Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/38—Boron-containing compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
  • C08K3/04—Carbon
• • 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
  • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
  • C09D5/18—Fireproof paints including high temperature resistant paints
• • 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
  • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
  • C09D5/18—Fireproof paints including high temperature resistant paints
  • C09D5/185—Intumescent paints
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S428/00—Stock material or miscellaneous articles
  • Y10S428/92—Fire or heat protection feature
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S428/00—Stock material or miscellaneous articles
  • Y10S428/92—Fire or heat protection feature
  • Y10S428/921—Fire or flameproofing

Definitions

• This invention relates to thermal protective compositions which form chars when exposed to fire or other thermal extremes.
• the invention is particularly well suited to use in solvent-based, thin-film intumescent coatings for substrates, but its usefulness is not limited thereto.
• compositions which provide protection against fire and other thermal extremes, such as temperatures above about 300° C.
• Some ofthe compositions are foamed inorganic passive insulative compositions which protect merely by their low thermal conductivity and their thickness as applied. These include, for example, foamed cement or intumesced silicates.
• the present invention is not concerned with such systems, but with systems which include a polymeric binder and which form a char when exposed to fire or hyperthermal conditions.
• the char-forming compositions may operate by various modalities.
• the compositions may be used in various forms, including thick film (mastic) coatings, thin film coatings, castings, extrusions, and others.
• the compositions may include organic or inorganic binders and various additives.
• the compositions Upon exposure to heat the compositions slowly lose weight as portions ofthe composition are volatilized, and a char is formed which provides a measure of protection against the transfer of heat energy.
• the char is consumed by physical erosion and by chemical processes, primarily oxidation by oxygen in the air and by free radicals produced by the coating or otherwise in a fire environment, and protection is lost.
• the length of time required for a given temperature rise across a predetermined thickness of the composition, under specified heat flux, environmental, and temperature conditions, is a measure ofthe effectiveness ofthe composition in providing thermal protection.
• different coatings behave differently. Ablative coatings swell to less than twice their original thickness. They provide limited passive thermal protection, but they tend to produce dense chars having good physical and chemical resistance.
• Intumescent coatings swell to produce a char more than five times the original thickness ofthe coating.
• This char provides an insulative blanket which provides superior thermal efficiency, but at the cost of some ofthe physical and chemical properties of the ablative coatings.
• the char of the intumescent materials tends to form coarse and irregular cell structures, cracks, and fissures as it expands, and the char may not expand uniformly at corners, leaving areas where the char provides far less protection than the average thermal protection of the underlying structure.
• Examples of the intumescent systems include silicate solutions or ammonium phosphate paints or mastic compositions such as those disclosed in Nielsen et al., U.S. Patent 2,680,077, Kaplan, U.S. Patent 3,284,216, or Ward et al., U.S. Patent 4,529,467.
• a third type of char-forming coating is disclosed in Feldman, U.S. Patent
• these compositions When subjected to thermal extremes, these compositions both undergo an endothermic phase change and expand two to five times their original thickness to form a continuous porosity matrix.
• These coatings tend to be tougher than intumescent coatings. They provide far longer thermal protection than ablative coatings, frequently longer than intumescent coatings, in part because the gasses formed by the endothermic phase change provide active cooling as they work their way through the open-cell matrix. These coatings may also have a tendency to crack and form voids and fissures.
• the present invention relates primarily to intumescent systems, particularly thin-film intumescent coating systems, i.e., those having a thickness as applied of less than five millimeters.
• intumescent systems particularly thin-film intumescent coating systems, i.e., those having a thickness as applied of less than five millimeters.
• Several aspects ofthe invention are also applicable to thick film intumescent compositions and to the Feldman type compositions which undergo an endothermic phase change and swell two to five times their original thickness.
• Some aspects ofthe invention are also applicable to ablative char-forming coatings.
• One object ofthe present invention is to provide char-forming compositions which provides better thermal efficiencies than previously known compositions.
• Another object is to provide such compositions which can be applied as a thin film to a substrate, but which provide remarkably long protection times to the underlying substrate.
• Another object is to provide such compositions which in both their applied form and as chars have a high degree of physical toughness and chemical integrity including adhesion and cohesion properties. Another object is to provide such compositions which in both their applied form and as chars resist oxidation and chemical attack.
• Another object is to provide such compositions which when exposed to fire and thermal extremes swell in all directions, to protect corners around which they are applied. Another object is to provide such compositions which resist cracking when exposed to fire and thermal extremes.
• a char- forming thermal protective composition comprising a binder, a source of carbon, and 0.5 to 10% elemental boron.
• the binder is one source of carbon, and more preferably an additional carbon source is provided such as in the form of chopped organic fibers like acrylonitrile fibers, or graphite, dispersed in the binder.
• the binder is preferably an organic polymer, most preferably a the ⁇ noplastic resin.
• the elemental boron comprises at least 2% by weight of the composition. The elemental boron provides unexpectedly high resistance to oxidation of the char, increasing the residual weight and strength of the char. In certain formulations, it has been found that the composition surprisingly gains weight and builds a tough, uniform char when heated from 750° to 850° C in the presence of oxygen. This aspect of the invention is applicable to numerous char-forming thermal protective systems.
• a thermal protective composition comprising a binder which softens when exposed to thermal extremes, a blowing agent which forms a gas when exposed to thermal extremes, and a drying oil.
• the oil is an unsaturated triacylglycerol or a conjugated fatty acid, most preferably a conjugated triglyceride.
• the unsaturated triacylglycerol contains from two to three conjugated double or triple bonds per chain, each chain having from twelve to twenty carbon atoms, illustratively oiticica oil containing licanic acid (4-keto-9,l l,13-octadecanoic acid) and isano oil containing isanic acid (17- octadecene-9,ll-diynoic acid).
