Ultrasensitive polyaniline-nickel oxide cladding modified with urease immobilized intrinsic optical fiber urea biosensor

Herein, we report a polyaniline-nickel oxide (PANI-NiO) nanocomposite as an efficient immobilization matrix for development the optical fiber urea biosensor. Optical fiber sensing probe was developed by removing some portion of optical fiber at middle and modified with PANI-NiO matrix. After the modification of cladding removed portion, it was immobilized with enzyme urease via glutaraldehyde as a bi-functional cross-linking agent. The physicochemical and optical properties of the PANI-NiO matrix were explored by X-ray diffraction, scanning electron microscopy, ultraviolet–visible, and Fourier transform infrared spectroscopic techniques. The characteristic features and performance of the developed sensor were evaluated via recording the output power and modal power distribution by means of a charge-coupled device camera. The developed urea biosensor exhibits a selective response towards urea concentrations in the linear range 1 nM–100 mM with a lower detection limit of 1 nM. Sensor recorded as a 40 days stability and response time ~1 min. Thus, the obtained experimental results of the developed sensor promote its applicability with practical prospects in diverse field.     

基于石墨烯光子晶体光纤的流体传感器

与传统的传感器设备阵列相比,由于结构更为简单,具有广泛检测兼容性的光纤系统逐渐成为分布式监测的有力候选者。然而,受工作机制的限制,大多数光纤传感器仍局限于对折射率等物理参数进行探测,一种用于环境化学监测的全光纤分布式传感系统亟待研发。本工作中,我们向化学气相沉积法生长的石墨烯光子晶体光纤(Gr-PCF)中引入了一种化学传感机制。初步结果表明,石墨烯光子晶体光纤可以选择性地检测浓度为ppb级的二氧化氮气体,并在液体中表现出离子敏感性。石墨烯光子晶体光纤与光纤通信系统的波分、时分复用技术结合后,将为实现分布式光学传感环境问题提供巨大的潜力和机会。     

Fiber-optic evanescent-field laser sensor for in-situ gas diagnostics

A compact, rugged and portable fiber-optic evanescent-field laser sensor is developed for the detection of gaseous species in harsh environments such as volcano fumaroles or industrial combustion of glass furnaces. The sensor consists of an optical multi-mode fused silica fiber with jacket and cladding removed and the bare fiber core in direct contact with the surrounding molecules. The beam of a single-mode DFB diode laser with an emission wavelength centered at 1.5705 microm is coupled into the fiber. At the other end of the fiber an infrared detector is used to record the transmitted infrared laser light intensity. Due to the frustrated total reflection (FTR) and the attenuated total reflection (ATR) the laser intensity is attenuated when passing through the fiber. The FTR is related to a change of the index of refraction while the latter one is related to a change of the absorption coefficient. While tuning the DFB laser wavelength across absorption lines of molecules surrounding the fiber a spectral intensity profile is measured. Voigt functions are fitted to the recorded intensity profiles to estimate relative molecule concentrations. In this paper results from first field measurements at the volcano site 'Solfatara' in Italy are reported that use such a sensor device for simultaneous detection of H2S, CO2 and H2O directly in the gas stream of a volcano fumarole.     

All-fiber-coupled laser-induced breakdown spectroscopy sensor for hazardous materials analysis

An all-fiber-coupled laser-induced breakdown spectroscopy (LIBS) sensor device is developed. A passively Q-switched Cr⁴⁺Nd³⁺:YAG microchip laser is amplified within an Yb fiber amplifier, thus generating high power laser pulses (pulse energy E_p = 0.8 mJ, wavelength λ = 1064 nm, repetition rate f_rep. = 5 kHz, pulse duration t_p = 1.2 ns). A passive (LMA) optical fiber is spliced to the active fiber of an Yb fiber amplifier for direct guiding of high power laser pulses to the sensor tip. In front of the sensor a plasma is generated on the surface to be analyzed. The plasma emission is collected by a set of optical fibers also integrated into the sensor tip. The spectrally resolved LIBS spectra are processed by application of principal component analysis (PCA) and analyzed together with the time-resolved spectra with neural networks. Such procedure allows accurate analysis of samples by LIBS even for materials with similar atomic composition. The system has been tested successfully during field measurements at the German Armed Forces test facility at Oberjettenberg.

The LIBS sensor is not restricted to anti-personnel mine detection but has also the potential to be suitable for analysis of bulk explosives and surface contaminations with explosives, e.g. for the detection of improvised explosive devices (IEDs).     

Development of an Optical Fiber Lactate Sensor

Lactate analysis is important in clinical diagnostics and the food industry. An ultrasensitive optical fiber lactate sensor with rapid response time and 50?μm size has been developed. Lactate dehydrogenase (LDH) has been directly immobilized onto an optical fiber probe surface through covalent binding mechanisms. The optical fiber surface is initially activated by silanization, which adds amine groups (–NH₂) to the surface. Aldehyde functional groups (–CHO) are then affixed to the optical fiber surface by employing a bifunctional cross-linking agent, glutaraldehyde. The amino acids of LDH enzyme molecules readily attach to these free -CHO groups on the fiber surface. Optimal immobilization of LDH occurs between 19 and 23 hours of exposure in the enzyme solution. The immobilized LDH enzyme molecules on the fiber surface show high enzymatic activity. The lactate sensor is able to detect lactate with a concentration detection limit of 0.5?μM and the absolute mass detection limit is 8.75 attomoles. Moreover, the sensor rapidly responds to lactate changes and exhibits good reproducibility. The lactate sensor is extremely selective. This immobilized enzyme sensor has been applied to accurately determine the lactate content in food samples.     

A fiber-optic absorption cell for remote determination of copper in industrial electroplating baths

A device for remote optical sensing is developed and evaluated for monitoring the concentration of copper(II) ions in an industrial plating bath. The sensor consists of an absorption cell which resides in the plating bath, and utilizes fiber optics to direct light into and out of the cell. The sensor is capable of being located in harsh environments for extended periods of time (on the order of weeks to years) and thus is ideal for long-term monitoring applications. The light source and detection electronics can be maintained in a controlled environment and can be multiplexed to several sensors of similar design, if desired. The sensor constructed operates by measuring the copper(II) absorbance with a near-infrared light-emitting diode (820 nm) as the light source. The device is capable of measuring copper(II) ion concentrations from 50 mM to 500 mM with relative standard deviations less than 1%. The construction and operation of the sensor are described and the effects of various interferences found in plating baths are evaluated, including those from temperature variations and variations in the concentrations of concomitant species in the plating bath. Also, drift compensation and noise sources are considered, with an evaluation of the long-term stability of the sensor and the feasibility of its use in an industrial environment.     

Photochemical modification of an optical fiber tip with a silver nanoparticle film: a SERS chemical sensor

We present a method of photochemical modification of an optical fiber tip with a silver nanoparticle film. The deposited silver nanoparticle film displays alternating light and dark circles, which are similar to a radial diffraction pattern. The modified optical fiber is examined as a chemical sensor for in situ detection. The modified fibers show excellent SERS activity, a low limit of detection (LOD), and good reproducibility. The maximum SERS activity of the sensor was achieved within 5.0 min of deposition. Thus, the method is also quite rapid.     

Theoretical and practical response evaluation of a fiber optic sensor for chlorinated hydrocarbons in water

The response behavior of a polymer-coated mid-infrared fiber optical sensor for chlorinated hydrocarbons in water is evaluated practically and theoretically. The sensor response to the target analytes tri- and tetrachloroethylene obtained in a muddy waste water sample is shown to be unaffected by other trace organic pollutants. A theoretical model is presented which can be used to predict the response of this sensing device. The use of this model allows to simulate the sensor response not only for increasing chlorinated hydrocarbon concentrations, but rather for any change in its concentration in the surrounding medium. In addition, the asymmetric sensor response, depending on the direction of the concentration change and the lag time after a concentration change can be explained by digital simulations and are shown to occur due to diffusion processes in the membrane.     

Portable fiber-optic immunosensor for detection of methsulfuron methyl

This fiber optic sensor, based on competitive immunoreactions between coating-haptens and free haptens in solutions with corresponding antibodies, was developed to determine the concentration of the free hapten, methsulfuron-methyl. The ovalbumin (OVA)-methsulfuron-methyl conjugate was immobilized on a microscope slide. Horseradish peroxidase (HRP) labeled goat anti-rabbit IgG was used to generate an optical signal. The portable optical device consisted of a 0.25-W tungsten-halogen light source and a photosensitive diode detector. A typical competitive-binding calibration curve was seen between 0.3 and 100 ng/ml of methsulfuron-methyl. The detection limit for methsulfuron-methyl was 0.1 ng/ml.     

