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Thanks to their good redox activity properties and exceptional conductivity, metal selenides (MSs) have attracted great attention as prospective positive electrodes for hybrid supercapacitors. However, they demonstrate low-rate capacities and poor endurance. Nanomaterials fabricated from MSs and reduced graphene oxide (rGO) with a porous skeleton can effectively mitigate the above-mentioned problems. Herein, porous MnSe@CoSe@FeSe 2 nanowires wrapped with rGO on nickel foam (NF@MCFS-rGO) are manufactured as a binder-free electrode for a hybrid supercapacitor. The obtained NF@MCFS-rGO, acting as a positive electrode, has distinct advantages such as (1) the porous nanowires are helpful for fast electrolyte penetration, (2) the conductivity of the MCFS is further improved when combined with rGO, and (3) wrapping MCFS within the rGO endows the nanomaterial with much better structural durability. Capitalizing on the high conductivity of the rGO and the porous morphology, the fabricated NF@MCFS-rGO manifests impressive characteristics with a capacitance of 1830 F g -1 at 1 A g -1 and only 6.75% capacitance loss within 10 000 cycles. By matching NF@MCFS-rGO with activated carbon (AC), the fabricated apparatus (AC\\NF@MCFS-rGO) reveals an energy density ( E D ) of 64.6 W h kg -1 and a long lastingness of 90.55% after 10 000 cycles.

Driven by their excellent conductivity and redox properties, metal tellurides (MTes) are increasingly capturing the spotlight across various fields. These properties position MTes as favorable materials for next-generation electrochemical devices. Herein, we introduce a novel, self-sustained approach to creating a yolk-shelled electrode material. Our process begins with a metal-organic framework, specifically a CoFe-layered double hydroxide-zeolitic imidazolate framework67 (ZIF67) yolk-shelled structure (CFLDH-ZIF67). This structure is synthesized in a single step and transformed into CuCoLDH nanocages. The resulting CuCoFeLDH-CuCoLDH yolk-shelled microrods (CCFLDH-CCLDHYSMRs) are formed through an ion-exchange reaction. These are then converted into CuCoFeTe-CuCoTe yolk-shelled microrods (CCFT-CCTYSMRs) by a tellurization reaction. Benefiting from their structural and compositional advantages, the CCFT-CCTYSMR electrode demonstrates superior performance. It exhibits a fabulous capacity of 1512 C g -1 and maintains an impressive 84.45% capacity retention at 45 A g -1 . Additionally, it shows a remarkable capacity retention of 91.86% after 10 000 cycles. A significant achievement of this research is the development of an activated carbon (AC)||CCFT-CCTYSMR hybrid supercapacitor. This supercapacitor achieves a good energy density ( E den ) of 63.46 W h kg -1 at a power density ( P den ) of 803.80 W kg -1 and retains 88.95% of its capacity after 10 000 cycles. These results highlight the potential of telluride-based materials in advanced energy storage applications, marking a step forward in the development of high-energy, long-life hybrid supercapacitors.

Transition metal phosphides (TMPs) demonstrate excellent potential for supercapacitor electrode materials owing to their good theoretical capacity and great electrical conductivity. The electrochemical features of the electrode materials based on monometallic or bimetallic phosphides are not desirable or satisfactory due to their low rate performance, unfavorable energy density, and short durability. One practical solution to overcome the above problems is to bring in heteroatoms to the structure of the bimetallic materials to create trimetallic phosphides. In this work, brand-new MnNiCoP yolk-shell spheres assembled with nanosheets are synthesized in a facile self-templated way using greatly uniform co-glycerate spheres as sacrificial templates, followed by a phosphorization process. Because of the existence of plenty of oxidation-reduction active sites, great surface area (SA) with mesoporous pathways, high electrical conductivity, and synergistic effect of Mn, Ni, and Co atoms, the fabricated MnNiCoP@NiF electrode demonstrates a considerably increased electrochemical efficiency compared with the bimetallic phosphide MnCoP@NiF electrode. Noticeably, the MnNiCoP@NiF electrode exhibits a great specific capacity of 291.24 mA h g -1 at an applied current density of 1 Ag -1 , 80% capacity retention at an applied current density of 20 Ag -1 , and 91.3% capacity retention after 14 000 cycles. In addition, a hybrid supercapacitor device with a brand-new positive electrode (MnNiCoP@NiF) and an appropriate negative electrode (AC@NiF) demonstrates an energy density of 57.03 W h kg -1 with a power density of 799.98 W kg -1 , plus superb cyclability with 88.41% of the primary capacitance after 14 000 cycles.

Owing to their metalloid characteristics with high electrical conductivity, transition metal phosphides (TMPs) have attracted considerable research attention as prospective cathodes for hybrid supercapacitors. Unfortunately, they usually exhibit low rate performance as well as poor longevity, which does not meet the demands of hybrid supercapacitors. The nanocomposite constructed from reduced graphene oxide (rGO) and TMPs with a highly porous nature can effectively overcome the above-mentioned issues, greatly widening their utilization. In this work, we fabricated nanosheet-assembled hollow copper-nickel phosphide spheres (NH-CNPSs) by the controllable phosphatizing of copper-nickel-ethylene glycol (CN-EG) precursors. Then, porous NH-CNPSs were embedded in rGO texture (NH-CNPS-rGO) to form a unique porous nanoarchitecture. The obtained NH-CNPS-rGO has several advantages benefiting as the cathode electrode, such as (i) the hollow structure as well as porous nanosheets are conducive to fast electrolyte diffusion, (ii) the electrical conductivity of NH-CNPS is further enhanced when coupled with the rGO texture, hence promoting electron transfer in the whole structure, (iii) wrapping NH-CNPSs within the rGO texture endows the nanocomposite with much better structural stability, resulting in longer durability of the electrode, And (iv) the porous structures generated in the nanocomposite provide a perfect space for reducing the mass transfer resistance and accessing the electrolyte, thereby boosting the reaction kinetics. The tests demonstrated that the optimal NH-CNPS-rGO electrode revealed a capacity of up to 1075 C g -1 , a superior rate capacity, and exceptional longevity of 94.7%. Moreover, a hybrid supercapacitor (NH-CNPS-rGO‖AC) equipped with the NH-CNPS-rGO-cathode electrode and activated carbon (AC)-anode electrode represented a satisfactory energy density of 64 W h kg -1 at 801 W kg -1 and amazing longevity (91.8% retention after 13 000 cycles), which endorses the promising potential of NH-CNPS-rGO for high-efficiency supercapacitors. This research showcases an appropriate method to engineer hollow TMP-rGO nanocomposites as effective materials for supercapacitors.

Design and fabrication of impressive and novel electrode materials for energy storage devices, especially supercapacitors, are of great importance. Herein, bimetallic CoSe 2 /FeSe 2 hollow nanocuboid nanostructures derived from Co/Fe-Prussian Blue analogues (denoted as CoSe 2 /FeSe 2 HNCs) are successfully designed and fabricated as a remarkable positive electrode material for high-performance supercapacitors. The bimetallic CoSe 2 /FeSe 2 HNC nanostructures can have increased active sites and short electron-ion diffusion pathways. Bimetallic CoSe 2 /FeSe 2 HNCs@NiF as a positive electrode showed efficient supercapacitive properties with a great specific capacity of 332.75 mA h g -1 (1197.90 C g -1 ) at 1 A g -1 , retaining 80.61% of its initial capacity at 20 A g -1 , considerable longevity (91.47% of its initial capacity after 10 000 cycles) and an excellent coulombic efficiency of 98.49%. Also, the designed and fabricated CoSe 2 /FeSe 2 HNCs@NiF||AC@NiF hybrid supercapacitor device using bimetallic CoSe 2 /FeSe 2 HNCs@NiF (positive electrode) and activated carbon@NiF (AC, negative electrode) exhibited an efficient energy density of 63.62 W h kg -1 and a superior durability of 91.14% after 10 000 cycles.

The development of durable, beneficial, and highly active non-precious metal-based electrocatalysts for hydrogen generation is a vital concern. This study proposes an effective strategy for the construction of Fe doped CoP nanosheet arrays wrapped by graphene (F 0.25 CP-G) on nickel foam as an efficient electrocatalyst for the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). In this design, the final catalyst possesses a combination of the high conductivity of graphene, great surface porosity, and the intrinsic electrocatalytic activity of the F 0.25 CP-G which results in high-performance electrocatalytic activity toward the HER and OER. Therefore, the as-synthesized F 0.25 CP-G catalyst can achieve overpotentials of 66 mV and 230 mV for the HER and OER, respectively, in KOH at 10 mA cm -2 . Furthermore, a practical electrolyzer (F 0.25 CP-G||F 0.25 CP-G) exhibits a current density of 10 mA cm -2 at 1.60 V along with good durability for 24 h.

