CS198299B2 - Method of incapsulation of the substances water non-miscible - Google Patents
Method of incapsulation of the substances water non-miscible Download PDFInfo
- Publication number
- CS198299B2 CS198299B2 CS783535A CS353578A CS198299B2 CS 198299 B2 CS198299 B2 CS 198299B2 CS 783535 A CS783535 A CS 783535A CS 353578 A CS353578 A CS 353578A CS 198299 B2 CS198299 B2 CS 198299B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- phase
- water
- bromide
- organic
- encapsulated
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 70
- 239000000126 substance Substances 0.000 title claims description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 21
- 230000008569 process Effects 0.000 claims abstract description 40
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 11
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 11
- 229920002396 Polyurea Polymers 0.000 claims abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 29
- 239000006185 dispersion Substances 0.000 claims description 24
- 230000001681 protective effect Effects 0.000 claims description 18
- 239000004094 surface-active agent Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 13
- -1 benzyltrifluorobutyl bromide Chemical compound 0.000 claims description 13
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 12
- 239000012948 isocyanate Substances 0.000 claims description 12
- 150000002513 isocyanates Chemical class 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 150000003839 salts Chemical group 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 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 claims description 4
- 125000005442 diisocyanate group Chemical group 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 239000000575 pesticide Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 3
- 239000000976 ink Substances 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000002563 ionic surfactant Substances 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 239000013043 chemical agent Substances 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001289 polyvinyl ether Polymers 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- XCXLEIPEAAEYTF-UHFFFAOYSA-M sodium fluorosulfate Chemical compound [Na+].[O-]S(F)(=O)=O XCXLEIPEAAEYTF-UHFFFAOYSA-M 0.000 claims 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 claims 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims 1
- 239000002775 capsule Substances 0.000 abstract description 39
- 239000003444 phase transfer catalyst Substances 0.000 abstract description 33
- 238000005538 encapsulation Methods 0.000 abstract description 14
- 239000000463 material Substances 0.000 abstract description 6
- 230000003197 catalytic effect Effects 0.000 abstract description 5
- 230000006872 improvement Effects 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 description 31
- 239000012074 organic phase Substances 0.000 description 30
- 239000008346 aqueous phase Substances 0.000 description 29
- 239000012071 phase Substances 0.000 description 28
- 239000007788 liquid Substances 0.000 description 16
- 239000004009 herbicide Substances 0.000 description 15
- 239000000084 colloidal system Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- 239000003054 catalyst Substances 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 230000002363 herbicidal effect Effects 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000000376 reactant Substances 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000000543 intermediate Substances 0.000 description 6
- 239000003094 microcapsule Substances 0.000 description 6
- 230000005501 phase interface Effects 0.000 description 6
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 239000002917 insecticide Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 238000004945 emulsification Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 238000010979 pH adjustment Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 238000013270 controlled release Methods 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000003223 protective agent Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 241000252233 Cyprinus carpio Species 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 239000000729 antidote Substances 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 239000012455 biphasic mixture Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 229940006460 bromide ion Drugs 0.000 description 1
- 239000007894 caplet Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 210000003238 esophagus Anatomy 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000008921 facial expression Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 210000001061 forehead Anatomy 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000005414 inactive ingredient Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/26—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
- A01N25/28—Microcapsules or nanocapsules
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Dentistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/801,932 US4140516A (en) | 1977-05-31 | 1977-05-31 | Encapsulation process employing phase transfer catalysts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS198299B2 true CS198299B2 (en) | 1980-05-30 |
Family
ID=25182388
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS783535A CS198299B2 (en) | 1977-05-31 | 1978-05-31 | Method of incapsulation of the substances water non-miscible |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US4140516A (fr) |
| JP (1) | JPS5826969B2 (fr) |
| AR (1) | AR217296A1 (fr) |
| AU (1) | AU514717B2 (fr) |
| BE (1) | BE867646A (fr) |
| BG (1) | BG29865A3 (fr) |
| BR (1) | BR7803468A (fr) |
| CA (1) | CA1110503A (fr) |
| CH (1) | CH640151A5 (fr) |
| CS (1) | CS198299B2 (fr) |
| DD (1) | DD137063A5 (fr) |
| DE (1) | DE2823377C2 (fr) |
| DK (1) | DK156989C (fr) |
| ES (1) | ES470373A1 (fr) |
| FR (1) | FR2392715A1 (fr) |
| GB (1) | GB1558460A (fr) |
| HU (1) | HU181952B (fr) |
| IL (1) | IL54804A (fr) |
| IT (1) | IT1115076B (fr) |
| MX (1) | MX5644E (fr) |
| NL (1) | NL7805878A (fr) |
| NZ (1) | NZ187429A (fr) |
| PH (1) | PH16196A (fr) |
| PL (1) | PL128464B1 (fr) |
| RO (1) | RO75293A (fr) |
| SU (1) | SU1022651A3 (fr) |
| YU (1) | YU40039B (fr) |
| ZA (1) | ZA783016B (fr) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4227917A (en) * | 1975-09-04 | 1980-10-14 | Ciba-Geigy Corporation | Phenylglyoxylonitrile-2-oxime-cyanomethyl ether as a crop safener |
| US4223070A (en) * | 1978-05-04 | 1980-09-16 | Stauffer Chemical Company | Impregnated porous granules with slow release pore membranes and process therefor |
| JPS5579867U (fr) * | 1978-11-29 | 1980-06-02 | ||
| DE2930409A1 (de) * | 1979-07-26 | 1981-02-12 | Bayer Ag | Spruehtrocknung von mikrokapseldispersionen |
| US4317743A (en) * | 1979-12-05 | 1982-03-02 | Wallace Business Forms, Inc. | Process for making microcapsules and resulting product |
| DE3020148A1 (de) | 1980-05-28 | 1981-12-03 | Bayer Ag, 5090 Leverkusen | Konzentrierte mikrokapselsuspensionen fuer reaktionsdurchschreibepapiere |
