US2961065A - Coke oven gas by-product recovery - Google Patents
Coke oven gas by-product recovery Download PDFInfo
- Publication number
- US2961065A US2961065A US711380A US71138058A US2961065A US 2961065 A US2961065 A US 2961065A US 711380 A US711380 A US 711380A US 71138058 A US71138058 A US 71138058A US 2961065 A US2961065 A US 2961065A
- Authority
- US
- United States
- Prior art keywords
- oil
- naphthalene
- gas
- wash
- wash oil
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000006227 byproduct Substances 0.000 title description 17
- 239000000571 coke Substances 0.000 title description 17
- 238000011027 product recovery Methods 0.000 title description 2
- 239000003921 oil Substances 0.000 description 271
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 257
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 142
- 229940075566 naphthalene Drugs 0.000 description 130
- 239000007789 gas Substances 0.000 description 101
- 229910021529 ammonia Inorganic materials 0.000 description 71
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 61
- 239000003245 coal Substances 0.000 description 27
- 239000002250 absorbent Substances 0.000 description 24
- 230000002745 absorbent Effects 0.000 description 24
- 238000011084 recovery Methods 0.000 description 21
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 19
- 238000000034 method Methods 0.000 description 18
- 230000008569 process Effects 0.000 description 18
- 239000011269 tar Substances 0.000 description 14
- 238000010521 absorption reaction Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 239000007921 spray Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000004939 coking Methods 0.000 description 9
- 238000011010 flushing procedure Methods 0.000 description 9
- 238000009835 boiling Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000010802 sludge Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000000356 contaminant Substances 0.000 description 4
- 238000000151 deposition Methods 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 238000005201 scrubbing Methods 0.000 description 4
- 230000008016 vaporization Effects 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 230000003134 recirculating effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 235000006173 Larrea tridentata Nutrition 0.000 description 2
- 244000073231 Larrea tridentata Species 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 235000011116 calcium hydroxide Nutrition 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 229960002126 creosote Drugs 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000011295 pitch Substances 0.000 description 2
- 239000012716 precipitator Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 241000380131 Ammophila arenaria Species 0.000 description 1
- 241001421757 Arcas Species 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 241001072332 Monia Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 201000003639 autosomal recessive cerebellar ataxia Diseases 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012717 electrostatic precipitator Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- -1 naphthalene compound Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/08—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors
- C10K1/16—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors with non-aqueous liquids
- C10K1/18—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors with non-aqueous liquids hydrocarbon oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/08—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors
- C10K1/085—Purifying combustible gases containing carbon monoxide by washing with liquids; Reviving the used wash liquors two direct washing treatments, one with an aqueous liquid and one with a non-aqueous liquid
Definitions
- This invention relates generally to the recovery of the gases from the coking of coal.
- An object of the present invention therefore is to provide a novel apparatus and process providing a system for the recovery of gases and other materials evolved during the coking of bltuminous coal and particularly adapted for the automation of such a system. Another object is to provide novel apparatus and process for removing the naphthalene from coke oven gas prior to the removal of the ammonia from the gas, thereby eliminating the possibility of naphthalene clogging the lines during subsequent steps of material removal from the gas.
- a further object is to provide novel apparatus and process for removing naphthalene from the gas in an absorbent oil, for removing the light oil from the gas in an absorbent oil, and for removing the naphthalene and the light oil from the absorbent oil simultaneously with minimum amount of heat and process steam.
- a still further object is to provide a novel process and apparatus for removing the ammonia from the gas With two liquors Which are kept separated whereby the am monia is stripped from each liquor separately.
- the absorbent oil used in the novel process of the invention is advantageously a petroleum type absorbent oil having a bo'ling range within the limits of 250 C. and 400 C., preferably Within the range of 300 C. to 370 C.
- a creosote type absorbent oil obtained by distillation of coal tar may also be used, but the corrosion problems generally encountered with creosote oil are avoided by use of the petroleum type.
- the aqueous liquors are used for removing the ammonia from the gas and are defined herein as fiushng liquor and ammonia wash liquor.
- the ammonia wash liquor may be stripped of its ammonia content and the liquor cooled and recycled for further ammonia absorption without ad ditlonal treatment, and thereby prevent even its small amount of phenol from going into sewage.
- This liquor ICC may be recirculated because it contains little or no fixed salts such as ammonium chloride.
- a naphthalene scrubber located immediately after the conventional primary coolers and tar preclpitators, removes naphthalene from the coke oven gas as soon as possible to prevent deposition of solid naphthalene in the gas piping and coal chemical recovery equipment.
- a minimum quantity of absorbent oil is used for the naphthalene absorption to minimize the introduction of ammonia and ammonia containing compounds into the subsequent light oil recovery system. It is also desirable that the ammonia absorbed by the minor quantity of absorbent oil leaving the naphthalene scrubber be removed before this oil mixes with the major quantity of wash oil from the benzol scrubbers.
- Contamination of the light oil recovery system with the ammonia containing rich oil from the naphthalene scrubber could be prevented by the use of a separate stripping still for each oil quantity, thereby keeping one absorbed oil entirely separated from the other.
- Such an arrangement would require a substantially greater quantity of stripping steam than is now used in conventional practice.
- naphthalene is one of the least volatile materials absorbed from the gas, it is one of the most difiicult to strip from the wash oil.
- naphthalene and benzene absorbed in wash oil a great deal more stripping steam is required for stripping the naphthalene than for the benzol.
- about 0.43 pound of naphthalene are removed in the benzol washers per ton of coal carbonized. This quantity will vary, depending upon the temperature of the wash oil and gas in the benzol washers and the efiiciency of stripping in the wash oil still, and the above quantity is estimated as being representative of an average condition.
- the quantity of wash oil circulated over the benzol washers in conventional operation is usually in the neighborhood of 165 gallons of wash oil per ton of coal carbonized.
- the normal quantity of stripping steam to the stripping still which is usually operated at C., is about 0.65 pound of steam per gallon of wash oil. This is equivalent to 107 pounds of steam per ton of coal carbonized.
- the steam used in the stripping still is sufiicient to remove the naphthalene absorbed in the benzol washers when the naphthalene content of the oil enterzng the stripping still is about 2% by weight.
- the quantity of naphthalene absorbed in the benzol washer and removed in the stripping still under these conditions is equivalent to about 0.035% by weight of the Wash oil circulating over the benzol washers. Under these conditions, the oil entering the stripping still would contain 2.0% by weight naphthalene and the oil leaving the stripping still for return to the benzol washers would contain 1.965% by weight of naphthalene. Thus, it is evident that the removal of naphthalene is limited by the quantity of steam used in the stripping still.
- the quantity of naphthalene removed from the gas depends upon the naphthalene content of the debenzolized oil circulated over the scrubbers, the temperature of the absorption, and the quantity of oil circulated. At a given absorption temperature and inlet concentraton of naphthalene in the gas, the amount of naphthalene absorbed is determined by the naphthalene content of the wash oil to the scrubbers. With other conditions being equal, therefore, it can be seen that the naphthalene removal from the gas is determined by the quantity of stripping steam used in the stripping still.
- the benzol washers are conventionally operated at slightly higher than atmospherc pressures, usually at about 800 mm. of mercury absolute. Operation at higher pressures, however, offers certain advantages. Op eration of the benzol washers at super atmospherc pressure of the gas permits a substantial reduction of the wash oil circulation rate and of the stripping steam; The higher gas pressure makes it possible to enrich the benzolized wash oil leaving the benzol washers to a greater extent, i.e., substantally proportional to the ratio of the absolute pressures. The enrichment of the wash oil when the gas pressure is 1450 mm. Hg absolute, for example, can be about 1.8 times that obtainable at the conventional lower pressure of 800 mm.
- the combined vapors that leave the top of the first stripping still pass through a conventional vapor to oil heat exchanger, light oil rectifier and light oil condenser.
- the purified wash oil thus is mixed with the wash oil circulation for the benzol scrubbers.
- the small amount of wash oil circulated over the naphthalene scrubber is taken from the oil pumped from the base of the wash oil still to the benzol washer.
