WO2009045432A1 - Boîtiers de pompe pour véhicules - Google Patents

Boîtiers de pompe pour véhicules Download PDF

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Publication number
WO2009045432A1
WO2009045432A1 PCT/US2008/011359 US2008011359W WO2009045432A1 WO 2009045432 A1 WO2009045432 A1 WO 2009045432A1 US 2008011359 W US2008011359 W US 2008011359W WO 2009045432 A1 WO2009045432 A1 WO 2009045432A1
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WO
WIPO (PCT)
Prior art keywords
metal
pump housing
coated
vehicular
composition
Prior art date
Application number
PCT/US2008/011359
Other languages
English (en)
Inventor
Andri E. Elia
Michael R. Day
Robert Espey
Glenn Steed
Andrew Wang
Jonathan Mccrea
Original Assignee
E.I. Du Pont De Nemours And Company
Morph Technologies, Inc.
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 E.I. Du Pont De Nemours And Company, Morph Technologies, Inc. filed Critical E.I. Du Pont De Nemours And Company
Publication of WO2009045432A1 publication Critical patent/WO2009045432A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/1601—Process or apparatus
    • C23C18/1633—Process of electroless plating
    • C23C18/1635—Composition of the substrate
    • C23C18/1639—Substrates other than metallic, e.g. inorganic or organic or non-conductive
    • C23C18/1641—Organic substrates, e.g. resin, plastic
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00—Electroplating characterised by the article coated
    • C25D7/04—Tubes; Rings; Hollow bodies
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02M—SUPPLYING COMBUSTION ENGINES IN GENERAL WITH COMBUSTIBLE MIXTURES OR CONSTITUENTS THEREOF
    • F02M37/00—Apparatus or systems for feeding liquid fuel from storage containers to carburettors or fuel-injection apparatus; Arrangements for purifying liquid fuel specially adapted for, or arranged on, internal-combustion engines
    • F02M37/0011—Constructional details; Manufacturing or assembly of elements of fuel systems; Materials therefor
    • F02M37/0017—Constructional details; Manufacturing or assembly of elements of fuel systems; Materials therefor related to fuel pipes or their connections, e.g. joints or sealings

Definitions

  • Vehicular pump housings comprising organic polymers which are metal plated.
  • Vehicles such as automobiles, boats, recreational vehicles, trucks, all terrain vehicles, farm equipment such as tractors, and construction equipment such as bulldozers and graders, are of course important items in modern society, and they are made of a myriad of parts. Many of these parts must have certain minimum physical properties such as stiffness and/or strength.
  • Traditional- ally these types of parts have been made from metals such as steel, but in recent decades organic polymers have been increasingly used for such parts for a variety of reasons.
  • Such polymeric parts are often lighter, and/or easier (cheaper) to fabricate especially in complicated shapes, and/or have better corrosion resistance.
  • Such polymeric parts have not replaced metals in some application because they are not stiff and/or strong enough, or have other property deficiencies compared to metal .
  • metal plated organic polymeric pump housings have the properties desired.
  • Metal plated polymeric parts have been used in vehicles, especially for ornamental purposes. Chrome or nickel plating of visible parts, including polymeric parts, has long been done. In this use the polymer is coated with a thin layer of metal to produce a pleasing visual effect. The amount of metal used is generally the minimum required to produce the desired visual effect and be durable.
  • US Patent 4,406,558 describes a gudgeon pin for an internal combustion engine which is metal plated polymer.
  • US Patent 6,595,341 describes an aluminum plated plastic part for a clutch. Neither of these patents mentions pump housings.
  • This invention concerns a vehicular pump housing, comprising an organic polymer composition which is coated at least in part by a metal.
  • This invention concerns a vehicle comprising a pump housing, which comprises an organic polymer composition which is coated at least in part by a metal.
  • organic polymer composition a composition which comprises one or more organic polymers.
  • one or more of the organic polymers is the continuous phase.
  • an “organic polymer” is meant a polymeric material which has carbon-carbon bonds in the polymeric chains and/or has groups in the polymeric chains which have carbon bound to hydrogen and/or halogen.
  • the organic polymer is synthetic, i.e., made by man.
  • the organic polymer may be for example a thermoplastic polymer (TPP) , or a thermoset polymer (TSP) .
  • TPP thermoplastic polymer
  • TPP thermoset polymer
  • TPP thermoset polymer
  • TPP thermoset polymer
  • TPP thermoset polymer
  • TSP thermoplastic polymeric material which is crosslinked, i.e., is insoluble in solvents and does not melt. It also refers to this type of polymeric material before it is crosslinked, but in the final pump housing, it is crosslinked.
  • the crosslinked TSP composition has a Heat Deflection Temperature of about 50 0 C, more preferably about 100 0 C, very preferably about 150 0 C or more at a load of 0.455 MPa (66 psi) when measured us- ing ASTM Method D648-07.
  • a polymeric “composition” is meant that the organic polymer is present together with any other additives usually used with such a type of polymer (see below) .
  • coated with a metal is meant part or all of one or more surfaces of the pump housing is coated with a metal.
  • the metal does not necessarily directly contact a surface of the organic polymer composition.
  • an adhesive may be applied to the surface of the organic polymer and the metal coated onto that. Any method of coating the metal may be used (see below) .
  • metal any pure metal or alloy or combination of metals. More than one layer of metal may be present, and the layers may have the same or different compositions .
  • Vehicular pumps serve many functions, pumping various fluids, often through or around the engine, to accom- push various tasks.
  • the pump housings are part of these pumping systems, which provide containment and transport of fluids for the purpose of heat transfer, pressuriza- tion, and energy transmission.
  • the housing materials must be resistant to the various fluids which may be present, such as antifreeze, oil, transmission fluid, power steering fluid, hydraulic oil, etc. These fluids may in some cases contain particulates which may cause erosion of polymeric parts.
  • pump housings may also contain op- erating portions of the pump such as bearings and rotating shafts, and therefore the housings may have to carry loads resulting from a drive pulley or other drive system.
  • the pump housing is advantageously metal coated to provide increased strength and stiffness to withstand such loads, and also possible loading from pressure generated within the housing.
  • the metal coating may also provide erosion protection against fluid and particulate flow. If the metal coating is copper or contains copper, anti-biofouling properties may be present, especially if the liquid is sea water. Copper is sometimes used in such applications, but here the metal coating is much lighter than used of copper (containing) objects, and may also serve more than one purpose.
  • the metal may be coated on one or both sides of the housing. If completely coated on the side which contacts the fluid, the coating may protect the OP composition from any deleterious effects of fluid, and/or lower permeability of the fluid through the housing.
  • the metal coating may also be in patterns to efficiently improve the particular physical property which is deficient, and the coating thickness may vary over different parts of the metal coating. For example bands of metal coating may be placed around the housing to prevent deformation when the housing is pressurized.
  • the OP composition be chosen so that its rated service temperature is at least as high as the highest operating temperature expected.
  • Useful pumps types for such housing are oil pumps, coolant (antifreeze) pumps, power steering pumps, transmission fluid pumps, hydraulic pumps, etc.
  • Organic polymeric compositions often do not have the requisite stiffness unless they are very thick, and thereby also heavy and expensive. However by using a metal coating the stiffness may be greatly increased with little additional weight. If the metal is coated on the interior of the pump housing it may also help to protect the organic polymer composition from being deleteriously affected by the fluids, and also will reduce fluid permeability through the organic polymeric composition. Metal coating both the interior and exterior of the pump hous- ing further improves the stiffness of the pump housing.
  • the portion of the pump housing which contacts the sealing gasket (s) be relatively stiff so as to maintain a good seal.
  • this thicker metal coating and/or coating on both sides may be employed in the areas near to or that will come in contact with the gasket (s), and/or the thickness of the OP molding may be somewhat thicker in this region.
  • Useful TSPs include epoxy, phenolic, and melamine resins. Parts may be formed from the thermoset resin by conventional methods such as reaction injection molding or compression molding.
  • Useful TPPs include poly (oxymethylene) and its copolymers; polyesters such as poly (ethylene terephtha- late) , poly (1, 4-butylene terephthalate) , poly (1,4- cyclohexyldimethylene terephthalate), and poly (1,3- poropyleneterephthalate) ; polyamides such as nylon-6, 6, nylon-6, nylon-12, nylon-11, and aromatic-aliphatic co- polyamides; polyolefins such as polyethylene (i.e.
  • LCP Thermotropic liquid crystalline polymer
  • Useful LCPs include polyesters, poly (ester-amides) , and poly (ester-imides) .
  • One pre- ferred form of LCP is "all aromatic", that is all of the groups in the polymer main chain are aromatic (except for the linking groups such as ester groups) , but side groups which are not aromatic may be present.
  • the TPPs may be formed into parts by the usual methods, such as injection molding, thermoforming, compression molding, extrusion, and the like.
  • the OP whether a TSP, TPP or other polymer composition may contain other ingredients normally found in such compositions such as fillers, reinforcing agents such as glass and carbon fibers, pigments, dyes, stabilizers, toughening agents, nucleating agents, antioxidants, flame retardants, process aids, and adhesion promoters.
  • Another class of materials may be substances that improve the adhesion to the resin of the metal to be coated onto the resin. Some of these may also fit into one or more of the classes named above.
  • the OP should preferably not soften significantly at the expected maximum operating temperature of the pump housing. Since it is often present at least in part for enhanced structural purposes, it will better maintain its overall physical properties if no softening occurs. Thus preferably the OP has a melting point and/or glass transition temperature and/or a Heat Deflection Temperature at or above the highest use tem- perature of the OP.
  • the OP composition (without metal coating) should also preferably have a relatively high flexural modulus, preferably at least about 1 GPa, more preferably at least about 2 GPa, and very preferably at least about 10 GPa. Since these are structural parts, and are usually preferred to be stiff, a higher flexural modulus improves the overall stiffness of the metal coated pump housing. Flexural modulus is measured by ASTM Method D790-03, Pro- cedure A, preferably on molded parts, 3.2 mm thick (1/8 inch), and 12.7 mm (0.5 inch) wide, under a standard laboratory atmosphere.
  • the OP composition may be coated with metal by any known methods for accomplishing that, such as vacuum deposition (including various methods of heating the metal to be deposited) , electroless plating, electroplating, chemical vapor deposition, metal sputtering, and electron beam deposition. Preferred methods are electroless plating and electroplating, and a combination of the two.
  • vacuum deposition including various methods of heating the metal to be deposited
  • electroless plating electroplating
  • chemical vapor deposition metal sputtering
  • electron beam deposition electron beam deposition
  • electroless plating and electroplating and a combination of the two.
  • the metal may adhere well to the OP composition without any special treatment, usually some method for improving adhesion will be used. This may range from simple abrasion of the OP composition surface to roughen it, addition of adhesion promotion agents, chemical etching, functionalization of the surface by exposure to plasma and/or radiation (for instance laser or UV radiation) or any combination of these.
  • More than one metal or metal alloy may be plated onto the organic resin, for example one metal or alloy may be plated directly onto the organic resin surface because of its good adhesion, and another metal or alloy may be plated on top of that because it has a higher strength and/or stiffness.
  • Useful metals and alloys to form the metal coating include copper, nickel, cobalt, cobalt-nickel, iron- nickel, and chromium, and combinations of these in dif- ferent layers.
  • Preferred metals and alloys are copper, nickel, and iron-nickel, cobalt, cobalt-nickel, and nickel is more preferred.
  • the surface of the organic resin of the structural part may be fully or partly coated with metal. In different areas of the part the thickness and/or the number of metal layers, and/or the composition of the metal layers may vary.
  • grain size of the metal deposited may be controlled by the electroplating conditions, see for instance U.S. Patents 5,352,266 and 5,433,797 and U.S. Patent Publications 20060125282 and 2005020525, all of which are hereby included by reference.
  • at least one of the metal layers deposited has an average grain size in the range of about 5 nm to about 200 nm, more preferably about 10 nm to about 100 nm.
  • the metal has an average grain size of at least 500 nm, preferably at least about 1000 nm, and/or has an average maximum grain size of about 5000 nm. For all these grain size preferences, it is preferred that that thickest metal layer, if there is more than one layer, be the specified grain size.
  • the thickness of the metal layer (s) deposited on the organic resin is not critical, being determined mostly by the desire to minimize weight while providing certain minimum physical properties such as modulus, strength and/or stiffness. These overall properties will depend to a certain extent not only on the thickness and type of metal or alloy used, but also on the design of the structural part and the properties of the organic resin composition.
  • the flexural modulus of the metal coated pump housing is at least about twice, more preferably at least about thrice the flexural modulus of the uncoated OP composition. This is measured in the following way.
  • the procedure used is ISO Method 178, using molded test bars with dimensions 4.0 mm thick and 10.0 mm wide. The testing speed is 2.0 mm/min.
  • the composition from which the pump housings are made is molded into the test bars, and then some of the bars are completely coated (optionally except for the ends which do not affect the test results) with the same metal using the same procedure used to coat the pump housings.
  • the thickness of the metal coating on the bars is the same as on the pump housings.
  • the test bars will be coated to the greatest metal thickness on the pump housings.
  • the flexural moduli of the coated and uncoated bars are then measured, and these values are used to determine the ratio of flexural moduli (flexural modulus of coated/flexural modulus of uncoated) .
  • the thicker the metal coating the greater the flexural modulus ratio between the uncoated and coated OP part.
  • the plated OP be tough, for example be able to withstand impacts. It has surprisingly been found that some of the metal plated OP compositions of the present invention are surprisingly tough. It has previously been reported (M. Corley, et al., Engineering Polyolefins for Metallized Decorative Applications, in Proceedings of TPOs in Automotive 2005, held June 21-23, 2005, Geneva Switzerland, Executive Conference Manage- ment, Madison, MI 48170 USA, p. 1-6) that unfilled or lightly filled polyolefin plaques have a higher impact energy to break than their Cr plated analog. Indeed the impact strength of the plated plaques range from 50 to 86 percent of the impact strength of the unplated plaques.
  • the impact maximum energies of the plated plaques are much higher than those of the unplated plaques. It is believed this is due to the higher filler levels of the OP compositions used, and in the present parts it is preferred that the OP composition have at least about 25 weight percent, more preferably about 35 weight percent, especially preferably at least about 45 weight percent of filler/reinforcing agent present. A preferred maximum amount of filler/reinforcing agent present is about 65 weight percent. These percentages are based on the total weight of all ingredients present.
  • Typical reinforcing agents/fillers include carbon fiber, glass fiber, aramid fiber, particulate minerals such as clays (various types), mica, silica, calcium carbonate (including limestone) , zinc oxide, wollastonite, carbon black, titanium dioxide, alumina, talc, kaolin, microspheres, alumina trihydrate, calcium sulfate, and other minerals.
  • particulate minerals such as clays (various types), mica, silica, calcium carbonate (including limestone) , zinc oxide, wollastonite, carbon black, titanium dioxide, alumina, talc, kaolin, microspheres, alumina trihydrate, calcium sulfate, and other minerals.
  • the ISO179 impact energy (see below for procedure) of the metal plated pump housing be 1.2 times or more the impact energy of the unplated OP composition, more preferably 1.5 times or more.
  • the test is run by making bars of the OP, and plating them by the same method used to make the pump housing, with the same thickness of metal applied. If the pump housing is metal plated on both sides (of the principal surfaces) , the test bars are plated on both sides, while if the pump housing is plated on one side (of the principal surfaces) the test bars are plated on one side. The impact energy of the plated bars are compared to the impact energy of bars of the unplated OP composition.
  • the metal coating will about 0.010 mm to about 1.3 mm thick, more preferably about 0.025 mm to about 1.1 mm thick, very preferably about 0.050 to about 1.0 mm thick, and especially preferably about 0.10 to about 0.7 mm thick. It is to be understood that any minimum thickness mentioned above may be combined with any maximum thickness mentioned above to form a different preferred thickness range.
  • the thickness required to attain a certain flexural modulus is also dependent on the metal chosen for the coating. Generally speaking the higher the tensile modulus of the metal, the less will be needed to achieve a given stiffness (flexural modulus) .
  • the flexural modulus of the uncoated OP composition is greater than about 200 MPa, more preferably greater than about 500 MPa, and very preferably greater than about 2.0 GPa.
  • Example 1 Zytel® 70G25, a nylon 6,6 product containing 25 weight percent chopped glass fiber available from E.I. DuPont de Nemours & Co., Inc. Wilmington, DE 19898 USA, was injection molded into bars whose central section was 10.0 mm wide and 4.0 mm thick. Before molding the poly- mer composition was dried at 80 0 C in a dehumidified dryer. Molding conditions were melt temperature 280-300 0 C and a mold temperature of 80 0 C. Some of the bars were etched using Addipost® PM847 etch, reported to be a blend of ethylene glycol and hydrochloric acid, and obtained from Rohm & Haas Chemicals Europe.
  • the flexural modulus was then determined, as described above, on the uncoated and metal coated bars.
  • the uncoated bars had a flexural modulus of 7.7 GPa, and the metal coated bars had a flexural modulus of 29.9 GPa.
  • Filler 1 - A calcined, aminosilane coated, kaolin, Polarite® 102A, available from Imerys Co., Paris, France .
  • Filler 3 - Nyad® G, a wollastonite from Nyco Minerals, Willsboro, NY 12996, USA.
  • Filler 4 - M10-52 talc manufactured by Barretts
  • GF 1 - Chopped (nominal length 3.2 mm) glass fi- ber PPG® 3660, available from PPG Industries, Pittsburgh, PA 15272, USA.
  • GF 2 - Chopped (nominal length 3.2 mm) glass fiber PPG® 3540, available from PPG Industries, Pittsburgh, PA 15272, USA.
  • HS2 - A thermal stabilizer contain 7 parts KI, 11 parts aluminum distearate, and 0.5 parts CuI (by weight) .
  • Polymer A Polyamide-6, 6, Zytel® 101 available from E.I. DuPont de Nemours & Co., Inc. Wilmington, DE 19810, USA.
  • Polymer C An ethylene/propylene copolymer grafted with 3 weight percent maleic anhydride.
  • Polymer D A copolyamide which is a copolymer of terephthalic acid, 1, 6-diaminohexane, and 2-methyl-l, 5- diaminopentane, in which each of the diamines is present in equimolar amounts.
  • Polymer E - Engage®8180 an ethylene/1-octene copolymer available by Dow Chemical Co., Midland, MI, USA.
  • Wax 2 - Licowax® OP available from Clariant Corp. Charlotte, NC 28205, USA.
  • the organic polymer compositions used in these examples are listed in Table 1.
  • the compositions were made by melt blending of the ingredients in a 30 mm Werner & Pfleiderer 30 mm twin screw extruder.
  • test pieces which were 7.62x12.70x0.30 cm plaques or ISO 527 test bars, 4 mm thick, gauge width 10 mm, were made by injection molding under the conditions given in Table 2. Before molding the polymer compositions were dried for 6-8 hr in dehumidified air under the temperatures indicated, and had a moisture content of ⁇ 0.1% before molding.
  • test specimens were then etched in sulfochro- mic acid or Rohm & Haas Chrome free etching solution, and rendered conductive on all surface by electroless deposition of a very thin layer of Ni.
  • Subsequent galvanic deposition of 8 ⁇ m of Cu was followed by deposition of a 100 ⁇ m thick layer of fine grain N-Fe (55-45 weight) using a pulsed electric current, as described in US Patent 5,352,266 for making fine grain size metal coatings.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrochemistry (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Compositions polymères organiques à plaquage métallique convenant pour la fabrication de boîtiers de pompe pour véhicules. De tels boîtiers sont plus légers et/ou plus résistants à la corrosion que des boîtiers de pompe classique en métal.
PCT/US2008/011359 2007-10-04 2008-10-01 Boîtiers de pompe pour véhicules WO2009045432A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US99758907P 2007-10-04 2007-10-04
US60/997,589 2007-10-04

Publications (1)

Publication Number Publication Date
WO2009045432A1 true WO2009045432A1 (fr) 2009-04-09

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PCT/US2008/011359 WO2009045432A1 (fr) 2007-10-04 2008-10-01 Boîtiers de pompe pour véhicules

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2438204A4 (fr) * 2009-06-02 2017-01-25 Integran Technologies Inc. Article polymere metallise a durabilite elevee et integrite par le vide et/ou la pression

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5168626A (en) * 1991-07-12 1992-12-08 General Motors Corporation Method for providing pump drip collector
US20070203271A1 (en) * 2006-01-27 2007-08-30 Alms Gregory R Coating process for thermoplastics

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5168626A (en) * 1991-07-12 1992-12-08 General Motors Corporation Method for providing pump drip collector
US20070203271A1 (en) * 2006-01-27 2007-08-30 Alms Gregory R Coating process for thermoplastics

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2438204A4 (fr) * 2009-06-02 2017-01-25 Integran Technologies Inc. Article polymere metallise a durabilite elevee et integrite par le vide et/ou la pression

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