| DC Field | Value | Language |
|---|
| dc.contributor.author | Chobit, M. | - |
| dc.contributor.author | Borova, S. | - |
| dc.contributor.author | Bukartyk, N. | - |
| dc.contributor.author | Shevchuk, О. | - |
| dc.contributor.author | Tokarev, V. | - |
| dc.date.accessioned | 2018-05-02T12:04:02Z | - |
| dc.date.available | 2018-05-02T12:04:02Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.citation | Obtain of carboxylic- and aminocontaining hydrogels based on acryl amide / M. Chobit, S. Borova, N. Bukartyk, О. Shevchuk, V. Tokarev // Litteris et Artibus : proceedings of the 6th International youth science forum, November 24–26, 2016, Lviv, Ukraine / Lviv Polytechnic National University. – Lviv : Lviv Polytechnic Publishing House, 2016. – P. 372–375. – Bibliography: 8 titles. | uk_UA |
| dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/40919 | - |
| dc.description.abstract | Cross-linked hydrogels based on functional copolymers of acryl amide with either acrylic acid or dimethylaminoethyl methacrylate were synthesized. It was studied the influence of the comonomer ratio onto copolymerization kinetics as well as the dependence of the physicochemical and physicomechanical properties of hydrogels on copolymer nature and cross-linking degree. The hydrogel obtained are highly flexible and elastic materials. In terms of swelling rate and degree, they can be attributed to super absorbent polymers. | uk_UA |
| dc.language.iso | en | uk_UA |
| dc.publisher | Lviv Polytechnic Publishing House | uk_UA |
| dc.subject | cross-linked hydrogels | uk_UA |
| dc.subject | functional copolymers | uk_UA |
| dc.subject | radical copolymerization | uk_UA |
| dc.subject | super absorbent polymers | uk_UA |
| dc.subject | swelling degree | uk_UA |
| dc.title | Obtain of carboxylic- and aminocontaining hydrogels based on acryl amide | uk_UA |
| dc.type | Conference Abstract | uk_UA |
| dc.contributor.affiliation | Lviv Polytechnic National University | uk_UA |
| dc.coverage.country | UA | uk_UA |
| dc.format.pages | 372-375 | - |
| dc.relation.referencesen | [1] Aamer Saeed, Ghulam Shabir, Iram Batool, "Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications" Journal of Fluorescence., vol. 24. pp.1119-1127, July 2014. [2] Raval J.P.,Rai A.R. "Synthesis and in vitro antimicrobial activityof N '- (4- (arylamino) - 6 - (pyridine – 2 - ylamino) - 1,3,5 – triazin – 2 - yl) benzohydrazide" International Journal of ChemTech Research., vol.1.pp.616-620, 2009. [3] Kaminski Z. J., "Triazine-Based Condensing Reagents" Biopolymers (PeptideScience)., vol. 55. pp. 140 – 164,2000. [4] Polovkovych S.V., [et al.] Synthesis of new 5- acetyl(arylmethyliden)-4-thiazolidones./ Heteroatom Chemistry – 2010. – Vol.21(6). – P.392-396. [5] Polovkovych S.V., [et al.] Synthesis of New Shiff Bases and Polycyclic Fused Thiopyranothia-zoles Containing 4,6-Dichloro-1,3,5-Triazine Moiety/ Journal of Heterocyclic Chemistry– 2013. – Vol. 50, № 6 – P. 1419-1424. [6] Saczewski F. Synthesis, structure and anticancer activity of novel 2,4-diamino-1,3,5-triazine derivatives. / Saczewski F., Bulakowska A., Bednarski P. [et al.] // Eur. J. Med. Chem - 2006. - Vol.41. – P.219-225. [7] Dinku W. Studies on transition metal complexes of herbicidal compounds. II: Transition metal complexes of derivatized 2-chloro-4-ethylamino-6-isopropylaminos- triazine (atrazine) / Dinku W., Megersa N., Raju V. J. T. [et al.] // Bulletin of The Chemical Society of Ethiopia - 2003. – Vol.17(3). – P.35-44. [8] Srinivas K. Synthesis and antibacterial activity of various substituted s-triazines. / Srinivas K., Srinivas U., Bhanuprakash K. [et al.] // Eur J Med Chem., - 2006. – Vol.41(11). – P.1240-6. | uk_UA |
| dc.citation.conference | Litteris et Artibus | - |
| dc.coverage.placename | Lviv | uk_UA |
| Appears in Collections: | Litteris et Artibus. – 2016 р.
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