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WO1982000651A1 - Poudres de revetement epoxy - Google Patents

Poudres de revetement epoxy Download PDF

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Publication number
WO1982000651A1
WO1982000651A1 PCT/US1980/001090 US8001090W WO8200651A1 WO 1982000651 A1 WO1982000651 A1 WO 1982000651A1 US 8001090 W US8001090 W US 8001090W WO 8200651 A1 WO8200651 A1 WO 8200651A1
Authority
WO
WIPO (PCT)
Prior art keywords
coating
epoxy
powder according
coating powder
powders
Prior art date
Application number
PCT/US1980/001090
Other languages
English (en)
Inventor
Corp Polymer
Original Assignee
Housenick J
Richart D
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
Application filed by Housenick J, Richart D filed Critical Housenick J
Priority to PCT/US1980/001090 priority Critical patent/WO1982000651A1/fr
Priority to EP19810900465 priority patent/EP0058149A4/fr
Priority to JP50076180A priority patent/JPS57501380A/ja
Priority to AU67807/81A priority patent/AU6780781A/en
Publication of WO1982000651A1 publication Critical patent/WO1982000651A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
    • C08G59/72—Complexes of boron halides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50—Amines
    • C08G59/5033—Amines aromatic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins

Definitions

  • This invention relates to high performance epoxy coating powders adapted for use in fusion coating processes. Coatings of these epoxy powders are highly resistant to chemical attack and are particularly well suited to extend the service life of oil field gear such as drill pipe, gas pipe, production tubing, transmission lines, sucker rods, filter screens and the like.
  • the coating compositions of this invention are dry, free-flowing powders that may be used in fusion coating processes.
  • Fusion coating processes are here defined as those coating processes in which coating powders are distributed over a substrate (which may be hot or cold) and heat, supplied from the substrate or an external source, fuses the powders into a continuous protective film. Examples of fusion coating processes include fluidized bed, electrostatic spraying, hot flocking (with or without electrostatic spray), cloud chambers, fluid transport of powder through pipe, and the like.
  • fusion coating processes include fluidized bed, electrostatic spraying, hot flocking (with or without electrostatic spray), cloud chambers, fluid transport of powder through pipe, and the like.
  • the coating compositions of this invention are distinguished by their unusual chemical and physical properties and are especially adapted to protect substrates in demanding applications such as pipe coating for "down hole” use in the oil fields; e.g., drill pipe, filter screens, and production or gas recovery tubing. It is not uncommon to encounter temperatures as high as 200°C. and pressures exceeding 700 kg/cm 2 in deep oil wells and an effective coating must give corrosion protection in these environments from such things as acid forming gases, particularly carbon dioxide and hydrogen sulfide, corrosive drilling muds, and chemicals that may be used to free a "frozen" drill string or open pores in oil bearing strata.
  • acid forming gases particularly carbon dioxide and hydrogen sulfide, corrosive drilling muds, and chemicals that may be used to free a "frozen" drill string or open pores in oil bearing strata.
  • a good coating should also have sufficient flexibility to bend with the string during drilling and be tough enough to withstand mechanical abuse (e.g., impact and abrasion) encountered in drilling operations. Because the requirements for coatings for oil field pipe, particularly drill pipe, are so demanding, it is convenient, for purposes of exposition, to discuss the invention in this context, although it should be understood that it is not intended that the invention be so limited, as the coating compositions here disclosed will be of utility in other applications in which a combination of good chemical, physical or electrical properties is required. It has become common practice to coat drill pipe and related gear with protective polymeric coatings. When properly formulated and applied, these coatings can increase the service life of mild steel pipe many times over.
  • 1 mm can only be achieved by performing a number of repetative steps including dipping or spraying the substrate with the liquid coating; evaporating volatile solvents or carriers; and at least partially curing the coating. Care must be exercised not to fully cure the resin until after the final coat has been applied, for otherwise, successive coating layers will not fuse together. More recently it has been recognized that fusion coating processes using dry powders offer a number of significant advantages over liquid systems. For example, powder coatings can be applied in film thickness of 1 mm or more in a single coating step. The energy requirements are reduced since only one bake cycle of 30 to 60 minutes is required as contrasted to multiple layer liquid coating systems which may require as many as six or more coats with each requiring an hour or cs partial baking cycle.
  • a further advantage of powder coatings is that they do not contain volatile solvents or carrier liquids that require costly collection and recovery systems to protect the environment.
  • Phenolics cure by condensation and the gaseous reaction products cause internal voids in the coating unless the coating is a relatively thin film.
  • Epoxy resins on the other hand, do not cure by condensation reactions, and are free from this problem.
  • epoxies as compared with phenolics, have many advantageous features: they are tougher and more flexible, they do not cure by condensation reactions, they can be applied as thick films and, therefore, are suitable for use in fusion coating processes. It is not surprising that a great deal of effort has been given to improving the chemical properties of the epoxies so that they can serve as effective replacements for phenolics in demanding applications such as drill pipe.
  • U.S. patent 4,122,060 discloses an epichlorohydrin-bisphenol-A type resin that is modified by the inclusion of a minor amount of an epoxidized novolac resin having a functionality greater than 2. This coating is adapted for rapid cures (e.g., less than two minutes) by the use of bifunctional hydroxyl terminated curing agents. Coating powders such as disclosed in this patent are much improved in chemical resistance when compared with straight epichlorohydrin-bisphenol-A resins but fall considerably short of meeting the demands imposed, for example, upon drill pipe coatings.
  • Another object of this invention is to formulate epoxy coating powders which yield coatings having improved chemical resistance at elevated temperatures and pressures. Another object of this invention is to provide epoxy coating powders that will form adherent chemically resistant protective films over substrates.
  • Another object of this invention is to provide adherent, chemically resistant epoxy coatings that have high cross-link densities, high glass transition temperatures and moderately good toughness and flexibility.
  • a specific object of this invention is to provide coating powders that, when applied in fusion coating processes, will materially extend the service life of metal gear used in the oil fields, including such things as flood pipe, recovery pipe, drill pipe, production tubing, sucker rods and filter screens.
  • coating powders comprised of:
  • An unmodified epoxy resin or a mixture of epoxy resins having an average functionality of greater than 3 and more preferably greater than 4;
  • An aromatic polyfunctional amine curing agent 3. At least 50 parts by weight per hundred parts of resin of a mineral filler; and
  • An essential property that must be considered when formulating a coating powder is the ability of the powder to fuse into a uniform, continuous and void free film.
  • two relatively simple test procedures have been established to measure the ability of a coating powder to fuse over a substrate.
  • One of these is gel time which provides a measure of the reactivity of a given system; and the other is inclined plate flow which is a combined measure of both the reactivity and melt viscosity of the coating powder.
  • ASTM Specification D-3451 (14) defines a procedure for measuring gel time in which a piece of aluminum foil is placed on a hot plate and heated to a given temperature, e.g. 190°C. A small quantity of powder is dropped onto the heated foil and stroked with a tongue depressor until continuous and readily breakable filaments are formed when the depressor is lifted from the foil. The elapsed time for this to occur is measured in seconds and is the gel time.
  • the Inclined Plate Flow Test is defined in ASTM D-3451 (17). In this test a small pellet of powder is placed on a glass or tin plate and inserted into a heated oven, e.g. 150°C. After the pellets and the plate have reached temperature equilibrium, the oven rack on which the plate rests is tilted to a 65° angle without opening the oven. After 30 minutes, the plate is removed from the oven, allowed to cool to room temperature and the length of the flow measured in millimeters. The distance the coating flows is dependent on the initial melt viscosity, rate of reaction, and the temperature at which the test is conducted. If the flow is too great, the coating may be expected to run and sag on a substrate; on the other hand, if the flow is too small, a rough, discontinuous, nonadherent film will probably result.
  • acceptable gel times are between 10 to 300 seconds when measured at 205°C, and useful inclined plate flows are bewteen 15mm and 100mm when measured at 150°C. It is generally true that the gel time and the inclined plate flow decrease as the functionality of an epoxy resin increases. It is also true that the gel time and the inclined plate flow increase with a decrease in molecular weight and functionality of the epoxy resin. By judiciously balancing the amount of a high functionality resin used with the amount of a low functionality, low molecular weight resin used, a formulating chemist can arrive at coating powder that has a useful gel time and inclined plate flow. Further control over the gel time and the inclined plate flow can be achieved in the selection of hardening agents and catalysts of varying reactivity.
  • Fillers can also play an important role in determining the melt viscosity and inclined plate flow of the coating material. Fillers generally increase the viscosity to a variable extent depending on the amount used, the particle size, the surface area and the surface chemistry of the filler.
  • the average functionality of the epoxy resins useful in the practice of this invention should be at least 3, and, preferably, at least 4.
  • a preferred class epoxy resins is the epoxy novolacs, which include both epoxy phenol novolacs and the epoxy cresol novolacs. These may be represented by the following general formula:
  • n may be from 1 to abqut 5 or more
  • the epoxy functionality is n + 2 and y is 0 for the epoxy phenol novolac and 1 for the epoxy cresol novolac.
  • Examples of other epoxies having functionalities of three or more include triglycidal p-aminophenol, triglycidal isocyanurate, tetra-p-hydroxyphenol-polyglycidal ether and the tetra functional epoxy based upon the reaction of methylene dianaline with epichlorohydrin.
  • the functionality of these resins makes them quite reactive and sufficient gel time and inclined plate flow may not be provided to yield satisfactory coatings.
  • the preferred curing agents for use in this invention are polyfunctional aromatic amines and particularly diamino diphenyl sulfone and bis (diaminophenyl) sulfone.
  • the reasons for their selection are several fold and the most important one is that they cure at comparatively slow rates.
  • the rapid rate at which high functionality epoxy novolac resins cure dictate the use of a slow curing agent in order to obtain long enough gel times and inclined plate flows.
  • a second advantage to the use of these curing agents is that they are polyfunctional and will increase the cross link density of the coating.
  • the chemical resistance of the coating is improved by the introduction of additional aromatic groups.
  • the amount of curing agent used is not extremely critical but generally it is useful to approximate a stoichometric quantity based on the functionality of the epoxy resin to a tolerance of about ⁇ 20%.
  • the Fillers Fillers are commonly included in coating powders to decrease raw material costs and to improve certain physical properties such as hardness and abrasion resistance. It has been believed by those skilled in the art that the use of fillers detracts from the chemical resistance of a pure epoxy coating, since fillers are generally more readily attacked by chemicals, particularly strong acides, than are cured epoxies. It has now been discovered, contrary to this conventional wisdom, that the performance of epoxy coatings, when exposed to corrosive environments at elevated temperatures and temperatures, can materially be increased through the use of selected mineral fillers in substantial amounts, i.e., at least 50 phr.
  • filler loadings as high as 200 phr have proved quite useful and, it is believed, even higher levels can be used.
  • the theoretical upper limit of the filler loading in a coating powder is the critical pigment volume concentration at which point there is no longer enough resin to wet out the pigment completely.
  • fillers are well known to the art, of which some of the more common are silica, barium sulphate, calcium carbonate, aluminum silicate, calcium silicate, mica, and the like.
  • the fillers should be in finely divided form, and, preferably their particle size should not exceed 10 microns. E. The Catalysts.
  • a better edge coverage is obtained when a small amount, e.g. less than 2% by weight, of a material having a high surface area is dry blended into the coating powder.
  • a material having a high surface area for example, fumed silica having an average diameter of 7 to 14 millimicrons and a surface area of between 200 and 400 square meters per gram is suitable, such as Cab-O-Sil® sold by the Cabot Corporation.
  • the coating powders of this invention can be pigmented as desired, and any conventional inorganic, organic, or filler pigments can be used. The amounts are not critical other than they should be present in a sufficient amount to provide the desired color density.
  • Flow control agents can be usefully included in the coating powders in amounts up to 2% by weight.
  • Typical flow control agents are polyalkylacrylates in which the alkyl group contains between 2 and 8 carbon atoms, such as ModaFlow® sold by Monsanto.
  • hydrophobic silicas may contribute useful chemical properties and are included in preferred formulations.
  • a coating powder was prepared in accordance with this invention by initially blending the following ingredients: Material phr
  • Diaminodiphenyl sulfone - curing 20 agent (Ciba-Giegy Eporal) Material phr
  • the coated panels were evaluated in autoclave tests in which the panels were immersed to 2/3 of their length in a given test solution and the solution was then purged with hydrogen sulfide. After the autoclave was sealed, it was charged with 140 psi of CO 2 and the pressure was increased to 2,800 psi with air. The temperature was raised to 300°F. and these conditions were maintained for 24 hours.
  • the test solutions used were four drilling muds including weighted lign ⁇ sulfate, Baroid K Plus (TM N. L. Baroid), salt water polymer and fresh water polymer. In these tests, the coatings were found to be superior to the industry standards for coatings for oil field drill pipe applied from previously known epoxy powder, liquid phenolics and liquid epoxy/phenolics.
  • the coated panels were bent and impacted and were found to have sufficient strength and toughness to withstand the abuse given drill pipe.
  • the gel time of the coating powder was about 60 seconds when measured at 205°C and the inclined plate flow was about 85 mm when measured at 150°C.
  • Two additional coating powders were prepared based upon the above formulation except in the first case 50 phr of both epoxy resins 1 and 2 were used and in the second case 90 phr of resin 1, 10 phr of resin 2 and 200 phr filler 5 were used.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)

Abstract

Poudres de revetement epoxy pouvant etre appliquees sur des substrats au moyen d'un procede de revetement par fusion. Le revetement resultant protege les substrats de la corrosion lors de l'utilisation dans des environnements hostiles. Les poudres de revetement epoxy comprennent a) des resines epoxydes non modifiees possedant un ensemble de fonctions dont le nombre moyen est superieur a 3; b) un agent de polymerisation d'amine aromatique polyfonctionnel; c) au moins 50 parties en poids de resine par 100 parties en poids d'un agent de remplissage; et d) un catalyseur de trichlorure de bore. Les poudres epoxydes de revetement conviennent particulierement a la protection des engrenages utilises dans les puits de petrole a l'interieur des forages, tels que les conduites de forages, les ecrans de filtre, la tuyauterie de production ou de recuperation de gaz et analogues.
PCT/US1980/001090 1980-08-22 1980-08-22 Poudres de revetement epoxy WO1982000651A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
PCT/US1980/001090 WO1982000651A1 (fr) 1980-08-22 1980-08-22 Poudres de revetement epoxy
EP19810900465 EP0058149A4 (fr) 1980-08-22 1980-08-22 Poudres de revetement epoxy.
JP50076180A JPS57501380A (fr) 1980-08-22 1980-08-22
AU67807/81A AU6780781A (en) 1980-08-22 1980-08-22 Epoxy coating powders

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
WOUS80/01090800822 1980-08-22
PCT/US1980/001090 WO1982000651A1 (fr) 1980-08-22 1980-08-22 Poudres de revetement epoxy

Publications (1)

Publication Number Publication Date
WO1982000651A1 true WO1982000651A1 (fr) 1982-03-04

Family

ID=22154507

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1980/001090 WO1982000651A1 (fr) 1980-08-22 1980-08-22 Poudres de revetement epoxy

Country Status (4)

Country Link
EP (1) EP0058149A4 (fr)
JP (1) JPS57501380A (fr)
AU (1) AU6780781A (fr)
WO (1) WO1982000651A1 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4757117A (en) * 1984-08-24 1988-07-12 Ciba-Geigy Corporation Powder coating compositions
US4844959A (en) * 1984-02-14 1989-07-04 Raychem Limited Heat curable adhesive coating
WO1991013683A1 (fr) * 1990-03-07 1991-09-19 Institut Khimii Akademii Nauk Moldavskoi Ssr Catalyseur de durcissement des resines epoxydes par des amines aromatiques
US5859096A (en) * 1996-03-22 1999-01-12 Ciba Specialty Chemicals Corporation Room temperature storage-stable, heat-curable, low CTE, one component epoxy resin tooling material
CN102181218A (zh) * 2011-03-18 2011-09-14 西北矿冶研究院 一种新型聚合物防腐涂层材料
EP2984142A4 (fr) * 2013-04-10 2017-04-19 Valspar Sourcing, Inc. Revêtement résistant au sulfure d'hydrogène

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61191214U (fr) * 1986-02-12 1986-11-28
JP5175509B2 (ja) * 2007-09-07 2013-04-03 日鉄住金ドラム株式会社 粉体塗料組成物

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3006890A (en) * 1958-07-21 1961-10-31 Tennessee Corp New resin compositions and curing agent therefor
US3755253A (en) * 1971-09-24 1973-08-28 Shell Oil Co Catalization of diaminodiphenylsulfone cure of polyepoxides with an imidazole compound or a salt thereof
US3784647A (en) * 1970-08-11 1974-01-08 Ciba Geigy Ag Curing epoxide resin with boron trichloride-amine complex
US3842035A (en) * 1971-10-01 1974-10-15 Shell Oil Co Powder coating composition

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3006890A (en) * 1958-07-21 1961-10-31 Tennessee Corp New resin compositions and curing agent therefor
US3784647A (en) * 1970-08-11 1974-01-08 Ciba Geigy Ag Curing epoxide resin with boron trichloride-amine complex
US3755253A (en) * 1971-09-24 1973-08-28 Shell Oil Co Catalization of diaminodiphenylsulfone cure of polyepoxides with an imidazole compound or a salt thereof
US3842035A (en) * 1971-10-01 1974-10-15 Shell Oil Co Powder coating composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4844959A (en) * 1984-02-14 1989-07-04 Raychem Limited Heat curable adhesive coating
US4757117A (en) * 1984-08-24 1988-07-12 Ciba-Geigy Corporation Powder coating compositions
WO1991013683A1 (fr) * 1990-03-07 1991-09-19 Institut Khimii Akademii Nauk Moldavskoi Ssr Catalyseur de durcissement des resines epoxydes par des amines aromatiques
US5859096A (en) * 1996-03-22 1999-01-12 Ciba Specialty Chemicals Corporation Room temperature storage-stable, heat-curable, low CTE, one component epoxy resin tooling material
CN102181218A (zh) * 2011-03-18 2011-09-14 西北矿冶研究院 一种新型聚合物防腐涂层材料
EP2984142A4 (fr) * 2013-04-10 2017-04-19 Valspar Sourcing, Inc. Revêtement résistant au sulfure d'hydrogène

Also Published As

Publication number Publication date
JPS57501380A (fr) 1982-08-05
EP0058149A1 (fr) 1982-08-25
EP0058149A4 (fr) 1982-12-20
AU6780781A (en) 1982-03-17

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