US2674756A - Plug for removing paraffin accumulating in oil conduits - Google Patents
Plug for removing paraffin accumulating in oil conduits Download PDFInfo
- Publication number
- US2674756A US2674756A US281056A US28105652A US2674756A US 2674756 A US2674756 A US 2674756A US 281056 A US281056 A US 281056A US 28105652 A US28105652 A US 28105652A US 2674756 A US2674756 A US 2674756A
- Authority
- US
- United States
- Prior art keywords
- oil
- plug
- weight
- acids
- paraffin
- 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
- 239000012188 paraffin wax Substances 0.000 title claims description 27
- 239000000463 material Substances 0.000 claims description 23
- 239000002253 acid Substances 0.000 claims description 15
- 150000007524 organic acids Chemical class 0.000 claims description 14
- 150000007513 acids Chemical class 0.000 claims description 12
- 230000003647 oxidation Effects 0.000 claims description 12
- 238000007254 oxidation reaction Methods 0.000 claims description 12
- 150000003460 sulfonic acids Chemical class 0.000 claims description 12
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 11
- 239000000194 fatty acid Substances 0.000 claims description 11
- 229930195729 fatty acid Natural products 0.000 claims description 11
- 150000004665 fatty acids Chemical class 0.000 claims description 11
- 150000001735 carboxylic acids Chemical class 0.000 claims description 10
- 239000001856 Ethyl cellulose Substances 0.000 claims description 8
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 8
- 229920001249 ethyl cellulose Polymers 0.000 claims description 8
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 2
- 229920003086 cellulose ether Polymers 0.000 description 34
- 239000003921 oil Substances 0.000 description 33
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 29
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 28
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 28
- -1 amine salt Chemical class 0.000 description 23
- 239000001993 wax Substances 0.000 description 17
- 239000002585 base Substances 0.000 description 15
- 239000010426 asphalt Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 125000005608 naphthenic acid group Chemical group 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 238000005984 hydrogenation reaction Methods 0.000 description 5
- 239000012170 montan wax Substances 0.000 description 5
- 150000002825 nitriles Chemical class 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- PTMRDOLOEDPHLB-UHFFFAOYSA-N 2,3-dipentylphenol Chemical compound CCCCCC1=CC=CC(O)=C1CCCCC PTMRDOLOEDPHLB-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001350 alkyl halides Chemical class 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical class CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000007790 scraping Methods 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical class CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000875 Dissolving pulp Polymers 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- MJEMIOXXNCZZFK-UHFFFAOYSA-N ethylone Chemical group CCNC(C)C(=O)C1=CC=C2OCOC2=C1 MJEMIOXXNCZZFK-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Chemical class CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 150000002943 palmitic acids Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/52—Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning
- C09K8/524—Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning organic depositions, e.g. paraffins or asphaltenes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/927—Well cleaning fluid
- Y10S507/929—Cleaning organic contaminant
- Y10S507/931—Organic contaminant is paraffinic
Definitions
- This invention relates generally to the removal of paraffin from production tubing, surface flow lines, and other conduits through which oil passes, and particularly to slowly soluble or disintegrable plugs adapted to be passed therethrough for removing paraffin deposits from the walls thereof.
- the present invention provides a plug of the same general type but Which has greater physical strength and ability to resist shattering. It has been found that the physical properties of oil soluble plugs can be materially improved by including in the composition thereof at least a minor quantity of an oil-soluble cellulose ether.
- one object of the present invention is to provide an oil-soluble paraffin-removing plug of improved strength and resistance to shattering during passage through production tubing,
- the forward end provides a cutting surface that will scrape or cut the parafiin upon contact therewith, to maintain shape and remain hard at temperatures in excess of the highest temperature expected to be encountered in temporary storage places, that is, in excess of approximately 150 F., to dissolve or disintegrate in the oil flowing through the conduit within a desired period of time, such as, for example, from one hour to a day or more after passing through the conduit and removing the paraffin from the interior thereof, and to be free from shattering or breaking under pressures required for propelling the plug through the production tubing or flow line.
