EP1060123A1 - Hydrogen production via the direct cracking of hydrocarbons - Google Patents
Hydrogen production via the direct cracking of hydrocarbonsInfo
- Publication number
- EP1060123A1 EP1060123A1 EP99907144A EP99907144A EP1060123A1 EP 1060123 A1 EP1060123 A1 EP 1060123A1 EP 99907144 A EP99907144 A EP 99907144A EP 99907144 A EP99907144 A EP 99907144A EP 1060123 A1 EP1060123 A1 EP 1060123A1
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- EP
- European Patent Office
- Prior art keywords
- catalyst
- nickel
- hydrogen
- carbon
- methane
- Prior art date
- Legal status (The legal status 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 status listed.)
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Classifications
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- 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
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- 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
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
- D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
- D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
- D01F9/127—Carbon filaments; Apparatus specially adapted for the manufacture thereof by thermal decomposition of hydrocarbon gases or vapours or other carbon-containing compounds in the form of gas or vapour, e.g. carbon monoxide, alcohols
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- 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
- C01B2203/02—Processes for making hydrogen or synthesis gas
- C01B2203/0266—Processes for making hydrogen or synthesis gas containing a decomposition step
- C01B2203/0277—Processes for making hydrogen or synthesis gas containing a decomposition step containing a catalytic decomposition step
-
- 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
- C01B2203/1052—Nickel or cobalt catalysts
-
- 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
- C01B2203/1076—Copper or zinc-based catalysts
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- 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
- C01B2203/1082—Composition of support materials
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- 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
- C01B2203/12—Feeding the process for making hydrogen or synthesis gas
- C01B2203/1205—Composition of the feed
- C01B2203/1211—Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
- C01B2203/1235—Hydrocarbons
- C01B2203/1241—Natural gas or methane
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- 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
- C01B2203/80—Aspect of integrated processes for the production of hydrogen or synthesis gas not covered by groups C01B2203/02 - C01B2203/1695
- C01B2203/84—Energy production
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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Definitions
- This invention relates generally to the production of hydrogen, and more specifically to hydrogen production by the direct cracking of hydrocarbons such as methane and natural gas.
- the current proton-exchange membrane (PEM) fuel cells utilize hydrogen as the energy source and require essential elimination (ideally below 20 ppmv) of carbon monoxide from the hydrogen stream to prevent poisoning of the electrocatalyst.
- Hydrogen is typically produced through steam reforming, partial oxidation or autothermal reforming of natural gas. In all these cases, however, carbon monoxide is a co-product, which has to be converted into carbon dioxide in subsequent steps which adds to the cost of the produced hydrogen.
- An alternative route is to directly crack the hydrocarbon fuel into hydrogen and carbon.
- the formation of carbon oxides is avoided and the need for downstream reactions such as water-gas shift and selective oxidation for the conversion of carbon monoxide to carbon dioxide is eliminated.
- this approach has not been extensively studied. While commercial processes exist that utilize thermal cracking of methane at extremely high temperatures for the -2- production of acetylene and carbon black, hydrogen production via the catalytic cracking of methane has been only briefly considered in the past.
- the rates of methane conversion and hydrogen formation were found to be in ratio of 1:2, thus, verifying the reaction stoichiometry for methane cracking.
- the amounts of carbon deposited on the spent catalyst and methane reacted indicated a good closure of the carbon balance (100 ⁇ 5%).
- catalyst activity may be fully restored by regenerating the catalyst through oxidation in air or steam gasification.
- the process of the invention may be applicable to any other suitable hydrocarbon such as ethane, ethylene, propane, propylene, butane, pentane, hexane and mixtures thereof, and hydrocarbons with molecular weights in the gasoline and diesel range. Nevertheless, it is anticipated that the preferred -4- hydrocarbons will be methane and natural gas. During the catalytic cracking of higher molecular weight hydrocarbons, it is expected that several other undesirable products will be formed in addition to the hydrogen.
- activity measurements for the methane cracking reaction were conducted over a set of 9 Ni-Cu/SIO 2 catalysts in which the total metal amount (on a molar basis) was maintained constant at 2.6 mmole of metal/g of support while the ratio of Ni:Cu was varied from approximately 8:1 to approximately 1 :8.
- the reaction was carried out in a pure methane stream, at 650 and 800 °C and at a gas hourly space velocity of 6000 hr 1. The results indicate that the presence of small amounts of Cu enhanced significantly the Ni activity at 800 °C.
- the promoting effect is also more pronounced when small amounts of Cu are added (i.e., Ni:Cu ratios greater than 1).
- the highest initial methane conversion observed with these set of catalysts is at the 8:1 Ni:Cu ratio. Even higher initial methane conversions are expected with higher Ni:Cu ratios up to about 20:1.
- FIG. 1 represents a plot of the deactivation of a Ni/SiO 2 catalyst at 550°C
- GHSN 30,000 h "1 in a stream containing 20% CH 4 , in He;
- FIG. 2 represents a plot of methane conversions obtained over fresh (•, ⁇ ) and regenerated (O in air, ⁇ in steam) ⁇ i/SiO 2 catalyst at 550°C at two different space velocities; -5-
- Fig. 4 represents a plot of initial methane conversion as a function of catalyst composition at two different temperatures over a series of Ni-Cu/SiO 2 catalysts (O at 650 °C and D at 800°C).
- the catalyst used in the first embodiment of this invention was prepared by incipient wetness impregnation of an aqueous solution of nickel nitrate onto the silica support, followed by calcination in air and in-situ reduction in flowing hydrogen.
- This is a standard method of preparation of supported metal catalysts and several different nickel salts can be used instead of nickel nitrate as the nickel precursor.
- other standard methods for the preparation of supported metal catalysts could be used without having a detrimental effect on the properties of the catalyst.
- silica we investigated other inorganic supports such as alumina and titania.
- the catalyst used in the present invention will eventually deactivate as a result of carbon deposition.
- Carbon may deposit on the surface to cover the active sites (site-blocking) or accumulate at the entrance of the pores to block further access of the reactants to the interior (pore-mouth plugging). It has been estimated that in both cases catalyst deactivation would occur within a short period of time. Even if 10 carbon atoms are needed to block each surface ⁇ i atom, for example, 11 mg of carbon deposition would be enough to completely deactivate one gram of the 16.4% ⁇ i/SiO 2 catalyst. Furthermore, if pore-mouth plugging was the main deactivation mechanism, approximately 250 mg of carbon would be sufficient to clog the external 10% of the pores, in one gram of the Ni/SiO 2 catalyst sample.
- SEM SEM and Transmission Electron Microscopy (TEM) analyses of the spent catalysts were utilized to further understand the deactivation mechanism.
- SEM micrographs indicate the formation of filamentous carbon on the catalyst surface. These filaments appear to grow out of the silica support surface, with their length increasing with time-on-stream. Each filament has a bright tip, identified by the use of SEM/EDS (Energy Dispersive X-Ray Spectroscopy) to be a nickel particle.
- SEM/EDS Energy Dispersive X-Ray Spectroscopy
- Spent catalyst samples were further studied by the use of X-Ray Diffraction (XRD). The XRD patterns, suggest that graphitic carbon constituents with different degrees of defect or distortion are present in the deactivated samples.
- TEM micrographs of the fully deactivated sample show that the growth of the carbon is terminated as a result of spatial limitations.
- the modes of filament termination include the nickel particle's restriction by the silica surface, the arm and the tip of another carbon filament. Formation of carbon filaments as a result of hydrocarbon cracking has been extensively reported in the literature with higher molecular weight hydrocarbons over supported nickel, iron, cobalt and several alloy catalysts.
- the carbon deposited on the catalyst in carrying out the present invention may be used in electrochemical applications such as superconductors, electrodes and fuel cells.
- the oxidation process was faster than the steam gasification, but caused a high temperature front. This front gradually moved through the catalyst bed, causing the collapse of the sample to a fine powder.
- XRD analysis suggests that the oxidation process completely removed -8- the deposited carbon and converted the metallic nickel into nickel oxide which had to be reduced in flowing hydrogen before the next reaction cycle shown in Figure 2.
- the catalyst bed maintained a uniform temperature profile during the steam regeneration process and the catalyst preserved its metallic nickel form at the end of the process.
- the set of Ni-Cu/SiO 2 catalysts used in the second embodiment of this invention had the total metal amount (on a molar basis) maintained constant at 2.6 mmole of metal/g of support while the ratio of Ni:Cu was varied from approximately 8:1 to approximately 1 :8.
- the catalysts were prepared by incipient wetness impregnation of nickel and copper nitrates (Ni(NO 3 ) 2 x6H 2 O and Cu(NO 3 ) 2 x2.5H 2 O) obtained from Aldrich (with a purity of 99.999%) onto commercially available SiO 2 (Davison Syloid 74).
- the silica support Prior to impregnation the silica support was dried, pressed into pellets under a pressure of 15,000 psig, crushed and sieved to obtain a granulometric fraction in the 20-35 mesh size.
- the impregnated samples were dried in a vacuum oven at 120 °C overnight and subsequently calcined in a muffler furnace at 700 °C for 6 hours.
- the Ni and Cu loadings were estimated by the weight difference between the blank support and the catalyst reduced overnight in a 1 :2 H 2 /N 2 mixture (total flow rate of 120 ml/min) at 650 °C .
Abstract
A process for producing substantially pure hydrogen by contacting a stream of a hydrocarbon gas with a nickel or nickel-copper containing catalyst at a temperature in the range of about 400 to 900 °C. This results in the conversion of the hydrocarbon gas to substantially pure hydrogen, with said process being carried out until the catalyst is deactivated due to the deposition of carbon on the catalyst. The deactivated catalyst may be regenerated by oxidation in air or by steam gasification of the deposited carbon. The carbon deposited on the catalyst also has separate utility for electrochemical and fuel storage applications and may be recovered for further use.
Description
Hydrogen Production via the Direct Cracking of Hydrocarbons
Field of the Invention
This invention relates generally to the production of hydrogen, and more specifically to hydrogen production by the direct cracking of hydrocarbons such as methane and natural gas.
Background of the Invention
Significant progress made in fuel cell technologies during the past decade has prompted exploration of replacing traditional central large power plants with so- called distributed power generators, consisting of a hydrogen generator and a membrane fuel cell power plant. This latter technology generates electricity at locations where it is aimed to be used, and therefore, eliminates the loss of electricity during its transmission. In addition, a fuel cell process does not emit any environmental pollutants such as NOx and SOx which are combustion by-products. Such a process becomes attractive for the automobile industry as well, since vehicles can be propelled by electricity produced from an on-board fuel cell power plant rather than by an internal combustion engine.
The current proton-exchange membrane (PEM) fuel cells utilize hydrogen as the energy source and require essential elimination (ideally below 20 ppmv) of carbon monoxide from the hydrogen stream to prevent poisoning of the electrocatalyst. Hydrogen is typically produced through steam reforming, partial oxidation or autothermal reforming of natural gas. In all these cases, however, carbon monoxide is a co-product, which has to be converted into carbon dioxide in subsequent steps which adds to the cost of the produced hydrogen.
An alternative route is to directly crack the hydrocarbon fuel into hydrogen and carbon. In this case, the formation of carbon oxides is avoided and the need for downstream reactions such as water-gas shift and selective oxidation for the conversion of carbon monoxide to carbon dioxide is eliminated. Surprisingly, this approach has not been extensively studied. While commercial processes exist that utilize thermal cracking of methane at extremely high temperatures for the
-2- production of acetylene and carbon black, hydrogen production via the catalytic cracking of methane has been only briefly considered in the past.
In U.S. Patent 3,361,535 high temperature catalytic cracking of methane is taught. The process taught by the 3,361,535 patent, however, results in the production of undesirable carbon monoxide co-product which requires elaborate additional processing for its conversion to carbon dioxide and results in additional cost.
Recently, Muradov Int. J. Hydrogen Energy 18,211(1993), studied the use of iron and nickel oxides supported on alumina as catalysts for the cracking of methane and reported that equilibrium conversions were achieved at temperatures above 800°C. The iron oxide, also appeared to maintain some part of its activity for several hours, in contrast to a Pt/Al2O3 catalyst which deactivated within minutes under similar conditions. Muradov Energy & Fuels 12,41(1998) has also reported the use of carbon-based catalysts for the same reaction. Although more stable, these catalysts exhibit a lower activity. Furthermore, Ishihara et al. Shokubai
35,324(1993); and Chem. Lett., 93(1995); reported that methane cracking takes place at low temperatures over a 10% Ni/SiO2 catalyst, which does not deactivate even after approximately 200 carbon per nickel atoms have been deposited on it. The results reported by Ishihara, et al., however, did not demonstrate a level of efficiency of hydrogen production which would result in potential commercial use.
Summary of the Invention
It can therefore be seen from the above review of the prior art that an efficient method of directly cracking hydrocarbons to produce hydrogen without the presence of undesirable co-products, such as carbon monoxide, has been an objective in the art.
It is therefore an object of the present invention to provide a method of producing hydrogen by the direct cracking of hydrocarbons.
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It is another object of the present invention to provide a method of producing pure hydrogen without carbon monoxide contamination by the direct cracking of hydrocarbons.
It is yet another object of the present invention to produce high purity hydrogen and carbon by the catalytic cracking of hydrocarbons. It is yet a further object of the present invention to provide a method of producing hydrogen by direct cracking of methane through the use of a highly efficient catalyst.
It is another object of the present invention to provide a method of producing hydrogen by direct cracking of methane or natural gas at low temperature using a nickel containing catalyst.
It is yet a further object of the present invention to provide a method of producing high purity hydrogen by direct cracking of methane at low temperature using a silica supported nickel-copper catalyst.
It has been discovered that the catalytic cracking of methane or natural gas as a potential route for efficient hydrogen production can be accomplished over silica- supported nickel containing catalysts. In one embodiment, activity measurements for the methane cracking reaction were conducted with a 16.4 wt.% Ni/SiO2 catalyst in a 20% CH4 in He stream at 550°C and a gas hourly space velocity (GHSN) of 30000 h"1. Under these conditions the catalyst exhibited a high initial activity for the cracking of methane (approximately 35% CH4 conversion). Hydrogen was the only gaseous product detected. In addition, the rates of methane conversion and hydrogen formation were found to be in ratio of 1:2, thus, verifying the reaction stoichiometry for methane cracking. The amounts of carbon deposited on the spent catalyst and methane reacted indicated a good closure of the carbon balance (100±5%). Upon deactivation of the catalyst due to carbon deposition; catalyst activity may be fully restored by regenerating the catalyst through oxidation in air or steam gasification. The process of the invention may be applicable to any other suitable hydrocarbon such as ethane, ethylene, propane, propylene, butane, pentane, hexane and mixtures thereof, and hydrocarbons with molecular weights in the gasoline and diesel range. Nevertheless, it is anticipated that the preferred
-4- hydrocarbons will be methane and natural gas. During the catalytic cracking of higher molecular weight hydrocarbons, it is expected that several other undesirable products will be formed in addition to the hydrogen.
In a second embodiment, activity measurements for the methane cracking reaction were conducted over a set of 9 Ni-Cu/SIO2 catalysts in which the total metal amount (on a molar basis) was maintained constant at 2.6 mmole of metal/g of support while the ratio of Ni:Cu was varied from approximately 8:1 to approximately 1 :8. The reaction was carried out in a pure methane stream, at 650 and 800 °C and at a gas hourly space velocity of 6000 hr1. The results indicate that the presence of small amounts of Cu enhanced significantly the Ni activity at 800 °C. The initial conversion over the 2.3 mmole Ni/0.3 mmole Cu/SiO2 composition for example, was measured at 63%, as compared to 14.4% for the 2.3 mmole Ni/SiO2 composition. This is a surprising result given that Cu alone is not active for the cracking of methane under these conditions (0.3% initial methane conversion for the 0.3 mmole Cu/SiO2 composition). The promoting effect is also more pronounced when small amounts of Cu are added (i.e., Ni:Cu ratios greater than 1). The highest initial methane conversion observed with these set of catalysts is at the 8:1 Ni:Cu ratio. Even higher initial methane conversions are expected with higher Ni:Cu ratios up to about 20:1. Brief Description of the Drawings
For a fuller understanding of the nature and objects of the invention, reference should be made to the following detailed description of a preferred mode of practicing the invention, read in connection with the accompanying drawings, in which: FIG. 1 represents a plot of the deactivation of a Ni/SiO2 catalyst at 550°C and
GHSN = 30,000 h"1 in a stream containing 20% CH4, in He;
FIG. 2 represents a plot of methane conversions obtained over fresh (•,♦) and regenerated (O in air, □ in steam) Νi/SiO2 catalyst at 550°C at two different space velocities;
-5-
FIG. 3 represents a plot of selectivities of hydrogen (• at GHSN = 15000 h"1, ♦ at GHSN =37500 h'1) and carbon dioxide (O at GHSN = 15000 h"1, Q at GHSN = 37500 h"1) during steam regeneration of the deactivated Νi/SiO2 catalyst at 550°C; and Fig. 4 represents a plot of initial methane conversion as a function of catalyst composition at two different temperatures over a series of Ni-Cu/SiO2 catalysts (O at 650 °C and D at 800°C).
Detailed Description of the Invention The catalyst used in the first embodiment of this invention was prepared by incipient wetness impregnation of an aqueous solution of nickel nitrate onto the silica support, followed by calcination in air and in-situ reduction in flowing hydrogen. This is a standard method of preparation of supported metal catalysts and several different nickel salts can be used instead of nickel nitrate as the nickel precursor. Furthermore, other standard methods for the preparation of supported metal catalysts could be used without having a detrimental effect on the properties of the catalyst. In addition to silica, we investigated other inorganic supports such as alumina and titania. Although nickel supported on these supports was also found to be effective for the catalytic cracking of methane, the performance of nickel supported on silica was superior to those of the other catalysts and therefore, this system was chosen to demonstrate the invention in this application. In addition, we examined the performance of other transition metals such as Co and Fe, supported on silica for this reaction. Although these catalysts were also found to be effective for the reaction, at 550°C the performance of nickel was again superior to the other catalysts. Finally, by examining several Ni/SiO2 catalysts of variable Ni content, it was determined that optimum performance for the catalytic cracking of methane can be obtained with a nickel content in excess of 5 wt.%, and, in particular a content of approximately 16 wt.%. As a result, a 16 wt.% Ni/SiO2 catalyst was chosen to demonstrate the invention in this application.
-6-
When the catalyst was placed in a conventional fixed bed reactor and exposed to a stream containing 20% CH4 (by volume) in He, at 550°C and under a GHSN of 30,000 h"1, a high initial activity was observed for the cracking of methane (approximately 35% CH4 conversion). Hydrogen was the only gaseous product detected and the rates of methane consumption and hydrogen production were found to be in a ratio of 1 :2, thus, verifying the reaction stoichiometry for methane cracking.
The catalyst used in the present invention will eventually deactivate as a result of carbon deposition. Carbon may deposit on the surface to cover the active sites (site-blocking) or accumulate at the entrance of the pores to block further access of the reactants to the interior (pore-mouth plugging). It has been estimated that in both cases catalyst deactivation would occur within a short period of time. Even if 10 carbon atoms are needed to block each surface Νi atom, for example, 11 mg of carbon deposition would be enough to completely deactivate one gram of the 16.4% Νi/SiO2 catalyst. Furthermore, if pore-mouth plugging was the main deactivation mechanism, approximately 250 mg of carbon would be sufficient to clog the external 10% of the pores, in one gram of the Ni/SiO2 catalyst sample.
It has been discovered that a significantly higher amount of carbon deposition on the Ni/SiO2 catalysts occurs before deactivation occurs. At a temperature of 550°C for example, a very slow deactivation of the Ni/SiO2 catalyst was observed for the first 2 hours (Figure 1) followed by a more rapid loss of activity during the third hour. By the time the catalyst was completely deactivated (200 minutes), approximately 0.59 g of carbon had accumulated on the 0.2 g of the Ni/SiO2 catalyst sample. This amount is in very good agreement with the amount of carbon calculated based on the integration of the methane conversion (0.61 g), and corresponds to approximately 2700 carbon atoms accumulated on the catalyst per surface nickel atom.
It is therefore apparent that the capability of the silica supported nickel catalyst to accommodate carbon is significantly higher than those predicted by either the site-blocking or pore-mouth plugging models. Scanning Electron Microscopy
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(SEM) and Transmission Electron Microscopy (TEM) analyses of the spent catalysts were utilized to further understand the deactivation mechanism. SEM micrographs indicate the formation of filamentous carbon on the catalyst surface. These filaments appear to grow out of the silica support surface, with their length increasing with time-on-stream. Each filament has a bright tip, identified by the use of SEM/EDS (Energy Dispersive X-Ray Spectroscopy) to be a nickel particle. Spent catalyst samples were further studied by the use of X-Ray Diffraction (XRD). The XRD patterns, suggest that graphitic carbon constituents with different degrees of defect or distortion are present in the deactivated samples. TEM micrographs of the fully deactivated sample show that the growth of the carbon is terminated as a result of spatial limitations. The modes of filament termination include the nickel particle's restriction by the silica surface, the arm and the tip of another carbon filament. Formation of carbon filaments as a result of hydrocarbon cracking has been extensively reported in the literature with higher molecular weight hydrocarbons over supported nickel, iron, cobalt and several alloy catalysts. The carbon deposited on the catalyst in carrying out the present invention may be used in electrochemical applications such as superconductors, electrodes and fuel cells.
The reversibility of filament growth and the regeneration of the catalyst has been previously considered by others, but no results have been reported on whether the catalyst activity can be restored. In fact, some workers have suggested that catalyst regeneration may be futile in view of the changes caused to the catalyst support structure as a result of the filament growth process. Conventional oxidation in air (C + O2 = CO2) and steam gasification (C + xH2O = COx + χH2) were considered as potential routes for the regeneration of the catalyst at 823 K. Surprisingly, both methods appear to be able to fully restore the activity of the catalyst, as shown in Figure 2 where the methane conversion is plotted against time- on-stream for the fresh and the regenerated catalysts. The oxidation process was faster than the steam gasification, but caused a high temperature front. This front gradually moved through the catalyst bed, causing the collapse of the sample to a fine powder. XRD analysis suggests that the oxidation process completely removed
-8- the deposited carbon and converted the metallic nickel into nickel oxide which had to be reduced in flowing hydrogen before the next reaction cycle shown in Figure 2. On the contrary, the catalyst bed maintained a uniform temperature profile during the steam regeneration process and the catalyst preserved its metallic nickel form at the end of the process.
Another difference between the two regeneration methods is that the steam gasification leads to the production of additional hydrogen. This is at the expense of external thermal energy, since the oxidation of carbon releases a large amount of heat. Nevertheless, the additional production of hydrogen may be of significant practical importance. Theoretical yields of four and three moles of hydrogen per mole of methane can be achieved respectively, with steam reforming and partial oxidation of methane, provided that all carbon monoxide is converted to carbon dioxide by the water-gas shift reaction. In comparison, methane cracking produces less hydrogen (two moles) from each mole of methane. The hydrogen yield however, can be dramatically improved if the hydrogen produced during the regeneration step is also accounted for. In this case, 2 moles of hydrogen were obtained from each mole of methane during the cracking step and an additional 1.4 moles were produced during the subsequent steam gasification of the deposited carbon, leading to an overall hydrogen yield of 3.4 moles for each mole of methane. This overall hydrogen yield is slightly less than that from steam reforming, but better than that for partial oxidation.
Formation of carbon monoxide and methane were also detected during the initial stage of the steam regeneration, where, as shown in Figure 3, the carbon dioxide and hydrogen selectivities are less than 100%. Increased selectivities of carbon dioxide and hydrogen, obtained when the regeneration was conducted at a higher space velocity, appear to suggest that carbon monoxide and methane may be secondary products, formed due to the reverse water-gas shift (H2 + CO2 = CO + H2O) and methanation (CO + 3 H2 = CH4 + H2O) reactions. These observations suggest that one may be able to efficiently control the selectivity of hydrogen production during the regeneration step by adjusting the space velocity.
-9-
TEM micrographs of the steam regenerated sample show that some remains of the large filaments are still present on this catalyst after the regeneration has been completed. The presence of these remains however, does not appear to have a negative effect on catalytic activity which is fully restored following the steam regeneration step (Figure 2). Following a few cycles of deactivation and steam regeneration however, an air oxidation step will be probably required, to completely remove the accumulated remains.
The set of Ni-Cu/SiO2 catalysts used in the second embodiment of this invention had the total metal amount (on a molar basis) maintained constant at 2.6 mmole of metal/g of support while the ratio of Ni:Cu was varied from approximately 8:1 to approximately 1 :8. The catalysts were prepared by incipient wetness impregnation of nickel and copper nitrates (Ni(NO3)2x6H2O and Cu(NO3)2x2.5H2O) obtained from Aldrich (with a purity of 99.999%) onto commercially available SiO2 (Davison Syloid 74). Prior to impregnation the silica support was dried, pressed into pellets under a pressure of 15,000 psig, crushed and sieved to obtain a granulometric fraction in the 20-35 mesh size. The impregnated samples were dried in a vacuum oven at 120 °C overnight and subsequently calcined in a muffler furnace at 700 °C for 6 hours. The Ni and Cu loadings were estimated by the weight difference between the blank support and the catalyst reduced overnight in a 1 :2 H2/N2 mixture (total flow rate of 120 ml/min) at 650 °C .
Following the reduction treatment, the samples were exposed to methane (GHSN - 6000 hr ') at 650 and 800 °C . Activity measurements were conducted at two different temperatures and the results are presented in Fig. 4. The results indicate that the presence of small amounts of Cu enhanced significantly the initial activity at 800 °C , while the presence of Cu had no significant effect at 650 °C. The initial conversion over the 2.3 mmole Νi/0.3 mmole Cu SiO2 composition for example, was measured at 63%, as compared to 14.4% for the 2.3 mmole Ni/SiO2 composition. This is a surprising result given that Cu alone is not active for the cracking of methane under these conditions (0.3% initial methane conversion for the
-10-
0.3 mmole Cu/SiO2 composition). The promoting effect is also more pronounced when small amounts of Cu are added (i.e., Ni:Cu ratios greater than 1).
While the present invention has been particularly shown and described with reference to the preferred mode as illustrated in the drawing, it will be understood by one skilled in the art that various changes in detail may be effected therein without departing from the spirit and scope of the invention as defined by the claims.
Claims
-11-
We Claim: 1. A process for producing hydrogen which comprises contacting a stream of a hydrocarbon gas with a nickel containing catalyst at a temperature in the range of about 400 to 900┬░C which results in the conversion of said gas to hydrogen, with said process being carried out until said catalyst is deactivated due to the deposition of carbon on said catalyst.
2. The process of claim 1 in which the catalyst contains at least 5 wt.% nickel.
3. The process of claim 1 in which the nickel containing catalyst is supported on an inorganic support.
4. The process of claim 1 in which the nickel containing catalyst is supported on silica.
5. The process of claim 1 in which the catalyst further contains copper.
6. The process of claim 5 in which the ratio of nicke copper varies from about 20:1 to 1:8.
7. The process of claim 1 in which the hydrocarbon gas is one selected from the group consisting of methane, natural gas, ethane, ethylene, propane, propylene, butane, pentane, hexane and mixtures thereof, and hydrocarbons with molecular weights in the gasoline and diesel range.
8. The process of claim 1 in which the deactivated catalyst is regenerated by oxidation in air.
9. The process of claim 1 in which the deactivated catalyst is regenerated by steam gasification of the deposited carbon. -12-
10. The process of claim 1 in which the hydrocarbon gas is mixed with an inert carrier gas.
1 1. A process for producing hydrogen which comprises contacting a stream of a hydrocarbon gas with a nickel containing catalyst at a temperature in the range of about 400 to 900┬░C which results in the conversion of said gas to hydrogen, and where said hydrocarbon gas is one selected from the group consisting of methane and natural gas.
12. The process of claim 11 in which the catalyst contains at least 5 wt.% nickel.
13. The process of claim 11 in which the nickel containing catalyst is supported on an inorganic support.
14. The process of claim 11 in which the nickel containing catalyst is supported on silica.
15. The process of claim 11 in which the catalyst further contains copper.
16. The process of claim 14 in which the ratio of nickel opper varies from about 20:1 to 1:8.
17. The process of claim 11 in which the catalyst is regenerated by oxidation in air.
18. The process of claim 11 in which the catalyst is regenerated by steam gasification of the deposited carbon. -13- 19. The process of claim 11 in which the hydrocarbon gas is mixed with an inert carrier gas.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7581998P | 1998-02-24 | 1998-02-24 | |
US75819P | 1998-02-24 | ||
US23186399A | 1999-01-14 | 1999-01-14 | |
US231863 | 1999-01-14 | ||
PCT/US1999/003556 WO1999043608A1 (en) | 1998-02-24 | 1999-02-19 | Hydrogen production via the direct cracking of hydrocarbons |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1060123A1 true EP1060123A1 (en) | 2000-12-20 |
Family
ID=26757315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP99907144A Withdrawn EP1060123A1 (en) | 1998-02-24 | 1999-02-19 | Hydrogen production via the direct cracking of hydrocarbons |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1060123A1 (en) |
CN (1) | CN1291165A (en) |
AU (1) | AU2687399A (en) |
CA (1) | CA2317395A1 (en) |
WO (1) | WO1999043608A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11434132B2 (en) | 2019-09-12 | 2022-09-06 | Saudi Arabian Oil Company | Process and means for decomposition of sour gas and hydrogen generation |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ITMI20010138A1 (en) * | 2001-01-26 | 2002-07-26 | Lentek S P A | METHANE HYDROGEN PRODUCTION AND PLANT USED IN THIS PROCEDURE |
CN100439238C (en) * | 2005-12-14 | 2008-12-03 | 微宏科技(湖州)有限公司 | Production of hydrogen by catalyzed decomposing magnesium and its mixture doped with other metals |
CN102274704B (en) * | 2010-06-11 | 2013-07-17 | 中国石油化工股份有限公司 | Stripping method of deactivated catalyst in preparation of alkene from methanol |
US20130224106A1 (en) * | 2012-01-23 | 2013-08-29 | King Abdullah University Of Science And Technology | Hydrogen generation |
CN102583242B (en) * | 2012-03-09 | 2014-02-05 | 大连理工大学 | Method for preparing hydrogen gas through catalytic cracking of methane |
CN106865498B (en) * | 2017-03-14 | 2019-05-21 | 大连理工大学 | A method of using Carbon Materials as catalyst preparation hydrogen and fibrous carbon |
NL2019407B1 (en) * | 2017-08-10 | 2019-02-21 | L2 Consultancy B V | Refueling station for supplying energy carriers to vehicles |
WO2019031966A1 (en) | 2017-08-10 | 2019-02-14 | L2 Consultancy B.V. | Refueling station for supplying energy carriers to vehicles |
JP2019182733A (en) * | 2018-04-01 | 2019-10-24 | 株式会社伊原工業 | Hydrogen generator, method for separating solid product material, system for discharging and collecting solid product material and method for manufacturing nickel based metal structure |
CN110342462A (en) * | 2019-08-27 | 2019-10-18 | 深圳市中科纳米科技有限公司 | A kind of method of hydrocarbon gas non-carbon-emitting hydrogen manufacturing |
CN111068688A (en) * | 2019-12-19 | 2020-04-28 | 南京理工大学 | Method for catalyzing methane cracking by using iron waste as catalyst |
CN111170764B (en) * | 2019-12-31 | 2021-11-23 | 娄底市安地亚斯电子陶瓷有限公司 | Wet hydrogen system and working method thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7811278A (en) * | 1978-11-15 | 1980-05-19 | Stamicarbon | METHOD FOR PROCESSING NITROGEN CONTAINING NATURAL GAS. |
US4435376A (en) * | 1982-03-26 | 1984-03-06 | Phillips Petroleum Company | Fibrous carbon production |
DD287015A5 (en) * | 1989-08-11 | 1991-02-14 | Leipzig Chemieanlagen | METHOD FOR PRODUCING PURE HYDROGEN AND METAL GROUT |
JP3211666B2 (en) * | 1996-06-25 | 2001-09-25 | トヨタ自動車株式会社 | Method for simultaneous production of hydrogen and carbon black |
-
1999
- 1999-02-19 CN CN99803169A patent/CN1291165A/en active Pending
- 1999-02-19 EP EP99907144A patent/EP1060123A1/en not_active Withdrawn
- 1999-02-19 CA CA002317395A patent/CA2317395A1/en not_active Abandoned
- 1999-02-19 WO PCT/US1999/003556 patent/WO1999043608A1/en not_active Application Discontinuation
- 1999-02-19 AU AU26873/99A patent/AU2687399A/en not_active Abandoned
Non-Patent Citations (1)
Title |
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See references of WO9943608A1 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11434132B2 (en) | 2019-09-12 | 2022-09-06 | Saudi Arabian Oil Company | Process and means for decomposition of sour gas and hydrogen generation |
Also Published As
Publication number | Publication date |
---|---|
AU2687399A (en) | 1999-09-15 |
CA2317395A1 (en) | 1999-09-02 |
WO1999043608A1 (en) | 1999-09-02 |
CN1291165A (en) | 2001-04-11 |
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