FIBRE COMPOSITION, USE OF SAID COMPOSITION AND ARTICLE COMPRISING SAID COMPOSITION

FIELD OF THE INVENTION

The present invention relates to a high-strength fibre composition comprising fibres up to 7 mm long with a viscosity of between 10 and 20 cP. The fibres present in said composition are distributed according to the length thereof, thereby guaranteeing high strength. The fibre composition of the invention can also be redispersible.

The use of the fibre composition according to the invention and an article comprising said composition are also disclosed.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a U.S. National Stage Entry of International Application No. PCT/BR2019/050530, filed Dec. 10, 2019, which claims priority to Brazilian Application No. BR 10 2018 075755, filed Dec. 11, 2018, the contents of both of which are hereby incorporated by reference in their entireties.

BACKGROUND OF THE INVENTION

Functional and process additives are commonly used in the paper and textile industry to improve material retention, sheet strength, hydrophobicity, among other features. Water-soluble synthetic polymers or emulsifiers, resins derived from petroleum or modified natural products, and cellulose derivatives obtained by dissolving cellulose pulp are usually used as additives.

On the other hand, materials using recyclable natural fibres have received attention recently due to the growing environmental awareness as a substitute to petroleum resources, as described in document US 2015/0225550. According to said document, among the natural fibres, a cellulose fibre having a fibre diameter of 10 to 50 μm, particularly a cellulose fibre derived from wood (pulp), has been widely used for this purpose, mainly as a paper product.

In view of the environmental and technical context presented, natural fibre products that have, among other advantages, high strength, redispersibility and fibre size that facilitates the easy bond between the fibres are sought.

There are state of the art documents which disclose compositions containing natural fibres. State of the art documents U.S. Pat. No. 9,856,607, WO 2013/183007, US 2015/0225550 and BR 11 2015 003819 0, for example, disclose cellulose fibre compositions (natural fibres) having different physical chemical properties and applications. However, conventional refining processes for fibre refining of cellulose fibre compositions are carried out with low energy levels, as described in document BR 11 2015 003819 0. The use of low energy levels does not guarantee the appropriate distribution of fibre sizes in order to provide high strength to the composition.

The present invention differs from all cited documents mainly by the distribution by fibres length. Fibre length and distribution present in the fibre composition of the invention allows an interaction between the fibres to occur, promoting better interlacing and greater bonding strength, which affects the composition's behavior and mechanical properties. Additionally, the viscosity range of the present invention and the fact that it is redispersible allow a better fibre availability to carry out their bonds, thus promoting better mechanical properties.

The present invention, by presenting these characteristics, when added to the paper sheet, for example, promotes greater wet or dry strength, even if applied in small quantities. Thus, a solution different from those already existing in the state of the art for an elevated strength fibre composition is described herein.

Additionally, fibre refining of the cellulose fibre compositions of the invention is carried out with a high level of energy. This guarantees the appropriate distribution of the fibre sizes, which favors the interaction between the fibres and improves their physical-mechanical properties.

There is still a need in art for compositions that, in addition to presenting high strength, also present a viscosity that allows the good redispersibility of the composition. As explained, redispersibility allows fibres to be more available to make the high number of bonds, resulting in high strength.

Therefore, the technical problem that the present invention solves is the difficulty of maintaining the wet sheet strength during the process and after drying, and to form strong bonds and interlaces between the fibres for this purpose. Thus, with the fibre size distribution of the fibre composition of the invention, there is a gain in (wet and dry) sheet strength, as the fibre arrangement and distribution favors interlacing and strong bonds.

SUMMARY OF THE INVENTION

A fibre composition is described herein comprising fibres having a length equal or inferior to 7 mm and a viscosity between 10 and 20 cP.

The fibre composition of the invention comprises the following fibre length distribution, based on dry weight:

i. 0 to 0.2 mm: 1.7 to 33.7%, preferably 16.5%;

ii. 0.2 to 0.5 mm: 12.0 to 44.0%, preferably 29%;

iii. 0.5 to 1.2 mm: 22.0 to 83.0%, preferably 52%;

iv. 1.2 to 2.0 mm: 0.10 to 3.8%, preferably 1.6%;

v. 2.0 to 3.2 mm: 0.06 to 0.10%; and

vi. 3.2 to 7.0 mm: 0.03 to 0.30%, preferably 0.13%.

