Method and Device for Flameless Stepwise Combustion
20220026058 · 2022-01-27
Inventors
Cpc classification
F23N1/02
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F23C9/006
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F23C2900/99001
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F23C6/042
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
Y02E20/34
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
International classification
Abstract
A method for heating a heating chamber to a temperature below the spontaneous ignition temperature of the fuel that is used, wherein fuel and air are reacted in flameless oxidation in a non-stoichiometric mixture ratio in a combustion chamber. The air ratio λ is at least lower than the stoichiometric ratio λ=1 such that the temperature in the combustion chamber does not exceed the temperature at which thermal nitrous oxide generation begins. Otherwise, λ is established such that the spontaneous ignition temperature of the fuel is exceeded. This results in two permissible air ratio ranges, between λ.sub.min and λ.sub.1 in sub-stoichiometric operation, and λ.sub.2 to λ.sub.max in superstoichiometric operation of the combustion chamber. The still-reactive gases released from the combustion chamber are made to react in the heating chamber, preferably by flameless oxidation. This avoids thermal nitrous oxide generation in the heating chamber.
Claims
1. A method for heating a heating chamber (12), comprising: heating the chamber to a temperature below a spontaneous ignition temperature of a fuel used to heat the chamber; reacting fuel and air in flameless oxidation in a nonstoichiometric ratio in a combustion chamber (11); and supplying the fuel and air in the heating chamber (12) as a reaction gas without heat withdrawal from the combustion chamber (11) apart from non-avoidable thermal losses; wherein the reaction gas is completely oxidized in the heating chamber (12), by adding air and/or fuel as necessary.
2. The method according to claim 1, wherein the oxidation in the heating chamber (12) is carried out with flame formation.
3. The method according to claim 1, wherein the oxidation in the heating chamber (12) is carried out without flame creation by gas guidance with large-scale recirculation.
4. The method according to claim 1, wherein a non-stoichiometric fuel/air ratio is adjusted in the combustion chamber (11) such that a temperature of 1400° C. is not exceeded in the combustion chamber (11).
5. The method according to claim 1, wherein a temperature between 1000° C. and 1300° C. is achieved in the combustion chamber (11) by adjustment or closed loop control of a fuel/air ratio.
6. The method according to claim 1, wherein the combustion chamber (11) is sub-stoichiometrically (λ<1) operated during full load operation and is super-stoichiometrically (λ>1) operated in a partial load operation.
7. The method according to claim 6, wherein a range (λ.sub.1, λ.sub.2) of non-used fuel/air ratios is defined between a fuel/air ratio in the super-stoichiometric operation and a fuel/air ratio in the sub-stoichiometric operation.
8. The method according to claim 1, further comprising extracting heat from the heating chamber (12).
9. A device (10) for heating a heating chamber (12), comprising: an adiabatic combustion chamber (11) that comprises at least one air supply device (15), at least one fuel supply device (14), and at least one discharge (16) wherein the adiabatic combustion chamber (11) is configured for flameless oxidation of fuel in a non-stoichiometric fuel/air ratio; and a heating chamber (12) in which the at least one discharge (16) of the combustion chamber (11) opens, wherein the heating chamber (12) includes a supply device for supplying air and/or fuel.
10. The device according to claim 9, wherein the adiabatic combustion chamber (11) has a volume that is smaller than a volume of the heating chamber (12).
11. The device according to claim 9, wherein the combustion chamber (11) is free of flame-maintaining structures.
12. The device according to claim 9, wherein the heating chamber (12) includes a heat withdrawal device (13).
13. The device according to claim 9, further comprising a heat exchanger (23) upstream of the combustion chamber (11) and/or the heating chamber (12).
14. The device according to claim 9, further comprising a regulating device for regulation of fuel and/or air supply to the combustion chamber (11) and/or heating chamber (12) that is configured such that a predefined upper temperature limit is not exceeded in the combustion chamber and/or the heating chamber (12).
15. The device according to claim 14, wherein the regulating device is configured to influence a fuel/air ratio for temperature regulation.
Description
[0026] In the drawings embodiments of an inventive device are illustrated. The drawings show:
[0027]
[0028]
[0029]
[0030]
[0031] For clarification of the inventive method reference is made to the device 10 according to
[0032] The combustion chamber 11 is supplied with fuel and air via a fuel line 14 and an air line 15. The ratio of fuel and air is thereby defined such that the air ratio is λ=1. Preferably λ is remarkably smaller than 1, i.e. the operation is executed in excess of fuel. For initiating the oxidation in the combustion chamber 11, it is preferably provided with a not further illustrated ignition device, e.g. with a spark ignition device or a pilot burner. It can be operated in continuous operation or can also be turned off after the flameless oxidation in the combustion chamber 11 has been established.
[0033] Preferably, the wall of the combustion chamber 11 comprises a high heat resistance. For example, the combustion chamber 11 can be lined with ceramic or can consist of ceramic. In doing so a quick heating of the combustion chamber 11 and a quick attainment of an operation manner with flameless oxidation shall be allowed after the ignition of the fuel in the combustion chamber 11.
