SYNTHESIS OF THIOCL OLIGOMERS BASED ON LOCAL RAW MATERIALS AND THEIR MODIFICATION WITH UNSATURATED COMPOUNDS

Annotasiya

The synthesis of thiocol oligomers based on local raw materials and their 
modification with unsaturated compounds belongs to the field of chemistry and 
materials science, and includes the processing of thiocol oligomers, raw materials and 
their modification with unsaturated compounds. These processes are an important way 
to produce environmentally friendly and economically efficient materials

SYNAPSES: Insights across the disciplines
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Zoirova Husnora Sakhomiddin kizi, & Normurodov Bakhtiyor Abdullayevich. (2025). SYNTHESIS OF THIOCL OLIGOMERS BASED ON LOCAL RAW MATERIALS AND THEIR MODIFICATION WITH UNSATURATED COMPOUNDS. SYNAPSES: Insights across the Disciplines, 2(1), 11–14. Retrieved from https://inlibrary.uz/index.php/siad/article/view/64576
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Annotasiya

The synthesis of thiocol oligomers based on local raw materials and their 
modification with unsaturated compounds belongs to the field of chemistry and 
materials science, and includes the processing of thiocol oligomers, raw materials and 
their modification with unsaturated compounds. These processes are an important way 
to produce environmentally friendly and economically efficient materials


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SYNTHESIS OF THIOCL OLIGOMERS BASED ON LOCAL RAW

MATERIALS AND THEIR MODIFICATION WITH UNSATURATED

COMPOUNDS

Zoirova Husnora Sakhomiddin kizi

Master's student at Termez State University

Normurodov Bakhtiyor Abdullayevich

Professor of Termez State University

Abstract.

The synthesis of thiocol oligomers based on local raw materials and their

modification with unsaturated compounds belongs to the field of chemistry and
materials science, and includes the processing of thiocol oligomers, raw materials and
their modification with unsaturated compounds. These processes are an important way
to produce environmentally friendly and economically efficient materials.

Key words.

Thiocol, polysulfide, acrylate, methacrylate, crosslinking, basalt, dolerite,

oceanite, platobasalt.

Аннотация

. Синтез тиоколовых олигомеров на основе местного сырья и их

модификация непредельными соединениями относится к области химии и
материаловедения и включает переработку тиоколовых олигомеров, сырья и их
модификацию непредельными соединениями. Эти процессы являются важным
способом получения экологически чистых и экономически эффективных
материалов.

Ключевые слова.

Тиокол, полисульфид, акрилат, метакрилат, сшивка, базальт,

долерит, океанит, платобазальт.

INTRODUCTION

Thiocol oligomers are organic compounds, often referred to as polysulfides or
thioxoolefins. They are usually present as oligonucleotides or oligomeric polymers and
contain thiol groups. The following steps can be used in the synthesis of thiocol
oligomers:
- Starting materials: Various starting materials, such as sulfides, thiol acids, or other
organic compounds, are used for the synthesis of thiocol oligomers.
- Synthesis process: This process is usually carried out by condensation reactions,
polymerization, or other chemical methods. Thiocol oligomers are often obtained by
the reaction of thiol groups during polymerization.


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Basalt is an igneous rock with a gray to black color and a specific gravity of 2.5-3. It
consists mainly of plagioclase; it also contains pyroxenes, olivine, and magnetite,
titanite, apatite, etc. Its chemical composition is close to its deep-seated analogue,
gabbro. Volcanic glass fills the spaces between the granular crystals. Fully crystallized
basalts are called dolerite. The type of basalt that formed on the ocean floor and is rich
in iron and magnesium is called oceanite, while the type that has flowed onto land
through tectonic faults and solidified is called plateau basalt. Basalt occupies a very
large area on the ocean floor and on land. Basalt lavas also flow from modern
volcanoes. Depending on the mineral content, they are called analcitic basalt, leucite
basalt, nepheline basalt, magnetite basalt, haiwinite basalt, apatite basalt, etc. Basalt is
used in the manufacture of acid-resistant chemical devices, pipes, electrical insulators,
in the production of cast stone products, and as a decorative coating material in
construction. Due to its good polishability, it has been used in sculpture since ancient
times in Egypt, Assyria, Rome, Byzantium, Armenia, and other places. It is found in
Kamchatka, Transbaikalia, Armenia, Ukraine, and the Kurama, Turkestan, and Tomdi
mountains of Uzbekistan.