In one aspect of the invention, the fibres of the composition are natural fibres.

In some embodiments of the invention, natural fibres are selected from cellulose fibres, cellulose fibre derivatives, wood derivatives or mixtures thereof. In a preferred embodiment, the natural fibres are cellulose fibres.

Natural fibres of the composition can be virgin, recycled or secondary natural fibres.

In one aspect of the invention, the natural fibres of the composition are obtained via kraft process. In a preferred embodiment of the invention, the natural fibres are kraft cellulose fibres.

Natural fibres of the composition can be whitened, semi-whitened or not whitened; they may comprise lignin and/or hemicellulose; and can be long or short.

In one embodiment of the invention, the fibre composition presents a dry content in the range between 3 and 70%. In a preferred embodiment, the fibre composition presents a dry content in the range between 20 and 50%.

In one aspect of the invention, the fibre composition is redispersible.

The fibre composition of the invention comprises 10,000 to 25 million fibres/g of the composition.

In one embodiment of the invention, the fibre composition has a fibre width of between 10 and 25 μm.

In one embodiment of the invention, the fibre composition has a polymerization degree of between 1,000 and 2,000 units.

In one embodiment of the invention, the fibre composition has a tensile index of between 70 and 100 Nm/g; elongation of between 2 and 5%; Scott Bond of between 180 and 300 ft.lb/in²; and bursting index of between 4 and 9 KPam²/g.

In one embodiment of the invention, the fibre composition has a body of between 1 and 2 cm³/g; Taber stiffness of between 0.3 and 5%; and wall thickness between 3 and 6 μm.

In one embodiment of the invention, the fibre composition has an opacity of between 30 and 80%.

In one embodiment of the invention, the fibre composition has a fines content of between 10 and 90% and fibrillation of between 5 and 20%.

In one embodiment of the invention, the fibre composition has Brookfield Viscosity at 1% of between 92 and 326 cP.

In one aspect of the invention, the fibre composition, when redispersed, presents at least 70% of the Brookfield Viscosity initial value at 1%.

In one aspect of the invention, the fibre composition is used in paper manufacturing, fibre cement, thermoplastic composites, inks, varnishes, adhesives, filters and wooden panels.

The use of the fibre composition of the invention for paper manufacturing, fibre cement, thermoplastic composites, inks, varnishes, adhesives, filters and wooden panels is also described herein.

An article comprising the fibre composition of the invention is also disclosed.

In one embodiment of the invention, the article is a paper, a fibre cement, a thermoplastic composite, an ink, a varnish, an adhesive, a filter or a wooden panel. In a preferred embodiment of the invention, the article is a paper.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 01 depicts a length graph, in mm, of the formulations from example 1 of the invention.

FIG. 02 depicts a fibres width graph, in μm, of the formulations from example 1 of the invention.

FIG. 03 depicts a fines content graph, in %, of the formulations from example 1 of the invention.

FIG. 04 depicts a graph of the number of fibres per mass from the composition, in millions/gram, of the formulations from example 1 of the invention.

FIG. 05 depicts a viscosity graph, in cP, of the formulations from example 1 of the invention.

FIG. 06 depicts a Brookfield viscosity (1%) graph, in cP, of the formulations from example 1 of the invention.

FIG. 07 depicts a polymerization degree graph, in units, of the formulations from example 1 of the invention.

FIG. 08 depicts a tensile graph, in Nm/g, of the formulations from example 1 of the invention.

FIG. 09 depicts an elongation graph, in %, of the formulations from example 1 of the invention.

FIG. 10 depicts a Scott Bond, in ft.lb/in², of the formulations from Example 1 of the invention.

FIG. 11 depicts a bursting index graph, in KPam²/g, of the formulations from example 1 of the invention.

FIG. 12 depicts a body graph, in cm³/g, of the formulations from Example 1 of the invention.

FIG. 13 depicts an opacity graph, in %, of the formulations from example 1 of the invention.

FIG. 14 depicts a Taber stiffness graph, in %, of the formulations from example 1 of the invention.

FIG. 15 depicts an air passage resistance (RPA) graph, in sec/100 mL air, of the formulations from example 1 of the invention.

FIG. 16 depicts a tensile graph, in Nm/g, of the formulations from example 2 of the invention.

FIG. 17 depicts an elongation graph, in %, of the formulations from example 2 of the invention.

FIG. 18 depicts a Scott Bond, in ft.lb/in², of the formulations from Example 2 of the invention.

FIG. 19 depicts a bursting index graph, in KPam²/g, of the formulations from example 2 of the invention.

FIG. 20 depicts an oSR graph of the formulations from example 2 of the invention.

FIG. 21 depicts a body graph, in cm³/g, of the formulations from Example 2 of the invention.

FIG. 22 depicts an air passage resistance graph, in sec/100 mL air, of the formulations from example 2 of the invention.

FIG. 23 depicts an opacity graph, in %, of the formulations from example 2 of the invention.

FIG. 24 depicts a fines content graph, in %, of the formulations from example 3 of the invention.

FIG. 25 depicts a fibres length graph, in mm, of the formulations from example 3 of the invention.

FIG. 26 depicts a fibres width graph, in μm, of the formulations from example 3 of the invention.

FIG. 27 depicts a graph of the number of fibres per mass from the composition, in millions/gram, of the formulations from example 3 of the invention.

FIG. 28 depicts a tensile index graph, in Nm/g, of the formulations from example 3 of the invention.

FIG. 29 depicts an elongation graph, in %, of the formulations from example 3 of the invention.

FIG. 30 depicts a bursting index graph, in KPam²/g, of the formulations from example 3 of the invention.

FIG. 31 depicts a Scott Bond, in ft.lb/in², of the formulations from Example 3 of the invention.

FIG. 32 depicts a body graph, in cm³/g, of the formulations from Example 3 of the invention.

FIG. 33 depicts an air passage resistance graph, in sec/100 mL air, of the formulations from example 3 of the invention.

FIG. 34 depicts a body graph, in cm³/g, of the formulations from Example 4 of the invention.

FIG. 35 depicts a tensile index graph, in Nm/g, of the formulations from example 4 of the invention.

FIG. 36 depicts a bursting index graph, in KPam²/g, of the formulations from example 4 of the invention.

FIG. 37 depicts a tear index graph, in mNm²/g, of the formulations from example 4 of the invention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides a fibre composition that presents elevated strength, good processability and redispersibility, for application on paper, fibre cement, thermoplastic composites, inks, varnishes, adhesives, filters and wooden panels.

The invention is based on a fibre composition comprising fibres of length equal or inferior to 7 mm and a viscosity between 10 and 20 cP.

In a preferred embodiment of the invention, the fibre composition has a viscosity of 13 cP.

The term “length”, as used herein, is defined as the largest fibre axis.

The term “viscosity” refers to the property which determines the fluid strength degree to a shear force.

The absolute (or dynamic) viscosity of a fluid is defined by the Newtonian equation:

η=τ/{dot over (y)}

wherein η is the absolute or dynamic viscosity, τ is the shear tension, and {dot over (y)} is the speed gradient dv/dz (v being the speed of a plane relative to the other and z the coordinate perpendicular to the two planes).

Kinematic viscosity is defined as the relationship between absolute viscosity and the fluid specific mass, both measured at the same temperature and pressure.

Specific mass, in turn, is defined as the mass-to-volume ratio.

The term “viscosity” as used herein refers to absolute viscosity.

The fibre composition of the present invention comprises the following fibre length distribution, based on dry weight:

i. 0 to 0.2 mm: 1.7 to 33.7%, preferably 16.5%;

ii. 0.2 to 0.5 mm: 12.0 to 44.0%, preferably 29%;

iii. 0.5 to 1.2 mm: 22.0 to 83.0%, preferably 52%;

iv. 1.2 to 2.0 mm: 0.10 to 3.8%, preferably 1.6%;

v. 2.0 to 3.2 mm: 0.06 to 0.10%; and

vi. 3.2 to 7.0 mm: 0.03 to 0.30%, preferably 0.13%.

This distribution by fibre length allows interaction between the fibres, affecting the behavior and mechanical properties of the composition that comprises them and guaranteeing their elevated strength. The fibres of the invention go through a refining using high energy levels (in the range of 700 to 1,200 kwh/t, preferably 1,000 kwh/t) and reach a size and length distribution different from that observed in the art. This causes the fibre interaction to be established by these sizes and distribution and, therefore, the behavior of physical-chemical and mechanical properties is defined according to these interactions.

Cellulose fibres have many hydroxyl groups in their structure, which makes it possible to easily establish hydrogen bonding. When microfibrilated or nanofibrilated, this bonding capacity increases due to fibre sizes, interlacing and contact surfaces. Therefore, it is important to have the fibre size distribution as defined in the present invention. This fibre size distribution leads to the necessary size balance to promote better composition strength.

Thus, the interactions provided by the fibre length distribution of the invention result in compositions having elevated strength, which is propagated to the final product added with said composition.

In one aspect of the invention, the fibres of the composition are natural fibres.

As used herein, the term “fibre” means an elongated particulate having an apparent length that considerably exceeds its apparent width.

The term “natural fibres”, as described herein, refers to cellulose fibres, cellulose fibre derivatives, wood derivatives or mixtures thereof.

In a preferred embodiment, the natural fibres are cellulose fibres.

Cellulose is the most abundant component of vegetables cell wall. The cellulose polymer empirical formula is (C₆H₁₀O₅)n, wherein n is the polymerization degree. This is one of the most abundant polymers on the planet. Cellulose is a long chain polymer and its repetition unit is called cellobiosis, which consists of two anhydroglucose rings joined by the β-1,4 glycosidic bond.

As used herein, the term “cellulose fibres” means fibres composed of or derived from cellulose.

In a preferred embodiment, the natural fibres are fibrillated cellulose fibres.

In a more preferred embodiment, the natural fibres are microfibrillated cellulose (MFC) fibres.

“Microfibrilated cellulose (MFC)” or “Microfibril” is a fibre or particle similar to a cellulose shank that is narrower and smaller than a pulp fibre normally used in paper applications.

Natural fibres can be virgin, recycled or secondary natural fibres.

As used herein, “recycled fibres” are non-smooth fibres that allow the fibres to separate from each other, resulting in less compact and more aerated compositions.

In one aspect of the invention, the natural fibres of the composition are obtained via kraft process. In a preferred embodiment of the invention, the natural fibres are kraft cellulose fibres.

The “kraft process” is the most dominant process in the paper and cellulose industry, in which wood chips are treated with a cooking liquor (a mixture of sodium hydroxide and sodium sulfide) over a temperature range of 150-180° C.

The composition natural fibres can be whitened, semi-whitened or not whitened; may comprise lignin and/or hemicellulose; and can be long (over 2 mm) or short (less than 2 mm).

Lignin is a phenolic polymeric material formed from phenolic precursors p-hydroxycinnamic alcohols, such as p-coumaryl alcohol, coniferyl alcohol and synaphyl alcohol through a metabolic pathway. Lignin and its derivatives are products of renewable origin that make up a green chemistry platform to replace raw materials of fossil origin, among other high value-added applications in various industries and segments.

The term “dry content”, as described herein, refers to the solid content of the composition.

In one embodiment of the invention, the fibre composition has Brookfield Viscosity at 1% of between 92 and 326 cP.

The expression “Brookfield Viscosity” refers to a viscosity measurement performed using a Brookfield Viscometer.

In one aspect of the invention, the fibre composition is redispersible. When redispersed, the composition presents at least 70% of the Brookfield Viscosity initial value at 1%.

The fibre composition of the invention comprises 10,000 to 25 million fibres per gram of the composition.

In one embodiment of the invention, the fibre composition has a fibre width of between 10 and 25 μm. In a preferred embodiment, the fibre composition has a fibre width of between 18 and 22 μm. In a more preferred embodiment, the fibre composition has a fibre width of 20 μm. Even with the refining and smaller fibre size, the fibre width does not change significantly.

The term “width”, as used herein, is defined as the smallest axis of the fibre.

