MULTILAYERED COMPOSITE MATERIAL USING NANOFIBRILATED CELLULOSE AND THERMOPLASTIC MATRIX POLYMER
20170028672 ยท 2017-02-02
Inventors
Cpc classification
B32B2307/54
PERFORMING OPERATIONS; TRANSPORTING
B29C51/00
PERFORMING OPERATIONS; TRANSPORTING
B32B2262/062
PERFORMING OPERATIONS; TRANSPORTING
D04H1/4374
TEXTILES; PAPER
B32B2250/20
PERFORMING OPERATIONS; TRANSPORTING
B32B5/26
PERFORMING OPERATIONS; TRANSPORTING
B32B2262/04
PERFORMING OPERATIONS; TRANSPORTING
B32B5/02
PERFORMING OPERATIONS; TRANSPORTING
D04H1/43835
TEXTILES; PAPER
B29C51/10
PERFORMING OPERATIONS; TRANSPORTING
B32B2260/021
PERFORMING OPERATIONS; TRANSPORTING
B32B2307/546
PERFORMING OPERATIONS; TRANSPORTING
International classification
B32B5/02
PERFORMING OPERATIONS; TRANSPORTING
D04H1/4374
TEXTILES; PAPER
D04H1/4382
TEXTILES; PAPER
B32B37/10
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The present invention relates to a multi-layered composite material manufactured by thermocompressing a multi-layered sheet, comprising: a first sheet layer formed from a solution containing nanofibrillated cellulose and a first thermoplastic matrix polymer; and a second sheet layer formed from a solution containing a second thermoplastic matrix polymer. The multi-layered composite material of the present invention has the high strength and high elastic modulus.
Claims
1. A multi-layered composite material manufactured by thermocompressing a multi-layered sheet comprising: a first sheet layer formed from a solution containing nanofibrillated cellulose and a first thermoplastic matrix polymer; and a second sheet layer formed from a solution containing a second thermoplastic matrix polymer, wherein the first thermoplastic matrix polymer and the second thermoplastic matrix polymer are hot-melt bonded, and the nanofibrillated cellulose is inserted between the hot-melt bonded polymers.
2. The multi-layered composite material of claim 1, wherein the first thermoplastic matrix polymer and the second thermoplastic matrix polymer are one of polyamide based resins.
3. The multi-layered composite material of claim 2, wherein the polyamide resin is polyamide 6 or polyamide 66.
4. The multi-layered composite material of claim 1, wherein the first sheet layer is prepared by mixing a suspension of nanofibrillated cellulose and the first thermoplastic matrix in a solid weight ratio of 3:7 to 5:5.
5. The multi-layered composite material of claim 1, wherein the second sheet layer is a hot-melt web, a meltblown nonwoven fabric, or a film.
6. The multi-layered composite material of claim 5, wherein the thermocompressing is performed at 100 C. to 200 C. when the second layer sheet is a hot-melt web, and at 170 C. to 270 C. when the second layer sheet is a meltblown nonwoven fabric or a film.
7. The multi-layered composite material of claim 1, wherein the thermocompression is performed at a pressure range of 4 MPa to 100 MPa.
8. The multi-layered composite material of claim 1, wherein the multi-layered composite material has a tensile strength of 20 MPa to 80 MPa.
9. A method of manufacturing a multi-layered composite material, comprising: a first step of preparing a multi-layered sheet by laminating at least one of a first sheet layer prepared by drying and compressing a solution containing nanofibrillated cellulose and a first thermoplastic matrix polymer; and at least one of a second sheet layer containing a second thermoplastic matrix polymer; and a second step of hot-melting the first thermoplastic matrix polymer and the second thermoplastic matrix polymer by applying a pressure at a temperature below the degradation temperature of nanofibrillated cellulose.
10. The method of claim 10, wherein the first thermoplastic matrix polymer and the second thermoplastic matrix polymer are the same or different polyamide resins.
11. A reinforced molded product comprising the multi-layered composite material according to claim 1.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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[0050]
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DETAILED DESCRIPTION OF THE INVENTION
[0054] Hereinafter, the present invention will be described in detail with reference to the following Examples. However, the Examples of the present invention may be embodied in many different forms and these Examples should not be construed as limiting the scope of the present invention.
Example 1
Preparation of a Composite Material Containing Nanofibrillated Cellulose and Thermoplastic Matrix Polymer
[0055] First, a pulp dispersion was prepared by dispersing a hardwood pulp of a fiber length of 1.0 mm into water, followed by dissociation via mechanical refining in a pulper for 30 minutes. A pulp dispersion of a solid concentration of 0.2 wt % was prepared, stirred for 30 minutes, and then fibrillated by a homogenizer.
[0056] The pulp dispersion was passed through three nozzles of different size, installed in a high pressure homogenizer, in a sequential order of nozzle diameter, as follows: 1) 5 times: nozzle diameter 250 m, pressure 70 MPa, 2) 5 times: nozzle diameter 200 m, pressure 240 MPa, and 3) 5 times: nozzle diameter 150 m, pressure 310 MPa. The cellulose dispersion was passed 5 times per nozzle (i.e., a total of 15 times of the homogenizing process), and a nano sized fibrillated cellulose (nanofibrillated cellulose, NC) suspension was thereby prepared.
[0057] The thus-prepared NC suspension and two kinds of polyamide (PA) fibers (PA6 or PA66) were mixed at a weight ratio of solid content of about 4:6, and the NC/PA composite material was prepared in the form of a sheet as illustrated in
Example 2
Preparation of a Multi-Layered Composite Material Using a Composite Material Containing Nanofibrillated Cellulose and Thermoplastic Matrix Polymer
[0058] For the preparation of a multi-layered composite material, as illustrated in
TABLE-US-00001 TABLE 1 Matrix or NC Total Adhesive Thermocompressing No. of Content Thickness Sample Layer Conditions Layers (wt %) (m) Name 1 40.0 40 N1 PA hot- 150 C./60 sec 2 38.0 160 L2 melt web 3 37.4 280 L3 4 37.1 400 L4 5 37.0 490 L5 PA a 210 C. to 2 34.7 260 M2 meltblown 230 C./60 sec 3 33.3 420 M3 nonwoven 4 32.6 620 M4 fabric 5 32.2 830 M5 PA Film 210 C. to 2 38.0 170 F2 230 C./120 sec 3 37.4 290 F3 4 37.1 400 F4 5 37.0 540 F5 190 C./600 sec 3 40.0 100 S3 Preheating followed by 240 C./1,200 sec (87 MPa)
Experiment 1
Physical Properties of the NC/PA Composite Materials and the Multi-Layered Composite Material Prepared Using the Same
(1) Tensile Modulus
[0059] The tensile modulus of the composite materials was evaluated according to ASTM D638-03 using a universal testing machine (H100KS, Tinius Olsen, UK), and in particular, under the crosshead speed of 1.0 mm/min and a load cell of 2.5 kN.
[0060]
[0061] Although the tensile modulus of PA66 sheet was 0.8 MPa, the tensile modulus of NC/PA6 and NC/PA66 composite materials was shown to be in the range of 1 MPa to 2 MPa and 3 MPa to 12 MPa according to NC contents. The tensile modulus of the NC/PA66 multi-layered composite material was higher than that of the NC/PA6 composite material, and the tensile modulus of the NC/PA6 composite material increased as the NC content increased. Additionally, the NC/PA multi-layered composite material subjected to thermocompressing at a pressure of 87 MPa was shown to have a higher tensile modulus compared to the NC/PA multi-layered composite material subjected to thermocompressing at a pressure of 4.8 MPa.
(2) Flexural Modulus
[0062] The flexural modulus of composite materials was evaluated according to ASTM D790-03 under the same conditions as in the evaluation of tensile modulus.