- a desired period of time such as, for example, from one hour to a day or more after passing through the conduit and removing the paraffin from the interior thereof, and to be free from shattering or breaking under pressures required for propelling the plug through the production tubing or flow line.
- the base materials may be exemplified by high melting point waxes, such as microcrystalline hydrocarbon waxes derived from petroleum and having melting points between 150 F. and 200 F.; ceresin; montan wax; chloro-waxes; waxes from the Fischer-Tropsch process; waxes from crude oil tank bottoms; high melting synthetic wax-like materials such as the anilides and amides of the higher fatty acids; ester gums; high melting petroleum resins derived from crude oil residues by solvent treatment and/or oxidation; petroleum asphalts having softening points (R. & B.) between 200 F. and 300 F. and having a maximum penetration at 77 F.
- high melting point waxes such as microcrystalline hydrocarbon waxes derived from petroleum and having melting points between 150 F. and 200 F.; ceresin; montan wax; chloro-waxes; waxes from the Fischer-Tropsch process; waxes from crude oil tank bottoms; high melting synthetic wax-like materials such as the anilides and amide
- waxy asphalts derived from petroleum residuum by propane treatment oxidized residues from thermal or catalytic oil cracking units; and residues from coal tar, coal tar pitch, and vegetable pitches; or mixture of two or more of these materials.
- the rosin amines used for the production of the rosin amine salts included'as a component of the plug may be prepared from dehydrogenated rosin, disproportionated rosin, or hydrogenated rosin by first reacting with ammonia to form the nitrile and then hydrogenating the nitrile to the amine.
- the step of making the nitrile may be carried out by passing gaseous ammonia into the molten rosin material and vaporizing the water as fast as it is formed or by heating the rosin material and ammonia in the presence of a dehydration catalyst.
- the nitrile is preferably purified by alkali extraction or by distillation to remove unconverted acid.”
- the hydrogenation of the nitrile may be carried out in the presence or absence of a solvent and in the presence or absence of ammonia.
- the catalyst may be any of the well-known hydrogenation catalysts such as Raney nickel, R-aney cobalt, activated nickel, cobalt, palladium or platinum, etc., and supports may be used if desired.
- the hydrogenation is usually carried out under a pressure of about 200 to about 8,0Qpounds per square inch at a temperature of about 20 C. to about 200 C.
- the rosin amine salts which may be used in accordance with this invention include the salts of organic acids such as the higher fatty acids, for example, lauric, stearic, and palmitic acids; naphthenic acids having a molecular weight preferably between 170 and 350; sulfonic acids derived by the treatment of petroleum fractions with sulfuric acid or other sulfonating agents.
- organic acids such as the higher fatty acids, for example, lauric, stearic, and palmitic acids
- naphthenic acids having a molecular weight preferably between 170 and 350
- sulfonic acids derived by the treatment of petroleum fractions with sulfuric acid or other sulfonating agents are preferred, and these acids usually have a molecular weight between 400 and 550 and acid numbers between 30 and 140 mg. KOl-I per gram.
- Sulfonic acids derived from higher alkyl benzenes, naphthalenes, and anthracenes may also be used, as well as carboxylic acids such as abietic acid, and acids from the oxidation of paraffin wax.
- Particularly suitable are the rosin amine salts of stearic acid, palmitic acid, and naphthenic acid.
- the rosin amine salts may be prepared simply by mixing the amine with an equivalent amount of organic acid and heating, or by dissolving the amine and acid in a suitable solvent, heating if necessary, and then removing the solvent.
- the cellulose ether employed as a component of the plugs made in accordance with this invention may be any oil-soluble cellulose ether such, for example, as ethyl, propyl, isopropyl, n-butyl, isobutyl, or benzyl cellulose. Some of these cellulose eth'ers are commercially available, and various processes are known for the preparation thereof. Thus, cellulose may be treated with a base, for example sodium hydroxide, to form alkali cellulose which is then heated with the appropriate alkyl halide or alkyl sulfate.
- a base for example sodium hydroxide
- a method more recently employed for preparation of cellulose ethers involves dissolving cellulose in a quaternary ammonium hydroxide and then treating the cellulose with a desired dialkyl sul fate or alkyl halide.
