ferric-ethylenediamineacetate (Fe(III)-EDTA) and H(2)O(2) as additives to produce additional hydroxyl radical (*OH) at low dose. In this process, aqueous electron and hydrogen atom rapidly react with O(2) molecules, thereby forming hydroperoxyl/superoxide anion radical (HO2*/O(2)(-)), which reduces the Fe(III)-EDTA into Fe(II)-EDTA.

A kinetic method for HO2*/O2*- determination in advanced oxidation processes.

A new kinetic method is developed for the determination of hydroperoxyl radical (HO(2)(*))/superoxide radical (O(2)(*)(-)) in aqueous solution, and the calibration using a kinetic half-life technique is also established for determining the concentration of HO(2)(*)/O(2)(*)(-) as produced in the UV/H(2)O(2) process. This new method is based on the reduction of Fe(3+)-EDTA into Fe(2+)-EDTA by HO(2)(*)/O(2)(*)(-) and the well-known Fenton-like reaction of H(2)O(2) and Fe(2+)-EDTA to yield the hydroxyl radicals (OH(*)). Benzoic acid scavenges the OH radicals to produce hydroxybenzoic acids, which are analyzed by fluorescence detection (lambda(ex) = 320 nm; lambda(em) = 400 nm).