01771nas a2200253   4500008004100000022001400041245009900055210006900154260007300223300001400296490000700310520087300317653003001190653000901220653001301229653002501242653000801267100002201275700002501297700002001322700001901342700002601361856013001387       2006                        eng d  a0167-577X00aElectron beam induced surface cross-linking of functional monomers coated on silicon substrate0 aElectron beam induced surface crosslinking of functional monomer  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcMAY  a1360-13650 v603 a<p>A 3: 1 composition of functional monomer: multifunctional acrylate was spin coated and later cross-linked under the influence of keV electron irradiation on the surface of silicon to generate a surface-anchored cross-linked network bearing functional moieties. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) as well as wetting angle measurements were used for the analysis of functional monomer cross-linked surfaces. Results of the surface reconstruction of surfaces and electron irradiated on coated silicon wafers reveal that long-term hydrophilic surfaces can be achieved. Thus, the surface architecture can be favorably manipulated by using this remarkable technique with a Suitable combination of functional monomers and cross-linkers. (c) 2005 Elsevier B.V. All rights reserved.</p>10aelectron beam irradiation10aFTIR10aPolymers10asurface modification10aXPS1 aMahapatra, S., K.1 aBodas, Dhananjay, S.1 aMandale, A., B.1 aGangal, S., A.1 aBhoraskar, Vasant, N.  uhttps://library.ncl.res.in/content/electron-beam-induced-surface-cross-linking-functional-monomers-coated-silicon-substrate-002512nas a2200241   4500008004100000022001400041245010100055210006900156260007700225300001400302490000700316520163400323653002101957653001301978653001301991653001302004100002502017700002402042700002602066700002102092700002502113856013202138       2007                        eng d  a0947-653900aExhaustive analysis of frontal copolymerization of functionalized monovinyl and divinyl monomers0 aExhaustive analysis of frontal copolymerization of functionalize  aBOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANYbWILEY-V C H VERLAG GMBHcAPR  a5862-58720 v133 a<p>A series of copolymers of 2-hydroxyethyl methacrylate (HEMA)/ glycidyl methacrylate (GMA) and ethylene dimethacrylate (EGDM) were synthesized by frontal polymerization (FP). This study was conducted to investigate the effect of crosslink density, type and concentration of initiator, the use of a complex initiator system, porogen, and diluent on the most relevant parameters of FP, such as sustainability of the front, temperature profile, front velocity, and yield. The products were also characterized for intruded pore volume, pore-size distribution, epoxy-functionality number, and surface morphology. Higher crosslink densities (CLDs) and initiator concentration produced higher front velocities, whereas no trend in front temperature was noted. A complex initiation system was effective in stabilizing and increasing the polymerization yield. Relative to suspension polymerization (SP), FP products synthesized without a solvent were microporous, whereas micro-to-macroporous products were obtained in the presence of a solvent (for HEMA-EGDM polymers). We also present, explain, and discuss the exotic patterns observed under a microscope. We observed two basic types of spatial patterns, namely, planar and nonplanar patterns. The type of planar pattern observed under scanning electron microscopy (SEM) has a spatial impulse that appears as a loop followed by regular periodic motion in the radial and axial directions. This behavior gives rise to a repeating pattern that is a few microns thick. Also, nonplanar patterns, namely, layered concentric rings and winding staircase patterns, were observed under SEM.