US3081355A - Substituted diphenyl - Google Patents

Substituted diphenyl Download PDF

Info

Publication number
US3081355A
US3081355A US30439A US3043960A US3081355A US 3081355 A US3081355 A US 3081355A US 30439 A US30439 A US 30439A US 3043960 A US3043960 A US 3043960A US 3081355 A US3081355 A US 3081355A
Authority
US
United States
Prior art keywords
diphenyl
compound
phenoxy
substituted diphenyl
melting
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US30439A
Other languages
English (en)
Inventor
Richard L Johnson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shell USA Inc
Original Assignee
Shell Oil Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to NL264937D priority Critical patent/NL264937A/xx
Application filed by Shell Oil Co filed Critical Shell Oil Co
Priority to US30439A priority patent/US3081355A/en
Priority to FR862131A priority patent/FR1290563A/fr
Priority to DES74046A priority patent/DE1242313B/de
Priority to GB18184/61A priority patent/GB916358A/en
Priority to US235902A priority patent/US3130162A/en
Application granted granted Critical
Publication of US3081355A publication Critical patent/US3081355A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C10N2030/08Resistance to extreme temperature
    • 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
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids
    • 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
    • C10N2040/12Gas-turbines
    • 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
    • C10N2040/12Gas-turbines
    • C10N2040/13Aircraft turbines
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention relates to a novel substituted diphenyl compound useful as a heatand oxidation-stable lubricant and to compositions containing the compound.
  • lubricants which are stable under the elevated temperatures of mllitary and commercial aircraft turbine engines.
  • One important class comprises diesters of alkane dioarboxylic acids; this type of compound is typified by d1-2- ethylhexyl sebacate.
  • the diesters are generally too volatile to be useful at temperatures above about 500 F. and begin to decompose at around 600 F.
  • This compound has the and has a molecular weight of 306 and a melting point of 505 1 C.
  • Inhibited Hercoflex 600 (mixed esters of pentearythritol) 19 o-(m-Phenoxy-phenoxy)diphenyl 122 Because of these desirable properties, the novel diphenyl described may readily be employed both as a lubricant and in admixture with other lubricants. For example, when it is added to another higher melting lubricant, the resulting mixture is characterized by a melting point considerably lower than that of the higher melting component.
  • diphenyl diphenyl oxides are those diphenyl oxides having a phenyl substituent on each of the phenyl rings att-ached to the oxyradical.
  • the preferred compositions are those wherein the o(m-phenoxy-phenoxy) diphenyl makes up at least about two-third of the total composition on a Weight basis.
  • Table III are presented the minimum melting points of binary systems containing the novel compound of the invention with the diphenyl oxides noted.
  • the melting points of the mixtures including the compound of the invention are considerably lower than that of the higher melting component and are about 10 C. lower than the melting point of the lower melting component.

Landscapes

  • 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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US30439A 1960-05-20 1960-05-20 Substituted diphenyl Expired - Lifetime US3081355A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
NL264937D NL264937A (bg) 1960-05-20
US30439A US3081355A (en) 1960-05-20 1960-05-20 Substituted diphenyl
FR862131A FR1290563A (fr) 1960-05-20 1961-05-17 Diphényle substitué et sa préparation
DES74046A DE1242313B (de) 1960-05-20 1961-05-18 Schmiermittel
GB18184/61A GB916358A (en) 1960-05-20 1961-05-18 A phenoxyphenoxy-diphenyl, its preparation and use in lubricating compositions and as hydraulic fluid
US235902A US3130162A (en) 1960-05-20 1962-08-10 Substituted diphenyl

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US30439A US3081355A (en) 1960-05-20 1960-05-20 Substituted diphenyl

Publications (1)

Publication Number Publication Date
US3081355A true US3081355A (en) 1963-03-12

Family

ID=21854215

Family Applications (1)

Application Number Title Priority Date Filing Date
US30439A Expired - Lifetime US3081355A (en) 1960-05-20 1960-05-20 Substituted diphenyl

Country Status (4)

Country Link
US (1) US3081355A (bg)
DE (1) DE1242313B (bg)
GB (1) GB916358A (bg)
NL (1) NL264937A (bg)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3321403A (en) * 1963-01-23 1967-05-23 Monsanto Co Polyphenyl thioethers
US3406207A (en) * 1963-09-20 1968-10-15 Monsanto Co Diphenoxybiphenyl compounds and process
US3429816A (en) * 1965-09-01 1969-02-25 Progil Thermostable mixtures of diphenoxybenzenes and mono- and diphenoxydiphenyls usable as functional liquids
US3471574A (en) * 1963-09-20 1969-10-07 Monsanto Co Phenoxybiphenyl compounds

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2263663A (en) * 1940-01-25 1941-11-25 Standard Oil Dev Co Mineral oil composition
US2429905A (en) * 1943-09-10 1947-10-28 Sun Oil Co Lubricant composition
US2862034A (en) * 1958-11-25 X-dibenzyloxy-x-nitrostyrenes
US2902518A (en) * 1959-09-01 Hydhoxyalkyl mothers of z

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL107472C (bg) * 1957-12-09

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2862034A (en) * 1958-11-25 X-dibenzyloxy-x-nitrostyrenes
US2902518A (en) * 1959-09-01 Hydhoxyalkyl mothers of z
US2263663A (en) * 1940-01-25 1941-11-25 Standard Oil Dev Co Mineral oil composition
US2429905A (en) * 1943-09-10 1947-10-28 Sun Oil Co Lubricant composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3321403A (en) * 1963-01-23 1967-05-23 Monsanto Co Polyphenyl thioethers
US3406207A (en) * 1963-09-20 1968-10-15 Monsanto Co Diphenoxybiphenyl compounds and process
US3471574A (en) * 1963-09-20 1969-10-07 Monsanto Co Phenoxybiphenyl compounds
US3429816A (en) * 1965-09-01 1969-02-25 Progil Thermostable mixtures of diphenoxybenzenes and mono- and diphenoxydiphenyls usable as functional liquids

Also Published As

Publication number Publication date
GB916358A (en) 1963-01-23
NL264937A (bg)
DE1242313B (de) 1967-06-15

Similar Documents

Publication Publication Date Title
US3360465A (en) Synthetic ester lubricants
US3426075A (en) Mixed polyphenyl ethers-thioethers
US3006852A (en) Lubricating compositions and process of lubrication utilizing certain polyoxyphenylene compounds
US3321403A (en) Polyphenyl thioethers
US3414618A (en) Mono-p-tertiary alkyl diarylamines
US3081355A (en) Substituted diphenyl
US3115519A (en) Stable esters
US2732406A (en) New asymmetric diphenylol methanes
US2451895A (en) Synthetic grease
US2477327A (en) Hydroxy alkyl thio succinic acids and esters
US3696851A (en) Chemical compounds and compositions
US2362767A (en) Lubricants
US3130162A (en) Substituted diphenyl
US3148147A (en) 2, 2-dialkyl-1, 3-propanediol diesters as functional fluids
US3451061A (en) Functional fluid compositions
US3449442A (en) 2,4-diphenoxybromobenzene and 2,4-diphenoxychlorobenzene as new compounds and synthetic lubricants
US3567783A (en) Process for preparing polyphenyl ethers
US2469469A (en) Oxidation inhibitors
US3080321A (en) Isomeric mixtures of diphenoxy-, ditoloxy-, and phenoxytoloxybenzenes as functional fluids
US2384323A (en) Aliphatic-ether-alcohol derivatives of cashew nut shell oil
US3260672A (en) Synthetic ester lubricating oil containing certain haloalkyl carboxylic acid esters
US2998454A (en) Substituted phenyl biphenylyl sulfones and their preparation
US3253042A (en) alpha, alpha'-polythiobis(2, 6-dialkylphenols)
US3423469A (en) Polyphenyl ether compositions
US3409552A (en) Alkyl aryl ether polymers in lubricants