US1953618A - Absorption of olefines - Google Patents
Absorption of olefines Download PDFInfo
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- US1953618A US1953618A US551970A US55197031A US1953618A US 1953618 A US1953618 A US 1953618A US 551970 A US551970 A US 551970A US 55197031 A US55197031 A US 55197031A US 1953618 A US1953618 A US 1953618A
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- 238000010521 absorption reaction Methods 0.000 title description 6
- 239000007788 liquid Substances 0.000 description 72
- 239000012530 fluid Substances 0.000 description 33
- 238000000034 method Methods 0.000 description 25
- 239000002253 acid Substances 0.000 description 22
- 229930195733 hydrocarbon Natural products 0.000 description 17
- 150000002430 hydrocarbons Chemical class 0.000 description 17
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 15
- 238000004891 communication Methods 0.000 description 15
- 230000002706 hydrostatic effect Effects 0.000 description 14
- 239000004215 Carbon black (E152) Substances 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 11
- 239000002480 mineral oil Substances 0.000 description 5
- 235000010446 mineral oil Nutrition 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- KOYGZROXUOTUEE-UHFFFAOYSA-N butane;but-1-ene Chemical compound CCCC.CCC=C KOYGZROXUOTUEE-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 3
- 238000001816 cooling Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000518994 Conta Species 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- SYRIRLOOSKFSFC-UHFFFAOYSA-N butane Chemical compound CCCC.CCCC SYRIRLOOSKFSFC-UHFFFAOYSA-N 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
Images
Classifications
-
- 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
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1862—Stationary reactors having moving elements inside placed in series
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D11/00—Solvent extraction
- B01D11/04—Solvent extraction of solutions which are liquid
- B01D11/0446—Juxtaposition of mixers-settlers
- B01D11/0457—Juxtaposition of mixers-settlers comprising rotating mechanisms, e.g. mixers, mixing pumps
-
- 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
- B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
- B01J2219/00076—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements inside the reactor
- B01J2219/00083—Coils
-
- 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
- B01J2219/00164—Controlling or regulating processes controlling the flow
Definitions
- This invention relates to a novel apparatus desired number which when revolving, agitate the and process for contacting immiscible liquids liquid contained in the mixing device, causing inwith each other for the purpose of extraction, termingling of otherwise not miscible liquids in chemical treatment or the like, and more parmore or less fine emulsions.
- Diaphragms 25 are ticularly to an apparatus and/or process wherein so spaced that one pair of them form a sub- 60 it is desired to carry out such contact in counterstantially enclosed space 26 in which the agicurrent relationship of the two liquids.
- the preferred process comprises passing two that the emulsions formed in the mixing comsubstantially immiscible liquids in counter-curpartments may separate due to differences in rent flow to each other through a plurality of specific gravity of the liquids in question.
- 65 stages arranged in contiguous relationship and Such diaphragms may be also placed between communicating with each ata plurality of points, each end rotor and end plates 11 and 12 of the each alternate stage containing an agitating mixing vessel, or they may be omitted and exmeans, the end stages being characterized as ternal separating vessels substituted for this pur- 15 quiescent or separating zones and each end stage pose.
- the diaphragms 25 are closed on shaft by dergoing treatment.
- Vanes 34 tend to increase the turbulence the accompanying drawings, generally illustratand eddy fiow in the agitating compartments ing at least one practical embodiment of a novel whereas vanes tend to straighten out eddy 30 systematic combination of means for carrying flow in the separating compartments thereby forth the steps of the method involved, although expediting stratification of the immiscible fluids.
- Openings 28, 29, 30 and 31 are provided for in which drawings feeding into and discharging from the vessel 10
- Fig. 1 is a sectional side elevation of the appathe materials to be inter-acted, while openings 35 ratus carried out according to this invention; 32 may be provided for sampling the liquids at Fig.
- Coil 33 may be Fig. 3 is a rear elevation of a diaphragm and provided for additional internal cooling, either Fig. 4 is a plan view of a diaphragm closing by water or by other refrigerating media or may piece. be utilized for heating purposes, if so desired,
- 10 is a cylindrical shell
- the operation of the device may possibly be provided with removable covers 11 and 12 and best understood by first considering the rotors at with an outer jacket 13 which may be utilized rest and supposing that two immiscible liquids 45 for heating or cooling the liquids in the mixer, of different specific gravities, e. g., sulfuric acid should this be necessary.
