Patent Application
20190040577
The invention relates to a new technology that controls slag and fouling deposits in a black liquor recovery boiler, which utilizes black liquor produced as a byproduct of pulp making to recover heat and pulping chemicals.
Paper production involves the treatment of wood chips with chemicals to digest chips into pulp, which is used as a feedstock for either paper manufacture or dissolving pulp. The digestion of wood chips by white liquor (i.e., NaOH and Na2S) produces Kraft pulp (often referred to as delignified or cellulosic pulp) and black residue called black liquor, which is a combination of organic residues and spent pulp digester chemical. As an approximate estimate, the production of 1,000 tons of Kraft pulp can result in the formation of 1,500 tons of black liquor. Owing to the large quantity of spent chemical generated and relative high cost of fresh digestion/pulping chemicals, black liquor can be fired in a recovery boiler to generate thermal steam and regenerate pulping chemicals to be recycled back into the pulping process.
Pulp produced by digestion with white liquor is washed, and spent digestion chemicals are recovered and recycled back to the digestion process. The original pulping chemicals (i.e., white liquor) can be regenerated following digestion by separating the black liquor from pulp, evaporating excess water from the black liquor, and burning the black liquor in a recovery boiler to create heat and smelt (i.e., molten sodium salts, predominantly Na2CO3 and Na2S). The smelt forms at the bottom of the boiler and is dissolved in water to produce “green liquor”. The clarified green liquor is reacted with calcium hydroxide to convert Na2CO3 to NaOH (i.e., causticizing) to produce a white liquor that contains Na2S and NaOH. The white liquor is subsequently recycled to the digester.
The black liquor, following evaporation, forms a high viscosity, black material, which is liquid only at elevated temperatures. Black liquor contains organic residues from the delignification process and—as a result—black liquor has a heating value and can be fired in a black liquor recovery boiler. The inorganic fraction of the black liquor primarily consists of relatively low melting temperature sodium salts, predominantly in the form of sodium hydroxide, sodium sulfide, sodium sulfate, and sodium carbonate. Owing to the low melting points of sodium salts (often <850° C.), firing black liquor can result in deposition of molten or vapor phase sodium salts on heat exchange surfaces (i.e., slagging and fouling, respectively). Deposition on heat exchanger surfaces decreases the boiler efficiency and ultimately leads to pluggage and mandatory boiler shutdown, resulting in loss of pulp production.
Black liquor is difficult to handle and burn, but engineering experience has determined that it can be sprayed into a combustion zone of a black liquor recovery boiler by nozzles of various design, including splash plate, swirlcone, V-type and beer can design. The spray enters the boiler at the correct temperature and droplet size distribution to permit best utilization. The injectors (often referred to as “liquor guns”) penetrate the vertical boiler walls above a char bed (also called a char pile) and desirably above the primary and secondary air ports, but below the tertiary and quaternary air ports. The injectors typically spray the black liquor from opposite walls with droplet velocity and momentum sufficient that a majority reaches beyond the midpoint of the boiler but none reaches the opposite wall by the time the droplets fall to the char pile. Some volatiles are removed in the descent to the pile and some carbonization is effected, but the main burning of the black liquor occurs under reducing conditions in the char pile (to promote reduction of Na2SO4 to Na2S). Primary air is introduced at the approximate elevation of the char pile and supplies about 40 percent or less of the stoichiometric oxygen. Secondary air is introduced below the injection points for the black liquor and adds another 30 to 50 percent of the needed air. Above the level of the black liquor guns are ports for additional air, typically tertiary air and sometimes quaternary air. These additional air ports are essential to supply sufficient air to complete the combustion process and produce process steam.
