CS269554B1 - Fumigant - Google Patents
Fumigant Download PDFInfo
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- CS269554B1 CS269554B1 CS877476A CS747687A CS269554B1 CS 269554 B1 CS269554 B1 CS 269554B1 CS 877476 A CS877476 A CS 877476A CS 747687 A CS747687 A CS 747687A CS 269554 B1 CS269554 B1 CS 269554B1
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- dinitroso
- regulator
- trioxane
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- 239000002316 fumigant Substances 0.000 title claims description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 239000010457 zeolite Substances 0.000 claims abstract description 7
- 239000003380 propellant Substances 0.000 claims abstract description 6
- 229920001732 Lignosulfonate Polymers 0.000 claims abstract description 4
- 230000035784 germination Effects 0.000 claims abstract description 4
- 235000002595 Solanum tuberosum Nutrition 0.000 claims abstract description 3
- 244000061456 Solanum tuberosum Species 0.000 claims abstract description 3
- 235000019357 lignosulphonate Nutrition 0.000 claims abstract description 3
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims abstract 4
- 239000000203 mixture Substances 0.000 claims description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 6
- 239000004156 Azodicarbonamide Substances 0.000 claims description 5
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 claims description 5
- 235000019399 azodicarbonamide Nutrition 0.000 claims description 5
- 239000005983 Maleic hydrazide Substances 0.000 claims description 3
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 239000003063 flame retardant Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 2
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims 2
- 239000002202 Polyethylene glycol Substances 0.000 claims 2
- 235000021317 phosphate Nutrition 0.000 claims 2
- HCNUDMZUISFCKU-UHFFFAOYSA-N (2,3,4-triphenylphenyl) dihydrogen phosphate Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC=CC=2)C(OP(O)(=O)O)=CC=C1C1=CC=CC=C1 HCNUDMZUISFCKU-UHFFFAOYSA-N 0.000 claims 1
- 239000004913 cyclooctene Substances 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract description 6
- PRPINYUDVPFIRX-UHFFFAOYSA-N 1-naphthaleneacetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CC=CC2=C1 PRPINYUDVPFIRX-UHFFFAOYSA-N 0.000 abstract description 4
- 239000005971 1-naphthylacetic acid Substances 0.000 abstract description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 abstract description 4
- 235000012015 potatoes Nutrition 0.000 abstract description 2
- CBXQCVZYHBHJRI-UHFFFAOYSA-N 2-oxidoazaniumylidyneacetonitrile Chemical class [O-][N+]#CC#N CBXQCVZYHBHJRI-UHFFFAOYSA-N 0.000 abstract 1
- 229920005610 lignin Chemical class 0.000 description 6
- -1 siloxanes Chemical class 0.000 description 5
- 229920001807 Urea-formaldehyde Polymers 0.000 description 4
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical class O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000005647 Chlorpropham Substances 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 description 2
- 238000010411 cooking Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- XHYWZUWPPUQDDR-UHFFFAOYSA-N 1-amino-1-carbamoylurea Chemical compound NC(=O)N(N)C(N)=O XHYWZUWPPUQDDR-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004117 Lignosulphonate Substances 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- UNYSKUBLZGJSLV-UHFFFAOYSA-L calcium;1,3,5,2,4,6$l^{2}-trioxadisilaluminane 2,4-dioxide;dihydroxide;hexahydrate Chemical compound O.O.O.O.O.O.[OH-].[OH-].[Ca+2].O=[Si]1O[Al]O[Si](=O)O1.O=[Si]1O[Al]O[Si](=O)O1 UNYSKUBLZGJSLV-UHFFFAOYSA-L 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000032823 cell division Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229910052676 chabazite Inorganic materials 0.000 description 1
- 238000009388 chemical precipitation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052675 erionite Inorganic materials 0.000 description 1
- 230000010437 erythropoiesis Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002972 pentoses Chemical class 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Riešenie je zaměřené na prostriedok určený k zaaedzeniu klíčivosti zemiakov. Proatriedok je tvořený prchavou účinnou létkou, napr. profémoa, chlorprofémom, metyleaterom kvseliny 1-naftyloctovej, hvdrazidoa kyseliny malelnovej atd., zápalnou pohonnou zmesou na béze 1,5 metano-3,7-dinitrózo-l,3,5,7-tetraazacyklooktšnu a regulátorem horenla. Podstatou je použitie, ako regulátore horenla, vodonerozpustných močovinoforoaldehvdových kondenzátov, zeolitov, trlerylfosfétov, N.NČblskarbamoylhydrazínu jednotlivo alebo v zmesiacn s sulfonovanými zlúčeninsmi ligninu, trioxanom alebo derivétmi sikylenoxidov, v množstve 0,1 až 40 % hmot. na celkovú hmotnost prostrledku.The solution is resource-focused intended to prevent germination potatoes. Proatriedok is made up of fleeting effective flight, e.g. profemaa, chlorpropema, 1-naphthylacetic acid methyl ether, the malodic acid hydrazide etc., with an incendiary propellant on the base 1,5 metano-3,7-dinitroso-1,3,5,7-tetraazacyclooctane and the regulator burned. The essence is the use as a regulator burning, water-insoluble urea-fluoroaldehvd condensates, zeolites, trlerylphosphates, N.N.blbarbamoylhydrazine individually or mixed with sulfonated lignin compounds, trioxane or cyanogen oxide derivatives, in amounts 0.1 to 40 wt. weight prostrledku.
Description
CS 269554 B1 1CS 269554 B1 1
Vynález sa týká proatriedku na zabránanie klíčivosti Jedlých a hospodářských·zemlakov v skladoch větraných ventilátoral. □oterajšie běžné proatriedky proti klíčivosti zemlakov eú aplikovaná vo forměprášku prl uskladňovaní dona. Použltie práškových prapatárov vo velkých skladoch nlsJe technicky nožná a prato sa použlvajú v kvepalnej formě. Tieto sú odpařená aleborozprášená, napr. stlačený· vzduchon. Uvedená netódy sú poruchová, pristrojovo nároč-né s nízkou produktivitou práce. Významná postavenie zaujinajú dýaovnica na zanedzenieklíčivosti, ktoró sú tvořená účinnou zložkou s psstlcidnya účinkom, a zápalnou pohon-nou zmesou. Pohonná znesi obsahujú zlúčeniny uvolňujúce dusík alebo oxid uhličitý, naj-ma azodlkarbonanid a/alebo Ν,Ν-dlnltrózopentametyléňtetranin /3ap. pat. č. 57, 55,378; 60 42,302 a č. 81 77,202 atd./. Za účelon zlepšenla stability a spolehlivosti uvedenéprostriedky obsahujú, napr. nltroqunldin, nitrocelulózu, CH-celulózu infusoriovú hlin-ku, granulovaný kovový vápník, práškový uhlik, oxid nanganičltý, dusičnan strontnatý,nastenec, 11 a skleněná vlékna /Oap. pat. č. 58 140,002; č. 58 32,801; č. 58 172,303;č. 81 75, 402/.The present invention relates to a composition for preventing germination of edible and economic seeds in ventilated fan stores. Šie Obvious common anti-germination agents eu applied in the form of powder dust. The use of powdered binder in large warehouses is technically foot and is used in quail. These are vaporized or dusted, eg compressed air. The aforementioned nodes are malfunctioning, machine-intensive with low labor productivity. Significant positions are impressed by the dagger on neglect of the germination, which are made up of an active ingredient with psstlcidnya effect, and an incendiary propellant. The propellants contain nitrogen-releasing or carbon dioxide-releasing compounds, most preferably azodlcarbonanide and / or Ν, Ν-dl-trisopentamethylenetetranine / 3ap. pat. No. 57, 55,378; 60 42,302 and No. 81 77,202 etc./. For the purpose of improving the stability and reliability, the compositions comprise, for example, nitrocellin, nitrocellulose, CH-cellulose, diatomaceous earth, granular calcium metal, carbon powder, nanganate, strontium nitrate, talc, 11 and glass fibers. pat. No. 58,140,002; No. 58 32,801; No. 58,172,303; 81, 75, 402).
