JPS5946541B2 - 活性成分の制御された放出を行うための固体重合体物品 - Google Patents

活性成分の制御された放出を行うための固体重合体物品

Info

Publication number: JPS5946541B2
Authority: JP; Japan
Prior art keywords: polymer; active ingredient; solid article; article according; solid
Prior art date: 1977-02-01
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

Application number

JP52013112A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5399252A (en

Inventor

ロバ−ト・デ−ビツト・クロス

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bush Boake Allen Ltd

Original Assignee

Bush Boake Allen Ltd

Priority date (The priority date 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 date listed.)

1977-02-01

Filing date

1977-02-10

Publication date

1984-11-13

1977-02-10 Application filed by Bush Boake Allen Ltd filed Critical Bush Boake Allen Ltd

1978-08-30 Publication of JPS5399252A publication Critical patent/JPS5399252A/ja

1984-11-13 Publication of JPS5946541B2 publication Critical patent/JPS5946541B2/ja

Status Expired legal-status Critical Current

Links

239000004480 active ingredient Substances 0.000 title claims description 74
239000007787 solid Substances 0.000 title claims description 26
238000013270 controlled release Methods 0.000 title description 2
229920000642 polymer Polymers 0.000 claims description 74
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 59
239000000203 mixture Substances 0.000 claims description 53
239000002904 solvent Substances 0.000 claims description 38
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 36
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 20
239000003205 fragrance Substances 0.000 claims description 19
-1 glycerol ester Chemical class 0.000 claims description 19
235000010323 ascorbic acid Nutrition 0.000 claims description 18
229960005070 ascorbic acid Drugs 0.000 claims description 18
239000011668 ascorbic acid Substances 0.000 claims description 18
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
239000000463 material Substances 0.000 claims description 11
150000002148 esters Chemical class 0.000 claims description 8
239000002917 insecticide Substances 0.000 claims description 8
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 7
239000003016 pheromone Substances 0.000 claims description 7
239000002685 polymerization catalyst Substances 0.000 claims description 7
239000000126 substance Substances 0.000 claims description 6
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
150000001735 carboxylic acids Chemical class 0.000 claims description 4
239000003638 chemical reducing agent Substances 0.000 claims description 4
235000014113 dietary fatty acids Nutrition 0.000 claims description 4
239000000194 fatty acid Substances 0.000 claims description 4
229930195729 fatty acid Natural products 0.000 claims description 4
229920002554 vinyl polymer Polymers 0.000 claims description 4
CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims description 3
230000000855 fungicidal effect Effects 0.000 claims description 3
239000000417 fungicide Substances 0.000 claims description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
150000004665 fatty acids Chemical class 0.000 claims description 2
150000002978 peroxides Chemical class 0.000 claims description 2
235000010352 sodium erythorbate Nutrition 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims 1
230000000379 polymerizing effect Effects 0.000 claims 1
239000000600 sorbitol Substances 0.000 claims 1
239000000178 monomer Substances 0.000 description 23
239000003921 oil Substances 0.000 description 21
235000019198 oils Nutrition 0.000 description 21
239000010692 aromatic oil Substances 0.000 description 19
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 16
239000000243 solution Substances 0.000 description 13
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 12
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 12
GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 11
238000006116 polymerization reaction Methods 0.000 description 11
FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 description 11
HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 10
239000003054 catalyst Substances 0.000 description 10
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 8
VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 8
229910001870 ammonium persulfate Inorganic materials 0.000 description 8
238000004132 cross linking Methods 0.000 description 8
238000001704 evaporation Methods 0.000 description 8
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 8
239000011347 resin Substances 0.000 description 8
229920005989 resin Polymers 0.000 description 8
DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 7
239000000853 adhesive Substances 0.000 description 7
239000007864 aqueous solution Substances 0.000 description 7
239000012298 atmosphere Substances 0.000 description 7
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 7
230000008020 evaporation Effects 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
229920001328 Polyvinylidene chloride Polymers 0.000 description 6
UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000005033 polyvinylidene chloride Substances 0.000 description 6
239000002202 Polyethylene glycol Substances 0.000 description 5
239000002253 acid Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
239000007800 oxidant agent Substances 0.000 description 5
229920001223 polyethylene glycol Polymers 0.000 description 5
239000010666 rose oil Substances 0.000 description 5
235000019719 rose oil Nutrition 0.000 description 5
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
241000220317 Rosa Species 0.000 description 4
229940022663 acetate Drugs 0.000 description 4
229910002092 carbon dioxide Inorganic materials 0.000 description 4
230000000694 effects Effects 0.000 description 4
125000000524 functional group Chemical group 0.000 description 4
DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000000344 soap Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
244000241235 Citrullus lanatus Species 0.000 description 3
235000012828 Citrullus lanatus var citroides Nutrition 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
235000016623 Fragaria vesca Nutrition 0.000 description 3
235000011363 Fragaria x ananassa Nutrition 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
239000001569 carbon dioxide Substances 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
239000001046 green dye Substances 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 3
239000002609 medium Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
150000007522 mineralic acids Chemical class 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
125000005702 oxyalkylene group Chemical group 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000002985 plastic film Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
125000002348 vinylic group Chemical group 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 2
OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 2
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
244000144730 Amygdalus persica Species 0.000 description 2
241000272525 Anas platyrhynchos Species 0.000 description 2
ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
241000167854 Bourreria succulenta Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
240000009088 Fragaria x ananassa Species 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
241000147041 Guaiacum officinale Species 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 description 2
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235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
235000011613 Pinus brutia Nutrition 0.000 description 2
241000018646 Pinus brutia Species 0.000 description 2
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DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
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NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
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238000000354 decomposition reaction Methods 0.000 description 2
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CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
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238000000465 moulding Methods 0.000 description 2
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239000001044 red dye Substances 0.000 description 2
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VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
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HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
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LVSQXDHWDCMMRJ-UHFFFAOYSA-N 4-hydroxybutan-2-one Chemical compound CC(=O)CCO LVSQXDHWDCMMRJ-UHFFFAOYSA-N 0.000 description 1
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DINKXUCRJBUQAZ-UHFFFAOYSA-N tert-butyl 5-bromopyridine-3-carboxylate Chemical compound CC(C)(C)OC(=O)C1=CN=CC(Br)=C1 DINKXUCRJBUQAZ-UHFFFAOYSA-N 0.000 description 1
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Classifications

