2021 (3) 5
https://doi.org/10.15407/polymerj.43.03.198
Synthesis and properties of oligodiuretanediols based on a mixture of (2,4–2,6) toluilendiisocyanate
S.M. Kuzmenko,
State Higher Educational Institution „Ukrainian State University of Chemical Technology”, 8, ave. Gagarin, Dnipro, 49005, Ukraine,
ORCID: 0000-0001-8527-1608
E.O. Sporyagin,
Dniprovs’kyy Natsional’nyy universytet im. O.Honchara, 72, ave. Gagarin, Dnipro, 49000, Ukraine,
ORCID: 0000-0001-9892-7258
O.M. Kuzmenko,
LLC „Research and development enterprise „UKRPOLIKHIMSYNTEZ”, 10, Komisar Krylov str., Dnipro, 49124, Ukraine,
A.Ya. Puzenko,
Dniprovs’kyy Natsional’nyy universytet im. O.Honchara, 72, ave. Gagarin, Dnipro, 49000, Ukraine,
Polym. J., 2021, 43, no. 3: 198-203.
Section: Polymer synthesis.
Language: Ukrainian.
Abstract:
The paper describes the synthesis, the reaction of a mixture of isomers (2,4–2,6) of toluilendiisocyanate with a double molar excess of aliphatic individual or oligomeric diols, a number of previously unknown oligodiuretanediols and their physicochemical constants. It is shown that with an increase in the synthesis temperature from 50 to 70 °C, the reaction time to complete depletion in the mixture of free NCO-groups decreases from 8–9 hours to 3–4 hours. The reaction temperature of 70–2 °С should be considered optimal, because at higher temperatures side reactions of free NCO-groups with already formed urethane ones are possible.
Because the presence of even a small amount of moisture in the diols can provoke side effects during the urethane formation reaction, all of the above diols were dried from the adsorbed moisture by azeotropic distillation with toluene before use in the reaction.
Since the final products are even at the synthesis temperature (68–70 °C) viscous liquids, and there are difficulties with the homogenization of the reaction mass during synthesis, and when unloading the finished product from the reaction plant, in all cases, the synthesis was performed in solution cyclohexanone by 50 % by weight of the final product.
Control of the reaction was performed by changing the % wt. free NCO-groups in time. The reaction was considered complete if the measured % wt. free NCO-groups in the reaction mixture for at least one hour twice showed zero.
The isolated oligodiuretanediols range from solid at room temperature to very viscous products, which significantly depends on the molecular weight of the diol used in the reaction (ie the concentration of urethane groups formed). They are homogeneous, transparent compounds that are readily soluble in esters, ethers, aromatic and halide-containing, aprotic solvents, ketones, poorly or completely insoluble in aliphatic saturated hydrocarbons.
The structure of the synthesized oligomeric products is confirmed by functional analysis, IR–spectra.
In the IR-spectra of each of the synthesized oligodiuretanediols there are no absorption bands in the region of 2270 cm-1, which confirms the complete completion of the reaction of urethane formation according to the scheme. At the same time, the absorption bands in the region of 3450 cm-1, 1720 cm-1, 1540 cm-1 are fixed, which are characteristic of the presence of urethane groups in the structure of the target products.
As the chain length of the diol component –R– increases in the target product (which synchronously leads to an increase in molecular weight), the intensity of these absorption bands decreases, which is associated with a decrease in the concentration of formed urethane groups in the structure of oligodiuretanediols. The refractive index also decreases synchronously.
Synthesized series of oligodiuretanediols can be used for synthesis on its basis of other classes of oligomers with the simultaneous presence in the structure of urethane groups.
The ability of such compounds to be soluble in solvents of different nature has been studied, which provides information for the directions of their further use (varnishes, enamels, primers).
Key words: toluilendiisocyanate, diol, reaction of joining, oligodiuretandiol, properties.
REFERENCES
1. Lyubartovich S.A., Morozov Yu.L., Tretyakov O.B. Reaktsionnoe formirovanie poliuretanov. M.: Himiya, 1990: 288.
2. Karabanova L.V., Gomza Yu. P., Nesin S. D., Bondaruk O. N., Geraschenko I.I. i dr. Nanostrukturirovannyie polimernyie materialyi i nanokompozityi na osnove vzaimopronikayuschih polimernyih setok dlya biomeditsinskogo primeneniya. Razdel: Nanorazmernyie sistemyi i nanorazmernyie materialyi. Рod redaktsiey Naumovtsa. Kiev: Akademika, 2014: 236.
3. Makarova M.A., Tereshapov V.V., Semichev V.Yu i dr. Razrabotka podhoda i printsipov formirovaniya novogo tipa uretansoderzhaschih multibloksopolimerov s reguliruemoy strukturoy polimernyih tsepey. Vestnik Permskogo federalnogo issledovatelskogo tsentra Rossiyskoy Federatsii. 2019, no. 3: 70–77.
4. Ostanin S.A., Zuev V.V., Mokeev M.V. Issledovanie vnutrennego stroeniya poliuretanov-polimochevin metodom spektroskopii yadernogo magnitnogo rezonansa. Nauchno-tehnicheskiy vestnik informatsionnyih tehnologiy mehaniki i optiki. 2018, 18, no. 1: 65–71. https://doi.org/10.17586/2226-1494-2018-18-1-65-71.
5. Tereshapov V.V., Makarova M.A. i dr. Novyie predstavleniya o vzaimosvyazi strukturyi predelnyih fiziko-mehanicheskih svoystv i deformatsionnogo povedeniya nanostrukturirovannyih polimernyih sistem na osnove oligodiizotsianatov. Vestnik Permskogo federalnogo issledovatelskogo tsentra Rossiyskoy Federatsii. 2017, 1: 81–86.
6. Sorokin M.F., Lyalyushko K.A. Praktikum po himii i tehnologii plYonkoobrazuyuschih veschestv . M.: Himiya, 1971: 288.
7. Kazitsina L.A., Kupletskaya N.B. Primenenie IK–, UF–, YaMR spektroskopii v organicheskoy himii. M.: Vyisshaya shkola, 1971: 264.
8. Dekhant I., Dants V., Kimmer R. Infrakrasnaya spektroskopiya polimerov. Shmolone. Perevod s nem. M.: Himiya, 1976: 472.