Regionalized chemical footprint method to identify aquatic ecotoxicity hotspots of hard disk drive rare-earth magnets.

The chemical footprint (ChF), which combines life cycle assessment (LCA) and quantitative risk assessment principles, shows promise for exploring localized toxicity impacts of manufacturing processes, which is not achievable with LCA alone. An updated ChF method was applied to the global annual production of a hard disk drive (HDD) rare-earth element (REE) magnet assembly, assuming a supply chain in East and Southeast Asia. Existing REE magnet assembly LCA inventories were combined with supplier manufacturing locations to create a cradle-to-gate spatial unit process inventory.

Comprehensive elemental analysis of consumer electronic devices: Rare earth, precious, and critical elements.

Over the past few decades, electronic devices of all kinds, and especially consumer electronics, have evolved in function and composition, in parallel to increasing manufacture and use. There is great potential for recovering economic value and reducing environmental impact by recycling devices and extracting various elements. However, there are few studies that comprehensively identify the elemental content of electronic devices or electronic waste.

Rational interface design of epoxy-organoclay nanocomposites: role of structure-property relationship for silane modifiers.

Montmorillonite was modified by three silane surfactants with different functionalities to investigate the role of surfactant structure on the properties of a final epoxy-organoclay nanocomposite. N-aminopropyldimethylethoxysilane (APDMES), an aminated monofunctional silane, was chosen as a promising surfactant for several reasons: (1) it will bond to silica in montmorillonite, (2) it will bond to epoxide groups, and (3) to overcome difficulties found with trifunctional aminosilane bonding clay layers together and preventing exfoliation. A trifunctional and non-aminated version of APDMES, 3-aminopropyltriethoxysilane (APTES) and n-propyldimethylmethoxysilane (PDMMS), respectively, was also studied to provide comparison to this rationally chosen surfactant.

Bioaccumulation and biotransformation of decabromodiphenyl ether and effects on daily growth in juvenile lake whitefish (Coregonus clupeaformis).

Decabromodiphenyl ether (BDE 209) is the main congener in the commonly used commercial flame retardant mixture, "deca-BDE". There is evidence showing that fish can debrominate BDE 209 into potentially more toxic congeners. The objective of this study was to evaluate BDE 209 uptake and its potential effects on juvenile lake whitefish (Coregonus clupeaformis).

Bioaccumulation and biomagnification of polybrominated diphenyl ethers in a food web of Lake Michigan.

Polybrominated diphenyl ethers are hydrophobic chemicals and can biomagnify in food chains. Little is known about the biomagnification of PBDEs in the Lake Michigan food web. Plankton, Diporeia, lake whitefish, lake trout, and Chinook salmon were collected from Lake Michigan in 2006 between April and August.

Hydrolysis and H2O2-assisted UV photolysis of 3-chloro-1,2-propanediol.

3-Chloro-1,2-propanediol (3-MCPD) is a chlorinated alcohol that is often formed as a by-product in the manufacturing of food products. In addition, 3-MCPD may be a disinfection by-product from wastewater treatment by chlorine and may be present in drinking waters from purification plants using epichlorohydrin-linked cationic polymer resins as flocculants. Due to concerns about the toxicity of 3-MCPD and its potential presence in water samples, the removal of 3-MCPD from water should be addressed and examined.

Hydrogen peroxide-assisted UV photodegradation of Lindane.

Aqueous solutions of gamma-hexachlorocyclohexane (Lindane) were photolyzed (lambda=254 nm) under a variety of solution conditions. The initial concentrations of hydrogen peroxide (H(2)O(2)) and Lindane varied from 0 to 20 mM and 0.21 to 0.

Birnessite mediated debromination of decabromodiphenyl ether.

Decabromodiphenyl ether (BDE-209) is a major component of a commercial flame retardant formulation; however, there is limited information on the fate of BDE-209 in the environment, including metal oxide mediated degradation. Laboratory experiments were conducted to investigate the birnessite (delta-MnO(2))-promoted debromination of BDE-209 in tetrahydrofuran (THF)-water systems as well as catechol solutions. Up to 100% (0.

Photodegradation of decabromodiphenyl ether adsorbed onto clay minerals, metal oxides, and sediment.

