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  • Volume 35, Issue 4

Low-concentrating CPC collectors for photocatalytic water detoxification: comparison with a medium concentrating solar collector

S. Malato, J. Blanco, C. Richter, D. Curcó, J. Giménez
Published February 1997, 35 (4) 157-164;
S. Malato
Centro de Investigaciones Energéticas, Mediambientales y Tecnológicas (CIEMAT), Plataforma Solar de Almeria, Box 22, Crta. Senés s/n, Tabernas, Almeria 04200, Spain
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J. Blanco
Centro de Investigaciones Energéticas, Mediambientales y Tecnológicas (CIEMAT), Plataforma Solar de Almeria, Box 22, Crta. Senés s/n, Tabernas, Almeria 04200, Spain
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C. Richter
Centro de Investigaciones Energéticas, Mediambientales y Tecnológicas (CIEMAT), Plataforma Solar de Almeria, Box 22, Crta. Senés s/n, Tabernas, Almeria 04200, Spain
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D. Curcó
Departamento de Ingeniería Química, Facultad de Química, Universidad de Barcelona, C/ Martí i Franqués 1, Barcelona 08028, Spain
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J. Giménez
Departamento de Ingeniería Química, Facultad de Química, Universidad de Barcelona, C/ Martí i Franqués 1, Barcelona 08028, Spain
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Abstract

The photocatalytic oxidation of 2,4-Dichlorophenol (DCP), using TiO2 suspensions under solar radiation, has been studied at pilot-plant scale at the Plataforma Solar de Almería (PSA). Two different reactor designs were tested: a medium concentrating radiation system called a Parabolic-Trough-Collector Reactor, PTCR, equipped with two motors (azimuth and elevation) to adjust the position of the module perpendicular to the sun, and a low-concentrating radiation system, the Compound-Parabolic-Concentrator Reactor, CPCR, facing south and inclined 37 degrees. Substrates were dissolved in water to required mg L−1 levels in a reservoir tank. In both cases, 0.2 g L−1 of the suspended TiO2 catalyst was used in a 250 L solution of the contaminant, which was recirculated through the photoreactors using a centrifugal pump and an intermediate reservoir tank. The advantages and disadvantages of the two types of photoreactors in DCP oxidation are compared and discussed. The strong potential of photocatalytic peroxydisulphate-assisted degradation in high DCP concentrations was demonstrated in both systems, and chemical actinometry (the decomposition reaction of oxalic acid by radiated uranyl salts) in the CPC reactor is compared with the results obtained in the PTC.

  • Dichlorophenol
  • peroxydisulphate
  • photocatalysis
  • solar collectors
  • solar actinometry
  • titanium dioxide
  • © IWA Publishing 1997

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Water Science and Technology: 2017 (2)
  Volume 35, Issue 4

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Low-concentrating CPC collectors for photocatalytic water detoxification: comparison with a medium concentrating solar collector
S. Malato, J. Blanco, C. Richter, D. Curcó, J. Giménez
Water Science and Technology Feb 1997, 35 (4) 157-164;
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Low-concentrating CPC collectors for photocatalytic water detoxification: comparison with a medium concentrating solar collector
S. Malato, J. Blanco, C. Richter, D. Curcó, J. Giménez
Water Science and Technology Feb 1997, 35 (4) 157-164;

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Keywords

Dichlorophenol
peroxydisulphate
photocatalysis
solar collectors
solar actinometry
titanium dioxide
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