EP1392452A4 - WOOD TREATMENT METHOD AND COMPOSITION - Google Patents
WOOD TREATMENT METHOD AND COMPOSITIONInfo
- Publication number
- EP1392452A4 EP1392452A4 EP02723715A EP02723715A EP1392452A4 EP 1392452 A4 EP1392452 A4 EP 1392452A4 EP 02723715 A EP02723715 A EP 02723715A EP 02723715 A EP02723715 A EP 02723715A EP 1392452 A4 EP1392452 A4 EP 1392452A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- wood
- composition
- containing salt
- boron
- silicon
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 132
- 239000002023 wood Substances 0.000 title claims abstract description 108
- 238000000034 method Methods 0.000 title claims abstract description 75
- 230000008569 process Effects 0.000 title claims abstract description 55
- 150000003839 salts Chemical class 0.000 claims abstract description 71
- 229910052796 boron Inorganic materials 0.000 claims abstract description 42
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 34
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 32
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 32
- 239000010703 silicon Substances 0.000 claims abstract description 32
- 239000003755 preservative agent Substances 0.000 claims abstract description 17
- 230000002335 preservative effect Effects 0.000 claims abstract description 15
- 230000006866 deterioration Effects 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 124
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 69
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 63
- 239000000243 solution Substances 0.000 claims description 58
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 35
- -1 boron ions Chemical class 0.000 claims description 33
- 229910021538 borax Inorganic materials 0.000 claims description 32
- 239000000377 silicon dioxide Substances 0.000 claims description 32
- 239000004328 sodium tetraborate Substances 0.000 claims description 30
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 29
- 239000004327 boric acid Substances 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- 229910052782 aluminium Inorganic materials 0.000 claims description 20
- 239000001508 potassium citrate Substances 0.000 claims description 19
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 claims description 19
- 235000015870 tripotassium citrate Nutrition 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 17
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 10
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 8
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000000378 calcium silicate Substances 0.000 claims description 4
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 3
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical group Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 claims description 2
- 230000001680 brushing effect Effects 0.000 claims description 2
- 239000008119 colloidal silica Substances 0.000 claims description 2
- 238000007654 immersion Methods 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims description 2
- 230000003247 decreasing effect Effects 0.000 claims 1
- 229910052914 metal silicate Inorganic materials 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 abstract description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract description 3
- 230000007613 environmental effect Effects 0.000 abstract description 3
- 239000008188 pellet Substances 0.000 description 30
- 238000003756 stirring Methods 0.000 description 26
- 239000004115 Sodium Silicate Substances 0.000 description 19
- 229910052911 sodium silicate Inorganic materials 0.000 description 19
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 18
- 238000012546 transfer Methods 0.000 description 18
- 239000000084 colloidal system Substances 0.000 description 12
- 241000256602 Isoptera Species 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000012530 fluid Substances 0.000 description 6
- 238000004321 preservation Methods 0.000 description 5
- 241000219289 Silene Species 0.000 description 4
- CDMADVZSLOHIFP-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 CDMADVZSLOHIFP-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 3
- 229920000592 inorganic polymer Polymers 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229910001414 potassium ion Inorganic materials 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 235000006173 Larrea tridentata Nutrition 0.000 description 2
- 244000073231 Larrea tridentata Species 0.000 description 2
- 229910007156 Si(OH)4 Inorganic materials 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229940063013 borate ion Drugs 0.000 description 2
- 229960002126 creosote Drugs 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009919 sequestration Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 2
- 239000010876 untreated wood Substances 0.000 description 2
- 239000003171 wood protecting agent Substances 0.000 description 2
- 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
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241001387505 Heterotermes tenuis Species 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229910004835 Na2B4O7 Inorganic materials 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000005018 Pinus echinata Nutrition 0.000 description 1
- 241001236219 Pinus echinata Species 0.000 description 1
- 235000011334 Pinus elliottii Nutrition 0.000 description 1
- 235000017339 Pinus palustris Nutrition 0.000 description 1
- 235000008566 Pinus taeda Nutrition 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- 244000274906 Quercus alba Species 0.000 description 1
- 235000009137 Quercus alba Nutrition 0.000 description 1
- 229910020489 SiO3 Inorganic materials 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical class [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000002457 bidirectional effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001638 boron Chemical class 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000004691 decahydrates Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 231100000584 environmental toxicity Toxicity 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000010875 treated wood Substances 0.000 description 1
- 239000002025 wood fiber Substances 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
- B27K3/16—Inorganic impregnating agents
- B27K3/32—Mixtures of different inorganic impregnating agents
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/14—Boron; Compounds thereof
-
- 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
- B27K3/163—Compounds of boron
-
- 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
- B27K3/52—Impregnating agents containing mixtures of inorganic and organic compounds
-
- 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
- C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/02—Inorganic materials
Definitions
- This invention relates to a process for improved wood preservation by the synthesis and use of a non-toxic, environmentally friendly aqueous composition with increased effectiveness over current technology.
