EP2106485B1 - Honeycomb structure based on lignocellulosic materials and process for producing the same - Google Patents
Honeycomb structure based on lignocellulosic materials and process for producing the same Download PDFInfo
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- EP2106485B1 EP2106485B1 EP08705093.6A EP08705093A EP2106485B1 EP 2106485 B1 EP2106485 B1 EP 2106485B1 EP 08705093 A EP08705093 A EP 08705093A EP 2106485 B1 EP2106485 B1 EP 2106485B1
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- European Patent Office
- Prior art keywords
- paper
- lignocellulosic
- sio
- honeycomb
- thickness
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- Not-in-force
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- 238000000034 method Methods 0.000 title description 8
- 239000012978 lignocellulosic material Substances 0.000 title description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 52
- 239000000377 silicon dioxide Substances 0.000 claims description 26
- 229910052681 coesite Inorganic materials 0.000 claims description 15
- 229910052906 cristobalite Inorganic materials 0.000 claims description 15
- 229910052682 stishovite Inorganic materials 0.000 claims description 15
- 229910052905 tridymite Inorganic materials 0.000 claims description 15
- 239000003063 flame retardant Substances 0.000 claims description 12
- -1 silicon alkoxide Chemical class 0.000 claims description 11
- 239000002243 precursor Substances 0.000 claims description 9
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 239000011574 phosphorus Substances 0.000 claims description 4
- 238000005516 engineering process Methods 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 239000000123 paper Substances 0.000 description 35
- 241000264877 Hippospongia communis Species 0.000 description 26
- 239000000203 mixture Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000835 fiber Substances 0.000 description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 5
- 239000002131 composite material Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000003014 phosphoric acid esters Chemical class 0.000 description 4
- 235000019353 potassium silicate Nutrition 0.000 description 4
- OWICEWMBIBPFAH-UHFFFAOYSA-N (3-diphenoxyphosphoryloxyphenyl) diphenyl phosphate Chemical group C=1C=CC=CC=1OP(OC=1C=C(OP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)C=CC=1)(=O)OC1=CC=CC=C1 OWICEWMBIBPFAH-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 239000012792 core layer Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000011087 paperboard Substances 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000009832 plasma treatment Methods 0.000 description 2
- 230000008092 positive effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000001878 scanning electron micrograph Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000004305 biphenyl Chemical group 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical compound CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
- ZMCWFMOZBTXGKI-UHFFFAOYSA-N tritert-butyl borate Chemical compound CC(C)(C)OB(OC(C)(C)C)OC(C)(C)C ZMCWFMOZBTXGKI-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/40—Coatings with pigments characterised by the pigments siliceous, e.g. clays
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/30—Multi-ply
- D21H27/40—Multi-ply at least one of the sheets being non-planar, e.g. crêped
Definitions
- the invention relates to honeycomb structures based on lignocellulosic materials.
- Honeycomb paper is applied as an intermediate (“sandwich”) layer having a low specific mass in various types of constructions.
- Honeycomb structures based on recycled paper provide certain advantages, such as a light weight and a relatively high compression strength, at low costs.
- Another advantage of paper based honeycomb structures is their high flexibility. This makes it possible to fold the honeycomb structures and reduce the diameter of the honeycomb structures, as a result of which the required amount of space for storage, transport and handling can be relatively low.
- honeycomb structures based on paper often have a limited biological stability ( viz . they are susceptible of attack by microorganisms, such as moulds), a limited water stability ( viz . their mechanical strength may drop considerably when wet or when in humid atmosphere) and have a limited fire resistance.
- substances are combined with the paper material, e.g. by impregnating the paper.
- these (fire resistant) resins this generally results in a product having an increased stiffness, as a result of which the honeycomb structures often can not be compacted by folding and so they take up a lot of space.
- EP-A-1 130 161 describes a method for producing a dehumidifying element, wherein paper is impregnated with a suspension of a molecular sieve, such as aluminium silicate, in water glass. This document does not disclose or suggest a lignocellulosic honeycomb structure.
