HK1085230B - Composition for the protection of a shaped article against corrosion - Google Patents
Composition for the protection of a shaped article against corrosion Download PDFInfo
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- HK1085230B HK1085230B HK06107503.9A HK06107503A HK1085230B HK 1085230 B HK1085230 B HK 1085230B HK 06107503 A HK06107503 A HK 06107503A HK 1085230 B HK1085230 B HK 1085230B
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Description
The present invention relates to a composition for the protection of a shaped article, in particular a shaped article made from or consisting essentially of one or more metals, metal compositions or alloys against corrosion. The present invention relates in particular to a composition for insulating and sealing a shaped article that is in contact with salts, moisture, water and other substances that are corrosive to a shaped article with the effect that said shaped article is protected against corrosion. The present invention also relates to a composition that can be used to protect subterranean shaped articles against corrosion. In the present invention, a shaped article is envisaged to encompass oil lines, oil pipes, gas lines, gas pipes, man hole covers, underground tanks, man hole covers, welding joints, flanges, crane hooks, thermit weldings in divisible shafts below the ground level and in T-joints.
For protecting shaped articles against corrosion a plurality of materials is employed. Shaped articles such as man hole covers, underground tanks, pipes, lines are often made of metal, metal compositions or alloys and such shaped articles are subject to corrosion since they are in contact with salts, moisture, water and other corrosive components. Corrosion is obviously not preferred since it is detrimental to strength and must therefore be prevented or inhibited to extend the life cycle of the shaped article as much as possible.
Obviously, materials for preventing corrosion, in particular long-term corrosion, must have a long-term chemical, physical, mechanical and thermal stability. Moreover, as is well known in the art, the application of such materials is often a laborious, time-consuming and expensive process. The materials must further have a good adhesion on metals and other materials like polyethylene and polypropylene. Another requirement is that they have a very low permeability for water, salts, moisture.
Several materials for inhibiting or preventing corrosion are known in the art. Examples of such materials are bitumen and synthetic, thermosetting resins, e.g. epoxy resins and polyurethane resins. These materials have the disadvantage that a hard coating or seal is produced which can easily split or tear under the influence of for example mechanical stress. Another disadvantage of these materials is that volatile solvents are required when such materials are applied. After application of these materials, the solvents evaporate thereby leading to the formation of a micro-porous seal or coating which is at least permeably for corrosive substances such as salts, water and moisture. Nor are the solvents friendly to the environment.
Bitumen are also permeable for water and do generally not meet the requirements laid down by the KIWA ("Keuringsinstituut voor Waterleidingartikelen"; Dutch Inspection Institute for Water Supply Articles). Moreover, bitumen have in general a glass transition temperature of more than about 10°C. As a consequence, removal of bitumen is difficult under high temperature conditions, e.g. the summer, and formation of cracks can easily occur during low temperature conditions, e.g, the winter.
Synthetic, thermosetting resins are also easily split or torn as a result of mechanical stress. Moreover, they are not easily removed from the shaped article and easy removal is important when repairs have to be carried out to the shaped article or when the level of protection provided by the thermosetting resin needs to be checked. In addition, cleaning of the shaped article is also difficult which is required when a new seal or coating is applied so that complex and laborious cleaning techniques such as sand blasting have to be employed for cleaning the shaped article to a sufficient extent. It is obvious to the person skilled in the art that if the shaped article is a gas or oil line or pipe line of several hundreds of miles long, replacing or repairing a seal or coating made of synthetic, thermosetting resins is a time-consuming and expensive operation. Finally, applying a seal or coaling based on synthetic, thermosetting resins in it self is difficult and laborious.
The present invention relates to a composition for the protection of a shaped article against corrosion, said composition comprising:
- (a) a polyisobutene having a glass transition temperature of less than -20°C and surface tension of less than 40 mM/m at a temperature above the glass transition temperature of said polyisobutene,
- (b) a filler material, and
- (c) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and/or a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol.
Advantages of the present invention are that the compositions have an improved setting on the shaped article to be sealed or coated including an improved deformability and a very good adhesion, i.e. a very good adhesive power to the surface of the shaped article. The composition according to the invention does not set and therefore remains soft and is impermeable for water, moisture, salts and is pore-tight. An additional and very important feature of the composition of the present invention that if a coating or seal made of the composition according to the invention is mechanically deformed to a relatively small extent, the damage is repaired automatically within a relatively short period time due to the fluid-like and/or visco-elastic nature of the composition of the invention. That is, the composition has self-recovering properties and any deformation or damage is repaired as a result of flow of the composition into holes or cavities caused by mechanical deformations or soil stresses. Consequently, the seal or coating comprising the composition according to the invention is not only smooth when applied, but even if indentations, imprints, dents, cavities are caused by mechanical forces, they will disappear in due course and the smooth surface of the seal or coating reappears. Obviously, because of this fluid-like nature any seal or coating comprising the composition according to the present invention does not tear or break and does not build up internal stresses. Likewise, irregularities on the surface of the shaped article are perfectly filled or enveloped by the composition according to the invention where materials according to the state of the art often give rise to problems in such circumstances. The fluid-like and/or visco-elastic nature of the composition according to the invention also implies that it has no pot-life whereas protective coatings need to be applied within a certain period of time.
