FI128885B - Catalyst for dehydrogenation, method for preparing the catalyst and use - Google Patents

Catalyst for dehydrogenation, method for preparing the catalyst and use Download PDF

Info

Publication number
FI128885B
FI128885B FI20185940A FI20185940A FI128885B FI 128885 B FI128885 B FI 128885B FI 20185940 A FI20185940 A FI 20185940A FI 20185940 A FI20185940 A FI 20185940A FI 128885 B FI128885 B FI 128885B
Authority
FI
Finland
Prior art keywords
catalyst
support
dehydrogenation
tio
precursor
Prior art date
Application number
FI20185940A
Other languages
Finnish (fi)
Swedish (sv)
Other versions
FI20185940A1 (en
FI20185940A (en
Inventor
Noora Kaisalo
Timo Repo
Juha Keskiväli
Päivi Aakko-Saksa
Pekka Simell
Matti Reinikainen
Matti Putkonen
Laura Keskiväli
Original Assignee
Teknologian Tutkimuskeskus Vtt Oy
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 Teknologian Tutkimuskeskus Vtt Oy filed Critical Teknologian Tutkimuskeskus Vtt Oy
Priority to FI20185940A priority Critical patent/FI128885B/en
Priority to PCT/FI2019/050784 priority patent/WO2020094921A1/en
Publication of FI20185940A1 publication Critical patent/FI20185940A1/en
Publication of FI20185940A publication Critical patent/FI20185940A/en
Application granted granted Critical
Publication of FI128885B publication Critical patent/FI128885B/en

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/063—Titanium; Oxides or hydroxides thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/42—Platinum
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/20—Catalysts, in general, characterised by their form or physical properties characterised by their non-solid state
    • B01J35/23—Catalysts, in general, characterised by their form or physical properties characterised by their non-solid state in a colloidal state
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0238—Impregnation, coating or precipitation via the gaseous phase-sublimation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/08—Heat treatment
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00—Manufacture or treatment of nanostructures
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/0005—Reversible uptake of hydrogen by an appropriate medium, i.e. based on physical or chemical sorption phenomena or on reversible chemical reactions, e.g. for hydrogen storage purposes ; Reversible gettering of hydrogen; Reversible uptake of hydrogen by electrodes
    • C01B3/001—Reversible uptake of hydrogen by an appropriate medium, i.e. based on physical or chemical sorption phenomena or on reversible chemical reactions, e.g. for hydrogen storage purposes ; Reversible gettering of hydrogen; Reversible uptake of hydrogen by electrodes characterised by the uptaking medium; Treatment thereof
    • C01B3/0015—Organic compounds; Solutions thereof
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/22—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds
    • C01B3/24—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds of hydrocarbons
    • C01B3/26—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds of hydrocarbons using catalysts
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
    • C07C5/333—Catalytic processes
    • C07C5/3335—Catalytic processes with metals
    • C07C5/3337—Catalytic processes with metals of the platinum group
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10—Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041—Composition of the catalyst
    • C01B2203/1047—Group VIII metal catalysts
    • C01B2203/1064—Platinum group metal catalysts
    • C01B2203/107—Platinum catalysts
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/32—Hydrogen storage

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Nanotechnology (AREA)
  • Physics & Mathematics (AREA)
  • Combustion & Propulsion (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Composite Materials (AREA)
  • Thermal Sciences (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

The invention relates to a catalyst for dehydrogenation. The catalyst is a Pt catalyst, in which Pt catalyst agent is formed by using a Pt-precursor and is arranged on a support, and the support is selected from TiO2 or γ-Al2O3. Further, the invention relates to a method for producing a catalyst and a use of the catalyst.

