EP1842944B3 - Biodegradable binding twine - Google Patents
Biodegradable binding twine Download PDFInfo
- Publication number
- EP1842944B3 EP1842944B3 EP07105204A EP07105204A EP1842944B3 EP 1842944 B3 EP1842944 B3 EP 1842944B3 EP 07105204 A EP07105204 A EP 07105204A EP 07105204 A EP07105204 A EP 07105204A EP 1842944 B3 EP1842944 B3 EP 1842944B3
- Authority
- EP
- European Patent Office
- Prior art keywords
- biodegradable
- core material
- oder
- und
- twine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000835 fiber Substances 0.000 claims abstract description 34
- 239000011162 core material Substances 0.000 claims abstract description 32
- 239000000463 material Substances 0.000 claims abstract description 26
- 229920001222 biopolymer Polymers 0.000 claims abstract description 16
- 244000198134 Agave sisalana Species 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 9
- 239000004626 polylactic acid Substances 0.000 claims abstract description 5
- 229920002472 Starch Polymers 0.000 claims description 15
- 125000001931 aliphatic group Chemical group 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 239000008107 starch Substances 0.000 claims description 14
- 235000019698 starch Nutrition 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 229920000728 polyester Polymers 0.000 claims description 9
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- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229920000747 poly(lactic acid) Polymers 0.000 claims description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- 229920000858 Cyclodextrin Polymers 0.000 claims description 2
- 102000014171 Milk Proteins Human genes 0.000 claims description 2
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- 239000005018 casein Substances 0.000 claims description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims description 2
- 235000021240 caseins Nutrition 0.000 claims description 2
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- 229940097362 cyclodextrins Drugs 0.000 claims description 2
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- 239000011257 shell material Substances 0.000 description 18
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- 150000007513 acids Chemical class 0.000 description 14
- 239000000853 adhesive Substances 0.000 description 12
- 230000001070 adhesive effect Effects 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
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- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 8
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
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- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
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- 244000025221 Humulus lupulus Species 0.000 description 5
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- JRHWHSJDIILJAT-UHFFFAOYSA-N 2-hydroxypentanoic acid Chemical compound CCCC(O)C(O)=O JRHWHSJDIILJAT-UHFFFAOYSA-N 0.000 description 4
- 235000008694 Humulus lupulus Nutrition 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 4
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
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- 239000005014 poly(hydroxyalkanoate) Substances 0.000 description 4
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 4
- 229920000903 polyhydroxyalkanoate Polymers 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 4
- 244000025254 Cannabis sativa Species 0.000 description 3
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 3
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 3
- 240000000491 Corchorus aestuans Species 0.000 description 3
- 235000011777 Corchorus aestuans Nutrition 0.000 description 3
- 235000010862 Corchorus capsularis Nutrition 0.000 description 3
- 229920002261 Corn starch Polymers 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 240000006240 Linum usitatissimum Species 0.000 description 3
- 235000004431 Linum usitatissimum Nutrition 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
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- 235000011037 adipic acid Nutrition 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 235000009120 camo Nutrition 0.000 description 3
- 235000005607 chanvre indien Nutrition 0.000 description 3
- 239000008120 corn starch Substances 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 239000011487 hemp Substances 0.000 description 3
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 3
- 229920005615 natural polymer Polymers 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- AFENDNXGAFYKQO-UHFFFAOYSA-N 2-hydroxybutyric acid Chemical compound CCC(O)C(O)=O AFENDNXGAFYKQO-UHFFFAOYSA-N 0.000 description 2
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 description 2
- 241001136792 Alle Species 0.000 description 2
- 240000008564 Boehmeria nivea Species 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
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- 241000219146 Gossypium Species 0.000 description 2
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 2
- 240000003183 Manihot esculenta Species 0.000 description 2
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 159000000032 aromatic acids Chemical class 0.000 description 2
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- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
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- 239000006185 dispersion Substances 0.000 description 2
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- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 2
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
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- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
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- 241000894006 Bacteria Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 244000078856 Prunus padus Species 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 229920000704 biodegradable plastic Polymers 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
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- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 238000009945 crocheting Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 229920005839 ecoflex® Polymers 0.000 description 1
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
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- 235000019426 modified starch Nutrition 0.000 description 1
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- 230000008635 plant growth Effects 0.000 description 1
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- 229920001592 potato starch Polymers 0.000 description 1
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- 239000004753 textile Substances 0.000 description 1
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Classifications
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/02—Yarns or threads characterised by the material or by the materials from which they are made
- D02G3/04—Blended or other yarns or threads containing components made from different materials
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/36—Cored or coated yarns or threads
Definitions
- the present patent application relates to a biodegradable yarn of a core material of biodegradable natural fibers and / or chemical fibers and a shell of a biodegradable plastic.
- Game are used for example in the form of tie cords in hop growing; their use is also in other areas z. B. in viticulture, the construction industry or packaging industry possible.
- hops from Elsen are used as a climbing aid for hop plants in hop growing.
- the plant can grow upwards and thus reach the desired heights, while hopping up to about 8 meters.
- the wires are knotted in the hop garden at the top of a cross wire and just below in the immediate vicinity of the hop plant stuck in the ground.
- the wire is cut by hand or machine down with the hop plant just above the ground and also topped off with the hop plant.
- the wire is shredded together with the plant remains of the hop plant and spent on the fields for rotting or rusting.
- a new hop wire is attached to each hop plant as described above.
- the hops are currently made of iron, usually of ST 37 and have a round cross section with a diameter of 1.1 and 1.5 mm.
- the hop plant needs a certain surface roughness on the wire surface in order to be able to hold tight to the wire. In the conventional iron wire mesh, this surface roughness is due to the manufacturing process and resulting flash rust.
- a first disadvantage is its very high specific gravity.
- Another disadvantage is that when chopping the wire a very high wear on the chopping knives occurs.
- hop spikes A particular disadvantage is the so-called "hop spikes".
- hop farmer drives the shredded material from his farm to the fields with the tractor and wagon with the pieces of iron wire approx. 2 to 5 centimeters long, it regularly happens that such "hop spikes” fall on the road.
- driving over these "hop spikes” with the car they then drill into the tires and cause high damage.
- the DE-OS 23 44 221 describes support cords for plants from z. B. polyolefin. A cross-sectional change is to be achieved by a melt fracture induced in the extrusion. However, this leads to strength variations over the length of the string. In addition, although the surface achievable by melt fracture is deformed, it is still smooth so that plants will find insufficient support.
- the DE 198 00 842 C2 describes a plastic thread, which is formed as a monofilament, wherein the monofilament consists of a polypropylene and is treated on the surface to reduce the surface smoothness, wherein the plastic thread made of biodegradable modified polypropylene and is stretched to increase strength, and wherein the surface of the plastic thread through Profiling and / or chemical and physical processes is reduced.
- the 1 October 2007 disclosed ES 2 282 021 discloses a recyclable vertical crop support applicable to the attachment of plants in an upright position by means of staples or similar devices and consisting of a braided or twisted cord of paper or cellulose which additionally includes waxes and resins.
- the waxes may be polyethylene waxes or paraffinic waxes, and the resins may be acrylic resins.
- the present invention is therefore based on the object to provide an improved yarn with controllable biodegradability and compostability and excellent tensile strength and elongation at break.
- the present invention thus provides a biodegradable and compostable yarn containing a core material of natural fibers and / or man-made fibers and comprising a shell material of biodegradable and compostable biopolymers.
- the materials forming the core of the yarn of the invention are those of natural fibers such as cotton, flax, hemp, sisal, jute, coconut, bast, ramie and / or man-made fibers, for example of natural polymers such as e.g. Viscose, cellulose, lyocell and / or Tencel, and fibers of biodegradable and compostable aliphatic and / or partially aromatic polyester amides and / or aliphatic and / or partially aromatic polyesters.
- natural fibers such as cotton, flax, hemp, sisal, jute, coconut, bast, ramie and / or man-made fibers
- natural polymers such as e.g. Viscose, cellulose, lyocell and / or Tencel
- the core fibers are selected from natural fibers consisting of cotton, flax (linen), hemp, sisal, cellulose and / or jute.
- the materials forming the core are particularly preferably natural fibers of sisal, since sisal has a natural water-repellent action.
- biodegradable and compostable means biodegradable and compostable yarns according to the invention which are completely biodegradable and compostable according to DIN EN 13 432.
- the yarn according to the invention disintegrates after a certain, predeterminable time and is converted under composting conditions by the bacteria and microbes in the soil into natural waste products, so that in this case even a natural fertilization is achieved.
- the time required for the yarn of the present invention to fully degrade is limited (e.g., by the weight fraction of shell material, based on the total weight of the yarn of the invention), i.e., adjustable.
- the yarn according to the invention can be defined in terms of its degradation time to each individual application.
- the tear strength of the yarn according to the invention can also be adjusted to any particular application.
- acids can also be used in the form of derivatives such as, for example, acid chlorides or esters, both as monomers and as oligomeric esters.
- the yarn according to the invention has the advantage that by the use of natural fibers, such as cotton, flax, hemp, sisal, jute, ramie and coconut, and / or man-made fibers of natural polymers, such as viscose (a definition of these terms eg in Römpp Chemie Lexikon, 9th edition, Thieme Verlag, Stuttgart , under the relevant keywords) and the envelope material from biopolymers because of the biodegradability of the yarn according to the invention a soil contamination is avoided, whereby the planting period is increased.
- the yarn of the present invention is sufficiently durable to ensure its durability throughout the growing season because it can withstand the rainfall during that time.
- the biopolymer material forming the shell material can be biopolymeric materials of starch (for example, corn starch, potato starch, wheat starch, rice starch, tapioca starch, sorghum starch, manioc starch, pea starch, modified starches, starch degradation products), cyclodextrins, polylactic acid, biodegradable resins, milk protein, casein , Sugar, vegetable oils, cellulose (for example cellulose acetate), aliphatic and / or (partially) aromatic polyesters (for example those described above), polyhydroxyalkanoates and / or polyvinyl alcohol / starch mixtures.
- starch for example, corn starch, potato starch, wheat starch, rice starch, tapioca starch, sorghum starch, manioc starch, pea starch, modified starches, starch degradation products
- cyclodextrins polylactic acid, biodegradable resins, milk protein, casein , Sugar, vegetable oils,
- the shell material is selected from vegetable biopolymeric materials and / or petroleum-based biopolymeric materials.
- the shell material is selected, for example, from starch, polylactic acid, cellulose, mixtures of aromatic and aliphatic polyesters and / or polyvinyl alcohol / starch mixtures.
- These biodegradable and compostable shell materials may further comprise other components, provided that the yarn according to the invention has the complete biodegradability and compostability according to DIN EN 13 432.
- Such shell materials are commercially available, e.g. under the trade name biomat by Pro-Tech, ECOFLEX by BASF, Materbi by Novamont, Natureflex by Inovia Films, or Biophan by Treofan.
- the proportion of the biopolymeric shell material, based on the total weight of the yarn according to the invention, is usually 5 to 40 wt .-%, preferably 10 to 30 wt .-%, in particular 15 to 25 wt .-%.
- the core material of the yarn according to the invention is subjected to one or more of the above-mentioned shell materials.
- the time period until the onset of the decomposition process of the yarn according to the invention can be precisely controlled in terms of time.
- the period of time until the onset of the decomposition process of the yarn according to the invention can be adjusted by suitable choice of the composition of the wrapping material, for example the mixing ratio of the wrapping materials used.
- the shell material preferably comprises a mixture of vegetable and petroleum-based biopolymers in a ratio of 1: 1 to 1: 5, in particular 1: 2 to 1: 4, more preferably 1: 2 to 1: 3.
- the vegetable biopolymers used may be, for example, starch, cellulose and / or vegetable oils; the petroleum-based biopolymers used are, for example, polyhydroxyalkanoates or polyesters.
- the shell material consists of a mixture of vegetable biopolymers such as corn starch and petroleum-based biopolymers such as polyhydroxyalkanoates or polyesters in a ratio of 1: 3. This ensures that the yarn according to the invention has a start of decomposition of within six months.
- the shell material consists of a mixture of vegetable biopolymers such as corn starch and petroleum-based biopolymers such as polyhydroxyalkanoates or polyesters in a ratio of 1: 2. This ensures that the yarn according to the invention has a decomposition start within four months. Other mixing ratios may prolong or shorten the degradation time.
- the application of the wrapping material to the core material of the yarn according to the invention can be done for example by wrapping, welding, fusing, gluing, machine bonding, shrinking or dip coating.
- the wrapping material may be wrapped in the form of a film around the core material.
- the film of the enveloping material may have a thickness in a range between 0.001 and 0.2 mm, preferably in a range of 0.01 to 0.1 mm, in particular in a range of 0.02 to 0.08 mm.
- an envelope can in another embodiment be made using a tubular film blowing device, wherein the envelope is inflated onto the core material.
- the yarn according to the invention can be produced, for example, by using textile processing methods known per se, such as spinning, twisting, braiding, crocheting, bobbins, knitting, weaving and / or knitting, for example in the form of staple fiber yarns (spun yarns) ) or filament yarns present core materials of natural fibers and / or man-made fibers of natural polymers are combined or solidified as a fiber, so that a strength of the yarn of the invention of at least 450 N is achieved.
- textile processing methods known per se such as spinning, twisting, braiding, crocheting, bobbins, knitting, weaving and / or knitting, for example in the form of staple fiber yarns (spun yarns) ) or filament yarns present core materials of natural fibers and / or man-made fibers of natural polymers are combined or solidified as a fiber, so that a strength of the yarn of the invention of at least 450 N is achieved.
- Lyocell is the generic term for solvent-spun cellulose fibers produced by the NMMO or lyocell process. Lyocell fibers are available, for example, from Lenzing AG and Courtaulds Fibers, Coventry / Great Britain. Tencel fibers are a further development and also available from the company Courtaulds. Tencel is a registered trademark. These fibers have the advantage that their dry strength is higher than any other commercial cellulose staple fiber; when wet, this strength is even more pronounced. Dry, the strength is twice as high as conventional viscose fibers and wet three times as high.
- the core material can be applied with an adhesive before application of the wrapping material.
- adhesive material according to the invention are those which combine with the core material and the shell material and are biodegradable.
- adhesives based on starch or based on polyvinyl alcohol These are known to those skilled in the art and commercially available. For example, the following may be mentioned: starch-based planatol-based adhesives, polyvinyl alcohol-based dispersions, e.g. Helmitin adhesive L 93 / 22-01 from Forbo Helmitin, or the dispersion adhesive Adhesin from Henkel.
- an adhesive can increase the tensile strength of the yarn according to the invention and improve the bond between the core material and the casing.
- the adhesive is applied in a proportion of 5 to 30% by weight, based on the weight of the core material.
- the application amount is in a range of 5 to 20, ideally 7 to 10 wt .-%.
- the yarn according to the invention can, for example, achieve a tensile strength of at least 500 N and an elongation at break of not more than 4%.
- the applied adhesive can be firmly incorporated into the core material.
- the adhesive is pressed into the fibers of the core material using a rope-making machine, whereby the strength of the yarn according to the invention increases significantly.
- the application of the cladding material to the core material occurs, for example, by melting, A natural roughness develops on the surface of the yarn according to the invention, whereby the plant growth on the yarn according to the invention is improved along.
- the melting of the shell material according to the invention for example, at temperatures between 50 and 200 ° C, preferably between 80 and 150 ° C, in particular between 100 and 130 ° C, depending on the shell material used.
- the yarn of the invention may have a variety of geometric shapes, such as round, flat, polygonal, oval, etc. Ideally, however, the yarn of the invention has a round shape.
- the thickness of the yarn according to the invention may be in a range of 0.5 to 10 mm, preferably 1 to 8 mm, in particular 2 to 6 mm.
- the yarn of the invention has an S twist. This supports the growth of the plant and can be generated, for example, using a rope machine. In this case, lay lengths in a range of 0.5 to 4 cm, preferably 1 to 3 cm, in particular 1.5 to 2.5 cm have proven to be favorable.
- sisal cord with a diameter of about 2.5 mm and a basic strength of about 400 N.
- the sisal cord is unrolled by a flyer from the supply spool and pulled through a glue bath, the excess glue before leaving the glue station of the cord is stripped off.
- the sisal cord becomes a 2 cm wide and 0.03 mm thick biopolymer Wannerra film WBA 2000 wrapped and pulled through a Nipper and pressed.
- the wrapped cord is fused together by means of hot air and solidified and, by turning back the cord / rope machine, its final strength of more than 500 N and its roughened surface are obtained.
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Abstract
Description
Die vorliegende Patentanmeldung betrifft ein biologisch abbaubares Garn aus einem Kernmaterial aus biologisch abbaubaren Naturfasern und/oder Chemiefasem und einer Hülle aus einem biologisch abbaubaren Kunststoff.The present patent application relates to a biodegradable yarn of a core material of biodegradable natural fibers and / or chemical fibers and a shell of a biodegradable plastic.
Game werden beispielsweise in Form von Bindeschnüren im Hopfenanbau verwendet; ihr Einsatz ist aber auch in anderen Gebieten z. B. im Weinbau, der Bauindustrie oder Verpackungsindustrie möglich.Game are used for example in the form of tie cords in hop growing; their use is also in other areas z. B. in viticulture, the construction industry or packaging industry possible.
Gegenwärtig werden im Hopfenanbau überwiegend Drähte aus Elsen als Kletterhilfe für Hopfenpflanzen eingesetzt. An den Drähten kann die Pflanze nach oben wachsen und damit die gewünschten Höhen, beim Hopfen bis zu ungefähr 8 Metern, erreichen.At present, mainly hops from Elsen are used as a climbing aid for hop plants in hop growing. On the wires, the plant can grow upwards and thus reach the desired heights, while hopping up to about 8 meters.
Die Drähte werden in der Hopfengartenanlage oben an einem Querdraht verknotet und unten in unmittelbarer Nähe der Hopfenpflanze knapp in den Boden gesteckt. Bei der Ernte des Hopfens wird der Draht von Hand oder maschinell unten mit der Hopfenpflanze knapp über der Erde abgeschnitten und oben ebenfalls mit der Hopfenpflanze abgerissen.The wires are knotted in the hop garden at the top of a cross wire and just below in the immediate vicinity of the hop plant stuck in the ground. When harvesting the hops, the wire is cut by hand or machine down with the hop plant just above the ground and also topped off with the hop plant.
In der Hopfenpflückmaschine wird der Draht zusammen mit den Pflanzenresten der Hopfenpflanze klein gehäckselt und zum Verrotten bzw. Verrosten auf die Felder verbracht. Bevor dann im nächsten Frühjahr die Hopfenpflanze erneut auszutreiben beginnt, wird für jede Hopfenpflanze wieder ein neuer Hopfendraht wie oben beschrieben angebracht.In the hop-picking machine, the wire is shredded together with the plant remains of the hop plant and spent on the fields for rotting or rusting. Before the hops plant begins to drive out again next spring, a new hop wire is attached to each hop plant as described above.
Die Hopfendrähte sind derzeit aus Eisen, und zwar in der Regel aus ST 37 und haben einen runden Querschnitt mit einem Durchmesser von 1,1 und 1,5 mm. Die Hopfenpflanze benötigt, um sich gut an den Draht festhalten zu können, eine bestimmte Oberflächenrauhigkeit auf der Drahtoberfläche. Bei dem herkömmlichen Eisendrahtergibt sich diese Oberflächenrauhigkeit durch den Herstellprozess und dadurch entstehenden Flugrost.The hops are currently made of iron, usually of ST 37 and have a round cross section with a diameter of 1.1 and 1.5 mm. The hop plant needs a certain surface roughness on the wire surface in order to be able to hold tight to the wire. In the conventional iron wire mesh, this surface roughness is due to the manufacturing process and resulting flash rust.
Der üblicherweise verwendete Eisendraht besitzt jedoch wesentliche Nachteile.However, the iron wire commonly used has significant disadvantages.
Ein erster Nachteil ist sein sehr hohes spezifisches Gewicht. Ein größerer Hopfenbauer besitzt ca. 100.000 Hopfenpflanzen, d.h. er muss jedes Jahr 100.000 Drähte neu anbringen. Hier hat er ungeheuere Gewichte zu transportieren und auch zu tragen.A first disadvantage is its very high specific gravity. A larger hop farmer owns about 100,000 hop plants, i. he has to rewire 100,000 wires every year. Here he has immense weights to transport and carry too.
Ein weiterer Nachteil ist der relativ hohe Preis.Another disadvantage is the relatively high price.
Ebenfalls nachteilig ist, dass beim Häckseln des Drahts ein sehr hoher Verschleiß an den Häckselmessern auftritt.Another disadvantage is that when chopping the wire a very high wear on the chopping knives occurs.
Ein besonderer Nachteil sind die sogenannten "Hopfen-Spikes". Wenn der Hopfenbauer mit dem Traktor und Wagen das Häckselgut mit den ca. 2 bis 5 Zentimeter langen Eisendrahtstücken von seinem Bauernhof auf die Felder fährt, kommt es regelmäßig vor, dass solche "Hopfen-Spikes" auf die Strasse fallen. Beim Überfahren dieser "Hopfen-Spikes" mit dem PKW bohren sich diese dann in die Reifen und führen zu hohen Schäden.A particular disadvantage is the so-called "hop spikes". When the hop farmer drives the shredded material from his farm to the fields with the tractor and wagon with the pieces of iron wire approx. 2 to 5 centimeters long, it regularly happens that such "hop spikes" fall on the road. When driving over these "hop spikes" with the car, they then drill into the tires and cause high damage.
Ein weiterer großer Nachteil ist die Anreicherung von umweltschädigenden Stoffen im Erdreich.Another major disadvantage is the accumulation of environmentally harmful substances in the soil.
Für die anderen oben angegebenen Anwendungsgebiete gilt bei Verwendung von Metalldrähten im Wesentlichen das gleiche.Essentially the same applies to the other fields of application given above when metal wires are used.
Zur Abhilfe der beschriebenen Probleme sind schon vielfach Kunststofffäden aus Monofilen oder multifile Fäden beschrieben worden. Keine der beschriebenen Fäden hat sich in der Praxis jedoch durchsetzen können. Dies liegt daran, dass bei allen Fäden aus Kunststoff jeweils nur eines der beschriebenen Vielzahl an Problemen mehr oder weniger gut gelöst wurde, die anderen jedoch geblieben sind.To remedy the problems described plastic threads of monofilaments or multifilament threads have been described many times. However, none of the described threads has prevailed in practice. This is because with all threads made of plastic only one of the described variety of problems was solved more or less well, but the others have remained.
So ist in der
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Der vorliegenden Erfindung liegt daher die Aufgabe zugrunde, ein verbessertes Garn mit steuerbarer biologischer Abbaubarkeit und Kompostierbarkeit sowie ausgezeichneter Reißfestigkeit und Reißdehnung bereitzustellen.The present invention is therefore based on the object to provide an improved yarn with controllable biodegradability and compostability and excellent tensile strength and elongation at break.
Außerdem soll ein Verfahren zur Herstellung derartiger Garne beschrieben werden.In addition, a method for producing such yarns will be described.
Überaschenderweise wurde erfindungsgemäß festgestellt, dass durch Kombination eines Kernmaterials aus biologisch abbaubaren und kompostierbaren Naturfasern und/oder Chemiefasern mit einem Hüllmaterial aus biologisch abbaubaren und kompostierbaren Biopolymeren ein Garn mit steuerbarer biologischer Abbaubarkeit und Kompostierbarkeit sowie ausgezeichneter Reißfestigkeit und Reißdehnung erhalten werden kann.Surprisingly, according to the invention, it has been found that by combining a core material of biodegradable and compostable natural fibers and / or man-made fibers with a shell material of biodegradable and compostable biopolymers, a yarn having controllable biodegradability and compostability as well as excellent tear strength and elongation at break can be obtained.
Gegenstand der vorliegenden Erfindung ist somit ein biologisch abbaubares und kompostierbares Garn, das ein Kernmaterial aus Naturfasern und/oder Chemiefasern enthält und ein Hüllmaterial aus biologisch abbaubaren und kompostierbaren Biopolymeren umfasst.The present invention thus provides a biodegradable and compostable yarn containing a core material of natural fibers and / or man-made fibers and comprising a shell material of biodegradable and compostable biopolymers.
Erfindungsgemäß handelt es sich bei den den Kern des erfindungsgemäßen Garns bildenden Werkstoffen um solche aus Naturfasern wie beispielsweise Baumwolle, Flachs (Leinen), Hanf, Sisal, Jute, Kokos, Bast, Ramie und/oder Chemiefasern beispielsweise aus natürlichen Polymeren wie z.B. Viskose, Cellulose, Lyocell und/oder Tencel, sowie Fasern von biologisch abbaubaren und kompostierbaren aliphatischen und/oder teilaromatischen Polyesteramiden und/oder aliphatischen und/oder teilaromatischen Polyestern.According to the invention, the materials forming the core of the yarn of the invention are those of natural fibers such as cotton, flax, hemp, sisal, jute, coconut, bast, ramie and / or man-made fibers, for example of natural polymers such as e.g. Viscose, cellulose, lyocell and / or Tencel, and fibers of biodegradable and compostable aliphatic and / or partially aromatic polyester amides and / or aliphatic and / or partially aromatic polyesters.
In einer bevorzugten Ausführungsform der vorliegenden Erfindung sind die Kernfasem aus Naturfasern, die aus Baumwolle, Flachs(Leinen), Hanf, Sisal, Cellulose und/oder Jute bestehen, ausgewählt. Besonders bevorzugt handelt es sich erfindungsgemäß bei den den Kern bildenden Materialien um Naturfasern aus Sisal, da Sisal eine natürliche wasserabweisende Wirkung hat.In a preferred embodiment of the present invention, the core fibers are selected from natural fibers consisting of cotton, flax (linen), hemp, sisal, cellulose and / or jute. According to the invention, the materials forming the core are particularly preferably natural fibers of sisal, since sisal has a natural water-repellent action.
Unter dem Begriff "biologisch abbaubar und kompostierbar" werden erfindungsgemäße biologisch abbaubare und kompostierbare Garne verstanden, die vollständig gemäß DIN EN 13 432 biologisch abbaubar und kompostierbar sind.The term "biodegradable and compostable" means biodegradable and compostable yarns according to the invention which are completely biodegradable and compostable according to DIN EN 13 432.
Das erfindungsgemäße Garn zerfällt nach einer bestimmten, vorgebbaren Zeit und wird unter Kompostierbedingungen durch die Bakterien und Mikroben im Erdreich in natürliche Ausscheidungsprodukte umgewandelt, so dass hierbei sogar noch eine natürliche Düngung erreicht wird.The yarn according to the invention disintegrates after a certain, predeterminable time and is converted under composting conditions by the bacteria and microbes in the soil into natural waste products, so that in this case even a natural fertilization is achieved.
Die Zeit, die das erfindungsgemäße Garn bis zum vollständigen Abbau benötigt, ist in Grenzen (beispielsweise durch den Gewichtsanteil an Hüllmaterial, bezogen auf das Gesamtgewicht des erfindungsgemäßen Garns) einstellbar, d.h. das erfindungsgemäße Garn kann definiert in seiner Abbauzeit auf jeden einzelnen Anwendungsfall eingestellt werden.The time required for the yarn of the present invention to fully degrade is limited (e.g., by the weight fraction of shell material, based on the total weight of the yarn of the invention), i.e., adjustable. The yarn according to the invention can be defined in terms of its degradation time to each individual application.
Durch Variation beispielsweise des Kernmaterials kann ferner die Reißfestigkeit des erfindungsgemäßen Garns ebenfalls auf jeden speziellen Anwendungsfall eingestellt werden.By varying, for example, the core material, the tear strength of the yarn according to the invention can also be adjusted to any particular application.
Werden als Kernmaterial biologisch abbaubare und kompostierbare Fasern aus aliphatischen und/oder teilaromatischen Polyesteramiden und/oder aliphatischen und/oder teilaromatischen Polyestern verwendet, kann es sich bei diesen um die folgenden Polymere handeln:
- Aliphatische und/oder teilaromatische Polyester:
- A) aus aliphatischen bifunktionellen Alkoholen, bevorzugt linearen C2 bis C10-Dialkoholen wie beispielsweise Ethandiol, Butandiol, Hexandiol oder besonders bevorzugt Butandiol und/oder gegebenenfalls cycloaliphatischen bifunktionellen Alkoholen, bevorzugt mit 5 oder 6 C-Atomen im cycloaliphatischen Ring, wie beispielsweise Cyclohexandimethanol, und/oder teilweise oder vollständig statt der Diole monomeren oder oligomeren Polyolen auf der Basis von Ethylenglykol, Propylenglykol, Tetrahydrofuran oder Copolymeren daraus mit Molekulargewichten bis 4000, bevorzugt bis 1000, und/oder gegebenenfalls geringen Mengen verzweigten bifunktionellen Alkoholen, bevorzugt C3-C12-Alkyldiolen, wie beispielsweise Neopentylglykol, und zusätzlich gegebenenfalls geringen Mengen höherfunktionellen Alkoholen wie beispielsweise 1,2,3-Propantriol oder Trimethylolpropan sowie aus aliphatischen bifunktionellen Säuren, vorzugsweise C2-C12-Alkyldicarbonsäuren, wie beispielsweise und bevorzugt Bernsteinsäure, Adipinsäure und/oder gegebenenfalls aromatischen bifunktionellen Säuren wie beispielsweise Terephthalsäure, Phthalsäure, Naphthalindicarbonsäure und zusätzlich gegebenenfalls geringen Mengen höherfunktionellen Säuren wie beispielsweise Trimellitsäure oder
- B) aus säure- und alkoholfunktionalisierten Bausteinen, vorzugsweise mit 2 bis 12 C-Atomen in der Alkylkette beispielsweise Hydroxybuttersäure, Hydroxyvaleriansäure, Milchsäure, oder deren Derivaten, beispielsweise ε-Caprolacton oder Dilactid,
oder einer Mischung und/oder einem Copolymer enthaltend A und B,
wobei die aromatischen Säuren nicht mehr als 50 Gew.-% Anteil, bezogen auf alle Säuren, ausmachen.
- Aliphatische und/oder teilaromatische Polyesteramide:
- C) aus aliphatischen bifunktionellen Alkoholen, bevorzugt linearen C2 bis C10-Dialkoholen wie beispielsweise Ethandiol, Butandiol, Hexandiol oder besonders bevorzugt Butandiol und/oder gegebenenfalls cycloaliphatischen bifunktionellen Alkoholen, vorzugsweise mit 5 bis 8 C-Atomen im cycloaliphatischen Ring, wie beispielsweise Cyclohexandimethanol, und/oder teilweise oder vollständig statt der Diole monomeren oder oligomeren Polyolen auf der Basis von Ethylenglykol, Propylenglykol, Tetrahydrofuran oder Copolymere daraus mit Molekulargewichten bis 4000, bevorzugt bis 1000, und/oder gegebenenfalls geringen Mengen verzweigten bifunktionellen Alkoholen, vorzugsweise mit C2-C12-Alkyldicarbonsäuren, wie beispielsweise Neopentylglykol und zusätzlich gegebenenfalls geringen Mengen höherfunktionellen Alkoholen wie beispielsweise 1,2,3-Propantriol, Trimethylolpropan sowie aus aliphatischen bifunktionellen Säuren wie beispielsweise und bevorzugt Bernteinsäure, Adipinsäure und/oder gegebenenfalls aromatischen bifunktionellen Säuren wie beispielsweise Terephthalsäure, Isophthalsäure, Naphthalindicarbonsäure und zusätzlich gegebenenfalls geringen Mengen höherfunktionellen Säuren wie beispielsweise Trimellitsäure oder
- D) aus säure- und alkoholfunktionalisierten Bausteinen, vorzugsweise mit 2 bis 12 C-Atomen in der Kohlenstoffkette, beispielsweise Hydroxybuttersäure, Hydroxyvaleriansäure, Milchsäure oder deren Derivaten, beispielsweise ε-Caprolacton oder Dilactid,
oder einer Mischung und/oder einem Copolymer enthaltend C) und D),
wobei die aromatischen Säuren nicht mehr als 50 Gew.-% Anteil. bezogen auf alle Säuren, ausmachen, - E) einem Amidanteil aus aliphatischen und/oder cycloaliphatischen bifunktionellen und/oder gegebenenfalls geringen Mengen verzweigten bifunktionellen Aminen, bevorzugt sind lineare aliphatische C2 bis C10-Diamine, und zusätzlich gegebenenfalls geringen Mengen höherfunktionellen Aminen, unter den Aminen bevorzugt Hexamethylendiamin, Isophorondiamin und besonders bevorzugt Hexamethylendiamin, sowie aus linearen und/oder cycloaliphatischen bifunktionellen Säuren, vorzugsweise mit 2 bis 12 C-Atomen in der Alkylkette bzw. C5- oder C6-Ring im Falle von cycloaliphatischen Säuren, bevorzugt Adipinsäure, und/oder gegebenenfalls geringen Mengen verzweigten bifunktionellen und/oder gegebenenfalls aromatischen bifunktionellen Säuren wie beispielsweise Terephthalsäure, Isophthalsäure, Naphthalindicarbonsäure und zusätzlich gegebenenfalls geringen Mengen höherfunktionellen Säuren, vorzugsweise mit 2 bis 10 C-Atomen, oder
- F) aus einem Amidanteil aus säure- und aminfunktionalisierten Bausteinen, vorzugsweise mit 4 bis 20 C-Atomen in dercycloaliphatischen Kette, bevorzugt ω-Laurinlactam, ε-Caprolactam, besonders bevorzugt ε-Caprolactam,
der Esteranteil C) und/oder D) mindestens 20 Gew.-%, bezogen auf die Summe aus C), D), E) und F) beträgt, vorzugsweise der Gewichtsanteil der Esterstrukturen 20 bis 80 Gew.-%, der Anteil der Amidstrukturen 80 bis 20 Gew.-% beträgt.
- Aliphatic and / or partially aromatic polyesters:
- A) from aliphatic bifunctional alcohols, preferably linear C 2 to C 10 dialcohols such as ethanediol, butanediol, hexanediol or more preferably butanediol and / or optionally cycloaliphatic bifunctional alcohols, preferably having 5 or 6 carbon atoms in the cycloaliphatic ring, such as cyclohexanedimethanol , and / or partially or completely instead of the diols of monomeric or oligomeric polyols based on ethylene glycol, propylene glycol, tetrahydrofuran or copolymers thereof with molecular weights up to 4000, preferably up to 1000, and / or optionally small amounts of branched bifunctional alcohols, preferably C 3 -C 12- Alkyldiolen, such as neopentyl glycol, and additionally optionally small amounts of higher functionality alcohols such as 1,2,3-propanetriol or trimethylolpropane and aliphatic bifunctional acids, preferably C 2 -C 12 alkyl dicarboxylic acids, such as and preferably Bernst acid, adipic acid and / or optionally aromatic bifunctional acids such as terephthalic acid, phthalic acid, naphthalenedicarboxylic acid and additionally optionally small amounts of higher-functional acids such as trimellitic acid or
- B) from acid- and alcohol-functionalized building blocks, preferably with 2 to 12 C atoms in the alkyl chain, for example hydroxybutyric acid, hydroxyvaleric acid, lactic acid, or derivatives thereof, for example ε-caprolactone or dilactide,
or a mixture and / or a copolymer comprising A and B,
wherein the aromatic acids constitute not more than 50% by weight, based on all acids.
- Aliphatic and / or partly aromatic polyesteramides:
- C) from aliphatic bifunctional alcohols, preferably linear C 2 to C 10 dialcohols such as ethanediol, butanediol, hexanediol or more preferably butanediol and / or optionally cycloaliphatic bifunctional alcohols, preferably having 5 to 8 carbon atoms in the cycloaliphatic ring, such as cyclohexanedimethanol and / or partially or completely instead of the diols monomeric or oligomeric polyols based on ethylene glycol, propylene glycol, tetrahydrofuran or copolymers thereof with molecular weights up to 4000, preferably up to 1000, and / or optionally small amounts of branched bifunctional alcohols, preferably with C 2 - C 12 -alkyldicarboxylic acids, such as neopentyl glycol and additionally optionally small amounts of higher functional alcohols such as 1,2,3-propanetriol, trimethylolpropane and aliphatic bifunctional acids such as and preferably Bernteinsäure, adipic acid and / or geg also aromatic bifunctional acids such as terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid and additionally optionally small amounts of higher-functional acids such as trimellitic acid or
- D) from acid- and alcohol-functionalized building blocks, preferably with 2 to 12 C atoms in the carbon chain, for example hydroxybutyric acid, hydroxyvaleric acid, lactic acid or derivatives thereof, for example ε-caprolactone or dilactide,
or a mixture and / or a copolymer comprising C) and D),
wherein the aromatic acids not more than 50 wt .-% share. based on all acids, make up, - E) an amide portion of aliphatic and / or cycloaliphatic bifunctional and / or optionally small amounts of branched bifunctional amines, preferably linear aliphatic C 2 to C 10 diamines, and additionally optionally small amounts of higher functional amines, among the amines preferably hexamethylenediamine, isophoronediamine and especially preferably hexamethylenediamine, and from linear and / or cycloaliphatic bifunctional acids, preferably branched with 2 to 12 C atoms in the alkyl chain or C 5 - or C 6 ring in the case of cycloaliphatic acids, preferably adipic acid, and / or optionally small amounts bifunctional and / or optionally aromatic bifunctional acids such as terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid and additionally optionally small amounts of higher-functional acids, preferably having 2 to 10 carbon atoms, or
- F) from an amide moiety of acid- and amine-functionalized building blocks, preferably with 4 to 20 C atoms in the cycloaliphatic chain, preferably ω-laurolactam, ε-caprolactam, particularly preferably ε-caprolactam,
the ester fraction C) and / or D) is at least 20% by weight, based on the sum of C), D), E) and F), preferably the weight fraction of the ester structures is from 20 to 80% by weight, the proportion of Amide structures 80 to 20 wt .-% is.
Alle als Säuren genannten Monomere können auch in Form von Derivaten wie beispielsweise Säurechloride oder Ester, sowohl als Monomere als auch als oligomere Ester, eingesetzt werden.All monomers mentioned as acids can also be used in the form of derivatives such as, for example, acid chlorides or esters, both as monomers and as oligomeric esters.
Das erfindungsgemäße Garn hat den Vorteil, dass durch die Verwendung von Naturfasern, wie beispielsweise Baumwolle, Flachs(Leinen), Hanf, Sisal, Jute, Ramie und Kokos, und/oder Chemiefasern aus natürlichen Polymeren, wie beispielsweise Viskose (eine Definition dieser Begriffe findet sich z.B. im
Um das Kernmaterial des erfindungsgemäßen Garns herum befindet sich ein Überzug aus einem biopolymeren Material. Bei dem das Hüllmaterial bildenden biopolymeren Material kann es sich um biopolymere Materialien aus Stärke (beispielsweise Maisstärke, Kartoffelstärke, Weizenstärke, Reisstärke, Tapiokastärke, Sorghumstärke, Maniokstärke, Erbsenstärke, modifizierte Stärken, Stärkeabbauprodukte), Cyclodextrinen, Polymilchsäure, biologisch abbaubaren Harzen, Milcheiweiß, Casein, Zucker, Pflanzenölen, Cellulose (beispielsweise Celluloseacetat), aliphatischen und/oder (teil)aromatischen Polyestern (beispielsweise den oben beschriebenen), Polyhydroxyalkanoaten und/oder Polyvinylalkohol/Stärke-Mischungen handeln. Vorzugsweise ist das Hüllmaterial aus pflanzlichen biopolymeren Materialien und/oder erdölbasierenden biopolymeren Materialien ausgewählt. In einer bevorzugten Ausführungsform ist das Hüllmaterial beispielsweise aus Stärke, Polymilchsäure, Cellulose, Gemischen aus aromatischen und aliphatischen Polyestern und/oder Polyvinylalkohol/Stärke-Mischungen ausgewählt. Diese biologisch abbaubaren und kompostierbaren Hüllmaterialien können ferner andere Bestandteile umfassen, vorausgesetzt, dass das erfindungsgemäße Garn die vollständige biologische Abbaubarkeit und Kompostierbarkeit gemäß DIN EN 13 432 aufweist. Derartige Hüllmaterialien sind beispielsweise im Handel erhältlich, z.B. unter der Handelsbezeichnung biomat von der Firma Pro-Tech, ECOFLEX von der Firma BASF, Materbi von der Firma Novamont, Natureflex von der Firma Inovia Films, oder Biophan von der Firma Treofan.Around the core material of the yarn according to the invention is a coating of a biopolymeric material. The biopolymer material forming the shell material can be biopolymeric materials of starch (for example, corn starch, potato starch, wheat starch, rice starch, tapioca starch, sorghum starch, manioc starch, pea starch, modified starches, starch degradation products), cyclodextrins, polylactic acid, biodegradable resins, milk protein, casein , Sugar, vegetable oils, cellulose (for example cellulose acetate), aliphatic and / or (partially) aromatic polyesters (for example those described above), polyhydroxyalkanoates and / or polyvinyl alcohol / starch mixtures. Preferably, the shell material is selected from vegetable biopolymeric materials and / or petroleum-based biopolymeric materials. In a preferred embodiment, the shell material is selected, for example, from starch, polylactic acid, cellulose, mixtures of aromatic and aliphatic polyesters and / or polyvinyl alcohol / starch mixtures. These biodegradable and compostable shell materials may further comprise other components, provided that the yarn according to the invention has the complete biodegradability and compostability according to DIN EN 13 432. Such shell materials are commercially available, e.g. under the trade name biomat by Pro-Tech, ECOFLEX by BASF, Materbi by Novamont, Natureflex by Inovia Films, or Biophan by Treofan.
Der Anteil des biopolymeren Hüllmaterials, bezogen auf das Gesamtgewicht des erfindungsgemäßen Garns, beträgt üblicherweise 5 bis 40 Gew.-%, vorzugsweise 10 bis 30 Gew.-%, insbesondere 15 bis 25 Gew.-%.The proportion of the biopolymeric shell material, based on the total weight of the yarn according to the invention, is usually 5 to 40 wt .-%, preferably 10 to 30 wt .-%, in particular 15 to 25 wt .-%.
Üblicherweise wird das Kernmaterial des erfindungsgemäßen Garns mit einem oder mehreren der obengenannten Hüllmaterialien beaufschlagt. Durch Wahl und/oder Zusammensetzung der geeigneten Materialien für das Hüllmaterial lässt sich die Zeitdauer bis zum Einsetzen des Zersetzungsprozesses des erfindungsgemäßen Garns zeitlich genau steuern. In einer bevorzugten Ausführungsform kann die Zeitdauer bis zum Einsetzen des Zersetzungsprozesses des erfindungsgemäßen Garns durch geeignete Wahl der Zusammensetzung des Hüllmaterials, beispielsweise des Mischungsverhältnisses der verwendeten Hüllmaterialien, eingestellt werden. Vorzugsweise weist das Hüllmaterial eine Mischung aus pflanzlichen und erdölbasierenden Biopolymeren in einem Verhältnis von 1:1 bis 1:5, insbesondere 1:2 bis 1:4, noch besser 1:2 bis 1:3 auf. Bei den verwendeten pflanzlichen Biopolymeren kann es sich beispielsweise um Stärke, Cellulose und/oder Pflanzenöle handeln, die verwendeten erdölbasierenden Biopolymere sind beispielsweise Polyhydroxyalkanoate oder Polyester. In einer speziellen Ausführungsform der vorliegenden Erfindung besteht das Hüllmaterial aus einer Mischung aus pflanzlichen Biopolymeren wie z.B Maisstärke und erdölbasierenden Biopolymeren wie Polyhydroxyalkanoaten oder Polyestern im Verhältnis von 1:3. Hierdurch wird erreicht, dass das erfindungsgemäße Garn einen Zersetzungsbeginn von innerhalb von sechs Monaten aufweist.Usually, the core material of the yarn according to the invention is subjected to one or more of the above-mentioned shell materials. By choice and / or composition of the suitable materials for the shell material, the time period until the onset of the decomposition process of the yarn according to the invention can be precisely controlled in terms of time. In a In a preferred embodiment, the period of time until the onset of the decomposition process of the yarn according to the invention can be adjusted by suitable choice of the composition of the wrapping material, for example the mixing ratio of the wrapping materials used. The shell material preferably comprises a mixture of vegetable and petroleum-based biopolymers in a ratio of 1: 1 to 1: 5, in particular 1: 2 to 1: 4, more preferably 1: 2 to 1: 3. The vegetable biopolymers used may be, for example, starch, cellulose and / or vegetable oils; the petroleum-based biopolymers used are, for example, polyhydroxyalkanoates or polyesters. In a specific embodiment of the present invention, the shell material consists of a mixture of vegetable biopolymers such as corn starch and petroleum-based biopolymers such as polyhydroxyalkanoates or polyesters in a ratio of 1: 3. This ensures that the yarn according to the invention has a start of decomposition of within six months.
In einer weiteren speziellen Ausführungsform der vorliegenden Erfindung besteht das Hüllmaterial aus einer Mischung aus pflanzlichen Biopolymeren wie z.B Maisstärke und erdölbasierenden Biopolymeren wie Polyhydroxyalkanoaten oder Polyestern im Verhältnis von 1:2. Hierdurch wird erreicht, dass das erfindungsgemäße Garn einen Zersetzungsbeginn innerhalb von vier Monaten aufweist. Andere Mischungsverhältnisse können zu einer Verlängerung oder Verkürzung der Abbauzeit führen.In a further specific embodiment of the present invention, the shell material consists of a mixture of vegetable biopolymers such as corn starch and petroleum-based biopolymers such as polyhydroxyalkanoates or polyesters in a ratio of 1: 2. This ensures that the yarn according to the invention has a decomposition start within four months. Other mixing ratios may prolong or shorten the degradation time.
Die Applikation des Hüllmaterials auf das Kernmaterial des erfindungsgemäßen Garns kann beispielsweise durch Umhüllen, Verschweißen, Verschmelzen, Verkleben, maschinelles Verbinden, Aufschrumpfen oder Tauchbeschichten erfolgen.The application of the wrapping material to the core material of the yarn according to the invention can be done for example by wrapping, welding, fusing, gluing, machine bonding, shrinking or dip coating.
In einer Ausführungsform der vorliegenden Erfindung kann das Hüllmaterial in Form einer Folie um das Kernmaterial herum gewickelt werden. Die Folie des Hüllmaterials kann dabei eine Dicke in einem Bereich zwischen 0,001 und 0,2 mm, vorzugsweise in einem Bereich von 0,01 bis 0,1 mm, insbesondere in einem Bereich von 0,02 bis 0,08 mm aufweisen.In one embodiment of the present invention, the wrapping material may be wrapped in the form of a film around the core material. The film of the enveloping material may have a thickness in a range between 0.001 and 0.2 mm, preferably in a range of 0.01 to 0.1 mm, in particular in a range of 0.02 to 0.08 mm.
Erfindungsgemäß haben sich beispielsweise Kordelmaschinen zum Wickeln des Hüllmaterials, das beispielsweise in Form von Folien vorliegt, auf das Kernmaterial als vorteilhaft erwiesen. Eine Umhüllung kann erfindungsgemäß in einer anderen Ausführungsform unter Verwendung einer Schlauchfolienblasvorrichtung erfolgen, wobei die Hülle auf das Kernmaterial aufgeblasen wird.According to the invention, for example, cordless machines for winding the wrapping material, which is present for example in the form of films, have proved to be advantageous on the core material. According to the invention, an envelope can in another embodiment be made using a tubular film blowing device, wherein the envelope is inflated onto the core material.
Wie oben ausgeführt, kann das erfindungsgemäße Garn beispielsweise hergestellt werden, indem unter Verwendung von an sich bekannten textilen Verarbeitungsverfahren, wie beispielsweise Spinnen, Zwirnen, Flechten, Häkeln, Klöppeln, Stricken, Weben und/oder Wirken, die beispielsweise in Form von Stapelfasergamen (Spinnfasergarnen) oder Filamentgarnen vorliegenden Kernmaterialien aus Naturfasern und/oder Chemiefasern aus natürlichen Polymeren zusammengeführt oder als Faser verfestigt werden, so dass eine Festigkeit des erfindungsgemäßen Garns von mindestens 450 N erreicht wird.As stated above, the yarn according to the invention can be produced, for example, by using textile processing methods known per se, such as spinning, twisting, braiding, crocheting, bobbins, knitting, weaving and / or knitting, for example in the form of staple fiber yarns (spun yarns) ) or filament yarns present core materials of natural fibers and / or man-made fibers of natural polymers are combined or solidified as a fiber, so that a strength of the yarn of the invention of at least 450 N is achieved.
Gute Ergebnisse wurden auch mit Lyocellfasem und Tencelfasern erzielt, die gesponnen, verzwirnt oder geflochten werden. Tencelfasern eignen sich gut. Lyocell ist der Gattungsbegriff für lösungsmittelgesponnene Cellulosefasern, die nach dem NMMO- bzw. Lyocell-Verfahren hergestellt werden. Lyocellfasern sind beispielsweise von den Firmen Lenzing AG und Courtaulds Fibres, Coventry/Großbritannien, erhältlich. Tencelfasern sind eine Weiterentwicklung und ebenfalls von der Firma Courtaulds erhältlich. Tencel ist ein eingetragenes Warenzeichen. Diese Fasern haben den Vorteil, dass ihre Trockenfestigkeit höher ist als die jeder anderen kommerziellen Cellulose-Stapelfaser, im nassen Zustand ist diese Festigkeit noch ausgeprägter. Trocken ist die Festigkeit zweimal so hoch wie bei herkömmlichen Viskosefasern und nass dreimal so hoch.Good results have also been obtained with lyocell fibers and tencel fibers that are spun, twisted or braided. Tencel fibers work well. Lyocell is the generic term for solvent-spun cellulose fibers produced by the NMMO or lyocell process. Lyocell fibers are available, for example, from Lenzing AG and Courtaulds Fibers, Coventry / Great Britain. Tencel fibers are a further development and also available from the company Courtaulds. Tencel is a registered trademark. These fibers have the advantage that their dry strength is higher than any other commercial cellulose staple fiber; when wet, this strength is even more pronounced. Dry, the strength is twice as high as conventional viscose fibers and wet three times as high.
In einer bevorzugten Ausführungsform kann das Kernmaterial vor Aufbringen des Hüllmaterials mit einem Kleber beaufschlagt werden. Als Klebematerial eignen sich erfindungsgemäß solche, die sich mit dem Kernmaterial und dem Hüllmaterial verbinden und biologisch abbaubar sind. Als Beispiele lassen sich Kleber auf Stärkebasis oder auf Basis von Polyvinylalkohol nennen. Diese sind dem Fachmann auf dem einschlägigen Fachgebiet bekannt und im Handel erhältlich. Beispielsweise lassen sich die folgenden nennen: Planatol-Kleber auf Stärkebasis, Dispersionen auf Basis von Polyvinylalkohol wie z.B. Helmitin Kleber L 93/22-01 der Firma Forbo Helmitin, oder der Dispersionskleber Adhesin der Fa. Henkel.In a preferred embodiment, the core material can be applied with an adhesive before application of the wrapping material. As adhesive material according to the invention are those which combine with the core material and the shell material and are biodegradable. Examples are adhesives based on starch or based on polyvinyl alcohol. These are known to those skilled in the art and commercially available. For example, the following may be mentioned: starch-based planatol-based adhesives, polyvinyl alcohol-based dispersions, e.g. Helmitin adhesive L 93 / 22-01 from Forbo Helmitin, or the dispersion adhesive Adhesin from Henkel.
Durch die Mitverwendung eines Klebers kann die Reißfestigkeit des erfindungsgemäßen Garns erhöht und die Verbindung zwischen Kernmaterial und Hülle verbessert werden. Beispielsweise wird der Kleber in einem Anteil von 5 bis 30 Gew.-%, bezogen auf das Gewicht des Kernmaterials, aufgetragen. Bevorzugt liegt die Auftragsmenge in einem Bereich von 5 bis 20, idealerweise zwischen 7 und 10 Gew.-%. Durch die Mitverwendung eines Klebers kann das erfindungsgemäße Garn beispielsweise eine Reißfestigkeit von mindestens 500 N und eine Reißdehnung von höchstens 4 % erreichen.The concomitant use of an adhesive can increase the tensile strength of the yarn according to the invention and improve the bond between the core material and the casing. For example, the adhesive is applied in a proportion of 5 to 30% by weight, based on the weight of the core material. Preferably, the application amount is in a range of 5 to 20, ideally 7 to 10 wt .-%. By using an adhesive, the yarn according to the invention can, for example, achieve a tensile strength of at least 500 N and an elongation at break of not more than 4%.
Ferner kann bei Mitverwendung eines Klebers beispielsweise durch Wahl des geeigneten Herstellungsverfahrens des erfindungsgemäßen Garns der applizierte Kleber in das Kernmaterial fest eingearbeitet werden. So wird der Kleber beispielsweise nach Applikation auf das Kernmaterial unter Verwendung einer Seilereimaschine in die Fasern des Kernmaterials eingepresst, wodurch die Festigkeit des erfindungsgemäßen Garns deutlich steigt.Furthermore, when an adhesive is used, for example by selecting the suitable production method of the yarn according to the invention, the applied adhesive can be firmly incorporated into the core material. For example, after application to the core material, the adhesive is pressed into the fibers of the core material using a rope-making machine, whereby the strength of the yarn according to the invention increases significantly.
Erfolgt die Aufbringung des Hüllmaterials auf das Kernmaterial beispielsweise durch Aufschmelzen, entsteht auf der Oberfläche des erfindungsgemäßen Garns eine natürliche Rauhigkeit, wodurch das Pflanzenwachstum an dem erfindungsgemäßen Garn entlang verbessert wird. Das Aufschmelzen des Hüllmaterials kann erfindungsgemäß beispielsweise bei Temperaturen zwischen 50 und 200 °C, vorzugsweise zwischen 80 und 150 °C, insbesondere zwischen 100 und 130°C, je nach verwendetem Hüllmaterial erfolgen.If the application of the cladding material to the core material occurs, for example, by melting, A natural roughness develops on the surface of the yarn according to the invention, whereby the plant growth on the yarn according to the invention is improved along. The melting of the shell material according to the invention, for example, at temperatures between 50 and 200 ° C, preferably between 80 and 150 ° C, in particular between 100 and 130 ° C, depending on the shell material used.
Das erfindungsgemäße Garn kann die verschiedensten geometrischen Formen haben, beispielsweise rund, flach, mehrkantig, oval usw. Idealerweise hat das erfindungsgemäße Garn jedoch eine runde Form. Die Dicke des erfindungsgemäßen Garns kann in einem Bereich von 0,5 bis 10 mm, vorzugsweise 1 bis 8 mm, insbesondere 2 bis 6 mm, liegen.The yarn of the invention may have a variety of geometric shapes, such as round, flat, polygonal, oval, etc. Ideally, however, the yarn of the invention has a round shape. The thickness of the yarn according to the invention may be in a range of 0.5 to 10 mm, preferably 1 to 8 mm, in particular 2 to 6 mm.
In einer bevorzugten Ausführungsform der vorliegenden Erfindung besitzt das erfindungsgemäße Garn eine S-Drehung. Diese unterstützt das Wachstum der Pflanze und kann beispielsweise unter Verwendung einer Seilereimaschine erzeugt werden. Erfindungsgemäß haben sich dabei Schlaglängen in einem Bereich von 0,5 bis 4 cm, vorzugsweise 1 bis 3 cm, insbesondere 1,5 bis 2,5 cm als günstig erwiesen.In a preferred embodiment of the present invention, the yarn of the invention has an S twist. This supports the growth of the plant and can be generated, for example, using a rope machine. In this case, lay lengths in a range of 0.5 to 4 cm, preferably 1 to 3 cm, in particular 1.5 to 2.5 cm have proven to be favorable.
Ausgangsmaterial ist eine Sisalkordel mit einem Durchmesser von ca. 2,5 mm und einer Grundfestigkeit von ca. 400 N. Die Sisalkordel wird mittels eines Flyers von der Vorlagespule abgerollt und durch ein Leimbad gezogen, wobei der überflüssige Leim vor Verlassen der Leimstation von der Kordel abgestreift wird. Unmittelbar vor dem Einzug in eine handelsübliche Kordel-/Seilereimaschine, die so eingerichtet ist, dass das fertige Garn eine S-Drehung mit einer Schlaglänge von 1,5 cm erhält, wird die Sisalkordel mit einer 2 cm breiten und 0,03 mm starken biopolymeren Folie der Fa. Wenterra mit der Bezeichnung WBA 2000 umwickelt und durch einen Nipper gezogen und verpresst. Direkt nach Verlassen des Nippers wird die umwickelte Kordel mittels Heißluft miteinander verschmolzen und verfestigt und erhält durch das Rückdrehen der Kordel-/Seilereimaschine seine Endfestigkeit von mehr als 500 N und seine aufgeraute Oberfläche.Starting material is a sisal cord with a diameter of about 2.5 mm and a basic strength of about 400 N. The sisal cord is unrolled by a flyer from the supply spool and pulled through a glue bath, the excess glue before leaving the glue station of the cord is stripped off. Immediately prior to insertion into a commercial cord / ropemaking machine designed to give the finished yarn an S twist with a lay length of 1.5 cm, the sisal cord becomes a 2 cm wide and 0.03 mm thick biopolymer Wannerra film WBA 2000 wrapped and pulled through a Nipper and pressed. Immediately after leaving the nipper, the wrapped cord is fused together by means of hot air and solidified and, by turning back the cord / rope machine, its final strength of more than 500 N and its roughened surface are obtained.
Claims (7)
- A biodegradable and compostable twine which contains a core material of natural fibers and/or chemical fibers and a sheath material of biodegradable and compostable biopolymers, wherein the biodegradable and compostable biopolymers are selected from the group consisting of starch, cyclodextrins, polylactic acid, biodegradable resins, milk protein, casein, sugar, vegetable oils, cellulose, aliphatic and/or (partially) aromatic polyesters, polyhydroxyalkenoates, and polyvinyl alcohol/starch mixtures.
- A twine according to claim 1, wherein the core material consists of sisal.
- A twine according to claim 1 or claim 2, wherein the sheath material consists of polylactic acid.
- A twine according to one of the preceding claims, wherein the amount of sheath material based on the total weight of the inventive twine is 5-40 wt.%.
- A method for the production of a twine according to one of claims 1-4, wherein a core material of natural fibers and/or chemical fibers is wrapped with a sheath material of biodegradable and compostable biopolymers on a cording machine.
- A method according to claim 5, wherein the method also comprises the stage of fusing the sheath material onto the core material.
- A method according to claim 6, wherein the fusion step is carried out by the application of hot air.
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WO2022058950A1 (en) * | 2020-09-17 | 2022-03-24 | Cordenka Innovations GmbH | Biodegradable plant-training string |
Also Published As
Publication number | Publication date |
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DE102006016538A1 (en) | 2007-11-08 |
DK1842944T3 (en) | 2010-08-16 |
EP1842944A3 (en) | 2008-05-28 |
ES2345677T3 (en) | 2010-09-29 |
ES2345677T7 (en) | 2012-06-14 |
EP1842944A2 (en) | 2007-10-10 |
EP1842944B1 (en) | 2010-05-26 |
ATE469253T1 (en) | 2010-06-15 |
PT1842944E (en) | 2010-08-09 |
EP1842944B9 (en) | 2012-07-25 |
ES2345677T9 (en) | 2012-12-26 |
DE502007003898D1 (en) | 2010-07-08 |
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