Other advantages of the composition according to the invention are a high chemical stability and resistance over a wide pH-range, excellent impact resistance, very good electrochemical impedance, a high cathodic protection performance, essentially no cathodic disbondment or undercreep corrosion. Additionally, the composition can be used within an operating temperature range of -50° to 85°C.
There are more important advantages of the composition according to the present invention. Most protecting systems require the use of a primer before these systems are applied to the shaped article to provide sufficient adhesion. The use of a primer is unnecessary with the composition according to the present invention which implies that the composition can be applied within a shorter period of time thereby making the operation less expensive.
Coating systems have the disadvantage that, in particular under high-temperature conditions, suffer from loss of material which is not only costly but also detrimental to the environment and health of the user. Such problems do not occur when the composition according to the present invention is used. Other problems that do arise when coating systems are applied are that air bubbles may be formed in the coating which easily burst open thereby leading to pinholes in the coating layer and a poor protection. The present inventors have found that when the composition of the present invention is used, any air bubble present between the surface of the shaped article and the surface of the protective layer of the composition according to the invention migrates to the outer surface of the protective layer of the composition and diffuses away. In locations where the shaped article is in contact with salt, e.g. sea water, salt crystals are formed on the surface of the shaped article and before a coating system is applied to said surface, it requires thorough cleaning, i.e. by sand blasting, whereas the composition according to the invention encapsulates the salt crystals and removal of these crystals is not required. The necessity that for prior art protecting systems the salt crystals must be removed is that these crystals are hygroscopic and absorb water that permeates the protective layer. As a consequence, the salt crystals swell thereby causing cracks in the protective layer which eventually leads to a deteriorated protection to corrosion. In practice these salt crystals cause serious problems in the operation of shaped articles which require that the state of the art protective coatings must be replaced regularly. The composition according to the invention, however, does not suffer from such problems and is therefore much more economical to the end-user.
In a desert-like environment sand storms regularly occur. Any protective systems that must be applied by spray techniques cannot be used under such circumstances. However, the present inventors have found that the composition according the present invention can be applied without leading to an inferior protective layer.
Shaped articles can also directly be coated with the composition according to the invention under humid conditions, provided that condensation does not occur, whereas most systems according to the prior art can generally not be used under such conditions.
Shaped articles protected by the composition according to the invention can be easily inspected since a protective layer of the composition according to the invention can easily be removed and, after inspection, be reapplied. Most materials according to the state of the art are far more difficult to remove. Moreover, when removed the surface of the shaped article needs to be thoroughly cleaned before such materials are reapplied. Obviously, a protective layer of the composition according to the invention is also more easily tested.
According to the invention, the polyisobutene employed in the composition according to the present invention has a glass transition temperature of less than -20°C, preferably less than -40°C and more preferably less than -60°C. The surface tension of the polyisobutene is according to the present invention less than 40 mM/m at a temperature above the glass transition temperature of said polyisobutene. According to the invention, mixtures of different polyisobutenes may be used.
It is well known in the art that the glass transition temperature (Tg) is dependent from the molecular weight of a polymer, i.e. the higher the molecular weight, the higher the Tg. Consequently, the upper limit of the Tg defines in fact a maximum for the molecular weight of the polyisobutene and excludes ultrahigh molecular weight polyisobutenes. Reference is for example made to Römpp Chemie Lexicon, 9th. edition, page 1587. According to Römpp Chemie Lexicon, 9th. edition, page 3539, polyisobutenes are commercially manufactured within a molecular weight range of 300 to 2.500.000. For example, BP manufactures Napvis and Hyvis (now sold under the trade name Indopol) having a Mn range of 180 to 6000 and BASF manufactures these polymers under the trade name Oppanol; the grade Oppanol B 200 G has a Mn of 600.000. Although not many data for the glass transition temperature vs. molecular weight of commercially available polyisobutenes are known, it can be estimated that at a Mn of 5000 or higher the glass transition temperature is becomes lower than -60°C.
The surface tension parameter is also used to define a certain class of polyisobutenes. In general, polymers having a relatively low surface tension have better flow, wetting and adhesion properties than polymers having a relatively high surface tension. Furthermore, it is also well known in the art that the surface tension increases with increasing molecular weight (and obviously also with increasing viscosity), although the increase above a molecular weight of 2000 - 3000 is in general negligible and reaches about 1 mN/m of the value at infinite molecular weight. Reference is for example made to J. Bandrup, E.H. Immergut, Polymer Handbook, third edition (1989), page VI/412. Hence, in the present invention the surface tension is used to distinguish between very low molecular weight polyisobutens from polyisobutenes according to the present invention and therefore defines a minimum of the molecular weight. The surface tension of polyisobutylene (Mn 2700) is 33.6 mN/m at 20°C (cf. J. Bandrup, E.H. Immergut, Polymer Handbook, third edition (1989), page VI/414) whereas the surface tension of the low molecular weight polyisobutenes (up to a Mn of 430) is 22 -27 mN/m. Hence, the polyisobutenes according to the invention have a surface tension less than 40 nM/m at a temperature that is higher than the glass transition temperature.
