GB873975A - Method for making foams - Google Patents
Method for making foamsInfo
- Publication number
- GB873975A GB873975A GB36515/57A GB3651557A GB873975A GB 873975 A GB873975 A GB 873975A GB 36515/57 A GB36515/57 A GB 36515/57A GB 3651557 A GB3651557 A GB 3651557A GB 873975 A GB873975 A GB 873975A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- dimethyl
- pentanol
- ethyl
- alkyd
- 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
Links
- 239000006260 foam Substances 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 12
- 229920000180 alkyd Polymers 0.000 abstract 8
- 239000002253 acid Substances 0.000 abstract 6
- WFRBDWRZVBPBDO-UHFFFAOYSA-N 2-methyl-2-pentanol Chemical group CCCC(C)(C)O WFRBDWRZVBPBDO-UHFFFAOYSA-N 0.000 abstract 4
- KYWJZCSJMOILIZ-UHFFFAOYSA-N 3-methylhexan-3-ol Chemical group CCCC(C)(O)CC KYWJZCSJMOILIZ-UHFFFAOYSA-N 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 4
- 150000007513 acids Chemical class 0.000 abstract 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 4
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 abstract 4
- 238000005187 foaming Methods 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 239000005056 polyisocyanate Substances 0.000 abstract 4
- 229920001228 polyisocyanate Polymers 0.000 abstract 4
- 150000005846 sugar alcohols Polymers 0.000 abstract 4
- 239000001117 sulphuric acid Substances 0.000 abstract 4
- 235000011149 sulphuric acid Nutrition 0.000 abstract 4
- 150000003509 tertiary alcohols Chemical class 0.000 abstract 4
- WUOACPNHFRMFPN-VIFPVBQESA-N (R)-(+)-alpha-terpineol Chemical compound CC1=CC[C@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-VIFPVBQESA-N 0.000 abstract 2
- HYRNQHVQTJQLFS-UHFFFAOYSA-N 1,1,2,2-tetraphenylethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C(C=1C=CC=CC=1)C1=CC=CC=C1 HYRNQHVQTJQLFS-UHFFFAOYSA-N 0.000 abstract 2
- SFRDIOSZMHLSFP-UHFFFAOYSA-N 1,1,2-triphenylpropan-1-ol Chemical compound C=1C=CC=CC=1C(O)(C=1C=CC=CC=1)C(C)C1=CC=CC=C1 SFRDIOSZMHLSFP-UHFFFAOYSA-N 0.000 abstract 2
- GIMDPFBLSKQRNP-UHFFFAOYSA-N 1,1-diphenylethanol Chemical compound C=1C=CC=CC=1C(O)(C)C1=CC=CC=C1 GIMDPFBLSKQRNP-UHFFFAOYSA-N 0.000 abstract 2
- OXLXSOPFNVKUMU-UHFFFAOYSA-N 1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC OXLXSOPFNVKUMU-UHFFFAOYSA-N 0.000 abstract 2
- QYLFHLNFIHBCPR-UHFFFAOYSA-N 1-ethynylcyclohexan-1-ol Chemical compound C#CC1(O)CCCCC1 QYLFHLNFIHBCPR-UHFFFAOYSA-N 0.000 abstract 2
- PLSMHHUFDLYURK-UHFFFAOYSA-N 2,3,4-trimethyl-3-pentanol Chemical group CC(C)C(C)(O)C(C)C PLSMHHUFDLYURK-UHFFFAOYSA-N 0.000 abstract 2
- IKECULIHBUCAKR-UHFFFAOYSA-N 2,3-dimethylbutan-2-ol Chemical group CC(C)C(C)(C)O IKECULIHBUCAKR-UHFFFAOYSA-N 0.000 abstract 2
- RFZHJHSNHYIRNE-UHFFFAOYSA-N 2,3-dimethylpentan-3-ol Chemical group CCC(C)(O)C(C)C RFZHJHSNHYIRNE-UHFFFAOYSA-N 0.000 abstract 2
- NCIAKSBPWVOMFR-UHFFFAOYSA-N 2,3-diphenylbutan-2-ol Chemical compound C=1C=CC=CC=1C(C)(O)C(C)C1=CC=CC=C1 NCIAKSBPWVOMFR-UHFFFAOYSA-N 0.000 abstract 2
- PSSOZTBFLMDWRE-UHFFFAOYSA-N 2,4-dimethyl-3-propan-2-ylpent-4-en-2-ol Chemical compound CC(C)(C(C(=C)C)C(C)C)O PSSOZTBFLMDWRE-UHFFFAOYSA-N 0.000 abstract 2
- IFXNWIUSZUHIDG-UHFFFAOYSA-N 2,4-dimethyl-3-propan-2-ylpentan-3-ol Chemical group CC(C)C(O)(C(C)C)C(C)C IFXNWIUSZUHIDG-UHFFFAOYSA-N 0.000 abstract 2
- CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical group CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 abstract 2
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 abstract 2
- UYOPRNGQFQWYER-UHFFFAOYSA-N 2-methylpent-4-en-2-ol Chemical compound CC(C)(O)CC=C UYOPRNGQFQWYER-UHFFFAOYSA-N 0.000 abstract 2
- BDCFWIDZNLCTMF-UHFFFAOYSA-N 2-phenylpropan-2-ol Chemical compound CC(C)(O)C1=CC=CC=C1 BDCFWIDZNLCTMF-UHFFFAOYSA-N 0.000 abstract 2
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 abstract 2
- PZPYIRQFCOFLGJ-UHFFFAOYSA-N 3-ethyl-2,4-dimethylpentan-3-ol Chemical group CCC(O)(C(C)C)C(C)C PZPYIRQFCOFLGJ-UHFFFAOYSA-N 0.000 abstract 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 abstract 2
- GNROHGFUVTWFNG-UHFFFAOYSA-N 4-ethylheptan-4-ol Chemical group CCCC(O)(CC)CCC GNROHGFUVTWFNG-UHFFFAOYSA-N 0.000 abstract 2
- DIFXCBNNWBBNCA-UHFFFAOYSA-N 4-methyl-3-propan-2-ylpent-1-yn-3-ol Chemical compound CC(C)C(O)(C#C)C(C)C DIFXCBNNWBBNCA-UHFFFAOYSA-N 0.000 abstract 2
- PYKQMQBNPLNLPS-UHFFFAOYSA-N 4-methylhept-1-en-4-ol Chemical compound CCCC(C)(O)CC=C PYKQMQBNPLNLPS-UHFFFAOYSA-N 0.000 abstract 2
- IQXKGRKRIRMQCQ-UHFFFAOYSA-N 4-methylheptan-4-ol Chemical group CCCC(C)(O)CCC IQXKGRKRIRMQCQ-UHFFFAOYSA-N 0.000 abstract 2
- SJTPBRMACCDJPZ-UHFFFAOYSA-N 4-propylheptan-4-ol Chemical group CCCC(O)(CCC)CCC SJTPBRMACCDJPZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000004254 Ammonium phosphate Substances 0.000 abstract 2
- 229910015900 BF3 Inorganic materials 0.000 abstract 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 abstract 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 2
- 229920005830 Polyurethane Foam Polymers 0.000 abstract 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical class OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 abstract 2
- GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 abstract 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 2
- 239000000654 additive Substances 0.000 abstract 2
- 239000001361 adipic acid Substances 0.000 abstract 2
- 235000011037 adipic acid Nutrition 0.000 abstract 2
- 150000001279 adipic acids Chemical class 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 229910000148 ammonium phosphate Inorganic materials 0.000 abstract 2
- 235000019289 ammonium phosphates Nutrition 0.000 abstract 2
- -1 amyl alcohols Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 239000010425 asbestos Substances 0.000 abstract 2
- 150000001536 azelaic acids Chemical class 0.000 abstract 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 abstract 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 235000011132 calcium sulphate Nutrition 0.000 abstract 2
- 239000001175 calcium sulphate Substances 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 2
- 229910052570 clay Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 239000004088 foaming agent Substances 0.000 abstract 2
- 239000003365 glass fiber Substances 0.000 abstract 2
- 150000002311 glutaric acids Chemical class 0.000 abstract 2
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 150000002691 malonic acids Chemical class 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- PRZYKDRCYOLTQA-UHFFFAOYSA-N methyl 2,5,11,14,18-pentachlorooctadecanoate Chemical compound COC(=O)C(Cl)CCC(Cl)CCCCCC(Cl)CCC(Cl)CCCCCl PRZYKDRCYOLTQA-UHFFFAOYSA-N 0.000 abstract 2
