Green Polymerization of Vinyl Acetate Using Maghnite-Na+, an Exchanged Montmorillonite Clay, as an Ecologic Catalyst

dc.citation.epage190
dc.citation.issue2
dc.citation.spage183
dc.contributor.affiliationUniversity Oran
dc.contributor.authorCherifi, Badia Imene
dc.contributor.authorBelbachir, Mohammed
dc.contributor.authorBennabi, Souad
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
dc.date.accessioned2024-01-09T10:19:10Z
dc.date.available2024-01-09T10:19:10Z
dc.date.created2021-03-16
dc.date.issued2021-03-16
dc.description.abstractПроведено «зелену» полімеризацію вінілацетату новим методом, який полягає у використанні глини під назвою Maghnite-Na+ як екологічного, нетоксичного, недорогого каталізатора, що регенерується простою фільтрацією. За допомогою рентгенівської дифракції та скануючої електронної мікроскопії доведено, що Maghnite-Na+ можна отримувати катіонним обробленням (натрієм) сирої глини maghnite. Показано, що такий каталізатор є ефективною альтернативою токсичним каталізаторам пероксид бензоїлу та азобісізобутиронітрилу, які в основному використовуються для синтезу полівінілацетату (ПВА). Встановлено, що синтез стає менш енергозатратним завдяки використанню як ємності для реакційної суміші утилізованого поліуретану, який є поновлюваним матеріалом та хорошим теплоізолятором, що підтримує температуру 273 К протягом 6 год. В контексті «зеленої» хімії, з метою уникнення використання розчинника реакцію проводили в масі. Структуру отриманого полімеру встановлено методами 1Н та 13С ядерно-магнітної резонансної спектроскопії. Для підтвердження структури ПВА застосовано Фур‘є-спектроскопію. За допомогою термогравіметричного аналізу показано, що синтезований полімер є термічно стабільним і починає руйнуватися за 603 К, а визначена за допомогою диференціальної скануючої калориметрії температура склування становить 323 К.
dc.description.abstractIn this work, the green polymerization of vinyl acetate is carried out by a new method which consists in the use of clay called Maghnite-Na+ as an ecological catalyst, non-toxic, inexpensive and recyclable by a simple filtration. X-ray diffraction and scanning electron microscopy showed that Maghnite-Na+ is successfully obtained after cationic treatment (sodium) on crude maghnite. It is an effective alternative to replace toxic catalysts such as benzoyl peroxide and azobisisobutyronitrile which are mostly used during the synthesis of polyvinyl acetate (PVAc) making the polymerization reaction less problematic for the environment. The synthesis reaction is less energetic by the use of recycled polyurethane as a container for the reaction mixture and is considered as a renewable material and a good thermal insulator maintaining the temperature of 273 K for 6 h. The reaction in bulk is also preferred to avoid the use of a solvent and therefore to stay in the context of green chemistry. In these conditions, the structure of obtained polymer is established by 1H NMR and 13C NMR. Infrared spectroscopy (FT-IR) was also used to confirm the structure of PVAc. Thermogravimetric analysis showed that it is thermally stable and starts to degrade at 603 K while differential scanning calorimetry showed that this polymer has a glass transition temperature Tg of 323 K.
dc.format.extent183-190
dc.format.pages8
dc.identifier.citationCherifi B. I. Green Polymerization of Vinyl Acetate Using Maghnite-Na+, an Exchanged Montmorillonite Clay, as an Ecologic Catalyst / Badia Imene Cherifi, Mohammed Belbachir, Souad Bennabi // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2021. — Vol 15. — No 2. — P. 183–190.
dc.identifier.citationenCherifi B. I. Green Polymerization of Vinyl Acetate Using Maghnite-Na+, an Exchanged Montmorillonite Clay, as an Ecologic Catalyst / Badia Imene Cherifi, Mohammed Belbachir, Souad Bennabi // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2021. — Vol 15. — No 2. — P. 183–190.
