PT841088E - Microcapsulas produzidas mediante uso de poli-isocianatos de imino-oxadiazinodiona - Google Patents
Microcapsulas produzidas mediante uso de poli-isocianatos de imino-oxadiazinodiona Download PDFInfo
- Publication number
- PT841088E PT841088E PT97118626T PT97118626T PT841088E PT 841088 E PT841088 E PT 841088E PT 97118626 T PT97118626 T PT 97118626T PT 97118626 T PT97118626 T PT 97118626T PT 841088 E PT841088 E PT 841088E
- Authority
- PT
- Portugal
- Prior art keywords
- isocyanates
- formula
- microcapsules
- weight
- groups
- Prior art date
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- 239000003094 microcapsule Substances 0.000 title claims description 49
- 239000005056 polyisocyanate Substances 0.000 title description 22
- 239000012948 isocyanate Substances 0.000 claims description 68
- 150000002513 isocyanates Chemical class 0.000 claims description 66
- 239000000839 emulsion Substances 0.000 claims description 33
- 239000003431 cross linking reagent Substances 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 31
- 238000002360 preparation method Methods 0.000 claims description 28
- 239000000126 substance Substances 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 26
- 239000003921 oil Substances 0.000 claims description 26
- 230000008569 process Effects 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000012071 phase Substances 0.000 claims description 14
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 11
- 239000008346 aqueous phase Substances 0.000 claims description 10
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical group NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 125000005442 diisocyanate group Chemical group 0.000 claims description 9
- PJMDLNIAGSYXLA-UHFFFAOYSA-N 6-iminooxadiazine-4,5-dione Chemical compound N=C1ON=NC(=O)C1=O PJMDLNIAGSYXLA-UHFFFAOYSA-N 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 8
- -1 oxadiazinotrione Chemical compound 0.000 claims description 8
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims description 7
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 7
- HXSACZWWBYWLIS-UHFFFAOYSA-N oxadiazine-4,5,6-trione Chemical compound O=C1ON=NC(=O)C1=O HXSACZWWBYWLIS-UHFFFAOYSA-N 0.000 claims description 7
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 6
- 239000003925 fat Substances 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 239000003995 emulsifying agent Substances 0.000 claims description 4
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 4
- 230000008030 elimination Effects 0.000 claims description 3
- 238000003379 elimination reaction Methods 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- 238000004581 coalescence Methods 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- 125000005498 phthalate group Chemical class 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000000243 solution Substances 0.000 description 32
- 239000002775 capsule Substances 0.000 description 30
- 239000006185 dispersion Substances 0.000 description 27
- 235000019198 oils Nutrition 0.000 description 25
- 239000000975 dye Substances 0.000 description 22
- 229920001228 polyisocyanate Polymers 0.000 description 21
- 150000001875 compounds Chemical class 0.000 description 15
- 150000003254 radicals Chemical class 0.000 description 14
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical class F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 11
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 11