• the conjugated drying oil reduces the surface tension of the coating and provides a blowing agent which begins to swell the composition at a lower temperature than would otherwise occur, thereby stretching the boundary between heat source and substrate quickly and forming a greater heat gradient to keep the substrate cool.
• a mixture of triglyceride fatty acids is employed in order to provide control of these properties.
• the mixture may include, for example, equal parts of oiticica oil, castor oil as an aerating agent, and linseed oil as a plasticizer and flow agent.
• a thermal protective composition comprising a binder which softens when exposed to thermal extremes, a blowing agent which forms a gas when exposed to thermal extremes, and a mixture of a metal salt of a medium chain (ten to thirty carbon) carboxylic acid with a metal oxide.
• the metal carboxylate is preferably a salt of a T-2 metal, most preferably zinc or copper stearate, and the metal oxide is preferably alumina.
• This additive provides a foam which spreads omnidirectionally to fill in exterior corners more effectively than previously known coatings.
• Combinations of the different aspects of the invention have been found to provide thin film coatings which yield remarkably thick chars, on the order of ten to thirty times the thickness of the original coating. These chars provide unexpected thermal efficiency; fine, uniform closed cell structure; greatly increased protection of corners and edges of underlying substrates; resistance to cracking and fissures; physical toughness; and resistance to oxidation.
• the preferred embodiments ofthe invention are solvent-based (as opposed to water- based or latex) systems, in which coatings having thicknesses on the order of 0.8 millimeters have been found to protect columns for an hour under the heating conditions of ASTM E-119.
• the additives of the present invention provide many of the same advantages without producing the thick, closed-cell chars of the thin film coatings.
• FIG. 1 is a graphical representation of the heating of a column section coated with 0.905 millimeters of a prior art thin film coating when exposed to an ASTM E-119 fire curve.
• FIG. 2 is a graphical representation of the heating of a column section coated with 0.802 millimeters of a thin film coating of the present invention when exposed to an ASTM E- 119 fire curve.
• FIG. 3 is a sectional view of a column, showing a thermal protective intumescent coating applied as a thin film to the column.
• FIG. 4 is a sectional view of the column of FIG. 3, coated with a prior art composition, after exposure to a thermal extreme.
• FIG. 5 is a sectional view of the column of FIG. 1, coated with a composition ofthe present invention, after exposure to a thermal extreme.
• FIG. 6 is a graphical representation of the effect of different percentage weights of elemental boron on a graphite cloth as a result of undergoing a thermogravimetric analysis.
• a drying oil additive consisting of equal mixture by volume of oiticica oil, castor oil, and linseed oil
• a metal stearate/metal oxide additive consisting of 5 parts of zinc stearate, 3 parts of alumina, together with small amounts of rheology agents, deaerating agents, and bentonite.
• the standard material was applied to a generally uniform thickness averaging 0.905 millimeters to a first W10x49 column section and a slightly thinner coating (average thickness 0.802 millimeters) of the material of the present invention was applied to an identical column section.
• the coatings were cured, and each column section was exposed to a standard ASTM E-119 simulated fire.
• Such a fire simulation involves the use of a flame whose temperature is continuously increased to 927°C (1700°F) during a one-hour period; the end point ofthe test occurs when the average temperature ofthe steel substrate reaches 538°C (1000° F).
• the ASTM furnace temperature is indicated by numeral 1
• the measured furnace temperature by numeral 3 triangles
• the temperature of a flange edge by numeral 5 the temperature of a flange by numeral 7
• the temperature of the column web by numeral 9 the average measured column temperature by numeral 11 (dots)
• the slope ofthe average column temperature by numeral 13 The column coated with the standard composition lasted just less than 30 minutes, but the column coated with the material ofthe present invention lasted one hour before the end point ofthe test was reached.
• the superiority of the composition of the preferred embodiment of the present invention is shown most clearly by the curve 13 in FIGS. 1 and 2.
• the curve 13 represents the rate at which the temperature ofthe column is rising.
• the temperature of the column protected with the preferred composition of the present invention is somewhat less than the temperature of the column protected by the control composition (both being between 200° and 250° C), but its rate of heating is approximately half (about eight degrees per minute against about sixteen). From ten minutes to beyond sixty minutes, this curve shows the continued suppression ofthe rate of heat rise produced by the prefe ⁇ ed composition of this invention.
• the char left by the composition of the present invention showed far greater uniformity of cell size, without large voids, less tendency to form fissures and cracks, and expanded more uniformly around exterior corners of the column's flanges.
• the thin coating 17 of a thermal protective composition on the column 15 FIGS. 3-5.
• FIGS. 4 and 5 responds to heat by swelling as shown in FIGS. 4 and 5.
• the exterior edges of the column's flanges showed expansion of the char 19 in horizontal and vertical directions, leaving a poorly protected area, indicated by numeral 21 of FIG. 4, which heated substantially faster than the flange faces or web, reaching a temperature of 538°C in about twenty-three minutes.
• the char 23 ofthe illustrative embodiment ofthe invention expanded more than the standard and largely filled the web area of the column.
• the char expanded more uniformly radially outward, providing a far thicker protective layer 25 along the exterior edge of the flange than the layer 21 of the standard.
• the coating also started to intumesce earlier in the heating process.
• the formulation thus showed its superiority in thermal efficiency, insulation, and char integrity.
• EXAMPLE 2 FORMULATION OF SAMPLE COMPOSITIONS
• Formula B suitable for exterior applications, utilized a polyol having more hydroxyl endings than Formula A.
• To these formulations were added differing quantities of additives in accordance with the present invention.
• the drying oil (“oils”) additive and the stearate/oxide (“st/o") additive were the same as were used in Example 1.
• the quantities ofthe additives shown in the following TABLE 1 are by weight.
• thermoplastics such as styrenes, polypropylenes, polyethylenes, ABS, polyamides, polyurethanes, vinylidenes, modified epoxies and copolymers of such thermoplastics may be used. These examples are merely illustrative.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Paints Or Removers (AREA)
• Fireproofing Substances (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Carbon And Carbon Compounds (AREA)
• Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Priority Applications (10)

