KR20230138803A - 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 - Google Patents
인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 Download PDFInfo
- Publication number
- KR20230138803A KR20230138803A KR1020220036878A KR20220036878A KR20230138803A KR 20230138803 A KR20230138803 A KR 20230138803A KR 1020220036878 A KR1020220036878 A KR 1020220036878A KR 20220036878 A KR20220036878 A KR 20220036878A KR 20230138803 A KR20230138803 A KR 20230138803A
- Authority
- KR
- South Korea
- Prior art keywords
- fermentation
- phosphoric acid
- hydrate
- phosphate
- ammonium phosphate
- Prior art date
Links
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title claims abstract description 306
- 229910000147 aluminium phosphate Inorganic materials 0.000 title claims abstract description 153
- 238000000855 fermentation Methods 0.000 title claims abstract description 145
- 230000004151 fermentation Effects 0.000 title claims abstract description 145
- 238000000034 method Methods 0.000 title claims abstract description 91
- 239000002921 fermentation waste Substances 0.000 title claims description 42
- 238000004064 recycling Methods 0.000 title 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims abstract description 62
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims abstract description 59
- 239000004254 Ammonium phosphate Substances 0.000 claims abstract description 58
- 235000019289 ammonium phosphates Nutrition 0.000 claims abstract description 58
- 239000007788 liquid Substances 0.000 claims description 57
- BZQFBWGGLXLEPQ-REOHCLBHSA-N phosphoserine Chemical compound OC(=O)[C@@H](N)COP(O)(O)=O BZQFBWGGLXLEPQ-REOHCLBHSA-N 0.000 claims description 51
- FXDNYOANAXWZHG-VKHMYHEASA-N O-phospho-L-homoserine Chemical compound OC(=O)[C@@H](N)CCOP(O)(O)=O FXDNYOANAXWZHG-VKHMYHEASA-N 0.000 claims description 43
- 244000005700 microbiome Species 0.000 claims description 33
- 239000012141 concentrate Substances 0.000 claims description 31
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 24
- 239000013078 crystal Substances 0.000 claims description 20
- 102000004190 Enzymes Human genes 0.000 claims description 19
- 108090000790 Enzymes Proteins 0.000 claims description 19
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 17
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 13
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 13
- 150000001413 amino acids Chemical class 0.000 claims description 12
- -1 diammonium hydrogen phosphate heptahydrate Chemical group 0.000 claims description 12
- 239000012452 mother liquor Substances 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- 229910000388 diammonium phosphate Inorganic materials 0.000 claims description 4
- 235000019838 diammonium phosphate Nutrition 0.000 claims description 4
- 239000010808 liquid waste Substances 0.000 claims description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 239000002699 waste material Substances 0.000 abstract description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 44
- 238000002425 crystallisation Methods 0.000 description 33
- 230000008025 crystallization Effects 0.000 description 33
- 229910019142 PO4 Inorganic materials 0.000 description 32
- 239000010452 phosphate Substances 0.000 description 32
- 238000011084 recovery Methods 0.000 description 31
- 238000010979 pH adjustment Methods 0.000 description 24
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 21
- 229960002433 cysteine Drugs 0.000 description 20
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 19
- 235000018417 cysteine Nutrition 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000000243 solution Substances 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 15
- 108030001910 O-phosphoserine sulfhydrylases Proteins 0.000 description 14
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 13
- 229930182817 methionine Natural products 0.000 description 13
- 239000002243 precursor Substances 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 12
- 229940024606 amino acid Drugs 0.000 description 11
- 235000001014 amino acid Nutrition 0.000 description 11
- 229910001415 sodium ion Inorganic materials 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- 239000013076 target substance Substances 0.000 description 10
- 102000011848 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase Human genes 0.000 description 9
- 108010075604 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase Proteins 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 9
- 230000001419 dependent effect Effects 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 239000011574 phosphorus Substances 0.000 description 9
- 229910052698 phosphorus Inorganic materials 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 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 6
