SU519214A1 - Catalyst for the conversion of cyclic hydrocarbons - Google Patents

Catalyst for the conversion of cyclic hydrocarbons

Info

Publication number
SU519214A1
SU519214A1 SU2052510A SU2052510A SU519214A1 SU 519214 A1 SU519214 A1 SU 519214A1 SU 2052510 A SU2052510 A SU 2052510A SU 2052510 A SU2052510 A SU 2052510A SU 519214 A1 SU519214 A1 SU 519214A1
Authority
SU
USSR - Soviet Union
Prior art keywords
catalyst
conversion
cyclic hydrocarbons
carbon fiber
composition
Prior art date
Application number
SU2052510A
Other languages
Russian (ru)
Inventor
Олег Владимирович Брагин
Татьяна Георгиевна Ольферьева
Игорь Николаевич Ермоленко
Алла Михайловна Сафонова
Original Assignee
Институт Органической Химии Им. Зелинского Ан Ссср
Институт общей и неорганической химии АН Белорусской ССР
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Институт Органической Химии Им. Зелинского Ан Ссср, Институт общей и неорганической химии АН Белорусской ССР filed Critical Институт Органической Химии Им. Зелинского Ан Ссср
Priority to SU2052510A priority Critical patent/SU519214A1/en
Application granted granted Critical
Publication of SU519214A1 publication Critical patent/SU519214A1/en

Links

Landscapes

  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Готовый катализатор содержит 3 вес. % платины.The finished catalyst contains 3 wt. % platinum.

Б. Испытание катализатора. Опыты провод т в микрокаталитической установке с импульсной подачей исходного углеводорода . В реактор загружают 40 мг (содержание платины 1,2 мг) платиноуглеродного волокна. Углеводород ввод т в реактор импульсами по 120 мкл. Скорость газаносител  (водород) составл ет 2000 .мл/час. Продукты реакции поступают в капилл рный хроматограф с пламенно-ионизационным детектором .B. Test catalyst. The experiments were carried out in a microcatalytic installation with a pulsed feed of the initial hydrocarbon. Charged to the reactor 40 mg (platinum content 1.2 mg) of platinum carbon fiber. Hydrocarbon is introduced into the reactor in pulses of 120 µl. The gas carrier rate (hydrogen) is 2000 ml / hour. The reaction products enter a capillary chromatograph with a flame ionization detector.

Состав продуктов реакции г#мс-1,2-диметилциклопентана при , %:The composition of the reaction products g # MS-1,2-dimethylcyclopentane at,%:

Углеводороды состава Hydrocarbons composition

0,8 Продукты гидрогенолиза0.8 Hydrogenolysis Products

состава С composition C

19,1 Гранс-изомер 65,6 Цис-изомер 14,519.1 Grans isomer 65.6 Cis isomer 14.5

Отношение изомеров цис-/транс0 ,22 в катализатеThe ratio of isomers CIS- / TRANS0, 22 in catalyzate

(равновесное отношение в этих услови х 0,215). Циклогексан на 83,6 дегидрируетс  до бензола.(equilibrium ratio in these conditions is 0.215). The cyclohexane is 83.6 dehydrated to benzene.

Бензол при 250°С и скорости водорода 7700 мл/час на 99,8% превращаетс  в циклогексан .Benzene at 250 ° C and a hydrogen rate of 7700 ml / hour is 99.8% converted to cyclohexane.

Конфигурационна  изомеризаци  г|«с-1-метил - 3 - этилциклобутана при 230°С в присутствии 10 мг катализатора проходит наConfiguration isomerization of g | "s-1-methyl-3-ethylcyclobutane at 230 ° C in the presence of 10 mg of catalyst passes on

20,.20,.

Состав продуктов превращени  ,4-№метилциклогексана в этих же услови х следующий: 23,1% г)анс-изомера, 72,1% цисизомера , 4,8% п-ксилола.The composition of the products of transformation, 4-methylcyclohexane under the same conditions, is as follows: 23.1% g) ans-isomer, 72.1% cis isomer, 4.8% p-xylene.

Предлагаемый катализатор про вл ет высокую активность в реакции конфигурационной изомеризации диалкилциклопентанов.The proposed catalyst exhibits high activity in the configurational isomerization reaction of dialkylcyclopentanes.

Состав продуктов превращени  1(ис-1,2-диметилциклопентана представлен в таблице.The composition of the conversion products 1 (is-1,2-dimethylcyclopentane is presented in the table.

) Равновесный состав стереоизомеров I, 2 - цис-/транс-равно 0,215.) The equilibrium composition of stereoisomers I, 2 - cis / trans is 0.215.

Благодар  иапользоваиию в (качестве носител  в предлагаемом катализаторе пиролитического углеродного волокна катализатор обладает высокой газопроницаемостью сло , доступностью активной фазы (платины) мочекулам реагирующих веществ. Платина в высокодисперсном состо нии равномерно распредел етс  по объему катализатора и жестко фиксируетс  в угольной матрице, что обеспечивает высокую активность и термостабильность катализатора. Катализатор можно получать в различных формах (волокно, ткань, лента, фильтр и т. д.)Due to its use (as a carrier in the proposed pyrolytic carbon fiber catalyst, the catalyst has a high gas permeability layer, the availability of the active phase (platinum) to reactant substances). Platinum in a highly dispersed state is uniformly distributed throughout the catalyst and is rigidly fixed in the carbon matrix, which ensures high activity and thermal stability of the catalyst. The catalyst can be obtained in various forms (fiber, cloth, tape, filter, etc.)

