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Publication numberUS3714111 A
Publication typeGrant
Publication dateJan 30, 1973
Filing dateAug 31, 1970
Priority dateAug 31, 1970
Publication numberUS 3714111 A, US 3714111A, US-A-3714111, US3714111 A, US3714111A
InventorsJ Economy, R Clark
Original AssigneeCarborundum Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Ablative composites containing novolac fibers
US 3714111 A
Abstract
A composite comprising a charrable resin or plastic reinforced by fibers prepared from the resin condensation products of phenols and aldehydes which can be fiberized and cured.
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Description  (OCR text may contain errors)

United States Patent [1 1 Economy et al.-

ABLATIVE COMPOSITES 1 CONTAINING NOVOLAC FIBERS Inventors: James Economy, Eggertsville; Rodger A. Clark, Youngstown, both of NY.

The Carbort'mbum Niagara Falls, NY.

Filed: Aug. 31, 1970 Appl. No.1 68,577

, Related U.S. Application Data Continuation of Ser. No. 764,73l, Oct. 3, 1968, abandoned.

Assignee: Company,

US. Cl 260/38, 260/D1G. 23 Int. Cl. .l ..C08k l/80 Field of Search ..260/38, DIG. 23

[ Jan. 30, 1973 OTHER PUBLlCATlONS H. A. Pohl, Reaction Spinning of Fibers," Textile Research Journal, June 1958 pp. 473-477.

Primary Examiner-Morris Liebman Assistant ExaminerS. M. Person Att0rney1(. W. Brownell A composite comprising a charrable resin or plastic reinforced by fibers prepared from the resin condensation products of phenols and aldehydes which can be fiberized and cured.

ABSTRACT 7 Claims, 1 Drawing Figure PATENIEflJAuaolms ABLATION OF COMPOSBTES BY OXYACETYLENE TORCH (approximate Wmpemium 2500 6) Carbon Fimws- /Snfl|ca Fubws- Phenolic Bonded Dm'usih L? Bonded DensiW 3 L35 Phenoli Fibws Phenoflic Bondad I I I I I DensijiwLO 8... :25;; moi v.95

IO 3O 4O 5O 6O 89 90 TIME (seconds) mm Appflicaflon of Twch INVENTORS JAMES ECONOMY *0 Hon? Face BY RODGER A. CLARK Arrow/v5) ABLATIVE COMPOSITES CONTAINING NOVOLAC FIBERS This is a continuation of application Ser. No. 764,731, filed October 3, 1968 and now abandoned.

THE BACKGROUND Composites are two-phase materials in which fibers that have excellent tensile strength are bonded by a matrix phase. When the composite is deformed under loads the fibers are constrained to take up the same deformation as the matrix phase thus effectively reinforcing the matrix. In addition, the presence of fibers helps to retard the propagation of cracks and thus to produce a material which is tough as well as of high strength. Organic resins are occasionally strengthened with organic polymer fibers, some of which are very strong with good strength to weight ratios. These composites must be used at room temperature because organic polymer fibers lose strength rapidly at temperatures only slightly above room temperature. For this reason,'r'nost plastics have been reinforced by glass fibers, asbestos fibers or carbon fibers.

Composites have been used in various structural and friction applications. An exotic use of composites is as ablative structures. The ablative structures are used primarily to enable the reentry of rockets and satellites. Other applications include the protection of rocket nozzle structures from attrition by hot propellant gases and the insulation of rocket motor case structures from the heat from the burning propellant.

The materials that have been found most useful for ablating heat protection systems for reentry vehicles and rocket nozzles usually do not merely melt or sublime in response to heating but rather decompose to give large volumes of gas leaving a porous refractory residue. When such materials are exposed to a stream of hot gas the surface temperature rises to the decomposition temperature of the material which then begins to char or carbonize and evolve rather low molecular weight gases. Then the interface between the char layer and the virgin material moves into the material away from the hot face. During this period, gases generated in the course of the char forming process move through the char and absorb heat. These heated gases are then ejected. As the char layer thickens, the amount of heat reaching the moving interface is reduced by the insulating effect of the porous char combined with the cooling effect of the diffusing gases. As a result, the surface temperature of the char eventually rises until the char itself begins to ablate.