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 150000001944 cysteine derivatives Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 150000002741 methionine derivatives Chemical class 0.000 description 5
- 229940085991 phosphate ion Drugs 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 3
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 3
- 229960003067 cystine Drugs 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 238000000638 solvent extraction Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- ROUPZXDBSPQFLE-UHFFFAOYSA-N triazanium;phosphate;hydrate Chemical compound [NH4+].[NH4+].[NH4+].O.[O-]P([O-])([O-])=O ROUPZXDBSPQFLE-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000003053 toxin Substances 0.000 description 2
- 231100000765 toxin Toxicity 0.000 description 2
- 108700012359 toxins Proteins 0.000 description 2
- QIJRTFXNRTXDIP-UHFFFAOYSA-N (1-carboxy-2-sulfanylethyl)azanium;chloride;hydrate Chemical compound O.Cl.SCC(N)C(O)=O QIJRTFXNRTXDIP-UHFFFAOYSA-N 0.000 description 1
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- JZCAHRHZFBBFRZ-WCCKRBBISA-N (2s)-2-amino-4-methylsulfanylbutanoic acid;copper Chemical compound [Cu].CSCC[C@H](N)C(O)=O JZCAHRHZFBBFRZ-WCCKRBBISA-N 0.000 description 1
- KDLLAIYWORQMSN-WCCKRBBISA-N (2s)-2-amino-4-methylsulfanylbutanoic acid;iron Chemical compound [Fe].CSCC[C@H](N)C(O)=O KDLLAIYWORQMSN-WCCKRBBISA-N 0.000 description 1
- LHJPJULTVBDZBN-WCCKRBBISA-N (2s)-2-amino-4-methylsulfanylbutanoic acid;magnesium Chemical compound [Mg].CSCC[C@H](N)C(O)=O LHJPJULTVBDZBN-WCCKRBBISA-N 0.000 description 1
- BZVFZBYIWNIHHL-WCCKRBBISA-N (2s)-2-amino-4-methylsulfanylbutanoic acid;manganese Chemical compound [Mn].CSCC[C@H](N)C(O)=O BZVFZBYIWNIHHL-WCCKRBBISA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 102100037579 D-3-phosphoglycerate dehydrogenase Human genes 0.000 description 1
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 1
- 239000004201 L-cysteine Substances 0.000 description 1
- 235000013878 L-cysteine Nutrition 0.000 description 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- XUYPXLNMDZIRQH-LURJTMIESA-N N-acetyl-L-methionine Chemical compound CSCC[C@@H](C(O)=O)NC(C)=O XUYPXLNMDZIRQH-LURJTMIESA-N 0.000 description 1
- 108010038555 Phosphoglycerate dehydrogenase Proteins 0.000 description 1
- 102100021762 Phosphoserine phosphatase Human genes 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 229960004308 acetylcysteine Drugs 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003862 amino acid derivatives Chemical class 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical compound [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-O azanium;hydron;hydroxide Chemical compound [NH4+].O VHUUQVKOLVNVRT-UHFFFAOYSA-O 0.000 description 1
- UUQMNUMQCIQDMZ-UHFFFAOYSA-N betahistine Chemical compound CNCCC1=CC=CC=N1 UUQMNUMQCIQDMZ-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 229960001305 cysteine hydrochloride Drugs 0.000 description 1
- KKEZAVVOJGHSFU-UHFFFAOYSA-N diazanium dihydrogen phosphate Chemical compound [NH4+].[NH4+].OP(O)([O-])=O.OP(O)([O-])=O KKEZAVVOJGHSFU-UHFFFAOYSA-N 0.000 description 1
- PYLIXCKOHOHGKQ-UHFFFAOYSA-L disodium;hydrogen phosphate;heptahydrate Chemical compound O.O.O.O.O.O.O.[Na+].[Na+].OP([O-])([O-])=O PYLIXCKOHOHGKQ-UHFFFAOYSA-L 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229940099459 n-acetylmethionine Drugs 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 102000030592 phosphoserine aminotransferase Human genes 0.000 description 1
- 108010088694 phosphoserine aminotransferase Proteins 0.000 description 1
- 108010076573 phosphoserine phosphatase Proteins 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229940110280 zinc methionine Drugs 0.000 description 1
- CNMFGFBWPBBGKX-SCGRZTRASA-L zinc;(2s)-2-amino-4-methylsulfanylbutanoate Chemical compound [Zn+2].CSCC[C@H](N)C([O-])=O.CSCC[C@H](N)C([O-])=O CNMFGFBWPBBGKX-SCGRZTRASA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P3/00—Preparation of elements or inorganic compounds except carbon dioxide
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/26—Phosphates
- C01B25/28—Ammonium phosphates
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/18—Phosphoric acid
- C01B25/234—Purification; Stabilisation; Concentration
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B7/00—Fertilisers based essentially on alkali or ammonium orthophosphates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/12—Methionine; Cysteine; Cystine
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Removal Of Specific Substances (AREA)
- Fertilizers (AREA)
Abstract
Description
도 2는 O-포스포세린(O-phosphoserine, OPS) 또는 O-포스포호모세린(O-phosphohomoserine, OPHS) 발효액으로부터 효소 전환 반응을 이용하여 생산된, 발효액; 또는 상기 발효액에서 시스테인, 시스테인 유도체, 메티오닌 또는 메티오닌 유도체를 제거하고 남은, 발효 폐액으로부터, 인산암모늄 또는 이의 수화물을 회수하고, 해당 인산 회수 물질을 다시 O-포스포세린 또는 O-포스포호모세린 발효에 사용하는 공정을 간략히 나타낸 것이다.