| US4956129A (en) * | 1984-03-30 | 1990-09-11 | Ici Americas Inc. | Microencapsulation process |
| US4500494A (en) * | 1983-02-18 | 1985-02-19 | Stauffer Chemical Company | Microencapsulated chelating agents and their use in removing metal ions from aqueous solutions |
| US4933167A (en) * | 1983-07-22 | 1990-06-12 | Scher Herbert B | Pesticide compositions |
| AR240875A1 (es) * | 1984-01-09 | 1991-03-27 | Stauffer Chemical Co | Procedimiento para producir capsulas de poliurea de dimensiones multiples que contienen un material inmiscible en agua en su interior y las capsulas resultantes |
| US4681806A (en) * | 1986-02-13 | 1987-07-21 | Minnesota Mining And Manufacturing Company | Particles containing releasable fill material and method of making same |
| US4994261A (en) * | 1986-03-31 | 1991-02-19 | Ici Americas Inc. | Pesticide compositions and method |
| US5049182A (en) * | 1989-02-03 | 1991-09-17 | Ici Americas Inc. | Single-package agricultural formulations combining immediate and time-delayed delivery |
| US5223477A (en) * | 1989-02-03 | 1993-06-29 | Imperial Chemical Industries Plc | Single-package agricultural formulations combining immediate and time-delayed delivery of thiocarbamate herbicides and dichlormid as safener |
| US5322862A (en) * | 1990-05-22 | 1994-06-21 | Nippon Kayaku Kabushiki Kaisha | Resin molding composition for preventing gnawing damage by animals |
| US5225118A (en) * | 1990-08-15 | 1993-07-06 | Boise Cascade Corporation | Process for manufacturing polyurea microcapsules and product therefrom |
| DK0570382T3 (da) * | 1991-02-06 | 1999-09-27 | Zeneca Ag Products Inc | Mikroindkapslet, herbicid sammensætning |
| US5164126A (en) * | 1991-03-05 | 1992-11-17 | Appleton Papers Inc. | Process for microencapsulation |
| JP3114321B2 (ja) * | 1992-01-29 | 2000-12-04 | 住友化学工業株式会社 | 飛翔性双翅目衛生害虫防除剤 |
| JP3306131B2 (ja) * | 1992-11-05 | 2002-07-24 | 富士写真フイルム株式会社 | マイクロカプセルの製造方法 |
| US5846554A (en) * | 1993-11-15 | 1998-12-08 | Zeneca Limited | Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant |
| ATE167980T1 (de) * | 1993-11-15 | 1998-07-15 | Zeneca Ltd | Mikrokapseln, die suspensionen von biologisch aktiven verbindungen enthalten |
| US5993842A (en) * | 1994-12-12 | 1999-11-30 | Zeneca Limited | Microcapsules containing suspensions of biologically active compounds |
| US5849412A (en) * | 1995-02-17 | 1998-12-15 | Medlogic Global Corporation | Encapsulated materials |
| US5932285A (en) * | 1995-02-17 | 1999-08-03 | Medlogic Global Corporation | Encapsulated materials |
| ZA974359B (en) * | 1996-05-23 | 1998-05-12 | Zeneca Ltd | Microencapsulated compositions. |
| DE19646880A1 (de) * | 1996-11-13 | 1998-05-14 | Hoechst Schering Agrevo Gmbh | Endosulfan-Mikrokapseldispersion |
| US6080418A (en) * | 1997-04-07 | 2000-06-27 | 3M Innovative Properties Company | Suspensions of microcapsules containing biologically active ingredients and adhesive microspheres |
| US6248364B1 (en) | 1997-04-07 | 2001-06-19 | 3M Innovative Properties Company | Encapsulation process and encapsulated products |
| EA200000150A1 (ru) * | 1997-07-22 | 2000-10-30 | Монсанто Компани | Составы, содержащие аммонний-глифосат в высокой концентрации |
| US5939324A (en) * | 1997-12-02 | 1999-08-17 | The United States Of America As Represented By The United States Department Of Energy | Performance evaluation soil samples utilizing encapsulation technology |
| KR100621474B1 (ko) * | 1998-07-29 | 2006-09-22 | 신젠타 리미티드 | 염기에 의해 방출이 자극되는 마이크로캡슐 |