- the wash oil circulation for the benzol washers is continuously bled off for absorption of naphthalene in the naphthalene absorbers; but before this oil is returned to the recirculating system for the benzol washers, any ammonia and other volatile consttuents are removed in the first stripping still and any high boiling non-volatile materials are rebe sent to the stripping still, the total naphthalene to be 7 removed in the stripping still is about 1.39 pounds of naphthalene per ton of coal. This is about 3.25 times the quantity of naphthalene nrmally required to be removed from the wash oil in the stripping still.
- the naphthalene in the benzolized wash oil and debenzolized wash oil build up to the point where it is mpossible to obtain satisfactory naphthalene removal in the scrubber and benzol washers.
- the novel process and apparatus of this invention permits satisfactory removal of the intween this limited quantity'of wash oil and the large amount of coke oven gas to be scrubbed, the oil may be recirculated from bottom to top of one or more recirculating stages in the naphthalene scrubber, advantageously at least two recirculated stages. These stages may be provided with packing or sprays.
- naphthalene rich wash oil from the naphthalene scrubber is fed to a first stripping still which may consist of from one to ten trays, although itis .beleved that the optimum number of stripping trays is between two and five.
- the naphthalene rich wash oil enters the top Stripping tray and flows from the bottom strpping tray to the wash oil purifier.
- the wash oil from the naphthalene stripper is kept sparate from the benzolized oil from the benzol washers.
- the benzolized wash oil from the benzol scrubbers is fed to theupper portion of a second stripping still and flws downwardly through the still.
- the wash oil flowing from 7 the first stripping still with most of its naphthalene stripped therefrom flows into a Wash oil purifier where the wash oil and residual naphthalene are vaporized with heat and live' steam and any tar, pitch, sludge, or polymerized material is removed as 1esidue in' the wash oil purifier and thus kept out of thewash oil circulatedover the benzol washers.
- the wash oil vapors from the purifier moved as residue in the purifier,thereby removing any contaminants which otherwise would build up in the wash oil system and enter the oil both from the benzol washers and from the naphthalene scrubber.
- the foregoing purifies the wash oil while removing the normal contaminartts and sludge which build up in the benzol washer system as well as the additional contaminants which are absorbed in the naphthalene scrubber.
- the quantity of stripping steam required for purfying the wash oil and for stripping the light oil Constituents and naphthalene from the wash oil from the benzol washers, and a relatively large quantity of naphthalene from the wash oil from the naphthalene scrubbers, is minimized, and the utilization of the wash oil purifier is increased to take care of the additional contaminants introduced in the naphthalene scrubbers without sacrificing its ability to keep the sludge and nonvolatle contaminants in the benzol Washer system at a satisfactory level.
- the fiushing liquor which cools the gases evolved during the cokng of coal and removes some phenol therefrom and some ammonia as free ammonia and some as fixed ammonia (such as in. ammonum chloride), and the wash liquor which is later used to remove the remainder of the free ammonia from the gas, are kept separate.
- materials such as milk of lime
- the ammonia recovered from both liquors may be combinedand used for production of frtilizer or burned.
- the gas is washed with an absorbent oil prior to the ammonia recovery step to remove the naphthalene from the gas, thereby preventing deposition of naphthalene during subsequen-t processng of the gas; this washing also removes the major part of the residual phenol from the gas whereby the phenol content of the wash liquor which contains the free ammonia is substantially reduced and phenol may be removed only from the surplus fiushing liquor prior to bengsent to waste.
- the gas is also s crubbed with wash oil to remove light oil after the step of washing to remove the ammonia.
- the naphthalene and the light oil are both stripped from'the absorbent oil in armanner wherein the vapors from a light oil stripping still'areapplied to a still for stripping the naphthalene fromthe naphthalene rich oil, the stripped absorbent oil from the naphthalene stripping still is then vaporized with steam and the resulting vapors are fed to the light oil stripping stll for stripping the light oil from the light oil rich oil.
- the byproduct system is combined with means for rendering the operation of the system automatic.
- a particular ad vantage of this by-product system of the invention is the fact that the early removal of naphthalene and the recovery of ammonia as a vapor rather than as a solid salt of ammonia substantially prevents unexpected flow stopp:ges and renders the process better adapted to automatic control.
- the single sheet of drawing schematcally illustrates a novel arrangement of apparatus for carrying out the in- Vention.
- the coal or other bituminous material is heated in a conventional coke oven battery in the absence of air.
- the gas evolved flows through conduit 12 to a collector main 13. Flushing liquor sprays into the conduits 12 and collector main 13 through injectors 15 cooling the hot gases and condensing some of the tar.
- the mixture of fiushing liquor, gas, and tar flow through conduit 17 to a downcorner where the gases separate from the liquor and tar.
- the liquor and tar flow through a line 21 from downcomer 19 to a fiushing liquor decanter tank 23 where the tar being heavier than the liquor settles to the bottom and is pumped by way of a conventional line (not shown) to storage.
- the pitch sludge is conveyed by scraper 25 to cart 27.
- the liquor overfiows through line 29 and is forced by a pump 31 through line 33, a screen 35, and line 37 to injectors 15.
- Circulating tank 38 serves as a reservoir for the flushing liquor.
- the gas flows through a conduit 41 from downcomer 19 to the lower section of a conventional primary cooler 43.
- the gas ascends the primary cooler countercurrent to the liquid descending from sprays 47.
- This liquor collects at the lower portion of primary cooler 43 and flows through a line 49 to a pump 51 which recirculates the liquid through a line 52, a cooler S3, and a line 54 back to the sprays 47.
- Excess liquor and condensed tar also overflow through line 56 to the decanter tank 23
- the gas leaves primary cooler 43 through a conduit 55, flows to an electrostatic precipitator 57 which removes substantially all the tar from the gas, and then flows through a conduit 59 to the lower portion of a naphthalene scrubber 63.
- the gas ascends naphthalene scrubber 63 countercurrent to the descent of absorbent or wash oil sprayed into the scrubber at sprays 64.
- Scrubber 63 is illustrated herein as being divided into two sections so that the absorbing oil from sprays 64 collect at the center of the scrubber and flow through conduit il to a pump 73 and through line 74, cooler 75, and lines 76 back to sprays 54. A portion of this oil also flows through line 78, a pump 79, line 81, cooler 82 and line 83 in the lower section.
- the wash oil collects in the bottom portion of the scrubber and flows through line S4 to a decanter 85 where the wash oil is separated from any aqueous condensate.
- the wash oil is sent by line to pump 79, and the condensate is sent to storage tank 159 through line 33.
- the gas which leaves at conduit 90 has the naphthalene content so reduced as to substantially eliminate the dan-ger of any naphthalene clogging the apparatus lines during the further processing of the gas.
- the volume of wash oil that entere the scrubber through line 238 leaves at line 209 as an equivalent volume with the naphthalene 'aud higher boiling hydrocarbons therein, i.e., as naphthalene rich oil.
- the naphthalenefree gas flows through conduit to a booster 91, which raises the gas to a pressure such that the pressure of the gas leaving the system at line 92 is substantially the pressure required to deliver the gas to the points of utilization at sufiicient pressure for use.
- This compression of the gas raises the temperature of the gas.
- the gas flows through conduit 90 to the lower portion of final cooler 93 where the gas flows upwardly countercurrent to the flow of water sprayed into the top by way of line 97.
- the water collects at the bottom of cooler 93 and flows back through line 90, pump 99, line 163, cooler 101, and line 97 into the cooler.
- the gas flows from cooler 93 through a line 35 to the lower portion of an ammonia washer 107.
- the gas flows upwardly through washer 107 and through a line 169 to the lower portion of a second washer 311 similar to washer 107.
- the gas leaves washer 111 at line 113 substantially free of ammonia.
- the gas ascending through the washer is contacted with water descending (not shown) within the washer from sprays connected to line 112F and 112S.
- Each washer is shown herein as having two sections. The water collects at the upper section and flows through line 118F, 3.18S, pump H9F, 119S, and line 112F, 112S back to the sprays.
- the excess liquor collecting in the upper section overfiows through line 122F, 1225 to the suction of pump 123F, 1233 where it joins with the liquor being recirculated through line 124F, 124S to sprays in the lower section of the washer.
