Dimethylformamide Impurities as Propylene Polymerization Inhibito
This research study examined how the use of dimethylformamide (DMF) as an inhibitor af fects the propylene polymerization process when using a Ziegler–Natta catalyst. Several experiments were carried out using TiCl4/MgCl2 as a catalyst, aluminum trialkyl as a cocatalyst, and different amounts of DMF...
- Autores:
-
Hernández Fernández, Joaquin
González-Cuello, Rafael
Ortega-Toro, Rodrigo
- Tipo de recurso:
- Fecha de publicación:
- 2023
- Institución:
- Universidad Tecnológica de Bolívar
- Repositorio:
- Repositorio Institucional UTB
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.utb.edu.co:20.500.12585/12539
- Palabra clave:
- Polypropylene
N,N-dimethylformamide (DMF)
Ziegler–Natta catalyst
Productivity
Melt flow index (MFI)
Molecular weight distribution (MW)
Catalyst inhibition
Density functional theory (DFT)
LEMB
- Rights
- openAccess
- License
- http://creativecommons.org/publicdomain/zero/1.0/
id |
UTB2_3fbc95ccc2364c3b9654d90c5a3c05e7 |
---|---|
oai_identifier_str |
oai:repositorio.utb.edu.co:20.500.12585/12539 |
network_acronym_str |
UTB2 |
network_name_str |
Repositorio Institucional UTB |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
dc.title.alternative.spa.fl_str_mv |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
title |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
spellingShingle |
Dimethylformamide Impurities as Propylene Polymerization Inhibito Polypropylene N,N-dimethylformamide (DMF) Ziegler–Natta catalyst Productivity Melt flow index (MFI) Molecular weight distribution (MW) Catalyst inhibition Density functional theory (DFT) LEMB |
title_short |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
title_full |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
title_fullStr |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
title_full_unstemmed |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
title_sort |
Dimethylformamide Impurities as Propylene Polymerization Inhibito |
dc.creator.fl_str_mv |
Hernández Fernández, Joaquin González-Cuello, Rafael Ortega-Toro, Rodrigo |
dc.contributor.author.none.fl_str_mv |
Hernández Fernández, Joaquin González-Cuello, Rafael Ortega-Toro, Rodrigo |
dc.subject.keywords.spa.fl_str_mv |
Polypropylene N,N-dimethylformamide (DMF) Ziegler–Natta catalyst Productivity Melt flow index (MFI) Molecular weight distribution (MW) Catalyst inhibition Density functional theory (DFT) |
topic |
Polypropylene N,N-dimethylformamide (DMF) Ziegler–Natta catalyst Productivity Melt flow index (MFI) Molecular weight distribution (MW) Catalyst inhibition Density functional theory (DFT) LEMB |
dc.subject.armarc.none.fl_str_mv |
LEMB |
description |
This research study examined how the use of dimethylformamide (DMF) as an inhibitor af fects the propylene polymerization process when using a Ziegler–Natta catalyst. Several experiments were carried out using TiCl4/MgCl2 as a catalyst, aluminum trialkyl as a cocatalyst, and different amounts of DMF. Then, we analyzed how DMF influences other aspects of the process, such as catalyst activity, molecular weight, and the number of branches in the polymer chains obtained, using experimental and computational methods. The results revealed that as the DMF/Ti ratio increases, the catalyst activity decreases. From a concentration of 5.11 ppm of DMF, a decrease in catalyst activity was observed, ranging from 45 TM/Kg to 44 TM/Kg. When the DMF concentration was increased to 40.23 ppm, the catalyst activity decreased to 43 TM/Kg, and with 75.32 ppm, it dropped even further to 39 TM/Kg. The highest concentration of DMF evaluated, 89.92 ppm, resulted in a catalyst productivity of 36.5 TM/Kg and lost productivity of 22%. In addition, significant changes in the polymer’s melt flow index (MFI) were noted as the DMF concentration increased. When 89.92 ppm of DMF was added, the MFI loss was 75%, indicating a higher flowability of the poly mer. In this study, it was found that dimethylformamide (DMF) exhibits a strong affinity for the titanium center of a Ziegler–Natta (ZN) catalyst, with an adsorption energy (Ead) of approximately −46.157 kcal/mol, indicating a robust interaction. This affinity is significantly higher compared to propylene, which has an Ead of approximately −5.2 kcal/mol. The study also revealed that the energy gap between the highest occupied molecular orbital (HOMO) of DMF and the lowest unoccupied molecular orbital (SOMO) of the Ziegler–Natta (ZN) catalyst is energetically favorable, with a value of approximately 0.311 eV. |