- Ethyl cellulose has been found to be especially suitable for use in the present invention. 7
- Oil-soluble cellulose ethers such as ethyl cellulose
- the cellulose ether solution may then be mixed immediately with the other components to form a homogeneous mass fromwhich the plugs-may be shaped, or may be cooled andstorechuzitil 4 ready for use, at which time it may be reheated to a melting temperature.
- cellulose ethers there are several substances which are mutually compatible with the oil-soluble cellulose ethers and with the other components of the parafiin-removing plug, and which are therefore suitable for forming the cellulose ether solution.
- beeswax, montan wax, stearic acid, phenolic resin, castor oil, or dibutyl phthalate may be used for this purpose.
- the oil-soluble cellulose other solution may be made by heating montan wax to'a temperature of approximately 250 F.
- Oil-soluble paraflin removing plugs may be made by melting the base material, the rosin amine salt, if necessary, and the cellulose ether or cellulose ether solution, depending on the base material employed, mixing these components in the desired proportions, and shaping the molten or plastic material to the desired contour and dimensions by molding or extrusion.
- the relative percentages of the components of the plugs may be varied considerably, depending upon the conditions under which they are to be used.
- the oil-soluble base material comprising wax or asphalt may constitute from about 90% to about 55% of the total weight of the plug
- the rosin amine salt of an organic acid may comprise from about 5% to about 45% of the total weight
- the amount of oil-soluble cellulose ether or cellulose ether solution employed may preferably :be that which is required to incorporate into the plugs from about 0.5% to about 5% by weight of the oil-soluble cellulose ether. While the percentage of cellulose ether employed in the plug may be increased considerably over the suggested 5%, little, if any, improvement in the physical properties of the plugs is noted by the inclusion of a greater amount of this material.
- Example II For removing paraffin deposits from oil lines at temperatures less than about 100 F., a suitable plug may be made consisting of 90% by weight of the same asphalt as employed in Example I, 5% by weight of rosin amine stearate, and 5% by weight of the same cellulose ether solution as employed in Example I. A plug of this composition subjected to the same shock test as described in connection with Example I was found to develop only a minor edge fracture.
- Example III A plug composed of 55% by weight of microcrystalline wax having a melting point between 190 F. and 195 F., 40% rosin amine stearate, and 5% of the same cellulose ether solution as employed in Example I will effectively remove parafiin deposits from the interior of an oil flow line and completely dissolve in the oil within a period of several hours at a temperature of approximately 130 F.
- Example IV Plugs composed of 50% of the same asphalt as employed in Example I, 35% microcrystalline wax, rosin amine stearate, and 5% of the same cellulose ether solution as used in Example I will effectively remove parafiin deposits and dissolve at a satisfactory rate in a surface oil line at temperatures between 80 F. and 100 F.
- Plugs provided in accordance with this invention are satisfactory for removing parafiin deposits from any production tubing or other conduit through which oil flows.
- the procedure is not one of using a plug of given percentages of base material such as wax or asphalt, or mixtures thereof, with the rosin amine salt and cellulose ether solution, but instead the percentages of such materials are varied to obtain, under the conditions of each case where it is desired to remove paraffin deposits, a plug having the aforementioned necessary characteristics, that is, sufficiently hard to provide an effective cutting surface, maintain shape and remain hard at temperatures in excess of those expected to be encountered in temporary storage places, sufficiently soluble to dissolve in oil within a desired period of time, and will not shatter or break under the compression forces necessary to propel the plug through the conduit.
- plugs may be provided preferably in accordance with this invention containing either asphalt alone, or wax alone as the base materials, or mixtures thereof. It is necessary in each case, however, to include at least 5% by weight of the rosin amine salt and sufiicient cellulose ether solution to provide at least about 0.5% oil-soluble cellulose ether in order to obtain the desired physical properties of the plug.
- a plug is formed by varying the percentages of the components until the necessary physical properties are obtained for the conditions under which the plug is to be employed.
- the plug is shaped to conform with the interior of the oil conduit and is adapted to fit snugly therein.
