AU2002247652A1 - Method for preparing composite materials containing natural binders - Google Patents
Method for preparing composite materials containing natural bindersInfo
- Publication number
- AU2002247652A1 AU2002247652A1 AU2002247652A AU2002247652A AU2002247652A1 AU 2002247652 A1 AU2002247652 A1 AU 2002247652A1 AU 2002247652 A AU2002247652 A AU 2002247652A AU 2002247652 A AU2002247652 A AU 2002247652A AU 2002247652 A1 AU2002247652 A1 AU 2002247652A1
- Authority
- AU
- Australia
- Prior art keywords
- moisture content
- fibres
- natural
- fibre
- protein
- 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
- 238000000034 method Methods 0.000 title claims description 55
- 239000002131 composite material Substances 0.000 title claims description 15
- 239000011230 binding agent Substances 0.000 title claims description 11
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- 102000004169 proteins and genes Human genes 0.000 claims description 47
- 239000000835 fiber Substances 0.000 claims description 35
- 239000000853 adhesive Substances 0.000 claims description 25
- 230000001070 adhesive effect Effects 0.000 claims description 25
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- 239000002023 wood Substances 0.000 claims description 20
- 238000002156 mixing Methods 0.000 claims description 12
- 239000000843 powder Substances 0.000 claims description 11
- 238000007731 hot pressing Methods 0.000 claims description 9
- 241001465754 Metazoa Species 0.000 claims description 8
- 235000013311 vegetables Nutrition 0.000 claims description 5
- 238000000748 compression moulding Methods 0.000 claims description 4
- 239000005022 packaging material Substances 0.000 claims description 4
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- 241000209140 Triticum Species 0.000 description 15
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- 238000003825 pressing Methods 0.000 description 11
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- 239000000047 product Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
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- 244000025254 Cannabis sativa Species 0.000 description 6
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 6
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 6
- 229920001807 Urea-formaldehyde Polymers 0.000 description 6
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- 235000005607 chanvre indien Nutrition 0.000 description 6
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- 238000012360 testing method Methods 0.000 description 5
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- 235000010469 Glycine max Nutrition 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
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- 238000005452 bending Methods 0.000 description 3
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- 239000006185 dispersion Substances 0.000 description 3
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- 229920001568 phenolic resin Polymers 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 2
- 235000021120 animal protein Nutrition 0.000 description 2
- 239000007767 bonding agent Substances 0.000 description 2
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- 239000012153 distilled water Substances 0.000 description 2
- -1 e.g. particleboard Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 235000012054 meals Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- 235000015099 wheat brans Nutrition 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
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- 108010017384 Blood Proteins Proteins 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010028690 Fish Proteins Proteins 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
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- 102000014171 Milk Proteins Human genes 0.000 description 1
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- 108010058846 Ovalbumin Proteins 0.000 description 1
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- 241000065615 Schinopsis balansae Species 0.000 description 1
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- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 235000019772 Sunflower meal Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000005862 Whey Substances 0.000 description 1
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- 108010046377 Whey Proteins Proteins 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 229920002494 Zein Polymers 0.000 description 1
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- 239000012736 aqueous medium Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
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- 239000004566 building material Substances 0.000 description 1
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- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
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- 239000012467 final product Substances 0.000 description 1
- 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 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000021239 milk protein Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000010944 pre-mature reactiony Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000004456 rapeseed meal Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 229940071440 soy protein isolate Drugs 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
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- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
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- 210000002268 wool Anatomy 0.000 description 1
- 239000005019 zein Substances 0.000 description 1
- 229940093612 zein Drugs 0.000 description 1
Description
METHOD FOR PREPARING COMPOSITE MATERIALS CONTAINING
NATURAL BINDERS
The invention relates to a method for preparing natural fibre-based composite materials containing natural binders and powdery proteins .
With this methods, products are made in the form of artefacts such as panels and boards, composed of wood and/or non-wood natural fibre materials and a protein as the sole binder component (added) .
Today, manufacture of the panels and boards is generally performed by means of hot pressing of wood or other vegetable fibres in presence of a reactive resin. Typical resins used during the mixing process are urea formaldehyde (UF) resins, phenol formaldehyde (PF) resins and melamine urea formaldehyde ( UF) resins. During the initial blending process aqueous resin is sprayed on the dry wood or vegetable fibres (2-4% moisture) and the whole is blended. The fibres dosed with resin can then be submitted to a further drying step. During this drying process the resin-dosed fibre is pneumatically or mechanically conveyed to the intermediate storage bins. From here, the fibre is transported to the mat forming line and to the pre-press. The thus formed mats are then entering the press and stacked. These mats are then submitted to hot pressing to consolidate the mat to a desirable panel density and thickness, to cure the resins and to heat stabilise the panel so that it will remain at the target thickness and density under normal service
conditions. Also continuous presses can be used. The thus obtained panels are then finished by shaving-off the edges by sanding the surfaces .
A disadvantage of this process is that the fibre material must be dried to a sufficient level to allow the blending with the liquid resin; otherwise homogeneous blending is not possible while lump formation occurs at too high moisture content .
An other disadvantage is that when adding the resin, the temperature during the blending and forming step must be controlled, because otherwise, a premature reaction occurs, and this is not desirable.
To reduce or avoid the use of the resin adhesives, the resin adhesives can be partially or fully replaced by renewable resources .
The use of animal or vegetable proteins in fibreboard is disclosed in Forest Products Journal (1998, vol.47, n°2, p.71-75), wherein the use of soya protein isolates in combination with synthetic resins is discussed. . Also the use of soya isolate powder is disclosed. In this method, wood particles are sprayed with 4% phenol formaldehyde resin, whereafter the mixture is further tumbled in a blender while 4% soya isolate powder is slowly added. Also the use of a soya isolate dispersion as the sole adhesive is disclosed.
However, the resultant fibreboard has the disadvantage that it has no moisture resistance.
The use of animal proteins in powder form is further disclosed in Sovjet patent application SU 1 813 640. In the disclosed method, lime milk (1,6-3,2%) and water (35- 45%) are added to a fibre material at about 4% moisture content. In a next step, 8-16% albumin or casein powder glue is added, and the whole is mixed until the glue is uniformly distributed into the fibre material . The composition is then heated between 140-170°C at a pressure of 1,4-2,5 Mpa, this during 0,6-1,0 min/mm.
The use of wheat gluten as an adhesive has been disclosed in Starch (1968, vol20, n°12 p.395-399). The gluten that is used is reduced with sodium sulphite or thioglycolic acid.
The disadvantage related to these products is that the wheat gluten adhesive is obtained through a chemical reaction in an aqueous medium.
In Dutch patent application NL 1 003 133, the use of an adhesive based on wheat gluten for preparing fibreboard is disclosed. The wheat gluten glue used is a dispersion at 55-60% d.s., obtained by dispersing gluten into a solution of urea, citric acid and sodium bisulpite. The gluten glue, which is first mixed with a cross-linker
(formaldehyde, glutardialdehyde or maleic anhydride) , is then sprayed on and mechanically mixed with the wood fibre substrate.
The disadvantage here is that dispersing aids are needed to prepare the gluten glue dispersion.
Also the use of proteins as formaldehyde scavenger is disclosed in Dutch patent application NL 1 003 133, whereby 10% of a standard urea formaldehyde resin is replaced by gluten glue.
The disadvantage is that above 10% replacement of the standard urea formaldehyde resin, there is a clear loss of Internal Bond Strength.
