DE1082402B - Process for the production of large-pored foams - Google Patents
Process for the production of large-pored foamsInfo
- Publication number
- DE1082402B DE1082402B DEF26449A DEF0026449A DE1082402B DE 1082402 B DE1082402 B DE 1082402B DE F26449 A DEF26449 A DE F26449A DE F0026449 A DEF0026449 A DE F0026449A DE 1082402 B DE1082402 B DE 1082402B
- Authority
- DE
- Germany
- Prior art keywords
- water
- foams
- disulfohydrazide
- production
- weight
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 5
- 239000006260 foam Substances 0.000 title description 11
- 238000004519 manufacturing process Methods 0.000 title description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000004014 plasticizer Substances 0.000 claims description 4
- 239000011148 porous material Substances 0.000 description 10
- 239000003380 propellant Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 150000001540 azides Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- YMGHPIVBMBXPCR-NXVVXOECSA-N (z)-n,n-dibutyloctadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCCC)CCCC YMGHPIVBMBXPCR-NXVVXOECSA-N 0.000 description 1
- LSRGVBOHVMLGKY-UHFFFAOYSA-N 2,3-dimethyl-5,6-dinitrosobenzene-1,4-dicarboxamide Chemical compound CC1=C(C)C(C(N)=O)=C(N=O)C(N=O)=C1C(N)=O LSRGVBOHVMLGKY-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 150000004008 N-nitroso compounds Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/125—Water, e.g. hydrated salts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of 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 a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use of 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
Verfahren zur Herstellung von grobporigen Schaumstoffen Es ist bekannt, daß man Schaumstoffe aus Polymerisaten oder Mischpolimerisaten des Vinylchlorids oder Vinylidenchlorids herstellen kann. Hierbeiwirdmeistens so verfahren, daß das Polymerisat-gegebenenfalls im Gemisch mit Weichmacher-zusammen mit einem Stabilisator und einem Treibmittel, und gegebenenfalls weiteren Zusätzen, in einer allseitig geschlossenen Form unter Druck bis zur Zersetzungstemperatur des Treibmittels und der Geliertemperatur des Polymerisates erhitzt wird, daraufhin in der Form abgekühlt und unter Atmosphärendruck bei etwa 100° C aufgetrieben wird. Process for the production of coarse-pored foams It is known that one foams from polymers or mixed polymers of vinyl chloride or vinylidene chloride can produce. This is usually done in such a way that the Polymer - optionally mixed with plasticizer - together with a stabilizer and a propellant, and optionally further additives, in one on all sides closed form under pressure up to the decomposition temperature of the propellant and the gelling temperature of the polymer is heated, then cooled in the mold and is expanded under atmospheric pressure at about 100 ° C.
Als Treibmittel kommen hierbei bevorzugt solche Verbindungen in Frage, die bei ihrer Zersetzung Stickstoff abspalten. Solche Treibmittel sind z. B. Azoverbindungen, wie Azoisobuttersäuredinitril, Azodicarbonamid oder Sulfohydrazide, wie z. B. Diphenylsulfon-3, 3'-disulfohydrazid, Benzol-1, 3-disulfohydrazid oder N-Nitrosoverbindungen, wie z. B. Dinitrosopentamethylentetramin, Dinitrosodimethylterephthalamid oder andere stickstoffabspaltende Verbindungen. Preferred propellants here are those compounds which split off nitrogen when they decompose. Such propellants are e.g. B. azo compounds, such as azoisobutyric acid dinitrile, azodicarbonamide or sulfohydrazides, such as. B. Diphenylsulfone-3, 3'-disulfohydrazide, benzene-1, 3-disulfohydrazide or N-nitroso compounds, such as z. B. dinitrosopentamethylenetetramine, dinitrosodimethylterephthalamide or others nitrogen-releasing compounds.
Die PorengröBe der hierbei erhaltenen Schaumstoffe wird in erster Linie durch die Art des verwendeten Treibmittels bestimmt. Es wird dabei beobachtet, daß sie abhängig ist von der Zersetzungstemperatur des Treibmittels, seiner Löslichkeit in der Kunststoffmischung sowie deren Gelierungsgeschwindigkeit. Es gelingt auf relativ einfache Weise, Schaumstoffe mit sehr feiner Porenstruktur herzustellen, indem Pigmentzusätze oder schnell gelierende Weichmacher, wie z. B. Trikresylphosphat, eingesetzt werden. Dagegen können die Poren bei einem gegebenen Treibmittel nur in sehr geiingem Maße vergrößert werden, z. B. durch Variation der Kunststoffmischung oder Veränderung der Verschäumungsbedingungen. Die Erzielung von großen Poren ist jedoch aus manchen technischen Gründen (z. B. bessere Rutschfestigkeit grobporiger Schaumstoffe usw.) sehr erwünscht. Man ist ferner bestrebt, bei Verwendung von ein und demselben Treibmittel möglichst verschiedenartige Porengrößen des Schaumstoffes einstellen zu konnen. The pore size of the foams obtained in this way is the first Line determined by the type of propellant used. It is observed that it depends on the decomposition temperature of the propellant and its solubility in the plastic mixture and its gelation rate. It succeeds on relatively simple way to produce foams with a very fine pore structure, by adding pigment or rapidly gelling plasticizers, such as. B. tricresyl phosphate, can be used. In contrast, with a given blowing agent, the pores can only be enlarged to a very small extent, e.g. B. by varying the plastic mixture or changing the foaming conditions. Achieving large pores is essential however, for some technical reasons (e.g. better slip resistance, larger pores Foams, etc.) are very desirable. One also strives when using a and the same blowing agent as different pore sizes as possible in the foam to be able to hire.
