Application of Sodium Ion Sensor Based on the SnO_2/ITO Glass in the Detection of Rinsing Solution for Contact Lenses

This paper presents the studying results of the sodium ion sensor device based on the SnO_2/ITO glass structure in the detection of rinsing solution for contact lenses.The selective membrane contains poly (vinyl chloride) (PVC),bis (2-ethylhexyl) sebacate (DOS),(12-crown-4) methylmalonate (B12C4),and sodium tetrakis (4-fluoropbenyl) borate dehydrate (NaTFBD). The final weight ratios are PVC:DOS:B12C4:NaTFBD=33:66:2:2.In this condition,the sensor has performances with linear sensitivity,short response time,good repeatability and selectivity.The sensor was used to measure the rinsing solution for the contact lenses.Because the experimental results show close to the accurate value for four commercial products,this sensor can preliminary be used in detecting the rinsing solution for the contact lenses.Using this structure and sodium-sensing membrane to construct the sodium sensor is proven successfully in this application.

Electrodeposited Cobalt-Iron Alloy Thin-Film for Potentiometric Hydrogen Phosphate-Ion Sensor

A cobalt-iron alloy thin-film electrode-based electrochemical hydrogen-phosphate-ion sensor was prepared by electrodepositing on an Au-coated Al2O3 substrate from an aqueous solution of metal-salts. The use of a cobalt-iron alloy electrode greatly improved the hydrogen-ion sensor response performance, i.e., the sensor worked stably for more than 7 weeks and showed a quick response time of several seconds. Among the cobalt and iron alloy systems tested, the electrodeposited Co58Fe42 thin-film electrode showed the best EMF response characteristics, i.e., the sensor exhibited a linear potentiometric response to hydrogen-phosphate ion at the concentration range between 1.0 × 10–5 and 1.0 × 10–2 M with the slope of –43 mV/decade at pH 5.0 and at 30℃. A sensing mechanism of the Co-based potentiometric hydrogen-phosphate ion sensor was proposed on the basis of results of instrumental analysis.

Highly Concentrated,Conductive,Defect-free Graphene Ink for Screen-Printed Sensor Application

Conductive inks based on graphene materials have received significant attention for the fabrication of a wide range of printed and flexible devices.However,the application of graphene fillers is limited by their restricted mass production and the low concentration of their suspensions.In this study,a highly concentrated and conductive ink based on defect-free graphene was developed by a scalable fluid dynamics process.A high shear exfoliation and mixing process enabled the production of graphene at a high concentration of 47.5 mg mL^(−1)for graphene ink.The screen-printed graphene conductor exhibits a high electrical conductivity of 1.49×10^(4)S m^(−1)and maintains high conductivity under mechanical bending,compressing,and fatigue tests.Based on the as-prepared graphene ink,a printed electrochemical sodium ion(Na^(+))sensor that shows high potentiometric sensing performance was fabricated.Further,by integrating a wireless electronic module,a prototype Na^(+)-sensing watch is demonstrated for the real-time monitoring of the sodium ion concentration in human sweat during the indoor exercise of a volunteer.The scalable and efficient procedure for the preparation of graphene ink presented in this work is very promising for the low-cost,reproducible,and large-scale printing of flexible and wearable electronic devices.

1-Pyrenecarboxaldehyde thiosemicarbazone:A novel fluorescent molecular sensor towards mercury(Ⅱ) ion

A novel and simple fluorescent molecular sensor,1-pyrenecarboxaldehyde thiosemicarbazone（Hpytsc）,was synthesized.Its higher sensitivity and selectivity to mercury（Ⅱ） ion were studied through absorption and emission channels.The UV-vis spectra show that the increasing mercury（Ⅱ） ion concentrations result in the decreasing absorption intensity.The fluorescence monomer emission of Hpytsc is enhanced upon binding mercury（Ⅱ） ion,which should be due to the 1：1 complex formation between Hpytsc and metal ion.

