Academic literature on the topic 'Imprimed polymers'

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Journal articles on the topic "Imprimed polymers"

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Becskereki, Gergely, George Horvai, and Blanka Tóth. "The Selectivity of Molecularly Imprinted Polymers." Polymers 13, no. 11 (2021): 1781. http://dx.doi.org/10.3390/polym13111781.

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The general claim about novel molecularly imprinted polymers is that they are selective for their template or for another target compound. This claim is usually proved by some kind of experiment, in which a performance parameter of the imprinted polymer is shown to be better towards its template than towards interferents. A closer look at such experiments shows, however, that different experiments may differ substantially in what they tell about the same imprinted polymer’s selectivity. Following a short general discussion of selectivity concepts, the selectivity of imprinted polymers is analy
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Chu, Hui Juan, Hong Liang Wei, Jing Zhu, and Chun Ping Nong. "Synthesis and Performance of Molecular Imprinted Polymers as Drug Release Controller." Applied Mechanics and Materials 130-134 (October 2011): 446–49. http://dx.doi.org/10.4028/www.scientific.net/amm.130-134.446.

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Molecular imprinted polymers were synthesized using α-methylacrylacid as monomer, acetylsalicylic acid as template. Polyethylene glycol dimethylacrylate was taken as cross-linker. UV-Vis spectrophotometer was used to detect the drug-loading and releasing performances of these polymers. The studies showed that the imprinted polymers could load more drugs than non-imprinted polymer, and exhibited a slower drug-releasing rate than the latter at pH 7.4. The content of cross-linker had influences on drug-loading amounts. The imprinted polymer released few drugs at the buffer solution of pH 1.2.
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Azodi-Deilamia, Saman, Majid Abdoussa, and S. Rezvaneh Seyedib. "Synthesis and characterization of molecularly imprinted polymer for controlled release of tramadol." Open Chemistry 8, no. 3 (2010): 687–95. http://dx.doi.org/10.2478/s11532-010-0035-x.

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AbstractIn this paper, we describe how to prepare a highly selective imprinted polymer by a bulk polymerization technique. We used tramadol as the template, (MAA) as functional monomers, and (EGDMA) as the cross-linker in chloroform as solvent. Results from Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA), Scanning Electron microscopy (SEM) show that this imprinted sorbent exhibits good recognition and high affinity for tramadol. Selectivity of molecularly imprinted polympers (MIP) was evaluated by comparing several substances with similar molecular structures t
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Jamoussi, Bassem, Radhouane Chakroun, Bandar A. Al-Mur, et al. "Design of a New Phthalocyanine-Based Ion-Imprinted Polymer for Selective Lithium Recovery from Desalination Plant Reverse Osmosis Waste." Polymers 15, no. 18 (2023): 3847. http://dx.doi.org/10.3390/polym15183847.

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In this study, a novel technique is introduced that involves the combination of an ion-imprinted polymer and solid-phase extraction to selectively adsorb lithium ions from reverse osmosis brine. In the process of synthesizing ion-imprinted polymers, phthalocyanine acrylate acted as the functional monomer responsible for lithium chelation. The structural and morphological characteristics of the molecularly imprinted polymers and non-imprinted polymers were assessed using Fourier transform infrared spectroscopy and scanning electron microscopy. The adsorption data for Li on an ion-imprinted poly
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Qiu, Hua Min, Chuan Nan Luo, Lu Lu Fan, Zhen Lv, and Fu Guang Lu. "Molecularly Imprinted Polymer Prepared by Precipitation Polymerization for Quercetin." Advanced Materials Research 306-307 (August 2011): 646–48. http://dx.doi.org/10.4028/www.scientific.net/amr.306-307.646.

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In this paper, molecular imprinted polymer for quercetin was synthesized by precipitation polymerization with acrylamide as functional monomer, ethylene glycol dimethacrylate as cross-linker, 2,2-azobisisobutyronitrile as initiator and acetone as the solvent. The polymers’ adsorption properties were characterized. As results shown that the synthesized imprinted polymer is microspheres with particle size in the nanometer scale, the adsorption capacity of quercetin imprinted polymers is 1.1×10-5mol/g, adsorption temperature is 60°C, adsorption time is 30 min. The molecular imprinting technology
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Bing, Nai Ci, Xiang Rong Zhu, Zhen Tian, Hong Yong Xie, and Li Jun Wang. "Controllable Imprinted Polymer Layer Coated Silica-Gel for S-1-(1-Naphthyl) Ethylamine Recognition by ATRP." Advanced Materials Research 508 (April 2012): 237–40. http://dx.doi.org/10.4028/www.scientific.net/amr.508.237.

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Controlled grafting ofS-1-(1-naphthyl) Ethylamine-imprinting polymer layer on the silica-gel was carried out by the surface-initiated atom transfer radical polymerization (ATRP). Polymerization time was used as the independent variable to manipulate the amount of grafted imprinting polymer on the silica-gel. For comparison, molecularly imprinted polymers (MIPs) without silica-gel also prepared at the same condition. SEM, FT-IR and UV spectrum were used to study the structural morphology and selectivity of polymers and probe the incorporation of imprinted polymer layer on the surface of substra
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Augustine, Anju, and Beena Mathew. "Synthesis of Carbon Nanotube Incorporated Molecular Imprinted Polymer with Binding Affinity towards Testosterone." ISRN Polymer Science 2014 (February 19, 2014): 1–7. http://dx.doi.org/10.1155/2014/790583.

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A novel polymer was synthesised using functionalized carbon nanotube and acrylamide as the polymer support for the separation of testosterone. The developed polymers were characterised using FT-IR, XRD, and SEM techniques. Imprinted polymer showed specificity towards the template testosterone. Among the various polymers, the MWCNT incorporated polymer showed high binding towards the used template. Investigation of the selectivity characteristics revealed that the developed polymer showed selectivity toward the template testosterone than similar compounds. The bound template could be totally re
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Thach, Ut Dong, Hong Hanh Nguyen Thi, Tuan Dung Pham, Hong Dao Mai, and Tran-Thi Nhu-Trang. "Synergetic Effect of Dual Functional Monomers in Molecularly Imprinted Polymer Preparation for Selective Solid Phase Extraction of Ciprofloxacin." Polymers 13, no. 16 (2021): 2788. http://dx.doi.org/10.3390/polym13162788.

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Background: Ciprofloxacin (CIP), an important broad-spectrum fluoroquinolone antibiotic, was often used as a template molecule for the preparation of imprinted materials. In this study, methacrylic acid and 2-vinylpyridine were employed for the first time as dual functional monomers for synthesizing ciprofloxacin imprinted polymers. Methods: The chemical and physicochemical properties of synthesized polymers were characterized using Fourier transform-infrared spectroscopy, thermogravimetric analysis-differential scanning calorimetry, scanning electron microscopy, and nitrogen adsorption-desorp
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Jiang, Xu Hong, and Zhan Mei Liu. "Uiformly-Sized, Molecularly Imprinted Polymers for Naproxen by Precipitation Polymerization." Advanced Materials Research 399-401 (November 2011): 713–17. http://dx.doi.org/10.4028/www.scientific.net/amr.399-401.713.

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Uniformly-sized, molecularly imprinted polymers (MIPs) for (D)-naproxen have been prepared by a precipitation polymerization method using methacrylic acid (MAA) as a functional monomer and divinylbenzene (DVB) as a cross-linker in acetonitrile or a mixture of toluene and acetonitrile(1:3). The (D)-naproxen-imprinted MAA-co-DVB polymers were monodispersed microspheres with size in the range of 1.5 to 3.6µm. Enantioseparation of naproxen was attained using the (D)-naproxen-imprinted MAA-co-DVB polymer microspheres. When Ethylene glycol dimethacrylate(EGDMA) was used as a cross-linker, the MAA-co
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Bhawani, Showkat Ahmad, Nur'Izzah Binti Juarah, Salma Bakhtiar, et al. "Synthesis of Molecularly Imprinted Polymer Nanoparticles for Removal of Sudan III Dye." Asian Journal of Chemistry 34, no. 12 (2022): 3269–74. http://dx.doi.org/10.14233/ajchem.2022.24052.

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Molecularly imprinted polymer (MIP) nanoparticles of Sudan III dye as template were synthesized by using non-covalent approach. The molecularly imprinted polymers were synthesized in a microemulsion contained Sudan III as a template, acrylic acid (AA) as a monomer, 1,4-butanediol dimethacrylate as a cross-linker and 2,2-azo-bisisobutyronitrile (AIBN) as an initiator. The synthesized beads were characterized by TEM and FTIR. The TEM results revealed the nanosize beads of polymers were produced. The efficiency of imprinted and non-imprinted polymers was evaluated by batch binding studies. The re
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Dissertations / Theses on the topic "Imprimed polymers"

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Sala, Alexandre. "Synthèse et caractérisation de polymères à empreintes ionique du cuivre pour la conception d'électrodes modifiées." Electronic Thesis or Diss., Toulon, 2022. http://www.theses.fr/2022TOUL0010.

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L’utilisation du cuivre en tant qu’agent biocide dans les revêtements anti-salissures sur les bateaux a provoqué son accumulation dans les eaux portuaires. Le but de ces travaux de thèse est de développer des capteurs électrochimiques permettant sa détection dans des échantillons marins. Pour cela des polymères à empreintes du cuivre(II) ont été élaborés et utilisés pour la modification d’électrodes.Dans un premier temps, des particules de polymères à empreintes ont été synthétisées à l’aide d’un agent réticulant (le diméthacrylate d’éthylène glycol ou le N,N’-méthylène-bis-acrylamide) et d’un
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Mandadi, Deepika. "A Characterization of Caffeine Imprinted Polypyrrole Electrode." TopSCHOLAR®, 2009. http://digitalcommons.wku.edu/theses/130.

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Nanotechnology holds great potential for improving our lives by creating many new materials and devices in medical sciences, electronics and also in energy production. Molecularly imprinted polymers (MIPs) are highly stable synthetic polymers that possess molecular recognition properties due to cavities created in the polymer matrix that are complementary to an analyte both in shape and in positioning of functional groups. These MIPs have been widely employed for diverse applications (e.g., in chromatographic separation, drug screening, chemosensors, catalysis, immunoassays etc) due to their s
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O'Donnell, Elizabeth Anne. "Water-compatible molecularly imprinted polymers." Thesis, University of Strathclyde, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438467.

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Robak, Andrew Joseph. "Development of coenzyme-imprinted molecularly imprinted polymers as catalysts /." view abstract or download file of text, 2007. http://proquest.umi.com/pqdweb?did=1276397881&sid=1&Fmt=2&clientId=11238&RQT=309&VName=PQD.

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Thesis (Ph. D.)--University of Oregon, 2007.<br>Typescript. Includes vita and abstract. Includes bibliographical references (leaves 94-100). Also available for download via the World Wide Web; free to University of Oregon users.
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Tsai, Mei-Hsuan. "Boron containing molecular imprinted polymer (MIP) templates from symmetric and asymmetric diboration of olefins and other boron containing functional polymers." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608235.

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Bates, Ferdia. "Design and development of molecularly imprinted polymers and imprinted sensors." Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/399170.

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Esta tesis se ha hecho principalmente para estudiar e investigar polímeros impresos (MIPs) con la intención de usarlos como sensores de larga vida. La línea de investigación de esta tesis es la dirigida a conseguir la integración de estas formaciones impresas dentro de una lengua electrónica (ET), que es la rama de especialización en la que se ha desarrollado principalmente este proyecto. Después de hacer una revisión de la literatura, que inicialmente se centraba en la aplicación de MIPs a un equipo electroquímico, un sensor voltamétrico impreso y un procedimiento sensitivo complementario, el
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Yvenou, Etienne. "Développement de modules thermoélectriques imprimés et flexibles pour des applications à température ambiante." Thesis, Université Grenoble Alpes (ComUE), 2017. http://www.theses.fr/2017GREAI071/document.

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L’effet thermoélectrique permet la conversion directe et réversible d’un flux de chaleur en courant électrique via l’utilisation de semi-conducteurs de type-p et de type n. Les polymères conjugués, comme le poly(3,4-éthylènedioxythiophène) (PEDOT) sont pressentis pour être des alternatives aux alliages de tellurure de bismuth (Bi2Te3) coûteux, toxiques et difficiles à synthétiser.Cette thèse se propose d’améliorer la conductivité électrique d’un PEDOT et de faciliter sa mise en œuvre par une technique d’impression grande surface comme le spray.La première partie porte sur l’amélioration de la
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Bonini, Francesca. "Molecularly imprinted polymers for protome analysis." Thesis, Cranfield University, 2008. http://dspace.lib.cranfield.ac.uk/handle/1826/2716.

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Fast and efficient methods for the detection of insurgence and progression of diseases are at the basis of modern diagnostics and medicine. In this concern, biomarkers represent a powerful diagnostic tool, as their expression profiles well correlate with the pathology progression. Thus, the pathological state could be diagnosed by measuring the altered presence of a biomarker. In this direction, conspicuous help has been given by proteomics, intended as the study of the protein pattern of a sample and most frequently performed by two-dimensional electrophoresis. Although the proteome approach
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Mistry, Reena. "Niacinamide analysis using molecularly imprinted polymers." Thesis, University of British Columbia, 2002. http://hdl.handle.net/2429/43182.

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The objectives of this research were to use molecularly imprinted polymers (MIP) and microfluidic chips as an approach to a rapid and low cost analytical method for niacinamide analysis. Lab-on-a-chip (microfluidics) devices are becoming increasingly popular due to their relatively low cost, sensitivity, and speed. MIPs may be able to serve as solid-phase extraction packing material in microfluidic chips. To reach the objectives, it was necessary to identify the mechanisms by which binding of analyte to polymer occur, determine the optimal functional monomer to cross-linker ratio, and gain
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Wang, Jinfang. "Xanthine-imprinted polymers for decaffeination applications." Thesis, University of Strathclyde, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.431777.

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Books on the topic "Imprimed polymers"

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Martín-Esteban, Antonio, ed. Molecularly Imprinted Polymers. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1629-1.

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Mattiasson, Bo, and Lei Ye, eds. Molecularly Imprinted Polymers in Biotechnology. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20729-2.

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Börje, Sellergren, ed. Molecularly imprinted polymers: Man-made mimics of antibodies and their applications in analytical chemistry. Elsevier, 2001.

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Bartsch, Richard A., and Mizuo Maeda, eds. Molecular and Ionic Recognition with Imprinted Polymers. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0703.

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Kutner, Wlodzimierz, and Piyush Sindhu Sharma, eds. Molecularly Imprinted Polymers for Analytical Chemistry Applications. Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788010474.

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A, Bartsch Richard, Maeda Mizuo, American Chemical Society. Division of Industrial and Engineering Chemistry., and American Chemical Society Meeting, eds. Molecular and ionic recognition with imprinted polymers. American Chemical Society, 1998.

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1967-, Yan Mingdi, and Ramström Olof, eds. Molecularly imprinted materials: Science and technology. Marcel Dekker, 2005.

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Liu, Zhaosheng, Yanping Huang, and Yi Yang, eds. Molecularly Imprinted Polymers as Advanced Drug Delivery Systems. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0227-6.

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1947-, Komiyama Makoto, ed. Molecular imprinting: From fundamentals to applications. Wiley-VCH, 2003.

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Davis, Fred J., ed. Polymer Chemistry. Oxford University Press, 2004. http://dx.doi.org/10.1093/oso/9780198503095.001.0001.

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Polymer Chemistry: A Practical Approach in Chemistry has been designed for both chemists working in and new to the area of polymer synthesis. It contains detailed instructions for preparation of a wide-range of polymers by a wide variety of different techniques, and describes how this synthetic methodology can be applied to the development of new materials. It includes details of well-established techniques, e.g. chain-growth or step-growth processes together with more up-to-date examples using methods such as atom-transfer radical polymerization. Less well-known procedures are also included,
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Book chapters on the topic "Imprimed polymers"

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Hall, Andrew J., Marco Emgenbroich, and Börje Sellergren. "Imprinted Polymers." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b104333.

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Whitcombe, Michael J., and Dhana Lakshmi. "Imprinted Polymers." In Electropolymerization. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527630592.ch7.

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Ulubayram, Kezban. "Molecularly Imprinted Polymers." In Advances in Experimental Medicine and Biology. Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48584-8_10.

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Piletsky, Sergey A., Iva Chianella, and Michael J. Whitcombe. "Molecularly Imprinted Polymers." In Encyclopedia of Biophysics. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_719.

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Takeuchi, Toshifumi, and Hirobumi Sunayama. "Molecularly Imprinted Polymers." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-36199-9_126-1.

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Haupt, Karsten, Ana V. Linares, Marc Bompart, and Bernadette Tse Sum Bui. "Molecularly Imprinted Polymers." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_307.

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Takeuchi, Toshifumi, and Hirobumi Sunayama. "Molecularly Imprinted Polymers." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_126.

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Rosa, Mariana Azevedo, Tássia Venga Mendes, and Eduardo Costa Figueiredo. "Restricted Access Molecularly Imprinted Polymers." In Molecularly Imprinted Polymers. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1629-1_5.

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Turiel Trujillo, Esther, and Myriam Díaz-Álvarez. "Preparation of Monolithic Fibers in Fused Silica Capillary Molds for Molecularly Imprinted Solid-Phase." In Molecularly Imprinted Polymers. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1629-1_13.

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Bossi, Alessandra Maria, and Laura Pasquardini. "The Search for Peptide Epitopes for Through." In Molecularly Imprinted Polymers. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1629-1_22.

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Conference papers on the topic "Imprimed polymers"

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Vitale, U., A. Rechichi, M. D’Alonzo, et al. "Selective Peptide Recognition With Molecularly Imprinted Polymers in Designing New Biomedical Devices." In ASME 8th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2006. http://dx.doi.org/10.1115/esda2006-95587.

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Molecular imprinting is a technique for the synthesis of polymers capable to bind selectively specific molecules. The imprinting of large proteins, like cell adhesion proteins or cell receptors, can lead to important and innovative biomedical applications. However such molecules show such important conformational changes in the polymerisation environment that the recognition sites are poorly specific. The “epitope approach” can overcome this limit by adopting, as template, a stable short peptide sequence representative of an accessible fragment of a larger protein. The resulting imprinted poly
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Zhenhe Chen, Bin Xue, Wentao Zhao, Linxia Zhang, Liquan Sun, and Aiqin Luo. "High porosity lysozyme imprinted polymers." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5964091.

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Ciardelli, G., F. M. Montevecchi, P. Giusti, et al. "Molecular Imprinted Nanostructures in Biomedical Applications." In ASME 8th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2006. http://dx.doi.org/10.1115/esda2006-95669.

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Molecular imprinting is an emerging technology that allows to introduce nanostructured cavities into a polymer. In preparing molecular imprinted polymers (MIPs), the functional monomer(s) is first prearranged around the template molecule by specific interactions; the polymerisation is then carried out with a high percentage of cross-linking agent (which “freezes” the macromolecular network). Molecular mechanics and dynamics can be used to gain indications on the best monomers to be used in order to maximize interactions with the template. Once the polymerization reaction has been completed, th
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Benito-Peña, Elena, Sergio Carrasco, Fernando Navarro-Villoslada, David R. Walt, and María C. Moreno-Bondi. "Optically-based Molecularly Imprinted Polymers Sensors." In Optical Sensors. OSA, 2017. http://dx.doi.org/10.1364/sensors.2017.setu2e.4.

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Lulinski, Piotr, and Dorota Maciejewska. "Preliminary Evaluation of Molsidomine Imprinted Polymers." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01269.

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Xie, Baiyi, and Aiqin Luo. "Research on the Lysozyme imprinted polymers." In 2015 2nd International Conference on Machinery, Materials Engineering, Chemical Engineering and Biotechnology. Atlantis Press, 2016. http://dx.doi.org/10.2991/mmeceb-15.2016.30.

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Tancharoen, Chompoonuch, Wannisa Sukjee, Chak Sangma, and Thipvaree Wangchareansak. "Molecularly Imprinted Polymer for explosive detection." In 2015 Asian Conference on Defence Technology (ACDT). IEEE, 2015. http://dx.doi.org/10.1109/acdt.2015.7111605.

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Murray, George M., Bradley R. Arnold, Craig A. Kelly, and O. Manuel Uy. "Imprinted polymer sensors for contamination detection." In Environmental and Industrial Sensing, edited by Yud-Ren Chen and Shu-I. Tu. SPIE, 2001. http://dx.doi.org/10.1117/12.418722.

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ZHANG, ZHUJUN. "MOLECULAR IMPRINTED POLYMER-BASED CHEMILUMINESCENCE SENSORS." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0037.

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Holthoff, Ellen L., Dimitra N. Stratis-Cullum, and Mikella E. Hankus. "Xerogel-based molecularly imprinted polymers for explosives detection." In SPIE Defense, Security, and Sensing, edited by Augustus W. Fountain III and Patrick J. Gardner. SPIE, 2010. http://dx.doi.org/10.1117/12.850129.

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Reports on the topic "Imprimed polymers"

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Holthoff, Ellen L., Lily Li, Tobias Hiller, and Kimberly L. Turner. A Molecularly Imprinted Polymer (MIP)-Coated Microbeam MEMS Sensor for Chemical Detection. Defense Technical Information Center, 2015. http://dx.doi.org/10.21236/ada622335.

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Harvey, Scott D. Ultraselective Sorbents. Task 2: Molecularly Imprinted Polymers (MIPs)/Stabilized Antibody Fragments (STABs). Final Report FY 2004. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/15016482.

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Holthoff, Ellen, and Dimitra Stratis-Cullum. A Nanosensor for Explosives Detection Based on Molecularly Imprinted Polymers (MIPs) and Surfaced-enhanced Raman Scattering (SERS). Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada516676.

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Harvey, Scott D. Ultraselective Sorbents. Task 2: Molecularly Imprinted Polymers (MIPs)/Stabilized Antibody Fragments (STABs). Final Report -- Fiscal Year (FY) 2005. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/860003.

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Bendikov, Michael, and Thomas C. Harmon. Development of Agricultural Sensors Based on Conductive Polymers. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7591738.bard.

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In this 1-year feasibility study, we tried polymerization of several different monomers, commercial as well as novel, specially designed and synthesized for this project in the presence of the nitrate ion to produce imprinted conductive polymers. Polymers 1 and 2 (shown below) produced a response to nitrate, but one inferior to that produced by a polypyrrole (Ppy)-based sensor (which we demonstrated prior to this study). Thus, we elected to proceed with improving the stability of the Ppy-based sensor. In order to improve stability of the Ppy-based sensor, we created a two-layer design which in
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Glasscott, Matthew, Johanna Jernberg, Erik Alberts, and Lee Moores. Toward the electrochemical detection of 2,4-dinitroanisole (DNAN) and pentaerythritol tetranitrate (PETN). Engineer Research and Development Center (U.S.), 2022. http://dx.doi.org/10.21079/11681/43826.

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Abstract:
Analytical methods to rapidly detect explosive compounds with high precision are paramount for applications ranging from national security to environmental remediation. This report demonstrates two proof-of-concept electroanalytical methods for the quantification of 2,4-dinitroanisol (DNAN) and pentaerythritol tetranitrate (PETN). For the first time, DNAN reduction was analyzed and compared at a bare graphitic carbon electrode, a polyaniline-modified (PANI) electrode, and a molecularly imprinted polymer (MIP) electrode utilizing PANI to explore the effect of surface-area and preconcentration a
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