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Polymers Based Sensors

A special issue of Sensors (ISSN 1424-8220). This special issue belongs to the section "Chemical Sensors".

Deadline for manuscript submissions: closed (15 September 2019) | Viewed by 13603

Special Issue Editors


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Guest Editor
Polymer Research Group, Faculty of Science, University of Burgos, 09001 Burgos, Spain
Interests: polymers; polymer sensors; high performance polymers; polymers for advanced applications; design and synthesis of advanced polymers; monomers; monomer synthesis; chemical sensors; supramolecular chemistry
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Polymer Research Group, Faculty of Science, University of Burgos, 09001 Burgos, Spain
Interests: polymers; micro and nanocellular polymers; design, synthesis and characterization of high performance polymers; nanoporous sensory polymers; polymer foaming processes
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Polymer Research Group, Faculty of Science, University of Burgos, 09001 Burgos, Spain
Interests: polymers; polymer sensors; high performance aramids; design, synthesis and characterization of polymers; polymers for advanced applications
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The development of supramolecular chemistry by Pedersen, Cram, and Lehn in the 1960s brought forth the growth of a new research field called chemical sensors or chemosensors. These molecules present a receptor which provides information about the chemical composition of its environment through selective interaction with target molecules or analytes. Although they present many advantages, especially their low weight, they are generally water insoluble, exhibit moderate to low light and thermal stability, and tend to migrate when they are dispersed in physical supports, thus limiting their applicability.

In the last few decades, the optimization of polymer-based chemistry has led to a completely new family of sensory materials and devices employing polymers, which have the ability to respond reversibly or irreversibly to different stimuli (temperature, pH, biological molecules, etc.) in their environment. The response can take place in several ways, such as through the modification of surface properties or changes in shape, solubility, color or fluorescence, and can be generally transduced to originate a measurable change through electrical, colorimetric, or piezoelectric variations. This kind of polymers shows interesting properties, combined to the recent optimization of their synthesis and fabrication processes, and can be manufactured into different shapes, such as micro/fibers, films, beads, coatings, or wires. For these reasons, polymer-based sensors are employed in a wide range of applications, with special interest in the use in medical devices and biomedical applications, drug delivery, tissue engineering, as well as bio/sensors.

This Special Issue on Polymer-Based Sensors is devoted to the discussion and dissemination of the latest research in this interesting and quick-evolving field. Special attention will be given to the last developments in the synthesis of specific polymers for recent sensing applications, such as the detection of biomedical and biological molecules, the design of new sensory devices based on polymers, and the optimization of the sensing characteristics of classical sensory polymers employed in the detection of cations and anionic species, explosives or pollutants, which are of particular interest in environmental, food security, and civil and military protection.

Prof. Dr. José Miguel García
Dr. José Antonio Reglero Ruiz
Dr. Miriam Trigo-López
Guest Editors

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Keywords

  • polymer chemosensors
  • colorimetric sensors
  • fluorescence sensors
  • electrochemical sensors
  • piezoelectric sensors
  • polymeric sensory devices
  • detection of explosives and chemical warfare agents
  • sensing of cations and anionic species
  • detection of biomolecules
  • detection of biomedical analytes
  • sensing of pollutants

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Published Papers (4 papers)

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Research

9 pages, 2490 KiB  
Article
Hydrogen Detection with SAW Polymer/Quantum Dots Sensitive Films
by Izabela Constantinoiu and Cristian Viespe
Sensors 2019, 19(20), 4481; https://doi.org/10.3390/s19204481 - 16 Oct 2019
Cited by 8 | Viewed by 3321
Abstract
Regarding the use of hydrogen as a fuel, it is necessary to measure its concentration in air at room temperature. In this paper, sensitive composite films have been developed for surface acoustic wave (SAW) sensors, using quantum dots (QDs) and polymers. Si/SiO2 [...] Read more.
Regarding the use of hydrogen as a fuel, it is necessary to measure its concentration in air at room temperature. In this paper, sensitive composite films have been developed for surface acoustic wave (SAW) sensors, using quantum dots (QDs) and polymers. Si/SiO2 QDs were used due to having a high specific surface area, which considerably improves the sensitivity of the sensors compared to those that only have a polymer. Si/SiO2 QDs were obtained by laser ablation and analyzed by X-ray diffraction and transmission electron microscopy (TEM). Two types of polymers were used: polydimethylsiloxane (PDMS) and polymethylmethacrylate (PMMA). Polymer and polymer with QDs compositions were deposited on the sensor substrate by drop casting. A heat treatment was performed on the films at 80 °C with a thermal dwell of two hours. The sensors obtained were tested at different hydrogen concentrations at room temperature. A limit of detection (LOD) of 452 ppm was obtained by the sensor with PDMS and Si/SiO2 QDs, which was heat treated. The results demonstrated the potential of using QDs to improve the sensitivity of the SAW sensors and to achieve a heat treatment that increases its adsorption capacity of the gas molecules. Full article
(This article belongs to the Special Issue Polymers Based Sensors)
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9 pages, 4344 KiB  
Communication
Room Temperature Hydrogen Gas Sensing via Reversible Hydrogenation of Electrochemically Deposited Polycarbazole on Interdigitated Pt Transducers
by Agnieszka Stolarczyk, Tomasz Jarosz and Marcin Procek
Sensors 2019, 19(5), 1098; https://doi.org/10.3390/s19051098 - 4 Mar 2019
Cited by 3 | Viewed by 3383
Abstract
In this study, polycarbazole (PCz) is presented as a receptor structure for chemoresistive hydrogen sensors. The fabrication of the proposed sensors via electropolymerisation of PCz on interdigitated Pt electrodes is an inexpensive, cost-efficient, and repeatable method. Preliminary results presented in this work show [...] Read more.
In this study, polycarbazole (PCz) is presented as a receptor structure for chemoresistive hydrogen sensors. The fabrication of the proposed sensors via electropolymerisation of PCz on interdigitated Pt electrodes is an inexpensive, cost-efficient, and repeatable method. Preliminary results presented in this work show that PCz-based sensors are sensitive to hydrogen gas in the range of 1–4% in air at room temperature. Notably, responses are both relatively high (from approximately 280% for 1% of H2) and rapid (response and recovery times for 1% H2 from 5 s and up to 32 s, respectively). Results of PCz structures on Pt and Au electrodes prove that the application of Pt electrodes is crucial for observation of sensing effect. A sensing mechanism based on reversible hydrogenation of PCz is proposed to explain the sensor operating principles. Full article
(This article belongs to the Special Issue Polymers Based Sensors)
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9 pages, 2491 KiB  
Article
Sensory Polymeric Foams as a Tool for Improving Sensing Performance of Sensory Polymers
by Blanca S. Pascual, Saúl Vallejos, Cipriano Ramos, María Teresa Sanz, José A. Reglero Ruiz, Félix C. García and José M. García
Sensors 2018, 18(12), 4378; https://doi.org/10.3390/s18124378 - 11 Dec 2018
Cited by 4 | Viewed by 2801
Abstract
Microcellular sensory polymers prepared from solid sensory polymeric films were tested in an aqueous Hg(II) detection process to analyze their sensory behavior. First, solid acrylic-based polymeric films of 100 µm thickness were obtained via radical copolymerization process. Secondly, dithizone sensoring motifs were anchored [...] Read more.
Microcellular sensory polymers prepared from solid sensory polymeric films were tested in an aqueous Hg(II) detection process to analyze their sensory behavior. First, solid acrylic-based polymeric films of 100 µm thickness were obtained via radical copolymerization process. Secondly, dithizone sensoring motifs were anchored in a simple five-step route, obtaining handleable colorimetric sensory films. To create the microporous structure, films were foamed in a ScCO2 batch process, carried out at 350 bar and 60 °C, resulting in homogeneous morphologies with cell sizes around 5 µm. The comparative behavior of the solid and foamed sensory films was tested in the detection of mercury in pure water media at 2.2 pH, resulting in a reduction of the response time (RT) around 25% and limits of detection and quantification (LOD and LOQ) four times lower when using foamed films, due to the increase of the specific surface associated to the microcellular structure. Full article
(This article belongs to the Special Issue Polymers Based Sensors)
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12 pages, 1636 KiB  
Article
Evidence of Reactivity in the Membrane for the Unstable Monochloramine during MIMS Analysis
by Essyllt Louarn, Abdoul. Monem Asri-Idlibi, Julien Leprovost, Michel Héninger and Hélène Mestdagh
Sensors 2018, 18(12), 4252; https://doi.org/10.3390/s18124252 - 3 Dec 2018
Cited by 5 | Viewed by 3535
Abstract
Membrane Inlet Mass Spectrometry (MIMS) was used to analyze monochloramine solutions (NH2Cl) and ammonia solutions in a compact FTICR. Chemical ionization enables identification and quantification of the products present in the permeate. The responses of protonated monochloramine and ammonium increase linearly [...] Read more.
Membrane Inlet Mass Spectrometry (MIMS) was used to analyze monochloramine solutions (NH2Cl) and ammonia solutions in a compact FTICR. Chemical ionization enables identification and quantification of the products present in the permeate. The responses of protonated monochloramine and ammonium increase linearly with the solution concentration. The enrichments were respectively 1.2 and 5.5. Pervaporation is dependent on pH and only the basic form of ammonia NH3 pervaporates through the membrane. Unexpectedly, the small ammonia molecule permeated very slowly. It could be due to interactions with water molecules inside the membrane that create clusters. Moreover, NH2Cl solutions, in addition to the NH3Cl+ signal, presented a strong NH4+ signal at m/z 18.034. Ammonia presence in the low-pressure zone before ionization is probable as NH4+ was detected with all the precursors used, particularly CF3+ and trimethylbenzene that presents a proton affinity higher than monochloramine. Ammonia may be formed inside the membrane due to the fact that NH2Cl is unstable and may react with the water present in the membrane. Those results highlight the need for caution when dealing with chloramines in MIMS and more generally with unstable molecules. Full article
(This article belongs to the Special Issue Polymers Based Sensors)
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