SU158066A1 - - Google Patents
Info
- Publication number
- SU158066A1 SU158066A1 SU789979A SU789979A SU158066A1 SU 158066 A1 SU158066 A1 SU 158066A1 SU 789979 A SU789979 A SU 789979A SU 789979 A SU789979 A SU 789979A SU 158066 A1 SU158066 A1 SU 158066A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- maleic anhydride
- water
- ethylene oxide
- temperature
- glycol
- Prior art date
Links
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU813302619A Addition SU995076A2 (ru) | 1981-06-19 | 1981-06-19 | Вторичный источник питани посто нного напр жени |
Publications (1)
Publication Number | Publication Date |
---|---|
SU158066A1 true SU158066A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2943096A (en) | Preparation of monomeric glycidyl polyethers of polyhydric phenols | |
US3450684A (en) | Fluorocarbon polyethers | |
US11548981B2 (en) | Polyphenylene ether, composition of the same, and manufacturing method of the same | |
CN110041238B (zh) | 一种降低多巯基羧酸酯气味的方法 | |
KR102069569B1 (ko) | 저분자량 충격 폴리에테르를 제조하는 개선된 방법 | |
US2211624A (en) | Organic substituted acetic acid | |
SU158066A1 (enrdf_load_stackoverflow) | ||
JPS59196853A (ja) | 2−シアンアクリレ−トの製造方法 | |
EP0008492A1 (en) | Method for manufacture of aromatic polyester-polycarbonate | |
US2188340A (en) | Process of reacting methyl vinyl ketone with hydrogen cyanide and products thereby obtained | |
US4005121A (en) | Process for the preparation of oligocarbonates with two catalysts | |
US3560529A (en) | Polymerization of itaconic anhydride | |
US3542815A (en) | Polymerization of aconitic anhydride | |
US2455722A (en) | Method for production of polymeric beta, gamma-olefinic alcohols | |
JP6957911B2 (ja) | ポリエーテルポリオールの製造方法 | |
CN113754876A (zh) | 一种双酚a聚醚多元醇及其制备方法 | |
US3465030A (en) | Process for the production of diallyl-phthalate | |
US2947761A (en) | Epoxtoation of aldehydes | |
US2625569A (en) | Trioxepane polymers | |
JPH0558012B2 (enrdf_load_stackoverflow) | ||
RU2757583C1 (ru) | Диглицидиловый эфир 4-хлорфталевой кислоты в качестве мономера для получения эпоксидных полимеров | |
US3513136A (en) | Polymerization of maleic anhydride | |
US2532036A (en) | Process of preparing polyhydric alcohols | |
PL29409B1 (pl) | Sposób wytwarzania kwasu glikolowego. | |
US2793221A (en) | Ozonolysis of primary amines |