Two-Dimensional pH Mapping of a Histamine-Stimulated Gastric Mucosa by Using an Ion Image Sensor in the Guinea Pig

In order to examine the hydronium ion （proton）-releasing functions in cells, [pH]out （extracellular pH） was measured using an ion image sensor composed of a 2D （two-dimensional） array of potential sensitive pixels. Using gastric tissues prepared from the stomach, pH distribution was observed during the histamine stimulation. The 2D distribution of [pH]out in the gastric tissues showed clear differences between the mucosal sides and the serous side. Even before the histamine stimulation, the mucosal side of the gastric mucosa showed a slightly lower pH than that of serous side. In the mucosal side, [pH]out decreased after the onset of the stimulation. The ion image sensor was capable of visualizing [pH]out in the gastric tissues. The present chemical-sensing technique realized a label-free microscopic assessment of the 2D distributions of biologically interesting substances, and consequently, [pH] out imaging via chemical microscopy has a future potential in medical fields for endoscopic analysis of gastric ulcers.

An ionic liquid supported CeO_2 nanoparticles-carbon nanotubes composite-enhanced electrochemical DNA-based sensor for the detection of Pb^(2+)

An electrochemical sensor incorporating a signal enhancement for the determination of lead （II） ions （Pb2＋） was designed on the basis of the thrombin-binding aptamer （TBA） as a molecular recog- nition element and ionic liquid supported cerium oxide （CeO2） nanoparticles-carbon nanotubes compo- site modification. The composite comprises nanoparticles CeO2, multi-waU carbon nanotubes （MWNTs） and hydrophobic room temperature ionic liquid （RTIL） 1-ethyl-3-methylimidazolium tetrafluoroborate （EMIMBF4）. The electrochemical sensors were fabricated by immersing the CeOa-MWNTs-EMIMBF4 modified glassy carbon electrode （GCE） into the solution of TBA probe. In the presence of Pb2＋, the TBA probe could form stable G-quartet structure by the specific binding interactions between Pb2＋ and TBA. The TBA-bound Pb2＋ can be electrochemically reduced, which provides a readout signal for quantitative detection of Pb2＋. The reduction peak current is linearly related to the concentration of Pb2＋ from 1.0 ＊ 10-8 M to 1.0 ＊ 105 M with a detection limit of 5 ＊ 109 M. This work demonstrates that the CeOz-MWNTs-EMIMBF4 nanocomposite modified GCE provides a promising platform for immobi- lizing the TBA probe and enhancing the sensitivity of the DNA-based sensors.

Studies on Non-potentiometric Piezoelectric Sensor System for Determination of Vitamin B_1

A piezoelectric sensor responsive to vitamin B 1 was fabricated based on the vitamin B 1 tetraphenylborate ion pair. The general performance characteristics of the sensor are presented here. The proposed sensor showed a wide working pH range, a good sensitivity and selectivity. The response range is between 1 0×10 -7 -4 9×10 -5 mol/L with a detection limit of 8×10 -8 mol/L at pH 4 0. The selectivity should be attributed to the preferential adsorption of the component ion on the membrane/solution interface. The adsorption behavior of vitamin B 1 on the crystal surface was investigated with a quartz crystal impedance(QCI) system.

Chemiluminescence flow Sensor for determination of the Ammonium ion

A novel chemiluminescence (CL) sensor for NH4+ combined with flow injection analysis is presented in this paper. It is based on the inhibition effect of NH4+ on the CL reaction between luminol, immobilized electrostatically on an anion-exchange column, and hypochlorous acid electrogenerated on-line. The sensor responds linearly to NH4+ concentration in 1.0x10(-6)-4.0x10(-9) g/ml range. A complete analysis could be performed in 1 min. The system is stable for 200 determination.

PVC Membrane Selective Electrode for Determination of Cadmium(Ⅱ) Ion in Chocolate Samples

