[0001] This invention relates to the manufacture of board of lignocellulose-containing material,
such as fiber board.
[0002] Board of this kind is manufactured by disintegrating the material to particles containing
fiber bundles and fibers. Glue is added to the disintegrated material and the material
is dried and a web is formed which finally is pressed at increased temperature for
curing the glue so that a board is formed. Fiber board is made of material which is
disintegrated by defibering, i.e. of more or less free fibers.
[0003] The binding agent normally used is urea formaldehyde glue, which is admixed to the
disintegrated material. The amount of glue can be 6% or more. The glue is relatively
expensive, and it is therefore desired to minimize the glue addition. A smaller amount
of glue, however, deteriorates the strength of the completed board. In view thereof,
the glue addition must be optimized.
[0004] At the drying of the glued material, a great or small amount of water soluble formaldehyde
is given off from the glue. After the separation of the drying gas from the fiber
material, for example in a cyclone, the liquid content is condensed out of the gas.
In conventional cleaning processes the water soluble formaldehyde then causes problems.
The formaldehyde following along with the material to the final pressing also can
cause problems when it is successively given off from the completed board. When glue
is added to the material after its drying, the problem with formaldehyde separation
arises at the pressing as well as from the completed board.
[0005] Fiber board manufactured according to the dry method normally is called MDF (Medium
Density Fiberboard) and is a board product made of wood fiber. The yield exceeds 95%.
The starting material preferably is wood chips, which are defibered with relatively
low energy input, 100-500 kWh/ton fibers, for freeing the fibers. The defibered fiber
material is glued, dried, formed to a web and pressed in a hot press. Alternatively,
the material can be dried prior to the gluing. The material normally is preheated
prior to the defibering to above 150°C whereafter the defibering is carried out under
pressure at this high temperature in order to facilitate the freeing of the fibers.
At such a high temperature, however, the material can be degradated and miscoloured
due to occurring hydrolysis. A short heating time reduces this shortcoming, but miscolouring
yet cannot be avoided, and at the same time the energy consumption increases.
[0006] The urea formaldehyde glue normally used can be mixed with the fiber material on
the conveying line (blow line) from the defibering apparatus or in a separate mixing
device. The amount of admixed glue can be 6% or more.
[0007] When the fiber material subsequently is dried in a tube drier by means of gas at
high temperature, a great or small amount of water soluble formaldehyde is given off
from the glue. As stated above, the formaldehyde following along with the fiber material
to the final pressing also can cause problems when it is given off successively from
the completed board. This applies especially to gluing after the drying of the material,
which can be carried out at the manufacture of fiber board.
[0008] The aforesaid problems can be reduced by the present invention, which simultaneously
offers further advantages. According to the invention, the fiber material is treated
with an impregnation liquid containing fiber surface activating chemicals and preheated
before it is finally disintegrated.
[0009] Examples of such chemicals are such which affect the lignin, such as Na
2SO
3 and NaHSO
3. These chemicals can be added in an amount of 1-30 kg/ton material expressed as Na
2SO
3. According to the invention, it is possible to increase the ISO-brightness of the
completed product, to reduce the energy consumption at the defibering, to reduce the
glue amount at maintained strength or to increase the strength at maintained glue
amount. Furthermore, also the formaldehyde separation can be reduced substantially.
[0010] The invention is described in greater detail in the following with reference to some
embodiments thereof.
[0011] Fiberboard is manufactured by impregnating the raw material in the form of chips
of, for example, softwood with lignin affecting chemicals, such as Na
2SO
3 and NaHSO
3, in an amount of 1-30, preferably 10-20 kg/ton fiber material expressed as Na
2SO
3.
[0012] The impregnation, which has to be carried out rapidly, can last some minute. Thereafter
the temperature is increased to 150-200°C, preferably 160-180°C, for 2-3 minutes.
However, the preheating can of course be performed prior to or at the same time as
the impregnation. The pH value is kept within 2-12. This implies, that an impregnation
solution with Na
2SO
3 and NaHSO
3 will contain sulphite in the form of HSO
3- and/or SO
32-. The pH value suitably can be controlled by NaOH. Due to this chemical treatment
(sulphonation), the subsequent defibering can be carried out to the desired defibering
degree with an energy input lower than normal. The energy consumption is in the interval
50-400 kWh/ton fiber material. The energy saving can amount to about 10% compared
with conventional defibering.
[0013] Owing to the impregnation, also the brightness of the completed fiber board increases.
[0014] As regards the fiber disintegration in the defibered material, it was found that
both the fine material content and the shives content were reduced, i.e. the proportion
of prima fiber has increased.
[0015] It was also found at the impregnation according to the invention that the strength
properties of the completed board have improved substantially. The tensile strength
as well as the elasticity modules and the fiber bond have increased by at least 10%.
Alternatively, this effect can be utilized for reducing the amount of glue addition
at maintained strength properties. A 10% increase in the fiber bond corresponds to
a 1% decrease in glue addition. The sulphonation according to the invention also implies,
that the separation of formaldehyde can be reduced, due to the fact, that the sulphite
ions in the impregnation solution react with the formaldehyde so that it is bound
in the fiber material instead of being given off from the completed board.
EXAMPLE
[0016] Raw material in the form of chips was exposed to different impregnation treatment.