According to the invention, the most preferred polyisobutenes have preferably a Mn (average molecular weight, viscosity average calculated according to Jo = 3.06 x 10-2 x Mv 0.65) in the range of 10000 to 100000, more preferably in the range of 15000 to 80000. The preferred molecular weight distribution Mw/Mn is preferably not more than 4, more preferably not more than 3.5.
The filler material according to the invention comprises preferably an inorganic material such as inorganic minerals, salts and oxides, e.g. chalk, boron sulphate, aluminium oxide, silicon dioxide, limestone, ground quartz, glass, talc, slate, bentonite. However, it is preferred that the filler material has a density of 2.0 to 4.0 kg/dm3, preferably 1.5 to 3.5 kg/dm3, at 20°C according to DIN ISO 787/10. It is furthermore preferred that the filler material consists essentially of an inorganic material, preferably at least 75 wt.%, more preferably at least 90 wt.% and most preferably at least 95 wt.%, based on the total weight of the filler material. It is furthermore preferred that the filler material has a very low water solubility, preferably of less than 0.1 g/l (20°C; according to DIN ISO 787/8), more preferably less than 0.05 g/l. According to a particular embodiment of the present invention, the filler material consists essentially of calcium carbonate and a very suitable commercially available material is Omyalite 95T (available from Omya GmbH, Köln, Germany).
According to the invention, the composition comprises 40 wt.% to 80 wt.% of the filler material, preferably 50 wt.% to 70 wt.%, calculated on the total weight of the composition.
Properties of polymers, e.g. polyisobutenes, are strongly influenced by degradation reactions that may occur during production and uses. In many cases these degradation reactions are initiated by the presence of oxygen which may be catalysed by light, heat, water and metal ions. In initiation reactions free radicals are formed that in propagation reactions lead to the formation of unstable hydroperoxides. The hydroperoxides are the main initiators of thermal degradation and photodegradation processes.
Anti-oxidants are commonly used to prevent such degradation reactions wherein primary anti-oxidants interfere directly with propagation reactions leading to degradation, i.e. that they terminate such propagation reactions, whereas secondary anti-oxidants induce decomposition of the hydroperoxides.
According to the invention, the anti-oxidant composition comprises a primary and/or a secondary anti-oxidant, wherein the primary anti-oxidant is selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol. Furthermore, the primary anti-oxidant may comprise mixtures of sterically hindered phenol compounds. Likewise, the secondary anti-oxidant may comprise more than one secondary anti-oxidants.
The sterically hindered phenol compounds are preferably selected from the compounds according to formula (I):
wherein R1 is a C1-C4-alkyl group;
n is 1, 2, 3 or 4;
X is -CH2-, -CH2-CH2-C(O)-Y- or -CH2-C(O)-CH2-CH2-;
Y is -O- or -NH- is; and
if n=2, then X is -CH2-CH2-C(O)-Y- wherein Y is bonded to R2, and R2 is a C2-C12-alkylene group, a C4-C12-alkylene group that is interrupted by one or more oxygen atoms or sulphur atoms, or is a direct bond; and
if n = 4, then X is -CH2-CH2-C(O)-Y- wherein Y is bonded to 2 and R2 is C4-C10 alkanetetrayl.
The C1-C4 group encompasses methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl and t-butyl. According to the invention, the preferred meaning for R1 is t-butyl.
The C2-C12-alkylene group is preferably branched or linear. Examples of such groups are ethylene, propylene, tetramethylene, pentamethylene, hexamethylene, heptamethylene, octamethylene, decamethylene and dodecamethylene. R2 is preferably a C2-C10-alkylene group, more preferably a C2-C8-alkylene group and in particualr a C4-C8-alkylene group, typically hexamethylene.
The C4-C12-alkylene group that is interrupted by one rmore oxygen atoms or sulphur atoms is preferably a C4-C10-alkylene group, more preferably a C4-C8-alkylene group and in particuar a C4-C6-alkylene group. Examples of suitable groups are:
- -CH2-O-CH2-CH2-O-CH2-,
- -CH2-(O-CH2-CH2)2-O-CH2-,
- -CH2-(O-CH2-CH2)3-O-CH2-,
- -CH2-(O-CH2-CH2-)4-O-CH2-,
- -CH2-CH2-O-CH2-CH2-O-CH2-CH2- and
- -CH2CH2-S-CH2-CH2-.
Particularly preferred C4-C12-alkylene groups that are interrupted by one or more oxygen atoms or sulphur atoms are -CH2-CH2-O-CH2-CH2-O-CH2-CH2- and -CH2-CH2-S-CH2-CH2-.
According to the invention, C4-C10 alkanetetrayl is preferably (-CH2)4C.
Preferred sterically hindered phenol compounds according to the invention are those wherein in formula (I) n = 1 and R2 is C2-C20 alkyl. However, compounds that are more preferred are those wherein in formula (I) n = 2, R2 is C2-C8 alkylene, C4-C8 alkylene that is interrupted by a sulphur atom or an oxygen atom, or, if Y is -NH-, R2 is additionally a direct bond and those wherein in formula (I) n = 4 and R2 is C4-C8 alkanetetrayl. Other preferred sterically hindered phenol compounds according to the invention are those wherein in formula (I) R1 is t-butyl, n = 1, 2 or 4, X is -CH2-CH2-C(O)-Y-, Y is an oxygen atom or -NH- and if n = 1, then R2 is C14-C18 alkyl; and if n=2, R2 is C4-C6 alkylene or C4-C6 alkylene interrupted by an oxygen atom; and if n = 4, R2 is C4-C8 alkanetetrayl.
Suitable sterically hindered phenol compounds are for example disclosed in US 5.763.512 ).
The sterically hindered phenol compounds are most preferably selected from the group consisting of Irganox™ 1330, Irganox™ 1010, Irganox™ 1098, Irganox™ 1076, Irganox™ 245, Irganox™ 259, Irganox™ 1035, Irganox™ 3114 and Irganox™ 3125. Even more preferably, the sterically hindered phenol compounds are selected from the group consisting of Irganox™ 1330, Irganox™ 1010.
Instead of or additional to the sterically hindered phenol compounds, a sterically hindered alkylthiomethylphenol or arylthiomethylphenol compound or a mixture of such compounds may be used. Such compounds are for example disclosed in US 4358.616 .
These sterically hindered thiomethylphenol compounds are represented by formula (II):
wherein R3 is a C1-C12 alkyl group,
m is 1,2 or 3,
R4 is a C1-C12 alkyl group, a C1-C2 cycloalkyl group, a C6-C12 aryl group, a C7-C12 aralkyl group or a C7-C12 alkaryl group, and
n is an integer (5-m).
A suitable and preferred example of the compounds according to formula (II) is Irganox 1520, i.e. 2,4-di-octylthiomethyl-6-methyl phenol.
According to the invention, the secondary anti-oxidant is preferably selected from the group consisting of phosphites and thioesters. Suitable phosphites are for example disclosed in US 5.763.512 .
According to the invention, the phosphites are preferably selected from the compounds according to formulae (III - V):
wherein R is a carbon atom, a nitrogen atom or an oxygen atom and wherein n is 2, 3 of 4;
wherein R5 is a C1-C4-alkyl group and X is a group as defined above for R2 of formula (I) or a C6-C18-hydrocarbyl group, wherein the hydrocarbyl group comprises one or more arylene groups. According to the invention, suitable fosfites are Irgafos™ 168, Irgafos™ 12 and Irgafos™ P-EPQ.
The thioesters are preferably selected from the group of compounds represented by formula (VI): S-(R6-COOR7)2 wherein R6 is a C1-C12 alkylene group, preferably a C1-C6 alkylene group, and wherein R7 is a C1-C12 alkyl group, a C6-C12 aryl group, a C7-C12 alkaryl group or a C7-C12 aralkyl group.
In addition to the primary and secondary anti-oxidants, the anti-oxidant composition preferably comprises a further anti-oxidant selected from the group of lactones represented by formula (VII):
wherein R8 - R11 are independently hydrogen, halogen or C1-C12 alkyl and wherein R12 - R16 are independently hydrogen, halogen or C1-C12 alkyl. Preferably, R8 - R11 and R12-R16 are independently hydrogen or C1-C12 alkyl. More preferably, R8 and R10 are C1-C6 alkyl groups, R9 and R11 are hydrogens and R12-R16 are independently hydrogen or C1-C12 alkyl groups. Even More preferably, R8 and R10 are C1-C6 alkyl groups, R9 and R11 are hydrogens, R14 and R15 are C1-C6 alkyl groups and R12, R13 and R16 are hydrogens. Such lactones are for example disclosed in US 6.310.220 .
The present invention also relates to a wrapping tape for the protection of a shaped article against corrosion, wherein the wrapping tape comprises:
- (a) a first layer comprising a film, said film comprising a polymer or a copolymer of one or more α-olefins and/or diolefins, and
- (b) a second layer comprising a composition comprising:
- (i) a polyisobutene having a glass transition temperature of less than -20°C and surface tension of less than 40 mM/m at a temperature above the glass transition temperature of said polyisobutene,
- (ii) a filler material, and
- (iii) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and/or a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol.
The wrapping tape according to the invention can be easily applied to the shaped article to be protected since the second layer (b) can easily be deformed. Moreover after being applied, the wrapping tape can also easily be removed. Although due to cohesive breakage it does leave some residuals on the surface of the shaped article, these residuals can be easily removed by scraping. Additionally, the wrapping tape can in particular be applied to T-joints. Furthermore, the wrapping tape according to the invention can suitably be used for repairing damaged or corroded shaped articles that were already provided with some protecting material according to the state of the art, provided that the surface of the shaped article is cleaned to a St-2 level according to the NEN-EN-ISO standard 8501-1. Finally, as described above, the wrapping tape has self repairing properties due to the fluid and/or visco-elastic nature of layer (b).
