Determination of Glyphosate and AMPA in Food Samples Using Membrane Extraction Technique for Analytes Preconcentration

The method for determining glyphosate (NPG) and its metabolite AMPA (aminomethyl phosphonic acid) in solid food samples using UAE-SLM-HPLC–PDA technique was developed. Firstly, ultrasonic-assisted solvent extraction (UAE) and protein precipitation step were used for the analyte isolation. Then, the supernatant was evaporated to dryness and redissolved in distilled water (100 mL). The obtained solution was alkalized to pH 11 (with 1 M NaOH) and used directly as donor phase in SLM (supported liquid membrane) extraction. The SLM extraction was performed using 2 M NaCl (5 mL) as an acceptor phase. The flow rate of both phases (donor and acceptor) was set at 0.2 mL/min. The membrane extraction took 24 h but did not require any additional workload. Finally, the SLM extracts were analyzed using the HPLC technique with photo-diode array detector (PDA) and an application of pre-column derivatization with p-toluenesulfonyl chloride. Glyphosate residues were determined in food samples of walnuts, soybeans, barley and lentil samples. The LOD values obtained for the studied food were 0.002 μg g−1 and 0.021 μg g−1 for NPG and AMPA, respectively. Recoveries values ranged from 32% to 69% for NPG, 29% to 56% for AMPA and depended on the type of sample matrix. In the case of buckwheat and rice flour samples, the content of NPG and AMPA was below the detection level of a used analytical method.

Separation of Boron from Geothermal Waters with Membrane System

This study presents the separation and recovery of boron from geothermal waters with a polymeric membrane system and suggests a transport mechanism. The optimum relative parameters of the transport were examined. The recovery value of boron was 60.46% by using polymeric membrane system from prepared aquatic solution to the acceptor phase. The membrane’s capacity and selectivity of the transport process were examined. Kinetics values were calculated for each transport parameter. The optimum kinetic values were 1.4785 × 10−6 (s−1), 7.3273 × 10−8 (m/s), 13.5691 × 10−8 (mol/m2.s), 5.8174 × 10−12 (m2/s) for constant rate, permeability coefficient, flux, and diffusion coefficient, respectively. Boron was transported selectively and successfully from geothermal waters in the presence of other metal cations with 59.85% recovery value. This study indicates the application of real samples in polymeric membrane systems, which are very practical, economic, and easy to use for large-scale applications. The chemical and physical properties of polymer inclusion membranes (PIMs) offer the opportunity to be specially designed for specific applications.

Preconcentration and Determination of Psychotropic Drugs in Urine Samples by Ion Mobility Spectrometry with Electrospray Ionization Coupling On-Line Single-Drop Liquid-Liquid-Liquid Microextraction

A method for analysis of psychotropic drugs in urine is investigated using a novel single-drop liquid-liquid-liquid microextraction (SDLLLME) apparatus as an electrospray emitter in ion mobility spectrometry (IMS). In this method, ketamine and pethidine are back-extracted into the acceptor phase (water and methanol) from the water and methanol immiscible organic phase. Sensitivity of extraction is improved as it does not require further methanol-adding procedure. Factors affecting the extraction of psychotropic drugs are characterized, including organic solvent type, extraction time, and concentration of NaOH/Ac in the donor/acceptor phase. The best extraction sensitivity is obtained with 600 μL dodecane as the organic phase, 30 minutes extraction time, and 10 mL donor phase with 0.01 M sodium hydroxide (NaOH) and 3 μL acceptor phase with 0.5 M acetic acid (Ac). Using this method, the two analytes can be extracted and analyzed simultaneously, showing this method is valuable for field application.

Ionic Liquid-based Hollow Fiber Liquid–Liquid–Liquid Microextraction Combined with Capillary Electrophoresis for the Determination of Sulfonamides in Aquaculture Waters

Ionic liquid-based hollow-fiber liquid–liquid–liquid microextraction (IL-HF-LLLME) coupled to capillary electrophoresis (CE) has been developed for the determination of six sulfonamides (SAs) in aquaculture waters. A series of extraction parameters was optimized to enhance the extraction efficiency, which included type and pore size of hollow fiber, type and composition of extraction solvent, pH value of donor phase, the concentration of acceptor phase and the mass ratio of donor phase to acceptor phase along with extraction temperature and time. Under optimal conditions, the IL-HF-LLLME-CE method provided a wide liner range for six SAs from 2 to 1,000 μg L−1 (r2 ≥ 0.9995), the limits of the detection from 0.25 to 0.48 and the enrichment factors from 122 to 230, respectively. Relative standard deviations for intra- and interday precision were 1.4–5.3% and 1.8–7.5% (n = 5), respectively. The proposed method was successfully applied for the determination of trace-level SAs in seven real-world aquaculture water samples with good recoveries (80.4–100.7%). Also, sulfamerazine and sulfamethoxazole were detected at the level of 0.52–1.60 μg L−1 in two water samples. Due to its good sensitivity, simple operation, short analysis time and eco-friendliness, the developed method has a great application potential in analysis of trace SA residues in aquaculture waters.

Fullerene derivative induced morphology of bulk heterojunction blends: PIPCP:PC61BM

The performance of organic solar cells depends on the morphology in bulk heterojunctions, including the polymer degree of crystallinity and the amount of each phase: aggregated donor, aggregated acceptor and molecularly mixed donor : acceptor phase.

Performance evaluation of hollow fiber renewal liquid membrane for extraction of uranium(VI) from acidic sulfate solution

The performance of the hollow fiber renewal liquid membrane (HFRLM) in the continuous and recycling modes for the extraction of uranium(VI) from the acidic sulfate solution has been investigated. Alamine 336 diluted in kerosene was used as a carrier in liquid membrane (LM) phase. In the batch experiments, the effects of sulfuric acid, extractant and uranium(VI) concentration were studied and the optimum concentration of the donor and LM phases were determined 0.15 mol L−1and 0.0125 mol L−1, respectively. Various parameters affecting the HFRLM performance including the lumen and shell side flow rate, organic/aqueous volume ratio, acceptor phase type and concentration of carrier and acceptor phase were studied. The mass transfer flux increases with increasing the lumen side flow rates and the shell side flow rate did not have any significant effect. The uranium transfer flux increases with increasing O/A ratio, acceptor and Alamine 336 concentration, and reaches a maximum value at 1/20, 0.5 mol L−1and 0.0125 mol L−1, respectively. Further increase in these parameters result in uranium transfer decrement. The results show that liquid membrane phase is a rate-controlling step. Among the investigated acceptor phases, 0.5 mol L−1NH4Cl result in 60.35% uranium(VI) recovery in the recycling mode.