Grabeel, Margaret N.2014-03-142014-03-141992-05-05etd-12232009-020452http://hdl.handle.net/10919/46394The concentrations of chlorine dioxide (CI02), chlorine, chlorite (CIO2), and chlorate (CI03) were evaluated following pretreatment of raw water by CI02 at water treatment plants in New Castle, Pennsylvania; Charleston, West Virginia; Skagit, Washington; and Columbus, Georgia. Chlorite and chlorate concentrations were unaffected by any of the water treatment processes and did not vary as a function of time of travel in the distribution system. Chlorine dioxide, which was analyzed on-site at two water treatment plants, reformed in the clear well and in the distribution system following post chlorination. The chlorite-removal capability of powdered activated carbon (PAC) was evaluated in both laboratory- and pilot-scale studies. Chlorite removal by PAC in laboratory studies decreased with increasing pH over a range from pH 5.5 to 7.5 and varied with the type of PAC. Chlorite was reduced to chloride at pHs ranging from 5.5 to 7.5, but CI03- formed at the pH 5.5 through 6.0. The pilot plant study; which was conducted at Newport News, Virginia; evaluated CI02 removal by PAC enmeshed in a floc blanket in a pulsed-bed, solids-contact clarifier. An average of 27 percent of the CI02 was removed when the PAC dose was 10 mg/L PAC and 57 percent when it was 20 mg/L PAC. Chlorate was not removed by PAC, but the concentrations could be reduced if the CIOz generator was properly operated.xi, 166 leavesBTDapplication/pdfenIn CopyrightLD5655.V855 1992.G72Carbon, ActivatedChlorine dioxideDrinking waterThesishttp://scholar.lib.vt.edu/theses/available/etd-12232009-020452/