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 11
- 229920002451 polyvinyl alcohol Polymers 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 8
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 description 7
- 230000001804 emulsifying effect Effects 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000008367 deionised water Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 4
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229920000768 polyamine Polymers 0.000 description 4
- IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 238000006555 catalytic reaction Methods 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 150000002357 guanidines Chemical class 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- PVXRCPDNJSFYBV-UHFFFAOYSA-N carbamoyl fluoride Chemical class NC(F)=O PVXRCPDNJSFYBV-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000007764 o/w emulsion Substances 0.000 description 2
- 238000006384 oligomerization reaction Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- DVQHRBFGRZHMSR-UHFFFAOYSA-N sodium methyl 2,2-dimethyl-4,6-dioxo-5-(N-prop-2-enoxy-C-propylcarbonimidoyl)cyclohexane-1-carboxylate Chemical compound [Na+].C=CCON=C(CCC)[C-]1C(=O)CC(C)(C)C(C(=O)OC)C1=O DVQHRBFGRZHMSR-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- GNPWYHFXSMINJQ-UHFFFAOYSA-N 1,2-dimethyl-3-(1-phenylethyl)benzene Chemical class C=1C=CC(C)=C(C)C=1C(C)C1=CC=CC=C1 GNPWYHFXSMINJQ-UHFFFAOYSA-N 0.000 description 1
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 1
- PAUHLEIGHAUFAK-UHFFFAOYSA-N 1-isocyanato-1-[(1-isocyanatocyclohexyl)methyl]cyclohexane Chemical compound C1CCCCC1(N=C=O)CC1(N=C=O)CCCCC1 PAUHLEIGHAUFAK-UHFFFAOYSA-N 0.000 description 1
- CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 description 1
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- FXSFKECPPGDGBN-UHFFFAOYSA-N 3,3-bis(1h-indol-2-yl)-2-benzofuran-1-one Chemical compound C12=CC=CC=C2C(=O)OC1(C=1NC2=CC=CC=C2C=1)C1=CC2=CC=CC=C2N1 FXSFKECPPGDGBN-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- KEZMBAQUUXDDDQ-UHFFFAOYSA-N CCC.N=C=O.N=C=O Chemical class CCC.N=C=O.N=C=O KEZMBAQUUXDDDQ-UHFFFAOYSA-N 0.000 description 1
- ZHESOIPTRUDICE-UHFFFAOYSA-N CCCCCCCCC.N=C=O.N=C=O.N=C=O Chemical class CCCCCCCCC.N=C=O.N=C=O.N=C=O ZHESOIPTRUDICE-UHFFFAOYSA-N 0.000 description 1
- QMFJYNOVTQYLTA-UHFFFAOYSA-N CCCCCCCCCCC.N=C=O.N=C=O.N=C=O Chemical class CCCCCCCCCCC.N=C=O.N=C=O.N=C=O QMFJYNOVTQYLTA-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- RTDFOQVLLJZRIH-JZAVHCKJSA-N Glycoursocholanic acid Chemical compound C([C@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC(O)=O)C)[C@@]2(C)CC1 RTDFOQVLLJZRIH-JZAVHCKJSA-N 0.000 description 1
- 102100033969 Guanylyl cyclase-activating protein 1 Human genes 0.000 description 1
- 101001068480 Homo sapiens Guanylyl cyclase-activating protein 1 Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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- 229920000877 Melamine resin Polymers 0.000 description 1
- HDONYZHVZVCMLR-UHFFFAOYSA-N N=C=O.N=C=O.CC1CCCCC1 Chemical class N=C=O.N=C=O.CC1CCCCC1 HDONYZHVZVCMLR-UHFFFAOYSA-N 0.000 description 1
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- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
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- 239000013638 trimer Substances 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/06—Making microcapsules or microballoons by phase separation
- B01J13/14—Polymerisation; cross-linking
- B01J13/16—Interfacial polymerisation
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/914—Transfer or decalcomania
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2984—Microcapsule with fluid core [includes liposome]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2984—Microcapsule with fluid core [includes liposome]
- Y10T428/2985—Solid-walled microcapsule from synthetic polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Polyurethanes Or Polyureas (AREA)
- Color Printing (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19646110A DE19646110A1 (de) | 1996-11-08 | 1996-11-08 | Mikrokapseln unter Verwendung von Iminooxadiazindion-Polyisocyanaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT841088E true PT841088E (pt) | 2001-11-30 |
Family
ID=7811048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT97118626T PT841088E (pt) | 1996-11-08 | 1997-10-27 | Microcapsulas produzidas mediante uso de poli-isocianatos de imino-oxadiazinodiona |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6020066A (cg-RX-API-DMAC10.html) |
| EP (1) | EP0841088B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JPH10137578A (cg-RX-API-DMAC10.html) |
| CN (1) | CN1100602C (cg-RX-API-DMAC10.html) |
| AR (1) | AR010555A1 (cg-RX-API-DMAC10.html) |
| BR (1) | BR9705447A (cg-RX-API-DMAC10.html) |
| DE (2) | DE19646110A1 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2157509T3 (cg-RX-API-DMAC10.html) |
| ID (1) | ID18090A (cg-RX-API-DMAC10.html) |
| IN (1) | IN186809B (cg-RX-API-DMAC10.html) |
| PT (1) | PT841088E (cg-RX-API-DMAC10.html) |
| TW (1) | TW341526B (cg-RX-API-DMAC10.html) |
| ZA (1) | ZA9710042B (cg-RX-API-DMAC10.html) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2185265T3 (es) * | 1998-06-02 | 2003-04-16 | Bayer Ag | Procedimiento para la preparacion de polisocianatos que contienen grupos imidooxadiazindiona. |
| DE19840583A1 (de) * | 1998-09-05 | 2000-03-09 | Bayer Ag | Mikrokapsel-Formulierungen |
| DE19840582A1 (de) * | 1998-09-05 | 2000-03-09 | Bayer Ag | Mikrokapsel-Formulierungen |
| US6653256B1 (en) | 1999-08-24 | 2003-11-25 | Bayer Aktiengesellschaft | Microcapsule formulations |
| BR0111465B1 (pt) | 2000-06-03 | 2012-12-11 | microcápsula, processo modificado para o encapsulamento de um material disperso dentro de uma casca permeável sólida de uma resina polimérica, produto da reação, e, método para a modificação da mobilidade do solo de um produto agroquìmico. | |
| DE10051194A1 (de) * | 2000-10-16 | 2002-04-25 | Bayer Ag | Mikrokapseln mit Wänden aus Polyharnstoff |
| DE10051190A1 (de) * | 2000-10-16 | 2002-04-25 | Bayer Ag | Mikrokapseln mit Wänden aus Polyharnstoff |
| DE10117671A1 (de) * | 2001-04-09 | 2002-10-10 | Bayer Ag | Mit duftstoffhaltigen Mikrokapseln ausgerüstetes Leder |
| EP1409125B1 (en) * | 2001-07-12 | 2016-04-20 | Reaxa Limited | Microencapsulated catalyst, methods of preparation and methods of use thereof |
| DE10241000A1 (de) * | 2001-09-10 | 2003-03-27 | Bayer Ag | Mikrokapsel-haltige Vliese |
| GB0128839D0 (en) * | 2001-12-01 | 2002-01-23 | Univ Cambridge Tech | Encapsulated transition metal reagents for reactions in supercritical carbon dioxide |
| US20040137031A1 (en) * | 2002-12-13 | 2004-07-15 | Monsanto Technology Llc | Microcapsules with amine adjusted release rates |
| US7704940B2 (en) | 2004-04-09 | 2010-04-27 | The Sun Products Corporation | Granulate for use in a cleaning product and process for its manufacture |
| MXPA06014671A (es) * | 2004-06-14 | 2007-03-12 | Monsanto Technology Llc | Microcapsulas de liberacion activada del material contenido en su nucleo. |
| ES2324359T3 (es) * | 2004-12-23 | 2009-08-05 | Unilever N.V. | Composiciones detergentes liquidas y uso de las mismas. |
| GB0524659D0 (en) * | 2005-12-02 | 2006-01-11 | Unilever Plc | Improvements relating to fabric treatment compositions |
| JP4739995B2 (ja) * | 2006-03-10 | 2011-08-03 | Ｊｘ日鉱日石エネルギー株式会社 | 感圧記録材料用マイクロカプセルとその製造方法及びそれを用いた感圧記録材料 |
| DE102008002145A1 (de) | 2008-06-02 | 2009-12-03 | Symrise Gmbh & Co. Kg | Kapsel mit organisch-anorganischer Hybridwand |
| PL2169042T3 (pl) | 2008-09-30 | 2012-09-28 | Procter & Gamble | Kompozycja zawierająca mikrokapsułki |
| EP2349551B2 (en) * | 2008-11-07 | 2023-07-26 | The Procter & Gamble Company | Benefit agent containing delivery particle |
| AU2010213530B2 (en) | 2009-02-13 | 2015-09-03 | Monsanto Technology Llc | Encapsulation of herbicides to reduce crop injury |
| GB0902634D0 (en) | 2009-02-18 | 2009-04-01 | Reaxa Ltd | Microencapsulated catalyst |
| ES2436720T3 (es) | 2009-12-18 | 2014-01-03 | The Procter & Gamble Company | Composición que comprende microcápsulas |
| EP2336286A1 (en) | 2009-12-18 | 2011-06-22 | The Procter & Gamble Company | Composition comprising microcapsules |
| EP2553081B1 (en) | 2010-03-31 | 2014-01-08 | Unilever PLC | Microcapsule incorporation in structured liquid detergents |
| WO2011120799A1 (en) | 2010-04-01 | 2011-10-06 | Unilever Plc | Structuring detergent liquids with hydrogenated castor oil |
| UY33563A (es) | 2010-08-18 | 2012-03-30 | Monsanto Technology Llc | Aplicacion temprana de acetamidas encapsuladas para reducir daños en los cultivos |
| FR2965190B1 (fr) * | 2010-09-24 | 2013-12-27 | Univ Tours Francois Rabelais | Procede de fabrication de microcapsules polysiloxane fonctionnalisees et peu poreuses. |
| CN102146219B (zh) * | 2011-01-19 | 2013-04-24 | 山西大学 | 活性染料微胶囊的制备方法 |
| US8936030B2 (en) | 2011-03-25 | 2015-01-20 | Katherine Rose Kovarik | Nail polish remover method and device |
| EP2495300A1 (en) | 2011-03-04 | 2012-09-05 | Unilever Plc, A Company Registered In England And Wales under company no. 41424 of Unilever House | Structuring detergent liquids with hydrogenated castor oil |
| US12245673B2 (en) | 2011-03-25 | 2025-03-11 | Seed Health, Inc. | Insect repellent pet collar |
| EP2841550B1 (en) | 2012-04-23 | 2016-01-20 | Unilever Plc. | Externally structured aqueous isotropic liquid detergent compositions |
| WO2013160023A1 (en) | 2012-04-23 | 2013-10-31 | Unilever Plc | Externally structured aqueous isotropic liquid laundry detergent compositions |
| WO2013160024A1 (en) | 2012-04-23 | 2013-10-31 | Unilever Plc | Externally structured aqueous isotropic liquid detergent compositions |
| US9221989B2 (en) * | 2013-08-28 | 2015-12-29 | P.H. Glatfelter Company | Tamper evident documents and inks |
| US20150037565A1 (en) * | 2013-07-31 | 2015-02-05 | P.H. Glatfelter Company | Tamper evident documents and inks |
| EP2839877A1 (de) * | 2013-08-21 | 2015-02-25 | Kwizda Agro GmbH | Verfahren zur Herstellung von Konzentraten von vorzugsweise wasserlöslichen Wirkstoffen |
| WO2015113015A1 (en) | 2014-01-27 | 2015-07-30 | Monsanto Technology Llc | Aqueous herbicidal concentrates |
| CN106400589B (zh) * | 2016-08-30 | 2018-09-28 | 苏州丰倍生物科技有限公司 | 一种环保型无碳复写纸压敏油的制备方法 |
| WO2018210523A1 (en) | 2017-05-15 | 2018-11-22 | Unilever Plc | Composition |
| WO2018210522A1 (en) | 2017-05-15 | 2018-11-22 | Unilever Plc | Composition |