dc.identifier.doidoi.org/10.23939/chcht15.02.183
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/60725
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 2 (15), 2021
dc.relation.references[1] Cui H., Du G.: Adv. Polym. Technol., 2012, 31, 130. https://doi.org/10.1002/adv.20244
dc.relation.references[2] Amann M., Minge O.: Adv. Polym. Sci., 2012, 245, 137. https://doi.org/10.1007/12_2011_153
dc.relation.references[3] Chen J., Zhao X., Zhang L. et al.: J. Polym. Sci. Pol. Chem., 2015, 53, 1430. https://doi.org/10.1002/pola.27582
dc.relation.references[4] Karakus G., Polat A., Yenidunya A. et al.: Polym. Int., 2012, 62, 492. https://doi.org/10.1002/pi.4341
dc.relation.references[5] Andersen F.: J. Am. Coll. Toxicol., 1996, 15, 166. https://doi.org/10.3109%2F10915819609043794
dc.relation.references[6] Abdollahi M., Bigdeli P.: Polym. Bull., 2018, 75, 1823. https://doi.org/10.1007/s00289-017-2130-z
dc.relation.references[7] Kattner H., Buback M.: Macromol. Chem. Phys., 2014, 215, 1180. https://doi.org/10.1002/macp.201400095
dc.relation.references[8] Pennarun P.-Y.: Pat. EP2552243A1, Publ. Febr. 06, 2013.
dc.relation.references[9] https://www.sciencepresse.qc.ca/blogue/2011/08/08/fautcraindre-gomme-macher
dc.relation.references[10] Morin A., Detrembleur C., Jerôme C. et al.: Macromolecules, 2013, 46, 4303. https://doi.org/10.1021/ma400651a
dc.relation.references[11] Geng S., Shah F., Liu P. et al.: RSC Adv., 2017, 7, 7483. https://doi.org/10.1039/c6ra28574k
dc.relation.references[12] Zhang Y., Pang B., Yang S. et al.: Materials, 2018, 11, 89. https://doi.org/10.3390/ma11010089
dc.relation.references[13] Dubininkas M., Buika G.: Chinese J. Polym. Sci., 2013, 31, 346. https://doi.org/10.1007/s10118-013-1220-0
dc.relation.references[14] Madras G., Chattopadhyay S.: Polym. Degrad. Stabil., 2001, 73, 33. https://doi.org/10.1016/S0141-3910(01)00064-7
dc.relation.references[15] Tewari N., Srivastava A.: Can. J. Chem., 1990, 68, 356. https://doi.org/10.1139/v90-052
dc.relation.references[16] Shaffei K., Moustafa A., Hamed A.: Int. J. Polym. Sci., 2009, 2009. https://doi.org/10.1155/2009/731971
dc.relation.references[17] http://www.labchem.com/tools/msds/msds/LC20070.pdf
dc.relation.references[18] https://pubchem.ncbi.nlm.nih.gov/compound/benzoyl_peroxide#section=Toxicity
dc.relation.references[19] https://pubchem.ncbi.nlm.nih.gov/compound/aibn#section=Human-Toxicity-Excerpts
dc.relation.references[20] https://snpu.fr/un-polyurethane-durable-contre-le-rechauffementclimatique/
dc.relation.references[21] Belbachir M., Bensaoula A.: Pat. US 6274527B1, Publ. Aug. 14, 2001.
