NO770891L - Fremgangsm}te for impregnering av tre - Google Patents

Fremgangsm}te for impregnering av tre

Info

Publication number: NO770891L
Authority: NO; Norway
Prior art keywords: wood; reactive solvent; impregnating agent; solvent; pentachlorophenol
Prior art date: 1976-03-15

Application number

NO770891A

Other languages

English (en)

Norwegian (no)

Inventor

William J Oberley

John J Kozak

Original Assignee

Koppers Co Inc

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.)

1976-03-15

Filing date

1977-03-14

Publication date

1977-09-16

1977-03-14 Application filed by Koppers Co Inc filed Critical Koppers Co Inc

1977-09-16 Publication of NO770891L publication Critical patent/NO770891L/no

Links

239000002023 wood Substances 0.000 title claims abstract description 149
238000000034 method Methods 0.000 title claims abstract description 68
238000005470 impregnation Methods 0.000 title claims description 49
239000002904 solvent Substances 0.000 claims description 144
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 claims description 125
239000003795 chemical substances by application Substances 0.000 claims description 116
239000007788 liquid Substances 0.000 claims description 80
238000011282 treatment Methods 0.000 claims description 47
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 45
239000000203 mixture Substances 0.000 claims description 39
239000003755 preservative agent Substances 0.000 claims description 34
239000000178 monomer Substances 0.000 claims description 26
230000002335 preservative effect Effects 0.000 claims description 25
239000001273 butane Substances 0.000 claims description 23
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 23
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 22
239000010875 treated wood Substances 0.000 claims description 22
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
239000003999 initiator Substances 0.000 claims description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
239000006184 cosolvent Substances 0.000 claims description 11
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 10
238000004090 dissolution Methods 0.000 claims description 10
239000003063 flame retardant Substances 0.000 claims description 10
238000010438 heat treatment Methods 0.000 claims description 9
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 8
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 8
239000002245 particle Substances 0.000 claims description 8
229920000642 polymer Polymers 0.000 claims description 8
239000004342 Benzoyl peroxide Substances 0.000 claims description 7
235000019400 benzoyl peroxide Nutrition 0.000 claims description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 6
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 5
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 5
230000015556 catabolic process Effects 0.000 claims description 5
229920002239 polyacrylonitrile Polymers 0.000 claims description 5
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 claims description 4
238000009835 boiling Methods 0.000 claims description 4
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 4
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims description 4
238000000354 decomposition reaction Methods 0.000 claims description 4
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims description 4
239000003505 polymerization initiator Substances 0.000 claims description 4
RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical class ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 claims description 3
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
-1 benzoyl- Chemical group 0.000 claims description 3
230000000149 penetrating effect Effects 0.000 claims description 3
238000005979 thermal decomposition reaction Methods 0.000 claims description 3
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims description 2
PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 claims description 2
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims description 2
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
150000004996 alkyl benzenes Chemical class 0.000 claims description 2
150000005204 hydroxybenzenes Chemical class 0.000 claims description 2
WSGCRAOTEDLMFQ-UHFFFAOYSA-N nonan-5-one Chemical compound CCCCC(=O)CCCC WSGCRAOTEDLMFQ-UHFFFAOYSA-N 0.000 claims description 2
150000002978 peroxides Chemical class 0.000 claims description 2
HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 claims description 2
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 claims description 2
239000008096 xylene Substances 0.000 claims description 2
238000001704 evaporation Methods 0.000 claims 2
230000008020 evaporation Effects 0.000 claims 2
229920002319 Poly(methyl acrylate) Polymers 0.000 claims 1
239000004793 Polystyrene Substances 0.000 claims 1
150000002500 ions Chemical class 0.000 claims 1
229920001485 poly(butyl acrylate) polymer Polymers 0.000 claims 1
229920003214 poly(methacrylonitrile) Polymers 0.000 claims 1
229920002223 polystyrene Polymers 0.000 claims 1
229920002689 polyvinyl acetate Polymers 0.000 claims 1
239000011118 polyvinyl acetate Substances 0.000 claims 1
230000007928 solubilization Effects 0.000 claims 1
238000005063 solubilization Methods 0.000 claims 1
230000003381 solubilizing effect Effects 0.000 claims 1
239000000243 solution Substances 0.000 description 30
239000011449 brick Substances 0.000 description 20
206010037844 rash Diseases 0.000 description 19
208000010201 Exanthema Diseases 0.000 description 15
201000005884 exanthem Diseases 0.000 description 15
230000035515 penetration Effects 0.000 description 12
239000011261 inert gas Substances 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
239000013078 crystal Substances 0.000 description 7
230000014759 maintenance of location Effects 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
239000007789 gas Substances 0.000 description 6
230000001105 regulatory effect Effects 0.000 description 6
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
238000002441 X-ray diffraction Methods 0.000 description 5
229910052802 copper Inorganic materials 0.000 description 5
239000010949 copper Substances 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
239000005871 repellent Substances 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
238000009826 distribution Methods 0.000 description 4
238000006253 efflorescence Methods 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
239000003607 modifier Substances 0.000 description 4
238000011084 recovery Methods 0.000 description 4
231100000331 toxic Toxicity 0.000 description 4
230000002588 toxic effect Effects 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
235000014466 Douglas bleu Nutrition 0.000 description 3
241000218683 Pseudotsuga Species 0.000 description 3
235000005386 Pseudotsuga menziesii var menziesii Nutrition 0.000 description 3
238000012644 addition polymerization Methods 0.000 description 3
238000006731 degradation reaction Methods 0.000 description 3
230000008021 deposition Effects 0.000 description 3
239000000975 dye Substances 0.000 description 3
150000008282 halocarbons Chemical class 0.000 description 3
GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 3
239000004137 magnesium phosphate Substances 0.000 description 3
229960002261 magnesium phosphate Drugs 0.000 description 3
229910000157 magnesium phosphate Inorganic materials 0.000 description 3
235000010994 magnesium phosphates Nutrition 0.000 description 3
238000013508 migration Methods 0.000 description 3
230000005012 migration Effects 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
150000002894 organic compounds Chemical class 0.000 description 3
239000011148 porous material Substances 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
230000002940 repellent Effects 0.000 description 3
230000000717 retained effect Effects 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
238000012546 transfer Methods 0.000 description 3
239000003171 wood protecting agent Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
229910001369 Brass Inorganic materials 0.000 description 2
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
241000222634 Lenzites Species 0.000 description 2
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
235000005018 Pinus echinata Nutrition 0.000 description 2
241001236219 Pinus echinata Species 0.000 description 2
235000017339 Pinus palustris Nutrition 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000002519 antifouling agent Substances 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
239000010951 brass Substances 0.000 description 2
230000006378 damage Effects 0.000 description 2
ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 2
229950006824 dieldrin Drugs 0.000 description 2
NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 2
FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
229940049964 oleate Drugs 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-M oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC([O-])=O ZQPPMHVWECSIRJ-KTKRTIGZSA-M 0.000 description 2
150000002902 organometallic compounds Chemical class 0.000 description 2
239000003209 petroleum derivative Substances 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 2
230000005855 radiation Effects 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
229920000638 styrene acrylonitrile Polymers 0.000 description 2
238000012360 testing method Methods 0.000 description 2
LMDKALUFKHCRFQ-UHFFFAOYSA-M tributylplumbyl acetate Chemical compound CCCC[Pb](CCCC)(CCCC)OC(C)=O LMDKALUFKHCRFQ-UHFFFAOYSA-M 0.000 description 2
PWBHRVGYSMBMIO-UHFFFAOYSA-M tributylstannanylium;acetate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(C)=O PWBHRVGYSMBMIO-UHFFFAOYSA-M 0.000 description 2
230000004580 weight loss Effects 0.000 description 2
JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