- the plug is then inserted in the conduit and oil under pressure is applied to one end thereof causing the plug to be propelled through the conduit, thereby removing parafiin deposits. While moving through the conduit and also after traveling to the end of the conduit with removal of all the parafiin deposited on the interior thereof, the plug will dissolve relatively slowly in the oil.
- the plugs may comprise solid, cylindrical shapes, or in the event that more rapid dissolution or disintegration is required, the plugs may be formed as hollow cylinders having one end closed so that the internal surface of the plug may be subjected to the solvent action of the oil in the conduit being cleaned. If necessary, the hollow, cylindrical plugs may be formed with internal webs to give added strength, or the leading end of the plug, be it either solid or hollow, may be recessed or dished rather than fiat.
- a plug for removing paraflin from the wall of a conduit through which oil flows including between 55% and 90% by weight of an oil-soluble base material, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of an oil-soluble cellulose ether.
- a plug for removing paraffin from the wall of a conduit through which oil flows including between 55% and 90% by weight of asphalt, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5 and 5% by weight of an oil-soluble cellulose ether.
- a plug for removing paraffin from the wall of a conduit through which oil flows including between 55% and 90% by weight of an oilsoluble wax, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids,
- naphthenic acids sulfonic acids, carboxylic acids; and acids derived from the oxidation of paraffin wax, and between 0.5% and by weight of an oil-soluble cellulose ether.
- a plug for removing parafiin from the wall of a conduit through which oil flows including between 55% and 90% by weight of an oil-soluble base material consisting of asphalt and wax, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of parafiin wax, and between 0.5% and 5% by weight of an oil-soluble cellulose ether.
- a plug for removing paraffin from the wall of a conduit through which oil flows including between 55% and 90% by weight of an oil-soluble base material, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of ethyl cellulose.
- a plug for removing paraffin from the wall of a conduit through which oil flows including between 55% and 90% by weight of asphalt, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of ethyl cellulose.
- a plug for removing parafiin from the wall of a conduit through which oil flows including between 55% and 90% by weight of an oil-soluble wax, between 5% and by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of ethyl cellulose.
- a plug for removing paraflin from the wall of a conduit through which oil flows including between and by weight of an oil-soluble base material consisting of asphalt and wax, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin Wax, and between 0.5% and 5% by weight of ethyl cellulose.
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Description
Patented Apr. 13, 1954 PLUG FOR REMOVING PARAFFIN ACCUMU- LATING IN OIL CONDUITS Harrell L. Bilhartz and Howard E. Greenwell, Dallas, Tex., assignors to The Atlantic Refining Company, Philadelphia, Pa., a corporation of Pennsylvania No Drawing. Application April 7, 1952, Serial No. 281,056
8 Claims.
This invention relates generally to the removal of paraffin from production tubing, surface flow lines, and other conduits through which oil passes, and particularly to slowly soluble or disintegrable plugs adapted to be passed therethrough for removing paraffin deposits from the walls thereof.
In co-pending application, Serial No. 137,478, filed January 7, 1950, by Harrell L. Bilhartz, Howard E. Greenwell, and Lawrence E. Davis, now Patent No. 2,603,804, said Bilhartz and Greenwell being co-inventors of the present invention, there is disclosed a paraffin-removing plug consisting of an oil-soluble base material and a rosin amine salt of an organic acid. The purpose of the invention disclosed therein was to provide slowly soluble or disintegrable plugs adapted to be passed through production tubing, surface flow lines, and other conduits through which oil flows thereby to remove, by cutting or scraping, paramn deposited on the walls thereof.
While the plugs disclosed in said application have proved to be generally satisfactory, the present invention provides a plug of the same general type but Which has greater physical strength and ability to resist shattering. It has been found that the physical properties of oil soluble plugs can be materially improved by including in the composition thereof at least a minor quantity of an oil-soluble cellulose ether.