- US-A-6 066 379 is directed to a paperboard that has a complex coating which is water repellant and allows re-pulping of the paperboard. This document does not disclose or suggest a lignocellulosic honeycomb structure.
- the paper should have a glueability that is sufficient to produce the honeycomb structures therefrom.
- a glueability that is sufficient to produce the honeycomb structures therefrom.
- water glass an aqueous solution of sodium silicate, is commonly employed as a glue in this type of applications.
- an endless honeycomb structure can be made, which would be very desirable from a process economic point of view.
- the paper itself has a certain elasticity (especially if compression pressure is applied), because this facilitates the production of composites with a core layer of honeycomb. If the core layer is more elastic, the compression strength can be better maintained in the composite after assembling the composites (gluing and pressing the skins onto the core layer).
- the amount of compounds that are brought into contact with the paper material should be as low as possible but still homogeneously distributed in a thin layer on surfaces of the paper (and fibers), viz . sufficient to bring about the desired effect, while avoiding any detrimental effect.
- the present invention aims at providing this.
- the present invention is directed to a lignocelluloisic structure comprising a layer with a thickness of 0.01 ⁇ m to 10 ⁇ m comprising SiO 2 on at least part of its surface, which structure is in the form of a honeycomb structure, and which structure is obtainable by contacting the lignocellulosic structure with a SiO 2 precursor.
- the thin SiO 2 based layer can be applied in various ways.
- a highly preferred method comprises contacting the lignocellulosic structure with a suitable precursor e.g . by submerging the lignocellulosic structures in a bath of SiO 2 precursor or by spraying the SiO 2 precursor on the structure or application of the silica using plasma technology.
- a suitable precursor e.g . by submerging the lignocellulosic structures in a bath of SiO 2 precursor or by spraying the SiO 2 precursor on the structure or application of the silica using plasma technology.
- SDBD surface dielectric barrier discharge
- Silica sol-gel is a suitable precursor.
- the silica sol-gel component is typically based on silicon alkoxide, Si(OR) 4 , wherein R is an alkyl, preferably methyl or ethyl. These compounds can be subjected to hydrolysis and gelation, whereby silane groups (Si-OH) and siloxane groups (Si-O-Si) are broken and formed, respectively.
- Commercially widely available sol-gel components are TEOS (tetraethylorthosilicate) and TMOS (tetramethylorthosilicate).
- the silica content of the SiO 2 precursor typically ranges from 1-10% silica and the solvent (such as ethanol, isopropanol or other alcohols, acetone or other ketones) content typically ranges from 10-70%.
- solvent such as ethanol, isopropanol or other alcohols, acetone or other ketones
- ethanol as a solvent has a very limited risk, because these solvents have limited toxicity.
- solvents tend to evaporate easily. It is highly preferred to collect the vapours comprising the evaporated solvents and thus recover the solvent therefrom so that it may be recycled.
- materials can be provided that provide excellent fire-retardant properties, while at the same time conserving all other requirements and where the transport volume of structures produced is minimized.
- the thin SiO 2 based layer has a thickness of 0.01 ⁇ m to 10 ⁇ m, preferably about 0.2 to 5 ⁇ m, more preferably about 0.5 to 2.5 ⁇ m.
- the paper surface may be treated with further substances, such as fire retardants.
- fire retardants such as fire retardants.
- These further components may be applied together with the SiO 2 film, but it is also possible to apply them in a separate process step e.g . a subsequent dipping or spraying step or a plasma treatment.
- Phosphorus based fire retardants are very suitable for this purpose.
- the combination of phosphorus based fire retardants and silica sol-gel provides materials that have excellent fire-retardant properties, while at the same time conserving all other above-mentioned requirements and where the transport volume of structures produced is minimized.
- the (phosphorus based) fire retardant which may be used in the present invention is preferably a phosphate ester and more preferably an oligomeric phosphate ester.
- the fire retardant that may be used in the composition of the present invention can be used to impregnate paper in order to create honeycomb structures.
- the structures thus obtained show excellent properties with respect to water resistance, fire retardant properties, compressibility and durability.
- the product can still be combined with water glass in the conventional method of lamination.