VUHNXENESAVFON-UHFFFAOYSA-N 2,3,4,5,6-pentachlorophenol;zinc Chemical compound [Zn].OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl VUHNXENESAVFON-UHFFFAOYSA-N 0.000 description 1
RULKYXXCCZZKDZ-UHFFFAOYSA-N 2,3,4,5-tetrachlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C(Cl)=C1Cl RULKYXXCCZZKDZ-UHFFFAOYSA-N 0.000 description 1
LHJGJYXLEPZJPM-UHFFFAOYSA-N 2,4,5-trichlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C=C1Cl LHJGJYXLEPZJPM-UHFFFAOYSA-N 0.000 description 1
LINPIYWFGCPVIE-UHFFFAOYSA-N 2,4,6-trichlorophenol Chemical compound OC1=C(Cl)C=C(Cl)C=C1Cl LINPIYWFGCPVIE-UHFFFAOYSA-N 0.000 description 1
BZWMYDJJDBFAPE-UHFFFAOYSA-N 2-chloro-4-phenylphenol Chemical compound C1=C(Cl)C(O)=CC=C1C1=CC=CC=C1 BZWMYDJJDBFAPE-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
KPFPEXKMIDAQNO-UHFFFAOYSA-N 3-chloro-2-phenylphenol Chemical compound OC1=CC=CC(Cl)=C1C1=CC=CC=C1 KPFPEXKMIDAQNO-UHFFFAOYSA-N 0.000 description 1
FPBMWSBRLLFCEG-UHFFFAOYSA-N 4-chloronaphthalen-2-ol Chemical compound C1=CC=CC2=CC(O)=CC(Cl)=C21 FPBMWSBRLLFCEG-UHFFFAOYSA-N 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
QATWRXACOFOJRC-UHFFFAOYSA-N ClC1=C(C(=C(C(=C1O)Cl)Cl)Cl)Cl.ClC1=C(C(=C(C2=CC=CC=C12)Cl)Cl)Cl Chemical compound ClC1=C(C(=C(C(=C1O)Cl)Cl)Cl)Cl.ClC1=C(C(=C(C2=CC=CC=C12)Cl)Cl)Cl QATWRXACOFOJRC-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 description 1
239000013032 Hydrocarbon resin Substances 0.000 description 1
DFBKLUNHFCTMDC-UHFFFAOYSA-N LSM-36947 Chemical compound C12C(C3(Cl)Cl)(Cl)C(Cl)=C(Cl)C3(Cl)C2C2CC1C1C2O1 DFBKLUNHFCTMDC-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
206010034960 Photophobia Diseases 0.000 description 1
235000011334 Pinus elliottii Nutrition 0.000 description 1
235000008566 Pinus taeda Nutrition 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
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
UVCFFGYNJOPUSF-UHFFFAOYSA-M acetyloxy(ethyl)mercury Chemical compound CC[Hg+].CC([O-])=O UVCFFGYNJOPUSF-UHFFFAOYSA-M 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000011021 bench scale process Methods 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
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AWGTVRDHKJQFAX-UHFFFAOYSA-M chloro(phenyl)mercury Chemical compound Cl[Hg]C1=CC=CC=C1 AWGTVRDHKJQFAX-UHFFFAOYSA-M 0.000 description 1
OOCCDEMITAIZTP-UHFFFAOYSA-N cinnamyl alcohol Chemical compound OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
239000003426 co-catalyst Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000008139 complexing agent Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
229940120693 copper naphthenate Drugs 0.000 description 1
LABRFZDGWLJDJS-UHFFFAOYSA-N copper;2,3,4,5,6-pentachlorophenol Chemical compound [Cu].OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LABRFZDGWLJDJS-UHFFFAOYSA-N 0.000 description 1
SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
230000007423 decrease Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
QWUGXIXRFGEYBD-UHFFFAOYSA-M ethylmercuric chloride Chemical compound CC[Hg]Cl QWUGXIXRFGEYBD-UHFFFAOYSA-M 0.000 description 1
MJOUBOKSWBMNGQ-UHFFFAOYSA-N ethylmercury(1+) Chemical compound CC[Hg+] MJOUBOKSWBMNGQ-UHFFFAOYSA-N 0.000 description 1
239000002360 explosive Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000000835 fiber Substances 0.000 description 1
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150000002432 hydroperoxides Chemical class 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Chemical class 0.000 description 1
238000012690 ionic polymerization Methods 0.000 description 1
239000001282 iso-butane Substances 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
238000002386 leaching Methods 0.000 description 1
208000013469 light sensitivity Diseases 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000003915 liquefied petroleum gas Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
230000007903 penetration ability Effects 0.000 description 1
230000002093 peripheral effect Effects 0.000 description 1
XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical compound CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 description 1
BODKAQWWZBLGOU-UHFFFAOYSA-N phenylmercury(1+) Chemical compound [Hg+]C1=CC=CC=C1 BODKAQWWZBLGOU-UHFFFAOYSA-N 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
238000012643 polycondensation polymerization Methods 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
238000004064 recycling Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002893 slag Substances 0.000 description 1
HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 1
WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
238000006557 surface reaction Methods 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
239000010876 untreated wood Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
MXODCLTZTIFYDV-UHFFFAOYSA-L zinc;1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Zn+2].C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O.C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O MXODCLTZTIFYDV-UHFFFAOYSA-L 0.000 description 1

Classifications

- 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
- B27K3/02—Processes; Apparatus
- B27K3/15—Impregnating involving polymerisation including use of polymer-containing impregnating agents
- B27K3/156—Combined with grafting onto wood fibres
- 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
- B27K3/16—Inorganic 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
- 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
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
- 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
- B27K2240/00—Purpose of the treatment
- B27K2240/30—Fireproofing
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/23—Azo-compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—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 an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
- C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C08L31/04—Homopolymers or copolymers of vinyl acetate
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/18—Homopolymers or copolymers of nitriles
- C08L33/20—Homopolymers or copolymers of acrylonitrile

Landscapes

Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Wood Science & Technology (AREA)
Forests & Forestry (AREA)
Materials Engineering (AREA)
Inorganic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)

NO770891A 1976-03-15 1977-03-14 Fremgangsm}te for impregnering av tre NO770891L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US66678876A	1976-03-15	1976-03-15

Publications (1)

Publication Number	Publication Date
NO770891L true NO770891L (no)	1977-09-16

Family

ID=24675478

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO770891A NO770891L (no)	1976-03-15	1977-03-14	Fremgangsm}te for impregnering av tre

Country Status (10)

Country	Link
JP (1)	JPS52110803A (da)
AU (1)	AU507381B2 (da)
CA (1)	CA1085106A (da)
DE (1)	DE2710530A1 (da)
DK (1)	DK106777A (da)
FI (1)	FI770788A7 (da)
FR (1)	FR2344384A1 (da)
GB (1)	GB1570311A (da)
NO (1)	NO770891L (da)
SE (1)	SE7702775L (da)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ZA797045B (en) *	1979-03-22	1981-11-25	Envirosol Syst Int	Wood treatment process and product thereof
GB8430354D0 (en) *	1984-11-30	1985-01-09	Brown D M H	Protected structure
EP0229176B1 (en) *	1985-07-16	1990-10-17	INNOFINANCE Altalános Innovácios Pénzintézet	Wood treatment composition
NO311246B1 (no)	2000-01-18	2001-11-05	Marc Schneider	Trepolymerkompositt, fremgangsmåte til fremstilling av trepolymerkompositten ved å impregnere tremateriale og/ellertrebasert materiale, og anvendelse derav
DE60102449T2 (de) *	2000-01-18	2005-03-24	Wood Polymer Technologies Asa	Verfahren zum imprägnieren von holz
AU2005328560B2 (en) *	2004-09-30	2011-09-01	Carter Holt Harvey Wood Products Australia Pty Limited	Impregnation apparatus and method
SI1799411T1 (sl) *	2004-09-30	2011-11-30	Solvents Australia Pty Ltd	Impregnacijska naprava in metode
EP3329046B1 (en) *	2015-07-30	2019-06-19	Green Theme Technologies, Inc.	Hyperbaric process for applying and curing an organic polymerizable treatment

