Classifications

• • 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
  • F16L58/02—Protection of pipes or pipe fittings against corrosion or incrustation by means of internal or external coatings
  • F16L58/04—Coatings characterised by the materials used
  • F16L58/10—Coatings characterised by the materials used by rubber or plastics
  • F16L58/1054—Coatings characterised by the materials used by rubber or plastics the coating being placed outside the pipe
  • F16L58/109—Coatings characterised by the materials used by rubber or plastics the coating being placed outside the pipe the coating being an extruded layer
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
  • B05D7/20—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to wires
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
  • B05D7/14—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies
  • B05D7/148—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies using epoxy-polyolefin systems in mono- or multilayers
• • 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
  • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
  • C09D151/06—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
• • 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
  • F16L58/02—Protection of pipes or pipe fittings against corrosion or incrustation by means of internal or external coatings
  • F16L58/04—Coatings characterised by the materials used
  • F16L58/10—Coatings characterised by the materials used by rubber or plastics
  • F16L58/1054—Coatings characterised by the materials used by rubber or plastics the coating being placed outside the pipe
  • F16L58/1072—Coatings characterised by the materials used by rubber or plastics the coating being placed outside the pipe the coating being a sprayed layer

Definitions

• This invention relates to a process for coating pipe in the field, i.e., at or near the point where the pipe is to be installed. It can be utilized in the coating of pipes which, after being in service for a period of time, need to have the previous coating material removed and a new coating material applied and is especially suited for field coating the areas around welded pipe joints and any defects in a previously applied pipe coating.
• pipes made from steel, iron and the like are employed to construct underground or underwater pipelines for carrying a vast number of different fluids or slurries in many different types of environments. Very high expenses must be incurred in association with their installation, surveillance, maintenance, and cathodic protection, not to mention the inherent danger and expense associated with damaged or broken pipelines. A number of different methods are therefore employed to protect the steel pipe from mechanical and chemical damage before, during and after its installation.
• the primary protection for this steel pipe is initially provided by either a factory-applied ("mill”) coating that is applied to the individual sections of pipe or a ditch-applied (“over-the-ditch”) coating that is applied to an entire pipeline after welding the individual sections together and immediately before laying.
• a factory-applied (“mill”) coating that is applied to the individual sections of pipe
• a ditch-applied (“over-the-ditch”) coating that is applied to an entire pipeline after welding the individual sections together and immediately before laying.
• ditch-applied coatings molten coal tar or the like is applied over the pipe (usually with a protective fabric covering) or adhesive plastic tapes are spirally wound onto the pipe.
• these coatings provide very inferior performance and especially in the areas of adhesive strength and resistance to corrosion.
• thick outer protective layers are generally applied by extruding a sheet of molten thermoplastic onto the heated pipe or sinter coating the heated pipe with a gravity fed or fluidized thermoplastic resin powder or the like.
• a mill coating usually, but not always, comprises a primer layer of epoxy resin which is applied to the cleaned and heated steel pipe.
• the epoxy primer can be applied in a number of ways and generally adheres quite well to the clean metal.
• the epoxy resin coating is about 0.02 to 0.1 millimeters thick. This layer functions primarily as protection against cathodic disbonding as well as being a substrate to which a thicker protective thermoplastic resin coating can be adhered using an intermediate adhesive layer.
• the application of mill coatings of this type and the use of various materials for their preparation is well-known.
• thermoplastic resin to the exterior of a pipe to form a coating
• thermoplastic resin a particulate olefin polymer resin coating composition comprising an adhesive olefin polymer having succinic acid or anhydride groups along the adhesive olefin polymer molecule backbone, is applied to the heated pipe.
• the invention relates to an improved field coating and an improved coated pipe obtained according to the process of this invention.
• the present invention can apply to the field coating of existing pipelines which, because of damage to the original coating, need to be removed for replacement of the existing coating.