- 150000002913 oxalic acids Chemical class 0.000 abstract 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 2
- 150000003047 pimelic acids Chemical class 0.000 abstract 2
- 239000011496 polyurethane foam Substances 0.000 abstract 2
- 229910052895 riebeckite Inorganic materials 0.000 abstract 2
- 235000012424 soybean oil Nutrition 0.000 abstract 2
- 239000003549 soybean oil Substances 0.000 abstract 2
- 150000003442 suberic acids Chemical class 0.000 abstract 2
- 150000003444 succinic acids Chemical class 0.000 abstract 2
- 229920002994 synthetic fiber Polymers 0.000 abstract 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract 2
- 125000005628 tolylene group Chemical group 0.000 abstract 2
- RBNWAMSGVWEHFP-UHFFFAOYSA-N trans-p-Menthane-1,8-diol Chemical group CC(C)(O)C1CCC(C)(O)CC1 RBNWAMSGVWEHFP-UHFFFAOYSA-N 0.000 abstract 2
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 abstract 2
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 abstract 2
- 239000000080 wetting agent Substances 0.000 abstract 2
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 abstract 1
- TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical group CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 abstract 1
- FRDAATYAJDYRNW-UHFFFAOYSA-N 3-methyl-3-pentanol Chemical group CCC(C)(O)CC FRDAATYAJDYRNW-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical group CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 abstract 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
- C08J9/14—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 organic
- C08J9/142—Compounds containing oxygen but no halogen atom
-
- 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
- C08J2207/00—Foams characterised by their intended use
- C08J2207/04—Aerosol, e.g. polyurethane foam spray
-
- 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
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/06—Polyurethanes from polyesters
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)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US873975XA | 1956-11-23 | 1956-11-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB873975A true GB873975A (en) | 1961-08-02 |
Family
ID=22204943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB36515/57A Expired GB873975A (en) | 1956-11-23 | 1957-11-22 | Method for making foams |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE562500A (enExample) |
| GB (1) | GB873975A (enExample) |
| NL (2) | NL103077C (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2325468A (en) * | 1997-05-22 | 1998-11-25 | Basf Corp | Self-skinning polyurethane foams |
| CN114420369A (zh) * | 2022-01-25 | 2022-04-29 | 上海金尔电线电缆有限公司 | 一种peek发泡绝缘高温稳相射频电缆及其制备工艺 |
-
0
- BE BE562500D patent/BE562500A/xx unknown
- NL NL222679D patent/NL222679A/xx unknown
- NL NL103077D patent/NL103077C/xx active
-
1957
- 1957-11-22 GB GB36515/57A patent/GB873975A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2325468A (en) * | 1997-05-22 | 1998-11-25 | Basf Corp | Self-skinning polyurethane foams |
| CN114420369A (zh) * | 2022-01-25 | 2022-04-29 | 上海金尔电线电缆有限公司 | 一种peek发泡绝缘高温稳相射频电缆及其制备工艺 |
Also Published As
| Publication number | Publication date |
|---|---|
| NL222679A (enExample) | |
| BE562500A (enExample) | |
| NL103077C (enExample) |
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