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4856295A (da) *	1971-11-17	1973-08-07

1977
- 1977-02-11 GB GB5929/77A patent/GB1570311A/en not_active Expired
- 1977-02-14 CA CA271,662A patent/CA1085106A/en not_active Expired
- 1977-02-24 AU AU22612/77A patent/AU507381B2/en not_active Expired
- 1977-03-10 DE DE19772710530 patent/DE2710530A1/de not_active Withdrawn
- 1977-03-11 DK DK106777A patent/DK106777A/da unknown
- 1977-03-11 SE SE7702775A patent/SE7702775L/xx unknown
- 1977-03-11 FI FI770788A patent/FI770788A7/fi not_active Application Discontinuation
- 1977-03-14 FR FR7707564A patent/FR2344384A1/fr active Pending
- 1977-03-14 NO NO770891A patent/NO770891L/no unknown
- 1977-03-15 JP JP2856777A patent/JPS52110803A/ja active Granted

Also Published As

Publication number	Publication date
CA1085106A (en)	1980-09-09
JPS5625362B2 (da)	1981-06-11
FI770788A7 (da)	1977-09-16
DK106777A (da)	1977-09-16
DE2710530A1 (de)	1977-09-22
AU507381B2 (en)	1980-02-14
SE7702775L (sv)	1977-09-16
GB1570311A (en)	1980-06-25
JPS52110803A (en)	1977-09-17
AU2261277A (en)	1978-08-31
FR2344384A1 (fr)	1977-10-14

Publication	Publication Date	Title
Kartal et al.	2004	Decay and termite resistance of boron-treated and chemically modified wood by in situ co-polymerization of allyl glycidyl ether (AGE) with methyl methacrylate (MMA)
Li et al.	2011	Improvement of decay resistance of wood via combination treatment on wood cell wall: Swell-bonding with maleic anhydride and graft copolymerization with glycidyl methacrylate and methyl methacrylate
CA2859731C (en)	2016-03-15	Pentachlorophenol/borate compositions and uses thereof
NO770891L (no)	1977-09-16	Fremgangsm}te for impregnering av tre
CN1938133A (zh)	2007-03-28	浸渍工艺
Grattan	2018	Treatment of waterlogged wood
Phillips et al.	1971	The graft copolymerization of styrene and lignin. I. Hydrochloric acid lignin
US4399195A (en)	1983-08-16	Preservation of wood
US4085251A (en)	1978-04-18	High retention wood preservative composition
US4433031A (en)	1984-02-21	Preservation of wood
Czvikovszky	1968	Wood-plastic combination. By monomer impregnation and radiation polymerization
Carlson et al.	1990	Residual solvents in wood-consolidant composites
EP4251383B1 (en)	2026-04-08	Method for treating wood
WITTE et al.	1977	A comparative study of three consolidation methods on limestone
Sheikh et al.	1993	Radiation induced polymerization of vinyl monomers and their application for preparation of wood-polymer composites
US3371058A (en)	1968-02-27	Flame retardant
Spindler et al.	1973	Polymer impregnated fibrous materials: The resistance of polymer-wood composites to chemical corrosion
Moustafa et al.	1977	Some wood polymer composites II
Šimůnková et al.	1983	Consolidation of wood by the method of monomer polymerization in the object
Nikulina et al.	2020	About the possibility of using 1-vinylnaphthalene to modify natural wood
EP1799411B1 (en)	2011-06-08	Impregnation apparatus and method
Turner et al.	1998	Treatment of timber products with gaseous borate esters: Part 2. Process improvement
US3278405A (en)	1966-10-11	Polyacrylonitrile containing keteneimine linkages produced by high energy radiation
Ibach et al.	1995	Low polymer levels containing bioactive monomer polymerized in situ provide resistance to Gloeophyllum trabeum
Burstall et al.	1984	Graft copolymerization as a method of preserving papers: problems and potentialities