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This thesis addresses the synthesis of two 2-oxazoline macromonomers, MKA-1 and MKA-2, functionalized with quaternary ammonium groups, and the subsequent polymerization of these prepolymers to obtain hydrogels and graft copolymers. The 2-oxazoline macromonomers were synthesized by cationic ring-opening polymerization of 2-ethyl-2-oxazoline using 4-chloromethylstyrene as the initiator, sodium iodide as the catalyst, and N,N-dimethyldodecylamine as the terminating agent. The quaternary ammonium group was thus incorporated into the macromonomer structure. The hydrogels were synthesized by free-radical polymerization of the 2-oxazoline macromonomer and hydroxyethyl methacrylate using ethylene bisacrylamide as the crosslinker. The polymerization was initiated by ammonium persulfate and N,N,N',N'-tetramethylethylenediamine. Graft copolymers were also synthesized via free radical polymerization from the 2-oxazoline and hydroxyethyl methacrylate macromonomers, using 2,2'-azoisobutyronitrile as the initiator. The macromonomers were characterized by nuclear magnetic resonance (NMR) and infrared (FTIR) spectroscopy. 1H-NMR spectroscopy determined that the MKA-1 and MKA-2 macromonomers had degrees of polymerization of 21 and 9%, values that were in excellent agreement with theoretical values. The degree of functionalization of MKA-1 and MKA-2 with quaternary ammonium groups was 98 and 99%, respectively. Using infrared spectrometry (FTIR), the hydrogels and graft copolymers were qualitatively characterized, demonstrating the presence of the macromonomer and hydroxyethyl methacrylate molecules in their structure.

To evaluate the antibacterial activity of the MKA-2 macromonomer and the hydrogels, the "Performance Standards for Antimicrobial Susceptibility Testing" (ATCC 6538P), a standard test strain for disinfectants, was applied. The biocidal capacity of the hydrogels against Staphylococcus aureus bacteria was determined. Some of the hydrogels developed showed excellent biocidal activity against this bacterium.

This thesis was developed as part of the PUCP-DFI-PI1000 research project: "Development of a polymeric material with antibacterial properties," with financial support from PUCP.

Details

1010268
Title
Elaboración de macromonómeros de 2-oxazolinas, funcionalizados con grupos amonio cuaternarios, y su posterior polimerización
Alternate title
Preparation of 2-Oxazoline Macromonomers, Functionalized With Quaternary Ammonium Groups, and Their Subsequent Polymerization
Number of pages
162
Publication year
2025
Degree date
2025
School code
1618
Source
MAI 87/1(E), Masters Abstracts International
ISBN
9798288810497
University/institution
Pontificia Universidad Catolica del Peru (Peru)
University location
Peru
Degree
Master's
Source type
Dissertation or Thesis
Language
Spanish
Document type
Dissertation/Thesis
Dissertation/thesis number
32208110
ProQuest document ID
3231604268
Document URL
https://www.proquest.com/dissertations-theses/elaboración-de-macromonómeros-2-oxazolinas/docview/3231604268/se-2?accountid=208611
Copyright
Database copyright ProQuest LLC; ProQuest does not claim copyright in the individual underlying works.
Database
2 databases
  • ProQuest One Academic
  • ProQuest One Academic