WO2001087584A1 - Sleeve for protecting polypropylene-covered pipe comprising bonding agent - Google Patents
Sleeve for protecting polypropylene-covered pipe comprising bonding agent Download PDFInfo
- Publication number
- WO2001087584A1 WO2001087584A1 PCT/CA2001/000710 CA0100710W WO0187584A1 WO 2001087584 A1 WO2001087584 A1 WO 2001087584A1 CA 0100710 W CA0100710 W CA 0100710W WO 0187584 A1 WO0187584 A1 WO 0187584A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- covering
- polypropylene
- article
- psi
- sleeve
- Prior art date
Links
- 239000007767 bonding agent Substances 0.000 title claims abstract description 13
- -1 polypropylene Polymers 0.000 claims abstract description 60
- 239000004743 Polypropylene Substances 0.000 claims abstract description 57
- 229920001155 polypropylene Polymers 0.000 claims abstract description 57
- 229920000098 polyolefin Polymers 0.000 claims abstract description 11
- 238000006073 displacement reaction Methods 0.000 claims abstract description 4
- 239000004634 thermosetting polymer Substances 0.000 claims abstract description 4
- 238000000576 coating method Methods 0.000 claims description 45
- 239000011248 coating agent Substances 0.000 claims description 35
- 239000000463 material Substances 0.000 claims description 28
- 229920001187 thermosetting polymer Polymers 0.000 claims description 23
- 239000013521 mastic Substances 0.000 claims description 18
- 239000004831 Hot glue Substances 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- 239000011342 resin composition Substances 0.000 claims description 4
- 229920002396 Polyurea Polymers 0.000 claims description 2
- 229920002050 silicone resin Polymers 0.000 claims description 2
- 229920001225 polyester resin Polymers 0.000 claims 1
- 239000004645 polyester resin Substances 0.000 claims 1
- 229920005749 polyurethane resin Polymers 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 27
- 240000005428 Pistacia lentiscus Species 0.000 description 17
- 239000000853 adhesive Substances 0.000 description 14
- 230000001070 adhesive effect Effects 0.000 description 14
- 230000035882 stress Effects 0.000 description 8
- 239000002689 soil Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000009434 installation Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920005615 natural polymer Polymers 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical compound CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 description 1
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 230000006355 external stress Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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
- F16L58/18—Protection of pipes or pipe fittings against corrosion or incrustation specially adapted for pipe fittings
- F16L58/181—Protection of pipes or pipe fittings against corrosion or incrustation specially adapted for pipe fittings for non-disconnectible pipe joints
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B1/00—Layered products having a non-planar shape
- B32B1/08—Tubular products
-
- 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
- F16L13/00—Non-disconnectible pipe-joints, e.g. soldered, adhesive or caulked joints
- F16L13/02—Welded joints
- F16L13/0254—Welded joints the pipes having an internal or external coating
- F16L13/0272—Welded joints the pipes having an internal or external coating having an external coating
-
- 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
- F16L58/1063—Coatings characterised by the materials used by rubber or plastics the coating being placed outside the pipe the coating being a sheet wrapped around the pipe
Definitions
- the present invention relates to improved arrangements for providing a secondary covering on a polypropylene covered tubular article.
- the invention is directed toward the application of a functional secondary coating over a polypropylene-coated substrate in circumstances where it is not possible to use a high shear strength adhesive that will bond to both polypropylene and the backing component of the secondary coating.
- a high shear strength adhesive that will bond to both polypropylene and the backing component of the secondary coating.
- the backing is a heat-shrinkable crosslinked polymer derived primarily from ethylene, which would be compatible with adhesives that bond to polyethylene, but not to polypropylene.
- the invention could also be used beneficially in circumstances wherein the high shear strength adhesive is compatible with both the backing of the secondary coating and with polypropylene, but the temperature required to achieve an adequate bond to the polypropylene-coated substrate would be so high as to damage the coating.
- polypropylene coatings are generally used for high temperature pipelines, and therefore require the use of joint-completion systems that will also withstand high temperatures .
- heat-shrinkable backing sheets suitable for anticorrosion applications are based on ethylene polymers or copolymers.
- Polypropylene is not crosslinkable by preferred conventional methods, and there are currently therefore no commercial heat-shrinkable polypropylene backing sheets available.
- those adhesives that bond well to both polypropylene and ethylene-based polymers are relatively low strength mastics or hybrid mastic/hot melt adhesives . These have excellent sealing properties, but inadequate shear resistance at elevated temperatures.
- polypropylene coatings are typically three- layer (epoxy/copolymer adhesive/polypropylene) constructions . Preheat temperatures in excess of about 200°C can severely damage the coating.
- an elongate tubular article extending along a longitudinal axis and having a covering comprising polypropylene thereon with an outer surface, a secondary covering comprising polyolefin with an outer surface at least partially superimposed over the polypropylene covering, said secondary covering having an edge with a face extending transverse said axis, a bonding agent capable of bonding to said polypropylene and secondary coverings interposed at least between said edge and said polypropylene covering, and a cured deposit of thermoset resin applied at least over said edge of the secondary covering and bonding to said outer surfaces of said polypropylene and secondary coverings and providing the secondary covering with increased stability against displacement radially outwardly with respect to said polypropylene covering.
- the bonding agent which may be, for example, a mastic or hybrid mastic/hot melt adhesive, provides excellent sealing between the polypropylene and secondary covering while the cured deposit creates a strong bond between the secondary covering and the polypropylene coating. Further, the cured deposit stabilizes the edge of the secondary covering against being lifted by axial stresses, such as soil stresses or other axial forces, such as travelling over a stinger in the course of laying pipe from a lay barge in the course of underwater pipeline installation.
- axial stresses such as soil stresses or other axial forces
- Fig. 1 is a partially sectional view through a pipe joint in the course of application of a heat shrinkable sleeve thereto;
- Fig. 2 is a partially sectional view showing the completed pipe joint
- Fig. 3 is a partially section view showing a modified completed pipe joint.
