US20150191674A1 - Tubular threaded joint and lubricating coating forming composition for use therein - Google Patents

Tubular threaded joint and lubricating coating forming composition for use therein Download PDF

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Publication number
US20150191674A1
US20150191674A1 US14/419,447 US201314419447A US2015191674A1 US 20150191674 A1 US20150191674 A1 US 20150191674A1 US 201314419447 A US201314419447 A US 201314419447A US 2015191674 A1 US2015191674 A1 US 2015191674A1
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Prior art keywords
threaded joint
lubricating coating
box
pin
lubricating
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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US14/419,447
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English (en)
Inventor
Kunio Goto
Yuuji Tanaka
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.)
Vallourec Oil and Gas France SAS
Nippon Steel Corp
Original Assignee
Vallourec Oil and Gas France SAS
Nippon Steel and Sumitomo Metal Corp
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Filing date
Publication date
Application filed by Vallourec Oil and Gas France SAS, Nippon Steel and Sumitomo Metal Corp filed Critical Vallourec Oil and Gas France SAS
Assigned to NIPPON STEEL & SUMITOMO METAL CORPORATION, VALLOUREC OIL AND GAS FRANCE reassignment NIPPON STEEL & SUMITOMO METAL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GOTO, KUNIO, TANAKA, YUUJI
Publication of US20150191674A1 publication Critical patent/US20150191674A1/en
Assigned to NIPPON STEEL CORPORATION reassignment NIPPON STEEL CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: NIPPON STEEL & SUMITOMO METAL CORPORATION
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
    • E—FIXED CONSTRUCTIONS
    • E21—EARTH OR ROCK DRILLING; MINING
    • E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B17/00—Drilling rods or pipes; Flexible drill strings; Kellies; Drill collars; Sucker rods; Cables; Casings; Tubings
    • E21B17/02—Couplings; joints
    • E21B17/04—Couplings; joints between rod or the like and bit or between rod and rod or the like
    • E21B17/042—Threaded
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04—Elements
    • C10M2201/041—Carbon; Graphite; Carbon black
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04—Elements
    • C10M2201/041—Carbon; Graphite; Carbon black
    • C10M2201/042—Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
    • C10M2205/163—Paraffin waxes; Petrolatum, e.g. slack wax used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/18—Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/1253—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C10M2207/2805—Esters used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/1003—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/221—Six-membered rings containing nitrogen and carbon only
    • C10M2215/222—Triazines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/0403—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046—Overbasedsulfonic acid salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/34—Lubricating-sealants
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/015—Dispersions of solid lubricants
    • C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/023—Multi-layer lubricant coatings
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10—Semi-solids; greasy
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2080/00—Special pretreatment of the material to be lubricated, e.g. phosphatising or chromatising of a metal
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
    • F16L58/00—Protection of pipes or pipe fittings against corrosion or incrustation
    • F16L58/18—Protection of pipes or pipe fittings against corrosion or incrustation specially adapted for pipe fittings
    • F16L58/182—Protection of pipes or pipe fittings against corrosion or incrustation specially adapted for pipe fittings for screw-threaded joints

Definitions

  • the present invention relates to a tubular threaded joint for use in connecting steel pipes and particularly oil country tubular goods, and a surface treatment method thereof.
  • Oil country tubular goods such as tubing and casing used in oil well drilling for excavation of crude oil or gas oil are usually connected (jointed) to each other by a tubular threaded joint.
  • the depth of the oil wells was 2,000 to 3,000 m, but in deep oil wells such as recent offshore oil fields, the depth may reach 8,000 to 10,000 m.
  • the length of the oil country tubular goods is typically several tens of meters, and the periphery of tubing through which a fluid such as crude oil flows is surrounded with a plurality of casings, and thus the number of the oil country tubular goods jointed by the threaded joint reaches a vast number.
  • a typical tubular threaded joint (also, called special threaded joint) used for connecting oil country tubular goods has a pin-box structure.
  • a pin which is a joint member having a male thread, is typically formed at both ends of the oil country tubular goods.
  • a box which is a counterpart joint member having a female thread that is screwed to the male thread is typically formed at both-side internal surfaces of a coupling that is a separate member.
  • seal portions 4 a and 4 b are provided at an outer peripheral portion close to an end surface on the front end side in relation to the male thread of the pin, and on an internal peripheral surface of the base portion of the female thread of the box, respectively.
  • Shoulder portions (also called torque shoulder) 5 a and 5 b are provided at the end surface of the front end of the pin 1 , and the deepest portion of the box 2 which corresponds to the end surface.
  • the seal portions 4 a and 4 b , and the shoulder portions 5 a and 5 b constitute an unthreaded metal contact portion of the tubular threaded joint, and the unthreaded metal contact portion and a threaded portion constitute a contact surface of the tubular threaded joint.
  • Patent Document 1 discloses an example of the special threaded joint.
  • one end (pin) of an oil country tubular good is inserted into a coupling (box), and the male thread and the female thread are fastened until the shoulder portions of the pin and the box come into contact with each other and interfere each other with appropriate torque. According to this, the seal portions of the pin and the box come into close contact with each other to form a metal-to-metal seal portion, and thus gastightness of the threaded joint is secured.
  • API American Petroleum Institute recommends seizure resistance such that seizure called galling does not occur and gastightness is maintained even when fastening (make-up) and loosening (break-out) are repeated ten times.
  • a viscous liquid lubricant which contains heavy metal powders called “compound grease” is applied to the contact surface of the threaded joint in advance whenever the fastening is performed so as to increase seizure resistance and gastightness.
  • compound grease is specified in API standard BUL 5A2.
  • the compound grease contains a large amount of heavy metal powders such as zinc, lead, and copper.
  • heavy metal powders such as zinc, lead, and copper.
  • grease which has been applied is washed off or overflows to an exterior surface, and thus there is a possibility in that particularly, harmful heavy metals such as lead may have an adverse effect on the environment and particularly on sea life.
  • a process of applying compound grease deteriorates a working environment and working efficiency, and there is also a concern of harmful effects on the human body.
  • Patent Document 1 Japanese Unexamined Patent Application, First Publication No. H5-87275
  • Patent Document 2 Japanese Unexamined Patent Application, First Publication No. 2002-173692
  • Patent Document 3 PCT International Publication No. WO2009/072486
  • seal portions 4 a and 4 b of a pin 1 and a box 2 form a metal-to-metal seal portion during fastening, and thus gastightness is secured.
  • FIG. 2 A torque chart (vertical axis: torque, and horizontal axis: turns) during fastening of this kind of threaded joint is shown in FIG. 2 .
  • torque vertical axis: torque
  • horizontal axis turns
  • Ts shouldering torque
  • Ty decreases compared to a case in which compound grease of the related art is applied, and thus ⁇ T decreases.
  • optimal fastening torque may not be determined depending on tolerance in an amount of thread interference.
