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1.
Water Sci Technol ; 77(3-4): 739-747, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-29431719

RESUMEN

Dieldrin and DDx removal through wastewater treatment, ozonation, and microfiltration was assessed for a water reuse project for groundwater replenishment in Monterey, California, USA. Full-scale sampling was conducted at the wastewater treatment plant, and physical wastewater treatment processes, ozonation, and microfiltration were tested at the bench scale. Removals observed through wastewater treatment, ozonation, and microfiltration were 84%, 44% to 63%, and 97% to 98%, respectively, for dieldrin, and 93%, 36% to 48%, and 92% to 94% for DDx. These were sufficient to meet California Ocean Plan water quality objectives after wastewater treatment alone. Levels in the secondary effluent, ahead of ozonation, microfiltration, reverse osmosis and advanced oxidation in the advanced water purification facility, met drinking water standards. Removal of dieldrin and DDx through wastewater treatment occurred by physical treatment processes; removal through the full-scale wastewater treatment plant, which included biological and physical treatment processes, matched removal through the physical bench-scale wastewater treatment processes. Dieldrin and DDx removal correlated with removal of volatile suspended solids, suggesting that volatile suspended solids could be used as an indicator for pesticide removal through wastewater treatment. Dieldrin and DDx concentrations were highest in the solids contact process, where biomass is accumulated for carbon removal.


Asunto(s)
Diclorodifenil Dicloroetileno/química , Dieldrín/química , Ozono/química , Plaguicidas/química , Eliminación de Residuos Líquidos/métodos , Contaminantes Químicos del Agua/química , Biomasa , Filtración , Aguas Residuales/química , Purificación del Agua/métodos
2.
Proc Natl Acad Sci U S A ; 78(3): 1321-2, 1981 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-16592988

RESUMEN

Through the use of (Cp(2)TiH)(x) or (Cp(2)Ti)(1-2), in which Cp is C(5)H(5) (cyclopentadienyl ligand), it is possible to effect not only the previously known direct reduction of aldehydes and esters to alkanes but also the one-step conversion to alkane of amides derived from selected primary aromatic amines.

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