- the solution collects at the bottom of the washer and flows through line 127F, 127S to the pump 123F, 1235.
- the solution from washer 111 also flows through line 1248 to line 129 to pump 119F and to washer 197.
- the solution from washer 107 flows through line 127F to pump 123F and then flows through line E31 to a storage tank 133.
- the solution from line 131 may alternately flow to tank 133 by way of line 134, the final cooler 93, and line 135.
- the gas which leaves washer 111 at line 113 is substantially free of ammonia and flows to a first benzol washer 138 and through conduit 141 to a second benzol washer 343.
- the gas which leaves washer 143 at conduit 145 is substantially free of valuable byproducts such as tar, naphthalene, ammonia, and light oil.
- This gas may then flow to a suitable gas holder 149 and through line 151 to a consumer for the production of chemicals such as synthetic ammonia or to a steel plant as fuel in open hearth fumaces, etc.
- Benzol washers 138 and 143 may be substantially identical to the ammonia washers 107, 111 except that where the gas is washed in the ammonia washers with water the gas in the benzol scrubbers is washed with the absorbent oil. Also, where such ammonia washers usually have two steps of wash, each benzol washer may have three or four stages.
- the light oil, i.e., the benzene, toluene, xylene components, of the coke oven gas is absorbed from the gas into the absorbent oil.
- the excess flushing liquor flows from recycle line 33 through line 153 to flushing liquor storage tank 160.
- This liquor contains in solution free ammonia, fixed ammonia (primarily as ammonium chiqprimary coolers from going to the sewer.
- dephenolizing stage 164 which may be of any conventional type, a particulardesirable type for this use is the dephenolizing system described in our copending application Serial No. 679,701. From the dephenolizing operation, the solution fiows through line 165 to a storage tank 166 and through pump 167 and line 162 to the upper portion of ammonia still 163.
- the milk of lime slurry is added to still 163 by way of a conventional lime leg 169 and steam is added at 170 to strip the ammonia from the solution.
- the solution substantially free of ammonia and phenol is then released through outlet 173 to sewerage.
- the steam and ammonia vapors from the upper portion of still 263 pass through a dephlegmator 175 where they are subjected to coolng so that the greater portion of the water vapor is removed from the ammonia vapor.
- the ammonia vapor then flows through line 178 to a line 179 which is connected to the outlet line 180 of a second ammonia still Most of the water vapor is removed from the vapor leaving the still by the dephlegmator 205, and the ammomia vapor flows through line 180 to line 179.
- the ammonia in line 179 may be sent to a conventional ammonia saturator of the type used in the indirect process of ammonia recovery, if there be a demand for ammoni um sulfate or ammonium phosphates. If the demand for such ammonium salts be low the ammonia may then be sent to a boilert or to a fiare to be burned.
- the deammoniated liquor from line 204 may be sent to the quenching station (not shown) for quenching the coke from the coke ovens 1), without any increase in corrosion of surrounding steelwork since the concentration of chlorides and, other corrosive salts is very low in thisstream.
- wash oil is etected in a novel manner with a pair of strip-.
- 2,946,655 is used to remove the phenol from the flushing liquor by extracton in a light oil solvent which s0lvent is then treated to re move the phenol; and in this manner, the light oil may then be purified to prevent substantial build-up of impurities therein.
- the wash oil which fiows from the benzol washers through line 213 and which is rich in light oil and less rich in naphthalene also flows through a vapor to oil heat exchanger 215 where the wash oil is heated by vapors from still 207, a final heater 2Il6, and a line 220 to the upper portion of still 208.
- the light oil rich wash oil descends through still 208, the light oil is stripped from the absorbent oil with steam which is supplied to the still 208 in a manner described hereinafter.
- the light oil and steam vapors from still 208 are fed by conduit 218 to the lower por: tion of still 207 and pass upwardly through still 207 to strip the naphthalene from the wash oil which is descend ing through this still.
- the combined steam, and naph thalene vapors, and light oil by way of conduit 223, pass through heat exchanger 215 and, by indirect heat exchange with the light-oil-rich wash oil from line 213 heat this oil.
- the condensate flows to a water separator 214 where the water is discharged and the oil pumped to a final heater 216.
- the vapors are sent to conventional rectifying and condensing equipment (not shown),
- the absorbent or wash oil stripped of light oil flows from the bottom of still 208 through line 230, pump 233, and line 234, to an indirect cooler 235 Where the absorbing medum is cooled to substantially ambient temperatures and then through line 237 to a circulating tank 238.
- a minor portion of the wash oil is withdrawn from tank 238 and is fed by way of line'238N to naphthalene scrubber 63 as the absorbent oil for the naphthalene scrubber, and a major portion of thewash oil is withdrawn and is fed by way of line 233B to benzol scrubber 143 as the absorbent oil for the benzol washers 138 and 143.
- the naphthalenestripped Wash oil from still 207 is conducted by way of line 241 to a wash oil purifier 243 where direct steam through line 244 is injected into this wash oil by way of nozzles 247 and additional indirect heat supplied by way of steam heated coils 249 vaporizes the wash oil and lower-boiling material to leave This resnous high-boiling residte material is 7 discharged through line 246.
- the vapors from the top of the purifier flow through line 248 to an inlet 251 to wash oil still 208.
- overfiow 242 is placed in this line so that in the event lation of wash oil over the naphthalene scrubber was 2.1 gallons per ton of coal carbonized, and this oil was recrculated over each of the recirculating stages at the rate of 200 gallons per ton of coal. Coolers 75 for each recirculatng stage maintained the oil at 30 C.
- the average pressure in the benzol washers was 1450 mm. Hg absolute and the temperature was 25 C.
- the wash oil from the naphthalene scrubber had a naphthalene content of by weight and was preheated to 120 C. by heater 210, before entering the top tray of a 4tray strippng still 267.
- This oil left the strippng still with a naphthalene content of 2% by weight and flowed to the wash oil purifier 243 which was maintained at a temperature of 190 C. by the use of an indirect heating coil 249 using high pressure steam.
- Low pressure strippng steam flowed through the purifier by way of line 244 and sparger 247 at the rate of 70 pounds of steam per ton of coal.
- the steam and oil vapor from the purifier entered below a 12tray still ntilized for strippng light oil from the bcnzolized wash oil from the benzol washers 138, 143.
- the circulation rate for wash oil to the benzol Washers was 91 gallons of wash oil per ton of coal carbonized.
- the naphthalene content of the wash oil to the benzol washers was 2% by weight and the naphthalene content of the wash oil from the benzol washers was 2.03% by weight.
- the wash oil pumped from the base of the wash oil still was 93.1 gallons per ton of coal carbonized.
- This quantity was split into two streams, one stream of 91 gallons per ton of coal was pumped to the benzol washer 143 and the other stream of 2.1 gallons per ton of coal carbonized was pumped to the naphthalene scrubber 63.
- Tne oil condensate from a light oil condenser was sent to storage for subsequent reotification and refining.
- This system in the naphthalene scrubber, removed naphthalene to a degree that no naphthalene depositions were encountered in the lines and chemical recovery equipment after the naphthalene scrubber.
- the quantity of wash oil circulated and strippng steam used was reduced substantially below that required for normal operation at lower pressure and with naphthalene scrubbing.
- the foregoing has presented a novel arrangement for the removal of by-products from the gas evolved during the coking of coal with absorbent oil and ammonia liquors.
- the naphthalene is removed from the gas early in the process so that the likelihood of the apparatus becoming clogged due to deposition of naphthalene during subsequent treatment of the gas is substantially eliminated.
- the absorbent or wash oil used for the recovery of naphthalene and light oils is continuously purified and the vapors from this purification are applied first to the wash oil from the benzol scrubbers and then to the wash oil from the naphthalene scrubber.
- each quantity of steam takes part in three operations, namely, strippng the wash oil from high boling impurities, strippng light oil from wash oil, and strippng naphthalene from wash oil. Efiiciency of operation is achieved by removing the absorbent oil to be purified at the point where the greatest possibility for buildup of resinous materials occurs.
- the tar precipitators and naphthalene scrubber can be located in the system beyond or after the booster or compressor. When so positioned, the naphthalene scrubber can additionally serve as a cooler for the gas. Additional advantages of so positioning the naphthalene scrubber are that the scrubbing is accomplishcd at high pressures, thereby reducing the size required for towers, lines, and pumps, and also thereby reducing the amount of wash oil required for the naphthalene removal and the amount of steam required for the strippng steps.
- the primary coolers may be of the indirect type and the naphthalene scrubbers, ammonia washers, and benzol washers may be of the packed, spray, bubble plate or perforated plate type.
- a process for the recovery of valuable by-products from the gas evolved from the coking of coal which comprises first contacting said gas with a first quantity of wash oil to remove the naphthalene from the gas by absorpton in the wash oil, whereby said first quantity of wash oil becomes rich in naphthalene, thereafter contacting said gas with a second quantity of wash oil to remove light oil from the gas by absorption in the wash oil, whereby said second quantity of wash oil becomes rich in light oil, applying the naphthalene rich wash oil to a first strippng zone where naphthalene is stripped therefrom, applying the light oil rich wash oil to a second strippng zone where the light oil is stripped therefrom, applying the vapors of said second zone to said first zone whereby said vapors strip the naphthalene from the wash oil therein, withdrawing stripped wash oil from said first zone and applying heat and steam thereto whereby the wash oil vaporizes, and applying the vapors of said wash oil and steam to said second strippng zone for
- a process for the recovery of valuable by-products from the gas evolved from the coking of coal which comprises coo'ing said gas with fiushing liquor and re covering the flushing liquor, contacting said gas with a minor quantity of wash oil to remove naphthalene from the gas by absorption, thereafter contacting said gas with ammonia wash liquor to remove ammonia from the gas by absorption, subsequently contacting said gas with a major quantity of wash oil to remove the light oil by absorption, applying said minor quantity of wash oil to a first strippng zone, applying said major quantity of wash oil to a second strippng zone, withdrawing stripped wash oil from said first zone, vaporizing said withdrawn wash oil with steam and feeding the vapors therefrom to said second zone to strip the light oil from said major quantity of wash oil, feeding the vapors from said second zone to said first zone for strippng the naphthalene from said minor quantity, removing phenol from said flushing liquor and removng ammonia from both of said liquors.
- a process for the recovery of valuable by-products from the gas evolved from the cokiug of coal which ll comprises first contacting said gas with a first quantity of wash oil to remove the naphthalene from the gas by absorption in the wash oil, whereby said first quantity of wash oil becomes rich in naphthalene, thereafter contacting said gas with a second quantity of wash oil to remove light oil from the gas by absorption in the wash soil, whereby said second quantity of wash oil becomes rich in light oil, applying the naphthalene rich wash oil to a first stripping zone where naphthalene is stripped therefrom, app.ying the light oil rich wash oil to a second stripping zone where the light oil is stripped therefrom, applying the vapors of said second zone to said first zone whereby said vapors strip the naphthalene from the wash oil therein, withdrawing stripped wash oil from said first zone and applying heat and steam thereto whereby the wash oil vaporizes, applying the vapors of said wash oil and steam to said second stripping zone for strip
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Industrial Gases (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Nov. 22, 1960 E. J. HELM EI'AL COKE OVEN GAS BYPRODUCT RECOVERY Filed Jan. 27, 1958 United States Patent O COKE OVEN GAS BY-PRGDUCT RECOVERY Edward J. Helm and Eiwood V. Schulte, Pittsburgh, Pa., assignors to Koppers Company, Inc., a corporafien of Delaware Filed Jan. 27, 1958, Ser. No. 711,380
6 Claims. (Cl. 183-114.6)
This invention relates generally to the recovery of the gases from the coking of coal.
When coal and other bituminous materials are heated in a coke oven in the absence of air, large volumes of gas, known as coke even gas are driven ofl the coal leaving a residue of carbonaceous material. This gas contains various valuable by-products such as ammonia, naphthalene, tar, and light oils such as benzene, toluene, and xylene, which by-products are recovered at the coke plant. The provisions for the recovery of these byproducts involves a large capital expense, and efforts are now being made to utilize these provisons and increase their capacity without changing their physical dimensions. Eiforts are also being made to automate these units and to decrease the down time during which the units are undergoing repars or maintenance. One of the problems existing heretofore in automating and increasing the capacity of the by-product recovery system has been that the naphthalene compound tends to settle out as a solid and thereby clog the lines.
An object of the present invention therefore is to provide a novel apparatus and process providing a system for the recovery of gases and other materials evolved during the coking of bltuminous coal and particularly adapted for the automation of such a system. Another object is to provide novel apparatus and process for removing the naphthalene from coke oven gas prior to the removal of the ammonia from the gas, thereby eliminating the possibility of naphthalene clogging the lines during subsequent steps of material removal from the gas.
A further object is to provide novel apparatus and process for removing naphthalene from the gas in an absorbent oil, for removing the light oil from the gas in an absorbent oil, and for removing the naphthalene and the light oil from the absorbent oil simultaneously with minimum amount of heat and process steam.
A still further object is to provide a novel process and apparatus for removing the ammonia from the gas With two liquors Which are kept separated whereby the am monia is stripped from each liquor separately.
The absorbent oil, known as wash oil, used in the novel process of the invention is advantageously a petroleum type absorbent oil having a bo'ling range within the limits of 250 C. and 400 C., preferably Within the range of 300 C. to 370 C. A creosote type absorbent oil obtained by distillation of coal tar may also be used, but the corrosion problems generally encountered with creosote oil are avoided by use of the petroleum type.
The aqueous liquors are used for removing the ammonia from the gas and are defined herein as fiushng liquor and ammonia wash liquor. In accordance with this invention, the ammonia wash liquor may be stripped of its ammonia content and the liquor cooled and recycled for further ammonia absorption without ad ditlonal treatment, and thereby prevent even its small amount of phenol from going into sewage. This liquor ICC may be recirculated because it contains little or no fixed salts such as ammonium chloride.
According to this invention, a naphthalene scrubber, located immediately after the conventional primary coolers and tar preclpitators, removes naphthalene from the coke oven gas as soon as possible to prevent deposition of solid naphthalene in the gas piping and coal chemical recovery equipment. With the naphthalene scrubber thus located ahead of the ammonia removal equipment, a minimum quantity of absorbent oil is used for the naphthalene absorption to minimize the introduction of ammonia and ammonia containing compounds into the subsequent light oil recovery system. It is also desirable that the ammonia absorbed by the minor quantity of absorbent oil leaving the naphthalene scrubber be removed before this oil mixes with the major quantity of wash oil from the benzol scrubbers. Contamination of the light oil recovery system with the ammonia containing rich oil from the naphthalene scrubber could be prevented by the use of a separate stripping still for each oil quantity, thereby keeping one absorbed oil entirely separated from the other. Such an arrangement, however, would require a substantially greater quantity of stripping steam than is now used in conventional practice.
Since naphthalene is one of the least volatile materials absorbed from the gas, it is one of the most difiicult to strip from the wash oil. For equal quantities of naphthalene and benzene absorbed in wash oil a great deal more stripping steam is required for stripping the naphthalene than for the benzol. In normal benzol washer operation, as known heretofore, about 0.43 pound of naphthalene are removed in the benzol washers per ton of coal carbonized. This quantity will vary, depending upon the temperature of the wash oil and gas in the benzol washers and the efiiciency of stripping in the wash oil still, and the above quantity is estimated as being representative of an average condition. The quantity of wash oil circulated over the benzol washers in conventional operation is usually in the neighborhood of 165 gallons of wash oil per ton of coal carbonized. The normal quantity of stripping steam to the stripping still, which is usually operated at C., is about 0.65 pound of steam per gallon of wash oil. This is equivalent to 107 pounds of steam per ton of coal carbonized. Under these conditions, the steam used in the stripping still is sufiicient to remove the naphthalene absorbed in the benzol washers when the naphthalene content of the oil enterzng the stripping still is about 2% by weight. The quantity of naphthalene absorbed in the benzol washer and removed in the stripping still under these conditions is equivalent to about 0.035% by weight of the Wash oil circulating over the benzol washers. Under these conditions, the oil entering the stripping still would contain 2.0% by weight naphthalene and the oil leaving the stripping still for return to the benzol washers would contain 1.965% by weight of naphthalene. Thus, it is evident that the removal of naphthalene is limited by the quantity of steam used in the stripping still.