• This invention is most preferably applicable to field coating the gaps or holes in the mill coatings, which gaps or holes result from partial removal of the mill coating for girth welding purposes or due to damage during transportation, installation and/or service of the coated pipe.
• the resulting field coating has uniformly excellent adhesion to the pipe and superior physical properties while being more economical in application time and labor than the currently available field pipe coating systems.
• a further surprising benefit of the invention is that, when used to coat the gaps or holes in the existing pipe coating, there is simultaneous adhesion to the pipe and the overlapped portions of the commonly used pipe mill-coating materials.
• the present invention will apply to steel or iron pipe such as that which is commonly used to transport oil, gas, water, and the like over long distances underground or underwater.
• Such pipes are typically subject to corrosion and are therefore provided with protective exterior coatings and connected to a negative electrical potential to provide cathodic protection.
• the process of the present invention may be applied to, and provides coatings which are suitable for use on, pipes which will operate in the normal range of service temperatures and in particular to such pipes which are operated at relatively high service temperatures, such as 50°C up to 90"C, especially pipes with a service temperature over 60°C.
• the present invention has been developed to apply a high performance pipe coating in the field. This includes situations where the coating of an existing pipeline needs to be at least partially replaced.
• the present invention offers even more surprising results when used to provide coatings over areas bordered by existing pipe coating such as gaps or holes in the existing mill coating of a pipe or pipeline.
• the gaps or holes can range in size and shape from a "hole” of a few square centimeters to a "gap" which occurs when the mill coating is not present around the entire circumference of the pipe for distances up to many meters. Such holes typically result from unintentional defects in or damage to the mill coating during production, transportation, installation or service.
• the gaps typically result from the intentional removal or deletion of the mill coating over a length of the pipe where the ends of two separate pipe sections have to be welded together (i.e., "girth welds").
• One of the key aspects of the present invention is the use of the olefin polymer resin coating composition in particulate form to coat pipes in the field.
• resin compositions are generally known in the art and comprise an adhesive olefin polymer having succinic acid or anhydride groups along the adhesive olefin polymer molecule backbone.
• suitable adhesive polymer resins which may be used in the process according to the invention is taught, for example, in US patents 3,873,643; 4,087,587; 4,416,944; 4,230,830; 4,684,576; 4,010,223; and 4,026,967.
• the adhesive olefin polymer has copolymerized therein or, preferably, grafted thereto maleic acid or anhydride or other monomeric unit which results in the prescribed succinic acid or anhydride groups along the backbone of the adhesive olefin polymer molecule.
• the base polymer in which the acid or anhydride groups are copolymerized or to which they are grafted is selected based upon a number of considerations such as: (a) the heat resistance desired in the final coating material, (b) compatibility with any other olefin polymer resin(s) with which it may be blended to produce the coating material, and (c) compatibility with the existing mill coating, if any, in situations where the coating material is used to coat holes or gaps in an existing mill coating.
• High density polyethylene (HDPE) has been found to provide very suitable base resins for the preparation of maleic anhydride or acid grafted adhesive resins.
• low density polyethylene (LDPE) low density polyethylene (LDPE)
• linear ethylene copolymers linear ethylene copolymers
• PP polypropylene
• the adhesive olefin polymer it has been found to be necessary to. obtain, grafted or copolymerized, from about 0.0001 to about 10 weight percent of the acid or anhydride. It has been found preferable to obtain from about 0.01 to about 5 weight percent acid or anhydride groups based on the weight of the adhesive olefin polymer, more preferably from about 0.5 to about 3 weight percent.
• the adhesive olefin polymer having the succinic acid or anhydride groups along the polymer molecule backbone is then mixed with additional amounts of one or more other olefin polymers.
• the selection of the amount and type of additional olefin polymer(s) is again based upon the above considerations to achieve the desired combination of processability and physical properties which are desired to be obtained in the olefin polymer resin coating composition.
