USH1147H - Method of inhibiting corrosion in oil field produced fluids - Google Patents
Method of inhibiting corrosion in oil field produced fluids Download PDFInfo
- Publication number
- USH1147H USH1147H US07/635,258 US63525890A USH1147H US H1147 H USH1147 H US H1147H US 63525890 A US63525890 A US 63525890A US H1147 H USH1147 H US H1147H
- Authority
- US
- United States
- Prior art keywords
- formulation
- corrosion
- dads
- corrosion inhibitor
- ppm
- 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.)
- Abandoned
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Classifications
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- 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
- C09K8/54—Compositions for in situ inhibition of corrosion in boreholes or wells
Definitions
- This invention relates generally to the use of corrosion inhibiting composition comprising diaryldisulfide in oil and gas field produced fluids.
- the invention relates to a method for inhibiting corrosion in wells producing gas containing hydrogen sulfide.
- solvents are sometimes added to the oil to dissolve the sulfur.
- solvents include amine based solvents and dimethyl disulfide (“DMDS").
- the method of the present invention involves the use of a formulation in the treatment of wells producing oil and gas with free sulfur.
- the formulation comprises a mixture of diaryldisulfides ("DADS") and a film forming corrosion inhibitor. Both components of the formulation contribute to the corrosion protection and the DADS also functions as solvent for the free sulfur.
- DADS diaryldisulfides
- a formulation useful in the treatment of sulfur producing oil wells and gas wells should have the following properties:
- the method of the present invention employs a corrosion inhibitor formulation containing an effective amount of DADS and a film forming corrosion inhibitor which satisfies most of the above properties.
- the method of the present invention has particular utility in the treatment of wells producing natural gas and free sulfur because of its dual function in dissolving the sulfur and protecting the well tubulars against corrosion.
- tubulars as used herein include both the well tubing and the well flow line.
- DADS Diaryldisulfide useable in the present invention has the following general formula
- R is an alkyl group or an aromatic group
- R' is an aromatic group.
- the preferred alkyl group contains from 1 to 12 carbon atoms and can be linear or branched.
- the preferred aromatic group for R and R' is a phenyl or substituted phenyl group wherein the substitution is an alkyl group containing from 1 to 3 carbon atoms.
- DADS is available as a waste product generated from the caustic wash of sour naphthas in oil refineries.
- DADS is a mixture of compounds having the R--S--S--R' formula, where R in some of the compounds is alkyl and aromatic in others. R' in the mixture of compounds includes unsubstituted and substituted phenyl groups. Most of the DADS compounds are those wherein R and R' are different aromatic groups (e.g., phenyl groups).
- DADS is commercially available from Merichem as a mixture of aryl, alkyl disulfides and diaryldisulfides, and can be produced by methods well known in the art.
- DADS typically is a mixture of the following components:
- Corrosion Inhibitor Film forming inhibitors are a well known class of corrosion inhibitors and operate by forming a barrier on the well tubulars. These inhibitors consist of one or more polar groups based on N,S, or O which are attracted to the metal or metal corrosion by-product surface. Nonpolar alkyl chains attached to the molecule are oleophilic and attract hydrocarbons to form an oily barrier on the metal surface of the well tubulars.
- the preferred film forming inhibitors for use in the present invention are the amine acid or salts and imidazoline derivatives.
- the fatty amine corrosion inhibitors are made by combining fatty amines with various fatty acids such as resin acids, tall oil acids, sulfurized tall oil fatty acids, dimer and trimer acids, naphthenic acids, lauric acids, oleic acids, and the like.
- R is an alkyl group containing from 10 to 20 carbon atoms
- R' is an alkyl group containing from 10 to 40 carbon atoms
- Y is H, C2H4OH, or C2H4NH2
- the formulation may also include solvents such as aromatic solvents and surfactants such as ethoxylated alcohols or ethoxylated alkyl phenols for dispersing the formulation in the produced fluids.
- solvents such as aromatic solvents
- surfactants such as ethoxylated alcohols or ethoxylated alkyl phenols for dispersing the formulation in the produced fluids.
- the formulation will generally include the following package that can be premixed:
- each of the main components of the corrosion inhibitor formulation may be added separately, it is preferred to package them in a single formulation for introduction into the production stream.
- the formulation may be batched into the stream but preferably is introduced continuously into the production stream at a subsurface location or at the surface.
- a conventional "macaroni" string fed by a chemical pump may be used to inject the formulation into the tubulars at a subsurface location.
- a chemical pump may be used to inject the chemical into the flow line.
- the amount of the formulation actives injected will depend on the application. In the preferred application in produced fluids containing free sulfur, the DADS component should be at least 4-5 times (by weight) the amount of free sulfur in the fluid treated. In most application the concentration of the formulation in the produced fluid may range from 200 to 10,000 ppm (vol), preferably 1000 to 5000 ppm. It is also preferred that the volume ratio of DADS to corrosion inhibitor ranges from 20:1 to 1:1 and preferably 10:1 to 2:1 and most preferably 7:1 to 3:1.
- Coupons were cleaned and dipped in the treatment fluid (e.g., DADS and or corrosion inhibitor) for several minutes. The coupons then were dipped in water and placed in Autoclave Engineering stainless steel cells, each containing brine. The cells were pressurized with a charge gas to 1000 psi. The cells were placed in a wheel test cabinet at the test conditions and exposure times. After exposure, the coupons were cleaned and weighed and the corrosion rate (mpy) for each coupon determined.
- the treatment fluid e.g., DADS and or corrosion inhibitor
- test materials and conditions were as follows:
- Tests were carried out to ascertain the corrosion inhibition properties of (a) DADS alone with no elemental sulfur present and (b) DADS alone in the presence of elemental sulfur.
- the test data are showing in Table I.
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- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Abstract
A method for treating a hydrocarbon stream containing free sulfur wherein a formulation comprising a diaryldisulfide and a film forming corrosion inhibitor are introduced into the hydrocarbon stream.
Description
This invention relates generally to the use of corrosion inhibiting composition comprising diaryldisulfide in oil and gas field produced fluids. In one aspect the invention relates to a method for inhibiting corrosion in wells producing gas containing hydrogen sulfide.
The production of oil and natural gas from subterranean formations sometimes contains hydrogen sulfide and/or free sulfur, both of which contribute to corrosion of well tubulars. In addition, free sulphur can deposit and plug the well tubulars (tubing or flow lines) and other production equipment. Tests have shown that corrosion is particularly severe in areas of sulfur deposition. For example, in local regions of the pipe or equipment which are not capable of being scraped, the sulfur deposits which could not be removed caused severe localized corrosion.
In order to prevent sulfur deposition, solvents are sometimes added to the oil to dissolve the sulfur. Such solvents include amine based solvents and dimethyl disulfide ("DMDS").
Laboratory tests have shown that the amine based solvents are not effective in certain applications, (e.g., in the presence of carbon dioxide) and the DMDS solvents are objectionable because of their odor and toxicity. Moreover, the DMDS solvents are expensive and present disposal problems.
Thus, there is a need for a well treatment which inhibits both the buildup of sulfur and the corrosion of production tubulars and equipment.
The method of the present invention involves the use of a formulation in the treatment of wells producing oil and gas with free sulfur. The formulation comprises a mixture of diaryldisulfides ("DADS") and a film forming corrosion inhibitor. Both components of the formulation contribute to the corrosion protection and the DADS also functions as solvent for the free sulfur.
Laboratory tests indicate that the combination of DADS and the film forming corrosion inhibitor provide better protection on the metal surface of the well tubulars than either compound alone. Although the reasons for the improved results are not fully understood, it is believed that the DADS may remove sulfur deposits thereby conditioning the metal surface for deposition of the film forming corrosion inhibitor.
As indicated above, the presence of free sulfur in oil and gas well produced fluids can create plugging and corrosion problems. These problems may be particularly severe in the presence of hydrogen sulfide, carbon dioxide, and brine. If not treated with chemicals, the well can be damaged and nonproductive.
A formulation useful in the treatment of sulfur producing oil wells and gas wells should have the following properties:
(a) good sulfur solvency
(b) good corrosion inhibition
(c) inexpensive
(d) nondamaging to equipment (non-metallic components)
(e) non-toxic
(f) easily disposable
The method of the present invention employs a corrosion inhibitor formulation containing an effective amount of DADS and a film forming corrosion inhibitor which satisfies most of the above properties.
The method of the present invention has particular utility in the treatment of wells producing natural gas and free sulfur because of its dual function in dissolving the sulfur and protecting the well tubulars against corrosion. The term "tubulars" as used herein include both the well tubing and the well flow line.
Each of the essential components of the formulation, as well as other constituents and additives, are described in detail below.
DADS: Diaryldisulfide useable in the present invention has the following general formula
R--S--S--R'
where:
R is an alkyl group or an aromatic group; and
R' is an aromatic group.
The preferred alkyl group contains from 1 to 12 carbon atoms and can be linear or branched. The preferred aromatic group for R and R' is a phenyl or substituted phenyl group wherein the substitution is an alkyl group containing from 1 to 3 carbon atoms.
DADS is available as a waste product generated from the caustic wash of sour naphthas in oil refineries. DADS is a mixture of compounds having the R--S--S--R' formula, where R in some of the compounds is alkyl and aromatic in others. R' in the mixture of compounds includes unsubstituted and substituted phenyl groups. Most of the DADS compounds are those wherein R and R' are different aromatic groups (e.g., phenyl groups).
DADS is commercially available from Merichem as a mixture of aryl, alkyl disulfides and diaryldisulfides, and can be produced by methods well known in the art.
DADS typically is a mixture of the following components:
______________________________________
COMPONENTS RANGE (wt %)
______________________________________
Alkyl phenyldisulfide
20-30
Diphenyldisulfide 1-5
Phenyltoluyldisulfide
10-15
Toluylethylphenyldisulfide
10-20
Diethylphenyldisulfide
5-15
Naphtha 5-15
______________________________________
Corrosion Inhibitor: Film forming inhibitors are a well known class of corrosion inhibitors and operate by forming a barrier on the well tubulars. These inhibitors consist of one or more polar groups based on N,S, or O which are attracted to the metal or metal corrosion by-product surface. Nonpolar alkyl chains attached to the molecule are oleophilic and attract hydrocarbons to form an oily barrier on the metal surface of the well tubulars.
The preferred film forming inhibitors for use in the present invention are the amine acid or salts and imidazoline derivatives.
The fatty amine corrosion inhibitors are made by combining fatty amines with various fatty acids such as resin acids, tall oil acids, sulfurized tall oil fatty acids, dimer and trimer acids, naphthenic acids, lauric acids, oleic acids, and the like.
The imidazolines of the following structure are particularly preferred: ##STR1## where: R is an alkyl group containing from 10 to 20 carbon atoms;
R' is an alkyl group containing from 10 to 40 carbon atoms; and
Y is H, C2H4OH, or C2H4NH2
A variety of these film forming corrosion inhibitors are commercially available.
Other constitutents: The formulation may also include solvents such as aromatic solvents and surfactants such as ethoxylated alcohols or ethoxylated alkyl phenols for dispersing the formulation in the produced fluids.
Formulation: The formulation will generally include the following package that can be premixed:
______________________________________
Broad Preferred
Most
Range Range Preferred
(vol %) (vol %) Range
______________________________________
DADS 60-99 75-95 75-93
Film Former
1-40 5-20 5-15
Solvent 0-30 0-5 1-5
Surfactant 0-20 0-5 0.5-3
______________________________________
Operation: Although each of the main components of the corrosion inhibitor formulation may be added separately, it is preferred to package them in a single formulation for introduction into the production stream.
The formulation may be batched into the stream but preferably is introduced continuously into the production stream at a subsurface location or at the surface. A conventional "macaroni" string fed by a chemical pump may be used to inject the formulation into the tubulars at a subsurface location. For surface injection, a chemical pump may be used to inject the chemical into the flow line.
The amount of the formulation actives injected will depend on the application. In the preferred application in produced fluids containing free sulfur, the DADS component should be at least 4-5 times (by weight) the amount of free sulfur in the fluid treated. In most application the concentration of the formulation in the produced fluid may range from 200 to 10,000 ppm (vol), preferably 1000 to 5000 ppm. It is also preferred that the volume ratio of DADS to corrosion inhibitor ranges from 20:1 to 1:1 and preferably 10:1 to 2:1 and most preferably 7:1 to 3:1.
Corrosivity tests were carried out in a rotating high pressure cell. The test equipment was as follows:
Coupons were cleaned and dipped in the treatment fluid (e.g., DADS and or corrosion inhibitor) for several minutes. The coupons then were dipped in water and placed in Autoclave Engineering stainless steel cells, each containing brine. The cells were pressurized with a charge gas to 1000 psi. The cells were placed in a wheel test cabinet at the test conditions and exposure times. After exposure, the coupons were cleaned and weighed and the corrosion rate (mpy) for each coupon determined.
The test materials and conditions were as follows:
______________________________________
Temperature 180 Degrees Fahrenheit
Brine 1000 ppm chloride + Sulfur
Brine 100% Brine
Hydrogen Sulfide
5% of charge gas
Carbon Dioxide
65% of charge gas
Nitrogen 30% of charge gas
Total Pressure
1000 psi at room temperature
Fluid Volume 50 cc
Agitation Rotation High Pressure Wheel Test
Coupon Type 6" × 1/8" Rod 1018 Carbon Steel
Run Time 24 Hours
______________________________________
Corrosion Inhibitor (CI)--a fatty amine film forming corrosion inhibitor
DADS--(produced by Merichem)
Tests were carried out to ascertain the corrosion inhibition properties of (a) DADS alone with no elemental sulfur present and (b) DADS alone in the presence of elemental sulfur. The test data are showing in Table I.
TABLE I ______________________________________ EXP DADS CONC. SULFUR CORROSION NO. (PPM) (WPPM) RATE (MPY) ______________________________________ 1 0 400 225.3 2 1000 400 42.2 3 2000 400 25.8 4 5000 400 15.5 5 0 NONE 122.8 6 1000 NONE 145.7 7 2000 NONE 12.5 8 5000 NONE 4.7 ______________________________________
These tests demonstrate unequivocally that DADS possess corrosion inhibition properties independent of its sulfur dissolution effects on corrosivity.
Additional tests were conducted to determine the corrosion protection obtained in the presence of both DADS and a film forming corrosion inhibitor. The environment contained 400 ppm sulfur.
TABLE II ______________________________________ EXP CI CONC. DADS CORROSION NO. (PPM) (PPM) RATE (MPY) ______________________________________ 9 0 0 196.0 10 1000 0 23.2 11 2000 0 19.1 12 0 5000 11.3 13 1000 5000 10.6 14 2000 5000 8.2 15 0 7000 -- ______________________________________
The combination of the corrosion inhibitor and DADS provided the most protection. Note that Experiment No. 13 gave almost twice the protection of Experiment No. 11 at half the CI concentration. Since DADS costs far less than the commercial corrosion inhibition currently used in production operations, the combination of the CI and DADS is very cost effective.
Additional tests were conducted to determine the effects on corrosion by varying the relative amounts of the DADS and the film forming corrosion inhibitor (CI). The data obtained from these test are presented in Table III.
TABLE III ______________________________________ EXP CI CONC. DADS CORROSION NO. (PPM) (PPM) RATE (MPY) ______________________________________ 16* 0 0 196.0 17 0 7000 12.5 18 1000 6000 6.9 19 2000 5000 6.3 20 3000 4000 6.1 21 4000 3000 6.6 22 5000 2000 7.0 23 6000 1000 8.2 24 7000 0 9.6 ______________________________________ *The blank (Experiment No. 16) was determined in Experiment No. 9.
The above data demonstrate the synergistic effect of the combination of the film forming corrosion inhibitor and DADS on corrosion. The corrosion rate in the presence of both the CI and DADS is lower than that in the presence of each component alone. Note Experiment 19 at a DADS/CI volume ratio of 6:1 was lower than the CI at the same total concentration (7000 ppm).
Claims (7)
1. A method of inhibiting the corrosion in the metal tubulars of a well producing oil or gas which contains corrosive amounts of hydrogen sulfide and free sulfur, said method comprises introducing into the produced oil or gas stream from 200 ppm to 10,000 ppm (vol) of a formulation comprising:
(a) a diaryldisulfide having the following formula:
R--S--S--R'
Where:
R is an alkyl group or an aromatic group; and
R' is an aromatic group; and
(b) a film forming amine-based corrosion inhibitor having polar groups capable of attaching to the surface of the tubulars; the volume ratio of (a)/(b) being between 2:1 and 10:1.
2. The method of claim 1 wherein R is an aromatic group.
3. The method of claim 1 wherein the diaryldisulfide is a mixture of alkylaryl disulfides and diaryldisulfides.
4. The method of claim 1 wherein said volume ratio is between 3:1 and 7:1.
5. The method of claim 1 wherein the film forming corrosion inhibitor is an imidazoline corrosion inhibitor.
6. The method of claim 1 wherein the concentration of the formulation in the produced fluids is between 1000 to 5000 ppm by volume.
7. The method of claim 1 wherein the formulation also includes a surfactant selected from the group consisting of ethoxylated alcohols and ethoxylated alkyl phenols for dispersing the formulation in the produced oil or gas stream.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/635,258 USH1147H (en) | 1990-12-28 | 1990-12-28 | Method of inhibiting corrosion in oil field produced fluids |
| CA002058266A CA2058266A1 (en) | 1990-12-28 | 1991-12-20 | Method of inhibiting corrosion in oil field produced fluids |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/635,258 USH1147H (en) | 1990-12-28 | 1990-12-28 | Method of inhibiting corrosion in oil field produced fluids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH1147H true USH1147H (en) | 1993-03-02 |
Family
ID=24547076
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/635,258 Abandoned USH1147H (en) | 1990-12-28 | 1990-12-28 | Method of inhibiting corrosion in oil field produced fluids |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | USH1147H (en) |
| CA (1) | CA2058266A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009143219A1 (en) | 2008-05-20 | 2009-11-26 | Bp Corporation North America Inc. | Mitigation of elemental sulfur deposition during production of hydrocarbon gases |
| US9238588B2 (en) | 2013-08-02 | 2016-01-19 | Ecolab USA, Inc. | Organic disulfide based corrosion inhibitors |
| US9834509B2 (en) | 2015-08-05 | 2017-12-05 | Ecolab Usa Inc. | Metal-catalyzed oxidative coupling of thiols |
| US11242480B2 (en) | 2017-08-03 | 2022-02-08 | Championx Usa Inc. | Thiol adducts for corrosion inhibition |
| US20230130247A1 (en) * | 2019-12-20 | 2023-04-27 | Cameron International Corporation | Corrosion inhibitor |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108929664B (en) * | 2018-08-16 | 2020-10-23 | 广汉市福客科技有限公司 | Foamless cleaning agent and preparation method and application thereof |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2768929A (en) | 1953-08-03 | 1956-10-30 | Gulf Research Development Co | Refining of sulfur bearing mineral oils with dialkylpolysulfide |
| US3846311A (en) | 1971-09-07 | 1974-11-05 | Amoco Prod Co | Method for removing elemental sulfur from wells and flowlines |
| US4020144A (en) | 1975-05-02 | 1977-04-26 | Exxon Research And Engineering Company | Method for removal of gaseous sulfur and nitrogen compounds from gas streams |
| US4239630A (en) | 1978-11-29 | 1980-12-16 | Standard Oil Company (Indiana) | Method for dissolving sulfur deposits rapidly |
| US4248717A (en) | 1979-05-29 | 1981-02-03 | Standard Oil Company (Indiana) | Method for removing elemental sulfur from high temperature, high pressure wells and flow lines |
| US4290900A (en) | 1979-05-29 | 1981-09-22 | Standard Oil Company (Indiana) | Method and composition for removing elemental sulfur from high temperature, high pressure wells and flow lines |
| US4295979A (en) | 1979-05-29 | 1981-10-20 | Standard Oil Company (Indiana) | Method and composition for inhibiting corrosion in high temperature, high pressure gas wells |
| DE3542551A1 (en) | 1984-12-03 | 1986-06-05 | Société Nationale Elf Aquitaine (Production), Courbevoie | METHOD FOR SOLVING SULFUR |
| US4804485A (en) | 1987-05-08 | 1989-02-14 | Pennwalt Corporation | Polyalkyleneoxyamine catalysts for dialkyl disulfides and/or polysulfides used in dissolving sulfur |
| US5028343A (en) | 1989-02-09 | 1991-07-02 | Atochem North America, Inc. | Stabilized sulfur dissolving compositions |
-
1990
- 1990-12-28 US US07/635,258 patent/USH1147H/en not_active Abandoned
-
1991
- 1991-12-20 CA CA002058266A patent/CA2058266A1/en not_active Abandoned
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2768929A (en) | 1953-08-03 | 1956-10-30 | Gulf Research Development Co | Refining of sulfur bearing mineral oils with dialkylpolysulfide |
| US3846311A (en) | 1971-09-07 | 1974-11-05 | Amoco Prod Co | Method for removing elemental sulfur from wells and flowlines |
| US4020144A (en) | 1975-05-02 | 1977-04-26 | Exxon Research And Engineering Company | Method for removal of gaseous sulfur and nitrogen compounds from gas streams |
| US4239630A (en) | 1978-11-29 | 1980-12-16 | Standard Oil Company (Indiana) | Method for dissolving sulfur deposits rapidly |
| US4248717A (en) | 1979-05-29 | 1981-02-03 | Standard Oil Company (Indiana) | Method for removing elemental sulfur from high temperature, high pressure wells and flow lines |
| US4290900A (en) | 1979-05-29 | 1981-09-22 | Standard Oil Company (Indiana) | Method and composition for removing elemental sulfur from high temperature, high pressure wells and flow lines |
| US4295979A (en) | 1979-05-29 | 1981-10-20 | Standard Oil Company (Indiana) | Method and composition for inhibiting corrosion in high temperature, high pressure gas wells |
| DE3542551A1 (en) | 1984-12-03 | 1986-06-05 | Société Nationale Elf Aquitaine (Production), Courbevoie | METHOD FOR SOLVING SULFUR |
| US4728447A (en) | 1984-12-03 | 1988-03-01 | Societe Nationale Elf Aquitaine | Process and product for dissolving sulfur |
| US4804485A (en) | 1987-05-08 | 1989-02-14 | Pennwalt Corporation | Polyalkyleneoxyamine catalysts for dialkyl disulfides and/or polysulfides used in dissolving sulfur |
| US5028343A (en) | 1989-02-09 | 1991-07-02 | Atochem North America, Inc. | Stabilized sulfur dissolving compositions |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009143219A1 (en) | 2008-05-20 | 2009-11-26 | Bp Corporation North America Inc. | Mitigation of elemental sulfur deposition during production of hydrocarbon gases |
| US8430161B2 (en) | 2008-05-20 | 2013-04-30 | Bp Corporation North America Inc. | Mitigation of elemental sulfur deposition during production of hydrocarbon gases |
| US9238588B2 (en) | 2013-08-02 | 2016-01-19 | Ecolab USA, Inc. | Organic disulfide based corrosion inhibitors |
| EP3027787A4 (en) * | 2013-08-02 | 2017-04-05 | Ecolab USA Inc. | Organic disulfide based corrosion inhibitors |
| US9834509B2 (en) | 2015-08-05 | 2017-12-05 | Ecolab Usa Inc. | Metal-catalyzed oxidative coupling of thiols |
| US11242480B2 (en) | 2017-08-03 | 2022-02-08 | Championx Usa Inc. | Thiol adducts for corrosion inhibition |
| US20230130247A1 (en) * | 2019-12-20 | 2023-04-27 | Cameron International Corporation | Corrosion inhibitor |
| US12024675B2 (en) * | 2019-12-20 | 2024-07-02 | Cameron International Corporation | Corrosion inhibitor |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2058266A1 (en) | 1992-06-29 |
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