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1.
Environ Technol ; 35(9-12): 1409-17, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24701939

RESUMO

A comparative study on the treatment of thermomechanical pulping (TMP) pressate was conducted under thermophilic (55 degrees C) and mesophilic (30 degrees C) temperatures to explore in-mill biological treatment, with the intention to operate under heat-efficient conditions. The experimental study involved sequencing batch reactors (SBRs) operated over 114 days. Receiving a total influent chemical oxygen demand (COD) of 3700-4100 mg L(-1), the COD removal efficiencies of 80-90% and 75-85% were achieved for the mesophilic and thermophilic SBRs, respectively, at a hydraulic retention time (HRT) of 12 and 24h. Excellent sludge settleability (sludge volume index < 100 mL g(-1) mixed liquor suspended solids) was obtained at both thermophilic and mesophilic SBRs. A higher level of effluent suspended solids was observed under thermophilic conditions. The results support the feasibility of applying thermophilic biological treatment of TMP pressate. The treated effluent has the potential for subsequent reuse as process water after polishing, thus addressing the long-standing desire to develop water system closure for the pulp and paper mill operation.


Assuntos
Reatores Biológicos , Resíduos Industriais , Gerenciamento de Resíduos , Análise da Demanda Biológica de Oxigênio , Floculação , Temperatura Alta , Papel , Tamanho da Partícula , Águas Residuárias/análise
2.
Beilstein J Org Chem ; 7: 1533-40, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22238529

RESUMO

A facile synthesis of hitherto unreported 3-(2-benzofuroyl)carbazoles 3a-k, 3,6-bis(2-benzofuroyl)carbazoles 5a-k, and naphtho[2,1-b]furoylcarbazoles 3l and 5l is described. The synthesis mainly relies on the ultrasound-assisted Rap-Stoermer reaction of 3-chloroacetyl- (1) or 3,6-dichloroacetyl-9-ethyl-9H-carbazole (4) with various salicylaldehydes 2a-k as well as 2-hydroxy-1-naphthaldehyde (2l) in CH(3)CN with the presence of PEG-400 as catalyst. The procedure offers easy access to benzofuroylcarbazoles in short reaction times and the products are obtained in moderate to good yields.

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