WO1997034879A1 - Method for the preparation of melamine - Google Patents
Method for the preparation of melamine Download PDFInfo
- Publication number
- WO1997034879A1 WO1997034879A1 PCT/NL1997/000146 NL9700146W WO9734879A1 WO 1997034879 A1 WO1997034879 A1 WO 1997034879A1 NL 9700146 W NL9700146 W NL 9700146W WO 9734879 A1 WO9734879 A1 WO 9734879A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- melamine
- ammonia
- post
- product
- urea
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/62—Purification of melamine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/56—Preparation of melamine
- C07D251/60—Preparation of melamine from urea or from carbon dioxide and ammonia
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
Definitions
- the invention relates to a method for the preparation of melamine from urea in which melamine is recovered from a reaction product containing melamine by cooling the reaction product with a cooling medium in a supercritical state to obtain, without washing or further purification, a commercially usable high purity solid melamine product. More particularly the invention relates to a method for the preparation of melamine from urea via a continuous, anhydrous, high-pressure process in which melamine is recovered from a melamine melt by cooling the melamine melt through direct contact with a cooling medium in a supercritical state to obtain a high purity solid melamine product without further washing or purification. The product thus obtained is commercially valuable.
- the gaseous stream contains C0 2 and NH 3 off-gases and also melamine vapor while the liquid stream consists substantially of liquid melamine.
- the gaseous product is sent to a melamine scrubber, while the liquid melamine is transferred to a product cooler.
- the melamine scrubber In the melamine scrubber the above-mentioned C0 2 and NH 3 off-gases and melamine vapor, are scrubbed, at virtually the same pressure as the reactor pressure, with molten urea so as to pre-heat the urea, cool said off-gases and remove the melamine.
- the pre-heated urea which contains the removed melamine, is then fed to the reactor.
- the product cooler the pressure and temperature of the liquid melamine from the gas-liquid separator are reduced by means of a liquid cooling medium, preferably liquid ammonia, so as to produce a solid melamine product.
- the drawback of this method is that the purity of the melamine obtained is typically in the range of 96 to 99.5%. Besides melamine, contaminants such as urea, C0 2 , ammeline-related compounds and other organic solids (melem and melam, for example) are present. The resulting purity of such a product is not high enough for some critical melamine applications, such as coatings. There is a need for a method to directly obtain, without further purification steps, higher purity melamine.
- An object of the present invention is an improved method for the preparation of very high purity melamine, generally 99.5 to 99.95 wt. %, from urea in which the melamine is recovered from the urea pyrolysis reaction product as a dry powder.
- One particular object is an improved, continuous, high-pressure, anhydrous process for the production of melamine from urea in which very high purity melamine is obtained directly as a dry powder from the melamine melt through cooling.
- a continuous, anhydrous, high-pressure process for recovering solid melamine from the reaction product of urea pyrolysis can utilize a melamine scrubber unit, a reactor vessel, a gas-liquid separator unit, and a product cooler unit.
- the process can also optionally utilize either or both of a post-reactor vessel or an evaporator unit. In such a process:
- Liquid urea melt is fed into the melamine scrubber unit at a pressure of about 5 to 25 MPa, preferably 8 to 20 MPa and at a temperature above the melting point of urea.
- the liquid urea comes into contact with off-gases from the gas- liquid separator unit.
- These off-gases are composed primarily of carbon dioxide and ammonia with small amounts of melamine vapor.
- the urea melt scrubs the melamine vapor out of the off-gas.
- the off-gases also pre-heat the urea melt prior to its transfer to the reactor vessel.
- the carbon dioxide and ammonia gases are removed from the scrubber and are preferably sent to a urea plant for conversion to urea.
- the preheated urea melt which now contains small amounts of melamine, is removed from the scrubber and fed to the reactor vessel.
- the scrubber can be provided with a cooling jacket so as to ensure extra cooling.
- the scrubber can also be provided with internal cooling bodies.
- the urea and melamine melt is fed to the reactor vessel using, for example, a high-pressure pump.
- Ammonia either in the form of a liquid or hot vapor, is fed into the bottom of the reactor vessel for the purposes of promoting mixing in the vessel, preventing clogging of the vessel bottom, and preventing formation of melamine condensation products, for example, melam, melem and melone.
- the reactor vessel containing the urea melt, melamine, and ammonia is heated to a temperature of about 325°C to 450°C, preferably of about 350°C to 425°C, and pressurized to a pressure of about 5 to 25 MPa, preferably of about 8 to 20 MPa. Under these conditions, liquid melamine, gaseous carbon dioxide and more gaseous ammonia are produced from the pyrolysis of the urea melt. The melamine, carbon dioxide, and ammonia are fed as a mixed stream to the gas-liquid separator .
- the liquid melamine is separated from the gaseous ammonia and carbon dioxide and sent to, for example, a post-reactor vessel, an evaporator unit or a product cooler.
- the gaseous ammonia and carbon dioxide which also contain a small amount of melamine vapor are sent to the scrubber unit.
- the gas-liquid separator is preferably at the same temperature and pressure as the reactor vessel.
- the liquid melamine is further reacted with more ammonia under the same temperature and pressure conditions as are present in the reactor vessel. This second reaction with ammonia further reduces the impurity level in the melamine. After completion of this post-reaction the liquid melamine is sent to either an evaporator unit or a product cooler.
- the liquid melamine is converted to gaseous melamine. Any impurities remain in the evaporator unit while the gaseous melamine is transferred to a product cooler.
- the liquid or gaseous melamine is cooled and solidified by contacting with a cooling medium in a supercritical state.
- the pressure during cooling of the liquid or gaseous melamine is preferably such that the reduced pressure is between about 0.9 and 2.5, more preferably between a reduced pressure of about 1 and the reactor pressure.
- the temperature during cooling is preferably such that the reduced temperature is between about 0.9 and 2, more preferably between about 1 and 1.5.
- the solid highly pure melamine is removed from the bottom of the cooling unit.
- Figure 1 is a flow diagram of an embodiment according to the present invention of a system for the production of melamine from urea which incorporates a post-reaction step prior to the cooling step.
- Figure 2 is a flow diagram of an embodiment according to the present invention of a system for the production of melamine from urea which incorporates an evaporation step prior to the cooling step.
- the purity of the melamine can be substantially increased by directly cooling the urea pyrolysis reaction product with a supercritical cooling medium. More particularly we have discovered that substantial increases in the purity of melamine can be obtained in the preparation of melamine from urea via a continuous, anhydrous, high-pressure process, in which melamine is recovered from the melamine melt leaving the urea pyrolysis reactor, by cooling the melamine melt through direct contact with a cooling medium which is in a supercritical state.
- supercritical ammonia is used as the cooling medium.
- This cooling can be effected at a pressure that is virtually the same as or lower than the urea pyrolysis reactor pressure, but generally higher than the critical pressure of the cooling medium.
- This method yields melamine having a purity, without further washing or purification, of greater than 99 wt. %, and more specifically having a purity of 99.5 to 99.95 wt. %.
- the pressure and temperature of the cooling medium should be such that both the reduced pressure and temperature are about 0.9 or greater.
- Reduced pressure is defined as the ratio (P/P c ) between the actual pressure (P in MPa) and the critical pressure (P c in MPa) and reduced temperature is defined as the ratio (T/T c ) between the actual temperature (T in °K) and the critical temperature (T c in °K).
- Critical pressure is defined as the pressure of the liquid-vapor critical point.
- Critical temperature is defined as the temperature of the liquid-vapor critical point.
- Urea preferably in the form of a melt, is the preferred starting material for the production of melamine. Ammonia and carbon dioxide are by-products obtained during the melamine preparation, which proceeds according to the following reaction equation:
- the preparation of the melamine can be carried out at low pressure, preferably between about 0.1 and 2.5 MPa, in the presence of a catalyst such as aluminum oxide, or at high pressure, preferably between about 5 and 25 MPa, without a catalyst.
- the temperature of the reaction varies between about 325°C and 450°C and preferably is between about 350°C and 425°C.
- the by-products ammonia and carbon dioxide are generally returned to an adjoining urea plant. The results reported herein can be obtained in a plant suited for the preparation of melamine from urea.
- a plant suitable for the present invention can comprise a melamine scrubber, a reactor vessel, optionally in combination with a gas-liquid separator or with a separate gas-liquid separator, optionally a downstream post-reactor vessel and a product cooler.
- a reactor vessel optionally in combination with a gas-liquid separator or with a separate gas-liquid separator, optionally a downstream post-reactor vessel and a product cooler.
- the reactor can be a high pressure reactor, such as described in U.S. Patent No. 3,271,116, 3,470,163 or 3,432,274.
- a post-reactor vessel in which the melamine melt is contacted with ammonia, after which the post-reacted melamine is transferred to the product cooler, for cooling by means of direct contact with a cooling medium in a supercritical state.
- the advantage of incorporating a post-reaction step is that even lower amounts of by-products such as melem and/or melam are obtained, which results in a higher purity melamine product.
- Suitable post-reactor vessels are described in Nitrogen No. 139, September/October 1982, Fig. 3.
- melamine can be prepared from urea in a plant comprising a melamine scrubber 1, a reactor vessel 2 which contains an internal gas-liquid separation unit 3, a post-reactor vessel 4, and a product cooler 5.
- Urea melt is fed to the gas scrubber 1 at a pressure of about 5 to 25 MPa, preferably 8 to 20 MPa and at a temperature above the melting point of urea.
- the gas scrubber 1 can be provided with a cooling jacket so as to ensure extra cooling.
- the melamine scrubber 1 can also be provided with internal cooling bodies.
- the liquid urea comes into contact with off-gases from the gas-liquid separation unit 3 of the reactor vessel 2. These off-gases are composed primarily of carbon dioxide and ammonia with small amounts of melamine vapor.
- the urea melt scrubs the melamine vapor out of the off-gas and carries this melamine to the reactor vessel 2.
- the off-gases are cooled down from about the temperature of the reactor 2, that is from about 350°C to 425°C, to about 175°C to 235°C, while the urea melt is heated to about 175°C to 235°C.
- the melamine scrubber 1 temperature should, in general, not exceed about 275°C.
- the carbon dioxide and ammonia waste gases are removed from the top of the melamine scrubber 1 and are preferably returned to a urea plant for use as starting material.
- the urea and melamine melt can then be withdrawn from the melamine scrubber 1 and fed, for example via a high-pressure pump, to the reactor vessel 2, which is at a pressure of about 5 to 25 MPa, and preferably of about 8 to 20 MPa. Gravity transfer of the urea melt can also be utilized by placing the melamine scrubber 1 above the reactor vessel 2.
- the molten urea is converted into melamine, carbon dioxide and ammonia by heating to a temperature of about 325°C to 450°C, preferably of about 350°C to 425°C, at a pressure of about 5 to 25 MPa, preferably of about 8 to 20 MPa.
- Ammonia can be fed to the reactor vessel 2 in the form of a liquid or a hot vapor.
- the ammonia feed can serve as a purification agent to prevent clogging of the reactor vessel 2 bottom or to prevent the formation of melamine condensation products such as melam, melem and melone, or to promote mixing in the reactor vessel 2.
- the amount of ammonia fed to the reactor is about 0.01 to 10 mol per mol urea; preferably, about 0.1 to 5 mol per mol urea, and in particular about 0.2 to 2 mol per mol urea.
- the carbon dioxide and ammonia formed in the reaction as well as any extra ammonia feed into the reactor vessel 2 can collect in an internal gas-liquid separation unit 3, for example in the top of the reactor vessel 2 and can be separated, in gaseous form, from the liquid melamine.
- the resulting gas mixture of carbon dioxide, ammonia and melamine is sent to the melamine scrubber 1 for removal of the melamine vapor and to preheat the urea melt.
- the liquid melamine is withdrawn from the reactor vessel 2 and transferred to a post-reactor vessel 4.
- the liquid melamine can again be contacted with about 0.01 to 10 mol ammonia per mol melamine and preferably about 0.1 to 2 mol ammonia per mol melamine.
- the contact time in the post-reactor vessel 4 is between about 1 minute and
- the liquid melamine is cooled by contacting it directly with a cooling medium at a temperature and pressure at which the cooling medium is in a supercritical state.
- a cooling medium at a temperature and pressure at which the cooling medium is in a supercritical state.
- supercritical ammonia is the cooling medium.
- the pressure of the cooling medium during cooling of the liquid melamine is preferably such that the reduced pressure of the cooling medium is between about 0.9 and 2.5, more preferably between a reduced pressure of about 1 and the reactor pressure.
- the temperature of the cooling medium during cooling is preferably such that the reduced temperature of the cooling medium is between about 0.9 and 2, more preferably between about 1 and 1.5.
- the melamine is converted into a powder and removed from the bottom of the product cooler 5.
- the melamine powder has a melamine content of greater than 99 wt. %, and more specifically a melamine content of 99.5 to 99.95 wt. %, and can be used, generally, without further washing or purification, in applications which require very high purity melamine, such as coatings.
- a separate gas-liquid separation unit can be installed after the reactor vessel instead of internally to the reactor vessel.
- an evaporation stage 6 is included between the post- reactor vessel 4 and the product cooler 5.
- liquid melamine melt is converted into gaseous melamine with any by-products remaining behind in the evaporator 6.
- gaseous melamine is then cooled in the product cooler 5 using a cooling medium in a supercritical state.
- This evaporation step has the advantage of further reducing the quantity of contaminating by-products and thus very high purity solid melamine is obtained. This may be advantageous especially in applications demanding a very high degree of purity.
- an evaporation stage can be included between the reactor vessel and the product cooler and the post-reaction stage can be bypassed.
- the following example was carried out in a pilot plant equipped with a melamine scrubber, a reactor vessel incorporating a gas-liquid separator, a post-reactor vessel and a product cooler.
- the bottom of the post-reactor vessel was fed with 10 kg/h of ammonia at a temperature of 400°C and a pressure of 15 MPa.
- This ammonia flowed from the post-reactor vessel to the reactor vessel and from there, together with the ammonia and carbon dioxide formed during the melamine synthesis, to the melamine scrubber.
- the gas scrubber was fed with 100 kg/h of liquid urea at a temperature of 140°C and a pressure of 15 MPa.
- the liquid urea was heated to about 200°C in the melamine scrubber by means of the C0 2 , NH 3 and melamine off-gases from the reactor vessel, which were at a temperature of about 400°C.
- the melamine vapor entrained by the off-gases leaving the reactor vessel was removed from the off-gas by the urea melt and was transferred, together with the urea melt, to the reactor vessel.
- the urea and scrubbed melamine melt was reacted at a temperature of about 400°C and a pressure of about 15 MPa in the reactor vessel.
- the reaction product was separated into a gaseous and a liquid stream.
- the gaseous stream which was comprised of C0 2 , NH 3 and melamine vapor was sent to the melamine scrubber while the liquid stream of melamine was sent to the post-reactor vessel.
- the liquid melamine was contacted with ammonia for about 25 minutes at a temperature of about 400°C and a pressure of about 15 MPa.
- the liquid melamine was transferred to the product cooler, where it was cooled by mixing it with supercritical ammonia at a temperature of about 150°C and a pressure of about 14 MPa.
- a solid material of 99.7 wt. % melamine was obtained.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002250270A CA2250270A1 (en) | 1996-03-21 | 1997-03-20 | Method for the preparation of melamine |
JP9533378A JP2000506882A (en) | 1996-03-21 | 1997-03-20 | How to get melamine |
AU19475/97A AU715825B2 (en) | 1996-03-21 | 1997-03-20 | Method for the preparation of melamine |
KR1019980707579A KR20000064783A (en) | 1996-03-21 | 1997-03-20 | Melamine manufacturing method |
EP97907484A EP0888315A1 (en) | 1996-03-21 | 1997-03-20 | Method for the preparation of melamine |
PL97328914A PL328914A1 (en) | 1996-03-21 | 1997-03-20 | Method of obtaining melamine |
NO19984324A NO310108B1 (en) | 1996-03-21 | 1998-09-17 | Process for producing melamine |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL1002669 | 1996-03-21 | ||
NL1002669A NL1002669C2 (en) | 1996-03-21 | 1996-03-21 | Process for the preparation of melamine. |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997034879A1 true WO1997034879A1 (en) | 1997-09-25 |
Family
ID=19762536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NL1997/000146 WO1997034879A1 (en) | 1996-03-21 | 1997-03-20 | Method for the preparation of melamine |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0888315A1 (en) |
JP (1) | JP2000506882A (en) |
KR (1) | KR20000064783A (en) |
CN (1) | CN1218458A (en) |
AU (1) | AU715825B2 (en) |
CA (1) | CA2250270A1 (en) |
NL (1) | NL1002669C2 (en) |
NO (1) | NO310108B1 (en) |
PL (1) | PL328914A1 (en) |
WO (1) | WO1997034879A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000040567A1 (en) * | 1998-12-31 | 2000-07-13 | Kemira Agro Oy | High-pressure process for the preparation of melamine from urea |
WO2000053587A1 (en) * | 1999-03-08 | 2000-09-14 | Dsm N.V. | Method for preparing melamine |
US6380385B1 (en) | 1995-12-07 | 2002-04-30 | Agrolinz Melanin Gmbh | Process for the preparation of pure melamine |
WO2004111016A1 (en) * | 2003-06-12 | 2004-12-23 | Ami Agrolinz Melamine International Gmbh | Method and device for producing melamine in a single-phase tubular reactor |
WO2007000176A1 (en) * | 2005-06-28 | 2007-01-04 | Casale Chemicals S.A. | Process for gently cooling and crystallizing melamine from a melamine melt or from the gaseous phase |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL8403843A (en) * | 1984-01-05 | 1985-08-01 | Melamine Chemicals Inc | PROCESS FOR PREPARING MELAMINE. |
US4565867A (en) * | 1984-01-05 | 1986-01-21 | Melamine Chemicals, Inc. | Anhydrous high-pressure melamine synthesis |
US5514796A (en) * | 1995-06-07 | 1996-05-07 | Melamine Chemicals, Inc. | Melamine of improved purity produced by high-pressure, non-catalytic process |
WO1996020182A1 (en) * | 1994-12-23 | 1996-07-04 | Agrolinz Melamin Gmbh | Process for producing high-purity melamine |
-
1996
- 1996-03-21 NL NL1002669A patent/NL1002669C2/en not_active IP Right Cessation
-
1997
- 1997-03-20 EP EP97907484A patent/EP0888315A1/en not_active Withdrawn
- 1997-03-20 CA CA002250270A patent/CA2250270A1/en not_active Abandoned
- 1997-03-20 WO PCT/NL1997/000146 patent/WO1997034879A1/en not_active Application Discontinuation
- 1997-03-20 AU AU19475/97A patent/AU715825B2/en not_active Ceased
- 1997-03-20 CN CN97194661A patent/CN1218458A/en active Pending
- 1997-03-20 PL PL97328914A patent/PL328914A1/en unknown
- 1997-03-20 JP JP9533378A patent/JP2000506882A/en active Pending
- 1997-03-20 KR KR1019980707579A patent/KR20000064783A/en not_active Application Discontinuation
-
1998
- 1998-09-17 NO NO19984324A patent/NO310108B1/en not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL8403843A (en) * | 1984-01-05 | 1985-08-01 | Melamine Chemicals Inc | PROCESS FOR PREPARING MELAMINE. |
US4565867A (en) * | 1984-01-05 | 1986-01-21 | Melamine Chemicals, Inc. | Anhydrous high-pressure melamine synthesis |
WO1996020182A1 (en) * | 1994-12-23 | 1996-07-04 | Agrolinz Melamin Gmbh | Process for producing high-purity melamine |
US5514796A (en) * | 1995-06-07 | 1996-05-07 | Melamine Chemicals, Inc. | Melamine of improved purity produced by high-pressure, non-catalytic process |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6380385B1 (en) | 1995-12-07 | 2002-04-30 | Agrolinz Melanin Gmbh | Process for the preparation of pure melamine |
WO2000040567A1 (en) * | 1998-12-31 | 2000-07-13 | Kemira Agro Oy | High-pressure process for the preparation of melamine from urea |
WO2000053587A1 (en) * | 1999-03-08 | 2000-09-14 | Dsm N.V. | Method for preparing melamine |
US6579980B2 (en) | 1999-03-08 | 2003-06-17 | Dsm N.V. | Method for preparing melamine |
WO2004111016A1 (en) * | 2003-06-12 | 2004-12-23 | Ami Agrolinz Melamine International Gmbh | Method and device for producing melamine in a single-phase tubular reactor |
US7385057B2 (en) | 2003-06-12 | 2008-06-10 | Ami Agrolinz Melamine International Gmbh | Method and device for producing melamine in a single-phase tubular reactor |
WO2007000176A1 (en) * | 2005-06-28 | 2007-01-04 | Casale Chemicals S.A. | Process for gently cooling and crystallizing melamine from a melamine melt or from the gaseous phase |
Also Published As
Publication number | Publication date |
---|---|
KR20000064783A (en) | 2000-11-06 |
NO310108B1 (en) | 2001-05-21 |
JP2000506882A (en) | 2000-06-06 |
NO984324L (en) | 1998-11-17 |
AU715825B2 (en) | 2000-02-10 |
NO984324D0 (en) | 1998-09-17 |
NL1002669C2 (en) | 1997-09-23 |
EP0888315A1 (en) | 1999-01-07 |
CA2250270A1 (en) | 1997-09-25 |
AU1947597A (en) | 1997-10-10 |
CN1218458A (en) | 1999-06-02 |
PL328914A1 (en) | 1999-03-01 |
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