SU331556A1 - - Google Patents
Info
- Publication number
- SU331556A1 SU331556A1 SU1447808A SU1447808A SU331556A1 SU 331556 A1 SU331556 A1 SU 331556A1 SU 1447808 A SU1447808 A SU 1447808A SU 1447808 A SU1447808 A SU 1447808A SU 331556 A1 SU331556 A1 SU 331556A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- aluminum
- strong
- solution
- alcohol
- water
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 18
- 235000019441 ethanol Nutrition 0.000 description 15
- 229910052782 aluminium Inorganic materials 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 11
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 235000011007 phosphoric acid Nutrition 0.000 description 9
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- 239000011574 phosphorus Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- -1 aluminum halide Chemical class 0.000 description 4
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 229940009859 aluminum phosphate Drugs 0.000 description 3
- 238000004455 differential thermal analysis Methods 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000001757 thermogravimetry curve Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- USJRLGNYCQWLPF-UHFFFAOYSA-N chlorophosphane Chemical class ClP USJRLGNYCQWLPF-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1628593A SU382274A3 (enrdf_load_stackoverflow) | 1969-06-12 | 1970-06-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU331556A1 true SU331556A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Schlesinger et al. | Reactions of diborane with alkali metal hydrides and their addition compounds. New syntheses of borohydrides. Sodium and potassium borohydrides1 | |
| KR101105618B1 (ko) | 시아노보레이트 음이온을 갖는 염 | |
| CN100584756C (zh) | 一种制备十二氢十二硼酸盐的方法 | |
| JPH09506329A (ja) | リチウムヘキサフルオロホスフェートの製造法 | |
| Desroches et al. | Design and synthesis of multifunctional thiacalixarenes and related metal derivatives for the preparation of sol–gel hybrid materials with non-linear optical properties | |
| SU331556A1 (enrdf_load_stackoverflow) | ||
| Nitschke et al. | Structural diversity and spectral and thermal properties of the first alkaline earth metal tetracyanidoborates:[Mg (H 2 O) 6][B (CN) 4] 2,[Mg (H 2 O) 2][B (CN) 4] 2,[Mg (DMF) 6][B (CN) 4] 2,[Ca (H 2 O) 3][B (CN) 4] 2, and [Ca (H 2 O) 2 (CH 3 CN)][B (CN) 4] 2 | |
| Des Marteau | Reaction of bromine (I) fluorosulfate with some covalent chlorides | |
| Kmecl et al. | Boron phosphate: its synthesis, gradual crystallisation and characterisation of bulk properties | |
| US3036087A (en) | Process for the preparation of phosphocreatine and/or phosphocreatinine | |
| DK149473B (da) | Fremgangsmaade til fremstilling af aminomethan-phosphonsyrer | |
| US3366510A (en) | Process for the manufacture of niobates and tantalates of alkali metals and alkalineearth metals and coating objects therewith | |
| Firth et al. | Reactions of Tetrafluorohydrazine with Di-and Triphenylphosphine. A New Method for Preparation of Fluorophosphoranes | |
| CN106829865A (zh) | 一种制备k2b12h12的方法 | |
| Osthoff et al. | Boron—Nitrogen Systems. II. Diethylaminoboron Dichloride1 | |
| JPH0218319A (ja) | Ｔｏｎ構造型の新規ゼオライト、それらの製造方法およびそれらの用途 | |
| US3592594A (en) | Process for the manufacture of phosphorus pentafluoride | |
| RU2282586C1 (ru) | Додекагидро-клозо-додекаборат уротропина и способ его получения | |
| JP2829048B2 (ja) | 難溶性半水セッコウ繊維の製造方法 | |
| Zrelli et al. | Synthesis, Characterization and Thermal Behavior of HYP2O7· 3H2O Electrical Properties of HYP2O7 | |
| JPS5838435B2 (ja) | リン酸モノエステルの製造法 | |
| Rowley et al. | Preparation and properties of calcium monofluorophosphate dihydrate | |
| Isbell et al. | Kinetic study of the reduction of trimethyl phosphate, triethyl phosphate, and tributyl phosphate by sodium in liquid ammonia | |
| JP4587529B2 (ja) | イピダクリン及び塩酸イピダクリン水和物の製造方法 | |
| Keller | Reaction of diborane with trimethylamine-alane and dimethylaminoalane |