publishDate |
2023 |
dc.date.accessioned.none.fl_str_mv |
2023-10-03T14:02:33Z |
dc.date.available.none.fl_str_mv |
2023-10-03T14:02:33Z |
dc.date.issued.none.fl_str_mv |
2023-09-18 |
dc.date.submitted.none.fl_str_mv |
2023-10-02 |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.hasversion.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.spa.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
status_str |
publishedVersion |
dc.identifier.citation.spa.fl_str_mv |
Hernández-Fernández, J.; González-Cuello, R.; Ortega-Toro, R. Dimethylformamide Impurities as Propylene Polymerization Inhibitor. Polymers 2023, 15, 3806. https://doi.org/10.3390/polym15183806. |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12585/12539 |
dc.identifier.url.none.fl_str_mv |
https://doi.org/10.3390/polym15183806 |
dc.identifier.instname.spa.fl_str_mv |
Universidad Tecnológica de Bolívar |
dc.identifier.reponame.spa.fl_str_mv |
Repositorio Universidad Tecnológica de Bolívar |
identifier_str_mv |
Hernández-Fernández, J.; González-Cuello, R.; Ortega-Toro, R. Dimethylformamide Impurities as Propylene Polymerization Inhibitor. Polymers 2023, 15, 3806. https://doi.org/10.3390/polym15183806. Universidad Tecnológica de Bolívar Repositorio Universidad Tecnológica de Bolívar |
url |
https://hdl.handle.net/20.500.12585/12539 https://doi.org/10.3390/polym15183806 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/publicdomain/zero/1.0/ |
dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.cc.*.fl_str_mv |
CC0 1.0 Universal |
rights_invalid_str_mv |
http://creativecommons.org/publicdomain/zero/1.0/ CC0 1.0 Universal http://purl.org/coar/access_right/c_abf2 |
eu_rights_str_mv |
openAccess |
dc.format.extent.none.fl_str_mv |
15 |
dc.format.mimetype.spa.fl_str_mv |
application/pdf |
dc.publisher.place.spa.fl_str_mv |
Cartagena de Indias |
dc.publisher.sede.spa.fl_str_mv |
Campus Tecnológico |
dc.source.spa.fl_str_mv |
Polymers |
institution |
Universidad Tecnológica de Bolívar |
bitstream.url.fl_str_mv |
https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/1/polymers-15-03806.pdf https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/2/license_rdf https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/3/license.txt https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/4/polymers-15-03806.pdf.txt https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/5/polymers-15-03806.pdf.jpg |
bitstream.checksum.fl_str_mv |
e1b59d5be608dc53b2cb78b993ac5e6b 42fd4ad1e89814f5e4a476b409eb708c e20ad307a1c5f3f25af9304a7a7c86b6 1047aab6f7c54f1cefb0ac1a08791697 deec3124e5c33b24502d38769bc9d44d |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositorio Institucional UTB |
repository.mail.fl_str_mv |
repositorioutb@utb.edu.co |
_version_ |
1814021581093994496 |
spelling |
Hernández Fernández, Joaquinc9c120ef-5174-40a7-b55e-d858079b16ceGonzález-Cuello, Rafael095663a6-3ad0-4976-b75b-0805d4de1e3bOrtega-Toro, Rodrigod594d4c1-6ec9-4782-a84b-cee2853ea3592023-10-03T14:02:33Z2023-10-03T14:02:33Z2023-09-182023-10-02Hernández-Fernández, J.; González-Cuello, R.; Ortega-Toro, R. Dimethylformamide Impurities as Propylene Polymerization Inhibitor. Polymers 2023, 15, 3806. https://doi.org/10.3390/polym15183806.https://hdl.handle.net/20.500.12585/12539https://doi.org/10.3390/polym15183806Universidad Tecnológica de BolívarRepositorio Universidad Tecnológica de BolívarThis research study examined how the use of dimethylformamide (DMF) as an inhibitor af fects the propylene polymerization process when using a Ziegler–Natta catalyst. Several experiments were carried out using TiCl4/MgCl2 as a catalyst, aluminum trialkyl as a cocatalyst, and different amounts of DMF. Then, we analyzed how DMF influences other aspects of the process, such as catalyst activity, molecular weight, and the number of branches in