DC Field | Value | Language |
dc.contributor.author | Bratychak, Michael | |
dc.contributor.author | Ripak, Oresta | |
dc.contributor.author | Namiesnik, Jacek | |
dc.contributor.author | Shyshchak, Olena | |
dc.contributor.author | Astakhova, Olena | |
dc.date.accessioned | 2019-01-29T12:53:37Z | - |
dc.date.available | 2019-01-29T12:53:37Z | - |
dc.date.created | 2018-01-20 | |
dc.date.issued | 2018-01-20 | |
dc.identifier.citation | Obtaining of coumarone-indene resins based on light fraction of coal tar. 2. Coumarone-indene resins with epoxy groups / Michael Bratychak, Oresta Ripak, Jacek Namiesnik, Olena Shyshchak, Olena Astakhova // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 93–100. | |
dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/43919 | - |
dc.description.abstract | З використанням легкої фракції кам’яно-
вугільної смоли та отриманої на її основі фракції, що википає
за температур 423–463 К з додаванням стиролу і гліцидил-
метакрилату розроблений метод одержання інден-кума-
ронових смол з епоксидними групами (ІКСЕ). ІКСЕ отримані за
радикальною коолігомеризацією з використанням як ініціатор
монопероксидної похідної дигліцидилового етеру діоксидифе-
нілпропану (ПО). Вивчена терміна стабільність ПО.
Встановлено вплив кількості ініціатора, температури та
тривалості реакції на вихід та температуру розм’якшення
ІКСЕ. Структура синтезованих ІКСЕ підтверджена ІЧ- та
1Н ЯМРспектроскопічними дослідженнями. | |
dc.description.abstract | Coumarone-indene resins with epoxy groups
(CIRE) have been obtained using light fraction of coal tar
or fraction with the distillation range of 423–463 K based
on it. Styrene and glycidyl methacrylate were used as
modifiers. CIRE were synthesized via radical
cooligomerization using monoperoxide derivative of
dioxyphenylpropane diglycidyl ether (PO) as an initiator.
Thermal stability of PO has been studied. The effect of
initiator amount, reaction temperature and time on the
yield and softening temperature of CIRE has been
determined. The structure of the synthesized CIRE was
confirmed by IR and 1H NMR spectroscopy. | |
dc.format.extent | 93-100 | |
dc.language.iso | en | |
dc.publisher | Lviv Politechnic Publishing House | |
dc.relation.ispartof | Chemistry & Chemical Technology, 1 (12), 2-18 | |
dc.relation.uri | https://doi.org/10.3103/S1068364X14120072 | |
dc.relation.uri | https://doi.org/10.23939/chcht10.04si.631 | |
dc.relation.uri | https://doi.org/10.23939/chcht11.04.509 | |
dc.relation.uri | https://www.chemicalbook.com/ChemicalProductProperty_ | |
dc.relation.uri | https://www.astm.org/Standards/D36.htm | |
dc.relation.uri | https://doi.org/10.1002/pola.24053 | |
dc.subject | інден-кумаронова смола | |
dc.subject | кам’яно- вугільна смола | |
dc.subject | стирол | |
dc.subject | малеїновий ангідрид | |
dc.subject | гліцидилметакри- лат | |
dc.subject | пероксид | |
dc.subject | термоліз | |
dc.subject | ІЧ-спектроскопія | |
dc.subject | 1Н ЯМР- спектроскопія | |
dc.subject | coumarone-indene resin | |
dc.subject | coal tar | |
dc.subject | glycidyl methacrylate | |
dc.subject | styrene | |
dc.subject | peroxide | |
dc.subject | thermolysis | |
dc.subject | infrared spectroscopy | |
dc.subject | 1H NMR spectroscopy | |
dc.title | Obtaining of coumarone-indene resins based on light fraction of coal tar. 2. Coumarone-indene resins with epoxy groups | |
dc.title.alternative | Одержання інден-кумаронових смол з легкої фракції кам‘яно-вугільної смоли. 2. Інден-кумаронові смоли з епоксидними групами | |
dc.type | Article | |
dc.rights.holder | © Національний університет „Львівська політехніка“, 2018 | |
dc.rights.holder | © Bratychak M., Ripak O., Namiesnik J., Shyshchak O., Astakhova O., 2018 | |
dc.contributor.affiliation | Lviv Polytechnic National University | |
dc.contributor.affiliation | Gdansk University of Technology | |
dc.format.pages | 8 | |