- Wood preservation is the technique of reducing the rate of deterioration of wood by: 1) biological agencies of fungi, insects, marine bares, 2) damaging sun rays and 3) fire. Wood preservation is generally achieved by a chemical treatment. Wood preservation increases the useful life of wood and reduces the cost of frequent replacement. Properly designed wood structures give long service without special protection, but large economic loss may result when wood in its natural state is used at high temperatures, in structures exposed to salt water, or under climate conditions that favor the development of harmful fungi and insects.
- the wood preservatives in general used today are oils, including oil borne and water borne chemicals. Oils are used widely for outdoor use. They do not smell in water but they contribute to staining and painting difficulties. Coal tar creosote alone, or in 5% pentachlorophenol in petroleum oil are used for treatment of products such as ties, posts, poles, pilings and construction timbers. Another common treatment solution is water based and contains copper, chromium and arsenic salts (CCA).
- CCA copper, chromium and arsenic salts
- One aspect of this invention is a process for reducing the rate of deterioration of wood.
- the process comprises contacting wood with an aqueous mixture comprising an alkaline, colloidal composition, of a silicon-containing salt having boron ions incorporated therein for time sufficient to impregnate at least a portion of the wood with the mixture.
- the wood may be contacted by immersing the wood in the aqueous mixture at a pressure above atmospheric pressure in a closed container or may be sprayed or brushed on. Once dried the wood is very resistant to rot, insects, and other environmental insults.
- Another aspect of this invention is an article of manufacture that comprises wood impregnated with a silicon-containing salt, a boron-containing salt, and optionally an aluminum halide.
- the silicon-containing salt is present at a level in the wood of about 1% w/w to about 30% w/w and the boron-containing salt is present at a level in the wood of about 1% w/w to about 30% w/w.
- the aluminum salt will be present at a level less than about 1% w/w.
- Still another aspect of this invention is a colloidal composition that comprises water, an alkali metal hydroxide in a quantity sufficient to bring the pH of the water to at least 10, a silicon-containing salt, a boron-containing salt, optionally aluminum halide, and optionally a preservative.
- a further aspect of this invention is a process for making a composition suitable for reducing the rate of deterioration of wood.
- the process comprises mixing a boron- containing salt with an alkali-metal silicate solution at a pH of at least 10, optionally adding an aluminum halide and a preservative, and mixing to form a uniform colloidal composition being supersaturated with the boron-containing salt.
- Figure 1 is a representation of the believed evolution of the polymer in an electret generator with a step gradient magnetic field with K + ions or the nucleus and stabilized by the K + ion with sequestration of the boron ion and water.
- Figure 2 is a representation of bound water on a typical colloidal particle made by standard activation techniques.
- Figure 3 is a schematic drawing of an electret generator useful for making the composition of the invention.
- Figure 4 is a schematic drawing of an electret generator of Figure 3 demonstrating the three magnetic quadripolar booster generators and other modifications.
- Figure 5 is a representation of a detailed schematic drawing of the magnetic quadripolar generator with its flux fields and gradients.
- Figure 6 is a representation of the sequestration of boron ions by the silica colloid in the composition of the invention.
- Figure 7 is a representation of the pressure treatment apparatus of the invention for treating a variety of wood products. Detailed Description of the Invention
- Wood as used for structures such as houses, decks, fences, marine pilings, utility poles, railroad ties, and the like tends to deteriorate over time due to a multiplicity of environmental insults.
