US2512464A - Manufacture of sponge rubber - Google Patents

Manufacture of sponge rubber Download PDF

Info

Publication number
US2512464A
US2512464A US101250A US10125049A US2512464A US 2512464 A US2512464 A US 2512464A US 101250 A US101250 A US 101250A US 10125049 A US10125049 A US 10125049A US 2512464 A US2512464 A US 2512464A
Authority
US
United States
Prior art keywords
froth
latex
mold
electrodes
sponge
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 - Lifetime
Application number
US101250A
Inventor
James U Mann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Uniroyal Inc
Original Assignee
United States Rubber Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by United States Rubber Co filed Critical United States Rubber Co
Priority to US101250A priority Critical patent/US2512464A/en
Application granted granted Critical
Publication of US2512464A publication Critical patent/US2512464A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C08J9/30Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by mixing gases into liquid compositions or plastisols, e.g. frothing with air
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C35/00Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
    • B29C35/02Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
    • B29C35/12Dielectric heating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/3415Heating or cooling
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00Compositions of unspecified rubbers
    • 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
    • C08J2321/00Characterised by the use of unspecified rubbers
    • C08J2321/02Latex
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S264/00Plastic and nonmetallic article shaping or treating: processes
    • Y10S264/46Molding using an electrical heat
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S521/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S521/915Utilizing electrical or wave energy during cell forming process