- Fig. 1 shows a partial longitudinal cross section through two pipeline sections 11 and 12 aligned along a longitudinal axis 13 and secured together at a weld joint 14.
- the sections 11 and 12 each carry a polypropylene coating 16 and 17 which covers the pipe 11 or 12 along its entire length except for a short section exposed at each end of the pipe to permit the above mentioned welding operation.
- Fig. 1 shows a sleeve-form protective covering 18 to be applied over the pipe weld area.
- the covering 18 is of sufficient length that it overlaps at each end on the coating 16 and 17.
- the covering 18 comprises a heat shrinkable backing 19 provided on its underside with a functional coating 21 which is typically a sealant or adhesive.
- the backing 19 is heated so that it shrinks down tightly onto the coating 16 and 17.
- the fluidity and tackiness of the functional coating 21 increases as the backing 19 becomes hotter, so that the functional coating tends to wet and coat the exposed surfaces of the metal pipes 11 and 12 and form a tight seal on the adjacent ends of the coatings 16 and 17.
- sleeve 18 may be of the cylindrical or wrap-around type. Many forms of heat shrinkable sleeve and known to those of ordinary skill in the art, and it is contemplated that the present invention may be used with all such sleeve.
- the backing sheet 19 may comprise a cross-linked polyolefin sheet.
- polyolefin materials comprise blends of polyethylene with suitable copolymers such as, for example, poly (ethylene-vinyl acetate), poly (ethylene-ethyl acrylate) , poly(ethylene-maleic anhydride) and poly (ethylene-vinyl acetate-maleic anhydride) .
- the backing sheet 19 may comprise other materials and may comprise polypropylene. Blends which aid in attaining adhesion to the curable thermosetting composition are preferred.
- the functional coating 21 may comprise a mastic, hot melt adhesive or a hybrid thereof. These materials are well known to those of ordinary skill in the art, and need not be described in detail herein.
- the functional coating 21 is a very high shear strength hot-melt adhesive, desirably having a shear strength as measured by ASTM D1002 at the operating temperature of the article of at least about 20 psi, more desirably at least about 100 psi.
- suitable high shear strength adhesives are the adhesive used on the heat shrinkable sleeve GTS-HT ® , sold by Canusa-CPS division of Shaw Industries Ltd., and the adhesive used on the heat- shrinkable sleeve WPC-120 ® , produced by Raychem Corporation.
- a bonding agent capable of bonding to the backing 19 as well as to the polypropylene coatings 16 and 17 is interposed between the end edges of the sleeve 19 and the coating 16 and 17.
- the bonding agent indicated at 22 and 23 in the accompanying drawings is preferably a mastic.
- the mastic materials comprise substantially amorphous natural or synthetic polymers, or mixtures thereof, in contrast to the hot melt adhesive materials, which typically exhibit marked crystallinity.
- Examples of typical mastic compositions include blends of substantially amorphous rubber materials, such as butyl rubber, natural rubber, latex SBR rubber, with tackifying resins, such as synthetic hydrocarbon tackifying resins, rosin ester tackifying resins, and inert fillers such as calcium carbonate, talc and carbon black, usually together with antioxidants, and with or without admixtures of other amorphous natural or synthetic polymers, such as asphalt, polybutene and amorphous polyolefins, such as amorphous polypropylene, styrene-isoprene copoly ers, and liquid butyl polymers.
- tackifying resins such as synthetic hydrocarbon tackifying resins, rosin ester tackifying resins, and inert fillers such as calcium carbonate, talc and carbon black, usually together with antioxidants, and with or without admixtures of other amorphous natural or synthetic polymers, such as asphalt, polybuten
- Such mastic compositions provide excellent properties of excluding ingress of water to the sealed area, and, as compared with hot melt adhesive and other functional coating materials, exhibit broader softening temperatures and substantial surface tack which contribute to considerably greater ease of application over a wide range of ambient temperature including very low ambient temperatures .
- the bonding agent may be a conventional mastic-hot melt adhesive hybrid.
- the mastic and hybrid materials bond well to polypropylene and other polyolefins, as well as to hot melt adhesives, and therefore form a strong water excluding bond between the polypropylene coatings 16 and 17 and the adjacent ends of the sleeve 18.
- the mastic portions 22 and 23 may be provided by, for example, applying a mastic tape circumferentially around the polypropylene coating 16 and 17 at the locations as indicated in Fig. 1, in register with the inner marginal portions of the sleeve 18.
- the mastic may be applied as a narrow band, leaving contact between adhesive 21 and coating 16 and 17, or preferably may be applied in sufficient width to cover all of the coating 16 and 17 which would otherwise come into contact with the adhesive 21, as shown in Figure 3. This ensures there is no unbonded, unsealed boundary between the polypropylene coating and the sleeve 18.
- the sleeve 18 In installation of the sleeve 18, in its preferred use, the sleeve 18 is heated in known manner to cause it to shrink down tightly onto the polypropylene coated pipe sections as seen in Figs. 2 and 3.
- the adhesive 21 bonds very well to the bare surface of the steel pipe 11 and 12, but cannot bond to the polypropylene pipe coatings 16 and 17.
- the layer of mastic or other bonding agent 22 and 23 which, as seen in Figs. 2 and 3 on shrinking down of the sleeve 18 may tend to be extruded somewhat outwardly from the ends of the sleeve 18, creates a weak but water- resistant bond between the sleeve 18 and the coating 16 and 17.
- the adhesive 21 is in contact with the coatings 16 and 17, as in Fig.
- the sleeve 18 cannot move as a whole because of the high shear bond between the steel pipe 11 and 12 and the sleeve 18, but the ends are susceptible to lifting.
- the ends of the sleeve 18 and the adjacent pipe coating 16 and 17 are over-coated with a layer of a hard, tough curable coating comprising a thermoset resin 24 and 26.