If necessary, the wrapping tape may comprise a further layer (c) to protect layer (b). Moreover, the wrapping tape preferably has between layers (a) and (b) a further layer (d) comprising a reinforcing net-like layer having a woven, knitted or spool-knitted structure and that can be deformed in two orthogonal directions. The reinforcing net-like layer can be manufactured from polyolefin fibres, e.g. fibres made from ethane homopolymers or copolymers or propene homopolymers or copolymers, as is well known in the art
Layer (a) of the wrapping tape preferably comprises a polymer or a copolymer of one or more α-olefins and/or diolefins. Examples of such polymers and copolymers are EP(D)M elastomers, ethylene homopolymers, ethylene-α-olefin copolymers, propylene homopolymers and propylene-α-olefin copolymers. If the copolymer is an ethylene copolymer which is a preferred embodiment of the invention, the α-olefin is then preferably a C3-C12 α-olefin, in particular a C3-C8 α-olefin. Examples of suitable α-olefins are propene, 1-butene, 1-hexene and 1-octene. The ethylene copolymers preferably comprise 0.1 to 30 wt.%, in particular 0.1 to 20 wt.% α-olefin. The density of the ethylene homopolymers or copolymers (as measured according to ASTM D 1248) is preferably 0.800 - 0.975 g/cm3, in particular 0.850 - 0.950 g/cm3. The melt index (as measured according to ASTM D 1238) of the ethylene homopolymers or copolymers is preferably 0.1 to 50 g/min., in particular 0.2 to 20 g/min. Layer (a) of the wrapping tape comprises preferably one or more of the following polymers: low density polyethylene (LDPE), linear low density polyethylene (LLDPE), high density polyethylene (HDPE), an ethene propene copolymer, an ethene propene diene copolymer. According to a preferred embodiment of the invention, layer (a) of the wrapping tape comprises LDPE, HDPE or LLDPE or a combination thereof.
Obviously, layer (a) may comprise more than one layer and can for example be a multilayer film comprising of LLDPE outer layers and a HDPE inner layer. Such multilayer films are well known in the art.
Layer (a) may further comprise different additives such as pigments and fillers.
The wrapping tape according to the invention has preferably a total thickness of 1.0 to 3.0 cm, more preferably 1.2 to 2.8 cm. The width of the wrapping tape ca obviously adjusted as desired or as suitable, but is preferably 3.0 to 50.0 cm, more preferably 4.0 to 40.0 cm. The thickness of layer (a) is preferably 10 µm to 500 µm, more preferably 20 µm to 300 µm.
The invention also relates to a process for the manufacture of a wrapping tape for the protection of a shaped article against corrosion, wherein a composition comprising:
- (i) a polyisobutene having a glass transition temperature of less than -20°C and surface tension of less than 40 mM/m at a temperature above the glass transition temperature of said polyisobutene,
- (ii) a filler material, and
- (iii) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and/or a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol,
After said lamination step, the surface of layer (b) not being in contact with layer (a) is preferably protected by a layer (c), wherein layer (c) may be any suitable material that comprises an olefin polymer or copolymer, paper.
If a layer (d) is present between layers (a) and (b) as described above, layers (a) and (d) are first laminated where after a layer (b) is applied to the surface of layer(d) opposite the surface of layer (d) that is in contact with layer (a). The thickness of layer (b) is controlled by e.g. a knife.
After the wrapping tape is manufactured, it is preferably wrapped around a bobbin or a spool.
Another important advantage of the wrapping tape according to the invention is the following. It is known in the art that sulphate-reducing bacteria are frequently encountered in defects in the protective layer of subterranean shaped articles. These bacteria are capable of producing hydrogen sulphide that is known to promote metal corrosion (cf. for example S. Grobe et al., Materials and Corrosion, Vol. 47, pages 413 - 424, 1996; M.J. Feijo et a., Materials and Corrosion, Vol. 651, pages 691 - 697, 2000). Since during the application of a protective layer infection and inclusion may occur, it is essential that components that promote bacterial growth do not permeate during the protective layer. Moreover, it is believed that at least one of the essential elements (in particular carbon, hydrogen, oxygen and nitrogen) are must be absent in order to prevent the growth of such bacteria. Since the wrapping tape according to the invention has a low permeability for gases (air, i.e. nitrogen, oxygen and water vapour) and is water resistant and is free of nitrogen containing compounds (unless a particular anti-oxidant is used that contains nitrogen; it is believed, however, that this is not detrimental given the fact that only small amounts of anti-oxidants are added), the inventors believe that with the wrapping tape according to the invention corrosive problems due to such micro-organisms do not occur.
Finally, the inventors have noted that with protective systems like butyl rubber (which is spirally applied to shaped articles such as pipe lines) corrosion occurs in the areas of overlap between different windings ("spiral corrosion") due to the fact that in the areas of overlap the rather stiff butyl rubber windings are not in intimate contact so that occlusion of air, water vapour occurs. Such problems do, however, not occur with the wrapping tape according to the invention because of the fluid and/or visco-elastic nature of layer (b).