도 3은 O-포스포세린 또는 O-포스포호모세린 발효액으로부터 효소 전환 반응을 이용하여 생산된, 발효액; 또는 상기 발효액에서 시스테인, 시스테인 유도체, 메티오닌 또는 메티오닌 유도체를 제거하고 남은, 발효 폐액으로부터, 인산암모늄 또는 이의 수화물을 2 단계에 걸쳐 회수하고, 회수한 인산을 다시 O-포스포세린 또는 O-포스포호모세린 발효에 사용하는 공정을 간략히 나타낸 것이다.
비교예 1 | 실험예 1 | |
나트륨 함량(%) | 18.3 | 11.0 |
암모늄 함량(%) | 2.1 | 7.1 |
인산염 함량(%) | 42.4 | 42.8 |
황산염 함량(%) | 2.2 | 4.1 |
비교예 1 | 실험예 1 | |
나트륨 농도(g/L) | 92.4 | 68.6 |
암모늄 농도(g/L) | 13.1 | 44.1 |
인산염 농도(g/L) | 61.2 | 59.2 |
황산염 농도(g/L) | 139.3 | 153.1 |
비교예 1 | 실험예 1 | |
초기 인산(g) | 85.0 | 85.0 |
인산염(g) | 126.0 | 134.0 |
회수 인산(g) | 54.0 | 57.0 |
인산 회수율(%) | 63.5 | 67.0 |
Claims (13)
- (a) 인산을 함유하는 발효액 또는 발효 폐액을 농축하는 단계;
(b) 상기 농축된 농축액에 암모니아 가스 또는 암모니아수를 첨가하여 농축액의 pH를 8 내지 11로 조정하는 단계; 및
(c) 상기 pH 조정된 농축액으로부터 인산암모늄 또는 이의 수화물을 분리하는 단계;를 포함하는,
인산을 발효액 또는 발효 폐액으로부터 회수하는 방법.
- (a) 인산을 함유하는 발효액 또는 발효 폐액을 농축하는 단계;
(b) 상기 농축된 농축액에 암모니아 가스 또는 암모니아수를 첨가하여 농축액의 pH를 8 내지 11로 조정하는 단계;
(c) 상기 pH 조정된 농축액으로부터 인산암모늄 또는 이의 수화물을 분리하는 단계; 및
(d) 상기 인산암모늄 또는 이의 수화물을 배지에 투여하는 단계를 포함하는, 인산을 발효액 또는 발효 폐액으로부터 재사용하는 방법.
- 제1항 또는 제2항에 있어서, 상기 인산암모늄은 인산수소이암모늄인, 방법.
- 제1항 또는 제2항에 있어서, 상기 발효액은 (i) O-포스포세린, (ii) O-포스포호모세린, 또는 (iii) O-포스포세린 또는 O-포스포호모세린, 전환효소 또는 이를 발현하는 미생물, 및 황화물을 첨가하여 제조한 아미노산 또는 이의 유도체;를 포함하는 것인, 방법.
- 제1항 또는 제2항에 있어서, 상기 (b) 단계와 (c) 단계 사이 또는 (c) 단계에서, 상기 pH 조정된 농축액을 냉각시키는 단계를 추가로 포함하는, 방법.
- 제1항 또는 제2항에 있어서, 상기 (b) 단계와 (c) 단계 사이 또는 (c) 단계에, 인산암모늄 또는 이의 수화물의 결정을 결정핵으로 첨가하는 단계를 추가로 포함하는, 방법.
