EP2607032A1 - Procédé destiné à la réduction de l'émission de composés organiques liquides à partir de matières dérivées du bois et matières dérivées du bois - Google Patents
Procédé destiné à la réduction de l'émission de composés organiques liquides à partir de matières dérivées du bois et matières dérivées du bois Download PDFInfo
- Publication number
- EP2607032A1 EP2607032A1 EP11194281.9A EP11194281A EP2607032A1 EP 2607032 A1 EP2607032 A1 EP 2607032A1 EP 11194281 A EP11194281 A EP 11194281A EP 2607032 A1 EP2607032 A1 EP 2607032A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- additive
- wood
- lignocellulose
- products
- organic compounds
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 35
- 150000002894 organic compounds Chemical class 0.000 title 1
- 239000000654 additive Substances 0.000 claims abstract description 113
- 239000002023 wood Substances 0.000 claims abstract description 95
- 230000000996 additive effect Effects 0.000 claims abstract description 72
- 239000012855 volatile organic compound Substances 0.000 claims abstract description 64
- 239000000853 adhesive Substances 0.000 claims abstract description 37
- 230000001070 adhesive effect Effects 0.000 claims abstract description 37
- 235000007586 terpenes Nutrition 0.000 claims abstract description 28
- 150000003505 terpenes Chemical class 0.000 claims abstract description 27
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical group [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000002253 acid Substances 0.000 claims abstract description 21
- 150000007513 acids Chemical class 0.000 claims abstract description 19
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 15
- 150000004645 aluminates Chemical class 0.000 claims abstract description 14
- 239000011094 fiberboard Substances 0.000 claims abstract description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 11
- 239000010452 phosphate Substances 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 125000003277 amino group Chemical group 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 238000004519 manufacturing process Methods 0.000 claims description 38
- 150000001409 amidines Chemical class 0.000 claims description 37
- 230000008569 process Effects 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 12
- 238000004026 adhesive bonding Methods 0.000 claims description 6
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 5
- 241000294754 Macroptilium atropurpureum Species 0.000 claims description 5
- 229920002522 Wood fibre Polymers 0.000 claims description 5
- 239000011093 chipboard Substances 0.000 claims description 5
- 239000002025 wood fiber Substances 0.000 claims description 5
- 125000000909 amidinium group Chemical group 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 claims description 3
- 238000003825 pressing Methods 0.000 claims description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 2
- GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 229910002651 NO3 Inorganic materials 0.000 claims 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- -1 amidine compound Chemical class 0.000 abstract description 11
- 239000000835 fiber Substances 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 description 25
- 150000001875 compounds Chemical class 0.000 description 15
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 13
- 150000001642 boronic acid derivatives Chemical class 0.000 description 13
- 150000001299 aldehydes Chemical class 0.000 description 12
- 235000021317 phosphate Nutrition 0.000 description 11
- 230000009467 reduction Effects 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 6
- 229920001807 Urea-formaldehyde Polymers 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 239000007857 degradation product Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 241000218631 Coniferophyta Species 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 4
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 3
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- BQOFWKZOCNGFEC-UHFFFAOYSA-N carene Chemical compound C1C(C)=CCC2C(C)(C)C12 BQOFWKZOCNGFEC-UHFFFAOYSA-N 0.000 description 3
- 239000012084 conversion product Substances 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 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 3
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 3
- 239000012978 lignocellulosic material Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 3
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 2
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 2
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 2
- 125000000320 amidine group Chemical group 0.000 description 2
- 229920003180 amino resin Polymers 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 229930006722 beta-pinene Natural products 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 238000002144 chemical decomposition reaction Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 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 2
- 235000019253 formic acid Nutrition 0.000 description 2