The present invention further relates to a process for covering a shaped article with a wrapping tape, wherein the wrapping tape comprises:
- (a) a first layer comprising a film, said film comprising a polymer or a copolymer of one or more α-olefins and/or diolefins, and
- (b) a second layer comprising a composition comprising:
- (i) a polyisobutene having a glass transition temperature of less than -20°C and surface tension of less than 40 mM/m at a temperature above the glass transition temperature of said polyisobutene,
- (ii) a filler material, and
- (iii) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and/or a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol
According to the invention, wherein the surface of the shaped article is preferably cleaned to a St-2 level according to NEN-EN-ISO Standard 8501-1 prior to the application of the wrapping tape. The St-2 level is defined as: "Thorough scraping and wire-brushing; hand tools and/or machine brushing/grinding is acceptable. Loose mill scale, rust and foreign matter must be fully removed. Finally, the surface should be cleaned with a vacuum cleaner, clean dry compressed air or a clean brush. Surface should have a faint metallic sheen (no anchor pattern is required)".
The wrapping tape is preferably wrapped around the shaped article such that subsequent layers of the wrapping tape overlap each other, wherein the overlap has preferably a width of at least 1.0 mm, more preferably a width of at least 5.0 mm and in particular a width of at least 10.0 mm. Obviously, greater widths, e.g. about 50.0 mm are also possible but that is also dependent from the width of the wrapping tape used as will be obvious to the person skilled in the art. It is, however, necessary that the width of the overlap is at least 1.0 mm to obtain a proper sealing. Moreover, the first and last windings are preferably applied essentially perpendicular to the wrapping direction, that is if the shaped article is for example a pipe line, the first and last windings are applied essentially circumferential and essentially perpendicular to the length of the pipe line. If the end of a first wrapping tape is reached, a second wrapping tape may be applied where the first wrapping tape expired, provided that the longitudinal overlap is at least 1.0 mm, preferably at least 5.0 mm and most preferably at least 10.0 mm. The wrapping tape is preferably applied without tension.
According to the invention, it is preferred that after the wrapping tape has been applied, an outerwrap film is wrapped around the shaped article. Preferably the outerwrap film is selected from films comprising one or more polyolefins that are preferably selected from the group consisting of ethylene homopolymers, ethylene copolymers, ethylene vinylchloride copolymers, vinylchloride polymers and ethylene vinylacetate copolymers. According to a preferred embodiment of the invention, the outerwrap film is a PVC film. The outerwrap film is preferably applied with tension.
Preferably, the outerwrap film is wrapped such that the width of the overlap is at least 20% of the width of the outerwrap film, preferably at least 40% of the width of the outerwrap film.
The invention will be further illustrated by the following examples which are, however, not intended to restrict the scope of the invention by any means.
In this example the water permeability of the wrapping tape according to the present invention was compared with that of several commercially available materials at similar thickness. The data show the excellent performance of the composition according to the invention, i.e. it has the lowest permeability for water.
| Material | |
| Bitumen | 840 |
| EPDM | 157 |
| Butyl rubber | 82.5 |
| LDPE | 68 |
| Polypropylene (95% isotactic) | 51 |
| Wrapping tape according to the invention | 35.5 |
In this example, a composition comprising polyisobutene and 2,6-di-t-butyl-4-methylphenol (BHT; supplied by Bax Chemicals B.V., The Netherlands) as the anti-oxidant were tested relative to the neat polyisobutene. The polyisobutylene was Oppanol B10 N (containing about 0.04 wt.% BHT) supplied by BASF, The Netherlands, having a Mn of 24000 and a Mv of 40000. The filler material was Omyalite 95T supplied by Omya GmbH, Germany.
The tests that were performed were:
- 1. Thermogravimetric analysis. This test provided data of the weight loss of the polyisobutene as function of the temperature. The analysis was performed in the presence of air at a temperature of 60° and 85°C. Data are shown in Table 1.
- 2. Determination of adhesion strength. The composition according to the invention was used in combination with a plastic tape. The composition contained 38.6 wt.% Oppanol B10 N, 60.3 wt.% Omyalite 95T, 0.06 wt.% pigment (green) and 1.0 wt.% BHT. The size of the sample was 4.9 x 13 cm of which 3.5 cm was applied to a steel plate having a size of 4.8 x 7.1 cm. The adhesion strength was determined by using a tensile testing machine (Zwick, 5 KN). The drawing rate was 300 mm/min. Data are shown in Table 2; the standard deviation of the load data is about 0.003 so that a load of 0.0562 ± 0.003 implies that the adhesive strength is unchanged.
| Formulations (wt%, calculated on weight of total composition) | ||
| A | B | |
| Oppanol B10 N | 100.00 | 99.00 |
| BHT | 0.00 | 1.00 |
| Weight loss (%) at 60°C | ||
| 1 Day | 0.02 | 0.07 |
| 3 Days | 0.06 | 0.09 |
| 5 Days | 0.04 | 0.09 |
| 10 Days | 0.06 | 0.15 |
| Weight loss (%) at 85°C | ||
| 1 Day | 0.00 | 0.08 |
| 3 Days | 0.09 | 0.12 |
| 5 Days | 0.08 | 0.12 |
| 10 Days | 0.13 | 0.23 |
The data of Table 1 show that BHT leaches out. Table 2
| Exp. | Subjected to | Max. load (kN) | Loss of adhesive strength |
| 1 | RT (reference) | 0.0562 | N.a. |
| 2 | 1 week, 60°C | 0.0558 | No |
| 3 | 1 week -20°C | 0.0551 | No |
| 4 | 5 days, 150°C | Brittle, break of seal | Yes |
| 5 | 1 week 85°C | 0.0491 | Yes |
| 6 | 2 weeks, 85°C | No adhesion | Yes |
| 7 | 1 week, -20°C | 0.0552 | No |
The data of Table 2 show that under various conditions the adhesive strength decreases over time. This is caused by the fact that BHT leaches out of the composition thereby providing insufficient protection to the polyisobutene.
The composition according to the invention was subjected to an ageing test and an accelerated ageing test. I these tests, the composition according to the invention was compared with a similar composition containing BHT as the anti-oxidant All tested compositions contained 1.0 wt.% of anti-oxidant or anti-oxidant composition, based on the total composition (cf. Table 3). Table 3
| Formulation | Anti-oxidant (1.0 wt.%) |
| E | BHT |
| F | Irganox 1010 / Irgaphos 168 (50:50 w/w) |
| G | Irganox 1010 |
| H | Irganox 1330 |
Corroded steal pipes were brushed clean by using a wire brush. The steal pipes were subsequently laminated with a wrapping tape comprising the compositions and a polyethylene film. In a climatic cabin the steal pipes were immersed in a brine solution and subjected to the following cycle: 4 h at 85°C, 6 h from -20°C to 85°C, 4 h at -20°C and 6 h from 85°C to -20°C. The cycle was repeated 135 times which according to the standard for cable sleeves of Deutsche Telekom AG corresponds with a life cycle of 107.5 years. After this test, the Mn of the polyisobutene (the polyisobutene had originally a Mn of 24000) was determined by GPC (the polyisobutene was isolated by soxhlet extraction using hexane as the solvent, the solvent was evaporated and the residue was dissolved in THF (2mg/ml). The GPC apparatus used was a Spectra Physics P 1000 (light diffraction detection). The flow was 1 ml/min. and the column used was a Waters F6. An increase of the Mn implies a reduced adhesive strength. Data are shown in Table 4.
Table 4
| Formulation | |
| E | 147 |
| F | 107 |
| G | 108 |
| H | 108 |
The data in Table 4 shows that formulation E (containing BHT) showed the largest increase of the Mn.
Formulations E - H were mixed with rust. The samples were stored in an oven at 85°C for six months. Thereafter, the polyisobutene was isolated as described above and analysed by FT-IR. The spectra of the formulations were superimposed on each other and the relative absorption was determined at the wavelength region of 1730 cm-1. In Table 5 the absorption data are shown.
Table 5
| Formulation | Absorption units (1729 cm-1) |
| E | 0.011 |
| F | 0.004 |
| G | 0.004 |
| H | 0.000 |
The data in Table demonstrate that oxidation of the polyisobutene in the formulation containing BHT occurred to a higher extent than in the other samples.
Pipe spools (diameter of about 10 cm; length of about 10 cm) were subsequently coated with a wrapping tape comprising the compositions (total thickness about 3 mm) and a PVC film. Coated test panels were also used in the field test. This test comprised the following tests:
- Holiday detection
- Chemical resistance tests
- Impact resistance tests
- Electrochemical impedance tests
This test was performed according to ASTM G 62 (Method B) using a Elcometer 236 Holiday Detector. At 3000 V no holidays could be detected in the coated spools and panels.
Samples of the compositions according to the invention were immersed in aqueous solutions at pH 4, 7 and 10 (pH adjusted by HCl or NaoH) and kept at about 23°C for one week. Thereafter, the pH of 4 was decreased to 3 whereas the pH of 10 was increased to 11 and the samples were again kept under these conditions for one week. After this period, the pH of 3 was decreased to 2 and the pH of 11 was increased to 12 and the samples were kept under these conditions for three weeks. At the end of the test (i.e. five weeks) no change in colour or in weight could be determined demonstrating that the compositions are stable under these conditions which is essential for long-term corrosion protection.
This test was performed according to ASTM G14. The tests were performed using 4 lb weight at two different force levels of 6, 10 and 15 Joule at room temperature. After testing, the areas (dents) were visually examined for damage and tested using a Elcometer 269 Pinhole detector. The dent obtained after testing at 6 Joule disappeared quickly whereas the dents obtained after testing at 10 and 15 Joule partially recovered. No holidays were detected. These results demonstrate the high impact resistance and self recovering characteristics of the compositions according to the invention.
Electrochemical impedance spectroscopy measurements were conducted on the coated spools and coated tests panels. Two commercially available corrosion protective materials were tested as well for comparison. The measurements were conducted by using a computer controlled EG & G Frequency Response Analyser (Model 1025) in conjunction with a EG & G potentiostat/galvanostat (Model 283). The impedance results are shown in Table 6.
Table 6
| Coating | |
| Composition according to invention | |
| Commercial material 1 ("tape" type) | |
| Commercial material 2 (liquid) |
This test revealed that the composition according to the invention has better corrosion protective characteristics than the commercially available materials.