- the composition 24 and 26 extends in the form of bands extending around the ends of the sleeve 18 and onto the adjacent surfaces of the pipe coating 16 and 17.
- the curable composition is preferably applied, for example by brushing or spraying, in sufficient thickness so that, in the cured state, as seen in Figs. 2 and 3, the bands 24 and 26 of the cured deposit extend continuously from the surface of the coatings 16 and 17 continuously to at least the outer surface of the backing sheet 19, and preferably above this surface, as seen in Fig. 2, so that, in effect, the cured deposit 24 and 26 forms a solid block or abutment extending over the full depth of the end surface of the backing sheet 19.
- the curable composition may be applied in the form of a tape of fibre mesh, weave or roving impregnated with the curable composition in uncured or partially cured (B-staged) form.
- thermoset material 24 and 26 creates a strong bond between the sleeve 18 and the polypropylene coatings 16 and 17. Further, the material 24 and 26 stabilizes the end portions of the sleeve 18, which would otherwise be bonded to the polypropylene coating 16 and 17 only by the low shear mastic or other bonding agent. This guards against the ends of the sleeve 18 being lifted radially outwardly by soil stress or by other forces, such as travelling over the stinger of a lay barge.
- thermoset composition 24 and 26 may crack or may in itself become incapable of providing a water-tight seal. In such condition, however, the thermoset material 24 and 26 continues to bond the ends of the sleeve 18 to the polypropylene coating 16 and 17, and continues to safeguard the integrity of the mastic or other bonding agent 22 and 23, so that the latter continues to maintain its f nction in providing a water tight seal .
- the thermoset material in its cured condition exhibits a flexural modulus (as measured by ASTM D790) of at least about 10 3 psi.
- Thermoset materials having a flexural modulus substantially less than about 10 3 psi tend to have insufficient stiffness to withstand the pressures generated by gross soil movements. Generally speaking, the stiffer and harder the thermoset material is, the better it will withstand external stresses.
- the use of thermoset materials having a flexural modulus in excess of about 10 7 psi does not appear to significantly increase the stability of the covering such as the sleeve 16, and may require use of thermosetting materials which are highly filled, excessively expensive and difficult to work with.
- the flexural modulus is in the range about 10 4 psi to about 10 6 psi, still more preferably about 5xl0 4 psi to about 7.5xl0 5 psi.
- the thermoset material has a shear strength (as measured by ASTM D 1002) of at least about 250 psi at the maximum operating temperature which the coverings are destined to encounter when the covered article is in service.
- Materials having a shear strength significantly less than about 250 psi tend to have insufficient strength to withstand soil stresses such as may typically be encountered in pipeline service.
- the shear strength at the maximum operating temperature is in the range about 500 to about 10,000 psi, still more preferably about 1000 to about 5000 psi.
- thermoset material since, essentially, the present invention utilizes the physical properties of the thermoset material, the nature of the thermoset material is not especially critical provided that it forms a bond of sufficient strength to the first and second coverings to be able to resist peeling, shearing and other stresses in service so as to improve the stability of the second coverings to be able to resist peeling, shearing and other stresses in service so as to improve the stability of the second covering against displacement relative to the first covering.
- the thermosetting material in its uncured condition should be sufficiently mobile or fluid, usually liquid or paste-like that it can be readily applied to provide the deposit having the required thickness along and preferably bridging over the edges of the sleeve 18 and the adjacent portions of the coatings 16 and 17.
- the composition in its uncured state has a certain degree of thixotropy so that the applied composition does not tend to flow down to a lower portion of the pipeline surface before curing.
- the thermosetting composition may be modified by addition of thixotroping agents, reinforcing fillers and the like.
- thermosetting composition is applied in the form of an impregnated tape
- the impregnation may take place prior to, during, or after wrapping.
- the curable composition may be applied thickly to the appropriate regions and the fibrous tape applied over it, after which the liquid curable composition is worked into the tape.
- the tape may be saturated with the liquid curable composition, then wrapped over the appropriate regions .
- a fibrous tape impregnated with a moisture-activated resin such as for example Master Wrap, which is sold by Patchmasters International Inc.
- the tape is first soaked in water, then wrapped on in one or more layers, with cure taking about 1 hour.
- Another preferred product is a fibreglass tape impregnated with a partially cured (or "B- staged") resin. After wrapping, the tape is gently heated to effect final cure.
- thermosetting composition which is sufficiently mobile and fluid in its uncured state for application in the manner above described, and which, in the cured condition has the hardness and shear strength discussed above, and which can be made to bond well to each of the substrates it contacts may be used in the present invention.
- thermosetting polyesters, polyurethanes, epoxy resins, silicone resins and polyurea resins may be employed.
- the presently preferred materials are epoxy resins based on bisphenol A-epichlorohydrins and cured with reactive hardeners such as primary or secondary amines.
- Other thermosetting compositions which may be used in the present invention will be readily apparent to those skilled in the art, and need not be described in.detail herein. For example, U.S. Pat. No.
- thermosetting compositions will comprise two components, namely a resin composition and a hardener which are mixed together shortly before application, in the preferred form, the thermosetting resin composition is applied, for example by brushing or spraying, to form the bands on the ends of the sleeve such as a sleeve 18 directly after heat shrinking of the sleeve, and while the sleeve is still hot, typically at a temperature of about 80°C, and is allowed to cure.
- the surfaces of the polypropylene coating 16 and 17 outwardly beyond the sleeve 18 are oxidized or otherwise treated so that they will bond more strongly to the curable composition.
- Such methods of modifying the surface of polypropylene are well known to those skilled in the art, and are used commonly in the printing of polypropylene films and articles.
- the coating 16 and 17 may be oxidized by, for example, playing on their surfaces the flame of a gas torch used for heating and shrinking down the sleeve 18, or by using a hot air blower, or the surfaces may be oxidized chemically, for example through application of chromic acid solution.
