NO129230B - - Google Patents
Download PDFInfo
- Publication number
- NO129230B NO129230B NO04358/70A NO435870A NO129230B NO 129230 B NO129230 B NO 129230B NO 04358/70 A NO04358/70 A NO 04358/70A NO 435870 A NO435870 A NO 435870A NO 129230 B NO129230 B NO 129230B
- Authority
- NO
- Norway
- Prior art keywords
- weight
- block
- carrier
- copolymer
- block copolymer
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 claims description 42
- 229920001400 block copolymer Polymers 0.000 claims description 40
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 30
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 29
- 238000002360 preparation method Methods 0.000 claims description 26
- 239000004800 polyvinyl chloride Substances 0.000 claims description 14
- -1 diene hydrocarbon Chemical class 0.000 claims description 13
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 12
- 239000004793 Polystyrene Substances 0.000 claims description 11
- 229920002223 polystyrene Polymers 0.000 claims description 11
- 239000000575 pesticide Substances 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 6
- 239000011574 phosphorus Substances 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 239000004709 Chlorinated polyethylene Substances 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 31
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 23
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 description 17
- 229920001577 copolymer Polymers 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 239000012071 phase Substances 0.000 description 11
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 239000008187 granular material Substances 0.000 description 8
- 239000002917 insecticide Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 230000001788 irregular Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 229910052744 lithium Inorganic materials 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- 239000005062 Polybutadiene Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000012876 carrier material Substances 0.000 description 3
- 238000000748 compression moulding Methods 0.000 description 3
- 150000001993 dienes Chemical class 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 229920001756 Polyvinyl chloride acetate Polymers 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229910052736 halogen Chemical group 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- BNKAXGCRDYRABM-UHFFFAOYSA-N ethenyl dihydrogen phosphate Chemical class OP(O)(=O)OC=C BNKAXGCRDYRABM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- VGMQZCPHUDXGFR-UHFFFAOYSA-N lithium;naphthalene Chemical compound [Li].[Li].C1=CC=CC2=CC=CC=C21 VGMQZCPHUDXGFR-UHFFFAOYSA-N 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur 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
- A01N25/08—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
- A01N25/10—Macromolecular compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5613069 | 1969-11-17 | ||
| GB2463470 | 1970-05-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO129230B true NO129230B (xx) | 1974-03-18 |
Family
ID=26257213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO04358/70A NO129230B (xx) | 1969-11-17 | 1970-11-16 |
Country Status (16)
| Country | Link |
|---|---|
| JP (1) | JPS5510561B1 (xx) |
| AR (1) | AR192867A1 (xx) |
| AT (1) | AT303455B (xx) |
| BE (1) | BE758889A (xx) |
| CA (1) | CA937164A (xx) |
| CH (1) | CH563115A5 (xx) |
| DE (1) | DE2056320C3 (xx) |
| DK (1) | DK128432B (xx) |
| ES (1) | ES385582A1 (xx) |
| FR (1) | FR2080883A1 (xx) |
| IE (1) | IE34733B1 (xx) |
| IL (1) | IL35655A (xx) |
| NL (1) | NL173815C (xx) |
| NO (1) | NO129230B (xx) |
| OA (1) | OA03522A (xx) |
| SE (1) | SE376536B (xx) |
-
0
- BE BE758889D patent/BE758889A/nl not_active IP Right Cessation
-
1970
- 1970-11-16 AT AT1030370A patent/AT303455B/de not_active IP Right Cessation
- 1970-11-16 NO NO04358/70A patent/NO129230B/no unknown