</p>10acopolymerization10apatterns10aPolymers10aporosity1 aPujari, Narahari, S.1 aInamdar, Satish, R.1 aAmbekar, Jalindar, D.1 aKulkarni, B., D.1 aPonrathnam, Surendra  uhttps://library.ncl.res.in/content/exhaustive-analysis-frontal-copolymerization-functionalized-monovinyl-and-divinyl-monomers-000833nas a2200217   4500008004100000022001400041245011100055210006900166260007700235300001400312490000700326653001500333653001400348653001400362653001300376653002100389100002100410700002800431700003000459856012600489       2008                        eng d  a1433-785100aPolymer electrolyte fuel cells using nafion-based composite membranes with functionalized carbon nanotubes0 aPolymer electrolyte fuel cells using nafionbased composite membr  aPO BOX 10 11 61, D-69451 WEINHEIM, GERMANYbWILEY-V C H VERLAG GMBHcFEB  a2653-26560 v4710afuel cells10amembranes10ananotubes10aPolymers10aproton transport1 aKannan, Ramaiyan1 aKakade, Bhalchandra, A.1 aPillai, Vijayamohanan, K.  uhttps://library.ncl.res.in/content/polymer-electrolyte-fuel-cells-using-nafion-based-composite-membranes-functionalized-002137nas a2200253   4500008004100000022001400041245006600055210006600121260009200187300001800279490000800297520129000305653001401595653002501609653001301634653001401647100001901661700002501680700001701705700001501722700002101737700002501758856010001783       2009                        eng d  a1042-015000aHigh energy electron irradiation effects on polystyrene films0 aHigh energy electron irradiation effects on polystyrene films  a4 PARK SQUARE, MILTON PARK, ABINGDON OX14 4RN, OXON, ENGLANDbTAYLOR & FRANCIS LTDcSEP  aPII 9144664970 v1643 a<p>The effect of an 8MeV electron-beam on the structural, optical and dielectric properties of polystyrene films has been investigated respectively by means of Fourier transform infrared (FTIR) spectroscopy, ultraviolet-visible (UV-VIS) spectroscopy and electrical impedance (LCR) analysis over a radiation dose in the range of 50-250kGy using a Microtron accelerator. The FTIR spectral analysis shows no change in the overall structure of the irradiated polystyrene films, except a minor change in the intensity of a few peaks in the FTIR spectrum, indicating that polystyrene is resistant to electron-beam irradiation over the range of radiation doses investigated. The optical band gap analysis using the UV-VIS absorption spectra of the polystyrene shows a small decrease in the optical band gap (Eg) and the activation energy with an increase in electron doses. Further, the dielectric measurements over a frequency range of 100Hz to 1MHz for the electron-beam-irradiated polystyrene films show that both the dielectric constant and the dielectric loss increase with an increase in electron radiation dose, which may be ascribed to the formation of defect sites in the band gap of polystyrene as a consequence of molecular chain scission in the polymer films upon irradiation.</p>10aelectrons10aoptical spectroscopy10aPolymers10aradiation1 aMathad, R., D.1 aKumar, H., G. Harish1 aSannakki, B.1 aGanesh, S.1 aSarma, K., S. S.1 aBadiger, Manohar, V.  uhttps://library.ncl.res.in/content/high-energy-electron-irradiation-effects-polystyrene-films-001889nas a2200229   4500008004100000022001400041245010200055210006900157260010000226300001400326490000700340520096800347653004401315653002601359653001301385653001301398653005301411100002501464700002601489700002201515856012201537       2010                        eng d  a0266-353800aPolyethersulfone-expanded graphite nanocomposites: charge transport and impedance characteristics0 aPolyethersulfoneexpanded graphite nanocomposites charge transpor  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLANDbELSEVIER SCI LTDcNOV0  a2111-21160 v703 a<p>Polyethersulfone (PES)-expanded graphite nanocomposites have been prepared by solution blending route after sonicating expanded graphite in dichloromethane. It has been observed that ultrasonication results in nanosheets formation leading to a low percolation threshold of 3 wt.%. At 5 wt.% filler loading the conductivity is of the order of 10(-2) S/cm. Hopping type of charge transport occurs at 3.2 wt.% expanded graphite in PES below which capacitive effects couple. The effective dielectric constant at low frequency increases with filler concentration. Impedance measurement has been carried out to evaluate interfacial capacitance which, for 3.2 wt.% expanded graphite addition in PES, increases to 110 pF from 32 pF for 1 wt.% expanded graphite in the polymer. DSC analysis shows an increment of 12 C in the T(g) of PES with 3 wt.% expanded graphite suggesting interaction between the polymer and filler. (C) 2010 Elsevier Ltd. All rights reserved.