- the end surfaces of the sleeve 18 on which the curable composition 24 and 26 is applied tend to be ozidized as a result of the normal surface oxidization that occurs during the shrinking operation, and therefore are receptive to forming a strong bond with the curable compositions.
- the principals of the invention described above may be applied in the application of other secondary coverings on a polypropylene coated article, such as, for example, in the application of a polyolefin patch on a polypropylene coated pipe.
- a central portion of the patch may be adhered to a holiday with a high shear hot melt adhesive, and mastic or like bonding agent may be applied on the underside of the margin of the patch, and the edges of the patch and the adjacent surfaces of the polypropylene coating may be covered with curable thermoset composition.
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Abstract
An elongate tubular article extending along a longitudinal axis has a polypropylene covering. A polyolefin secondary covering is at least partially superimposed over the polypropylene. The secondary covering has an edge with a face extending transverse to the axis. A bonding agent capable of bonding to the polypropylene and to the secondary covering is interposed at least between the edge and the polypropylene covering. A cured deposit of thermoset resin is applied at least over the edge of the secondary covering and bonds to the outer surfaces of the polypropylene and secondary coverings. This provides the secondary covering with increased stability against displacement radially outwardly with respect to the polypropylene covering.
Description
SLEEVE FOR PROTECTING POLYPROPYLENE-COVERED PIPE COMPRISING BONDING AGENT-
The present invention relates to improved arrangements for providing a secondary covering on a polypropylene covered tubular article.
More especially, the invention is directed toward the application of a functional secondary coating over a polypropylene-coated substrate in circumstances where it is not possible to use a high shear strength adhesive that will bond to both polypropylene and the backing component of the secondary coating. This is true, for example, when the backing is a heat-shrinkable crosslinked polymer derived primarily from ethylene, which would be compatible with adhesives that bond to polyethylene, but not to polypropylene. However, the invention could also be used beneficially in circumstances wherein the high shear strength adhesive is compatible with both the backing of the secondary coating and with polypropylene, but the temperature required to achieve an adequate bond to the polypropylene-coated substrate would be so high as to damage the coating.
The following problems arise, for example, in the provision of a heat shrinkable polyolefin sleeve on a polypropylene coated pipe in the course of completion of a pipe joint between polypropylene coated pipe sections.
Firstly polypropylene coatings are generally used for high temperature pipelines, and therefore require the use of joint-completion systems that will also withstand high temperatures .
Secondly high strength adhesives that bond to polyethylene-based polymers do not generally bond well to polypropylene .
Thirdly, currently preferred heat-shrinkable backing
sheets suitable for anticorrosion applications are based on ethylene polymers or copolymers. Polypropylene is not crosslinkable by preferred conventional methods, and there are currently therefore no commercial heat-shrinkable polypropylene backing sheets available.
Fourthly, those adhesives that bond well to both polypropylene and ethylene-based polymers are relatively low strength mastics or hybrid mastic/hot melt adhesives . These have excellent sealing properties, but inadequate shear resistance at elevated temperatures.
Fifthly, polypropylene coatings are typically three- layer (epoxy/copolymer adhesive/polypropylene) constructions . Preheat temperatures in excess of about 200°C can severely damage the coating.
Similar problems may also arise in applying other polyolefin secondary coverings over a polypropylene coated pipe section, for example in applying a polyolefin patch over a holiday in the polypropylene coating.
According to the present invention, there is provided an elongate tubular article extending along a longitudinal axis and having a covering comprising polypropylene thereon with an outer surface, a secondary covering comprising polyolefin with an outer surface at least partially superimposed over the polypropylene covering, said secondary covering having an edge with a face extending transverse said axis, a bonding agent capable of bonding to said polypropylene and secondary coverings interposed at least between said edge and said polypropylene covering, and a cured deposit of thermoset resin applied at least over said edge of the secondary covering and bonding to said outer surfaces of said polypropylene and secondary coverings and providing the secondary covering with increased stability against displacement radially outwardly with respect to said polypropylene covering.
With this arrangement, the bonding agent, which may be, for example, a mastic or hybrid mastic/hot melt adhesive, provides excellent sealing between the polypropylene and secondary covering while the cured deposit creates a strong bond between the secondary covering and the polypropylene coating. Further, the cured deposit stabilizes the edge of the secondary covering against being lifted by axial stresses, such as soil stresses or other axial forces, such as travelling over a stinger in the course of laying pipe from a lay barge in the course of underwater pipeline installation.
The invention will now be described in more detail, by way of example only, with reference to the accompanying drawings, wherein
Fig. 1 is a partially sectional view through a pipe joint in the course of application of a heat shrinkable sleeve thereto;
Fig. 2 is a partially sectional view showing the completed pipe joint; and
Fig. 3 is a partially section view showing a modified completed pipe joint.
Fig. 1 shows a partial longitudinal cross section through two pipeline sections 11 and 12 aligned along a longitudinal axis 13 and secured together at a weld joint 14. The sections 11 and 12 each carry a polypropylene coating 16 and 17 which covers the pipe 11 or 12 along its entire length except for a short section exposed at each end of the pipe to permit the above mentioned welding operation.
Fig. 1 shows a sleeve-form protective covering 18 to be applied over the pipe weld area. The covering 18 is of sufficient length that it overlaps at each end on the
coating 16 and 17. In the preferred form, the covering 18 comprises a heat shrinkable backing 19 provided on its underside with a functional coating 21 which is typically a sealant or adhesive. In the course of installation, the backing 19 is heated so that it shrinks down tightly onto the coating 16 and 17. Usually, the fluidity and tackiness of the functional coating 21 increases as the backing 19 becomes hotter, so that the functional coating tends to wet and coat the exposed surfaces of the metal pipes 11 and 12 and form a tight seal on the adjacent ends of the coatings 16 and 17. The intimacy of the contact between the functional coating material 21 and the underlying surfaces is enhanced by the hoop stress imparted by the sleeve backing 19 as it shrinks down. Such sleeve 18 may be of the cylindrical or wrap-around type. Many forms of heat shrinkable sleeve and known to those of ordinary skill in the art, and it is contemplated that the present invention may be used with all such sleeve.
