FI65012C - Medel foer konservering av trae och traematerial samt foerfarande foer framstaellning av konserveringsmedlet - Google Patents
Medel foer konservering av trae och traematerial samt foerfarande foer framstaellning av konserveringsmedlet Download PDFInfo
- Publication number
- FI65012C FI65012C FI802164A FI802164A FI65012C FI 65012 C FI65012 C FI 65012C FI 802164 A FI802164 A FI 802164A FI 802164 A FI802164 A FI 802164A FI 65012 C FI65012 C FI 65012C
- Authority
- FI
- Finland
- Prior art keywords
- weight
- solvent
- organic
- dimethyl
- wood
- Prior art date
Links
- 101100148710 Clarkia breweri SAMT gene Proteins 0.000 title 1
- 239000002904 solvent Substances 0.000 claims abstract description 41
- 239000002023 wood Substances 0.000 claims abstract description 31
- 239000000417 fungicide Substances 0.000 claims abstract description 25
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000126 substance Substances 0.000 claims abstract description 17
- 239000000203 mixture Substances 0.000 claims abstract description 16
- 239000002917 insecticide Substances 0.000 claims abstract description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 40
- 230000000855 fungicidal effect Effects 0.000 claims description 31
- 239000011877 solvent mixture Substances 0.000 claims description 16
- 239000003171 wood protecting agent Substances 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000003755 preservative agent Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000010426 asphalt Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 4
- 239000004035 construction material Substances 0.000 abstract 1
- -1 dichlorofluoromethylthio Chemical group 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 8
- 239000003849 aromatic solvent Substances 0.000 description 7
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 7
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 7
- 229960002809 lindane Drugs 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 230000000749 insecticidal effect Effects 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000013543 active substance Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 239000002274 desiccant Substances 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- LLVCJAQYTNSMRB-UHFFFAOYSA-N dichloro-fluoro-(sulfamoylamino)sulfanylmethane Chemical compound NS(=O)(=O)NSC(F)(Cl)Cl LLVCJAQYTNSMRB-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 125000005609 naphthenate group Chemical group 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000003791 organic solvent mixture Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- XDIPOBQVBXLETD-UHFFFAOYSA-N 1,2,3,4-tetrachloro-5,6-dinitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1[N+]([O-])=O XDIPOBQVBXLETD-UHFFFAOYSA-N 0.000 description 1
- BFCFYVKQTRLZHA-UHFFFAOYSA-N 1-chloro-2-nitrobenzene Chemical class [O-][N+](=O)C1=CC=CC=C1Cl BFCFYVKQTRLZHA-UHFFFAOYSA-N 0.000 description 1
- RULKYXXCCZZKDZ-UHFFFAOYSA-N 2,3,4,5-tetrachlorophenol Chemical class OC1=CC(Cl)=C(Cl)C(Cl)=C1Cl RULKYXXCCZZKDZ-UHFFFAOYSA-N 0.000 description 1
- XLIOSTKZVOKGMB-UHFFFAOYSA-M 2,3-dichlorophenolate;tributylstannanylium Chemical compound [O-]C1=CC=CC(Cl)=C1Cl.CCCC[Sn+](CCCC)CCCC XLIOSTKZVOKGMB-UHFFFAOYSA-M 0.000 description 1
- WCBYIQXROKIJLD-UHFFFAOYSA-N 2-carbamothioylsulfanylpropyl carbamodithioate;zinc Chemical compound [Zn].NC(=S)SC(C)CSC(N)=S WCBYIQXROKIJLD-UHFFFAOYSA-N 0.000 description 1
- QBGLHYQUZJDZOO-UHFFFAOYSA-N 2-chloro-3-nitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1Cl QBGLHYQUZJDZOO-UHFFFAOYSA-N 0.000 description 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- GLMHLMZCDUFDAU-UHFFFAOYSA-N FNS(=O)(=S)NC(Cl)Cl Chemical compound FNS(=O)(=S)NC(Cl)Cl GLMHLMZCDUFDAU-UHFFFAOYSA-N 0.000 description 1
- LXMQMMSGERCRSU-UHFFFAOYSA-N Fluotrimazole Chemical compound FC(F)(F)C1=CC=CC(C(C=2C=CC=CC=2)(C=2C=CC=CC=2)N2N=CN=C2)=C1 LXMQMMSGERCRSU-UHFFFAOYSA-N 0.000 description 1
- QTDRLOKFLJJHTG-UHFFFAOYSA-N Furmecyclox Chemical compound C1=C(C)OC(C)=C1C(=O)N(OC)C1CCCCC1 QTDRLOKFLJJHTG-UHFFFAOYSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical compound ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 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
- 150000003949 imides Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- LXCJGJYAOVCKLO-UHFFFAOYSA-N n-cyclohexyl-n-hydroxynitrous amide Chemical compound O=NN(O)C1CCCCC1 LXCJGJYAOVCKLO-UHFFFAOYSA-N 0.000 description 1
- SVIKNKPDPGCMAE-UHFFFAOYSA-N n-phenyl-n-(1,1,2,2-tetrachloro-2-fluoroethyl)sulfanylmethanesulfonamide Chemical compound FC(Cl)(Cl)C(Cl)(Cl)SN(S(=O)(=O)C)C1=CC=CC=C1 SVIKNKPDPGCMAE-UHFFFAOYSA-N 0.000 description 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical class CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000013324 preserved food Nutrition 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010875 treated wood Substances 0.000 description 1
- YSUXTNDMKYYZPR-UHFFFAOYSA-M tributylstannyl prop-2-enoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C=C YSUXTNDMKYYZPR-UHFFFAOYSA-M 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing >N—S—C≡(Hal)3 groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
- B27K3/42—Aromatic compounds nitrated, or nitrated and halogenated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/50—Mixtures of different organic impregnating agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K5/00—Treating of wood not provided for in groups B27K1/00, B27K3/00
- B27K5/02—Staining or dyeing wood; Bleaching wood
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Environmental Sciences (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
- Two-Way Televisions, Distribution Of Moving Picture Or The Like (AREA)
- Shovels (AREA)
Claims (6)
1. Medel för konservering av trä och trämaterial bestäende av mer än 65 vikt %, fördelaktigt mer än 72 vikt % av minst ett svärflyktigt organiskkemiskt lösningsmedel med en flampunkt över 30 C, och mellan 0. 35 och 10 vikt %, fördelaktigt mellan 1 och 7 vikt % av minst en fungicid, som är löslig eller delvis löslig i det organiskkemiska svarflyktiga lösningsmedlet med flampunkten över 30 °C, samt even-tuellt mellan 0,1 och 7 vikt %, fördelaktigt mellan 0,3 och 3 vikt % av minst en insekticid, som är löslig i det organiskkemiska svarflyktiga lösningsmedlet med flampunkten över 30 °C, känneteck-n a t av att fungiciden bestär av NjN-dimetyl-N'-fenyl-N'-ifluordi-klormetyltio)-sulfamid och N,N-dimetyl-N'-p-tolyl-N'-(diklorfluor-metyltio)-sulfamid i ett viktförhällande mellan 25:10 och 10:30, fördelaktigt mellan 15:10 och 10:15.
2. Medel för konservering av trä och trämaterial enligt patentkravet 1, kännetecknat av att mellan 0,5 och 23 vikt %, fördelaktigt mellan 2 och 15 vikt %, av det organiska svarflyktiga lösningsmedlet eller lösningsmedelsblandningen med flampunkten över 30 °C ersatts med en lika stor mängd av ett eller flere organiskkemiska bindemedel och/eller fixermedel, varvid som organiskkemiska binde-medel och/eller fixermedel använts sädana, som är fördelbara eller emulgerbara, företrädesvis dock lösliga i lösningsmedlet eller lösningsmedelsblandningen, varvid ersättandet utförs sä, att den erhäll-na blandningen eller den erhällna lösningsmedelsblandningen likasä har en flampunkt över 30 °C och det organiskkemiska lösningsmedlet eller lösningsmedelsblandningen är ett oljigt eller ett oljeartat lösningsmedel.
3. Medel för konservering av trä eller trämaterial enligt patentkravet 1 eller 2, kännetecknat därav att mellan 0,05 och 6 vikt %, fördelaktigt mellan 0,1 och 4 vikt %, av det organiska svarflyktiga lösningsmedlet eller lösningsmedelblandningen, företrädesvis av det oljiga eller oljeartade lösningsmedlet eller lösningsmedelsblandingen, ersatts med en lika stor mängd av ett eller flere färgämnen, som är oljelösliga i det organiska svärflyktiga lösningsmedlet eller lösningsmedelsblandningen, och/eller med bitumen, och/eller organiska och eller oorganiska färgpigment, som är olösliga i vatten och/eller i organiskkemiska lösningsmedel eller lösningsmedelsblandningar.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792927349 DE2927349A1 (de) | 1979-07-06 | 1979-07-06 | Mittel zum konservieren von holz und holzwerkstoffen sowie verfahren zur herstellung des konservierungsmittels |
| DE2927349 | 1979-07-06 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI802164A FI802164A (fi) | 1981-01-07 |
| FI65012B FI65012B (fi) | 1983-11-30 |
| FI65012C true FI65012C (fi) | 1984-03-12 |
Family
ID=6075079