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- OQLZINXFSUDMHM-UHFFFAOYSA-N Acetamidine Chemical compound CC(N)=N OQLZINXFSUDMHM-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000771208 Buchanania arborescens Species 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 229910004844 Na2B4O7.10H2O Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 125000005619 boric acid group Chemical class 0.000 description 1
- 235000021170 buffet Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- ZZTURJAZCMUWEP-UHFFFAOYSA-N diaminomethylideneazanium;hydrogen sulfate Chemical compound NC(N)=N.OS(O)(=O)=O ZZTURJAZCMUWEP-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- RSCACTKJFSTWPV-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;pentahydrate Chemical compound O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 RSCACTKJFSTWPV-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- HMJMQKOTEHYCRN-UHFFFAOYSA-N formaldehyde;phenol;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.OC1=CC=CC=C1.NC1=NC(N)=NC(N)=N1 HMJMQKOTEHYCRN-UHFFFAOYSA-N 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- RCNGYCUXXUWXBF-UHFFFAOYSA-N hexanal;pentanal Chemical compound CCCCC=O.CCCCCC=O RCNGYCUXXUWXBF-UHFFFAOYSA-N 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000563 toxic property Toxicity 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N1/00—Pretreatment of moulding material
- B27N1/003—Pretreatment of moulding material for reducing formaldehyde gas emission
Definitions
- the present application relates to processes for the production of wood materials from lignocellulose, in particular for the production of chipboard, fiberboard or OSB boards, these wood materials to prevent or reduce the emission of volatile organic compounds and possibly very volatile organic compounds, especially terpenes and acids, be treated with at least one additive during manufacture.
- these additives are amidines and / or borates.
- the present application is directed to the use of amidines and / or borates as additives in the production of wood-based materials from lignocellulose for reducing the emission of VOC and optionally VVOC, in particular for reducing the emission of terpenes and acids.
- the application is directed to obtainable by the process according to the invention wood materials, or by using the additives produced wood materials with reduced emission of volatile organic compounds, in particular terpenes and acids.
- Lignocellulosic or lignocellulosic materials such as wood and wood pulp products, and derived timber products, such as wood-based panels, contain, among other things, volatile organic compounds (VOCs) and very volatile organic compounds (VVOCs).
- VOCs volatile organic compounds
- VVOCs very volatile organic compounds
- the emission of these VOC and VVOC also referred to as the total amount of volatile compounds
- volatile organic compounds (VOCs) in addition to saturated and unsaturated aldehydes, include all volatile organic compounds whose retention time in the glass chromatograph is between C 6 (Hexane) and C 16 (hexadecane).
- VOCs are not a homogeneous class of substances but a smorgasbord of compounds.
- VVOC very volatile organic compounds
- these VVOC include organic acids, saturated and unsaturated aldehydes, eg. As pentanal, hexanal, etc., alcohols, terpenes, aliphatic and aromatic hydrocarbons and much more.
- VVOC very volatile organic compounds
- formaldehyde or formic acid also occur in the production but also in the use of wood-based materials.
- these compounds can occur during curing from the adhesives.
- these compounds can occur by reaction of compounds present in the wood material. The emission of these volatile and highly volatile wood constituents or constituents of the adhesives from wood products, including wood-based panels, is becoming more and more of a problem due to stricter limits or greater sensitization of the end users.
- the volatile organic compounds and volatile organic compounds are dependent on the type and condition of the lignocelluloses; such as the type of wood, the storage period, the storage conditions of the wood or the crushed products of the wood, in different chemical compositions and quantities.
- the VOC originate essentially from extractives of lignocelluloses, eg. As the wood or conversion products thereof. Prominent representatives of these are substances such as alpha-pinene, beta-pinene, delta-3-carene. Especially in wood conifers, these components are found again. Conversion products, the z. B. occur during storage and processing of the wood and the crushing products, z. B. aldehydes, such as pentanal and hexanal.
- Mainly particleboard, medium density fibreboard (MDF) or OSB boards are used to produce large quantities of resins and fats that lead to the formation of volatile organic terpene compounds and aldehydes. Some of these substances are also formed by degradation of the main components of the wood, such as lignin, cellulose and hemicellulose.
- TVOCs with VOCs including aldehydes as well as VVOCs including formaldehyde can also arise when using certain adhesives for making the wood-based material.
- VOC emissions are composed of the so-called primary emissions of volatile wood constituents, such as terpenes, or chemical degradation products, such as acetic acid, and so-called secondary or tertiary emissions, as listed above.
- conversion products eg. B. by fragmentation of the resins and fats
- a permanent secondary or tertiary emission of said compounds takes place.
- So z. B. especially in OSB panels in the design field this release of great disadvantage, since in this application, the OSB panels have no emission-reducing coating and installed in large quantities, especially as the area of the plate, based on the total cubic meters of the room or building becomes.
- Adhesives currently used in the manufacture of wood-based materials such as OSB boards, medium density fiberboard, etc. include aminoplast adhesives such as urea-formaldehyde (UF) adhesives, melamine-urea-phenol-formaldehyde (UF) adhesives.
- Other adhesives typically used in wood-based materials include diisocyanate-based adhesives (PMDI), polyurethane adhesives (PU adhesives), phenol-formaldehyde (PF) adhesives, and / or tannin-formaldehyde (TF) adhesives
- Adhesives or mixtures thereof. In the fibreboard area find z. B.
- VOCs and VVOCs mainly aminoplast adhesives use.
- the release of the VOCs and VVOCs takes place both during the production of the wood-based materials as well as after their production or in their application.
- it may, for. B. come in the thermo-mechanical treatment of lignocellulosic materials to a partial chemical degradation of the wood.
- the resulting VOC and VVOC, such as aldehydes and acids or terpenes then emit during the manufacturing process or later use of the wood-based materials produced. They can also have a negative influence on the bond strength and thus adversely affect the property of the produced wood materials.
- VOC volatile organic compound
- US Pat. VVOC highly volatile organic compounds
- the emission of VOCs and also of VVOCs should be significantly reduced both during production and during later use become.
- the additives themselves should not show any toxic properties and should not adversely affect the production process itself.
- the production costs of wood-based materials themselves must not be significantly increased.
- the agents or additives used should as far as possible be reacted with the heterogeneous classes of volatile organic compounds as well as the very volatile organic compounds or prevent their formation from constituents of the wood-based materials.
- additives are added at certain times in the process according to the invention for the production of wood materials from lignocellulose, in particular for the production of chipboard, fiberboard or OSB boards.
- additives are an amidine and / or borate, aluminate and / or phosphate, in particular borate.
- the compounds obtained by the reaction are such that they are no longer volatile and thus no longer contribute to the TVOC emissions, or the toxicity of the resulting compounds is significantly reduced. As a result, the emission is also after the production, d. H. in daily use, significantly reduced.
- the expression also includes the corresponding amidinium salts.
- Other possible anions as counterions are halide ions, such as chloride, bromide and iodide, as well as thiocyanate.
- amidines d. H. Additive I
- amidine in the form of a solution in particular an aqueous solution containing 5-40 wt .-% of amidine, on the lignocellulose-containing crushing products by z. B. impregnation of this is applied before the drying step.
- Other preferred methods for incorporating the additive I into the lignocellulosic crushing products include methods in which the amidine is added in the form of a solid, such as salt, in the scattering of the lignocellulose-containing comminution products, and preferably the construction of the additive relative to bare wood in the range from 2 to 30% by weight, such as in a range of 5 to 25% by weight, e.g. B. 10 -20 wt .-%.
- the additive can be used differently depending on the layer used, for. B. to 20 wt .-% in the middle layers and 10 wt .-% in the outer layers.
- the additive I can be used in the form of a powder.
- it may be interspersed as a powder.
- additive I from the group of amidines or alone an additive II selected from borate, aluminum and / or phosphate.
- borate is understood in the present case to be salts or esters of boric acids, these may be present in the form of simple borates or polyborates. Unless otherwise stated, are present under the Term “borate” means both borates and polyborates.
- the borates are salts of monoborates (BO 3 3- ), diborates (B 2 O 5 4- ) triborates (B 3 O 5 - ), tetraborates (B 4 O 7 2- ), pentaborates (B 5 O 9 3- ), hexaborates (B 6 O 11 4- and B 6 O 10 2- ).
- the borates according to the invention comprise longer-chain polyborates.
- borates are usually present as salts with alkali or alkaline earth metals (eg sodium tetraborate Na 2 B 4 O 7 .10H 2 O), or zinc ions as countercations (eg zinc borate, 2 (ZnO) 3 (B 2 O 3 ) ⁇ XH 2 O).
- alkali or alkaline earth metals eg sodium tetraborate Na 2 B 4 O 7 .10H 2 O
- zinc ions eg zinc borate, 2 (ZnO) 3 (B 2 O 3 ) ⁇ XH 2 O.
- those having an ammonium group are also possible and may contain hydrate groups.
- the polyborate acts catalytically in the reaction of the amidines or amines with the aldehydes.
- the borate acts as an antioxidant and thus prevents the oxidative degradation of resins and fats and other wood components that are responsible for the secondary and tertiary emission of terpenes and acids or their degradation products.
- the borates and polyborates as additives not only prevent the emission of VOC by reacting with or prevent the degradation of VOC, but also form a mechanical barrier to prevent the emission of VOC and VVOC. That is, it is assumed that the borates form an amorphous glassy melt due to the high pressing temperatures, which closes the open surfaces of the wood materials, such as the OSB, and thus also mechanically prevents emission.
- the borates / polyborates as well as the aluminates and phosphates as additive II allow terpene reduction, presumably due to their property as Lewis acid. These act as catalysts for the addition of the double bond in terpenes. Thus, degradation of the terpenes into volatile organic degradation products that contribute to secondary and tertiary emission is prevented.
- the borates, as well as the aluminates and phosphates are introduced at least as additive II into the topcoat-forming lignocellulose-containing comminution products.
- the additives may be present in different layers of the wood material.
- the amidines may be present as additives in the middle layers, while the borates are introduced into the layers forming the cover layer.
- both additives may be present as a combination in at least one layer of the wood materials, particularly preferably both additives I and II are at least in the outer layer.
- at least the amidine may be present in the topcoat.
- none of the additives mentioned may be present in a middle layer.
- an aluminate or phosphate can be used as additive II.
- Preferred compounds thereof are alkali and alkaline earth aluminates and phosphates, and those having a zinc ion or ammonium ion as a cation.
- the additives are preferably introduced separately in a combined use.
- the introduction of the amidine as additive I, z. Example as an aqueous solution, done before the drying step of the crushed products or alternatively as a solid in scattering the crushed products, while the borate is added separately in the scattering of the crushed products of amidine or added as a solution after the dryer in the gluing.
- the additive II such as the borate, z. B. introduced in the form of a solution after the dryer in particular in the cover layer.
- the additive II can be introduced as a solution in the gluing of the cover layer.
- the concentration of the additive II, based on atro wood at 2-30 wt .-%, such as 5-25 wt .-%, z. B. 10 - 20 wt .-%.
- the process according to the invention is one in which wood chips, wood strands or wood fibers are used as lignocellulose-containing comminution products.
- the inventive method is used in particular for the production of OSB boards, MDF boards or chipboard.
- the additives are added in such a way that at least one of the two additives I and II is added as a solution in front of the dryer. Furthermore, one or both additives I and II can be introduced after the dryer in the gluing or topcoat.
- the application of the additives can be carried out by known methods, such as spraying, impregnation or immersion.
- the addition of the additives may generally be carried out before or after the comminution and working up of the comminuted products, e.g. B. after the refiner in fibers done.
- the application of the amidine additives takes place immediately before the hot pressing or before the dryer.
- the addition of the adhesive can be carried out before or after the application of the additives.
- the additives are, as stated above, preferably applied separately. Alternatively, however, the additives can also be applied simultaneously.
- the adhesive can also be between the application of the first additive and the application of the second additive. In particular, as stated above, the combination of both additives is preferred.
- the addition of a solution of additives to the spread mat can take place via nozzles directly in front of the hot press.
- the additives are introduced via customary equipment, such as binder dosing, Beleimtrommel, blow-line gluing or dry gluing.
- the present invention is directed to the use of amidine as an additive (also referred to herein as additive I) in the production of wood-based materials from lignocellulose to reduce the emission of VOC and possibly VVOC, so TVOC, in particular the reduction of the emission of terpenes and acids not only in the manufacturing process itself, but also in the later use.
- amidine also referred to herein as additive I
- VOC the emission of VOC and possibly VVOC, so TVOC
- the use is characterized by the fact that the additive during the manufacturing process of the wood material is registered or applied.
- the present invention is directed to the use of borate, aluminate and / or phosphate as an additive (also referred to herein as additive II) for reducing the emission of VOC and optionally VVOC, in particular for reducing the emission of terpenes and acids , in the production and use of wood materials from lignocellulose, characterized in that the additive during the manufacturing process of the wood material can be applied or applied, in particular, that the additive is introduced at least in the outer layer of the wood material.
- additive II additive for reducing the emission of VOC and optionally VVOC, in particular for reducing the emission of terpenes and acids
- additive I and additive II such as amidine and borate, aluminate and / or phosphate as an additive instead.
- the present invention is directed to the use of amidine and / or borate, aluminate and / or phosphate as a reducing additive the emission of VOC and possibly VVOC in the manufacture and use of lignocellulosic wood materials, the additive being used at least in the top layer of OSB boards and fiberboards.
- a treatment agent is provided for reducing the emission of VOC and possibly VVOC, in particular of terpenes and acids, from lignocellulose-containing comminution products and wood-based materials from lignocellulose-containing comminution products.
- This treatment agent comprises at least one additive I according to the invention and at least one additive II according to the invention.
- the present invention is directed to a wood material obtainable by a method according to the invention.
- This wood-based material is preferably a fiberboard, in particular a lightweight and super-lightweight MDF board, or an OSB board.
- Lignocelluloses are understood to mean lignocellulose-containing materials, such as wood.
- the resulting comminution products of lignocelluloses include in particular wood strands, wood chips, wood fibers but also wood veneer.
- the lignocelluloses such as the wood-based materials or the comminuted products thereof, may be both conifers and hardwoods. Even mixtures of these two types of wood are possible.
- the wood chips, strands or wood fibers come from conifers.
- the wood materials which can be produced by the production process according to the invention can be prepared according to known processes.
- the method may additionally be supplemented by other methods known to the person skilled in the art for reducing the emission of volatile organic compounds or very volatile organic compounds.
- the adhesives used in the process of the invention include the conventional adhesives, as used for the production of cervical spine and as stated above.
- the adhesives include as adhesives PF adhesives, isocyanate-based adhesives, UF adhesives, MUF adhesives, MUPF adhesive, TF adhesive, PU adhesive, or mixtures thereof.
- the VOC determination is carried out by means of testing in accordance with the AgBB (Construction Health Assessment Committee, May 2010) in a large ISO 16000 chamber. During the test, a surface-specific ventilation rate of 1 m 3 / (m 2 * h) was determined. Here was a dosage of amidine (guanidine sulfate) as a 40% solution before the dryer, ie the amidine is in the top and middle layer. The borate (sodium tetraborate) is also dosed as a 40% solution, but only in the topcoat. The adhesive used is one based on PMDI. The OSB is produced on a production line.
- Trial 1 Test results (AgBB): C [ ⁇ g / m 3 ] 28 days OSB hexanal pentanal ⁇ -pinene ⁇ -pinene 3-Caren TVOC Reference 100% PMDI 1305 201 353 44 205 2932 Amidine / borate 12 mm 148 48 106 13 60 554 Amidine / borate 18 mm 172 44 80 13 54 457
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Wood Science & Technology (AREA)
- Forests & Forestry (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11194281.9A EP2607032B1 (fr) | 2011-12-19 | 2011-12-19 | Procédé destiné à la réduction de l'émission de composés organiques liquides à partir de matières dérivées du bois et matières dérivées du bois |
PL11194281T PL2607032T3 (pl) | 2011-12-19 | 2011-12-19 | Sposób zmniejszania emisji lotnych związków organicznych z tworzyw drzewnych i tworzywa drzewne |
ES11194281T ES2773350T3 (es) | 2011-12-19 | 2011-12-19 | Procedimiento para reducir la emisión de compuestos orgánicos volátiles de materiales a base de madera y materiales a base de madera |
HUE11194281A HUE049225T2 (hu) | 2011-12-19 | 2011-12-19 | Eljárás illékony szerves vegyületek kibocsátásának csökkentésére fatermékekbõl, és fatermékek |
PT111942819T PT2607032T (pt) | 2011-12-19 | 2011-12-19 | Processo para reduzir as emissões de compostos orgânicos voláteis em materiais à base de madeira e material de madeira |
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EP11194281.9A EP2607032B1 (fr) | 2011-12-19 | 2011-12-19 | Procédé destiné à la réduction de l'émission de composés organiques liquides à partir de matières dérivées du bois et matières dérivées du bois |
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EP2607032A1 true EP2607032A1 (fr) | 2013-06-26 |
EP2607032B1 EP2607032B1 (fr) | 2020-01-22 |
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EP11194281.9A Active EP2607032B1 (fr) | 2011-12-19 | 2011-12-19 | Procédé destiné à la réduction de l'émission de composés organiques liquides à partir de matières dérivées du bois et matières dérivées du bois |
Country Status (5)
Country | Link |
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EP (1) | EP2607032B1 (fr) |
ES (1) | ES2773350T3 (fr) |
HU (1) | HUE049225T2 (fr) |
PL (1) | PL2607032T3 (fr) |
PT (1) | PT2607032T (fr) |
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Publication number | Priority date | Publication date | Assignee | Title |
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EP3290172A1 (fr) * | 2016-09-02 | 2018-03-07 | SWISS KRONO Tec AG | Utilisation de résine coulée pour la réduction des émissions de composés organiques volatiles provenant de matériaux dérivés du bois |
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EP0255950A2 (fr) * | 1986-08-07 | 1988-02-17 | Homanit GmbH & Co.KG | Procédé de fabrication de panneaux de fibres de bois |
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WO2006032267A1 (fr) | 2004-09-21 | 2006-03-30 | Institut für Holztechnologie Dresden gGmbH | Bois ou materiau en bois et procede de fabrication associe |
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JPS594465B2 (ja) * | 1973-08-15 | 1984-01-30 | カブシキガイシヤ サンワケミカル | ボウネンザイ |
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ATE354540T1 (de) * | 2000-01-21 | 2007-03-15 | United States Borax Inc | Nonaboratzusammensetzung und ihre herstellung |
KR101098517B1 (ko) * | 2008-12-24 | 2011-12-26 | 한국과학기술연구원 | 목재용 보존처리제 |
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2011
- 2011-12-19 PL PL11194281T patent/PL2607032T3/pl unknown
- 2011-12-19 EP EP11194281.9A patent/EP2607032B1/fr active Active
- 2011-12-19 HU HUE11194281A patent/HUE049225T2/hu unknown
- 2011-12-19 ES ES11194281T patent/ES2773350T3/es active Active
- 2011-12-19 PT PT111942819T patent/PT2607032T/pt unknown
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EP3290172A1 (fr) * | 2016-09-02 | 2018-03-07 | SWISS KRONO Tec AG | Utilisation de résine coulée pour la réduction des émissions de composés organiques volatiles provenant de matériaux dérivés du bois |
Also Published As
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PL2607032T3 (pl) | 2020-07-27 |
PT2607032T (pt) | 2020-04-29 |
EP2607032B1 (fr) | 2020-01-22 |
ES2773350T3 (es) | 2020-07-10 |
HUE049225T2 (hu) | 2020-09-28 |
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