- 20 is a shaft running and hydrocarbon oil have been placed. into the parallel to the center line of shell 10 but preferapparatus so that practically the entire space ably eccentrically located therein and supported. with-in the shell 10 is filled with liquid.
- the in bearings 21 are examples of bearings 21.
- Stufiing glands 22 preventleaktwo liquids will naturally rest in the device in 50 age of liquids along the shaft when in motion, such a manner that the heavier one occupies a and specially formed end or ends-of the shaft lower layer, the lighter one resting on top as, as shown at 23 permit connection to a prime for example, shown by the dividing line drawn mover by means of pulleys or couplings or the in Fig. 1. like.
- the shaft carries within the space enclosed If now the rotors are set in motion, the two 55 by vessel 10, suitably spaced rotors 24 of any liquids in the mixing compartments will be emulsified, but no substantial disturbance of the separated liquids occurs in the separating compartments because the total hydraulic head acting on openings 27 from the mixing compartment is still the same as that from the neighboring separating compartment. If we now remove some of the heavy liquid through opening 31, the deficiency will be made up by additional liquid flowing in through the openings of diaphragm 25. However, this incoming liquid contains not only sulfuric acid, but also admixed hydrocarbon, so that after separation of the two, the level of sulfuric acid in this compartment will be lower than that corresponding to the hydraulic head necessary to maintain equilibrium.
- the relative time of contact may be varied independent of the throughput. Assume the volu metric capacity of the shell to be 200 gallons and that it contains 100 gallons of each liquid, the hourly feed also being 100 gallons of each. The average contact time of each of the liquids will then be one hour. If the contents of the shell are changed to 50 gallons of the light liquid and 150 gallons of the heavy liquid, the throughput being kept at 100 gallons per hour for each of the liquids, then the average contact time for the light liquid will be reduced to one-half hour and that for .the heavy liquid increased to one and one-half hours; the ratio of the contact times of the two liquids thereby.
- the relative time of contact of the light or heavy liquid may be either increased or decreased, depending on'the character of the substantially immiscible liquids and the economic conditions of operation.
- the number of agitating and settling chambers employed is dependent on the character of the liquids undergoing treatment and the nature of the process. For example, in parallel flow, an agitating chamber in communication with two settling chambers may suflice whereas in counter-current flow a plurality of agitating chambers is desirable, the efhciency of the process increasing with the number of agitating compartments.
- Pentane-pentene and hexane-hexene fractions are very suitable for treatment by my process for the selective absorption and removal of tertiary-base olefines (olefines capable of yielding tertiary alcohols upon hydrolysis).
- a butane-butene fraction containing approximately 15 to 20% by wt. of tertiary or gamma butylene is introduced at 30 while an equivalent amount of 65 to H2804 is introduced at 29.
- about a 10% excess of 65 to 70% H2804 is introduced at 29 (the amount of H2804 to be added being calculated on the amount of isobutylene to be absorbed).
- the vessel 10 in the meantime has been filled with 65 to 70% H2804 and the butane-butene fraction to be treated, the exact proportion of the contents of the vessel being dependent on the desired relative time of contact.
- the liquids flow in countercurrent fashion, the efilux at 28 comprising the butane-butane fraction from which the isobutylene has been substantially removed while the efflux at 31 comprises H2804 relatively saturated with isobutylene.
- the temperature is maintained between about to 90 F. to avoid substantial polymerization of the butene-l and butane-2.
- the pressure in the vessel is approximately the vapor pressure of the butane-butene fraction at the operating temperature.
- the process and/or apparatus assure ease of control, simplicity and flexibility of operation and maximum yield in the optimum minimum time of contact.
- a process for the treatment of immiscible fluids comprising: flowing a tertiary-base olefinecontaining fluid and an acid in counter-current through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other, the ratioof the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the end'product from a settling zone.
- a process for the treatment or substantially immiscible liquids comprising: flowing a tertiarybase olefine-containing fluid and an acid in counter-current through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the propertions of the two liquids in the agitating zones' and removing the dissolved tertiary-base olefine from an end settling zone.