In one embodiment of the invention, the fibre composition has a polymerization degree of between 1,000 and 2,000 units. In a preferred embodiment, the composition has a polymerization degree of between 1131 and 1710 units. In a more preferred embodiment, the fibre composition has a polymerization degree of 1248 units.

The polymerization degree (DP) is measured by the equation:

DP=1.75×[η],

wherein [η] is the intrinsic viscosity and is calculated using the following equation:

[η]=ηsp/(c(1+0.28×ηsp)),

wherein ηsp is the specific viscosity and c represents the cellulose content at the time of the viscosity measurement.

Since this polymerization degree is also the average polymerization degree measured according to viscosimetry, this polymerization degree is also called “average polymerization viscosity degree”.

In one embodiment of the invention, the fibre composition has a tensile index of between 70 and 100 Nm/g, preferably of between 70.8 and 94.6 Nm/g, more preferably of 93.1 Nm/g; elongation of between 2 and 5%, preferably of between 2.6 and 4.4%, more preferably 4.2%; Scott Bond of between 180 to 300 ft.lb/in², preferably between 198.5 and 248.0 ft.lb/in², more preferably 228 ft.lb/in²; and bursting index of between 4 and 9 KPam²/g, preferably of between 4.7 and 7.5 KPam²/g, more preferably 7.5 KPam²/g.

The expression “tensile index” is defined as the quotient between tensile strength and glue spread. Glue spread is the relationship between the paper mass and the area.

The term “elongation”, as used herein, means how much the fibre composition can be elongated without breaking.

The expression “Scott Bond” means a type of mechanical physical test that determines the material's strength in the Z direction.

The expression “bursting index” means the quotient between the bursting strength, when the sheet is subjected to a specific pressure, by glue spread.

In one embodiment of the invention, the fibre composition has a body of between 1 and 2 cm³/g, preferably of between 1 to 1.5 cm³/g, more preferably of 1 cm³/g; Taber stiffness of between 0.3 and 5%, preferably of between 0.4 and 1.1%, more preferably of 0.4%; and wall thickness of between 3 and 6 μm, preferably of between 3 and 4 μm, more preferably of 3.5 μm.

The expression “body” is defined as the volume-to-mass ratio. The body is a quantity inverse to the specific mass.

The expression “Taber stiffness” means the flexural strength of a material at a given angle. In the present invention the angle of 150 was used.

The expression “wall thickness” represents the wall width.

In one embodiment of the invention, the fibre composition has an opacity of between 30 and 80%, preferably of between 37.2 to 70.5%, more preferably of 41.7%.

The term “opacity” means the absence of transparency and determines the amount of light that can pass through the sheet and/or product.

In one embodiment of the invention, the fibre composition has a fines content of between 10 and 90%, preferably between 14 and 65%, more preferably of 60%, and fibrillation of between 5 and 20%, preferably of between 6 and 12%, more preferably of 8.6%.

The term “fines” means very small fibres and fibre fragments, for example, inferior to 2 mm in length.

The “fibrillation” is promoted by the fibre refining, which can be internal or external.

Internal fibrillation is the fibre swelling caused by water penetration into the cellulose fibres during the refining process, promoting the fibre swelling due to water molecules accommodation between the fibrils. Internal fibrillation makes fibres more flexible.

External fibrillation, in turn, is the fibrils or fibrillar units exposure during the mass refining operation, increasing the fibre specific surface for developing interfibrillary bonds during the formation of the paper sheet.

The fibre composition of the invention can alternatively be additivities with unrefined cellulose.

The fibre composition of the present invention is used in paper manufacturing, fibre cement, thermoplastic composites, inks, varnishes, adhesives, filters and wooden panels.

The invention is also based on the use of fibre composition for paper manufacturing, fibre cement, thermoplastic composites, inks, varnishes, adhesives, filters and wooden panels.

As used herein, the term “thermoplastic” means a plastic having the ability to soften and flow when subjected to a temperature and pressure increase, becoming a piece with defined shapes after cooling and solidification.

New temperature and pressure applications promote the same softening and flow effect and new coolings solidify the plastic in definite shapes. Thus, thermoplastics have the capacity to undergo physical transformations in a reversible way, being able to go through this process more than once, thus maintaining the same features.

Additionally, the invention is based on an article comprising the fibre composition of the invention.

In one embodiment of the invention, the article is a paper, a fibre cement, a thermoplastic composite, an ink, a varnish, an adhesive, a filter or a wooden panel.

In a preferred embodiment of the invention, the article is a paper.

The use of the composition of the present invention promotes a significant gain in strength due to the fibres small size and the length distribution thereof, and a consequent increase in the number of bonds among them. As explained above, cellulose fibres have many hydroxyl groups in their structure, which allows for easy hydrogen bonding. When microfibrilated or nanofibrilated, this bonding capacity increases due to fibre sizes, interlacing and contact surfaces. Therefore, it is important to have the fibre size distribution as defined herein. Such fibre size distribution results in the necessary size balance to promote better sheet strength.

Other advantages of the fibre composition of the present invention are that it has good processability and promotes good redispersibility, due to its viscosity value combined with the distribution of fibre lengths.

EXAMPLES

The examples presented herein are non-exhaustive, serve only to illustrate the invention and should not be used as a basis for limiting it.

Example 1

This study assesses the morphological, physical and mechanical properties of the fibre composition of the invention comprising microfibrillated cellulose (MFC) fibres, whether or not additivated with kraft cellulose.

Formulation C0 represents the MFC fibre composition of the invention, without whitened eucalyptus kraft cellulose additivation.

Formulations C5, C10, C20, C35, C50 and C75 represent MFC fibre compositions according to the invention, additivated with, respectively, 5%, 10%, 20%, 35%, 50% and 75% of whitened eucalyptus kraft cellulose.

Formulation C100 represents a formulation having 100% cellulose.

The morphological properties of the formulations are shown in Table 1.

TABLE 1

Length
Width
Fines
# of fibres

Formulation
(mm)
(μm)
(%)
(million/g)

C100
0.79
18.80
10.71
23.56

C0
0.35
21.70
64.06
11.14

C5
0.49
20.60
54.08
13.57

C10
0.56
20.00
47.60
12.25

C20
0.63
19.60
40.88
15.74

C35
0.67
19.50
31.40
15.44

C50
0.72
19.00
22.08
17.19

C75
0.76
18.70
14.64
20.89

The results obtained are presented in the graphs of FIGS. 01, 02, 03 and 04.

The viscosity values and polymerization degree (GP) of the formulations are shown in Table 2.

TABLE 2

Brookfield
Polymerization

Viscosity
Viscosity
Degree

Formulation
(cP)
(1%) (P)
(units)

C100
19.4
92
1773

C0
12.0
326
1131

C5
12.5
317
1218

C10
13.0
309
1248

C20
13.5
238
1311

C35
14.3
174
1347

C50
16.0
125
1514

C75
18.0
102
1710

The results obtained are presented in the graphs of FIGS. 05, 06 and 07.

The physical-mechanical properties of the formulations are shown in Tables 3 and 4.

TABLE 3

Tension
Elongation
Scott Bond
Bursting index

Formulation
(Nm/g)
(%)
(ft · lb/in²)
(KPam²/g)

C100
28.06
2.83
76
1.64

C0
88.0
4.4
209.5
7.5

C5
88.6
4.0
224.5
7.4

C10
93.1
4.2
228.0
7.5

C20
94.6
3.8
237.5
7.5

C35
91.8
3.7
248.0
6.9

C50
92.2
3.2
241.5
6.2

C75
70.8
2.6
198.5
4.7

TABLE 4

Air passage

Body
Opacity
Taber
resistance

Formulation
(cm³/g)
(%)
Stiffness (%)
(sec/100 mL air)

C100
1.67
78.09
0.78
8.0

C0
1.0
37.2
0.4
42300.0

C5
1.0
40.4
0.4
42300.0

C10
1.0
41.7
0.4
42300.0

C20
1.0
44.7
0.4
42300.0

C35
1.1
46.8
0.6
42300.0

C50
1.2
55.7
0.6
42300.0

C75
1.5
70.5
1.1
2134.0

The results presented in tables 3 and 4 are depicted in the graphs of FIGS. 08, 09, 10, 11, 12, 13, 14, and 15.

The results obtained show that with up to 50% additivation, there is no loss of mechanical or physical-mechanical strength properties in relation to C0, except for elongation and bursting index properties, with significant opacity gain.

Example 2

This second study evaluates the physical-mechanical properties of paper sheets (article—final product), in which the fibre composition of the invention was applied. Sheets of paper were analyzed with the addition of 5% of the MFC fibre composition of the invention, additivated or not with cellulose. Sheets of paper treated with the MFC fibre composition of the invention were compared to Sheets of paper to which only cellulose was added.

Formulation C0 represents the MFC fibre composition of the invention, without whitened eucalyptus kraft cellulose additivation.

Formulation C100 represents a formulation having 100% cellulose.

The paper sheet physical-mechanical properties, in which the fibre composition of the invention and only cellulose were applied, are found in Tables 5 and 6.

TABLE 5

Tension
Elongation
Scott Bond
Bursting index

Formulation
(Nm/g)
(%)
(ft · lb/in²)
(KPam²/g)

C100
17.06
1.40
45
0.66

C0
30.16
2.95
69
1.69

C5
27.36
2.58
65
1.31

C10
26.60
2.70
66
1.39

C20
25.56
2.71
64
1.37

C35
24.84
2.33
60
1.19

C50
22.69
2.29
53
1.16

C75
21.36
1.85
50
0.86

TABLE 6

Air passage

resistance

Body
(sec/100 mL

Formulation
oSR*
(cm³/g)
air)
Opacity (%)

C100
21
1.78
0.66
77.73

C0
46
1.71
1.69
78.39

C5
41
1.70
1.31
78.72

C10
40
1.70
1.39
78.41

C20
38
1.72
1.37
78.23

C35
36
1.77
1.19
78.58

C50
32
1.76
1.16
77.69

C75
27
1.77
0.86
77.59

*oSR, also called grinding degree, dewatering degree or refining degree, is the measure of a sheet depletion when formed in a specific apparatus called Schopper-Riegler.

The results obtained in the present study are presented in the graphs from FIGS. 16, 17, 18, 19, 20, 21, 22, and 23.

The results obtained show that when applied to the paper, the addition of the composition of the invention generates an average traction gain of almost 50% in relation to pure cellulose; and 100% gain in bursting index.

Example 3

A study is presented herein which demonstrates the redispersion effect of the fibre composition of the invention.

Tested formulations represent MFC fibre compositions without whitened eucalyptus kraft cellulose additivation; compositions of MFC fibres having 5%, 10% and 20% whitened eucalyptus kraft cellulose; and formulation with 100% cellulose.

The morphological and mechanical properties of the formulations were analyzed before and after the pressing step.

The morphological properties analyzed were: fines content (%), fibre length (mm), fibre width (μm) and number of fibres per mass of the composition (millions of fibres/gram).

The analyzed mechanical properties were: tensile index (Nm/g), elongation (%), bursting index (KPam²/g), Scott Bond (ft.lb/in²), body (cm³/g) and air passage resistance (s/100 mL air).

The obtained results are presented in the graphs from FIGS. 24, 25, 26, 27, 28, 29, 30, 31, 32 and 33.

Through the obtained results, it is concluded that there is retention of cellulose in the MFC maintaining the properties of the fibre proportion in the composition with regard to its morphology. Furthermore, no significant differences were observed in formulations before and after pressing.

Example 4

A verification study for dry content levels of the fibre composition of the invention is presented herein.

The physical-mechanical properties of the body (cm³/g), tensile index (Nm/g), bursting index (KPam²/g) and tear index (mNm²/g) for different dry content (%) were analyzed.

The results obtained in this study are portrayed in FIGS. 34, 35, 36 and 37.

Through the results, it was concluded that there was a significant body gain after 30% dry content and a loss of tensile strength after 30% dry content. Additionally, it was observed that the dry content did not significantly affect the tear strength. Regarding the bursting rate, no significant changes were observed between the dry content levels of 10, 20, 30, and 50%. Therefore, it is clear that redispersibility was achieved up to a maximum of 50% dry content.

FIBRE COMPOSITION, USE OF SAID COMPOSITION AND ARTICLE COMPRISING SAID COMPOSITION

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