Photoassisted Fenton degradation of polystyrene.

Fenton and photoassisted Fenton degradation of ordinary hydrophobic cross-linked polystyrene microspheres and sulfonated polystyrene beads (DOWEX 50WX8) have been attempted. While the Fenton process was not able to degrade these polystyrene materials, photoassisted Fenton reaction (mediated by broad-band UV irradiation from a 250 W Hg(Xe) light source) was found to be efficient in mineralizing cross-linked sulfonated polystyrene materials. The optimal loadings of the Fe(III) catalyst and the H(2)O(2) oxidant for such a photoassisted Fenton degradation were found to be 42 µmol-Fe(III) and 14.1 mmol-H(2)O(2) per gram of the sulfonated polystyrene material. The initial pH for the degradation was set at pH 2.0. This photoassisted Fenton degradation process was also able to mineralize commonly encountered polystyrene wastes. After a simple sulfonation pretreatment, a mineralization efficiency of >99% (by net polymer weight) was achieved within 250 min. The mechanism of this advanced oxidative degradation process was investigated. Sulfonate groups introduced to the surface of the treated polystyrene polymer chains were capable of rapidly binding the cationic Fe(III) catalyst, probably via a cation-exchange mechanism. Such a sorption of the photoassisted Fenton catalyst was crucial to the heterogeneous degradation process.

Analysis of adsorption characteristics of 2,4-dichlorophenol from aqueous solutions by activated carbon fiber.

In this study experiments were conducted to investigate the adsorption of 2,4-dichlorophenol (2,4-DCP) by activated carbon fiber (ACF) activated by static air. With the results of batch experiments at various temperatures, the adsorption isotherms, kinetics and thermodynamics of this adsorption process were evaluated. Four adsorption isotherm models, Langmuir, Freundlich, Redlich-Peterson and Toth equations, were used to fit the experimental data and the results reveal that the adsorption isotherm models fitted the data in the order of: Langmuir>Redlich-Peterson>Toth>Freundlich isotherms. A pseudo second-order adsorption model was better to describe the adsorption data than the pseudo first-order model and the Bangham model at the temperatures tested. The activation energy was calculated to be 40.90 kJ/mol, while the thermodynamic parameters DeltaH and DeltaS were estimated to be -5.82 kJ/mol and 0.07 kJ/(molK), respectively.

The occurrence and distribution of pharmaceutical compounds in the effluents of a major sewage treatment plant in Northern Taiwan and the receiving coastal waters.

The pharmaceutical residues in waste water from the largest sewage treatment plant (STP) in Northern Taiwan and in seawater around the effluent discharged area were determined. An environmental risk assessment for the marine environment was conducted based on the environment risk quotient (ERQ). The concentrations of the analyzed compounds in STP influent and effluent were generally higher than those found in coastal seawater. Relatively higher values were found at the estuarine mouth and the discharged area, suggesting that the STP effluent is a point source. The removal efficiency and half life of the analyzed compounds were 6.3-46.8% and 3-18 days, respectively. The ERQ value theoretical calculation was generally greater than 1. However, when the measured concentrations replaced the predicated concentrations, the ERQ values were considerably lower than 1. Therefore, our results call for a re-evaluation of the risks posed by pharmaceuticals to coastal marine ecosystems in Northern Taiwan.