In the European patent application EP 976 790, a process for the manufacture of composite materials is disclosed, in which a vegetable material containing fibre, or a mixture of such vegetable materials, are subjected to at least one thermoplastic processing step. The thermoplastic processing may be carried out in the presence of a bonding agent, for example a chemical bonding agent such as urea-formaldehyde, or a protein
(which protein may be contained in the vegetable material or added to it) . Prior to the thermoplastic processing step(s), the vegetable material (s) are subjected to at least one preliminary treatment . The product of the thermoplastic processing step(s) may be subjected to an after-treatment. The vegetable material (s) may be mixed with additives prior to and/or during the thermoplastic processing step(s) . The composites may be formed in a variety of configurations, including board, sheets and films, and may find use as constructional items.
The disadvantage is that when proteins are used as the sole binder, relative to the total of the fibrous vegetable material and protein, the amount of water may be in the range of 25 to 50% by weight. As a result thereof, the compression-moulded articles must be submitted to an additional time and energy consuming drying step.
The purpose of the invention is to resolve the abovementioned disadvantages. This purpose is achieved by providing a method for preparing natural fibre-based composite materials containing natural binders and powdery proteins, comprising the following steps:
• adding a powdery protein adhesive binder to natural fibres having a moisture content of 1 -
15%;
• mixing the natural fibres together with the powdery protein adhesive;
• adjusting the moisture content of the composition to 6 - 24% w/w; and
• submitting the mixture to a heat pressure treatment to form the natural fibre-based material .
In a preferred method according the invention, the ratio of natural fibres and protein powder adhesive varies between 19:1 up to 1:1.
In a preferred method according the invention, the heat pressure treatment is performed within a temperature range of 100 - 250 °C.
In a preferred method according to the invention, the proteins added to the fibres have a moisture content varying between 4 and 14 % w/w.
In a more preferred method according the invention, the proteins added to the natural fibres have a moisture content between 8 and 12 % w/w.
In a specific method according to the invention, the wood or plant fibres have a moisture content between 1 and 20 % w/w.
In a more specific method according to the invention, the wood or plant fibres have a moisture content between 2 and 15 % w/w.
Preferably, the natural fibre-based composite materials include one of the products selected from packaging materials, decorative items, backing materials or structural materials.
In a preferred method according to the invention, said natural fibres can be obtained from whole plants or various parts thereof.
In a preferred method according to the invention, said natural fibres can be of animal origin.
In a preferred method according to the invention, said powdery protein adhesive can be of animal origin.
In another preferred method according to the invention, said powdery protein adhesive can be of vegetable origin.
In a preferred method according to the invention, the final moisture content of the composition is adjusted to 12 - 20% w/w.
In a more preferred method according to the invention, the final moisture content of the composition is adjusted to 14 - 18 % w/w.
In a preferred method according to the invention, the ratio of natural fibres and protein powder adhesive vary between 9:1 and 2:1.
In a more preferred method according the invention, the ratio of natural fibres and protein powder adhesive vary between 9 : 1 and 2,5:1.
In a preferred method according to the invention, the heat pressure treatment is performed within a temperature range of 175 - 225 °C.
In a specific method according to the invention, the heat pressure treatment is performed by means of compression moulding or by hot pressing in open presses.
In a specific method according to the invention, during hot pressing treatment a pressure is exercised that is sufficient to obtain a natural fibre-based composite
material with a density varying between 0,5 kg/dm3 and 1,5 kg/dm3.
In general, the term natural fibre-based composite materials concerns reconstituted products containing natural fibres originating from wood and/or annual plants, and an adhesive. Such composite materials include e.g. packaging materials, decorative items, backing materials, structural materials. More particularly, it refers to construction or building materials such as e.g. particleboard, medium density and high-density fibreboard, oriented strand board or chipboard. Other compositions comprise e.g. packaging materials (bottles, containers) , decorative items (door panels) , backing materials (carpet tiles, roofing materials) , or structural materials (e.g. car bumpers) .
Apart from wood, natural fibre materials can be obtained from whole plants or from various parts thereof. Textile fibres such as cotton, flax hemp or ramie can be used, but also meal products from the cereals or oilseed processing industry. Typical examples thereof are wheat bran, corn bran, wheat straw, barley husks, rapemeal, sunflower meal, soybean meal, etc. The natural fibre materials can also be of animal origin such as wool, silk or keratin-waste, etc.