Accordingly, one object of the present invention is to provide an oil-soluble paraffin-removing plug of improved strength and resistance to shattering during passage through production tubing,
surface flow lines and other conduits through i lines, or other oil conduits, and which comprises a slowly soluble or disintegrable base material, a rosin amine salt of an organic acid, and a small proportion of an oil soluble cellulose ether. The plug is formed so as to fit snugly in the conduit through which it is caused to be propelled by applying fluid pressure on one end thereof. In order for the plug to effectively remove paraffin, it is necessary for it to be sufiiciently hard that the forward end provides a cutting surface that will scrape or cut the parafiin upon contact therewith, to maintain shape and remain hard at temperatures in excess of the highest temperature expected to be encountered in temporary storage places, that is, in excess of approximately 150 F., to dissolve or disintegrate in the oil flowing through the conduit within a desired period of time, such as, for example, from one hour to a day or more after passing through the conduit and removing the paraffin from the interior thereof, and to be free from shattering or breaking under pressures required for propelling the plug through the production tubing or flow line. This is accomplished in accordance with the invention by varying the percentages of the above mentioned components of the plug, dependent upon the conditions in each particular case.
The base materials may be exemplified by high melting point waxes, such as microcrystalline hydrocarbon waxes derived from petroleum and having melting points between 150 F. and 200 F.; ceresin; montan wax; chloro-waxes; waxes from the Fischer-Tropsch process; waxes from crude oil tank bottoms; high melting synthetic wax-like materials such as the anilides and amides of the higher fatty acids; ester gums; high melting petroleum resins derived from crude oil residues by solvent treatment and/or oxidation; petroleum asphalts having softening points (R. & B.) between 200 F. and 300 F. and having a maximum penetration at 77 F. of 10, and preferably between 5 and 10; waxy asphalts derived from petroleum residuum by propane treatment; oxidized residues from thermal or catalytic oil cracking units; and residues from coal tar, coal tar pitch, and vegetable pitches; or mixture of two or more of these materials.
The rosin amines used for the production of the rosin amine salts included'as a component of the plug may be prepared from dehydrogenated rosin, disproportionated rosin, or hydrogenated rosin by first reacting with ammonia to form the nitrile and then hydrogenating the nitrile to the amine. The step of making the nitrile may be carried out by passing gaseous ammonia into the molten rosin material and vaporizing the water as fast as it is formed or by heating the rosin material and ammonia in the presence of a dehydration catalyst. The nitrile is preferably purified by alkali extraction or by distillation to remove unconverted acid."
prior to hydrogenation to the amine, since the acidic materials frequently destroy the activity of the hydrogenation catalyst. The hydrogenation of the nitrile may be carried out in the presence or absence of a solvent and in the presence or absence of ammonia. The catalyst may be any of the well-known hydrogenation catalysts such as Raney nickel, R-aney cobalt, activated nickel, cobalt, palladium or platinum, etc., and supports may be used if desired. The hydrogenation is usually carried out under a pressure of about 200 to about 8,0Qpounds per square inch at a temperature of about 20 C. to about 200 C.
The rosin amine salts which may be used in accordance with this invention include the salts of organic acids such as the higher fatty acids, for example, lauric, stearic, and palmitic acids; naphthenic acids having a molecular weight preferably between 170 and 350; sulfonic acids derived by the treatment of petroleum fractions with sulfuric acid or other sulfonating agents. Of these, the oil-soluble sulfonic acids obtained as a by-product in the manufacture of mineral white oils are preferred, and these acids usually have a molecular weight between 400 and 550 and acid numbers between 30 and 140 mg. KOl-I per gram. Sulfonic acids derived from higher alkyl benzenes, naphthalenes, and anthracenes may also be used, as well as carboxylic acids such as abietic acid, and acids from the oxidation of paraffin wax. Particularly suitable are the rosin amine salts of stearic acid, palmitic acid, and naphthenic acid. The rosin amine salts may be prepared simply by mixing the amine with an equivalent amount of organic acid and heating, or by dissolving the amine and acid in a suitable solvent, heating if necessary, and then removing the solvent.
The cellulose ether employed as a component of the plugs made in accordance with this invention may be any oil-soluble cellulose ether such, for example, as ethyl, propyl, isopropyl, n-butyl, isobutyl, or benzyl cellulose. Some of these cellulose eth'ers are commercially available, and various processes are known for the preparation thereof. Thus, cellulose may be treated with a base, for example sodium hydroxide, to form alkali cellulose which is then heated with the appropriate alkyl halide or alkyl sulfate. A method more recently employed for preparation of cellulose ethers involves dissolving cellulose in a quaternary ammonium hydroxide and then treating the cellulose with a desired dialkyl sul fate or alkyl halide. Ethyl cellulose has been found to be especially suitable for use in the present invention. 7
Oil-soluble cellulose ethers, such as ethyl cellulose, have been found to be incompatible with asphalts, paraffin base waxes, andcertain other waxes useful as components of oil-soluble paraffin removing plugs, and therefore may not be readily mixed therewith. It has been found, however, that the oil-soluble cellulose ethers may be readily mixed with the incompatible asphalt or wax base materials by first dissolving the cellulose ether in a substance which is compatible both with the cellulose ether and with the base material to form a mixture which shall hereinafter be referred to as a cellulose ether solution. The cellulose ether solution may then be mixed immediately with the other components to form a homogeneous mass fromwhich the plugs-may be shaped, or may be cooled andstorechuzitil 4 ready for use, at which time it may be reheated to a melting temperature.
There are several substances which are mutually compatible with the oil-soluble cellulose ethers and with the other components of the parafiin-removing plug, and which are therefore suitable for forming the cellulose ether solution. For example, beeswax, montan wax, stearic acid, phenolic resin, castor oil, or dibutyl phthalate may be used for this purpose. The oil-soluble cellulose other solution may be made by heating montan wax to'a temperature of approximately 250 F. and slowly adding thereto as much oilsoluble cellulose ether as will readily dissolve therein, adding also a very small quantity of an anti-oxidant, such as diamylphenol, which serves the purpose of preventing oxidation of the cellulose ether when exposed to the high temperature required for melting the montan wax and dissolving the cellulose ether therein. Although it will [be understood that the percentages of the several components of the solution are not criti cal, a satisfactory solution has been found to be one consisting of 87 parts montan wax to 12 parts of ethyl cellulose and one part of diamylphenol.
Oil-soluble paraflin removing plugs, according to this invention, may be made by melting the base material, the rosin amine salt, if necessary, and the cellulose ether or cellulose ether solution, depending on the base material employed, mixing these components in the desired proportions, and shaping the molten or plastic material to the desired contour and dimensions by molding or extrusion. The relative percentages of the components of the plugs may be varied considerably, depending upon the conditions under which they are to be used. In general, the oil-soluble base material comprising wax or asphaltmay constitute from about 90% to about 55% of the total weight of the plug, the rosin amine salt of an organic acid may comprise from about 5% to about 45% of the total weight, while the amount of oil-soluble cellulose ether or cellulose ether solution employed may preferably :be that which is required to incorporate into the plugs from about 0.5% to about 5% by weight of the oil-soluble cellulose ether. While the percentage of cellulose ether employed in the plug may be increased considerably over the suggested 5%, little, if any, improvement in the physical properties of the plugs is noted by the inclusion of a greater amount of this material.
The following examples are illustrative of plugs which will satisfactorily remove paramn under the various conditions indicated, which are sufficiently oil soluble to dissolve in oil within a period of several hours, which have sufficient physical strength to resist shattering or breakage during normally expected conditions of storage and use, and which will retain their physical shape and remain hard at the highest temperatures expected to be encountered in temporary storage places.
Erarnple I teristics making it suitable for use in removing L-1 A \ln paraffin deposits from the interior of an oil flow line at temperatures in the'range of 120 F. to 125 F. A plug of this composition immersed in a typical crude oil at a temperature of approximately 110 F. was found to dissolve to about half its weight in one hour. When a plug of this composition one inch in diameter and 1 inches long was subjected to the shock imposed thereon by dropping of a 621 gram weight from a height of 32 inches, said plug showed only a very slight crack on one edge which did not substantially decrease the paraffin-removing properties of the plug.
Example II For removing paraffin deposits from oil lines at temperatures less than about 100 F., a suitable plug may be made consisting of 90% by weight of the same asphalt as employed in Example I, 5% by weight of rosin amine stearate, and 5% by weight of the same cellulose ether solution as employed in Example I. A plug of this composition subjected to the same shock test as described in connection with Example I was found to develop only a minor edge fracture.
Example III A plug composed of 55% by weight of microcrystalline wax having a melting point between 190 F. and 195 F., 40% rosin amine stearate, and 5% of the same cellulose ether solution as employed in Example I will effectively remove parafiin deposits from the interior of an oil flow line and completely dissolve in the oil within a period of several hours at a temperature of approximately 130 F.
Example IV Plugs composed of 50% of the same asphalt as employed in Example I, 35% microcrystalline wax, rosin amine stearate, and 5% of the same cellulose ether solution as used in Example I will effectively remove parafiin deposits and dissolve at a satisfactory rate in a surface oil line at temperatures between 80 F. and 100 F.
Plugs provided in accordance with this invention are satisfactory for removing parafiin deposits from any production tubing or other conduit through which oil flows. In the actual operation of scraping or cutting paraffin from the interior of such oil flow lines, the procedure is not one of using a plug of given percentages of base material such as wax or asphalt, or mixtures thereof, with the rosin amine salt and cellulose ether solution, but instead the percentages of such materials are varied to obtain, under the conditions of each case where it is desired to remove paraffin deposits, a plug having the aforementioned necessary characteristics, that is, sufficiently hard to provide an effective cutting surface, maintain shape and remain hard at temperatures in excess of those expected to be encountered in temporary storage places, sufficiently soluble to dissolve in oil within a desired period of time, and will not shatter or break under the compression forces necessary to propel the plug through the conduit. This will be apparent when consideration is given to the fact from location to location there are variations in the temperatures encountered in the oil flow lines, the composition of the oil in which the soluble plug is required to dissolve, the time in which it is desirable that the plug dissolve, the amount of paraffin deposited and other fac tors, which need not be mentioned. Field tests have indicated, for example, that the wax content may vary from 0% to 55% by weight, asphalt content from 0% to rosin amine salt from 5% to 5%, and the cellulose ether solution sufiicient to incorporate into the plugs from about 0.5% to 5% of cellulose ether, dependent upon the particular conditions encountered.
It is to be noted that plugs may be provided preferably in accordance with this invention containing either asphalt alone, or wax alone as the base materials, or mixtures thereof. It is necessary in each case, however, to include at least 5% by weight of the rosin amine salt and sufiicient cellulose ether solution to provide at least about 0.5% oil-soluble cellulose ether in order to obtain the desired physical properties of the plug.
In the practice of the invention, a plug is formed by varying the percentages of the components until the necessary physical properties are obtained for the conditions under which the plug is to be employed. The plug is shaped to conform with the interior of the oil conduit and is adapted to fit snugly therein. The plug is then inserted in the conduit and oil under pressure is applied to one end thereof causing the plug to be propelled through the conduit, thereby removing parafiin deposits. While moving through the conduit and also after traveling to the end of the conduit with removal of all the parafiin deposited on the interior thereof, the plug will dissolve relatively slowly in the oil.
While a number of embodiments have been described above, it will be understood that this invention is susceptible of various other embodiments within the scope of the appended claims. For example, the plugs may comprise solid, cylindrical shapes, or in the event that more rapid dissolution or disintegration is required, the plugs may be formed as hollow cylinders having one end closed so that the internal surface of the plug may be subjected to the solvent action of the oil in the conduit being cleaned. If necessary, the hollow, cylindrical plugs may be formed with internal webs to give added strength, or the leading end of the plug, be it either solid or hollow, may be recessed or dished rather than fiat.
We claim:
1. A plug for removing paraflin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of an oil-soluble base material, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of an oil-soluble cellulose ether.
2. A plug for removing paraffin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of asphalt, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5 and 5% by weight of an oil-soluble cellulose ether.