Merely by way of example, various forms of backing and functional coating are described in U.S. Pat. Nos. 4,472,468 (Tailor et al) , 5,134,000 (Smythe et al) , 5,175,032 (Steele et al) and 5,411,777 (Steele et al) . Reference should be made to these for disclosures of suitable sleeves for use in connection with the present invention.
In preferred forms, for example, the backing sheet 19 may comprise a cross-linked polyolefin sheet. Presently preferred polyolefin materials comprise blends of polyethylene with suitable copolymers such as, for example, poly (ethylene-vinyl acetate), poly (ethylene-ethyl acrylate) , poly(ethylene-maleic anhydride) and poly (ethylene-vinyl acetate-maleic anhydride) . However, the backing sheet 19 may comprise other materials and may comprise polypropylene. Blends which aid in attaining adhesion to the curable thermosetting composition are preferred.
The functional coating 21 may comprise a mastic, hot melt adhesive or a hybrid thereof. These materials are well known to those of ordinary skill in the art, and need not be described in detail herein.
Preferably, the functional coating 21 is a very high shear strength hot-melt adhesive, desirably having a shear strength as measured by ASTM D1002 at the operating temperature of the article of at least about 20 psi, more desirably at least about 100 psi. Examples of suitable high shear strength adhesives are the adhesive used on the heat shrinkable sleeve GTS-HT®, sold by Canusa-CPS division of Shaw Industries Ltd., and the adhesive used on the heat- shrinkable sleeve WPC-120®, produced by Raychem Corporation.
Before the sleeve 18 is shrunk down onto the pipe joint area, a bonding agent capable of bonding to the backing 19 as well as to the polypropylene coatings 16 and 17 is interposed between the end edges of the sleeve 19 and the coating 16 and 17. The bonding agent, indicated at 22 and 23 in the accompanying drawings is preferably a mastic. Usually, the mastic materials comprise substantially amorphous natural or synthetic polymers, or mixtures thereof, in contrast to the hot melt adhesive materials, which typically exhibit marked crystallinity.
Examples of typical mastic compositions include blends of substantially amorphous rubber materials, such as butyl rubber, natural rubber, latex SBR rubber, with tackifying resins, such as synthetic hydrocarbon tackifying resins, rosin ester tackifying resins, and inert fillers such as calcium carbonate, talc and carbon black, usually together with antioxidants, and with or without admixtures of other amorphous natural or synthetic polymers, such as asphalt, polybutene and amorphous polyolefins, such as amorphous polypropylene, styrene-isoprene copoly ers, and liquid butyl polymers. Such mastic compositions provide excellent
properties of excluding ingress of water to the sealed area, and, as compared with hot melt adhesive and other functional coating materials, exhibit broader softening temperatures and substantial surface tack which contribute to considerably greater ease of application over a wide range of ambient temperature including very low ambient temperatures .
The bonding agent may be a conventional mastic-hot melt adhesive hybrid.
The mastic and hybrid materials bond well to polypropylene and other polyolefins, as well as to hot melt adhesives, and therefore form a strong water excluding bond between the polypropylene coatings 16 and 17 and the adjacent ends of the sleeve 18.
The mastic portions 22 and 23 may be provided by, for example, applying a mastic tape circumferentially around the polypropylene coating 16 and 17 at the locations as indicated in Fig. 1, in register with the inner marginal portions of the sleeve 18. The mastic may be applied as a narrow band, leaving contact between adhesive 21 and coating 16 and 17, or preferably may be applied in sufficient width to cover all of the coating 16 and 17 which would otherwise come into contact with the adhesive 21, as shown in Figure 3. This ensures there is no unbonded, unsealed boundary between the polypropylene coating and the sleeve 18.
In installation of the sleeve 18, in its preferred use, the sleeve 18 is heated in known manner to cause it to shrink down tightly onto the polypropylene coated pipe sections as seen in Figs. 2 and 3. The adhesive 21 bonds very well to the bare surface of the steel pipe 11 and 12, but cannot bond to the polypropylene pipe coatings 16 and 17. The layer of mastic or other bonding agent 22 and 23 which, as seen in Figs. 2 and 3 on shrinking down of the
sleeve 18 may tend to be extruded somewhat outwardly from the ends of the sleeve 18, creates a weak but water- resistant bond between the sleeve 18 and the coating 16 and 17. However, where the adhesive 21 is in contact with the coatings 16 and 17, as in Fig. 2, there is effectively no bond. As installed, the sleeve 18 cannot move as a whole because of the high shear bond between the steel pipe 11 and 12 and the sleeve 18, but the ends are susceptible to lifting. To overcome this, the ends of the sleeve 18 and the adjacent pipe coating 16 and 17 are over-coated with a layer of a hard, tough curable coating comprising a thermoset resin 24 and 26. In the examples illustrated, the composition 24 and 26 extends in the form of bands extending around the ends of the sleeve 18 and onto the adjacent surfaces of the pipe coating 16 and 17.
The curable composition is preferably applied, for example by brushing or spraying, in sufficient thickness so that, in the cured state, as seen in Figs. 2 and 3, the bands 24 and 26 of the cured deposit extend continuously from the surface of the coatings 16 and 17 continuously to at least the outer surface of the backing sheet 19, and preferably above this surface, as seen in Fig. 2, so that, in effect, the cured deposit 24 and 26 forms a solid block or abutment extending over the full depth of the end surface of the backing sheet 19. Alternatively, the curable composition may be applied in the form of a tape of fibre mesh, weave or roving impregnated with the curable composition in uncured or partially cured (B-staged) form.