The photodebromination of decabromodiphenyl ether (BDE-209) adsorbed onto six different solid matrixes was investigated in sunlight and by irradiation with 350 +/- 50 nm lamps (four lamps at 24 W each). After 14 days of lamp irradiation, BDE-209 degraded with a half-life of 36 and 44 days, respectively, on montmorillonite or kaolinite, with much slower degradation occurring when sorbed on organic carbon-rich natural sediment (t1/2 = 150 days). In late summer and fall sunlight (40.

Enhanced Fenton's destruction of non-aqueous phase perchloroethylene in soil systems.

The Fenton's system is applied to the destruction of perchloroethylene (PCE) present as a dense non-aqueous phase liquid (DNAPL) in soil slurry systems; the initial concentration of PCE was 45 times higher than its aqueous solubility. Studies were conducted in two matrices: Ottawa sand and soil from Warsaw, IN. In Ottawa sand, a 60-62% decrease in PCE concentration was observed, and Cl(-) recovery was 47-58%, whereas in Warsaw soil, a 44-49% decrease in PCE concentration and a Cl(-) recovery of 40-42% were observed after the addition of 600 mM H(2)O(2) and 10 mM dissolved iron.

Enhanced chemical oxidation of aromatic hydrocarbons in soil systems.

Fenton's destruction of benzene, toluene, ethylbenzene, and xylene (BTEX) was investigated in soil slurry batch reactors. The purpose of the investigation was to quantify the enhancement of oxidation rates and efficiency by varying process conditions such as iron catalyst (Fe(II) or Fe(III); 2, 5, and 10mM), hydrogen peroxide (H2O2; 30, 150, 300 mM), and metal chelating agents (l-ascorbic acid, gallic acid, or N-(2-hydroxyethyl)iminodiacetic acid). Rapid contaminant mass destruction (97% after 3h) occurred in the presence of 300 mM H2O2 and 10 mM Fe(III).

Cosolvent-enhanced chemical oxidation of perchloroethylene by potassium permanganate.

A laboratory study was conducted to examine cosolvent-enhanced in-situ chemical oxidation (ISCO) of perchloroethylene (PCE) using potassium permanganate (KMnO4). The conceptual basis for this new technique is to enhance permanganate oxidation of dense non-aqueous phase liquids (DNAPLs) with the addition of a cosolvent, thereby increasing DNAPL solubility while avoiding mobilization. Among 17 cosolvent candidates screened, tertiary butyl alcohol (TBA) and acetone were the most stable in the presence of KMnO4, both of which increased PCE aqueous solubility significantly, and therefore are suitable to be used as cosolvent in this study.

Solar photodecomposition of decabromodiphenyl ether: products and quantum yield.

Decabromodiphenyl ether (BDE209) is a widely used flame retardant, yet information regarding its environmental transformation rates and pathways are largely unknown. Because photochemical transformation is often suggested as a potentially important fate process for BDE209, the reaction rate and products of the solar degradation under favorable solvent conditions were determined in this study. Decabromodiphenyl ether (BDE209), dissolved in hexane, reacts in minutes via direct solar irradiation, at midlatitude (40 degrees 29' N, 86 degrees 59.

Enhanced sonochemical decomposition of 1,4-dioxane by ferrous iron.

The enhanced ultrasonic decomposition of 1,4-dioxane by the addition of ferrous iron (Fe(II)) was investigated at 205, 358, 618, and 1071 kHz. The total organic carbon (TOC) remaining was also determined at each frequency. Addition of Fe(II) improved the 1,4-dioxane decomposition rate and mineralization efficiency at all frequencies studied.

Heterogeneous photochemical reactions of decabromodiphenyl ether.

Brominated diphenyl ethers are a major class of brominated flame retardants, with production of decabromodiphenyl ether (DBDPE) contributing significantly to this total. Although little is known about the mechanisms and rates of DBDPE decay in the natural environment, photochemical transformation is often suggested as a potentially important fate process. In this study, photochemical reactions of DBDPE precipitated onto hydrated surfaces (quartz glass, silica particles, and humic acid-coated silica particles) were measured.

The impact of particulates on the aqueous sonication of bromobenzene.

Sonodegradation of bromobenzene, bromophenolate ion, and 2,4,5-trichlorobiphenyl was studied in the presence of various types of solid particles suspended in water. Three particle diameters (10 nm, 15 microm, and 35 microm) and two particle types (silica particles and organic resin) were investigated over a range of particle concentrations (0.05-10 g l(-1)).