A. B. Arbuzov, V. Drozdov, D. A. Shlyapin, A. Lavrenov
{"title":"液体镓-铟共晶活化铝-钴和铝-镍合金与叔丁基氯的相互作用,形成催化金属-铝-氯配合物","authors":"A. B. Arbuzov, V. Drozdov, D. A. Shlyapin, A. Lavrenov","doi":"10.6060/IVKKT20186109-10.5862A","DOIUrl":null,"url":null,"abstract":"It is known that binary alloys of aluminum and metals of the iron group (cobalt, nickel) after their activation with the liquid eutectic gallium-indium by the removal of “passivating” oxide layers sharply increase the reactivity with respect to organochlorines. Corresponding reactions lead to the formation of metal – alumo - chloride complexes as inorganic products, which are active in many practically important catalytic reactions of liquid-phase conversion of hydrocarbons such as: alkylation, isomerization, oligomerization. This approach which was previously developed by the authors for the polycrystalline aluminum, is of interest in metal-complex catalysis since the formation of catalytic alumo-chloride and/or metal-alumo-chloride complexes can be carried out directly in the reaction medium, i.e. in situ. In this work, the local composition, structure and morphology of surface layers of aluminum-cobalt and aluminum-nickel alloys activated with liquid gallium-indium eutectic were studied using the methods of scanning electron microscopy and X-ray energy-dispersive spectrometry to determine the physicochemical regularities of the dynamics of their interaction with tert-butyl chloride at room temperatures. The formation of metal chloride complexes in the interphase area “activated alloy - tert-butyl chloride” was studied by ATR-FT-IR method in situ. The results obtained indicate that mono- and bi- nuclear alumo-chloride anions stabilized by cobalt and nickel cations are formed during the interaction. It is assumed that the ionic complex pairs formed are the active centers in liquid-phase reactions of hydrocarbons transformation at low temperatures. These structures are responsible for significantly change in the selectivity of catalytic processes compared to aluminum chloride catalyst. \nFor citation: \nArbuzov A.B., Drozdov V.A., Shlyapin D.A., Lavrenov A.V. Interaction of aluminum-cobalt and aluminum-nickel alloys activated by liquid gallium-indium eutectic with tert-butyl chloride for formation of catalytic metal - alumo-chloride complexes. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 64-69","PeriodicalId":45993,"journal":{"name":"Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya i Khimicheskaya Tekhnologiya","volume":null,"pages":null},"PeriodicalIF":0.6000,"publicationDate":"2018-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"INTERACTION OF ALUMINUM-COBALT AND ALUMINUM-NICKEL ALLOYS ACTIVATED BY LIQUID GALLIUM-INDIUM EUTECTIC WITH TERT-BUTYL CHLORIDE FOR FORMATION OF CATALYTIC METAL - ALUMO-CHLORIDE COMPLEXES\",\"authors\":\"A. B. Arbuzov, V. Drozdov, D. A. Shlyapin, A. Lavrenov\",\"doi\":\"10.6060/IVKKT20186109-10.5862A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"It is known that binary alloys of aluminum and metals of the iron group (cobalt, nickel) after their activation with the liquid eutectic gallium-indium by the removal of “passivating” oxide layers sharply increase the reactivity with respect to organochlorines. Corresponding reactions lead to the formation of metal – alumo - chloride complexes as inorganic products, which are active in many practically important catalytic reactions of liquid-phase conversion of hydrocarbons such as: alkylation, isomerization, oligomerization. This approach which was previously developed by the authors for the polycrystalline aluminum, is of interest in metal-complex catalysis since the formation of catalytic alumo-chloride and/or metal-alumo-chloride complexes can be carried out directly in the reaction medium, i.e. in situ. In this work, the local composition, structure and morphology of surface layers of aluminum-cobalt and aluminum-nickel alloys activated with liquid gallium-indium eutectic were studied using the methods of scanning electron microscopy and X-ray energy-dispersive spectrometry to determine the physicochemical regularities of the dynamics of their interaction with tert-butyl chloride at room temperatures. The formation of metal chloride complexes in the interphase area “activated alloy - tert-butyl chloride” was studied by ATR-FT-IR method in situ. The results obtained indicate that mono- and bi- nuclear alumo-chloride anions stabilized by cobalt and nickel cations are formed during the interaction. It is assumed that the ionic complex pairs formed are the active centers in liquid-phase reactions of hydrocarbons transformation at low temperatures. These structures are responsible for significantly change in the selectivity of catalytic processes compared to aluminum chloride catalyst. \\nFor citation: \\nArbuzov A.B., Drozdov V.A., Shlyapin D.A., Lavrenov A.V. Interaction of aluminum-cobalt and aluminum-nickel alloys activated by liquid gallium-indium eutectic with tert-butyl chloride for formation of catalytic metal - alumo-chloride complexes. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. 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INTERACTION OF ALUMINUM-COBALT AND ALUMINUM-NICKEL ALLOYS ACTIVATED BY LIQUID GALLIUM-INDIUM EUTECTIC WITH TERT-BUTYL CHLORIDE FOR FORMATION OF CATALYTIC METAL - ALUMO-CHLORIDE COMPLEXES
It is known that binary alloys of aluminum and metals of the iron group (cobalt, nickel) after their activation with the liquid eutectic gallium-indium by the removal of “passivating” oxide layers sharply increase the reactivity with respect to organochlorines. Corresponding reactions lead to the formation of metal – alumo - chloride complexes as inorganic products, which are active in many practically important catalytic reactions of liquid-phase conversion of hydrocarbons such as: alkylation, isomerization, oligomerization. This approach which was previously developed by the authors for the polycrystalline aluminum, is of interest in metal-complex catalysis since the formation of catalytic alumo-chloride and/or metal-alumo-chloride complexes can be carried out directly in the reaction medium, i.e. in situ. In this work, the local composition, structure and morphology of surface layers of aluminum-cobalt and aluminum-nickel alloys activated with liquid gallium-indium eutectic were studied using the methods of scanning electron microscopy and X-ray energy-dispersive spectrometry to determine the physicochemical regularities of the dynamics of their interaction with tert-butyl chloride at room temperatures. The formation of metal chloride complexes in the interphase area “activated alloy - tert-butyl chloride” was studied by ATR-FT-IR method in situ. The results obtained indicate that mono- and bi- nuclear alumo-chloride anions stabilized by cobalt and nickel cations are formed during the interaction. It is assumed that the ionic complex pairs formed are the active centers in liquid-phase reactions of hydrocarbons transformation at low temperatures. These structures are responsible for significantly change in the selectivity of catalytic processes compared to aluminum chloride catalyst.
For citation:
Arbuzov A.B., Drozdov V.A., Shlyapin D.A., Lavrenov A.V. Interaction of aluminum-cobalt and aluminum-nickel alloys activated by liquid gallium-indium eutectic with tert-butyl chloride for formation of catalytic metal - alumo-chloride complexes. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2018. V. 61. N 9-10. P. 64-69