This invention relates to a method and an apparatus for the decomposition of natural gas or methane into its gaseous constituents and carbon using cold arc discharge. More particularly, the invention relates to the use of a cold arc discharge in order to achieve the decomposition of natural gas or methane into carbon in the form of solid particles and gaseous products consisting mainly of hydrogen and acetylene in admixture with unreacted methane.
Arc discharge has been known for a long time. A sustained arc will generate hot plasma. However, by controlling the arc, one can generate a cold arc discharge producing a very dense plasma, but with considerably less heat. In the past, a small pulse width using a flyback transformer produced such dense plasma, but it was a rather difficult and expensive way of generating a “cold arc”.
In Canadian patent application No. 2,353,752 there is disclosed a method and an apparatus for producing hydrogen and carbon from natural gas or methane using a barrier discharge non-thermal plasma, which is also called “cold plasma”. Such process requires, however, the use of precisely designed and formulated ceramic materials as the dielectric barrier. Such materials may be difficult and expensive to obtain or produce. There is, therefore, a need for a method and an apparatus that would transform natural gas or methane primarily into hydrogen and carbon without requiring such materials.
It has been surprisingly found that hydrogen and carbon can be produced from natural gas or methane by using cold arc discharge instead of dielectric barrier discharge. It should be noted that the chemical reaction mechanism remains similar in both the dielectric barrier discharge (DBD) and cold arc discharge (CAD), namely the general chemical reaction is:
CH4(g)→C(s)+H2(g)
However, the microdischarges in DBD are specifically produced so as not to fall into an arcing mode, whereas in CAD arcs of controlled time duration and frequency are produced to carry out the reaction.
A cold arc discharge may be defined as an intermittent arc discharge that makes it possible for the reactor to operate at relatively low temperatures, typically below 200° C. On the other hand, the hot arc discharge produces a continuous plasma arc which generates temperatures within the reactor in the range of 1700° C. to 4000° C. and higher, since the temperature of the hot plasma is in excess of 4000 K.
The present applicant has found that it is possible to generate a cold arc discharge by limiting the lifetime of an arc during a discharge by using a capacitor in series with a high voltage electrode while using a pulsating high voltage discharge, and further that the cold arc so produced is well suited for promoting the reaction mentioned above, namely dissociation of natural gas or methane into its components. It should be noted that the resulting products contain in addition to hydrogen and carbon, a small but measurable amount of acetylene and trace amounts of some other hydrocarbons that are usually produced in such reactions.
The resulting gas flow exiting from the reactor is then normally passed through a solids collector, such as a HEPA (high efficiency particle arrester) to collect the typically nanoscale solid carbon particles that occur as a result of the process and the remaining gaseous mixture comprising essentially unreacted natural gas, hydrogen and acetylene proceeds to equipment that measures the gas composition and collects or further processes that gaseous mixture.
Thus, in essence, the method of the present invention for decomposing natural gas or methane into its gaseous constituents and carbon comprises passing a flow of natural gas or methane through a reaction zone and generating a cold arc discharge in said reaction zone adapted to decompose the natural gas or methane into its gaseous constituents and carbon in the form of solid particles.
In a more specific embodiment, the method comprises:
In order to make the system more efficient, a plurality of HV electrodes with capacitors in series therewith may be installed in the reaction zone and arranged in such a manner as to produce a high degree of conversion. The wall of dielectric material through which the HV electrode or electrodes are projected need not be of any special material, and may be, for example, made of plastic that would resist temperatures of the order of 200° C.-400° C. If desired, however, walls of ceramic material may also be used.
In another embodiment, the method comprises:
In this embodiment, a plurality of capacitor-connected electrodes may also be installed in the reaction zone. This may be done by mounting them on a central cylindrical shaft made of dielectric material and surrounding this shaft with the HV electrode in the form of a tubular metal wall which is connected to the HV source.
The basic apparatus in accordance with the present invention comprises a reactor with a reaction zone, means for passing a flow of natural gas or methane through said reaction zone and means for generating a cold arc discharge or a plurality of cold arc discharges in said reaction zone such as to convert the natural gas or methane into its gaseous constituents and carbon.
In one non-limitative embodiment, the reactor has a tubular shape with a rotatable cylindrical ground electrode made of a conducting material, such as aluminum or steel, in the middle and with an outer wall of dielectric material, such as a plastic or ceramic, through which a plurality of HV electrodes extend into the reaction zone formed in the space between the ground electrode and the outer wall. Each of the HV electrodes is provided with a capacitor in series and is connected through the capacitor to a pulsating high voltage source adapted to produce a high frequency cold arc discharge between each HV electrode and the ground electrode. This enables conversion of the natural gas or methane introduced through an inlet port or ports and flowing through the reaction zone, into its gaseous constituents and carbon. The ground electrode is normally rotated during the operation of the reactor so that carbon would not form conducting bridges between the electrodes. Rotating speeds between 60 RPM and 200 RPM may be used. Outside of the reactor, means are provided to separate the solid particles of carbon from the gaseous products and to analyse the latter to determine the gaseous constituents.
In another embodiment, the reactor again has a tubular shape, but with a rotatable cylinder of dielectric material in the middle, in which are embedded a plurality of electrodes extending outwardly from the cylindrical surface. Each such electrode is provided with a capacitor in series and is connected to a common ground. This is surrounded by a metal tube acting as a high voltage electrode. The reaction zone is formed between the capacitor-connected electrodes and the HV tube which can be made of any conducting metal, such as aluminum or steel. As in the previous embodiment, means are provided for passing a flow of natural gas or methane through the reaction zone while connecting the conductive metal tube to a pulsating HV source. In this manner, arc discharges are generated in the reaction zone between the metal tube, namely the HV electrode, and the rotating capacitor-connected electrodes. Thus, when AC high potential is applied to a number of capacitor-connected electrodes through the common HV electrode (metal tube), the arc discharge occurs homogeneously at each electrode area. Because the capacitor-connected electrodes are mounted on the central shaft and are rotating, the arc discharges are also rotating, which increases the reaction area and, therefore, the decomposition efficiency.
It should be noted that the International PCT Publication WO 2004/061929 A1 describes a plasma generator for producing ozone which uses a pair of electrodes without interposition of a dielectric body, and a capacitor in series therewith. It also requires a second capacitor in parallel with the electrodes for supplementing the power supply. Furthermore, it is indicated that the capacitor in series with the electrodes is an arc-suppression capacitor producing an arc-suppressing discharge between the electrodes, thereby generating plasma. Moreover, according to this prior art disclosure, the electrode unit is composed of a floating electrode, and insulator arranged around the floating electrode and a ground electrode arranged around the insulator. This prior art system is therefore clearly different from the one of the present invention and is used for a completely different purpose.
The present invention will now be further described with reference to the appended drawings which illustrate various embodiments of the invention.
In the drawings in which the same elements are designated by the same reference numbers,
An exemplary high voltage source 28 is a high voltage line generating a pulsating high voltage discharge. The pulsating high voltage discharge is bi-polar; i.e., it generates both positive and negative pulses. A schematic for an exemplary high voltage source 28 is depicted in
The capacitor 26 blocks the current during the discharge and produces a cold arc discharge in the reaction zone between the HV electrode 24 and the ground electrode 20. This cold arc discharge is adapted to decompose the natural gas or methane flowing through the reaction zone into its gaseous constituents and solid carbon particles, which is achieved by controlling the frequency and duration of the cold arc discharge. The frequency of the arc is controlled by a microcontroller. There is no specific limit to the frequency that can be used, but at a certain point, the cold arc discharge will transform into thermal plasma and this should be avoided. Frequencies in the range of about 1 kHz to about 20 kHz are quite suitable. As far as the arc duration is concerned, it is mainly a function of the capacitor, although the power supply impedance will also have an effect on the arc duration. The arc duration may be determined by the current waveform during a discharge. A small capacitor will give very short current pulses, while a large capacitor will give longer current pulses. For example, a capacitor of 1000 pF gives a current pulse width of approximately 3 μs, whereas a capacitor of 100 pF gives a current pulse width of approximately 40 ns. Capacitors from about 100 pF to about 3000 pF have been found quite suitable for the purposes of the present invention, although this range is not limitative. Exemplary time constants that can be used in the circuit range from about 0.1 μs to about 0.2 μs. It should also be noted that the size of the gap has an effect on the current pulse duration because the discharge impedance is higher. Generally, pulse width durations between about 40 ns and about 3 μs are satisfactory and produce good results in conjunction with frequencies of about 1 kHz to about 12 kHz, although again they are not limitative for the purposes of the present invention.
The polarity of the capacitor 26 has been set as shown in
During the arc discharge, illustrated in
In
The numbers shown on the left side of the graph in both
1—plasma current
2—high voltage before the capacitor in reference to ground—transformer voltage
3—high voltage after the capacitor in reference to ground—gap voltage
In
At the bottom of both
The time scale along the horizontal axis of the waveforms depicted in
In
Capacitance, gap discharge size and voltage level have an effect on conversion levels. Increasing capacitance has increased conversion levels, but at the same time it increases the production of heat. By increasing the capacitance, it takes more time to charge the capacitor, therefore the arc is sustained longer and more power from the source is needed. Gap distance also increases the conversion since the plasma volume is increased. As a consequence to gap increase, the voltage will also be increased because of higher potential needed to create breakdown.
It should be noted that the breakdown voltage is mainly a function of gap and frequency. For example, at a frequency of 8 kHz, the initial breakdown voltage can drop to about 6 kV and sustain a discharge with a gap of 5 mm and a capacitor of 100 pF. In another example, a continuous discharge (not initial) is obtained at 11 kV with a capacitor of 500 pF at the same frequency of 8 kHz. For the purposes of the present invention, gaps can be between about 2.5 mm and about 20 mm with initial voltages between about 15 kV and about 25 kV depending on the gap and frequency used. The duration of each pulse can be between about 10% to about 50% of the period of the input voltage. For example, assume an input voltage having a frequency of 20 kHz that transitions between OV and positive (during a positive pulse) and negative (during a negative pulse) values Vmax and Vmin, respectively. This translates to an input voltage having a period of 50 μs. If using a pulse of 10% duration, the input voltage would be at Vmax for 5 μs and then return to 0 V for 20 μs, following which the input voltage would transition to Vmin and hold for 5 μs and then return to 0 V for another 20 μs. The pulse duration will depend on, for example, the selected frequency and on the voltage source 28's ability to generate the desired voltage waveform.
The configuration shown in
A still further embodiment is illustrated in
Further embodiments of the invention are illustrated in
As shown in
On the other hand, as shown in
In a further embodiment of the present invention, illustrated in
A further, more detailed design of this system is illustrated in
Apart from the change in configuration set out in
A non-limitative example of the method of operation of the system of the present invention is now described in conjunction with
The process resulting from this operation has converted natural gas or methane into its two main constituents, according to the following reaction:
CH4→C(s)+H2
Various other complementary reactions that also occur during the process give trace amounts of other compounds. However, these unwanted compounds are very minute with the exception of acetylene (C2H2) which is produced in a measurable amount. The resulting gas is then passed from the bottom part of the reactor 40 via line 2 through a HEPA (high efficiency particle arrester) 42 to collect the solid carbon particles that proceed via line 4 to a vessel 44. The remaining mixture of H2 and C2H2 as well as unreacted CH4 proceed via line 5 to equipment 46 that measures the gas composition. In the present example, the concentration of gases in the product stream was as follows: H2=17.48 mol %; C2H2=3.07 mol % and CH4=79.45 mol % Although the gas portion resulting from the above process could further be treated to separate hydrogen from the other two gases in the mixture, it should be noted that the resulting gas is essentially hythane which is a gas consisting of about 80% methane and 20% hydrogen, and is a product in its own right since it can be used as a fuel for internal combustion engines. For example, U.S. Pat. No. 5,516,967 discloses a direct conversion of methane to hythane by subjecting methane to a controlled oxidation with water vapor at a temperature of 400 to 500° C. and at a pressure from 1 to 5 atmospheres, in the presence of a particular catalyst. In the present process, hythane is also produced directly but using cold arc discharge instead of controlled oxidation. In the example given above, 0.9 kilowatts were used to produce 1 cubic meter of hythane which included a minor proportion of acetylene.
It should be understood that various modifications that would be obvious to those skilled in the art can be made to the method and apparatus of the present invention without departing from the following claims.
The present invention is not to be limited in terms of the particular embodiments described in this application, which are intended as single illustrations of individual aspects of the invention. Many modifications and variations of this invention can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. Functionally equivalent methods and apparatuses within the scope of the invention, in addition to those enumerated herein, will be apparent to those skilled in the art from the foregoing descriptions. Such modifications and variations are intended to fall within the scope of the appended claims. The present invention is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled. It is to be understood that this invention is not limited to particular methods, reagents, compounds compositions or biological systems, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting.
Other embodiments are set forth within the following claims.
Number | Date | Country | Kind |
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2516499 | Aug 2005 | CA | national |
This application is a continuation-in-part of copending U.S. patent application Ser. No. 11/795,372, filed Apr. 28, 2006, which is a US National Stage Application of PCT/CA2006/000671, filed Apr. 28, 2006, which claims benefit of priority to Canadian patent application 2,516,499, filed Aug. 19, 2005, the contents of which are incorporated herein by reference in their entireties.
Number | Date | Country | |
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Parent | 11795372 | Jul 2007 | US |
Child | 12033818 | US |