US3558417A - Water-repellant resinous foam - Google Patents

Water-repellant resinous foam Download PDF

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Publication number
US3558417A
US3558417A US3558417DA US3558417A US 3558417 A US3558417 A US 3558417A US 3558417D A US3558417D A US 3558417DA US 3558417 A US3558417 A US 3558417A
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United States
Prior art keywords
foam
water
raft
repellant
zinc stearate
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Expired - Lifetime
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Inventor
Ival O Salyer
James L Schwendeman
Charles E Mcclung
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Monsanto Research Corp
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Monsanto Research Corp
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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/14Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36After-treatment
    • C08J9/365Coating
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249987With nonvoid component of specified composition

Abstract

A BUOYANT MEMBER FOR A COLLAPSIBLE BUOYANT DEVICE, COMPRISING (1) AN INNER OPEN-CELL FLEXIBLE RESINOUS FOAM SURFACE-COATED WITH A COMPOUND SELECTED FROM THE GROUP CONSISTING OF STEARIC ACID, LEAD STEARATE, AND ZINC STEARATE AND (2) AN OUTER WATER-IMPERMEABLE MEMBRANE.

Description

United States Patent Patented Jan. 2.6, 1971 3,558,417 WATER-REPELLANT RESINOUS FOAM [Va] 0. Salyer, James L. Schwendeman, and Charles E.
McCluug, Dayton, Ohio, assignors to Monsanto Research Corporation, St. Louis, Mo., a corporation of Delaware No Drawing. Filed Feb. 14, 1968, Ser. No. 705,312
Int. Cl. B32b 7/00; B44d 1/08, 1/94 US. Cl. 161-160 4 'Claims ABSTRACT OF THE DISCLOSURE A buoyant member for a collapsible buoyant device, comprising (1) an inner open-cell flexible resinous foam surface-coated with a compound selected from the group consisting of stearic acid, lead stearate, and zinc stearate and (2) an outer water-impermeable membrane.
The invention herein described was made in the course of or under a contract or subcontract thereunder, with the Department of Navy.
BACKGROUND OF THE INVENTION This invention pertains to a foamed synthetic resin which has been surface-treated to render it water-repellant and compression-set-resistant, and more particularly to an open-cell flexible urethane foam treated with stearic acid, lead stearate, or zinc stearate. It further pertains to an improvement in a life raft wherein the buoyant member is collapsible and resistant to compression set at moderately elevated temperatures.
For certain applications such as floats, buoys, life rafts, life preservers, etc., open-cell flexible resinous foams have inherent advantages of flexibility, compactibility, lightness, buoyancy, etc. For such uses they may be enclosed in water-impermeable covers such as rubberized fabric. One disadvantage is that their open-cell structure is permeable to liquids and they may quickly become water-logged if the outer cover is torn. A further disadvantage is that, although they are easily compactible by compression and folding, they may develop compression set if stored at moderately elevated temperatures, say 60-80 C. (140- 180 F.)
Life rafts utilizing a buoyant member, such as a flotation tube, are well-known (e.g., the PK-2 raft of Specification MilL-I8664A(Aer)). -In the past the flotation tube has been filled with a gas when the raft was deployed.
SUMMARY OF THE INVENTION An object of this invention is to provide a waterrepellant, compression-set-resistant open cell flexible urethane foam. Another object is to provide a buoyant member for a collapsible life raft, utilizing water-repellant, compression-semesistant open cell flexible urethane foam.
These and other objects hereinafter defined are met by the invention wherein there is provided a composition comprising an open-cell flexible resinous foam surfacecoated with a compound selected from the group consisting of stearic acid, lead stearate, and zinc stearate.
Although the invention is directed particularly to urethane foams, it encompasses any other flexible resinous foams. Thus, foams of rubber, cellulose acetate, polyvinyl chloride, styrenebutadiene copolymers, etc., may be used in combination with stearic acid or zinc stearate. For optimum water-repellancy it is preferred that the pore size of the foam be smaller than about 1 mm.
The process for surface-treating the foam is simply to coat the foam with a solution or suspension of stearic acid, lead stearate, or zinc stearate in a low-boiling organic liquid and evaporate off the liquid. To avoid dusting problems the coating may be heated above the melting point of the stearic acid (melting point 69 (3.), lead stearate (melting point C.) or zinc stearate (melting point (3.). The add-on of the coating may be in the range of 3 to 30% by weight of the foam, but preferably 5 to 20%. Other methods of application include dusting the powdered additive over the surface, followed by a melting step to cause adherence; or immersion of the foam in molten additive.
The treated foam is both water-repellant and compression-set-resistant. It may be collapsed and stored for many days, even at moderately high temperatures where compression set would normally be objectionable within a few days, thereafter quickly and positively snapping back to its full extended shape when released. It is water-repellant and resists the normal capillary flow of water through its porous structure.
In utilizing the surface-treated foam in a life raft, the surface-coated foam serves as the inner part of a buoyant member as flotation tube. Itis preferably enclosed in an outer thin, low-density, water-impermeable, flexible membrane, e.g., a barrier such as a film, or coated or rubberized cloth. To allow compressing and expanding, the cover may contain air vents which are closeable or scalable. The buoyant member may encircle a circular or somewhat elliptical shaped area and may be provided with a floor consisting of a water-impermeable fiexible fabric. The entire assembly may be collapsed into a relatively small volume for storage, from which it is readily deployed into full volume for use.