- 제1항 또는 제2항에 있어서, 상기 수화물은 인산수소이암모늄 7수화물 또는 인산수소이암모늄 12수화물인, 방법.
- 제1항 또는 제2항에 있어서, 상기 (c) 단계의 인산암모늄 또는 이의 수화물을 모액으로부터 결정화하는 단계를 추가적으로 포함하는, 방법.
- 제8항에 있어서, 상기 (c) 단계는, (i) 모액을 농축하는 단계, (ii) 상기 모액의 pH를 8 내지 11로 조정하는 단계, 및 (iii) 상기 pH 조정된 모액으로부터 인산암모늄 또는 이의 수화물을 결정화하여 분리하는 단계를 포함하는, 방법.
- 제9항에 있어서, 상기 (ii) 단계와 (iii) 단계 사이 또는 (iii) 단계에, 모액에 인산암모늄 또는 이의 수화물 결정을 결정핵으로 첨가하는 단계를 추가로 포함하는, 방법.
- 제1항 또는 제2항에 있어서, 상기 (a) 단계 전에, 발효액 또는 발효 폐액을 pH 8 내지 11로 조정하는 단계를 추가로 포함하는, 방법.
- 제1항 또는 제2항에 있어서, 상기 (b) 단계; 또는 (b) 단계와 (c) 단계 사이에, 알코올을 첨가하는 단계를 추가로 포함하는, 방법.
- 제12항에 있어서, 상기 알코올은 메탄올, 에탄올, 프로판올, 부탄올 또는 이들의 조합인 것인, 방법.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020220036878A KR102744891B1 (ko) | 2022-03-24 | 2022-03-24 | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 |
CN202380029432.2A CN118922552A (zh) | 2022-03-24 | 2023-03-20 | 从发酵液或发酵废液中回收磷酸以及再利用磷酸的方法 |
PCT/KR2023/003652 WO2023182744A1 (ko) | 2022-03-24 | 2023-03-20 | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 |
EP23775241.5A EP4474481A1 (en) | 2022-03-24 | 2023-03-20 | Method for recovering phosphoric acid from fermentation broth or fermentation waste liquid and reusing same |
TW112110740A TWI866124B (zh) | 2022-03-24 | 2023-03-22 | 用於自醱酵液或醱酵廢液回收及再循環磷酸的方法 |
ARP230100739A AR128882A1 (es) | 2022-03-24 | 2023-03-27 | Método de recuperación y reutilización del ácido fosfórico del caldo de fermentación o líquido de desecho de fermentación |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020220036878A KR102744891B1 (ko) | 2022-03-24 | 2022-03-24 | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20230138803A true KR20230138803A (ko) | 2023-10-05 |
KR102744891B1 KR102744891B1 (ko) | 2024-12-19 |
Family
ID=88101800
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020220036878A KR102744891B1 (ko) | 2022-03-24 | 2022-03-24 | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP4474481A1 (ko) |
KR (1) | KR102744891B1 (ko) |
CN (1) | CN118922552A (ko) |
AR (1) | AR128882A1 (ko) |
WO (1) | WO2023182744A1 (ko) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101857210A (zh) * | 2010-06-04 | 2010-10-13 | 广西明利集团有限公司 | 用湿法磷酸生产工业级磷酸二铵的方法 |
KR20190008465A (ko) * | 2017-07-13 | 2019-01-24 | 씨제이제일제당 (주) | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3375068A (en) | 1965-03-01 | 1968-03-26 | St Paul Ammonia Products Inc | Phosphoric acid extraction |
US3466141A (en) | 1966-02-22 | 1969-09-09 | Mini Ind Chimice | Process for the production of sodium phosphates |
EP0087323B1 (en) | 1982-02-23 | 1986-09-03 | The Dharamsi Morarji Chemical Company Limited | A process to manufacture commercially acceptable phosphoric acid and gypsum from rock phosphate |
US4543239A (en) | 1984-08-21 | 1985-09-24 | International Minerals & Chemical Corp. | Phosphoric acid extraction process |
US7687046B2 (en) | 2002-06-28 | 2010-03-30 | Ecophos | Method of producing phosphoric acid salt |
WO2005099854A1 (en) * | 2004-04-13 | 2005-10-27 | Iogen Energy Corporation | Recovery of inorganic salt during processing of lignocellulosic feedstocks |
MA33379B1 (fr) | 2009-05-27 | 2012-06-01 | Easymining Sweden Ab | Production de phosphates d'ammonium |
