BR112017017246A2 - método para preparação contínua de cristal de metionia de alta densidade aparente - Google Patents
método para preparação contínua de cristal de metionia de alta densidade aparenteInfo
- Publication number
- BR112017017246A2 BR112017017246A2 BR112017017246A BR112017017246A BR112017017246A2 BR 112017017246 A2 BR112017017246 A2 BR 112017017246A2 BR 112017017246 A BR112017017246 A BR 112017017246A BR 112017017246 A BR112017017246 A BR 112017017246A BR 112017017246 A2 BR112017017246 A2 BR 112017017246A2
- Authority
- BR
- Brazil
- Prior art keywords
- crystals
- elutriation
- region
- mixture
- collector
- Prior art date
Links
- 239000013078 crystal Substances 0.000 title abstract 9
- 238000000034 method Methods 0.000 title abstract 4
- 238000002360 preparation method Methods 0.000 title abstract 2
- 239000000463 material Substances 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 238000006386 neutralization reaction Methods 0.000 abstract 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 abstract 2
- 238000002425 crystallisation Methods 0.000 abstract 2
- 230000008025 crystallization Effects 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 229930182817 methionine Natural products 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- SBKRXUMXMKBCLD-UHFFFAOYSA-N 5-(2-methylsulfanylethyl)imidazolidine-2,4-dione Chemical compound CSCCC1NC(=O)NC1=O SBKRXUMXMKBCLD-UHFFFAOYSA-N 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 230000003472 neutralizing effect Effects 0.000 abstract 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D9/00—Crystallisation
- B01D9/0036—Crystallisation on to a bed of product crystals; Seeding
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/57—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
- C07C323/58—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D9/00—Crystallisation
- B01D9/0004—Crystallisation cooling by heat exchange
- B01D9/0013—Crystallisation cooling by heat exchange by indirect heat exchange
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D9/00—Crystallisation
- B01D9/0018—Evaporation of components of the mixture to be separated
- B01D9/0027—Evaporation of components of the mixture to be separated by means of conveying fluid, e.g. spray-crystallisation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D9/00—Crystallisation
- B01D9/005—Selection of auxiliary, e.g. for control of crystallisation nuclei, of crystal growth, of adherence to walls; Arrangements for introduction thereof
- B01D9/0054—Use of anti-solvent
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/26—Separation; Purification; Stabilisation; Use of additives
- C07C319/28—Separation; Purification
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D9/00—Crystallisation
- B01D2009/0086—Processes or apparatus therefor
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
a presente invenção diz respeito a um método para a preparação contínua de cristais de metionina de alta densidade aparente. o processo do método é da seguinte forma: um hidrolisado, o qual é obtido a partir de uma reação de 5-(ß-metiltioetil)hidantoína e uma solução de carbonato de potássio, é misturado com um material de circulação externa a partir de um cristalizador de neutralização dtb com uma seção de neutralização de fase gasosa; depois que a mistura é resfriada, a mistura entra em um distribuidor de líquido de uma região de neutralização na parte superior do cristalizador; a mistura é pulverizada em gotículas ou gotas de líquido em gás de dióxido de carbono para a reação de neutralização e, então, naturalmente cai em uma região de cristalização na parte inferior a ser misturada com um material na região; a mistura cresce em pequenos cristais em um sistema para formar cristais com diâmetros de partícula maiores e, entretanto, novos núcleos de cristal são formados; em uma região de decantação na parte mediana da região de cristalização, os cristais com diâmetros de partícula maiores afundam em um coletor de elutriação, enquanto os cristais pequenos circulam com o material de circulação externa, e uma parte do material de circulação externa é usada para elutriação dos cristais no coletor de elutriação, e outra parte desta é usada para misturar com o hidrolisado; e os cristais no coletor de elutriação são separados, lavados e secos para obter produto de metionina de alta densidade aparente.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510078388.1A CN104744326B (zh) | 2015-02-12 | 2015-02-12 | 一种连续制备高堆积密度甲硫氨酸结晶的方法 |
CN201510078388.1 | 2015-02-12 | ||
PCT/CN2015/098368 WO2016127707A1 (zh) | 2015-02-12 | 2015-12-23 | 一种连续制备高堆积密度甲硫氨酸结晶的方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
BR112017017246A2 true BR112017017246A2 (pt) | 2018-04-17 |
BR112017017246B1 BR112017017246B1 (pt) | 2021-06-01 |
Family
ID=53584679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112017017246-1A BR112017017246B1 (pt) | 2015-02-12 | 2015-12-23 | Método para preparação contínua de cristal de metionia de alta densidade aparente |
Country Status (14)
Country | Link |
---|---|
US (1) | US10293273B2 (pt) |
EP (1) | EP3246310B1 (pt) |
JP (1) | JP6423109B2 (pt) |
KR (1) | KR101975189B1 (pt) |
CN (1) | CN104744326B (pt) |
AU (1) | AU2015382630B2 (pt) |
BR (1) | BR112017017246B1 (pt) |
CA (1) | CA2974447A1 (pt) |
MX (1) | MX2017010418A (pt) |
MY (1) | MY183295A (pt) |
RU (1) | RU2678585C2 (pt) |
SG (1) | SG11201705530VA (pt) |
WO (1) | WO2016127707A1 (pt) |
ZA (1) | ZA201705902B (pt) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104744326B (zh) * | 2015-02-12 | 2016-08-10 | 山东新和成氨基酸有限公司 | 一种连续制备高堆积密度甲硫氨酸结晶的方法 |
CN106008297B (zh) * | 2016-06-03 | 2018-11-30 | 宁夏紫光天化蛋氨酸有限责任公司 | 一种蛋氨酸新晶型ⅱ及其制备方法 |
CN106083675B (zh) * | 2016-06-03 | 2018-07-27 | 宁夏紫光天化蛋氨酸有限责任公司 | 一种蛋氨酸新晶型i及其制备方法 |
KR20180078621A (ko) * | 2016-12-30 | 2018-07-10 | 씨제이제일제당 (주) | 결정화 기술을 이용한 l-메티오닌 결정의 제조방법 |
CN108794363A (zh) * | 2017-05-02 | 2018-11-13 | 宁夏紫光天化蛋氨酸有限责任公司 | 一种蛋氨酸结晶方法 |
EP3636633B1 (en) * | 2017-05-16 | 2022-06-01 | Sumitomo Chemical Company, Limited | Pneumatic conveyance method for methionine |
CN109384696A (zh) * | 2017-08-03 | 2019-02-26 | 宁夏紫光天化蛋氨酸有限责任公司 | 一种获得高纯度高堆积密度蛋氨酸的方法 |
CN111542512A (zh) * | 2017-12-27 | 2020-08-14 | 住友化学株式会社 | 纯化甲硫氨酸的制造方法 |
CN108939603B (zh) * | 2018-09-06 | 2021-06-18 | 四川金象赛瑞化工股份有限公司 | 一种分离硫酸钠和硫酸铵过程中直接冷却结晶的方法 |
CN109173329B (zh) * | 2018-10-31 | 2023-08-29 | 浙江新和成股份有限公司 | 用于蒸发结晶的装置 |
WO2020254403A1 (en) | 2019-06-18 | 2020-12-24 | Evonik Operations Gmbh | Process for the preparation of d,l-methionine |
CN111389044A (zh) * | 2020-04-16 | 2020-07-10 | 天津天大清能环境工程有限公司 | 一种防结垢蒸发结晶系统及方法 |
JP2023545162A (ja) | 2020-10-13 | 2023-10-26 | エボニック オペレーションズ ゲーエムベーハー | 最適化された粒度分布を有するd,l-メチオニン |
CN114426298B (zh) * | 2020-10-29 | 2023-08-01 | 中国石油化工股份有限公司 | 碳化法制备氢氧化铝的系统及其碳化反应器 |
CN113289372A (zh) * | 2021-06-23 | 2021-08-24 | 江苏派克斯特纤维素有限公司 | 非食用盐加工用蒸发结晶装置 |
CN115043763B (zh) * | 2022-06-14 | 2024-04-05 | 天津大学 | 一种dl-蛋氨酸的气液连续结晶方法 |
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CA866570A (en) * | 1968-07-19 | 1971-03-23 | Werner Hans-Helmut | Recovery of minerals from saturated solutions by crystallization |
JPS5818122B2 (ja) * | 1975-05-23 | 1983-04-11 | 日石三菱株式会社 | シヨウセキハンノウソウチ |
SU1428406A1 (ru) * | 1986-10-08 | 1988-10-07 | Предприятие П/Я Р-6273 | Способ регулировани процесса кристаллизации в циркул ционном кристаллизаторе |
JP2921097B2 (ja) | 1990-10-30 | 1999-07-19 | 住友化学工業株式会社 | メチオニンの製造方法 |
FR2708267B1 (fr) | 1993-07-28 | 1995-09-01 | Rhone Poulenc Nutrition Animal | Méthode de cristallisation de la méthionine. |
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DE69709526T2 (de) * | 1996-10-31 | 2002-08-01 | Sumitomo Chemical Co | Verfahren zur Herstellung von Methionin |
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JP4338524B2 (ja) * | 2001-11-29 | 2009-10-07 | 日本曹達株式会社 | メチオニンの製造方法 |
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JP2008297251A (ja) * | 2007-05-31 | 2008-12-11 | Mitsui Chemicals Inc | ビスフェノール類の晶析方法 |
JP2009292795A (ja) * | 2008-06-09 | 2009-12-17 | Sumitomo Chemical Co Ltd | メチオニンの製造方法 |
JP2009292796A (ja) | 2008-06-09 | 2009-12-17 | Sumitomo Chemical Co Ltd | メチオニンの製造方法 |
DE102008029050A1 (de) * | 2008-06-18 | 2009-12-24 | Gea Messo Gmbh | Verfahren und Vorrichtung zur kontinuierlichen Herstellung eines Kristallisats mit konstanter Korngrößenverteilung |
JP2010111640A (ja) * | 2008-11-07 | 2010-05-20 | Sumitomo Chemical Co Ltd | メチオニンの製造方法 |
WO2012091479A2 (en) * | 2010-12-29 | 2012-07-05 | Cj Cheiljedang Corporation | Methods for production of l-methionine and related products |
EP2641898A1 (de) | 2012-03-20 | 2013-09-25 | Evonik Industries AG | Verfahren zur Herstellung von Methionin |
CN102897795B (zh) * | 2012-11-12 | 2015-02-25 | 中国石油化工股份有限公司 | 一种大颗粒硫酸铵晶体的生产方法 |
CN202983275U (zh) * | 2012-11-22 | 2013-06-12 | 中节能六合天融环保科技有限公司 | 一种具有dtb特性的真空结晶器 |
CN204170452U (zh) * | 2014-05-14 | 2015-02-25 | 重庆紫光化工股份有限公司 | 一种有机合成料液的分离纯化系统 |
CN104744326B (zh) | 2015-02-12 | 2016-08-10 | 山东新和成氨基酸有限公司 | 一种连续制备高堆积密度甲硫氨酸结晶的方法 |
-
2015
- 2015-02-12 CN CN201510078388.1A patent/CN104744326B/zh active Active
- 2015-12-23 SG SG11201705530VA patent/SG11201705530VA/en unknown
- 2015-12-23 AU AU2015382630A patent/AU2015382630B2/en active Active
- 2015-12-23 RU RU2017121649A patent/RU2678585C2/ru active
- 2015-12-23 WO PCT/CN2015/098368 patent/WO2016127707A1/zh active Application Filing
- 2015-12-23 JP JP2017552207A patent/JP6423109B2/ja active Active
- 2015-12-23 MY MYPI2017001156A patent/MY183295A/en unknown
- 2015-12-23 CA CA2974447A patent/CA2974447A1/en not_active Abandoned
- 2015-12-23 KR KR1020177022736A patent/KR101975189B1/ko active IP Right Grant
- 2015-12-23 MX MX2017010418A patent/MX2017010418A/es active IP Right Grant
- 2015-12-23 US US15/549,833 patent/US10293273B2/en active Active
- 2015-12-23 EP EP15881855.9A patent/EP3246310B1/en not_active Not-in-force
- 2015-12-23 BR BR112017017246-1A patent/BR112017017246B1/pt active IP Right Grant
-
2017
- 2017-08-30 ZA ZA2017/05902A patent/ZA201705902B/en unknown
Also Published As
Publication number | Publication date |
---|---|
ZA201705902B (en) | 2018-12-19 |
CN104744326B (zh) | 2016-08-10 |
EP3246310A1 (en) | 2017-11-22 |
WO2016127707A1 (zh) | 2016-08-18 |
KR20170106400A (ko) | 2017-09-20 |
KR101975189B1 (ko) | 2019-05-07 |
RU2017121649A (ru) | 2018-12-21 |
AU2015382630B2 (en) | 2018-05-17 |
SG11201705530VA (en) | 2017-08-30 |
EP3246310A4 (en) | 2018-01-10 |
EP3246310B1 (en) | 2019-08-07 |
BR112017017246B1 (pt) | 2021-06-01 |
MX2017010418A (es) | 2018-06-07 |
RU2678585C2 (ru) | 2019-01-30 |
AU2015382630A1 (en) | 2017-08-24 |
MY183295A (en) | 2021-02-18 |
CN104744326A (zh) | 2015-07-01 |
US20180043281A1 (en) | 2018-02-15 |
JP6423109B2 (ja) | 2018-11-14 |
CA2974447A1 (en) | 2016-08-18 |
RU2017121649A3 (pt) | 2018-12-21 |
US10293273B2 (en) | 2019-05-21 |
JP2018504453A (ja) | 2018-02-15 |
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Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 23/12/2015, OBSERVADAS AS CONDICOES LEGAIS. |