Mixed C18 and C1 modification on an optical fiber for chromatographic sensing

An optical fiber-chromatographic sensor, aiming at simultaneous and selective response to multiple components following a chromatographic separation, is described. We report an improved approach for immobilization of octadecyl (C(18)) and methyl (C(1)) moieties as stationary phase on an optical fiber suitable as a sensing phase for organic solutes. By this approach, the stability and lifetime of the sensing layer as well as the detectability and retention behavior of the chromatographic sensor could be improved. Infrared spectroscopy was employed to confirm the presence of C(18) and C(1) moieties on the modified surface of the optical fiber. The chromatographic sensor was applied, with good sensitivity and chemical selectivity, to the simultaneous separation and detection of bromobenzene and toluene, using water as the mobile phase.     

Characterization of Optical Fiber Dissolved Oxygen Sensor for Aquaculture Sensing and Monitoring

Optical fiber sensor using sol gel membrane incorporated RTV silicon rubber was fabricated and developed for the characterization of dissolved oxygen in aqueous solution. The sol gel materials used consists of Tetraethylorthosilicate (TEOS) and Triethoxyoctylsilane (Octyl-triEOS) as the precursor compound for the preparation of the sol gel structures, while tris-BP Ruthenium (II) chloride as the fluorescent lifetime of the oxygen indicator. Dip coating techniques is utilized to position the sol gel technology at the distal end of the optical fiber. Dissolved oxygen gas sensor characterizations include a study on the sensitivity, temperature effects and drift rate of the sensor performance when measured in 40ppt salt water. Potential applications of the optical fiber sensor are including aquaculture, river monitoring and environment sector.     

一种新的基于折射率变化的光纤化学传感器

在光纤化学传感器中,基于样品折射率变化的传感器是其中的重要分支,并获得了广泛的实际应用^[1].根据敏感部件的不同可将其分为两大类:一类的敏感部件是裸光纤,这类传感器已用于检测苯、甲醇和丙酮^[2],测定血样中葡萄糖浓度^[3],鉴定燃油质量.     

Vapor zone velocities measurement using a capillary optical fiber sensor with an application to gas chromatography

A fiber optic sensor has been used for real-time measurement of the migration rates of all the compounds in a mixture separated by gas chromatography. The sensor makes use of a coated capillary optical fiber as the column. This new type of waveguide consists in a polarization-maintaining optical core positioned close to the capillary edge along the entire fiber length. The optical detection is performed through the coupling of the two polarization modes of the waveguide and this coupling is detected by a polarimetric interferometry technique. Through some signal processing, the resulting interferogram provides the migration rates of the various compounds of a gas mixture flowing in the capillary. One of the major benefits of this optical migration rate sensing is that the detection of each velocity peak appears as soon as the analyte enters the capillary fiber and the peaks are constantly measured during the whole separation process. Carrier gas acceleration occurring in the column is plainly demonstrated. This paper presents a proof-of-concept on a qualitative basis. The experiments were done at 29 °C because the current opto-fluidic set-up cannot withstand a higher temperature.     

大型仪器功能开发(151~159)瓦里安300XP离子注入机改造及功能开发

在完全掌握瓦里安300XP离子注入机各部件的工作原理后, 将原离子源供电系统中500 W电流源和450 W起弧电源升级为1 500 W电流源和1 500 W起弧电源, 并集成到当前系统中.将现有不稳定的气体流量、离子源电源、分析器、源磁场和吸极高压塑料光纤隔离控制线路, 升级成多通道光纤通讯光端机隔离控制系统.将一个10 cm进样终端改造成15 cm的样品卡盘, 并开发了一套独立控制剂量监测系统.改造后, 硼最大束流超过150 μA, 且可调节. 15 cm圆片的片内及片间电阻不均匀性小于3.5%.利用大束流硼离子注入制备浓硼掺杂单晶硅结构层, 应用到微电子机械系统压力传感器、热电器件以及纳米谐振子器件中.     

Fiber-optic dual Fabry-Pérot interferometric carbon monoxide sensor with polyaniline/Co3O4/graphene oxide sensing membrane

An optical fiber dual Fabry-Pérot interferometric carbon monoxide gas sensor based on PANI/Co₃O₄/GO (PCG) sensing membrane coated on the end face of the optical fiber is proposed and fabricated. One end face of photonic crystal fiber (PCF) without cut-off wavelength is fused with a single-mode fiber (SMF), and the other end face of the PCF is coated with PCG sensing membrane. The collapsed layer formed during the air hole fusion of PCF is used as the first reflector, the interface between PCF and sensing membrane is used as the second reflector, and the interface between the sensing membrane and the air is used as the third reflector, thus the dual Fabry-Pérot structure sensor is formed. The results show that the sensor has excellent sensitivity and selectivity to carbon monoxide. With the increasing concentration of carbon monoxide gas in the range of 0−60 ppm, the intensity of interference spectrum decreases. The sensitivity of the sensor is 0.3473 dB m/ppm, and its linearity is good. The response time and recovery time are 68 s and 106 s, respectively. The sensor has the advantages of the compact size, low cost, high sensitivity, strong selectivity and simple structure. It is suitable for the sensing detection of low concentration carbon monoxide gas.     

