Title of article
Model reactor for photocatalytic degradation of persistent chemicals in ponds and waste water
Author/Authors
George R. Franke، نويسنده , , C. Franke، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1999
Pages
9
From page
2651
To page
2659
Abstract
A laboratory scale flow-through model reactor for the degradation of persistent chemicals using titanium dioxide (TiO2) as photocatalyst immobilized on glass beads is presented. In the test system with a volume of 18 L contaminated water is pumped to the upper part of the floating reactor and flows over the coated beads which are exposed to UV-radiation. The degradation of two dyes of different persistance was investigated. Primary degradation of methylene blue did not fit a first order kinetic due to coincident adsorption onto the photocatalyst and direct photolysis, resulting in a half-life of 6 h. A filtrate of a green algae suspension accelerated the colour removal. In contrast, reactive red 2 was degraded only by photocatalysis; neither adsorption nor direct photolysis led to a colour removal. The course of primary degradation followed a first order kinetic with a half-life of 18 h and a rate constant of 0.04 h−1. Analysis of the degradation products indicated mineralization by detection of NO2− and NO3−, accompanied by a decrease of pH and an increase of conductivity. A successful adaptation of the model reactor (scale 1:10) to dimensions required for surface waters and waste water treatment plants would be a costefficient and environmentally sustainable application of photocatalysis for the treatment of industrially polluted water and could be of relevance for third world contries, particularly those favoured by high solar radiation.
Keywords
model reactor , photocatalysis , Solar energy , degradation , waste water treatment , titanium dioxide , persistent chemicals
Journal title
Chemosphere
Serial Year
1999
Journal title
Chemosphere
Record number
724473
Link To Document