CN112899800A - Graphene and nanocellulose modified composite fiber and preparation method thereof - Google Patents
Graphene and nanocellulose modified composite fiber and preparation method thereof Download PDFInfo
- Publication number
- CN112899800A CN112899800A CN201911133904.0A CN201911133904A CN112899800A CN 112899800 A CN112899800 A CN 112899800A CN 201911133904 A CN201911133904 A CN 201911133904A CN 112899800 A CN112899800 A CN 112899800A
- Authority
- CN
- China
- Prior art keywords
- graphene
- cellulose
- nano
- nanocellulose
- unmodified
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 95
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 94
- 239000000835 fiber Substances 0.000 title claims abstract description 84
- 239000002131 composite material Substances 0.000 title claims abstract description 48
- 229920001046 Nanocellulose Polymers 0.000 title claims abstract description 39
- 238000002360 preparation method Methods 0.000 title claims abstract description 7
- 229920002678 cellulose Polymers 0.000 claims abstract description 59
- 239000001913 cellulose Substances 0.000 claims abstract description 59
- 229920005989 resin Polymers 0.000 claims abstract description 45
- 239000011347 resin Substances 0.000 claims abstract description 45
- 238000009987 spinning Methods 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 8
- 238000001125 extrusion Methods 0.000 claims description 20
- 230000003179 granulation Effects 0.000 claims description 20
- 238000005469 granulation Methods 0.000 claims description 20
- 238000002844 melting Methods 0.000 claims description 19
- 230000008018 melting Effects 0.000 claims description 19
- 238000002074 melt spinning Methods 0.000 claims description 14
- 239000004594 Masterbatch (MB) Substances 0.000 claims description 13
- 238000002156 mixing Methods 0.000 claims description 12
- 229920002292 Nylon 6 Polymers 0.000 claims description 9
- 239000010410 layer Substances 0.000 claims description 7
- -1 polyethylene terephthalate Polymers 0.000 claims description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 7
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 7
- 229920001707 polybutylene terephthalate Polymers 0.000 claims description 6
- 239000002356 single layer Substances 0.000 claims description 6
- 229920002749 Bacterial cellulose Polymers 0.000 claims description 5
- 239000005016 bacterial cellulose Substances 0.000 claims description 5
- 125000000524 functional group Chemical group 0.000 claims description 4
- 210000001724 microfibril Anatomy 0.000 claims description 4
- 239000002023 wood Substances 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 3
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 3
- 229920003043 Cellulose fiber Polymers 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 abstract description 10
- 239000000945 filler Substances 0.000 abstract description 5
- 230000008569 process Effects 0.000 abstract description 5
- 230000035699 permeability Effects 0.000 abstract description 4
- 239000004753 textile Substances 0.000 abstract description 3
- 241000894006 Bacteria Species 0.000 abstract description 2
- 230000009881 electrostatic interaction Effects 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 230000003068 static effect Effects 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 description 50
- 239000002826 coolant Substances 0.000 description 9
- 238000001914 filtration Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 238000012545 processing Methods 0.000 description 9
- 238000004804 winding Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- 239000012209 synthetic fiber Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 230000005661 hydrophobic surface Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001263 acyl chlorides Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- AWSFEOSAIZJXLG-UHFFFAOYSA-N azepan-2-one;hydrate Chemical compound O.O=C1CCCCCN1 AWSFEOSAIZJXLG-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920006350 polyacrylonitrile resin Polymers 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Images
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
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- 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
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/09—Addition of substances to the spinning solution or to the melt for making electroconductive or anti-static filaments
-
- 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
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D01F1/103—Agents inhibiting growth of microorganisms
-
- 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
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/54—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of unsaturated nitriles
-
- 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
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/90—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyamides
-
- 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
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/92—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
Abstract
The invention belongs to the field of textiles, and particularly relates to a graphene and nanocellulose modified composite fiber and a preparation method thereof. The graphene nano-modified composite fiber provided by the invention comprises 99.0-99.9% of resin, graphene and nano-cellulose are used as nano-modified fillers, the total mass addition content of the graphene and the nano-cellulose is 0.1-1.0%, and the mass ratio of the graphene to the nano-cellulose is 1: 9-9: 1. graphene and nanocellulose can improve the dispersibility of a single filler in a resin matrix due to electrostatic interaction. The composite material is spun into fiber through functional fiber prepared with spinning equipment, and the fiber has the advantages of high strength, wear resistance, air permeability, static resistance, far infrared heating, bacteria resistance and the like. The invention has simple process and excellent product performance, and is suitable for special requirements of functional clothes.
Description
Technical Field
The invention belongs to the field of textiles, and particularly relates to a graphene and nanocellulose modified composite fiber and a preparation method thereof.
Background
Over 100 years ago, the raw materials of the textile are mainly derived from natural substances, such as cotton, hemp, silk, wool and the like, and the natural fibers are obtained with higher cost and longer growth cycle. Later, with the development of the polymer synthesis industry, synthetic fibers, which are chemical fibers prepared by spinning, molding and post-treating synthetic linear polymers having suitable molecular weights, have gradually appeared and become widely used. Compared with natural fibers, the synthetic fibers have the advantages of high strength, good elasticity, mildew and moth resistance and the like, but have the defects of poor air permeability, poor heat retention and the like.
Graphene is a two-dimensional carbon material with the highest strength and the best electrical property, and the mechanical strength, the wear resistance and the antistatic effect of the fiber can be obviously improved by adding the graphene into a resin matrix. In addition, research results show that the graphene has good antibacterial performance and a far infrared absorption function, so that the synthetic fiber is expected to have better antibacterial performance and self-warming property when the graphene is added into resin to prepare the fiber. However, graphene has a large specific surface area (generally 2630 m)2About/g), and the two-dimensional sheet layers are easy to agglomerate in the resin due to the existence of Van der Waals force, so that the dispersion effect is damaged, and the fiber performance of the composite material is seriously reduced.
To address this problem, researchers have adopted many different approaches to improve. The patent application with the application number of 201710952633.6 disperses graphene into caprolactam water solution, then carries out polymerization reaction to obtain graphene/nylon 6 with high dispersibility, and then obtains graphene nylon 6 composite fibers through melt spinning. In the patent application with the patent application number of 201711007680.X, a surfactant and a coupling agent are used for carrying out surface dispersion treatment on graphene, and the treated graphene, nylon and a heat stabilizer are granulated in a double-screw extruder to obtain the composite material. The patent application with the patent application number of 201810903390.1 blends graphene fiber with the graphene content of 0.4-0.8% with cotton fiber to obtain the composite fiber blended by the two fibers.
The methods improve the dispersibility of graphene to a certain extent, but simultaneously change the process route of the fiber synthesis industry (adding graphene in the polymerization process), or introduce more chemical substances (heat stabilizer, coupling agent and the like) or increase the spinning process (blending), and have different defects.
Disclosure of Invention
The invention aims to develop a formula and a preparation method of a graphene and nanocellulose modified composite fiber, which can obviously improve the dispersibility of graphene and nanocellulose in a resin matrix. In addition, the addition of the functional nano-filler graphene and the nano-cellulose can obviously improve the strength, the wear resistance, the antistatic property, the antibacterial property and the heat retention property of the composite fiber. In addition, the whole spinning process does not need to add extra process and equipment, and the energy is saved and the environment is protected.
The specific technical scheme of the invention is as follows:
the graphene and nano-cellulose modified composite fiber comprises the following components in percentage by weight: 99.0% -99.9% of resin and 0.1% -1.0% of graphene and nano-cellulose in total, wherein the weight ratio of the added graphene to the added nano-cellulose is 1: 9-9: 1.
further preferably, the graphene and nanocellulose modified composite fiber comprises the following components in percentage by weight: 99.4-99.8% of resin and 0.2-0.6% of graphene and nano-cellulose in total, wherein the weight ratio of the added graphene to the added nano-cellulose is 3: 1-1: 3.
The graphene and nano-cellulose modified composite fiber is characterized in that one or more of nylon 6(PA6), polyethylene terephthalate (PET), polybutylene terephthalate (PBT) and Polyacrylonitrile (PAN) are adopted.
The graphene and nanocellulose modified composite fiber according to the invention, wherein the graphene includes but is not limited to single-layer graphene and/or few-layer graphene.
The graphene and nanocellulose modified composite fiber is characterized in that the nanocellulose comprises unmodified nanocellulose and/or modified nanocellulose; wherein the unmodified nano-cellulose comprises one or more of unmodified nano-cellulose whiskers, unmodified nano-cellulose fibers, unmodified wood nano-cellulose, unmodified cellulose microfibrils, unmodified wood cellulose microfibrils and unmodified bacterial cellulose; the modified nano-cellulose is obtained by modifying functional groups of unmodified micro-nano-cellulose on the basis of the unmodified micro-nano-cellulose, wherein the functional groups of the modified micro-nano-cellulose comprise one or more of alkyl, cycloalkyl, heterocyclic groups, aromatic groups, alkoxy groups, ester groups, acyl, amino and isocyanate groups.
The invention also provides a preparation method of any one of the graphene and nanocellulose modified composite fibers, which specifically comprises the following steps:
1) carrying out melt blending extrusion granulation on graphene, nano cellulose and resin on a double-screw extruder to obtain a composite material master batch;
2) and carrying out melt spinning on the dried composite material master batch on spinning equipment to obtain the graphene nano cellulose modified composite fiber.
The melt blending extrusion granulation and melt spinning involved in the present invention can be performed using techniques well known in the art. As a preference and not a limitation, the melt blending extrusion granulation and melt spinning may be specifically: mixing and stirring the graphene, the nano cellulose powder and the resin in a high-speed blender for 10-20 minutes to uniformly mix the materials, taking out the mixed material, and carrying out extrusion granulation in a double-screw extruder, wherein the processing temperature of the extruder is preferably higher than the melting temperature of the resin by 20-40 ℃. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is drawn into as-spun fiber silk at high speed through a winding device, and the as-spun fiber is post-processed into the required fiber.
Cellulose molecules are linear polymers formed by repeatedly connecting beta-D-glucose through beta (1-4) glycosidic bonds, in a cellulose crystal structure, a large number of hydroxyl groups exist in a glucose ring plane between two parallel molecular chains, so that the cellulose molecular chains are hydrophilic due to more-OH, -O and other groups in a direction parallel to the glucose ring, and are hydrophobic due to more C-H groups in a direction vertical to the glucose ring. When cellulose and graphene are dispersed in a resin matrix, the hydrophobic surface of the cellulose chain follows the graphene SP2Aromatic ring arrangement of hybrid orbitals, CH-and graphene SP on the hydrophobic surface of cellulose molecular chains2The hybridized pi bonds are interacted, namely CH-pi interaction, graphene and nano cellulose are added into the resin matrix together, and the stability of the graphene and the nano cellulose in the resin matrix can be improved through the coordination interaction of the two fillers. According to the invention, the dispersion of graphene in the resin matrix is effectively improved by adding the environment-friendly nano-cellulose, and in addition, the air permeability of the synthetic fiber is improved by adding the biomass-based nano-cellulose.
Graphene and nanocellulose can improve the dispersibility of a single filler in a resin matrix due to electrostatic interaction. The composite material is spun into fiber through functional fiber prepared with spinning equipment, and the fiber has the advantages of high strength, wear resistance, air permeability, static resistance, far infrared heating, bacteria resistance and the like. The invention has simple process and excellent product performance, and is suitable for special requirements of functional clothes.
Specifically, the present invention has the following advantages:
1. according to the technical scheme provided by the invention, the nano-cellulose and the graphene are utilized to endow the fibers with functionality, and the graphene and the nano-cellulose can synergistically improve the dispersibility of the graphene and the nano-cellulose in a resin matrix due to an electrostatic effect.
2. The nano-cellulose and the graphene can obviously improve the strength, the wear resistance, the antistatic property, the antibacterial property and the heat preservation property of the resin matrix.
3. The raw materials for preparing the nano-cellulose and the graphene are natural fibers and graphite, and have rich sources and low price.
4. The technical scheme provided by the invention is simple in process and environment-friendly.
Drawings
Fig. 1 is a schematic diagram of a graphene and nanocellulose modified composite fiber according to the present invention.
Detailed Description
The present invention will be further described with reference to the following specific examples.
Example 1
Mixing 2 parts of nano cellulose whisker, 3 parts of single-layer graphene and 999 parts of polybutylene terephthalate (PBT) resin in a mixer for 15 minutes, taking out the mixed material, and carrying out extrusion granulation in a double-screw extruder, wherein the processing temperature of the extruder is higher than the melting temperature of the resin by 30 ℃. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed to prepare the graphene and nano-cellulose modified composite fiber. The prepared graphene and nanocellulose modified composite fiber is shown in fig. 1. Compared with the original PBT fiber, the tensile strength of the fiber is improved by 15 percent, and the modulus is improved by 10 percent.
Example 2
Mixing 0.5 part of nano cellulose whisker, 0.5 part of few-layer graphene and 999 parts of nylon 6 resin in a mixer for 10 minutes, taking out the mixed material, and carrying out extrusion granulation in a double-screw extruder, wherein the processing temperature of the extruder is 20 ℃ higher than the melting temperature of the resin. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed to prepare the graphene and nano-cellulose modified composite fiber.
Example 3
After 0.5 part of nano cellulose fiber, 4.5 parts of few-layer graphene and 995 parts of nylon 6 resin are mixed in a mixer for 20 minutes, the mixture is taken out and extruded and granulated in a double-screw extruder, and the processing temperature of the extruder is higher than the melting temperature of the resin by 40 ℃. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed into graphene and nano-cellulose modified composite fiber, so that the graphene and nano-cellulose modified composite fiber is prepared.
Example 4
Mixing 2 parts of acyl chloride modified nano cellulose fiber, 8 parts of few-layer graphene and 990 parts of polyacrylonitrile resin in a mixer for 15 minutes, taking out the mixed material, and performing extrusion granulation in a double-screw extruder, wherein the processing temperature of the extruder is 25 ℃ higher than the melting temperature of the resin. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed into graphene and nano-cellulose modified composite fiber, so that the graphene and nano-cellulose modified composite fiber is prepared.
Example 5
Mixing 1 part of anhydride modified nano cellulose fiber, 4 parts of few-layer graphene and 995 parts of nylon 6 resin in a mixer for 12 minutes, taking out the mixed material, and performing extrusion granulation in a double-screw extruder, wherein the processing temperature of the extruder is higher than the melting temperature of the resin by 35 ℃. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed into graphene and nano-cellulose modified composite fiber, so that the graphene and nano-cellulose modified composite fiber is prepared.
Example 6
After 4 parts of bacterial cellulose fiber, 1 part of single-layer graphene and 995 parts of polyethylene terephthalate (PET) are mixed in a mixer for 15 minutes, the mixture is taken out and extruded and granulated in a double-screw extruder, and the processing temperature of the extruder is 30 ℃ higher than the melting temperature of the resin. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed into graphene and nano-cellulose modified composite fiber, so that the graphene and nano-cellulose modified composite fiber is prepared.
Example 7
After 4.5 parts of bacterial cellulose fiber, 0.5 part of single-layer graphene and 995 parts of polyethylene terephthalate (PET) are mixed in a mixer for 10 minutes, the mixture is taken out and extruded and granulated in a double-screw extruder, and the processing temperature of the extruder is 20 ℃ higher than the melting temperature of the resin. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, and the nascent fiber is post-processed into graphene and nano-cellulose modified composite fiber, so that the graphene and nano-cellulose modified composite fiber is prepared.
Example 8
Mixing 2 parts of bacterial cellulose fiber, 2 parts of single-layer graphene and 996 parts of nylon 6 resin in a mixer for 20 minutes, taking out the mixed material, and performing extrusion granulation in a double-screw extruder, wherein the processing temperature of the extruder is 25 ℃ higher than the melting temperature of the resin. And adding the resin master batch obtained by extrusion granulation into a melt spinning machine, melting the mixture, conveying the mixture into a spinning part, conveying the mixture into a spinning assembly through a metering pump, and filtering the mixture and then extruding the mixture through capillary holes of a spinneret plate. The liquid silk is gradually solidified through a cooling medium, and is stretched into nascent fiber silk at a high speed through a winding device, the nascent fiber is post-processed into graphene and nano-cellulose modified composite fiber, and the graphene and nano-cellulose modified composite fiber is prepared.
Finally, it should be noted that the above embodiments are only used for illustrating the technical solutions of the present invention and are not limited. Although the present invention has been described in detail with reference to the embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the spirit and scope of the invention as defined in the appended claims.
Claims (7)
1. The graphene and nanocellulose modified composite fiber is characterized by comprising the following components in percentage by weight: 99.0% -99.9% of resin and 0.1% -1.0% of graphene and nano-cellulose in total, wherein the weight ratio of the added graphene to the added nano-cellulose is 1: 9-9: 1.
2. the graphene and nanocellulose modified composite fibre according to claim 1, wherein said graphene and nanocellulose modified composite fibre comprises, in weight percent: 99.4-99.8% of resin and 0.2-0.6% of graphene and nano-cellulose in total, wherein the weight ratio of the added graphene to the added nano-cellulose is 3: 1-1: 3.
3. The graphene and nanocellulose modified composite fiber according to claim 1 or 2, wherein the resin comprises one or more of nylon 6, polyethylene terephthalate, polybutylene terephthalate and polyacrylonitrile.
4. The graphene and nanocellulose modified composite fibre according to claim 1 or 2, wherein said graphene comprises single-layer graphene and/or few-layer graphene.
5. The graphene and nanocellulose modified composite fibre according to claim 1 or 2, wherein said nanocellulose comprises unmodified nanocellulose and/or modified nanocellulose; wherein the unmodified nano-cellulose comprises one or more of unmodified nano-cellulose whiskers, unmodified nano-cellulose fibers, unmodified wood nano-cellulose, unmodified cellulose microfibrils, unmodified wood cellulose microfibrils and unmodified bacterial cellulose; the modified nano-cellulose is obtained by modifying functional groups of unmodified micro-nano-cellulose on the basis of the unmodified micro-nano-cellulose, wherein the functional groups of the modified micro-nano-cellulose comprise one or more of alkyl, cycloalkyl, heterocyclic groups, aromatic groups, alkoxy groups, ester groups, acyl, amino and isocyanate groups.
6. A method for preparing the graphene and nanocellulose modified composite fiber according to any one of claims 1 to 5, comprising the steps of:
1) carrying out melt blending extrusion granulation on graphene, nano cellulose and resin on a double-screw extruder to obtain a composite material master batch;
2) and carrying out melt spinning on the dried composite material master batch on spinning equipment to obtain the graphene nano cellulose modified composite fiber.
7. The preparation method according to claim 6, wherein the melt blending extrusion granulation temperature in the step 1) is 20-40 ℃ higher than the melting temperature of the resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911133904.0A CN112899800B (en) | 2019-11-19 | 2019-11-19 | Graphene and nanocellulose modified composite fiber and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911133904.0A CN112899800B (en) | 2019-11-19 | 2019-11-19 | Graphene and nanocellulose modified composite fiber and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN112899800A true CN112899800A (en) | 2021-06-04 |
CN112899800B CN112899800B (en) | 2022-12-13 |
Family
ID=76103374
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201911133904.0A Active CN112899800B (en) | 2019-11-19 | 2019-11-19 | Graphene and nanocellulose modified composite fiber and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112899800B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN117362946A (en) * | 2023-10-16 | 2024-01-09 | 江苏蜀扬春新材料科技有限公司 | Nanocellulose modified polyester composite material and preparation method thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106757511A (en) * | 2017-01-11 | 2017-05-31 | 珠海泓利服饰股份有限公司 | The modified nylon fiber and its preparation technology of a kind of platelet of Graphene containing polymolecularity and liquid phase surface conductance film |
US20170241049A1 (en) * | 2016-02-24 | 2017-08-24 | Tingying Zeng | Method to Massively Manufacture Carbon Fibers through Graphene Composites and the Use Thereof |
CN107254722A (en) * | 2017-07-28 | 2017-10-17 | 广州市中诚新型材料科技有限公司 | A kind of graphene composite fibre |
CN107641280A (en) * | 2017-06-13 | 2018-01-30 | 华烯新材料科技无锡有限公司 | A kind of compound PP master batches of graphene and preparation method |
CN108707992A (en) * | 2018-06-04 | 2018-10-26 | 刘逸新 | A kind of regenerated cellulose/graphene oxide it is composite modified have can thermoplastic processability fiber producing processes |
CN108842221A (en) * | 2018-07-12 | 2018-11-20 | 山东联星能源集团有限公司 | A kind of ultrahigh-strength graphene modified fiber materials and preparation method thereof |
-
2019
- 2019-11-19 CN CN201911133904.0A patent/CN112899800B/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20170241049A1 (en) * | 2016-02-24 | 2017-08-24 | Tingying Zeng | Method to Massively Manufacture Carbon Fibers through Graphene Composites and the Use Thereof |
CN106757511A (en) * | 2017-01-11 | 2017-05-31 | 珠海泓利服饰股份有限公司 | The modified nylon fiber and its preparation technology of a kind of platelet of Graphene containing polymolecularity and liquid phase surface conductance film |
CN107641280A (en) * | 2017-06-13 | 2018-01-30 | 华烯新材料科技无锡有限公司 | A kind of compound PP master batches of graphene and preparation method |
CN107254722A (en) * | 2017-07-28 | 2017-10-17 | 广州市中诚新型材料科技有限公司 | A kind of graphene composite fibre |
CN108707992A (en) * | 2018-06-04 | 2018-10-26 | 刘逸新 | A kind of regenerated cellulose/graphene oxide it is composite modified have can thermoplastic processability fiber producing processes |
CN108842221A (en) * | 2018-07-12 | 2018-11-20 | 山东联星能源集团有限公司 | A kind of ultrahigh-strength graphene modified fiber materials and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
林东瀚: "基于纳米纤维素—石墨烯—聚苯胺复合电极的超级电容器的研究", 《工程科技Ⅰ辑;工程科技Ⅱ辑》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN117362946A (en) * | 2023-10-16 | 2024-01-09 | 江苏蜀扬春新材料科技有限公司 | Nanocellulose modified polyester composite material and preparation method thereof |
CN117362946B (en) * | 2023-10-16 | 2024-05-03 | 江苏蜀扬春新材料科技有限公司 | Nanocellulose modified polyester composite material and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN112899800B (en) | 2022-12-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Panyasart et al. | Effect of surface treatment on the properties of pineapple leaf fibers reinforced polyamide 6 composites | |
Chirayil et al. | Nanofibril reinforced unsaturated polyester nanocomposites: Morphology, mechanical and barrier properties, viscoelastic behavior and polymer chain confinement | |
CN105802019B (en) | A kind of graphene/glass fiber reinforced polypropylene composite material and preparation method thereof | |
US20200325328A1 (en) | Polyester Composites and Their Preparation Methods | |
CN106009056B (en) | A kind of polymer nanofiber-based aerogel material and preparation method thereof | |
Song et al. | Mechanical properties of poly (lactic acid)/hemp fiber composites prepared with a novel method | |
Ogunsona et al. | A critical review on the fabrication processes and performance of polyamide biocomposites from a biofiller perspective | |
Ma et al. | Preparing cellulose nanocrystal/acrylonitrile-butadiene-styrene nanocomposites using the master-batch method | |
Zhang et al. | Lignocellulose nanofiber/polylactic acid (LCNF/PLA) composite with internal lignin for enhanced performance as 3D printable filament | |
CN111875940B (en) | Toughened heat-resistant polylactic acid 3D printing wire and preparation method thereof | |
CN114044978A (en) | Quaternary ammonium salt functionalized nano SiO2Antibacterial modified polypropylene material and preparation method thereof | |
Li et al. | Homogeneous dispersion of chitin nanofibers in polylactic acid with different pretreatment methods | |
CN112899800B (en) | Graphene and nanocellulose modified composite fiber and preparation method thereof | |
CN102311616A (en) | Carbon-fiber-reinforced polyester composite material and preparation method thereof | |
CN111040442A (en) | Whisker-reinforced hydrophobic nylon 66 composite material and preparation method thereof | |
Liang et al. | Nanocellulose reinforced lightweight composites produced from cotton waste via integrated nanofibrillation and compounding | |
Sucharitpong et al. | Production of nylon-6/cellulose nanocrystal composite films using solvent dissolution | |
CN105239204A (en) | Novel polylactic acid fiber fabric | |
Yu et al. | Mechanical Properties of Cellulose Nanofibril (CNF)‐and Cellulose Nanocrystal (CNC)‐Based Nanocomposites | |
Mahmoudian et al. | Bionanocomposite fibers based on cellulose and montmorillonite using ionic liquid 1-ethyl-3-methylimidazolium acetate | |
CN105239202A (en) | High temperature resistant and high-strength modified polylactic acid fiber | |
CN110066497A (en) | A kind of low smell, it is low distribute, high abrasion polyethylene terephthalate composition and preparation method thereof | |
CN104845150A (en) | PET/PTT/carbon nano-tube composite material and preparation method thereof | |
CN111087787A (en) | Biodegradable fiber reinforced PC/ABS composite material | |
CN107841105A (en) | Heat-proof combustion-resistant PLA graphene composite material and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |