Porous membrane structures as stationary phase for capillary electrochromatography

This work presents the application of membrane technology for the fabrication of stationary phase for CEC columns using the technique based on phase inversion of polymer solution. A blend of polyimide P84 and sulphonated poly(ether ether ketone was processed via immersion precipitation dry‐wet spinning into small‐bore porous fiber. The morphology, zeta potential, and performance of the porous structure in the CEC separation were investigated. Noncharged molecules (as markers of the electroosmotic flow) and small organic compounds were injected into the column, driven under the application of voltage, and detected on the electropherogram. The proof of concept of applying porous membrane structure as stationary phase for CEC was shown and possible optimization to improve efficiency and selectivity was suggested.     

Rapid Capillary‐Assisted Solution Printing of Perovskite Nanowire Arrays Enables Scalable Production of Photodetectors

Despite recent progress in producing perovskite nanowires (NWs) for optoelectronics, it remains challenging to solution‐print an array of NWs with precisely controlled position and orientation. Herein, we report a robust capillary‐assisted solution printing (CASP) strategy to rapidly access aligned and highly crystalline perovskite NW arrays. The key to the CASP approach lies in the integration of capillary‐directed assembly through periodic nanochannels and solution printing through the programmably moving substrate to rapidly guide the deposition of perovskite NWs. The growth kinetics of perovskite NWs was closely examined by in situ optical microscopy. Intriguingly, the as‐printed perovskite NWs array exhibit excellent optical and optoelectronic properties and can be conveniently implemented for the scalable fabrication of photodetectors.     

PVC Supported Liquid Membrane and Carbon Paste Potentiometric Sensors Incorporating a Mn(III)‐Porphyrin for the Direct Determination of Undissociated Paracetamol

PVC supported liquid membrane and carbon paste potentiometric sensors incorporating an Mn(III)‐porphyrin complex as a neutral host molecule were developed for the determination of paracetamol. The measurements were carried out in solution at pH 5.5. Under such conditions paracetamol exists as a neutral molecule. The mechanism of molecular recognition between the Mn(III)‐porphyrin and paracetamol, leading to potentiometric signal generation, is discussed.     

A Study on Operational Parameters for Advanced Use of Bismuth Film Electrode in Anodic Stripping Voltammetry

A study is presented on the characterization, evaluation and optimization of several key operational parameters for a reliable and effective use of a bismuth film electrode (BiFE) as an advanced replacement of the mercury film electrode in anodic stripping voltammetric measurements of trace heavy metals. Applying in situ preparation of the BiFE and employing lead(II) and cadmium(II) as model analyte ions, key parameters including bismuth precursor salt and substrate surface (platinum, gold, glassy carbon, carbon paste, carbon fiber) for bismuth plating, concentration as well as cationic and anionic composition of the measurement solution, solution pH and temperature, potential interferents, and stripping modes were carefully examined for their effects in the preconcentration and stripping steps. Parameters such as substrate surface (except platinum), precursor salt, solution matrix and temperature showed no or little impact on the BiFE performance in stripping analysis. On the other hand, the BiFE performance was found to be dependent on the solution pH (with maximum efficiency in the range of 4 to 5), on the stripping mode (with square‐wave voltammetry as the best choice) and to a certain degree on the presence of surface active substances. The results revealed that the non‐toxic solid‐state BiFE is applicable under a wide variety of conditions which proves it highly suitable for practical work in environmental trace heavy metal analysis.     

多荧光光纤传感器及其在混合溶剂检测中的应用

微纳光纤与其他微纳结构的集成可以拓展荧光光纤传感器检测范围和集成度,是光纤传感领域的研究热点。目前,国际上关于荧光光纤传感器这一领域的研究还处于单一检测物荧光响应的阶段,对多检测物的多通道荧光响应仍存在很大挑战。本文结合微纳光纤的光波导性能以及有机荧光材料的光功能特性,制备了能够同时激发和收集多种荧光的微纳光纤,并将之应用于高性能荧光光纤传感器的制备。通过选用不同荧光波长的有机材料与凝胶掺杂,制备了多荧光发射的光纤涂层材料,可控构筑了多组分荧光检测剂掺杂凝胶涂层。利用荧光光谱结合色度图分析,确定检测物与色坐标的关系,实现了多检测物的多通道荧光响应,为实现多荧光光纤传感器的可控构筑提供了有益的借鉴和指导意义。     

Modified carbon paste sensor for cetyltrimethylammonium ion based on its ion-associate with tetrachloropalladate(II).

A comparative study was made between developed chemically modified carbon paste electrodes and PVC membrane electrodes for the cationic surfactant cetyltrimethylammonium bromide (CTAB). The carbon paste electrode modified with cetyltrimethylammonium-tetrachloropalladate(II) (CTA-TClP) provides a more sensitive and stable device than that shown by electrodes with an inner reference solution. The best performance was obtained by an electrode based on the paste containing 3.6 wt% CTA-TCIP, 1.8 wt% ethylhexadecyldimethylammonium bromide, 37.6 wt% graphite and 57 wt% tricresyl phosphate. The sensor exhibited a Nernstian response for CTAB over a wide concentration range of 3.5 x 10(-7) to 1.0 x 10(-3) M with a detection limit of 2.0 x 10(-7) M between pH 2.7 and 8.2 with a fast response time of 相似文献   

Enantioselective,Potentiometric Memberane Electrodes Based on Different Cyclodextrins as Chiral Selectors for the Assay of S‐Flurbiprofen

Four enantioselective, potentiometric membrane electrodes (EPMEs) based on carbon paste impregnated with α‐, β‐, 2‐hydroxyl‐3‐trimethylammoniopropyl‐β‐(as chloride salt) and γ‐cyclodextrins, were proposed as a chiral selectors for assay of S‐flurbiprofen raw materials and in its pharmaceutical formulation Froben 100 tablets. The best response was obtained when β‐cyclodextrin was used for the electrode design. The four EPMEs showed very low detection limits (of 10^?8 to 10^?9 mol/L magnitude orders). The surfaces of the electrodes are easily renewable by simply polishing on an alumina paper.     

Trace determination of organophosphate esters in environmental water samples with an ionogel‐based nanoconfined ionic liquid fiber coating for solid‐phase microextraction with gas chromatography and flame photometric detection

Organophosphate esters, widely used as flame retardants and plasticizers, are regarded as a class of emerging pollutants. In this work, a novel approach was developed for the fabrication of a solid‐phase microextraction fiber by using hybrid silica‐based materials with immobilized ionic liquids with sol–gel technology, and the prepared solid‐phase microextraction fiber was then coupled with gas chromatography and flame photometric detection for the analysis of six organophosphate esters. The high loading of 1‐hexadecyl‐3‐methylimidazolium bis(trifluoromethylsulfonyl)imide was confined within the hybrid network. The developed solid‐phase microextraction fiber possesses a coating thickness of ～35 μm with good thermal stability and long lifetime. The parameters affecting the extraction efficiency such as extraction time, temperature, pH, and ionic strength of the sample solution were optimized. Under the optimized conditions, the limits of detection were in the range of 0.04?0.95 μg L^?1, and the precision of the method assessed with repeatability and reproducibility of (RSD%) ?13 and ?29%, respectively. The proposed method was successfully applied to determine the six organophosphate esters in three real water samples, with recoveries in the range of 64.8?125.4% at two different spiking concentration levels. As a result, the proposed method demonstrated its potential for application in trace determination of organophosphate esters in actual water samples.     

Surface-enhanced Raman scattering (SERS) optrodes for multiplexed on-chip sensing of nile blue A and oxazine 720

The fabrication and on-chip integration of surface-enhanced Raman scattering (SERS) optrodes are presented. In the optrode configuration, both the laser excitation and the back-scattered Raman signal are transmitted through the same optical fiber. The SERS-active component of the optrode was fabricated through the self-assembly of silver nanoparticles on the tip of optical fibers. The application of SERS optrodes to detect dyes in aqueous solution indicated a limit of quantification below 1 nM, using nile blue A as a molecular probe. Using the optrode-integrated microfluidic chip, it was possible to detect several different dyes from solutions sequentially injected into the same channel. This approach for sequential detection of different analytes is applicable to monitoring on-chip chemical processes. The narrow bandwidth of the vibrational information generated by SERS allowed solutions of different compositions of two chemically similar dyes to be distinguished using a dilution microfluidic chip. These results demonstrate the advantages of the SERS-optrode for microfluidics applications by illustrating the potential of this vibrational method to quantify components in a mixture.     

In‐situ Fabrication of Functional Materials inside Porous Fiber using Microwave Selective Heating

We developed a simple fabrication method, which can emplace functional materials inside porous fibers. In contrast to conventional impregnation methods or surface coating, various functions can be included inside of natural or synthetic fibers. This fabrication method has three steps. First, the raw material solution is absorbed to the fiber. Then the fiber is immersed and pressurized in immiscible liquids with the raw material solution. Finally, the functional particles are fabricated in‐situ inside of the fiber by a chemical reaction such as microwave selective heating. As a model reaction, we fabricated silver‐nanoparticle‐containing cotton fiber. The elemental silver was distributed inside of the fiber in a cross‐sectional distribution as confirmed by SEM‐EDS. Furthermore, we fabricated fibers with zeolite particles inside of porous PTFE fibers.     

Dynamical behavior of magnetic polarizable microsphere using whispering gallery mode

In this article, analytical and experimental studies are carried out to investigate the dynamical behavior of polymer microspheres that are doped with magnetic polarizable microparticles. The effect of a static and harmonic inductive magnetic field on the elastic deformation of the microsphere is investigated. The elastic deformation that is induced by the magnetic forces (magnetostrictive effect) acting on the microsphere is measured using an optical technique that is based on the whispering gallery mode (WGM) of the microsphere. The WGMs experience a shift when the morphology of the resonator is perturbed by the elastic deformation. Therefore, the elastic deformation of the microsphere is measured by monitoring the shift of the optical resonances. For these studies, the microsphere has a radius of ∼600 µm and is fabricated by mixing polyvinyl chloride (PVC) with magnetic polarizable microparticles. The microsphere is further coated with a thin layer of pure PVC that serves as a wave‐guide for the optical modes. Experiments are carried out to validate the analysis. Measurements are taken up to a frequency of 200 Hz, showing that the microspheres can be used as magnetic field sensors or as element for the fabrication of smart structures. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 598–603     

A Simple Strategy for Easily Assembling 3D Printed Miniaturized Cells Suitable for Simultaneous Electrochemical and Spectrophotometric Analyses

A rapid and user‐friendly approach is here presented for assembling smart and versatile platforms for simultaneous electrochemical and spectrophotometric measurements. They consist of an optically transparent pencil‐drawn electrochemical cell, including reference, counter and working carbon electrodes, assembled on flexible PVC supports, exploiting a commercial desktop digitally controlled plotter/cutter. This cell is installed on a U shaped 3D printed polylactic frame where a second transparent window consisting of an unmodified PVC layer was also applied. After optimization of the fabrication procedure, the electrochemical and optical characterization of the assembled miniaturized platforms was performed by using aqueous electrolytes and potassium hexacyanoferrate(II) as redox probe. These devices were then tested by a proof‐of‐concept direct and simultaneous electrochemical and spectrophotometric quantification of a commonly used food dye (Brilliant Blue, E‐133) in soft‐drinks and candies. Spectrophotometric and electrochemical determinations can be performed at the same time, providing simultaneous information and enabling a concomitant comparison and validation of the results obtained.     

PVC膜离子选择电极检测下限的优化

价格低廉、携带方便、适用浓度宽、操作简单快捷、能耗低的离子选择电极在医院、分析实验室、野外等领域得到了越来越广泛的应用。尽管如此,由于PVC膜中存在的离子流严重破坏了更低检测下限的获取,限制了离子选择电极的进一步发展。因此,本文从减小甚至消除PVC膜中存在的离子流角度出发,系统论述了优化PVC膜离子选择电极检测下限的原理和优良策略,根据收集归纳的大量数据定量阐述传感膜组成的优化、电极组装和调制、应用旋转电极以及电流极化处理等对检测下限的优化提升作用,进一步总结出各种方法的改善规律,分析它们的优势和面临的问题。提出在PVC铸膜液中要突破传统配方,减小增塑剂和离子交换剂用量,以抑制传感膜两侧的离子流,同时外加电流补偿处理等也是降低电极检测下限的有效方法,对检测下限的改善最好的可降低5个数量级。这一总结为PVC膜离子选择电极的高性能化明确了研究方向。     

Formulation of Composite Resistive Pastes for Micro-Heater Manufacturing

We investigate in this work the formulation of composite resistive pastes based on epoxy resins and graphite for micro-heater manufacturing via thick-film technology. The resistive paste is first screen-printed onto a printed circuit board (PCB) substrate, and then coated with expandable polydimethylsiloxane (PDMS), a composite based on an elastomeric matrix and expandable microspheres, resulting into one-shot thermal actuators allowing pumping and sealing in microfluidic devices. The resistive paste must therefore have controlled properties, such as rheology, resistivity and temperature stability. This paper details the formulation and characterization of suitable epoxy-graphite resistive composites, and the control of their properties through additives.     

Harnessing Light with Photonic Nanowires: Fundamentals and Applications to Quantum Optics

The efficient feeding of spontaneous emission (SE) into a controlled optical mode lies at the heart of a new generation of advanced optoelectronic devices, such as low‐threshold microlasers and bright sources of quantum light. In the solid state, single‐mode emission was first demonstrated by using the Purcell effect that arises in a resonant microcavity. Recently, the need to relax the constraints inherent to such a narrow‐band approach has motivated large effort to develop structures ensuring broadband and efficient SE control. This minireview deals with fiber‐like photonic nanowires, a class of high‐index waveguides that features key assets in this context. Combining theoretical predictions and experimental results, the paper details the SE dynamics in such tiny wires. In addition, it shows how the far‐field emission of a single wire can be tailored through proper engineering of the two wire ends. As an application in the field of quantum optics, we review the realization of an ultrabright single‐photon source. This first device was based on a self‐assembled quantum dot embedded in a wire antenna realized with a top‐down fabrication process. Considering recent advances in the direct growth of tapered photonic wires, we also propose a bottom‐up fabrication route to realize a complete device. In particular, this proposal ensures the optimal 3D positioning of a single emitter inside the antenna. Finally, future research and application prospects are also reviewed.     

Room Temperature Ionic Liquids (RTILs) and Multiwalled Carbon Nanotubes (MWCNTs) as Modifiers for Improvement of Carbon Paste Ion Selective Electrode Response; A Comparison Study with PVC Membrane

Room temperature ionic liquids (RTILs), 1‐n‐butyl‐3‐methylimidazolium tetrafluoroborate, [bmim]BF₄, and multiwalled carbon nanotubes (MWCNTs) were used for improvement of a praseodymium carbon paste ion selective sensor response. [bmim]BF₄ can be a better binder than mineral oils. MWCNTs have a good conductivity which helps the transduction of the signal in carbon paste electrode. The characteristics of these electrodes as potentiometric sensors were evaluated and compared with PVC membrane sensor. The results indicate that potentiometric sensor constructed with ionic liquid shows an increase in performance in terms of Nernstian slope, selectivity, response time, and response stability compared to Pr(III) PVC membrane sensor.     

Dual‐curable fluorinated poly(methacrylate) copolymers for optical adhesives

In pursuit of photo‐curable adhesive for optical communication, dual‐curable acrylic oligomers (AOs) having alkoxy silane group, fluorine atoms and vinyl group as a pendent group were synthesized by two‐stage reactions. The isocyanate group containing oligomers were firstly synthesized via radical polymerization of acrylic monomers, and followed by urethane reaction with 2‐hydroxy ethyl methacrylate. The dual curing behaviors, e.g. thermal and photo‐cure, were studied by using photo‐differential scanning calorimetry (DSC) and real‐time IR. An optimum adhesive formulation, based on AO (15 g), epoxy acrylate (80 g), isobonyl methacrylate (17 g) and photo‐initiator (3 g), was obtained. As the content of AO was increased in the optical adhesive formulation, refractive index decreased but transmittance increased due to the increase in fluorine content. The optical transmittance at the range of 1.3 to 1.55 μm was higher than 90%. The addition of colloidal silica with the earlier mentioned formulation was helpful in decreasing crosslinking volume shrinkage and the increasing of glass fiber adhesion. The required properties for the optical adhesive, including chemical resistance and thermal resistance, dimension stability, etc. were also investigated. Copyright © 2005 John Wiley & Sons, Ltd.     

Application of nanostructure ZnLI2 complex in construction of optical pH sensor

This is for the first time that application of complex nanostructure is reported as pH indicator in PVC matrix. This new optical pH sensor was constructed based on incorporation of ZnLI₂ complex nanostructure in PVC matrix. The synthesized nanostructure ZnLI₂ complex was characterized by SEM and XRD technique. The membrane solution was speared on the glass plate to provide thin film and the membrane surface morphology was investigated via field emission scanning microscope (FE‐SEM) technique. Central composite design (CCD) combined with desirability function (DF) was applied to find the best experimental composition of membrane providing the highest absorbance. These conditions were found in correspondence with 3 mg of pH indicator, 3 mg of ionic additive and 1.5 mg/mg of DBP/PVC weight ratio. Under optimum conditions, the proposed pH sensor has two linear working ranges of 4 ‐ 8 at 393 nm (R² = 0.9897) and 5 ‐ 8 (R² = 0.9982) at 570 nm with response time of 4 min. The pK_a of proposed pH optical sensor was calculated through three methods that found to be 5.63. The present optical sensor shows stability after 2 months without any significant divergence in response properties (less than 5% RSD). Furthermore, current pH optode was exhibited good repeatability (RSD = 1.14%) as well as reproducibility (RSD = 4.06%). No significant variation was observed on sensor response with increasing the ionic strength in the range of 0.0–0.5 M of sodium chloride. All above features indicated that the proposed sensor can be successfully used for detection of pH in solutions with different ionic strength.     

FET‐Based Chemical Sensor Systems Fabricated with Standard Technologies

Miniaturized solid‐state ion sensors based on field‐effect transistors on silicon can take advantage of the capabilities of microelectronics and microsystems technology for the integration of combined functionalities. Optimized solid‐state chemical sensors usually require specific materials and fabrication processes. However, if standard fabrication processes can be used, integrated chemical sensor systems can be developed in a shorter time and in a cost effective way. We show that, for applications in which a long operating time is not required, such as in disposable biomedical sensors, good integrated sensor systems can be fabricated with standard materials and processes. Specific examples are presented, such as multisensor systems, sensors with integrated signal‐processing circuits and sensors with particle manipulation electrodes.     

Tellurite Carbon Paste Sensors: Microscopic Analysis Provides New Insights on the Nature of the Interaction Between the Ionophore and Analytical Species

In this work, scanning electron microscopy (SEM) was used for the characterization of chemically modified carbon paste sensors (CMCPSs), with the aim of understanding their chemical and electrochemical properties. The work also provides a microscopic study on the role of the binder, type of carbon, amount and nature of modifier, composition of the carbon paste and its impact on the electrochemical performance of the sensor. In addition, energy dispersive X‐ray spectroscopy (EDX) was utilized for the direct observation of the interaction between the chemical modifier and the carbon paste. This has enabled the fabrication of new sensitive and selective chemically modified carbon paste sensors that were successfully applied for the detection of tellurite ions in pure solutions, environmental and biological samples. This work provides new insights on the rational design and integration of carbon paste sensors for a variety of applications.