Көмір мен тақтатасты бірлесіп гидрлеу арқылы отын өнімдерін алу

Толық мәтін

Introduction

Recently, researchers have been paying great attention to the study of the processes of joint thermocatalytic processing of coal and shale. This is most relevant for the deposits of the Republic of Kazakhstan, where both coal and shale are present at the same time. Numerous studies have shown that the organic and mineral parts of oil shale have an activating effect on the thermocatalytic transformation of coals, heavy residual petroleum products, liquid high-boiling waste and some oil and chemical industries [1–2].

A number of processes of thermochemical processing of coal and oil shale have been developed in NJSC al-Farabi Kazakh National university, the Faculty of chemistry and chemical technology, the Department of physical chemistry, catalysis and petrochemistry, as well as the Research Institute of New chemical technologies and materials [3–14], which are based on the results of our research on the complex chemical and technological processing of hard and brown coals of Kazakhstan, conducted in 1990–2020 [15–19]. As the research results have shown, the catalytic properties of oil shales allow for the hydrogenolysis of the organic mass of coals and heavy petroleum raw materials with a high degree of their transformation into liquid distillate products without intensive coke and pellet formation under optimal conditions [3–6, 9, 20].

The mineral part of the shale, containing aluminosilicates, iron oxides and other catalytically active forms of metals, in turn activates the cracking reactions [21]. The presence of such a complex of properties in oil shales causes a change not only in the reactivity of the components of hydrocarbon raw materials, but also in the sizes of supramolecular structures that are an integral part of such a dispersed system, and the preparation of the raw mixture, during its heating and hydrogenolysis [22–24].

It is proved [21, 25, 26] that an important indicator of the possibility of obtaining synthetic liquid products from solid hydrocarbon raw materials is the ratio C : H. In coal it is 0.6–0.8%, while in shale oil it reaches 1.5%, which is similar to the indicators for natural oil. In the process of coal liquefaction, the presence of a hydrogen donor is necessary, for which heavy oil fractions can be used. On this basis, work has begun on the study of joint processing of coal and shale oil, during which it is possible to use them as a “supplier” of hydrogen for coal liquefaction in parallel with the liquefaction of shale oil. This technology will make it possible to obtain a wider range of liquid products with a high content of “light” fractions.

Materials and methods

In this paper, the process of joint processing of brown coal of Taldykol deposit and oil shale of Kiin deposit is studied.

The Taldykol deposit is located in Bayanaul district of Pavlodar region, 65 km south-east of Ekibastuz and 160 km south-west of the regional center of Pavlodar. Taldykol coal has the following physical and chemical characteristics: W^a = 12.0% (moisture analytical), A^daf = 7.4% (dry ash), V^daf = 41.2% (volatile substances), C^daf = 74.5% (carbon of the dry ashless state), H^daf = 5.43% (dry state hydrogen), S^daf = 0.53% (total dry state sulfur), O + N = 19.54% (amount of carbon and nitrogen), H/C = 0.87% (the ratio of hydrogen to carbon). The insignificant content of ash (7.4%) and a fairly high content of hydrogen (5.43%) make it possible to consider the coal of the Taldykol deposit as a favorable raw material for hydrogenation processing into liquid fuel [27].

The Kiin deposit is located on the territory of the Stepnoy district of the Aktobe region in the upper reaches of the Kiya River, the left tributary of the Ural River. It was opened in 1940 by A.L. Yanshin. Kiin shale has the following physicochemical characteristics: A^daf = 72% (dry ash), V^daf = 19.3% (volatile substances), C^daf = 74% (carbon of the dry ashless state), H^daf = 7.6% (dry state hydrogen), S^daf = 1.04% (total dry state sulfur), H/C = 0.103% (the ratio of hydrogen to carbon), calorific value per dry substance 265–1537 kcal/kg, heat of combustion of combustible mass 7314–7744 kcal/kg, resin yield per organic mass 21–27%. Yield of semi-coking products in the retort: resin – 4.1–6.5%, semi-coke – 86–93%, pyrogenic water – 2.0–3.7% and gas + losses 1.0–4.3% [27].

The process of liquefaction of coal and shale was carried out at a laboratory installation under a pressure of 5.0 MPa and a temperature of 425°C. To intensify the coal liquefaction process, a catalytic system consisting of fine solid particles of polymetallic ore enrichment sludge was introduced. Destructive processes are additionally implemented on the surface of these particles. Under the conditions of experiments in the process of catalytic processing of a mixture of coal and shale, coke-shaped products on the walls of the installation and in the volume of the reaction mixture were not formed. Liquid products obtained in the process were subjected to distillation with fraction selection with boiling point up to 200°С, fractions with boiling point up to 200–370°С. The residue from the boiling point above 370°C contained in its composition the insoluble organic matter of shale and coal and their mineral part [3–4].

Results

Based on the data of Table 1, it follows that the optimal amount of shale added to coal is 15.0%. When using Kiin shale in the accepted conditions of thermocatalytic processing (test 1), a high yield of the gasoline fraction with boiling point up to 200°C – 15.3% is obtained based on coal and diesel fraction with boiling point up to 200–370°C – 26.4%. With a decrease in Kiin shale additives to 10.0%, the total yield of gasoline and diesel fraction decreases from 41.7% to 38.4%. A further decrease in the amount of shale added to 8.0% and 5.2% leads to a significant decrease in the yield of the fractions of motor fuels to 36.8% and 33.2%, respectively, the yield of the heavy residue and coke increases with boiling point above 370°C.

 

Table 1. Results of thermal catalytic processing of coal with different shale content (425°C, 5.0 MPa, reaction time 1.0 h, intensively shaken reactor)

Product Yield	No. of tests
	1	2	3	4
Taken, wt.%:
Coal	85.0	90.0	92.0	94.8
Shale, including:	15.0	10.0	8.0	5.2
Obtained based on coal, wt.%:
Gas	11.2	14.1	11.0	11.2
Water	5.3	4.7	4.6	4.9
Fraction with boiling point up to 200°C	15.3	12.5	12.1	11.9
Fraction with boiling point up to 200–370°C	26.4	25.9	24.7	21.3
Total yield of light distillates	41.7	38.4	36.8	33.2
Balance with boiling point above 370°C	38.8	39.3	42.5	43.5
Coke content on the mineral part of shale, wt.%	3.0	3.5	5.1	7.2

 

An increase in the content of shale in the co- al shale mixture above 15.0% is impractical, since this will lead to a complication of the process technology, an increase in erosion of the equipment by the mineral part of the shale, a delamination of the reaction mixture into liquid and solid phases and a complication of the hardware design of the unit for isolating solid components from liquid products of thermocatalytic processing.

The results of the joint thermal catalytic processing of brown coal of the Taldykol deposit and shale of the Kiin deposit are summarized in Table 2.

 

Table 2. Thermocatalytic processing of Taldykol coal and Kiin shale mixture

Process indicators	Coal	Coal +Oil shale
Process Conditions
Coal: Paste Former (shale + coal): pasting agent	1 : 1.3	(0.6 + 0.4) : 1.3
Shale Organic Mass: Coal Organic Mass		1 : 0.9
Temperature, °C	420	420
Pressure, MPa	5.0	5.0
Duration, min	15	30
Product Yield, %
Fraction with boiling point up to 200°C	14.9	15.3
Fraction with boiling point up to 200–370°C	22.1	26.4
Fraction with boiling point above 370°C	34.6	38.8
Solid products, gas + water	26.8	18.0
Losses	1.6	1.5

 

As shown in Table 2, the addition of shale to coal under optimal process conditions makes it possible to carry out the process of co-hydrogenation of the organic mass of coal with a high degree of conversion into liquid products without coke formation. In comparison with the process of hydrogenation of coal alone, the degree of transformation of the process of co-hydrogenation of coal and shale is high, since as a result, there is an increase in the yield of liquid products, namely fractions with boiling point up to 200°C from 14.9% to 15.3%, fractions with boiling point 200–370°C from 22.1% to 26.4%, fraction with boiling point above 370°C from 34.6% to 38.8%. The solid residue was used as an organic binder for road construction. The bitumen obtained on the basis of products of thermocatalytic processing of a mixture of shale and coal meets the requirements of GOST 22245-76 for petroleum bitumen [17].

The fuel products obtained were investigated using gas chromatographic and elemental analysis. The results are shown in Table 3.

 

Table 3. Characteristics of distillate products of thermal catalytic processing of coal in a mixture with shale

Indicator	Fractions with boiling point
	up to 200°C	200–370°C	above 370°C
Density at 20°C, g/cm³	0.7547	0.8891	0.9394
Contents, Vol. %:
Phenols	2.7	1.8	–
Nitrogenous bases	1.5	4.5	–
Group hydrocarbon composition, wt. %
paraffinic + naphthenic	73.5	48.3	23.1
aromatic	26.5	51.7	57.1
silica gel resins	–	–	16.5
asphaltenes	–	–	3.3
Iodine number, g I2/100g of product	25.6	34.2	12.3
Elemental composition, wt. %:
С	85.71	86.30	86.65
H	13.93	12.40	11.24
S	0.27	1.11	1.83
N	0.09	0.19	0.28
Content, g/t
V	–	–	6
Ni	–	–	19

 

According to the results of gas chro- matographic analysis, it can be seen that the content of paraffin-naphthenic hydrocarbons in the fractions with a boiling point up to 200°C is high (73.5 wt.%) compared to fractions of boiling point 200–370°C (48.3 wt.%) and with a boiling point above 370°C (23.1 wt.%). And the content of aromatic hydrocarbons has an inverse correlation, that is in fractions with a boiling point above 370°C – 57.1 wt.%, in fractions with a boiling point 200–370°C – 51.7 wt.%, in fractions with a boiling point up to 200°C – 26.5 wt.%. And also in fractions with a boiling point above 370°C resins were found (16.5 wt.%) and asphaltenes (3.3 wt.%).

The content of nitrogenous bases in light distillates (1.5–4.5 vol.%), phenols (2.7–1.8 vol.%), high sulfur content (0.27–1.83 wt.%), as well as the presence of vanadium and nickel indicate that the distillates obtained do not meet the requirements for the quality of motor fuels and need additional processing, such as hydrotreating, cracking, reforming, etc.

Conclusions

Thus, the results of studies of the joint hydrogenation of coal and shale showed that the implementation of the process in the presence of shale of the Kiin deposit increased the total yield of liquid products. The optimal amount of shale added to coal is 15.0%. In this case, there is an increase in the total yield of liquid products by 10%. The solid residue with a boiling point above 370°C has been tested as an organic binder for road construction. The proposed process technology also makes it possible to obtain gasoline and diesel fractions, which after appropriate hydrotreating can be used as motor fuels. Gasoline fraction obtained has a high content of paraffin-naphthenic hydrocarbons (73.5 wt.%) and a moderate amount of aromatic hydrocarbons (26.5 wt.%), as well as unsaturated compounds. The addition of oil shale to coal allows the process to be carried out under optimal conditions with a high degree of conversion into liquid products without coke formation. The degree of transformation of the mixture of organic mass of shale and coal is much higher than just coal.

ДОПОЛНИТЕЛЬНО

Источник финансирования. Работа выполнена в рамках проекта грантового финансирования АР14869180 «Разработка эффективных технологии совместной гидрогенизационной переработки углей и горючих сланцев РК для получения компонентов моторных топлив и химических веществ».

Конфликт интересов. Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с публикацией настоящей статьи.

Вклад авторов. Все авторы подтверждают соответствие своего авторства международным критериям ICMJE (все авторы внесли существенный вклад в разработку концепции, проведение исследования и подготовку статьи, прочли и одобрили финальную версию перед публикацией). Наибольший вклад распределён следующий образом: Каирбеков Ж.К. – интерпретация данных исследования, проверка результатов, написание и редактирование рукописи, Сармурзина Р.Г. – концепция исследования, Есеналиева М.З. – интерпретация данных, контроль за выполнением работы, Каирбеков А.Ж. – проведение исследования, Суймбаева С.М. – проведение экспериментов, Джелдыбаева И.М. – сбор, анализ, интерпретация данных, написание и редактирование рукописи.

ADDITIONAL INFORMATION

Funding source. The work was carried out within the framework of the grant financing project AP14869180 «Development of effective technologies with joint hydrogenаtion processing of coal and oil shаle of the Republic of Kаzаkhstаn for the production of motor fuel components and chemicаls».

Competing interests. The authors declare that they have no competing interests.

Authors’ contribution. All authors made a substantial contribution to the conception of the work, acquisition, analysis, interpretation of data for the work, drafting and revising the work, final approval of the version to be publi- shed and agree to be accountable for all aspects of the work. The largest contribution is distributed as follows: Zhaksyntay K. Kairbekov – interpretation of research data, verification of results, writing and editing of the manuscript; Raushan G. Sarmurzina – research concept; Manshuk Z. Esenalieva – interpretation of data, control over the per- formance of work; Altay Zh. Kairbekov – conducting research; Saltanat M. Suimbaeva – conducting experiments; Indira M. Dzheldybaeva – data collection, analysis, interpretation, writing and editing of the manuscript.

Авторлар туралы

Ж. Қ. Қайырбеков

Әл-Фараби атындағы Қазақ Ұлттық Университеті

Email: zh_kairbekov@mail.ru
ORCID iD: 0000-0002-0255-2330
Scopus Author ID: 5591070520
ResearcherId: A-5389-2015

Sc. (Chemistry), professor

Қазақстан, Алматы қаласы

Р. Ғ. Сармурзина

Мұнай-химия өнімдерін өндірушілер мен тұтынушылар қауымдастығы

Email: sarmurzina_r@mail.ru
ORCID iD: 0000-0002-9572-9712
Scopus Author ID: 6603381995

Sc. (Chemistry), professor

Қазақстан, Астана қаласы

М. З. Есеналиева

Әл-Фараби атындағы Қазақ Ұлттық Университеті

Email: esenalieva@mail.ru
ORCID iD: 0000-0002-0817-2048
Scopus Author ID: 6507284187

Cand. Sc. (Chemistry), Ass. Professor

Қазақстан, Алматы қаласы

А. Ж. Қайырбеков

Әл-Фараби атындағы Қазақ Ұлттық Университеті

Email: altay_kairbekov@gmail.com
Scopus Author ID: 56600640700

Cand. Sc. (Technology)

Қазақстан, Алматы қаласы

С. М. Суймбаева

Әл-Фараби атындағы Қазақ Ұлттық Университеті

Email: saltanat_suimbayeva@mail.ru
ORCID iD: 0000-0003-3990-4974
Scopus Author ID: 57201691853
ResearcherId: EBK-0532-2022
Қазақстан, Алматы қаласы

І. М. Джелдыбаева

Әл-Фараби атындағы Қазақ Ұлттық Университеті

Хат алмасуға жауапты Автор.
Email: indiko_87@mail.ru
ORCID iD: 0000-0002-1524-4046
SPIN-код: 8666-3303
Scopus Author ID: 56600659100
ResearcherId: CPH-4244-2022
Қазақстан, Алматы қаласы

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