LITERATURE ANALYSIS AND METHODOLOGY

Synthesis of thiocol oligomers based on sodium tetrasulfide, monochlorohydrin and
urea adducts. (MKA-1) In a 500 ml three-necked flask equipped with an automated
mixer, reflux condenser, thermometer and additional funnel, 31.5 g (0.40 mol) of
sodium sulfide is dissolved in 150 ml of water. 37.5 g (1.17 mol) of sulfur is added to
the solution, the mixture is heated and stirred with a stirrer for 1 hour. Then the solution
is filtered and 0.22 g (0.0013 mol) of ionic liquid (tetraethylammonium chloride) is
added. To this solution, 33.2 g (0.30 mol) of monochlorohydrin is stirred at 700 °C for
1 hour. Then 0.3 g (0.0013 mol) of urea adduct is added and the reaction mixture is
kept at 80 °C for another 1 hour. After that, the mixture is cooled. The resulting light
yellow gummy product is washed three times with warm water. Then it is dried in a
fume hood. The product obtained is 62 g (94% of theory). Sulfur content is 37.4%.)
Synthesis of polysulfide oligomers based on sodium tetrasulfide, dichlorohydrin and
urea adducts. DKA-4
In a 500 ml three-necked flask equipped with a stirrer, reflux condenser, thermometer
and additional funnel, 31.5 g (0.40 mol) of sodium sulfide is dissolved in 150 ml of
water. 37.5 g (1.17 mol) of sulfur is added to the solution, the mixture is boiled with
stirring for 1 hour. Then the solution is filtered and 0.22 g (0.0013 mol) of ionic liquid
(tetraethylammonium chloride) is added. To this solution, 38.7 g (0.30 mol) of
dichlorohydrin is poured into it at 65-70°C with stirring for 1 hour. Then 0.3 g (0.0013


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mol) of urea is added and the reaction mixture is heated at 80-85°C for another 1 hour.
After that, the mixture is cooled. The resulting pale yellow viscous mass is washed
three to four times with warm distilled water and dried in a fume hood. Obtain 62 g of
oligomer (96% theoretical). The sulfur content is 55.1%.

RESULTS.

Synthesis of thiocol oligomers based on sodium tetrasulfide,

epichlorohydrin and urea adducts. EKA-7 In a 500 ml three-necked flask equipped with
a stirrer, reflux condenser, thermometer and additional funnel, 31.5 g (0.40 mol) of
sodium sulfide is dissolved in 150 ml of water. 37.5 g (1.17 mol) of sulfur is added to
the solution, the resulting mixture is boiled for 1 hour with stirring. Then the solution
is filtered and 0.22 g (0.0013 mol) of ionic liquid (tetraethylammonium chloride) is
added. To this solution, 27.8 g (0.30 mol) of epichlorohydrin is poured into it with
stirring at 700C for 1 hour. Then 0.3 g (0.0013 mol) of urea adduct is added and the
reaction mixture is kept at 800C for another 1 hour. The resulting dark brown viscous
mass is washed three times with boiling water and dried in a fume hood. The resulting
product is 67g. (93% theoretical). The sulfur content is 55.2%.
Synthesis of polysulfide oligomers with sodium tetrasulfide, monochlorohydrin and
metal-containing adducts. (MMA-2) A 500 ml three-necked flask is equipped with a
stirring rod, a reflux condenser, a thermometer and a dropping funnel. Initially, 31.5 g
(0.40 mol) of sodium sulfide is placed in the flask and dissolved in 150 ml of water.
37.5 g (1.17 mol) of sulfur is added to the solution and the mixture is heated at 800 C
for 1 hour with stirring. After that, 0.22 g (0.0013

mol) of ionic solution of tetraethylammonium chloride is added to the mixture.

Time dependence of polysulfide oligomer reaction yield at 80°C


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The dependence of the reaction yield on time during the synthesis of polysulfide
oligomers was studied at a temperature of 80°C. When the reaction time was two hours,
the reaction oligomer was obtained in high yield.

CONCLUSION

The synthesis of thiocol oligomers and their modification with unsaturated compounds
is an important method for creating new, highly effective materials. These processes
can be used to develop environmentally friendly and energy-efficient technologies.
Materials produced from local raw materials can be economically viable and suitable
for long-term use.

LIST OF REFERENCES

1.

Хакимуллин Ю.И. Герметики на основе полисульфидных олигомеров:

синтез, свойства, применение / Ю. И. Хакимуллин, В. С. Минкин. Ф. М. Малютин
[и др.] - М.: Наука, 2007.- С.301.