The surface-coated foam may also be used in floats, buoys, life preservers, buoyant vests, buoyant jackets, etc.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The invention is further illustrated by, but not limited to, the following examples.
Example 1 This example illustrates the block foam test for waterproofing.
iBlocks of urethane open-cell foam measuring 2 in. x 4 in. x 8 in. were cut from larger blocks. The properties of the foam were as follows:
Density (lb./cu. ft.) 1.59 Tensile strength (p.s.i.) 10.0 Elongation (percent) 175.0 Compression set (percent) at 90% compression 15.0 Cell size (cells/linear inch) 50-60 Open cells (percent) 90-95 Block No. 1 was left untreated for a control. Block No. 2 was treated with a coating of stearic acid by saturating the foam with a 5% by weight solution of stearic acid in hexane and allowing the hexane to evaporate. The add-on was estimated to be about 5.0%. Block No. 3 was treatel with a coating of zinc stearate by spraying with a zinc stearate dry powder mold release spray. The add-0n was estimated to be about 5.0%.
A comparison of the effectiveness in water-proofing was made by floating the blocks on calm water. The depth of foam immersion was noted after 21 days as follows: No. 1, 1.5 inch; No. 2, none; No. 3, none.
Example 2 This example illustrates the /a-scale model life raft test.
A model raft was constructed to one-third linear scale of the Navy PK-2 life raft (MILI-8664A(Aer)). The full-size raft is approximately 3' wide x 5' long in size. A nylon base cloth or bottom cloth was used for the 3 floor as specified in MIL-C-21109. An encircling'buoyant tube fabricated from nylon fabric, Specification MIL-C- 6819, served as a gunwale. Inside the tube was a core of open-cell flexable urethane form having the properties tabulated in Example 1. All joints and laps of the fabric were sealed with cement, Specification MILC-5539.
Prior to closure within the buoyant tube, the urethane foam was surface-coated with zinc stearate by saturating with a by weight suspension of zinc stearate in hexane, and the hexane removed by evaporation. The add-on of Zinc stearate was about The model raft floated easily in water and was capable of supporting a 10 lb. weight even when the raft was filled with water to its topsides. The 10 lb. load is equivalent to a 270 lb. load on the full-size raft.
To test the buoyancy of the raft when the outer fabric was torn, a cut was made 1 /2 inches in length on the bottom side of the buoyant tube. This permitted water to enter the foam-filled buoyancy chamber. To further simulate service conditions, the water on which the raft floated was agitated as short choppy waves. Under these conditions the raft and 10 lb. load remained afloat for the duration of the test (11 days).
By comparison, a model raft which contained untreated urethane foam in the buoyant tube sank within several hours after a 1 /2 inch cut was made on the bottom side of the buoyant tube.
Example 3 where:
C=compression set t =original thickness t =thickness after removal from clamp r =thickness of spacer bar in clamp Blocks of open-cell flexible polyurethane foam having the properties tabulated in Example 1 were cut, measuring 2 in. x 4 in. x 4 in. Block No. l was tested with no surface treatment. Block No. 2 was treated with a surface coating of zinc stearate by the procedure of Example 2. The
estimated add-on was about 5.0%. Each block was compressed by clamps to 10% of its original height, i.e., to 0.2 inch. It was then stored at 71 C. (160 F.) for 56 days under compression. At the end of this time the clamps were removed and the height measured (a) immediately upon release and (b) after 1 hour. Results for the two blocks are summarized in the following table:
COMPRESSION SET (PERCENT) Measured i\'leasurcd immediately after 1 hr.
Untreated foam 95 Zinc stearate treated foam 22 17 It is to be understood that although the invention has r been described with specific reference to particular embodiments thereof, it is not to be so limited since changes and alterations therein may be made which are within the full intended scope of this invention as defined by the appended claims.
What we claim is:
1. A composition comprising an open-cell flexible resinous foam surface-coated with a compound selected from the group consisting of stearic acid, lead stearate,
F and zinc stearate.
References Cited UNITED STATES PATENTS 2,642,920 6/1953 Simon et al. 16l--l90 WILLIAM J. VAN BALEN, Primary Examiner US. Cl. X.R.
96, 11; ll7138.8, 167; 161-164, 190, 411; 260-2.S
US3558417D 1968-02-14 1968-02-14 Water-repellant resinous foam Expired - Lifetime US3558417A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3675377A (en) * 1970-09-02 1972-07-11 Goodyear Tire & Rubber Inflatable-deflatable flexible structural component
US3984887A (en) * 1974-07-23 1976-10-12 Keigo Tanemoto Portable collapsible boat
US4161460A (en) * 1974-11-08 1979-07-17 R. B. Cybernetris (1970) Ltd. Method of enhancing oleophilic and hydrophobic properties of absorbent material
US4194041A (en) * 1978-06-29 1980-03-18 W. L. Gore & Associates, Inc. Waterproof laminate
USRE31898E (en) * 1970-09-02 1985-05-28 Goodyear Aerospace Corporation Inflatable-deflatable flexible structural component

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3675377A (en) * 1970-09-02 1972-07-11 Goodyear Tire & Rubber Inflatable-deflatable flexible structural component
USRE31898E (en) * 1970-09-02 1985-05-28 Goodyear Aerospace Corporation Inflatable-deflatable flexible structural component
US3984887A (en) * 1974-07-23 1976-10-12 Keigo Tanemoto Portable collapsible boat
US4161460A (en) * 1974-11-08 1979-07-17 R. B. Cybernetris (1970) Ltd. Method of enhancing oleophilic and hydrophobic properties of absorbent material
US4194041A (en) * 1978-06-29 1980-03-18 W. L. Gore & Associates, Inc. Waterproof laminate

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