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US2249626A - Lubricating composition - Google Patents

Lubricating composition Download PDF

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Publication number
US2249626A
US2249626A US383167A US38316741A US2249626A US 2249626 A US2249626 A US 2249626A US 383167 A US383167 A US 383167A US 38316741 A US38316741 A US 38316741A US 2249626 A US2249626 A US 2249626A
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Prior art keywords
corrosion
salts
barium
metal
bearing
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Expired - Lifetime
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US383167A
Inventor
Cook Elmer William
Jr William David Thomas
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Wyeth Holdings LLC
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American Cyanamid Co
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Priority to US383167A priority Critical patent/US2249626A/en
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Publication of US2249626A publication Critical patent/US2249626A/en
Priority to GB3221/42A priority patent/GB561801A/en
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Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/088Neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/089Overbased salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/08Groups 4 or 14
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings

Definitions

  • This invention relates to lubricating oil compositions containing corrosion inhibitors.
  • phenol sulfides are particularly useful. They are very cheap relatively, and in the form of .their salts show complete solubility in Pennsylvania oils.
  • other 2, 4-dialkylphenol sulfides may be used such as those obtained from p-amylphenol which has been condensed with the.
  • R, R R and R are alkyl radicals and X is hydrogen or a metal.
  • sulfur atoms can also be used but it is not practical to use them in the form of their salts with strongly basic metals such as alkaline earth metals.
  • salts of more weakly basic metals such as tin can be'employed.'
  • the mono sulfides are in' general more effective than the corresponding disulfides, and are therefore preferred. 1
  • the products used in the present invention may be prepared in various ways, for example, by reacting the respective dialkyl phenol with sulfur dichloride in solution in carbon tetrachloride, ethylene chloride, or trichlorethylene, or other suitable solvent.
  • the dialkylphenol sulfides and their methods of preparation are not claimed per se in the presentapplication, forming the subject matter of our copending application, Serial No. 383,166, filed March 13, 194.1.
  • the phenol sulfides are preferably used in the form of their salts such as tin, barium, or zinc salts.
  • a l of the salts are effective corrosion inhibitors but they will difier somewhat, and curiously enoughithey difier with the different alloys used. Thus, for example, with silver-cadmium alloys and most lubricating oils, the tin salts appear to give maximum protection. With other alloy bearings, barium and zinc salts are preferable. We have not determined the reason for this difference in effectiveness with the diflerent' salts when used with certain alloys. It should be Essentially they are understood, however, that while the difieren't metal salts differ among themselves, they are all efiective corrosion inhibitors and sludge dispersors.
  • compositions of the present invention reduce sludge formation. Probably this isdue, at least in part, to the fact that the dialkylphenol sulfides of the present invention tend to wet bearing surfaces and thus to coat them with a thin film which removes the metal surface from actual contact of the bulk of. the oil and it is believed that the metal of the bearing acts as a catalyst in sludge formation.
  • the operation of compounds of the present invention is difiicult to determine exactly and it is possible that other factors may be involved, and hence, the invention is not intended to be limited to any theory of action.
  • dialkylphenol sulfides of the present invention show uniformly good sludge dispersing powers, .their corrosion inhibiting effect varies greatly with different oils and different bearings. Therefore, no one compound is best for all oils and all bearings. In some cases,'more advantageous results are obtained from a mixture of dififerent metal salts of the dialkylphenol sulfides. Thus, mixtures of the barium salts with zinc or tin salts are particularly effective and in some cases are more efl'ective with certain oils than either alone.
  • the salts may be prepared either by direct action of the metal hydroxide or metal alcoholate, in the case of strongly basic metals, with the phenol sulfide, or in the case of some of the heavy metals by double decomposition of the sodium salt of the dialkylphenol sulfide and an alcoholic solution of the metal in question.
  • the products used in the present invention also have a further peculiar property in that they tend to render certain other compounds having corrosion inhibiting power, soluble in oil in which the other compounds will not dissolve when used alone.
  • the reason why certain other compounds are rendered soluble when associated with the 2,4-dialkylphenol sulfides of the present invention has not as yet been completely determined and no theoretical explanation is therefore advanced.
  • EXAMPLE 1 A solvent refined Mid-continent lubricating oil was subjected to the conventional Indiana oxidation test modified by suspending alloy bearing sections in the test ,oil samples. Loss of weight of the alloy bearing strips was taken as a measure of corrosion tendency of the lubricating composition. The test period was for 70 hours at 341 F., air being pumped through the lubricating compositions at the rate of 10 liters per hour. The corrosion effects are shown in the following table.
  • EXAMPLE 2 A Pennsylvania oil of predominantly parafiin base was tested as described in Example 1. The corrosion inhibiing effects of the various products are shown in the following table.
  • Example 3 the barium compound did not show improved corrosion resistance over the controlsample although corrosion was not increased.
  • the barium compound was the only one that showed high corrosion inhibiting tendencies; It is-notable, however, thatmixed compounds containing both barium and other metal salts show uniformly good results in all formula:
  • R, R, R. and R are alkyl radicals and M is a metal, in amounts suflicient to exert sludge dispersing properties under heavy duty service without increasing bearing corrosion.
  • a paraffin base lubricating oil composition are used, part being the barium salt containing a 2,4-dialkylphenol sulfide having 0 M 0 M U 407R,
  • R, R RF and R are alkyl radicals and M is a metal, in amounts sufllcient to exert sludge dispersing properties under heavy duty service without increasing bearing corrosion.
  • a composition according to claim-1 M is barium.
  • a composition according to claim 3 in which a mixture of diamylphenol sulfide salts are used, part of them being a barium salt and part a different metal salt.
  • composition according to claim 3 in which a mixture of diamylphenol sulfide salts the zinc salt.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

Patented July 15, 1941 UNITED'STATES PATENT OFFICE 'LUBRICATING COMPOSITION Elmer William Cook, New York, N. Y., and William David Thomas, Jr., Stamford, Conn., assignors to American Cyanamid Company, New York, N. Y., a corporation 01' Maine No Drawing. Application March 13, 1941,
Serial No. 383,167
16 Claims.
This invention relates to lubricating oil compositions containing corrosion inhibitors.
When lubricating oil is used under conditions of extremely hard surfaces such as heavy duty- Diesel engines, tractor and airplane engines, a serious problem is presented due to the fact that the oil tends to form sludges which causes sticking on rings and also corrosive decomposition products are formed which present a serious corrosion problem with bearings, especially the new heavy duty alloy bearings such as silvercadmium and copper-lead bearings.
It has been proposed to decrease the bad effect phenol sulfides are particularly useful. They are very cheap relatively, and in the form of .their salts show complete solubility in Pennsylvania oils. However, other 2, 4-dialkylphenol sulfides may be used such as those obtained from p-amylphenol which has been condensed with the.
chlorinated residues of waxes and in which the alkyl radical in the Z-posltio'n maycontain from 20-21, carbon atoms. of course the sulfides may of sludging by adding metal salts of various organic acids which have a detergent action on the sludge. However, the addition of such metal salts has the very grave disadvantage that they greatly accelerate corrosion of bearings and this has seriously reduced their field of utility.
It has also been proposed in the past to use certain p-alkylphenol sulfides as corrosion inhibitors. These compounds do have considerable corrosion inhibiting power but are open to seri'-- phenol sulfides are used in the form of their metal salts as bearing corrosion inhibitors and anti-sludging agents. These compounds show high solubility when the alkyl groups are sufficiently large, for example five carbon atoms or more; they do not decompose with heat, and give a protection against corrosion which is of a different order of magnitude than corrosion inhibitors which have hitherto been used. Even in such extreme tests as heating the lubricating oil to 340 F. and blowing air through it for days, the corrosion of bearing alloys is not increased and in many cases is less than 1% of that which resuits with standard so-called corrosion inhibitors. While any of the 2, 4-dialkylphenol sulfides may be' used, I have found that the.2, 4-diamylhave different phenols. represented by the formula:
in which R, R R and R are alkyl radicals and X is hydrogen or a metal.
Disulfides in which two phenol radicals are united through two. sulfur atoms can also be used but it is not practical to use them in the form of their salts with strongly basic metals such as alkaline earth metals. However, salts of more weakly basic metals such as tin can be'employed.'
The mono sulfides are in' general more effective than the corresponding disulfides, and are therefore preferred. 1
The products used in the present invention may be prepared in various ways, for example, by reacting the respective dialkyl phenol with sulfur dichloride in solution in carbon tetrachloride, ethylene chloride, or trichlorethylene, or other suitable solvent. The dialkylphenol sulfides and their methods of preparation are not claimed per se in the presentapplication, forming the subject matter of our copending application, Serial No. 383,166, filed March 13, 194.1.
The phenol sulfides are preferably used in the form of their salts such as tin, barium, or zinc salts. A l of the salts are effective corrosion inhibitors but they will difier somewhat, and curiously enoughithey difier with the different alloys used. Thus, for example, with silver-cadmium alloys and most lubricating oils, the tin salts appear to give maximum protection. With other alloy bearings, barium and zinc salts are preferable. We have not determined the reason for this difference in effectiveness with the diflerent' salts when used with certain alloys. It should be Essentially they are understood, however, that while the difieren't metal salts differ among themselves, they are all efiective corrosion inhibitors and sludge dispersors.
In addition to excellent dispersion characteristics, the compositions of the present invention reduce sludge formation. Probably this isdue, at least in part, to the fact that the dialkylphenol sulfides of the present invention tend to wet bearing surfaces and thus to coat them with a thin film which removes the metal surface from actual contact of the bulk of. the oil and it is believed that the metal of the bearing acts as a catalyst in sludge formation. The operation of compounds of the present invention is difiicult to determine exactly and it is possible that other factors may be involved, and hence, the invention is not intended to be limited to any theory of action.
While the dialkylphenol sulfides of the present invention show uniformly good sludge dispersing powers, .their corrosion inhibiting effect varies greatly with different oils and different bearings. Therefore, no one compound is best for all oils and all bearings. In some cases,'more advantageous results are obtained from a mixture of dififerent metal salts of the dialkylphenol sulfides. Thus, mixtures of the barium salts with zinc or tin salts are particularly effective and in some cases are more efl'ective with certain oils than either alone.
The salts may be prepared either by direct action of the metal hydroxide or metal alcoholate, in the case of strongly basic metals, with the phenol sulfide, or in the case of some of the heavy metals by double decomposition of the sodium salt of the dialkylphenol sulfide and an alcoholic solution of the metal in question.
It is an important advantage of the present invention that the products can be used in very small quantities in lubricating oils. Thus the cost of protecting lubricating oils against corrosion in heavy duty service is negligible.
The products used in the present invention also have a further peculiar property in that they tend to render certain other compounds having corrosion inhibiting power, soluble in oil in which the other compounds will not dissolve when used alone. The reason why certain other compounds are rendered soluble when associated with the 2,4-dialkylphenol sulfides of the present invention has not as yet been completely determined and no theoretical explanation is therefore advanced.
While one of the outstanding fields of the present invention is in the protection of parafiin base and highly refined lubricating oils for which many known corrosion inhibitors are unsuitable, it should be understood that the present invention is not limited to paraflln base and highly refined lubricating oils entirely. On the contrary, the ,same desirable corrosion inhibiting and anti-sludging effect is to be noted with asphalt and naphthenic base lubricating oils although the advantage is not so outstanding because other corrosion inhibitors, even though less effective, can-be used with such oils.
The invention will be described in greater detail'in conjunction with the following specific.
examples.
EXAMPLE 1 A solvent refined Mid-continent lubricating oil was subjected to the conventional Indiana oxidation test modified by suspending alloy bearing sections in the test ,oil samples. Loss of weight of the alloy bearing strips was taken as a measure of corrosion tendency of the lubricating composition. The test period was for 70 hours at 341 F., air being pumped through the lubricating compositions at the rate of 10 liters per hour. The corrosion effects are shown in the following table.
In every case sludging was reduced materially as compared with the control and such sludge as was formed was soft and for the most part readily removed from the glass tube in which the test was carried out by a single wash with kerosene.
EXAMPLE 2 A Pennsylvania oil of predominantly parafiin base was tested as described in Example 1. The corrosion inhibi ing effects of the various products are shown in the following table.
Table 2 CADMIUM-SILVER BEARING Additive Conccn- Bearing tration loss Percen JV 5.
None (control) 5005000 Tin dlnmyl henol monosulfido.-- U. 3 533 Zinc diamy phenol monosulfldel 0.3 83
Barium diamylphenol monosulfidm. 0. 15
Zinc diamylphenol monosulfide. 0. l5 17 Barium diamylphenol monosulildo 0. l5
Tin diamylphenol monosulflde. 0. 15 2 COPPER-LEAD BEARING None (control) 201 Zinc diamylphenol monosulflde 0. 3 33 Barium diamylphenol monosulflde 0.3 50 Barium 2-dodecyl-4-tert. amylphenol monosulfldo 0. 5 136 COPPER-SILVER-OADMIUM BEARING None (control) 389 Barium dlamglphenol monosulfida- 0.3 Zinc diamylp enol monosulfide 0.3 43 Tin diamylphenol monosulflde 0; 3 +11 In every case sludging was reduced materially as compared with the control and such sludge as was formed was soft, and for the most part, readily removed from the glass tube in which the test was carried out by a single wash with kerosene.
'th-test was carried out by-a singlewash with 'of the classes. 'We claim: a 1. A lubricating oil composition containing a ,2,4-dialkylphenolsulfide having. the following Exmrns 3 A Pennsylvania base oil highly refined by the aluminum chloride process was tested as described in Example 1. The corrosion inhibiting results are shown in the following table.
means gain.
In every case sludging wasreduced materially as compared with the control andsuch sludge as was formed was soft, and. for the most part, readily removed from the glass tube in which kerosene.
An examination of the specific examples will show that awhiledn every case corrosion was no worse as compared with the control, it is not possible to correlate corrosion inhibitance with chemical structure. Thus, .for. instance, in
- Example 3 the barium compound did not show improved corrosion resistance over the controlsample although corrosion was not increased. On the other hand, in Example 1 with the silvercadmium bearing, the barium compound was the only one that showed high corrosion inhibiting tendencies; It is-notable, however, thatmixed compounds containing both barium and other metal salts show uniformly good results in all formula:
OM OM 2-OsUm I m R,
in which R, R, R. and R are alkyl radicals and M is a metal, in amounts suflicient to exert sludge dispersing properties under heavy duty service without increasing bearing corrosion.
2. A paraffin base lubricating oil composition are used, part being the barium salt containing a 2,4-dialkylphenol sulfide having 0 M 0 M U 407R,
' the formula:
in which R, R RF and R are alkyl radicals and M is a metal, in amounts sufllcient to exert sludge dispersing properties under heavy duty service without increasing bearing corrosion.
3. A lubricating oil composition containing a zA-diamylphenol sulfide having the following formula:
O M OM C sHnUS U0 5H1! in which M is a metal, in amounts sufiicient to exert sludge dispersing properties under heavy duty service without increasing bearing corrosion.
4. A composition according to claim 1 in which M is tin.
5. A composition according to claim 2 in which M is tin.
6. A composition according to claim 3 in which M is tin.
7. A composition according to claim-1 M is barium.
8. A composition according to claim 2 in which M is barium.
- 9. A composition according to claim 3 in which in which M is barium.
10. A composition I 1 in which M is zinc.
11. A composition which M is zinc.
12. A composition according to claim which M is zinc.
13. A composition which a mixture of according to claim according to claim in dialkylphenol sulfide salts are used, part of them being a barium salt and part a difierent metal salt.
14. A composition according to claim 3 in which a mixture of diamylphenol sulfide salts are used, part of them being a barium salt and part a different metal salt.
15. A composition according to claim 3 in which a mixture or diamylphenol sulfide salts are used, part being the barium salt and part the zinc salt. 7
16. A composition according to claim 3 in which a mixture of diamylphenol sulfide salts the zinc salt.
ELMER WILLIAM COOK.' WILLIAM DAVID THOMAS, JR.
according to claim 2 in and part
US383167A 1941-03-13 1941-03-13 Lubricating composition Expired - Lifetime US2249626A (en)

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GB3221/42A GB561801A (en) 1941-03-13 1942-03-11 Improvements in lubricating compositions

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2415833A (en) * 1942-01-01 1947-02-18 Standard Oil Dev Co Lubricant
US2417118A (en) * 1941-08-16 1947-03-11 Texas Co Composition of matter
US2424204A (en) * 1941-08-09 1947-07-15 Standard Oil Dev Co Extreme pressure lubricants
US2459754A (en) * 1946-05-23 1949-01-18 Firestone Tire & Rubber Co Purification of phenol sulfides and preparation of metallic salts thereof
US2480664A (en) * 1946-09-06 1949-08-30 Standard Oil Dev Co Lubricating oil composition
US2488134A (en) * 1943-05-26 1949-11-15 Standard Oil Dev Co Sulfur-containing aromatic compounds
US2553183A (en) * 1948-07-03 1951-05-15 Shell Dev Fuel oil composition
US2944020A (en) * 1956-05-11 1960-07-05 Sinclair Refining Co Anti-wear lubricating oil composition
US3200135A (en) * 1959-07-29 1965-08-10 Sterling Drug Inc Copper, cadmium, and zinc salts of halo-2, 2'-dihydroxydiphenyl sulfides and sulfoxides
US4309293A (en) * 1979-12-10 1982-01-05 Mobil Oil Corporation Process for reducing the corrosivity of phenol sulfides
US4443381A (en) * 1980-07-07 1984-04-17 Milton Braid Direct exchange process

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2424204A (en) * 1941-08-09 1947-07-15 Standard Oil Dev Co Extreme pressure lubricants
US2417118A (en) * 1941-08-16 1947-03-11 Texas Co Composition of matter
US2415833A (en) * 1942-01-01 1947-02-18 Standard Oil Dev Co Lubricant
US2488134A (en) * 1943-05-26 1949-11-15 Standard Oil Dev Co Sulfur-containing aromatic compounds
US2459754A (en) * 1946-05-23 1949-01-18 Firestone Tire & Rubber Co Purification of phenol sulfides and preparation of metallic salts thereof
US2480664A (en) * 1946-09-06 1949-08-30 Standard Oil Dev Co Lubricating oil composition
US2553183A (en) * 1948-07-03 1951-05-15 Shell Dev Fuel oil composition
US2944020A (en) * 1956-05-11 1960-07-05 Sinclair Refining Co Anti-wear lubricating oil composition
US3200135A (en) * 1959-07-29 1965-08-10 Sterling Drug Inc Copper, cadmium, and zinc salts of halo-2, 2'-dihydroxydiphenyl sulfides and sulfoxides
US4309293A (en) * 1979-12-10 1982-01-05 Mobil Oil Corporation Process for reducing the corrosivity of phenol sulfides
US4443381A (en) * 1980-07-07 1984-04-17 Milton Braid Direct exchange process

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Publication number Publication date
GB561801A (en) 1944-06-06

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