- One aspect of this invention is a process for reducing the rate of deterioration of wood. The process comprises contacting wood with an aqueous, alkaline, colloidal composition of a silicon-containing salt having boron ions incorporated therein for time sufficient to impregnate at least a portion of the wood with the mixture.
- the wood is contacted by immersing the wood in the aqueous mixture at a pressure of above atmospheric pressure for a period of time that is sufficient to ensure at least a portion of the silicon-containing salt and a boron-containing salt is deposited on or within the wood being treated.
- the process is carried out at a pressure of about 125 psi to about 175 psi, and the temperature may be ambient or elevated. The pressure is maintained for a time sufficient to impregnate most of the wood, e.g. about 30 minutes to about 2 hours.
- the wood may be cotreated with aqueous calcium silicate for improved results.
- the pressure is maintained for a period of time dependant on the quantity, the porosity, and the length of wood being treated to impregnate the wood throughout its entire structure.
- the wood is removed from contact with the aqueous composition and dried to provide a product having the silicon-containing salt and the boron-containing salt deposited therein. Drying may be done at ambient or elevated temperatures and pressures.
- the drying may take 30 days or more. It appears that by pressure-treating wood in accordance with the invention, the silicon-containing salt and the boron-containing salt are deposited throughout the wood, resulting in a weight increase that may vary from 20% to 70% increase over the untreated wood. It is thought that the colloidal composition is drawn into the wood, perhaps by capillary action, and the salts are deposited throughout the fibrous structure of the wood. The weight increase will depend on the temperature, pressure, wood porosity, wood size, colloid composition and the like.
- the process is carried out using an alkaline colloidal composition
- an alkaline colloidal composition comprising water made basic to a pH of at least about 10 with an alkali metal hydroxide, a silicon-containing salt, a boron-containing salt, and optionally an aluminum halide.
- the details of the composition will be discussed hereinafter.
- the process of this invention is particularly applicable to immersion of wood within the aqueous composition
- the wood may also be impregnated by contacting through application at ambient pressure and temperature of the aqueous composition to the surface of the wood and allowing it to dry. Such application may be done by application with a brush, pouring the composition onto the wood surface, spraying the composition on, and the like. Once the composition is applied, the wood is dried for a period of time to ensure the impregnation of the wood at the surface is complete.
- Another aspect of this invention is an article of manufacture that comprises wood impregnated with a silicon-containing salt, a boron-containing salt, and optionally an aluminum halide.
- the silicon-containing salt is present in the wood at a level of about 1% w/w to about 30% w/w and the boron-containing salt (e.g. metal borate or boric acid) is present at a level in the wood of about 1% w/w to about 30% w/w, with the aluminum halide present up to about 1% w/w.
- the dry weight of an article of this invention (made by pressure treatment) will be 20% to about 70% greater than comparable untreated wood. If the article is prepared by brushing or spraying, the impregnation is primarily surface, and the weight increase is less, i.e. no more than 10%. The ultimate increase will depend on a number of factors discussed hereinbefore.
- Another aspect of this invention is a colloidal composition that comprises water, an alkali metal hydroxide in a quantity sufficient to bring the pH of the water to at least 10, a silicon-containing salt, a boron-containing salt, optionally an aluminum halide, and optionally a preservative.
- the silicon-containing salt will preferably be silica or sodium silicate, while the boron-containing salt will be borax or boric acid.
- the composition is the combination of an alkali metal hydroxide and a silicon-containing salt, preferably a colloid solution (or suspension), an alkali metal silicate such as sodium or potassium silicate, or silica dissolved in an aqueous solution of an alkali metal hydroxide.
- the composition will be an aqueous colloidal suspension.
- colloidal silica A useful description of the properties of colloidal silica can be found in "The Chemistry of Silica” by Ralph K. Her, John Wiley & Sons, N.Y. (1979).
- the alkali metal hydroxide is sodium hydroxide or potassium hydroxide, particularly the latter. Mixtures of the two are also useful.
- the silicon-containing salt is present at a level of about 2% w/v to about 20% w/v, at least about 4% w/v
- the boron-containing salt e.g., borax
- the composition may include a preservative such as tripotassium citrate present in a stabilizing amount and an aluminum halide, e.g. aluminum trichloride or aluminum trifluoride, present in up to about 1.0% w/v.
- a preservative such as tripotassium citrate present in a stabilizing amount
- an aluminum halide e.g. aluminum trichloride or aluminum trifluoride, present in up to about 1.0% w/v.
- the colloid particles will exhibit a high zeta potential, i.e. about -40 to -75 mV.
- the process for making the composition of this invention involves
- the most plentiful silicon-containing salt occurs in nature as silica and is also known as silicon dioxide (SiO 2 ). It comprises nearly sixty percent of the earth's crust, either in the free form (e.g., sand) or combined with other oxides in the form of silicates. Silica is not known to have any significant toxic effects when ingested in small quantities (as SiO 2 or as a silicate) by humans and is regularly found in drinking water in most public water systems throughout the U.S.
- the preferred composition useful in this invention is an alkaline aqueous silica colloidal composition, which can be referred to as a solution or a colloidal suspension.
- the aqueous composition is prepared by dissolving particulate silica in highly alkaline water which is prepared by dissolving a strong base in water to provide an aqueous solution that is basic (i.e., a pH of more than 7, preferably at least 10).
- the strong base will be sodium hydroxide or potassium hydroxide, preferably the latter.
- a molar quantity of at least 3 will generally be used to prepare the alkaline solution with no more than 4 molar generally being needed. Because the solubility (its ability to form a stable colloidal composition) of silica increases with increasing temperature, it is preferred that the alkaline solution be heated to a temperature above ambient, up to and including the boiling point of the solution.
- egg preserver A well-known solution is known as "egg preserver" which may be prepared by this method and is calculated to contain about 40% by weight of Na 2 Si 3 O 7 (a commonly available dry form of a sodium silicate).
- Na 2 Si 3 O 7 a commonly available dry form of a sodium silicate.
- a standard commercially available sodium silicate is one that is 27% w/v sodium silicate.
- a boron-containing salt e.g. boric acid or a metal borate such as sodium borate, i.e. borax
- a metal borate such as sodium borate, i.e. borax
- borax a metal borate
- an aluminum halide and a preservative may also be added.
- the addition of the source of B ions, a preservative such as tripotassium citrate, and the aluminum halide may be lead to polymerization of the Si(OH) as visualized below:
- the alkaline used could be potassium hydroxide, which provides the K+ ions, along with TPC.
- the colloid of this composition is thought to be more tightly bound and more extensively branched than known colloid systems.
- Figure 2 is representative of the typical double layer of water found on a typical silica colloid particle.
- the boron-containing salt is preferably borax, i.e. sodium borate, also known as sodium biborate and other names, with a formula of Na 2 B 4 O 7 . It is often found as the decahydrate.
- the aqueous composition of this invention is preferably further treated to provide a supersaturated solution of the boron salt.
- the composition is treated to increase the electrostatic charge on the particles.
- it is important to maintain the temperature above ambient to maintain solubility of the salts.
- conduit means (7) The fluid flows through conduit means (7) and exits through holes (8) into conduit means (13), the fluid then flows in the opposite direction, it then exits through holes (9), and reverses direction again through conduit means (14).
- the fluid exits conduit means (14) through orifices (10) into conduit means (15), this fluid enters chamber (11) and exits the generator proper through conduit (12) and is carried back to containment means (5) through conduit (4a) and (4b).
- Figure 4 illustrates the function and location of the magnetic booster units of the generator along with the "off line” chemical mixing containment means (22).
- High velocity prolonged flow through the counter current device of the invention will generate the colloid of the invention because of the counter current charge effect which generates multiple bidirectional magnetic fields which generate on electrostatic charge on the adjacent moving charged colloidal particle moving in the counter current process. If one adds the magnetic booster units of Figure A, the electrostatic charge builds on the colloid much faster.
- valve (17) of conduit (4a) is closed and valve (16) of conduit (18) is opened as well as valve (20) of conduit (19) is opened.
- the chemical containment means (22) is heated with electric heater (21) which is powered by cord (25) and is agitated by paddle (23) via shaft (24) which is rotated by pulley (26) pulled by belt (33) on pulley (27) powered by motor (28).
- the heated fluid with dissolved chemicals is pumped via pump (32) through conduit (19) into conduit (4) and back to containment means (5).
- Upper portion of Figure 5 illustrates a top cross sectional view of the concentric conduits shown in Figure 4.
- a magnetic booster unit e.g., unit A
- magnets are shown arranged in a plane and form vertices of a quadrilateral shape (e.g., a rectangle or square) in that plane. Poles of adjacent magnets are of opposite orientation as indicated by the "+" and "-" signs shown in Figure 5. As shown in the lower portion of Figure 5, this arrangement of the four magnets creates multiple gradients for the magnetic field in the z axis (i.e., component of the magnetic field along axis extending out of the plane shown in the upper portion of Figure 5). Here, measurements are shown for the magnetic field in the z axis along line A-A' that is displaced about an inch above the plane of the magnets.
- Gradients can also exist for the magnetic field in the x axis and y axis (i.e., component of magnetic field along lines A-A' and B-B'). These multiple gradients are responsible for the significant electrostatic charge that can build on the silica colloidal particle as the generator continues to process the aqueous composition.
- the generator shown in Figure A one can produce silica colloidal particles having sizes in the range of about 1 ⁇ m to about 200 ⁇ m, typically in the range of about 1 ⁇ m to about 150 ⁇ m or from about 1 ⁇ m to about 110 ⁇ m.
- the silica colloidal particles may have zeta potentials in the range of about -5 millivolts (mV) to over about -75 mV, and typically in the range of about -30 mV to about -40 to -75 mV.
- a zeta potential represents an electrostatic charge exhibited by a colloidal particle, and a zeta potential of greater magnitude typically corresponds to a more stable colloidal system (e.g., as a result of inter-particle repulsion).
- This example describes a process for making a representative composition of the invention.
- the detailed preparation of the composition may be visualized by referring to Figure 5.
- a starting solution is added to container means (5).
- the solution contains 1,846.2 ml of 26.0% sodium silicate with quantity sufficient of water to bring the volume to 6,500 ml.
- the solution is circulated through the generator with valve (16) and valve (20) closed but with valve (17) open. 500 Grams of KOH granules are slowly added to the solution in the running generator.
- the composition is circulated for 30 minutes at 60° C. 2 Liters of solution flow into containment (22) by opening valve (16) and closing valve (17).
- valve (20) When 2 liters have flowed into containment means (22) valve (20) is opened and 800 grams of tripotassium citrate is slowly added to the solutions in containment means (22) through chemical feeder (29) and stirred with paddle (23) and rod (24) until dissolved. 1000 Gm of borax (sodium tetraborate decahydrate) is added to solution through chemical feed (29). The borax is dissolved by stirring with paddle (21) on shaft (24). The generator runs for 1 hour. A second 1,000 grams of borax is added and circulated until it is dissolved. The temperature is kept at 60° C. The generator is run for 1 hour and a third 1,000 grams of borax is added, stirred and circulated until it is dissolved.
- borax sodium tetraborate decahydrate
- Example 2 This example describes a process of the invention for the pressure treatment of wood.
- lumber to be treated (56) is placed in pressure chamber (54) and sealed with door (55).
- Valves (58) and (64) are closed.
- Valve (68) is opened and vacuum pump (67) is powered through power conduit (19b).
- the vacuum pump (67) is a 26 inch vacuum pump.
- the vacuum pump can be a vacuum pump of any size, such as a 30 inch vacuum pump.
- the vacuum pump (67) is pumped on the chamber (54) to eliminate the gases that are contained within the wood fibers.
- the vacuum eliminates the gases from the ends of the wood.
- the amount of time that the vacuum is required to be maintained on the chamber (54) depends on the quantity, the type, and the length of wood that is being treated. For example, for a small amount of wood the vacuum may be maintained for 15 minutes and for a large amount of wood, or a long piece of wood, the vacuum may be maintained for 45 minutes.
- Valve (58) is then opened and a composition of the invention (e.g. 6% Si0 2 and
- 8%o boron-containing salt for the boron ion is sucked from a containment means (62) and/or a storage means (66) into the chamber (4) and subsequently into the wood.
- the composition travels from the storage means (66) to the containment means (62) through conduit (65).
- the composition travels from the containment means (62) to the chamber (54) through conduits (57) and (60).
