JP5122289B2 - 結晶形態のメラミンシアヌレート - Google Patents
結晶形態のメラミンシアヌレート Download PDFInfo
- Publication number
- JP5122289B2 JP5122289B2 JP2007536152A JP2007536152A JP5122289B2 JP 5122289 B2 JP5122289 B2 JP 5122289B2 JP 2007536152 A JP2007536152 A JP 2007536152A JP 2007536152 A JP2007536152 A JP 2007536152A JP 5122289 B2 JP5122289 B2 JP 5122289B2
- Authority
- JP
- Japan
- Prior art keywords
- particles
- melamine
- mixture
- melamine cyanurate
- solid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 239000002245 particle Substances 0.000 claims abstract description 96
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 239000007787 solid Substances 0.000 claims abstract description 45
- 239000006185 dispersion Substances 0.000 claims abstract description 41
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 30
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims abstract description 30
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims description 55
- 229920001577 copolymer Polymers 0.000 claims description 22
- 239000000654 additive Substances 0.000 claims description 14
- 239000008187 granular material Substances 0.000 claims description 12
- 230000000996 additive effect Effects 0.000 claims description 9
- 229920001519 homopolymer Polymers 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 13
- 239000004094 surface-active agent Substances 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- 229920000642 polymer Polymers 0.000 description 20
- 239000013078 crystal Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 15
- FFWREGAZKSCJFZ-UHFFFAOYSA-N 1,3,5-triazinane-2,4,6-trione;dihydrate Chemical compound O.O.O=C1NC(=O)NC(=O)N1 FFWREGAZKSCJFZ-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000003063 flame retardant Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 150000002148 esters Chemical class 0.000 description 10
- 239000012071 phase Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 7
- 150000004683 dihydrates Chemical class 0.000 description 7
- 238000009826 distribution Methods 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 5
- 238000000113 differential scanning calorimetry Methods 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 238000002411 thermogravimetry Methods 0.000 description 5
- 239000000428 dust Substances 0.000 description 4
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 4
- 239000007909 solid dosage form Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 238000010923 batch production Methods 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 238000000149 argon plasma sintering Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 238000000634 powder X-ray diffraction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 238000000859 sublimation Methods 0.000 description 2
- 230000008022 sublimation Effects 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
- 239000004908 Emulsion polymer Substances 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
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000252141 Semionotiformes Species 0.000 description 1
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 238000005421 electrostatic potential Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000002356 laser light scattering Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000007431 microscopic evaluation Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 1
- PZNOBXVHZYGUEX-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine;hydrochloride Chemical compound Cl.C=CCNCC=C PZNOBXVHZYGUEX-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005550 wet granulation Methods 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
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
-
- 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
- C07D251/70—Other substituted melamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34928—Salts
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/06—Organic materials
- C09K21/10—Organic materials containing nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04105066.7 | 2004-10-15 | ||
| EP04105066 | 2004-10-15 | ||
| PCT/EP2005/055036 WO2006040289A1 (en) | 2004-10-15 | 2005-10-06 | Melamine cyanurate in crystalline form |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008516924A JP2008516924A (ja) | 2008-05-22 |
| JP2008516924A5 JP2008516924A5 (enExample) | 2008-11-27 |
| JP5122289B2 true JP5122289B2 (ja) | 2013-01-16 |
Family
ID=34929705
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007536152A Expired - Fee Related JP5122289B2 (ja) | 2004-10-15 | 2005-10-06 | 結晶形態のメラミンシアヌレート |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8765864B2 (enExample) |
| EP (1) | EP1799655B1 (enExample) |
| JP (1) | JP5122289B2 (enExample) |
| CN (1) | CN101039923B (enExample) |
| AT (1) | ATE551331T1 (enExample) |
| WO (1) | WO2006040289A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1856064A4 (en) * | 2005-03-07 | 2010-08-04 | Bromine Compounds Ltd | METHOD FOR PRODUCING MELAMINE CYANURATE |
| CN102276963A (zh) * | 2010-06-11 | 2011-12-14 | 东丽纤维研究所（中国）有限公司 | 一种阻燃性聚酯树脂组合物及成型品 |
| RU2471788C1 (ru) * | 2011-07-07 | 2013-01-10 | Лев Давидович Раснецов | Способ получения цианурата меламина |
| CN104311500B (zh) * | 2014-09-29 | 2016-07-06 | 济南泰星精细化工有限公司 | 溶胶改性法制备三聚氰胺氰尿酸盐的方法 |
| CN106588799A (zh) * | 2016-11-15 | 2017-04-26 | 广东聚航新材料研究院有限公司 | 一种三聚氰胺氰尿酸盐的酸式高效制备方法 |
| CN110317181B (zh) * | 2019-06-13 | 2022-04-08 | 山东泰星新材料股份有限公司 | 一种三聚氰胺氰尿酸盐纳米片微球的制备方法及其应用 |
| EP3896043B1 (en) * | 2020-04-17 | 2025-04-02 | Depco-Trh Pty Ltd | High opacity laminate surface |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3532635A (en) * | 1966-12-29 | 1970-10-06 | Purex Corp Ltd | Opacified liquid products and methods for their productions |
| JPS5455588A (en) * | 1977-10-04 | 1979-05-02 | Asahi Chem Ind Co Ltd | Production of melamine cyanurate |
| JPS5632470A (en) * | 1979-08-28 | 1981-04-01 | Yuka Meramin Kk | Preparation of melamine-cyanuric acid adduct |
| JP2834221B2 (ja) * | 1989-10-05 | 1998-12-09 | 三菱化学株式会社 | 表面処理されたメラミン・シアヌル酸付加物の製造法 |
| AT394565B (de) * | 1990-01-30 | 1992-05-11 | Chemie Linz Gmbh | Cyanursaeure oder deren derivate enthaltende melaminzubereitung und stabile dispersion von melamin in polyetherolen, verfahren zu ihrer herstellung und ihre verwendung |
| FR2674852B1 (fr) * | 1991-04-04 | 1993-07-02 | Atochem | Procede de synthese du cyanurate de melamine. |
| US5135974A (en) * | 1991-09-23 | 1992-08-04 | Fr Polymers, Inc. | Cyanurate based fire retardant concentrates |
| JP3127936B2 (ja) * | 1992-05-08 | 2001-01-29 | 日産化学工業株式会社 | メラミンシアヌレートの製造方法 |
| JPH06157820A (ja) * | 1992-11-18 | 1994-06-07 | Nissan Chem Ind Ltd | 表面処理されたメラミンシアヌレート粉末の製法及び該粉末を用いた難燃性樹脂組成物 |
| US5493023A (en) * | 1992-12-09 | 1996-02-20 | Mitsui Toatsu Chemicals, Inc. | Granular melamine cyanurate and preparation process thereof |
| JP3684585B2 (ja) * | 1993-11-26 | 2005-08-17 | 日産化学工業株式会社 | メラミンシアヌレート顆粒およびその製造方法 |
| JP3118359B2 (ja) * | 1993-12-27 | 2000-12-18 | 三井化学株式会社 | メラミンシアヌレートの製造方法 |
| DE69432398T2 (de) * | 1993-12-28 | 2003-11-27 | Kanegafuchi Kagaku Kogyo K.K., Osaka | Additiv für thermoplastische Harze und flammhemmende Harzzusammensetzungen |
| AT400031B (de) * | 1994-02-08 | 1995-09-25 | Chemie Linz Gmbh | Verfahren zur herstellung von melamincyanurat |
| JPH08157595A (ja) * | 1994-12-09 | 1996-06-18 | Japan Energy Corp | Ｍｃａ微粒子の製造方法 |
| ITMI991539A1 (it) * | 1999-07-13 | 2001-01-13 | Alcantara Spa | Additivo utile per rendere ignifughi materiali tessili in particolaretessuti non tessuti microfribrosi sintetici procedimento per la sua pr |
| TWI284126B (en) * | 2001-10-25 | 2007-07-21 | Ciba Sc Holding Ag | Free flowing melamine cyanurate agglomerate, method for producing same and use in flame retardant polymer compositions and polymer compositions containing melamine cyanurate |
-
2005
- 2005-10-06 EP EP05794769A patent/EP1799655B1/en not_active Expired - Lifetime
- 2005-10-06 CN CN200580035253.1A patent/CN101039923B/zh not_active Expired - Fee Related
- 2005-10-06 AT AT05794769T patent/ATE551331T1/de active
- 2005-10-06 US US11/664,660 patent/US8765864B2/en not_active Expired - Fee Related
- 2005-10-06 WO PCT/EP2005/055036 patent/WO2006040289A1/en not_active Ceased
- 2005-10-06 JP JP2007536152A patent/JP5122289B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006040289A1 (en) | 2006-04-20 |
| US8765864B2 (en) | 2014-07-01 |
| ATE551331T1 (de) | 2012-04-15 |
| JP2008516924A (ja) | 2008-05-22 |
| EP1799655A1 (en) | 2007-06-27 |
| EP1799655B1 (en) | 2012-03-28 |
| CN101039923B (zh) | 2010-08-11 |
| US20080312360A1 (en) | 2008-12-18 |
| CN101039923A (zh) | 2007-09-19 |
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