The usefulness of an ablating material does not depend altogether on the rateof ablation, but rather on the net ability to prevent heat from the environment from damaging the structure or payload on which it is applied. The effect of this in a given composite may depend on the temperature of the hot face. That is, composites of one composition may be superior at temperatures between 2,000 and 3,000 C but inferior to other composites at higher temperatures and vice versa.

According to this invention, there is provided an organic polymer fiber reinforced plastic or resin composite which does not rapidly lose strength on heating above room temperature and which has outstanding ablation properties.

THE INVENTION Composites with superior ablating properties according to this invention comprise a charrable resin reinforced by fibers prepared from the resin condensation products of phenols and aldehydes which can be fiberized and cured. (Hereafter, these synthetic fibers will be referred to as phenolic fibers.) Preferably, the charrable resin is a phenolic resin. Alternatively, any other resin which produces a high char yield may be used, such as furane resins or polybenzimidaz'ole resins. To a certain extent the fibers may include not only phenolic fibers but, in addition thereto, asbestos, glass, silica, boron nitride, or carbon fibers or other similar refractory fibers which do not degrade below about 500 C. It is also permissible to include limited quantities of some other fibers, such as polyamides, in the composite. This, of course, depends on the particular application.

The figure is a graph comparing the ablation properties of several composites described in detail hereinafter.

Phenolic resins are prepared by the condensation reaction between phenols and aldehydes. The most common reactants are phenol, itself, and formaldehyde. The various phenols and aldehydes that can be used to make phenolic resins are well-known. See, for example, Phenolic Resins by D. F. Gould, Reinhold Publishing Co., New York (1959). The condensation reaction proceeds very slowly in the absence of a catalyst.

When alkaline catalysts are used and the molar ratio of formaldehyde to phenol is greater than l:l, the primary reaction products are phenol alcohols which are called resoles. When acid catalysts are used and the molar ratio of formaldehyde to phenol is somewhat less than 1:1, the primary reaction products are probably also phenol alcohols but they rearrange rapidly to yield diphenyl methane derivatives to which the name novolac has been given Resoles are thermal setting whereas novolacs are permanently fusible. However, novolacs can be cured by treatment with aldehydes or hexamethylene tetramine, among others, in the presence of an appropriate catalyst. The fundamental difference between resoles and novolacs is the presence of one or more free methylol groups on the former; it is through reactions of these methylol groups that the cross-linking occurs.

Phenolic fibers can be made from resoles and novolacs or combinations of each in varying proportions. Additives and modifiers, either reactive or nonreactive, can be used to alter the fiber characteristics either for attenuation or the end use properties. When resoles are used as a starting material, they should be dried prior to fiberization. The fibers may be drawn from a viscous mass or may be formed by forcing the viscous mass into a turbulent air stream. Heating will cause curing of the resoles. Novolacs may be fiberized in a similar manner. When a pure novolac is fiberized, curing is accomplished by treating the fibers with an aldehyde in the presence of an appropriate catalyst. Fibers can be made from novolacs according to the process described in US. patent application Ser. No.

Composite phenolic fiber-resin structures can be fabricated by mixing the fibers with the uncured resins prior to casting or shaping. The ratio of fiber to resin matrix can be varied to obtain optimum results. Preferably, the fibers should constitute at least about 35 percent, by volume, of the composite. Practically, the maximum attainable fiber content is about 85 percent by volume.

Composites according to the teachings of this invention have outstanding properties even at elevated temperatures. The ultimate tensile strength of phenolic fibers is three to six times the strength of the bulk phenolic resins. The fibers have a modulus of elasticity at least as high as or greater than the bulk resin. Therefore, on deformation the fibers being constrained to take up the deformation of the matrix effectively reinforce the matrix. The strength and the modulus of elasticity of phenolic fibers is about the same at 250 C as at room temperature. At even higher temperatures,

the phenolic fibers char or carbonize resulting in car-.

bon fibers that have even higher tensile strengths. Other organic fibers rapidly lose their strength on heating above room temperature. The very best polyamide fibers retain their strengths only to temperatures of about 225 C and at about 325 C decompose into a friable char. Hence, composites according to the teachings of this invention, maintain good tensile strengths on heating. This is especially important where the composites are used as ablating materials as well as in many other applications.