Uvedený výpočet modifikátorov rozšiřuje tento vynález, ktorý sa týká funigantutvořeného prchavým insakticldom a/alebo fungicldoa, bakterlcidoa, alebo druhým pesti-cldom, zápalnou pohonnou zmesou a regulátoroa horenia. Ako regulátory horenia sú pou-žité vodonarozpustné'močovinoformaldehydové kondenzáty, aulfonovaná zlúčeniny , ligni-nu, zeolity, triarylfoefáty, deriváty alkylenoxidov alebo siloxanov, trloxan, N,N-biskarbamoylhydrazin Jednotlivá alebo v zmesiach navzájem v množstva 0,1 až 40 % hmot.na calkovú hmotnost funigantu. Výhodou tohto vynálezu Je technická a ekonomická dostupnost priaad modifikujúcichpropagáclu bezplameňového horenia. Výrobok má dobrú fyzlkólno-cheelckú stabilitu vzhla-dom k segregácii a tepelným účinkoa. Správná interakcle pohonnej zaesl a regulátorahorenia zabezpečuje uvolnenle aerosolu v podobě huetej hasly, v ktorej je rovnoměrněrozptýlená účinná látka, napr. profám, chlórprofám, metyleater kyseliny 1-naftylocto-vej, hydrazid kyseliny maleinovej et3. Účinná látka ee„v prúde vzduchu vnáša do ven-tilátorom větraného skladu zemlakov, kde ea usedzuje. Táto Játka z_abijá_buňky výhonkovočiek, takže delenie buniek a tým rast kllčkov je inhibover.ý. Potlačanie dýchania atranspirácle vedle k zachovanlu výživných látok a k znlženiu strát na hmotnosti ccao 20 %. Skladované zemlaky sú plnohodnotná ako potravina do obdobla preklenutia za-čiatku novej úrody. Mimo zachovaní· kvality Jedlých zemlakov je možná uviesf ňalšiavýhody, napr. to, že vyakladňovacia technika móže byť použitá bezporuchovo až do kon-ce času skladovania a v čase preklenutia prl opracovaných zemiakoch sa výrazné skrátičas lúpanla v lúpaclch prevádzkách.The aforementioned calculation of the modifiers extends the present invention, which relates to the funcant formed by the volatile insecticide and / or fungicidal, bactericidal, or second pesticide, inflammatory propellant and flame regulator. The flame retardants used are water-soluble urea-formaldehyde condensates, sulfonated compounds, lignin, zeolites, triarylphosphates, derivatives of alkylene oxides or siloxanes, trloxane, N, N-biscarbamoylhydrazine. to the weight of the funcant. An advantage of the present invention is the technical and economical availability of a modification modifying flame-retardant flame. The product has good physico-chelating stability due to segregation and thermal efficiency. The proper interaction of the propellant and the regulator provides for the release of the aerosol in the form of a hub, in which the active substance is uniformly dispersed, e.g. prof, chlorpropham, 1-naphthylacetic acid methyl ether, maleic hydrazide et 3. The active ingredient ee in the air stream introduces the ventilated storage of earths to the fans, where it is settled. This is a cell from the cells of the shoots, so that cell division and hence growth of the clusters is inhibited. Suppressing atranspircle in addition to maintaining nutrients and reducing weight loss by about 20%. The stored earths are full-fledged as a food to the brink of a new crop. In addition to preserving the quality of Edible Ears, there are some other advantages, for example, that the refining technique can be used without fail until the end of storage time, and at the time of bridging the processed potatoes, a significant reduction in peel in peeling operations.
Pod pojaom vodonerozpustný močovlnoformaldehydový kondenzát sa rozuoejú polyme-tylánmočoviny charakterizované východzim molárnym pomerom formaldehydu k močovina 0,7až 2,5, a výhodou 0,85 až 1,9.Under the water-insoluble urea-formaldehyde condensate form, the polymeric ureas are characterized by an initial mole ratio of formaldehyde to urea of 0.7 to 2.5, and preferably 0.85 to 1.9.
Zdrojom eylfonovaných zlúčenin ligninu Je najma výroba buničin. Pri týchto vý-robách dochádza k chemickým reakciám ligninu s varnými chemikáliemi. Podstatou týchtoreakcii Je rozštiepenle lignin-celulfi^ového komplexu a makromolekuly ligninu, pričomsa zvyšuje Jeho rozpustnost vplyvom vzniklých hydrofilným skupin. Kyseliny lignosulfo-novó reagujú ešte vnútri bunačnej etany s katiónmi varných roztokov za vzniku lignosul-fonátov, ktoré potom íahko difundujú do varného média. Materiál výluhu z kyslých var-ných postupov Je vodný roztok anorganických a organických zlúčenin so sušinou 9 až14 % hmot. Asi 65 % obsahu sušiny tvoria ligninové zlúčeniny, 25 X sacharidické podlely,medzl ktoré patria Jednoduché pentózy a hexózy, kyseliny aldonová a alduronovó