A wrapping tape comprising the composition according to the invention (total thickness 1.8 mm; polyethylene film used as backing) was applied to a cleaned (St-2 level according to NEN-EN-ISO standard 8501-1) steel pipe surface by wrapping spirally without tension. The subsequent turns had an overlap of about 10 mm. Next a PVC film (thickness 0.5 mm; 50 % overlap of the turns) was applied using tension ensuring good contact between the composition according to the invention and the surface of the steel pipe. A holiday test at 20 kV revealed that holidays were not present
Further evaluations were performed according to the European Standard EN 12068, "External organic coatings for the corrosion protection of buried and immersed steel pipelines used ion conjunction with cathodic protection - Tapes and Shrinkable Materials", 1998. The composition according to the invention was compared to the C-class products (highest class). Impact resistance tests (ASTM G14) showed an impact resistance of 16.8 Joule (requirement at least 15 Joule). Indentation resistance tests revealed a residual thickness after indentation of 0.74 mm (requirement at least 0.6 mm). The electrical insulation resistance was at least 1.15 x 108 ohm.m-2 (requirement at least 108 ohm.m-2). Cathodic Disbonding tests (ASTM G 95 and ASTM G 8) revealed a disbonding of 3.1 mm at room temperature and 6.8 mm at 50°C (requirement less than 10 mm which is the most stringent requirement).
Claims (17)
- Use of a composition comprising:(a) a polyisobutene having a glass transition temperature of less than -20°C and surface tension of less than 40 mN/m at a temperature above the glass transition temperature of said polyisobutene,(b) a filler material, and(c) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol.for the protection of a shaped article against corrosion.
- Use according to claim 1, wherein the sterically hindered phenol compound comprises at least two sterically hindered phenol groups.
- Use according to claims 1 or claim 2, wherein the secondary anti-oxidant is selected from the group consisting of phosphites and thioesters.
- Use according to any one of claims 1 - 3, wherein the anti-oxidant composition further comprises a lactone.
- Use according to any one of the preceding claims, wherein the shaped article is an oil or gas line or pipe.
- Wrapping tape for the protection of a shaped article against corrosion, wherein the wrapping tape comprises:(a) a first layer comprising a film, said film comprising a polymer or a copolymer of one or more α-olefins and/or diolefins, and(b) a second layer comprising a composition comprising:(i) a polyisobutene having a glass transition temperature of less than - 20°C and surface tension of less than 40 mN/m at a temperature above the glass transition temperature of said polyisobutene,(ii) a filler material, and(iii) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t butyl-4-methylphenol.
- Wrapping tape according to claim 6, wherein the total thickness of the wrapping tape is 1,0 to 3.0 cm.
- Process for the manufacturing of a wrapping tape wherein a composition is laminated onto a film, said film comprising a polymer or a copolymer of one or more α-olefins and/or diolefins and said composition comprising;(a) a polyisobutene having a glass transition temperature of less than -20°C and surface tension of less than 40 mN/m at a temperature above the glass transition temperature of said polyisobutene,(b) a filler material, and(c) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2,6-di-t-butyl-4-methylphenol.
- Process according to claim 8, wherein the total thickness of the wrapping tape is 1.0 to 3.0 cm.
- A shaped article comprising the composition according to any one of claims 1 -5 or comprising the wrapping tape according to claim 6 or claim 7 or comprising the wrapping tape obtainable by the process according to claim 8 or claim 9.
- Shaped article according to claim 10, wherein the shaped article is an oil or gas line or pipe.
- Process for covering a shaped article with a wrapping tape, wherein the wrapping tape comprises:(a) a first layer comprising a film, said film comprising a polymer or a copolymer of one or more α-olefins and/or diolefins, and(b) a second layer comprising a composition comprising:(i) a polyisobutene having a glass transition temperature of less than - 20°C and surface tension of less than 40 mN/m at a temperature above the glass transition temperature of said polyisobutene,(ii) a filler material, and(iii) an anti-oxidant composition, wherein said anti-oxidant composition comprises a primary and a secondary anti-oxidant, the primary anti-oxidant being selected from the group consisting of sterically hindered phenol compounds, provided that the sterically hindered phenol compound is not 2.6-di-t-butyl-4-methylphenoI.
- Process according to claim 12, wherein the surface of the shaped article is cleaned to a St-2 level according to NEN-EN-ISO Standard 8501-1 prior to the application of the wrapping tape.
- Process according to claim 12 or claim 13, wherein the wrapping tape is wrapped around the shaped article such that subsequent layers of the wrapping tape overlap each other.
- Process according to any one of claims 12 - 14, wherein after the wrapping tape has been applied, an outerwrap film is wrapped around the shaped article.
- Process according to claim 15, wherein the outerwrap film is selected from films comprising one or more polyolefins.
- Process according to claim 16, wherein the polyolefin is selected from the group consisting of ethylene homopolymers, ethylene copolymers, ethylene vinylchloride copolymers, ethylene vinylacetate copolymers.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03077214.9 | 2003-07-14 | ||
| EP03077214 | 2003-07-14 | ||
| PCT/NL2004/000510 WO2005005528A1 (en) | 2003-07-14 | 2004-07-14 | Composition for the protection of a shaped article against corrosion |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HK1085230A1 HK1085230A1 (en) | 2006-08-18 |
| HK1085230B true HK1085230B (en) | 2007-10-18 |
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