The quantity of naphthalene removed from the gas depends upon the naphthalene content of the debenzolized oil circulated over the scrubbers, the temperature of the absorption, and the quantity of oil circulated. At a given absorption temperature and inlet concentraton of naphthalene in the gas, the amount of naphthalene absorbed is determined by the naphthalene content of the wash oil to the scrubbers. With other conditions being equal, therefore, it can be seen that the naphthalene removal from the gas is determined by the quantity of stripping steam used in the stripping still.
The benzol washers are conventionally operated at slightly higher than atmospherc pressures, usually at about 800 mm. of mercury absolute. Operation at higher pressures, however, offers certain advantages. Op eration of the benzol washers at super atmospherc pressure of the gas permits a substantial reduction of the wash oil circulation rate and of the stripping steam; The higher gas pressure makes it possible to enrich the benzolized wash oil leaving the benzol washers to a greater extent, i.e., substantally proportional to the ratio of the absolute pressures. The enrichment of the wash oil when the gas pressure is 1450 mm. Hg absolute, for example, can be about 1.8 times that obtainable at the conventional lower pressure of 800 mm. The higher concentration of light oil constituents in the benzolized wash oil in turn makes it possibleto reduce the stripping steam requirements substantially in inverse proportion to the ratio of the absolute pressure. It will be understood, of course, that these pressures carry through the am momia washers and any other gas treating units beyond the pressure side of the booster which takes the gas from the coke oven and forces it through the units beyond the boosters. This invention functions well with either the conventional or the higher pressure operations.
It has been found that if the small quantity of rich wash oil from the naphthalene scrubber is mixed with the benzolized oil from the benzol washers and the mixture are fed to the second still and condensed in the latter still. Stripping steam and wash oil vapors enter the bottom of the second still and flow upwardly in countercurrent contact with the wash oil from the benzol scrubbers, thus strippng the light oil products from the wash oil from the benzol scrubbers. The wash oil vapors condense in the second still. The steam and light oil vapors then flow from the second still upwardly through the first stripping still and strip the naphthalene from the oil from the naphthalene scrubbers. The combined vapors that leave the top of the first stripping still pass through a conventional vapor to oil heat exchanger, light oil rectifier and light oil condenser. The purified wash oil thus is mixed with the wash oil circulation for the benzol scrubbers. The small amount of wash oil circulated over the naphthalene scrubber is taken from the oil pumped from the base of the wash oil still to the benzol washer. Thus, a small percentage of the wash oil circulation for the benzol washers is continuously bled off for absorption of naphthalene in the naphthalene absorbers; but before this oil is returned to the recirculating system for the benzol washers, any ammonia and other volatile consttuents are removed in the first stripping still and any high boiling non-volatile materials are rebe sent to the stripping still, the total naphthalene to be 7 removed in the stripping still is about 1.39 pounds of naphthalene per ton of coal. This is about 3.25 times the quantity of naphthalene nrmally required to be removed from the wash oil in the stripping still. If it Were attempted to operate in this manner with the reduced quantity of steam required for strip-ping the light oil products absorbed at the higher pressure, the naphthalene in the benzolized wash oil and debenzolized wash oil build up to the point where it is mpossible to obtain satisfactory naphthalene removal in the scrubber and benzol washers. The novel process and apparatus of this invention permits satisfactory removal of the intween this limited quantity'of wash oil and the large amount of coke oven gas to be scrubbed, the oil may be recirculated from bottom to top of one or more recirculating stages in the naphthalene scrubber, advantageously at least two recirculated stages. These stages may be provided with packing or sprays.
In accordance with this invention, naphthalene rich wash oil from the naphthalene scrubber is fed to a first stripping still which may consist of from one to ten trays, although itis .beleved that the optimum number of stripping trays is between two and five. The naphthalene rich wash oil enters the top Stripping tray and flows from the bottom strpping tray to the wash oil purifier.
The wash oil from the naphthalene stripper is kept sparate from the benzolized oil from the benzol washers.
The benzolized wash oil from the benzol scrubbers is fed to theupper portion of a second stripping still and flws downwardly through the still. The wash oil flowing from 7 the first stripping still with most of its naphthalene stripped therefrom flows into a Wash oil purifier where the wash oil and residual naphthalene are vaporized with heat and live' steam and any tar, pitch, sludge, or polymerized material is removed as 1esidue in' the wash oil purifier and thus kept out of thewash oil circulatedover the benzol washers. The wash oil vapors from the purifier moved as residue in the purifier,thereby removing any contaminants which otherwise Would build up in the wash oil system and enter the oil both from the benzol washers and from the naphthalene scrubber. The foregoing purifies the wash oil while removing the normal contaminartts and sludge which build up in the benzol washer system as well as the additional contaminants which are absorbed in the naphthalene scrubber. By utilizing the same stripping steam three times in the wash oil purifier, in the second stripping still, and in the fuel stripping still, the quantity of stripping steam required for purfying the wash oil and for stripping the light oil Constituents and naphthalene from the wash oil from the benzol washers, and a relatively large quantity of naphthalene from the wash oil from the naphthalene scrubbers, is minimized, and the utilization of the wash oil purifier is increased to take care of the additional contaminants introduced in the naphthalene scrubbers without sacrificing its ability to keep the sludge and nonvolatle contaminants in the benzol Washer system at a satisfactory level.
In accordance with this invention, the fiushing liquor Which cools the gases evolved during the cokng of coal and removes some phenol therefrom and some ammonia as free ammonia and some as fixed ammonia (such as in. ammonum chloride), and the wash liquor which is later used to remove the remainder of the free ammonia from the gas, are kept separate. Thus; when the ammonia isrecovered from the liquor, it is necessary to add materials, such as milk of lime, only to the fiushing liquor to free the fixed ammonia, since the wash liquor will contain little or no fixed ammonia. The ammonia recovered from both liquors may be combinedand used for production of frtilizer or burned. The gas is washed with an absorbent oil prior to the ammonia recovery step to remove the naphthalene from the gas, thereby preventing deposition of naphthalene during subsequen-t processng of the gas; this washing also removes the major part of the residual phenol from the gas whereby the phenol content of the wash liquor which contains the free ammonia is substantially reduced and phenol may be removed only from the surplus fiushing liquor prior to bengsent to waste. The gas is also s crubbed with wash oil to remove light oil after the step of washing to remove the ammonia. The naphthalene and the light oil are both stripped from'the absorbent oil in armanner wherein the vapors from a light oil stripping still'areapplied to a still for stripping the naphthalene fromthe naphthalene rich oil, the stripped absorbent oil from the naphthalene stripping still is then vaporized with steam and the resulting vapors are fed to the light oil stripping stll for stripping the light oil from the light oil rich oil.
and a major portion of the stipped absorbent oil from the light oil stripping still is used for the benzene or light oil scrubbing and a minor portion used for the naphthalene scrubbing.
In a preferred embodiment of this invention, the byproduct system is combined with means for rendering the operation of the system automatic. A particular ad vantage of this by-product system of the invention is the fact that the early removal of naphthalene and the recovery of ammonia as a vapor rather than as a solid salt of ammonia substantially prevents unexpected flow stopp:ges and renders the process better adapted to automatic control.
The above and further objects and novel features will appear more fully from the following detailed description when the same is read in connection with the accompanying drawing. It is to be understood, however, that the drawing is not intended as a definition of the invention but is for the purpose of illustration only.
The single sheet of drawing schematcally illustrates a novel arrangement of apparatus for carrying out the in- Vention.
Turning now to the novel arrangement of apparatus for carrying out the process of the invention, the coal or other bituminous material is heated in a conventional coke oven battery in the absence of air. The gas evolved flows through conduit 12 to a collector main 13. Flushing liquor sprays into the conduits 12 and collector main 13 through injectors 15 cooling the hot gases and condensing some of the tar. The mixture of fiushing liquor, gas, and tar flow through conduit 17 to a downcorner where the gases separate from the liquor and tar.