| NO20021592D0 (no) * | 2002-04-04 | 2002-04-04 | Fmc Biopolymer As | Polysakkaridkapsler og fremgangsmåte ved fremstilling derav |
| RU2347608C2 (ru) * | 2003-05-11 | 2009-02-27 | Бен-Гурион Юниверсити Оф Дзе Негев Рисерч Энд Дивелопмент Оторити | Инкапсулированные эфирные масла |
| PE20061029A1 (es) * | 2005-03-01 | 2006-11-27 | Basf Ag | Procedimiento para la preparacion de composiciones de microcapsula de liberacion rapida |
| US7678847B2 (en) * | 2005-07-22 | 2010-03-16 | Appleton Papers Inc. | Encapsulated structural adhesive |
| US7629394B2 (en) * | 2006-02-21 | 2009-12-08 | Appleton Papers Inc. | UV curable coating material of encapsulated water dispersed core material |
| WO2007103186A2 (fr) * | 2006-03-03 | 2007-09-13 | Fmc Corporation | Procede et appareil de preparation de capsules |
| ME02956B (fr) | 2006-03-30 | 2018-07-20 | Fmc Corp | Microcapsules de polymères acétylène-carbamid-polyurée et formulations à liberation controlée |
| DE102006015940A1 (de) * | 2006-04-05 | 2007-10-11 | Bayer Cropscience Ag | Flüssige Formulierungen im Pflanzenschutz und deren Verwendung |
| JP5439952B2 (ja) * | 2009-05-29 | 2014-03-12 | 住友化学株式会社 | マイクロカプセルの製造方法 |
| WO2012074588A2 (fr) | 2010-08-30 | 2012-06-07 | President And Fellows Of Harvard College | Libération contrôlée par cisaillement pour lésions sténosées et traitements thrombolytiques |
| US9206381B2 (en) | 2011-09-21 | 2015-12-08 | Ecolab Usa Inc. | Reduced misting alkaline cleaners using elongational viscosity modifiers |
| BR112015001697A2 (pt) | 2012-07-27 | 2017-07-04 | Fmc Corp | formulações de clomazona |
| US9637708B2 (en) | 2014-02-14 | 2017-05-02 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
| ES2774793T3 (es) * | 2014-10-24 | 2020-07-22 | Basf Se | Partículas pesticidas orgánicas |
| AU2017272086B2 (en) | 2016-05-23 | 2019-06-27 | Ecolab Usa Inc. | Reduced misting alkaline and neutral cleaning, sanitizing, and disinfecting compositions via the use of high molecular weight water-in-oil emulsion polymers |
| CN109153948B (zh) | 2016-05-23 | 2021-03-16 | 埃科莱布美国股份有限公司 | 通过使用高分子量油包水乳液聚合物的减少雾化的酸性清洁、消毒和杀菌组合物 |
| AU2018227539B2 (en) | 2017-03-01 | 2020-04-09 | Ecolab Usa Inc. | Reduced inhalation hazard sanitizers and disinfectants via high molecular weight polymers |
| CN114096650A (zh) | 2019-07-12 | 2022-02-25 | 埃科莱布美国股份有限公司 | 使用碱溶性乳液聚合物的减少雾化的碱性清洁剂 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1112755A (en) * | 1913-11-08 | 1914-10-06 | John A Bergstrom | Poisonous tablet and antidote. |
| DE1120131B (de) * | 1958-12-08 | 1961-12-21 | Union Carbide Corp | Verfahren zur Herstellung von Urethangruppen aufweisenden Schaumstoffen |
| GB1001458A (en) * | 1962-12-03 | 1965-08-18 | Ici Ltd | Catalysts for isocyanate reactions |
| CH453305A (fr) * | 1963-10-21 | 1968-06-14 | Pilot Pen Co Ltd | Procédé pour encapsuler de fines gouttelettes de liquides dispersées |
| US3577515A (en) * | 1963-12-13 | 1971-05-04 | Pennwalt Corp | Encapsulation by interfacial polycondensation |
| JPS5212150B1 (fr) * | 1968-06-04 | 1977-04-05 | ||
| US3701759A (en) * | 1969-04-10 | 1972-10-31 | Stauffer Chemical Co | Certain geranyl phenyl ethers and their epoxides and their use in controlling insects |
| US3576760A (en) * | 1969-06-13 | 1971-04-27 | Nat Patent Dev Corp | Water soluble entrapping |
| JPS5022507B1 (fr) * | 1969-09-02 | 1975-07-31 | ||
| GB1330227A (en) * | 1970-07-08 | 1973-09-12 | Gen Tire & Rubber Co | Catalytic system for waterblown flexible polyetherurethane foams and foams made therefrom |