- the composition of the invention typically comprises 1 to 90 wt.% oligomeric phosphate esster, preferably from 5 to 50 wt.%, based on weight of the total composition.
- the contacting of the lignocellulosic material with the SiO 2 precursor can be carried out in a continuous fashion by using a conventional paper treatment process, e.g . by submerging a continuous belt of lignocellulosic material (paper) through a bath containing the sol-gel composition and optionally the fire retardant composition, application of coating processes as used in the paper industry or plasma treatment under atmospheric pressure.
- the impregnated paper maintains its flexibility in the length direction, by which it can be stored and transported without requiring much space, due to its compactness.
- the structures that are thus produced have dimensions that are "endless", viz . up to e.g . 50 m or more. Also no emission of harmful compounds occurs during the production process. If a silica sol-gel comprising ethanol is used, the solvent can be collected as vapor and recycled.
- Suitable (oligomeric or monomeric) phosphate esters may be represented by the following formula I: wherein each of R 1 , R' 1 , R 2 , R' 2 and R 3 is independently hydrogen or hydrocarbon side chain, in particular straight, branched or cyclic C 1 -C 10 alkyl or alkenyl (preferably C 2 -C 8 alkyl or alkenyl), optionally substituted, e.g. with halogen, epoxide hydroxyl, amino; and n is an integer from 0 to typically about 10. In case n is zero, the compounds of formula I are monomeric phosphate esters. Examples of suitable oligomeric phosphate ester compounds and their production are given e.g. in US-A-3 767 732 and US-A-4 382 042 .
- Single compositions of the present invention can be prepared by admixing the ingredients in any order.
- the (oligomeric) phosphate esters are mixed into the sol-gel composition.
- a boric acid derivative is present in the compositions of the present invention, in particular those described in DE-A-198 33 479 . It was found that the addition of these boric acid compounds has a positive effect on the durability of the lignocellulosic products that are impregnated with the compositions of the present invention.
- Suitable boric acid derivatives for this purpose are boric acid, trialkylborate ( e.g. tributyl borate; tri-isopropyl borate; or tri-tert-butyl borate).
- the boric acid derivatives may be present in amounts of typically 0 to 10 wt.%, preferably 0.5 to 5 wt.%, based on weight of the total composition.
- the boric acid provides further protection against biological degradation (that may be caused by degrading organisms like fungi and insects) and has positive effects on the fire resistance.
- Honeycomb structures can be prepared by known process, e.g . the paper honeycomb production processes described in Pflug et al. (5th Global Wood and Natural Fibre Composites Symposium, Kassel (DE), 27-28 April 2004 ) typically out of low cost recycled paper (e.g. Testliner).
- Figure 3 shows schematically the different process steps in a suitable production process for making expanded honeycombs.
- adhesive lines are printed on the paper, which may come from one or several paper rolls (1).
- a stack of several sheets is made and bonded together (2). Those sheets can be cut to strips prior or after stacking to a slice (3).
- the third step many slices are stacked and bonded together to produce an unexpanded endless paper honeycomb core (4).
- the sheets are pulled apart (5) expanding the stack into a hexagonal honeycomb core (6).
- the residual stresses in paper honeycombs can be relaxed after expansion by a controlled application of heat.
- the structures that are produced in this way comprise walls formed of paper strips having a width of several cm, e.g. about 1-6 cm.
- a typical honeycomb structure is has a diameter of the cells of e.g. 5 - 50 mm and a thickness of the total honeycomb layer of e.g. 5 - 60 mm.
- the paper weight is usually between 80 g/m 2 and 250 g/m 2 .
- Figure 4 shows a scanning electron micrograph (SEM), of a sample that is prepared in accordance with the present invention. A thin silica film on a cell wall of a paper fiber can be seen.
- Paper 140 g/m 2 was treated with silica in ethanol (concentration 18 %) using a coating treatment.
- the coated paper was dried at 105 °C over a period of 12 hours.
- the paper that is treated in accordance with the present invention maintains it strength after the first and second measurement. Furthermore, the flexibility of the honeycomb structure in the length direction was maintained. Also the paper had an excellent glueability so that it could be easily glued with water glass.
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- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Laminated Bodies (AREA)
Description
- The invention relates to honeycomb structures based on lignocellulosic materials.
- Honeycomb paper is applied as an intermediate ("sandwich") layer having a low specific mass in various types of constructions.
- Honeycomb structures based on recycled paper ("ligno-fibers") provide certain advantages, such as a light weight and a relatively high compression strength, at low costs. Another advantage of paper based honeycomb structures is their high flexibility. This makes it possible to fold the honeycomb structures and reduce the diameter of the honeycomb structures, as a result of which the required amount of space for storage, transport and handling can be relatively low.
- On the other hand, honeycomb structures based on paper often have a limited biological stability (viz. they are susceptible of attack by microorganisms, such as moulds), a limited water stability (viz. their mechanical strength may drop considerably when wet or when in humid atmosphere) and have a limited fire resistance. In order to compensate these effects, substances are combined with the paper material, e.g. by impregnating the paper. When the paper is impregnated with these (fire resistant) resins, this generally results in a product having an increased stiffness, as a result of which the honeycomb structures often can not be compacted by folding and so they take up a lot of space. Also, some frequently used resins, such as phenol based resins, that need to be heated at high temperatures release formaldehyde, which is a hazardous compound and this must be avoided, especially for indoor applications. After curing, the honeycomb structures maintain their stiffness, which presents another drawback. Because of this bulkiness, large transport volumes are required.
-
EP-A-1 130 161 describes a method for producing a dehumidifying element, wherein paper is impregnated with a suspension of a molecular sieve, such as aluminium silicate, in water glass. This document does not disclose or suggest a lignocellulosic honeycomb structure. -
US-A-6 066 379 is directed to a paperboard that has a complex coating which is water repellant and allows re-pulping of the paperboard. This document does not disclose or suggest a lignocellulosic honeycomb structure. - The paper should have a glueability that is sufficient to produce the honeycomb structures therefrom. For instance water glass, an aqueous solution of sodium silicate, is commonly employed as a glue in this type of applications. As long as the paper remains its flexibility during the processing, in principle an endless honeycomb structure can be made, which would be very desirable from a process economic point of view.
- It is furthermore very desirable if the paper itself has a certain elasticity (especially if compression pressure is applied), because this facilitates the production of composites with a core layer of honeycomb. If the core layer is more elastic, the compression strength can be better maintained in the composite after assembling the composites (gluing and pressing the skins onto the core layer).
- Furthermore, the amount of compounds that are brought into contact with the paper material should be as low as possible but still homogeneously distributed in a thin layer on surfaces of the paper (and fibers), viz. sufficient to bring about the desired effect, while avoiding any detrimental effect.
- It would be highly desirable to provide a lignocellulose based honeycomb structure that meets all the above-mentioned needs. The present invention aims at providing this.
- It was found that this object can be met by applying silica in thin layers to the lignocellulosic fibers (paper surface). Thus, in a first aspect, the present invention is directed to a lignocelluloisic structure comprising a layer with a thickness of 0.01 µm to 10 µm comprising SiO2 on at least part of its surface, which structure is in the form of a honeycomb structure, and which structure is obtainable by contacting the lignocellulosic structure with a SiO2 precursor.
- The thin SiO2 based layer can be applied in various ways.
- A highly preferred method comprises contacting the lignocellulosic structure with a suitable precursor e.g. by submerging the lignocellulosic structures in a bath of SiO2 precursor or by spraying the SiO2 precursor on the structure or application of the silica using plasma technology.
- A suitable plasma technology is the surface dielectric barrier discharge (SDBD) which works under atmospheric pressure and is therefore suitable for continuous production processes.
