About: 3-Chlorophenol is a research topic. Over the lifetime, 22 publications have been published within this topic receiving 791 citations. The topic is also known as: 3-Chlorophenol.
TL;DR: In this paper, the photocatalytic degradations of 2-chlorophenol (2CP) and 3-chlorphenol (3CP) in TiO{sub 2} aqueous suspensions at {λ > 340 nm have been studied.
Abstract: The photocatalytic degradations of 2-chlorophenol (2CP) and 3-chlorophenol (3CP) in TiO{sub 2} aqueous suspensions at {lambda} > 340 nm have been studied. They are faster than direct photolysis at {lambda} > 290 nm despite the additional number of photons available in this wavelength region and produce lower maximal concentrations of intermediates. Complete mineralization is achieved eventually; however, it requires a much longer time than dechlorination and dearomatization. Effects of radiant flux, wavelength, initial concentrations, and pH are examined. Para hydroxylation is the main pathway, so that 2CP and 3CP both give rise to chlorohydroquinone (CHQ), whereas formation of catechol (CT) is a very minor pathway in the degradation of 2CP. Further hydroxylation of CHQ and CT forms hydroxyhydroquinone, which rapidly decomposes to carboxylic acids and carbonyl compounds not identified yet.
TL;DR: The results suggest that rice-straw-based carbon may be effectively used as a low-cost substitute for activated carbon for removal of chlorophenols from water.
TL;DR: In this article, a β-cyclodextrin (β-CD) functionalized graphene modified carbon paste electrode (CD/GRs/CPE) was prepared and characterized by atomic force microscopy (AFM), Fourier transform infrared (FT-IR) and electrochemical impedance spectroscopy (EIS).
Abstract: In the present paper, a β-cyclodextrin (β-CD) functionalized graphene modified carbon paste electrode (CD/GRs/CPE) was prepared and characterized by atomic force microscopy (AFM), Fourier transform infrared (FT-IR) and electrochemical impedance spectroscopy (EIS). The electrochemical behaviors of 2-chlorophenol (2-CP) and 3-chlorophenol (3-CP) on different electrodes were investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The results demonstrated that the CD/GRs/CPE exhibited remarkable enhancement effects towards these two chlorophenols, especially for 3-CP. Importantly, their oxidation peaks could be well separated by CVs and DPVs. Under the optimized conditions, the oxidation peak currents displayed a good linear relationship to concentration in the ranges from 0.5 to 40 μM for 2-CP and 0.4 to 77 μM for 3-CP, with detection limits of 0.2 and 0.09 μM, respectively. As a practical application, the proposed sensor was applied to quantitatively determine 2-CP and 3-CP in water samples with satisfying results.
TL;DR: The proposed reactivity scale proved to be effective for comparing the different operating conditions for the same soil, but failed when used to compare the oxidation performances for different soils, since the different adsorptive behavior of the tested soils may have influenced the contaminant removal rate.
TL;DR: A commercial multiwall carbon nanotube and its carboxylated derivate was used after purification to study the competitive adsorption of phenol (P) and m-chlorophenol from 0.1 M aqueous NaCl solutions without external pH control.
Abstract: A commercial multiwall carbon nanotube and its carboxylated derivate (CNTC and COOHC, respectively) was used after purification to study the competitive adsorption of phenol (P) and m-chlorophenol (CP) from 0.1 M aqueous NaCl solutions without external pH control. The adsorption takes place practically exclusively on the external surface of the nanotubes. The uptake of P is suppressed in comparison to its single solute behaviour on both nanotubes, independently of the initial pollutant concentration. The uptake of CP however is more sensitive to the concentration and the surface chemistry of the nanotube. The measured co-adsorption isotherms were compared to the isotherms calculated from the competitive Langmuir model (CLM). Preferential adsorption of CP was observed in about 95% of the relative concentration range. The total adsorption may exceed the corresponding single component sorption capacity.