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In the present study, we used two popular radio communication SAW resonators as a base for gas sensors and tested their performance. Taking into account issues related to sensor sensitivity, the possibility of applying a sensor layer, the availability of devices, and other related issues, we selected two popular single-port resonators with center frequencies of 315 and 433 MHz (models R315 and R433, respectively) for testing purposes. Both resonators were equipped with a sensitive film of hexafluoroisopropanol-substituted polydimethylsiloxane, a material that selectively absorbs molecules with a high ability to form basic hydrogen bonds. Fabricated sensors were used to detect trace amounts of dimethyl methylphosphonate (DMMP) vapor, which has often been used in similar studies as a nerve chemical warfare agent simulant. Sensors using both devices loaded with sensor layers of an optimal thickness rapidly reacted to a gas containing DMMP at a concentration of 3 mg/m3, generating a stable analytical signal ranging from several to several dozen kilohertz. In the case of R433, the frequency signal was 20.5 kHz at 1 min from the beginning of exposure to DMMP. The obtained results showed that the used transducers exhibited good performance as a base for gas sensors. Finally, their suitability for sensing applications was confirmed by a comparison with the results obtained in previous similar studies.
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The latest trends in the field of the on-site detection of chemical warfare agents (CWAs) involve increasing the availability of point detectors to enhance the operational awareness of commanders and soldiers. Among the intensively developed concepts aimed at meeting these requirements, wearable detectors, gas analyzers as equipment for micro- and mini-class unmanned aerial vehicles (UAVs), and distributed sensor networks can be mentioned. One of the analytical techniques well suited for use in this field is surface acoustic wave sensors, which can be utilized to construct lightweight, inexpensive, and undemanding gas analyzers for detecting CWAs. This review focuses on the intensively researched and developed variant of this technique, utilizing absorptive sensor layers dedicated for nerve CWAs' detection. The paper describes the mechanism of the specific interaction occurring between the target analyte and the sensing layer, which serves as the foundation for their selective detection. The main section of this paper includes a chronological review of individual achievements in the field, largely based on the peer-reviewed scientific literature dating back to the mid-1980s to the present day. The final section presents conclusions regarding the prospects for the development of this analytical technique in the targeted application.
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A Love-type acoustic wave sensor (AT-cut quartz substrate, SiO2 guiding layer) with a center frequency of approximately 120 MHz was used to detect a simulant of pathogenic botulinum neurotoxin type A-recombinant of BoNT-A light chain-in liquid samples. The sensor was prepared by immobilizing monoclonal antibodies specific for botulinum neurotoxin via a thiol monolayer deposited on a gold substrate. Studies have shown that the sensor enables selective analyte detection within a few minutes. In addition, the sensor can be used several times (regeneration of the sensor is possible using a low pH buffer). Nevertheless, the detectability of the analyte is relatively low compared to other analytical techniques that can be used for rapid detection of botulinum neurotoxin. The obtained results confirm the operation of the proposed sensor and give hope for further development of this label-free technique for detecting botulinum neurotoxin.
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Técnicas Biossensoriais , Dióxido de Silício , Imunoensaio , Anticorpos Monoclonais , SomRESUMO
On-site detection of chemical warfare agents (CWAs) can be performed by various analytical techniques. Devices using well-established techniques such as ion mobility spectrometry, flame photometry, infrared and Raman spectroscopy or mass spectrometry (usually combined with gas chromatography) are quite complex and expensive to purchase and operate. For this reason, other solutions based on analytical techniques well suited to portable devices are still being sought. Analyzers based on simple semiconductor sensors may be a potential alternative to the currently used CWA field detectors. In sensors of this type, the conductivity of the semiconductor layer changes upon interaction with the analyte. Metal oxides (both in the form of polycrystalline powders and various nanostructures), organic semiconductors, carbon nanostructures, silicon and various composites that are a combination of these materials are used as a semiconductor material. The selectivity of a single oxide sensor can be adjusted to specific analytes within certain limits by using the appropriate semiconductor material and sensitizers. This review presents the current state of knowledge and achievements in the field of semiconductor sensors for CWA detection. The article describes the principles of operation of semiconductor sensors, discusses individual solutions used for CWA detection present in the scientific literature and makes a critical comparison of them. The prospects for the development and practical application of this analytical technique in CWA field analysis are also discussed.
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One of the most important methods of measuring the concentration of gaseous oxygen uses its paramagnetic properties, thanks to which oxygen molecules are drawn into the area of a strong magnetic field. This Review presents the current state of knowledge, achievements, and development prospects in the field of magnetic oxygen sensors using this phenomenon. We present the theoretical basis of the physical phenomena used in the paramagnetic oxygen sensors. The principles of operation of individual types of paramagnetic oxygen sensors, including the well-established and widely used magnetoacoustic and magnetopneumatic devices as well as the Pauling cells, are also described. In addition, this Review presents the existing and conceptual innovative sensors known mainly from the scientific and patent literature, including refractometric, interferometric, and ultrasonic sensors. This Review also discusses the advantages and limitations of individual devices, indicating the potential areas of their application.
