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State of Palladium in Palladium–Aluminosilicate Catalysts As Studied by XPS and the Catalytic Activity of the Catalysts in the Deep Oxidation of Methane Научная публикация

Журнал Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Вых. Данные Год: 2007, Том: 48, Номер: 5, Страницы: 728-734 Страниц : 7 DOI: 10.1134/S0023158407050187
Ключевые слова Palladium; Aluminosilicate; Palladium Catalyst; Deep Oxidation; Palladium Particle
Авторы Tsyrulʹnikov P.G. 1 , Afonasenko T.N. 1 , Koshcheev S.V. 2 , Boronin A.I. 2
Организации
1 Institute of Hydrocarbon Processing Problems, Siberian Branch, Russian Academy of Sciences, Omsk, Russia
2 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russia

Реферат: Palladium catalysts based on Siralox and AS aluminosilicate supports for the deep oxidation of methane were studied. With the use of XRD analysis, it was found that they were heterophase systems consisting of an amorphous aluminosilicate and γ-Al2O3 stabilized against agglomeration. It was found that the catalytic activity of palladium-aluminosilicate catalysts in the deep oxidation of methane at 500°C depended on the support precalcination temperature. X-ray photoelectron spectroscopy (XPS) was used to study the states of the AS-30 aluminosilicate support calcined at 600, 800, or 1000°C and palladium supported on it. It was found that the action of an acid impregnation solution of palladium nitrate on the aluminosilicate calcined at 800°C resulted in a structural rearrangement of the aluminosilicate surface. This rearrangement resulted in the stabilization of both palladium oxide and palladium metal particles at surface defects and the incorporation of these particles into the aluminosilicate after catalyst calcination. As a result, an anomalous decrease in catalytic activity was observed in aluminosilicate samples calcined at 800°C. According to XPS data, palladium in the catalyst was stabilized in the following three phases: metal (E b(Pd 3d 5/2) = 334.8 eV), oxide (E b(Pd 3d 5/2) = 336.8 eV), and “interaction” (E b(Pd 3d 5/2) = 335.8 eV) phases. The ratio between these phases depended on support and catalyst calcination temperatures. The interaction phase, which consisted of PdOx clusters stabilized in the aluminosilicate structure, was responsible for the retention of activity after calcination at high temperatures (800°C). Based on an analysis of XPS data, it was hypothesized that palladium in the interaction phase occurred in a charged state with the formal charge on the Pd atom close to 1 + (δ+ phase).
Библиографическая ссылка: Tsyrulʹnikov P.G. , Afonasenko T.N. , Koshcheev S.V. , Boronin A.I.
State of Palladium in Palladium–Aluminosilicate Catalysts As Studied by XPS and the Catalytic Activity of the Catalysts in the Deep Oxidation of Methane
Kinetics and Catalysis. 2007. V.48. N5. P.728-734. DOI: 10.1134/S0023158407050187 WOS Scopus РИНЦ OpenAlex CAPlusCA
Оригинальная: Цырульников П.Г. , Афонасенко Т.Н. , Кощеев С.В. , Боронин А.И.
Исследование методом РФЭС состояния палладия в палладийалюмосиликатных катализаторах и их каталитическая активность в глубоком окислении метана
Кинетика и катализ. 2007. Т.48. №5. С.778-784. РИНЦ
Даты:
Поступила в редакцию: 14 авг. 2006 г.
Опубликована в печати: 1 сент. 2007 г.
Идентификаторы БД:
≡ Web of science: WOS:000249971500018
≡ Scopus: 2-s2.0-35148885212
≡ РИНЦ: 13540324
≡ OpenAlex: W1994373361
≡ Chemical Abstracts: 2007:1138068
≡ Chemical Abstracts (print): 150:263382
Цитирование в БД:
≡ Web of science 45 Сбор данных от 20.02.2026
≡ Scopus 44 Сбор данных от 15.02.2026
≡ РИНЦ 37 Сбор данных от 15.02.2026
≡ OpenAlex 43 Сбор данных от 15.02.2026
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