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CEPATEC AB
Knut-Erik Persson

WOOD FIBRE
Page
1. Physical properties of wood 1

2.1 Chemical composition of wood 10

2.2 Structure of fibre 24

3. Interfibre bonds 28

1. Physical properties of wood

The stem of the tree has three


important functions

− to carry the crown


− to be a piping for liquid
transports
− to store nutrients.

Fig. 1. Pine forest. (1-001.tif)


The exterior and the interior
bark contain dark-coloured
material, which can be difficult to
remove during the cooking and
the bleaching process.

The high content of e.g. silicon


easily leads to crust problems at
the production of pulp.
Fig. 2. Cut up of trunk.
Birch bark contains a large amount Marking of the exterior and
of extractives that can be very interior bark. (1-002.tif)
difficult to dissolve and wash off.

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In the border between the interior bark


and wood there is a thin layer called
cambium. Here the tree grows by cell-
division.

Fig. 3. Cut up of trunk.


Marking of cambium.
(1-003.tif)

Inside the cambium there is the


sapwood, which is the youngest and
most living part of the tree trunk. The
necessary liquid transport from the root
to the crown of the tree goes through this
layer.

Fig. 4. Cut up of trunk.


Marking of the sapwood.
(1-004.tif)

The interior part of the trunk consists of


heartwood. This type of wood is formed
when the tree is about 20 years old.
Heartwood grows out through the oldest
sapwood, which dies and is filled with
resin. In hardwood there is no heart-
wood.

At the centre of the trunk there is the pith Fig. 5. Cut up of trunk.
Marking of the heartwood.
or medulla, a living nutritious substance, (1-005.tif)
from which the tree grows in height.

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Wood mainly consists of wood cells, fibres, which may be of


different types in softwood and in hardwood. The pictures show
where the fibres are located in the different types of wood.

1
1

2 2

Fig. 6. Softwood. Fig. 7. Hardwood.


1. Tracheids 1. Libriform cells
2. Parenchyma cells 2. Parenchyma cells
(1-006.tif) (1-007.tif)

Regarding fibre dimensions and fibre properties in general terms,


there are tracheids when it concerns softwood and libriform cells
when it concerns hardwood; "real paper making fibres”.

The most frequent species of trees in Scandinavia is spruce, pine


and birch.

The fibres are different regarding appearance and size but the
similarity is that they have sharp tips and an interior cavity, called
lumen.

Spruce

Pine

Birch

1 mm

Fig. 8. Sketch. Fibres in spruce, pine and birch. (1-008.tif)

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The fibres give the tree


trunk its mechanical
strength. In softwood, the
tracheids take care of the
necessary liquid
transports. To be able to
do this, the tracheids are
connected to each other
through pits, which are
Fig. 9. Microscope photo. Unbleached
recesses in the fibre wall. softwood sulphate. (1-009.tif)

Parenchyma cells are much smaller. This type of fibre is called


”fines” when it is found in pulp. The fines may deteriorate the
dewatering capacities and cause problem later during the paper
making process. Another disadvantage could be high content of
wood resin.

At the heartwood forming the pits in the fibre


wall of the tracheids will close. This may also
happen if the wood dries too quickly,
particularly sprucewood.

At the production of chemical pulp the cooking


liquor must have the ability of penetrating the fibre
wall. Heartwood and very dry sprucewood may
cause problems.

Fig. 10. Closed pit in heart-wood of


pine. (Pekka Saranpää)
(1-010.tif)

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It is the properties of the tracheids and libriform cells which


determine the mechanical strength development of the finished
pulp.

The average length of a


tracheid is, in Swedish
coniferous trees, 3–3.5 mm
and the diameter is
0.025–0.035 mm.

Fig. 11. Fibres in pine sulphate


pulp. (STFI) (1-012.tif)

Compared to the tracheids,


the libriform cells of birch
are considerably shorter
and thinner. The average
length is 1.1 mm and the
diameter is 0.022 mm.
Another difference is that
the thickness of the fibre Fig. 12. Fibres in birch sulphate
wall is smaller. pulp. (STFI) (1-013.tif)

Libriform-
cells.