dc.relation.references[22] Benharrats N., Belbachir M., Legrand A. et al.: Clay Miner., 2003, 38, 49. https://doi.org/10.1180/0009855033810078
dc.relation.references[23] Breen C., Madejovii J., Komadel P.: Appl. Clay. Sci., 1995, 10, 219. https://doi.org/10.1016/0169-1317(95)00024-X
dc.relation.references[24] Ayat M., Belbachir M., Rahmouni A.: Bull. Chem. React. Eng. Catal., 2016, 11, 376. https://doi.org/10.9767/bcrec.11.3.578.376-388
dc.relation.references[25] Bensaada N., Ayat M., Meghabar R. et al.: Current. Chem. Lett., 2015, 4, 55. https://doi.org/10.5267/j.ccl.2015.3.002
dc.relation.references[26] Rahmouni A., Belbachir M., Ayat M.: Bull. Chem. React. Eng. Catal., 2018, 13, 262. https://doi.org/10.9767/bcrec.13.2.1308.262-274
dc.relation.references[27] Kim B., Jung J., Hong S. et al.: Macromolecules, 2002, 35, 1419. https://doi.org/10.1021/ma010497c
dc.relation.references[28] Abd El-Ghaffar M., Youssef A., Abd El-Hakim A.: Arab. J. Chem., 2015, 8, 771. https://doi.org/10.1016/j.arabjc.2014.01.001
dc.relation.references[29] Nuruzzaman Md., Rahman M., Liu Y. et al.:J. Agric. Food Chem., 2016, 64, 1447. https://doi.org/10.1021/acs.jafc.5b05214
dc.relation.references[30] Zenasni M., Benfarhi S., Merlin A. et al.: Nat. Sci., 2012, 4, 856. https://doi.org/10.4236/ns.2012.411114
dc.relation.references[31] https://www.chemicalbook.com/SpectrumEN_108-05-4_1HNMR.htm
dc.relation.references[32] Itab Y.: Doct. thesis. The University of Lorraine, 2012.
dc.relation.references[33] Poljansek I., Fabjan E., Burja K. et al.: Prog. Org. Coat., 2013, 76, 1798. https://doi.org/10.1016/j.porgcoat.2013.05.019
dc.relation.references[34] Rimez B., Rahier H., Van Assche G. et al.: Polym. Degrad. Stabil., 2008, 93, 800. https://doi.org/10.1016/j.polymdegradstab.2008.01.010
dc.relation.references[35] Daniels W.: Vinyl Acetate Polymers, Encyclopedia of Polymer Science & Engineering, 2nd edn. Wiley Interscience 1990, 402-442.
dc.relation.referencesen[1] Cui H., Du G., Adv. Polym. Technol., 2012, 31, 130. https://doi.org/10.1002/adv.20244
dc.relation.referencesen[2] Amann M., Minge O., Adv. Polym. Sci., 2012, 245, 137. https://doi.org/10.1007/12_2011_153
dc.relation.referencesen[3] Chen J., Zhao X., Zhang L. et al., J. Polym. Sci. Pol. Chem., 2015, 53, 1430. https://doi.org/10.1002/pola.27582
dc.relation.referencesen[4] Karakus G., Polat A., Yenidunya A. et al., Polym. Int., 2012, 62, 492. https://doi.org/10.1002/pi.4341
dc.relation.referencesen[5] Andersen F., J. Am. Coll. Toxicol., 1996, 15, 166. https://doi.org/10.3109%2F10915819609043794
dc.relation.referencesen[6] Abdollahi M., Bigdeli P., Polym. Bull., 2018, 75, 1823. https://doi.org/10.1007/s00289-017-2130-z
dc.relation.referencesen[7] Kattner H., Buback M., Macromol. Chem. Phys., 2014, 215, 1180. https://doi.org/10.1002/macp.201400095
dc.relation.referencesen[8] Pennarun P.-Y., Pat. EP2552243A1, Publ. Febr. 06, 2013.
