Related Experiment Video
Updated: May 2, 2026

Physical, Chemical and Biological Characterization of Six Biochars Produced for the Remediation of Contaminated Sites
Published on: November 28, 2014
Effect of reductive property of activated carbon on total organic halogen analysis
Yao Li1, Xiangru Zhang, Chii Shang
1Department of Civil and Environmental Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.
Abstract:
Total organic halogen (TOX) is a collective parameter and a toxicity indicator for all the halogenated organic disinfection byproducts (DBPs) in a water sample. TOX can be measured with the adsorption-pyrolysis method based on Standard Method 5320B. This method involves concentration of organic halogens from water by adsorption onto activated carbon (AC) and removal of inorganic halides present on the AC by competitive displacement by nitrate ions. Since AC can also act as a reductant, this work studied whether the reduction of chlorinated DBPs by AC occurs during the TOX measurement, to what extent the reduction affects the measurement of TOX, what type of chlorinated DBPs can be reduced by AC, and whether the method for the TOX measurement can be improved. Initially, chlorinated Suwannee River fulvic acid samples were prepared and pretreated with precipitation/dialysis/ultrafiltration to minimize the chloride levels in the samples. It was found that the fractions of TOX in the precipitated, dialyzed, and ultrafiltered samples that were reduced by AC in 5 min were around 13%, 20% and 24%, respectively. The formation of some N-chloroamino compounds and their reactivity with AC were examined. The results indicate that organic chloramines are one type of DBPs in TOX that could be reduced by AC. It was demonstrated that slight oxidation of AC with ozone basically inhibited its reduction for TOX and meanwhile maintained its adsorption capacity for TOX.
More Related Videos
08:12Characterization, Quantification and Compound-specific Isotopic Analysis of Pyrogenic Carbon Using Benzene Polycarboxylic Acids BPCA
Published on: May 16, 2016
09:46Reducing Willow Wood Fuel Emission by Low Temperature Microwave Assisted Hydrothermal Carbonization
Published on: May 19, 2019
Related Concept Videos
Alkyl Halides
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
ortho–para-Directing Deactivators: Halogens
Reactions at the Benzylic Position: Halogenation
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Radical Halogenation: Thermodynamics