[0034] The reaction gases created in the combustion chamber are introduced in the heating chamber 12 via a reaction gas passage 16. In addition, air and/or fuel are introduced in the heating chamber 12 via a line 17 in order to mix with the hot reaction gases there and to effect a complete oxidation of the used fuel. The heating chamber 12 is preferably remarkably larger than the combustion chamber 11, wherein an average temperature is obtained in the heating chamber 12 that is remarkably lower than in the combustion chamber 11 and that can be preferably also below the spontaneous ignition temperature of the used fuel. The created exhaust gases are discharged via a line 18 from the heating chamber 12.
[0035] Preferably the combustion chamber 11 is operated in a temperature range that is at least such high that the spontaneous ignition temperature of the used fuel is exceeded, whereby it is however concurrently so low that the nitrogen oxide formation is nearly completely suppressed. The useable temperature range in the combustion chamber 11 can be, for example, defined such that the lower temperature limit is between 800° C. and 1100° C., preferably 850° C. and 1100° C., whereas the upper temperature limit is, for example, between 1100° C. and 1400° C., preferably 1100° C. and 1300° C. and has, for example, an amount of 1200° C. The desired temperature range is preferably adjusted by a respective definition or regulation of the air ratio λ. Thereby the combustion chamber 11 operates, for example (and preferably), in excess of air. In doing so, comparably small constructions of the combustion chamber 11 can be achieved. In addition, the impulse of secondary air that has to be supplied via line 17 and that is required for the complete oxidation is available for establishment of a large-scale and sufficiently quick recirculation flow in the downstream heating chamber 12.
[0036] The temperature in the combustion chamber 11 depends during adiabatic operation only from the fuel/air ratio, i.e. the air ratio, and thus from the cross-section ratio of the air inlet nozzles of the combustion chamber 11 and secondary air nozzles in the heating chamber 12. In case of a ratio of, for example, 1:1, which corresponds to an air shortage of about 50%, a temperature of about 1100° C. is achieved with natural gas as fuel in the nearly adiabatic combustion chamber 11. In addition, a temperature closed loop control can be established that influences the stoichiometry, i.e. the air ratio in the combustion chamber 11, in order to maintain the temperature in the combustion chamber 11 within a desired range. This is particularly appropriate during use of lean gases with changing calorific value as fuel. Then the temperature in the combustion chamber 11 can be controlled in closed loop via the air ratio λ.
[0037] The control of the temperature in the combustion chamber 11 by appropriate definition of the stoichiometry (of the air ratio λ) can also be applied for the cold start such that the combustion chamber 11 can be quickly brought to the desired operation temperature of, e.g. 1000° C. For cold start the combustion chamber 11 can be, for example, operated in stoichiometric operation (λ=1), until the desired temperature is reached, after which the operation is continued in an sub-stoichiometric manner. In order to allow the desired flameless operation in the combustion chamber 11, the combustion chamber 11 is configured for creation of a large-scale recirculation vortex. Flame-holding structures are, however, not present. For this suitable flow guide devices can be arranged in the combustion chamber 11 that support the formation of a recirculation flow.
[0038] Flameless operation can also be realized in the downstream heating chamber 12, if required, although the temperature thereof is less than the spontaneous ignition temperature of the used fuel in the area of the heat withdrawing structures, e.g. the heating coil 13. For this reference is made to
[0039] The device 10 and the method explained based thereon have numerous advantages compared with conventional heating devices, particularly those based on the operation with flame. Due to the operation of the combustion chamber 11 in flameless oxidation and preferably also the heating chamber 12 with flameless oxidation, the thermal NOx-formation can be nearly completely suppressed and thus values of below 10 mg/m.sup.3 can be achieved. This applies independent from the temperature of the zones of the heating chamber 12 serving for heat withdrawal that can also be below the spontaneous ignition temperature of the used fuel, e.g. below 850° C.
[0040] In the case of use of lean gases with changing calorific value, problems of flame stabilization that are otherwise present can be avoided by operation of the combustion chamber 11 with flameless oxidation. It is shown that the combustion chamber 11 can be adapted to different power ranges of 10 kW to some MW in a manner being identical in construction and cheap.
[0041] In the combustion chamber 11 operated without heat withdrawal a temperature can be substantially maintained constant, also during partial load, such that large control ratio is obtained without specific effort.
[0042] If the combustion chamber 11 is provided with a heat transition impeding lining, e.g. a ceramic lining, or consists itself of ceramic or another material with a high thermal resistance, the combustion chamber 11 can also operate flamelessly during cold start. With the technique of flameless oxidation local temperature peaks in flames are avoided, which has a material-conserving effect on the combustion chamber 11 as well as the heating chamber 12.
[0043]
[0044] The combustion chamber 11 can be provided with a temperature sensor 30 that is connected with control 28. A task of the temperature sensor 30 is the monitoring of the operation of the combustion chamber 11, where usual flame sensors cannot be used due to lack of flames in the flameless oxidation. Preferably the temperature sensor is a “quick” sensor, that means it comprises a remarkably small thermal inertia.
[0045] In the system according to
[0046] The system 22 illustrated in
[0047] First, a full load operation is illustrated. For this the control 28 adjusts the fuel flow according to the desired load by means of the flow rate regulating device 29 and then regulates the air flow by means of the flow rate regulating device 26, i.e. the air ratio, such that the temperature in the combustion chamber 11 is in a desired operation range, e.g. between 850° C. and 1300° C., for example at about 1100° C. Thereby a flameless oxidation is achieved in the combustion chamber 11. By means of the temperature sensor 30 the control 28 detects the temperature and reduces the air flow in the air line 15, if the temperature increases above a desired amount and increases the air flow, if the temperature decreases too far. The temperature closed loop control is thus carried out by means of a variation of the air ratio λ in the sub-stoichiometric range. This is apparent from the right section of the abscissa in
[0048] During transition into the partial load the control 28 reduces the fuel flow by means of the flow rate regulating device 29 to smaller values. The air ratio λ is thereby adjusted such that the spontaneous ignition temperature is reliably exceeded in the combustion chamber 11. Potentially necessary air for the complete oxidation of still present remaining fuel in the heating chamber 12 is again supplied via line 17.
[0049] During extreme low load the control can transition from the sub-stoichiometric operation of the combustion chamber 11 described so far to the super-stoichiometric operation thereof, as illustrated in
[0050] The range between the two limit values λ.sub.1 and λ.sub.2 is avoided by control 28 at least as soon as the combustion chamber 11 is heated in that this range is passed in a short period during switching from sub-stoichiometric operation to super-stoichiometric operation or is switched without transition from sub-stoichiometric operation to super-stoichiometric operation (and vice versa). In doing so, the increase of the temperature in the combustion chamber 11 above a critical limit value of, e.g. 1300° C. or 1400° C. and the accompanying thermal NOx-formation is avoided.
[0051] Numerous modifications can be made to the presented embodiments. For example, the air preheating by means of the heat exchanger 23 can be limited to the air supplied to the combustion chamber 11 via line 15. As an alternative the air preheating can be limited to the air supplied to the heating chamber 12 via line 17. It is also possible to supply a mixture of preheated and not preheated air via line 15 and/or line 17. Further, also a preheating of the fuel supplied to the combustion chamber 11 via line 14 is basically possible. In addition, particularly for sub-stoichiometric operation of the combustion chamber 11 an additional fuel supply can be provided for the heating chamber 12 in order to effectuate an increased ratio of the heat creation in the heating chamber 12. In all presented embodiments it is, however, considered to be advantageous to effectuate the majority of the heat creation in the combustion chamber 11 by means of flameless oxidation. The further oxidation in the heating chamber 12 can be carried out with or without flame, wherein the flameless oxidation allows the decrease of the nitrogen oxide creation down to values below 10 mg/m.sup.3.
[0052] In the inventive method for heating a heating chamber 12 with a temperature below the spontaneous ignition temperature of the used fuel a combustion chamber 11 is provided in which fuel and air are brought to reaction with one another in flameless oxidation in a non-stoichiometric mixture ratio. The air ratio λ is thereby at least so far away from the stoichiometric ratio λ=1 that a temperature in the combustion chamber 11 is not exceeded beginning with which a thermal nitrogen oxide creation starts. This temperature is, e.g. 1300° C. to 1400° C. On the other hand the air ratio λ is defined such that the spontaneous ignition temperature of the used fuel is reliably exceeded in the combustion chamber 11. Thus, two reliable air ratio ranges are obtained, namely a first range between λ.sub.min and λ.sub.1 in the sub-stoichiometric operation and a second range λ.sub.2 to λ.sub.max in the super-stoichiometric operation of the combustion chamber 11. The still reactive gases released from the combustion chamber 11 are brought to reaction with additional air and/or additional fuel in a zone of the heating chamber 12, whereby it is preferably carried out with flameless oxidation. The named zone is particularly formed within the gas jet 21. Due to the flameless oxidation, a thermal nitrogen oxide creation is avoided also in the heating chamber 12.
LIST OF REFERENCE SIGNS
[0053] 10 device [0054] 11 combustion chamber [0055] 12 heating chamber [0056] 13 heating coil [0057] 14 fuel line [0058] 15 air line [0059] 16 reaction gas passage [0060] 17 line [0061] 18 exhaust gas [0062] 19-a flow guide device [0063] 19 recirculation vortex [0064] 20 air [0065] 21 gas jet [0066] 22 system [0067] 23 heat exchanger [0068] 24 outlet [0069] 25 fresh air inlet [0070] 26, 27 flow rate regulating device [0071] 28 control [0072] λ air ratio [0073] λ.sub.1, λ.sub.2, λ.sub.min, λ.sub.max, λ.sub.v air ratio limit values [0074] 29 flow rate regulating device [0075] 30 temperature sensor