One batch was treated with 10 kg Na
2SO
3 per ton chips, and one batch with 10 kg NaHSO
3 per ton chips. A reference batch was not impregnated.
[0017] The different batches were preheated to about 170°C and thereafter defibered. In
the blow line after the defibering, urea formaldehyde glue of the type E2 was added
in an amount of 10% dry glue calculated on dry fiber. The material was thereafter
dried to a dry matter content of about 90%. The fibers were dry formed to a mat, which
was prepressed with a pressure of about 1.5 MPa and hot pressed for 5-6 minutes at
170°C. The board thus manufactured was tested on strength, ISO-brightness and formaldehyde
content (perforator value). The relative energy consumption for the different batches
was also measured. The results were as follows:
| Property |
Reference batch |
Na2SO3 batch |
NaHSO3 batch |
| Bending strength MPa |
38.4 |
43.8 |
40.0 |
| Internal bond strength MPa |
1.8 |
2.1 |
2.0 |
| ISO-brightness % |
24 |
26 |
26 |
| Formaldehyde content mg CH2O/100 g |
27 |
20 |
18 |
| Relative energy consumption |
1.0 |
0.95 |
0.95 |
[0018] The results confirm the technical effects stated above.
[0019] The invention, of course, is not restricted to the embodiments described above, but
can be varied within the scope of the invention idea as defined by the appendant claims.
1. A method of manufacturing fiberboard according to the dry method starting with lignocellulose-containing
material which is disintegrated, glued, dried, formed to a web and pressed,
characterized in that the material, before it is finally disintegrated is treated with an impregnation
solution containing fiber surface activating chemicals in an amount of 1-30 kg/ton
fiber material, expressed as Na2SO3, and preheated to 150-200°C whereby the pH value is kept within 2-12 and that the
disintegration is performed with an energy input of 50-400 kWh/ton fiber material.
2. A method as defined in claim 1,
characterized in that the fiber surface activating chemicals are of a type affecting the lignin.
3. A method as defined in claim 2,
characterized in that the impregnation solution contains Na2SO3 and/or NaHSO3.
4. A method as defined in anyone of claims 1-3,
characterized in that the disintegrated material first is glued and thereafter dried before it
is formed to a web.
5. A method as defined in anyone of claims 1-3,
characterized in that the disintegrated material first is dried and thereafter glued before it
is formed to a web.
1. Verfahren zur Herstellung einer Faserplatte nach den Trockenverfahren, ausgehend von
Lignozellulose enthaltendem Material, das zerkleinert, geleimt, getrocknet und zu
einem Flächengebilde geformt und verpreßt wird, dadurch gekennzeichnet, daß das Material,
bevor es schließlich zerkleinert wird, mit einer Imprägnierlösung behandelt wird,
die die Faseroberfläche aktivierende Chemikalien in einer Menge von 1-30 kg/Tonne
Fasermaterial, ausgedrückt als Na2SO3, enthält, und auf 150-200°C vorerhitzt wird, wobei der pH-Wert zwischen 2-12 gehalten
wird und daß die Zerkleinerung mit einer Energiezufuhr von 50-400 kWh/Tonne Fasermaterial
ausgeführt wird.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die die Faseroberfläche aktivierenden
Chemikalien von einer Art sind, die Lignin beeinflußt.
3. Verfahren nach Anspruch 2, dadurch gekennzeichnet, daß die Imprägnierlösung Na2SO3 und/oder NaHSO3 enthält.
4. Verfahren nach einem der Ansprüche 1-3, dadurch gekennzeichnet, daß das zerkleinerte
Material zuerst geleimt und anschließend getrocknet wird, bevor es zu einem Flächengebilde
geformt wird.
5. Verfahren nach einem der Ansprüche 1-3, dadurch gekennzeichnet, daß das zerkleinerte
Material zuerst getrocknet und anschließend geleimt wird, bevor es zu einem Flächengebilde
geformt wird.
1. Procédé de fabrication de panneau de fibres selon la méthode sèche en partant d'un
matériau contenant de la lignocellulose qui est désintégré, collé, séché et conformé
en un ruban puis comprimé, caractérisé en ce que le matériau, avant qu'il soit finalement
désintégré est traité avec une solution d'imprégnation contenant des agents chimiques
d'activation de la surface des fibres en une quantité de 1-30 kg/tonne du matériau
en fibres, exprimée en tant que Na2SO3 et, préchauffé jusqu'à 150-200°C de manière que la valeur du pH soit maintenue entre
2-12 et en ce que la désintégration est effectuée avec une admission d'énergie de
50-400 KWh/tonne de matériau en fibres.
2. Procédé selon la revendication 1, caractérisé en ce que les agents chimiques d'activation
de la surface des fibres sont d'un type affectant la lignine.
3. Procédé selon la revendication 2, caractérisé en ce que la solution d'imprégnation
contient Na2SO3 et/ou NaHSO3.
4. Procédé selon l'une quelconque des revendications 1-3, caractérisé en ce que le matériau
désintégré est tout d'abord collé et ensuite séché avant d'être conformé en un ruban.
5. Procédé selon l'une quelconque des revendications 1-3, caractérisé en ce que le matériau
désintégré est tout d'abord séché et ensuite collé avant d'être conformé en un ruban.