On curing, the thermoset material 24 and 26 creates a strong bond between the sleeve 18 and the polypropylene coatings 16 and 17. Further, the material 24 and 26 stabilizes the end portions of the sleeve 18, which would otherwise be bonded to the polypropylene coating 16 and 17 only by the low shear mastic or other bonding agent. This guards against the ends of the sleeve 18 being lifted radially outwardly by soil stress or by other forces, such
as travelling over the stinger of a lay barge.
In prolonged service, the thermoset composition 24 and 26 may crack or may in itself become incapable of providing a water-tight seal. In such condition, however, the thermoset material 24 and 26 continues to bond the ends of the sleeve 18 to the polypropylene coating 16 and 17, and continues to safeguard the integrity of the mastic or other bonding agent 22 and 23, so that the latter continues to maintain its f nction in providing a water tight seal .
In the preferred form, the thermoset material, in its cured condition exhibits a flexural modulus (as measured by ASTM D790) of at least about 103 psi. Thermoset materials having a flexural modulus substantially less than about 103 psi tend to have insufficient stiffness to withstand the pressures generated by gross soil movements. Generally speaking, the stiffer and harder the thermoset material is, the better it will withstand external stresses. However, the use of thermoset materials having a flexural modulus in excess of about 107 psi does not appear to significantly increase the stability of the covering such as the sleeve 16, and may require use of thermosetting materials which are highly filled, excessively expensive and difficult to work with. More preferably, the flexural modulus is in the range about 104 psi to about 106 psi, still more preferably about 5xl04 psi to about 7.5xl05 psi.
Desirably, the thermoset material has a shear strength (as measured by ASTM D 1002) of at least about 250 psi at the maximum operating temperature which the coverings are destined to encounter when the covered article is in service. Materials having a shear strength significantly less than about 250 psi tend to have insufficient strength to withstand soil stresses such as may typically be encountered in pipeline service. The higher the shear strength, the better the material will perform, but the use of materials having shear strengths in excess of the shear
strength of the bond between the thermoset deposit and the first covering (typically up to about 20,000 psi) do not contribute significantly to increased resistance to soil stresses, and may involve the use of highly reinforced or excessively expensive materials. More preferably, the shear strength at the maximum operating temperature is in the range about 500 to about 10,000 psi, still more preferably about 1000 to about 5000 psi.
Since, essentially, the present invention utilizes the physical properties of the thermoset material, the nature of the thermoset material is not especially critical provided that it forms a bond of sufficient strength to the first and second coverings to be able to resist peeling, shearing and other stresses in service so as to improve the stability of the second coverings to be able to resist peeling, shearing and other stresses in service so as to improve the stability of the second covering against displacement relative to the first covering. The thermosetting material in its uncured condition should be sufficiently mobile or fluid, usually liquid or paste-like that it can be readily applied to provide the deposit having the required thickness along and preferably bridging over the edges of the sleeve 18 and the adjacent portions of the coatings 16 and 17. Desirably, the composition in its uncured state has a certain degree of thixotropy so that the applied composition does not tend to flow down to a lower portion of the pipeline surface before curing. If necessary or desirable, the thermosetting composition may be modified by addition of thixotroping agents, reinforcing fillers and the like.
If the thermosetting composition is applied in the form of an impregnated tape, the impregnation may take place prior to, during, or after wrapping. For example, the curable composition may be applied thickly to the appropriate regions and the fibrous tape applied over it, after which the liquid curable composition is worked into
the tape. Alternatively, the tape may be saturated with the liquid curable composition, then wrapped over the appropriate regions . One particularly preferably method is to use a fibrous tape impregnated with a moisture-activated resin, such as for example Master Wrap, which is sold by Patchmasters International Inc. The tape is first soaked in water, then wrapped on in one or more layers, with cure taking about 1 hour. Another preferred product is a fibreglass tape impregnated with a partially cured (or "B- staged") resin. After wrapping, the tape is gently heated to effect final cure.
It is contemplated that any thermosetting composition which is sufficiently mobile and fluid in its uncured state for application in the manner above described, and which, in the cured condition has the hardness and shear strength discussed above, and which can be made to bond well to each of the substrates it contacts may be used in the present invention. For example, thermosetting polyesters, polyurethanes, epoxy resins, silicone resins and polyurea resins may be employed. The presently preferred materials are epoxy resins based on bisphenol A-epichlorohydrins and cured with reactive hardeners such as primary or secondary amines. Other thermosetting compositions which may be used in the present invention will be readily apparent to those skilled in the art, and need not be described in.detail herein. For example, U.S. Pat. No. 4,732,632 in the name Pieslak et al describe numerous epoxy resin compositions, and may be referred to for its disclosure of resin compositions suitable for use in the present invention. Generally, the thermosetting compositions will comprise two components, namely a resin composition and a hardener which are mixed together shortly before application, in the preferred form, the thermosetting resin composition is applied, for example by brushing or spraying, to form the bands on the ends of the sleeve such as a sleeve 18 directly after heat shrinking of the sleeve, and while the sleeve is still hot, typically at a temperature of about
80°C, and is allowed to cure.
Preferably., the surfaces of the polypropylene coating 16 and 17 outwardly beyond the sleeve 18 are oxidized or otherwise treated so that they will bond more strongly to the curable composition. Such methods of modifying the surface of polypropylene are well known to those skilled in the art, and are used commonly in the printing of polypropylene films and articles. The coating 16 and 17 may be oxidized by, for example, playing on their surfaces the flame of a gas torch used for heating and shrinking down the sleeve 18, or by using a hot air blower, or the surfaces may be oxidized chemically, for example through application of chromic acid solution.
The end surfaces of the sleeve 18 on which the curable composition 24 and 26 is applied tend to be ozidized as a result of the normal surface oxidization that occurs during the shrinking operation, and therefore are receptive to forming a strong bond with the curable compositions.
