Graft Copolymerization of Acrylonitrile onto Sodium Salt of Partially Carboxymethylated Tamarind Kernel Powder Using Ceric Ammonium Nitrate as a Photo‐Initiator in an Aqueous Medium Under Ultraviolet‐Radiation

Ultraviolet (UV) radiation‐induced graft copolymerization of acrylonitrile (AN) onto sodium salt of partially carboxymethylated tamarind kernel powder (Na‐PCMTKP, DS¯=0.15) has been carried out using ceric ammonium nitrate (CAN) as a photo‐initiator. The optimal UV‐radiation‐induced grafting conditi...

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Veröffentlicht in:Macromolecular symposia. 2021-08, Vol.398 (1), p.n/a
Hauptverfasser: Trivedi, Jignesh H., Joshi, Harshil A., Trivedi, Harikrishna C.
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description Ultraviolet (UV) radiation‐induced graft copolymerization of acrylonitrile (AN) onto sodium salt of partially carboxymethylated tamarind kernel powder (Na‐PCMTKP, DS¯=0.15) has been carried out using ceric ammonium nitrate (CAN) as a photo‐initiator. The optimal UV‐radiation‐induced grafting conditions have been established with Na‐PCMTKP = 0.5 g (dry basis), [HNO3] = 0.2 mol L−1, [AN] = 0.295 mol L−1, [CAN] = 6.0 × 10−3 mol L−1, time = 6 h, temperature = 30 °C, volume of water = 144.58 mL, and total volume = 150 mL. The maximum percentage of grafting (%G) and percentage grafting efficiency (%GE) achieved under these established optimum reaction conditions are 361.16% and 89.33%, respectively. The various reaction conditions have been varied with a view to study their influence on the grafting yields (%G and %GE). A plausible mechanism to explain initiation, propagation, and termination of UV‐radiation‐initiated graft copolymerization has also been suggested. The influence of the efficiency of the photo‐initiator on the grafting yields has been investigated. Fourier transform infrared, thermogravimetric analysis, differential scanning calorimeter (DSC), and scanning electron microscopy techniques have been successfully used to provide the evidence of grafting of polyacrylonitrile onto Na‐PCMTKP. The kinetics of thermal decomposition of the graft copolymer, Na‐PCMTKP‐g‐PAN, has also been investigated with the help of the DSC curves obtained at different heating rates. The Ozawa and the Kissinger methods have been utilized for the evaluation of the kinetic parameters for the thermal decomposition of the graft copolymer sample. The synthesized graft copolymer after saponification may be used as a superabsorbent hydrogel for potential applications.
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The optimal UV‐radiation‐induced grafting conditions have been established with Na‐PCMTKP = 0.5 g (dry basis), [HNO3] = 0.2 mol L−1, [AN] = 0.295 mol L−1, [CAN] = 6.0 × 10−3 mol L−1, time = 6 h, temperature = 30 °C, volume of water = 144.58 mL, and total volume = 150 mL. The maximum percentage of grafting (%G) and percentage grafting efficiency (%GE) achieved under these established optimum reaction conditions are 361.16% and 89.33%, respectively. The various reaction conditions have been varied with a view to study their influence on the grafting yields (%G and %GE). A plausible mechanism to explain initiation, propagation, and termination of UV‐radiation‐initiated graft copolymerization has also been suggested. The influence of the efficiency of the photo‐initiator on the grafting yields has been investigated. Fourier transform infrared, thermogravimetric analysis, differential scanning calorimeter (DSC), and scanning electron microscopy techniques have been successfully used to provide the evidence of grafting of polyacrylonitrile onto Na‐PCMTKP. The kinetics of thermal decomposition of the graft copolymer, Na‐PCMTKP‐g‐PAN, has also been investigated with the help of the DSC curves obtained at different heating rates. The Ozawa and the Kissinger methods have been utilized for the evaluation of the kinetic parameters for the thermal decomposition of the graft copolymer sample. 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The optimal UV‐radiation‐induced grafting conditions have been established with Na‐PCMTKP = 0.5 g (dry basis), [HNO3] = 0.2 mol L−1, [AN] = 0.295 mol L−1, [CAN] = 6.0 × 10−3 mol L−1, time = 6 h, temperature = 30 °C, volume of water = 144.58 mL, and total volume = 150 mL. The maximum percentage of grafting (%G) and percentage grafting efficiency (%GE) achieved under these established optimum reaction conditions are 361.16% and 89.33%, respectively. The various reaction conditions have been varied with a view to study their influence on the grafting yields (%G and %GE). A plausible mechanism to explain initiation, propagation, and termination of UV‐radiation‐initiated graft copolymerization has also been suggested. The influence of the efficiency of the photo‐initiator on the grafting yields has been investigated. Fourier transform infrared, thermogravimetric analysis, differential scanning calorimeter (DSC), and scanning electron microscopy techniques have been successfully used to provide the evidence of grafting of polyacrylonitrile onto Na‐PCMTKP. The kinetics of thermal decomposition of the graft copolymer, Na‐PCMTKP‐g‐PAN, has also been investigated with the help of the DSC curves obtained at different heating rates. The Ozawa and the Kissinger methods have been utilized for the evaluation of the kinetic parameters for the thermal decomposition of the graft copolymer sample. The synthesized graft copolymer after saponification may be used as a superabsorbent hydrogel for potential applications.