Physicochemical investigation of mercury sorption on mesoporous thioacetamide/chitosan from wastewater.

Mercury is a toxic environmental element, so it was necessary to prepare a new, highly efficient, cheap sorbent to remove it. A mesoporous thioacetamide/chitosan (MTA/CS) was manufactured via a simplistic strategy; the chitin deacetylation to gain chitosan (CS) and the addition of thioacetamide. The as-prepared MTA/CS was characterized using X-ray diffraction, EDX, SEM, FTIR, and BET surface analysis. According to the findings, the MTA/CS was effectively synthesized. The removal behaviors of Hg2+ onto MTA/CS composite were inspected, which suggested that the MTA/CS composite exhibited great sorption properties for Hg2+ in liquid solutions. The maximal Hg2+ sorption capacity was 195 mg/g. The effects of temperature, Hg2+ concentration, contacting time, and MTA/CS concentration on sorption were analyzed. The 2nd-order model and Langmuir isotherm were suitable for the physicochemical adsorption processes. Thermodynamic analysis showed that the Hg2+ adsorption process onto the MTA/CS composite is exothermic and occurred spontaneously. The desorption condition of Hg2+ from its loaded MTA/CS was also gained. Likewise, the MTA/CS sorbent was undoubtedly regenerated by 0.8 M NaNO3 80 min contacting and 1:50 S:L ratio. The versatility and durability of MTA/CS sorbent were investigated via nine sorption-extraction cycles. The optimum parameters were applied to wastewater. Based on the result, the as-prepared MTA/CS might be a potential sorbent for removing Hg2+ from liquid solutions.

Development of a maleic acid-based material to selectively solid-phase extract basic compounds from environmental samples.

This study presents a novel mixed-mode weak cation-exchange (WCX) material. This material was prepared by means of the functionalization of a mesoporous divinylbenzene (DVB) resin with maleic acid (maleic acid-DVB), which yielded a high carboxylic moiety content resulting in WCX interactions as well as suitable specific surface area for reversed-phase interactions. After the optimization of the solid-phase extraction (SPE) protocol to enhance the selectivity of the sorbent, this material was evaluated as a novel WCX sorbent in the SPE of a group of drugs from environmental water samples. The method is based on SPE followed by liquid chromatography (LC) coupled to high resolution mass spectrometry (HRMS) with an Orbitrap analyzer, and was validated and applied for the determination of basic drugs in river, effluent and influent wastewater samples. Maleic acid-DVB sorbent yielded suitable recovery rates (57% to 89%) and an acceptable matrix effect (<32%) thanks to the effective washing step included when these environmental waters were loaded through the novel resin. The method was applied to different environmental water samples and some basic drugs were suitably quantified in these environmental samples.

Dispersive micro solid phase extraction of busulfan from plasma samples using novel mesoporous sorbent prior to determination by HPLC-MS/MS.

Determination of busulfan concentration in patients undergoing bone marrow transplantation is necessary in order to reduce toxic effects and/or graft rejection due to unadjusted dose exposure. A new extraction method namely dispersive micro solid phase extraction (DMSPE) based on mesoporous sorbent was used for cleaning-up the plasma samples. DMSPE coupling with liquid chromatography with tandem mass spectrometry (LC-MS/MS) was implemented for the determination of busulfan dosage in plasma samples. The linear range was found from 10 to 2000 ng/ml. The precision and accuracy were found better than 15% according to Food and drug Administration (FDA) guideline. This method was successfully used to determine the busulfan in patients administrated busulfan as part of the preparative regimen for bone marrow transplantation.