WO2012053794A2 (en) | 2010-10-20 | 2012-04-26 | Cj Cheiljedang Corporation | Microorganism producing o-phosphoserine and method of producing l-cysteine or derivatives thereof from o-phosphoserine using the same |
KR101208267B1 (ko) | 2010-10-20 | 2012-12-04 | 씨제이제일제당 (주) | O-포스포세린 설피드릴라제 변이체 |
KR101404376B1 (ko) | 2011-12-15 | 2014-06-11 | 씨제이제일제당 (주) | 신규 o-포스포세린 설프하이드릴라아제를 이용하여 시스테인 또는 이의 유도체를 생산하는 방법 |
KR101397555B1 (ko) * | 2012-07-24 | 2014-05-20 | 한국화학연구원 | 암모늄락테이트로부터 젖산 및 락타이드의 제조방법 |
US9803225B2 (en) | 2012-10-26 | 2017-10-31 | Adisseo France S.A.S. | Means and methods for the enzymatic production of L-methionine from O-phospho-L-homoserine and methanethiol |
KR101493154B1 (ko) | 2013-05-10 | 2015-02-13 | 씨제이제일제당 (주) | 신규 RhtB 단백질 변이체 및 이를 이용한 O-포스포세린의 생산방법 |
KR101525663B1 (ko) | 2013-05-10 | 2015-06-04 | 씨제이제일제당 (주) | 신규 o-포스포세린 배출 단백질 및 이를 이용한 o-포스포세린의 생산방법 |
CA3024212C (en) * | 2016-05-20 | 2020-03-31 | Cambi Technology As | Method for recovery of phosphate |
-
2022
- 2022-03-24 KR KR1020220036878A patent/KR102744891B1/ko active IP Right Grant
-
2023
- 2023-03-20 EP EP23775241.5A patent/EP4474481A1/en active Pending
- 2023-03-20 WO PCT/KR2023/003652 patent/WO2023182744A1/ko active Application Filing
- 2023-03-20 CN CN202380029432.2A patent/CN118922552A/zh active Pending
- 2023-03-27 AR ARP230100739A patent/AR128882A1/es unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101857210A (zh) * | 2010-06-04 | 2010-10-13 | 广西明利集团有限公司 | 用湿法磷酸生产工业级磷酸二铵的方法 |
KR20190008465A (ko) * | 2017-07-13 | 2019-01-24 | 씨제이제일제당 (주) | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 |
Also Published As
Publication number | Publication date |
---|---|
EP4474481A1 (en) | 2024-12-11 |
CN118922552A (zh) | 2024-11-08 |
WO2023182744A1 (ko) | 2023-09-28 |
TW202403050A (zh) | 2024-01-16 |
KR102744891B1 (ko) | 2024-12-19 |
AR128882A1 (es) | 2024-06-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9752167B2 (en) | Methods for production of L-methionine and related products | |
US8372606B2 (en) | Methods for obtaining crystals of a basic amino acid hydrochloride | |
AU2018299607B2 (en) | Method Of Recovering Phosphoric Acid From Fermentation Broth Or Fermentation Waste Liquid And Reusing The Same | |
JP2005139156A (ja) | コハク酸モノアンモニウム塩の製造法 | |
KR102744891B1 (ko) | 인산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 | |
CN108101791B (zh) | 从发酵溶液分离和纯化1,4-二氨基丁烷的方法 | |
CN108558908B (zh) | 一种头孢他啶母液的除盐方法及头孢他啶的制备方法 | |
TWI866124B (zh) | 用於自醱酵液或醱酵廢液回收及再循環磷酸的方法 | |
CN112391424A (zh) | 一种l-天冬氨酸的清洁提取工艺 | |
KR20230030600A (ko) | 아세트산을 발효액 또는 발효 폐액으로부터 회수 및 재사용하는 방법 | |
JP2018520698A (ja) | セルロース、ヘミセルロース及びリグニンを含む物質の酸加水分解物から発酵性糖を単離する方法 | |
KR101395558B1 (ko) | 퀴놀린산의 정제방법 | |
KR20230079987A (ko) | 3-하이드록시프로피온산의 회수 공정 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20220324 |
|
PA0201 | Request for examination | ||
PG1501 | Laying open of application | ||
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20240320 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20241129 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20241216 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20241217 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration |