US3276519A - Paraffin control method - Google Patents
Paraffin control method Download PDFInfo
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- US3276519A US3276519A US283971A US28397163A US3276519A US 3276519 A US3276519 A US 3276519A US 283971 A US283971 A US 283971A US 28397163 A US28397163 A US 28397163A US 3276519 A US3276519 A US 3276519A
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- derivatives
- well
- paraffin
- inhibiting
- compounds
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- 238000000034 method Methods 0.000 title claims description 21
- 239000012188 paraffin wax Substances 0.000 title description 25
- 239000000203 mixture Substances 0.000 claims description 36
- 230000002401 inhibitory effect Effects 0.000 claims description 28
- 239000007788 liquid Substances 0.000 claims description 25
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims description 24
- 239000010426 asphalt Substances 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 23
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 19
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 16
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 claims description 16
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims description 16
- 230000008021 deposition Effects 0.000 claims description 11
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 claims description 9
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 claims description 9
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- 150000001491 aromatic compounds Chemical class 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 30
- 239000012530 fluid Substances 0.000 description 20
- 239000000126 substance Substances 0.000 description 19
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 12
- 238000000151 deposition Methods 0.000 description 12
- -1 fiuorene Chemical compound 0.000 description 12
- 238000005755 formation reaction Methods 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 229950011260 betanaphthol Drugs 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 230000001276 controlling effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 6
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 239000004305 biphenyl Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 239000003849 aromatic solvent Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- CBMXCNPQDUJNHT-UHFFFAOYSA-N 1,6-dimethylnaphthalene Chemical compound CC1=CC=CC2=CC(C)=CC=C21 CBMXCNPQDUJNHT-UHFFFAOYSA-N 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- WWGUMAYGTYQSGA-UHFFFAOYSA-N 2,3-dimethylnaphthalene Chemical compound C1=CC=C2C=C(C)C(C)=CC2=C1 WWGUMAYGTYQSGA-UHFFFAOYSA-N 0.000 description 2
- YGYNBBAUIYTWBF-UHFFFAOYSA-N 2,6-dimethylnaphthalene Chemical compound C1=C(C)C=CC2=CC(C)=CC=C21 YGYNBBAUIYTWBF-UHFFFAOYSA-N 0.000 description 2
- AUKRYONWZHRJRE-UHFFFAOYSA-N 9-anthrol Chemical compound C1=CC=C2C(O)=C(C=CC=C3)C3=CC2=C1 AUKRYONWZHRJRE-UHFFFAOYSA-N 0.000 description 2
- 150000001454 anthracenes Chemical class 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000011344 liquid material Substances 0.000 description 2
- 150000002790 naphthalenes Chemical class 0.000 description 2
- 150000002987 phenanthrenes Chemical class 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- SXWIAEOZZQADEY-UHFFFAOYSA-N 1,3,5-triphenylbenzene Chemical compound C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=CC(C=2C=CC=CC=2)=C1 SXWIAEOZZQADEY-UHFFFAOYSA-N 0.000 description 1
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- GTBXZWADMKOZQJ-UHFFFAOYSA-N 1-phenanthrol Chemical compound C1=CC2=CC=CC=C2C2=C1C(O)=CC=C2 GTBXZWADMKOZQJ-UHFFFAOYSA-N 0.000 description 1
- XLHGZXJNKKTXGY-UHFFFAOYSA-N 2,3,4-triphenylcyclohexa-1,5-diene-1,4-diol Chemical compound C=1C=CC=CC=1C1(O)C=CC(O)=C(C=2C=CC=CC=2)C1C1=CC=CC=C1 XLHGZXJNKKTXGY-UHFFFAOYSA-N 0.000 description 1
- LRQYSMQNJLZKPS-UHFFFAOYSA-N 2,7-dimethylnaphthalene Chemical compound C1=CC(C)=CC2=CC(C)=CC=C21 LRQYSMQNJLZKPS-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
- 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 1
- 241001449342 Chlorocrambe hastata Species 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- TUAHORSUHVUKBD-UHFFFAOYSA-N benzo[c]phenanthrene Chemical compound C1=CC=CC2=C3C4=CC=CC=C4C=CC3=CC=C21 TUAHORSUHVUKBD-UHFFFAOYSA-N 0.000 description 1
- TXVHTIQJNYSSKO-UHFFFAOYSA-N benzo[e]pyrene Chemical compound C1=CC=C2C3=CC=CC=C3C3=CC=CC4=CC=C1C2=C34 TXVHTIQJNYSSKO-UHFFFAOYSA-N 0.000 description 1
- 150000001846 chrysenes Chemical class 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- LHRCREOYAASXPZ-UHFFFAOYSA-N dibenz[a,h]anthracene Chemical compound C1=CC=C2C(C=C3C=CC=4C(C3=C3)=CC=CC=4)=C3C=CC2=C1 LHRCREOYAASXPZ-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 150000003220 pyrenes Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 239000002023 wood Substances 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
- Y10S507/922—Fracture fluid
-
- 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
- Y10S507/93—Organic contaminant is asphaltic
-
- 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
- the present invention relates to new and improved compositions for control-ling or inhibiting the deposition of paraffin and the like substances on surfaces of pipes, formations and the like, past which liquid hydrocarbons are conducted, and the methods of using such compositions.
- the present invention is particularly adapted to the treating of oil and gas wells and the like.
- the present invention is an improvement over the composition and process disclosed in US. Patent No. 3,051,653.
- Another object of the present invention is to provide a paraflin control composition which is a liquid under ambient conditions and which will act to prevent paraffin from depositing in surface and down hole equipment where is is desirable to place the product in the system with a chemical pump. This enables a 100% active chemical to be introduced into the system rather than a mixture of an unactive solvent and an active paraflin preventing chemical.
- Still another object of the present invention is to provide a new and improved paraffin inhibiting composition which will not freeze under atmospheric conditions and which will also provide a 100% active parafiin preventing chemical.
- Yet a further object of the present invention is to provide a new and improved paraflin control composition comprising liquids, readily oil soluble solids, solids which dissolve during placement thereof, as well as slowly soluble solids.
- thracene pyrene, phenanthrene, fluoranthene, fiuorene, chrysene, acenaphthene, diphenyl or biphenyl, indene, naphthacene, and naphthanthracene.
- acids nitrogen containing compounds, compounds which are derivations of any combinations of any ofthe. above substituents and aryl'derivatives, of these classes of compounds may be used within the skill of a person skilled in the art.
- Some examples of the chemicals are compounds which may be used in the present invention are l-methy-l phenanthrene, phenanthrol, Z-hydroxy phenanthrene, Z-methyl anthracene, anthranol, naphthanthracene, naphthacene, 1,2,5,6 dibenzanthracene, 1,2 benzopyrene, 3,4 benzophenanthrene, diphenyl, 4-hydroxy diphenyl (p-phenyl phenol), 1,3,5-triphenyl benzene, l-methyl naphthalene, Z-methyl naphthalene, 1,6-dimethyl naphthalene, 2,3-dimethyl naphthalene, 2,6-dimethyl naphthalene, 2,7-dimethyl naphthalene, l-naphthoic acid, Z-naphthoic acid, l-naphthol, Z-naphthol, abi
- mono substituted and disubstituted derivatives of phenanthrene alkylated, hydroxylated and arylated derivatives of phenanthrene; mono substituted and disubstituted derivatives of anthracene; alkylated, hydroxylated and arylated derivatives of anthracene; alkylated and hydroxylated derivatives of chrysene; alkylated and hydroxylated, derivatives of pyrene; hydroxy and alkyl derivatives of diphenyl; alkyl and hydroxy derivatives of acenaphthene; alkyl and hydroxy derivatives of liuorene; mono substituted and isomeric disubstituted derivatives of naphthalene; and alkylated and hydroxylated derivatives of naphthalene.
- Some of the above materials having relatively low melting point-s can be used as solvents for the materials having higher melting points, and thereby provide a product which will not freeze under atmospheric conditions and/or provide a 100% active parafiin deposition prevention chemical.
- the above compounds may be dissolved in a suitable solvent and injected into an oil producing system in a manner which will provide a concentration of from about 1 ppm. to about 10,000 ppm. in the produced oil to act as a paraffin inhibiting chemical.
- concentrations of paraifin inhibiting composition varying from about 1 ppm. (parts per million) to about 20 ppm. of Well fluids have been found to be satisfactory.
- the compounds or mixtures of the present invention may be used in either liquid or solid form, and the solid 3 form may be particulated, in sticks, balls, or other desired forms without departing from the scope of the invention.
- the present invention may be utilized in decreasing or removing paraffin depositions in tank bottoms.
- It may also be used in combination with other chemicals, such as corrosion inhibitors, emulsion preventers and others when they are introduced into an oil producing system.
- liquid paraffin control compounds and mixtures thereof may also be used in the manner disclosed in copending application, Serial No. 278,327, filed May 6, 1963.
- the treating or fracturing fluid containing the paraflin inhibitor is injected or pumped into the well bore at a sufficient pressure and rate to create the horizontal fracture.
- the treating agent is preferably a high fluid loss fluid and is also introduced into the well bore and fracture in such manner that it is lost to the face of the fracture and into the formation within the first few feet of the fracture.
- the treated fluid may be further displaced into the formation by the injection of either additional treated fluid or untreated fluid.
- the untreated fluid should preferably be of low fluid loss to limit displacement of fluid.
- the amount of fluid injected into the formations will govern the extent the fluids are extended into the formation, but the flow pattern will exist without regard to the amounts of fluid injected into such formation.
- the fluids injected into the well and the natural well fluids will be produced from the formation, through the fracture and into the well bore in a particular pattern.
- the compounds of the present invention act on the asphalt in a slightly different manner than on the paraflins, actually dissolving them or solvating them so they have little effect on the amount of paraflin which comes out of solution.
- a number of field jobs have been successfully performed in the Odessa area of West Texas using a liquid paraffin control material, a mixture of naphthalene and beta naphthol in an aromatic solvent.
- the use of this liquid material was particularly successful when used with hydraulic pump installations.
- the liquid paraffin inhibiting agent was injected into the suction of the power unit with a standard chemical pump. A reduction and a stabilization in the power oil pressure, as well as an increase in production, were reported in most instances.
- Table I shows the softening point lowering obtained by adding 5% by weight of a variety of materials to the asphalt sample.
- Naphthalene lowered the softening point considerably more than did the other solids and even a little more than the same weight of liquid kerosene. This indicates a strong interaction between these two substances.
- the wax had very little effect on the softening point of the asphalt, as expected.
- the other three solids all have considerably higher melting points than either the wax or naphthalene and the softening point lowerings obtained with them were greater than with the wax, and less than with naphthalene.
- Table II shows the effect of naphthalene concentration on the softening points of several samples of the Donna Spears asphalt and also on several samples of another asphalt identified as Rock Island Tussy. The effect appears to be similar with either type of asphalt.
- paraflin control material be tailored to the particular Well to be treated and that mixtures of two or more of such compounds be used, such as a mixture comprising naphthalene, beta naphthol and an aromatic solvent or a mixture compris ing naphthalene, beta naphthol, and xylene bottoms.
- the present invention relates to a new and improved method of controlling or inhibiting the deposition of paraffin in wells by the treating therewith of certain polycyclic aromatic compounds, principally fused ring compounds, in either liquid or solid form.
- a method of treating oil and gas Wells and other equipment for inhibiting the formation of paraflin on surfaces past which liquid hydrocarbons are conducted comprising the step of introducing into the well or other equipment a treating composition consisting of at least one polycyclic aromatic compound having at least two rings of carbon atoms, said polycyclic aromatic compound selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen-containing compounds derived therefrom and the arylated derivatives thereof and said composition having been tailored for the conditions of the well being treated.
- a method of treating oil and gas wells and other equipment for inhibiting the formation of paraflin on surfaces past which liquid hydrocarbons are conducted comprising the step of introducing into the well or other equipment a treating composition consisting of a mixture of at least two polycyclic aromatic compounds, said polycyclic aromatic compound selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylrated derivatives thereof, the acid derivatives thereof, the nitrogen-containing compound derived therefrom and the arylated derivatives thereof, each of said compounds having at least two rings of carbon atoms, and said composition having been tailored for the conditions of the well being treated.
- a method of inhibiting or controlling the formation of paraffin on surfaces past which hydrocarbons flow in a well, over a prolonged period of time comprising the step of, introducing into the well a relatively high fluid loss paraflin inhibiting liquid, the active ingredient of which is selected from the group of polycyclic aromatic compounds consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen containing compounds derived therefrom, the arylated derivatives thereof and mixtures thereof.
- the active ingredient of which is selected from the group of polycyclic aromatic compounds consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthan
- paraffin inhibiting liquid is a composition comprising naphthalene, beta naphthol and an aromatic solvent.
- paraffin inhibiting liquid is a composition comprising naphthalene, beta naphthol and xylene bottoms.
- a method of hydraulically producing fractures in underground strata penetrated by the bore of a well comprising the steps of:
- paraffin inhibiting liquid selected from the group of polycyclic aromatic compounds consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen containing compounds derived therefrom, the arylated derivatives thereof and mixtures thereof;
- paraffin inhibiting liquid is a composition comprising naphthalene, beta naphthol and an aromatic solvent.
- paraflin inhibiting liquid is a composition comprising naphthalene, beta naphthol and xylene bottoms.
- a method of treating oil and gas wells and the like for inhibiting the deposition of asphalt on surfaces past which liquid hydrocarbons are conducted comprising the step of introducing into the well a treating composition consisting of at least one polycyclic aromatic compound having at least two rings of carbon atoms, said polycyclic aromatic compound selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogencontaining compounds derived therefrom and the arylated derivatives thereof.
- a method of treating oil and gas wells and the like for inhibiting the deposition of asphalt on surfaces past which liquid hydrocarbons are conducted comprising the step of introducing into the well a treating com-position selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen containing compounds derived therefrom, the arylated derivatives thereof and mixtures thereof.
- a treating com-position selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivative
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
United States Patent Ofiice 3,276,519 Fatented Oct. 4, 1966 No Drawing. Filed May 29,4963, Ser. No. 283,971
Claims. (Cl. 166-41) The present invention relates to new and improved compositions for control-ling or inhibiting the deposition of paraffin and the like substances on surfaces of pipes, formations and the like, past which liquid hydrocarbons are conducted, and the methods of using such compositions.
The present invention is particularly adapted to the treating of oil and gas wells and the like.
The present invention is an improvement over the composition and process disclosed in US. Patent No. 3,051,653.
Although the slowly soluble solid naphthalenic compounds or mixtures as disclosed in said Patent No. 3,051,653 have been found to be highly effective in most instances of application, there are some well conditions in which a liquid material or a slowly soluble material more compatible with or attuned to such well conditions is required.
It is, therefore, a primary object of the present invention to provide a composition and method for controlling or inhibiting the deposition of paraffin on surfaces pas-t which liquid hydrocarbons are conducted, which may be applied in such variations or combinations to meet various well conditions, that optimum properties of placement can be obtained.
Another object of the present invention is to provide a paraflin control composition which is a liquid under ambient conditions and which will act to prevent paraffin from depositing in surface and down hole equipment where is is desirable to place the product in the system with a chemical pump. This enables a 100% active chemical to be introduced into the system rather than a mixture of an unactive solvent and an active paraflin preventing chemical.
Still another object of the present invention is to provide a new and improved paraffin inhibiting composition which will not freeze under atmospheric conditions and which will also provide a 100% active parafiin preventing chemical.
Yet a further object of the present invention is to provide a new and improved paraflin control composition comprising liquids, readily oil soluble solids, solids which dissolve during placement thereof, as well as slowly soluble solids.
Other objects and advantages will be readily apparent from the description of the invention set forth hereinbelow.
It has been discovered that two or more of certain polycyclic coal tar products and/ or their derivatives may be combined in such manner that the compounds with the highest melting points and the lowest solubilities in crude oils, for which treatment for paraflin deposition is proposed, are obtained, thereby providing optimum properties of placement of the compounds.
Some of the classes of compounds and their alkylated and/or hydroxylated derivatives which may be used in carrying out the present invention are naphthalene, an-
thracene, pyrene, phenanthrene, fluoranthene, fiuorene, chrysene, acenaphthene, diphenyl or biphenyl, indene, naphthacene, and naphthanthracene.
Also the acids, nitrogen containing compounds, compounds which are derivations of any combinations of any ofthe. above substituents and aryl'derivatives, of these classes of compounds may be used within the skill of a person skilled in the art.
Some examples of the chemicals are compounds which may be used in the present invention are l-methy-l phenanthrene, phenanthrol, Z-hydroxy phenanthrene, Z-methyl anthracene, anthranol, naphthanthracene, naphthacene, 1,2,5,6 dibenzanthracene, 1,2 benzopyrene, 3,4 benzophenanthrene, diphenyl, 4-hydroxy diphenyl (p-phenyl phenol), 1,3,5-triphenyl benzene, l-methyl naphthalene, Z-methyl naphthalene, 1,6-dimethyl naphthalene, 2,3-dimethyl naphthalene, 2,6-dimethyl naphthalene, 2,7-dimethyl naphthalene, l-naphthoic acid, Z-naphthoic acid, l-naphthol, Z-naphthol, abietic acid and l-methyl 7-isopropyl phenanthrene.
In addition to the specific compounds enumerated above, the following may also be used in the present invention: mono substituted and disubstituted derivatives of phenanthrene; alkylated, hydroxylated and arylated derivatives of phenanthrene; mono substituted and disubstituted derivatives of anthracene; alkylated, hydroxylated and arylated derivatives of anthracene; alkylated and hydroxylated derivatives of chrysene; alkylated and hydroxylated, derivatives of pyrene; hydroxy and alkyl derivatives of diphenyl; alkyl and hydroxy derivatives of acenaphthene; alkyl and hydroxy derivatives of liuorene; mono substituted and isomeric disubstituted derivatives of naphthalene; and alkylated and hydroxylated derivatives of naphthalene.
It should be noted, that with the exception of diphenyl and its derivatives, all of the above compounds are fused ring compounds.
By selecting from the above groups, those compounds which are liquid under ambient conditions, it is possible to provide a material which will act to prevent or inhibit paraffin from depositing on surface equipment or down hole equipment, and which can be desirably placed in the system with a chemical pump. This enables a active chemical to be introduced rather than a mixture of an unactive solvent and an active paraffin inhibiting or preventing chemical. An example of this type of chemical is l-methyl naphthalene which melts at 19 C.
Some of the above materials having relatively low melting point-s can be used as solvents for the materials having higher melting points, and thereby provide a product which will not freeze under atmospheric conditions and/or provide a 100% active parafiin deposition prevention chemical.
It should also be noted that the above compounds may be dissolved in a suitable solvent and injected into an oil producing system in a manner which will provide a concentration of from about 1 ppm. to about 10,000 ppm. in the produced oil to act as a paraffin inhibiting chemical.
In actual field applications, concentrations of paraifin inhibiting composition varying from about 1 ppm. (parts per million) to about 20 ppm. of Well fluids have been found to be satisfactory.
The compounds or mixtures of the present invention may be used in either liquid or solid form, and the solid 3 form may be particulated, in sticks, balls, or other desired forms without departing from the scope of the invention.
The present invention may be utilized in decreasing or removing paraffin depositions in tank bottoms.
It may also be used in combination with other chemicals, such as corrosion inhibitors, emulsion preventers and others when they are introduced into an oil producing system.
The inventors have authored two papers which relate to the theory they believe explains how these chemicals function as paraffin inhibiting or control agents, and which disclose in detail the various ways in which these chemicals may be used. These papers are entitled Checking Paraflin Deposition by Crystal Growth Inhibition and A New Approach to the Paraffin Problem and were presented at the 37th Annual Fall Meeting of the Society of Petroleum Engineers of AIME in Los Angeles, California, October 7-10, 1962, and at the Spring Meeting of the Mid-Continent District Division of Production in Amarillo, Texas, March 27-29, 1963, respectively.
The liquid paraffin control compounds and mixtures thereof may also be used in the manner disclosed in copending application, Serial No. 278,327, filed May 6, 1963.
In such well treating method, the treating or fracturing fluid containing the paraflin inhibitor is injected or pumped into the well bore at a sufficient pressure and rate to create the horizontal fracture. The treating agent is preferably a high fluid loss fluid and is also introduced into the well bore and fracture in such manner that it is lost to the face of the fracture and into the formation within the first few feet of the fracture.
The treated fluid may be further displaced into the formation by the injection of either additional treated fluid or untreated fluid. The untreated fluid should preferably be of low fluid loss to limit displacement of fluid. The amount of fluid injected into the formations will govern the extent the fluids are extended into the formation, but the flow pattern will exist without regard to the amounts of fluid injected into such formation.
After the fluids have been introduced into the formation and the well has been placed on production, the fluids injected into the well and the natural well fluids will be produced from the formation, through the fracture and into the well bore in a particular pattern.
The treating liquid which has been lost to the formation nearest the well bore will therefore be slowly produced back with the producing fluids. As only a few parts per million are required of most paraffin inhibitors to provide an effective control over the paraflin problems, a continuing control of the paraffin problem is maintained over a long period of time.
The compounds disclosed hereinabove, as well as those disclosed in U.S. Patent No. 3,051,653, and naphthalene can be used in preventing or inhibiting asphalt deposits which are found in many wells in California. These asphalt deposits are different from the ordinary paraffin deposits found in wells throughout most of the United States and the rest of the world, in that they contain little, if any, normal paraffins.
The compounds of the present invention act on the asphalt in a slightly different manner than on the paraflins, actually dissolving them or solvating them so they have little effect on the amount of paraflin which comes out of solution.
These compounds may be used for controlling or removing asphalt in methods similarly to those employed in inhibiting or controlling paraflin, and are particularly suited to be used with a hot oil, well stimulation process. US. Patents No. 2,300,348 and 3,014,531 are illustrative of hot oil, well stimulation processes.
A number of field jobs have been successfully performed in the Odessa area of West Texas using a liquid paraffin control material, a mixture of naphthalene and beta naphthol in an aromatic solvent. The use of this liquid material was particularly successful when used with hydraulic pump installations. The liquid paraffin inhibiting agent was injected into the suction of the power unit with a standard chemical pump. A reduction and a stabilization in the power oil pressure, as well as an increase in production, were reported in most instances.
A laboratory project was conducted to study the effect of various substances on the softening points of asphalt. It is believed that colloidal asphalt plays an important role in paraflin depositions, and a large lowering of the softening point of the asphalt indicates a strong interaction of the additive tested with the asphalt.
Samples of Donna Spears asphalt were obtained from the Kerr-McGee Refining Company located at Wynne- Wood, Oklahoma. The softening points of these asphalts were determined with a TGA-A.S.T.M. ring and ball tester according to the procedure given in A.S.T.M., Serial D3 6-26.
Table I shows the softening point lowering obtained by adding 5% by weight of a variety of materials to the asphalt sample.
TABLE I.EFFECT OF VARIOUS ADDITIVES ON THE SOFT- ENING POINT OF ASPHALT Type of Asphalt Donna Spears. Softening point of asphalt 111 F. Concentration of additives "5% by wt.
Melting Softening Softening Percent Additive Point of Point of Point Lowering Additive, Mixture, Lowering, F. F. F.
P-12fi Wax 126 103 8 7. 2 Anthracene 423 11 9. 9 Para-phenyl phenoL. 329 99 12 10. 8 Beta-Naphthol 252 93 18 16. 3 Kerosene liquid 89 -22 19. 8 Naphthalene 176 86 -25 22. 5
1 A paraffinic wax having a melting point of 126 F.
Naphthalene lowered the softening point considerably more than did the other solids and even a little more than the same weight of liquid kerosene. This indicates a strong interaction between these two substances. The wax had very little effect on the softening point of the asphalt, as expected.
The other three solids all have considerably higher melting points than either the wax or naphthalene and the softening point lowerings obtained with them were greater than with the wax, and less than with naphthalene.
Table II shows the effect of naphthalene concentration on the softening points of several samples of the Donna Spears asphalt and also on several samples of another asphalt identified as Rock Island Tussy. The effect appears to be similar with either type of asphalt.
TABLE II.-EFFECT OF NAPH'IHALENE ON SOFTENING POINTS OF ASPHALTS Percent Softening Softening Percent Asphalt Naphtha- Point of Point Lowering lene Mixture, Lowering, by Weight F. F.
Rock Island Tussy. 0 121 0 0 Do 1 114 7 5. 8
Using the testing procedures as disclosed hereinabove,
another sample of asphalt, having a softening point of 5 167 F., and obtained from the Kerr-McGee Refining Company was tested. The results of these tests are shown in Table III, wherein each compound was added to the asphalt sample in the stated percentage thereof and the softening point for each mixture was determined.
TABLE III Percent Softening Compound Compound Point of by Weight Mixture, F.
1 166. Naphthalene g f 20 86. 5 1 158. 0 Anthracene 5 150. 0 159.0 7 a 1 161.0 Alpha methyl naphthalene 5 137. O 10 117.0 1 158. 0 Beta naphthol 5 147. 0 10 120. 0 1 160. O Para-phenyl phenol 5 144. 0 10 0 1 5 0 Xylene bottoms 5 In 0 10 110. 0 1 162. 0 Acintene Dipentene 5 134. 0 10 115.0
Although there are some wells having paraflin problems which can be helped by the addition thereto of a small amount of a single one of the compounds disclosed hereinabove, it is preferred that the paraflin control material be tailored to the particular Well to be treated and that mixtures of two or more of such compounds be used, such as a mixture comprising naphthalene, beta naphthol and an aromatic solvent or a mixture compris ing naphthalene, beta naphthol, and xylene bottoms.