| EP3625320A1 (en) | 2017-05-15 | 2020-03-25 | Unilever PLC | Composition |
| WO2018210524A1 (en) | 2017-05-15 | 2018-11-22 | Unilever Plc | Composition |
| US10464948B2 (en) | 2017-05-30 | 2019-11-05 | Covestro Deutschland Ag | Polycyclic diiminooxadiazinones |
| AU2018284252B2 (en) | 2017-06-13 | 2023-08-17 | Monsanto Technology Llc | Microencapsulated herbicides |
| SG10201806031VA (en) * | 2018-07-13 | 2020-02-27 | Mitsui Chemicals Inc | Re-dispersible polyurea microcapsules and method of preparing re-dispersible polyurea microcapsules |
| UA129154C2 (uk) | 2019-01-30 | 2025-01-29 | Монсанто Текнолоджі Ллс | Мікрокапсульовані ацетамідні гербіциди |
| EP4339121A1 (en) | 2022-09-14 | 2024-03-20 | The Procter & Gamble Company | Consumer product |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2909906A1 (de) * | 1979-03-14 | 1980-10-02 | Bayer Ag | Verfahren zur kontinuierlichen herstellung von mikrokapseln |
| DE2909950A1 (de) * | 1979-03-14 | 1980-10-02 | Bayer Ag | Mikrokapseln |
| DE3421865A1 (de) * | 1984-06-13 | 1985-12-19 | Bayer Ag, 5090 Leverkusen | Kontinuierliche herstellung von mikrokapseldispersionen |
| FR2591124B1 (fr) * | 1985-12-10 | 1988-02-12 | Rhone Poulenc Spec Chim | Procede de microencapsulation par polyaddition-interfaciale. |
| DE3902078A1 (de) * | 1989-01-25 | 1990-07-26 | Bayer Ag | Verfahren zur herstellung von modifizierten, isocyanuratgruppen aufweisenden polyisocyanaten und ihre verwendung |
| US5164126A (en) * | 1991-03-05 | 1992-11-17 | Appleton Papers Inc. | Process for microencapsulation |
| DE19532060A1 (de) * | 1995-08-31 | 1997-03-06 | Bayer Ag | Polycyclische Iminooxadiazindione, deren Herstellung und Verwendung |
| DE19607632A1 (de) * | 1996-02-29 | 1997-09-04 | Bayer Ag | Mikrokapseln mit Wänden aus Umsetzungsprodukten von Biuret-Polyisocyanaten und Guanidinen |
-
1996
- 1996-11-08 DE DE19646110A patent/DE19646110A1/de not_active Withdrawn
-
1997
- 1997-09-25 TW TW086113943A patent/TW341526B/zh active
- 1997-10-09 IN IN2903DE1997 patent/IN186809B/en unknown
- 1997-10-23 US US08/956,821 patent/US6020066A/en not_active Expired - Fee Related
- 1997-10-27 PT PT97118626T patent/PT841088E/pt unknown
- 1997-10-27 ES ES97118626T patent/ES2157509T3/es not_active Expired - Lifetime
- 1997-10-27 DE DE59703664T patent/DE59703664D1/de not_active Expired - Lifetime
- 1997-10-27 EP EP97118626A patent/EP0841088B1/de not_active Expired - Lifetime
- 1997-10-31 JP JP9315901A patent/JPH10137578A/ja active Pending
- 1997-11-07 ZA ZA9710042A patent/ZA9710042B/xx unknown
- 1997-11-07 AR ARP970105196A patent/AR010555A1/es unknown
- 1997-11-07 CN CN97122266A patent/CN1100602C/zh not_active Expired - Fee Related
- 1997-11-07 BR BR9705447-0A patent/BR9705447A/pt not_active Application Discontinuation
- 1997-11-07 ID IDP973626A patent/ID18090A/id unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1100602C (zh) | 2003-02-05 |
| AR010555A1 (es) | 2000-06-28 |
| MX9708588A (es) | 1998-09-30 |
| ID18090A (id) | 1998-02-26 |
| JPH10137578A (ja) | 1998-05-26 |
| IN186809B (cg-RX-API-DMAC10.html) | 2001-11-10 |
| TW341526B (en) | 1998-10-01 |
| EP0841088A3 (de) | 1998-07-22 |
| CN1189393A (zh) | 1998-08-05 |
| DE19646110A1 (de) | 1998-05-14 |
| BR9705447A (pt) | 2000-02-29 |
| ZA9710042B (en) | 1998-05-25 |
| US6020066A (en) | 2000-02-01 |
| ES2157509T3 (es) | 2001-08-16 |
| EP0841088B1 (de) | 2001-05-30 |
| EP0841088A2 (de) | 1998-05-13 |
| DE59703664D1 (de) | 2001-07-05 |
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