- a process for the treatment of substantially immiscible liquids comprising: flowing a mineral oil fraction containing oleflnes in counter-current with an acid through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions oi the two liquids in the agitating zones and removing the treated material from a settling zone.
- a process for the treatment of substantially immiscible liquids comprising: flowing a mineral oil fraction containing oleflnes in counter-current with an acid through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed tertiary-base oleflnes from an end settling zone.
- a process for the treatment of substantially immiscible fluids comprising: flowing a mineral oil fraction consisting essentially of hydrocarbons containing more than three carbon atoms to the molecule and also containing the corresponding tertiary-base oleflnes in counter-current with an acid through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed tertiary-base oleflnes from an end settling zone.
- a process for the treatment'of substantially immiscible liquids comprising: flowing a mixture of paraflin and olefine hydrocarbons consisting essentially of hydrocarbons containing more than three carbon atoms to the molecule and also containing the corresponding tertiary-base oleflnes in counter-current with an acid through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the set tling zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed tertiarybase oleflnes from an end settling zone.
- a process for the treatment of substantially immiscible fluids comprising: flowing a hydrocarbon mixture containing isobutylene in countercurrent with H2SO4 through a series of alternate agitating and settling zones only the conall times substantially equal to the proportions of the liquids in the agitating zones and removing the absorbed isobutylene from an end settling zone.
- a process for the treatment of substantially immiscible fluids comprising: flowing a hydrocarbon mixture consisting essentially of Cd-Iio and C4H8 and containing isobutylene in countercurrent with H2804 through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads 01 the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones andremoving the absorbed isobutylene from an end settling zone.
- a process for the treatment of substantially immiscible fluids comprising: flowing a hydrocarbon mixture conta'ming isobutylene in countercurrent with 65% to H2804 through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other at a temperature below that at which polymerization of secondarybase butylene takes place, the ratio of the hydrostatic heads of the two liquids in the separating zones being, at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed isobutylene from an end settling zone.
- a process for the treatment 01 substantially immiscible fluids comprising: flowing a hydrocarbon mixture consisting essentially of C'lHliJ and 04 H3 and containing isobutylene in countercurrent with 65% to 70% H2304 through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones at a temperature below that at which polymerization of secondarybase butylene takes place, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed isobutylene from an end settling zone.
- a process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the height of an acid layer in a settling zone which also contains an olefine-containing fluid substantially immiscible with said acid, agitating the two liquids in'a mixing zone which is in communication with only two contiguous settling zones, the ratio of the hydrostatic heads of the two liquids in the settling zone being at all times substantially equal to the proportions of the two liquids in the mixing zone and hydrostatically controlling the flow of fluid from the settling zone to the mixing zone and vice versa while continuously feeding the immiscible fluids to the treating zones in countercurrent.
- a process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of acid layers in a series of horizontally arranged, settling zones which also contain olefine-containing fluid substantially immiscible with said acid, continuously agitating the two liquids in a series of mixing zones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio 01' the hydrostatic heads oi. the two liquids in the settling zones being at all times substantially equal to the proportions of the two liquids in the mixing zones and hydrostatically controlling the flow.
- a process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of acid layers in a series of horizontally arranged settling zones which also contain tertiary-base olefinecontaining fluid substantially immiscible with said acid, continuously agitating-the liquids in a series of mixingzones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the settling zones being at all times substantially equal to the proportions of the two liquids in the mixing zones and hydro statically controlling the flow of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in counter-current.
- a process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of H2304 layers in a series of horizontally arranged settling zones which also contain tertiary-base olefine-containing fluid substantially immiscible with the HzSOi, continuously agitating the liquids in a series of mixing zones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio of the hydrostatic heads of .the two liquids in the settling zones being at all times substantially equal to the proportions of the two liquids in the mixing zones and hydrostatically controlling the flow of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in counter-current.
- a process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of H280; layers in a series of horizontally arranged settling zones which also contain isobutylene-containing fluid substantially immiscible vnth the H2804, continuously agitating the liquids in a series of mixing zones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the settling zones being at all time substantially equal to the proportions of the two liquids in the mixing zones and hydrostatically controlling the flow of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in countercurrent.
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Description
April 3, 1934. G. A. KRAMER 3,
ABSORPTION or OLEFINES Filed July 20, 1931 2' Sheets-Sheet 1' lnvenror fiusTav AKfamer A ril 3, 1934.