the polymer chains obtained, using experimental and computational methods. The results revealed that as the DMF/Ti ratio increases, the catalyst activity decreases. From a concentration of 5.11 ppm of DMF, a decrease in catalyst activity was observed, ranging from 45 TM/Kg to 44 TM/Kg. When the DMF concentration was increased to 40.23 ppm, the catalyst activity decreased to 43 TM/Kg, and with 75.32 ppm, it dropped even further to 39 TM/Kg. The highest concentration of DMF evaluated, 89.92 ppm, resulted in a catalyst productivity of 36.5 TM/Kg and lost productivity of 22%. In addition, significant changes in the polymer’s melt flow index (MFI) were noted as the DMF concentration increased. When 89.92 ppm of DMF was added, the MFI loss was 75%, indicating a higher flowability of the poly mer. In this study, it was found that dimethylformamide (DMF) exhibits a strong affinity for the titanium center of a Ziegler–Natta (ZN) catalyst, with an adsorption energy (Ead) of approximately −46.157 kcal/mol, indicating a robust interaction. This affinity is significantly higher compared to propylene, which has an Ead of approximately −5.2 kcal/mol. The study also revealed that the energy gap between the highest occupied molecular orbital (HOMO) of DMF and the lowest unoccupied molecular orbital (SOMO) of the Ziegler–Natta (ZN) catalyst is energetically favorable, with a value of approximately 0.311 eV.Universidad Tecnológica de Bolivar, Universidad de Cartagena, Universidad de la Costa15application/pdfenghttp://creativecommons.org/publicdomain/zero/1.0/info:eu-repo/semantics/openAccessCC0 1.0 Universalhttp://purl.org/coar/access_right/c_abf2PolymersDimethylformamide Impurities as Propylene Polymerization InhibitoDimethylformamide Impurities as Propylene Polymerization Inhibitoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85PolypropyleneN,N-dimethylformamide (DMF)Ziegler–Natta catalystProductivityMelt flow index (MFI)Molecular weight distribution (MW)Catalyst inhibitionDensity functional theory (DFT)LEMBCartagena de IndiasCampus TecnológicoInvestigadoresJuber, F.A.H.; Jawad, Z.A.; Chin, B.L.F.; Yeap, S.P.; Chew, T.L. The prospect of synthesis of PES/PEG blend membranes using blend NMP/DMF for CO2/N2 separation. J. Polym. Res. 2021, 28, 177.Publishing, S.; Scrivener, M.; Carmical, P. Introduction to Industrial Polypropylene. 2005. Available online: https://www.eng.uc. edu/~beaucag/Classes/Properties/Books/Dennis%20B.%20Malpass,%20Elliot%20I.%20Band(auth.)%20-%20Introduction% 20to%20Industrial%20Polypropylene_%20Properties,%20Catalysts%20Processes%20(2012)%20-%20libgen.lc.pdf (accessed on 19 June 2023).Joaquin, H.F.; Juan, L. Quantification of poisons for Ziegler Natta catalysts and effects on the production of polypropylene by gas chromatographic with simultaneous detection: Pulsed discharge helium ionization, mass spectrometry and flame ionization. J. Chromatogr. A 2020, 1614, 460736.Albizzati, E.; Giannini, U.; Morini, G.; Smith, C.A.; Zeigler, R.C. Advances in propylene polymerization with MgCl2 supported catalysts. In Ziegler Catalysts: Recent Scientific Innovations and Technological Improvements; Springer: Berlin/Heidelberg, Germany, 1995; pp. 415–425Zhang, B.; Zhang, L.; Fu, Z.; Fan, Z. Effect of internal electron donor on the active center distribution in MgCl2 -supported Ziegler–Natta catalyst. Catal. Commun. 2015, 69, 147–149.Nikolaeva, M.; Mikenas, T.; Matsko, M.; Zakharov, V. Effect of AlEt3 and an External Donor on the Distribution of Active Sites According to Their Stereospecificity in Propylene Polymerization over TiCl4/MgCl2 Catalysts with Different Titanium Content. Macromol. Chem. Phys. 2016, 217, 1384–1395.Hernández-Fernández, J.; Vivas-Reyes, R.; Toloza, C.A.T. Experimental Study of the Impact of Trace Amounts of Acetylene and Methylacetylene on the Synthesis, Mechanical and Thermal Properties of Polypropylene. Int. J. Mol. Sci. 2022, 23, 12148.Bahri-Laleh, N. Interaction of different poisons with MgCl2/TiCl4 based Ziegler-Natta catalysts. Appl. Surf. Sci. 2016, 379, 395–401.Pernusch, D.C.; Spiegel, G.; Paulik, C.; Hofer, W. Influence of Poisons Originating from Chemically Recycled Plastic Waste on the Performance of Ziegler–Natta