WO2015015331A1 - Solution spinning of fibers - Google Patents
Solution spinning of fibers Download PDFInfo
- Publication number
- WO2015015331A1 WO2015015331A1 PCT/IB2014/062485 IB2014062485W WO2015015331A1 WO 2015015331 A1 WO2015015331 A1 WO 2015015331A1 IB 2014062485 W IB2014062485 W IB 2014062485W WO 2015015331 A1 WO2015015331 A1 WO 2015015331A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fibers
- level
- water
- polymer
- spinning
- Prior art date
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 109
- 238000009987 spinning Methods 0.000 title claims abstract description 60
- 229920000642 polymer Polymers 0.000 claims abstract description 65
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 30
- 229920001410 Microfiber Polymers 0.000 claims abstract description 7
- 239000003658 microfiber Substances 0.000 claims abstract description 7
- 239000002121 nanofiber Substances 0.000 claims abstract description 7
- 239000003002 pH adjusting agent Substances 0.000 claims description 20
- 239000002904 solvent Substances 0.000 claims description 16
- 239000002250 absorbent Substances 0.000 claims description 14
- 230000002745 absorbent Effects 0.000 claims description 14
- 230000002378 acidificating effect Effects 0.000 claims description 12
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- 239000002131 composite material Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 125000000524 functional group Chemical group 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims 1
- 239000000243 solution Substances 0.000 description 56
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
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- 230000008569 process Effects 0.000 description 5
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- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
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- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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- 230000015572 biosynthetic process Effects 0.000 description 3
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
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- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- JGRXEBOFWPLEAV-UHFFFAOYSA-N 2-ethylbutyl prop-2-enoate Chemical compound CCC(CC)COC(=O)C=C JGRXEBOFWPLEAV-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
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- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 1
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- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
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- 108010035532 Collagen Proteins 0.000 description 1
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- 206010021639 Incontinence Diseases 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
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- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
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- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
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- OXOPJTLVRHRSDJ-SNAWJCMRSA-N [(e)-but-2-enyl] 2-methylprop-2-enoate Chemical compound C\C=C\COC(=O)C(C)=C OXOPJTLVRHRSDJ-SNAWJCMRSA-N 0.000 description 1
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- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
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- 238000005266 casting Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 125000000490 cinnamyl group Chemical group C(C=CC1=CC=CC=C1)* 0.000 description 1
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
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- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
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- 150000004665 fatty acids Chemical class 0.000 description 1
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- 150000004676 glycans Chemical class 0.000 description 1
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- 239000011121 hardwood Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 150000007524 organic acids Chemical class 0.000 description 1
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- 239000001814 pectin Substances 0.000 description 1
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- 235000010987 pectin Nutrition 0.000 description 1
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- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
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- 239000004094 surface-active agent Substances 0.000 description 1
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- 229920001897 terpolymer Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/16—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated carboxylic acids or unsaturated organic esters, e.g. polyacrylic esters, polyvinyl acetate
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/04—Dry spinning methods
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/18—Formation of filaments, threads, or the like by means of rotating spinnerets
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/005—Synthetic yarns or filaments
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/02—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of yarns or filaments
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/659—Including an additional nonwoven fabric
Definitions
- Fig. 1 illustrates a device that may be employed in the present invention to centrifugally spin fibers
- amine-containing basic polymers may include, for instance, poiyamides (e.g., N-substituted polyamides), po!yimides, polyimines (e.g., poiyethyieneimine), polyureas, etc.
- the fiber web may also be employed in a multi-layered laminate structure.
- the other layers of the laminate may include a nonwoven web (e.g., a me!t-spun web, such as a me!tblown or spunbond web), film, strands, etc.
- the laminate may contain a fiber web positioned between two spunbond webs.
- the wipe may be a "wet wipe” in that it contains a solution for cleaning, disinfecting, sanitizing, etc.
- the particular wet wipe solutions are not critical to the present invention and are described in more detail in U.S. Patent Nos. 6,440,437 to Krzysik, et al.; 8,028,018 to Amundson, et al; 5,888,524 to Cole; 5,867,835 to Win, et al.; 5,540,332 to Kopacz, et al.; and 4,741 ,944 to Jackson, et al.
Abstract
A technique for forming fibers (e.g., nanofibers, microfibers, etc.) from an aqueous spinning solution is provided. Through careful control over the nature and relative concentration of the components in the solution, fibers can be formed that remain relatively water resistant. To help accomplish these unique features, a pH-sensitive polymer is employed in the spinning solution that is generally soluble in water at a certain pH value, yet generally insoluble in water at a different pH value. This property allows for selective adjustment of the pH both before and after spinning to control the water-solubility of the polymer as desired.
Description
SOLUTION SPINNING OF FIBERS
Related . A jp 8catjon
The present application claims priority to U.S. application serial no.
13/953,097, filed on July 29, 2013, which is incorporated herein in its entirety by reference thereto.
Backgroun of the Invention
Solution spinning has become an important process for forming fibers, such as nanofibers and microfibers. To ensure good homogeneity of the polymer in the spinning solution, which aids in fiber formation, many traditional fiber processes employ the use of organic solvents, such as acetone, formic acid, methylene chloride, ethylene chloride, tetrahydrofuran, toluene, hexafiuoroisopropanoi, and trifluoroacetic acid. Due to the potential environmental concerns associated with such organic solvents, attempts have also been recently made to spin fibers from aqueous solutions. Unfortunately, aqueous solutions are often problematic in that they typically require the use of fiber-forming polymers that are generally soluble in water. While fibers can be readily spun from such polymers, the resulting fibers are highly susceptible to property degradation upon exposure to water due to the presence of a high concentration of water-soluble materials. As such, a need currently exists for a method of forming fibers from an aqueous spinning solution.
Summary of ' the i Invention
In accordance with one embodiment of the present invention, a method for forming fibers from an aqueous spinning solution is disclosed. The spinning solution contains a pH-sensitive polymer and a solvent that includes water. The pH-sensitive polymer is generally soluble in water at a first pH level and generally insoluble in water at a second pH level. The method comprises spinning the solution into fibers while at the first pH level and selectively adjusting the pH of the fibers during and/or after spinning so the pH is at the second pH level.
In accordance with another embodiment of the present invention, a fiber that is formed from an aqueous spinning solution is disclosed. The fiber contains one or more pH-sensitive polymers that are generally soluble in water at a first pH level and generally insoluble in water at a second pH level and optionally one or more hydrophiiic polymers that are generally soluble in water at the first pH level
and the second pH level The pH-sensitive polymers constitute about 50 wt.% or more of the polymer content of the fiber and the hydrophiiic polymers constitute less than about 50 wt.% of the polymer content of the fiber.
Other features and aspects of the present invention are discussed in greater detail below.
ief .OescrjBtjoo of the Dr wj fl
A fuli and enabling disclosure of the present invention, including the best mode thereof, directed to one of ordinary skill in the art, is set forth more
particularly in the remainder of the specification, which makes reference to the appended figures in which:
Fig. 1 illustrates a device that may be employed in the present invention to centrifugally spin fibers;
Fig. 2 is an SEM mi crop holograph showing the fibers formed in Example 2 at a magnification of 51 OX; and
Fig, 3 is an SEM microphotograph showing the fibers formed in Example 2 at magnification of 1850X.
Detailed Description of Representative Embodiments
Definjtjons
As used herein, the term "fibers" refer to elongated structures having a definite length or that are substantially continuous in nature. The fibers may be, for example, "nanofibers" or "microfibers." The term "nanofibers" generally refers to fibers having an average diameter of less than about 1 micrometer, in some embodiments about 800 nanometers or less, in some embodiments from about 5 nanometers to about 500 nanometers, and in some embodiments, from about 10 nanometers to about 100 nanometers, while the term "microfibers" generally refers to fibers having an average diameter of from about 1 micrometer to about 100 micrometers, in some embodiments about 2 micrometers to about 50 micrometers, in some embodiments from about 3 micrometers to about 40 micrometers, and in some embodiments, from about 5 micrometers to about 25 micrometers.
As used herein, the term "meitb!own" web generally refers to a nonwoven web that is formed by a process in which a molten thermoplastic material is extruded through a plurality of fine, usually circular, die capillaries as molten fibers into converging high velocity gas (e.g., air) streams that attenuate the fibers of
molten thermoplastic material to reduce their diameter. Thereafter, the meltb!own fibers are carried by the high velocity gas stream and are deposited on a collecting surface to form a web of randomly dispersed meltblown fibers,
As used herein, the term "spunbond" web generally refers to a nonwoven web containing substantially continuous filaments. The filaments are formed by extruding a molten thermoplastic material from a plurality of fine, usually circular, capillaries of a spinnerette with the diameter of the extruded filaments then being rapidly reduced as by, for example, eductive drawing and/or other well-known spunbonding mechanisms.
Detailed Description
Reference now will be made in detail to various embodiments of the invention, one or more examples of which are set forth below. Each example is provided by way of explanation of the invention, not limitation of the invention. Sn fact, it will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. For instance, features illustrated or described as part of one embodiment, can be used on another embodiment to yield a still further embodiment. Thus, it is intended that the present invention covers such modifications and variations within the scope of the appended claims and their equivalents.
Generally speaking, the present invention is directed to a technique for forming fibers (e.g., nanofibers, microfibers, etc.) from an aqueous spinning solution, The present inventors have discovered that through careful control over the nature and relative concentration of the components in the solution, fibers can be formed that remain relatively water resistant. To help accompiish these unique features, a pH-sensitive polymer is employed in the spinning solution that is generally soluble in water at a first pH level, yet generally insoluble in water at a second pH level. This property allows for selective adjustment of the pH both before and after spinning to control the water-solubility of the polymer as desired. Namely, the pH can be controlled prior to spinning so that the pH~sensitive polymer is dissolved in the solution in a substantially homogeneous fashion. After spinning, however, the pH may be altered so that when contacted with water, the
resulting fibers do not readily dissolve. Among other things, this allows the fibe to substantially retain their mechanical strength and integrity even when wet.
Various embodiments of the present invention will now be described in more detail.
I. Solution
As noted, the spinning solution of the present invention contains a pH- sensitive polymer. Typically, such polymers constitute from about 30 wt.% to about 90 wt.%, in some embodiments from about 40 wt.% to about 80 wt.%, and in some embodiments, from about 50 wt.% to about 70 wt.% of the spinning solution. The particular nature of the polymer may vary so long as it is generally soluble in water (e.g., at 25°C) at a certain pH level, yet generally insoluble in water (e.g., at 25°C) at a different pH level. The polymer may contain a relatively acidic functional group (e.g., carboxylic, sulfonic, etc.) and/or relatively basic functional group (e.g., tertiary amine) that imparts the desired pH sensitivity.
Acidic pH-sensitive polymers, for instance, often contain carboxylic groups. Examples of such carboxylic-containing acidic polymers may include, for instance, {meth)acry!ic acid polymers, vinyl acetate polymers, vinyl ether polymers, etc. As used herein, the term "(meth)acrylic" includes acrylic and methacryiic monomers, as well as salts or esters thereof, such as acrylate and methacrylate monomers. Particular examples of such (meth)acryiic monomers may include, for instance, acrylic acid, methacryiic acid, methyl acrylate, ethyl acrylate, n-propyl acrylate, \- propyl acrylate, n-butyl acrylate, s-buiyl acrylate, i-butyl acrylate, t-butyl acrylate, n- amyi acrylate, i-amyl acrylate, isobornyl acrylate, n-hexy! acrylate, 2-ethylbutyl acrylate, 2-ethylhexyl acrylate, n-octyS acrylate, n-decyi acrylate, methyicyclohexyl acrylate, cyciopentyl acrylate, cyclohexyl acrylate, methyl methacrylate, ethyl methacrylate, 2-hydroxyethyl methacryiate, n-propy! methacryiate, n-butyl methacrylate, i-propyi methacrylate, i-butyl methacrylate, n-amyi methacrylate, n- hexyl methacrylate, i-amy! methacrylate, s-butyl-methacryiate, t-butyl methacryiate, 2-ethy!butyl methacrylate, methyicyclohexyl methacrylate, cinnamyl methacryiate, crotyl methacrylate, cyclohexyl methacryiate, cyciopentyl methacrylate, 2- ethoxyethyl methacrylate, isobornyl methacryiate, etc., as well as combinations thereof. In one particular of the present invention, an acidic polymer may be
employed that is a terpolymer formed from an acrylate component (e.g., ethyl acry!ate), methacry!ate component (e.g., methyl mefhacrylate) and (meth)acry!ic acid component (e.g., acrylic acid or methacry!ic acid). Such polymers are commercially available under the name CARBOSET® from Lubrizoi. Basic pH- sensitive polymers may also be employed in the present invention. For instance, basic pH-sensitive polymers often contain primary, secondary, and/or tertiary amine groups. Examples of such amine-containing basic polymers may include, for instance, poiyamides (e.g., N-substituted polyamides), po!yimides, polyimines (e.g., poiyethyieneimine), polyureas, etc.
The pH at which the polymer is capable of being dissolved in water as a relatively homogenous solution will of course vary depending on the nature of the pH-sensitive polymer. When acidic polymers are employed, for instance, the pH at which a transition from solution to colloid occurs is typically from about 5 to about 15, in some embodiments from about 7 to about 14, and in some embodiments, from about 8 to about 12. The acidic poiymer may, for instance, remain in solution at a first pH level of about 5 or more, in some embodiments about 7 or more, in some embodiments about 8 or more, and in some embodiments, about 9 or more. Of course, at a second pH level of less than about 5, the acidic polymer may instead form a colloidal system with water and thus remain generally water- insoluble. In stark contrast, when basic polymers are employed, the pH level at which a transition from solution to colloid occurs is typically from about 1 to about 5. The basic polymer may, for instance, remain in solution within a pH range of about 5 or less, in some embodiments about 4 or less, and in some embodiments, about 3 or less. Within a pH range of greater than about 5, however, the basic poiymer may form a colloidal system with water and thus remain generally water- insoluble.
To aid in the desired pH transition, a pH modifier is also typically employed in the spinning solution. Such pH modifiers may be present in any effective amount needed to achieve the desired pH level, in some embodiments, for example, pH modifier(s) are present in an amount from about 0.001 wt.% to about 5 wt.%, in some embodiments from about 0.005 wt.% to about 2 wt.%, and in some embodiments, from about 0.01 wt.% to about 1 wt.% of the solution.
Various H modifiers may be utilized to achieve the desired pH level, Basic pH modifiers, for instance, may be employed in combination with acidic pH- sensitive polymers, while acidic pH modifiers may be employed in combination with basic pH-sensitive polymers. Examples of suitable basic pH modifiers may include, for instance, ammonia; mono-, di~, and tri-alkyl amines (e.g.,
triethylamine); mono-, di-, and tri-alkanolamines (e.g., monoethanolamine, isopropanolamine, diethanolamine, and triethanolamine); etc., as well as mixtures of basic pH modifiers. Examples of suitable acidic pH modifiers may likewise include, for instance, inorganic acids, such as hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, and po!yphosphoric acid; organic acids, as well as mixtures of acidic pH modifiers. Prior to spinning, the pH modifier helps ensure that the pH- sensitive polymer remains in solution. However, the present inventors have discovered that certain types of pH modifiers can be employed that readily evaporate from the fibers during and/or after their formation due to their relatively low boiling point. Of course, the boiling point is normally selected so that the modifier can be readily removed during and/or after spinning, but not to such an extent that a significant portion of the modifier is inadvertently released from the solution prior to spinning, in this regard, the pH modifier typically has a boiling point in water (atmospheric pressure) of from about 10°C to about 50°C, in some embodiments from about 15°C to about 45°C, and In some embodiments, from about 25°C to about 35°C. The boiling point of ammonia in water (ammonium hydroxide) is, for instance, about 37.7°C.
B, Solvent
In addition to a pH-sensitive polymer and optional pH modifier, a solvent may also be employed in the spinning solution. As indicated above, the spinning solution used to form the fibers of the present invention is generally aqueous in nature. In this regard, water (e.g., deionized water) typically constitutes about 50 wt.% or more, in some embodiments, about 70 wt.% or more, and in some embodiments, about 90 wt.% to 100 wt.% of the solvent(s) used in the solution. In some embodiments, a secondary solvent may also be employed in conjunction with water to form a solvent mixture. Suitable secondary solvents may include, for instance, glycols (e.g., ethylene glycol, propylene glycol, butylene glycol, triethylene glycol, hexylene glycol, polyethylene glycols, ethoxydiglycol,
dipropyienegiycol, etc.); glycol ethers (e.g., methyl glycol ether, ethyl glycol ether, isopropyl glycol ether, etc.); alcohols (e.g., methanol, ethanol, n-propanol, iso- propanol, and butanoi); ketones (e.g., acetone, methyl ethyl ketone, and methyl isobutyl ketone); esters (e.g.. ethyl acetate, butyl acetate, diethy!ene glycol ether acetate, methoxypropyl acetate, ethylene carbonate, propylene carbonate, etc.): amides (e.g., dimeihylformamide, dimethy!acetamide, dimethyicaprylic/capric fatty acid amide and N-aikylpyrrolldones); sulfoxides or suffones (e.g., dimethyl sulfoxide (DMSO) and sulfolane); and so forth. It should be understood, however, that such secondary solvents are by no means required in the present invention. In fact, as indicated above, one benefit of the present invention is that conventiona! organic solvents, such as acetone, formic acid, methylene chloride, ethylene chloride, tetrahydrofuran, toluene, hexafluoroisopropanol, and trifluoroacetic acid, are not required in the present invention. Thus, in certain embodiments, the spinning solution may be generally free of organic solvents such that they constitute, for example, about 10 wt.% or less, in some embodiments, about 5 wt.% or less, and in some embodiments, 0 to about 1 wt.% of solvent(s) used in the solution.
The total amount of solvent(s) employed in the spinning solution may vary, but is generally such that the resulting solution has a relatively high viscosity, such as from about 50,000 to about 800,000 centipoise, in some embodiments from about 80,000 to about 500,000 centipoise, and in some embodiments, from about 100,000 to about 400,000 centipoise, as determined using a Brookfield
programmable rheometer (Mode! DV-III). As is well known in the art, the speed and spindle size of the rheometer may be selected based on the general range of expected viscosities for the solution and to achieve a torque value between 10% and 100%. For example, in certain embodiments, the viscosity of the spinning solution may be determined with spindle number 7 and at a speed of 1 rpm. The total amount of soivent(s) employed in the spinning solution typically ranges from about 10 wt.% to about 60 wt.%, in some embodiments from about 15 wt.% to about 50 wt.%, and in some embodiments, from about 20 wt.% to about 40 wt.%, based on the total weight of the spinning solution.
C. Other Components
Although not required, a variety of other additives may also be employed in the spinning solution, such as catalysts, antioxidants, stabilizers, surfactants, spinning aids, waxes, nucleating agents, particulates, and other materials added to enhance processability or Impart other properties to the fibers. In one
embodiment, for example, a hydrophilic polymer is employed in the solution that is generally soluble in water (e.g., 25°C) at both the first and second pH ranges noted above. Among other things, such polymers can facilitate the ability of the pH- sensitive polymer to be spun. The hydrophilic polymer typically has a relatively high molecular weight to ensure that the resulting fibers can remain relatively water resistant, For instance, the hydrophilic polymer may have a weight average molecular weight of about 100,000 to about 5,000,000 grams per mole, in some embodiments from about 500,000 to about 3,000,000 grams per mole, and in some embodiments, from about 1 ,000,000 to about 2,000,000 grams per mole. When employed, such hydrophilic polymers typically constitute from about 0.5 wt.% to about 20 wt.%, in some embodiments from about 1 wt.% to about 15 wt.%, and in some embodiments, from about 2 wt.% to about 10 wt.% of the solution. Any suitable hydrophilic polymer may generaSlybe employed, such as polyvinyl alcohol, poSyacrylamide, collagen, pectin, chitin, chitosan, poly(a-amino acids), polyvinylpyrrolidone, polyethers, polysaccharides, polyurethanes, etc. Polyethers may be particularly suitable, such as polyalkyiene oxides (e.g., polyethylene oxide ("PEG") and polypropylene oxide ("PPG")). Polyalkyiene oxides may, for instance, have on average about 30 to about 15,000 oxide units (e.g., glycol units) per polymeric molecule.
II. Spinning
Generally speaking, any of a variety of known solution spinning techniques may generally be employed in the present invention, such as electrospinnlng, centrifugal spinning, etc. Centrifugal spinning, for instance, involves the
application of the spinning solution to a rotary sprayer having a rotating nozzle. The nozzle may have a concave inner surface and a forward surface discharge edge. The spinning solution moves through the rotary sprayer along the concave inner surface so that it is distributed toward the forward surface of the discharge edge of the nozzle. Separate fibrous streams are formed from the spinning
solution while the solvent vaporizes to produce fibers. A shaping fluid can flow around the nozzle to direct the spinning solution away from the rotary sprayer. The fibers may be collected on the surface in the form of a coherent nonwoven web of fibers. Optionally, an electrical field can be added to the process, such as between the spin disk and the collector, which creates a voltage potential between an electrode and the spin disk and/or the collector. While having a minimal impact on their formation, such an electric field may help the fibers separate and produce a more uniform web structure.
Referring to Fig. 1 , one particular embodiment of a device that may be employed to centrifugally spin fibers is shown. As shown, the device may include a rotating spin disk 10 having a flat surface 1 1 and a forward surface discharge edge 12 mounted on a drive shaft 13, which is connected to a high speed motor (not shown). The spinning solution may be pumped through a supply tube 14 running coaxially with the drive shaft 13 and in close proximity to the center of the spin disk 10. opposite to the side of the disk attached to the drive shaft 13. As the spinning solution exits the supply tube 14, it is directed into contact with the rotating spin disk 10 and travels along the flat surface 1 1 , which fully wets the flat surface and distributes the spinning solution as a film until it reaches the forward surface discharge edge 12. The rotational speed of the spin disk 10 is typically from about 4,000 to about 100,000 rpm, in some embodiments from about 6,000 to about 100,000 rpm, and in some embodiments, from about 8,000 to about 100,000 rpm. The forward surface discharge edge 12 can be sharp or rounded and can include serrations or dividing ridges. The rotation speed of the spin disk 10 propels the spinning solution along the flat surface 1 1 and past the forward surface discharge edge 12 to form separate fibrous streams, which are thrown off the discharge edge by centrifugal force. If desired, the fibrous streams may be collected on a surface to form a fibrous web.
Regardless of the particular technique employed, the solvent and pH modifier may be removed from the fibers during and/or after spinning, in certain embodiments, for example, the solvent and pH modifier are vaporized during the spinning process. Alternatively, however, the fibers (or a web containing the fibers) may simply be dried or heated to remove these components, it should also be understood that the solvent and pH modifier may be removed in separate steps
if so desired. In any event, the pH-sensitive polymer generally constitutes a majority of the polymers present in the resulting fibers. That is, pH-sensitive polymers typically constitute about 50 wt.% or more, in some embodiments, about 70 wt.% or more, and in some embodiments, from about 90 wt.% to 100 wt.% of the polymer content of the fibers. Because the pH-sensitive polymer within the fibers is generally insoluble in water at a second pH level due to the removal of the pH modifier, the resulting fibers are able to better retain good mechanical and physical properties after exposure to water due to its presence at high
concentrations. To the contrary, hydrophilic polymers (e.g., polyethylene oxide) that are generally soluble within the first and second pH ranges noted above typically constitute less than about 50 wt.%, in some embodiments, about 30 wt.% or less, and in some embodiments, from 0 wt.% to about 10 wt.% of the polymer content of the fibers.
The fibers of the present invention may be used alone or in the form of a coherent fibrous web structure. Typically, the fibrous web is a "nonwoven" web to the extent that individual fibers are randomly interlaid, not in an identifiable manner as in a knitted fabric. The basis weight of the fiber web may generally vary, but is typically from about 1 gram per square meter ("gsm") to 150 gsm, in some embodiments from about 2 gsm to about 100 gsm, and in some embodiments, from about 5 gsm to about 50 gsm.
If desired, the fibers may also be employed in a composite that contains a combination of the fibers with other types of fibers (e.g., staple fibers, filaments, etc.). For example, additional synthetic fibers may be utilized, such as those formed from polyolefins (e.g., polyethylene, polypropylene, polybutylene, etc.); polytetrafluoroethylene; polyesters (e.g., polyethylene terephthalate. polylactic acid, etc.); polyamides (e.g., nylon); polyvinyl chloride; polyviny!idene chloride; polystyrene; and so forth. The composite may also contain pulp fibers, such as high-average fiber length pulp, low-average fiber length pulp, or mixtures thereof. One example of suitable high-average length fluff pulp fibers includes softwood kraft pulp fibers. Low-average length fibers may also be used in the composite. An example of suitable low-average length pulp fibers is hardwood kraft pulp fibers. Such composites may be formed using a variety of known techniques. The relative percentages of the additional fibers may vary over a wide range depending
on the desired characteristics of the composite. For example, the composite may contain from about 1 wt.% to about 60 wt.%, in some embodiments from 5 wt.% to about 50 wt.%, and in some embodiments, from about 10 wt.% to about 40 wt.% fibers of the present invention, as well as from about 40 wt.% to about 99 wt.%, in some embodiments from 50 wt.% to about 95 wt.%, and in some embodiments, from about 80 wt.% to about 90 wt.% additional fibers.
If desired, the fiber web may also be employed in a multi-layered laminate structure. The other layers of the laminate may include a nonwoven web (e.g., a me!t-spun web, such as a me!tblown or spunbond web), film, strands, etc. In one embodiment, for example, the laminate may contain a fiber web positioned between two spunbond webs. Various techniques for forming laminates of this nature are described in U.S. Patent Nos. 4,041 ,203 to Brock et al.;, 5,213,881 to Timmons, et al.; 5,484,888 to Timmons, et al; 4,374,888 to Bornslaeger;
5,169.706 to Collier, et aL; and 4,788,029 to Brock et al. Of course, the laminate may have other configurations and possess any desired number of layers, such as a spunbond/fiber web/meftb!own web/spunbond laminate, spunbond/fiber web laminate, etc. In yet another embodiment, the laminate may include a fiber web positioned adjacent to a film. Any known technique may be used to form a film, including blowing, casting, flat die extruding, etc. The film may be a mono- or multi-layered film. Any of a variety of polymers may generally be used to form a melt-spun nonwoven web or film used in the laminate structure, such as poiyolefins (e.g., polyethylene, polypropylene, polybutylene, etc.);
polytetrafluoroethylene; polyesters {e.g., polyethylene terephthalate, polylactic acid, etc.); polyamides (e.g., nylon); polyvinyl chloride; polyvinylidene chloride; polystyrene; and so forth.
111. Articles
The fibers and fiber webs of the present invention may be used in a wide variety of applications. For example, the fibers may be incorporated into filtration media, medical products, such as gowns, surgical drapes, facemasks, head coverings, surgical caps, shoe coverings, sterilization wraps, warming blankets, heating pads, etc., absorbent articles, and so forth. For example, the fibers may be incorporated into an "absorbent article" thai is capable of absorbing water or other fluids. Examples of some absorbent articles include, but are not limited to,
persona! care absorbent articles, such as diapers, training pants, absorbent underpants, incontinence articles, feminine hygiene products (e.g., sanitary napkins), swim wear, baby wipes, mitt wipe, and so forth; medical absorbent articles, such as garments, fenestration materials, underpads, bedpads, bandages, absorbent drapes, and medica! wipes; food service wipers; clothing articles;
pouches, and so forth.
Materials and processes suitable for forming such artic!es are well known to those skilled in the art. Absorbent articles, for instance, typically include a substantially liquid-impermeable layer (e.g., outer cover), a liquid-permeable layer (e.g., topsheet, surge management layer, ventilation layer, wrap, etc.), and an absorbent core. The topsheet, for instance, is generally employed to help isolate the wearer's skin from liquids held in the absorbent core. Due to its proximity to the skin, a fibrous web is generally employed in the topsheet to provide a cloth-like feeling. If desired, the fibrous web used in the topsheet may be formed from the fibers of the present invention. The outer cover is likewise designed to be liquid- impermeable, but yet typically permeable to gases and water vapor (i.e.,
"breathable"). This permits vapors to escape from the absorbent core, but still prevents liquid exudates from passing through the outer cover. While the outer cover generally contains a film to impart the desired impermeability to liquids, a fibrous web is often laminated to the film as a facing to impart a more cloth-like feeling. If desired, the fibrous web used in the outer cover may be formed from the fibers of the present invention.
In yet another embodiment, the fibers of the present invention may be incorporated into a wipe configured for use on skin, such as a baby wipe, adult wipe, hand wipe, face wipe, cosmetic wipe, household wipe, industrial wipe, personal cleansing wipe, cotton ball, cotton-tipped swab, and so forth. The wipe may assume a variety of shapes, including but not limited to, generally circular, oval, square, rectangular, or irregularly shaped. Each individual wipe may be arranged in a foided configuration and stacked one on top of the other to provide a stack of wet wipes. Such folded configurations are well known to those skilled in the art and include c-folded, z-folded, quarter-folded configurations and so forth. For example, the wipe may have an unfolded length of from about 2.0 to about 80.0 centimeters, and in some embodiments, from about 10.0 to about 25.0
centimeters. The wipes may likewise have an unfolded width of from about 2,0 to about 80.0 centimeters, and in some embodiments, from about 10.0 to about 25.0 centimeters. The stack of folded wipes may be placed in the interior of a container, such as a plastic tub, to provide a package of wipes for eventual sale to the consumer. Alternatively, the wipes may include a continuous strip of material which has perforations between each wipe and which may be arranged in a stack or wound into a roll for dispensing. The wipe may be a "wet wipe" in that it contains a solution for cleaning, disinfecting, sanitizing, etc. The particular wet wipe solutions are not critical to the present invention and are described in more detail in U.S. Patent Nos. 6,440,437 to Krzysik, et al.; 8,028,018 to Amundson, et al; 5,888,524 to Cole; 5,867,835 to Win, et al.; 5,540,332 to Kopacz, et al.; and 4,741 ,944 to Jackson, et al. The amount of the wet wipe solution employed may depending upon the type of wipe material utilized, the type of container used to store the wipes, the nature of the cleaning formulation, and the desired end use of the wipes. Generally, each wipe contains from about 150 to about 600 wt.% and desirably from about 300 to about 500 wt.% of a wet wipe solution based on the dry weight of the wipe. When employed, the cleaning formulation is typically kept at the second pH level so as not to have a substantial adverse impact on the integrity of the fibers.
The present invention may be better understood with reference to the following examples.
EXAMPLEJ,
The ability to form fibers in accordance with the present invention was demonstrated. Initially, 18.6 grams of polyethylene oxide (weight average molecular weight of 1.6 x 106 g/moi, Afla) was dissolved in 100.5 grams of deionized water. Thereafter, 201 grams of a pH-sensitive polymer was added to the solution and stirred for 15 minutes using a paddle-type mixer (Caframo, BDC Series) at a speed setting of 300 rpm. The pH-sensitive polymer was an acrylic polymer available from Lubrizol under the name CARBOSET® 514H. The mixture was left in a sealed bottle overnight to degas. The viscosity of the mixture was determined to be 83,000 centipoise, based on an average of three samples using a Brookfie!d programmable rheometer {Model DV-III), with spindle number 6 and speed of 1 rpm, and at ambient temperature and pressure.
EXAMPLE 2
The ability to form fibers in accordance with the present invention was demonstrated, initially, 18.6 grams of polyethylene oxide (weight average molecular weight of 1.6 x 106 g/mol, Afla) was dissolved in 100.5 grams of deionized water. Thereafter, 201 grams of CARBOSET® 514H and 6.3 grams of ammonia (14% in an aqueous solution) was added to the solution and mixed for about 15 to 20 minutes until homogenous. The viscosity of the mixture was determined to be 292,000 centipoise, based on an average of three samples using a Brookfield programmable rheometer (Mode! DV-ΠΙ), with spindle number 7 and speed of 1 rpm.
Prior to spinning, the solution was left overnight in a sealed container to degas (no vacuum or heat was employed). Two (2) milliliters of the degassed solution were then loaded into a Forcespinning® L-IOOO system (FibeRio® Technology Corporation), which spun the solution into fibers for 1 minute at 5000 to 6000 rpm using a cotton-candy collector (no vacuum). Two needles (26G, 1.27 cm) were attached to each end of the spinneret, which was mounted on a spinning shaft. The distance from the tip of the needles to the collector was set to 8.9 centimeters. Once collected, the fibers were allowed to air dry. SE
microphotographs (51 OX and 1850X) of the resulting fibers are shown in Figs. 2-3. The average fiber diameter was 1.5 micrometers (standard deviation of 0.6 micrometers). To test the resistance of the fibers to water, a dissolution test was also performed on three separate samples from Example 2. More particularly, a bundle of the fibers was cut and weighed, put in a glass vial, submerged in deionized water, and then left at room temperature for 7 days. Fibers were not oven dried before or after the test. After 7 days, the contents of the vials (water and fibers) were poured on a filter paper (Whatman filter paper, 90 mm diameter), which was disposed on a glass dish. The samples were left under a hood with a funnel on top and then allowed to dry for 7 days. Thereafter, the contents were weighed to determine the percent of fibers dissolved, which is equal to the [Fiber Weight - Weight of Dried Fibers]/fFiber Weight] x 100. The results are shown in Table 1 below.
Table 1 : Sample Characteristics
As indicated, the fibers are generally water resistant in that only a minimal amount dissolved in water.
While the invention has been described in detail with respect to the specific embodiments thereof, it will be appreciated that those skilled in the art, upon attaining an understanding of the foregoing, may readily conceive of alterations to, variations of, and equivalents to these embodiments. Accordingly, the scope of the present invention should be assessed as that of the appended claims and any equivalents thereto.
Claims
1. A method for forming fibers from an aqueous spinning solution, wherein the spinning solution contains a pH-sensitive polymer and a solvent that includes water, wherein the pH-sensitive polymer is generally soluble in water at a first pH level and generally insoluble in water at a second pH level the method comprising spinning the solution into fibers while at the first pH level and selectively adjusting the pH of the fibers during and/or after spinning so the pH is at the second pH level.
2. The method of claim 1 , wherein pH-sensitive polymers constitute from about 30 wt.% to about 90 wt.% of the solution and solvents constitute from about 10 wt.% to about 60 wt.% of the solution.
3. The method of claim 1 or 2, wherein the pH-sensitive polymer is an acidic polymer, and preferably a polymer containing carboxyiic functional groups, such as a (meth)acry!ic acid polymer.
4. The method of claim 3, wherein the first pH level is about 5 or more and the second pH level is less than about 5.
5. The method of any of the foregoing claims, wherein the pH-sensitive polymer is a basic polymer, and preferably a polymer containing amine functional groups.
6. The method of claim 5, wherein first pH level is about 5 or less and the second pH level is greater than about 5.
7. The method of any of the foregoing claims, wherein the spinning solution further contains a pH modifier.
8. The method of claim 7, wherein the pH modifier is removed from the fibers during and/or after spinning.
9. The method of claim 7, wherein the pH modifier has a boiling point in water of from about 10°C to about 50°C at atmospheric pressure.
10. The method of any of the foregoing claims, wherein water constitutes about 50 wt.% or more of the solvents in the spinning solution,
11 . The method of any of the foregoing claims, wherein the spinning solution is generally free of organic solvents.
18
12. The method of any of the foregoing ciaims, wherein the spinning solution further contains a hydrophilic polymer that is generaily soluble in water at the first pH level and the second pH level.
13. The method of any of the foregoing claims, wherein the fibers are formed by centrifugal spinning.
14. A fiber formed according to the method of any of the foregoing ciaims, wherein the fiber is a nanofiber or microfiber.
15. A fiber that is formed from an aqueous spinning solution, the fiber containing one or more pH-sensitive polymers that are generally soluble in water at a first pH level and generally insoluble in water at a second pH level and optionally one or more hydrophilic polymers that are generaily soluble in water at the first pH level and the second pH ievei, and wherein the pH-sensitive polymers constitute about 50 wt.% or more of the polymer content of the fiber and the hydrophilic polymers constitute less than about 50 wt.% of the polymer content of the fiber, wherein the fiber is a nanofiber or a microfiber.
18. A composite that comprises the fiber of claim 14 or 15 in combination with additional fibers.
17. A nonwoven web comprising the fiber of claim 14 or 15.
18. A laminate comprising the nonwoven web of claim 17 and Iayer of a melt-spun nonwoven web, film, strands, or combination thereof.
19. An absorbent article comprising an absorbent core positioned between a liquid-permeable Iayer and a substantially liquid-impermeable Iayer, wherein the absorbent core, liquid-permeable Iayer, the liquid-impermeable Iayer, or a combination thereof, comprise the nonwoven web of ciaim 17.
20. A wipe comprising the nonwoven web of claim 17.
Applications Claiming Priority (2)
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US13/953,097 US20150031261A1 (en) | 2013-07-29 | 2013-07-29 | Solution Spinning of Fibers |
US13/953,097 | 2013-07-29 |
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WO2015015331A1 true WO2015015331A1 (en) | 2015-02-05 |
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PCT/IB2014/062485 WO2015015331A1 (en) | 2013-07-29 | 2014-06-20 | Solution spinning of fibers |
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WO (1) | WO2015015331A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3190216B1 (en) | 2015-09-04 | 2019-05-08 | LG Chem, Ltd. | Method for manufacturing super absorbent polymer fiber |
US10760184B2 (en) | 2016-03-24 | 2020-09-01 | Lg Chem, Ltd. | Preparation method of superabsorbent polymer fiber |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3413936A4 (en) | 2016-02-12 | 2019-11-20 | Tricol Biomedical, Inc. | Chitosan superfine fiber systems |
CN113622082B (en) * | 2020-05-06 | 2022-09-23 | 深圳陶陶科技有限公司 | Preparation method and application of centrifugal spinning non-woven fabric |
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US6753454B1 (en) * | 1999-10-08 | 2004-06-22 | The University Of Akron | Electrospun fibers and an apparatus therefor |
US20070077427A1 (en) * | 2004-10-18 | 2007-04-05 | Fiber Innovation Technology, Inc. | Soluble Microfilament-Generating Multicomponent Fibers |
US20090218059A1 (en) * | 2008-03-03 | 2009-09-03 | Rajeev Farwaha | Salt-sensitive cationic polymeric binders for nonwoven webs and method of making the same |
US20100055438A1 (en) * | 2003-04-10 | 2010-03-04 | Trustees Of Tufts College | Concentrated aqueous silk fibroin solution and use thereof |
US20130175729A1 (en) * | 2007-04-20 | 2013-07-11 | Coloplast A/S | Multi-Component Non-Woven |
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2013
- 2013-07-29 US US13/953,097 patent/US20150031261A1/en not_active Abandoned
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US6753454B1 (en) * | 1999-10-08 | 2004-06-22 | The University Of Akron | Electrospun fibers and an apparatus therefor |
US20100055438A1 (en) * | 2003-04-10 | 2010-03-04 | Trustees Of Tufts College | Concentrated aqueous silk fibroin solution and use thereof |
US20070077427A1 (en) * | 2004-10-18 | 2007-04-05 | Fiber Innovation Technology, Inc. | Soluble Microfilament-Generating Multicomponent Fibers |
US20130175729A1 (en) * | 2007-04-20 | 2013-07-11 | Coloplast A/S | Multi-Component Non-Woven |
US20090218059A1 (en) * | 2008-03-03 | 2009-09-03 | Rajeev Farwaha | Salt-sensitive cationic polymeric binders for nonwoven webs and method of making the same |
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Publication number | Priority date | Publication date | Assignee | Title |
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EP3190216B1 (en) | 2015-09-04 | 2019-05-08 | LG Chem, Ltd. | Method for manufacturing super absorbent polymer fiber |
US10760184B2 (en) | 2016-03-24 | 2020-09-01 | Lg Chem, Ltd. | Preparation method of superabsorbent polymer fiber |
EP3336226B1 (en) * | 2016-03-24 | 2021-04-07 | LG Chem, Ltd. | Method for producing superabsorbent polymer fiber |
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