dc.relation.referencesen[9] https://www.sciencepresse.qc.ca/blogue/2011/08/08/fautcraindre-gomme-macher
dc.relation.referencesen[10] Morin A., Detrembleur C., Jerôme C. et al., Macromolecules, 2013, 46, 4303. https://doi.org/10.1021/ma400651a
dc.relation.referencesen[11] Geng S., Shah F., Liu P. et al., RSC Adv., 2017, 7, 7483. https://doi.org/10.1039/P.6ra28574k
dc.relation.referencesen[12] Zhang Y., Pang B., Yang S. et al., Materials, 2018, 11, 89. https://doi.org/10.3390/ma11010089
dc.relation.referencesen[13] Dubininkas M., Buika G., Chinese J. Polym. Sci., 2013, 31, 346. https://doi.org/10.1007/s10118-013-1220-0
dc.relation.referencesen[14] Madras G., Chattopadhyay S., Polym. Degrad. Stabil., 2001, 73, 33. https://doi.org/10.1016/S0141-3910(01)00064-7
dc.relation.referencesen[15] Tewari N., Srivastava A., Can. J. Chem., 1990, 68, 356. https://doi.org/10.1139/v90-052
dc.relation.referencesen[16] Shaffei K., Moustafa A., Hamed A., Int. J. Polym. Sci., 2009, 2009. https://doi.org/10.1155/2009/731971
dc.relation.referencesen[17] http://www.labchem.com/tools/msds/msds/LC20070.pdf
dc.relation.referencesen[18] https://pubchem.ncbi.nlm.nih.gov/compound/benzoyl_peroxide#section=Toxicity
dc.relation.referencesen[19] https://pubchem.ncbi.nlm.nih.gov/compound/aibn#section=Human-Toxicity-Excerpts
dc.relation.referencesen[20] https://snpu.fr/un-polyurethane-durable-contre-le-rechauffementclimatique/
dc.relation.referencesen[21] Belbachir M., Bensaoula A., Pat. US 6274527B1, Publ. Aug. 14, 2001.
dc.relation.referencesen[22] Benharrats N., Belbachir M., Legrand A. et al., Clay Miner., 2003, 38, 49. https://doi.org/10.1180/0009855033810078
dc.relation.referencesen[23] Breen C., Madejovii J., Komadel P., Appl. Clay. Sci., 1995, 10, 219. https://doi.org/10.1016/0169-1317(95)00024-X
dc.relation.referencesen[24] Ayat M., Belbachir M., Rahmouni A., Bull. Chem. React. Eng. Catal., 2016, 11, 376. https://doi.org/10.9767/bcrec.11.3.578.376-388
dc.relation.referencesen[25] Bensaada N., Ayat M., Meghabar R. et al., Current. Chem. Lett., 2015, 4, 55. https://doi.org/10.5267/j.ccl.2015.3.002
dc.relation.referencesen[26] Rahmouni A., Belbachir M., Ayat M., Bull. Chem. React. Eng. Catal., 2018, 13, 262. https://doi.org/10.9767/bcrec.13.2.1308.262-274
dc.relation.referencesen[27] Kim B., Jung J., Hong S. et al., Macromolecules, 2002, 35, 1419. https://doi.org/10.1021/ma010497c
dc.relation.referencesen[28] Abd El-Ghaffar M., Youssef A., Abd El-Hakim A., Arab. J. Chem., 2015, 8, 771. https://doi.org/10.1016/j.arabjc.2014.01.001
dc.relation.referencesen[29] Nuruzzaman Md., Rahman M., Liu Y. et al.:J. Agric. Food Chem., 2016, 64, 1447. https://doi.org/10.1021/acs.jafc.5b05214
dc.relation.referencesen[30] Zenasni M., Benfarhi S., Merlin A. et al., Nat. Sci., 2012, 4, 856. https://doi.org/10.4236/ns.2012.411114
dc.relation.referencesen[31] https://www.chemicalbook.com/SpectrumEN_108-05-4_1HNMR.htm
dc.relation.referencesen[32] Itab Y., Doct. thesis. The University of Lorraine, 2012.
dc.relation.referencesen[33] Poljansek I., Fabjan E., Burja K. et al., Prog. Org. Coat., 2013, 76, 1798. https://doi.org/10.1016/j.porgcoat.2013.05.019
dc.relation.referencesen[34] Rimez B., Rahier H., Van Assche G. et al., Polym. Degrad. Stabil., 2008, 93, 800. https://doi.org/10.1016/j.polymdegradstab.2008.01.010
dc.relation.referencesen[35] Daniels W., Vinyl Acetate Polymers, Encyclopedia of Polymer Science & Engineering, 2nd edn. Wiley Interscience 1990, 402-442.