Claims (1)

Формула изобретени Invention Formula Катализатор дл  превращени  циклических углеводородов, содержащий платину на носителе, отличающийс  тем, что, .с целью повышени  активности и термостабильности Катализатора, в качестве носител  он содержит пиролитическое углеродное волокно ери следующем содержании компонентов, вес. %:A catalyst for the conversion of cyclic hydrocarbons containing platinum on a carrier, characterized in that, in order to increase the activity and thermal stability of the catalyst, it contains pyrolytic carbon fiber as the carrier for the following components, by weight. %: Платина2,7-3,2Platinum2,7-3,2 Пиролитическое углеродное волокноОстальное. диметилциклопеитана при 310°С; цис-ПJ, транс-82,3; отношение Pyrolytic carbon fiber Else. dimethylcyclopeitan at 310 ° C; cis-PJ, trans-82.3; an attitude
SU2052510A 1974-08-13 1974-08-13 Catalyst for the conversion of cyclic hydrocarbons SU519214A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU2052510A SU519214A1 (en) 1974-08-13 1974-08-13 Catalyst for the conversion of cyclic hydrocarbons

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU2052510A SU519214A1 (en) 1974-08-13 1974-08-13 Catalyst for the conversion of cyclic hydrocarbons

Publications (1)

Publication Number Publication Date
SU519214A1 true SU519214A1 (en) 1976-06-30

Family

ID=20593735

Family Applications (1)

Application Number Title Priority Date Filing Date
SU2052510A SU519214A1 (en) 1974-08-13 1974-08-13 Catalyst for the conversion of cyclic hydrocarbons

Country Status (1)

Country Link
SU (1) SU519214A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4233763A1 (en) * 1992-10-07 1994-04-14 Hasso Von Bluecher Reactivation of noble metal activated carbon catalyst - by e.g. reforming or platforming catalyst by pyrolysis, activation and opt. redn without burning carbon support

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4233763A1 (en) * 1992-10-07 1994-04-14 Hasso Von Bluecher Reactivation of noble metal activated carbon catalyst - by e.g. reforming or platforming catalyst by pyrolysis, activation and opt. redn without burning carbon support

Similar Documents

Publication Publication Date Title
Siegel et al. The Stereochemistry of the Hydrogenation of Cycloölefins on Supported Palladium Catalysts1, 2
US4056576A (en) Chemical process over gallium catalyst converting saturated hydrocarbons to olefins
Farkas Part. II.—Catalytic reactions of hydrocarbons. The activation of hydrogen in catalytic reactions of hydrocarbons
US3409702A (en) Catalytic olefin isomerization process
US3303235A (en) Unsaturated hydrocarbons by oxidative dehydrogenation over a catalyst comprising zinc and iron
PINES et al. Alumina: Catalyst and Support. VII. 1 Aromatization of n-Heptane-1-C14 Over Chromia-Alumina Catalysts2, 3
SU519214A1 (en) Catalyst for the conversion of cyclic hydrocarbons
US3898297A (en) Alkyl benzene isomerisation process
IL23403A (en) Dehydrogenation of hydrocarbons and catalyst therefor
US3864425A (en) Ruthenium-promoted fluorided alumina as a support for SBF{HD 5{B -HF in paraffin isomerization
US2600379A (en) Supported group viii-carbon dehydrogenation catalyst
US3574076A (en) Conversion of unsaturated hydrocarbons in the presence of a catalyst and ultraviolet radiation
GB1125324A (en) Process for the manufacture of n-vinyl compounds
Sondheimer et al. UNSATURATED MACROCYCLIC COMPOUNDS. XIII. 1 CYCLOTRIACONTAPENTADECAENE
ES310402A1 (en) A continuous procedure for the catalytic hydrogenation of an aromatic polynitro compound. (Machine-translation by Google Translate, not legally binding)
ES311270A1 (en) The continuous procedure for the catalytic hydrogenation of an aromatic polynitro compound. (Machine-translation by Google Translate, not legally binding)
US2379697A (en) Production of diolefins
US2908656A (en) Pretreatment of noble metal catalysts
US2272266A (en) Manufacture of polycyclic hydrocarbons
Imizu et al. Isomerization of butenes over thorium dioxide.
US2857439A (en) Dehydrogenation of sulfur-contaminated monocyclic terpenes
Lietz et al. Low temperature hydrogenolysis and hydrogenation of alkylbenzenes on platinum catalysts
US3840608A (en) Hydrogenation of aromatic hydrocarbons
ES280295A1 (en) Fenol catalytic preparation procedure (Machine-translation by Google Translate, not legally binding)
US4041093A (en) Method of dehydrogeneration, dehydrocyclization and hydrodealkylation