Catalysts. Macromol. React. Eng. 2022, 16, 2100020.Hernández-Fernández, J.; Ortega-Toro, R.; Castro-Suarez, J.R. Theoretical–Experimental Study of the Action of Trace Amounts of Formaldehyde, Propionaldehyde, and Butyraldehyde as Inhibitors of the Ziegler–Natta Catalyst and the Synthesis of an Ethylene–Propylene Copolymer. Polymers 2023, 15, 1098.Obot, I.B.; Macdonald, D.D.; Gasem, Z.M. Density functional theory (DFT) as a powerful tool for designing new organic corrosion inhibitors. Part 1: An overview. Corros. Sci. 2015, 99, 1–30.Stukalov, D.V.; Zakharov, V.A. Active Site Formation in MgCl2−Supported Ziegler−Natta Catalysts. A Density Functional Theory Study. J. Phys. Chem. C 2009, 113, 21376–21382Hernández-Fernández, J.; Guerra, Y.; Puello-Polo, E.; Marquez, E. Effects of Different Concentrations of Arsine on the Synthesis and Final Properties of Polypropylene. Polymers 2022, 14, 3123.Joaquin, H.F.; Juan, L.M. Autocatalytic influence of different levels of arsine on the thermal stability and pyrolysis of polypropylene. J. Anal. Appl. Pyrolysis 2022, 161, 105385.Hernández-Fernández, J.; López-Martínez, J. Experimental study of the auto-catalytic effect of triethylaluminum and TiCl4 residuals at the onset of non-additive polypropylene degradation and their impact on thermo-oxidative degradation and pyrolysis. J. Anal. Appl. Pyrolysis 2021, 155, 105052.Hernández-Fernández, J.; Cano, H.; Aldas, M. Impact of Traces of Hydrogen Sulfide on the Efficiency of Ziegler–Natta Catalyst on the Final Properties of Polypropylene. Polymers 2022, 14, 3910.Torabi, S.R.; Fazeli, N.; Zarand, M.G. Effect of dimethyl formamide in the synthesis of linear low density polyethylene on branched and molecular structure. J. Appl. Polym. Sci. 2012, 123, 1267–1272Heravi, M.M.; Ghavidel, M.; Mohammadkhani, L. Beyond a solvent: Triple roles of dimethylformamide in organic chemistry. RSC Adv. 2018, 8, 27832–27862.Louvis, A.R.; Silva, N.A.A. N,N-dimethylformamide (CAS No. 68-12-2). Rev. Virtual Química 2016, 8, 1764–1785.Marsella, J.A. Dimethylformamide. In Kirk-Othmer Encyclopedia of Chemical Technology; Wiley Online Library: Hoboken, NJ, USA, 2013.Varnava, K.G.; Sarojini, V. Making Solid-Phase Peptide Synthesis Greener: A Review of the Literature. Chem. Asian J. 2019, 14, 1088–1097.Kim, T.H.; Kim, S.G. Clinical Outcomes of Occupational Exposure to N,N-Dimethylformamide: Perspectives from Experimental Toxicology. Saf. Health Work 2011, 2, 97–104Li, M.-J.; Zeng, T. The deleterious effects of N,N-dimethylformamide on liver: A mini-review. Chem. Biol. Interact. 2019, 298, 129–136.Zhou, Z.; Sang, L.; Wang, J.; Song, L.; Zhu, L.; Wang, Y.; Xiao, J.; Lian, Y. Relationships among N,N-dimethylformamide exposure, CYP2E1 and TM6SF2 genes, and non-alcoholic fatty liver disease. Ecotoxicol. Environ. Saf. 2021, 228, 112986.Hernández-Fernández, J.; González-Cuello, R.; Ortega-Toro, R. Parts per Million of Propanol and Arsine as Responsible for the Poisoning of the Propylene Polymerization Reaction. Polymers 2023, 15, 3619.http://purl.org/coar/resource_type/c_2df8fbb1ORIGINALpolymers-15-03806.pdfpolymers-15-03806.pdfapplication/pdf4391733https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/1/polymers-15-03806.pdfe1b59d5be608dc53b2cb78b993ac5e6bMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8701https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/2/license_rdf42fd4ad1e89814f5e4a476b409eb708cMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-83182https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/3/license.txte20ad307a1c5f3f25af9304a7a7c86b6MD53TEXTpolymers-15-03806.pdf.txtpolymers-15-03806.pdf.txtExtracted texttext/plain62244https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/4/polymers-15-03806.pdf.txt1047aab6f7c54f1cefb0ac1a08791697MD54THUMBNAILpolymers-15-03806.pdf.jpgpolymers-15-03806.pdf.jpgGenerated Thumbnailimage/jpeg7661https://repositorio.utb.edu.co/bitstream/20.500.12585/12539/5/polymers-15-03806.pdf.jpgdeec3124e5c33b24502d38769bc9d44dMD5520.500.12585/12539oai:repositorio.utb.edu.co:20.500.12585/125392023-10-04 00:18:32.164Repositorio Institucional UTBrepositorioutb@utb.edu.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 |