Vessel cells.

Fig. 13. Liberated libriform and vessel cells in a birch sulphate pulp. (STFI)
(1-011.tif)

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The libriform cells have no


pits. In hardwood the liquid is
transported in special cells,
called vessel cells.

The vessel cells are vital to


transport the large quantities
of liquid which are a
consequence of the excessive
evaporation from the leaf
Fig. 14. Vessel cells in birch-
surfaces.
wood. (STFI) (1-014.tif)

The vessels are long pipes with


thin walls, which easily break at
the pulping process.

Fig. 15. Vessel cells in birch


sulphate pulp. (STFI) (1-015.tif)

Another type of channels is to


be found in pine, but here the
channels are used for resin
storage; resin ducts or
channels.

Fig. 16. Resin channels in


pinewood. (STFI) (1-016.tif)

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The majority fibre types Fibre types in Spruce/Pine and Birch


are ”real fibres” in pine- (Percent by weight)
Tracheids Parencyma-cells
and sprucewood, while it Libriform-cells Vessels

is less in birchwood.
86%

98%
2%
9%

5%

Spruce/Pine Birch

Fig. 17. (1-017.tif)

The wood fibres are


cemented to each other with
the help of a binding
material, lignin. To some
extent, this substance can be
found in the fibre walls too.
The proportion of lignin in
the fibre wall is higher in
pine- and sprucewood than in
birchwood. Fig. 18. Illustration. Fibres in wood.
(1-018.tif)

The separate fibres are formed


like tubes and have an interior
cavity, called lumen. In a living
tree it is filled with water and
nutrients.

Fig. 19. Illustration of wood


fibres. (1-019.tif)

The thickness of the


fibre wall can differ if
the fibres are formed the Spring Summer
early, or during the late wood wood
growth period of the
year. Here, the names Fig. 20. Illustration. Spring and summer
used are spring wood and wood fibres. (1-020.tif)
summer wood.

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During the early growth


period much of the
nutriment intake is used for
production of new foliage
and new branches. After
this there is a period when
the main part of the
nutriments is used to form
fibres. Compared with the
spring fibres, the summer Fig. 21. Cross-section of pinewood with
fibres grow longer, the visible zones of spring and summer wood.
walls thicker and the (STFI) (1-021.tif)
diameter smaller.

The fibre length can vary depending on


the locality, climate, soils, etc. Slow
growth develops long fibres.

Besides, a slow growth produces fibres


with an, on average, thin fibre wall. The
fibre becomes slim and is because of that
easy to form. The weight of each
separate fibre is reduced, meaning that
the number of fibres at a given weight of
wood will increase. Fig. 22. South Swedish
forest. (1-022.tif)

The fibre length varies Fibre length vs. age of the tree (Spruce /Picea abies)
Fibre length mm
within the tree trunk. 4,0

The fibre length in the 3,5


3,0
exterior part of the trunk 2,5
is always greater than in 2,0
the interior part. 1,5
1,0

Full fibre length is 0,5


0,0
not reached until after 0 5 10 15 20 25
Year
about 15 years.
Fig. 23. (1-023.tif)

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A slow growth means that the


average felling age increases and
accordingly also the average fibre
length of a fallen stand of trees.

Fig. 24. Felling. (1-024.tif)

A slower growth develops

− an increased fibre length

− a slimmer and by that a more pliable fibre

− lighter fibres and by that a larger number of these in a given


pulp quantity.

The Nordic softwood trees grow slowly. Thus, the raw material is
well suited for production of paper with good mechanical strength
properties.

Sawmill chips mainly


originate from the exterior
parts of the tree trunk.
They have a long fibre on
average and are therefore a
good raw material for pulp
production.
Fig. 25. Wood chips from sawmill.
(1-025.tif)

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2.1 Chemical composition of wood

The wood mainly consists of


Pinewood.
cellulose, hemicellulose and (1-026a.tif)
lignin.

