基于定向纳米碳管气体放电的气敏传感器研究

介绍了一种基于定向纳米碳管的气敏传感器,以生长定向纳米碳管的氧化铝模板作为阳极,铝板作为阴极,利用纳米碳管的尖端发射效应,在较低的电压下使气体产生放电现象。通过对纳米碳管在气体中击穿电压和放电电流的测量,实现对气体的定性定量检测。同时纳米碳管气敏传感器还具有体积小、灵敏度高、稳定性好、响应速度快、在常温常压下即可进行检测等优点,具有较好的应用前景。     

溴化四-(4-N,N,N-二甲基,正庚烷基氨基苯基)卟啉钴的合成,L-B膜及其气敏、湿敏特性

卟啉和酞菁是一类大环共轭化合物,由于其结构和性能以及在生命科学中所起的作用,使得用L-B膜技术研究其结构和功能越来越引起人们的重视.自从Jones等发现原卟啉L-B膜具有较好的光导性以来,卟啉L-B膜的电导性和气体敏感特性相继有人进行过研究。发现卟啉铜L-B膜对二氧化氮有很高的敏感性,而且有良好的选择性.人工合成的     

The physical properties of pressure sensitive rubber composites

Nitrile butadiene rubber, NBR, structural foam of different apparent densities was obtained by using different concentrations of foaming agent, azodicarbonamide, ADC/K. The true stress-strain characteristics, in case of compression, of foamed samples after the application of cyclic stress-strain were measured. The effect of the cyclic stress-strain on strain energy density of ADC/K foaming agent-filled NBR rubber composites was studied. The mechanical parameters were found to depend on the foaming agent concentration and on the pre-cyclic fatigue number. Results also indicated that the strain energy decreased with filler concentration.The effects of the cyclic stress-strain on the conductivity of ADC/K foaming agent-filled NBR rubber composites were studied. The electrical properties were found to depend on the foaming agent concentration, the strain amplitude and the number of stress-strain cycles of pre-strain. This study was assisted by the current-voltage characteristics which were measured under the effect of different compression ratios: 0%, 5%, 10%, 15%, 20%, 25% and 30%. The free current carrier mobility and the equilibrium concentration of charge carriers in the conduction band were produced as functions of compressive strain. Results also indicate that there is a linear variation between pressure and conductivity for all samples, which means that these samples can be used as a pressure sensor.     

Analysis of sorption and bioavailability of different species of mercury on model soil components using XAS techniques and sensor bacteria

The present work studies the adsorption behaviour of mercury species on different soil components (montmorillonite, kaolinite and humic acid) spiked with CH₃HgCl and CH₃HgOH at different pH values, by using XAS techniques and bacterial mercury sensors in order to evaluate the availability of methyl mercury on soil components. The study details and discusses different aspects of the adsorption process, including sample preparation (with analysis of adsorbed methyl mercury by ICP-OES), the various adsorption conditions, and the characterization of spiked samples by XAS techniques performed at two synchrotron facilities (ESRF in Grenoble, France and HASYLAB in Hamburg, Germany), as well as bioavailability studies using mercury-specific sensor bacteria. Results show that XAS is a valuable qualitative technique that can be used to identify the bonding character of the Hg in mercury environment. The amount of methyl in mercury adsorbed to montmorillonite was pH-dependent while for all soil components studied, the bond character was not affected by pH. On the other hand, clays exhibited more ionic bonding character than humic acids did with methyl mercury. This interaction has a higher covalent character and so it is more stable for CH₃HgOH than for CH₃HgCl, due to the higher reactivity of the hydroxyl group arising from the possible formation of hydrogen bonds.The bioavailability of methyl mercury adsorbed to montmorillonite, kaolinite and humic acids was measured using recombinant luminescent sensor bacterium Escherichia coli MC1061 (pmerBR_BSluc). In case of contact exposure (suspension assays), the results showed that the bioavailability was higher than it was for exposure to particle-free extracts prepared from these suspensions. The highest bioavailability of methyl mercury was found in suspensions of montmorillonite (about 50% of the total amount), while the bioavailabilities of kaolinite and humic acids were five times lower (about 10%). The behaviour of methyl mercury in the presence of montmorillonite could be explained by the more ionic bonding character of this system, in contrast to the more covalent bonding character observed for humic acids. Thus, XAS techniques seem to provide promising tools for investigating the mechanisms behind the observed bioavailabilities of metals in various environmental matrices, an important topic in environmental toxicology.     

A highly selective fluorescent sensor for Cu based on 2-(2′-hydroxyphenyl)benzoxazole in a poly(vinyl chloride) matrix

This paper describes a copper selective optical chemical sensor based on static quenching of the fluorescence of 2-(2′-hydroxyphenyl)benzoxazole entrapped in a poly(vinyl chloride) (PVC) membrane. The effect of the composition of the sensing membrane was studied, and experimental conditions were optimized. The sensors exhibit stable response over the concentration range from 4.0 × 10⁻⁸ M to 5.0 × 10⁻⁵ M Cu²⁺ at pH 4.0-6.5, and a high selectivity. The response time for Cu²⁺ with concentration ≤5 × 10⁻⁶ M is less than 7 min. The optode can be regenerated using 0.1 M HCl and acetate buffer solution. The sensor has been used for direct measurement of copper content in river water samples with a relative error less than 4% with reference to that obtained by atomic absorption spectrometry.     

Calibration coefficient of a heat-flow DSC; Part II. Optimal calibration procedure

One-point (Mettler) and many-point (Netzsch) heat flow calibration of a DSC is discussed. It is shown that the two types of calibration are the alternative extremes between quick but rough procedure and time-consuming but accurate one. One-point calibration compares a typical function k(T) at the melting point of indium with the measured value for particular DSC and multiplies k(T) by a scaling factor. Many-point calibration is based on general mathematical procedure, namely fitting a set of experimental values of sensitivity to a polynomial. The polynomial coefficients are evaluated by the method of least squares. Based on the relationship between the sensitivity of a thermocouple and calibration coefficient of a DSC sensor made from it, two-point heat flow calibration is suggested. This is an optimal calibration procedure, for the relationship contains only two unknown coefficients. An example of how to perform the two-point calibration with Netzsch-Proteus Software is described in the Appendix.     

Solid-state pH nanoelectrode based on polyaniline thin film electrodeposited onto ion-beam etched carbon fiber

An ultramicro pH sensor has been constructed based on a thin polyaniline film that was electrochemically deposited onto a carbon fiber nanometer-size electrode. The substrate nanoelectrodes were fabricated using ion-beam conically etched carbon fibers with tip diameters ranging ca. from 100 to 500 nm. The polyaniline film was deposited from HCl solution containing the aniline monomer by cycling the potential between −0.2 and +1.0 V. The electromotive force (emf) signal between the pH sensitive polyaniline-coated nanoelectrode and an Ag/AgCl reference electrode was linear over the pH range of 2.0-12.5 with a slightly super-Nernstian slope of ca. −60 mV/pH unit. Response times ranged from several sec at pHs around 7 up to 2 min at pH 12.5. The proposed pH nanoelectrode displayed high ion selectivity with respect to K⁺, Na⁺, Ca²⁺, and Li⁺, with log K_H,M values around −12 and has a working lifetime of about 20 days. Key parameters important for the pH nanoelectrode performance, including polyaniline film preparation, selectivity, response time, temperature dependence, relative coating thickness, stability, and reproducibility, have been characterized and optimized. The performance of the pH nanoelectrode was examined by measuring the pH of several real samples including body fluids (serum, urine) and low ionic strength water samples (rain, deionized and tap water). The results agreed very well with those obtained by using commercial glass pH electrodes. The proposed pH nanoelectrode demonstrated attractive properties and seems particularly promising for use under physiological conditions.     