heaice-lulózy a zbývajúcich 10 % připadá na anorganické zlúčeniny ako sú oxid siřičitý, siriči-tany a sírany sodné, horečnaté, vápenaté a amonné. Obsah sacharldov Je možné měnit napr.cestou biologického apracovanla, po ktorom obsah redukujúcich sacharldov sa znižujs nahodnotu 0,1 až 0,2 % hmot. vztlahnuté na sulfitový výluh. Pře lzoláciu kyselin ligno- 2 CS 269554 B1 eulfónových xo sulfltových výlubov existuje celý red metód, z ktorých preetaarnosímožno spoeenút: metody membránovej eeperácle, edeorpčná, -elektrochemické, irystllcTOnie, chemického zrážania a pod. Sulfonovaná zlúčenlny ligninu ako regulátor·’ horenieJe možná použit vo forma lignoaulfonovanej kyseliny. Os potřebná uviest, že.hymsllnalignosulfonová obsiahnutá v eulfitovom výluhu Je vysoko polydiaperzný materiál· OeJpriemsrná relativná molekulová hmotnost sa pohybuje od niekolko stoviek až do niakol-ko stoviek tisíc. VSeobecne Je známe, že nizkomolekulárne frakcia kyselin lignosulfo-nových sú vise sulfonovaná a majú skoro lineárnu Struktúru makromolskulováho rečazea.So zvýiujúcou sa molekulovou haotnosfou klesá relativné zeetúpenie sulfoskupiny v mak-romolekule ligninu v přepočte na jednu aonomernu Jednotku a fragmenty ligninu zleka-vajú trojrozměrná Struktúru. Výhodná je aplikácia lignosulfonovsj kyseliny vo formě Jej soli sodných vápe-natých, horečnatých a pod. samostatné elebo v zmesi. Pozornosf mi zaslúžia produktyzrážania kyseliny lignosulfonovej, resp. jej soli, predkondenzátom připraveným konden-záciou amidových derivátov kyseliny uhličitej, či tiouhličitej s aldehydmí.The source of the lyophilized lignin compounds is in particular the production of pulps. These products have chemical reactions of lignin with cooking chemicals. The essence of these reactions is the cleavage of the lignin-celulfite complex and the lignin macromolecule, while increasing its solubility by the resulting hydrophilic groups. Lignosulfonate acids still react within the cell ethane with the cation of the boiling solutions to form lignosulphonates, which then easily diffuse into the boiling medium. Leaching material from acidic cooking processes is an aqueous solution of inorganic and organic compounds with a dry weight of 9 to 14% by weight. About 65% of the dry matter content is represented by lignin compounds, 25% of the carbohydrate content, including simple pentoses and hexoses, aldonic acid and alduronic hyaluronic acid, and the remaining 10% are inorganic compounds such as sulfur dioxide, sulphite and sodium sulphate, magnesium , calcium and ammonium. The content of saccharides can be altered by, for example, a biological treatment, after which the content of reducing saccharides is reduced to a value of 0.1 to 0.2% by weight. based on sulphite leachate. For the isolation of ligno-2 acids of 269554 B1 sulphonic oily sulphide voids, there are a number of red methods that can be utilized: membrane eerectomy, erythropoiesis, electrochemical, irystllotin, chemical precipitation, and the like. The sulphonated lignin compound as a regulator may be used in the form of a ligno-sulphonated acid. It should be noted that the sulfonium sulfonate contained in the sulphite liquor is highly polydisperse material. The average relative molecular weight ranges from several hundreds to less than hundreds of thousands. Generally, it is known that low molecular weight fractions of lignosulfonic acids are sulfonated and have a nearly linear structure. . Preference is given to the application of lignosulfonic acid in the form of its sodium salt, calcium, magnesium, and the like. separate elebo in a mixture. The products of the lignosulfonic acid precipitation, respectively. a salt thereof, a precondensate prepared by condensation of amide derivatives of carbonic acid or thiocarbonate with aldehyde.
Zo zeolitov, ktorá majú praktický význam k priprave fumigantov, je možná uvlesfnapr. z prirodných klinoptllolit, modernit, chabazit, erionitj zo syntetických zeolitA, v Ha-, K- a Ca- formách, X v Ne-, Ca- a Ba- formách, Y v Na, Ca-, a NH4- formách,syntetický mordenit v Na- a H- formách, omega v Na- a H- formách a ZSM zeolity.Of the zeolites that are of practical importance for the preparation of fumigants, perhaps uvlesfnapr. from natural clinoptololite, moderne, chabazite, erionite from synthetic zeolites, in Ha-, K- and Caforms, X in Ne-, Ca- and Ba-forms, Y in Na, Ca-, and NH 4 -forms, synthetic mordenite in Na- and H-forms, omega in Na- and H- forms and ZSM zeolites.