Description

CATALYST FOR DEHYDROGENATION, METHOD FOR PREPARING THE CATALYST AND USE
FIELD The application relates to a catalyst for de- hydrogenation as defined in claim 1 and a method for preparing the catalyst as defined in claim 7. Further, the application relates to a use of the catalyst as defined in claim 13.
BACKGROUND Known from the prior art is that hydrogen is a flexible energy carrier, however, its production and storage is challenging in compressed and liquid form, or as adsorbed physically or binded chemically in sol- id materials. Liguid organic hydrogen carriers (LOHCs) are suggested as reversible, effective, safe, user- friendly and economical hydrogen storages compatible with the existing fuel infrastructure. Many LOHC com- pounds are stabile at normal temperature and pressure. The LOHC system is promising particularly for applica- tions, where safety, robustness and fast kinetics of the system are priorities. Catalytic dehydrogenation of some perhydrogenated LOHC candidates are mature in- dustrial processes. DBT (dibenzyl toluenes) is a com- — mercial LOHC hydrogen storage system. O Reforming of cycloalkanes is based on noble —- metals, particulartly Pt, or on lower-cost Ni and Mo 7 30 and their combinations with alkali reagents. Alumina T is a common support in these reactions. In the prior E art, Pt on carbon has been observed to be the most ac- S tive amongst the tested catalysts for hydrogen release 3 from perhydrogenated dibenzyl toluenes (H18-DBT). = 35 From CN 107185525, KR 20130082272, KR N 20160014180, CN 108114717, CN 108435203 and KR
20180081659 are known different catalysts comprising Pt.
OBJECTIVE The objective is to disclose a new type cata- lyst for dehydrogenation. Further, the objective is to disclose a new type method for preparing the catalyst. Further, the objective is to improve a dehydrogenation process. Further, the objective is to provide effi- cient process and catalyst for releasing hydrogen in the dehydrogenation.
SUMMARY The catalyst and method and use are charac- terized by what are presented in the claims.
A catalyst for dehydrogenation is a Pt cata- lyst. The catalyst is prepared from a support and a Pt catalyst agent which arranged onto the support.
BRIEF DESCRIPTION OF THE DRAWINGS The accompanying drawings, which are included to provide a further understanding of the invention and constitutes a part of this specification, illus- trate some embodiments of the invention and together with the description help to explain the principles of the invention. In the drawings: — Fig. 1 shows results from the tests according O to three embodiments at Pt contents of 1 — 1.5 wt%. 5 LO 30 DETAILED DESCRIPTION - A catalyst for dehydrogenation is a Pt cata- E lyst, in which Pt catalyst agent is formed by using a 3 Pt-precursor and is arranged on a support, and the 3 support is selected from TiO, or y-Al,0s. > 35 In a method for preparing a catalyst for de- hydrogenation, Pt catalyst agent is formed from a Pt-
precursor, the catalyst agent is arranged onto a sup- port which is selected from TiO; or vyv-Al,0s3 in order to form the catalyst, and the catalyst is calcinated. In this context, the support means any sup- port or carrier material, onto which any Pt catalyst agent is arranged. In an embodiment, the support is in the form of powder. In an embodiment, the support is selected from TiO,. In an embodiment, the TiO, support consists of anatase-rutile system. In a further embodiment, the TiO, support is formed from a mixture of anatase and rutile forms. In an embodiment, the TiO, support consists of powder. In an embodiment, particles of the powder have particle size which may vary and which may be in large size range. In an embodiment, particles of the powder are nanoparticles, microparticles and/or other particles. In an embodiment, particles of the powder are nanoparticles and/or microparticles. In an embodi- ment, the TiO, support consists of the powder with particles which have particle size over 0.015 um, over
0.035 um or larger. In an embodiment, the TiO; support consists of the powder with nanoparticles. In an em- bodiment, the TiO, support consists of the powder with nanoparticles which have particle size 0.015 - 0.100 um, or in an embodiment the powder with larger parti- — cle sizes. In a further embodiment, the TiO, support O consists of the powder with nanoparticles which have — particle size 0.015 — 0.035 pm. In a further embodi- 7 30 ment, the TiO, support consists of the powder with na- = noparticles which have particle size selected from E: 0.015 — 0.035 pm or over 0.035 um. In a further embod- 2 iment, the TiO, support consists of the nanopowder. 3 In an embodiment, the support is selected > 35 from vV-Al03. In an embodiment, the v-Al,03 support consists of the powder.