Metal-organic framework (MOF) derived nanoarchitectures have special features, such as high surface area (SA), abundant active sites, exclusive porous networks, and remarkable supercapacitive performance when compared to traditional nanoarchitectures. Herein, we propose a viable strategy for the synthesis of hollow manganese nickel selenide spheres comprising nanosheets supported on the nickel foam (denoted as MNSe@NF) from the MOF. The MNSe nanostructures can demonstrate enriched active sites, and shorten the ion-electron diffusion pathways. When the MNSe@NF electrode is used as a cathode electrode for a hybrid supercapacitor, the electrode reflected impressive supercapacitive properties with a high capacity of 325.6 mA h g-1 (1172.16 C g-1) at 2 A g-1, an exceptional rate performance of 86.6% at 60 A g-1, and remarkable longevity (3.2% capacity decline after 15 000 cycles). Also, the assembled MNSe@NF∥AC@NF hybrid supercapacitors employing activated carbon on the nickel foam (AC@NF, anode electrode) and MNSe@NF (cathode electrode) revealed an impressive energy density of 66.1 W h kg-1 at 858.45 W kg-1 and an excellent durability of 94.1% after 15 000 cycles.

Thanks to the attractive structural characteristics and unique physicochemical properties, mixed metal selenides (MMSes) can be considered as encouraging electrode materials for energy storage devices. Herein, a straightforward and efficient approach is used to construct multi-shelled nickel-manganese selenide hollow spheres (MSNMSeHSs) as cathode and double-shell nickel-iron selenide hollow spheres (DSNFSeHSs) as anode electrode materials by tuning shell numbers for supercapacitors. The as-designed MSNMSeHS electrode can deliver a splendid capacity of ∼339.2 mA h g-1/1221.1 C g-1, impressive rate performances of 78.8%, and considerable longevity of 95.7%. The considerable performance is also observed for the DSNFSeHS electrode with a capacity of 258.4 mA h g-1/930.25 C g-1, rate performance of 75.5%, and longevity of 90.9%. An efficient asymmetric apparatus (MSNMSeHS||DSNFSeHS) fabricated by these two electrodes depicts the excellent electrochemical features (energy density of ≈112.6 W h kg-1 at 900.8 W kg-1) with desirable longevity of ≈94.4%.

Agarose gel as a green membrane has been proposed for use in electromembrane extraction of five hypothalamic-related peptides without an ionic carrier. Octreotide, goserelin, triptorelin, cetrorelix, and somatostatin were extracted from 5.0 mL of sample solution (adjusted to pH 5.0) into a microvolume acceptor solution (HCl, 100 mM) under the applied voltage of 30 V in 15 min. The pH of the agarose gel 3.0% (w/v) was adjusted to 4.0 to facilitate the movement of peptides through the membrane. Quantification was performed using an HPLC-UV system on a C18 column. Quantification and detection limits were found to be in the range of 15.0-20.0 ng mL -1 and 4.5-6.0 ng mL -1 , respectively. Dynamic linear ranges were found to be in the range of 15.0-1000 ng mL -1  (R 2  > 0.995) and recoveries were in the range of 62.3-77.6%. The optimized method was applied to spiked human plasma samples. The method showed relative recoveries in the range of 44.8-66.0%. Finally, the proposed method was compared with and shown to have higher recoveries than, the conventional electromembrane extraction method for the peptides under study., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Porous structures have attracted considerable attention as promising electrode designs for supercapacitor applications. Herein, we introduce a procedure towards the construction of nanoporous CuCoNi-P nanotube arrays (CCNP-NAs) by a metal-organic framework and hierarchical CoFe 2 Se 4 nanosheet arrays (CFS-NAs) through a hydrothermal strategy, followed by selenization for the flexible asymmetric device. Due to the unique design of the electrode materials, the CCNP-NA and CFS-NA electrodes show exceptional specific capacities of ∼406.73 and 248.2 mA h g -1 at 2 A g -1 , reasonable rate capabilities of 84.2 and 71.2% at 50 A g -1 , and remarkable durability of 98.9% and 95.1%, respectively. Remarkably, an advanced flexible device was constructed using the CCNP-NA positive electrode and CFS-NA negative electrode. Our flexible device demonstrates tremendous energy density (∼153.5 W h kg -1 at 852.8 W kg -1 ), super-high durability of 96.2%, and considerable flexibility under bending conditions. This work proposes insight into the rational construction of porous nanostructures for next-generation electronic devices.

Objective: This study was conducted to determine the effect of intramuscular ondansetron on ketamine-associated vomiting in children undergoing procedural sedation., Methods: This randomized, double-blind, placebo-controlled, parallel-group clinical trial was conducted at the emergency departments of two university-affiliated tertiary care hospitals. Eligible participants included all 6-month to 16-year-old children who received IM ketamine for PSA in the ED. A convenience sampling approach was used and a block randomization method was applied (blocks of four) using a computer-generated random sequence. Patients received ketamine 4 mg/kg or ketamine 4 mg/kg plus ondansetron 0.1 mg/kg intramuscularly. All findings including the occurrence of vomiting and its frequency were then recorded in the data collection sheets., Results: Of 56 patients who received ondansetron plus ketamin, 7 (12.5%) and 1 (1.8%) experienced vomiting during recovery and before discharge and Of 65 patients in the control group, 14 (21.5%) and 6 (9.2%) experienced vomiting during recovery and before discharge, respectively. The observed differences in the rates of vomiting during recovery and at discharge were statistically significant between the two groups (P-value of 0.03 and <0.001, respectively)., Conclusion: Intramuscular ondansetron is effective in controlling ketamine-associated vomiting., (Copyright © 2019 Elsevier Inc. All rights reserved.)

The practical exploration of electrode materials with complex hollow structures is of considerable significance in energy storage applications. Mixed-metal selenides (MMSs) with favorable architectures emerge as new electrode materials for supercapacitor (SC) applications owing to their excellent conductivity. Herein, a facile and effective metal-organic framework (MOF)-derived strategy is introduced to encapsulate multi-shelled zinc-cobalt-selenide hollow nanosphere positive and yolk-double shell cobalt-iron-selenide hollow nanosphere negative electrode materials with controlled shell numbers in a graphene network (denoted as G/MSZCS-HS and G/YDSCFS-HS, respectively) for SC applications. Due to the considerable electrical conductivity and unique structures of both electrodes, the G/MSZCS-HS positive and G/YDSCFS-HS negative electrodes exhibit remarkable capacities (∼376.75 mA h g -1 and 293.1 mA h g -1 , respectively, at 2 A g -1 ), superior rate performances (83.4% and 74%, respectively), and an excellent cyclability (96.8% and 92.9%, respectively). Furthermore, an asymmetric device (G/MSZCS-HS//G/YDSCFS-HS) has been fabricated with the ability to deliver an exceptional energy density (126.3 W h kg -1 at 902.15 W kg -1 ), high robustness of 91.7%, and a reasonable capacity of 140.3 mA h g -1 .

Owing to the increased requirement for efficient energy storage systems (ESs), investigating favorable electrodes with porous nanoarchitecture for supercapacitors (SCs) is vital. Nonetheless, the development of these kinds of electrodes to obtain high energy density remains a difficult task. Low specific capacitances of positive (cathode) and negative (anode) electrode materials are a serious obstacle that limits the performance of asymmetric SCs (ASCs). Herein, we proposed the preparation of yolk-shell Cu-Co-P hollow nanospheres (Y-CCP HN) as a positive electrode using a metal-organic framework (MOF) and CuFeS 2 nanosheet (CFS NS) arrays as a negative electrode via a low-cost and simple hydrothermal route for ASCs. The Y-CCP HN and CFS NS electrodes exhibited significant specific capacitances (∼2043.3 F g -1 (340.55 mA h g -1 ) and 654.3 F g -1 (218.1 mA h g -1 ), respectively), considerable rate performances (∼77.55% and 63.2%, respectively, even at 24 A g -1 ), and exceptional durability (96.7% and 95.3% after 8000 cycles, respectively). Most notably, the Y-CCP HN//CFS device delivers a wonderful energy density of 158.4 W h kg -1 at a power density of 900.3 W kg -1 , a notable specific capacitance of 352.1 F g -1 (176.05 mA h g -1 ), and excellent cyclability (96.1% after 8000 cycles). This exploration demonstrates a good strategy for the construction of other metal phosphides and sulfides with porous nature, emphasizing considerable prospects for next-generation ESs.

To construct a supercapacitor (SC) with considerable performance, synthesis of an electrode material with a highly porous structure is necessary. Herein, an efficient metal-organic framework (MOF)-derived procedure is offered to construct a graphene wrapped multi-shelled NiGa2O4 hollow sphere (GW-MSNGOHS) positive electrode material and a graphene-wrapped yolk-shell NiFe2O4 hollow sphere (GW-YS-NFOHS) negative electrode material with a highly porous nature in SCs. The GW-MSNGOHS and GW-YS-NFOHS electrodes exhibit excellent capacities (∼411.25 mA h g-1 and 254.25 mA h g-1, respectively, at 1 A g-1), reasonable rate performances (75.85%, and 62.7%, respectively), and outstanding cyclability (98.9% and 90.9%, respectively). Benefiting from the reasonably engineered negative and positive electrodes, the fabricated asymmetric device (GW-MSNGOHS//GW-YS-NFOHS) can show an excellent energy density (ED) of 118.97 W h kg-1 at a power density (PD) of 1702 W kg-1, an exceptional robustness of 92.1%, and an excellent capacity (Cs) of 140.2 mA g-1.

Herein, electromembrane extraction was combined with ultraviolet spectrophotometry using a customized manifold for preconcentration and simultaneous determination of morphine, codeine, and papaverine in water and human urine samples. Absorption spectra of the extracts were recorded inside the lumen of the hollow fiber using two fiber optics connected to a miniature spectrophotometer. Partial least squares regression was applied to resolve the overlapped spectra of the analytes. Performance of the model was validated by an independent test set. Central composite design was applied to optimize the extraction parameters. The optimized extraction conditions are as follows; supporting liquid membrane: 2-nitrophenyl octyl ether containing 15% v/v bis(2-ethylhexyl) phosphate, applied voltage: 80 V, donor pH: 3.0, acceptor pH: 1.0, extraction time: 20 min. Finally, the optimized extraction method was validated for determination of the mentioned alkaloids in human urine samples. The method showed good linearity (R 2  > 0.995) for all of the mentioned alkaloids. The limits of detection for morphine, codeine, and papaverine in diluted human urine were found to be 0.6, 1.1, and 0.6 ng/mL, respectively with acceptable relative standard deviations. Enrichment factors of 104, 108, and 102 were achieved for morphine, codeine, and papaverine, respectively., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

An electromembrane extraction followed by HPLC-UV technique was developed and validated for quantification of leuprolide and triptorelin in rabbit plasma. The influencing parameters on the extraction efficiency were optimized using experimental design methodology. The optimized conditions were found to be; supported liquid membrane: a mixture of 1-octanol and 2-ethyl hexanol (1:1) containing 10% v/v di(2-ethylhexyl) phosphate, applied voltage: 5 V, extraction time: 5 min, pH of the donor phase: 4.5 and pH of the acceptor phase: 1.0. The optimized method was validated for linearity, intraday and interday precision, and accuracy in rabbit plasma. The range of quantification for both peptides was 0.5-1000 ng/mL with regression coefficients higher than 0.994. Relative recoveries of leuprolide and triptorelin were found to be 80.3 and 75.5%, respectively. Limits of quantification and detection for both peptides were found to be 0.5 and 0.15 ng/mL, respectively. The validated method was successfully applied to pharmacokinetic study of the 1-month depot formulations of each peptide after subcutaneous administration to rabbits., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Herein, we proposed a desirable strategy for the synthesis of graphene-wrapped NiCo2Se4 microspheres (positive electrode) and petal-like iron disulfide (FeS2) (negative electrode) on nickel foam substrates. The positive electrode represents a substantial specific capacitance of 2112.30 F g-1 and excellent durability (6.8% loss after 5000 cycles). Furthermore, the negative electrode reflects good electrochemical performance with a specific capacitance of 321.30 F g-1 and a satisfactory rate capability of 47% capacitance retention. Considering the notable properties of the electrodes, a flexible asymmetric all-solid-state device based on graphene-wrapped NiCo2Se4 microspheres (positive electrode) and petal-like iron disulfide (negative electrode) was assembled. Our flexible device exhibits the high specific capacitance of 221.30 F g-1, the significant energy density of 78.68 W h kg-1 and excellent flexibility.

Objective: Assessment of Corrected Flow Time (FTc) in carotid artery has been suggested recently as a measure of intravascular volume status. This study aimed to determine the reference values of FTc in carotid artery in a normal population., Methods: A total number of 142 healthy volunteers (73 females and 69 males) with a mean age of 36.65±10.52years were included., Results: The mean FTc in carotid artery was 325.18±22.15ms 0.5 . The mean value of FTc differed significantly between females and males both before and after passive leg raise (PLR) (330.18±21.61ms 0.5 vs. 319.88±21.62, P=0.005 before PLR, and 336.89±22.95ms 0.5 vs. 326.51±21.21, P=0.006 after PLR)., Conclusion: This study would potentially pave the way to determine clinically significant cutoff points in order to assess the diagnostic accuracy of FTc in predicting intravascular volume status and fluid therapy responsiveness., (Copyright © 2017 Elsevier Inc. All rights reserved.)

A new zinc complex, [Zn (9-AC) 2 ] (1) (9-AC = 9-anthracenecarboxylic acid), was prepared via conventional electrochemical method in a fast and facile process and fully characterized by 1 H NMR, 13 C NMR, IR spectroscopy and elemental analysis. The nano structures of the same compound were successfully produced by a facile and environment-friendly sonoelectrochemical route at different current densities (0.5, 1.2, 1.8, 2.5 and 3.5 mA/cm 2 ). The new nano-structure particles were characterized by scanning electron microscopy, X-ray powder diffraction, IR spectroscopy and elemental analysis. Thermal stability of single crystal and nano-size samples of the prepared compound was studied by thermogravimetric and differential thermal analysis. The comparison of the effect of current density without and with ultrasonic irradiation on particle size has been investigated in convectional electrochemical and sonoelectrochemical method respectively. The results showed that using ultrasonic irradiation with increasing the current density lead to decrease the particle sizes unlike conventional electrochemical method. In other words, when the current density increase from 0.5 to 3.5 mA/cm 2 , in sonoelectrochemical method, the particle sizes decrease from 100 to 48 nm while, in convectional electrochemical method, the particle sizes increase from 400 to 1200 nm and possible explanation offered. Photoluminescence properties of the nano-structured and crystalline bulk of the prepared complex at room temperature in the solid state have been investigated in detail. The results indicate that the size of the complex particles has an important effect on their optical properties.

In this work, a novel microextraction technique using molecularly imprinted polymer-coated multi-walled carbon nanotubes (MIP-MWCNTs) in electromembrane extraction (EME) procedure is described. The method in combination with HPLC-UV was utilized to determine naproxen, as an acidic model drug, in urine, plasma and wastewater samples. For this purpose, MIP-MWCNTs were placed in the pores of polypropylene hollow fiber. The MIP-MWCNTs-EME method has the advantages of high selectivity and cleanup of MIP along with high enrichment ability of the EME in a single step extraction. Continuing with the research, optimization of the factors affecting the migration of naproxen from sample solutions to MIP-MWCNTs sites and then into the lumen of hollow fiber was explored. Under the optimized conditions, the limit of detection (LOD) of the developed method was calculated to be 0.3μgL -1 . All relative standard deviations (RSDs) were lower than 3%. Linearity of the method was obtained within the range of 1-1000μgL -1 with the coefficient of determination (r 2 ) being higher than 0.999. Under the optimized conditions, an extraction recovery of 66% was obtained, which corresponded to a preconcentration factor of 88. Finally, the developed method was satisfactorily used to determine naproxen in urine, plasma and wastewater samples., (Copyright © 2016 Elsevier B.V. All rights reserved.)

In this work, a new solid-phase microextraction fiber was prepared based on nitrogen-doped graphene (N-doped G). Moreover, a new strategy was proposed to solve problems dealt in direct coating of N-doped G. For this purpose, first, Graphene oxide (GO) was coated on Pt wire by electrophoretic deposition method. Then, chemical reduction of coated GO to N-doped G was accomplished by hydrazine and NH3. The prepared fiber showed good mechanical and thermal stabilities. The obtained fiber was used in two different modes (conventional headspace solid-phase microextraction and cold-fiber headspace solid-phase microextraction (CF-HS-SPME)). Both modes were optimized and applied for the extraction of benzene and xylenes from different aqueous samples. All effective parameters including extraction time, salt content, stirring rate, and desorption time were optimized. The optimized CF-HS-SPME combined with GC-FID showed good limit of detections (LODs) (0.3-2.3 μg/L), limit of quantifications (LOQs) (1.0-7.0 μg/L) and linear ranges (1.0-5000 μg/L). The developed method was applied for the analysis of benzene and xylenes in rainwater and some wastewater samples., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Electromembrane extraction (EME) was carried out using a novel instrumentation capable of impedometric monitoring of the system during the extraction. This instrumentation involves a classical two-electrode assembly fed by two time-resolved potential functions, the first for the extraction of analyte and the second for obtaining the impedance information. The impedometric analysis of the system was achieved by Laplace transformation of the current recorded during the extraction. It has been shown that the obtained impedance information can be converted to very useful knowledge about time dependence of double layer capacitance, kinetics of analyte depletion, total permeability of the SLM and the effect of experimental parameters on system behavior. It has also been shown that the impedance analysis is a powerful tool for the estimation of optimum experimental parameters without determination of analyte in the acceptor phase., (Copyright © 2016 Elsevier B.V. All rights reserved.)

In this work, a simple and efficient surfactant assisted pulsed two-phase electromembrane extraction (SA-PEME) procedure combined with gas chromatography (GC) has been developed for the determination of alfentanil, sufentanil and methadone in various samples. It has been found that the addition of anionic surfactant causes the accumulation of the cationic analytes at the SLM/solution interface resulting in an easier transfer of the analytes into the organic phase. The method was accomplished with 1-octanol as the acceptor phase and supported liquid membrane (SLM) by means of an 80 V pulsed electrical driving force and the extraction time of 20 min. The model analytes were extracted from 3.0 mL sample solution (pH 4.0) containing 0.02% w/v surfactant (sodium dodecyl sulfate). The duty cycle of 92% and frequency of 0.357 Hz gave the best performance. Extraction recoveries in the range of 70.5-95.2% and satisfactory repeatability (7.6

Electromembrane extraction (EME) of model analytes was carried out using a virtually rotating supported liquid membrane (SLM). The virtual (nonmechanical) rotating of the SLM was achieved using a novel electrode assembly including a central electrode immersed inside the lumen of the SLM and five counter electrodes surrounding the SLM. A particular electronic circuit was designed to distribute the potential among five counter electrodes in a rotating pattern. The effect of the experimental parameters on the recovery of the extraction was investigated for verapamil (VPL), trimipramine (TRP), and clomipramine (CLP) as the model analytes and 2-ethyl hexanol as the SLM solvent. The results showed that the recovery of the extraction is a function of the angular velocity of the virtual rotation. The best results were obtained at an angular velocity of 1.83 RadS(-1) (or a rotation frequency of 0.29 Hz).The optimization of the parameters gave higher recoveries up to 50% greater than those of a conventional EME method. The rotating also allowed the extraction to be carried out at shorter time (15 min) and lower voltage (200 V) with respect to the conventional extraction. The model analytes were successfully extracted from wastewater and human urine samples with recoveries ranging from 38 to 85%. The RSD of the determinations was in the range of 12.6 to 14.8%., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Purpose: The purpose of this study is to investigate the possible correlation between corrected flow time (FTc) in carotid artery and changes in volume status., Materials and Methods: Ninety-three patients with end-stage renal failure who underwent fluid removal via hemodialysis were enrolled prospectively. The volume of fluid removed as well as prehemodialysis and posthemodialysis measures of FTc in the carotid artery, heart rate, and mean arterial pressure was evaluated. All imaging measurements were performed with patients at supine position, 15 minutes before and after the hemodialysis session, by evaluating the right common carotid artery at the level of the lower border of thyroid cartilage., Results: The mean FTc before fluid removal was 345.07±37.19 milliseconds. This measure decreased significantly after the volume removal with a posthemodialysis mean of 307.77±31.76 milliseconds (P<.0001). There was a statistically significant and negative association between the volume of fluid removed by hemodialysis and the changes in FTc (Pearson correlation, -0.39; P<.0001)., Conclusion: The assessment of changes in FTc of carotid artery via Doppler waveform analysis may predict the changes in intravascular volume. The use of this diagnostic modality may be an accurate and noninvasive alternative to currently available methods., (Copyright © 2015 Elsevier Inc. All rights reserved.)

The distribution of electric field vectors was first calculated for electromembrane extraction (EME) systems in classical and cylindrical electrode geometries. The results showed that supported liquid membrane (SLM) has a general field amplifying effect due to its lower dielectric constant in comparison with aqueous donor/acceptor solutions. The calculated norms of the electric field vector showed that a DC voltage of 50 V can create huge electric field strengths up to 64 kV m(-1) and 111 kV m(-1) in classical and cylindrical geometries respectively. In both cases, the electric field strength reached its peak value on the inner wall of the SLM. In the case of classical geometry, the field strength was a function of the polar position of the SLM whereas the field strength in cylindrical geometry was angularly uniform. In order to investigate the effect of the electrode geometry on the performance of real EME systems, the analysis was carried out in three different geometries including classical, helical and cylindrical arrangements using naproxen and sodium diclofenac as the model analytes. Despite higher field strength and extended cross sectional area, the helical and cylindrical geometries gave lower recoveries with respect to the classical EME. The observed decline of the signal was proved to be against the relations governing migration and diffusion processes, which means that a third driving force is involved in EME. The third driving force is the interaction between the radially inhomogeneous electric field and the analyte in its neutral form., (Copyright © 2015 Elsevier B.V. All rights reserved.)

We are introducing mercapto-mesoporous carbon modified carbon paste electrode (mercapto-MP-C-CPE) as a new sensor for trace determination of omeprazole (OM) in biological samples. The synthesized modifier was characterized by thermogravimetry analysis (TGA), differential thermal analysis (DTA), transmission electron microscopy (TEM), Fourier transform infrared spectrometry (FT-IR), X-ray diffraction (XRD), elemental analysis (CHN) and N2 adsorption surface area measurement (BET). The electrochemical response characteristic of the modified-CPE toward OM was investigated by cyclic and differential pulse voltammetry (CV and DPV). The proposed sensor displayed a good electrooxidation response to the OM, its linear range is 0.25nM to 25μM with a detection limit of 0.04nM under the optimized conditions. The prepared modified electrode shows several advantages such as high sensitivity, long-time stability, wide linear range, ease of preparation and regeneration of the electrode surface by simple polishing and excellent reproducibility., (Copyright © 2014 Elsevier B.V. All rights reserved.)

A new lead complex, [Pb(Q)2] (1) (Q=quinoline-2-carboxylic acid), was prepared via conventional electrochemical method in a fast and facile process and fully characterized by (1)H and (13)C NMR, IR, UV spectroscopies and elemental analysis. The nano-structures of same compound were successfully prepared at 25, 48 and 60°C by a facile and environment-friendly sonoelectrochemical route. The new nano-structure particles were characterized by scanning electron microscopy, X-ray powder diffraction, IR spectroscopy and elemental analysis. Thermal stability of single-crystal and nano-size samples of the prepared compound was studied by thermogravimetric and differential thermal analysis. The effect of sonoelectrochemical temperature on particle size has been investigated, and possible explanations offered. The photoluminescence properties of the nano-structured and crystalline bulk of the prepared complex at room temperature in the solid state have been investigated in detail. The results indicate that the size of the complex particles has an important effect on the optical properties of it. The prepared complexes, as bulk and as nano-particles, were utilized as a precursor for preparation of PbO nanoparticles by direct thermal decomposition at 600°C in air. The nano-structures of PbO were characterized by scanning electron microscopy, X-ray powder diffraction and IR spectroscopy., (Copyright © 2014 Elsevier B.V. All rights reserved.)