Broadly, the present invention relates to a new and improved method of controlling or inhibiting the deposition of paraffin in wells by the treating therewith of certain polycyclic aromatic compounds, principally fused ring compounds, in either liquid or solid form.
What is claimed is:
1. A method of treating oil and gas Wells and other equipment for inhibiting the formation of paraflin on surfaces past which liquid hydrocarbons are conducted, comprising the step of introducing into the well or other equipment a treating composition consisting of at least one polycyclic aromatic compound having at least two rings of carbon atoms, said polycyclic aromatic compound selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen-containing compounds derived therefrom and the arylated derivatives thereof and said composition having been tailored for the conditions of the well being treated.
2. A method of treating oil and gas wells and other equipment for inhibiting the formation of paraflin on surfaces past which liquid hydrocarbons are conducted, comprising the step of introducing into the well or other equipment a treating composition consisting of a mixture of at least two polycyclic aromatic compounds, said polycyclic aromatic compound selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylrated derivatives thereof, the acid derivatives thereof, the nitrogen-containing compound derived therefrom and the arylated derivatives thereof, each of said compounds having at least two rings of carbon atoms, and said composition having been tailored for the conditions of the well being treated.
3. A method of inhibiting or controlling the formation of paraffin on surfaces past which hydrocarbons flow in a well, over a prolonged period of time, comprising the step of, introducing into the well a relatively high fluid loss paraflin inhibiting liquid, the active ingredient of which is selected from the group of polycyclic aromatic compounds consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen containing compounds derived therefrom, the arylated derivatives thereof and mixtures thereof.
4. The method of claim 3, wherein said paraffin inhibiting liquid is a composition comprising naphthalene, beta naphthol and an aromatic solvent.
5. The method of claim 3, wherein said paraffin inhibiting liquid is a composition comprising naphthalene, beta naphthol and xylene bottoms.
6. A method of hydraulically producing fractures in underground strata penetrated by the bore of a well, comprising the steps of:
(a) introducing into the well a fracturing fluid having a paraffin inhibiting liquid dispersed in at least the spearhead thereof, said paraffin inhibiting liquid being selected from the group of polycyclic aromatic compounds consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen containing compounds derived therefrom, the arylated derivatives thereof and mixtures thereof;
(b) causing said fluid to contact a section of the underground strata to be fractured;
(c) applying suflicient pressure to said fluid to fracture said strata section and inject thereinto fluid containin g said paraffin inhibiting liquid, whereby said paraffin inhibiting liquid is lost to the face of the fracture and into the strata section; and
(d) allowing the paraffin inhibiting liquid to be produced back with the well fluids thereby providing a continuing paraffin inhibiting treatment.
7. The method of claim 6, wherein said paraffin inhibiting liquid is a composition comprising naphthalene, beta naphthol and an aromatic solvent.
8. The method of claim 6, wherein said paraflin inhibiting liquid is a composition comprising naphthalene, beta naphthol and xylene bottoms.
9. A method of treating oil and gas wells and the like for inhibiting the deposition of asphalt on surfaces past which liquid hydrocarbons are conducted, comprising the step of introducing into the well a treating composition consisting of at least one polycyclic aromatic compound having at least two rings of carbon atoms, said polycyclic aromatic compound selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogencontaining compounds derived therefrom and the arylated derivatives thereof.
10. A method of treating oil and gas wells and the like for inhibiting the deposition of asphalt on surfaces past which liquid hydrocarbons are conducted, comprising the step of introducing into the well a treating com-position selected from the group consisting of pyrene, phenanthrene, fluoranthene, fluorene, chrysene, acenaphthene, indene, naphthacene, naphthanthracene, the alkylated derivatives thereof, the hydroxylated derivatives thereof, the acid derivatives thereof, the nitrogen containing compounds derived therefrom, the arylated derivatives thereof and mixtures thereof.
(References on following page) References Cited by the Examiner UNITED STATES PATENTS Peski 166-41 Dana 16641 Kaufman 16641 Carpenter et a1. 16641 Irwin 16642.1 Skolaut et a1 252-8.3 Fast et a1 166 42.1
V 8 3,127,345 3/1964 De Groote et :11.
3,172,473 3/1965 Crowley et a1. 166-41 OTHER REFERENCES Kirk-Oth'mer Encyclopedia, of Chemical Technology, The Interscience Encyclopedia Inc., N.Y., vol. 13, p. 625.
CHARLES E. OCONNELL, Primdry Examiizrf T. A. ZALENSKI, s. I. NOVOSAD,
. ss antExamin n-n
Claims (1)
- 9. A METHOD OF TREATING OIL AND GAS WELLS AND THE LIKE FOR INHIBITING THE DEPOSITION OF ASPHALT ON SURFACES PAST WHICH LIQUID HYDROCARBONS ARE CONDUCTED, COMPRISING THE STEP OF INTRODUCING INTO THE WELL A TREATING COMPOSITION CONSISTING OF AT LEAST ONE POLYCYCLIC AROMATIC COMPOUND HAVING AT LEAST TWO RINGS OF CARBON ATOMS SAID POLYCYCLIC AROMATIC COMPOUND SELECTED FROM THE GROUP CONSISTING OF PYRENE, PHENANTHRENE, FLUORANTHENE, FLUORINE, CHRYSENE, ACENAPHTHENE, INDENE, NAPHTHACENE, NAPHTHANTHRACENE, THE ALKYLATED DERIVATIVES THEREOF, THE HYDROXYLATED DERIVATIVES THEREOF, THE ACID DERIVATIVES THEREOF, THE NITROGENCONTAINING COMPOUNDS DERIVED THEREFROM AND THE ARYLATED DERIVATIVES THEREOF.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US283971A US3276519A (en) | 1963-05-29 | 1963-05-29 | Paraffin control method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US283971A US3276519A (en) | 1963-05-29 | 1963-05-29 | Paraffin control method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3276519A true US3276519A (en) | 1966-10-04 |
Family
ID=23088356
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US283971A Expired - Lifetime US3276519A (en) | 1963-05-29 | 1963-05-29 | Paraffin control method |
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| US (1) | US3276519A (en) |
Cited By (10)
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|---|---|---|---|---|
| US3437146A (en) * | 1968-01-11 | 1969-04-08 | Midwest Chem & Processing Co I | Method of removing paraffin from a well with heated solvent |
| US3574319A (en) * | 1969-12-30 | 1971-04-13 | Tenneco Oil Co | Paraffin control method |
| US3640824A (en) * | 1965-11-19 | 1972-02-08 | Sinclair Oil & Gas Co | Paraffin inhibitor in crude oil with high-molecular weight highly branched polyethylene |
| EP0644315A1 (en) * | 1993-09-17 | 1995-03-22 | AGIP S.p.A. | Effective hydrocarbon blend for removing asphaltenes |
| US5696058A (en) * | 1992-09-21 | 1997-12-09 | Union Oil Company Of California | Solids-free, essentially all-oil wellbore fluid |
| WO1998030784A1 (en) * | 1997-01-09 | 1998-07-16 | Imperial College Of Science, Technology & Medicine | Method of controlling asphaltene precipitation in a fluid |
| WO2004111383A1 (en) * | 2003-06-13 | 2004-12-23 | Nicolae Slemcu | Substances to stimulate the extraction of crude oil and a method of processing them |
| US20050082231A1 (en) * | 2001-07-31 | 2005-04-21 | Gochin John J. | Method of controlling asphaltene precipitation in a fluid |
| NO341486B1 (en) * | 2004-06-16 | 2017-11-27 | Champion Tech Inc | Process for inhibiting the formation of naphthenate precipitates or naphthenate stabilized emulsions |
| WO2018177619A1 (en) * | 2017-03-30 | 2018-10-04 | Clariant International Ltd | Fluids for fracking of paraffinic oil bearing formations |
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| US7401653B2 (en) * | 2003-06-13 | 2008-07-22 | Nicolae Slemcu | Substances to stimulate the extraction of crudeoil and a method of processing them |
| NO341486B1 (en) * | 2004-06-16 | 2017-11-27 | Champion Tech Inc | Process for inhibiting the formation of naphthenate precipitates or naphthenate stabilized emulsions |
| WO2018177619A1 (en) * | 2017-03-30 | 2018-10-04 | Clariant International Ltd | Fluids for fracking of paraffinic oil bearing formations |
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