| DE2312059C2 (de) * | 1972-03-15 | 1987-04-02 | Stauffer Chemical Co., Westport, Conn. | Verfahren zum Einkapseln eines mit Wasser nicht mischbaren organischen Materials in einer Polyharnstoffkapsel |
| CA1104882A (fr) * | 1972-03-15 | 1981-07-14 | Herbert B. Scher | Methode de mise en capsule |
| GB1452504A (en) * | 1973-11-15 | 1976-10-13 | Wiggins Teape Ld | Method of making microcapsules |
| US4046741A (en) * | 1976-02-17 | 1977-09-06 | Stauffer Chemical Company | Post-treatment of polyurea microcapsules |
-
1977
- 1977-05-31 US US05/801,932 patent/US4140516A/en not_active Expired - Lifetime
-
1978
- 1978-05-24 GB GB21921/78A patent/GB1558460A/en not_active Expired
- 1978-05-25 ZA ZA00783016A patent/ZA783016B/xx unknown
- 1978-05-29 PH PH21203A patent/PH16196A/en unknown
- 1978-05-29 IL IL54804A patent/IL54804A/xx unknown
- 1978-05-29 DE DE2823377A patent/DE2823377C2/de not_active Expired
- 1978-05-29 CH CH586478A patent/CH640151A5/de not_active IP Right Cessation
- 1978-05-30 BG BG039913A patent/BG29865A3/xx unknown
- 1978-05-30 AR AR272388A patent/AR217296A1/es active
- 1978-05-30 IT IT49597/78A patent/IT1115076B/it active
- 1978-05-30 CA CA304,452A patent/CA1110503A/fr not_active Expired
- 1978-05-30 HU HU78SA3113A patent/HU181952B/hu not_active IP Right Cessation
- 1978-05-30 MX MX787113U patent/MX5644E/es unknown
- 1978-05-30 BR BR7803468A patent/BR7803468A/pt unknown
- 1978-05-30 NZ NZ187429A patent/NZ187429A/xx unknown
- 1978-05-30 FR FR7816025A patent/FR2392715A1/fr active Granted
- 1978-05-30 AU AU36639/78A patent/AU514717B2/en not_active Expired
- 1978-05-30 NL NL7805878A patent/NL7805878A/xx not_active Application Discontinuation
- 1978-05-31 PL PL1978207239A patent/PL128464B1/pl unknown
- 1978-05-31 DK DK241678A patent/DK156989C/da active
- 1978-05-31 DD DD78205691A patent/DD137063A5/xx unknown
- 1978-05-31 RO RO7894233A patent/RO75293A/fr unknown
- 1978-05-31 JP JP53065627A patent/JPS5826969B2/ja not_active Expired
- 1978-05-31 CS CS783535A patent/CS198299B2/cs unknown
- 1978-05-31 SU SU782625405A patent/SU1022651A3/ru active
- 1978-05-31 BE BE2057024A patent/BE867646A/xx not_active IP Right Cessation
- 1978-05-31 YU YU1303/78A patent/YU40039B/xx unknown
- 1978-05-31 ES ES470373A patent/ES470373A1/es not_active Expired
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CS198299B2 (en) | Method of incapsulation of the substances water non-miscible | |
| JP3848676B2 (ja) | 生物学的に活性な化合物の懸濁液を含有するマイクロカプセル | |
| EP1292386B1 (fr) | Nouvelles microcapsules | |
| RU2443723C2 (ru) | Микрокапсулы с ацетиленкарбамид-полимочевинными полимерами и их композиции для регулированного высвобождения | |
| US4309213A (en) | Process of encapsulation by interfacial polycondensation | |
| JPH0568300B2 (fr) | ||
| JPS585697B2 (ja) | カプセル化方法 | |
| SK1362001A3 (en) | Acid-triggered release microcapsules | |
| CN104619173A (zh) | 农用化学组合物,其制备方法及其用途 | |
| AU716412B2 (en) | Microencapsulation process and product | |
| HU194504B (en) | Method for filling inmiscibles in water materials into microcapsules | |
| JPH052370B2 (fr) | ||
| US5993842A (en) | Microcapsules containing suspensions of biologically active compounds | |
| JPS61249904A (ja) | シロアリ防除剤 | |
| JP2895562B2 (ja) | 多段カプセル化によるマイクロカプセルの製造方法 | |
| RU2212797C2 (ru) | Способ получения препарата для уничтожения бытовых насекомых в виде водной суспензии на основе микрокапсулированного раствора хлорпирифоса | |
| MXPA97005484A (es) | Proceso de microencapsulacion y producto |