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI802164A FI65012C (fi) | 1979-07-06 | 1980-07-07 | Medel foer konservering av trae och traematerial samt foerfarande foer framstaellning av konserveringsmedlet |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4337093A (sv) |
| EP (1) | EP0022900B1 (sv) |
| JP (1) | JPS5638202A (sv) |
| AT (1) | ATE2727T1 (sv) |
| CA (1) | CA1133655A (sv) |
| DE (2) | DE2927349A1 (sv) |
| FI (1) | FI65012C (sv) |
| HU (1) | HU189466B (sv) |
| YU (1) | YU42671B (sv) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3122270A1 (de) * | 1981-06-04 | 1982-12-23 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Bakterizides und fungizides mittel |
| DE3139252A1 (de) * | 1981-10-02 | 1983-04-21 | Basf Ag, 6700 Ludwigshafen | Holzschutzmittel |
| US4652558A (en) * | 1985-06-26 | 1987-03-24 | Chevron Research Company | 2-thio-organotin-4(3H)-quinazolinone |
| DE3531363A1 (de) * | 1985-09-03 | 1987-03-12 | Bayer Ag | Materialschutzmittel |
| DE3609589A1 (de) * | 1986-03-21 | 1987-09-24 | Ruetgerswerke Ag | Mittel und verfahren zur dimensionsstabilisierung von holz oder holzwerkstoffen |
| CA1329311C (en) * | 1987-04-28 | 1994-05-10 | David Lloyd Evans | Compositions and methods of treatment of timber |
| CH681439A5 (sv) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv | |
| CH681440A5 (sv) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv | |
| CH681438A5 (sv) * | 1990-04-26 | 1993-03-31 | Warmoctro Bv | |
| DE4104023A1 (de) * | 1991-02-09 | 1992-08-13 | Ostermann & Scheiwe Gmbh & Co | Konservierungsmittel fuer holz- und holzwerkstoffe |
| US6623552B1 (en) * | 2002-11-12 | 2003-09-23 | Michael Howard West | Aluminum salt-amine complex UV inhibitor for wood |
| RU2650685C2 (ru) * | 2016-05-18 | 2018-04-17 | Сергей Анатольевич Максименко | Огнебиозащитный трудновымываемый препарат для древесины и материалов на ее основе |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2769006A (en) * | 1951-02-17 | 1956-10-30 | Scient Oil Compounding Company | Solubilizing metal-8-hydroxy quinolates |
| US2966440A (en) * | 1956-05-07 | 1960-12-27 | Shell Oil Co | Insecticidal compositions |
| FR1310083A (sv) | 1960-11-03 | 1963-03-04 | ||
| DE1238139B (de) * | 1964-04-11 | 1967-04-06 | Bayer Ag | Mikrobizide Mittel fuer Anstriche und Kunststoffueberzuege |
| US3492256A (en) * | 1967-10-24 | 1970-01-27 | Ppg Industries Inc | Resinous coating compositions containing alkyd-amine resins |
| FI56499C (fi) * | 1973-07-17 | 1980-02-11 | Basf Ag | Synergistiskt medel foer skyddande av trae mot av svampar och insekter foerorsakad foerstoering |
| FR2355451A1 (fr) * | 1976-02-20 | 1978-01-20 | Sarpap | Procede de preparation de compositions biocides pour la preservation des bois |
| DE2655330A1 (de) * | 1976-12-07 | 1978-06-08 | Bayer Ag | Mittel zum konservieren von holz und werkstoffen |
| DE2844605A1 (de) * | 1978-10-13 | 1980-04-24 | Bayer Ag | Verwendung von n,n-dimethyl-n'-p- tolyl-n'-dichlorfluormethylthiosulfamid zur bekaempfung von holzschaedigenden pilzen |
-
1979
- 1979-07-06 DE DE19792927349 patent/DE2927349A1/de not_active Withdrawn
-
1980
- 1980-03-29 EP EP80101694A patent/EP0022900B1/de not_active Expired
- 1980-03-29 AT AT80101694T patent/ATE2727T1/de not_active IP Right Cessation
- 1980-03-29 DE DE8080101694T patent/DE3062252D1/de not_active Expired
- 1980-06-24 HU HU801564A patent/HU189466B/hu not_active IP Right Cessation
- 1980-07-01 YU YU1712/80A patent/YU42671B/xx unknown
- 1980-07-03 US US06/165,791 patent/US4337093A/en not_active Expired - Lifetime
- 1980-07-04 CA CA355,424A patent/CA1133655A/en not_active Expired
- 1980-07-07 FI FI802164A patent/FI65012C/fi not_active IP Right Cessation
- 1980-07-07 JP JP9182080A patent/JPS5638202A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| HU189466B (en) | 1986-07-28 |
| ATE2727T1 (de) | 1983-03-15 |
| DE2927349A1 (de) | 1981-01-29 |
| DE3062252D1 (en) | 1983-04-14 |
| YU42671B (en) | 1988-10-31 |
| FI65012B (fi) | 1983-11-30 |
| JPS6233923B2 (sv) | 1987-07-23 |
| EP0022900A1 (de) | 1981-01-28 |
| JPS5638202A (en) | 1981-04-13 |
| EP0022900B1 (de) | 1983-03-09 |
| US4337093A (en) | 1982-06-29 |
| CA1133655A (en) | 1982-10-19 |
| YU171280A (en) | 1983-12-31 |
| FI802164A (fi) | 1981-01-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: DEUTSCHE SOLVAY-WERKE GMBH |