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- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
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- 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
- A01N25/08—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 containing solids as carriers or diluents
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- 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
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- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
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- A61L9/044—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating with the help of an organic compound other than a macromolecular compound
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
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- C—CHEMISTRY; METALLURGY
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Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Epidemiology (AREA)
Medicinal Chemistry (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Polymers & Plastics (AREA)
Plant Pathology (AREA)
Toxicology (AREA)
Agronomy & Crop Science (AREA)
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Pulmonology (AREA)
Fats And Perfumes (AREA)
Compositions Of Macromolecular Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
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Cosmetics (AREA)

JP52013112A 1977-02-01 1977-02-10 活性成分の制御された放出を行うための固体重合体物品 Expired JPS5946541B2 (ja)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE7701076A SE421531B (sv)	1977-02-01	1977-02-01	Polymer komposition innehallande en for reglerad avgivning aktiv, flyktig bestandsdel, forfarande for framstellning av kompositionen samt anvendning derav

Publications (2)

Publication Number	Publication Date
JPS5399252A JPS5399252A (en)	1978-08-30
JPS5946541B2 true JPS5946541B2 (ja)	1984-11-13

Family

ID=20330329

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP52013112A Expired JPS5946541B2 (ja)	1977-02-01	1977-02-10	活性成分の制御された放出を行うための固体重合体物品

Country Status (9)

Country	Link
JP (1)	JPS5946541B2 (fr)
AU (1)	AU513822B2 (fr)
BE (1)	BE881972Q (fr)
CA (1)	CA1099429A (fr)
CH (1)	CH633304A5 (fr)
DE (1)	DE2705218A1 (fr)
FR (1)	FR2380328A1 (fr)
NL (1)	NL7701526A (fr)
SE (1)	SE421531B (fr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0011924A1 (fr) *	1978-10-23	1980-06-11	BUSH BOAKE ALLEN Limited	Compositions polymères libérant un parfum et procédés pour leur préparation
US4320873A (en) *	1979-05-21	1982-03-23	S. C. Johnson & Son, Inc.	Controlled release air freshener using an absorbent generator
CA1150635A (fr) *	1979-10-23	1983-07-26	Philip L. Williams	Monomere lipophyle d'un polymere hydrophyle contenant un ingredient volatif captif
IT1129711B (it) *	1980-01-23	1986-06-11	Montedison Spa	Formulazioni solide contenenti ferormoni
US4724240A (en) *	1981-03-23	1988-02-09	Wickhen Products, Inc.	Lattice-entrapped emollient-moisturizer composition
US4880617A (en) *	1981-03-23	1989-11-14	Dow Corning Corporation	Lattice-entrapped composition
CA1168157A (fr) *	1981-03-23	1984-05-29	Eric S. Abrutyn	Composition adoucissante-humidifiante, fixee dans un polymere
USRE33429E (en) *	1981-03-23	1990-11-06	Dow Corning Corporation	Lattice-entrapped emollient-moisturizer composition
US4729190A (en) *	1983-10-27	1988-03-08	Ciba-Geigy Corporation	Membrane-forming polymeric systems
US4855127A (en) *	1986-07-07	1989-08-08	Dow Corning Corporation	Lattice-entrapped composition
CA2037282C (fr) *	1990-04-02	1997-01-28	Nuno M. Rei	Microbicides immobilises dans des resines polymeres thermoplastiques hydrosolubles et dispersions aqueuses de microbicides ainsi produites
DE4416672A1 (de) *	1994-05-11	1995-11-16	Grillmayer Juergen	Duftender Gegenstand
JP7846623B2 (ja) *	2021-06-21	2026-04-15	積水化学工業株式会社	（メタ）アクリル樹脂組成物、無機微粒子分散スラリー組成物及び無機微粒子分散成形物