[0063]
(3) Fracture Properties
[0064] The fracture properties of the NC/PA composite material were evaluated according to ASTM D671-71 using an electrodynamic test system (Acumen 1, MTS system, USA), the load cell used was 3 kN, and the test was performed at a frequency of 20 Hz for 10.sup.6 cycles.
[0065]
[0066] Accordingly, it was confirmed that an NC/PA composite material with increased tensile modulus, flexural modulus, and service life can be prepared using the NC as a reinforcing material for PA.
Experiment 2
Physical Properties of a Multi-Layered Composite Material Comprising NC/PA Composite Materials and a Thermoplastic Panel
[0067] The method of preparing the NC with a homogenizer under high pressure and preparing the NC/PA sheets was the same as described in Example 1, and illustrated in
[0068] The thus-prepared NC/PA/NY and NC/PA/AB composite materials, a single NY panel (sample code: NY-N), and a single AB panel (sample code: AB-N), both without attaching the NC/PA sheet thereto, and an NC/PA thermocompressed sheet without the adhesive layer (sample code: S) were compared by their tensile characteristics, flexural characteristics, fracture properties, and impact characteristics.
[0069] In the preparation of the multi-layered composite materials, the thermocompressing between the composite materials and the adhesive layer for the samples of NY-S, NY-F, and NY-M was performed under the conditions of 210 C./40 seconds, and for the samples of NY-L and AB-L the thermocompressing was performed under the conditions of 130 C./60 seconds.
(1) Tensile Strength and Tensile Modulus
[0070] The tensile modulus of the NC/PA/NY and NC/PA/AB composite materials was evaluated according to ASTM D638-03 using a universal strength testing machine (H100KS, Tinius Olsen, UK), under the speed of 1.0 mm/min and a load cell of 50 kN.
[0071]
(2) Flexural Strength and Flexural Modulus
[0072] The flexural modulus of the prepared composite material was evaluated according to ASTM D790-03, under the same conditions of Experimental 1.
[0073]
(3) Fracture Fatigue Properties
[0074] The fracture properties of the NC/PA/NY and NC/PA/AB composite materials were evaluated according to ASTM D671-71 using an electrodynamic test system (Acumen 1, MTS system, USA). The load cell used was 3 kN and the test was performed at a frequency of 10 Hz for 10.sup.6 cycles.
[0075] The fracture fatigue properties of the NC/PA/NY and NC/PA/AB composite materials are illustrated in Table 2 below. When tests were performed for 10.sup.6 cycles with a strength of 70%, 50%, and 30% of the maximum flexural force, the fracture cycle of the AB-L sample, in which NC/PA/AB was adhered with a PA hot-melt film, was shown to be highest with a strength of 70%. With a strength of 50%, the NY-F sample, in which the NC/PA/NY was attached with a PA film, showed the highest increase of the maximum fracture cycle. Additionally, with a strength of 30%, all samples passed the 10.sup.6 cycle test. It was confirmed that the number of the fracture cycles significantly increased in all case of the NC/PA/NY and NC/PA/AB composite materials regardless of the kinds of the adhesive.
TABLE-US-00002 TABLE 2 Max. flexural force Sample Number of cycles codes 70% 50% 30% NY-N 19 559 Pass NY-S 35 704 Pass NY-L 25 1739 Pass NY-F 1796 29823 Pass NY-M 19 844 pass AB-N 2798 43892 Pass AB-L 4443 78627 Pass
(4) Impact Characteristics
[0076] The impact characteristics of the prepared composite materials were tested according to ASTM D 5420 using the Gardner impact test method (falling weight), which was performed by dropping a ball having a diameter of 50 mm from a height of 1,520 mm by a steel ball drop test machine.
[0077]
[0078] Accordingly, it was confirmed that tensile, flexural, fracture, and impact characteristics can be improved by attaching the NC/PA sheet to the NY and AB panels.