Definitions

  • This invention relates to the manufactureof sponge rubber from latex andmore, particularly to heat-setting, ahlatexfroth by means. of a low frequencybalanced. alternating, electric current.
  • the heat-settingof. shaped. latex. froths. 0011-. taining heat-setting, agents bypassing low frequency, balanced. alternating, electric currents from electrodes through the. froths to generate the desired amount of heat in the frothtoset or gel the same,.prior tosubjectingthe gelled froth to conventional vulcanizingconditions, is, known.
  • aheatsettable latex. froth is introduced into a-mold by, forming themfroth in the mold as Joy -chemical. blowing byv evolving. ages in the latexin the mold; or by.chemically blowingthelatex in-bulk or mechanicallywhipping a body of llatex intoas froth and pouring; the. froth into individual stactionary or traveling-mold: or by pouring'or otherwise introducingthe: froth into atraveling; con-,- tinuous mold.
  • the secondelectrode could. be embedded in the body of the frothbeing molded andremoved aftergellin-g of the froth;.bumbleerally each electrode will be comprise'd in' onerofi' the twoparts of a two-part mold, usually the bodypart and the cover part.
  • the bot-'- tom and top plates of a'box type mold may-be composed of metal with the sides made of 'woodr or other insulating material, or the mold may be all made of wood-withmetal plates secured to the opposite inner faces of the top and bottom sections, the metal plates, of course, being made the electrodes for the low frequency electric current to be passed through the froth. Also, the
  • body' of the mold may be of metal 'andcomprise. one electrodaand the cover of, the moldmay also be of "metal and.comprise the other electrode, such cover and body being separated by a gasketor. spacer of insulating material, such as wood, rubberor'th'e like.
  • One or both of such electrodes. may "be made wholly of zinc or cadmium, ormay; beLmade ofany'desired'metal with a' surface coating of zinc or cadmium" on the' face'of' the elec* trode which contacts thefoam'.
  • the latex-for preparing: sponge rubbberaccordxingctorthe present invention may 'be a natural: rubberdatex; or 1 aconjugated 'diene polymer synthetic rubber. latex; or'mixtures-of any ofithesame. Such-conjugated: di'ene polymer synthetic: rubber: latex. may.
  • aqueous emulsion poly-' merizate ot one or: almixture of butadienes-1,3-,; for example; buta-diene-LB; 2-methyl-butadiene- 1,3: (isoprene); 2-chloro-butadiene-L3: (chloro prene), piperylena;2,3-dimethyl butadiene-1,'3.;'
  • amides such as acrylic acid, methyl acrylate, methyl methacrylate, acrylonitrile, methacrylonitrile, methacrylamide; methyl vinyl ether; methyl vinyl ketone; vinylidene chloride.
  • the latex may be compounded with the usual vulcanizing and other compounding ingredients and the froth will contain a conventional heatsetting agent which may be added to the latex before frothing, or to the froth, as before pouring into the molds.
  • a conventional heatsetting agent which may be added to the latex before frothing, or to the froth, as before pouring into the molds.
  • heat-setting agent may be an alkali-metal silicofiuoride, or ammonium sulfate or other ammonium salt which together with zinc oxide forms a heat-setting combination.
  • the latex compound may be converted into a froth by whipping in a beater, such as a Hobart mixer, or by the evolution of a gas in the latex, as by the decomposicarbonate and an acid in the latex in the presing the latex and preparing the froth are well known.
  • a beater such as a Hobart mixer
  • both sections of the above referred mold could be made of zinc or have the interior faces made of zinc coating, as by spraying on an tion of hydrogen peroxide or the reaction of a i 16.. ence of a stabilizer.
  • the body of the electrodes could be of other metals than the aluminum used, provided, of course, at least the pan portion had a p zinc coating on the interior surface of the same.
  • the following is illustrative of the present inafter which water was added to a final concentration of 60% solids.
  • the latex was whipped to a froth in a conventional Hobart mixer to a density of .103 grams per cubic centimeter.
  • Four parts of potassium silicofluoride gelling agent were added at the end of the whipping operation.
  • the whipped froth was poured into a mold comprising a bottom metal pan 13%" x 17 and 3 /4" deep, which served as one electrode.
  • This path was made of aluminum and the interior surface of the same was a sprayed zinc coating.
  • a 13 x 17 1;" metal top plate was used, to which was fastened ten rows of fourteen closed end cores, each core being /2 diameter and 2 1 long, the cores projecting into the pan or mold space to form tubular openings in the finished sponge cushion in the usual manner.
  • the top plate served as the other electrode and the electrodes comprising the top plate and bottom pan section of the mold were separated by a rubber gasket.
  • the top plate was of aluminum, and not surfaced with zinc.
  • the froth was heated by passing a low frequency (60 cycles, 110 volts) electric current through the same.
  • the heating cycle was characterized by a rapid increase in current to about 16 amperes during the first three minutes. The current then fell off to 10 amperes, and after ten minutes no current flowed, the temperature of the latex foam reaching 90 C. to 100 C. in the ten minutes. After such heating the sponge had become permanently set. It was then placed in an air oven at 100 C. for 15 minutes to vulcanize the sponge, after which it was removed from the mold.
  • the resultant cured sponge had an undistorted outer surface free from pitting and devoid of coloration, wherever the surface had been in contact with the bottom pan electrode which was zinc-sprayed.
  • the process of producing sponge rubber from a latex which comprises introducing a heatsettable latex froth into a mold, and setting the froth in the mold by passage of a low frequency alternating electric current through the froth between metal electrodes, at least one of said electrodes being in contact with a portion of the outer surface of the sponge article being molded and the surface of which electrode in contact with the foam is composed of a metal selected from the group consisting of zinc and cadmium.
  • the process of producing sponge rubber from a latex which comprises introducing a heatsettable latex froth into a mold, and setting the froth in the mold by passage of a low frequency alternating electric current through the froth between metal electrodes, at least one of said electrodes being in contact with a portion of the outer surface of the sponge article being molded and the surface of which electrode in contact with the foam is composed of zinc.
  • the process of producing sponge rubber from a latex which comprises introducing a heats'ettable latex froth into a mold, and setting the froth in the mold by passage of a low frequency alternating electric current through the froth between metal electrodes, at least one of' said electrodes being in contact with a portion of the outer surface of the sponge article being moldedand the surface of which electrode in contact with the foam is composed of cadmium.

Description

Patented June 20, 1950 UNITED STATES PM orrrcr James UL- Mann,,Kearny, N. J .',,assign0r to United States Rubber Company, New York; N. Y., a corporation of New Jersey No Drawing; Application-June24, 1949.- SeriaLNo. 101,250.-
3 Claims; (Cl. 18 53) This invention relates to the manufactureof sponge rubber from latex andmore, particularly to heat-setting, ahlatexfroth by means. of a low frequencybalanced. alternating, electric current.
The heat-settingof. shaped. latex. froths. 0011-. taining heat-setting, agents bypassing low frequency, balanced. alternating, electric currents from electrodes through the. froths to generate the desired amount of heat in the frothtoset or gel the same,.prior tosubjectingthe gelled froth to conventional vulcanizingconditions, is, known. The use of various. metals as the electrodes,. gives rise to unsightlypitting or discoloration, tor. both, of the surface of the sponge rubber molded against thelelectrodes. For instance, aluminum, which is commonly used for molds, gives .very .bad. pitting; ironor.stainlesssteel, whichais alsoused for molds, gives pitting accompanied by, brown discoloration; and tin, which has been suggested for electrodes in lowv frequency alternating current heating, leaves yellow. and. black. spots. on. the surface of the finalsponge rubber article.
I have found that if the surface of the electrode in contactwith the froth in such low frequency balanced alternating current heatingis. made of. zinc or cadmium, the surface of the sponge article which was in contact with the zinc or cadmium electrode duringits setting or gelling will be free from pits and discoloration.
Incarrying out the present invention. aheatsettable latex. froth: is introduced into a-mold by, forming themfroth in the mold as Joy -chemical. blowing byv evolving. ages in the latexin the mold; or by.chemically blowingthelatex in-bulk or mechanicallywhipping a body of llatex intoas froth and pouring; the. froth into individual stactionary or traveling-mold: or by pouring'or otherwise introducingthe: froth into atraveling; con-,- tinuous mold. Such molds'will contain two'electrodes; at least one of which will be in contact with a portionv of the outer'surface of :thersponge: article being molded;v The secondelectrode could. be embedded in the body of the frothbeing molded andremoved aftergellin-g of the froth;.butigenerally each electrode will be comprise'd in' onerofi' the twoparts of a two-part mold, usually the bodypart and the cover part. Forexample, the bot-'- tom and top plates of a'box type mold may-be composed of metal with the sides made of 'woodr or other insulating material, or the mold may be all made of wood-withmetal plates secured to the opposite inner faces of the top and bottom sections, the metal plates, of course, being made the electrodes for the low frequency electric current to be passed through the froth. Also, the
body' of the mold may be of metal 'andcomprise. one electrodaand the cover of, the moldmay also be of "metal and.comprise the other electrode, such cover and body being separated by a gasketor. spacer of insulating material, such as wood, rubberor'th'e like. One or both of such electrodes. may "be made wholly of zinc or cadmium, ormay; beLmade ofany'desired'metal with a' surface coating of zinc or cadmium" on the' face'of' the elec* trode which contacts thefoam'.
The function of "the electrodes, in the low fre-.' quency balanced alternating current heating of the latex'froth of:therpresentdnvention; is very difi'erent' fromzthatz'in: the. deposition 0f'S01idiIl1b-'- ber masses ion electrodes; in theso-called: electro deposition of rubber from" liquid: latex by l the use of direct 'electriclicurrent onunbalanced alternat--' lug-current: Also; of course;.the low frequency: electric: current heating: to; which the present i inventionrelates; wherezthe: lowfrequency 1 electric" current for heating thel'foam isvcarriedcthrough the-foam, .is very different fDGHIJthBiSOECaIISdThiQH frequency dielectric: heatingi Where the. heat. is oreatedsin the latex foam asiancelectric insulator wh-iclmis placed-in: a: varying electrostatic field-Jot. higlrfrequency; suchas radio-frequency.
The latex-for preparing: sponge rubbberaccordxingctorthe present invention may 'be a natural: rubberdatex; or 1 aconjugated 'diene polymer synthetic rubber. latex; or'mixtures-of any ofithesame. Such-conjugated: di'ene polymer synthetic: rubber: latex. may. be: an aqueous emulsion poly-' merizate ot one or: almixture of butadienes-1,3-,; for example; buta-diene-LB; 2-methyl-butadiene- 1,3: (isoprene); 2-chloro-butadiene-L3: (chloro prene), piperylena;2,3-dimethyl butadiene-1,'3.;'
The. conjugated. dienevpolymerr synthetic rubber latex;v as known, maysalso benarmixture .of 'one or. more: of? such butadienes-l ,3.-:with wone or' more: other polymerizable compounds :which are capable of formi'ng rubberyycopolymers With :butadi'enes l,3-,-.for-"example,; up tou'70%- of such mixture of one :or'more compounds which contain a. single GHZ1==G group; whereaat least one of the disconnected valences is attached to an-electro negative group; that is, a. group-which substantially increases theelectrical .dissymmetry; or-polanchar ester: of, the molecule. Examples or compounds; whiclrconta-in EttCHz=C group and are copoly merizable with hutadienes-LB are aryl olefins: SdGhiflS styrene;;and-vinyl naphthalene; thealphas methylene carboxylicacids, and-their esters, .ni-
triles and amides, such as acrylic acid, methyl acrylate, methyl methacrylate, acrylonitrile, methacrylonitrile, methacrylamide; methyl vinyl ether; methyl vinyl ketone; vinylidene chloride.
The latex may be compounded with the usual vulcanizing and other compounding ingredients and the froth will contain a conventional heatsetting agent which may be added to the latex before frothing, or to the froth, as before pouring into the molds. such heat-setting agent, as is well known, may be an alkali-metal silicofiuoride, or ammonium sulfate or other ammonium salt which together with zinc oxide forms a heat-setting combination. The latex compound may be converted into a froth by whipping in a beater, such as a Hobart mixer, or by the evolution of a gas in the latex, as by the decomposicarbonate and an acid in the latex in the presing the latex and preparing the froth are well known.
vention, the parts referred to therein being by weight:
Sixty-three per cent natural rubber latex was compounded according to the following formulation:
Parts by weight Rubber (in latex) 100 Potassium oleate 2.8 Sulfur 2.5 Accelerator 2.7 Zinc oxide 5 Antioxidant 1 The compounding ingredients were added as aqueous solutions or pastes in known manner,
tion of the surface which was in contact with the top plate and the cores was badly pitted. In that this surface acts as the bottom of a seat cushion, such pitting on the bottom surface of the cushion and in the tubular openings extending into the body of the cushion, was not objectionaible. Such pitting, however, would be very objectionable in the main exposed surface portion of the cushion corresponding to the bottom or pan portion of the mold.
If desired both sections of the above referred mold could be made of zinc or have the interior faces made of zinc coating, as by spraying on an tion of hydrogen peroxide or the reaction of a i 16.. ence of a stabilizer. Such methods of compound-,
aluminum mold, or dipping in case of a sheet steel mold. The body of the electrodes could be of other metals than the aluminum used, provided, of course, at least the pan portion had a p zinc coating on the interior surface of the same. The following is illustrative of the present inafter which water was added to a final concentration of 60% solids. The latex was whipped to a froth in a conventional Hobart mixer to a density of .103 grams per cubic centimeter. Four parts of potassium silicofluoride gelling agent were added at the end of the whipping operation.
The whipped froth was poured into a mold comprising a bottom metal pan 13%" x 17 and 3 /4" deep, which served as one electrode. This path was made of aluminum and the interior surface of the same was a sprayed zinc coating. A 13 x 17 1;" metal top plate was used, to which was fastened ten rows of fourteen closed end cores, each core being /2 diameter and 2 1 long, the cores projecting into the pan or mold space to form tubular openings in the finished sponge cushion in the usual manner. The top plate served as the other electrode and the electrodes comprising the top plate and bottom pan section of the mold were separated by a rubber gasket. The top plate was of aluminum, and not surfaced with zinc. The froth was heated by passing a low frequency (60 cycles, 110 volts) electric current through the same. The heating cycle was characterized by a rapid increase in current to about 16 amperes during the first three minutes. The current then fell off to 10 amperes, and after ten minutes no current flowed, the temperature of the latex foam reaching 90 C. to 100 C. in the ten minutes. After such heating the sponge had become permanently set. It was then placed in an air oven at 100 C. for 15 minutes to vulcanize the sponge, after which it was removed from the mold. The resultant cured sponge had an undistorted outer surface free from pitting and devoid of coloration, wherever the surface had been in contact with the bottom pan electrode which was zinc-sprayed. The por- As stated above, tests on stainless steel and iron show pitting and brown discoloration of the sponge surface. Copper shows very bad pitting and black discoloration. Lead shows black discoloration. Tin and nickel show yellow and black spots. Silver shows bad pitting and black spots. Chromium shows bad pitting and green discoloration. Magnesium shows bad pitting. Where the inner electrode surface is composed of cadmium, similarly to the zinc coated bottom mold section above, the surface of the sponge rubber molded against it was devoid of any surface distortion or pitting or discoloration.
In view of the many changes and modifications that may be made without departing from the principles underlying the invention, reference should be made to the appended claims for an understanding of the scope of the invention.
Having thus described my invention, what I claim and desire to protect by Letters Patent is:
1. The process of producing sponge rubber from a latex which comprises introducing a heatsettable latex froth into a mold, and setting the froth in the mold by passage of a low frequency alternating electric current through the froth between metal electrodes, at least one of said electrodes being in contact with a portion of the outer surface of the sponge article being molded and the surface of which electrode in contact with the foam is composed of a metal selected from the group consisting of zinc and cadmium.
2. The process of producing sponge rubber from a latex which comprises introducing a heatsettable latex froth into a mold, and setting the froth in the mold by passage of a low frequency alternating electric current through the froth between metal electrodes, at least one of said electrodes being in contact with a portion of the outer surface of the sponge article being molded and the surface of which electrode in contact with the foam is composed of zinc.
3. The process of producing sponge rubber from a latex which comprises introducing a heats'ettable latex froth into a mold, and setting the froth in the mold by passage of a low frequency alternating electric current through the froth between metal electrodes, at least one of' said electrodes being in contact with a portion of the outer surface of the sponge article being moldedand the surface of which electrode in contact with the foam is composed of cadmium.
JAMES U. MANN.
No references cited.