• the principal features of polypropylene (PP) , low density polyethylene (LDPE) , high density polyethylene (HDPE) , and linear ethylene copolymer are well-known to practitioners in this art and are described, for example, in U.S. Patent No. 4,327,009. In general, any of these resins or other olefin copolymers can be employed as the additional olefin polymer(s) for use in this invention.
• the linear ethylene copolymer may have a density in the range of from about 0.88 g/cc to about 0.935 g/cc, preferably from about 0.90 g/cc to about 0.925 g/cc.
• LLDPE linear low density polyethylene
• ULDPE ultra low density polyethylene
• LLDPE linear medium density polyethylene
• At least one olefinically unsaturated alkene of from C 3 -C._, 0 most preferably from C.-C- is copolymerized with ethylene to make the linear ethylene polymer.
• 1-octene is the especially preferred alkene.
• the amount of said alkene may constitute from about 0.5% to about 35% by weight of the copolymer, preferably from about 1% to about 20%, most preferably from
• the linear ethylene copolymer may have a melt flow value (MFV) in the range of from about 0.1 g/10 min to about 2000 g/10 min as measured in accordance with ASTM D-1238(E).
• MMV melt flow value
• the melt flow value is in the range of from about
• melt flow value is inversely related to the molecular weight of the polymer.
• the LDPE which can be employed in accordance with the
• melt flow value in the range of from about 0.5 g/10 min to about 120 g/10 min according to ASTM D-1238(E) and a density in the range of from about 0.90 g/cc to about 0.94 g/cc, preferably a MFV of from about 0.7 g/10 min to about 40 g/10 min and a
• the HDPE which is used in accordance with the present invention is characterized as having a melt flow value in the range of from about 0.1 g/10 min to about 500 g/10 min according to ASTM D-1238(E) and a density in the range of
• the olefin polymer resin coating composition needs to be in particulate form, also referred to as powder or microgranule form. It has been found that when the adhesive polymer and additional olefin polymer have been selected to achieve good combinations of heat resistance and toughness, in order to achieve sufficient wetting of the heated steel pipe to be coated, the olefin polymer resin coating composition should have an average particle size of less than 0.5 millimeters, preferably less than 0.4 millimeters and most preferably 0.2 to 0.3 millimeters. Particle sizes of this order can be obtained using standard polymer grinding equipment. Such coating compositions may be prepared by any suitable method.
• One method of preparing such compositions is by dry-blending pellets of the adhesive polymer and the additional olefin polymer and optional additives. Then this mixture is extruded into pellets which subsequently are ground to the appropriate particle size.
• the particulate olefin polymer resin coating composition is applied to a heated pipe surface.
• the necessary pipe preparation procedures are generally well-known to those knowledgeable in this area of technology. Typically, such cleaning procedures require grit blasting or some similar type of impact cleaning to remove all traces of prior coating materials, dirt, rust and the like which may be present. If needed chemical cleaning means can be applied to "degrease" and properly prepare the pipe surface.
• a chemical pretreatment can be performed, such as by treating the steel surface with a chrome-iron-silicon oxide barrier layer that improves the long term adhesion and corrosion resistance of the coating system.
• an epoxy primer can be preliminary applied to the pipe by spray coating or the like. Where an epoxy primer coating is used, the selection of such epoxy primer and the heating of the pipe will need to take into account the curing characteristics for the resin and the need to have the pipe surface at the proper temperature at the point in time when the particulate olefin polymer resin coating composition is applied. Though in one aspect of the invention it has been found that the epoxy primer coating of the pipe is not needed for providing excellent field coatings, in a preferred aspect, the particulate olefin polymer resin coating composition is applied over the primer layer. Examples of epoxy primers which may advantageously used in the present process are Eurokote 714.31 of Bitumes Speciaux and epoxy primer D-1003 of Corrocoat.