Birchwood.
(1-026b.tif)
Fig. 26. Pine and birchwood.

In spruce, pine and Chemical composition of wood


birch, the content of 50

cellulose is almost the 40


42 41 41

same. In birch the 34

content of hemi- 30 28 28 27 27

cellulose is higher than 20


21

in spruce and pine and


the content of lignin is 10
4 4
Spruce

correspondingly lower. 0
3 Pine
Birch

Cellulose Hemicellulose Lignin Extractives

Fig. 27. (1-027.tif)

Cellulose, hemicellulose and lignin are all composed of carbon,


hydrogen and oxygen.

Carbon, hydrogen and oxygen are called elements; atoms.

The atoms create molecules. The molecules then are building blocks
in the connected large molecules, polymers, forming different
types of wood material.

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The separate building elements are called monomers (mono=


=one/single). The chemical reaction connecting the monomers is
called polymerisation, and the macro molecule achieved is called
polymer. (poly=many).

The polymers have properties quite different from the original


monomers.

Monomer
Polymer

Fig. 28. Illustration of


the termes monomer and
polymer. (1-028.tif)

The wood contains not only cellulose, hemicellulose and lignin but
also group of substances, called extractives or wood resin.
Quantity and chemical composition vary between different types of
wood. Here too, the atoms carbon and hydrogen and in most cases
oxygen are included.

Cellulose

The cellulose molecule is composed of a great number of glucose


molecules that have connected and formed a long chained poly-
saccharide. Glucose is the same as dextrose and is an example of a
”monosaccharide”. The product is soluble in water.
H OH

Fig. 29 shows a glucose molecule. OH C C OH


Carbon=C
The molecule is composed OH H
of carbon, hydrogen and oxygen
C H C Oxygen=O
atoms and has a ring-shaped H C O H
Hydrogen= H
structure. CH2OH

Fig. 29. Glucose molecule.


(1-029.tif)

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In cellulose the glucose molecules have connected to a chain that


may contain more than 10 000 glucose molecules.

A number of monomers has formed a polymer, which has quite


different properties compared with the original monomers.
Here, a very important difference is that the polymer formation, the
cellulose, is completely insoluble in water.

H OH

C
OH C OH
Glucose
Glukos
OH H
C H C

H C O H

CH2OH

Cellulose
Cellulosa

Fig. 30. Illustration showing how glucose molecules build up the


cellulose. (1-030.tif)

The OH groups on the glucose


molecules bind to each other by
an attraction between hydrogen
and oxygen atoms, placed on the
opposite molecules; the cellulose
molecules bind to each other
with hydrogen bonds.
Fig. 31. Illustration showing how
two cellulose molecules bind to
each other with hydrogen bonds.
(1-031.tif)

The cellulose molecules connect


and form small, elongated
units, micro fibrils.

Fig. 32. Illustration. Micro fibril.


(1-032.tif)

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The micro fibrils then connect and


form larger fibrils.

Fig. 33. Illustration. Fibril.


(1-033.tif)

The cellulose gives the fibre wall its strength and structure. The
task of the cellulose fibrils in a fibre wall can be compared with the
reinforcement bar in concrete.

At all production of paper pulp the


goal is to include cellulose
in the finished product in
an original form.

Fig. 34. Paper pulp.


(1-034.tif)

A chemical influence may break down the molecule chains and


make them shorter. Short molecule chains give the fibrils lower
mechanical strength and weaker fibre walls.

Fig. 35. Illustration. Broken


cellulose chain.
(1-035.tif)

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The smaller chain fragments that are broken the more their
properties will resemble the properties of the original monomers.
Consequently, some of the small chain fragments created during
the cooking process may be dissolved or dispersed in the cooking
liquor. The wood yield will decrease.

The cellulose molecules are normally


well arranged and closely packed
together. The distance between the
molecules becomes so small that no
water can penetrate.
Fig. 36. Illustration.
Closely packed cellulose
chains. (1-036.tif)

There are some small areas where this


order is broken. In these areas the
cellulose molecules are not so closely
packed together. The distance between
the molecule chains becomes larger and
water can penetrate.
Fig. 37. Illustration.
Disordered cellulose
chains. (1-037.tif)

However, when the distance between the cellulose molecules is that


small, a very limited amount of water can penetrate the chains. A
fibre wall built of only cellulose would therefore swell very little in
water.

