Oxidizing oxygen-fuel burner firing for reducing NOx...

Combustion – Fuel disperser installed in furnace – Plural feed means extending to common wall opening of furnace

Reexamination Certificate

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C431S186000, C431S189000

Reexamination Certificate

active

06171100

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention pertains to methods and apparatus for introducing an oxidizing oxygen-fuel combustion in air-fuel fired furnaces to reduce NOx emissions and improve thermal efficiency without any substantial detrimental effect on furnace life or product quality.
2. Related Art
The most common method to reduce NOx emissions is to use 100% oxygen-fuel combustion where use of oxygen instead of air eliminates nitrogen and thus significantly lower NOx emissions are achieved. This method has been successfully used on several types of glass furnaces. However, the use of 100% oxygen-fuel firing on large glass furnaces (450 to 1000 ton/day melted glass production capacity), such as float glass furnaces, has not been achieved so far due to overall economics with the oxygen use and uncertainty over glass quality and furnace life.
There are several other NOx control methods available in the market such as 3-R process (European Patent No. 0 599 547 A1), gas reburn process (U.S. Pat. No. 5,139,755) and oxygen-enriched air staging (U.S. Pat. No. 5,203,859).
The 3-R process and the gas reburn process use additional or reburn fuel injection (5% to 15% of total fuel use) in the exhaust stream to create gas reburn reactions and reduce NOx emissions. This is a post combustion method. This method requires injecting reburn fuel (natural gas) in the exhaust stream, which may be difficult for certain furnaces which cannot use reducing conditions in the regenerator due to refractories containing various oxides. Further the reburn fuel is an energy penalty and no thermal efficiency benefit is derived by injection of 5% to 15% reburn fuel in the exhaust stream outside the melt area. Here the additional fuel does not release any heat for the productivity increase and it is simply used as emissions cleaning medium. There are also concerns of higher CO emissions from the furnace.
In oxygen-enriched air staging, the secondary oxidant (oxygen or oxygen-enriched air) is introduced proximate to the exhaust of the industrial furnace to reduce NOx emissions. In these applications the furnace is operated using lower stoichiometry on the firing side to reduce thermal NOx formation. The secondary oxidant is injected into the exhaust stream (using exhaust port) to burnout CO and other hydrocarbons. This concept is illustrated in FIG.
1
. In
FIG. 1
a typical side fired regenerative furnace
1
having regenerators (checkers) A and B is illustrated schematically with both firing
2
and exhaust
4
ports. The firing is from left-to-right and secondary oxidant injection
6
is from right-to-left.
In U.S. Pat. No. 5,203,859 (as illustrated in FIG.
1
), the preferred embodiment includes withdrawal of preheated secondary combustion air
7
from firing side regenerator using an oxygen aspirator
8
. The oxygen is used as a prime mover for withdrawing secondary combustion air
7
. The secondary oxidant
6
is then injected proximate to the exhaust
4
. The disadvantages of above scheme include:
Space constraints due to large secondary air piping
7
carrying 2400° F. [1315° C.] air.
Complex flow reversal cycle to switch secondary preheated air from left-to-right side depending on the reversal cycle.
Difficulties in the burnout of CO and hydrocarbons in the melter space due to premature combustion in the exhaust port
4
leading to overheating of exhaust port
4
.
Design limitations of aspirator
8
in providing correct secondary oxidant mixture
High capital cost system.
Other known embodiments of the above include secondary oxidant as oxygen-enriched ambient air, which would create difficult mixing conditions due to smaller relative volume of the cold or ambient oxidant stream compared to primary exhaust stream. Here the exhaust gas volume is approximately 60 times greater than the secondary oxidant leading to inefficient mixing and poor thermal efficiency due to quenching of the melter combustion space by an ambient mixture. This can further result in poor product quality.
Additional known embodiments include use of oxygen as a secondary oxidant, which also creates difficult mixing conditions due to small gas volume (300 times smaller than the primary exhaust stream). This creates non-homogeneous burnout and creation of hot spots in the melter combustion space and exhaust port.
It would be a great benefit to glass and other manufacturers if NOx production could be decreased, while transferring heat to the load and avoiding some of the problems mentioned above.
SUMMARY OF THE INVENTION
In accordance with the present invention the above limitations are largely overcome using a much simpler approach for NOx reduction.
A first aspect of the invention is a method of heating a load in a furnace, the method comprising the steps of:
a) combusting a first fuel in at least one air-fuel burner, heat from the air-fuel burner being substantially transmitted to the load;
b) combusting a second fuel in at least one oxy-fuel burner, heat from the oxy-fuel burner being substantially transmitted to the load; wherein the air-fuel burner is operated in fuel-rich mode, and the oxy-fuel burner is operated in fuel-lean mode.
Preferred are methods wherein the combusting of step (a) creates an air-fuel flame that is substantially parallel to a horizontal surface of a load; wherein the combusting of step (b) creates an oxy-fuel flame that intersects the air-fuel flame; wherein the oxy-fuel flame projects from a flat bottom port toward the air-fuel flame at an angle &agr; measured from horizontal, the angle &agr;, ranging from about 1° to about 30°; methods wherein the oxy-fuel flame projects from below the air-fuel flame; and methods wherein the oxy-fuel flame intersects the air-fuel flame near a tail of the air-fuel flame.
Other preferred methods in accordance with the invention are those wherein the oxy-fuel flame projects from inclined ports toward the air-fuel flame at an angle &agr;, measured from horizontal ranging from about −10 to about 30°; methods wherein multiple oxy-fuel burners are present for each air-fuel burner; and methods wherein the first and second fuels are the same.
A second aspect of the invention is a method of temperature control in a furnace heating a load, the furnace having both air-fuel burners and oxy-fuel burners, said method comprising the steps of:
a) operating one or more air-fuel burners at constant fuel input; and
b) operating one or more oxy-fuel burners to increase or decrease temperature of the load without substantially changing production of NOx from the furnace.
A third aspect of the invention is an oxy-fuel burner comprising:
a) a central conduit adapted to deliver an oxidant;
b) an annular region external of the central conduit, the annular region adapted to deliver a fuel;
c) the central conduit having a nozzle attached at a central conduit end, wherein either the nozzle or the central conduit are adapted to be adjusted axially.
Preferred burners in accordance with this aspect of the invention are those wherein the central conduit has an oxidant exit end, and the burner annular region is defined by a refractory nozzle, the refractory nozzle having a furnace hot face, the oxidant exit end being positionable from the furnace hot face by a distance ranging from about D/4 to about 10D, wherein D is a diameter of a burner flame exit region.
The inventive methods are preferred for regenerative or recuperative glass furnaces which are known to produce high (thermal) NOx emissions due to the high flame temperatures and large availability of nitrogen in the atmosphere. The high flame temperatures arise from the higher combustion air preheat temperatures (1200° F. to 2400° F.) [649° C. to 1315° C.] and higher process temperatures (2700° F. to 2900° F.) [1482° C. to 1593° C.]. The nitrogen is available because the typical oxidant is air (~79% nitrogen).


REFERENCES:
patent: 1165835 (1915-12-01), Birkholz
patent: 1166451 (1916-01-01), Dreffein et al.
patent: 3934522 (1976-01-01), Booker
patent: 4531960 (1985-07-01), Desprez

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