Individual and simultaneous degradation of brominated high impact polystyrene and brominated acrylonitrile-butadiene-styrene and removal of heteroelements (Br,N, and O) from degradation oil by multiphase catalytic systems

Brominated high-impact polystyrene (HIPS-Br), which contained decabromodiphenyl ether flame retardant, and brominated acrylonitrile butadiene styrene (ABS-Br), which contained bromine-containing epoxy-type flame retardant, were degraded at 450°C individually and in a 1/1 mixture by a thermal and catalytic procedure using folded sheet mesoporous (FSM) and ZSM-5 zeolite in liquid phase contact mode. The two polymers produced similar degradation oils but at a higher yield for HIPS-Br. However, the composition and distribution of Br-, N-, and O-containing compounds depended on the type of flame retardant in HIPS-Br and ABS-Br. Multiphase catalytic systems consisting of FSM in liquid phase contact mode and various CaH-, FeO-, CoMo-, and NiMo-based catalysts, or combinations of these catalysts, in vapor phase contact mode were used to decrease the amount of heteroatoms (Br, N, and O) in the degradation oils. Each system gave particular results in terms of mass balance and concentrations of heteroatoms. A FSM (liquid phase contact)/CaHC (vapor phase contact) combination was the best catalytic system to remove Br-, N-, and O-containing compounds from degradation oils.     

Removal of trace arsenic（V） and phosphate from water by a highly selective ligand exchange adsorbent

The ligand exchange adsorbent could be used to remove the toxic arsenic(V) and phosphate efficiently from water even in the presence of foreign anions and possible to apply in chemical industry.     

Characteristic of organic aerosol in a remote area of Okinawa Island

A continuous investigation of aerosol pollutants in Cape Hedo, Japan was conducted from October 2005 to August 2006 by Aerodyne aerosol mass spectrometer (AMS). This article focused on the analysis of long-range transport of organic aerosol from continental origin to the remote island. Based on the transport distance and air mass origin, four main air mass origins were considered, including North China, South China, Japan and Korea. Although the mass concentration and air mass origin were quite different during study period, the mass spectrum and size distribution of organic matter and oxidized organics were similar, which showed uni-modal distribution with modal diameter of around 500 nm. The loss rate of organics was (5.15 ± 0.55) × 10-⁶ s-¹ obtained by plotting the concentration against the transport time. Conversion rate of SO₂ to sulfate and oxidation rate of organics were (1.07 ± 0.15) × 10-⁵ and (1.09 ± 0.52) × 10-⁶s-¹, respectively.     

Organophosphorus flame retardants in house dust from the Philippines: occurrence and assessment of human exposure

The use of organophosphorus flame retardants (PFRs) as flame retardants and plasticizers has increased due to the ban on common polybrominated diphenyl ether mixtures. However, only limited information on PFR contamination is available so far from Southeast Asia. In the present study, residual levels of PFRs in house dust and exposure through dust ingestion were investigated in the Philippines. House dust samples (n?=?37) were collected from Malate (residential area) and Payatas (municipal dumping area) in the Philippines and analyzed using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry. Among the targeted seven PFRs, triphenyl phosphate (TPP) was the predominant compound. Median levels of ΣPFRs in Malate (530 ng/g) were two times higher (p?<?0.05) than in Payatas (240 ng/g). The estimated daily intake of PFRs in the Philippines (of areas studied) via house dust ingestion was below the guideline values. House dust may be an important contributor in the overall exposure of humans to TPP even when considering dietary sources. To our knowledge, this is a first report on PFR contamination in house dust from developing country. PFRs were ubiquitously detected in the home environments in the Philippines. Although estimated exposure levels through dust ingestion were below the guideline, it was suggested that toddlers are at higher risk. Therefore, further investigations to understand the behavior of PFRs in house and other microenvironments and overall exposure pathways for the country’s populace to PFRs are necessary.     

Evaluating of arsenic(V) removal from water by weak-base anion exchange adsorbents

Arsenic contamination of groundwater has been called the largest mass poisoning calamity in human history and creates severe health problems. The effective adsorbents are imperative in response to the widespread removal of toxic arsenic exposure through drinking water. Evaluation of arsenic(V) removal from water by weak-base anion exchange adsorbents was studied in this paper, aiming at the determination of the effects of pH, competing anions, and feed flow rates to improvement on remediation. Two types of weak-base adsorbents were used to evaluate arsenic(V) removal efficiency both in batch and column approaches. Anion selectivity was determined by both adsorbents in batch method as equilibrium As(V) adsorption capacities. Column studies were performed in fixed-bed experiments using both adsorbent packed columns, and kinetic performance was dependent on the feed flow rate and competing anions. The weak-base adsorbents clarified that these are selective to arsenic(V) over competition of chloride, nitrate, and sulfate anions. The solution pH played an important role in arsenic(V) removal, and a higher pH can cause lower adsorption capacities. A low concentration level of arsenic(V) was also removed by these adsorbents even at a high flow rate of 250–350 h^?1. Adsorbed arsenic(V) was quantitatively eluted with 1 M HCl acid and regenerated into hydrochloride form simultaneously for the next adsorption operation after rinsing with water. The weak-base anion exchange adsorbents are to be an effective means to remove arsenic(V) from drinking water. The fast adsorption rate and the excellent adsorption capacity in the neutral pH range will render this removal technique attractive in practical use in chemical industry.     

Concentrations of various elements and inorganic ions in rice straw and ash

Various elements and inorganic ions in rice straw and ash samples were analyzed by using inductively coupled plasma atomic emission spectrometry (ICP‐AES) and ion chromatography (IC). Five major elements: Mg, Mn, Al, Ca, and Fe and eight minor and trace elements: Cr, Cu, Ti, Zn, La, Sr, Ba, and Hg were detected in these samples, at more than ppm‐level. In ash samples the trace elements such as Y, As, V, Se, and Sc were also identified. The concentrations of SO₄, PO₄, Cl, Na, and K ions in these samples were higher than those of other ions measured. These elements and inorganic ion concentrations were approximately one order of magnitude higher in the ash than in the straw samples. Gas chromatography/mass spectrometry (GC/MS) and library search showed the presence of fatty‐, carboxylic‐ and nicotinic acids, and their derivatives in small quantities in the straw samples.     

Interspecific comparisons of growth and diet among late larvae of three co-occurring clupeoid species in the Kii Channel,Japan

Growth and diet were compared among larvae of Japanese anchovy Engraulis japonicus, Japanese sardine Sardinops melanostictus and Pacific round herring Etrumeus teres. Compositions of prey items of the three species in the same month showed greater similarity than for the same species in different months. Prey size as well as prey taxa of the three species overlapped considerably with one another. Therefore, interspecific prey competition is likely in the case of limited food availability. The most abundant species tended to change from anchovy to round herring in early winter, from round herring to sardine in late winter and from sardine to anchovy in early spring, indicating a temporal segregation in use of the nursery grounds. Similar seasonal changes in growth rates were observed for the three species. Although interspecific prey competition is likely, the temporal segregation and similar temporal changes in growth rates could favor their coexistence.     

Imputing Unknown Market Values: A Different Perspective on the Disparity Between WTP and WTA

In the process of economic development, governments often expropriate private property and compensate the owners accordingly. Using the application of environmental regulation, this paper suggests a method to impute the price of an expropriated good when the price is not available, due to the lack of markets.