GB835801A - Improvements in or relating to mastics - Google Patents
Improvements in or relating to masticsInfo
- Publication number
- GB835801A GB835801A GB19841/57A GB1984157A GB835801A GB 835801 A GB835801 A GB 835801A GB 19841/57 A GB19841/57 A GB 19841/57A GB 1984157 A GB1984157 A GB 1984157A GB 835801 A GB835801 A GB 835801A
- Authority
- GB
- United Kingdom
- Prior art keywords
- binder
- isobutylene
- fibrous filler
- copolymer
- isobutylene polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 240000005428 Pistacia lentiscus Species 0.000 title 1
- 239000011230 binding agent Substances 0.000 abstract 10
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- 238000000576 coating method Methods 0.000 abstract 4
- 229920001577 copolymer Polymers 0.000 abstract 4
- 239000012765 fibrous filler Substances 0.000 abstract 4
- 238000009413 insulation Methods 0.000 abstract 4
- 229920000642 polymer Polymers 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000007799 cork Substances 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 abstract 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 abstract 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 2
- 229910000410 antimony oxide Inorganic materials 0.000 abstract 2
- 239000010425 asbestos Substances 0.000 abstract 2
- 229920005549 butyl rubber Polymers 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 abstract 2
- 239000008199 coating composition Substances 0.000 abstract 2
- 239000007859 condensation product Substances 0.000 abstract 2
- 239000010779 crude oil Substances 0.000 abstract 2
- 239000011928 denatured alcohol Substances 0.000 abstract 2
- 238000004821 distillation Methods 0.000 abstract 2
- 239000003063 flame retardant Substances 0.000 abstract 2
- 239000003349 gelling agent Substances 0.000 abstract 2
- 239000011630 iodine Substances 0.000 abstract 2
- 229910052740 iodine Inorganic materials 0.000 abstract 2
- 239000013521 mastic Substances 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- 238000007254 oxidation reaction Methods 0.000 abstract 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 abstract 2
- 239000012188 paraffin wax Substances 0.000 abstract 2
- 230000035515 penetration Effects 0.000 abstract 2
- 239000003208 petroleum Substances 0.000 abstract 2
- 229910052895 riebeckite Inorganic materials 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- 239000000454 talc Substances 0.000 abstract 2
- 229910052623 talc Inorganic materials 0.000 abstract 2
- 230000009974 thixotropic effect Effects 0.000 abstract 2
- KNXVOGGZOFOROK-UHFFFAOYSA-N trimagnesium;dioxido(oxo)silane;hydroxy-oxido-oxosilane Chemical compound [Mg+2].[Mg+2].[Mg+2].O[Si]([O-])=O.O[Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O KNXVOGGZOFOROK-UHFFFAOYSA-N 0.000 abstract 2
- 235000013311 vegetables Nutrition 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- 239000000080 wetting agent Substances 0.000 abstract 2
- 239000001836 Dioctyl sodium sulphosuccinate Substances 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 230000001680 brushing effect Effects 0.000 abstract 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 239000011152 fibreglass Substances 0.000 abstract 1
- 239000011494 foam glass Substances 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 239000000395 magnesium oxide Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000011490 mineral wool Substances 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 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
- F16L59/00—Thermal insulation in general
- F16L59/02—Shape or form of insulating materials, with or without coverings integral with the insulating materials
- F16L59/021—Shape or form of insulating materials, with or without coverings integral with the insulating materials comprising a single piece or sleeve, e.g. split sleeves; consisting of two half sleeves; comprising more than two segments
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D125/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
- C09D125/02—Homopolymers or copolymers of hydrocarbons
- C09D125/04—Homopolymers or copolymers of styrene
- C09D125/08—Copolymers of styrene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C09J123/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- C09J123/22—Copolymers of isobutene; Butyl rubber ; Homo- or copolymers of other iso-olefines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
Abstract
A mastic coating composition comprises a binder, said binder including from 20 to 40% of the binder of an isobutylene polymer or copolymer plasticized with from 20 to 60% of the binder of an asphaltene-free chemical condensation product obtained by subjecting a precipitated fraction of a natural paraffinic crude oil distillation residue to air oxidation having an iodine number below 40, a ball and ring softening point above 110 DEG F. and up to 200 DEG F., an average molecular weight of at least 1900, at least 40 carbon atoms per double bond, a susceptibility to penetration with temperature change of less than 2 units per DEG F. within the range of 30 DEG F. to 60 DEG F. and substantially complete solubility in 88 DEG Baume Naphtha. The isobutylene polymer may be a copolymer of isobutylene with styrene or isoprene, e.g. butyl rubber. The binder may also comprise a flame retardant such as chlorinated paraffin wax, a fibrous filler such as asbestine or asbestos, a non-fibrous filler such as micaceous talc, antimony oxide, ground vegetable cork or a gelling agent, e.g. of the bentonitic type, to render the composition thixotropic. The binder may be applied e.g. by brushing, spraying or trowelling, to form coatings on moulded and other thermal insulation in solution in an organic solvent, e.g. xylol, petroleum fraction or methyl isobutyl ketone, to which denatured alcohol or water and a wetting agent may be added to control the flow. The surface of the insulation, e.g. magnesia block, fibre glass, foam glass, mineral wool or cork board, may be covered with wire netting or a similar material such as woven glass fabric prior to coating to secure the coating to the insulation. U.S.A. Specification 2,337,336 is referred to.ALSO:A mastic coating composition comprises a binder containing from 20 to 40% of an isobutylene polymer or copolymer plasticized with from 20 to 60% of the binder of an asphaltene-free chemical condensation product obtained by subjecting a precipitated fraction of a natural paraffinic crude oil distillation residue to air oxidation, having an iodine number below 40, a ball and ring softening point above 110 DEG F. and up to 200 DEG F., an average molecular weight of at least 1900, at least 40 carbon atoms per double bond, a susceptibility to penetration with temperature change of less than 2 units per DEG F. within the range of 30 DEG F. to 60 DEG F. and substantially complete solubility in 88 DEG Baume Naphtha. The isobutylene polymer may be a copolymer of isobutylene and styrene or isoprene, e.g. butyl rubber. The binder may also comprise a flame-retardant such as chlorinated paraffin wax, a fibrous filler such as asbestine or asbestos, a non-fibrous filler such as micaceous talc, antimony oxide, ground vegetable cork or a gelling agent e.g. of the bentonitic type, to render the composition thixotropic. The binder may be applied to form coatings on moulded and other thermal insulation in solution in an organic solvent, e.g. xylol, petroleum fractions or methyl isobutyl ketone, to which denatured alcohol or water and a wetting agent, e.g. alkyl aryl polyether alcohol or dioctyl sodium sulphosuccinate, may be added to control the flow of the composition. U.S.A. Specification 2,337,336 is referred to.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB19841/57A GB835801A (en) | 1957-06-24 | 1957-06-24 | Improvements in or relating to mastics |
DEF23407A DE1192766B (en) | 1957-06-24 | 1957-07-05 | Coating agent for the production of heat-resistant coatings |
FR784014A FR1220976A (en) | 1957-06-24 | 1959-01-14 | Improvements to sealants |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB19841/57A GB835801A (en) | 1957-06-24 | 1957-06-24 | Improvements in or relating to mastics |
Publications (1)
Publication Number | Publication Date |
---|---|
GB835801A true GB835801A (en) | 1960-05-25 |
Family
ID=10136121
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19841/57A Expired GB835801A (en) | 1957-06-24 | 1957-06-24 | Improvements in or relating to mastics |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB835801A (en) |
-
1957
- 1957-06-24 GB GB19841/57A patent/GB835801A/en not_active Expired
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