Compact fluorescence detection using in-fiber microchannels-its potential for lab-on-a-chip applications

This paper reports a compact and practical fluorescence sensor using an in-fiber microchannel. A blue LED, a multimode PMMA or silica fiber and a mini-PMT were used as an excitation source, a light guide and a fluorescence detector, respectively. Microfluidic channels of 100 microm width and 210 microm depth were fabricated in the optical fibers using a direct-write CO(2) laser system. The experimental results show that the sensor has high sensitivity, able to detect 0.005 microg L(-1) of fluorescein in the PBS solution, and the results are reproducible. The results also show that the silica fiber sensor has better sensitivity than that of the PMMA fiber sensor. This could be due to the fouling effect of the frosty layer formed at the microchannel made within the PMMA fiber. It is believed that this fiber sensor has the potential to be integrated into microfluidic chips for lab-on-a-chip applications.     

An optical reflected device using a molecularly imprinted polymer film sensor

A novel and highly selective optical sensor with molecularly imprinted polymer (MIP) film was fabricated and investigated. The optical sensor head employing a medium finesse molecularly imprinted polymer film has been fabricated and characterised. A blank polymer and formaldehyde imprinted polymer were using methacrylic acid as the functional monomer and the ethylene glycol dimethacrylate as a crosslinker. The transduction mechanism is discussed based on the changes of optical intensity of molecularly imprinted polymer film acting as an optical reflected sensor. Template molecules, which diffused into MIP, could cause film density, and refractive index change, and then induce measurable optical reflective intensity shifts. Based on the reflective intensity shifts, an optical reflection detection of formaldehyde was achieved by illuminating MIP with a laser beam. For the same MIP, the reflective intensity shift was proportional to the amount of template molecule. This optical sensor, based on an artificial recognition system, demonstrates long-time stability and resistance to harsh chemical environments. As the research moves forward gradually, we establish the possibilities of quantitative analysis primly, setting the groundwork to the synthesis of the molecular imprinted optical fiber sensor. The techniques show good reproducibility and sensitivity and will be of significant interest to the MIPcommunity.     

Gas chromatographic sensing on an optical fiber by mode-filtered light detection

A chemical sensor for gas phase measurements is reported which combines the principles of chemical separation and fiber optic detection. The analyzer incorporates an annular column Chromatographic sensor, constructed by inserting a polymer-clad optical fiber into a silica capillary. Light from a helium-neon laser is launched down the fiber, producing a steady intensity distribution within the fiber, but a low background of scattered light. When sample vapor is introduced to the sensor, and an analyte-rich volume interacts with the polymer cladding, Chromatographic retention is observed simultaneously with a change in the local refractive index of the cladding. An increase in cladding refractive index (RI) causes light to be coupled out of the fiber, with detection at a right-angle to the annular column length to provide optimum S/N ratio. This detection mechanism is called mode-filtered light detection. We report a gas Chromatographic separation on a 3.1 m annular column (320 microm i.d. silica tube, 228 microm o.d. fiber with a 12 microm fluorinated silicone clad) of methane, benzene, butanone and chlorobenzene in 6 min. The annular column length was reduced to 22 cm to function as a sensor, with selected organic vapors exhibiting unique retention times and detection selectivity. The detection selectivity is determined by the analyte RI and the partition coefficient into the cladding. The calculated limit of detection (LOD) for benzene vapor is 0.03% by volume in nitrogen, and several chlorinated species had LOD values less than 1%. For binary mixtures of organic vapors, the detected response appears to be the linear combination of the two organic standards, suggesting that the annular column may be useful as a general approach for designing chemical sensors that incorporate separation and optical detection principles simultaneously.     

Fiber optic evanescent field sensors for gaseous species using MIR transparent fibers

A new method of optical gas sensing is presented which uses evanescent waves of optical fibers. Gas detection can be done in a simple, flexible, and possibly distributed way using a single optical fiber as both the sensor with an active element of 10 cm and the transmission line for optical signals. The detection of several single gaseous species — such as hexane, trichloro-trifluoro-ethane, methane, acetone, etc. — as well as gaseous mixtures in a concentration range of 1–10% could be achieved with an average reproducibility of 2–3% with a chalcogenide fiber optic coupled to an IFS 88 Bruker spectrometer.