Applications Claiming Priority (2)

Publications (1)

Family

ID=23966805

Family Applications (1)

Country Status (15)

Cited By (2)

Families Citing this family (15)

Citations (2)

Family Cites Families (12)

• 1995
  • 1995-06-27 US US08/494,993 patent/US5591791A/en not_active Expired - Lifetime
• 1996
  • 1996-06-20 IN IN1152CA1996 patent/IN189533B/en unknown
  • 1996-06-24 IL IL11872496A patent/IL118724A/xx not_active IP Right Cessation
  • 1996-06-25 BR BR9609375-7A patent/BR9609375A/pt not_active IP Right Cessation
  • 1996-06-25 KR KR1019970709808A patent/KR100462540B1/ko not_active Expired - Lifetime
  • 1996-06-25 CN CNB021479283A patent/CN100379829C/zh not_active Expired - Lifetime
  • 1996-06-25 NZ NZ311938A patent/NZ311938A/en unknown
  • 1996-06-25 AR ARP960103315A patent/AR002599A1/es unknown
  • 1996-06-25 AU AU63355/96A patent/AU698323B2/en not_active Ceased
  • 1996-06-25 EP EP96922501A patent/EP0835281A4/en not_active Withdrawn
  • 1996-06-25 CN CN96196082A patent/CN1125847C/zh not_active Expired - Fee Related
  • 1996-06-25 JP JP9504465A patent/JPH11508623A/ja not_active Ceased
  • 1996-06-25 WO PCT/US1996/010552 patent/WO1997001596A1/en not_active Application Discontinuation
  • 1996-06-25 CA CA002220704A patent/CA2220704C/en not_active Expired - Fee Related
• 1997
  • 1997-12-23 NO NO19976059A patent/NO311606B1/no not_active IP Right Cessation
• 1998
  • 1998-01-07 MX MX9800045A patent/MX9800045A/es unknown
• 2001
  • 2001-02-15 NO NO20010765A patent/NO313202B1/no not_active IP Right Cessation

Patent Citations (2)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events