The powdery protein adhesive can be of animal or vegetable origin. Animal protein sources are e.g. milk proteins, caseinates, whey concentrates and isolates, gelatine, fish proteins, egg albumin, plasma proteins,
animal flours, etc. The vegetable proteins can be selected among e.g. cereal proteins, tuberous proteins, proteins from leguminous origin, or oilseed proteins. Typical cereal proteins that can be used are wheat gluten, or maize gluten and derivatives thereof. Among the oilseed proteins, soy protein concentrates and isolates, rapeseed protein concentrates or sunflower protein concentrates, or derivatives thereof can be used, also. This list must not be considered as limiting, but merely as an illustration of the protein sources that can be used.
The proteins added to the natural fibres have a moisture content varying between 4 and 14% w/w, preferably varying between 8 and 12 % w/w. The wood or plant fibres may have a moisture content between 1 and 20 % w/w, 2 to 15% w/w being preferred. In contrast with standard conditions used during e.g. panel manufacture, the moisture content of the fibres can be higher because no additional moisture is added via the binding agent. This can offer an additional advantage with regard to drying cost reduction of the wood or plant fibres.
The natural fibres together with the powdery adhesive are mixed, and the final moisture content of the fibre/protein composition, before the heat pressure treatment, may vary between 6 and 24% w/w. Preferred ranges of moisture content are between 12 and 20% w/w, more preferably between 14 and 18% w/w. It is believed that his moisture content activates an initial sticking process, in which there occurs an interaction between the
proteins and the fibres. In this way, there is already a stabilisation before the heat pressure treatment. When the moisture content of the protein/fibre composition is too low, the phases can separate. When the moisture content of the fibre/protein composition is too high, more heat is needed to remove the water, and the final product has a less mechanical strength. With a moisture content between 6 and 24% w/w, the fibre/protein composition is already sufficiently homogeneous, which avoids an extra kneading step.
The ratio of natural fibre material and protein powder adhesive may vary between 19:1 up to 1:1, preferably between 9 : 1 and 2 : 1 and more preferably between 9 : 1 and 2,5:1.
Heat pressure treatment of the fibre/adhesive composition is performed within a temperature range of 100-250 °C, preferably between 175°C and 225°C. Pressure exercised during hot pressing must be sufficient to obtain densities varying between 0,5 kg/dm3 and 1,5 kg/dm3.
The heat pressure treatment of the compositions may be performed by means of compression moulding or by hot pressing of the fibre/protein composition. The processing parameters, in particular temperature, pressure, and processing time will depend in any given case upon the nature of the starting materials and desired properties of the end products. It is observed that temperature evolution in the core of the product
during hot pressing or compression moulding is quite fast, as illustrated by figure 1 (see example 4) .
The panel products obtained by means of the processes according to the invention do show excellent mechanical properties and sufficiently low water sensitivity.
It can be considered as an additional advantage that the prepared composites according to the invention are composed of biodegradable compounds. This can be of importance where materials are difficult to recycle.
The invention will now be further illustrated by way of specific examples, which are purely illustrative and not intended to limit the scope of the invention.
Example 1 :
In this example the influence of the gluten fraction (GF) , moisture content (MC) and pressing temperature (T) , on the density (D) and the thickness swelling (TS) of panel boards, containing hemp fibres, is illustrated. Especially the thickness swelling (water sensitivity) is a measure for the quality of adhesion between fibres and matrix.
Materials used:
• vital wheat gluten, moisture content 8,6% (Amylum Aquitaine, Bordeaux, France) • Hemp fibres, moisture content 8,9%, mean size 3 mm (Agricultural cooperative "La Chanvriere de l'Aube"
The hemp fibres are mixed with wheat gluten in a tumbling mixer (Heidolph Rheax 2, Germany) for 10 minutes. The volume of the mixing bowls is 100 ml, the total mass is 10g, the fibre weight fraction is 0.6, 0.7, 0.8, 0.9 w/w. Water is sprayed in the mixing bowl in order to raise the final water content to 18 %, the water content of the mixture without water addition being 9%. The fibre/gluten mix is poured into a cylindrical mould (diameter 35 mm) and pressed for 10 minutes at 100, 125, 150, 175, and 200°C under 10T load.
The samples thus obtained are immersed in distilled water
(at 25°C) for 24h. The thickness swelling is then determined as the percentage increase of the sample thickness as measured at the centre of the disks with a digital calliper square.
The material density is determined after measuring the sample thickness and diameter with a digital calliper square to the nearest 0,01mm and weighting the sample on a precision balance.
The moisture content of raw materials and samples is determined by weight difference after 24h drying at 104°C.
The results are given in table 1.
TABLE 1: Gluten/hemp fibre compositions: influence moisture content (MC) and pressing temperature (T) on density (D) and thickness swelling (TS)
Example 2
In this example different types of natural fibres are used. The method of preparing them is analogous to the process described in example 1. Also here, density and thickness swelling are determined in function of pressing temperature and moisture content. The following materials are used: wheat straw, wheat bran, and quebracho wood flour.
The gluten fraction is always 0,3. In table 2, the results of thickness swelling and density are given.
TABLE 2: Comparison of different fibres: influence moisture content (MC) and pressing temperature (T) on density (D) and thickness swelling (TS)
Example 3
In this example, mechanical properties of gluten /fibre compositions are determined. The same method as in example 1 is used, except that the panels are formed in a rectangular mould of 120mm x 10mm. The thickness obtained is between 5 and 6 mm.
The mechanical properties are investigated according to norm EN IS014125 in bending mode with TAXT2 texture analyser (Stable Microsystems, UK) . The distance between flexion points is 100 mm. The samples are analysed directly after fabrication.
Materials used:
• vital wheat gluten, moisture content 8,6% (Amylum Aquitaine, Bordeaux, France)
• Hemp fibres, moisture content 8,9%, mean size 2 and 6 mm (Agricultural cooperative "La Chanvriere de
1 ■Aube" )
• Linen straw (8,9% MC, Unilin NV, B-8710 Wielsbeke)
The results of the mechanical testing are given in table 3.
TABLE 3: Influence of fibre type, moisture content (MC) , ressing temperature (T) and gluten fraction (GF) on modulus of elasticity (MOE) and modulus of rupture (MOR) . Mean values of 4 replicates.
Example 4 :
Materials Vital wheat gluten, (8.6% Moisture content, Amylum Aquitaine, Bordeaux, Fr)
Wood particles (8.5 % MC, Unilin NV, Schaapdreef 36, B- 8710 Wielsbeke)
Methods - Mixing: The fibres are mixed with wheat gluten in a 5 1 rectangular mixing bowl by hand for 10 min, simulating the movements of a tumbling mixer. Pressing: A rectangular fibre mat of dimensions 17x26 cm and about 4cm height is formed by hand using a wooden frame. A k type thermocouple is placed in the centre of the fibre mat. After removal of the wooden frame, the mat is placed into the heated press (regulated at 175°C) and the temperature recording is started. The mat is compressed to 11 mm final thickness in a hand pump hydraulic press. The time needed for press closure to 11 mm is 60s, the load is maintained for 120s, then the load is relaxed gradually to zero during 1 min. The total pressing time is 4 min. 4 flexion specimens (30*170 mm) and 2 specimens (50*50 mm) for thickness swelling and determination of density are cut of each board.
The mechanical properties are investigated in bending mode with a ZWICK 500N universal testing machine. The distance between flexion points is 100 mm, cross-head
speed is 2mm/min. The samples are tested immediately after their fabrication.
Thickness swelling is investigated according to norm EN 319. The test specimens are immersed in distilled water (20°C) , thickness is determined in the centre of the test specimen after 2 and 24h of immersion.
Results
Core temperature evolution
0 60 120 180 240 300 Time (s)
FIGURE 1: Core temperature evolution during pressing of gluten and wood particles. 175° "C regulation temperature, 300g wood (9%MC) , 60g gluten (7%MC)
Figure 1 shows the core temperature evolution during the fabrication of a gluten wood particleboard. It is
observed that temperature rises very rapid as soon as the press is closed and the nominal thickness is reached. Core temperature reaches 150°C in 30 sec after press closure (90s total press time) .
- Mechanical properties
TABLE 4: Mechanical properties and water sensitivity of gluten wood particleboards .
Sample N° E F G H Specifications
Composition EN 312-2
Fibres g 300 300 300 300
Gluten g 60 75 75 33,3
Thickness mm 11,4 11,5 11,2 11,7
Density kg/m3 762,4 693,3 553
Mechanical properties
MOE G a 0,976 1,029 1,077 0,636 sdev 0,094 0,188 0,201 0,184
MOR Mpa 10,58 12,26 12,29 5,94 12,5 sdev 10,58 2,78 2,59 1, 04
Thickness swelling
TS (2h) 48,8 52,2 40,5 sdev 3,9 6 2,6
TS (24h) 60,3 63,9 53, 6 sdev 1,7 1,9 0,1
MOE is modulus of elasticity, MOR is modulus at break, TS is thickness swelling after immersion in 20°C water.
Specifications are EN 312-2, general purose particleboard
The production of gluten wood particleboard is feasible. Until now boards with a gluten weight fraction of 0.2 comply with the specifications of general purpose particleboard (EN 312-2) .
Example 5 :
In this example mechanical properties of different protein /fibre compositions are determined. The same method as in example 1 is used, except that the panels were formed in a rectangular mould of 120mm x 10mm. Moulding temperature is 175°C and moisture content is 9%. The fibre fraction is 0,8. Thickness obtained is between 5 and 6 mm. Mechanical properties are investigated according to norm EN ISO 14125 in bending mode with TAXT2 texture analyser (Stable Microsystems, UK) . The distance between flexion points is 100 mm. The samples are analysed directly after fabrication. The results are displayed in table 5.
Materials used:
• vital wheat gluten, moisture content 8,6% (Amylum ■Aquitaine, Bordeaux, France)
• Linen straw (8,9% MC, Unilin NV, B-8710 Wielsbeke)
• Zein (8% MC, Sigma Chemicals) • Corn gluten meal (8,5% MC)
• Soy protein isolate (7,8% MC PTI)
TABLE 5: Modulus of elasticity (MOE) and modulus of rupture (MOR) of protein/linen straw composite materials, moulded at 175°C, 9%MC, and 10 min press time:
Example 6 :
This example illustrates the effect of the pressing temperature on the mechanical properties of the fibre boards prepared with wheat gluten as the sole binder.
The boards in this example are prepared by mixing 300g wood fibres (2% moisture) with 33, 3g wheat gluten (7% moisture) in a T-bar rotating mixer for 3 minutes. Then 25g water, mixed with 5 , 5g parrafin emulsion was added and mixed for an additional 7 minutes.
The pressing procedure as described in example 4 is slightly modified, whereby the pressing temperature was increased to values of 200°C and 225°C and pressing time was lOs/mm. Density of the boards thus prepared varied between 0,732 and 0,735.
The boards thus obtained were submitted to mechanical testing, as already described in example 4.
Claims (19)
1. Method for preparing natural fibre-based composite materials containing natural binders and powdery proteins, comprising the following steps:
• adding a powdery protein adhesive binder to natural fibres having a moisture content of 1 - 15%; • mixing the natural fibres together with the powdery protein adhesive;
• adjusting the moisture content of the composition to 6 - 24% w/w; and
• submitting the mixture to a heat pressure treatment to form the natural fibre-based material .
2. Method according to claim 1, characterised in that the ratio of natural fibres and protein powder adhesive varies between 19:1 up to 1:1.
3. Method according to any one of claims 1 and 2, characterised in that the heat pressure treatment is performed within a temperature range of 100 - 250 °C.
Method according to any one of claims 1 up to and including 3, characterised in that the proteins added to the natural fibres have a moisture content varying between 4 and 14 % w/w.
5. Method according to claim 4, characterised in that the proteins added to the fibres have a moisture content between 8 and 12 % w/w.
6. Method according to any one of claims 1 up to and including 5, characterised in that the wood or plant fibres have a moisture content between 1 and 20 % w/w.
7. Method according to any one of claims 1 up to and including 6, characterised in that the wood or plant fibres have a moisture content between 2 and 15 % w/w.
8. Method according to any one of claims 1 up to and including 7, characterised in that the natural fibre- based composite materials include one of the products selected from packaging materials, decorative items, backing materials or structural materials.
9. Method according to any one of claims 1 up to and including 8, characterised in that said natural fibres can be obtained from whole plants or various parts thereof.
10. Method according to any one of claims 1 up to and including 8, characterised in that said natural fibres can be of animal origin.
11. Method according to any one of claims 1 up to and including 10, characterised in that said powdery protein adhesive can be of animal origin.
12. Method according to any one of claims 1 up to and including 10, characterised in that said powdery protein adhesive can be of vegetable origin.
13. Method according to any one of claims 1 up to and including 11, characterised in that the final moisture content of the composition is adjusted to 12 - 20% w/w.
14. Method according to claim 13, characterised in that the final moisture content of the composition is adjusted to 14 - 18 % w/w.
15. Method according to any one of claims 1 up to and including 14, characterised in that the ratio of natural fibres and protein powder adhesive vary between 9 : 1 and 2:1.
16. Method according to claim 15, characterised in that the ratio of natural fibres and protein powder adhesive vary between 9:1 and 2,5:1.
17. Method according to any one of claims 1 up to and including 16, characterised in that the heat pressure treatment is performed within a temperature range of 175 - 225
18. Method according to any one of claims 1 up to and including 17, characterised in that the heat pressure treatment is performed by means of compression moulding or by hot pressing in open presses.
19. Method according to any one of claims 18, characterised in that during hot pressing a pressure is exercised that is sufficient to obtain a natural fibre-based composite material with a density varying between 0,5 kg/dm3 and 1,5 kg/dm3.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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GB0101630.2 | 2001-01-23 | ||
GB0101630A GB0101630D0 (en) | 2001-01-23 | 2001-01-23 | Method for preparing composite materials containing natural binders |
PCT/EP2002/000665 WO2002059212A1 (en) | 2001-01-23 | 2002-01-21 | Method for preparing composite materials containing natural binders |
Publications (2)
Publication Number | Publication Date |
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AU2002247652A1 true AU2002247652A1 (en) | 2003-02-06 |
AU2002247652B2 AU2002247652B2 (en) | 2007-01-18 |
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AU2002247652A Ceased AU2002247652B2 (en) | 2001-01-23 | 2002-01-21 | Method for preparing composite materials containing natural binders |
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US (1) | US7387756B2 (en) |
EP (1) | EP1363974B1 (en) |
JP (1) | JP4170760B2 (en) |
CN (1) | CN1243060C (en) |
AT (1) | ATE370198T1 (en) |
AU (1) | AU2002247652B2 (en) |
CA (1) | CA2434895C (en) |
DE (1) | DE60221799T2 (en) |
DK (1) | DK1363974T3 (en) |
ES (1) | ES2292739T3 (en) |
GB (1) | GB0101630D0 (en) |
PT (1) | PT1363974E (en) |
WO (1) | WO2002059212A1 (en) |
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FR2863193B1 (en) * | 2003-12-05 | 2006-03-10 | Bsm Dev | PLANAR, BIODEGRADABLE AND MASSIVE STRUCTURAL ELEMENT IN MATERIAL OF CEREAL ORIGIN, AND METHOD FOR MANUFACTURING SUCH A COMPONENT |
DE102006006656A1 (en) * | 2005-08-26 | 2007-03-01 | Degussa Ag | Silane-containing binder for composites |
US7875655B2 (en) | 2006-01-20 | 2011-01-25 | Material Innovations, Llc | Carpet waste composite |
US7465332B2 (en) * | 2006-04-21 | 2008-12-16 | Gemchar, Llc | Disposable grease filter for air filtration system and method of manufacturing same |
US20080213562A1 (en) * | 2006-11-22 | 2008-09-04 | Przybylinski James P | Plastic Composites Using Recycled Carpet Waste and Systems and Methods of Recycling Carpet Waste |
DE102007050935A1 (en) * | 2007-10-23 | 2009-04-30 | Kronotec Ag | A method for reducing the emission of aldehydes and other volatile organic compounds from wood-based materials and compositions therefor |
DK2376283T3 (en) * | 2008-12-19 | 2017-08-21 | Fiber Composites Llc | WOOD PLASTIC COMPOSITIONS WITH IONOMER COAT MATERIALS AND METHODS OF MANUFACTURING |
FR2942234B1 (en) * | 2009-02-17 | 2012-03-09 | Univ Picardie | PROCESS FOR OBTAINING AGRO MATERIAL, IN PARTICULAR AGRO BINDER OR AGRO COMPOSITE, AND AGRO MATERIAL OBTAINED BY SUCH A METHOD |
CH701959B1 (en) * | 2009-10-01 | 2012-04-30 | Kremlin Group Corp | Cellulosic mass. |
GB2484545A (en) * | 2010-10-15 | 2012-04-18 | Glenn Williams | Panel comprising sustainable material |
US9428648B2 (en) * | 2010-12-03 | 2016-08-30 | Green Materials, Llc | Wheat gluten based compositions and articles made therefrom |
WO2012075489A1 (en) * | 2010-12-03 | 2012-06-07 | R&D Green Materials, Llc | Wheat gluten based compositions and articles made therefrom |
FR2976298B1 (en) | 2011-06-09 | 2014-08-22 | A P C A Assemblee Permanente Des Chambres D Agriculture | PROTECTIVE AND / OR COMBUSTION MATERIAL FROM CELLULOSIC PLANT MATERIAL AND METHOD OF MANUFACTURING THE SAME |
EP2766156A4 (en) | 2011-10-13 | 2015-11-11 | Univ Connecticut | Process for particleboard manufacture |
US20130202843A1 (en) * | 2012-02-06 | 2013-08-08 | Shawn M. Agosta | Green material based article, composition, and method of producing same |
US20160177067A1 (en) * | 2012-02-06 | 2016-06-23 | Shawn M. Agosta | Green Material Based Article, Composition, and Method of Producing Same |
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-
2001
- 2001-01-23 GB GB0101630A patent/GB0101630D0/en not_active Ceased
-
2002
- 2002-01-21 ES ES02716681T patent/ES2292739T3/en not_active Expired - Lifetime
- 2002-01-21 PT PT02716681T patent/PT1363974E/en unknown
- 2002-01-21 JP JP2002559504A patent/JP4170760B2/en not_active Expired - Fee Related
- 2002-01-21 US US10/466,915 patent/US7387756B2/en not_active Expired - Fee Related
- 2002-01-21 EP EP02716681A patent/EP1363974B1/en not_active Expired - Lifetime
- 2002-01-21 DE DE2002621799 patent/DE60221799T2/en not_active Expired - Lifetime
- 2002-01-21 CA CA2434895A patent/CA2434895C/en not_active Expired - Fee Related
- 2002-01-21 AU AU2002247652A patent/AU2002247652B2/en not_active Ceased
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- 2002-01-21 WO PCT/EP2002/000665 patent/WO2002059212A1/en active IP Right Grant
- 2002-01-21 CN CNB028040341A patent/CN1243060C/en not_active Expired - Fee Related
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