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1205768A (en) *	1966-07-26	1970-09-16	Nat Patent Dev Corp	Marine protective coatings
GR34006B (el) *	1966-07-26	1968-03-06	National Patent Development Corporation	Υδροφιλα πολυμερη, ειδη και μεθοδοι παρασκευης αυτων.
FR2022100A6 (en) *	1967-07-05	1970-07-31	Nat Patent Developm	Acrylate polymer as binder in cosmetic composns
US3655129A (en) *	1968-07-17	1972-04-11	Ppg Industries Inc	Slow release films and methods of making same
US3567118A (en) *	1968-09-05	1971-03-02	Nat Patent Dev Corp	Entrapped essences in dry composite fiber base products giving a strong fragrance when wet in water
US3868447A (en) *	1972-02-02	1975-02-25	Nat Patent Dev Corp	Hema paste
ES445695A1 (es) *	1975-03-03	1977-06-16	Airwick Ag	Un metodo para producir un sistema difusor solido liberador de vapores mejoradores del olor del aire provisto de una ma-triz polimerica.

1977
- 1977-02-01 SE SE7701076A patent/SE421531B/xx not_active IP Right Cessation
- 1977-02-04 CA CA271,072A patent/CA1099429A/fr not_active Expired
- 1977-02-07 AU AU22023/77A patent/AU513822B2/en not_active Expired
- 1977-02-08 DE DE19772705218 patent/DE2705218A1/de not_active Ceased
- 1977-02-10 JP JP52013112A patent/JPS5946541B2/ja not_active Expired
- 1977-02-14 CH CH181477A patent/CH633304A5/de not_active IP Right Cessation
- 1977-02-14 NL NL7701526A patent/NL7701526A/xx not_active Application Discontinuation
- 1977-02-14 FR FR7704127A patent/FR2380328A1/fr active Granted
1980
- 1980-02-28 BE BE0/199591A patent/BE881972Q/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
JPS5399252A (en)	1978-08-30
SE7701076L (sv)	1978-08-02
FR2380328B1 (fr)	1980-03-07
AU513822B2 (en)	1981-01-08
BE881972Q (fr)	1980-08-28
SE421531B (sv)	1982-01-04
CA1099429A (fr)	1981-04-14
AU2202377A (en)	1978-08-17
CH633304A5 (en)	1982-11-30
DE2705218A1 (de)	1978-08-10
NL7701526A (nl)	1978-08-16
FR2380328A1 (fr)	1978-09-08

Publication	Publication Date	Title
US4649046A (en)	1987-03-10	Air freshener
US4587129A (en)	1986-05-06	Hydrophilic gels containing high amounts of fragrance
EP0028118B1 (fr)	1986-01-15	Articles conformés à base de polymère et d'ingrédients volatils occlus
JPS5946541B2 (ja)	1984-11-13	活性成分の制御された放出を行うための固体重合体物品
US3966902A (en)	1976-06-29	Polymer complex carriers for an active ingredient
RU2585849C9 (ru)	2017-01-30	Бумага, пропитанная инсектицидными действующими веществами
CN102845416B (zh)	2016-08-03	芳香性防虫驱虫剂
US7754198B2 (en)	2010-07-13	Aroma-releasing polymeric gel matrix
WO1989001948A1 (fr)	1989-03-09	Compositions polymeres
JP4829589B2 (ja)	2011-12-07	飛翔害虫忌避剤
US4842853A (en)	1989-06-27	Solid which releases a fragrant substance and/or a disinfectant
JP4999310B2 (ja)	2012-08-15	飛翔害虫忌避剤
JPH0226982B2 (fr)	1990-06-13
US20020004033A1 (en)	2002-01-10	Emulsion type vapor generator
JPH01315402A (ja)	1989-12-20	揮散性物質を含有するゲル組成物およびゲル基材
JP2000319104A (ja)	2000-11-21	徐放性複合体およびその二次製品
JP4823645B2 (ja)	2011-11-24	飛翔害虫忌避剤
JPH0228221A (ja)	1990-01-30	徐放性膜及びその製造法
GB2061308A (en)	1981-05-13	Polymer compositions containing entrapped volatile ingredients
JP2005126393A (ja)	2005-05-19	放香防虫製品
JP3730697B2 (ja)	2006-01-05	動物忌避性光硬化成形物および有害動物の忌避方法
JP3749785B2 (ja)	2006-03-01	脱臭効力増強剤およびこれを用いた脱臭剤
JPS5892357A (ja)	1983-06-01	収容体
JP2000084956A (ja)	2000-03-28	人工大理石成形体
JPH02164368A (ja)	1990-06-25	抗菌・芳香性膜及びその製造法