As will be appreciated, the principals of the invention described above may be applied in the application of other secondary coverings on a polypropylene coated article, such as, for example, in the application of a polyolefin patch on a polypropylene coated pipe. In such a case, a central portion of the patch may be adhered to a holiday with a high shear hot melt adhesive, and mastic or like bonding agent may be applied on the underside of the margin of the patch, and the edges of the patch and the adjacent surfaces of the polypropylene coating may be covered with curable thermoset composition.
Claims
1. An elongate tubular article extending along a longitudinal axis and having a covering comprising polypropylene thereon with an outer surface, a secondary covering comprising polyolefin with an outer surface at least partially superimposed over the polypropylene covering, said secondary covering having an edge with a face extending transverse said axis, a bonding agent capable of bonding to said polypropylene and secondary coverings interposed at least between said edge and said polypropylene covering, and a cured deposit of thermoset resin applied at least over said edge of the secondary covering and bonding to said outer surfaces of said polypropylene and secondary coverings and providing the secondary covering with increased stability against displacement radially outwardly with respect to said polypropylene covering.
2. An article as claimed in claim 1 wherein the secondary covering has a functional, coating on an underside applied on the polypropylene covering.
3. An article as claimed in claim 2 wherein the functional coating is a very high shear strength hot melt adhesive.
4. An article as claimed in claim 3 wherein the functional coating has a shear strength of at least about 20 psi.
5. An article as claimed in claim 4 wherein the shear strength is at least about 100 psi.
6. An article as claimed in claim 1 wherein the bonding agent is a mastic or a mastic/hot melt adhesive hybrid.
7. An article as claimed in claim 1 wherein said deposit has a flexural modulus of about 103 to about 107 psi.
8. An article as claimed in claim 7 wherein said flexural modulus is about 104 to about 106 psi .
9. An article as claimed in claim 8 wherein said flexural modulus is about 5xl04to about 7.5xl05 psi.
10. An article as claimed in claim 1 wherein said deposit has a shear strength about 250 psi to about 20,000 psi.
11. An article as claimed in claim 10 wherein said shear strength is about 500 psi to about 10,000 psi.
12. An article as claimed in claim 11 wherein said shear strength is about 1000 psi to about 5000 psi.
13. An article as claimed in claim 1 wherein said cured thermoset deposit comprises an epoxy resin, a polyester resin, a polyurethane resin, a silicone resin or a polyurea resin.
14. An article as claimed in claim 1 wherein said secondary covering comprises sheet material and said covering has a thickness around the margins of the covering at least equal to the thickness of the sheet material .
15. An article as claimed in claim 1 wherein said secondary covering comprises a sleeve or a patch.
16. An article as claimed in claim 1 wherein said deposit is applied as a fibrous tape impregnated with a curable resin composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2001261942A AU2001261942A1 (en) | 2000-05-18 | 2001-05-18 | Sleeve for protecting polypropylene-covered pipe comprising bonding agent |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2,308,802 | 2000-05-18 | ||
CA002308802A CA2308802A1 (en) | 2000-05-18 | 2000-05-18 | Polypropylene-covered article having a secondary covering |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001087584A1 true WO2001087584A1 (en) | 2001-11-22 |
Family
ID=4166175
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CA2001/000710 WO2001087584A1 (en) | 2000-05-18 | 2001-05-18 | Sleeve for protecting polypropylene-covered pipe comprising bonding agent |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU2001261942A1 (en) |
CA (1) | CA2308802A1 (en) |
WO (1) | WO2001087584A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002047892A2 (en) * | 2000-12-15 | 2002-06-20 | Shawcor Ltd. | Method and apparatus for heating a zone of an elongate tubular article |
ITMI20110053A1 (en) * | 2011-01-20 | 2012-07-21 | Saipem Spa | METHOD OF JUNCTION OF TUBE CUTTINGS TO CREATE PIPES FOR HYDROCARBONS, IN PARTICULAR SUBMARINE PIPES |
WO2015054786A1 (en) * | 2013-10-16 | 2015-04-23 | Shawcor Ltd. | Heat shrinkable multilayer sleeve |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE370186T1 (en) | 2003-07-14 | 2007-09-15 | Frans Nooren Afdichtingssystem | COMPOSITION FOR PROTECTING A MOLDED BODY FROM CORROSION |
DK2081761T3 (en) | 2006-11-08 | 2010-06-07 | Frans Nooren Afdichtingssystem | Process for providing an elongated tubular article with a corrosion-protective coating system having self-repairing properties |
EP2204427A1 (en) | 2008-12-23 | 2010-07-07 | J. van Beugen Beheer B.V. | Adhesive compound |
JP6274674B2 (en) | 2012-07-13 | 2018-02-07 | フランス ノーレン アフディクティングスシステメン ビー.ブイ.Frans Nooren Afdichtingssystemen B.V. | Method for protecting articles in a moist environment against corrosion and compositions therefor |
EP3059485A1 (en) | 2015-02-17 | 2016-08-24 | J. van Beugen Beheer B.V. | Metal pipes with anticorrosive polyolefin covering layer |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4472468A (en) | 1982-11-12 | 1984-09-18 | Shaw Industries Limited | Heat shrinkable covering and method for applying same |
EP0188363A1 (en) * | 1985-01-14 | 1986-07-23 | Shaw Industries Ltd. | Preinsulated pipeline joint |
US4732632A (en) | 1984-11-09 | 1988-03-22 | Raychem Corporation | Protecting elongated substrate with multiple-layer polymer covering |