- Prior to entering the chamber (54) the composition may be passed through a boiler (59).
- the boiler (59) is any type of heating element that will allow the temperature of the composition to be maintained as it is circulated through the system.
- SILENE® calcium silicate
- V/2% concentration of SILENE
- the wood is treated with the SILENE composition and the composition of the invention.
- the system undergoes a pressure stage.
- liquid pressure is applied to the system.
- the vacuum is pulled, valve (68) is closed, valve (58) is opened, and a liquid pressure pump (P) is turned on.
- P liquid pressure pump
- the liquid pressure is maintained at about 150 pounds per square inch and the temperature is maintained at about 140° F for a period of time between 30 minutes and 2 hours.
- other pressures, other temperatures, and other times may be used.
- a gas pressure is applied to the system.
- the system is circulated under pressure pump (P).
- the pressure is applied by CO 2 container (51) through conduit (53) and valve (69) to the wood chamber (4).
- the composition which is a small particle colloid at high pH, is partially converted to a gel by the CO 2 . This is thought to lower pH at the surface of the wood.
- the pressure is applied to the system for anywhere from about 30 minutes to about 2 hours. The amount of time that the pressure is applied to the system depends on the quantity, the type, and the length of the wood that is being treated.
- the chamber is drained.
- the treated wood is then removed from the chamber (54) and is allowed to dry for a period of about 30 days.
- the formula of the composition may be altered for better penetration.
- Boric acid may be substituted for borax (sodium tetraborate decahydrate) if boric acid is used the amount is 1.22 more by weight than borax.
- Example 3 This composition of the invention is designed to paint or spray on decks or lumber.
- Example 2 5. Add 1000 ml of above solution to a container with constant stirring at pH 11.33 and T 22.2° C. Titrate with HC1 1:3 (use 150 ml HC1 x 150 ml) and slowly add 4 liters of above pressure treatment solution to 4 liters of the present solution (Example 2) and stir. This solution is clear and penetrates wood well.
- Example 4
- the above-described composition (Example 3) of the invention is combined with a wood sealer.
- the wood sealer is a 10% active blend of Silene (calcium silicate) blended with anhydrous alcohol.
- the spray on composition (from Example 3) is applied to the decking and allowed to dry for 3 - 4 hours.
- the wood sealer is then applied to the deck.
- the wood sealer chemically reacts with the decking treatment by reacting with the silica.
- the resultant is treated lumber with a water repellant sealer.
- Another embodiment of the invention is perfected by the synthesis of a saturated solution of 21% borax and 21% Si0 2 .
- the solution is very viscous. It is heated and mixed with fiber of any type and dried under hot roller presses to make a very strong and fire proof sheet of building material. All of the products treated with the invention are fire retardant.
- Southern yellow pine 2" x 4" wood pieces and white oak of similar size was pressure treated according to the invention. The immediate wt gain and wt gain after 1 month is prorated.
- composition that may be used to spray on a wood deck is produced.
- the composition may be produced using the following procedure.
- composition produced using this procedure has silica (probably as sodium silicate) present at a level of about 6% by weight calculated by known weight/volumes and has borax (as boron ions) present at a level of about 4.5% by weight calculated by known weight volumes.
- the composition produced using this procedure has a pH of about 10.
- composition that may be used to spray on a wood deck that has been treated with CCA is produced.
- the composition may be produced using the following procedure. A. Prepare solution A
- Example 9 hi this example of the present invention, a composition that may be used to pressure treat wood is produced. This composition provides a termite resistance to the wood.
- the composition may be produced using the following procedure.
- composition produced using this procedure has silica present at a level of about 8%> by weight calculated by known weight/volumes and a level of borate ion of about 4% by weight calculated by known weight/volumes.
- the composition produced using this procedure has a pH of about 10.5 to about 11.5.
- composition that may be used to pressure treat utility ties such as railroad ties and structural timbers and fence posts used in marine environments is produced.
- the composition may be produced using the following procedure.
- composition produced using this procedure has silica present at a level of about 10% by weight calculated by known weight/volumes and borate ions present at a level of about 10% by weight calculated at known weight/volumes.
- the composition produced by this process has a pH of about 10.5 or higher.