• the portion of the steel pipe which has been cleaned and is to be coated should be heated by any of the well-known steel pipe heating means. Where larger areas of pipe are required to be coated, an induction heating coil should preferably be used. In situations where smaller pipe areas such as a hole or defect in the mill coating need to be recoated, the pipe surface could be heated with a hot gas (preferably air) or other type of convection heating means.
• a hot gas preferably air
• the coating composition is applied to an area bordered by an existing mill coating, also that portion of the existing mill coating to be overlapped by the field coating is preferably heat-plastified.
• the pipe should be heated to a temperature of at least 100 ⁇ C and preferably at least 200°C.
• the maximum temperature to which the pipe should be heated is dependent on the expoxy primer (if any) and olefin polymer resin coating composition being used and the existing mill coating, if any, adjacent to the areas that are currently being coated.
• the pipe can be heated to temperatures up to about 260°C for the practice of the present invention.
• the minimum temperature it should be noted that insufficient heating (i.e., too low of a pipe temperature) will result in poor melting of the applied olefin polymer resin coating composition and poor wetting of the substrate surface.
• the application of the particulate olefin polymer resin coating composition can be accomplished in any of several ways.
• the olefin polymer resin coating material is preferably applied in the same fashion and before the epoxy primer is fully cured.
• a fluidizing device and application means such as normally used for applying an epoxy primer coating, can be used to first apply such epoxy primer coat and then to apply a subsequent coating of the particulate olefin polymer resin.
• the application means is mounted on the pipe and has a dispensing head that rotates around the circumference of the pipe and dispenses the fluidized particulate olefin polymer resin coating composition in circular or spiral pattern.
• Other olefin polymer resin application means are possible.
• the pipe heat will be used to cure the epoxy primer and melt the olefin polymer coating composition.
• additional heat is provided during at least part, preferably all of the particulate olefin polymer resin application by a supplemental source of flowing hot air at a temperature above the melting temperature of the resin.
• the hot air source is associated with the application means which is applying the particulate olefin polymer resin and applied simultaneously. It is also preferable if the air which is used for fluidized particulate transport is heated to an elevated temperature, preferably a temperature somewhat lower than the softening temperature of the particulate olefin polymer resin. This is advantageous as it reduces as much as possible air encapsulation in the coating.
• a coating of the olefin polymer resin coating material is applied to the pipe.
• the coating can generally be applied according to applicable coating specifications. Generally the material should be applied to achieve coating thicknesses of from 0.01 millimeters up to 7 millimeters. It is not necessary, according to the present invention, that further external layers are applied. Preferably the coating thickness is in the range 0.1 millimeter to 5 millimeters and most preferably it is in the range of 1 to 3 millimeters. The coating thickness will obviously be selected to correspond to the thickness of any mill coatings which are adjacent and the coating material applied in a way that a smooth overlap with any existing mill coating is obtained. It should also be noted that some portions of the pipe surface may be somewhat raised, such as where joints or seams are welded.
• the overall coating thickness or at least the localized coating thickness in such areas should be adjusted accordingly in order to achieve the necessary coating thickness in the direction directly perpendicular to the seam along the whole length of the seam.
• the applied coating material surprisingly, without further shaping or forming steps, provides a very smooth, shiny coating surface and overlap with the existing mill coating. A slight surplus of coating material is formed in the area around the welded seam.
• applicable coating specifications will prescribe the necessary coating thicknesses and the amount of overlap with any existing mill coating. Generally from 2 to 20 centimeters overlap with the existing coating is made with 2 to 10 centimeters usually being sufficient.
• the particulate olefin polymer resin coating material can also advantageously contain stabilizers and additives of the known types such as antioxidants, U.V. radiation absorbers, pigments, rust inhibitors, fillers and flame retardants. Carbon black is one of the preferred additives.
• Field pipe coatings applied as described above are found to provide surprisingly improved performance and can unexpectedly be obtained via a simplified application rocedure as compared to the field coatings that are currently known or suggested for use.
• the field coatings have surprising combinations of adhesive strength, resistance to cathodic disbonding, chemical and moisture resistance, physical strength, and high potential service temperature.
• the coating process surprisingly reduces the time and labor required for the field coating process and provides uniformly excellent coatings over extended lengths and/or for large numbers of individually coated areas.
• the adhesive olefin polymer resin prepared above and described in Table I are then combined with additional amounts of other olefin polymer resins to prepare the specific particulate olefin polymer resin coating compositions evaluated below.
• Table II below shows the amount and type of additional olefin polymer which is added and the physical properties of the resulting coating composition.
• the resultant particulate olefin polymer resin coating compositions had average particle sizes of about 0.25 to 0.30 millimeters.
• Irganox 1010 brand primary antioxidant 30stabilizer 8 percent Irgafos 168 brand secondary antioxidant stabilizer and the balance HDPE.
• Irganox and Irgafos are registered trademarks of Ciba-Geigy.
• Carbon steel pipe was initially prepared for coating by grit blasting until "near white metal" was obtained.
• the coating compositions are applied in a stream of hot air by an application device rotating back and forth around the circumference of the area to be coated, while supplying additional heat by means of a hot air steam, until a layer thickness of 3 mm is obtained.
• the results observed in testing the coated pipes are reported below.
• the comparative Experiment A (which is not an example of the present invention) one of the most commonly recommended shrinkable sleeve field coatings was tested. It was applied directly to the similarly cleaned steel pipe in accordance with the manufacturer's instructions.
• the sleeve material is believed to be a mono-directional oriented, semi-crosslinked polyethylene with a soft butylene-type adhesive layer.
• the adhesion test was performed according to DIN 30670 where the peeling strength in Newtons per 5 centimeter (N/5 cm) is determined.
• N/5 cm the peeling strength in Newtons per 5 centimeter
• For ambient temperature testing a strip 5 cm wide was cut down to the metal along the circumference of the pipe. Weights were attached to the strip to produce a 90° peel angle and the adhesion was determined by measuring the force (amount of weight) required to further peel the strip.
• an Instron tension testing apparatus (trademark of Instron Co., U.S.A.) was used at a peeling rate of 50 millimeters per minute with a peeling angle of 90°.
• a strip 2.5 cm wide was cut down to the metal surface and peeled partially away by hand. This was then mounted in the Instron and at the indicated temperatures, the tensile force measured while 2 to 3 inches were peeled. The average of five peeling tests is given as the adhesive strength.
• the labor requirement for the field coating process is simultaneously reduced. For example, 30 workers are typically able to apply 120 girth weld joint coatings in 10 hours for a 42 inch diameter pipeline. The same number of joints can be coated in the same time period with a one or two layer coating according to the presently claimed process by 6 workers, an 80 percent labor savings.

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• Engineering & Computer Science (AREA)
• General Engineering & Computer Science (AREA)
• Life Sciences & Earth Sciences (AREA)
• Wood Science & Technology (AREA)
• Chemical & Material Sciences (AREA)
• Mechanical Engineering (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Application Of Or Painting With Fluid Materials (AREA)
• Laminated Bodies (AREA)

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• 1988
  • 1988-10-03 GB GB888823194A patent/GB8823194D0/en active Pending
• 1989
  • 1989-09-21 AU AU42155/89A patent/AU4215589A/en not_active Abandoned
  • 1989-09-21 KR KR1019900701166A patent/KR900701414A/ko not_active Application Discontinuation
  • 1989-09-21 EP EP89910082A patent/EP0436573A1/de active Pending
  • 1989-09-21 BR BR898907688A patent/BR8907688A/pt not_active Application Discontinuation
  • 1989-09-21 JP JP1509432A patent/JPH04500924A/ja active Pending
  • 1989-09-21 EP EP89202376A patent/EP0366168A1/de not_active Withdrawn
  • 1989-09-21 WO PCT/EP1989/001094 patent/WO1990003850A1/en not_active Application Discontinuation

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