- 1970-11-16 OA OA54087A patent/OA03522A/xx unknown
- 1970-11-16 JP JP10027670A patent/JPS5510561B1/ja active Pending
- 1970-11-16 ES ES385582A patent/ES385582A1/es not_active Expired
- 1970-11-16 DK DK580470AA patent/DK128432B/da unknown
- 1970-11-16 AR AR232385A patent/AR192867A1/es active
- 1970-11-16 CH CH1695570A patent/CH563115A5/xx not_active IP Right Cessation
- 1970-11-16 DE DE2056320A patent/DE2056320C3/de not_active Expired
- 1970-11-16 IE IE1462/70A patent/IE34733B1/xx unknown
- 1970-11-16 NL NLAANVRAGE7016733,A patent/NL173815C/xx not_active IP Right Cessation
- 1970-11-16 FR FR7040958A patent/FR2080883A1/fr active Granted
- 1970-11-16 CA CA098248A patent/CA937164A/en not_active Expired
- 1970-11-16 SE SE7015427A patent/SE376536B/xx unknown
- 1970-11-16 IL IL35655A patent/IL35655A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2056320B2 (de) | 1979-08-30 |
| JPS5510561B1 (xx) | 1980-03-17 |
| DK128432B (da) | 1974-05-06 |
| AT303455B (de) | 1972-11-27 |
| CA937164A (en) | 1973-11-20 |
| NL173815B (nl) | 1983-10-17 |
| IE34733L (en) | 1971-05-17 |
| FR2080883B1 (xx) | 1973-02-02 |
| IL35655A (en) | 1974-05-16 |
| CH563115A5 (xx) | 1975-06-30 |
| FR2080883A1 (en) | 1971-11-26 |
| NL173815C (nl) | 1984-03-16 |
| AR192867A1 (es) | 1973-03-21 |
| ES385582A1 (es) | 1973-03-16 |
| OA03522A (fr) | 1971-03-30 |
| DE2056320A1 (de) | 1971-06-03 |
| IL35655A0 (en) | 1971-01-28 |
| IE34733B1 (en) | 1975-08-06 |
| SE376536B (xx) | 1975-06-02 |
| DE2056320C3 (de) | 1980-05-14 |
| BE758889A (nl) | 1971-05-13 |
| NL7016733A (xx) | 1971-05-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69731466T2 (de) | Nichtwassriges insektizides gel mit kontrollierter wirkstoffabgabe | |
| Arrieta et al. | Functional properties of sodium and calcium caseinate antimicrobial active films containing carvacrol | |
| WO2008127435A2 (en) | Controlled gas release from a melt processable compatible polymer blend | |
| EA027090B1 (ru) | Гранулы гидрированного блок-сополимера, полиолефиновая полимерная композиция и формованное из нее изделие | |
| TW200934842A (en) | Process for the production of insecticide-modified bead material composed of expandable polystyrene and insecticide-modified moldings obtainable therefrom | |
| WO2010072640A1 (de) | Verfahren zur stabilisierung von polymeren | |
| Holcapkova et al. | Thermal stability of bacteriocin nisin in polylactide-based films | |
| AU3915597A (en) | Method of making controlled release devices | |
| Gozzelino et al. | Quaternary ammonium monomers for UV crosslinked antibacterial surfaces | |
| Peppas et al. | Controlled release of perfumes from polymers. II. Incorporation and release of essential oils from glassy polymers | |
| CN106700383A (zh) | 一种止血带用tpe材料及其制备工艺 | |
| CN107041144B (zh) | 制备热塑性树脂的方法 | |
| NO169780B (no) | Polymerblanding omfattende polystyren, polypropylen og enblokk-kopolymer, samt anvendelse av denne til fremstilling av innpakningsmateriale | |
| NO129230B (xx) | ||
| CN107099031B (zh) | 一种耐高温改性聚六亚甲基胍及其制备方法和用途 | |
| Prasetya et al. | Synthesis of copolymer eugenol crosslinked with divinyl benzene and preliminary study on its antibacterial activity | |
| Zhang et al. | Design and in vitro evaluation of a film-controlled dosage form self-converted from monolithic tablet in gastrointestinal environment | |
| US3769417A (en) | Biocidal polymeric compositions for controlling invertebrate pests | |
| Jai‐eau et al. | Cure behavior and antimicrobial performance of sulfur‐cured natural rubber vulcanizates containing 2‐hydroxypropyl‐3‐piperazinylquinolinecarboxylic acid methacrylate or silver‐substituted zeolite | |
| JPS62232402A (ja) | 重合体の製造方法 | |
| JP3643151B2 (ja) | 抗菌性含リン樹脂およびその製造方法 | |
| JPS60231717A (ja) | 重合体の製造方法 | |
| Zhang et al. | Synthesis and antimicrobial activity of some cross‐linked copolymers with alkyl chains of various lengths | |
| JPH03200704A (ja) | 薬剤徐放性樹脂成形体 | |
| KR930000594A (ko) | 전자비임이 조사된 중합체 이물 조성물의 제조방법 및 이에의해 얻은 조형품 |