G. A. KRAMER ABSORPTION 0F OLEFINES Filed July 20, 1951 2 Sheets-Sheet 2 IFIGJ FIG.4
'Flel lnvemor- Gustav A. Kramer UNITED STATES PATENT OFF'IQE ABSORPTION F OLEFINES Gustav A. Kramer, Oakland, Calif., assignor to Shell Development Company, San Francisco, Calif., acorporation of Delaware Application July 20, 1931, Serial No. 551,970
15 Claims. (01. 26099.12)
This invention relates to a novel apparatus desired number which when revolving, agitate the and process for contacting immiscible liquids liquid contained in the mixing device, causing inwith each other for the purpose of extraction, termingling of otherwise not miscible liquids in chemical treatment or the like, and more parmore or less fine emulsions. Diaphragms 25 are ticularly to an apparatus and/or process wherein so spaced that one pair of them form a sub- 60 it is desired to carry out such contact in counterstantially enclosed space 26 in which the agicurrent relationship of the two liquids. tation of rotors 24 is not felt and is of such size The preferred process comprises passing two that the emulsions formed in the mixing comsubstantially immiscible liquids in counter-curpartments may separate due to differences in rent flow to each other through a plurality of specific gravity of the liquids in question. 65 stages arranged in contiguous relationship and Such diaphragms may be also placed between communicating with each ata plurality of points, each end rotor and end plates 11 and 12 of the each alternate stage containing an agitating mixing vessel, or they may be omitted and exmeans, the end stages being characterized as ternal separating vessels substituted for this pur- 15 quiescent or separating zones and each end stage pose. containing an inlet and outlet for the liquids un- The diaphragms 25 are closed on shaft by dergoing treatment. The emulsified liquids in means of diaphragm closing piece 36 which perthe agitating zones are maintained in a hydromits rotation of the shaft without substantial static balance with the stratified liquidsin the leakage of fluids between compartments.
20 adjacent separating zones. The agitating and separating stages are in 75 The foregoing and other objects and advancommunication through openings 27 suitably tages of the invention, however, will be so clearly placed near the upper and lower peripheries of apparent to those skilled in the industry, as incithe diaphragms and of such a size that they dental to the following disclosure, that it would permit liquid to circulate between the two stages serve no useful purpose to further enlarge upon without causing the turbulence of the mixing 0 the same initially, and with these prefacing re"- zones to be communicated to the separating marks, therefore, reference will now be had to zones. Vanes 34 tend to increase the turbulence the accompanying drawings, generally illustratand eddy fiow in the agitating compartments ing at least one practical embodiment of a novel whereas vanes tend to straighten out eddy 30 systematic combination of means for carrying flow in the separating compartments thereby forth the steps of the method involved, although expediting stratification of the immiscible fluids. not essentially the only apparatus for doing so, Openings 28, 29, 30 and 31 are provided for in which drawings feeding into and discharging from the vessel 10, Fig. 1 is a sectional side elevation of the appathe materials to be inter-acted, while openings 35 ratus carried out according to this invention; 32 may be provided for sampling the liquids at Fig. 2 is a front elevation of a diaphragm; various steps of the process. Coil 33 may be Fig. 3 is a rear elevation of a diaphragm and provided for additional internal cooling, either Fig. 4 is a plan view of a diaphragm closing by water or by other refrigerating media or may piece. be utilized for heating purposes, if so desired,
40 In the drawings, wherein like characters of by the passage therethrough of hot water, steam reference designate corresponding parts throughor other heating media. out the several views: 10 is a cylindrical shell The operation of the device may possibly be provided with removable covers 11 and 12 and best understood by first considering the rotors at with an outer jacket 13 which may be utilized rest and supposing that two immiscible liquids 45 for heating or cooling the liquids in the mixer, of different specific gravities, e. g., sulfuric acid should this be necessary. 