- composition that may be used to pressure treat wood is produced.
- This composition provides a high termite barrier to the wood.
- the composition may be produced using the following procedure.
- composition produced using this procedure has silica present at a level of about 8% by weight calculated by known weight/volumes and a level of borate ions of about 8% by weight calculated by known weight/volumes.
- the composition produced using this procedure has apH of about 10.5 or higher.
- composition that may be sprayed on wood to help protect the wood against termites is produced.
- the composition may be produced using the following procedure.
- composition produced using this procedure has silica present at a level of about 4% by weight calculated by known weight/volumes and a level of borate ions of about 8% by weight calculated by known weight/volumes.
- the composition produced using this procedure has a pH of about 10.2 or higher.
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Forests & Forestry (AREA)
- Agronomy & Crop Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28062001P | 2001-03-30 | 2001-03-30 | |
| US280620P | 2001-03-30 | ||
| PCT/US2002/010128 WO2002078865A1 (en) | 2001-03-30 | 2002-03-29 | Process and composition for treating wood |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1392452A1 EP1392452A1 (en) | 2004-03-03 |
| EP1392452A4 true EP1392452A4 (en) | 2004-12-01 |
Family
ID=31495495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP02723715A Withdrawn EP1392452A4 (en) | 2001-03-30 | 2002-03-29 | WOOD TREATMENT METHOD AND COMPOSITION |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1392452A4 (enExample) |
| JP (1) | JP2005511262A (enExample) |
| KR (1) | KR20040054612A (enExample) |
| CN (1) | CN1304124C (enExample) |
| BR (1) | BR0208766A (enExample) |
| MX (1) | MXPA03008943A (enExample) |
| PL (1) | PL368948A1 (enExample) |
| RU (1) | RU2291049C2 (enExample) |
| WO (1) | WO2002078865A1 (enExample) |
| ZA (1) | ZA200308424B (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1385925A4 (en) * | 2001-03-28 | 2007-03-21 | Sgt Technology Holdings Llc | REDUCTION OF SULFUR DIOXIDE EMISSIONS FROM HOT COMBUSTION |
| EP1817394A1 (en) * | 2004-10-11 | 2007-08-15 | Advanced Timber Technologies Pty Ltd | Fire retardant compositions and methods of use |
| WO2008124871A1 (en) * | 2007-04-11 | 2008-10-23 | Advanced Timber Technologies Pty Ltd | Fire retardant compositions and method of use |
| UA84117C2 (ru) * | 2008-04-17 | 2008-09-10 | Генрик Генрикович Шуминский | Устройство для получения электрической энергии |
| CA2734294A1 (fr) * | 2008-08-13 | 2010-02-18 | Long Lasting Innovation - L2I (Societe A Responsabilite Limitee) | Procede pour la fixation de molecules actives sur un support, element actif obtenu par ce procede et composition chimique pour la mise en oeuvre de ce procede |
| EP3262937A1 (en) | 2009-12-09 | 2018-01-03 | Barlaa B.V. | Micro-colloidal silicic acid composition |
| RU2441114C2 (ru) * | 2010-03-02 | 2012-01-27 | Государственное образовательное учреждение высшего профессионального образования Московский государственный строительный университет (ГОУ ВПО МГСУ) | Способ укрепления и био-влагозащиты деревянных свайных фундаментов |
| SE535622C2 (sv) | 2010-11-29 | 2012-10-16 | Organowood Ab | Miljövänlig träbehandlingsprocess |
| FR3000420B1 (fr) * | 2013-01-02 | 2015-07-31 | Ind Bois | Produit et procede de preparation du bois au traitement par trempage |
| CN105619558B (zh) * | 2016-03-01 | 2017-03-22 | 山东农业大学 | 有机‑无机杂化超疏水疏油防霉杀菌阻燃耐候木材改性剂的制备方法 |
| US20180195968A1 (en) * | 2017-01-10 | 2018-07-12 | Troy Corporation | Indicating penetration of non-aqueous solvent |
| KR101982550B1 (ko) * | 2018-10-05 | 2019-05-27 | 이용규 | LPM(Low Pressure Melamine) 판상재의 가공 방법 |
| JP7038441B2 (ja) * | 2018-12-28 | 2022-03-18 | 四国ケージ株式会社 | 殺有害生物剤を含有する散布剤 |
| CN114654550B (zh) * | 2022-01-10 | 2023-09-26 | 东北林业大学 | 一种阻燃木材及其制备方法、金属卤化物的用途 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB540642A (en) * | 1940-03-23 | 1941-10-24 | Hugo Johann Strausz | Flameproof and fire-retarding material for wood |
| US3180746A (en) * | 1961-08-03 | 1965-04-27 | Exxon Research Engineering Co | Protective coating |
| EP0636461A1 (en) * | 1993-07-28 | 1995-02-01 | Kabushiki Kaisha Koshii Preserving | A wood preservative composition, process for treating wood with the same, and wood treated with the same |
| EP0699644A1 (en) * | 1993-03-01 | 1996-03-06 | Toshinori Morizane | Modifier for porous materials and method of modifying porous materials |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3306765A (en) * | 1963-09-03 | 1967-02-28 | Gen Dynamics Corp | Method for fireproofing wood and the treated wood |
| US3725544A (en) * | 1969-12-09 | 1973-04-03 | Basf Ag | Fungicide for protecting wood |
| JPS4846195A (enExample) * | 1971-10-13 | 1973-07-02 | ||
| NZ211005A (en) * | 1984-02-02 | 1988-03-30 | Terje Rosenlund | Impregnating wood |
| SU1541056A1 (ru) * | 1987-12-30 | 1990-02-07 | Белорусский технологический институт им.С.М.Кирова | Способ получени огнестойкой древесины |
| DE19513903A1 (de) * | 1995-04-12 | 1996-10-17 | Bayer Ag | Holzschutzmittel enthaltend eine Kupferverbindung |
-
2002
- 2002-03-29 RU RU2003131872/04A patent/RU2291049C2/ru not_active IP Right Cessation
- 2002-03-29 MX MXPA03008943A patent/MXPA03008943A/es not_active Application Discontinuation
- 2002-03-29 BR BR0208766-9A patent/BR0208766A/pt not_active Application Discontinuation
- 2002-03-29 KR KR10-2003-7012870A patent/KR20040054612A/ko not_active Withdrawn
- 2002-03-29 CN CNB028094085A patent/CN1304124C/zh not_active Expired - Fee Related
- 2002-03-29 ZA ZA200308424A patent/ZA200308424B/en unknown
- 2002-03-29 WO PCT/US2002/010128 patent/WO2002078865A1/en not_active Ceased
- 2002-03-29 EP EP02723715A patent/EP1392452A4/en not_active Withdrawn
- 2002-03-29 JP JP2002577119A patent/JP2005511262A/ja active Pending
- 2002-03-29 PL PL02368948A patent/PL368948A1/xx unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB540642A (en) * | 1940-03-23 | 1941-10-24 | Hugo Johann Strausz | Flameproof and fire-retarding material for wood |
| US3180746A (en) * | 1961-08-03 | 1965-04-27 | Exxon Research Engineering Co | Protective coating |
| EP0699644A1 (en) * | 1993-03-01 | 1996-03-06 | Toshinori Morizane | Modifier for porous materials and method of modifying porous materials |
| EP0636461A1 (en) * | 1993-07-28 | 1995-02-01 | Kabushiki Kaisha Koshii Preserving | A wood preservative composition, process for treating wood with the same, and wood treated with the same |
Non-Patent Citations (1)
| Title |
|---|
| See also references of WO02078865A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2003131872A (ru) | 2005-03-27 |
| CN1511068A (zh) | 2004-07-07 |
| BR0208766A (pt) | 2004-07-06 |
| WO2002078865A1 (en) | 2002-10-10 |
| JP2005511262A (ja) | 2005-04-28 |
| CN1304124C (zh) | 2007-03-14 |
| EP1392452A1 (en) | 2004-03-03 |
| RU2291049C2 (ru) | 2007-01-10 |
| ZA200308424B (en) | 2004-10-29 |
| MXPA03008943A (es) | 2012-05-08 |
| WO2002078865A8 (en) | 2004-06-24 |
| KR20040054612A (ko) | 2004-06-25 |
| PL368948A1 (en) | 2005-04-04 |
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