JP6873310B2 - メチオニン−金属キレート及びその製造方法 - Google Patents
メチオニン−金属キレート及びその製造方法 Download PDFInfo
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- JP6873310B2 JP6873310B2 JP2020501488A JP2020501488A JP6873310B2 JP 6873310 B2 JP6873310 B2 JP 6873310B2 JP 2020501488 A JP2020501488 A JP 2020501488A JP 2020501488 A JP2020501488 A JP 2020501488A JP 6873310 B2 JP6873310 B2 JP 6873310B2
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- Prior art keywords
- methionine
- metal
- chelate
- metal chelate
- zinc
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- 238000001035 drying Methods 0.000 claims description 22
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- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic System
- C07F3/003—Compounds containing elements of Groups 2 or 12 of the Periodic System without C-Metal linkages
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
- C07C319/20—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by reactions not involving the formation of sulfide groups
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/142—Amino acids; Derivatives thereof
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- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F11/00—Compounds of calcium, strontium, or barium
- C01F11/36—Nitrates
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- C05C—NITROGENOUS FERTILISERS
- C05C5/00—Fertilisers containing other nitrates
- C05C5/04—Fertilisers containing other nitrates containing calcium nitrate
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
- C07F1/005—Compounds containing elements of Groups 1 or 11 of the Periodic System without C-Metal linkages
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic System
- C07F1/08—Copper compounds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic System
- C07F13/005—Compounds without a metal-carbon linkage
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic System
- C07F3/06—Zinc compounds
Description
特許文献1に記載の方法によりメチオニン−亜鉛キレートを製造した。具体的には、ZnCl2水溶液2Lを調製し、それにL−メチオニンの濃度が120g/LとなるようにZnCl2:L−メチオニン=1:2のモル比でL−メチオニンを溶解した。当該水溶液にNaOHをL−メチオニンと同じ当量比で投入し、L−メチオニン−亜鉛キレート粒子を含む懸濁液を作製した。当該懸濁液を真空濾過器で分離してL−メチオニン−亜鉛キレートを得た。乾燥後の含有量はメチオニン79.1%、亜鉛17.8%であり、ここで、純度は96.9%、回収率は78.3%であった。
特許文献2に記載の方法によりメチオニン−亜鉛キレートを製造した。具体的には、L−メチオニン120gにCa(OH)2とZnSO4七水和物をL−メチオニンに対する当量比0.5で混合して粉末混合物を作製した。当該混合物を密閉容器に入れ、80℃で12時間反応させた。その後、常温まで冷却し、L−メチオニン−亜鉛キレートとCaSO4混合物を得た。乾燥後の含有量はメチオニン59.2%、亜鉛13.0%、カルシウム7.8%、SO418.0%であり、ここで、メチオニン−亜鉛キレートは不溶性塩(CaSO4)と共に析出し、メチオニンと亜鉛の含有量を加算した純度は73.7%であったので、95%以上の純度を得るためにはさらなる精製工程が必要であった。最終回収率は97.2%であった。
特許文献1に記載の方法によりメチオニン−マンガンキレートを製造した。具体的には、MnCl2水溶液2Lを調製し、それにL−メチオニンの濃度が120g/LとなるようにMnCl2:L−メチオニン=1:2のモル比でL−メチオニンを溶解した。当該水溶液にNaOHをL−メチオニンと同じ当量比で投入し、L−メチオニン−マンガンキレート粒子を含む懸濁液を作製した。当該懸濁液を真空濾過器で分離してL−メチオニン−マンガンキレートを得た。乾燥後の含有量はメチオニン67.2%、マンガン8.8%であり、ここで、純度は76.0%、回収率は7.1%であった。
特許文献1に記載の方法によりメチオニン−銅キレートを製造した。具体的には、CuCl2水溶液2Lを調製し、それにL−メチオニンの濃度が120g/LとなるようにCuCl2:L−メチオニン=1:2のモル比でL−メチオニンを溶解した。当該水溶液にNaOHをL−メチオニンと同じ当量比で投入し、L−メチオニン−銅キレート粒子を含む懸濁液を作製した。当該懸濁液を真空濾過器で分離してL−メチオニン−銅キレートを得た。乾燥後の含有量はメチオニン82.4%、銅16.8%であり、ここで、純度は99.2%、回収率は28.9%であった。
L−メチオニン濃度150g/Lの水溶性懸濁液2Lに前記L−メチオニンに対する当量比0.5でCa(OH)2を投入し、L−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にL−メチオニンに対する当量比0.4で六水和物であるZn(NO3)2・6H2Oを投入し、L−メチオニン−亜鉛キレートを得た。乾燥後の含有量はメチオニン81.8%、亜鉛17.8%であり、ここで、純度は99.6%、回収率は90.2%であった。
L−メチオニン濃度154g/Lの水溶性懸濁液2Lに前記L−メチオニンに対する当量比0.5でCa(OH)2を投入し、L−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にL−メチオニンに対する当量比0.5でZn(NO3)2・6H2Oを投入し、L−メチオニン−亜鉛キレートを得た。乾燥後の含有量はメチオニン81.4%、亜鉛18.1%であり、ここで、純度は99.5%、回収率は93.6%であった。
L−メチオニン濃度154g/Lの水溶性懸濁液2Lに前記L−メチオニンに対する当量比0.5でCa(OH)2を投入し、L−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にL−メチオニンに対する当量比0.7でZn(NO3)2・6H2Oを投入し、L−メチオニン−亜鉛キレートを得た。乾燥後の含有量はメチオニン81.4%、亜鉛18.2%であり、ここで、純度は99.6%、回収率は94.6%であった。
DL−メチオニン濃度154g/Lの水溶性懸濁液2Lに前記DL−メチオニンに対する当量比0.5でCa(OH)2を投入し、DL−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にDL−メチオニンに対する当量比0.5でZn(NO3)2・6H2Oを投入し、DL−メチオニン−亜鉛キレートを得た。乾燥後の含有量はメチオニン81.9%、亜鉛17.9%であり、ここで、純度は99.8%、回収率は93.9%であった。
L−メチオニン濃度240g/Lの水溶性懸濁液2Lに前記L−メチオニンに対する当量比0.5でCa(OH)2を投入し、L−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にL−メチオニンに対する当量比0.5でZn(NO3)2・6H2Oを投入し、L−メチオニン−亜鉛キレートを得た。乾燥後の含有量はメチオニン81.6%、亜鉛18.0%であり、ここで、純度は99.6%、回収率は94.9%であった。
L−メチオニン濃度120g/Lの水溶性懸濁液2Lに前記L−メチオニンに対する当量比0.5でCa(OH)2を投入し、L−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にL−メチオニンに対する当量比0.5でMn(NO3)2を投入し、L−メチオニン−マンガンキレートを得た。乾燥後の含有量はメチオニン59.4%、マンガン9.9%であり、ここで、純度は69.3%、回収率は45.4%であった。
L−メチオニン濃度120g/Lの水溶性懸濁液2Lに前記L−メチオニンに対する当量比0.5でCa(OH)2を投入し、L−メチオニン−カルシウムキレート水溶液を作製した。その後、当該水溶液にL−メチオニンに対する当量比0.5でCu(NO3)2三水和物を投入し、L−メチオニン−銅キレートを得た。乾燥後の含有量はメチオニン82.0%、銅17.1%であり、ここで、純度は99.1%、回収率は95.7%であった。
実施例2によるL−メチオニン−亜鉛キレートの製造後に、表題化合物であるL−メチオニン−亜鉛キレートを分離して残った母液を8倍にさらに濃縮することにより、反応副産物であるCa(NO3)2を主成分として含む液体肥料を製造した。120℃で前記液体肥料副産物の水分を全て蒸発させた後に残った固形分の含有量は、カルシウム22.2%、NO368.6%、メチオニン7.6%、亜鉛1.2%であった。
実施例2によるL−メチオニン−亜鉛キレートの製造後に、表題化合物であるL−メチオニン−亜鉛キレートを分離して残った母液を濃縮した液体肥料を流動層乾燥機(180℃)に噴射して顆粒結晶形態の固形肥料を製造した。
Claims (10)
- メチオニンとCa(OH)2を混合するステップと、
前記混合物に硝酸金属塩を添加してメチオニン−金属キレートを生成するステップとを含む、メチオニン−金属キレートの製造方法。 - 前記メチオニンは、L−メチオニン又はDL−メチオニンである、請求項1に記載のメチオニン−金属キレートの製造方法。
- 前記硝酸金属塩における金属は、銅(Cu)、亜鉛(Zn)及びマンガン(Mn)からなる群から選択される少なくとも1つの金属である、請求項1に記載のメチオニン−金属キレートの製造方法。
- 前記硝酸金属塩は、メチオニンに対して0.3以上3.0以下の当量比で添加する、請求項1に記載のメチオニン−金属キレートの製造方法。
- 前記生成したメチオニン−金属キレートを精製するステップをさらに含む、請求項1に記載のメチオニン−金属キレートの製造方法。
- 前記メチオニン−金属キレートを乾燥するステップをさらに含む、請求項1に記載のメチオニン−金属キレートの製造方法。
- メチオニンとCa(OH)2を混合するステップと、
前記混合物に硝酸金属塩を添加してメチオニン−金属キレートを生成するステップと、
生成したメチオニン−金属キレートを分離するステップと、
メチオニン−金属キレートを分離した濾液を濃縮するステップとを含む、硝酸カルシウム(Ca(NO3)2)の製造方法。 - 前記硝酸金属塩における金属は、銅(Cu)、亜鉛(Zn)及びマンガン(Mn)からなる群から選択される少なくとも1つの金属である、請求項7に記載の硝酸カルシウムの製造方法。
- 前記濃縮するステップの後に、乾燥、顆粒化又は結晶化するステップをさらに含む、請求項7に記載の硝酸カルシウムの製造方法。
- 前記硝酸カルシウムは肥料添加剤である、請求項7に記載の硝酸カルシウムの製造方法。
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CN111094301A (zh) | 2020-05-01 |
SG11202000339WA (en) | 2020-02-27 |
MY193003A (en) | 2022-09-21 |
EP3653632A1 (en) | 2020-05-20 |
EP3653632B1 (en) | 2023-02-22 |
KR20190008477A (ko) | 2019-01-24 |
BR112020000856A2 (pt) | 2020-10-06 |
KR102068016B1 (ko) | 2020-01-21 |
BR112020000856B1 (pt) | 2024-03-05 |
US10981937B2 (en) | 2021-04-20 |
CN111094301B (zh) | 2022-11-15 |
JP2020526563A (ja) | 2020-08-31 |
EP3653632A4 (en) | 2021-01-13 |
ES2941532T3 (es) | 2023-05-23 |
US20200270276A1 (en) | 2020-08-27 |
RU2748499C1 (ru) | 2021-05-26 |
WO2019013497A1 (ko) | 2019-01-17 |
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