US3655343A - Apparatus for oxidizing a spent pulping liquor - Google Patents
Apparatus for oxidizing a spent pulping liquor Download PDFInfo
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- US3655343A US3655343A US27496A US3655343DA US3655343A US 3655343 A US3655343 A US 3655343A US 27496 A US27496 A US 27496A US 3655343D A US3655343D A US 3655343DA US 3655343 A US3655343 A US 3655343A
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C11/00—Regeneration of pulp liquors or effluent waste waters
- D21C11/0057—Oxidation of liquors, e.g. in order to reduce the losses of sulfur compounds, followed by evaporation or combustion if the liquor in question is a black liquor
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/26—Nozzle-type reactors, i.e. the distribution of the initial reactants within the reactor is effected by their introduction or injection through nozzles
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00054—Controlling or regulating the heat exchange system
- B01J2219/00056—Controlling or regulating the heat exchange system involving measured parameters
- B01J2219/00069—Flow rate measurement
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S261/00—Gas and liquid contact apparatus
- Y10S261/75—Flowing liquid aspirates gas
Definitions
- ABSTRACT A dual stage oxidation apparatus having a first and a second oxidation chamber arranged so that the first chamber convergingly extends in a pipelike manner and discharges into the second chamber, an inlet conduit for supplying spent pulping liquor into the first chamber, an atomizing nozzle attached to the end of the inlet conduit for spraying the spent liquor into the first chamber, the first chamber converging from a large radius to a lesser radius and fonning a conduit, a second atomizing nozzle attached to the converging conduit end formed from the first chamber and terminating in the second chamber for spraying the now partially oxidized spent liquor leaving the first chamber into the second camber, for essentially complete oxidation, an outlet formed by the converging of the second reaction chamber from a large radius to a lesser radius forming thereby the exit conduit, an externally mounted oxygen line supplying oxygen to both the first chamber and the second chamber, an externally mounted circulating conduit connecting the inlet spent liquor conduit with the second reaction chamber, detection means for measuring the liquid volume flow and detection means
- This invention relates to an apparatus for the oxidation of a spent or weak/or strong black liquor produced in the pulping of wood. More particularly, the present invention pertains to a multi-stage tubular reactor by which the oxidation with molecular oxygen of the spent or weak/or strong black liquor, produced, for example, in a kraft pulping process, is efficiently and economically performed without any undesireable foam formation and without the concentrated accumulation of inactive sulfate type compounds. Specifically, the subject invention concerns the direct and intimate oxidation of weak/or strong black liquor in a two-stage tubular reactor and wherein the liquor originated in a kraft pulping process using southern pine, or in any other wood species suitable for pulping.
- Another purpose of this invention is to provide an apparatus for the oxidation of a spent pulping liquor with molecular oxygen.
- Still another object of the invention is to make available to the prior art a multi-stage reactor, in which design, the better utilization of the principles of mass transfer and chemical reaction for regulating the oxidation of black liquor are successfully utilized.
- Yet still another object of the invention is to provide a novel apparatus which while performing the oxidation of the spent liquor does not generate foam and objectionable gaseous emissions as they are generated and released at the oxidation tower of systems practicing the prior art.
- a further purpose of the invention is to make available an apparatus which eliminates the possibility of cooling the treated spent liquor by storage time or the efiect of air flow.
- Yet another object of the invention is to effect an oxidation reactor in which the temperature of the spent liquor is increased to F. in the first stage, thereby promoting better efficiency in the second stage of the reactor and generally helping in the operation of the evaporators used in conventional recovery systems.
- the invention concerns a two stage device for the molecular oxidation of a spent pulping liquor, mainly a black liquor.
- the two-stage device consists essentially of two reaction chambers connected one into the other as a series.
- the spent liquor is first atomized and turbulently mixed and intimately contacted with molecular oxygen to oxidize a high percentage of the spent liquor.
- the first oxidation stage occurs in the first reaction chamber.
- the just oxygen treated liquor is again atomized, that is, for a second time, and again turbulently mixed and intimately contacted with molecular oxygen to further oxidize any unoxidized spent liquor remaining from the first oxidation in the first stage of the reactor.
- the second oxidation occurs in the second reaction chamber of the two-stage device.
- FIG. 1 graphically indicates how the efficiency of oxygen utilization linearlly decreases as the ratio of oxygen injected into initial sulfide content increases above the stoichiometric ratio of 1.00.
- FIG. 2 depicts how the efficiency of the oxygen utilization decreases with a decrease in retention time in the reactor for a ratio of oxygen to sulfide ranging between 1.05 to 1.15.
- FIG. 3 illustrates how the oxygen efficiency remains constant at different retention time since the ratio oxygen injected to sulfide content is below the stoichiometric value of 1.0, generally 0.75 to 0.85.
- FIG. 4 is an elevational view of the reaction apparatus with injection means and control means for performing the subject matter of the present invention.
- d C is the differential of the concentration of sulfide
- k is the chemical reaction rate constant
- C and C are the concentration of the oxygen and sulfide in the reaction zone.
- the data set forth in FIG. 1 indicates how the efi'iciency of oxygen utilization decreases when the ratio of oxygen injected into initial sulfide content increases above the value 1.00.
- the numbers along the X-axis represent the ratio of oxygen injected into initial sulfide content in black liquor.
- the numbers along the Y-axis represent the stoichiometric efficiency of oxygen utilization. The results were obtained in a single stage tubular reactor. The results plotted in FIG.
- the X-axis represents flow in the tubular reactor in gallons per minute for the ratio of O /S between 1.05 and 1.15.
- the Y-axis is as with FIG. 1.
- FIG. 3 The presence of two rates of conversion is further demonstrated in FIG. 3.
- the oxygen to sulfide ratio are below the stoichiometric value of 1.00; that is, at 0.75 to 0.85, indicating that theoretically all sulfides cannot be exidized for lack of enough oxygen.
- the efficiency of oxygen utilization remains practically constant, at different velocities, because the remaining concentration of sulfide, not oxidized, has not reached a value low enough to induce the first order reaction as the controlling one.
- the X-axis represents the flow of the spent liquor in the two-stage reactor in gallons per minute and the Y-axis, the oxygen utilization efficiency, as in FIGS. 1 and 2, for a ratio of 0 /5 between 0.75 and 0.85.
- FIG. 4 wherein a twostage reactor is depicted for use of oxygen absorption and chemical reaction in the oxidation of black liquor.
- a pipeline 20 which is connected to source of spent liquor to be treated (not shown) and also connects to the first stage of a reactor 35 where the essentially bulk oxidation of the spent liquor occurs.
- the black liquor flow in pipeline 20 passes an oxidation-reduction-potential (ORP) cell or sulfide electrode 22 suitably mounted in the wall 23 of feed pipeline 20.
- the pipeline 20 is made of stainless steel or any other duct or c0nduit material that does not chemically react or is adversely affected by the spent black liquor.
- the described cell 22 is commercially available from Beckman Instrument Co., of Fullerton, California, and it protrudes into the black liquor wherein, in operation, it relays a current signal through line 25 to an ORP Beckman 900 analyzer, for determining the sulfide content as ascertained by analyzer 24.
- the analyzer 24 provides essentially for a sulfide concentration signal, which is relayed to a primary control 26 which, in turn, is connected to a secondary controller or control 27.
- the primary control 26 is the first cascade of a two pen cascade controller made by Honeywell Manufacturing Co., of Philadelphia, Pennsylvania, and sold under the commercial designation S-320-l and No. 32631.
- the secondary controller 27 is an integral part of the control station 27 which contains the primary controller.
- the secondary controller 27 is designed to interpret a signal which measures the flow of liquor in pipeline 20.
- the flow of liquor is ascertained by an orifice meter 28 which is pneumatically connected through lines 29 to a pressure differential cell 30.
- This cell is commercially available and it is manufactured by Honeywell Manufacturing Co. and made available as 8-292-3, No. 29212.
- the pressure differential cell 30, in turn, is connected to a transducer, which converts the pneumatic signal to a current signal to be supplied through electrical line 31 to the secondary controller 27.
- the secondary controller 27 is connected through an electrical line 31a to a conventional control valve 32 such as a double-seated, diaphragm, cage in line type, which is part of an oxygen feedline 33.
- spent liquor flows in pipeline 20 past cell 22 which measures the amount of sulfide in the spent liquor while the flow rate of the spent liquor in the pipeline 20 is also being measured by an orifice meter 28.
- the two data are evaluated by the signals sent to the primary and secondary controllers 26 and 27 which send a command signal to valve 32 through line 31a for letting a now predetermined amount of oxygen enter into the system by a tee pipe 34 which permits some of the oxygen to enter the first stage reactor 35 and also permits some of the oxygen to travel in a conduit or pipe 36 suitably equipped with an in line gate valve 360 to a second stage reactor 37.
- the first stage reactor 35 is connected to the second stage reactor 37 by a pipeline 43, and pipeline 20 extends into a flange 39 and enters the first stage reactor shortly thereafter.
- the pipeline narrows and terminates with a nozzle 40 attached thereto for atomizing the spent liquor in the first stage reactor 35.
- the first stage reactor 35 has a joint 41 for converging into a flange 42 which leads into a pipe section 43 through a flange 44 and into second stage reactor 37
- the length of the pipeline 43 is determined by use of the equation previously indicated.
- Second stage reactor 37 is constructed in a manner similar to first stage reactor 35 by having a converging section leading into a flange 46 and then into a pipe 48 for transporting oxidized black liquor to storage tanks, not shown.
- the second stage reactor 37 is also externally connected to inlet pipeline 20 through a circulating conduit 38 suitably equipped with an inline gate valve 38a.
- the circulating conduit 38 circulates the spent liquor to aid in the oxidation of the spent liquor.
- the pressure in pipeline 20 forces the liquor into conduit 38 for circulation into reactor 37.
- the tubular reactor is operated at a high Reynolds number, above 500,000 to guarantee turbulent conditions in the reactor.
- the relative dimensions of a typical reactor are for example, as follows; the nozzle diameter is 0.5 times the pipeline diameter, the reaction chamber, for example, 35, has a diameter 1.8 times the pipeline diameter, the length of reaction chamber is 5.5 times the pipeline diameter, the length of the converging zone is 3 times the pipeline diameter.
- the diameter of the oxygen line 36 and spent liquor lines 43 to the second stage reactor are 0.33 times the respective diameters of the incoming oxygen pipelines 33 and the incoming liquor pipeline 20 which latter line has a diameter of any predetermined size, for example, according to the installation of 4, 6, 8 and inches, etc.
- the oxygen absorption process and the subsequent chemical reaction takes place in the reactor in three phases.
- oxygen molecules are transferred to the liquid black liquor surface.
- the liquid interphase has a definite thickness, usually a few molecules.
- oxygen must pass through this layer by diffusion.
- oxygen diffuses into the bulk of the spent liquor and the oxidation reaction takes place.
- the speed of the phases can be increased by turbulence.
- a fraction of the black liquor that is, 80 to 90 percent of the total flow in incoming pipeline 20, is atomized at nozzle 40 at a high Reynolds number above 500,000.
- the necessary oxygen is injected at 34 for oxidation, about 1.05 times the required stoichiometric amount used.
- Intimate mixing and diffusion of the spent liquor takes place in chamber 35, with oxidation taking place therein and in tubular section 43.
- Section 43 leads to the second reactor where the remaining fraction of unoxidized liquor is introduced and atomized by nozzle 40a.
- Oxygen for the oxidation of the remaining liquor is introduced by line 36.
- the mixing again takes place in the second stage reactor 37, and the liguor passes out in pipe 48.
- the process can be run on a ltmite quantity of liquor or on a continuous basis.
- a two-stage oxidation apparatus for the oxidation of sodium sulfide and mercaptide in spent black pulping liquor, the apparatus comprising a first oxidation reaction chamber in series with a second oxidation reaction chamber, a liquid inlet conduit extending into and terminating in the first chamber, means for supplying the black pulping liquor from the inlet conduit into and through the first reaction chamber, a nozzle integrally fixed to the end of the inlet conduit terminating in the first chamber, the first chamber converging inwardly and forming directly into a second fluid transport conduit that terminates in the second reaction chamber, the second transport conduit being a tubular reactor and having a substantial tubular section in the end that terminates in the second reaction chamber, a nozzle integrally fixed to the end of the second fluid transport conduit, the second chamber converging inwardly and extending outwardly into an outlet flow conduit from the second chamber, an external oxygen supply conduit for molecular oxygen divisibly connected to both the first and second chamber, means for controlling the amount of molecular oxygen delivered to the
Abstract
A dual stage oxidation apparatus having a first and a second oxidation chamber arranged so that the first chamber convergingly extends in a pipelike manner and discharges into the second chamber, an inlet conduit for supplying spent pulping liquor into the first chamber, an atomizing nozzle attached to the end of the inlet conduit for spraying the spent liquor into the first chamber, the first chamber converging from a large radius to a lesser radius and forming a conduit, a second atomizing nozzle attached to the converging conduit end formed from the first chamber and terminating in the second chamber for spraying the now partially oxidized spent liquor leaving the first chamber into the second camber, for essentially complete oxidation, an outlet formed by the converging of the second reaction chamber from a large radius to a lesser radius forming thereby the exit conduit, an externally mounted oxygen line supplying oxygen to both the first chamber and the second chamber, an externally mounted circulating conduit connecting the inlet spent liquor conduit with the second reaction chamber, detection means for measuring the liquid volume flow and detection means for measuring the sulfide concentration of the spent liquor with both means mounted on the inlet conduit and measuring the flow and sulfide concentration before the spent liquor enters into the first chamber, and said detection means governing the amount of oxygen supplied to both the first chamber and to the second for oxidizing the spent pulping liquor.
Description
Unite States atent Galeano 154] APPARATUS FOR OXIDIZING A SPENT PULPING LIQUOR [72] Inventor: Sergio F. Galeano, Toledo, Ohio [7 3] Assignee: Owens-Illinois, Inc.
[22] Filed: Apr. 13, 1970 [21] Appl. No.: 27,496
52 u.s.c1 ..23/284,23/252,23/49,
23/253 A, 261/76, 259/4, 210/63, 162/31 511 1m.c1. ..B01jl/00,D2lcll/14 [58] FieldofSearch ..23/284,285,252,49,253A;
261/75, 76, 77, 116, DIG. 26; 259/4; 196/126, 127; 210/63; 162/31 Primary Examiner-James H. Tayman, Jr. Attorney-Paul L. Sabatine, R. F. Rywalski and E. J. Holler 1151 3,655,343 1451 Apr. 11,1972
[57] ABSTRACT A dual stage oxidation apparatus having a first and a second oxidation chamber arranged so that the first chamber convergingly extends in a pipelike manner and discharges into the second chamber, an inlet conduit for supplying spent pulping liquor into the first chamber, an atomizing nozzle attached to the end of the inlet conduit for spraying the spent liquor into the first chamber, the first chamber converging from a large radius to a lesser radius and fonning a conduit, a second atomizing nozzle attached to the converging conduit end formed from the first chamber and terminating in the second chamber for spraying the now partially oxidized spent liquor leaving the first chamber into the second camber, for essentially complete oxidation, an outlet formed by the converging of the second reaction chamber from a large radius to a lesser radius forming thereby the exit conduit, an externally mounted oxygen line supplying oxygen to both the first chamber and the second chamber, an externally mounted circulating conduit connecting the inlet spent liquor conduit with the second reaction chamber, detection means for measuring the liquid volume flow and detection means for measuring the sulfide concentration of the spent liquor with both means mounted on the inlet conduit and measuring the flow and sulfide concentration before the spent liquor enters into the first chamber, and said detection means governing the amount of oxygen supplied to both the first chamber and to the second for oxidizing the spent pulping liquor.
2 Claims, 4 Drawing Figures PATENTEDAPR 11 I972 3,665,343
INVENTOR. SERGIO GALEAMQ A-rrORIAQQK PATENTEDAPR 11 1972 3; 655,343
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SERQKB mALEAMQ BACKGROUND OF THE INVENTION This invention relates to an apparatus for the oxidation of a spent or weak/or strong black liquor produced in the pulping of wood. More particularly, the present invention pertains to a multi-stage tubular reactor by which the oxidation with molecular oxygen of the spent or weak/or strong black liquor, produced, for example, in a kraft pulping process, is efficiently and economically performed without any undesireable foam formation and without the concentrated accumulation of inactive sulfate type compounds. Specifically, the subject invention concerns the direct and intimate oxidation of weak/or strong black liquor in a two-stage tubular reactor and wherein the liquor originated in a kraft pulping process using southern pine, or in any other wood species suitable for pulping.
The oxidation of a spent or black pulping liquor produced in the conventional art known kraft pulping processes has been heretobefore carried out by employing air as the oxidizing agent. In the prior art, oxidation is also being carried out on spent liquors produced from hardwoods on both the weak liquor, that is a spent liquor containing about 12 to 16 percent solids and on strong spent liquors, that is, liquors containing 30 to 36 percent solids. Generally, in the pulping installations employing the cooking of southern pine, there are only a few installations wherein the oxidation of a strong black liquor is practiced with air. Also, as far as is known, there does not appear to be any practice of the oxidation of the weak liquor due to excessive foaming. The oxidation of a spent liquor produced from a southern pine often is accompanied by a most objectionable characteristic, that is, the formation of excessive amounts of foam. Different methods of air oxidation have been suggested by the prior art for controlling the foam; however, the methods have not received universal acceptance and the attempts have generally led to the fact of uncontrolled foam formation and attempts to use the foam in a better economical way. In view of this prior art discussion, the fact seemingly remains that the presently employed processes for the oxidation air of weak black liquor is not very feasible at this time. It has been suggested by those versed in the art that a solution to this problem may reside in the employment of molecular oxygen for the oxidation of black liquor, especially the oxidation of a kraft weak black liquor from a kraft process using southern pine. However, the subject suggestion has not found acceptance in the pulping art because of the lack of a suitable means for effecting the oxidation.
Accordingly, it is a purpose of the present invention to provide an economical and more simple apparatus that is easy to operate for overcoming the difficulties associated with the prior art.
Another purpose of this invention is to provide an apparatus for the oxidation of a spent pulping liquor with molecular oxygen.
Still another object of the invention is to make available to the prior art a multi-stage reactor, in which design, the better utilization of the principles of mass transfer and chemical reaction for regulating the oxidation of black liquor are successfully utilized.
Yet still another object of the invention is to provide a novel apparatus which while performing the oxidation of the spent liquor does not generate foam and objectionable gaseous emissions as they are generated and released at the oxidation tower of systems practicing the prior art.
A further purpose of the invention is to make available an apparatus which eliminates the possibility of cooling the treated spent liquor by storage time or the efiect of air flow.
Yet another object of the invention is to effect an oxidation reactor in which the temperature of the spent liquor is increased to F. in the first stage, thereby promoting better efficiency in the second stage of the reactor and generally helping in the operation of the evaporators used in conventional recovery systems.
The invention also consists of the novel construction and arrangement of the parts and combination of parts hereinafter more fully set forth in the following detailed drawings, detailed specification and the accompanying claims.
SUMMARY OF THE INVENTION The invention concerns a two stage device for the molecular oxidation of a spent pulping liquor, mainly a black liquor. The two-stage device consists essentially of two reaction chambers connected one into the other as a series. In using the device, the spent liquor is first atomized and turbulently mixed and intimately contacted with molecular oxygen to oxidize a high percentage of the spent liquor. The first oxidation stage occurs in the first reaction chamber. Next, the just oxygen treated liquor is again atomized, that is, for a second time, and again turbulently mixed and intimately contacted with molecular oxygen to further oxidize any unoxidized spent liquor remaining from the first oxidation in the first stage of the reactor. The second oxidation occurs in the second reaction chamber of the two-stage device.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 graphically indicates how the efficiency of oxygen utilization linearlly decreases as the ratio of oxygen injected into initial sulfide content increases above the stoichiometric ratio of 1.00.
FIG. 2 depicts how the efficiency of the oxygen utilization decreases with a decrease in retention time in the reactor for a ratio of oxygen to sulfide ranging between 1.05 to 1.15.
FIG. 3 illustrates how the oxygen efficiency remains constant at different retention time since the ratio oxygen injected to sulfide content is below the stoichiometric value of 1.0, generally 0.75 to 0.85. These graphs, depicting the interpretation of data collected at a mill, indicate the employment of a controlled operation in which time, oxygen injected and sulfide content are utilized to achieve better oxygen efficiency and oxidation.
FIG. 4 is an elevational view of the reaction apparatus with injection means and control means for performing the subject matter of the present invention.
DETAILED DESCRIPTION OF THE DISCLOSURE In attaining the features, advantages and purposes of the invention it has now been found that a simple, efficient and relatively inexpensive tubular chemical oxidation reactor can be made available to the art for performing the purpose of the invention. In addition to the novel apparatus, the use of existing pipeline in a pulping facility can be used for connecting the pulping area with the weak liquor storage tanks or the pipeline connecting the weak liquor storage tanks with the evaporators, or the pipelines connecting the strong liquor tanks to the direct contact evaporator or the multiple effect evaporator can, if desired, be used as a functional part of the apparatus. Thus, the pipeline can be used according to its diameter and liquor flow as an integral part of the tubular reactor. These features, coupled with the reactor can reach efficient utilization of oxygen levels above percent. For the apparatus object of this invention an equation indicates the necessary design value. This equation is expressed as: C,=C;e""- in which C, and C are the desired final and initial sulfide concentration of the liquor, v the velocity flow in the reactor, k the rate constant equal to 5.7 min. and e Naperian base logarithm, and L is the length of pipeline required between the first and second reactor stages. This equation permits designing the unit according to existing or new conditions at any mill.
In the oxidation of black liquor with molecular oxygen, or 0 the rate of oxidation is governed by the combined effect of oxygen absorption and the chemical reaction rate. The chemical reaction rate is first order with relation to both oxygen and sulfide concentration according to the equation:
where d C, is the differential of the concentration of sulfide; with respect to time, k, is the chemical reaction rate constant; C and C, are the concentration of the oxygen and sulfide in the reaction zone. Oxygen absorption in most of the cases tested by experiments has shown to be liquid flow controlling, thus the rate of oxygen transfer 0' M0 is defined according to the equation:
where d M0 is the mass transfer differential of oxygen with respect to time; and e denotes the equilibrium concentration of oxygen in the liquor surface, and k is the mass transfer rate constant. A combined expression for both the effects is given Thus, a change in rate orders of the reaction suggest the convenience of a two-stage reactor in which in both stages a rapid absorption of oxygen is promoted and an increase in final constant rate value is provoked. In this manner in the second stage a fraction of both the oxygen and black liquor are again mixed with the bulk of the reacting liquor.
The feasibility of the above was carried out experimentally on a single stage tubular reactor and a two stage reactor. The trials were conducted in a southern kraft mill where for the first time weak black liquor was oxidized satisfactorily for several weeks at flow rates ranging from 850 to 1,550 gallons per minute. In Table l is set forth the black liquor oxidation in a tubular reactor which shows the effects of the ratio of 0 in terms of oxidation efficiency expressed in percent. The column Na s indicates the concentration of the Na S in the spent liquor; the phrase oxygen injected" is the amount of oxygen mixed with the spent liquor, with the oxygen efficiency of the oxidation expressed in percent, and, in the final column is set forth the flow of the spent black liquor in gallons per minute.
TABLE 1 Lb. mole/hr.
Oxygen Initial Oxygen 02/5 efficiency Flow Nags injected ratio (percent) gpm The data set forth in FIG. 1 indicates how the efi'iciency of oxygen utilization decreases when the ratio of oxygen injected into initial sulfide content increases above the value 1.00. The numbers along the X-axis represent the ratio of oxygen injected into initial sulfide content in black liquor. The numbers along the Y-axis represent the stoichiometric efficiency of oxygen utilization. The results were obtained in a single stage tubular reactor. The results plotted in FIG. 2, indicate that when the ratio of oxygen to sulfide ranges between 1.05 to 1.15 the efficiency of oxygen utilization decreases with a decrease in retention time in the two-stage reactor, because time is also needed to complete the reaction. This fact seemingly suggests that the chemical reaction is controlling since time is needed to complete a reaction that stoichiometrically should otherwise occur. Also, the increase in turbulence by decreasing the retention time does not appear to improve the completeness of the reaction, as there is need, besides diffusing the oxygen in the liquid, to give adequate time. In FIG. 2, the X-axis represents flow in the tubular reactor in gallons per minute for the ratio of O /S between 1.05 and 1.15. The Y-axis is as with FIG. 1. The presence of two rates of conversion is further demonstrated in FIG. 3. In FIG. 3, the oxygen to sulfide ratio are below the stoichiometric value of 1.00; that is, at 0.75 to 0.85, indicating that theoretically all sulfides cannot be exidized for lack of enough oxygen. The efficiency of oxygen utilization remains practically constant, at different velocities, because the remaining concentration of sulfide, not oxidized, has not reached a value low enough to induce the first order reaction as the controlling one. In FIG. 3, the X-axis represents the flow of the spent liquor in the two-stage reactor in gallons per minute and the Y-axis, the oxygen utilization efficiency, as in FIGS. 1 and 2, for a ratio of 0 /5 between 0.75 and 0.85. This evidence seemingly indicates the soundness for a dual step reactor, and desireability for turbulent diffusion and oxygen mass transfer, and of the apparatus design as set forth in the use of the nozzle, the reactor and the like.
Referring now to drawing FIG. 4 in detail, wherein a twostage reactor is depicted for use of oxygen absorption and chemical reaction in the oxidation of black liquor. In FIG. 4, a pipeline 20 which is connected to source of spent liquor to be treated (not shown) and also connects to the first stage of a reactor 35 where the essentially bulk oxidation of the spent liquor occurs. The black liquor flow in pipeline 20 passes an oxidation-reduction-potential (ORP) cell or sulfide electrode 22 suitably mounted in the wall 23 of feed pipeline 20. The pipeline 20 is made of stainless steel or any other duct or c0nduit material that does not chemically react or is adversely affected by the spent black liquor. The described cell 22 is commercially available from Beckman Instrument Co., of Fullerton, California, and it protrudes into the black liquor wherein, in operation, it relays a current signal through line 25 to an ORP Beckman 900 analyzer, for determining the sulfide content as ascertained by analyzer 24. The analyzer 24 provides essentially for a sulfide concentration signal, which is relayed to a primary control 26 which, in turn, is connected to a secondary controller or control 27. The primary control 26 is the first cascade of a two pen cascade controller made by Honeywell Manufacturing Co., of Philadelphia, Pennsylvania, and sold under the commercial designation S-320-l and No. 32631. The secondary controller 27 is an integral part of the control station 27 which contains the primary controller. The secondary controller 27 is designed to interpret a signal which measures the flow of liquor in pipeline 20. The flow of liquor is ascertained by an orifice meter 28 which is pneumatically connected through lines 29 to a pressure differential cell 30. This cell is commercially available and it is manufactured by Honeywell Manufacturing Co. and made available as 8-292-3, No. 29212. The pressure differential cell 30, in turn, is connected to a transducer, which converts the pneumatic signal to a current signal to be supplied through electrical line 31 to the secondary controller 27. The secondary controller 27 is connected through an electrical line 31a to a conventional control valve 32 such as a double-seated, diaphragm, cage in line type, which is part of an oxygen feedline 33. Thus, in operation thus far, spent liquor flows in pipeline 20 past cell 22 which measures the amount of sulfide in the spent liquor while the flow rate of the spent liquor in the pipeline 20 is also being measured by an orifice meter 28. The two data are evaluated by the signals sent to the primary and secondary controllers 26 and 27 which send a command signal to valve 32 through line 31a for letting a now predetermined amount of oxygen enter into the system by a tee pipe 34 which permits some of the oxygen to enter the first stage reactor 35 and also permits some of the oxygen to travel in a conduit or pipe 36 suitably equipped with an in line gate valve 360 to a second stage reactor 37. The first stage reactor 35 is connected to the second stage reactor 37 by a pipeline 43, and pipeline 20 extends into a flange 39 and enters the first stage reactor shortly thereafter. The pipeline narrows and terminates with a nozzle 40 attached thereto for atomizing the spent liquor in the first stage reactor 35. The first stage reactor 35 has a joint 41 for converging into a flange 42 which leads into a pipe section 43 through a flange 44 and into second stage reactor 37 The length of the pipeline 43 is determined by use of the equation previously indicated. Second stage reactor 37 is constructed in a manner similar to first stage reactor 35 by having a converging section leading into a flange 46 and then into a pipe 48 for transporting oxidized black liquor to storage tanks, not shown. The second stage reactor 37 is also externally connected to inlet pipeline 20 through a circulating conduit 38 suitably equipped with an inline gate valve 38a. The circulating conduit 38 circulates the spent liquor to aid in the oxidation of the spent liquor. In operation, the pressure in pipeline 20 forces the liquor into conduit 38 for circulation into reactor 37.
In actual operation, the tubular reactor is operated at a high Reynolds number, above 500,000 to guarantee turbulent conditions in the reactor. The relative dimensions of a typical reactor are for example, as follows; the nozzle diameter is 0.5 times the pipeline diameter, the reaction chamber, for example, 35, has a diameter 1.8 times the pipeline diameter, the length of reaction chamber is 5.5 times the pipeline diameter, the length of the converging zone is 3 times the pipeline diameter. The diameter of the oxygen line 36 and spent liquor lines 43 to the second stage reactor are 0.33 times the respective diameters of the incoming oxygen pipelines 33 and the incoming liquor pipeline 20 which latter line has a diameter of any predetermined size, for example, according to the installation of 4, 6, 8 and inches, etc. Of course, these dimensions are by way of example, and they can be varied by those skilled in the art as larger multi-stage reactors or smaller multi-stage reactors can be constructed in the light of the present broad disclosure. The oxygen absorption process and the subsequent chemical reaction takes place in the reactor in three phases. In the first phase, oxygen molecules are transferred to the liquid black liquor surface. The liquid interphase has a definite thickness, usually a few molecules. Next, the second phase, oxygen must pass through this layer by diffusion. Finally, in the third phase, oxygen diffuses into the bulk of the spent liquor and the oxidation reaction takes place. The speed of the phases can be increased by turbulence. In the first stage, a fraction of the black liquor, that is, 80 to 90 percent of the total flow in incoming pipeline 20, is atomized at nozzle 40 at a high Reynolds number above 500,000. The necessary oxygen is injected at 34 for oxidation, about 1.05 times the required stoichiometric amount used. Intimate mixing and diffusion of the spent liquor takes place in chamber 35, with oxidation taking place therein and in tubular section 43. Section 43 leads to the second reactor where the remaining fraction of unoxidized liquor is introduced and atomized by nozzle 40a. Oxygen, for the oxidation of the remaining liquor is introduced by line 36. The mixing again takes place in the second stage reactor 37, and the liguor passes out in pipe 48. The process can be run on a ltmite quantity of liquor or on a continuous basis.
The present invention may be embodied in other forms without departing from the spirit or essential attributes thereof and, accordingly, such embodiments as would be obvious to those versed in the present art in the light of this application are indicated as within the scope of the invention.
What is claimed is:
1. A two-stage oxidation apparatus for the oxidation of sodium sulfide and mercaptide in spent black pulping liquor, the apparatus comprising a first oxidation reaction chamber in series with a second oxidation reaction chamber, a liquid inlet conduit extending into and terminating in the first chamber, means for supplying the black pulping liquor from the inlet conduit into and through the first reaction chamber, a nozzle integrally fixed to the end of the inlet conduit terminating in the first chamber, the first chamber converging inwardly and forming directly into a second fluid transport conduit that terminates in the second reaction chamber, the second transport conduit being a tubular reactor and having a substantial tubular section in the end that terminates in the second reaction chamber, a nozzle integrally fixed to the end of the second fluid transport conduit, the second chamber converging inwardly and extending outwardly into an outlet flow conduit from the second chamber, an external oxygen supply conduit for molecular oxygen divisibly connected to both the first and second chamber, means for controlling the amount of molecular oxygen delivered to the first and second reactors flowing through the external oxygen supply conduit, the means for controlling the oxygen responsive to the sulfide content of the black liquor and the flow rate thereof in the inlet conduit that extends into the first reaction chamber, an externally mounted fluid circulating conduit connecting the inlet feed conduit before it enters the first reaction chamber with the second chamber for supplying the second chamber with some black liquor that has not been oxidized, and wherein said apparatus is used for efficient oxidation of the spent black pulping liquor at relatively low temperatures and pressures.
2. An oxidation apparatus for the oxidation of sodium sulfide and mercaptide and spent black pulping liquor, the apparatus comprising an oxidation reaction chamber, a liquid inlet conduit extending into and terminating in the reaction chamber, means for supplying black liquor from the inlet conduit into and through the reaction chamber, an oxygen supply conduit connected to the reaction chamber, means for supplying molecular oxygen through the oxygen supply conduit into the reaction chamber, a tubular reactor at the exit end of the reaction chamber, the tubular reactor having a length according to the following equation: C, =C, e where C, is the final sulfide concentration of the oxidized black liquor, C, is the initial sulfide concentration of the black liquor, e is the Naparian base logarithm, v is the velocity of flow in gallons per minute of the liquor in the tubular reactor, and L is the length in feet of the tubular reactor, and control means for controlling the amount of molecular oxygen to the reaction chamber through the oxygen supply conduit, the control means responsive to the sulfide content of the black liquor and the flow thereof in the inlet conduit.
Claims (1)
- 2. An oxidation apparatus for the oxidation of sodium sulfide and mercaptide and spent black pulping liquor, the apparatus comprising an oxidation reaction chamber, a liquid inlet conduit extending into and terminating in the reaction chamber, means for supplying black liquor from the inlet conduit into and through the reaction chamber, an oxygen supply conduit connected to the reaction chamber, means for supplying molecular oxygen through the oxygen supply conduit into the reaction chamber, a tubular reactor at the exit end of the reaction chamber, the tubular reactor having a length according to the following equation: Cf Ci e kL/v where Cf is the final sulfide concentration of the oxidized black liquor, Ci is the initial sulfide concentration of the black liquor, e is the Naparian base logarithm, v is the velocity of flow in gallons per minute of the liquor in the tubular reactor, and L is the length in feet of the tubular reactor, and control means for controlling the amount of molecular oxygen to the reaction chamber through the oxygen supply conduit, the control means responsive to the sulfide content of the black liquor and the flow thereof in the inlet conduit.
Applications Claiming Priority (1)
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US2749670A | 1970-04-13 | 1970-04-13 |
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US3655343A true US3655343A (en) | 1972-04-11 |
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US27496A Expired - Lifetime US3655343A (en) | 1970-04-13 | 1970-04-13 | Apparatus for oxidizing a spent pulping liquor |
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Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3852192A (en) * | 1973-03-29 | 1974-12-03 | Barber Colman Co | Reactor for wet oxidation of organic matter |
US3870631A (en) * | 1973-03-29 | 1975-03-11 | Barber Colman Co | Apparatus and method for wet oxidation of organic matter |
US3907678A (en) * | 1973-01-12 | 1975-09-23 | Sterling Winthrop Research Ins | Split air stream before and after the heat exchanger in a wet oxidation process |
US3917460A (en) * | 1970-08-31 | 1975-11-04 | Ass Pulp & Paper Mills | Wet combustion of waste liquors |
US3996139A (en) * | 1973-02-05 | 1976-12-07 | Prince Jack E | Liquid waste treatment apparatus |
US4058433A (en) * | 1975-03-06 | 1977-11-15 | Gulf States Paper Corporation | Conversion of sulfur in blank liquor to eliminate odorous emissions and facilitate the collection of sulfate soaps |
US4101286A (en) * | 1977-02-04 | 1978-07-18 | Dowa Mining Co., Ltd. | Bubble forming device having no moving parts |
US4217211A (en) * | 1979-07-09 | 1980-08-12 | BioMass Fuel Conversion Associates, Inc. | Pressurized treatment of sewage |
US4491551A (en) * | 1981-12-02 | 1985-01-01 | Johnson Dennis E J | Method and device for in-line mass dispersion transfer of a gas flow into a liquid flow |
US4515655A (en) * | 1983-08-15 | 1985-05-07 | Westvaco Corporation | Method of bleaching paper pulp by blending chlorine with a flow volume of paper pulp slurry |
US4662993A (en) * | 1983-08-15 | 1987-05-05 | Westvaco Corporation | Bleach system for dissolving chlorine gas into a bleach filtrate |
EP0279288A2 (en) * | 1987-02-14 | 1988-08-24 | Hüls Aktiengesellschaft | Process and apparatus for producing benzene-carboxylic acids or benzene-dicarboxylic-acid esters |
US5061377A (en) * | 1989-07-25 | 1991-10-29 | Canadian Liquid Air Ltd./Air Liquide Canada | Pipeline reactor and method |
US5102104A (en) * | 1990-03-05 | 1992-04-07 | U.S. Gold Corporation | Biological conversion apparatus |
US5143543A (en) * | 1991-08-23 | 1992-09-01 | U.S. Gold Corporation | Biological conversion method |
US5160458A (en) * | 1991-07-25 | 1992-11-03 | The Boc Group, Inc. | Gas injection apparatus and method |
US5169293A (en) * | 1990-06-18 | 1992-12-08 | Inax Corporation | Ejector with high vacuum force in a vacuum chamber |
US5382322A (en) * | 1991-10-18 | 1995-01-17 | Air Products And Chemicals, Inc. | Selective white liquor oxidation |
US5443799A (en) * | 1993-08-03 | 1995-08-22 | Orgral International Technologies Corporation | Process for the alkylation of olefins and apparatus for carrying out this process and others |
US5451324A (en) * | 1992-03-19 | 1995-09-19 | Eastman Kodak Company | Method of treating liquid effluents containing organic compounds |
EP0730491A1 (en) * | 1993-11-26 | 1996-09-11 | Hyperno Proprietary Limited | Chemical waste treatment |
US5772886A (en) * | 1996-07-22 | 1998-06-30 | Bettle; Griscom | Aquaculture process |
US5928521A (en) * | 1995-04-05 | 1999-07-27 | Mannesmann Aktiengesellschaft | Arrangement and process for oxidizing an aqueous medium |
US6199834B1 (en) * | 1997-06-16 | 2001-03-13 | Serguei A. Popov | Operation method for a gas-liquid ejector |
US6533499B2 (en) * | 2001-03-13 | 2003-03-18 | Boyd Breeding | Soil and groundwater remediation system |
US20060254987A1 (en) * | 2004-07-07 | 2006-11-16 | Ivey Burns | Process control oxidation |
US20070133346A1 (en) * | 2005-12-14 | 2007-06-14 | Tommy Jacobson | Mixing of chemicals into a thin stock pipe |
WO2013178885A1 (en) * | 2012-05-31 | 2013-12-05 | Wetend Technologies Oy | A method of and an arrangement for oxidizing white liquor |
CN111247293A (en) * | 2017-10-20 | 2020-06-05 | 维美德技术有限公司 | Method and system for removal of hydrogen sulfide ions (HS-) from a liquor of a pulping process |
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Cited By (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3917460A (en) * | 1970-08-31 | 1975-11-04 | Ass Pulp & Paper Mills | Wet combustion of waste liquors |
US3907678A (en) * | 1973-01-12 | 1975-09-23 | Sterling Winthrop Research Ins | Split air stream before and after the heat exchanger in a wet oxidation process |
US3996139A (en) * | 1973-02-05 | 1976-12-07 | Prince Jack E | Liquid waste treatment apparatus |
US3852192A (en) * | 1973-03-29 | 1974-12-03 | Barber Colman Co | Reactor for wet oxidation of organic matter |
US3870631A (en) * | 1973-03-29 | 1975-03-11 | Barber Colman Co | Apparatus and method for wet oxidation of organic matter |
US4058433A (en) * | 1975-03-06 | 1977-11-15 | Gulf States Paper Corporation | Conversion of sulfur in blank liquor to eliminate odorous emissions and facilitate the collection of sulfate soaps |
US4101286A (en) * | 1977-02-04 | 1978-07-18 | Dowa Mining Co., Ltd. | Bubble forming device having no moving parts |
US4217211A (en) * | 1979-07-09 | 1980-08-12 | BioMass Fuel Conversion Associates, Inc. | Pressurized treatment of sewage |
US4491551A (en) * | 1981-12-02 | 1985-01-01 | Johnson Dennis E J | Method and device for in-line mass dispersion transfer of a gas flow into a liquid flow |
US4515655A (en) * | 1983-08-15 | 1985-05-07 | Westvaco Corporation | Method of bleaching paper pulp by blending chlorine with a flow volume of paper pulp slurry |
US4662993A (en) * | 1983-08-15 | 1987-05-05 | Westvaco Corporation | Bleach system for dissolving chlorine gas into a bleach filtrate |
EP0279288A2 (en) * | 1987-02-14 | 1988-08-24 | Hüls Aktiengesellschaft | Process and apparatus for producing benzene-carboxylic acids or benzene-dicarboxylic-acid esters |
EP0279288A3 (en) * | 1987-02-14 | 1990-02-28 | Hüls Aktiengesellschaft | Process and apparatus for producing benzene-carboxylic acids or benzene-dicarboxylic-acid esters |
US5061377A (en) * | 1989-07-25 | 1991-10-29 | Canadian Liquid Air Ltd./Air Liquide Canada | Pipeline reactor and method |
US5102104A (en) * | 1990-03-05 | 1992-04-07 | U.S. Gold Corporation | Biological conversion apparatus |
US5169293A (en) * | 1990-06-18 | 1992-12-08 | Inax Corporation | Ejector with high vacuum force in a vacuum chamber |
AU636815B2 (en) * | 1991-07-25 | 1993-05-06 | Boc Group, Inc., The | Gas injection apparatus and method |
US5160458A (en) * | 1991-07-25 | 1992-11-03 | The Boc Group, Inc. | Gas injection apparatus and method |
US5143543A (en) * | 1991-08-23 | 1992-09-01 | U.S. Gold Corporation | Biological conversion method |
US5382322A (en) * | 1991-10-18 | 1995-01-17 | Air Products And Chemicals, Inc. | Selective white liquor oxidation |
US5500085A (en) * | 1991-10-18 | 1996-03-19 | Air Products And Chemicals, Inc. | Method for producing fully oxidized white liquor |
US5451324A (en) * | 1992-03-19 | 1995-09-19 | Eastman Kodak Company | Method of treating liquid effluents containing organic compounds |
US5777189A (en) * | 1993-08-03 | 1998-07-07 | Orgral International Technologies Corporation | Process for the alkylation of olefins |
US5443799A (en) * | 1993-08-03 | 1995-08-22 | Orgral International Technologies Corporation | Process for the alkylation of olefins and apparatus for carrying out this process and others |
EP0730491A1 (en) * | 1993-11-26 | 1996-09-11 | Hyperno Proprietary Limited | Chemical waste treatment |
EP0730491A4 (en) * | 1993-11-26 | 1997-12-17 | Hyperno Proprietary Limited | Chemical waste treatment |
US5928521A (en) * | 1995-04-05 | 1999-07-27 | Mannesmann Aktiengesellschaft | Arrangement and process for oxidizing an aqueous medium |
US5772886A (en) * | 1996-07-22 | 1998-06-30 | Bettle; Griscom | Aquaculture process |
US6199834B1 (en) * | 1997-06-16 | 2001-03-13 | Serguei A. Popov | Operation method for a gas-liquid ejector |
US6533499B2 (en) * | 2001-03-13 | 2003-03-18 | Boyd Breeding | Soil and groundwater remediation system |
US20060254987A1 (en) * | 2004-07-07 | 2006-11-16 | Ivey Burns | Process control oxidation |
US20080296233A1 (en) * | 2004-07-07 | 2008-12-04 | Disney Enterprises, Inc. | Process control oxidation |
US7514008B2 (en) * | 2004-07-07 | 2009-04-07 | Disney Enterprises, Inc. | Process control oxidation |
US7686962B2 (en) | 2004-07-07 | 2010-03-30 | Disney Enterprises, Inc. | Process control oxidation |
US20070133346A1 (en) * | 2005-12-14 | 2007-06-14 | Tommy Jacobson | Mixing of chemicals into a thin stock pipe |
WO2013178885A1 (en) * | 2012-05-31 | 2013-12-05 | Wetend Technologies Oy | A method of and an arrangement for oxidizing white liquor |
CN111247293A (en) * | 2017-10-20 | 2020-06-05 | 维美德技术有限公司 | Method and system for removal of hydrogen sulfide ions (HS-) from a liquor of a pulping process |
US11473243B2 (en) * | 2017-10-20 | 2022-10-18 | Valmet Technologies Oy | Method and a system for removing hydrogen sulphide ions (HS−) from a liquor of a pulp mill process |
CN111247293B (en) * | 2017-10-20 | 2023-07-28 | 维美德技术有限公司 | Method and system for removing sulfhydryl ions (HS-) from a liquor of a pulping process |
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Owner name: OI FOREST PRODUCTS STS INC., OHIO Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:OWENS-ILLINOIS, INC.;REEL/FRAME:004744/0811 Effective date: 19870323 Owner name: OI FOREST PRODUCTS STS INC., ONE SEAGATE, TOLEDO, Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:OWENS-ILLINOIS, INC.;REEL/FRAME:004744/0811 Effective date: 19870323 |