</description><subject>Acrylonitrile</subject><subject>Ammonium</subject><subject>Ammonium nitrate</subject><subject>Aqueous solutions</subject><subject>Cerium ammonium nitrate</subject><subject>Copolymerization</subject><subject>Differential scanning calorimetry</subject><subject>evidence of grafting</subject><subject>Fourier analysis</subject><subject>Fourier transforms</subject><subject>graft copolymerization</subject><subject>Graft copolymers</subject><subject>Hydrogels</subject><subject>Infrared analysis</subject><subject>Initiators</subject><subject>Kernels</subject><subject>kinetic parameters</subject><subject>Optimization</subject><subject>Polyacrylonitrile</subject><subject>Radiation</subject><subject>Scanning electron microscopy</subject><subject>Sodium</subject><subject>sodium salt of partially carboxymethylated tamarind kernel powder</subject><subject>Sodium salts</subject><subject>Tamarind</subject><subject>Thermal decomposition</subject><subject>Thermogravimetric analysis</subject><subject>Ultraviolet radiation</subject><subject>ultraviolet‐induced</subject><issn>1022-1360</issn><issn>1521-3900</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkc2O0zAQxyMEEsvClfNInFNsp4mbYxTBsmIXKro9cIomscN65djFdlnCiUfg5XgBnoRpi-DIyR_6_T80k2XPOVtwxsTLCeO8EEwwegj5IDvjpeB5UTP2kO70l_OiYo-zJzHeEVPXkp9lPy8Cjglav_N2nnQw3zAZ78CP0Axhtt6ZFIzV4F3ysPHK7CfYoE0HYo0hGbR2hhZD77-SQbqdLSat4AYnDMYpeKuD0xbW_l7pANto3CdoKWiAZprInvzeUQaJACMgrG998r--_7ikZIPJBzAO0EHzea_9PsK1PnbYuqOdJeUX461OJPmAyhzrP80ejWijfvbnPM-2r1_dtG_yq_cXl21zlQ9CCpljKSupZVlJVVW8wKEolBxWyAemFYpe1hz1oPpyqXTPe4UjL8tlWRWyqFUvdXGevTj57oKnejF1d34fHEV2grBlvVpxTtTiRA3Bxxj02O2CoenMHWfdYXXdYXXd39WRoD4J7mny83_o7rrZfPyn_Q1fYaWq</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Trivedi, Jignesh H.</creator><creator>Joshi, Harshil A.</creator><creator>Trivedi, Harikrishna C.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0002-7976-1181</orcidid></search><sort><creationdate>202108</creationdate><title>Graft Copolymerization of Acrylonitrile onto Sodium Salt of Partially Carboxymethylated Tamarind Kernel Powder Using Ceric Ammonium Nitrate as a Photo‐Initiator in an Aqueous Medium Under Ultraviolet‐Radiation</title><author>Trivedi, Jignesh H. ; 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The optimal UV‐radiation‐induced grafting conditions have been established with Na‐PCMTKP = 0.5 g (dry basis), [HNO3] = 0.2 mol L−1, [AN] = 0.295 mol L−1, [CAN] = 6.0 × 10−3 mol L−1, time = 6 h, temperature = 30 °C, volume of water = 144.58 mL, and total volume = 150 mL. The maximum percentage of grafting (%G) and percentage grafting efficiency (%GE) achieved under these established optimum reaction conditions are 361.16% and 89.33%, respectively. The various reaction conditions have been varied with a view to study their influence on the grafting yields (%G and %GE). A plausible mechanism to explain initiation, propagation, and termination of UV‐radiation‐initiated graft copolymerization has also been suggested. The influence of the efficiency of the photo‐initiator on the grafting yields has been investigated. Fourier transform infrared, thermogravimetric analysis, differential scanning calorimeter (DSC), and scanning electron microscopy techniques have been successfully used to provide the evidence of grafting of polyacrylonitrile onto Na‐PCMTKP. The kinetics of thermal decomposition of the graft copolymer, Na‐PCMTKP‐g‐PAN, has also been investigated with the help of the DSC curves obtained at different heating rates. The Ozawa and the Kissinger methods have been utilized for the evaluation of the kinetic parameters for the thermal decomposition of the graft copolymer sample. The synthesized graft copolymer after saponification may be used as a superabsorbent hydrogel for potential applications.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/masy.202000227</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7976-1181</orcidid></addata></record>
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subjects Acrylonitrile
Ammonium
Ammonium nitrate
Aqueous solutions
Cerium ammonium nitrate
Copolymerization
Differential scanning calorimetry
evidence of grafting
Fourier analysis
Fourier transforms
graft copolymerization
Graft copolymers
Hydrogels
Infrared analysis
Initiators
Kernels
kinetic parameters
Optimization
Polyacrylonitrile
Radiation
Scanning electron microscopy
Sodium
sodium salt of partially carboxymethylated tamarind kernel powder
Sodium salts
Tamarind
Thermal decomposition
Thermogravimetric analysis
Ultraviolet radiation
ultraviolet‐induced
title Graft Copolymerization of Acrylonitrile onto Sodium Salt of Partially Carboxymethylated Tamarind Kernel Powder Using Ceric Ammonium Nitrate as a Photo‐Initiator in an Aqueous Medium Under Ultraviolet‐Radiation
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