Pod pojmom trierylfosfáty sú uvažovaná substancie vSsobecnáho vzorce /R-O-/3 « P O, kde ft je fenyl, chlór, resp. polychlórfenyl, bróm, resp; polybrómfenyl, metyl,resp. dimetylfenyl, izopropyl, resp. diizopropylfenyl, Izobutyl, resp. dilzobutyl-fenyl, bifenyl, alkylchlór, resp. alkylbrómfenyl a pod. Táto skupina je charakterizo-vaná obsahom 5 až 10 X hmot. fosforu.The term trierylphosphates is intended to include compounds of the general formula (R-O- / 3-PO), where ft is phenyl, chlorine, respectively. polychlorophenyl, bromine, respectively; polybromophenyl, methyl, resp. dimethylphenyl, isopropyl, resp. diisopropylphenyl, isobutyl, respectively. dilzobutyl-phenyl, biphenyl, alkylchlor, resp. alkyl bromophenyl and the like. This group is characterized by a content of 5 to 10% by weight. phosphorus.
Ako oligomáry a/alebo polymáry na báze derivátov alkylenoxidov alebo slloxanovsú uvažovaná, najma polyetylánglykoly, polypropylánglykoly, polydímetylsiloxány at3.,ktorých středná molekulová hmotnost nepřesahuje 25 000. K parametrom, ktorá ovplyvnujó potřebná množstvá regulátorov horenia patři kva-lita a množství daliich zlo$lek, najma zloženie pohonnej změti. Obsah regulátorovhorenie sa pohybuje až do 40 % hmot., len výnimoSne je horná hranice překročená.As oligomers and / or polymers based on alkylene oxide or slloxane derivatives, polyethylene glycols, polypropylene glycols, polydimethylsiloxanes and the like, having an average molecular weight not exceeding 25,000 are contemplated. , especially the composition of propulsion. The content of the regulator burns up to 40% by weight, only the upper limit is exceeded.
Vynález je óalej objasněný na nasledujúcich příkladech, ktorými ovSem rozsah nieje obasdzený ani vyčerpaný. Přiklad 1 K dispozici! je azo-dlkarbonamld, l,5-metano-3,7-dinltrózo-l,3,5,7-tetraazacyklo-oktán s obsahom 5,0 % hmot. l,3,5-trlnitrózo-l,3,5-triazacyklohexánu, chlórprofám,vodonerozpustný močovinoformaldehydový kondenzát a sulfitová výluhy. Z týchto surovinje připravený na malaxári fumigant s nasledujúcim zloženims 50 hmot. d. azodikarbonamid 15 hmot. d. l,5-oeteno-3,7-dinitrózo-l,3,5,7-tetraezacyklooktán 10 hmot. d. chlórprofám 20 hmot. d. močovinoformaldehydový kondenzát5 hmot. d. vysuáený aulfitový výluh Přiklad 2The invention is further illustrated by the following examples, which are not to be construed as exhaustive or exhausted. Example 1 Available! is azo-dicarbonamide, 1,5-methano-3,7-dinoltrose-1,3,5,7-tetraazacyclo-octane containing 5.0 wt. 1,3,5-trlnitroso-1,3,5-triazacyclohexane, chlorpropham, water-insoluble urea-formaldehyde condensate and sulfite leachates. Of these raw materials, fumigant is prepared on malaxari with the following composition of 50% by weight. d. azodicarbonamide 15 wt. d. 1,5-oeteno-3,7-dinitroso-1,3,5,7-tetraesacyclooctane 10 wt. d. chlorprofam 20 wt. d. urea-formaldehyde condensate 5 wt. d. dried sulphite leachate Example 2
Zo surovin azo-dikarbonamid, l,5-mstano-3,7-dinitrózo-l,3,5,7-tetraazacyklooktánako v přiklade 1, metyleater kyseliny 1-naftyloctovsj a zeolitu klinoptllolitu je pripravený fumigant s nasledujúcim zložsnlm: 35 hmot. d. azo-dikarbonamid 30 hmot. d. l,5-metano-3,7-dinitrózo-l,3,5,7-totraazacyklooktán 10 hmot. d. metyleater kyseliny 1-naftyloctovsj 25 hmot. d. zeolit klinoptllolit.A fumigant is prepared from the raw materials of azodicarbonamide, 1,5-methano-3,7-dinitroso-1,3,5,7-tetraazacyclooctane as in Example 1, 1-naphthyl acetic acid methyl ether and zeolite clinoptololite. d. Azo dicarbonamide 30 wt. d. 1,5-Metano-3,7-dinitroso-1,3,5,7-totraazacyclooctane 10 wt. d. 1-naphthylacetic acid methyl ether 25 wt. d. zeolite clinoptllolite.
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CS877476A CS269554B1 (en) | 1987-10-16 | 1987-10-16 | Fumigant |
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