dc.relation.urihttps://doi.org/10.1002/adv.20244
dc.relation.urihttps://doi.org/10.1007/12_2011_153
dc.relation.urihttps://doi.org/10.1002/pola.27582
dc.relation.urihttps://doi.org/10.1002/pi.4341
dc.relation.urihttps://doi.org/10.3109%2F10915819609043794
dc.relation.urihttps://doi.org/10.1007/s00289-017-2130-z
dc.relation.urihttps://doi.org/10.1002/macp.201400095
dc.relation.urihttps://www.sciencepresse.qc.ca/blogue/2011/08/08/fautcraindre-gomme-macher
dc.relation.urihttps://doi.org/10.1021/ma400651a
dc.relation.urihttps://doi.org/10.1039/c6ra28574k
dc.relation.urihttps://doi.org/10.3390/ma11010089
dc.relation.urihttps://doi.org/10.1007/s10118-013-1220-0
dc.relation.urihttps://doi.org/10.1016/S0141-3910(01)00064-7
dc.relation.urihttps://doi.org/10.1139/v90-052
dc.relation.urihttps://doi.org/10.1155/2009/731971
dc.relation.urihttp://www.labchem.com/tools/msds/msds/LC20070.pdf
dc.relation.urihttps://pubchem.ncbi.nlm.nih.gov/compound/benzoyl_peroxide#section=Toxicity
dc.relation.urihttps://pubchem.ncbi.nlm.nih.gov/compound/aibn#section=Human-Toxicity-Excerpts
dc.relation.urihttps://snpu.fr/un-polyurethane-durable-contre-le-rechauffementclimatique/
dc.relation.urihttps://doi.org/10.1180/0009855033810078
dc.relation.urihttps://doi.org/10.1016/0169-1317(95)00024-X
dc.relation.urihttps://doi.org/10.9767/bcrec.11.3.578.376-388
dc.relation.urihttps://doi.org/10.5267/j.ccl.2015.3.002
dc.relation.urihttps://doi.org/10.9767/bcrec.13.2.1308.262-274
dc.relation.urihttps://doi.org/10.1021/ma010497c
dc.relation.urihttps://doi.org/10.1016/j.arabjc.2014.01.001
dc.relation.urihttps://doi.org/10.1021/acs.jafc.5b05214
dc.relation.urihttps://doi.org/10.4236/ns.2012.411114
dc.relation.urihttps://www.chemicalbook.com/SpectrumEN_108-05-4_1HNMR.htm
dc.relation.urihttps://doi.org/10.1016/j.porgcoat.2013.05.019
dc.relation.urihttps://doi.org/10.1016/j.polymdegradstab.2008.01.010
dc.rights.holder© Національний університет “Львівська політехніка”, 2021
dc.rights.holder© Cherifi B., Belbachir M., Bennabi S., 2021
dc.subjectполівінілацетат
dc.subjectекологічний каталізатор
dc.subjectМaghnite-Na+
dc.subjectполімеризація
dc.subject«зелена» хімія
dc.subjectтермічна стабільність
dc.subjectpolyvinyl acetate
dc.subjectecologic catalyst
dc.subjectMaghnite-Na+
dc.subjectpolymerization
dc.subjectgreen chemistry
dc.subjectthermal stability
dc.titleGreen Polymerization of Vinyl Acetate Using Maghnite-Na+, an Exchanged Montmorillonite Clay, as an Ecologic Catalyst
dc.title.alternative«Зелена» полімерізація вінілацетату з використанням як екокаталізатора монтморилонітової глини Maghnite-Na+
dc.typeArticle

Files

Original bundle

Now showing 1 - 2 of 2
Thumbnail Image
Name:
2021v15n2_Cherifi_B_I-Green_Polymerization_183-190.pdf
Size:
706.78 KB
Format:
Adobe Portable Document Format
Thumbnail Image
Name:
2021v15n2_Cherifi_B_I-Green_Polymerization_183-190__COVER.png
Size:
547.64 KB
Format:
Portable Network Graphics

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.78 KB
Format:
Plain Text
Description: