阅读说明：本技术 可生物降解的纺织品、母料和制造可生物降解的纤维的方法 (Biodegradable textiles, masterbatches and method for producing biodegradable fibers ) 是由 A·费里斯 A·麦金托什 S·M·饶 小R·A·亚瑟 于 2019-05-10 设计创作，主要内容包括：公开了一种母料和相关方法,以及可生物降解的长丝、纤维、纱线和织物。母料包括0.2至5质量％的CaCO-3；脂肪族聚酯,其具有在酯基团之间的链中具有二至六个碳的重复单元,条件是链中的2至6个碳不包括侧链碳；以及载体聚合物,其选自由以下组成的群组：PET、尼龙、其他热塑性聚合物及其组合。(A masterbatch and related methods, and biodegradable filaments, fibers, yarns, and fabrics are disclosed. The master batch comprises 0.2 to 5 mass% of CaCO 3 (ii) a An aliphatic polyester having repeating units with two to six carbons in the chain between ester groups, with the proviso that 2 to 6 carbons in the chain do not include pendant carbons; and a carrier polymer selected from the group consisting of: PET, nylon, other thermoplastic polymers, and combinations thereof.)

1. A method of making a fiber comprising:

a masterbatch consisting essentially of:

0.2 to 5 mass% of CaCO₃；

An aliphatic polyester comprising repeating units having two to six carbons in the chain between ester groups, with the proviso that 2 to 6 carbons in the chain do not include pendant carbons;

and a carrier polymer selected from the group consisting of: PET, nylon, olefins, other thermoplastic polymers, and combinations thereof,

blending into a polymer selected from the group consisting of: PET, nylon, olefins, other thermoplastic polymers, and combinations thereof, to form a molten mixture; and subsequently extruding the molten mixture into filaments.

2. A method of making a fiber according to claim 1, comprising adding the masterbatch to a polymer production line after the polymer is made but while the polymer remains in a molten state.

3. The method of making a fiber of claim 1, comprising adding the masterbatch to a continuous polymer production line during polymerization of a target polymer.

4. The method of making a fiber of claim 1, further comprising quenching the extruded filaments.

5. The method of making a fiber of claim 4, further comprising deforming the filament.

6. A method of making a fiber as set forth in claim 5 comprising cutting the textured filament into staple fibers.

7. The method of making a fiber of claim 6, further comprising spinning the staple fiber into a yarn.

8. The method of claim 7, further comprising weaving the yarn machine into a fabric.

9. The method of claim 7, further comprising weaving the yarn into a fabric.

10. The method of claim 6, further comprising laying a nonwoven batt from the staple fibers.

11. The method of claim 1, comprising extruding the molten mixture into pellets, and

the pellets are then remelted prior to the step of extruding the mixture to form filaments.

12. The method of claim 1, wherein the masterbatch to be blended consists essentially of:

between 0.9 and 1.1 mass% calcium carbonate; and is

Wherein the aliphatic ester with 2-6 carbons is polycaprolactone, and the amount is 44-54 percent by mass;

further comprises polybutylene succinate with the amount of 9-11 mass%; and is

Wherein the remainder of the masterbatch is polyethylene terephthalate as the carrier polymer.

13. The method of claim 1, wherein the molten mixture consists essentially of:

0.39 to 0.48 weight percent of a polyester;

0.39-0.49 wt% PLC; and

0.01% by weight calcium carbonate; and

at least 90 mass% of PET.

14. The method of claim 1, wherein the molten mixture of claim 13 further comprises a composition selected from the group consisting of: 0.05-0.1 wt% PLA, 0.05-0.1 wt% PHA, 0.05-0.1 wt% PBAT, 0.10-0.20 wt% PBS, 0.01 wt% silica, and combinations of these compositions.

Technical Field

The present invention relates to polymer compositions suitable for textiles which are also biodegradable within a reasonably beneficial short time span compared to the most common polymers.

Background

Textiles are the foundation of human culture and have been manufactured and used by mankind for thousands of years. The earliest textiles were and will continue to be woven from natural fibers such as flax, wool, silk and cotton. More recently, polymers such as polyesters, nylon olefins, other thermoplastic polymers, and combinations thereof have also been employed in the industry to produce textile fibers, yarns, and fabrics. Many modern polymers can be made into an almost endless variety of shapes and products that are attractive, durable, and water resistant. In many cases, these synthetic fibers or yarns (depending on the desired technique and the end product) can be mixed with natural fibers to obtain an end product having the desired characteristics of natural and synthetic materials.

While durability and water resistance are desirable, these properties can lead to secondary environmental issues. Textiles made from polymer fibers do not naturally biodegrade like natural fibers (such as cotton and wool) and can remain in landfills and waters (e.g., lakes, oceans) for hundreds of years or longer. According to the U.S. environmental protection agency, approximately 4400 thousand pounds of synthetic (polymer) textiles are shipped to landfills daily. Furthermore, during the laundry washing cycle, most of the microfibers released from the clothes are captured by the sludge of the wastewater treatment plant. The sludge eventually becomes a biosolid that is sent to landfills or used as fertilizer. These polymer microfibers then accumulate in soil or other ground environments and may even become mobile, eventually passing from the terrestrial environment into the aquatic environment. According to some estimates, about 50 million tons per year of plastic microfibers produced from laundering textiles are released into the ocean. Certain high surface area microfibers can absorb large amounts of toxin loading and resemble micro-plankton, thereby increasing the accumulation of organisms in the food chain by several orders of magnitude. Conversely, because humans typically consume top-grade predatory species, such microfiber contamination may have adverse effects on human health.

As an additional problem, items such as carpet and upholstery (residential and commercial) are bulky relative to apparel and often incorporate larger, bulkier yarns, and therefore can occupy a significant amount of landfill space.

In the non-woven environment, all types of "wipes" (typically a non-woven sheet or several sheets) that are now ubiquitous also take up a lot of space, even when considered "flushable", and can clog municipal sewage systems, which is a problem for small volume, low flow toilets that are increasingly used.

In view of these environmental issues, the generation of biodegradable polymers has been the subject of considerable academic and industrial interest. These include the following examples, which are representative and not comprehensive.

Shah et al in "Microbial degradation of aliphatic and aliphatic-aromatic polyesters," appl. Microbiol. Biotechnol (2014)98: 3437-. Some polyesters (such as PET) are not biodegradable, as that term is used in the invention described herein.

Many patents have described biodegradable polymer compositions. For example, in WO2016/079724 to Rhodia Poliamida, a polyamide composition is modified to produce a biodegradable polyamide fiber. In this patent, the biodegradation rate is measured according to astm d5511 test standard. On pages 8-9, prior art methods of biodegradation are discussed, including: photodegradation, prodegradant additives such as transition metal salts, and rapid degradation leaving a biodegradable polymer with a porous structure with high interfacial area and low structural strength; these biodegradable polymers 10 are listed as including starch-based polymers, polylactic acid, polycaprolactone, polybutylene succinate, polybutylene terephthalate-co-adipate, and several other polymers; however, this patent application states that "unfortunately, higher amounts are required to make the polymer biodegradable, and compatible and plasticizing additives are also required". As an exemplary biodegradation agent, reference is made to Lake et al, U.S. published patent application No. 2008/010323215. The biodegradable agent is advantageously a masterbatch comprising at least six additives: (1) a chemoattractant or chemochemotactic compound; (2) glutaric acid; (3) carboxylic acids having a chain length of 5-18 carbons; (4) is biodegradableThe polymer of (a); (5) a carrier resin; and (6) a swelling agent. The present invention is exemplified using 2% of a commercially available biodegradation agentThe masterbatch of (4) for preparing a polyamide fiber by melt spinning. The resulting fibers were tested by astm d5511 standard and found to degrade 13.9% or 15.5% after 300 days. Fibers without the biodegradation agent degraded by 2.2% and 2.3% under the same astm d5511 test.

LaPray et al in US 2018/0100060 produce biodegradable articles such as films, bags, bottles, caps, sheets, boxes or other containers, plates, and the like, made from a blend of a polymer and a carbohydrate-based polymer. Biodegradability is tested according to established standards such as ASTM D-5511 and ASTM D-6691 (simulated ocean conditions)).

Tokiwa et al describe biodegradable resin compositions comprising a biodegradable resin and mannan (polysaccharide) digestion products. Tokiwa et al list biodegradable mannan digestion products, including various mannooligosaccharides.

Bastioli et al, in U.S. Pat. No. 308,466,237, describe a biodegradable aliphatic-aromatic copolyester made from 51 to 37% of an aliphatic acid containing at least 50% of brassylic acid (1, 11-undecabocarboxylic acid) and 49-63% of an aromatic carboxylic acid. The biodegradable polymers may be additionally modified by the addition of starch or polybutylene succinate and copolymerization with lactic acid or polycaprolactone.

Lake et al, in U.S. patent No. 9,382,416, describe a biodegradable additive for polymeric materials comprising a chemoattractant compound, glutaric acid, 5-carboxylic acid, and a swelling agent. Furanone compounds are considered as attractants for bacteria.

Wnuk et al, in U.S. patent No. 5,939,467, describe a biodegradable polyhydroxyalkanoate polymer containing a second biodegradable polymer, such as polycaprolactone, and examples of cast and blown films.

Various biodegradable formulations are known, but generally not in the textile field, and do not solve the problem of washability, some of which may utilize calcium carbonate. For example, Yoshikawa et al in U.S. published patent application No. 2013/0288322, Jeong et al in WO2005/017015, Tashiro et al in U.S. patent 9,617,462, and Whitehouse in U.S. patent application No. 2007/0259584.

Despite the considerable efforts, there remains a need for new methods and materials to provide synthetic textiles that are durable, waterproof, and degrade in wastewater treatment anaerobic digesters, landfill conditions, and marine environments. Therefore, it would be beneficial to manufacture synthetic textiles that maintain their desired properties and degrade more rapidly than conventional synthetic textile materials during wastewater treatment, in anaerobic digesters, under landfill conditions, and in marine environments.

Disclosure of Invention

In one aspect, the present invention provides a masterbatch comprising: 0.2 to 5 mass% of CaCO₃(ii) a An aliphatic polyester comprising repeating units having two to six carbons in the chain between ester groups, wherein the chain repeating units of 2 to 6 carbons do not include pendant carbons; and a carrier polymer comprising PET, nylon, olefins, other thermoplastic polymers, and combinations thereof. The 2 to 6 carbons in the chain repeat unit do not include carbons in the ester (COOR) moiety, and if a side chain carbon is present, more than 6 carbons (plus an ester carbon) may be present in the repeat group.

In some preferred embodiments of any of the inventive aspects, the aliphatic polyester comprises repeating units having three to six carbons or 2 to 4 carbons in the chain between ester groups. In a particularly preferred embodiment, the aliphatic polyester comprises polycaprolactone. In some preferred embodiments, the masterbatch further comprises polybutylene succinate (PBS), polybutylene succinate adipate (PBSA), polylactic acid (PLA), Polyethersulfone (PES), Polyhydroxybutyrate (PHB), poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), polybutylene adipate terephthalate (PBAT), polybutylene succinate adipate (PBSA), poly (butylene succinate-co-terephthalate) (PBST), poly (butylene succinate/terephthalate/isophthalate) -co- (lactate) PBSTIL, and combinations thereof.

Preferably, the masterbatch (and textile) is substantially free of saccharides.

In another aspect, the present invention provides a molten intermediate comprising: an aliphatic polyester other than PET comprising repeat units having two to six carbons in the chain between ester groups, wherein the 2 to 6 carbon chain repeat units do not include pendant carbons; 0.01 to 0.2 mass% of CaCO₃(ii) a And at least 90 mass% of PET, nylon, olefins, other thermoplastic polymers, and combinations thereof. As used herein, the phrase "other than PET" may be expressed as "other than polyethylene terephthalate", or "provided that the aliphatic polyester is not polyethylene terephthalate".

In a further aspect, the present invention provides a fiber comprising: an aliphatic polyester other than PET comprising repeat units having two to six carbons in the chain between ester groups, wherein the 2 to 6 carbon chain repeat units do not include pendant carbons; 0.01 to 0.2 mass% of CaCO₃(ii) a And at least 90 mass% of PET, nylon, olefins, other thermoplastic polymers, and combinations thereof.

In various embodiments, the textile may have one or any combination of the following properties: biodegradability such that when subjected to astm d5511 conditions for 266 days, the textile decomposes by at least 40%, or at least 50%, or in the range of from 40% to about 80%, or in the range of from 40% to about 75%; wherein the decomposition products from the ASTM test are primarily methane and carbon dioxide; dimensional stability such that the textile retains its shape and shrinks less than 10%, or less than 5%, or less than 3% when subjected to conditions of the home laundering test AATCC 135-20151 IIAii (80 ° F machine wash, drum dry, five wash cycles); wherein the textile is colored and has a color fastness of at least grade 3, or at least grade 4, or grade 5 when subjected to conditions of AATCC 61-20132A (mod 105 ° f) or AATCC 8-2016 or AATCC 16.3-2014 (option 3, 20 AFU); a burst strength of at least 20psi, preferably at least 50psi, or at least 100psi, or in the range of 50 to about 200psi, or 50 to about 150psi when subjected to the conditions of ASTM D3786/D3886M-13; and a wicking capability such that when subjected to the conditions of AATCC 197-2013, option B, the textile draws the water core out a distance of at least 10mm or at least 20mm, or in the range of about 10mm or about 20mm to about 150mm within 2 minutes.

In yet another aspect, the present invention provides a method of making a fiber, yarn or fabric comprising: mixing the masterbatch described herein into a polymer comprising PET, nylon, olefins, other thermoplastic polymers, and combinations thereof to form a molten mixture; extruding the mixture to form filaments; and cooling the filaments. These filaments can be woven and knitted ("filament yarns"), formed into nonwoven webs, or cut into staple fibers for woven, nonwoven, and knit fabric applications. Alternatively, the molten mixture may be extruded to form pellets, and the pellets may be subsequently remelted prior to the step of extruding the mixture to form the fibers. In a further aspect, the present invention provides a textile product comprising: fibers comprising CaCO₃And at least 90 mass% of PET, nylon, olefins, other thermoplastic polymers, and combinations thereof, and having biodegradability such that when subjected to conditions of ASTM D5511 for 266 days, the textile decomposes by at least 40%, or at least 50%, or in the range of 40% to about 80%, or in the range of 40% to about 75%; and wherein the textile comprises one or more of the following properties: dimensional stability such that the textile retains its shape and shrinks less than 10%, or less than 5%, or less than 3% when subjected to the conditions of the home laundering test 5AATCC 135-; wherein the textile is coloured and has a colour fastness of at least grade 3, or at least grade 4, or grade 5 when subjected to conditions of AATCC 61-20132A (mod 105F) or AATCC 8-2016 or AATCC 16.3-2014 (option 3, 20 AFU); when subjected to the conditions of ASTM D3786/D3886M-13, at least 20psi, preferably at least 50psi, or at least 100psi, or in the range of 50 to about 200psiOr a burst strength of 50 to about 150 psi; and a wicking capability such that when subjected to the conditions of AATCC 197-2013, option B, the textile absorbs water over a distance of at least 10mm or at least 20mm in 2 minutes, or in the range of about 10 or about 20mm to about 150 mm.

In some preferred embodiments, advantages of the present invention may include enhanced biodegradability per mass% masterbatch; higher durability of the fiber or textile compared to other biodegradable treatments; the performance of the fiber or textile is better maintained.

The foregoing and other objects and advantages of the invention and the manner of attaining them will become more apparent upon consideration of the following detailed description taken in conjunction with the accompanying drawings.

Drawings

Figures 1-5 are graphs of percent (%) biodegradation versus elapsed time (expressed in days) for several examples of the present invention and control examples of cellulosic materials and conventional polymers.

Fig. 6 is an SEM micrograph of partially digested fibers according to the present invention.

Fig. 7 is a series of photographs showing the testing of plants of the present invention.

Detailed Description

Glossary

"aliphatic polyesters" contain repeating ester units in which the hydrocarbon chain comprises an open (non-aromatic) chain. These may be homopolymers, copolymers containing only aliphatic groups or copolymers containing both aliphatic and aromatic groups.

A "carrier polymer" is a polymer in a masterbatch that is the same as or compatible and miscible with the polymer in which the masterbatch is incorporated.

Denier (Dpi) is the grammage of 9,000 meters of an individual filament. Can be calculated by taking the yarn denier and dividing it by the number of filaments in the bundle.

For the purposes of the present invention, a non-biodegradable polymer is a polymer that degrades by 10% or less after 266 days of testing according to ASTM D-5511.

PET, nylon and Spandex (Spandex) have conventional meanings. Nylon is polyamide; one preferred nylon is nylon 6, 6. Spandex is a polyether-polyurea copolymer.

Polymers are macromolecules (molecular weight in excess of 100 daltons, usually thousands of daltons) containing many repeating units.

A textile is a material composed of natural and/or synthetic 5 fibers, filaments or yarns, and may be in the form of a knit, woven or nonwoven.

The term "nonwoven fabric" is well known to those of ordinary skill in the art and is used herein consistent with this understanding, including definitions such as those in torora, Phyllis g, and Robert s.merkel.fairchild's Dictionary of textiles.7th ed.new York, NY: Fairchild Publications,2009, page 387.

Thus, a nonwoven fabric is "created by the bonding or interlocking of fibers, or both; textile structures achieved by mechanical, chemical, thermal or solvent means, and combinations thereof ". Exemplary methods of forming the base web include carding fibers, air laying, and wet forming. These webs may be secured or bonded by the use of adhesives, including low melt fibers dispersed in the web, thermal bonding for suitable thermoplastic polymers, needling, hydroentangling (hydroentanglement), and spunbond processes.

Those skilled in the art will understand that in the textile field, the word "spinning" has two different definitions, both of which are clear in context. In forming synthetic filaments, the term "spinning" refers to the step of extruding molten polymer into filaments.

In the context of natural fibers or staple fibers cut from textured synthetic filaments, the term "spun" is used in its most historical sense (dating back to the ancient times) to twist the filaments into a coherent yarn structure from which fabrics can be woven.

For general reference, Phylis G.Totora and Robert S.Merkel, Fairchild's Dictionary of Textiles 7th Edition, New York, Fairchild Publications 2009 provides many other definitions recognized by those of ordinary skill in the art.

ASTM and AATCC test protocols are considered industry standards. These protocols typically do not change significantly over time; however, if any question arises about the date of these criteria (not specified herein), the criteria will be selected to be in effect in month 1 of 2018.

Unless defined to the contrary, the term "percentage" or symbol "%" refers to a percentage by mass ("mass%"), which has the same meaning as "weight percent" or "weight percent" in the present specification. These uses are well understood by the skilled artisan in this context.

Masterbatch formulations capable of achieving biodegradation generally comprise a carrier polymer. The carrier polymer is preferably formulated to match the matrix (i.e., the non-biodegradable polymer). Thus, in exemplary embodiments, the carrier polymer is selected from the group consisting of: PET, nylon, olefins, other thermoplastic polymers, and combinations thereof. As shown by way of example, PET and nylon, in combination with other components of the present invention, have been shown to produce excellent biodegradability in launderable textiles.

Surprisingly, the inventors have found that the addition of calcium carbonate to the masterbatch significantly improves the biodegradability of the resulting textile while avoiding negative effects on washability.

Although the present invention is not limited by the mechanism by which calcium carbonate acts, and although the inventors do not wish to be bound by any particular theory, the following assumptions seem to be reasonable. The presence of microscopic inorganic particles of calcium carbonate mixed in a homogenous organic polymer matrix introduces excessive nucleation sites for biodegradation. This calcium carbonate is dosed simultaneously with other biodegradable components so that the nucleation points are very close to these components. Calcium ions may play an important role in bacterial growth. The presence of calcium binding proteins in bacteria contributes to signal transduction and may contribute to important processes of positive chemotaxis where bacteria move towards higher concentrations of chemical substances.

According to this hypothesis, the rate of decomposition of the polymer into monomers and oligomers by hydrolysis of ester bonds under the action of anaerobic bacteria is accelerated by the presence of dispersed calcium carbonate. The presence of carbon dioxide, a metabolic byproduct, may also enhance the dissolution of calcium carbonate present in the polymer matrix.

Another mechanism in which calcium and calcium binding proteins in bacteria can play an important role is quorum sensing, a means of communication by bacteria optimized for population growth. Individual bacteria strive to create a hydrogel, which is composed of bacteria and extracellular polymeric materials, forming a coordinated functional community. This macrostructure amplifies the action of bacteria and contributes to causing the biodegradation of the polymer according to the invention, in particular the high surface area microfibrils that can be incorporated into such hydrogels.

The masterbatch formulation is embedded in a polymer matrix. As a further aspect of the hypothesis, the chemical moiety of the hydrolytic attack on the polymer chain starts from the inside. The masterbatch dispersed in the matrix creates nucleation sites for erosion and exponentially increases the fiber surface area. Bacterial enzymes erode from the outside and enter the body. Bacteria (in the 1 micron range) will initially act on the textile fibres from the outside, but as the polymer matrix dissolves and disintegrates, new surface area is exposed. With the formation of a synergistic bacterial community in the hydrogel, the large polymer chains break down into oligomeric chains and further into monomers, which then digest to CO₂And CH₄。

Thus, the masterbatch of the invention can be considered to function in two stages: physicochemical action, which breaks down into smaller fragments at the beginning, and biochemical action, which digests 25 substances in the second half.

In some embodiments, the fibers in the yarn or textile have a denier per filament (dpf) of from 1 to 50 or from 2 to 30 or up to 1,000. The denier of the fiber is not considered important for biodegradability, as fibrous textiles will generally have sufficient surface area to support bacterial growth.

In exemplary embodiments, the masterbatch comprises at least 0.5 mass% calcium carbonate, in some embodiments up to 10% calcium carbonate, in some cases inBetween about 0.5% and 5% calcium carbonate, and typically at least about 1.0% calcium carbonate. The compositions of the present invention preferably use fine calcium carbonate powder, preferably having a mass average particle size of 15 microns (μm) or less, 10 μm or less, in some embodiments 7 μm or less, and may range from a mass average particle size of between 0.1 μm and 10 μm, or between 1 μm and 8 μm, or between 5 μm and 8 μm. Particle size may be measured by commercial light analysis equipment or other conventional means, as is conventional. The calcium carbonate powder has a particle size of at least 0.5 square meter per gram (m)²Surface area of/g); in some cases at least 1.0m²G, and in some embodiments between 0.5 and 10m²Between/g. As is conventional, surface area can be determined by methods such as ISO 9277 standard for calculating the specific surface area of solids, which in turn is based on Brunauer-Emmett-teller (bet) theory.

In some preferred embodiments, the masterbatch formulation contains one or any combination of the following: polycaprolactone (PCL), Polyhydroxybutyrate (PHB), polybutylene succinate (PBS), polylactic acid (PLA) and poly (tetramethylene adipate-co-phthalate). Polycaprolactone or blends comprising PCL as the main aliphatic polyester component appear to be advantageous because, surprisingly, PCL was found to be superior to polylactic acid (PLA), PHB and PBS.

Because textiles need to be durable, the masterbatch and textile composition should avoid components that adversely affect durability. Preferably, the composition has less than 5% by mass of saccharides, more preferably less than 2%, or less than 1%; or less than these amounts of furanones; or below these amounts of these organic (carbon-based) components that leach out during washing. In some embodiments, the compositions of the present invention lack any component that significantly reduces wash durability.