2.

Deryagina E. N., Levanova E. P., Grabel’nykh V. A., Sukhomazova E. N.,

Russavskaya N. V., Korchevin N. A. Thiylation of Polyelectrophiles with Sulfur in
Hydrazine Hydrate Amine Systems // Russian Journal of General Chemistry, - 2005, -
V.75, -I. 2, p.194 -199.

3.

Levanova Е. P., Nikonova V. S., Grabel’nykh V. А., Russavskaya N. V., Albanov

А. I., Rozentsveig I. B., Korchevin N. А. Reactions of Dichloroethenes with Sulfur in
the System Hydrazine Hydrate–KОН // Russian Journal of General Chemistry, 2018,
V. 88, I. 3, p. 383–388.
4.

Khakimullin Y.N. et al. New alternative to liquid thiokol in commercial sealants

// Polym. Sci. Ser. D 2017 101. Springer, 2017. Vol. 10, № 1. P. 1–3.
5.

Трофимов Б. А., Малькина А. Г., Дорофеев И. А., Мячина Г. Ф., Родионова

И. В., Вакульская Т. И., Синеговская Л. М., Skotheim T. A. Синтез и свойства
полиенолигосульфидов - производных этиндитиола из ацэтилена и элементной
серы // Ж. общ. Химии, №9, 2007, т.77, с.1485-1492.
6.

Беев А. А., Микитаев А. К., Беева Д. А., Козлов Г. В., Балкаров А. М.

Серосодержащие эпоксиолигомеры и полимеры // Новые полимерные
композиционные материалы, -2007, -с.60-64.
7.

V.M Abbasov, H.M Abd El-Lateef, S.A. Mamedxanova, L.I Aliyeva, T.A.

Ismayilov, M.J. Ilham, O.A. Aydamirov and F.A.A. “Inhibitive Effect of Some Natural
Naphthenates as Corrosion Inhibitors on the Corrosive Performance of Carbon Steel in
CO2-Saturated Brine.” // Int. J. Sci. Res. Environ. Sci. 2013. Vol. 1, № 8,. P. 166-178,.

Bibliografik manbalar

Хакимуллин Ю.И. Герметики на основе полисульфидных олигомеров:

синтез, свойства, применение / Ю. И. Хакимуллин, В. С. Минкин. Ф. М. Малютин

[и др.] - М.: Наука, 2007.- С.301.

Deryagina E. N., Levanova E. P., Grabel’nykh V. A., Sukhomazova E. N.,

Russavskaya N. V., Korchevin N. A. Thiylation of Polyelectrophiles with Sulfur in

Hydrazine Hydrate Amine Systems // Russian Journal of General Chemistry, - 2005, -

V.75, -I. 2, p.194 -199.

Levanova Е. P., Nikonova V. S., Grabel’nykh V. А., Russavskaya N. V., Albanov

А. I., Rozentsveig I. B., Korchevin N. А. Reactions of Dichloroethenes with Sulfur in

the System Hydrazine Hydrate–KОН // Russian Journal of General Chemistry, 2018,

V. 88, I. 3, p. 383–388.

Khakimullin Y.N. et al. New alternative to liquid thiokol in commercial sealants

// Polym. Sci. Ser. D 2017 101. Springer, 2017. Vol. 10, № 1. P. 1–3.

Трофимов Б. А., Малькина А. Г., Дорофеев И. А., Мячина Г. Ф., Родионова

И. В., Вакульская Т. И., Синеговская Л. М., Skotheim T. A. Синтез и свойства

полиенолигосульфидов - производных этиндитиола из ацэтилена и элементной

серы // Ж. общ. Химии, №9, 2007, т.77, с.1485-1492.

Беев А. А., Микитаев А. К., Беева Д. А., Козлов Г. В., Балкаров А. М.

Серосодержащие эпоксиолигомеры и полимеры // Новые полимерные

композиционные материалы, -2007, -с.60-64.

V.M Abbasov, H.M Abd El-Lateef, S.A. Mamedxanova, L.I Aliyeva, T.A.

Ismayilov, M.J. Ilham, O.A. Aydamirov and F.A.A. “Inhibitive Effect of Some Natural

Naphthenates as Corrosion Inhibitors on the Corrosive Performance of Carbon Steel in

CO2-Saturated Brine.” // Int. J. Sci. Res. Environ. Sci. 2013. Vol. 1, № 8,. P. 166-178,