The liquor and tar flow through a line 21 from downcomer 19 to a fiushing liquor decanter tank 23 where the tar being heavier than the liquor settles to the bottom and is pumped by way of a conventional line (not shown) to storage. The pitch sludge is conveyed by scraper 25 to cart 27. The liquor overfiows through line 29 and is forced by a pump 31 through line 33, a screen 35, and line 37 to injectors 15. Circulating tank 38 serves as a reservoir for the flushing liquor.
The gas flows through a conduit 41 from downcomer 19 to the lower section of a conventional primary cooler 43. The gas ascends the primary cooler countercurrent to the liquid descending from sprays 47. This liquor collects at the lower portion of primary cooler 43 and flows through a line 49 to a pump 51 which recirculates the liquid through a line 52, a cooler S3, and a line 54 back to the sprays 47. Excess liquor and condensed tar also overflow through line 56 to the decanter tank 23 The gas leaves primary cooler 43 through a conduit 55, flows to an electrostatic precipitator 57 which removes substantially all the tar from the gas, and then flows through a conduit 59 to the lower portion of a naphthalene scrubber 63.
The gas ascends naphthalene scrubber 63 countercurrent to the descent of absorbent or wash oil sprayed into the scrubber at sprays 64. Scrubber 63 is illustrated herein as being divided into two sections so that the absorbing oil from sprays 64 collect at the center of the scrubber and flow through conduit il to a pump 73 and through line 74, cooler 75, and lines 76 back to sprays 54. A portion of this oil also flows through line 78, a pump 79, line 81, cooler 82 and line 83 in the lower section. The wash oil collects in the bottom portion of the scrubber and flows through line S4 to a decanter 85 where the wash oil is separated from any aqueous condensate. The wash oil is sent by line to pump 79, and the condensate is sent to storage tank 159 through line 33. The gas which leaves at conduit 90 has the naphthalene content so reduced as to substantially eliminate the dan-ger of any naphthalene clogging the apparatus lines during the further processing of the gas. The volume of wash oil that entere the scrubber through line 238 leaves at line 209 as an equivalent volume with the naphthalene 'aud higher boiling hydrocarbons therein, i.e., as naphthalene rich oil.
The naphthalenefree gas flows through conduit to a booster 91, which raises the gas to a pressure such that the pressure of the gas leaving the system at line 92 is substantially the pressure required to deliver the gas to the points of utilization at sufiicient pressure for use. This compression of the gas raises the temperature of the gas. Accordingly, the gas flows through conduit 90 to the lower portion of final cooler 93 where the gas flows upwardly countercurrent to the flow of water sprayed into the top by way of line 97. The water collects at the bottom of cooler 93 and flows back through line 90, pump 99, line 163, cooler 101, and line 97 into the cooler. The gas flows from cooler 93 through a line 35 to the lower portion of an ammonia washer 107.
The gas flows upwardly through washer 107 and through a line 169 to the lower portion of a second washer 311 similar to washer 107. The gas leaves washer 111 at line 113 substantially free of ammonia. In washer 107, 111 the gas ascending through the washer is contacted with water descending (not shown) within the washer from sprays connected to line 112F and 112S. Each washer is shown herein as having two sections. The water collects at the upper section and flows through line 118F, 3.18S, pump H9F, 119S, and line 112F, 112S back to the sprays. The excess liquor collecting in the upper section overfiows through line 122F, 1225 to the suction of pump 123F, 1233 where it joins with the liquor being recirculated through line 124F, 124S to sprays in the lower section of the washer. The solution collects at the bottom of the washer and flows through line 127F, 127S to the pump 123F, 1235. The solution from washer 111 also flows through line 1248 to line 129 to pump 119F and to washer 197. The solution from washer 107 flows through line 127F to pump 123F and then flows through line E31 to a storage tank 133. The solution from line 131 may alternately flow to tank 133 by way of line 134, the final cooler 93, and line 135.
The gas which leaves washer 111 at line 113 is substantially free of ammonia and flows to a first benzol washer 138 and through conduit 141 to a second benzol washer 343. The gas which leaves washer 143 at conduit 145 is substantially free of valuable byproducts such as tar, naphthalene, ammonia, and light oil. This gas may then flow to a suitable gas holder 149 and through line 151 to a consumer for the production of chemicals such as synthetic ammonia or to a steel plant as fuel in open hearth fumaces, etc.
The foregoing has described the flow of gas from the coke oven battery to the point of utilization and the removal of the valuaole constituents from the gas with an absorbing medium, i.e., water or absorbent oil. It will be clear to those skilled in the art that this novel arrangement involves various elements such as coke oven battery 3h, decanter tank 23, primary cooler 43, naphthalene scrubber 63, tar precipitators 57, final cooler 93 ammonia washers 107, 111, benzol scrubbers 138, 143 and gas holder 149 that are conventional units for the coking of coal and the recovery of by-products from the gases evolved during the coking.
Considering now the recovery of the by-products from the absorbing medium, the excess flushing liquor flows from recycle line 33 through line 153 to flushing liquor storage tank 160. This liquor contains in solution free ammonia, fixed ammonia (primarily as ammonium chiqprimary coolers from going to the sewer.
ride),and -phenol, as well as other mpurities such as pyridine, hydrogen sulfide, and cyanides. The ammonia is stripped from the liquor in an ammonia still 163; but, in those arcas in which the deammoniated liquor can not be released to sewerage without removal of the phenol, the liquor must be sent through dephenolizing stage 164 which may be of any conventional type, a particulardesirable type for this use is the dephenolizing system described in our copending application Serial No. 679,701. From the dephenolizing operation, the solution fiows through line 165 to a storage tank 166 and through pump 167 and line 162 to the upper portion of ammonia still 163. The milk of lime slurry is added to still 163 by way of a conventional lime leg 169 and steam is added at 170 to strip the ammonia from the solution. The solution substantially free of ammonia and phenol is then released through outlet 173 to sewerage. The steam and ammonia vapors from the upper portion of still 263 pass through a dephlegmator 175 where they are subjected to coolng so that the greater portion of the water vapor is removed from the ammonia vapor. The ammonia vapor then flows through line 178 to a line 179 Which is connected to the outlet line 180 of a second ammonia still Most of the water vapor is removed from the vapor leaving the still by the dephlegmator 205, and the ammomia vapor flows through line 180 to line 179. The ammonia in line 179 may be sent to a conventional ammonia saturator of the type used in the indirect process of ammonia recovery, if there be a demand for ammoni um sulfate or ammonium phosphates. If the demand for such ammonium salts be low the ammonia may then be sent to a boilert or to a fiare to be burned.
r The foregoing has presented ;a novel arrangement wheren the fiushing liquor which contains both fixed and free ammonia and the solution from the ammonia washers which contains only free ammonia is maintained separate and the ammonia is stripped separately from the solutions. Thus, it is necessary to apply a lime slurry only to the still wheren fixed ammonia is being stripped from the fiushing liquor as the solution from the ammonia washers contains little if any fixed ammonia. Also it has been found necessary in accordnce with this inventn to remove the phenol only from the flushing liquor containing the fixed ammonia as the naphthalene scrubber removes most of the phenol, as well as the naphthalene, which remains in the gas after leaving the For this reason, the concentration of phenol in the solution from the ammonia washers is low and recovery of the phenol from this solution will not be required. r
It has been found that 70-90% of the total phenol in the efiiuents from the coal chemical recovery operations is contained in the flushingliquor. Most of the phenol remaining in the gas after the primary coolers is absorbed in the absorbent oil in the naphthalene scrubber. Thus the ammonia wash liquor will have absorbed therein only 7 between 5% of the total phenol content in the coal chemical recovery effiuents. Since the phenol content of the dearnmoniated liquor leaving still 191 at line 204 is low, this liquor can oe cooled, and, if desired, without further treatment be recycled to the ammonia washers and thereby prevent even its small content of phenol Alternatively, the deammoniated liquor from line 204 may be sent to the quenching station (not shown) for quenching the coke from the coke ovens 1), without any increase in corrosion of surrounding steelwork since the concentration of chlorides and, other corrosive salts is very low in thisstream.
The removal of naphthalene and light oil from the the resnous high-boiling material as a residue.
wash oil is etected in a novel manner with a pair of strip-.
The absorbent or wash oil stripped of light oil flows from the bottom of still 208 through line 230, pump 233, and line 234, to an indirect cooler 235 Where the absorbing medum is cooled to substantially ambient temperatures and then through line 237 to a circulating tank 238. A minor portion of the wash oil is withdrawn from tank 238 and is fed by way of line'238N to naphthalene scrubber 63 as the absorbent oil for the naphthalene scrubber, and a major portion of thewash oil is withdrawn and is fed by way of line 233B to benzol scrubber 143 as the absorbent oil for the benzol washers 138 and 143.
The naphthalenestripped Wash oil from still 207 is conducted by way of line 241 to a wash oil purifier 243 where direct steam through line 244 is injected into this wash oil by way of nozzles 247 and additional indirect heat supplied by way of steam heated coils 249 vaporizes the wash oil and lower-boiling material to leave This resnous high-boiling residte material is 7 discharged through line 246. The vapors from the top of the purifier flow through line 248 to an inlet 251 to wash oil still 208. The wash oil vapors condense in still 208 and the light oil and steam pass upwar dly through still 208 countercurrent to the light oil rich wash oil passing down- 7 wardly through still 208 and strip the lightoil from the wash oil. Additional steam from line 252 may be passed through line 248 if needed.
Normally all of the discharg from still 207 passes through line 241 to purifier 243, the rate of, flow being controlled by a conventional level controller 254; An
, overfiow 242 is placed in this line so that in the event lation of wash oil over the naphthalene scrubber was 2.1 gallons per ton of coal carbonized, and this oil was recrculated over each of the recirculating stages at the rate of 200 gallons per ton of coal. Coolers 75 for each recirculatng stage maintained the oil at 30 C. The gas entered the benzol washers with a naphthalene content of 13 grains per 100 s.c.f. and left with a naphthalene content of 1.5 grains per 100 s.c.f. The average pressure in the benzol washers was 1450 mm. Hg absolute and the temperature was 25 C. The wash oil from the naphthalene scrubber had a naphthalene content of by weight and was preheated to 120 C. by heater 210, before entering the top tray of a 4tray strippng still 267. This oil left the strippng still with a naphthalene content of 2% by weight and flowed to the wash oil purifier 243 which was maintained at a temperature of 190 C. by the use of an indirect heating coil 249 using high pressure steam. Low pressure strippng steam flowed through the purifier by way of line 244 and sparger 247 at the rate of 70 pounds of steam per ton of coal. The steam and oil vapor from the purifier entered below a 12tray still ntilized for strippng light oil from the bcnzolized wash oil from the benzol washers 138, 143. The circulation rate for wash oil to the benzol Washers was 91 gallons of wash oil per ton of coal carbonized. The naphthalene content of the wash oil to the benzol washers was 2% by weight and the naphthalene content of the wash oil from the benzol washers was 2.03% by weight. The wash oil pumped from the base of the wash oil still was 93.1 gallons per ton of coal carbonized. This quantity was split into two streams, one stream of 91 gallons per ton of coal was pumped to the benzol washer 143 and the other stream of 2.1 gallons per ton of coal carbonized was pumped to the naphthalene scrubber 63. Tne oil condensate from a light oil condenser was sent to storage for subsequent reotification and refining. This system, in the naphthalene scrubber, removed naphthalene to a degree that no naphthalene depositions were encountered in the lines and chemical recovery equipment after the naphthalene scrubber. The quantity of wash oil circulated and strippng steam used was reduced substantially below that required for normal operation at lower pressure and with naphthalene scrubbing. The removal of ammonia and volatile compounds from the rich oil from the naphthalene scrubber in the strippng still 297 prevented contamination of the main wash oil circulating system for the benzol washers with these compounds. Vaporization of the wash oil from the naphthalene stripping still in the wash oil purifier 243 removed the traces of tar, pitch, and sludge absorbed in the naphthalene scrubber and at the same time maintained the sludge content of the main wash oil circulating system for the benzol washers at a satisfactory level, averaging about 10 to 15 grains per gallon, as determined by precipitation with isopentane, by continuous bleeding of wash oil from the benzol washer system and returning this bleed by way of the purifier after having passed through the naphthalene scrubber.
The foregoing has presented a novel arrangement for the removal of by-products from the gas evolved during the coking of coal with absorbent oil and ammonia liquors. The naphthalene is removed from the gas early in the process so that the likelihood of the apparatus becoming clogged due to deposition of naphthalene during subsequent treatment of the gas is substantially eliminated. The absorbent or wash oil used for the recovery of naphthalene and light oils is continuously purified and the vapors from this purification are applied first to the wash oil from the benzol scrubbers and then to the wash oil from the naphthalene scrubber. Economy is etected in that each quantity of steam takes part in three operations, namely, strippng the wash oil from high boling impurities, strippng light oil from wash oil, and strippng naphthalene from wash oil. Efiiciency of operation is achieved by removing the absorbent oil to be purified at the point where the greatest possibility for buildup of resinous materials occurs. Further economy and efficiency is achieved by maintaining the flushing liquor separate from the ammonia wash liquor and separately strippng each liquor of its ammonia content so that the ammonia strippng stills can be made smaller, the lime slurry need be applied only to one of the stlls, namely the still to which is fed liquor containing fixed ammonia, and the small quantity of solution to be dephenolized permits economy in the size of dephenolizer for a given size coke plant.
Although the foregong has illustrated and described the invention in detail, it is to be expressly understood that the invention is not limited thereto. As will now be understood by those skilled in the art, various changes can be made in the design and arrangement of the parts without departing from the spirit and scope of the n vention.
The tar precipitators and naphthalene scrubber, for example, can be located in the system beyond or after the booster or compressor. When so positioned, the naphthalene scrubber can additionally serve as a cooler for the gas. Additional advantages of so positioning the naphthalene scrubber are that the scrubbing is accomplishcd at high pressures, thereby reducing the size required for towers, lines, and pumps, and also thereby reducing the amount of wash oil required for the naphthalene removal and the amount of steam required for the strippng steps. The primary coolers may be of the indirect type and the naphthalene scrubbers, ammonia washers, and benzol washers may be of the packed, spray, bubble plate or perforated plate type.
What is claimed is:
I. A process for the recovery of valuable by-products from the gas evolved from the coking of coal which comprises first contacting said gas with a first quantity of wash oil to remove the naphthalene from the gas by absorpton in the wash oil, whereby said first quantity of wash oil becomes rich in naphthalene, thereafter contacting said gas with a second quantity of wash oil to remove light oil from the gas by absorption in the wash oil, whereby said second quantity of wash oil becomes rich in light oil, applying the naphthalene rich wash oil to a first strippng zone where naphthalene is stripped therefrom, applying the light oil rich wash oil to a second strippng zone where the light oil is stripped therefrom, applying the vapors of said second zone to said first zone whereby said vapors strip the naphthalene from the wash oil therein, withdrawing stripped wash oil from said first zone and applying heat and steam thereto whereby the wash oil vaporizes, and applying the vapors of said wash oil and steam to said second strippng zone for strippng the light ols from the wash oil therein.
2. A process for the recovery of valuable by-products from the gas evolved from the coking of coal which comprises coo'ing said gas with fiushing liquor and re covering the flushing liquor, contacting said gas with a minor quantity of wash oil to remove naphthalene from the gas by absorption, thereafter contacting said gas with ammonia wash liquor to remove ammonia from the gas by absorption, subsequently contacting said gas with a major quantity of wash oil to remove the light oil by absorption, applying said minor quantity of wash oil to a first strippng zone, applying said major quantity of wash oil to a second strippng zone, withdrawing stripped wash oil from said first zone, vaporizing said withdrawn wash oil with steam and feeding the vapors therefrom to said second zone to strip the light oil from said major quantity of wash oil, feeding the vapors from said second zone to said first zone for strippng the naphthalene from said minor quantity, removing phenol from said flushing liquor and removng ammonia from both of said liquors.
3. A process for the recovery of valuable by-products from the gas evolved from the cokiug of coal which ll comprises first contacting said gas with a first quantity of wash oil to remove the naphthalene from the gas by absorption in the wash oil, whereby said first quantity of wash oil becomes rich in naphthalene, thereafter contacting said gas with a second quantity of wash oil to remove light oil from the gas by absorption in the wash soil, whereby said second quantity of wash oil becomes rich in light oil, applying the naphthalene rich wash oil to a first stripping zone where naphthalene is stripped therefrom, app.ying the light oil rich wash oil to a second stripping zone where the light oil is stripped therefrom, applying the vapors of said second zone to said first zone whereby said vapors strip the naphthalene from the wash oil therein, withdrawing stripped wash oil from said first zone and applying heat and steam thereto whereby the wash oil vaporizes, applying the vapors of said wash oil and steam to said second stripping zone for stripping the light oils from the wash oil therein, whereby the wash oil vapors condense in said second zone, withdrawing the stripped wash oil from said second zone, and dividing said wash oil so withdrawn for use as said first and second quantities. r V
4. In a process wherein by-products such as naphthalene and light oil are recovered continuously from the gas evolved from the coking of coal by absorption in a wash oil, the improvement which comprises contacting said gas with a first wash oil to absorb the naphthalene therein, thereafter contacting said gas with a second wash oil to absorb the light oil therein, stripping the first wash oil also being subject to also absorbing high boiling compounds therein, vaporizing with steam in a r second zone said first wash oil from said high boiling compounds, applying the vapors so formed to said second wash oil in a third zone to strip the light oil therefrom with said steam and to condense said vaporized wash oil, applying the stripped vapors of light oil and steam to said first zone for stripping the naphthalene from wash oil in said first zone whereby the same quan:
tity of steam vaporizes the wash oil from high boilng compounds, strips the light oil from the second wash oil, and strips the naphthalene from the first wash oil.
5. The process of claim 4 wherein the stripped wash oil from the third zone is divided in said first and second wash oils for continuing the process. r
6. In a process wherein by-products such asnaphthalene and light oil are absorbed in a wash oil from the gas evolved from the coking of coal and recovered by stripping the by-prodcts from the wash oil with steam, the improvement which comprises contacting said gas with a first wash oil to absorb the naphthalene from the gas, thereafter contacting said gas with a second wash oil to absorb the light oil from said gas, withdrawing and ,subjecting wash oil from which the naphthalene has been stripped to steam thereby vaporizing said wash oil, applying the vapors of wash oil and steam to said second wash oil to remove the light oil therefrom as vapors of light oil, and applying the vapors of light oil and steam to said first wash oil to strip the naphthalene from said first wash whereby one quantity of steam serves to vaporize the wash oil from which the naphthalene has been withdrawn, strip the light oil from the second wash oil, and strip the naphthalene from the first wash oil.
References Cited in the file of this patent UNITED STATES PATENTS 932,758 Collins Aug. 31, 1909 1,487,768 Torrey Mar. 25, 1924 1,823,364 Knapp Sept. 15, 1931 2,067,029 Van Ackeren Jan. 5, 1937 2,710,663 Wilson June 14, 1955 OTHER REFERENCES Chem. and Met.s Chemical Engineering Flow Sheets, Fourth edition, Chemical and Met. Engineering, McGraw-Hill Publishing Co., Inc., New York, N.Y., page 61. 7
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US711380A US2961065A (en) | 1958-01-27 | 1958-01-27 | Coke oven gas by-product recovery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US711380A US2961065A (en) | 1958-01-27 | 1958-01-27 | Coke oven gas by-product recovery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2961065A true US2961065A (en) | 1960-11-22 |
Family
ID=24857856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US711380A Expired - Lifetime US2961065A (en) | 1958-01-27 | 1958-01-27 | Coke oven gas by-product recovery |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2961065A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1206870B (en) * | 1963-02-28 | 1965-12-16 | Dr Guenter Wunderlich | Process for incinerating the ammonia produced during coking |
| US3581472A (en) * | 1969-08-08 | 1971-06-01 | Koppers Co Inc | System for the removal of naphthalene from coke oven gas |
| DE2238805A1 (en) * | 1971-08-18 | 1973-02-22 | Koppers Co Inc | METHOD OF REMOVING AMMONIA FROM COK OVEN GAS |
| US4286971A (en) * | 1979-10-05 | 1981-09-01 | Bethlehem Steel Corporation | Removal of naphthalene from recirculated wash oil |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US932758A (en) * | 1909-03-13 | 1909-08-31 | Francis Joseph Collin | Method of recovering ammonia from coal-gases. |
| US1487768A (en) * | 1924-03-25 | Process op and apparatus for recovering the ammonia content of coal gas | ||
| US1823364A (en) * | 1926-12-02 | 1931-09-15 | Semet Solvay Co | Process for the elimination of waste liquors and the recovery of ammonium salts and phenols from said liquors |
| US2067029A (en) * | 1932-06-18 | 1937-01-05 | Koppers Co Inc | Elimination of poisonous waste liquors |
| US2710663A (en) * | 1952-04-17 | 1955-06-14 | United States Steel Corp | Method and apparatus for removing naphthalene from coke oven gas |
-
1958
- 1958-01-27 US US711380A patent/US2961065A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1487768A (en) * | 1924-03-25 | Process op and apparatus for recovering the ammonia content of coal gas | ||
| US932758A (en) * | 1909-03-13 | 1909-08-31 | Francis Joseph Collin | Method of recovering ammonia from coal-gases. |
| US1823364A (en) * | 1926-12-02 | 1931-09-15 | Semet Solvay Co | Process for the elimination of waste liquors and the recovery of ammonium salts and phenols from said liquors |
| US2067029A (en) * | 1932-06-18 | 1937-01-05 | Koppers Co Inc | Elimination of poisonous waste liquors |
| US2710663A (en) * | 1952-04-17 | 1955-06-14 | United States Steel Corp | Method and apparatus for removing naphthalene from coke oven gas |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1206870B (en) * | 1963-02-28 | 1965-12-16 | Dr Guenter Wunderlich | Process for incinerating the ammonia produced during coking |
| US3581472A (en) * | 1969-08-08 | 1971-06-01 | Koppers Co Inc | System for the removal of naphthalene from coke oven gas |
| DE2238805A1 (en) * | 1971-08-18 | 1973-02-22 | Koppers Co Inc | METHOD OF REMOVING AMMONIA FROM COK OVEN GAS |
| US4286971A (en) * | 1979-10-05 | 1981-09-01 | Bethlehem Steel Corporation | Removal of naphthalene from recirculated wash oil |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4140586A (en) | Method and apparatus for distillation | |
| US3120993A (en) | Gas purification process | |
| US3000693A (en) | Method of removing and disposing of ammonia from coke oven gas | |
| US2961065A (en) | Coke oven gas by-product recovery | |
| US2419225A (en) | Hydrogen cyanide recovery | |
| US2649403A (en) | Method of coke-oven by-product recovery | |
| US4277311A (en) | Apparatus for distillation | |
| US1830178A (en) | Removal of naphthalene and tar from fuel gas | |
| US1973913A (en) | Process of quenching hot coke | |
| US4244711A (en) | Process for minimizing the deposition of materials in the ammonia liquor coolers in the coking of carbonaceous materials | |
| US2966394A (en) | Method and apparatus for producing ammonium sulfate | |
| US1936864A (en) | Ammonia recovery | |
| US2675296A (en) | Gas purification process | |
| US2786082A (en) | Dephenolization process and apparatus | |
| US2059494A (en) | Method of rectification | |
| CN111825258B (en) | Coking residual ammonia water treatment device and method | |
| US1958583A (en) | Dehydration of tar, etc. | |
| US2010003A (en) | Coke-oven gas by-product recovery | |
| US2922751A (en) | Debenzolizing wash oil | |
| US1989177A (en) | Process for the recovery of phenols from gas liquors | |
| US2697067A (en) | Method and apparatus for coke oven by-product recovery | |
| US2785114A (en) | Schmalenbach | |
| EP0245814B1 (en) | Cooling, dehumidifying, de-naphthenizing and detarring plant for coal distillation gases | |
| US1747616A (en) | Ammonia-recovery process | |
| US1892654A (en) | Method and apparatus for distilling tar |