In an embodiment, the vy-A1,203 support has particle size of 0.02 - 32000 um.
In an embodiment, Pt-content is below 2 % by weight in the catalyst.
In an embodiment, the Pt-precursor is select- ed from %H,PtClgc (chloroplatinic acid) or Pt(NO3), (platinium nitrate). In an embodiment, the Pt- precursor is HPtCle.
In an embodiment, the Pt- precursor is Pt(N03),. When HPtCle or PL (NOs), is used as the precursor, an efficient catalyst can be formed for the dehydrogenation, especially for the dehydro- genation of H18-DRBT.
In an embodiment, the catalyst agent is ar- ranged by an impregnation onto the support.
In a fur- ther embodiment, the catalyst agent, preferably in the form of powder or alternatively in the form which is manufactured from the powder, is arranged by an im- pregnation onto the support.
In an embodiment, the catalyst is prepared by an incipient wetness impregna- tion.
In an embodiment, the catalyst is prepared by an AID-coating (atomic layer deposition coating). In a further embodiment, the catalyst agent is arranged by the ALD-coating method onto the support, e.g. onto the support powder.
In a further embodiment, the AID- coating is carried out so that at least the support is — in the powder form.
In a further embodiment, the O formed catalyst, preferably in the form of powder, is — arranged by means of the ALD-coating method on the 7 30 substrate in order to form a catalyst system.
In this = application, any suitable ALD-coating method can be = used, which is preferably suitable for the ALD-coating S of the powder material.
By means of the ALD-coating D method an amount of noble metal needed can be reduced > 35 in the catalyst.
In an embodiment, the catalyst is calcinated at 450 — 540 °C. In a further embodiment, the catalyst is calcinated at 480 — 520 °C.
An Important property of the dehydrogenation 5 catalyst is its capability to desorb hydrogen to avoid reverse reaction. In an embodiment, the dehydrogena- tion is a dehydrogenation of Hl18-DBT (perhydrogenated dibenzyl toluenes). Alternatively, the dehydrogenation is another dehydrogenation in which hydrogen is re- leased from other compounds, which are, for example, monocyclic or polycyclic alkanes.
In the dehydrogenation, a product composition is produced. The product composition means any product from the dehydrogenation. The product composition can comprise one or more product components, e.g. hydro- gen, hydrocarbons, organic liguids and/or other organ- ic compounds. The product composition may contain also other components. In an embodiment, the product compo- sition mainly consists of hydrocarbons and hydrogen.
Preferably, the hydrogen can be released from the product composition. In one embodiment, the product composition can be post-treated after the dehydrogena- tion, e.g. after releasing hydrogen. In one embodi- ment, the product composition can be supplied to a de- sired treatment process, e.g. for energy or for refin- ing the hydrocarbons or other compounds.
— In an embodiment, the catalyst is used or uti- O lized in a dehydrogenation in which hydrogen is re- — leased, in a dehydrogenation of H18-DBT, in a dehydro- 7 30 genation of the compounds which are monocyclic or pol- = ycyclic alkanes, in use of hydrogen for different pur- = poses, such as for energy or for manufacturing organic 2 gas or liquid, in a production of hydrocarbons or 3 fuel, or in their combinations.
O 35 Thanks to the invention, very efficient cata- N lysts can be produced for dehydrogenation of H18-DBT.
Further, the present catalysts are effective also for dehydrogenation of other substrates. The present cata- lysts are capable to fast release of hydrogen. Thus, the present catalysts improve efficiency of the LOHC hydrogen release system.
The present catalyst offers a possibility to release hydrogen easily and effectively. The present invention provides an industrially applicable, simple and affordable way to release hydrogen in the dehydro- genation.
EXAMPLES Example 1 This example presents a Pt catalyst with a TiO, support for dehydrogenation. Further, in this ex- ample, the catalyst for the dehydrogenation was pro- duced from the TiO; support and a Pt catalyst agent.
The Pt catalyst agent is formed from a Pt- precursor which is HPtCl6, or alternatively Pt(N03),. The Pt-precursor is arranged onto the support which is TiO,. The TiO, support consists of anatase-rutile sys- tem which comprises a mixture of anatase and rutile forms. The TiO, support is nanopowder which has parti- cle size about 0.020 — 0.030 jm. The catalyst agent is arranged by an incipient wetness impregnation onto the — support. In addition to the impregnated catalyst, ALD O technology can be used for forming platinum layer on — the titania support powder. 7 30 The Pt catalyst is calcinated at about 500 = °C, preferably for about two hours. i S Example 2 D This example presents a Pt catalyst with a y- > 35 Alo03 support for dehydrogenation. Further, in this ex-
ample, the catalyst for the dehydrogenation was pro- duced from the y-A1,03 support and a Pt catalyst agent.
The Pt catalyst agent is formed from a Pt- precursor which is HoPtCl6, or alternatively Pt(NO3)>,.
The Pt-precursor is arranged onto the support which is V-Al203. The vy-A1,03 support has particle size of 25 - 40 um. The catalyst agent is arranged by an incipient wetness impregnation onto the support. In addition to the impregnated catalyst, AID technology can be used for forming platinum layer on the alumina support pow- der.
The Pt catalyst is calcinated at about 500 *C, preferably for about two hours.
Example 3 In this example different catalysts were studied. Further, the effect of different Pt precur- sors in combination with alumina and titania supports on activity of the prepared catalysts for hydrogen re- lease from H18-DBT in comparison with commercial Pt on carbon catalyst.
Carbon supported Pt catalyst showed the high- est efficiency for the dehydrogenation of H18-DBT amongst the catalysts studied. It is known that carbon has a high surface area (200-300 m?/g) and typically dispersion of Pt on carbon is good, which are favora- — ble features for the dehydrogenation catalysts. Carbon O support is also low cost and abundant, but its dura- — bility is weak at high temperatures in the presence of 7 30 oxygen. Different hydrogen release rates were observed > between two different H18-DBT batches, one at 100% and = the other at 95% hydrogenation degree. For 100% hydro- S genated H18-DBT batch, Pt/C 1 wt% catalyst released 91 D % of the theoretical maximum of hydrogen in 45 o 35 minutes. When using the batch of H18-DBT having 95% N hydrogenation degree, commercial Pt/C (lwt%) catalyst was capable to release only 74% of hydrogen stored in substrate at 290 °C in 45 minutes.
Activity of the in- house catalysts prepared were compared to the activity of commercial Pt/C l1wt% for hydrogen release from H18- DBT (95%), thus the reference dehydrogenation degree in our study is 74% at 290 °C in 45 minutes (share of hydrogen released from the theoretical maximum). How- ever, we note that complete hydrogenation release was possible in reasonable time from fully hydrogenated H18-DBT (100%), whereas this level of dehydrogenation was not achieved with H18-DBT (95%). Using fully hy- drogenated substrate could increase efficiency of to-
tal process in practical applications.
Metal oxides are more durable supports than carbon, and thus interesting for the dehydrogenation of H18-DBT.
Alumina support is used in the commercial LOHC solution.
First, it is noted that the commercial Pt on alumina (5wt%) catalyst was not active for dehy- drogenation of H18-DBT showing only 9% hydrogen re- lease degree at 290 °C in 45 minutes.
Instead, many in-house Pt on alumina catalysts were active towards hydrogen release from H18-DBT.
However, only catalysts prepared on vy-Al,03 supports were active, while that prepared on o,y-Al,03 support was not particularly ac- tive.
In the tests, for different y-Al»03 supports, no consistent dependences between catalyst activity and — different particle sizes or surface areas of alumina O were found.
In the tests, the most active catalysts — were those prepared on vy-A1,03 having 40 jm particle 7 30 size and surface area of 100 m?/g, or 25 um particle = size and surface area of 200 m?/g.
Also other Pt/y- E Al,03; catalysts were active regardless of large varia- 2 tion of their particle sizes (from 0.02 to 32000 um) 3 and surface areas (from 100 and 200 m?/g). Particle > 35 sizes and surface areas indicated here are for the fresh supports. Surface area of alumina may decrease in calcination.
The best activity amongst the metal supported Pt catalyst was found for that prepared on titania na- nopowder support having rutile and anatase forms. This catalyst was active regardless of the Pt precursor used, although particularly high activity was observed when using H,PtClc precursor of Pt.
Using HPtCl; as a precursor led to higher ac- tivity of the dehydrogenation catalyst than using Pt (NOs) >. However, in the best case the nitrate precur- sor led to almost as high activity of catalyst as when using the acid precursor.
The titania nanopowder support is a mixture of anatase and rutile forms. Thus, we studied also ac- tivity of Pt catalyst prepared on titania nanopowder having anatase only form. However, activity of Pt on anatase titania was modest. TiO, is characterised by strong metal support interaction, chemical stability, and acid-base property. However, surface area of titania is relatively low, only up to about 80 m?/g.
In the tests, activity of catalyst was good only for TiO, containing both anatase and rutile forms, while anatase only was not active.
Example 4 — In this example, catalysts were prepared us- O ing incipient wetness impregnation method.
— Catalysts were calcinated at 500 °C tempera- 7 30 ture. For v-Al03, higher calcination temperatures = starting from 600 °C would lead to phase transition to = low-surface area 0«-Al,»03 (completed at 1200 °C). For 2 titania, phase transition from anatase to low-surface 3 area rutile starts already at about 550 °C. The calci- o 35 nation temperature of 500 °C is optimum for TiO, na- N nopowder used to increase its photocatalytic activity.
Simultaneously, a small part of anatase transformed to rutile, and surface area of TiO, decreased. Two Pt precursors used for the catalysts were choroplatinic acid (H2PtCl6, 38% (m/m) Pt content) and platinum nitrate (Pt(N0O3),). Pt on y-A1,03 and TiO, supports were studied in comparison with commercial Pt on carbon catalyst. Besides these catalysts, also commercial Pt/C and Pt/Al03 were tested.
Example 5 In this example, activities of catalysts, prepared according to example 3, were tested by heat- ing a mixture of H18-DBT and selected catalyst in a molar ratio of 400:1 in a round bottom flask while stirring with a magnetic stirrer at 500 mint. For some nanocatalysts stirring was reduced due to inertia caused by catalyst sludge. Limited tests indicated that stirring rate did not affect the results on cata- lyst activity. Two different H18-DBT substrates were used. In the first phase, Marlotherm SH, Sasol was hydrogen- ated in laboratory to 100% H18-DBT (hydrogenation pro- cedure, SI). Later on, HI8-DBT with a hydrogenation degree of 95% was purchased from Hydrogenious GmbH. All the results were obtained with the latter sub- — strate, H18-DBT 95%. O Formed hydrogen was collected in the measur- — ing glass and readings were recorded periodically. 7 30 Volumetric measurement of hydrogen release rate is = semi-quantitative due to the substantial effect of = temperature on hydrogen density, and consequently, to 2 hydrogen volume. Quantitative dehydrogenation degree 3 was analysed using NMR (Varian 300 Hz, dichloro- > 35 methane-d2 solvent, filtered samples). All hydrogen release rates were interpolated to 45 minutes for equal comparison of different catalysts. Fig. 1 shows some hydrogen release results from some tests with three catalysts in which Pt contents were 1 - 1.5 wt-%. The Pt/TiO, and Pt/Al,0; according to the invention and commercial Pt/C were tested. It was observed from the tests that the effi- cient catalysts can be produced for dehydrogenation of H18-DBT, and also for dehydrogenation of other sub- strates. Further, it was observed that the formed Pt/Ti0, catalyst is capable to faster release of hy- drogen than the previously known alumina catalysts. Further, from Fig. 1 can be observed that the Pt- catalyst with TiO;-support, which contains anatase- rutile system, has very high efficiency. Pt/Alo03 - catalyst has also high efficiency, but clearly lower efficiency than the Pt-catalyst with Ti0,-support.
The catalyst is suitable in different embodi- ments for different kinds of dehydrogenations. The method for producing a catalyst for dehydrogenation is suitable in different embodiments for forming differ- ent kinds of catalysts.
The invention is not limited merely to the examples referred to above; instead many variations — are possible within the scope of the inventive idea O defined by the claims.
5
O = a = co
N

Claims (13)

1. A catalyst for dehydrogenation, char - acterized in that - the catalyst is a Pt catalyst, in which Pt cata- lyst agent is formed by using a Pt-precursor and is arranged on a support, and - the support is selected from TiO; or vy-Al,03, in which the Ti0, support consists of anatase-rutile system and the v-A1,03 support has particle size of 0.02 — 32000 um.
2. The catalyst according to claim 1, characterized in that the TiO, support con- sists of a powder with nanoparticles which have parti- cle size 0.015 - 0.100 um.
3. The catalyst according to claim 1 or 2, characterized in that the Pt-precursor is se- lected from HPtClc or Pt(N03),.
4. The catalyst according to any one of claims 1 to 3, characterized in that the cat- alyst agent is arranged by an impregnation onto the support.
5. The catalyst according to any one of claims 1 to 4, characterized in that the cat- alyst is prepared by an ALD-coating.
6. The catalyst according to any one of claims 1 to 5, characterized in that the de- o hydrogenation is a dehydrogenation of H18-DBT or of > other compounds which are monocyclic or polycyclic al- AN kanes.
A 30
7. A method for preparing a catalyst for de- N hydrogenation, characterized in that the E method comprises steps S - forming Pt catalyst agent from a Pt-precursor, D - arranging the catalyst agent onto a support which o 35 is selected from TiO, or y-A1,203, in which the TiO; N support consists of anatase-rutile system and the
V-Al203 support has particle size of 0.02 —- 32000 pm, in order to form the catalyst, and - calcinating the catalyst.
8. The method according to claim 7, char - acterized in that the Pt-precursor is selected from H,PtClg or Pt (NOs).
9. The method according to claim 7 or 8, characterized in that the catalyst is calci- nated at 450 — 540 °C.
10. The method according to any one of claims 7 to 9, characterized in that the catalyst agent is arranged by an impregnation onto the support.
11. The method according to any one of claims 7 to 10, characterized in that the catalyst is prepared by an incipient wetness impregnation.
12. The method according to any one of claims 7 to 11, characterized in that the catalyst is prepared by an ALD-coating.
13. A use of the catalyst according to any one of claims 1 to 6, characterized in that the catalyst is used in a dehydrogenation in which hy- drogen is released, in a dehydrogenation of H18-DBT, in a dehydrogenation of the compounds which are mono- cyclic or polycyclic alkanes, in use of hydrogen for different purposes, for energy or for manufacturing organic gas or liquid, in a production of hydrocarbons o or fuel, or in their combinations.
O
N
N 0)
N
I jami a oO +
O
LO 00
O
N
FI20185940A 2018-11-06 2018-11-06 Catalyst for dehydrogenation, method for preparing the catalyst and use FI128885B (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
FI20185940A FI128885B (en) 2018-11-06 2018-11-06 Catalyst for dehydrogenation, method for preparing the catalyst and use
PCT/FI2019/050784 WO2020094921A1 (en) 2018-11-06 2019-11-05 Catalyst for dehydrogenation, method for preparing the catalyst and use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FI20185940A FI128885B (en) 2018-11-06 2018-11-06 Catalyst for dehydrogenation, method for preparing the catalyst and use

Publications (3)

Publication Number Publication Date
FI20185940A1 FI20185940A1 (en) 2020-05-07
FI20185940A FI20185940A (en) 2020-05-07
FI128885B true FI128885B (en) 2021-02-15

Family

ID=68621328

Family Applications (1)

Application Number Title Priority Date Filing Date
FI20185940A FI128885B (en) 2018-11-06 2018-11-06 Catalyst for dehydrogenation, method for preparing the catalyst and use

Country Status (2)

Country Link
FI (1) FI128885B (en)
WO (1) WO2020094921A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3192137A1 (en) * 2020-09-11 2022-03-17 Georgievich Dmitri BESSARABOV Dehydrogenation catalyst
CN113941328B (en) * 2021-11-11 2022-12-09 苏州金宏气体股份有限公司 Platinum/molybdenum dehydrogenation catalytic material, preparation method and application thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4219447A (en) * 1978-12-19 1980-08-26 Exxon Research & Engineering Co. Catalyst and a process for its preparation
DE4300297C2 (en) * 1993-01-08 1998-01-29 Degussa Process for the selective catalytic hydrogenation of the carbonyl group of 4-carboxylbenzaldehyde
US8366907B2 (en) * 2010-08-02 2013-02-05 Battelle Memorial Institute Deoxygenation of fatty acids for preparation of hydrocarbons
JP6583735B2 (en) * 2014-09-09 2019-10-02 国立大学法人静岡大学 Dehydrogenation catalyst for organic hydride and method for producing the same

Also Published As

Publication number Publication date
FI20185940A1 (en) 2020-05-07
WO2020094921A1 (en) 2020-05-14
FI20185940A (en) 2020-05-07

Similar Documents

Publication Publication Date Title
Sápi et al. In situ DRIFTS and NAP-XPS exploration of the complexity of CO2 hydrogenation over size-controlled Pt nanoparticles supported on mesoporous NiO
RU2292238C2 (en) Fischer-tropsch process catalyst (variations) and a method for preparation thereof
Tan et al. Support morphology-dependent catalytic activity of Pd/CeO2 for formaldehyde oxidation
Cauqui et al. Application of the sol-gel methods to catalyst preparation
CN101180124B (en) Catalyst manufacture
Xie et al. Efficient removal of methane over cobalt-monoxide-doped AuPd nanocatalysts
JP4906261B2 (en) Method for producing cobalt catalyst supported on titania support
CN101616733B (en) Catalysts based on sintered metal fibers coated by zinc oxide layer impregnated with palladium nanoparticles for the hydrogenation of alkynols
ZA200503464B (en) Improved supports for high surface area catalysts
CA2483942A1 (en) Catalyst for partial oxidation of hydrocarbon, process for producing the catalyst, process for producing hydrogen-containing gas with a use of the catalyst, and method of using hydrogen-containing gas produced with the use of the catalyst
Cui et al. High reactivity and sintering resistance of CH4 oxidation over modified Pd/Al2O3
Ismagilov et al. Synthesis and characterization of uranium-containing catalysts
FI128885B (en) Catalyst for dehydrogenation, method for preparing the catalyst and use
Wang et al. Ruthenium/cobalt binary oxides supported on hollow alumina microspheres as highly efficient catalyst for vinyl chloride oxidation
Zhang et al. Spherical Ni nanoparticles supported by nanosheet-assembled Al2O3 for dry reforming of CH4: elucidating the induction period and its excellent resistance to coking
US3668148A (en) Catalyst prepared by homogeneous precipitation under high temperature and pressure
CN107262112A (en) New structural catalyst
Hao et al. Hierarchically porous silica supported ceria and platinum nanoparticles for catalytic combustion of toluene
KR20130013568A (en) Manufacturing method for metal or metal oxide supported catalyst using melt-infiltration process of metal hydrate salt and metal or metal oxide supported catalyst thereof
Liang et al. A superior strategy for CO2 methanation under atmospheric pressure: Organic acid-assisted Co nanoparticles assembly on diatomite
EP3496850B1 (en) Catalytically active compositions of matter
Wang et al. Syngas production via CO2 reforming of methane over aluminum-promoted NiO–10Al2O3–ZrO2 catalyst
KR20140028400A (en) The modified catalyst for co2 conversion
Heupel et al. Sol-gel synthesis and application of NiO, NiTiO3 and Ni5TiO4 (BO3) 2 on open-cell TiO2 foams for CO2 methanation
CN116075363A (en) Modified catalyst support and catalyst supported thereon

Legal Events

Date Code Title Description
FG Patent granted

Ref document number: 128885

Country of ref document: FI

Kind code of ref document: B

MM Patent lapsed