The cellulose is uncoloured (white).

Hemicellulose

Hemicellulose is, like cellulose, a polysaccharide consisting of


different monosaccarides. The composition can vary between
different types of wood.

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The number of monomers in a


hemicellulose chain is
considerably less than in
cellulose and therefore the chain
becomes shorter. Another
difference is that the hemi-
cellulose chain is branched.

Fig. 38. Illustration. Branched


cellulose chain. (1-038.tif)

The molecule chains in the


hemicellulose are not as well-
arranged as in the cellulose. This,
and the fact that they are branched,
make them pack less closely.

Fig. 39. Illustration. Hemicellulose


chains. (1-039.tif)

Water can penetrate the molecule chains.


The hemicellulose layer swells greatly
and develops a gel-like character.

Fig. 40. Illustration showing how


the water has penetrated the
hemicellulose chains. (1-040.tif)

The role of the hemicellulose in the fibre wall is, together with the
lignin, to keep the small fibrils together. The function resembles
that of concrete in a concrete construction.

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A fibre wall built from both cellulose


and hemicellulose will have a more open
structure compared with a fibre wall of
cellulose fibrils, only. This open
structure allows the fibre wall to absorb
water and to swell.

Fig. 41. Illustration. Chemical


fibre. (1-041.tif)

The fibre wall becomes soft and the


fibres will form well in the sheet.

Fig. 42. Illustration. Soft pliable


fibres. (1-042.tif)

At the production of Chemical composition


(Percent by weight of the original dry substance in
chemical pulp, the chains Composition %
the wood).

of the hemicellulose may 50

40
42

be broken down in the 30 27


34 34

same way as the cellulose


24

20

chains. Actually, this risk 10


4
11

1,5
9

is considerably greater
0,4 0,1 0,05
0
Wood After cooking After bleaching

than with cellulose


Cellulose Lignin
Hemicellulose Extractives

chains. Fig. 43. (1-043.tif)

In practice, the risk of breaking down the hemicellulose determines


how far the removal of the lignin can be driven during the cooking
process.

The hemicellulose, like the cellulose, is uncoloured (white).

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Lignin

In comparison with cellulose and hemicellulose the lignin molecule has


quite different structural elements. The molecule is built like a three-
dimensional network. The exact composition can vary.

The main part of lignin is located


to the connective layer, the
middle lamella, which binds the
fibres in the wood, but some of it
is found in the fibre wall.

The lignin can be made water


soluble by letting it react with acid
or alkaline sulphur compounds at a Fig.44. Illustration. Wood fibres.
high temperature. (1-044.tif)

The chemical reactions during


the cooking process, which
transfer lignin to a soluble
form, can not be done without
also influencing the other wood
components. The more the
cellulose and the hemicellulose
chains are broken down, the
lower the fibre strength becomes.

Fig. 45. Pulp digester.


(1-045.tif)

To avoid this, there will always


be a certain part of lignin
remaining in the pulp when it
leaves the digester and enters the
washing stage.

Fig. 46. Washing filters in a pulp


mill. (1-046.tif)

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The conditions during the


bleaching are more lenient to the
cellulose and the hemicellulose
than during the previous cooking
and the risk in breaking down the
molecules is not likely. So, if
it is desirable to remove the rest
of the lignin, it has to be done in
a bleaching stage.

Fig. 47. Sheets made of pulp, taken


before, during and after the
bleaching. (1-047.tif)

When heated, the lignin will


soften. When the fibres are
separated with mechanical
methods this property is
utilised.

Fig. 48. Illustration. Chemically


liberated fibres. (1-048.tif)

The lignin has a water repellent (hydrophobic) character. This


property may be changed during the pulping process, but the quantity
of water that can be absorbed will still be very low.

In mechanical pulp, the fibre


surface is to a great extent
covered with lignin and the
number of OH groups is low.
Thus, if there is lignin on the
contact surfaces between the
fibres in a paper web, the
number of hydrogen bonds
between the fibres will be
low. The fibres bind weakly Fig. 49. Illustration. Fibre surface,
to each other. partially covered by lignin, with few
OH groups. (1-049.tif)

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Natural lignin is slightly


yellow. When exposed to
sunlight the lignin becomes
deep yellowish to brownish.

Fig. 50. Parts of a paper page yellowed


in strong sunlight. (1-050.tif)

Cooking wood in alkaline


conditions gives dark
coloured reaction
products and the pulp
leaving the digester is
dark brown.

Also when cooking in


acid conditions there is a
certain dark dyeing of the
lignin.

Fig. 51. Sheet produced of pulp


taken after washing. (1-051.tif)

A large content of lignin in the finished pulp gives a lower strength and,
concerning chemical pulps, also a considerably lower brightness.

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Extractives, wood resin

Chemically, extractives consist of

• fatty and resin acids

• different compounds of fatty and resin acids with glycerol or


other alcohols

• free higher alcohols

• hydrocarbon compounds (waxlike material).

The free higher alcohols and the hydrocarbon compounds are


sometimes called unsaponifiable. This means that they can not, in
the same way as the other components, be transferred to a soluble
form (saponified) at the alkaline conditions during a sulphate
cooking.

The total quantity of 50


Chemical composition of wood
extractives is higher 42 41 41

in pinewood than in 40
34

sprucewood. 30 28 28 27 27

21
20

10
Spruce
3 4 4
Pine
Birch
0
Cellulose Hemicellulose Lignin Extractives

Fig. 52. (1-052.tif)

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The composition of Chemical composition of the resin components


(Laman 1979)
the extractives in 100

pinewood differs from 75

that of sprucewood.
The high content of 50

resin acids and the 25


small quantity of
unsaponifiable makes 0
Pine Spruce Birch
the pine resin easier to Unsaponifiable Fatty acids
Fatty acid esters Resin acids
dissolve in the
Fig. 53. (1-053.tif)
cooking chemicals.

Vertical resin
channels.

Horizontal resin
channels.
In pine most resin is
located to the special
resin channels that run
vertically in the wood.
The location in channels
makes the pine resin
easy to access for the
cooking chemicals.

Fig. 54. Softwood, schematically


reproduced structure. (STFI)
(1-054.tif)

The sprucewood resin is mainly located in narrow, horizontal


channels. The deposition makes the liquor penetration during the
pulping process more difficult than in resin channels. Consequently,
the resin content in a spruce pulp is in most cases higher than in
pine pulp.

It is easier to dissolve and remove the pine resin than the spruce
resin during the pulping process.

The resin content in bark and branches is larger than in trunk


wood. A good barking makes it easier to produce a pulp with a low
resin content.

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The resin content in 50


Chemical composition of wood
birchwood may be on 42 41 41

the same level as in 40


34
pinewood. 30 28 28 27 27

21
20

10
Spruce
4 4
3 Pine
Birch
0
Cellulose Hemicellulose Lignin Extractives

Fig. 55. (1-055.tif)

The composition Chemical composition of the resin components


of the birch resin 100
(Laman 1979)

differs from that


of the softwood. 75

50
The content of
free resin acids 25
and fatty acids is
lower and the 0
Pine Spruce Birch
content of Unsaponifiable Fatty acids

esterified fatty Fatty acid esters Resin acids

acid and un-


saponifiable is higher*.
Fig. 56. (1-056.tif)

The unfavourable chemical composition of the birch resin makes it


difficult to dissolve. But there is also a mechanical reason, why it is
exceptionally difficult to remove the birch resin during the pulping
process.

i
(Esters mean reaction products between fatty acids and alcohol.)

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In birchwood most of the resin


is located in the thin paren-
chyma cells. The cooking
liquor has difficulties
penetrating the narrow
channels.
Parenchyma
cells.

Fig. 57. Hardwood, schematically


reproduced structure. (1-057.tif)

The resin located in the


birch bark has a still more
unfavourable composition.
Therefore, a good barking is
necessary for the production
of a birch pulp with a low
resin content.

Fig. 58. Birchwood. (1-058.tif)

If birch chips are stored in a


chip pile the wood resin is
chemically transformed. The
fatty acid esters break down
into free acids and alcohols.
This process increases the
solubility of the wood resin.

Fig. 59. Chip pile. (1-059.tif)

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Unsaponifiable resin will not be influenced during the storage.


When producing birch sulphate pulp, the unsaponifiable resin
therefore has to be transformed into a soluble form by addition of
softwood resin (pine oil) to the digester. In spite of that, the resin
content in birch pulp is often higher than in pine and spruce pulp.

High content of wood


resin in the paper pulp
deteriorates paper
strength and brightness
and causes dots and
deposits.

Fig. 60. Resin particles in a paper


sheet. (40 times.) (1-060.tif)

At the production of chemical pulp a larger quantity of the wood


resin is removed during the pulping process. More resin is removed
if the pulp is cooked at alkaline conditions than at acid conditions.

Mechanical pulps contain a large quantity of the original wood


resin.

2.2 Structure of fibre

Looking at the fibre from a physical perspective, it can be seen that


it is built up of a number of cell layers with different properties.

L= Lumen.

S3 = Interior layer in the secondary


wall.
S2 = Middle layer in the secondary
wall.
S1= Exterior layer in the secondary
wall.

P= The primary wall.


Fig. 61. The different layers
of the wood fibre. The M= Middle lamella.
direction of the cellulose
fibrils in the different layers
is marked. (1-061.tif)

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Primary wall

The exterior layer, the primary wall,


is thin, 0.1−0.3 µm.
Primary wall
The lignin content is high. The
capacity to swell in water is low.
The number of OH groups on the
surface is low and therefore the
capacity to form hydrogen bonds is Fig. 62. (1-062.tif)
limited. Because of that, to be able
to form inter fibre bonds the primary wall must be removed.

Secondary walls (S 1, S2, S3)

The exterior layer, S 1, of the three Exterior secondary


secondary walls is very thin and has wall. S1
a low swelling capacity. The
thickness varies between
0.1 and 0.2 µm.

Fig. 63. (1-063.tif)

The number of OH groups on the surface of the S 1 layer is low.


Thus, S1 has a limited capacity to form hydrogen bonds. The layer
also prevents the inner part of the fibre wall from absorbing water
and to swell. To counteract this, during paper making the S 1 layer
has to be split up or partially removed.

The middle layer of the secondary Middle


walls, S2, is much thicker than the secondary
outer layers P and S1. This layer is wall,S2.
about 80% of the fibre weight and
it will have a conclusive influence
on the properties of the finished
pulp. The thickness varies between
1 and 5 µm.
Fig. 64. (1-064.tif)
The number of OH-groups on
the surface of the S2 layer is high.

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In contrast to the other layers, the fibrils in S 2 are parallelly


orientated, in a main direction, which is the same as the
longitudinal direction of the fibre. Such an orientation favourably
influences the strength and stiffness of the fibre.

A low growth increases the lengthwise orientation of the fibrils.


Thus, another positive effect of a slow growth can be noted.

The S2 layer has a good swelling capacity. A release of this layer


makes the fibre wall soft. More intimate contact between the fibres
in a paper web is developed and the ability to form strong interfibre
bonds is increased.

The fibre layer is mainly built up of cellulose and hemicellulose.


The content of hemicellulose can vary in the finished pulp, but
generally it is higher than in the exterior layers P and S 1. The more
hemicellulose, the more the fibre wall will swell.

The interior layer of the Interior secondary wall, S3


secondary walls, S3, which
borders to the inner cavity of
the fibre, lumen, has a
thickness of about 0.1 µm and
thus it is very thin. The layer
S3 is sometimes also
referred to as the ”tertiary
wall”.
Fig. 65. (1-065.tif)

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Lumen Lumen

In the interior of the fibre there is


a cavity, lumen.

Fig. 66. (1-066.tif)

When paper is produced, the


fibres will be flattened and the
lumen will more or less disappear.
The fibres will then get a band-
like appearance (especially the
thin walled spring wood fibres).

Fig. 67. Illustration. Flattened


fibres. (1-067.tif)

Middle lamella

The adhesive zone located Middle lamella


between the primary walls of
adjacent cells is termed the middle
lamella. Chemically it consists
primarily of lignin. Normally the
lignin is hard and brittle but can
be softened with the help of heat
or chemicals. Fig. 68. (1-068.tif)

The capacity of lignin to absorb water is low. Besides, the number


of free OH-groups in lignin is low. Consequently, lignin, on the
fibre surfaces and inside the fibre wall weakens the bonds between
the fibres in a paper sheet.

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At all pulp production the fibres must be processed in such a way


that the lignin does not cover the entire fibre surfaces.

3. Interfibre bonds

When producing paper the reactions between the fibres and water
are of great importance. Paper making without water is completely
impossible.

The concept of hydrogen bonds is explained in a previous


description.

How paper fibres bind to


each other has been of
special interest to the experts
for a long time. A number of
different theories are listed
and today there seems to be a
common support for the
thesis that the hydrogen
bonds are the dominating
uniting power. Fig. 69. Illustration. Fibres in a paper
web. (1-069.tif)

The water molecules, closest to the fibre surfaces, will be attracted


by the OH groups on the fibre surfaces; bound water molecules.
The further away from the fibre surface the water molecule is, the
less attractive the force. Thus, as long as the paper web is wet
most of the water molecules can move freely; free water
molecules.

When the web dries, firstly the free water


molecules will disappear.

The adjacent fibre surfaces will then be attracted


to each other through the hydrogen bonds
formed between the water molecules bound to
OH-groups.

Fig. 70. Illustration. Water molecules


binding to the OH groups on the fibre
surfaces. (1-070.tif)

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After a while even part of the bound water will


disappear and more and more hydrogen bonds
directly between the OH groups on the fibre
surfaces are formed. The more such direct
hydrogen bonds, the stronger the fibres will bind
to each other.

Fig. 71. Illustration.


Hydrogen bonds
between fibre
surfaces. (1-071.tif.)

How many hydrogen bonds that can be formed, depends on the


amount of OH groups on the fibre surface. The necessary OH
groups are to be found in cellulose and hemicellulose but hardly-
in lignin. Thus fibres, surrounded by lignin, can not develop
strong hydrogen bonds.

Consequently, the amount of OH


groups on the surface, depends on
the kind of pulp which is used. In
chemical pulps, refined until the
primary wall and the outer
secondary wall S1 have split up, the
amount of OH groups is high.

Fig. 72. Illustration. Refined


fibre. (1-072.tif)

In mechanical pulp, with a lot


of lignin on the fibre surfaces, the
amount of OH groups is, however,
considerably lower.

Fig. 73. Illustration. Mechanical


fibre. (1-073.tif)

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To be able to create many


hydrogen bonds the direct contact
area between the fibres must be as
large as possible. The softer the
fibre wall is, the easier the fibre
forms and the direct contact
surface between the fibres
increases.

Fig. 74. Microscope photo. Liner.


(1-074.tif)

The softness of a fibre wall depends on the capacity to absorb


water. If chemical fibres are used, the fibres are refined to increase
the water absorbency.

During the refining:

− The primary wall and the


outer secondary wall, S1
will be broken up. Then the
surface of the swelling
disposed fibrewall, S2, will
be released (Exterior
fibrillation).
Fig. 75. Illustration. Refined
fibre. (1-075.tif)

− The fibre wall, S2 will be split up


(Interior fibrillation).

Fig. 76. Illustration. Decomposed


fibre wall. (1-076.tif)

The exterior- and interior fibrillation make it easier for the water
to penetrate into the fibre wall. The fibre will be soft and pliable.

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