The kinetics of heat-facilitated persulfate oxidation of p-chloroaniline（PCA） in aqueous solutions was measured at five different temperature conditions and at four different oxidant concentrations.The PCA degradati...The kinetics of heat-facilitated persulfate oxidation of p-chloroaniline（PCA） in aqueous solutions was measured at five different temperature conditions and at four different oxidant concentrations.The PCA degradation was found to follow a pseudo-first-order decay model when the persulfate was excessive.The pseudo-first-order rate constants of PCA degradation by persulfate（50 mmol/ L） at pH 7.0 are 0.12×10^-4,0.28×10^-4,0.43×10^-4,0.83×10^-4,1.32×10^-4 s^-1 at 10,20,30,40 and 50℃,respectively. Under the above reaction conditions,the reaction has activation energy of 49.97 kJ/mol.The observed rate was found to be function of temperature and oxidant concentration.Raising temperature and increasing persulfate concentration can significantly accelerate the PCA degradation.展开更多
Adsorption of Cr(Ⅵ) and p-chloroaniline on three typical soil colloids and pH influence were studied using batch equilibrium method. Both of Cr(Ⅵ) and p-chloroaniline adsorption on the colloids could be well describ...Adsorption of Cr(Ⅵ) and p-chloroaniline on three typical soil colloids and pH influence were studied using batch equilibrium method. Both of Cr(Ⅵ) and p-chloroaniline adsorption on the colloids could be well described by general adsorption simulation equations. The adsorption processes changed with media pH. When Cr(Ⅵ) and p-chloroaniline coexisted on soil colloids, their interactions could be observed in a certain pH range to be accompanied with Cr(Ⅵ) reduction, which clearly suggested that a surface catalytic reaction occurred in this system. Soil colloid acted as an efficient catalyst for the interaction of Cr(Ⅵ) and p-chloroaniline. The pH values at which no interaction was observed were 4.0, 4.5 and 5.0 for the colloids of indigotic black soil, yellow-brown soil and latosol, respectively. Capillary electrophoresis used to analyze p-chloroaniline provided a high separation efficiency and short separation time, and needed no more extensive pretreatment of samples.展开更多
基金supported financially by the Foundation of Science and Technology Planning Project of Guangdong Province(No2007A020100001-13)the Key Laboratory of Environmental Protection and Eco-Remediation of Guangdong Higher Education Institutions(China)
文摘The kinetics of heat-facilitated persulfate oxidation of p-chloroaniline（PCA） in aqueous solutions was measured at five different temperature conditions and at four different oxidant concentrations.The PCA degradation was found to follow a pseudo-first-order decay model when the persulfate was excessive.The pseudo-first-order rate constants of PCA degradation by persulfate（50 mmol/ L） at pH 7.0 are 0.12×10^-4,0.28×10^-4,0.43×10^-4,0.83×10^-4,1.32×10^-4 s^-1 at 10,20,30,40 and 50℃,respectively. Under the above reaction conditions,the reaction has activation energy of 49.97 kJ/mol.The observed rate was found to be function of temperature and oxidant concentration.Raising temperature and increasing persulfate concentration can significantly accelerate the PCA degradation.
文摘Adsorption of Cr(Ⅵ) and p-chloroaniline on three typical soil colloids and pH influence were studied using batch equilibrium method. Both of Cr(Ⅵ) and p-chloroaniline adsorption on the colloids could be well described by general adsorption simulation equations. The adsorption processes changed with media pH. When Cr(Ⅵ) and p-chloroaniline coexisted on soil colloids, their interactions could be observed in a certain pH range to be accompanied with Cr(Ⅵ) reduction, which clearly suggested that a surface catalytic reaction occurred in this system. Soil colloid acted as an efficient catalyst for the interaction of Cr(Ⅵ) and p-chloroaniline. The pH values at which no interaction was observed were 4.0, 4.5 and 5.0 for the colloids of indigotic black soil, yellow-brown soil and latosol, respectively. Capillary electrophoresis used to analyze p-chloroaniline provided a high separation efficiency and short separation time, and needed no more extensive pretreatment of samples.