EP0309597A1 (en) * | 1987-09-29 | 1989-04-05 | Blome GmbH & Co. Kommanditgesellschaft | Coating of the jointing area of steel pipes welded together |
US5134000A (en) | 1989-08-10 | 1992-07-28 | Shaw Industries Ltd. | Heat shrinkable protective sheets and methods for their manufacture |
US5175032A (en) | 1991-05-02 | 1992-12-29 | Shaw Industries Ltd. | Heat shrinkable closure sheets and sleeve structures and methods employing the same |
US5411777A (en) | 1989-08-10 | 1995-05-02 | Shaw Industries, Ltd. | Heat shrinkable protective sheets |
WO1995035461A1 (en) * | 1994-06-17 | 1995-12-28 | Shaw Industries Ltd. | Superimposed coverings having increased stability |
WO1999056055A1 (en) * | 1998-04-24 | 1999-11-04 | Raychem Limited | Pipe corrosion protection |
-
2000
- 2000-05-18 CA CA002308802A patent/CA2308802A1/en not_active Abandoned
-
2001
- 2001-05-18 AU AU2001261942A patent/AU2001261942A1/en not_active Abandoned
- 2001-05-18 WO PCT/CA2001/000710 patent/WO2001087584A1/en active Application Filing
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4472468A (en) | 1982-11-12 | 1984-09-18 | Shaw Industries Limited | Heat shrinkable covering and method for applying same |
US4732632A (en) | 1984-11-09 | 1988-03-22 | Raychem Corporation | Protecting elongated substrate with multiple-layer polymer covering |
EP0188363A1 (en) * | 1985-01-14 | 1986-07-23 | Shaw Industries Ltd. | Preinsulated pipeline joint |
EP0309597A1 (en) * | 1987-09-29 | 1989-04-05 | Blome GmbH & Co. Kommanditgesellschaft | Coating of the jointing area of steel pipes welded together |
US5134000A (en) | 1989-08-10 | 1992-07-28 | Shaw Industries Ltd. | Heat shrinkable protective sheets and methods for their manufacture |
US5411777A (en) | 1989-08-10 | 1995-05-02 | Shaw Industries, Ltd. | Heat shrinkable protective sheets |
US5175032A (en) | 1991-05-02 | 1992-12-29 | Shaw Industries Ltd. | Heat shrinkable closure sheets and sleeve structures and methods employing the same |
WO1995035461A1 (en) * | 1994-06-17 | 1995-12-28 | Shaw Industries Ltd. | Superimposed coverings having increased stability |
WO1999056055A1 (en) * | 1998-04-24 | 1999-11-04 | Raychem Limited | Pipe corrosion protection |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002047892A2 (en) * | 2000-12-15 | 2002-06-20 | Shawcor Ltd. | Method and apparatus for heating a zone of an elongate tubular article |
WO2002047892A3 (en) * | 2000-12-15 | 2003-11-20 | Shawcor Ltd | Method and apparatus for heating a zone of an elongate tubular article |
US6846176B2 (en) | 2000-12-15 | 2005-01-25 | Shawcor Ltd. | Method and apparatus for heating a zone of an elongate tubular article |
ITMI20110053A1 (en) * | 2011-01-20 | 2012-07-21 | Saipem Spa | METHOD OF JUNCTION OF TUBE CUTTINGS TO CREATE PIPES FOR HYDROCARBONS, IN PARTICULAR SUBMARINE PIPES |
WO2012098528A1 (en) * | 2011-01-20 | 2012-07-26 | Saipem S.P.A. | Pipe-joining method for building hydrocarbon pipelines, in particular, underwater pipelines |
CN103328872A (en) * | 2011-01-20 | 2013-09-25 | 塞彭公司 | Pipe-joining method for building hydrocarbon pipelines, in particular, underwater pipelines |
AU2012208268B2 (en) * | 2011-01-20 | 2016-12-01 | Saipem S.P.A. | Pipe-joining method for building hydrocarbon pipelines, in particular, underwater pipelines |
US10527206B2 (en) | 2011-01-20 | 2020-01-07 | Saipem S.P.A. | Pipe-joining method for building hydrocarbon pipelines, in particular, underwater pipelines |
WO2015054786A1 (en) * | 2013-10-16 | 2015-04-23 | Shawcor Ltd. | Heat shrinkable multilayer sleeve |
Also Published As
Publication number | Publication date |
---|---|
CA2308802A1 (en) | 2001-11-18 |
AU2001261942A1 (en) | 2001-11-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0765451B1 (en) | Superimposed coverings having increased stability | |
US5482087A (en) | Method of environmentally protecting a pipeline | |
CA2482706C (en) | Heat-recoverable composition and article | |
US4472468A (en) | Heat shrinkable covering and method for applying same | |
AU648661B2 (en) | Heat shrinkable closure sheets and sleeve structures and methods employing the same | |
CN1220839C (en) | Method of sealing a joint between two pipes | |
EP0195683A2 (en) | Coated recoverable articles | |
EP0100170B1 (en) | Heat shrinkable covering and method of applying same | |
WO2001087584A1 (en) | Sleeve for protecting polypropylene-covered pipe comprising bonding agent | |
US20040028862A1 (en) | Fibrous closure for heat-shrinkable covers | |
EP0134491A1 (en) | Heat-shrinkable covering material for special shape pipes and other articles | |
EP0465150A1 (en) | Tape coatings | |
NO850316L (en) | ENCAPPING DEVICE, EX. FOR A CABLE CHAIN. | |
JPH0493378A (en) | Novel tape coating | |
JPH0353875Y2 (en) | ||
JPS61193832A (en) | Corrosion preventive covering method of exposed steel surface of steel pipe covered with polyolefin corrosion preventive covering | |
GB2071258A (en) | Pipe seal | |
JPS61197077A (en) | Anticorrosive coating method of exposed surface of anticorrosive polyolefin-coated steel pipe | |
JPH07260085A (en) | Corrosionproof covering method of metal pipe connecting part | |
JPS6090739A (en) | Covering method of t-shaped tube | |
JPS6110190A (en) | Method of coating t pipe | |
JPH05305665A (en) | Heat shrinkable sealing sheet and sleeve structure and using method of sheet thereof | |
JPS6251724B2 (en) | ||
JPH0913181A (en) | Corrosion preventive method and corrosion preventive structure of weld zone of steel pipe | |
JPS6024924A (en) | Anticorrosive covering method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
122 | Ep: pct application non-entry in european phase | ||
NENP | Non-entry into the national phase |
Ref country code: JP |