dc.identifier.citationen | Obtaining of coumarone-indene resins based on light fraction of coal tar. 2. Coumarone-indene resins with epoxy groups / Michael Bratychak, Oresta Ripak, Jacek Namiesnik, Olena Shyshchak, Olena Astakhova // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 93–100. | |
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dc.relation.referencesen | [1] Hetmanchuk Yu., BratychakM., Khimiya ta Technologiya Polimeriv. Beskyd-Bit, Lviv 2006. | |
dc.relation.referencesen | [2] BratychakM., Hetmanchuk Yu., Khimichna Technologiya Syntezu Vysokomolekuliarnykh Spoluk. Vyd-vo NULP, Lviv 2009. | |
dc.relation.referencesen | [3] BratychakM., GaginM., Shyshchak O., Waclawek W., Chemia i Inzyneria Ekologiczna, 2004, 11, 15. | |
dc.relation.referencesen | [4] BratychakM., GaginM., Shyshchak O., Brostow W., Chemia i Inzyneria Ekologiczna, 2004, 11, 21. | |
dc.relation.referencesen | [5] GaginM., BratychakM., Shyshchak O., Waclawek W., Chemia i Inzyneria Ekologiczna, 2004, 11, 27. | |
dc.relation.referencesen | [6] Skibitskiy V., Grynyshyn O., BratychakM., Brostow W., Chemia i Inzyneria Ekologiczna, 2004, 11, 41. | |
dc.relation.referencesen | [7] BratychakM., Romashko I., Shyshchak O., WaclawekW., Ecolog. Chem. Eng., 2006, 13, 7. | |
dc.relation.referencesen | [8] BratychakM., Shyshchak O., Romashko I., WaclawekW., Ecolog. Chem. Eng., 2006, 13, 17. | |
dc.relation.referencesen | [9] BratychakM., Romashko I., Shyshchak O. et al., Ecolog. Chem. Eng., 2007, 14, 245. | |
dc.relation.referencesen | [10] BratychakM., Brostow W., Pietkiewicz D., Topilnytskiy P., Chem. Chem. Technol., 2007, 1, 155. | |
dc.relation.referencesen | [11] BratychakM., Grynyshyn O., Astakhova O. et al., Ecolog. Chem. Eng., 2008, 15, 387. | |
dc.relation.referencesen | [12] BratychakM., Shust O., Chervinskyy T. et al., Ecolog. Chem. Eng., 2011, 18, 49. | |
dc.relation.referencesen | [13] Chervinskyy T., BratychakM., GaginM., Waclawek W., Chemia i Inzyneria Ekologiczna, 2004, 11, 1225. | |
dc.relation.referencesen | [14] BratychakM., Grynyshyn O., Shyshchak O. et al., Ecolog. Chem. Eng., 2007, 14, 225. | |
dc.relation.referencesen | [15] Grynyshyn O., BratychakM., Krynytskiy V., Donchak V., Chem. Chem. Technol., 2008, 2, 47. | |
dc.relation.referencesen | [16] BratychakM., Grynyshyn O., Astakhova O. et al., Ecolog. Chem. Eng., 2010, 17, 309. | |
dc.relation.referencesen | [17] Tiwari H., Sharma R., Kumar R. et al., Coke Chem., 2014, 57, 477. https://doi.org/10.3103/S1068364X14120072. | |
dc.relation.referencesen | [18] Pyshyev S., Gunka V., Grytsenko Y., BratychakM., Chem. Chem. Technol., 2016, 10, 631.https://doi.org/10.23939/chcht10.04si.631 | |
dc.relation.referencesen | [19] BratychakM., Astakhova O., Shyshchak O. et al., Chem. Chem. Technol., 2017, 11, 509.https://doi.org/10.23939/chcht11.04.509 | |
dc.relation.referencesen | [20] https://www.chemicalbook.com/ChemicalProductProperty_ EN_CB3415111.htm. | |
dc.relation.referencesen | [21] BratychakM., Chervinskyy T., GaginM. et al., Ukr. Khim. Zh., 2005, 71, 50. | |
dc.relation.referencesen | [22] Braun D., Cherdron H., RehahnM. et al., Polymer Synthesis: Theory and Practice: Fundamentals, Methods, Experiments, 5th edn. Springer-Verlag, Berlin Heidelberg 2013. https:/doi.org/10.1007/978-3-642-28980-4_1 | |
dc.relation.referencesen | [23] ASTM- D36/D36M - 14e1. Standard Test Method for Softening Point of Bitumen (Ring-and-Ball Apparatus).https://www.astm.org/Standards/D36.htm | |
dc.relation.referencesen | [24] Wilson G., Henderson J., Caruso M. et al., J. Polym. Sci. A,2010, 48, 2698. https://doi.org/10.1002/pola.24053 | |
dc.citation.volume | 12 | |
dc.citation.issue | 1 | |
dc.citation.spage | 93 | |
dc.citation.epage | 100 | |
dc.coverage.placename | Lviv | |
Appears in Collections: | Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1
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