  • the optimal torque in FIG. 2 represents torque with which an amount of interference necessary for securing gastightness in the seal portions is accomplished to terminate fastening, and the optimal torque is determined in advance for each internal size of a joint or type of a joint.
  • the invention is to provide a tubular threaded joint provided with a lubricating coating which does not contain a harmful heavy metal, is excellent in seizure resistance, gastightness, and anticorrosive properties, and is capable of securing a large ⁇ T, and in which yielding of a shoulder portion is not likely to occur even in fastening with high torque.
  • a tubular threaded joint provided with a lubricating coating which does not contain a harmful heavy metal imposing a load on the global environment
  • a composition which contains melamine cyanurate (MCA, melamine cyanuric acid) and a basic metal salt of an aromatic organic acid as an essential component and which further contains one or more kinds selected from the group consisting of a pine resin-based material (including pine resin and a derivative thereof), wax, a metal soap, and a lubricating powder
  • a tubular threaded joint which has sufficient seizure resistance, gastightness, and anticorrosive properties, and a large ⁇ T, and which does not have a danger of causing no shouldering, may be obtained.
  • a composition for forming a lubricating coating to a tubular threaded joint contains a melamine cyanurate (hereinafter, abbreviated as MCA), a basic metal salt of an aromatic organic acid, and one or more kinds selected from the group consisting of a pine resin-based material, a wax, a metal soap, a lubricating powder.
  • MCA melamine cyanurate
  • the amount of the MCA be 0.5% by mass to 30% by mass on the basis of the total amount of non-volatile components of the composition.
  • the non-volatile components represent components other than a solvent in the composition.
  • an average particle size of the MCA contained in the composition be 10 ⁇ m to 40 ⁇ m.
  • the average particle size is defined as a median diameter (50% particle size: D50) of a volume-based particle size distribution obtained by a particle size distribution measuring device using a laser diffraction scattering method as a measurement principle.
  • the composition may contain a volatile organic solvent for low viscosity. It is preferable that the composition substantially do not contain a heavy metal such as lead that is harmful to the human body (specifically, in an amount exceeding 1% by mass on the basis of the total amount of non-volatile components of the composition).
  • a tubular threaded joint including a pin and a box, each being provided with a contact surface including a threaded portion and an unthreaded metal contact portion.
  • the lubricating coating formed using the composition is provided on the contact surface of at least one member of the pin and the box.
  • a film thickness of the lubricating coating be 10 ⁇ m to 500 ⁇ m.
  • the contact surface of at least one member of the pin and the box which is provided with the lubricating coating be subjected to a surface treatment by blasting, pickling, a phosphate chemical conversion treatment, an oxalate chemical conversion treatment, a borate chemical conversion treatment, electroplating, impact plating, or a surface treatment method selected from two or more kinds thereof before forming the lubricating coating.
  • the contact surface of one member of the pin and the box is provided with the lubricating coating, it is preferable that the contact surface of the other member of the pin and the box be subjected to the surface treatment by the surface treatment method.
  • the tubular threaded joint according to the invention is preferably suitable for connecting oil country tubular goods.
  • an operation mechanism of the lubricating coating formed from the composition according to the invention is considered as follows.
  • Fastening (make-up) of the tubular threaded joint is performed by inserting the pin into the box, and by rotating the pin or the box. First, only threaded portions come into contact with each other to screw together, and at a final stage of the fastening, when seal portions and shoulder portions start to come into contact, respectively, and thus a predetermined amount of interference is obtained in the seal portion and the shoulder portion, the fastening is completed.
  • the tubular threaded joint of the invention may reliably exhibit excellent seizure resistance during fastening of oil country tubular goods without applying grease lubricating oil such as compound grease which has been applied to the treaded joint. Accordingly, the tubular threaded joint of the invention may avoid an adverse effect on the global environment and the human body which is caused by the compound grease. In addition, it is not likely for a shoulder portion to yield during the fastening at high torque, and thus a stable metal-to-metal seal portion may be realized with a margin.
  • the lubricating coating formed on the contact surface thereof exhibits as a large ⁇ T as the coating of the grease lubricating oil such as the compound grease containing a harmful heavy metal in the related art, and thus it is possible to perform a fastening process without causing yield or seizure at the shoulder portion even during fastening with high torque.
  • the seizure may be suppressed even under severe conditions such as unstable drilling work in the sea.
  • the lubricating coating substantially does not contain a harmful heavy metal such as lead, and thus there is little impact on the global environment.
  • formation of rust is suppressed. Accordingly, even when fastening and loosening are repeated, a lubricating function is continuously exhibited, and gastightness may be secured after the fastening.
  • FIG. 1 is a diagram schematically illustrating an unthreaded metal contact portion (a shoulder portion and a seal portion) of a premium threaded joint.
  • FIG. 2 is a typical torque chart during fastening of a premium tubular threaded joint
  • FIG. 3 is a diagram schematically illustrating an assembling configuration of a steel pipe at the time of shipment and a coupling.
  • FIG. 4 is a diagram schematically illustrating a cross-section of the premium tubular threaded joint.
  • FIG. 3 schematically shows a state of a steel pipe for oil country tubular goods at the time of shipment and a coupling.
  • a pin 1 having a male threaded portion 3 a on an external surface is formed on both ends of a steel pipe A, and a box 2 having a female threaded portion 3 b on an internal surface is formed on both sides of a coupling B.
  • the pin represents a threaded joint member on a side having the male thread
  • the box represents a threaded joint member on a side having the female thread.
  • the coupling B may be tightly fastened in advance to one end of the steel pipe A.
  • protectors for protection of threaded portions are mounted to both of the pin in another end of the steel pipe A and the box in another end of the coupling B each of which is not fastened, before shipment, and those protectors are detached before using the threaded joint.
  • the pin is formed on the external surface of both ends of the steel pipe, and the box is formed on the internal surface of the coupling that is a separate component.
  • the box is formed on the internal surface of the coupling that is a separate component.
  • an integral type tubular threaded joint in which one end of the steel pipe is formed as a pin, and the other end is formed as a box without using the coupling.
  • the tubular threaded joint of the invention is applicable to any of these types.
  • FIG. 4 schematically illustrates a configuration of a representative tubular threaded joint (hereinafter, referred to as simply “threaded joint”).
  • the threaded joint is constituted by a pin 1 that is formed on an external surface of an end of the steel pipe A, and a box 2 that is formed on an internal surface of the coupling B.
  • the pin 1 includes a male threaded portion 3 a , a seal portion 4 a that is positioned at the front end of the steel pipe, and a shoulder portion 5 a of an end surface.
  • the box 2 includes a female threaded portion 3 b , and a seal portion 4 b and a shoulder portion 5 b on an inner side of the female threaded portion 3 b .
  • the seal portion and the shoulder portion constitute an unthreaded metal contact portion.
  • the threaded portions 3 a and 3 b , the seal portions 4 a and 4 b , and the shoulder portions 5 a and 5 b of the pin 1 and the box 2 become contact surfaces of the threaded joint. Seizure resistance, gastightness, and anticorrosive properties are required for the contact surface. Therefore, in the related art, compound grease containing a heavy metal powder is applied to the contact surface or viscous liquid or semisolid lubricating coating is formed on the contact surface.
  • the former has an adverse effect on the human body or the environment, and in the latter, ⁇ T is low during fastening with high torque, and thus there is a problem in that the shoulder portion may yield before fastening.
  • the contact surface of at least one member of the pin and the box is covered with the lubricating coating.
  • the lubricating coating exhibits an excellent lubricating performance and an gastightness maintaining effect during fastening of the threaded joint like the compound grease in the related art. Accordingly, even when the compound grease is not used, and fastening and loosening are repeated with high torque, the threaded joint of the invention may prevent the seizure of the threaded joint without yield of the shoulder portions, and gastightness after the fastening may be secured.
  • an underlayer (that is, the contact surface of the threaded joint) of the lubricating coating be roughened.
  • the roughening may be accomplished by directly roughening a steel surface by blasting or pickling, or by forming an underlayer coating having a rough surface on the steel surface before forming the lubricating coating.
  • the lubricating coating may be formed as follows. A lubricating coating forming composition that is diluted with an appropriate volatile organic solvent as necessary is prepared, and the composition is applied by an appropriate method such as brush application, spraying, and immersion, and then the solvent is vaporized and dried according to circumstances.
  • the lubricating coating may be formed on both of the contact surfaces of the pin and the box. However, as shown in FIG. 3 , in a case where the pin and the box are fastened at the time of shipment, it is sufficient that the lubricating coating is formed on a contact surface of either the pin or the box. In this case, since a surface treatment or application work for forming the lubricating coating in the short coupling is easier than that in the long steel pipe, the lubricating coating is preferably formed on the contact surface of the coupling (commonly, the contact surface of the box).
  • the lubricating coating be formed on the contact surfaces of both of the pin and the box to add anticorrosive properties in combination with a lubricating surface. According to this, a decrease in lubricating properties or gastightness due to formation of rust may be prevented.
  • the lubricating coating it is necessary for the lubricating coating to be coated on the entirety of the contact surface of the pin and/or the box, but a case in which a part (for example, only the unthreaded metal contact portion) of the contact surface is coated is also included in the invention.
  • the lubricating coating is formed on the contact surface of at least one of the pin and the box of the threaded joint so as to prevent the seizure during fastening between the steel pipes using the threaded joint, and formation of rust during storage.
  • the lubricating coating contains MCA (melamine cyanurate) and a basic metal salt of an aromatic organic acid.
  • the MCA is an organic salt formed from melamine and cyanuric acid, and is a white powder which has a chemical formula expressed by C 3 H 6 N 6 .C 3 H 3 N 3 O 3 and which is considered to have a mica-shaped crystal structure in which the melamine and the cyanuric acid are hydrogen-bonded.
  • the MCA has a heat-resistant temperature as high as 250° C. to 350° C., and a non-flammable gas (N 2 ) is generated during combustion, and thus the MCA is mainly used as a non-halogen flame retardant, and a flame retardant promoter with respect to various kinds of thermoplastic or thermosetting resins.
  • the MCA has a mica-shaped layered crystal structure, and thus the MCA is also used as a white lubricating oil additive.
  • a lubricating system of the MCA is not well known except that the MCA has a cleavable layered crystal structure.
  • the lubricating coating is formed on the contact surface of the tubular threaded joint in combination of the MCA and the basic metal salt of an aromatic organic acid. Accordingly, a specific frictional behavior in which coefficient of friction during low surface pressure sliding is low, and coefficient of friction during high surface pressure sliding is high is exhibited. This behavior becomes apparent for the first time in the invention, and the mechanism has not been clear yet.
  • MCA that is subjected to a surface treatment by a coupling agent such as a silane coupling agent and a titanium coupling agent is commercially available.
  • the surface-treated MCA has also the above-described effect, and thus may be used in the same manner.
  • the amount of the MCA in the lubricating coating (that is, the amount on the basis of the total amount of non-volatile components in the lubricating coating forming composition) is preferably set to be within a range of 0.5% by mass to 30% by mass. When the amount is less than 0.5% by mass, the effect of increasing ⁇ T becomes insufficient. On the other hand, when the amount exceeds 30% by mass, flowability as a lubricating coating decreases, and thus lubricating properties such as seizure resistance may be deficient. More preferably, the amount of MCA is 1% by mass or more, and still more preferably 2% by mass or more. The upper limit thereof is preferably set to 20% by mass or less.
  • the basic metal salt of an aromatic organic acid increases the seizure prevention effect and anticorrosive effect of the lubricating coating formed on the contact surface of the tubular threaded joint, and exhibits specific frictional behavior in which the coefficient of friction is low during the low surface pressure sliding, and the coefficient of friction is high during the high surface pressure sliding when being used in combination with MCA. Accordingly, the basic metal salt exhibits an effect of increasing ⁇ T.
  • the MCA having an average particle size of approximately 0.5 ⁇ m to 5 ⁇ m is commonly used from the viewpoint of dispersibility to a base.
  • the MCA is frequently classified as a solid lubricating agent.
  • an effect of improving lubricating properties is not sufficiently verified, and with regard to conditions under which the operation mechanism and effect are exhibited, and the like, there are many unclear points.
  • MCA contained in the lubricating coating MCA having a large average particle size is preferable so as to obtain a more sufficient ⁇ T improving effect.
  • a preferable average particle size of the MCA is 10 ⁇ m to 40 ⁇ m.
  • the average particle size is 10 ⁇ m or less, the ⁇ T improving effect is not sufficient.
  • the average particle size exceeds 40 ⁇ m, the MCA is not likely to be uniformly distributed on a frictional sliding interface during screw fastening, and thus the ⁇ T improving effect is not sufficiently obtained.
  • the average particle size is defined as a median diameter (50% particle size: D50) of a volume-based particle size distribution obtained by a particle size distribution measuring device using a laser diffraction scattering method as a measurement principle.
  • a basic organic metal salt having both of a lipophilic group and a hydrophilic group that is, a basic organic metal salt considered to have the same operation as a surfactant is aligned on a surface of MCA having slightly high hydrophilicity, and allows coarse MCA to be uniformly dispersed to a base that is an oil base.
  • the coarse MCA is reliably introduced to the high surface pressure sliding interface during fastening of the threaded joint.
  • the coarse MCA that is introduced to the sliding interface exhibits an operation of increasing a frictional resistance of the sliding interface during a process of being pressed and being deformed while preventing seizure (preventing contact between metals).
  • the basic metal salt of an aromatic organic acid is a salt constituted by an aromatic organic acid and a surplus alkali (alkali metal or alkali earth metal). Specific example thereof includes basic sulfonate, basic salicylate, basic phenate, and basic carboxylate. All of the basic metal salts of an aromatic organic acid are materials in which a surplus content of alkali is dispersed in oil as a metal salt of a colloidal fine particle and which are present in a grease form or a semisolid form at ambient temperature.
  • the basic metal salts of an aromatic organic acid show a significant heavy-duty anticorrosion performance, and exhibit a lubricating operation by physical absorption of surplus metal salts in a colloidal fine particle state, or chemical absorption of organic acid groups, and the like.
  • Alkali that constitutes a cation portion of the basic metal salts of an aromatic organic acid may be an alkali metal or alkali earth metal.
  • the alkali is preferably alkali earth metal, particularly, calcium, barium, or magnesium. Even when any of these is used, the same effect may be obtained.
  • basic oil having a base value JIS K2501 (in a case of using two or more kinds, a weighted average value of base values for which an amount is taken into consideration) of 50 mgKOH/g or more be used.
  • a preferable base value is 100 mgKOH/g to 500 mgKOH/g, and more preferably 250 mgKOH/g to 450 mgKOH/g.
  • the basic metal salts of an aromatic organic acid are grease type or semisolid materials, and may achieve a function of a base of the lubricating coating. Accordingly, the basic metal salts may be contained as much as 75% by mass in the lubricating coating.
  • the amount is preferably 70% by mass or less.
  • the lower limit of the amount is not particularly limited, but 20% by mass or more is preferable, and more preferably 40% by mass or more.
  • the total amount of the MCA and the basic metal salts of an aromatic organic acid in the lubricating coating is preferably set to 45% by mass to 95% by mass, and more preferably 50% by mass to 90% by mass.
  • the lubricating coating forming composition according to to the invention further contains one or more kinds selected from the group consisting of a pine resin-based material, a wax, a metal soap, and a lubricating powder in addition to the two kinds of essential components.
  • these components are collectively referred to as a lubricating selective component.
  • the lubricating coating does not contain at least one kind of lubricating selective component selected from the above components, adhesiveness between the lubricating coating that is formed and a surface of a base material, or sufficient coating strength against the high surface pressure during frictional sliding may not be obtained, and as a result, a lubricating performance, particularly, seizure resistance becomes deficient.
  • the pine resin-based material that is a material selected from pine resin and a derivative thereof
  • the pine resin-based material undergoes a high surface pressure in a friction surface, and becomes highly viscous, and thus the pine resin-based material is effective for increasing ⁇ T of the coating.
  • the pine resin is a natural resin secreted from wood of genus pinus .
  • the pine resin is constituted by three elements of carbon, hydrogen, and oxygen.
  • Main components of the fine tree include resin acid (rosin acid) expressed by C 20 H 30 O 2 , and colophane acid expressed by C n H n+10 O 4 .
  • resin acid Rosin acid
  • colophane acid expressed by C n H n+10 O 4
  • Examples of a representative resin acid include abietic acid, d-pimaric acid, and i-pimaric acid.
  • the pine resin (rosin) is largely classified into tall rosin, gum rosin, and wood rosin according to a collection method, and any of these may be used.
  • various kinds of pine rosin derivatives such as rosin ester, hydrogenated rosin, polymerized rosin, and dismutated rosin are commercially available, and these pine rosin derivatives may also be used as the pine resin-based material.
  • the amount of the pine resin-based material including the rosin and a derivative thereof in the lubricating coating is preferably set to 30% by mass or less. When the amount exceeds 30% by mass, the composition that is used for forming the coating becomes highly viscous, and thus there is a concern that coating forming properties may be damaged. To sufficiently obtain the above-described effect of the pine resin-based material, it is preferable that 5% by mass or more of rosins be contained in the lubricating coating, and more preferably 5% by mass to 20% by mass.
  • Wax not only has a seizure prevention effect due to a decrease in friction of the lubricating coating, but also decreases flowability of the lubricating coating. Accordingly, the wax is helpful to increase coating strength. Any of animal wax, vegetable wax, mineral wax, and synthetic wax may be used.
  • wax examples include beeswax, spermaceti (the above, animal wax), Japan wax, carnauba wax, candelilla wax, rice wax (the above, vegetable wax), paraffin wax, microcrystalline wax, petrolatum, montan wax, ozocerite, ceresin (the above, mineral wax), oxidation wax, polyethylene wax, Fischer-Tropsch wax, amide wax, hydrogenated castor oil (castor wax) (the above, synthetic wax), and the like.
  • the paraffin wax having a molecular weight of 150 to 500 is preferable.
  • the amount of wax in the lubricating coating is preferably set to 25% by mass or less. When the amount exceeds 25% by mass, adhesiveness or strength of the lubricating coating may decrease.
  • the amount is preferably 20% by mass or less.
  • the lower limit of the amount of the wax is not particularly limited, but it is preferable that 2% by mass or more of wax be contained so as to reliably obtain the effect of the wax.
  • the metal soap that is a salt of a fatty acid with a metal other than alkali metal may be contained in the lubricating coating so as to increase the seizure prevention effect and the anticorrosive effect of the lubricating coating.
  • the amount thereof in the coating is set to 30% by mass or less. When the amount exceeds 30% by mass, adhesiveness or strength of the lubricating coating may decrease.
  • the lower limit of the amount of the metal soap is not particularly limited, but it is preferable that 2% by mass or more of metal soap be contained so as to reliably obtain the above-described effect.
  • the fatty acid of the metal soap be a fatty acid having 12 to 30 carbon atoms.
  • the fatty acid may be either a saturated fatty acid or an unsaturated fatty acid.
  • the fatty acid may be any of a mixed fatty acid derived from natural fat and oil such as beef tallow, lard, wool fat, palm oil, rapeseed oil, and coconut oil, and a single compound such as lauric acid, tridecylic acid, myristic acid, palmitic acid, lanopalmitic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, arachic acid, behenic acid, erucic acid, lignoceric acid, lanoceric acid, sulfonic acid, salicylic acid, and carboxylic acid.
  • a type of the metal salt a calcium salt is preferable, but other alkali earth metal salts or zinc salts may be used.
  • the salt may be either a neutral salt or a basic salt.
  • the lubricating powder improves the strength of the lubricating coating or suppresses flowability thereof at a high temperature while maintaining Ts of the lubricating coating to be low, and thus the lubricating powder may improve the seizure resistance.
  • a nontoxic and harmless powder which is used as a solid lubricant is preferably used.
  • a preferable lubricating powder include graphite, tungsten disulfide (WS 2 ), molybdenum disulfide (MoS 2 ), tin disulfide, graphite fluoride, boron nitride (BN), cryolite, and PTFE (polytetrafluoroethylene).
  • Graphite is preferable in view of stability in a corrosive environment, an environment aspect, and the like.
  • Graphite is largely classified into natural graphite and artificial graphite. Natural graphite is less expensive. Natural graphite is classified into flake graphite, vein graphite, and amorphous graphite according to the shape thereof. Among these, amorphous graphite having the lowest crystallinity is preferable in terms of making an increase in ⁇ T and improvement in seizure resistance compatible with each other. Furthermore, when taking electrical properties or thermal properties into account, amorphous graphite in which an ash amount is 0.2% by mass to 5.5% by mass, and crystallinity is 98% or less is more preferable. Particularly, amorphous graphite in which crystallinity is 90% to 98% is preferable.
  • the average particle size of graphite is preferably 1 ⁇ m to 20 ⁇ m, and more preferably 1 ⁇ m to 15 ⁇ m.
  • the amount thereof is preferably 0.5% by mass to 20% by mass.
  • the amount is less than 0.5% by mass, the effect is not sufficient.
  • the amount exceeds 20% by mass there is a concern that the operation of other components may be deteriorated.
  • uniform dispersibility of the lubricating powder or flowability of the lubricating coating during friction may decrease.
  • the amount of the lubricating powder is more preferably 0.5% by mass to 10% by mass.
  • an average particle size of the lubricating powder which improves seizure resistance is preferably 0.1 ⁇ m to 10 and more preferably 1 ⁇ m to 5 ⁇ m.
  • Components other than the above-described components for example, one or more kinds of components selected from organic resins, and various kinds of oils and additives (for example, an extreme pressure agent) that are commonly used in lubricating oil may be mixed in the lubricating coating to increase uniform dispersibility of the lubricating powder in the lubricating coating, or to improve characteristics or properties of the lubricating coating.
  • the oils represent lubricating components (viscous liquid material (including greasy material)) which may be used in the lubricating oil and which are in a liquid form at room temperature, and the oils themselves have lubricating properties. Examples of the oils that may be used include synthetic ester, natural fats and oils, mineral oil, and the like.
  • An organic resin particularly, a thermoplastic resin functions to suppress surface tackiness of the lubricating coating, and to increase a film thickness.
  • the organic resin when being introduced to a frictional interface, the organic resin functions to increase seizure resistance, or to reduce friction even when receiving high fastening torque (high surface pressure) when metal portions come into contact with each other. Accordingly, the organic resin may be contained in the lubricating coating.
  • thermoplastic resin examples include polyethylene resins, polypropylene resins, polystyrene resins, polymethyl acrylate resins, styrene/acrylic acid ester copolymer resins, polyamide resin, polybutene (polybutylene) resins, and the like. Copolymers or blends of these may be used, or copolymers or blends of these with other thermoplastic resins may also be used.
  • the thermoplastic resin preferably has a density (JIS K 7112) in a range of 0.9 to 1.2, and thermal deformation temperature (JIS K 7206) is preferably in a range of 50° C. to 150° C. to easily deform at a frictional surface so as to allow the lubricating properties to be exhibited.
  • the polybutene resins having high viscosity at a high surface pressure are preferable.
  • thermoplastic resin is preferably in the form of powders of 0.05 ⁇ m to 30 ⁇ m, and the amount of the thermoplastic resin in the coating is preferably set to 10% by mass or less.
  • oils examples include beef tallow, lard, wool fat, palm oil, rapeseed oil, coconut oil, and the like.
  • mineral oil including synthetic mineral oil
  • synthetic ester examples include fatty acid monoester, dibasic acid diester, and fatty acid ester of trimethylol propane or pentaerythritol, and the like.
  • the amount of the oil in the lubricating coating is preferably set to 5% by mass or less.
  • the extreme pressure agent examples include, but are not limited to, sulfurized fats and oils, polysulfide, phosphate, phosphite, thiophosphate, and dithiophosphoric acid metal salt, and the like.
  • the amount thereof in the lubricating coating is preferably set within a range of 0.05% by mass to 5% by mass.
  • the lubricating coating substantially do not contain a harmful heavy metal.
  • the compound grease contains a large amount of powders of a soft heavy metal such as lead and zinc is to prevent seizure (galling) by suppressing contact between metals.
  • this function is provided in combination of the MCA and the basic metal salt of an aromatic organic acid which are contained in the lubricating coating, and thus even when the heavy metal powder is not contained at all, the coating may exhibit a sufficient lubricating performance.
  • the lubricating coating is formed as follows. A mixture of the constituent components is made into liquid by solvent addition and/or heating, and the liquid mixture is applied to the contact surface of at least one member of the pin and the box of the threaded joint, and the coated film is dried as necessary.
  • the application by heating may be realized by a so-called hot melt application method.
  • the mixture of the constituent components of the lubricating coating is heated to a temperature at which applicable viscosity is obtained, and the mixture is sprayed onto an application surface from a sprayer provided with a heat retention function.
  • the application surface may be preheated, for example, to approximately the same temperature as that of a material to be applied.
  • the lubricating coating forming composition is prepared by adding a volatile organic solvent to the mixture of the constituent components of the lubricating coating.
  • the volatile organic solvent is different from base oil of the lubricating oil, and evaporates during a coating forming process, and thus the volatile organic solvent substantially does not remain in the lubricating coating.
  • Volatile represents that there is a tendency for the organic solvent to evaporate at a coating state at a temperature of room temperature to 150° C.
  • the lubricating coating of the invention may be a viscous liquid or semisolid, and thus a little amount solvent is permitted to remain.
  • Examples of the solvent is not particularly limited, but examples of a volatile organic solvent which is suitable for use in the invention include petroleum solvents such as a solvent corresponding to industrial gasoline defined by JIS K 2201, mineral sprit, aromatic petroleum naphtha, xylene, and Cellosolve. A mixture of two or more kinds of these may be used.
  • a solvent having the flash point of 30° C. or higher, an initial boiling point of 150° C. or higher, and a final boiling point of 210° C. or higher is preferable from the viewpoints that it is relatively easy to handle, and evaporates rapidly, and thus the drying time may be short.
  • the lubricating coating forming composition may contain an antioxidant, a preservative, and a colorant, in addition to the above-described components.
  • Viscosity (dynamic viscosity: unit is cSt, B-type viscosity form) of the lubricating coating forming composition may be appropriately selected by adding an organic solvent or the like in accordance with an application method.
  • viscosity at 40° C. is preferably 4,000 cSt or less
  • viscosity at 60° C. is preferably 1,000 cSt or less.
  • the film thickness of the lubricating coating is preferably set within a range of 10 ⁇ m to 500 ⁇ m as described later. It is preferable that the lubricating coating have a thickness sufficient to bury minute gaps such as a gap between thread ridges in the contact surface. When the film thickness is too small, an effect provided to the frictional surface may not be expected. From the reason, the film thickness of the lubricating coating is preferably set to 10 ⁇ m or more.
  • the upper limit of the film thickness of the lubricating coating be set to approximately 500 ⁇ m.
  • the film thickness of the lubricating coating is more preferably 15 ⁇ m to 200 ⁇ m.
  • the film thickness of the lubricating coating be made to be larger than Rmax of the underlayer.
  • the film thickness in a case where the underlayer is rough is an average value of the film thickness of the entirety of the coating which may be calculated from the area, mass, and density of the coating.
  • the lubricating coating when oil is contained to a certain degree, the lubricating coating becomes a viscous liquid. In a case where an amount of oil is small, or oil is not contained, the lubricating coating becomes a semisolid.
  • the contact surface covered with the coating when the contact surface covered with the coating is subjected to a surface treatment for roughening, and thus surface roughness is made to be larger than 3 ⁇ m to 5 ⁇ m that is surface roughness after grinding, the seizure resistance is improved in many cases. Accordingly, it is preferable that the contact surface be subjected to the surface treatment for roughening before forming the lubricating coating.
  • Examples of the surface treatment include blasting by shooting a blasting material such as spherical shot and angular grit, and pickling by immersion in a strong acid solution such as sulfuric acid, hydrochloric acid, nitric acid, and hydrofluoric acid for roughening the surface.
  • the examples include a chemical conversion treatment such as a phosphate treatment, an oxalate treatment, and a borate treatment (roughness on a crystal surface increases along with growth of crystals that are generated), electroplating with metals such as Cu, Fe, Sn, and Zn, or alloys thereof (convex portions are preferentially plated, and thus the surface is slightly roughened), impact plating capable of forming a porous plated coating.
  • composite plating to form a plated coating in which solid fine particles are dispersed in metal is possible as a method of forming a roughened surface in order for the solid fine particles to project from plated coating.
  • Any surface treatment method of the contact surface is preferably performed in such a manner that the surface roughness Rmax obtained by the roughening of the surface treatment becomes 5 ⁇ m to 40 ⁇ m.
  • Rmax is less than 5 ⁇ m, adhesiveness with the lubricating coating or coating retention properties may not be sufficient.
  • Rmax exceeds 40 ⁇ m, friction increases, and thus when undergoing a high surface pressure, the coating may not withstand a shearing force and a compressive force. Therefore, the coating may be fractured or be peeled off.
  • the surface treatment for the roughening may be performed in combination of two or more kinds of the treatments, and as a treatment method thereof, a method known in the related art may be used.
  • the film thickness of the porous coating is preferably set to 5 ⁇ m or more so as to allow Rmax of the porous coating to be 5 ⁇ m or more.
  • the upper limit of the film thickness is not particularly specified, but the upper limit is commonly 50 ⁇ m or less, and preferably 40 ⁇ m or less.
  • Examples of particularly preferable surface treatment for forming the porous coating include formation of a coating of zinc or a zinc-iron alloy (porous metal coating) by a phosphate chemical conversion treatment (treatment using manganese phosphate, zinc phosphate, iron manganese phosphate, or zinc calcium phosphate), and impact plating.
  • a phosphate chemical conversion treatment treatment using manganese phosphate, zinc phosphate, iron manganese phosphate, or zinc calcium phosphate
  • impact plating from the viewpoint of adhesiveness, the manganese phosphate coating is preferable, and from the viewpoint of corrosion resistance, the coating of zinc or a zinc-iron alloy on which sacrificial protection due to zinc may be expected is more preferable.
  • the phosphate chemical conversion treatment may be performed by immersion or spraying according to a common method.
  • a chemical treatment solution an acidic phosphate treatment solution for use in general galvanizing material may be used.
  • a chemical conversion treatment of a zinc phosphate-based solution containing 1 g/L to 150 g/L of phosphate ions, 3 g/L to 70 g/L of zinc ions, 1 g/L to 100 g/L of nitrate ions, and 0 g/L to 30 g/L of nickel ions may be exemplified.
  • a manganese phosphate-based chemical conversion treatment solution that is commonly used in the threaded joint may be used.
  • the temperature of the solution may be from an ambient temperature to 100° C., and a treatment time may be up to 15 minutes depending on a desired film thickness.
  • an aqueous surface conditioning solution containing colloidal titanium may be supplied to the surface to be treated. After the phosphate treatment, the treated surface is preferably washed with cold or warm water prior to drying.
  • the impact plating may be performed by mechanical plating in which particles are allowed to collide with a material to be plated inside a rotating barrel, or by shooting plating in which particles are allowed to collide with a material to be plated using a blasting apparatus.
  • it is sufficient to perform the plating only on the contact surface, and thus it is preferable to employ the shooting plating capable of performing localized plating.
  • a material to be shot which is constituted by a powder in which an iron-based core is coated with zinc or a zinc alloy, is shot against a contact surface to be coated.
  • the amount of zinc or a zinc alloy in the particles is preferably within a range of 20% by mass to 60% by mass, and a particle size of the particles is preferably within a range of 0.2 mm to 1.5 mm. Only the zinc or zinc alloy that is a covering layer of the particles adheres to the contact surface of a base body by the shooting, and a porous coating of zinc or a zinc alloy is formed on the contact surface.
  • the shooting plating may form a porous plated metal coating with good adhesiveness on a steel surface regardless of a material quality of the steel.
  • the thickness of the zinc or zinc alloy layer formed by the impact plating is preferably 5 ⁇ m to 40 ⁇ m from the viewpoints of both of the corrosion resistance and the adhesiveness. When the thickness is less than 5 ⁇ m, sufficient corrosion resistance is not secured, and when the thickness exceeds 40 ⁇ m, the adhesiveness with the lubricating coating may deteriorate.
  • the above-described surface treatment may be performed in combination of two or more kinds thereof.
  • electroplating of metals such as Cu, Sn, and Ni, or alloys thereof may be exemplified.
  • Plating may be single-layer plating, or multi-layer plating of two or more layers.
  • Specific examples of this kind of electroplating include Cu plating, Sn plating, and Ni plating, as well as Cu—Sn alloy plating, Cu—Sn—Zn alloy plating, two-layer plating by Cu plating-Sn plating, and three-layer plating by Ni plating-Cu plating-Sn plating which are disclosed in Japanese Unexamined Patent Application, First Publication No. 2003-74763.
  • seizure may significantly occur, and thus it is preferable to perform single-layer plating of a Cu—Sn alloy or a Cu—Sn—Zn alloy, or multi-layer metal plating in combination of two or more layer plating selected from the alloy plating, Cu plating, Sn plating, and Ni plating, for example, two-layer plating of Cu plating-Sn plating, two-layer plating of Ni plating-Sn plating, or two-layer plating of Ni plating-Cu/Sn/Zn alloy plating, and three-layer plating of Ni plating-Cu plating-Sn plating as the surface treatment.
  • Such plating may be formed according to a method disclosed in Japanese Unexamined Patent Application, First Publication No. 2003-74763.
  • a coated film (commonly, Ni plating) of the lowest layer is preferably formed as a very thin coated layer having a film thickness less than 1 ⁇ m which is called strike plating.
  • the film thickness (in a case of multi-layer plating, the total film thickness) of the plating is preferably set within a range of 5 ⁇ m to 15 ⁇ m.
  • the contact surface of the other member (for example, the pin) which is not coated with the solid coating may be left in an untreated state, but preferably, the other member is subjected to the above-described surface treatment to roughen the contact surface. That is, the surface roughening may be performed by employing a method selected from blasting, pickling, a phosphate chemical conversion treatment, an oxalate chemical conversion treatment, a borate chemical conversion treatment, electroplating, impact plating, and a combination of two or more of these methods.
  • the contact surface of the other member not having a solid coating exhibits a satisfactory solid coating retention properties due to the anchor effect produced by the surface roughening, thereby increasing the seizure resistance of the tubular threaded joint.
  • a known anticorrosive coating such as a coating of a UV-curable resin or a thermosetting resin may be formed after the surface treatment as required.
  • the contact surface may be subjected to another surface treatment.
  • various kinds of solid coatings for example, solid lubricating coating
  • solid lubricating coating different from that of the invention may be formed.
  • a contact surface including a threaded portion and an unthreaded metal contact portion of the pin is referred to as “pin surface”
  • a contact surface including a threaded portion and an unthreaded metal contact portion of the box is referred to as “box surface”.
  • Surface roughness is Rmax.
  • % represents % by mass unless otherwise stated.
  • a surface treatment shown in Table 2 was performed with respect to a pin surface and a box surface of a premium threaded joint VAM TOP (registered trademark) (outer diameter: 17.78 cm (7 inches), thickness: 1.036 cm (0.408 inches) formed from Cr—Mo steel A or 13% Cr steel B shown in Table 1. Then, a lubricating coating was formed on the pin surface and the box surface, which was subjected to the surface treatment, by an illustrated application method using a composition shown in Table 3 (MCA and a basic metal salt of an aromatic organic acid are illustrated as an essential component, and a pine resin-based material, a wax, a metal soap, and a lubricating powder are illustrated as a selective component). Accordingly, the lubricating coating formed on the pin surface and the box surface had the same composition.
  • VAM TOP registered trademark
  • MCA and a basic metal salt of an aromatic organic acid are illustrated as an essential component
  • the lubricating coating were formed by the following several application methods except for Comparative Example 1 using compound grease, all of the lubricating coatings has the same thickness of 50 ⁇ m.
  • Ambient-temperature spray method a lubricating coating forming composition prepared by adding 30 parts by mass of a volatile organic solvent (mineral sprit: ExxsolTM D40 manufactured by ExxonMobil Chemical) to total of 100 parts by mass of lubricating coating components having a predetermined composition to decrease viscosity was spray-applied at an ambient temperature, and the organic solvent was allowed to vaporize by natural drying to form a lubricating coating;
  • a volatile organic solvent mineral sprit: ExxsolTM D40 manufactured by ExxonMobil Chemical
  • Heating spray method a lubricating coating forming composition, which contained lubricating coating components having a predetermined composition and did not contain a solvent, was heated to 130° C. to obtain a low viscosity liquid, and was spray-applied from a sprayer provided with a heat retention function onto the pin surface or the box surface which was preheated to 130° C. by induction heating. Then, the resultant applied composition was cooled to form a lubricating coating. This is a hot melt method.
  • Materials used for preparation of the lubricating coating forming composition are as follows.
  • MCA MC-4000 manufactured by NISSAN CHEMICAL INDUSTRIES, LTD. (average particle size: 14 ⁇ m);
  • Pine resin-based material rosin ester (ester gum H) manufactured by Arakawa Chemical Industries, Ltd.;
  • Basic metal salt of an aromatic organic acid basic Ca sulfonate (Calcinate C400CLR) (base value: 400 mgKOH/g) manufactured by CHEMTURA Corporation.
  • Metal soap Ca stearate (manufactured by DIC Corporation);
  • wax paraffin wax manufactured by NIPPON SEIRO CO., LTD;
  • Graphite amorphous graphite, a graphite powder manufactured by Nippon Graphite Industries, ltd., blue P (an ash content: 3.79% by mass, crystallinity: 96.9%, average particle size: 7 ⁇ m);
  • a manganese phosphate coating is executed by immersion in a manganese phosphate chemical conversion treatment solution (PALPHOS M1A manufactured by Nihon Parkerizing Co., Ltd., the same shall apply hereinafter) at 80° C. to 95° C. for 10 minutes
  • zinc phosphate coating is executed by immersion in a chemical conversion treatment solution for zinc phosphate (PALBOND 181X manufactured by Nihon Parkerzing Co., Ltd, the same shall apply hereinafter) at 75° C. to 85° C. for 10 minutes.
  • composition of non-volatile components of lubricating coating forming composition (numerical value in parentheses represents amount in % by mass)
  • Organic solvent Essential component (per 100 parts of Basic metal salt of Selective component total amount of aromatic organic Pine resin- Lubricating non-volatile No.
  • tubular threaded joint formed from Cr—Mo steel having a composition A shown in Table 1 a manganese phosphate coating (Rz: 12 ⁇ m) having a thickness of 15 ⁇ m was formed on a box surface after grinding finish, and then a lubricating coating having a film thickness of 50 ⁇ m and a composition indicated in each of Examples and Comparative Examples of Table 3 was formed thereon by ambient temperature spray application.
  • a zinc phosphate coating (Rz: 8 ⁇ m) having a thickness of 12 ⁇ m was formed on a pin surface after grinding finish, and then a lubricating coating was formed thereon in the same manner as the box surface.
  • Ni strike plating was formed on the box surface by electroplating after grinding finish, and then Cu plating having a thickness of 7 ⁇ m was formed thereon (total plating thickness: 8 ⁇ m).
  • Rz of the plated surface was 2 p.m.
  • a lubricating coating having a film thickness of 50 ⁇ m and a composition indicated in Example 2 of Table 3 was formed on the plated coating by ambient temperature spray application.
  • Ni strike plating was formed on the box surface by electroplating after grinding finish, and then Copper-Tin-Zinc alloy plating coating (Rz: 2 ⁇ m) was formed thereon (total plating thickness: 8 ⁇ m).
  • a lubricating coating having a film thickness of 50 ⁇ m and a composition indicated in Example 3 of Table 3 was formed on the plated coating.
  • tubular threaded joint formed from Cr—Mo steel having a composition A shown in Table 1 a manganese phosphate coating (Rz: 12 ⁇ m) having a thickness of 15 ⁇ m was formed on a box surface after grinding finish, and then a lubricating coating having a film thickness of 50 ⁇ m and a composition indicated in Example 5 of Table 3 was formed thereon by heating spray application.
  • a zinc phosphate coating (Rz: 8 ⁇ m) having a thickness of 12 ⁇ m was formed on a pin surface after grinding finish, and then a lubricating coating was formed thereon in the same manner as the box surface.
  • a manganese phosphate coating (Rz: 12 ⁇ m) having a thickness of 15 ⁇ m was formed on a box surface after grinding finish. Viscous liquid type compound grease according to API standard was applied onto the manganese phosphate coating (a total application amount in the pin and the box was 50 g, and a total application area was approximately 1,400 cm 2 ). The pin surface was left as it was after the grinding finish, and then the above-described compound grease was applied onto the pin surface.
  • Ts was torque when a shoulder portion began to interfere, specifically, torque when a torque variation, which was exhibited after the shoulder portion interfered, began to enter a linear region (elastic deformation region) was set as Ts.
  • Ty was torque when plastic deformation began to start, specifically, torque when linearity in a torque variation disappeared together with rotation after reaching Ts, and it began to be away from the linear region was set as Ty.
  • Example 2 in which the amount of MCA was as high as 30%, and very satisfactory results were obtained.
  • seizure occurred during the ninth fastening, and thus the test was stopped.
  • the number of times of fastening and loosening is five or more, there is no problem in a practical use, and thus the tubular threaded joint of Example 2 is also sufficiently useful.
  • ⁇ T relative value a relative value of ⁇ T when ⁇ T of Comparative Example 1 using the compound grease was set to 100 (hereinafter, referred to simply as ⁇ T relative value) was higher than 100% in each case, and it could be understood that in the tubular threaded joints of examples, fastening with high torque was possible without causing yielding of the shoulder portion.
  • the ⁇ T relative value was as very high as 124% or more except for Example 6.
  • the small amount 0.8% of MCA may be the reason why the ⁇ T relative value in Example 6 was 108% lower than that of other examples. Accordingly, to improve high torque fastening properties, it is preferable for the amount of MCA to be 1% or more, and more preferably 2% or more. As can be understood from results of the examples, as the amount of MCA increases, the ⁇ T relative value may increase.
  • Comparative Examples 2 to 3 it could be understood that when the lubricating coating does not contain any one of the MCA and the basic metal salt of an aromatic organic acid, the seizure resistance significantly deteriorates, and the ⁇ T relative value is much less than 100, and thus not only the seizure resistance but also the high torque fastening properties significantly deteriorate when compared to the compound grease.
  • tubular threaded joints of the respective examples were verified by an gastightness test or an operational suitability test in an actual drilling apparatus, all of the joints exhibited a satisfactory result. Since ⁇ T is larger than that of the compound grease used in the related art, it is verified that even when the fastening torque increases, fastening may be stably performed.

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  • Non-Disconnectible Joints And Screw-Threaded Joints (AREA)
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US14/419,447 2012-08-06 2013-07-31 Tubular threaded joint and lubricating coating forming composition for use therein Abandoned US20150191674A1 (en)

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JP2012174117 2012-08-06
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CN108949301A (zh) * 2018-08-01 2018-12-07 苏州力森克液压设备有限公司 一种用于液压缸的非皂基烃基型润滑脂
US20190056055A1 (en) * 2017-08-18 2019-02-21 Baker Hughes, A Ge Company, Llc Corrosion protection element for downhole connections
US20200157459A1 (en) * 2018-11-20 2020-05-21 Nch Corporation Composition and Method of Manufacturing Sulfonate-Based Greases Using a Glycerol Derivative
US20200181528A1 (en) * 2016-02-26 2020-06-11 Kyodo Yushi Co., Ltd. Grease composition for ball joint
US11591539B2 (en) 2018-04-26 2023-02-28 Shell Usa, Inc. Lubricant composition and use of the same as a pipe dope
US11987765B2 (en) 2019-01-07 2024-05-21 Nippon Steel Corporation Composition, and threaded connection for pipes including lubricant coating layer formed from the composition
EP4332204A4 (en) * 2021-05-31 2024-08-28 Jfe Steel Corp CHEMICAL AGENT, OIL WELL PIPE AND SCREW JOINT FOR OIL WELL PIPE

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CA2998097C (en) 2015-09-18 2020-12-22 Nippon Steel & Sumitomo Metal Corporation Composition, threaded joint for pipes including solid lubricant coating formed from the composition, and method for producing the threaded joint for pipes
AR107043A1 (es) * 2015-12-25 2018-03-14 Nippon Steel & Sumitomo Metal Corp Conexión roscada para caño o tubo y método para producir la conexión roscada para caño o tubo
EP3633256B1 (en) * 2017-05-22 2021-09-29 Nippon Steel Corporation Threaded connection for pipes or tubes and method for producing the threaded connection for pipes or tubes
CN107418683A (zh) * 2017-08-09 2017-12-01 广东尔航实业有限公司 螺丝润滑蜡及其制备方法、应用
MX2020004447A (es) 2017-10-13 2020-07-24 Nippon Steel Corp Composicion y conexion roscada para tubos o tuberias, incluyendo la capa de recubrimiento lubricante formada a partir de la composicion.
CN109868179A (zh) * 2019-02-26 2019-06-11 天津市金海利油脂有限公司 一种极压润滑脂的制造方法
NL2023042B1 (en) * 2019-04-30 2020-11-23 Tenaris Connections Bv Threaded connection for hammering interconnected tubular members
RU2771368C1 (ru) * 2021-11-16 2022-05-04 Федеральное государственное бюджетное образовательное учреждение высшего образования "Поволжский государственный технологический университет" Нагельное соединение деревянных элементов строительных конструкций

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US20200181528A1 (en) * 2016-02-26 2020-06-11 Kyodo Yushi Co., Ltd. Grease composition for ball joint
US11702613B2 (en) * 2016-02-26 2023-07-18 Kyodo Yushi Co., Ltd. Grease composition for ball joint
US20190056055A1 (en) * 2017-08-18 2019-02-21 Baker Hughes, A Ge Company, Llc Corrosion protection element for downhole connections
US10781962B2 (en) * 2017-08-18 2020-09-22 Baker Hughes, A Ge Company, Llc Corrosion protection element for downhole connections
US11591539B2 (en) 2018-04-26 2023-02-28 Shell Usa, Inc. Lubricant composition and use of the same as a pipe dope
CN108949301A (zh) * 2018-08-01 2018-12-07 苏州力森克液压设备有限公司 一种用于液压缸的非皂基烃基型润滑脂
US20200157459A1 (en) * 2018-11-20 2020-05-21 Nch Corporation Composition and Method of Manufacturing Sulfonate-Based Greases Using a Glycerol Derivative
US11987765B2 (en) 2019-01-07 2024-05-21 Nippon Steel Corporation Composition, and threaded connection for pipes including lubricant coating layer formed from the composition
EP4332204A4 (en) * 2021-05-31 2024-08-28 Jfe Steel Corp CHEMICAL AGENT, OIL WELL PIPE AND SCREW JOINT FOR OIL WELL PIPE

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AR091966A1 (es) 2015-03-11
RU2604526C2 (ru) 2016-12-10
CN104520414A (zh) 2015-04-15
RU2015103520A (ru) 2016-09-27
MX2015001584A (es) 2015-05-11
CA2880414A1 (en) 2014-02-13
EP2881454B1 (en) 2019-10-30
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WO2014024755A1 (ja) 2014-02-13
EP2881454A1 (en) 2015-06-10
CA2880414C (en) 2017-02-14
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JPWO2014024755A1 (ja) 2016-07-25
BR112015002181A2 (pt) 2017-07-04

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