The following experiments demonstrate that phenolic fiber composites having a phenolic resin matrix have excellent ablative properties. Specimens of the following composites were prepared:

Fibers Matrix Density Carbon Phenolic resin 1.35 gm/cc Silica Phenolic resin 1.70 gm/cc Phenolic resin Phenolic resin 0.5 gm/cc Phenolic resin Phenolic resin gm/cc measured and plotted against time after application of the torch to the front face. The results of this test are shown graphically in FIG. 1. The figure shows that phenolic fibers bonded with phenolic resins excelled in their capacity to maintain low back face temperatures over long times. The denser phenolic fiber-phenolic resin composite was superior to the less dense composite. The temperature of the oxyacetylene flame in this experiment is estimated between 2,200 and 2,700 C or about 2,500 C. It had been considered that organic fiber containing composites were inferior to silica or carbon fiber containing composites in this temperature range.

Phenolic fibers in phenolic resin matrices are superior to other organic fiber fillers as they do not generate gas prior to the time at which the matrices begin to degrade. Where the organic fiber starts to generate gas prior to the time the matrix begins to degrade and develop porosity, pressure build-ups are caused in the composites which can result in premature failure of the composite.

Having thus described our invention in detail and with the particularity required by the patent laws, what is desired to have covered by Letters Patent is as follows.

We claim:

1. A composite comprising a charrable resin reinforced by cured phenolic fibers prepared from novolac resin condensation products of phenols and aldehydes which can be fiberized and cured.

2. A composite according to claim 1 in which the charrable resin is a phenolic resin.

3. A composite according to claim 1 which comprises, in addition to phenolic fibers, refractory fibers that do not degrade below about 500 C.

4. A composite according to claim 1 which comprises in addition to the phenolic fibers, fibers selected from the group consisting of asbestos, glass, silica, boron nitride and carbon and mixtures thereof.

5. A composite according to claim 1 in which the fibers are present in an amount of from about 35 percent to about percent by volume of the composite.

6. A composite according to claim 2 having a density in excess'of 0.5 gm/cc.

7. An ablative heat shield comprising a composite according to claim 1.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US3314915 *Nov 2, 1962Apr 18, 1967Taylor CorpMolding composition for making thermal barriers and method of making same
US3553002 *Jul 31, 1967Jan 5, 1971NasaThermal protection ablation spray system
Non-Patent Citations
Reference
1 *H. A. Pohl, Reaction Spinning of Fibers, Textile Research Journal, June 1958 pp. 473 477.
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4267285 *Aug 20, 1979May 12, 1981Broutman L JComposites of polymeric material and thermosetting resinous fibers and particles and method
US4330442 *May 7, 1980May 18, 1982Armstrong World Industries, Inc.Asbestos free gasket forming compositions
US5401793 *Mar 18, 1992Mar 28, 1995Dainippon Ink And Chemicals, Inc.Intumescent fire-resistant coating, fire-resistant material, and process for producing the fire-resistant material
CN101290836BJun 13, 2008Sep 29, 2010陕西师范大学Method for enhancing specific capacitance of phenolic resin based activated carbon fiber
WO1983000338A1 *Jul 22, 1982Feb 3, 1983Martin Marietta CorpRefractory hard material-carbon fiber cathode coatings for aluminum reduction cells
Classifications
U.S. Classification523/138, 260/DIG.230, 524/404, 524/593, 523/179
International ClassificationC08J5/04
Cooperative ClassificationY10S260/23, C08J5/04
European ClassificationC08J5/04
Legal Events
DateCodeEventDescription
Jun 25, 1987ASAssignment
Owner name: KENNECOTT MINING CORPORATION
Free format text: CHANGE OF NAME;ASSIGNOR:KENNECOTT CORPORATION;REEL/FRAME:004815/0036
Effective date: 19870220
Owner name: STEMCOR CORPORATION, 200 PUBLIC SQUARE, CLEVELAND,
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:KENNECOTT MINING CORPORATION;REEL/FRAME:004815/0091
Effective date: 19870320
Jul 1, 1981ASAssignment
Owner name: KENNECOTT CORPORATION
Free format text: MERGER;ASSIGNORS:BEAR CREEK MINING COMPANY;BEAR TOOTH MINING COMPANY;CARBORUNDUM COMPANY THE;AND OTHERS;REEL/FRAME:003961/0672
Effective date: 19801230