BE372395A - - Google Patents
Info
- Publication number
- BE372395A BE372395A BE372395DA BE372395A BE 372395 A BE372395 A BE 372395A BE 372395D A BE372395D A BE 372395DA BE 372395 A BE372395 A BE 372395A
- Authority
- BE
- Belgium
- Prior art keywords
- alcohol
- phosphoric acid
- liters
- acid
- salt
- Prior art date
Links
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 38
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
- 235000019441 ethanol Nutrition 0.000 description 21
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 150000003839 salts Chemical class 0.000 description 17
- 239000000203 mixture Substances 0.000 description 13
- 229910019142 PO4 Inorganic materials 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 235000021317 phosphate Nutrition 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 229910052700 potassium Inorganic materials 0.000 description 8
- 239000011591 potassium Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 7
- 239000003513 alkali Substances 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 7
- 239000010452 phosphate Substances 0.000 description 7
- 238000004821 distillation Methods 0.000 description 5
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 5
- 235000019796 monopotassium phosphate Nutrition 0.000 description 5
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 5
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000001476 alcoholic effect Effects 0.000 description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 241000283074 Equus asinus Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- PIWKPBJCKXDKJR-UHFFFAOYSA-N Isoflurane Chemical compound FC(F)OC(Cl)C(F)(F)F PIWKPBJCKXDKJR-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B7/00—Fertilisers based essentially on alkali or ammonium orthophosphates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE372395A true BE372395A (d) |
Family
ID=43506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE372395D BE372395A (d) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE372395A (d) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2018552A1 (d) * | 1968-09-20 | 1970-05-29 | Goulding Ltd |
-
0
- BE BE372395D patent/BE372395A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2018552A1 (d) * | 1968-09-20 | 1970-05-29 | Goulding Ltd |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS59193845A (ja) | （＋）―および（―）―６―メトキシ―α―メチル―２―ナフタレン酢酸・Ｎ―メチル―Ｄ―グルカミン塩 | |
| JPS6233223B2 (d) | ||
| BE372395A (d) | ||
| EP0469742B1 (en) | Production of acetaminophen | |
| Higson et al. | CXLII.—A method for the formation of succinic acid and of its alkyl derivatives | |
| Bailey et al. | The Action of Monochloroacetic Acid on Semicarbazide and Hydrazine. | |
| JPH01186838A (ja) | ３−（４’−ブロモビフェニル）−４−フェニル酪酸の製造方法 | |
| CH395110A (de) | Procédé de préparation de la dibenzyloxyphosphorylcréatinine | |
| JPS6112640A (ja) | ビスフエノ−ル類の製法 | |
| US2069546A (en) | Separation of chloranisidine isomers | |
| KR800001177B1 (ko) | 초산유도체류의 제조방법 | |
| RU2203263C2 (ru) | Способ выделения диэтилового эфира | |
| BE533435A (d) | ||
| JPS58172326A (ja) | ２，２−ジシクロヘキセニルプロパンの製法 | |
| BE854097Q (fr) | Procede de preparation industrielle du tri (hydroxymathyl) amino-methane-gluconate-di-hydroxy-aluminate | |
| KR800001176B1 (ko) | 아세트 아마이드 유도체의 제조방법 | |
| Ingold | XLII.—Experiments on the synthesis of the polyacetic acids of methane. Part I. The conditions controlling synthesis by the cyanoacetic ester method, and the preparation of methanetriacetic acid | |
| US707178A (en) | Methylene di-aceto di-salicylic acid and process of making same. | |
| Perkin et al. | CXXXI.—cyclo Butane-1: 3-dicarboxylic acid and some of its derivatives | |
| Ingold et al. | CLXVII.—Experiments on the synthesis of the polyacetic acids of methane. Part VI. Methanetriacetic acid and its unstable esters | |
| Goodwin et al. | LXXXVII.—The reduction of iso phthalic acid. Part II | |
| Stephen et al. | XXXII.—αδ-Derivatives of adipic and β-methyladipic acids, and the preparation of muconic and β-methylmuconic acids | |
| Hahn et al. | Synthesis of Polypeptide Hydantoins. Tyrosyl-Alanine Hydantoin | |
| Gardner et al. | CCXV.—The condensation of ketones and aldehydes with the sodium derivative of ethyl cyanoacetate. Part II | |
| BE445556A (fr) | Procédé pour la préparation, à l'état pur, d'acides aminocarboniques à partir d'oximes |