The textile preferably has dimensional stability such that the textile retains its shape and shrinks less than 10%, or less than 5%, or less than 3%, as measured by the home laundering test AATCC 135-.

The textile or fiber may be colored (such as red, blue, green, etc.) and preferably has a color fastness of at least grade 3, or at least grade 4, or grade 5, as measured by AATCC 61-20132A (mod 105F) or AATCC 8-2016, or AATCC 16.3-2014 (option 3, 20 AFU). The textile sheet (e.g., a fabric sample cut from a shirt or pant) preferably has a burst strength of at least 20psi, preferably at least 50psi, or at least 100psi, or in the range of 50 to about 200psi, or 50 to about 150psi, wherein the burst strength 30 is measured according to ASTM D3786/D3886M-13.

In some preferred embodiments, the fabric is free of fuzz or fuzz (grade 5 according to ASTM D3512M-16).

In some embodiments, the textile core absorbs water; this is particularly desirable in garments that wick perspiration away from the wearer; in some preferred embodiments, the fabric wicks water over a distance of at least 10mm or at least 20mm, or in the range of about 10mm or about 20mm to about 150mm, in 2 minutes; as measured by AATCC 197-2013. Measured values for textiles manufactured according to some embodiments of the present invention are shown in the performance test comparison tables (i.e., tables 1-7).

In some cases, the precise chemical structure within the fiber may not be known, and one or a combination of the above properties is the most accurate and/or precise method of characterizing a textile. The masterbatch is mixed with a non-biodegradable polymer such as polyethylene terephthalate, nylon, olefins, other thermoplastic polymers, and combinations thereof. For the purposes of the present invention, a non-biodegradable polymer is a polymer that degrades by 10% or less (preferably 5% or less, in some embodiments 3% or less, and in some embodiments between 2% and 10% or between 2% and 5%) after 266 days of testing according to ASTM D-5511 when the polymer is free of additives (in other words, prior to mixing with the masterbatch). the fiber comprises at least 50 mass%, more preferably at least 70%, still more preferably at least 90%, or at least 95%, and in some embodiments at least 99% of a polymer selected from the group consisting of polyethylene terephthalate (PET), nylon, olefins, other thermoplastic polymers, and combinations thereof.

The invention includes textiles comprising these fibers (either as a monocomponent textile, or mixed with other fibers). Many textiles comprise a mixture (blend) of fibers, for example, textiles containing spandex typically include cotton fibers. In some embodiments, the textile comprises at least 10%, or at least 20%, or at least 50%, or at least 80%, or at least 90%, or 100% fibers made from polyethylene terephthalate (PET), nylon, olefins, other thermoplastic polymers, and combinations thereof.

The fibers produced from the masterbatch generally comprise at least 90 mass% of a non-biodegradable polymer. Because the masterbatch is preferably added in an amount of between 0.5% and 5%, preferably at least 1%, and in some embodiments between 1% and 5%, and in some embodiments between 2% and 5%, and because all of the masterbatch is present in the resulting composition, the resulting fiber will contain a corresponding amount of material.

The invention also includes blended intermediates, fibers, yarns, and textiles. Examples of finished products according to the invention include: knitted fabrics, woven fabrics, non-woven fabrics, garments, upholstery, carpets, bedding articles such as bed sheets or pillowcases, agricultural or construction industrial fabrics. Examples of garments include: shirts, pants, bras, underpants, hats, undergarments, coats, skirts, dresses, tights, stretch pants, and scarves.

Of course, the calcium carbonate particles are ground to a size useful in the present invention. Functionally, the milled particles can be as small as possible, and very small particles do not present disadvantages.

However, the upper limit of the particle size is defined in part by the denier, and the layman will be described by diameter. In these terms, the average particle size of the calcium carbonate should be no greater than 10% of the diameter of the extruded filaments, and the maximum particle size should be no greater than 20% of the diameter of the extruded filaments, since particle sizes greater than about 10% of the filament diameter are more likely to cause breakage at all stages of production and use.

As noted above, the lower limit is less important, with the main consideration being that the difficulty and cost of producing smaller and smaller particles increases.

Thus, as a practical example, once a (1 denier) polyester fiber has a diameter of 10 microns (μ), this means that the particle size of the calcium carbonate should not exceed about 1 μ. The skilled person will be able to select the relevant particle size based on this general 10% relationship.

In a similar relationship, the masterbatch composition may be produced in the form of solid chips for storage and transportation. The end user can then grind the chips to the desired size for their particular end use application.

In some embodiments, the milled masterbatch particles are then mixed with a liquid, which is then in turn miscible with the desired final polymer. For example, but not limited to, polyethylene glycol or ethanol are suitable for the polyester process.

As a further consideration, the prepared masterbatch may be added to the target polymer at an alternate stage of production. As an option, the masterbatch may be added to the polymer production line after the polymer is made, but while the polymer remains molten.

Alternatively, the masterbatch may be added to a continuous polymer production line during polymerization of the target polymer. In such an arrangement, the masterbatch works well if it is miscible with the final stages of polymerization, for example in a high polymerization kettle of a continuous production line.

In the context of the present invention, spandex can be the target polymer of a masterbatch process, so long as the spandex is melt-spinnable. Those skilled in the art recognize that the spandex variant is solvent spun rather than melt spun, and that the present invention is used with melt spun versions.

The examples throughout this specification are not intended to be limiting, but in various embodiments the invention may be characterized by any selected combination of features. In some embodiments, the composition may be defined in part by the absence of certain components. In some embodiments, the composition avoids including starch or sugars; such components may be excessively soluble and result in textiles lacking sufficient durability. Additives such as polybutylene succinate are preferably not copolymerized with the non-biodegradable polymer, but form a degradable phase in the composition.

In some embodiments, the compositions of the present invention avoid aliphatic aromatic polyesters.

The fibers, yarns and fabrics of the present invention may be characterized by their physical properties, such as by the ASTM and/or AATCC tests described in the examples. For example, fibers, yarns, and fabrics may be defined by the degree of degradation according to ASTM testing based on the mass% of the biodegradable agent in the fiber. The molecular composition of the precursors, intermediates and final products can be determined by conventional methods such as gel permeation chromatography, more preferably gradient analysis of polymer blends.

Of course, the skilled artisan will appreciate that once the masterbatch is used in combination with the host polymer, the number of components will vary in proportion to the relative amount of masterbatch added to the host polymer.

It will also be understood by those skilled in the art that when the present invention is considered in its examples as a molten intermediate, in the most common textile applications, the melt may be extruded in the form of pellets or filaments. Extruding and quenching the melt into pellets provides the opportunity to store, transport, and re-melt the pellets at different locations (e.g., at the customer's location).

When quenched, the filaments from the composition can be texturized using techniques well known to those skilled in the art, and the fabric can then be formed directly from the texturized filaments ("filament yarns"), or the texturized filaments can be cut into staple fibers. Such staple fibers can in turn be spun into yarns, most commonly in open-end systems, but obviously also in loop spinning. The yarn may in turn be formed into a fabric (woven, knitted, non-woven), or may be blended with another polymer (e.g., rayon) or natural fiber (cotton or wool) to form a blended yarn, which in turn may be made into a fabric having the characteristics of the blended fiber.

Any of the formulations from table 1 may be used for any of the filaments, pellets, staple fibers, textured filaments, or fabrics mentioned herein.

As used herein, the terms "napping" and "napping" or "napping" refer to well-known finishing steps on manufactured textiles (e.g., torora, see pages 378-79, above). In this case, the invention can also be used for polar fleece, i.e. a soft, fluffy insulating fabric, usually made of polyester.

When formed into suitable filaments, the compositions according to the invention are expected to function well as a filler for thermal insulating garments.

The nature, structure and many variations of the insulating garment will be well understood by the skilled person. Basically, the insulation is encased in a lightweight shell, for which low denier nylon is typical, often including a water repellent treatment that can withstand at least some precipitation.

Down is of course the best insulation, in terms of compressibility, bulk and warmth to weight ratio, but even slightly heavier and less compressible, such as the synthetic wadding of the present invention is less costly and has better insulating properties when wet.

As another example, filaments, fibers and yarns according to the present invention are expected to perform very well as biodegradable carpets or parts of such carpets. As is well known to those skilled in the art, a carpet is a textile floor covering that is typically formed from pile or tufted yarns attached to a backing. Before the advent of synthetic materials, and still currently in use, the typical pile was made of wool, and the backing was made of a woven fabric to which the yarns could be woven, tufted or otherwise attached.

Those skilled in the art often use the terms "carpet" and "carpet tile" interchangeably, although in some cases "carpet" covers the entire room ("carpet that is a floor covering), while" carpet tile "covers less than the entire area of the room.

Because synthetic materials such as nylon, polypropylene, polyester, and blends thereof with wool are useful carpet materials, the fibers or yarns formed by the present invention are fully suitable and useful for carpets. Those skilled in the art recognize a variety of backing materials, backing structures, and means of attaching the pile or tufts to the backing. Repetition of all such possibilities would be redundant, not explicit, and one of ordinary skill in the art may employ the necessary materials and steps in any given context and without undue experimentation.

Examples of the invention

Various masterbatch compositions having the compositions shown in table 1 were prepared.

These masterbatches were blended into polyethylene terephthalate (1% masterbatch is typical) and fed in a closed loop with a gravimetric feeder into a melt extruder equipped with twin screws. The additive batches were mixed at 250 ℃ and extruded through a strand die into a water bath or equivalent quenching device. After the classifier removed the particles at the very end of the pellet size distribution, the pellets were dried and bagged.

The calcium carbonate used in the test had a mass average particle size of 6.5 microns and a surface area of about 1.5 square meters per gram.

The formulation was extruded into PET at a loading rate of 1% and tested for degradation according to ASTM D5511 for the formulation most compatible with the extrusion process. The results for 266 days are shown in fig. 1 and table 2, and the results for 353 days are shown in fig. 2 and table 3.

Initial readings were taken on day 59; in this very early reading, it appears that formulation 13 (table 1) shows 3.9% degradation, while formulation 14 does not appear to start degrading at all. However, based on the air pressure events and noise in the data, the data from formulations 13 and 14 appears to be unreliable and irreproducible. Furthermore, such low degradation readings are too close to baseline to be reliable (3% degradation for PET without additives), thus stopping testing of these formulations.

The results shown above indicate an advantage over the prior art. Under these landfill conditions, the PET fibers degrade to methane and carbon dioxide. After 266 days, the PET samples prepared with 1 mass% of masterbatch formulations #2, 3, 6, 7 and 11 in the table degraded 43.6%, 66.1%, 56.5%, 21.3% and 38.3%, respectively. Under the same conditions, unmodified PET was degraded by 3.2%. The highest degradation occurred with a masterbatch containing 49% polycaprolactone and 10% polyhydroxybutyrate, while the lowest degradation occurred with a masterbatch containing 39% polycaprolactone and 20% polybutylene succinate. The material made from 49% polycaprolactone and 10% polyhydroxybutyrate also degraded significantly better than PET modified with a 1% masterbatch containing 39% polycaprolactone, 10% polyhydroxybutyrate and 10% polybutylene succinate.

The above results can be compared with the results reported in WO2016/079724 ("results after days 1-300 of Table"), in WO2016/079724, the polyamide fibers are obtained using 2% of a commercially available biodegradation agent(https:// ecological-Iic. com/about/eco-one-video-court; visited 2.11.2019) was melt spun. The resulting fibers were tested by ASTM D5511 standard and found to degrade by 13.9% ("PA 6.6") or 15.5% ("PA 5.6") after 300 days. Fibers of WO2016/079724 without biodegradation agent under the same ASTM D5511 test2.2% and 2.3% degradation.

Based on unmodified fibres and ignoring the difference between 266 and 300 days, conventional PET (table 2 herein) appears to be 3.2/2.25 to 1.42 times more degradable than polyamide fibres in WO 2016/079724. In contrast, the modified PET according to the invention has a degradability of 21.3/15.5 to 4.26 times higher than that of the modified polyamide fiber in WO 2016/079724. Correcting for the fact that in WO2016/079724 the polyamide fibres are modified by twice as much masterbatch (2% relative to 1%), the degradability of the PET according to the invention is between 2.74 and 8.52 times. Correcting for the 2.74/1.42 difference between unmodified polyester and polyimide, the present invention shows greater biodegradability between 1.92 times and 3.00 times.

Table 4 and figure 3 show the improvement in biodegradation of the fabrics made from formulation 2 (table 1) and the control polyester.

ASTM D5210-anaerobic degradation in the Presence of sludge

The finished fabric from both formulations was stonewashed to form microfibers and the degradation of the microfibers was determined according to ASTM D5210 for 55 days, which mimics the conditions typically experienced in water treatment facilities. The results are shown in table 5 and fig. 4.

ASTM D6691-aerobic degradation model 5a Marine Environment

The finished fabric from one formulation was stonewashed to form microfibers and tested for degradation according to ASTM D6691 for 112 days. The results are summarized in table 6 and fig. 5.

Example-non-toxicity

The compositions were tested using the ASTM E1963 method, a protocol for phytotoxicity testing using terrestrial plant species (such as beans, corn and peas) to determine the effect of the test substances on plant growth and development. Peas are good indicators because they are very sensitive to soil conditions. In this ASTM E1963 test, leachate containing residual soil from the ASTM D5511 test of formulation 2 was used. Fig. 7 shows results from ASTM E1963 testing.

Plant growth was examined in both the background (column 1) and the sample (column 3), indicating that percolate with the relevant byproduct sample had no inhibitory effect on plant growth.

TABLE 7 examples of properties of textiles with and without masterbatch

Microscopic analysis of fibers subjected to bacterial decomposition

Electron microscopy imaging of fibers subjected to bacterial decomposition of fibers according to the invention in ASTM D5511 (SEM IIV: 15 kv; field of view 173 microns; SEM magnification 1.5 times; Tescan)^TM Vega 3^TMTungsten thermionic emission SEM system (https:// www.tescan.com/en-us/technology/SEM/vega 3); visit 2.12.2019) and show bacterial colonies on the surface of the polyester fiber according to the invention after > 1 year exposure to bacteria.

In the drawings and specification, there have been set forth preferred embodiments of the invention and, although specific terms are employed, they are used in a generic and descriptive sense only and not for purposes of limitation, the scope of the invention being defined by the following claims.