Benzil bis(carbohydrazone)(BBC) is prepared and explored as new N N Schiff's base, which plays the role of an excellent ion carrier in the construction of a Cd(II) ion membrane sensor. The tris(2-ethylhexyl) phosphate best performance corresponds to a membrane composition of 30% poly(vinyl chloride), 65%(TEHP), 3.5% BBC and 1.5% tetradodecyl-ammoniumtetrakis(4-chlorophenyl) borate(ETH 500). This sensor shows very good selectivity and sensitivity towards cadmium ion over a wide variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The effect of membrane composition, selectivity, pH and influence of additive on the response properties of electrode were investigated. The response mechanism was discussed in the view of UV-spectroscopy. The electrode exhibits a Nernstian behavior(with slope of 29.7 mV per decade) over a very wide concentration range from 1.0×10?1 to 1.0×10?8 mol·L?1 with a detection limit of 3.2×10?8 mol·L?1. It shows rela-tively fast response time in whole concentration range(<8 s) and can be used for at least 10 weeks in the pH range of 2.0-9.0. The proposed sensor is successfully used for the determination of cadmium in different chocolate sam-ples and as indicator electrode in titration with ethylene diamine tetraacetate(EDTA).

Thiocyanate Ion Selective Solid Contact Electrode Based on Mn Complex of N,N'-BIs-(4-Phenylazosalicylidene)-O-Phenylene Diamine Ionophore

A thiocyanate ion selective poly(aniline) solid contact electrode based on manganese complex of N,N’-bis-(4-phenylazosalicylidene)-o-phenylene diamine ionophore was successfully developed. The electrode exhibits a good linear response of 58.1 mV/decade (at 20?C ± 0.2?C, r2 = 0.998) with in the concentration range of 1 × 10–1.0 ~ 1 × 10–5.8 M thiocyanate solution. The composition of this electrode was: ionophore 0.040, polyvinylchloride 0.300, dibutylphthalate 0.660 (mass). This dibutylphthalate plasticizer provides the best response characteristics. The electrode shows good selectivity for thiocyanate ion in comparison with any other anions and is suitable for use with aqueous solutions of pH 4.0 ~ 6.0. The standard deviations of the measured emf difference were ±1.70 and ±2.01 mV for thiocyanate sample solutions of 1.0 × 10–2 M and 1.0 × 10–3 M, respectively. The stabilization time was less than 170 sec. and response time was less than 17 sec.

Design and Synthetic Scheme of Water Dispersible Graphene Oxide-Coumarin Complex for Ultra-Sensitive Fluorescence Based Detection of Copper (Cu2+) Ion in Aqueous Environment

Copper oxides and its salts are now widely used as pesticides to control fungal and bacterial diseases of field crops. Copper toxicity is often a major contributor of human health problems caused through accumulation of excess copper ions in various organs via drinking water, fruits and vegetables. So, detection and estimation of cupric ions in biological organs, drinking water, fruits and vegetables are extremely important. Recently, a fluorescence based sensor using coumarin dye (high quantum yield) has been proposed to detect micromolar Cu++ ion in biological organs. But major problem with coumarin dye is that it is insoluble in water and undergoes dye-dye aggregation in organic solvents. We proposed here a synthetic scheme of preparation of graphene oxide conjugated coumarin dye derivative which would be water dispersible and expected to be an ideal candidate for Cu2+ ion estimation in biological organs and drinking water.

Effect of ion-beam assisted deposition on the film stresses of TiO_2 and SiO_2 and stress control

Based on Hartmann-Shack sensor technique, an online thin film stress measuring system was introduced to measure the film stresses of TiO2 and SiO2, and comparison was made between the film stresses prepared respectively by the conventional process and the ion-beam assisted deposition. The effect of ion-beam assisted deposition on the film stresses of TiO2 and SiO2 was investigated in details, and the stress control methodologies using on-line adjustment and film doping were put forward. The results show that the film stress value of TiO2 prepared by ion-beam assisted deposition is 40 MPa lower than that prepared by conventional process, and the stress of TiO2 film changes gradually from tensile stress into compressive stress with increasing ion energy; while the film stress of SiO2 is a tensile stress under ion-beam assisted deposition because of the ion-beam sputtering effect, and the film refractive index decreases with increasing ion energy. A dynamic film stress control can be achieved through in-situ adjustment of the processing parameters based on the online film stress measuring technique, and the intrinsic stress of film can be effectively changed through film doping.

6-(N,N-Dimethylamino)-2-naphthoylacryl Acid:a Highly Selective and Sensitive Fluorescent Sensor of Copper(Ⅱ)

A novel fluorescent probe,6-（N,N-dimethylamino）-2-naphthoylacryl acid（ACADAN） was designed and synthesized as a fluorescent sensor for Cu^2＋ in aqueous media.Significant amplification of fluorescence signals without causing any discernible change of maximum fluorescence emission wavelength（λ max） was observed upon the addition of Cu^2＋.Importantly,ACADAN is capable of recognizing Cu^2＋ selectively in aqueous media in the presence of various biologically relevant metal ions and the prevalent toxic metal ions in the environment with high sensitivity（detection limit was 0.1 μmol/L）.

Porous Silicon as a Carrier of Sensing Materials in Sensors

Novel potassium ion selective electrodes (K^+ISEs) and cDNA array sensors based on porous silicon (PS) have been developed.The calibration curve for the K^+ISEs is linear within a wide range of pK=2.0～6.0 with the slope of 56 mV per decade,which is near Nernst response.The response time and detection limit are within 31 s and 0.5μmol/L,respectively.The selective coefficient for Na^+ is-3.8,satisfies the requirement for the assay of blood potassium.The response variation is within 2 mV during 2 months.The binding capacity,the dynamic range and the detection limit of the DNA sensors were improved by replacing glass slide with PS substrates.The cDNA array sensors can bear 80℃of high temperature,75% of humidity,3.6 kLx of irradiation and keep stable within 10 days when they are exposed in air.Good performances of the K^+ISE and the cDNA array sensor are attributed to the large internal surface area and the easily modified microstructure of PS.

基于QCM的工业废水中重金属检测

锌离子(Zn^(2+))的检测涉及到食品,水土环境,人体病理等多方面人类安全问题,越发受到国内外学者的关注。为方便且准确地检测排放污水中Zn^(2+)是否达标,采用涂覆能够特异性吸附Zn^(2+)的含醚键离子交换树脂薄膜到石英晶体微天平(QCM)电极上,制备了重金属传感器。通过测量QCM的共振频移,研究了传感器的选择特性,检测精度,检测响应时间和重复性。实验结果表明:制备的涂覆含醚键树脂薄膜石英晶体传感器频率随Zn^(2+)的含量变化明显,检测精确度约为95%,可重复多次检测,检测时长适度。该传感器研究成果在重金属实际检测方面中有潜在的应用前景。

氨基化石墨烯电化学传感器在重金属离子检测中的运用分析

本研究旨在探讨氨基化石墨烯电化学传感器在重金属离子检测中的应用,特别是针对Cd^(2+)和Pb^(2+)的检测。研究内容主要包括氨基化石墨烯(NH_(2)-rGO)、壳聚糖(CS)和聚谷氨酸(Glu)复合材料修饰电极的制备,以及其在电化学检测中的性能评估。通过对不同修饰电极的表征与性能分析,本研究揭示了NH_(2)-rGO/CS/Glu复合材料修饰电极在提高检测灵敏度和选择性方面的显著效果。研究结果表明,相比于裸电极和单一材料修饰电极,NH_(2)-rGO/CS/Glu修饰电极对Cd^(2+)和Pb^(2+)展现出了更高的灵敏度和优异的选择性。此项研究为开发新型高效电化学传感器提供了有价值的参考,对于环境监测和重金属污染控制具有重要意义。

ZIF-8封装AuNCs荧光传感器用于铁离子的检测

介绍一个适合于本科教学使用的综合创新实验,设计合成了一种荧光传感器Au NCs@ZIF-8,并将其用于铁离子(Fe^(3+))的检测。MOFs具有高效吸附、聚集检测物的特点,因此选择将Au NCs封装到ZIF-8中,从而实现目标物的定量检测。封装后,由于Au NCs具有AIE特性,所以Au NCs@ZIF-8的荧光强度明显增强。ZIF-8是一种多孔材料,加入Fe^(3+)后,Fe^(3+)能够进入ZIF-8内部,导致Au NCs的荧光被Fe^(3+)猝灭,成功用于实际水样中Fe^(3+)的检测。尽管该实验步骤复杂并涉及新型纳米材料的合成和表征,但它成功地整合了无机化学、分析化学以及材料化学的相关知识,且操作难度适宜。这为提升学生的动手能力和科技前沿理解提供了一次宝贵的机会。