The combustion gases rising through the recovery boiler contain carryover ash formers (which cool to form ash) which are desirably recovered as solids in an electrostatic precipitator or other solids recovery equipment. Unfortunately, the ash from burning the black liquor will often contain components that cause it to act as an adhesive mass until it passes beyond a bull nose at the top of the combustion zone and into contact with an array of heat exchangers, such as those that form the screen tubes, super heater, the boiler bank (or reheat) and the economizer. The adhesive molten and gaseous sodium salts that are entrained within the flue gas condense on cooler heat exchange surfaces, resulting in deposition. Deposit formations continue to grow as the black liquor recovery boiler is operated, resulting in pluggage and hazardous slag falls, which result in boiler shutdowns and potentially dangerous conditions. For example, large slag falls can puncture or crack exposed screen tubes and release water onto the char bed. Owing to reducing conditions at the char bed, water is converted to hydrogen and oxygen, which pose a serious explosion hazard. Keeping the black liquor recovery boiler free of deposits is critical to maintain safe continuous operations and minimize explosion risks. Deposit control chemicals/additives and processes are known, but it is always a challenge to introduce them in a manner effective for black liquor recovery boilers. This problem has existed since the first such boilers were made and there have been only a few successes, and none which have universal effectiveness.
One established technology for achieving effective slag control in some black liquor recovery boilers is described in U.S. Pat. No. 5,740,745 to Smyrniotis, et al.; however, due to the way combustion occurs in a black liquor recovery boiler, there appears to be a unique set of requirements for introducing slag control chemicals. Because of internal structural variations among boilers, the flow of gases in the boilers is not always sufficiently regular to permit accurate and effective computational fluid dynamic solutions. Some physical obstructions such as internal support trusses or beams (and other structures added as retrofit for reasons peculiar to individual boilers) and heat transfer anomalies cannot be reliably modeled in some cases. The introduction of air at multiple levels can cause problems that are not easily seen and addressed. In addition, many predicted solutions require creating openings in boiler walls, often through water walls or other difficult locations. Accordingly, there is a need for a process that can supply the necessary chemical or chemicals despite the problems.
There is a need for an improved process that more effectively applies chemical additives to control deposit formation in a black liquor recovery boiler.
It is an object of the invention to provide a new technology that controls slag in a black liquor recovery boiler.
It is another object to provide a process that controls slag in a black liquor recovery boiler with minimal modification of boiler walls.
In one aspect, the invention provides a process for reducing deposits in a black liquor recovery boiler, the process comprising: injecting and burning black liquor in a boiler by injecting it into the boiler and into contact with primary air and secondary air before collecting on a char bed in the boiler near the bottom; introducing deposit-reducing chemical into the gases above the black liquor guns through secondary, tertiary, and/or quaternary air ports, which are often present in an interlaced configuration or at the corners of boiler walls (often called tangential or concentric air pattern).
In another aspect, the apparatus for introducing the deposit-reducing chemical is provided.
Other preferred aspects and their advantages are set out in the description which follows.
The invention will be better understood and its advantages will become more apparent when the following detailed description is read in conjunction with the accompanying drawings, in which:
Reference will first be made to
In similar arrangements, deposit-reducing chemical can be introduced through the secondary air ports 14 or quaternary air ports 18. In each case described, a similar effect is achieved using the air flow from the noted ports as a driver to provide excellent mixing and distribution within the combustion chamber 20 in advance of the bull nose 15.
The spray of black liquor from each of nozzles 21 positioned below the tertiary air ports enters the combustion chamber 20 of the boiler 10 at the correct temperature and droplet size to permit best utilization. Typical temperatures of the black liquor will be from 300° F. to 400° F., and droplets will be in the range of from 0.5 mm to 5 mm following impingement onto the splash plates of the injectors. The sprays from the injectors penetrate the vertical boiler walls above a char bed 36 and desirably above primary and secondary air ports, 12 and 14, respectively. The injectors typically spray the black liquor from opposite walls with droplet velocity and momentum sufficient that a majority reach beyond the midpoint of boiler but none reach the opposite wall by the time the droplets fall to the char bed 36.
The elevated temperatures in the combustion chamber 12, cause some volatiles to be removed in the fall of the black liquor to the char bed 36 and some carbonization is effected, but the main burning of the black liquor occurs under reducing conditions in the char pile. Primary air is introduced at the approximate elevation of the char pile and supplies about 40 percent or less of the stoichiometric oxygen. Secondary air is introduced below the black liquor guns and adds another 30 to 50 percent of the needed air. Above the black liquor injectors are ports for additional air (e.g., from 30 to 50 percent), typically tertiary air and sometimes quaternary air. These additional air ports are essential to supply sufficient air to obtain maximum combustion without unduly cooling combustion gases which are required to heat steam to produce utilizable energy. Quaternary air may comprise 20 to 50 percent of the needed air.