- Silica sol-gel is a suitable precursor. The silica sol-gel component is typically based on silicon alkoxide, Si(OR)4, wherein R is an alkyl, preferably methyl or ethyl. These compounds can be subjected to hydrolysis and gelation, whereby silane groups (Si-OH) and siloxane groups (Si-O-Si) are broken and formed, respectively. Commercially widely available sol-gel components are TEOS (tetraethylorthosilicate) and TMOS (tetramethylorthosilicate). The silica content of the SiO2 precursor typically ranges from 1-10% silica and the solvent (such as ethanol, isopropanol or other alcohols, acetone or other ketones) content typically ranges from 10-70%. Using these types of solvents, in particular ethanol as a solvent has a very limited risk, because these solvents have limited toxicity. These solvents tend to evaporate easily. It is highly preferred to collect the vapours comprising the evaporated solvents and thus recover the solvent therefrom so that it may be recycled.
- According to the present invention materials can be provided that provide excellent fire-retardant properties, while at the same time conserving all other requirements and where the transport volume of structures produced is minimized.
- The thin SiO2 based layer has a thickness of 0.01 µm to 10 µm, preferably about 0.2 to 5 µm, more preferably about 0.5 to 2.5 µm.
- The paper surface may be treated with further substances, such as fire retardants. These further components may be applied together with the SiO2 film, but it is also possible to apply them in a separate process step e.g. a subsequent dipping or spraying step or a plasma treatment. Phosphorus based fire retardants are very suitable for this purpose. The combination of phosphorus based fire retardants and silica sol-gel provides materials that have excellent fire-retardant properties, while at the same time conserving all other above-mentioned requirements and where the transport volume of structures produced is minimized.
- The (phosphorus based) fire retardant which may be used in the present invention is preferably a phosphate ester and more preferably an oligomeric phosphate ester. The fire retardant that may be used in the composition of the present invention can be used to impregnate paper in order to create honeycomb structures. The structures thus obtained show excellent properties with respect to water resistance, fire retardant properties, compressibility and durability. At the same time, the product can still be combined with water glass in the conventional method of lamination. When applied the composition of the invention typically comprises 1 to 90 wt.% oligomeric phosphate esster, preferably from 5 to 50 wt.%, based on weight of the total composition.
- The contacting of the lignocellulosic material with the SiO2 precursor can be carried out in a continuous fashion by using a conventional paper treatment process, e.g. by submerging a continuous belt of lignocellulosic material (paper) through a bath containing the sol-gel composition and optionally the fire retardant composition, application of coating processes as used in the paper industry or plasma treatment under atmospheric pressure. The impregnated paper maintains its flexibility in the length direction, by which it can be stored and transported without requiring much space, due to its compactness. The structures that are thus produced have dimensions that are "endless", viz. up to e.g. 50 m or more. Also no emission of harmful compounds occurs during the production process. If a silica sol-gel comprising ethanol is used, the solvent can be collected as vapor and recycled.
- The phosphate esters that find use in the present invention are commercially known fire-retardants. Suitable (oligomeric or monomeric) phosphate esters may be represented by the following formula I:
wherein each of R1, R'1, R2, R'2 and R3 is independently hydrogen or hydrocarbon side chain, in particular straight, branched or cyclic C1-C10 alkyl or alkenyl (preferably C2-C8 alkyl or alkenyl), optionally substituted, e.g. with halogen, epoxide hydroxyl, amino; and n is an integer from 0 to typically about 10. In case n is zero, the compounds of formula I are monomeric phosphate esters. Examples of suitable oligomeric phosphate ester compounds and their production are given e.g. inUS-A-3 767 732 andUS-A-4 382 042 . - Preferred compounds are those of formula I having R1 and/or R'1= (substituted) phenyl, hydrogen, methyl, ethyl, propyl, butyl or pentyl; R2 and/or R'2 = (substituted) phenyl, methyl, ethyl, propyl, butyl or pentyl; and R3= (substituted) phenyl, bisphenol A or biphenyl. A suitable monomeric compound is triphenyl phosphate, which corresponds to a compound of Formula I having R1=R1'=R2=phenyl and n=0. A suitable oligomeric phosphate ester is resorcinol bis(diphenyl phosphate) (RDP), commercially available as Fyrolflex™ RDP (Akzo Nobel), which corresponds to a compound of formula I having R1=R1'=R2=R2'=R3=phenyl and n=1.
- Single compositions of the present invention can be prepared by admixing the ingredients in any order. Preferably, the (oligomeric) phosphate esters are mixed into the sol-gel composition.
- In a preferred embodiment a boric acid derivative is present in the compositions of the present invention, in particular those described in
DE-A-198 33 479 . It was found that the addition of these boric acid compounds has a positive effect on the durability of the lignocellulosic products that are impregnated with the compositions of the present invention. Suitable boric acid derivatives for this purpose are boric acid, trialkylborate (e.g. tributyl borate; tri-isopropyl borate; or tri-tert-butyl borate). The boric acid derivatives may be present in amounts of typically 0 to 10 wt.%, preferably 0.5 to 5 wt.%, based on weight of the total composition. The boric acid provides further protection against biological degradation (that may be caused by degrading organisms like fungi and insects) and has positive effects on the fire resistance. - It was found that the leaching of the boric acid that commonly occurs can be reduced by using the SiO2 in accordance with the present invention.
- Honeycomb structures can be prepared by known process, e.g. the paper honeycomb production processes described in Pflug et al. (5th Global Wood and Natural Fibre Composites Symposium, Kassel (DE), 27-28 April 2004) typically out of low cost recycled paper (e.g. Testliner).
Figure 3 shows schematically the different process steps in a suitable production process for making expanded honeycombs. In a first step adhesive lines are printed on the paper, which may come from one or several paper rolls (1). Then a stack of several sheets is made and bonded together (2). Those sheets can be cut to strips prior or after stacking to a slice (3). In the third step many slices are stacked and bonded together to produce an unexpanded endless paper honeycomb core (4). Finally, the sheets are pulled apart (5) expanding the stack into a hexagonal honeycomb core (6). The residual stresses in paper honeycombs can be relaxed after expansion by a controlled application of heat. - Typically the structures that are produced in this way comprise walls formed of paper strips having a width of several cm, e.g. about 1-6 cm. A typical honeycomb structure is has a diameter of the cells of e.g. 5 - 50 mm and a thickness of the total honeycomb layer of e.g. 5 - 60 mm. The paper weight is usually between 80 g/m2 and 250 g/m2.
-
Figure 4 shows a scanning electron micrograph (SEM), of a sample that is prepared in accordance with the present invention. A thin silica film on a cell wall of a paper fiber can be seen. - The invention will now be illustrated by the following examples.
- Paper (140 g/m2) was treated with silica in ethanol (concentration 18 %) using a coating treatment. The coated paper was dried at 105 °C over a period of 12 hours.
- After being exposed to a humid atmosphere (relative humidity of 96%) at 20 °C for 5 days, the paper was subjected to a repeated stress/strain measurement. Three repeated measurements were carried out on each sample wherein the stress was increased to the maximum that could be achieved and then released again. The results for an untreated sample are given in
Figure 1 . - The results of the paper that was treated as described above are given in
Figure 2 . - From these results it clearly follows that the paper that is treated in accordance with the present invention maintains it strength after the first and second measurement. Furthermore, the flexibility of the honeycomb structure in the length direction was maintained. Also the paper had an excellent glueability so that it could be easily glued with water glass.
Claims (6)
- Lignocellulosic structure comprising a layer with a thickness of 0.01 µm to 10 µm comprising SiO2 on at least part of its surface, which structure is in the form of a honeycomb structure, and which structure is obtainable by contacting the lignocellulosic structure with a SiO2 precursor.
- Lignocellulosic structure according to claim 1, wherein said layer with a thickness of 0.01 µm to 10 µm comprising SiO2 has a thickness of 0.2 µm to 5 µm, preferably 0.5 µm to 2.5 µm.
- Lignocellulosic structure according to any of the previous claims, wherein the layer with a thickness of 0.01 µm to 10 µm comprising SiO2 is obtained by contacting the lignocellulosic structure with a silica sol-gel component, which is preferably a silicon alkoxide, Si(OR)4, wherein R is an alkyl, more preferably methyl or ethyl.
- Lignocellulosic structure according to any of the previous claims, further comprising a fire retardant, which is preferably a phosphorus based fire retardant, more preferably an oligomeric phosphate ester.
- Lignocellulosic structure according to any of the previous claims, which is produced by contacting the lignocellulosic structure with the SiO2 precursor using plasma technology.
- Lignocellulosic structure according to any of the previous claims, wherein the cells have an average diameter of 5 mm - 50 mm and wherein the thickness of the honeycomb layer is 5 mm - 60 mm.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08705093.6A EP2106485B1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
| EP12164779.6A EP2479343B1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07075034A EP1944413A1 (en) | 2007-01-12 | 2007-01-12 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
| EP08705093.6A EP2106485B1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
| PCT/NL2008/050024 WO2008085054A1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12164779.6 Division-Into | 2012-04-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2106485A1 EP2106485A1 (en) | 2009-10-07 |
| EP2106485B1 true EP2106485B1 (en) | 2013-05-15 |
Family
ID=37998264
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07075034A Withdrawn EP1944413A1 (en) | 2007-01-12 | 2007-01-12 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
| EP08705093.6A Not-in-force EP2106485B1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
| EP12164779.6A Not-in-force EP2479343B1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07075034A Withdrawn EP1944413A1 (en) | 2007-01-12 | 2007-01-12 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12164779.6A Not-in-force EP2479343B1 (en) | 2007-01-12 | 2008-01-14 | Honeycomb structure based on lignocellulosic materials and process for producing the same |
Country Status (3)
| Country | Link |
|---|---|
| EP (3) | EP1944413A1 (en) |
| CN (1) | CN101627162A (en) |
| WO (1) | WO2008085054A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102516786B (en) * | 2011-12-19 | 2014-02-19 | 南京林业大学 | Silicon-modified lignin expansion flame-retardant charcoal agent and its preparation method and application |
| CN103321098B (en) * | 2013-05-24 | 2016-04-13 | 吴江曦屹欧阻燃纸有限公司 | A kind of novel flame-retardant paper honeycomb combustion inhibitor special and preparation method thereof |
| JP6241843B2 (en) * | 2013-06-06 | 2017-12-06 | 国立研究開発法人産業技術総合研究所 | Paper honeycomb structure with silica coating and method for producing the same |
| CN107244087A (en) * | 2017-07-14 | 2017-10-13 | 苏州云逸航空复合材料结构有限公司 | The manufacture method of composite honeycomb and the equipment for manufacturing composite honeycomb |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1323381A (en) | 1970-07-23 | 1973-07-11 | Knapsack Ag | Polyols containing halogen and phosphorus and process for making them |
| US4382042A (en) | 1978-04-03 | 1983-05-03 | Stauffer Chemical Company | Method of preparing oligomeric phosphate esters |
| US5254195A (en) * | 1992-05-08 | 1993-10-19 | Industrial Technology Research Institute | Process for manufacturing moisture exchange element |
| US5626945A (en) * | 1993-09-28 | 1997-05-06 | International Paper Company | Repulpable, water repellant paperboard |
| DE19833479C2 (en) | 1998-07-24 | 2003-06-26 | Kallies Feinchemie Ag | Wood preservative, wood treatment method and use of wood preservative |
| SE515614E (en) * | 2000-03-01 | 2009-06-16 | Proflute Ab | Process for making dehumidifying elements and using a suspension for impregnating paper in the process |
-
2007
- 2007-01-12 EP EP07075034A patent/EP1944413A1/en not_active Withdrawn
-
2008
- 2008-01-14 EP EP08705093.6A patent/EP2106485B1/en not_active Not-in-force
- 2008-01-14 WO PCT/NL2008/050024 patent/WO2008085054A1/en not_active Ceased
- 2008-01-14 CN CN200880002206A patent/CN101627162A/en active Pending
- 2008-01-14 EP EP12164779.6A patent/EP2479343B1/en not_active Not-in-force
Also Published As
| Publication number | Publication date |
|---|---|
| CN101627162A (en) | 2010-01-13 |
| EP2479343A1 (en) | 2012-07-25 |
| WO2008085054A1 (en) | 2008-07-17 |
| EP1944413A1 (en) | 2008-07-16 |
| EP2479343B1 (en) | 2013-07-24 |
| EP2106485A1 (en) | 2009-10-07 |
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