Es wurde nun gefunden, daß man Schaumstoffe aus Polymerisaten oder Mischpolymerisaten des Vinylchlorids oder Vinylidenchlorids mit großen Poren erhält, wenn die Formasse bei der üblichen Verschäumung geringe Mengen von Wasser enthält. Überraschenderweise werden bei der Verschäumung in Gegenwart des Wassers wesentlich größere Poren erzielt als bei Abwesenheit des Wassers. It has now been found that you can make foams from polymers or Contains copolymers of vinyl chloride or vinylidene chloride with large pores, if the molding compound contains small amounts of water during the usual foaming. Surprisingly, they become essential when foaming in the presence of water larger pores achieved than in the absence of water.
Die porenvergrößemde Wirkung des Wasserzusatzes tritt bereits bei geringen Zusätzen von Wasser ein. Im allgemeinen werden jedoch die besten Ergebnisse erzielt, wenn der Wasserzusatz 2 bis 10 Gewichtsprozent der zu verschäumenden Mischung beträgt. Weiterhin hat es sich gezeigt, daß es vorteilhaft sein kann, wenn man dem Wasser noch oberflächenaktive Substanzen zusetzt, die eine bessere Einmischung des Wassers in die zu verschäumenden Substanzen gewährleisten. Als oberflächenaktive Substanzen kommen alle die Verbindungen in Frage, die in der Lage sind, die Oberflächenspannung des Wassers oder der zu verschäumenden Kunststoffmischung zu verändern, d. h. anion-und kationaktive sowie nichtionogene Verbindungen und z. B. Siliconöle. The pore-enlarging effect of the addition of water already occurs small additions of water. In general, however, it will give the best results achieved when the addition of water is 2 to 10 percent by weight of the mixture to be foamed amounts to. Furthermore, it has been shown that it can be advantageous if one to the Water still adds surface-active substances that allow better mixing of the Ensure water in the substances to be foamed. As a surface-active Substances are all those compounds that are capable of reducing surface tension to change the water or the plastic mixture to be foamed, d. H. anion and cationic and nonionic compounds and z. B. silicone oils.
Die oberflächenaktiven Substanzen können dem Wasser dabei in Mengen von z. B. 10 bis 40 °/0 zugesetzt werden.The surface-active substances can be added to the water in quantities from Z. B. 10 to 40 ° / 0 can be added.
Beispiel Eine Paste, bestehend aus 100 Gewichtsteilen eines in Emulsion hergestellten Polyvinylchlorids (K-Wert 66-75), 100 Gewichtsteilen Weichmacher, 0, 7 Gewichtsteilen Stabilisator und den in der nachfolgenden Tabelle angegebenen Mengen (in Gewichtsprozent, bezogen auf die vorstehend aufgeführte Mischung) an Treibmittel und Wasser, gegebenenfalls unter zusätzlicher Verwendung einer oberflächenaktiven Verbindung, wurde auf einem Dreiwalzenstuhl homogen vermischt, in eine dicht verschließbare Form (100-100-10 mm) eingefüllt und in der Presse 10 Minuten auf 165° C erhitzt. Nach dem Abkühlen der Form wurde der Rohling im Umluftheizschrank 20 Minuten auf 100° C geheizt, wobei der Schaumstoff seine endgültige Größe erhielt. Example A paste consisting of 100 parts by weight of one in emulsion manufactured polyvinyl chloride (K value 66-75), 100 parts by weight plasticizer, 0.7 parts by weight of stabilizer and those given in the table below Quantities (in percent by weight, based on the mixture listed above) Propellant and water, optionally with the additional use of a surface-active one Compound, was mixed homogeneously on a three-roll mill, into a sealable one Form (100-100-10 mm) filled and heated in the press to 165 ° C for 10 minutes. After the mold had cooled, the blank was placed in a circulating air heater for 20 minutes Heated to 100 ° C, whereby the foam got its final size.
Die Poren der dabei erhaltenen Schaumstoffe hatten die aus der nachfolgenden
Tabelle hervorgehenden Durchmesser :
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF26449A DE1082402B (en) | 1958-08-20 | 1958-08-20 | Process for the production of large-pored foams |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF26449A DE1082402B (en) | 1958-08-20 | 1958-08-20 | Process for the production of large-pored foams |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1082402B true DE1082402B (en) | 1960-05-25 |
Family
ID=7092030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF26449A Pending DE1082402B (en) | 1958-08-20 | 1958-08-20 | Process for the production of large-pored foams |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE1082402B (en) |
-
1958
- 1958-08-20 DE DEF26449A patent/DE1082402B/en active Pending
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