Claims (1)

1. THE PROCESS OF PRODUCING SPONGE RUBBER FROM A LATEX WHICH COMPRISES INTRODUCING A HEATSETTABLE LATEX FROTH INTO A MOLD, AND SETTING THE FROTH IN THE MOLD BY PASSAGE OF A LOW FREQUENCY ALTERNATING ELECTRIC CURRENT THROUGH THE FROTH BETWEEN METAL ELECTRODES, AT LEAST ONE OF SAID ELECTRODES BEING IN CONTACT WITH A PORTION OF THE OUTER SURFACE OF THE SPONGE ARTICLE BEING MOLDED AND THE SURFACE OF WHICH ELECTRODE IN CONTACT WITH THE FOAM IS COMPOSED OF A METAL SELECTED FROM THE GROUP CONSISTING OF ZINC AND CADMIUM.
US101250A 1949-06-24 1949-06-24 Manufacture of sponge rubber Expired - Lifetime US2512464A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US101250A US2512464A (en) 1949-06-24 1949-06-24 Manufacture of sponge rubber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US101250A US2512464A (en) 1949-06-24 1949-06-24 Manufacture of sponge rubber

Publications (1)

Publication Number Publication Date
US2512464A true US2512464A (en) 1950-06-20

Family

ID=22283696

Family Applications (1)

Application Number Title Priority Date Filing Date
US101250A Expired - Lifetime US2512464A (en) 1949-06-24 1949-06-24 Manufacture of sponge rubber

Country Status (1)

Country Link
US (1) US2512464A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2832997A (en) * 1953-09-24 1958-05-06 Goodyear Tire & Rubber Porous sheet material
US3215647A (en) * 1962-06-19 1965-11-02 Dow Chemical Co Synthetic rubber latex foam containing a coreactive material and process of making same
US3737488A (en) * 1969-07-04 1973-06-05 Int Synthetic Rubber Process for producing moulded foams from rubber latices by using microwave heating

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2832997A (en) * 1953-09-24 1958-05-06 Goodyear Tire & Rubber Porous sheet material
US3215647A (en) * 1962-06-19 1965-11-02 Dow Chemical Co Synthetic rubber latex foam containing a coreactive material and process of making same
US3737488A (en) * 1969-07-04 1973-06-05 Int Synthetic Rubber Process for producing moulded foams from rubber latices by using microwave heating

Similar Documents

Publication Publication Date Title
US2280771A (en) Method of baking or vulcanizing india-rubber or similar materials
US2293928A (en) Article comprising porous rubber
US2283316A (en) One-stage process for the manufacture of rubber
US2512464A (en) Manufacture of sponge rubber
US2138081A (en) Process for the production of sponge rubber from aqueous rubber dispersions
US2469894A (en) Method for improving the surface of synthetic rubber sponge
US2567988A (en) Latex foamed with hydrogen peroxide and a polyamine
US2290622A (en) Method of manufacturing cellular rubber
US2524039A (en) Process of producing cellular rubber
US1484731A (en) Manufacture of sponge-rubber articles
US2832997A (en) Porous sheet material
US2845659A (en) Production of foam rubber
US2858282A (en) Method of making latex sponge rubber
US2216785A (en) Gas expanded latex
US2476827A (en) Process of molding rubber sponges
US2801274A (en) Manufacture of sponge rubber from foamed rubber latex
US2711969A (en) Method of treating sheet sponge rubber
US2558860A (en) Manufacture of golf balls
US2613189A (en) Cellular material and blowing agent therefor
US2605509A (en) Method of producing elastic thread
US2776330A (en) Production of sponge rubber
US2246315A (en) Method of making sponge rubber
US1994165A (en) Composite product and method of making the same
US2933768A (en) Improved oil and heat resistant elastomer foamed products and their manufacture
US1959160A (en) Microporous rubber and method of making the same