3. A plug for removing paraffin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of an oilsoluble wax, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids,
naphthenic acids, sulfonic acids, carboxylic acids; and acids derived from the oxidation of paraffin wax, and between 0.5% and by weight of an oil-soluble cellulose ether.
4. A plug for removing parafiin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of an oil-soluble base material consisting of asphalt and wax, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of parafiin wax, and between 0.5% and 5% by weight of an oil-soluble cellulose ether.
5. A plug for removing paraffin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of an oil-soluble base material, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of ethyl cellulose.
-6. A plug for removing paraffin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of asphalt, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of ethyl cellulose.
7. A plug for removing parafiin from the wall of a conduit through which oil flows, including between 55% and 90% by weight of an oil-soluble wax, between 5% and by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin wax, and between 0.5% and 5% by weight of ethyl cellulose.
8. A plug for removing paraflin from the wall of a conduit through which oil flows, including between and by weight of an oil-soluble base material consisting of asphalt and wax, between 5% and 45% by weight of a rosin amine salt of an organic acid selected from the group comprising the higher fatty acids, naphthenic acids, sulfonic acids, carboxylic acids, and acids derived from the oxidation of paraffin Wax, and between 0.5% and 5% by weight of ethyl cellulose.
References Cited in the file of this patent UNITED STATES PATENTS Name Date Gross et al. June 3, 1952 Bilhartz et a1 June 22. 1952 Number m ;-fj
Claims (1)
- 5. A PLUG FOR REMOVING PARAFFIN FROM THE WALL OF A CONDUIT THROUGH WHICH OIL FLOWS, INCLUDING BETWEEN 55% AND 90% BY WEIGHT OF AN OIL-SOLUBLE BASE MATERIAL, BETWEEN 5% AND 45% BY WEIGHT OF A ROSIN AMINE SALT OF AN ORGANIC ACID SELECTED FROM THE GROUP COMPRISING THE HIGHER FATTY ACIDS, NAPHTHENIC ACIDS, SULFONIC ACIDS, CARBOXYLIC ACIDS, AND ACIDS DERIVED FROM THE OXIDATION OF PARAFFIN WAX, AND BETWEEN 0.5% AND 5% BY WEIGHT OF ETHYL CELLULOSE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US281056A US2674756A (en) | 1952-04-07 | 1952-04-07 | Plug for removing paraffin accumulating in oil conduits |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US281056A US2674756A (en) | 1952-04-07 | 1952-04-07 | Plug for removing paraffin accumulating in oil conduits |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2674756A true US2674756A (en) | 1954-04-13 |
Family
ID=23075764
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US281056A Expired - Lifetime US2674756A (en) | 1952-04-07 | 1952-04-07 | Plug for removing paraffin accumulating in oil conduits |
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| Country | Link |
|---|---|
| US (1) | US2674756A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2879847A (en) * | 1954-11-29 | 1959-03-31 | August W Willert Jr | Process for increasing the flow in oil wells |
| US5696058A (en) * | 1992-09-21 | 1997-12-09 | Union Oil Company Of California | Solids-free, essentially all-oil wellbore fluid |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2599385A (en) * | 1951-07-09 | 1952-06-03 | Petrolite Corp | Solid stick corrosion inhibitors and a process for preventing corrosion of oil and gas well equipment |
| US2603804A (en) * | 1950-01-07 | 1952-07-22 | Atlantie Refining Company | Plug for removing paraffing accumulating in oil conduits |
-
1952
- 1952-04-07 US US281056A patent/US2674756A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2603804A (en) * | 1950-01-07 | 1952-07-22 | Atlantie Refining Company | Plug for removing paraffing accumulating in oil conduits |
| US2599385A (en) * | 1951-07-09 | 1952-06-03 | Petrolite Corp | Solid stick corrosion inhibitors and a process for preventing corrosion of oil and gas well equipment |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2879847A (en) * | 1954-11-29 | 1959-03-31 | August W Willert Jr | Process for increasing the flow in oil wells |
| US5696058A (en) * | 1992-09-21 | 1997-12-09 | Union Oil Company Of California | Solids-free, essentially all-oil wellbore fluid |
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