</p>10aDifferential scanning calorimetry (DSC)10aElectrical properties10aModeling10aPolymers10aScanning/transmission electron microscopy (STEM)1 aRamanujam, B., T. S.1 aMahale, Rajashree, Y.1 aRadhakrishnan, S.  uhttps://library.ncl.res.in/content/polyethersulfone-expanded-graphite-nanocomposites-charge-transport-and-impedance-001844nas a2200253   4500008004100000022001400041245011700055210006900172260007300241300001400314490000800328520092800336653002501264653002301289653002201312653001301334653001101347653002301358100002401381700002301405700002001428700002001448856012201468       2011                        eng d  a0168-583X00aMorphological changes in nanoparticulate silver films due to electron beam irradiation of polystyrene substrates0 aMorphological changes in nanoparticulate silver films due to ele  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcJUL  a1534-15390 v2693 a<p>Results of the studies on the effect of 8 MeV electron beam irradiation of polystyrene substrates on the morphology of silver particulate films deposited at 455 K in a vacuum of 8 x 10(-6) Torr are reported. Optical absorption studies show the presence of transverse and longitudinal plasmon resonance for films deposited on irradiated polystyrene. Scanning electron microscopy reveals a decrease in particle size with smaller inter-particle separation for irradiated films. Larger clusters are formed in the case of films deposited on polystyrene after 300 h of irradiation. In this paper, we show that the morphology of silver nanoparticulate films can be modified by electron irradiation of inert polymer substrates like polystyrene. The change observed due to irradiation is attributed to the formation of free radicals, thereby altering the polymer-metal interaction. (C) 2011 Elsevier B.V. All rights reserved.</p>10aElectron bombardment10aOptical properties10aParticulate films10aPolymers10aSilver10asurface morphology1 aPattabi, Manjunatha1 aGurumurthy, S., C.1 aSanjeev, Ganesh1 aGaikwad, A., B.  uhttps://library.ncl.res.in/content/morphological-changes-nanoparticulate-silver-films-due-electron-beam-irradiation-002351nas a2200229   4500008004100000022001400041245006400055210006300119260010600182300001200288490000800300520156300308653002301871653001601894653001301910653002301923100001901946700001801965700002001983700002102003856009702024       2014                        eng d  a0009-250900aModeling chain-end scission using the fixed pivot technique0 aModeling chainend scission using the fixed pivot technique  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcSEP  a601-6100 v1163 a<p>Chain-end scission of polymer molecules is the breakage of a fixed-size oligomer or monomer from either end of the macromolecule. A common example is the generation of the glucose monomer from the hydrolysis of starch by glucoamylase. Modeling the dynamics of chain-end scission from first principles by considering each molecular size is challenging due to the large number of differential equations to be solved. The Population Balance Modeling (PBM) is a helpful framework as it could be formulated to lump a few molecular sizes together. However, it is then not obvious how to accurately account for the temporal evolution of the low molecular weight species, which is often of the greatest industrial interest. Here, the Fixed Pivot (FP) technique - one of the methods to solve PBM equations was appropriately modified to address this difficulty. By treating the lower molecular size range as a discrete domain in conjunction with a continuous domain in the upper ranges, the modified FP technique not only retains its original strengths, but also captures accurately the distribution of oligomers including the monomer. The results, which were obtained at a fraction of computational expense, benchmarked very well against the exact solutions for a polymer with a broad size distribution at different Degrees of Polymerization up to similar to O(10(5)). To facilitate wider adoption, guidelines on choice of pivots and observations of the performance of the modified FP technique are also deliberated. (C) 2014 Elsevier Ltd. All rights reserved.</p>10aChain-end scission10aFixed Pivot10aPolymers10aPopulation balance1 aHo, Yong, Kuen1 aDoshi, Pankaj1 aYeoh, Hak, Koon1 aNgoh, Gek, Cheng  uhttps://library.ncl.res.in/content/modeling-chain-end-scission-using-fixed-pivot-technique-001734nas a2200217   4500008004100000022001400041245011900055210006900174260007700243300001400320520087400334653002601208653003601234653002801270653001401298653001301312100001901325700002701344700001701371856012801388       2014                        eng d  a1434-194800aNature of the active site in ziegler-natta olefin polymerization catalysis systems - a computational investigation0 aNature of the active site in zieglernatta olefin polymerization   aBOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANYbWILEY-V C H VERLAG GMBHcOCT  a5063-50763 a<p>Pull quantum chemical calculations with density functional theory (DET) show that a principal role of donors in Ziegler-Nana (ZN) oh-din polymerization catalysts is to coordinate to the metal center at the active sites on the MgCl2 surface. Thereby, the behavior of the catalyst is modulated to favor insertion over termination and, thus, polymerization occurs. This is shown to be true for a range of different donors. The calculations indicate that active sites that feature anionic chloride ligands at the titanium center (the conventional model for the active site) would lead to lower-molecular-weight riolymers. If an -OC2H5 group were present instead of a chloride ligand, the active site would much more effectively produce long chain polymers. Therefore, the current work provides important new insights into the nature of the ZN polymerization process.</p>10aAlkene polymerization10aDensity functional calculations10aheterogeneous catalysis10aInsertion10aPolymers1 aKumawat, Jugal1 aGupta, Virendra, Kumar1 aVanka, Kumar  uhttps://library.ncl.res.in/content/nature-active-site-ziegler-natta-olefin-polymerization-catalysis-systems-computational-002744nas a2200433   4500008004100000022001400041245012800055210006900183260000800252300001200260490000900272520135800281653001901639653000601658653000601664653001901670653002501689653001401714653001901728653002801747653002301775653002301798653002401821653002801845653002501873653003101898653001301929653002801942653002001970653002901990653002102019653002202040100002302062700003002085700002402115700002002139700002002159856013102179       2017                        eng d  a0022-286000aSynthesis, characterization and electrochemical investigations of mixed-ligand copper(II)-organic supramolecular frameworks0 aSynthesis characterization and electrochemical investigations of  cNOV  a549-5570 v11473 a<p><span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);">Two mixed-ligand copper(II)-organic coordination compounds with 5,5'-dimethyl-2,2'-bipyridine (5,5'-Me(2)bpy) as a primary ligand while aliphatic malonate (Hmal) and aromatic 2-hydroxynicotinate (2-OHNA) as secondary ligands, were synthesized. These complexes are formulated as: [Cu(Hmal)(5,5'-Me(2)bPY)(H2O)](ClO4) 1 and [Cu-2(2-OHNA)(2)(5,5'-Me(2)bpy)(2)(NO3)KNO3) 2. These two complexes were structurally characterized by single crystal X-ray diffraction analysis. Characterization was further supported by powder X-ray diffraction analysis, elemental analyses, FT-IR, FAB-MASS and TGA, DSC studies. Cyclic voltammetric and UV-visible spectral studies of these two complexes have also been done. The electrochemical studies of complex 1 in DMSO and DMF have shown that this complex undergoes quasi reversible diffusion-controlled one-electron transfer reaction without any chemical complication while complex 2 in DMSO undergoes quasi-reversible diffusion-controlled one electron transfer reaction, following EC mechanism. The electrochemical behaviour of complex 2 in DMF is complicated probably due to presence of more than one species in solution phase. (C) 2017 Elsevier B.V. All rights reserved.</span></p>10a2 '-bipyridine10a310a510a5 '-dimethyl-210a5-Tricarboxylic acid10aBenzene-110aclassification10aCo-ordination-Compounds10aCrystal-structures10acyclic voltammetry10amagnetic properties10ametal organic framework10aMixed-ligand complex10api-pi stacking interaction10aPolymers10aSecondery Building Unit10aStructural data10aSupramolecular framework10aTernare Komplexe10aX-ray diffraction1 aSingh, Sandeep, K.1 aSrivastava, Ashish, Kumar1 aSrivastava, Krishna1 aBanerjee, Rahul1 aPrasad, Jagdish  uhttps://library.ncl.res.in/content/synthesis-characterization-and-electrochemical-investigations-mixed-ligand-copperii-organic02767nas a2200277   4500008004100000245008200041210006900123260000800192490000800200520188500208653000902093653004202102653002102144653001402165653001502179653001502194653001302209653004702222653001002269100002102279700001702300700002202317700001902339700001902358856011202377       2017                        eng d00aThermotropic liquid crystalline polyesters derived from 2-chloro hydroquinone0 aThermotropic liquid crystalline polyesters derived from 2chloro   cSEP0 v1293 a<p><span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);">Synthesis of thermotropic liquid crystalline polyesters derived from bis[4-hydroxy benzoyloxy]-2-chloro-1,4-benzene (BHBOCB) and aliphatic dicarboxylic acid chlorides by interfacial polycondensation methodology is presented. Synthesised polyesters consist of bis[4-hydroxy benzoyloxy]-2-chloro-1,4-benzene as a mesogen and aliphatic diacid chloride as flexible spacer. The length of oligomethylene units in the polymer was varied from the trimethylene to the dodecamethylene groups. Synthesized polyesters were characterized by differential scanning calorimetry and optical microscopy. The transition temperatures and thermodynamic properties were studied for all these polymers. These polyesters exhibited thermotropic liquid crystalline behavior and showed nematic texture except decamethylene spacer. Decamethylene spacer based polyester showed marble texture of smectic C. Mesophase stability of these polyesters was higher than (except first heating cycle of PE-1).&nbsp;</span><br style="margin: 0px; list-style: none; padding: 0px; color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);"><br style="margin: 0px; list-style: none; padding: 0px; color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);"><span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; background-color: rgb(248, 248, 248);">SYNOPSIS The present study deals with the synthesis of thermotropic liquid crystalline polyesters derived from bis[4-hydroxy benzoyloxy]-2-chloro-1,4-benzene (BHBOCB) and aliphatic dicarboxylic acid chlorides by interfacial polycondensation methodology.</span></p>10aacid10aAliphatic Flexible Spacers Main-chain10aAromatic Mesogen10aElastomer10aMorphology10aPolydomain10aPolymers10aThermotropic Liquid Crystalline Polyesters10aUnits1 aManurkar, Nagesh1 aMore, Sayaji1 aMulani, Khudbudin1 aGanjave, Nitin1 aChavan, Nayaku  uhttps://library.ncl.res.in/content/thermotropic-liquid-crystalline-polyesters-derived-2-chloro-hydroquinone02210nas a2200277   4500008004100000022001300041245014900054210006900203260000900272300001600281490000600297520121800303653003101521653003401552653001801586653003701604653001301641653001301654653002201667653002201689653001501711653002301726100002201749700003101771856013001802       2018                        eng d  a2470134300aSurface modification of polymers for tissue engineering applications: arginine acts as a sticky protein equivalent for viable cell accommodation0 aSurface modification of polymers for tissue engineering applicat  cAPR   a4242–42510 v33 a<p>Hydrophobic polymers, for their favorable mechanical properties, are a popular choice as permanent bioimplants. These materials remain absolutely bioinert for years, but throw up challenges when it comes to fast integration with healthy tissue. Addressing this, herein, we present a surface-modification technique of converting the hydrophobic surface of a polymeric film into a hydrophilic one using a layer-by-layer assembly process involving gold nanoparticles and small molecules like amino acids. These films showed much improved animal cell (murine fibroblast) adherence properties compared to commercially available tissue culture plates. Moreover, arginine-modified films exhibited a nearly equivalent cell viability compared to the films modified with the natural extracellular matrix component fibronectin. The surface hydrophilicity and roughness of our novel film were characterized by contact angle measurement and atomic force microscopy. Cell counting, fluorescence microscopy, cell viability, and collagen estimation assay were employed to demonstrate that our film favored a much improved cell adherence, and accommodation in comparison to the commercially available tissue culture plates.