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

Badia Imene Cherifi1, Mohammed Belbachir1, Souad Bennabi1
Affiliation: 
1 Laboratory of Polymer Chemistry, Department of Chemistry, Faculty of Exact and Applied Sciences, University Oran1 Ahmed Ben Bella, BP 1524 El M'Naouar, 31000 Oran, Algeria cherifi.imene@edu.univ-oran1.dz
DOI: 
https://doi.org/10.23939/chcht15.02.183
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Abstract: 
In 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.
References: 

[1] Cui H., Du G.: Adv. Polym. Technol., 2012, 31, 130. https://doi.org/10.1002/adv.20244
https://doi.org/10.1002/adv.20244

[2] Amann M., Minge O.: Adv. Polym. Sci., 2012, 245, 137. https://doi.org/10.1007/12_2011_153
https://doi.org/10.1007/12_2011_153

[3] Chen J., Zhao X., Zhang L. et al.: J. Polym. Sci. Pol. Chem., 2015, 53, 1430. https://doi.org/10.1002/pola.27582
https://doi.org/10.1002/pola.27582

[4] Karakus G., Polat A., Yenidunya A. et al.: Polym. Int., 2012, 62, 492. https://doi.org/10.1002/pi.4341
https://doi.org/10.1002/pi.4341

[5] Andersen F.: J. Am. Coll. Toxicol., 1996, 15, 166. https://doi.org/10.3109%2F10915819609043794

[6] Abdollahi M., Bigdeli P.: Polym. Bull., 2018, 75, 1823. https://doi.org/10.1007/s00289-017-2130-z
https://doi.org/10.1007/s00289-017-2130-z

[7] Kattner H., Buback M.: Macromol. Chem. Phys., 2014, 215, 1180. https://doi.org/10.1002/macp.201400095
https://doi.org/10.1002/macp.201400095

[8] Pennarun P.-Y.: Pat. EP2552243A1, Publ. Febr. 06, 2013.

[9] https://www.sciencepresse.qc.ca/blogue/2011/08/08/faut-craindre-gomme-ma...

[10] Morin A., Detrembleur C., Jerôme C. et al.: Macromolecules, 2013, 46, 4303. https://doi.org/10.1021/ma400651a
https://doi.org/10.1021/ma400651a

[11] Geng S., Shah F., Liu P. et al.: RSC Adv., 2017, 7, 7483. https://doi.org/10.1039/c6ra28574k
https://doi.org/10.1039/C6RA28574K

[12] Zhang Y., Pang B., Yang S. et al.: Materials, 2018, 11, 89. https://doi.org/10.3390/ma11010089
https://doi.org/10.3390/ma11010089

[13] Dubininkas M., Buika G.: Chinese J. Polym. Sci., 2013, 31, 346. https://doi.org/10.1007/s10118-013-1220-0
https://doi.org/10.1007/s10118-013-1220-0

[14] Madras G., Chattopadhyay S.: Polym. Degrad. Stabil., 2001, 73, 33. https://doi.org/10.1016/S0141-3910(01)00064-7
https://doi.org/10.1016/S0141-3910(01)00064-7

[15] Tewari N., Srivastava A.: Can. J. Chem., 1990, 68, 356. https://doi.org/10.1139/v90-052
https://doi.org/10.1139/v90-052

[16] Shaffei K., Moustafa A., Hamed A.: Int. J. Polym. Sci., 2009, 2009. https://doi.org/10.1155/2009/731971
https://doi.org/10.1155/2009/731971

[17] http://www.labchem.com/tools/msds/msds/LC20070.pdf

[18] https://pubchem.ncbi.nlm.nih.gov/compound/benzoyl_peroxide#section=Toxicity

[19] https://pubchem.ncbi.nlm.nih.gov/compound/aibn#section=Human-Toxicity-Ex...

[20] https://snpu.fr/un-polyurethane-durable-contre-le-rechauffement-climatique/

[21] Belbachir M., Bensaoula A.: Pat. US 6274527B1, Publ. Aug. 14, 2001.

[22] Benharrats N., Belbachir M., Legrand A. et al.: Clay Miner., 2003, 38, 49. https://doi.org/10.1180/0009855033810078
https://doi.org/10.1180/0009855033810078

[23] Breen C., Madejovii J., Komadel P.: Appl. Clay. Sci., 1995, 10, 219. https://doi.org/10.1016/0169-1317(95)00024-X
https://doi.org/10.1016/0169-1317(95)00024-X

[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
https://doi.org/10.9767/bcrec.11.3.578.376-388

[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
https://doi.org/10.5267/j.ccl.2015.3.002

[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
https://doi.org/10.9767/bcrec.13.2.1308.262-274

[27] Kim B., Jung J., Hong S. et al.: Macromolecules, 2002, 35, 1419. https://doi.org/10.1021/ma010497c
https://doi.org/10.1021/ma010497c

[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
https://doi.org/10.1016/j.arabjc.2014.01.001

[29] Nuruzzaman Md., Rahman M., Liu Y. et al.: J. Agric. Food Chem., 2016, 64, 1447.
https://doi.org/10.1021/acs.jafc.5b05214

https://doi.org/10.1021/acs.jafc.5b05214
https://doi.org/10.1021/acs.jafc.5b05214

[30] Zenasni M., Benfarhi S., Merlin A. et al.: Nat. Sci., 2012, 4, 856. https://doi.org/10.4236/ns.2012.411114
https://doi.org/10.4236/ns.2012.411114

[31] https://www.chemicalbook.com/SpectrumEN_108-05-4_1HNMR.htm

[32] Itab Y.: Doct. thesis. The University of Lorraine, 2012.

[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
https://doi.org/10.1016/j.porgcoat.2013.05.019

[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
https://doi.org/10.1016/j.polymdegradstab.2008.01.010

[35] Daniels W.: Vinyl Acetate Polymers, Encyclopedia of Polymer Science & Engineering, 2nd edn. Wiley Interscience 1990, 402-442.