Ionic Liquids Modify the Performance of Carbon Based Potentiometric Sensors

A new type of potentiometric sensor based on a recently constructed carbon ionic liquid electrode (CILE) is described. Two kinds of ionic liquids, i.e., N‐octylpyridinium hexafluorophosphate (OPFP) and 1‐butyl‐3‐methylimidazoluim hexafluorophosphate (BMFP) were tested as binder for construction of the carbon composite electrode. The characteristics of these electrodes as potentiometric sensors were evaluated and compared with those of the traditional carbon paste electrode (CPE). The results indicate that potentiometric sensors constructed with ionic liquid show an increase in performance in terms of Nernstian slope, selectivity, response time, and response stability compared to CPE.     

Comparison of Methionine α,γ‐Lyase and Homocysteine α,γ‐Lyase for Electrochemical Determination of Homocysteine

Recently, a novel enzymatic method was developed for determination of homocysteine. This method utilizes the electrochemical hydrogen sulfide sensor along with methionine α,γ‐lyase to accomplish the fast, accurate, sensitive and selective measurements. As a continuation of this work, another enzyme, homocysteine α,γ‐lyase, was used and the parallel experiments of using both enzymes were carried out against the effect of pH, sensitivity, linearity, and interferences, in an intended comparison between these two enzymes. The excellent linearity of amperometric currents against homocysteine concentrations, high sensitivities and low detection limits for both enzymes reconfirmed that the electrochemical method is superior over other analytical means. The high enzymatic activity of methionine α,γ‐lyase surpassing homocysteine α,γ‐lyase endowed the former higher sensitivity, lower detection limit and faster response than the latter, suggesting methionine α,γ‐lyase a better candidate for homocysteine measurement by electrochemical method. The differences between these two enzymes on the trends of response time and sensitivity at different pH environments, reactivity toward several forms of homocysteine as well as on the interference from several agents were also addressed and discussed.     

Comparative Studies of Tridentate Sulfur and Nitrogen‐Containing Ligands as Ionophores for Construction of Cadmium Ion‐Selective Membrane Sensors

New polymeric membrane cadmium‐ion selective sensors have been prepared by incorporating nitrogen and sulfur containing tridentate ligands as the ionophores into the plasticized PVC membranes. Poly(vinyl chloride) (PVC) based membranes of potassium hydrotris[N‐(2,6‐xylyl)thioimdazolyl) borate] (KTt^2,6‐xylyl) and potassium hydrotris(3‐phenyl‐5‐methylpyrazolyl) borate (KTp^Ph,Me) with sodium tetraphenyl borate (NaTPB) as an anionic excluder and dibutylphthalate (DBP), tributylphthalate (TBP), dioctylsebacate (DOS), and o‐nitrophenyloctyl ether (o‐NPOE) as plasticizing solvent mediators were investigated in different compositions. KTt^2,6‐xylyl was found to be a selective and sensitive ion carrier for Cd(II) membrane sensor. A membrane composed of KTt^2,6‐xylyl:NaTPB:PVC:DBP with the % mole ratio 2.3 : 1.1 : 34.8 : 61.8 (w/w) works well over a very wide concentration range (7.8×10^?8–1.0×10^?2 M) with a Nernstian slope of 29.4±0.2 mV/decades of activity between pH values of 3.5 to 9.0 with a detection limit of 4.37×10^?8 M. The sensor displays very good discrimination toward Cd(II) ions with regard to most common cations. The proposed sensor shows a short response time for whole concentration range (ca. 8 s). The effects of the cationic (tetrabutylammonium chloride, TBC), anionic (sodium dodecyl sulfate, SDS) and nonionic (Triton X‐100) surfactants were investigated on the potentiometric properties of proposed cadmium‐selective sensor. The proposed sensor based on KTt^2,6‐xylyl ionophore has also been used for the direct determination of cadmium ions in different water samples and human urine samples.