</p>10aCell and Molecular biology10aExtracellular matrix proteins10aNanoparticles10aPhysical and chemical properties10aPolymers10aProteins10aSurface structure10aSurface treatment10aThin films10atissue engineering1 aSengupta, Poulomi1 aPrasad, Bhagavatula, L. V.  uhttps://library.ncl.res.in/content/surface-modification-polymers-tissue-engineering-applications-arginine-acts-sticky-protein02204nas a2200205   4500008004100000022001400041245014700055210006900202260000900271300001200280490000700292520144700299653003301746653003401779653001301813653001101826100002001837700001501857856012601872       2020                        eng d  a1539-445X00aGlass transition temperature of polybutadiene and polyisoprene from high temperature segmental relaxation correlation using molecular dynamics0 aGlass transition temperature of polybutadiene and polyisoprene f  cJUL   a290-2960 v183 a<p>Predicting glass transition temperature for rubber and rubber composites is immensely important for tire industry for the development of products and fine-tune process conditions. Molecular dynamics simulation is been used to predict glass transition temperature as a function of molecular-level structural changes, e.g., composition (functional groups), topology, and polymerization. However, prediction of glass transition temperature within experimental error bar from molecular dynamics simulation is only possible from all atomistic description (model) of the system as united atom and coarse-grained models under-predict the values. Conventional way of calculation of glass transition temperature from density (or any other properties which show sharp transition)-temperature plots are computationally very demanding because of atomistic simulations and simulations below the glass transition point, i.e., in glassy state. Here we report a novel method for calculation of glass transition temperature using only segmental relaxation correlation functions calculated at higher temperatures, i.e., above glass transition temperature. We have presented a protocol here and shown for two polymeric systems polybutadiene and polyisoprene. We believe this method cuts the computational cost of predicting glass transition temperature by one-third and will be applicable for industrial applications for structure-property validations.</p>
10aGlass transition temperature10amolecular dynamics simulation10aPolymers10arubber1 aSharma, Pragati1 aRoy, Sudip  uhttps://library.ncl.res.in/content/glass-transition-temperature-polybutadiene-and-polyisoprene-high-temperature-segmental02461nas a2200409   4500008004100000022001400041245008800055210006900143260000900212300001600221490000700237520122100244653001601465653002501481653001701506653001501523653002601538653001901564653002201583653001301605653002101618653001601639653004201655653001201697653001301709653002401722100002001746700002401766700002201790700002001812700001601832700002101848700002201869700002101891700002101912856011801933       2024                        eng d  a1530-437X00aPolymeric PEI/PEG coated optical fiber fabry-perot interferometer for CO2 detection0 aPolymeric PEIPEG coated optical fiber fabryperot interferometer   cDEC   a40883-408890 v243 a<p>
	Monitoring carbon dioxide (CO2) gas is essential for numerous applications, but the detection of CO2 in miniaturized devices presents significant challenges. In this study, a polyethyleneimine/poly(ethylene glycol) (PEI/PEG) coated optical fiber Fabry-Perot interferometer (FPI) and its charge transfer process toward CO2 are investigated. Scanning electron microscopy and Fourier transform infrared spectroscopy were used to analyze the surface morphology and vibration bands of the PEI/PEG composite. The PEI/PEG composite Fabry-Perot (FP) cavity of length similar to 13 mu m is coated at the distal end of the single-mode fiber using a dip coating technique. A highly sensitive optical and low-cost FPI probe fabrication has displayed a linear sensitivity of 17.10 nm/% in the range of 0.31%-1.25% CO2 gas. The response and recovery times of the sensor are in a few tens of seconds. The enhanced performance of the sensor is primarily due to the protonation and charge transfer between CO2 gas molecules and PEI/PEG composite. Due to low-cost fabrication and high sensitivity, this FPI sensor can be used in a range of potential applications in bioprocessing, healthcare, and environmental monitoring.</p>
10adip coating10aFresnel's reflection10aInterference10amonitoring10aOptical fiber sensors10aOptical fibers10apolymer composite10aPolymers10arefractive index10asensitivity10aSensor phenomena and characterization10asensors10aswelling10aTemperature sensors1 aPawar, Dnyandeo1 aPresti, Daniela, Lo1 aLemma, Enrico, D.1 aRainer, Alberto1 aKumar, Ajay1 aKanawade, Rajesh1 aSilvestri, Sergio1 aSchena, Emiliano1 aMassaroni, Carlo  uhttps://library.ncl.res.in/content/polymeric-peipeg-coated-optical-fiber-fabry-perot-interferometer-co2-detection