20 is a shaft running and hydrocarbon oil have been placed. into the parallel to the center line of shell 10 but preferapparatus so that practically the entire space ably eccentrically located therein and supported. with-in the shell 10 is filled with liquid. The in bearings 21. Stufiing glands 22 preventleaktwo liquids will naturally rest in the device in 50 age of liquids along the shaft when in motion, such a manner that the heavier one occupies a and specially formed end or ends-of the shaft lower layer, the lighter one resting on top as, as shown at 23 permit connection to a prime for example, shown by the dividing line drawn mover by means of pulleys or couplings or the in Fig. 1. like. The shaft carries within the space enclosed If now the rotors are set in motion, the two 55 by vessel 10, suitably spaced rotors 24 of any liquids in the mixing compartments will be emulsified, but no substantial disturbance of the separated liquids occurs in the separating compartments because the total hydraulic head acting on openings 27 from the mixing compartment is still the same as that from the neighboring separating compartment. If we now remove some of the heavy liquid through opening 31, the deficiency will be made up by additional liquid flowing in through the openings of diaphragm 25. However, this incoming liquid contains not only sulfuric acid, but also admixed hydrocarbon, so that after separation of the two, the level of sulfuric acid in this compartment will be lower than that corresponding to the hydraulic head necessary to maintain equilibrium. Consequently, some additional liquid will flow into this separating compartment through the lower openings of the diaphragm 25 and some hydrocarbon through the upper openings of the diaphragm 25 back into the neighboring mixing compartment, until by separation of the incoming emulsion, sufficient acid has been accumulated to again establish equilibrium. Similarly, if the equilibrium were disturbed by feeding some additional acid into the opening 29, this acid will again disturb the hydraulic equilibrium and will force more acid through the lower openings of the neighboring diaphragm and so on through the entire device until equilibrium has again been reached.
By the same way, additional hydrocarbon fed into opening 30 would again be gradually distributed through the entire system, meanwhile being successively agitated with acid by the rotors in the mixing chambers.
If hydrocarbon is fed continuously into opening 30 and is being continuously removed at the same rate through opening 28, at the same time acid is being fed into nozzle 29 and being removed at the same rate through nozzle 31, it is easily understood that while the dividing levels in the separating compartments remain substantially unchanged, the acid and hydrocarbon come into thorough contact with each other in countercurrent, fresh acid always being contacted with nearly fully treated hydrocarbon and untreated hydrocarbon with nearly fully spent acid.
The relative time of contact may be varied independent of the throughput. Assume the volu metric capacity of the shell to be 200 gallons and that it contains 100 gallons of each liquid, the hourly feed also being 100 gallons of each. The average contact time of each of the liquids will then be one hour. If the contents of the shell are changed to 50 gallons of the light liquid and 150 gallons of the heavy liquid, the throughput being kept at 100 gallons per hour for each of the liquids, then the average contact time for the light liquid will be reduced to one-half hour and that for .the heavy liquid increased to one and one-half hours; the ratio of the contact times of the two liquids thereby.
decreasing from 1 to In similar manner, the relative time of contact of the light or heavy liquid may be either increased or decreased, depending on'the character of the substantially immiscible liquids and the economic conditions of operation.
Under certain circumstances, it may be desirable to effect the contact of the two substantially immiscible fluids by means of parallel flow, in which case the lighter fluid is introduced at 30 and removed at the same rate through 28,
while the heavier fluid is fed in at 31 and 18- moved at the same rate through 29,
,The number of agitating and settling chambers employed is dependent on the character of the liquids undergoing treatment and the nature of the process. For example, in parallel flow, an agitating chamber in communication with two settling chambers may suflice whereas in counter-current flow a plurality of agitating chambers is desirable, the efhciency of the process increasing with the number of agitating compartments.
By way of example only, reference will be had to the treatment of a mineral oil fraction consisting essentially of hydrocarbons containing four carbon atoms to the molecule with sulfuric acid of such strength, that the tertiary-base olefines contained therein, such as isobutylene, are selectively absorbed by the sulfuric acid and removed therewith, although it is to be understood that the process and apparatus is applicable to the treatment of any mineral oil fraction containing hydrocarbons of any number of carbon atoms to the molecule with an acid which may comprise H2804, H2PO4, HCl, etc.
Pentane-pentene and hexane-hexene fractions are very suitable for treatment by my process for the selective absorption and removal of tertiary-base olefines (olefines capable of yielding tertiary alcohols upon hydrolysis).
A butane-butene fraction containing approximately 15 to 20% by wt. of tertiary or gamma butylene is introduced at 30 while an equivalent amount of 65 to H2804 is introduced at 29. To insure the complete absorption and removal of the gamma butylene, about a 10% excess of 65 to 70% H2804 is introduced at 29 (the amount of H2804 to be added being calculated on the amount of isobutylene to be absorbed). The vessel 10 in the meantime has been filled with 65 to 70% H2804 and the butane-butene fraction to be treated, the exact proportion of the contents of the vessel being dependent on the desired relative time of contact. The liquids flow in countercurrent fashion, the efilux at 28 comprising the butane-butane fraction from which the isobutylene has been substantially removed while the efflux at 31 comprises H2804 relatively saturated with isobutylene. The temperature is maintained between about to 90 F. to avoid substantial polymerization of the butene-l and butane-2. The pressure in the vessel is approximately the vapor pressure of the butane-butene fraction at the operating temperature.
The process and/or apparatus assure ease of control, simplicity and flexibility of operation and maximum yield in the optimum minimum time of contact.
It will be obvious that various substitutions in the materials treated and in the liquids used, as well as modifications in the order and manner of execution may be made in the practical application of the invention, but such substitutions and modifications are to be considered as comprehended by the above disclosure and included within the purview of the following claims.
I claim as my invention:
1. A process for the treatment of immiscible fluids comprising: flowing a tertiary-base olefinecontaining fluid and an acid in counter-current through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other, the ratioof the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the end'product from a settling zone.
2. A process for the treatment or substantially immiscible liquids comprising: flowing a tertiarybase olefine-containing fluid and an acid in counter-current through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the propertions of the two liquids in the agitating zones' and removing the dissolved tertiary-base olefine from an end settling zone. I
3. A process for the treatment of substantially immiscible liquids comprising: flowing a mineral oil fraction containing oleflnes in counter-current with an acid through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions oi the two liquids in the agitating zones and removing the treated material from a settling zone.
4. A process for the treatment of substantially immiscible liquids comprising: flowing a mineral oil fraction containing oleflnes in counter-current with an acid through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed tertiary-base oleflnes from an end settling zone.
5. A process for the treatment of substantially immiscible fluids comprising: flowing a mineral oil fraction consisting essentially of hydrocarbons containing more than three carbon atoms to the molecule and also containing the corresponding tertiary-base oleflnes in counter-current with an acid through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed tertiary-base oleflnes from an end settling zone.
6. A process for the treatment'of substantially immiscible liquids comprising: flowing a mixture of paraflin and olefine hydrocarbons consisting essentially of hydrocarbons containing more than three carbon atoms to the molecule and also containing the corresponding tertiary-base oleflnes in counter-current with an acid through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the set tling zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed tertiarybase oleflnes from an end settling zone.
'7. A process for the treatment of substantially immiscible fluids comprising: flowing a hydrocarbon mixture containing isobutylene in countercurrent with H2SO4 through a series of alternate agitating and settling zones only the conall times substantially equal to the proportions of the liquids in the agitating zones and removing the absorbed isobutylene from an end settling zone.
8. A process for the treatment of substantially immiscible fluids comprising: flowing a hydrocarbon mixture consisting essentially of Cd-Iio and C4H8 and containing isobutylene in countercurrent with H2804 through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones, the ratio of the hydrostatic heads 01 the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones andremoving the absorbed isobutylene from an end settling zone.
9. A process for the treatment of substantially immiscible fluids comprising: flowing a hydrocarbon mixture conta'ming isobutylene in countercurrent with 65% to H2804 through a series of alternate agitating and settling zones only the contiguous zones of which are in communication with each other at a temperature below that at which polymerization of secondarybase butylene takes place, the ratio of the hydrostatic heads of the two liquids in the separating zones being, at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed isobutylene from an end settling zone.
10. A process for the treatment 01 substantially immiscible fluids comprising: flowing a hydrocarbon mixture consisting essentially of C'lHliJ and 04 H3 and containing isobutylene in countercurrent with 65% to 70% H2304 through a series of alternate agitating and settling zones each agitating zone being in communication with no more than two settling zones at a temperature below that at which polymerization of secondarybase butylene takes place, the ratio of the hydrostatic heads of the two liquids in the separating zones being at all times substantially equal to the proportions of the two liquids in the agitating zones and removing the absorbed isobutylene from an end settling zone.
11. A process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the height of an acid layer in a settling zone which also contains an olefine-containing fluid substantially immiscible with said acid, agitating the two liquids in'a mixing zone which is in communication with only two contiguous settling zones, the ratio of the hydrostatic heads of the two liquids in the settling zone being at all times substantially equal to the proportions of the two liquids in the mixing zone and hydrostatically controlling the flow of fluid from the settling zone to the mixing zone and vice versa while continuously feeding the immiscible fluids to the treating zones in countercurrent.
12. A process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of acid layers in a series of horizontally arranged, settling zones which also contain olefine-containing fluid substantially immiscible with said acid, continuously agitating the two liquids in a series of mixing zones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio 01' the hydrostatic heads oi. the two liquids in the settling zones being at all times substantially equal to the proportions of the two liquids in the mixing zones and hydrostatically controlling the flow.
of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in countercurrent.
13. A process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of acid layers in a series of horizontally arranged settling zones which also contain tertiary-base olefinecontaining fluid substantially immiscible with said acid, continuously agitating-the liquids in a series of mixingzones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the settling zones being at all times substantially equal to the proportions of the two liquids in the mixing zones and hydro statically controlling the flow of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in counter-current.
14. A process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of H2304 layers in a series of horizontally arranged settling zones which also contain tertiary-base olefine-containing fluid substantially immiscible with the HzSOi, continuously agitating the liquids in a series of mixing zones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio of the hydrostatic heads of .the two liquids in the settling zones being at all times substantially equal to the proportions of the two liquids in the mixing zones and hydrostatically controlling the flow of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in counter-current.
15. A process for the treatment of substantially immiscible fluids comprising: maintaining at a substantially constant level the heights of H280; layers in a series of horizontally arranged settling zones which also contain isobutylene-containing fluid substantially immiscible vnth the H2804, continuously agitating the liquids in a series of mixing zones alternately disposed with respect to the settling zones and in communication with no more than two settling zones, the ratio of the hydrostatic heads of the two liquids in the settling zones being at all time substantially equal to the proportions of the two liquids in the mixing zones and hydrostatically controlling the flow of fluid from the settling zones to the mixing zones and vice versa while continuously feeding the immiscible fluids to the treating zones in countercurrent.
GUSTAV h. KRAMER.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US551970A US1953618A (en) | 1931-07-20 | 1931-07-20 | Absorption of olefines |
US713359A US2022205A (en) | 1931-07-20 | 1934-02-28 | Apparatus for the treatment of immiscible liquids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US551970A US1953618A (en) | 1931-07-20 | 1931-07-20 | Absorption of olefines |
Publications (1)
Publication Number | Publication Date |
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US1953618A true US1953618A (en) | 1934-04-03 |
Family
ID=24203420
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US551970A Expired - Lifetime US1953618A (en) | 1931-07-20 | 1931-07-20 | Absorption of olefines |
Country Status (1)
Country | Link |
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US (1) | US1953618A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2424186A (en) * | 1944-09-12 | 1947-07-15 | Standard Oil Dev Co | Sulfuric acid extraction of isobutylene from hydrocarbon mixtures |
US2778717A (en) * | 1950-11-21 | 1957-01-22 | Decker Peter | Process and apparatus for the separation of mixtures of substances by continuous countercurrent distribution in solvents |
US2779537A (en) * | 1950-08-01 | 1957-01-29 | Samuel D Jarvis | Fluid contacting apparatus |
US3617382A (en) * | 1968-07-17 | 1971-11-02 | Christos B Natsis | Mixing apparatus as used in mass and heat transfer processes |
-
1931
- 1931-07-20 US US551970A patent/US1953618A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2424186A (en) * | 1944-09-12 | 1947-07-15 | Standard Oil Dev Co | Sulfuric acid extraction of isobutylene from hydrocarbon mixtures |
US2779537A (en) * | 1950-08-01 | 1957-01-29 | Samuel D Jarvis | Fluid contacting apparatus |
US2778717A (en) * | 1950-11-21 | 1957-01-22 | Decker Peter | Process and apparatus for the separation of mixtures of substances by continuous countercurrent distribution in solvents |
US3617382A (en) * | 1968-07-17 | 1971-11-02 | Christos B Natsis | Mixing apparatus as used in mass and heat transfer processes |
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