Data for persulfate activation by UV light to degrade theophylline in a water effluent.

The aim of this study was to degrade theophylline (TP) drug in a pharmaceutical effluent solution utilizing persulfate (PS). A simulated and a real effluent solution were used, with different conditions tested to optimize the degradation process. HPLC analyses and a modified-HPLC method were used to track concentrations of TP and PS respectively in the treatment process.

Chemically and thermally activated persulfate for theophylline degradation and application to pharmaceutical factory effluent.

Degradation of PPCPs by AOPs has gained major interest in the past decade. In this work, theophylline (TP) oxidation was studied in thermally (TAP) and chemically (CAP) activated persulfate systems, separately and in combination (TCAP). For [TP] = 10 mg L, (i) TAP resulted in 60% TP degradation at [PS] = 5 mM and = 60 °C after 60 min of reaction and (ii) CAP showed slight degradation at room temperature; however, (iii) TCAP resulted in complete TP degradation for [PS] = [Fe] = 2 mM at = 60 °C following a pseudo-first order reaction rate with calculated = 5.

A rapid and economical method for the quantification of hydrogen peroxide (HO) using a modified HPLC apparatus.

HO is one of the most commonly used oxidants for the degradation of recalcitrant organic contaminants in advanced oxidation processes (AOPs). However, most research aiming to optimize AOPs is missing the monitoring of the remaining HO, an important parameter to assess the efficiency of the process. In this work, a novel method for [HO] quantification was developed using simple modifications of an HPLC-DAD setup that is available in most analytical chemistry laboratories.

Rapid quantification of persulfate in aqueous systems using a modified HPLC unit.

Existing analytical techniques used for the quantification of persulfate (PS) in water mostly rely on polarography, reductometry or spectrophotometry. Although acceptable to a certain extent, these methods did not satisfy environmental chemists seeking rapid, reproducible and accurate quantification of PS upon the application of ISCO and AOPs technologies. Accordingly, a novel flow injection/spectroscopy analytical technique is developed via the use of an HPLC coupled to bypass capillary columns and a DAD detector.

The fate of selected pharmaceuticals in solar stills: Transfer, thermal degradation or photolysis?

The increase in demand for, and disposal of, pharmaceuticals, positively correlated with the growing human population, has led to the emergence of contaminants with high environmental and health impacts. Several developing countries that endure problems related to water sufficiency and/or quality resort to the use solar stills as an affordable water treatment method. This research is aimed at investigating the fate of five chemically distinct pharmaceuticals that might pervade solar stills; ibuprofen (IBU), diclofenac (DCF), carbamazepine (CBZ), ampicillin (AMP) and naproxen (NPX).

Aqueous removal of diclofenac by plated elemental iron: bimetallic systems.

The aqueous removal of diclofenac (DF) by micrometric iron particles (Fe(0)) and amended Fe(0) (Me(0)(Fe(0))) under oxic and anoxic conditions was investigated. Bimetallic systems were obtained by plating the surface of Fe with Co, Cu, Ir, Ni, Pd and Sn. Experimental results confirmed the superiority of (Me(0)(Fe(0))) for DF removal except for IrFe (oxic) and SnFe (anoxic).

Investigating the mechanism of clofibric acid removal in Fe(0)/H2O systems.

Since the introduction of iron wall technology, the inherent relationship between contaminant removal and iron corrosion has been mostly attributed to electron transfer from the metal body (direct reduction). This thermodynamically founded premise has failed to explain several experimental facts. Recently, a new concept considering adsorption and co-precipitation as fundamental contaminant removal mechanisms was introduced.

Antibiotic removal from water: elimination of amoxicillin and ampicillin by microscale and nanoscale iron particles.

Zerovalent iron powder (ZVI or Fe(0)) and nanoparticulate ZVI (nZVI or nFe(0)) are proposed as cost-effective materials for the removal of aqueous antibiotics. Results showed complete removal of Amoxicillin (AMX) and Ampicillin (AMP) upon contact with Fe(0) and nFe(0). Antibiotics removal was attributed to three different mechanisms: (i) a rapid rupture of the beta-lactam ring (reduction), (ii) an adsorption of AMX and AMP onto iron corrosion products and (iii) sequestration of AMX and AMP in the matrix of precipitating iron hydroxides (co-precipitation with iron corrosion products).

Use of FTIR spectroscopy coupled with ATR for the determination of atmospheric compounds.

Attenuated total reflection Fourier transformed infrared spectroscopy (ATR-FTIR) can be successfully used for the quantitative determination of small amounts of pollutants like the organic fraction of aerosols. The relation between sample concentration and reflectance is described by the Kubelka-Munk equation and was found to be linearly proportional to the absorption band of some functional group. Several parameters like the matter of solid matrix, the cleaning of the sampling support, the treatment of reflectance spectra and the base line correction considerably influenced the reflectance spectra and facilitated data interpretations.

Reductive destruction and decontamination of aqueous solutions of chlorinated antimicrobial agent using bimetallic systems.

Palladium, ruthenium and silver were investigated as catalysts for the dechlorination of dichlorophen (DCP, 2,2'-methylenebis(4-chlorophenol)), an antimicrobial and anthelmintic agent largely used as algicide, fungicide and bactericide. Experiments were undertaken under oxic and anoxic conditions for experimental durations up to 180 min (3h). The anoxic conditions were achieved by purging the solutions with nitrogen gas.

Catalytic degradation of chlorothalonil in water using bimetallic iron-based systems.

Modified zero valent iron (MZVI) was used to study the transformation of a chlorothalonil (CLT) solution and the variation of the observed degradation rate of the reduction reactions. This was carried out when transition metals e.g.

Rapid removal of flutriafol in water by zero-valent iron powder.

A study of the effect of zero-valent iron (ZVI) powder is carried out for the first time on the degradation of flutriafol ((RS)-2,4'-difluoro-alpha-(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl alcohol, C(16)H(13)F(2)N(3)O), a bifluorinated soil and water persistent triazole pesticide using a laboratory scale device consisting of a 20 ml pyrex serum vials fixed to a Vortex agitator. Different amounts of ZVI powder (10-50 g l(-1)) at pH 6.6 and room temperature were investigated.