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Gases , OxigênioRESUMO
On-site detection and initial identification of chemical warfare agents (CWAs) remain difficult despite the many available devices designed for this type of analysis. Devices using well-established analytical techniques such as ion mobility spectrometry, gas chromatography coupled with mass spectrometry, or flame photometry, in addition to unquestionable advantages, also have some limitations (complexity, high unit cost, lack of selectivity). One of the emerging techniques of CWA detection is based on acoustic wave sensors, among which surface acoustic wave (SAW) devices and quartz crystal microbalances (QCM) are of particular importance. These devices allow for the construction of undemanding and affordable gas sensors whose selectivity, sensitivity, and other metrological parameters can be tailored by application of particular coating material. This review article presents the current state of knowledge and achievements in the field of SAW and QCM-based gas sensors used for the detection of blister agents as well as simulants of these substances. The scope of the review covers the detection of blister agents and their simulants only, as in the available literature no similar paper was found, in contrast to the detection of nerve agents. The article includes description of the principles of operation of acoustic wave sensors, a critical review of individual studies and solutions, and discusses development prospects of this analytical technique in the field of blister agent detection.
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Substâncias para a Guerra Química , Agentes Neurotóxicos , Vesícula , Substâncias para a Guerra Química/análise , Humanos , Técnicas de Microbalança de Cristal de Quartzo , SomRESUMO
In this work, the synthesis of a new polysiloxane, poly {dimethylsiloxane-co-[4-(2,3-difluoro-4-hydroxyphenoxy) butyl] methylsiloxane} (dubbed PMFOS), is presented. This polymer exhibits high hydrogen bond acidity and was designed to be used as a sensor layer in gas sensors. The description of the synthetic route of the PMFOS has been divided into two main stages: the synthesis of the functional substituent 4-(but-3-en-1-yloxy)-2,3-difluorophenol, and the post-polymerization functionalization of the polysiloxane chain (methylhydrosiloxane-dimethylsiloxane copolymer) via hydrosilylation. The synthesized material was subjected to instrumental analysis, which confirmed its structure. The performed thermal analysis made it possible to determine some properties important for the sensor application, such as glass transition temperature and decomposition temperature. The results showed that PMFOS meets the requirements for materials intended for use in gas sensors based on acoustoelectric transducers.
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The paper presents the results of inverse gas chromatographic (IGC) research on two novel polysiloxanes: poly{dimethylsiloxane-co -[4-(2,3-difluoro-4-hydroxyphenoxy)butyl]methylsiloxane} and poly{dimethylsiloxane-co -[4-(4-hydroxyphenoxy)butyl]methylsiloxane}, dubbed PMFOS and PMOS respectively, designed for use as chemosensitive coatings for acoustoelectronic sensors. These materials contain phenolic functional substituents that differ by the presence of fluorine atoms. The materials' solvation properties were identified by IGC with application of an LSER solvation model at temperatures ranging from 40 to 120⯰C. In the case of both polysiloxanes, the research revealed that the dominant type of intermolecular interaction was the formation of acidic hydrogen bonds. The material with fluorine-activated hydroxyl groups, PMFOS, is much more acidic and less basic than the other one and thus more interesting. According to LSER, PMFOS exhibits high affinity and selectivity to hydrogen bond bases. In addition, the material retains its properties even at a temperature of 120⯰C.
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Fenóis , Siloxanas , Cromatografia Gasosa , Ligação de Hidrogênio , TemperaturaRESUMO
Electron capture detectors (ECDs) and detectors used in ion mobility spectrometry (IMS) have been successfully used for the detection of numerous compounds including hazardous substances. The general principles of their operations are similar and based on sample component ionization and measurement of the signal using the differences in the mobility of electric charge carriers. Differences in sensitivity result from various parameters of these instruments. Value of electric field intensity in ionic reactors have an influence on ionization process. The main goal of the performed tests was to compare the analytical properties of ECD and two types of IMS detectors: a drift tube spectrometer (DT IMS) and a differential mobility spectrometer (DMS). In the work performed, the efficiency of ionization and the response of detectors to selected analytes were compared. ECD, DT IMS and DMS were equipped with 63-Ni radioactive sources. Analytes have been ionized via electron capture process or dissociative electron transfer. Results obtained for oxygen and chloro-substituted organic compounds (carbon tetrachloride, benzyl chloride, chloroform, 2-chloroethyl ethyl sulfide) were used to calculate the relative signal and to compare the ionization efficiency for three detectors. The phenomena observed experimentally were related to energy dependencies and electron capture cross-sections of analytes. The efficiency of ionization in DT IMS was also compared for electron capture when nitrogen was used as the carrier gas, and when the ionization process was based on the collisions of the analyte molecules with the O2- with the use of air.
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We report on the absorption measurements of the liquid-filled pure-silica microstructured optical fibers. The measurements concentrate on spectroscopic analysis of the water solutions of a cationic dye, oxazine 725 perchlorate which, when filling the fiber, demonstrates much stronger absorption signals than observed in bulk with regular cuvettes. The effect is also seen in another cationic dye, but not in anionic dyes. Our investigations reveal that the effect originates from the adsorption of the dye molecules on the fiber inner walls. This effect also significantly enhances the sensitivity of spectroscopic measurements enabling the detection of molecules at very low concentrations. In particular, the detection of a 1 nM concentration of oxazine 725 perchlorate was demonstrated.
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We report a novel fiber-optic sensing architecture for the detection of paramagnetic gases. By interacting a modulated magnetic field with guided light within a microstructured optical fiber, it is possible to exploit Faraday Rotation Spectroscopy (FRS) within unprecedentedly small sample volumes. This approach, which utilizes magnetic circular birefringence and magnetic circular dichroism effects, is applied to a photonic bandgap fiber to detect molecular oxygen and operates at a wavelength of 762.309 nm. The optical fiber sensor has a 4.2 nL detection volume and 14.8 cm long sensing region. The observed FRS spectra are compared with a theoretical model that provides a first understanding of guided-mode FRS signals. This FRS guided-wave sensor offers the prospect of new compact sensing schemes.