The combustion gases rising through the boiler contain ash formers (carryover and fume) and unburned char which are desirably recovered as solids in an electrostatic precipitator or other solids recovery equipment, e.g., generally shown as 48. Unfortunately, the ash from burning the black liquor will often contain components that maintain it as an adhesive mass until in passes beyond a bull nose 15 at the top of the combustion chamber 20 and into contact with an array of heat exchangers 40, such as those that form the screen tubes, super heater 42, the boiler bank 44 (or reheat) and the economizer 46 prior to exiting the combustor via stack 50. Deposit control chemicals and processes are known, but it is always a challenge to introduce them in a manner effective for treatment of deposits in black liquor recovery boilers. This problem has existed since the first such boilers were made and there have been only a few successes, and none which have universal effectiveness.
The art has endeavored to solve the slagging problem by the introduction of various chemicals, such as magnesium oxide or hydroxide. Magnesium hydroxide has the ability to survive the hot environment of the furnace and react with the deposit-forming compounds, raising their ash fusion temperature and thereby modifying the texture and friability of the resulting deposits.
While all effective deposit-reducing chemicals are included, such as, without limitation magnesium oxide, magnesium hydroxide, magnesium carbonate, manganese oxide, manganese hydroxide, aluminum oxide and aluminum hydroxide, magnesium hydroxide is the chemical of choice for many black liquor recovery boilers and will be used in this description as exemplary. The magnesium hydroxide reagent can be prepared in any effective manner, e.g., from brines containing calcium and other salts, usually from underground brine pools or seawater. Dolomitic lime is mixed with these brines to form calcium chloride solution, and magnesium hydroxide which is precipitated and filtered out of the solution. This form of magnesium hydroxide can be mixed with water, with or without stabilizers, to concentrations suitable for storage and handling, e.g., from 25 to 65% solids by weight. For use in the process, it is diluted as determined by computational fluid dynamics (CFD) to within the range of from 0.1 to 10%, more narrowly from 1 to 5%. When it contacts the hot gases in the combustor, it is believed reduced to submicron and/or nano-sized particles, e.g., under 200 nanometers and preferably below about 100 nanometers. Median particle sizes of from 50 to about 150 nanometers are useful ranges for the process of the invention. Other forms of MgO can also be employed where necessary or desired, e.g., “light burn” or “caustic” can be employed where it is available in the desired particle size range.
To best achieve these effects, the invention will preferably take advantage of CFD to project initial flow rates and select initial reagent introduction rates, reagent introduction location(s), reagent concentration, reagent droplet size and reagent droplet momentum. CFD is a well understood science, and it is utilized with full benefit in this case, where it is desired to supply a minimum amount of chemical for maximum effect.
The following examples are presented to further explain and illustrate the invention and are not to be taken as limiting in any regard. Unless otherwise indicated, all parts and percentages are by weight.
This example illustrates the effect of introducing Mg(OH)2 (magnesium hydroxide) into a furnace burning 2,000 tons of black liquor per day.
The magnesium hydroxide was fed as a slurry at 2 pounds of 60 weight % slurry per ton of black liquor consumed. Density of the magnesium hydroxide slurry was approximately 12.7 pounds/gallon. Therefore, the feed rate was about 315 gallons per day for the Mg(OH)2 slurry.
We have seen that the invention provides at least the following advantages: (1) tertiary air protects the nozzles used to introduce the slag-reducing chemicals from the temperatures that exist in the area above the main combustion in the lower part of the furnace, (2) extremely good mixing is achieved and (3) high utilization of deposit-reducing chemicals is achieved due to the good mixing and the ability of deposit-reducing chemical to mix with slag formers by reaching the bull nose of the boiler in the zone just preceding the heat exchangers.
The above description is for the purpose of teaching the person of ordinary skill in the art how to practice the invention. It is not intended to detail all of those obvious modifications and variations, which will become apparent to the skilled worker upon reading the description. It is intended, however, that all such obvious modifications and variations be included within the scope of the invention which is defined by the following claims. The claims are meant to cover the claimed components and steps in any sequence that is effective to meet the objectives there intended, unless the context specifically indicates the contrary.
