NO332831B1 - Nye naturharpiksformuleringer - Google Patents

Nye naturharpiksformuleringer Download PDF

Info

Publication number: NO332831B1
Authority: NO; Norway
Prior art keywords: resin; phenol; product; formaldehyde; resins
Prior art date: 1999-07-29

Application number

NO20020449A

Other languages

English (en)

Norwegian (no)

Other versions

NO20020449L (no

NO20020449D0 (no

Inventor

Barry A Freel

Robert Graham

Regi Giroux

Original Assignee

Ensyn Renewables 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.)

1999-07-29

Filing date

2002-01-28

Publication date

2013-01-21

2002-01-28 Application filed by Ensyn Renewables Inc filed Critical Ensyn Renewables Inc

2002-01-28 Publication of NO20020449D0 publication Critical patent/NO20020449D0/no

2002-04-02 Publication of NO20020449L publication Critical patent/NO20020449L/no

2013-01-21 Publication of NO332831B1 publication Critical patent/NO332831B1/no

Links

239000000025 natural resin Substances 0.000 title claims abstract description 278
239000000203 mixture Substances 0.000 title claims abstract description 101
238000009472 formulation Methods 0.000 title abstract description 40
229920005989 resin Polymers 0.000 claims abstract description 267
239000011347 resin Substances 0.000 claims abstract description 267
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 145
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 141
238000000034 method Methods 0.000 claims abstract description 80
238000001704 evaporation Methods 0.000 claims abstract description 68
230000008020 evaporation Effects 0.000 claims abstract description 68
238000004821 distillation Methods 0.000 claims abstract description 58
238000000197 pyrolysis Methods 0.000 claims abstract description 56
239000002023 wood Substances 0.000 claims abstract description 55
238000000605 extraction Methods 0.000 claims abstract description 30
239000007787 solid Substances 0.000 claims abstract description 24
239000002028 Biomass Substances 0.000 claims abstract description 21
239000000047 product Substances 0.000 claims description 127
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 65
229920005610 lignin Polymers 0.000 claims description 51
239000000853 adhesive Substances 0.000 claims description 48
230000001070 adhesive effect Effects 0.000 claims description 48
238000012545 processing Methods 0.000 claims description 29
229920001568 phenolic resin Polymers 0.000 claims description 26
239000011120 plywood Substances 0.000 claims description 26
239000012263 liquid product Substances 0.000 claims description 24
239000002253 acid Substances 0.000 claims description 19
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 15
239000011093 chipboard Substances 0.000 claims description 15
238000005266 casting Methods 0.000 claims description 14
239000004567 concrete Substances 0.000 claims description 14
239000011094 fiberboard Substances 0.000 claims description 12
239000010426 asphalt Substances 0.000 claims description 11
239000011230 binding agent Substances 0.000 claims description 11
239000011121 hardwood Substances 0.000 claims description 10
239000004576 sand Substances 0.000 claims description 10
150000007513 acids Chemical class 0.000 claims description 9
239000004840 adhesive resin Substances 0.000 claims description 8
229920006223 adhesive resin Polymers 0.000 claims description 8
238000009413 insulation Methods 0.000 claims description 8
238000002203 pretreatment Methods 0.000 claims description 7
239000011342 resin composition Substances 0.000 claims 5
238000004519 manufacturing process Methods 0.000 abstract description 65
239000007788 liquid Substances 0.000 abstract description 43
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract description 29
239000004202 carbamide Substances 0.000 abstract description 15
150000001875 compounds Chemical class 0.000 abstract description 14
238000005194 fractionation Methods 0.000 abstract description 5
239000003921 oil Substances 0.000 description 122
235000013824 polyphenols Nutrition 0.000 description 44
229920001807 Urea-formaldehyde Polymers 0.000 description 28
238000011084 recovery Methods 0.000 description 28
238000012360 testing method Methods 0.000 description 27
239000000654 additive Substances 0.000 description 25
230000008569 process Effects 0.000 description 23
ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 20
150000002989 phenols Chemical class 0.000 description 18
239000012075 bio-oil Substances 0.000 description 17
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
238000003825 pressing Methods 0.000 description 15
239000003623 enhancer Substances 0.000 description 13
239000000835 fiber Substances 0.000 description 13
238000004458 analytical method Methods 0.000 description 11
239000003518 caustics Substances 0.000 description 10
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
206010042674 Swelling Diseases 0.000 description 9
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 9
239000000463 material Substances 0.000 description 9
238000002844 melting Methods 0.000 description 9
230000008018 melting Effects 0.000 description 9
239000002904 solvent Substances 0.000 description 9
230000008961 swelling Effects 0.000 description 9
238000006116 polymerization reaction Methods 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
150000001299 aldehydes Chemical class 0.000 description 7
239000003995 emulsifying agent Substances 0.000 description 7
HANVTCGOAROXMV-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.NC1=NC(N)=NC(N)=N1 HANVTCGOAROXMV-UHFFFAOYSA-N 0.000 description 7
239000010410 layer Substances 0.000 description 7
150000007524 organic acids Chemical class 0.000 description 7
238000002390 rotary evaporation Methods 0.000 description 7
238000012546 transfer Methods 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
230000000996 additive effect Effects 0.000 description 6
238000004132 cross linking Methods 0.000 description 6
238000002156 mixing Methods 0.000 description 6
235000013339 cereals Nutrition 0.000 description 5
238000006482 condensation reaction Methods 0.000 description 5
238000001816 cooling Methods 0.000 description 5
239000005011 phenolic resin Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
240000004144 Acer rubrum Species 0.000 description 4
235000011772 Acer rubrum var tomentosum Nutrition 0.000 description 4
235000009057 Acer rubrum var tridens Nutrition 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
230000003750 conditioning effect Effects 0.000 description 4
238000010586 diagram Methods 0.000 description 4
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
239000010408 film Substances 0.000 description 4
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
239000000843 powder Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
229930040373 Paraformaldehyde Natural products 0.000 description 3
239000003082 abrasive agent Substances 0.000 description 3
238000005273 aeration Methods 0.000 description 3
238000005452 bending Methods 0.000 description 3
-1 brake linings Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000000470 constituent Substances 0.000 description 3
238000010276 construction Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
238000012544 monitoring process Methods 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
235000005985 organic acids Nutrition 0.000 description 3
229920002866 paraformaldehyde Polymers 0.000 description 3
239000004014 plasticizer Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
230000009257 reactivity Effects 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
238000000926 separation method Methods 0.000 description 3
238000000638 solvent extraction Methods 0.000 description 3
229920001169 thermoplastic Polymers 0.000 description 3
239000004416 thermosoftening plastic Substances 0.000 description 3
KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical compound COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 description 2
241000609240 Ambelania acida Species 0.000 description 2
239000004606 Fillers/Extenders Substances 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
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
229920002522 Wood fibre Polymers 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
238000004026 adhesive bonding Methods 0.000 description 2
239000003513 alkali Substances 0.000 description 2
239000010905 bagasse Substances 0.000 description 2
239000003990 capacitor Substances 0.000 description 2
150000001728 carbonyl compounds Chemical class 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000005119 centrifugation Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000002826 coolant Substances 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
230000036541 health Effects 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
238000011068 loading method Methods 0.000 description 2
229920002521 macromolecule Polymers 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
230000000149 penetrating effect Effects 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
238000007158 vacuum pyrolysis Methods 0.000 description 2
TVZRAEYQIKYCPH-UHFFFAOYSA-N 3-(trimethylsilyl)propane-1-sulfonic acid Chemical compound C[Si](C)(C)CCCS(O)(=O)=O TVZRAEYQIKYCPH-UHFFFAOYSA-N 0.000 description 1
235000009414 Elaeocarpus kirtonii Nutrition 0.000 description 1
229920002488 Hemicellulose Polymers 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
229920001131 Pulp (paper) Polymers 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
239000004826 Synthetic adhesive Substances 0.000 description 1
244000236151 Tabebuia pallida Species 0.000 description 1
235000013584 Tabebuia pallida Nutrition 0.000 description 1
239000004809 Teflon Substances 0.000 description 1
229920006362 Teflon® Polymers 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000012223 aqueous fraction Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
239000000227 bioadhesive Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000837 carbohydrate group Chemical group 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
238000001311 chemical methods and process Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000002131 composite material Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000012792 core layer Substances 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
230000032798 delamination Effects 0.000 description 1
230000001066 destructive effect Effects 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000011552 falling film Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000001722 flash pyrolysis Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
238000002304 fractionated pyrolysis Methods 0.000 description 1
239000012634 fragment Substances 0.000 description 1
239000002783 friction material Substances 0.000 description 1
239000000446 fuel Substances 0.000 description 1
HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
239000003292 glue Substances 0.000 description 1
229960001867 guaiacol Drugs 0.000 description 1
238000007731 hot pressing Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000009434 installation Methods 0.000 description 1
229920005611 kraft lignin Polymers 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000002029 lignocellulosic biomass Substances 0.000 description 1
235000014666 liquid concentrate Nutrition 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000000178 monomer Substances 0.000 description 1
239000003345 natural gas Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
235000020030 perry Nutrition 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
JYIZNFVTKLARKT-UHFFFAOYSA-N phenol;1,3,5-triazine-2,4,6-triamine Chemical compound OC1=CC=CC=C1.NC1=NC(N)=NC(N)=N1 JYIZNFVTKLARKT-UHFFFAOYSA-N 0.000 description 1
239000003495 polar organic solvent Substances 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000010734 process oil Substances 0.000 description 1
ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical group CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000003303 reheating Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000005201 scrubbing Methods 0.000 description 1
238000002791 soaking Methods 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
239000011122 softwood Substances 0.000 description 1
230000007928 solubilization Effects 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000003809 water extraction Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08L61/22—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08L61/24—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urea or thiourea
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/0293—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with natural products, oils, bitumens, residues
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H8/00—Macromolecular compounds derived from lignocellulosic materials
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- 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
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J161/00—Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
- C09J161/04—Condensation polymers of aldehydes or ketones with phenols only
- C09J161/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J161/00—Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
- C09J161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C09J161/22—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C09J161/24—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urea or thiourea
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B53/00—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
- C10B53/02—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of cellulose-containing material
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10C—WORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
- C10C5/00—Production of pyroligneous acid distillation of wood, dry distillation of organic waste
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
- Y02P20/133—Renewable energy sources, e.g. sunlight

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Materials Engineering (AREA)
Oil, Petroleum & Natural Gas (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Biochemistry (AREA)
Phenolic Resins Or Amino Resins (AREA)
Compositions Of Macromolecular Compounds (AREA)
Macromonomer-Based Addition Polymer (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)

NO20020449A 1999-07-29 2002-01-28 Nye naturharpiksformuleringer NO332831B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US09/364,610 US6326461B1 (en)	1998-01-30	1999-07-29	Natural resin formulations
PCT/CA2000/000868 WO2001009243A1 (en)	1999-07-29	2000-07-28	Novel natural resin formulations

Publications (3)

Publication Number	Publication Date
NO20020449D0 NO20020449D0 (no)	2002-01-28
NO20020449L NO20020449L (no)	2002-04-02
NO332831B1 true NO332831B1 (no)	2013-01-21

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Application Number	Title	Priority Date	Filing Date
NO20020449A NO332831B1 (no)	1999-07-29	2002-01-28	Nye naturharpiksformuleringer

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US (3)	US6326461B1 (de)
EP (1)	EP1311615B1 (de)
AT (1)	ATE370990T1 (de)
AU (1)	AU779394C (de)
BR (1)	BR0012819B1 (de)
CA (1)	CA2380486C (de)
DE (1)	DE60036136T2 (de)
DK (1)	DK1311615T3 (de)
ES (1)	ES2292459T3 (de)
MX (1)	MXPA02001087A (de)
NO (1)	NO332831B1 (de)
PT (1)	PT1311615E (de)
WO (1)	WO2001009243A1 (de)

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2000
- 2000-07-28 DE DE60036136T patent/DE60036136T2/de not_active Expired - Lifetime
- 2000-07-28 WO PCT/CA2000/000868 patent/WO2001009243A1/en not_active Ceased
- 2000-07-28 AT AT00951134T patent/ATE370990T1/de active
- 2000-07-28 DK DK00951134T patent/DK1311615T3/da active
- 2000-07-28 CA CA002380486A patent/CA2380486C/en not_active Expired - Fee Related
- 2000-07-28 BR BRPI0012819-8A patent/BR0012819B1/pt not_active IP Right Cessation
- 2000-07-28 ES ES00951134T patent/ES2292459T3/es not_active Expired - Lifetime
- 2000-07-28 US US10/048,184 patent/US6844420B1/en not_active Expired - Lifetime
- 2000-07-28 MX MXPA02001087A patent/MXPA02001087A/es active IP Right Grant
- 2000-07-28 PT PT00951134T patent/PT1311615E/pt unknown
- 2000-07-28 EP EP00951134A patent/EP1311615B1/de not_active Expired - Lifetime
- 2000-07-28 AU AU64185/00A patent/AU779394C/en not_active Ceased
2001
- 2001-11-16 US US09/990,746 patent/US6555649B2/en not_active Expired - Lifetime
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Publication number	Publication date
ES2292459T3 (es)	2008-03-16
NO20020449L (no)	2002-04-02
DK1311615T3 (da)	2007-12-27
US20020132972A1 (en)	2002-09-19
EP1311615B1 (de)	2007-08-22
WO2001009243A1 (en)	2001-02-08
US6555649B2 (en)	2003-04-29
US6844420B1 (en)	2005-01-18
US6326461B1 (en)	2001-12-04
NO20020449D0 (no)	2002-01-28
AU779394B2 (en)	2005-01-20
AU779394C (en)	2005-06-16
BR0012819B1 (pt)	2011-01-25
CA2380486C (en)	2009-10-27
BR0012819A (pt)	2002-05-28
AU6418500A (en)	2001-02-19
ATE370990T1 (de)	2007-09-15
DE60036136T2 (de)	2008-05-15
CA2380486A1 (en)	2001-02-08
PT1311615E (pt)	2007-12-05
DE60036136D1 (de)	2007-10-04
EP1311615A1 (de)	2003-05-21
MXPA02001087A (es)	2003-08-20

Legal Events

Date	Code	Title	Description
2015-02-23	MM1K	Lapsed by not paying the annual fees

Publication	Publication Date	Title
US6326461B1 (en)	2001-12-04	Natural resin formulations
Effendi et al.	2008	Production of renewable phenolic resins by thermochemical conversion of biomass: A review
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EP3052549A1 (de)	2016-08-10	Verfahren zur erhöhung der reaktivität von lignin
Amen-Chen et al.	2002	Softwood bark pyrolysis oil-PF resols
Mao et al.	2017	Preparation, properties, and bonding utilization of pyrolysis bio-oil
DK3099485T3 (en)	2019-01-21	PLYWOOD LAMINATE MANUFACTURING
Nakos et al.	2001	Wood adhesives made with pyrolysis oils
Zhao et al.	2014	Recent development in forest biomass derived phenol formaldehyde (PF) resol resin for wood adhesives application
EP1045890B1 (de)	2004-09-29	Naturharz-formulierungen
CA2319416C (en)	2003-10-21	Natural resin formulations
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Roslan et al.	2017	Bio-Based Phenol Formaldehyde from Lignocellulosic Biomass
Papadopoulou	2008	Study on Synthetic and Bio-Based Phenol-Formaldehyde Adhesives for the Wood-Based Industry
CA2260570A1 (en)	2000-07-29	Process for the production of phenolic-rich pryolysis oils for use in making phenol-formaldehyde resole resins
MXPA01003926A (en)	2003-02-17	Bonding resins