Patent Application
20150259830
The invention relates to a new method for the manufacture of fibrous yarn, and particularly for the manufacture of paper yarn. Further, the invention relates to fibrous yarn obtainable by said method, as well as uses of said fibrous yarn.
Many different types of yarns made of natural fibers are known in the art. One well known example is paper yarn, which is traditionally manufactured from paper sheets. The first and only industrial method was developed in the late 19th century in Germany. It has been refined over time but the basic principle has remained the same and it is still in use today. Typically, paper manufactured from chemical, mechanical or chemi-mechanical pulp is slit to strips (width typically from 5 to 40 mm), which are twisted to thread. Said thread may be subjected to dyeing and finishing. The product (paper yarn) has limited applications because of deficiencies in its properties, such as limited strength, unsuitable thickness, layered or folded structure, and further, the manufacturing method is inefficient.
Cotton is very widely used as raw material in the manufacture of yarns and ropes. However, the cultivation of cotton requires significant water resources and it is widely carried out in regions where there is shortage of water and food. When available water is used for the irrigation of cotton fields, the situation with regard to food supply becomes worse. Thus the use of cotton does not support sustainable development, and there is a need for alternative sources of fiber, suitable for replacing cotton at least partly.
An object of the present invention is to provide a new method for the manufacture of fibrous yarn.
A further object is to provide a sustainable source of fibers for fibrous yarn.
A still further object is to provide fibrous yarn with improved and adjustable properties, suitable for varying applications of yarn.
Aspects of the invention are thus directed to a method for the manufacture of fibrous yarn, said method comprising the steps of providing an aqueous suspension comprising fibers and at least one rheology modifier, directing said suspension through at least one nozzle having an inner diameter of the outlet smaller than or equal to the maximum length weighed fiber length of the fibers, to form at least one yarn, and subjecting said yarn to dewatering.
Aspects of the invention are also directed to a yarn comprising fibers and at least one rheology modifier. Said yarn is obtainable by the method described above.
Aspects of the invention are also directed to the use and method of use of the obtained yarn in decoration, interior decor, furniture, clothes, bandages, dressings, textiles, in construction materials etc.
Particularly, the ease of manufacture of the fibrous yarn, applicability of the yarn to various sites of use, possibility to design the properties of the yarn according to the intended use, small water footprint, biodegradabilityare some examples of the desired benefits achieved by the present invention.
The characteristic features of the invention are presented in the appended claims.
Unless otherwise specified, the terms, which are used in the specification and claims, have the meanings commonly used in the field of paper and pulp manufacture, as well as in the field of yarn manufacture. Specifically, the following terms have the meanings indicated below.
The term “yarn” refers here to thread, yarn, chord, filament, wire, string, rope and strand.
The term “rheology modifier” is understood to mean here a compound or agent capable of modifying the viscosity, yield stress, thixotropy of the suspension.
It was surprisingly found that fibrous yarn can be manufactured in a very simple and efficient way directly from a suspension comprising fibres and at least one rheology modifier, whereby it not necessary to manufacture first paper or other fibrous product, which is sliced into strips and wound to a yarn.
The method according to the invention, for the manufacture of fibrous yarn comprises the steps, where an aqueous suspension comprising fibers and at least one rheology modifier is provided, followed by directing said suspension through at least one nozzle having an inner diameter of the outlet smaller than or equal to the maximum length weighed fiber length of the fibers, to form at least one yarn, and then subjecting said yarn to dewatering.
Here “maximum length weighed fiber length of the fibers” means length weighted fiber length where 90% of fibers are shorter or equal to this length. Fiber length may be measured with any suitable method used in the art.
The aqueous suspension in understood to mean any suspension comprising water and fibers originating from any and at least one plant based raw material source, including cellulose pulp, refined pulp, waste paper pulp, peat, fruit pulp, or pulp from annual plants. The fibers may be isolated from any cellulose containing material using chemical, mechanical, thermo-mechanical, or chemi-thermo-mechanical pulping processes.
The plant based raw material source may be a virgin source or recycled source or any combination thereof. It may be wood or non-wood material. The wood can be softwood tree such as spruce, pine, fir, larch, douglas-fir or hemlock, or hardwood tree such as birch, aspen, poplar, alder, eucalyptus or acacia, or a mixture of softwoods and hardwoods. The non-wood material can be plant, such as straw, leaves, bark, seeds, hulls, flowers, vegetables or fruits from corn, cotton, wheat, oat, rye, barley, rice, flax, hemp, manilla hemp, sisal hemp, jute, ramie, kenaf, bagasse, bamboo, reed or peat.
Suitably virgin fibers originating from pine may be used. Said fibers typically may have average length weighed fiber length from 2 to 3 mm. Also combinations of longer fibers with shorter ones may be used, for example fibers from pine with fibers from eucalyptus.
The aqueous suspension may comprise from 0.1 to 10% w/w, preferably from 0.2 to 2% w/w of fibers originating from any plant based raw material source.
Additionally the suspension may optionally comprise virgin or recycled fibers originating from synthetic materials, such as glass fibers, polymeric fibers, metal fibers, or from natural materials, such as wool fibers, or silk fibers.
The aqueous suspension may comprise at least one rheology modifier that forms a gel by cross linking the suspension, suitably selected from alginic acid, alginates such as sodium alginate, pectin, carrageenan, and nanofibrillar cellulose (NFC), or a combination of rheology modifiers. In the presence of cations, particularly divalent or multivalent cations, suitably such as Ca2+, Mg2+, Sr2+ or Ba2+, alginate, pectin and carrageenan (carrageenan cross-links also with K+) readily form a stable and strong gel. In the cross-linking of these polysaccharides calcium chloride is preferably used. The concentration of salt solution may vary from 1% w/w to 10% w/w.
Typically the poly-L-guluronic acid (G-block) content of alginate, poly-D-galacturonic acid content of pectin or carrageenan and the amount of divalent or multivalent cations (calcium ions) are regarded as being involved in determining gel strength.
The term “nanofibrillar cellulose” or “nanofibrillated cellulose” refers to a collection of isolated cellulose microfibrils or microfibril bundles derived from cellulose raw material. Microfibrils have typically high aspect ratio: the length might exceed one micrometer while the number-average diameter is typically below 200 nm. The diameter of microfibril bundles can also be larger but generally less than 1 μm. The smallest microfibrils are similar to so called elementary fibrils, which are typically 2-12 nm in diameter. The dimensions of the fibrils or fibril bundles are dependent on raw material and disintegration method. The nanofibrillar cellulose may also contain some hemicelluloses; the amount is dependent on the plant source. Mechanical disintegration of microfibrillar cellulose from cellulose raw material, cellulose pulp, or refined pulp is carried out with suitable equipment such as a refiner, grinder, homogenizer, colloider, friction grinder, ultrasoundsonicator, fluidizer such as microfluidizer, macrofluidizer or fluidizer-type homogenizer. In this case the nanofibrillar cellulose is obtained through disintegration of plant cellulose material and can be called “nanofibrillated cellulose”. “Nanofibrillar cellulose” can also be directly isolated from certain fermentation processes. The cellulose-producing micro-organism of the present invention may be of the genus Acetobacter, Agrobacterium, Rhizobium, Pseudomonas or Alcaligenes, preferably of the genus Acetobacter and more preferably of the species Acetobacterxylinum or Acetobacterpasteurianus. “Nanofibrillar cellulose” can also be any chemically or physically modified derivate of cellulose nanofibrils or nanofibril bundles. The chemical modification could be based for example on carboxymethylation, oxidation, esterification, or etherification reaction of cellulose molecules. Modification could also be realized by physical adsorption of anionic, cationic, or non-ionic substances or any combination of these on cellulose surface. The described modification can be carried out before, after, or during the production of microfibrillar cellulose.
The nanofibrillated cellulose can be made of cellulose which is chemically premodified to make it more labile. The starting material of this kind of nanofibrillated cellulose is labile cellulose pulp or cellulose raw material, which results from certain modifications of cellulose raw material or cellulose pulp. For example N-oxyl mediated oxidation (e.g. 2,2,6,6-tetramethyl-1-piperidine N-oxide) leads to very labile cellulose material, which is easy to disintegrate to microfibrillar cellulose. For example patent applications WO 09/084566 and JP 20070340371 disclose such modifications. The nanofibrillated cellulose manufactures through this kind of premodification or “labilization” is called “NFC-L” for short, in contrast to nanofibrillated cellulose which is made of not labilized or “normal” cellulose, NFC-N.
The nanofibrillated cellulose is preferably made of plant material where the nanofibrils can be obtained from secondary cell walls. One abundant source is wood fibres. The nanofobrillated cellulose is manufactured by homogenizing wood-derived fibrous raw material, which may be chemical pulp. When NFC-L is manufactured from wood fibres, the cellulose is labilized by oxidation before the disintegration to nanofibrils. The disintegration in some of the above-mentioned equipment produces nanofibrils which have the diameter of only some nanometers, which is 50 nm at the most and gives a clear dispersion in water. The nanofibrils can be reduced to size where the diameter of most of the fibrils is in the range of only 2-20 nm only. The fibrils originating in secondary cell walls are essentially crystalline with degree of crystallinity of at least 55%.
Said rheology modifier may be used in an amount from 0.1 to 20 weight %. Concentration of the rheology modifier, such as alginate is preferably 0.5-20% w/w.
The suspension may comprise also at least one dispersion agent that is typically anionic long chained polymer or NFC, or a combination of dispersion agents. Examples of suitable dispersion agents are carboxymethyl cellulose (CMC), starch (anionic or neutral) and anionic polyacrylamides (APAM), having high molecular weight. Dispersion agent modifies the suspension rheology to make the suspension shear thinning. Preferably at high shear rates (500 1/s) shear viscosity is less than 10% of zero shear viscosity of the suspension.
Said dispersion agent may be used in an amount from 0.1 to 20 weight %.
Optionally the aqueous suspension may be in the form of foam, and in that case the suspension comprises at least one surfactant selected from anionic surfactants and non-ionic surfactants and any combinations thereof, typically in an amount from 0.001 to 1% w/w.
Further, the suspension may comprise other additives selected from hydrophobicity or hydrophilicity agents, colorants, decorative agents, elasticity modifiers, tensile strength modifiers, or strength modifiers, such as starch, gums or water-soluble polyelectrolytes, decorative pieces such as metal powder etc.
The aqueous suspension is obtained using any suitable mixing method known in the art.
In the method suspension is directed through at least one nozzle. Suitably the amount of nozzles is selected depending on the manufacturing equipment used and on the product which is manufactured.
Any nozzle or extruder suitable for liquids and viscous fluids may be used. When the suspension contains alginates, pectin or carrageenan, suitably a nozzle is used comprising an inner die or orifice for the suspension and outer die or orifice for an aqueous solution comprising at least one cation (as a salt, such as calcium chloride or magnesium sulphite). Alternatively, the solution comprising the cation(salt) may be provided as a spray or mist when using nozzles with one orifice. The cation, when brought with contact for example with alginate or alginic acid, effects very rapid increase on the viscosity of the aqueous suspension whereby the strength of the yarn is increased, making the embodiment of the method utilizing gravitational force very attractive.
The inner diameter of the outlet of the nozzle is smaller than or equal to the maximum length weighed fiber length of the fibers. This helps to orientate the fibers essentially in the direction of the yarn and provides strength and flexibility to the product.
The suspension is conducted through the nozzle(s), which is arranged suitably vertically to provide a continuous yearn of the suspension below each nozzle, falling freely with the aid of gravitational force. In this embodiment it is preferable to use a suspension comprising a rheology modifier selected from alginic acid, sodium alginate, pectin and carrageenan, together with a solution comprising a cation. Particularly preferably the suspension comprises also a dispersion agent. The yarn has sufficient strength and thus no supporting bodies are needed, it can be dewatered and subjected to finishing and other optional steps if needed.
The nozzle(s) may also be arranged in a direction deviating from the vertical direction. The nozzle(s) may be arranged in the vicinity of pieces comprising gutters, where the nozzle directs the flow of the suspension in the gutters, acting as supporting bodies, to provide the yarn. Suitably the gutters are arranged spirally on the surface cylindrical drums as presented in
After the nozzle the yarn is subjected to dewatering which may include methods based on vacuum, mechanical pressing and/or thermal drying. The dewatering may be carried out by methods utilizing vacuum, mechanical pressing, convection, conduction or radiation of heat, by any suitable heating means such as heated airflow, IR, or contact with heated surface.
After the dry yarn is obtained, it may be subjected to optional finishing selected from pressing, twisting, shredding, pleating, coloring, waxing and any combinations thereof.
The yarn may also be treated with dyes, wax, or silicon oil to provide transparent yarn.
In
In
Moist yarn obtained from the nozzle initially contains water typically from 30 to 99.5% w/w. In the dewatering step the yarn may be dried to desired water content.
The invention provides several advantages. The manufacturing method is very simple and effective, and the equipment needed is simple and relatively cheap. The yarn is produced directly from the fiber suspension; it is not necessary to manufacture first paper. Traditional paper yarn may be replaced with the product obtainable by the method, for use as replacer for traditional yarns in textiles, decorative products, construction and composite materials. Thinner and thicker yarns may be produced ad the properties of the yarns may be varied, such as strength, flexibility, colour, hydrophobicity, hydrophilicity etc.
The rheology of the fiber suspension may be adjusted using rheology modifiers to the viscosity and thixotropyrange where the fiber suspension can be pumped through the nozzle without clogging it, but simultaneously to provide a moist yarn typically in gel form, which has sufficient strength to maintain its form during the drying step. Thus the rheology modifier gives shear thinning nature and strength to the yarn; in the case alginate is used a dispersion agent is typically also needed and the treatment of the moist yarn with a salt solution to provide sufficient strength.
The selection of the inner diameter of the outlet of the nozzle to smaller than or equal to the maximum length weighed fiber length of the fibers achieves the fibers to orientate in the direction of the yarn, which provides the final product flexibility and strength.
The water released after drying may be recovered by condensing and recycled in the method, for example by using a closed system, and thus practically no wastewater is formed. Also the amount of water needed in the process is very limited, particularly in the embodiment where the fiber suspension is provided in the form of foam.
Very thin to very thick yarns and ropes may be produced, which may be twisted together to provide products suitable for weaving, knitting, manufacture of carpets, blankets, textiles, dressings etc. Also very soft yarns may be produced for example from bamboo with alginates, particularly suitable for the manufacture or textiles and clothes. Further, very thick ropes may be produced, which may be used for example in interior decoration etc. purposes, as well as yarn and rope suitable for construction industry and in the manufacture of composite structures where the yarn is embedded in a matrix, such as a polymer. The composition of the fiber suspension may be adjusted according to the product that is manufactured.
The product is completely biodegradable if the starting materials used are natural materials.
The need of cotton may be reduced with the method and products of the present invention, where the fibers originate at least partly from more ecological plant material, such as wood and recycled paper.
Particularly, long fiber pulp, suitably manufactured from Nordic pine, may be used in the method to provide a yarn having the thickness of less than 0.1 mm and very good strength properties.
While the invention has been described with respect to specific examples presented in the figures, including presently preferred modes of carrying out the invention, those skilled in the art will appreciate that there are numerous variations and permutations of the above described embodiments that fall within the spirit and scope of the invention. It should be understood that the invention is not limited in its application to the details of construction and arrangements of the components set forth herein. Variations and modifications of the foregoing are within the scope of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20115882 | Sep 2011 | FI | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14343928 | Jul 2014 | US |
| Child | 14727118 | US |
