Cellulose Nanofiber-reinforced Unsaturated Polyester as a Potential Substitute for Glass Fiber-reinforced Plastics.

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Cellulose Nanofiber-reinforced Unsaturated Polyester as a Potential Substitute for Glass Fiber-reinforced Plastics. A. N. Nakagaito a,b, S. Sato a,c, A. Sato a,d and H. Yano a a Research Institute for Sustainable Humanosphere, Kyoto University, Japan b Department of Chemistry and Biotechnology, Tottori University, Japan c NIPPON PAPER Chemicals CO., LTD., Japan d SEIKO PMC Corp., Japan ABSTRACT Nanocomposites of unsaturated polyester (UP) reinforced with nanofibers obtained by applying shear stress to pulp fibers through extrusion were produced. Paper-like sheets of nanofibers were impregnated with UP, stacked in layers and hot pressed at 1.5 MPa, a compressing pressure typical of plywood manufacturing. When nanofibers extracted from needle-leaf unbleached pulp (NUKP) fibers were used, composites with 14 wt% UP content exhibited flexural modulus of 13.6 GPa and strength of 26 MPa, with an Izod impact strength of 38 kj/m 2. INTRODUCTION Cellulose nanofibers are composed of amorphous and crystalline portions, the latter possessing tensile modulus of 138 GPa [1]. Despite the presence of amorphous portions along their length, the practical tensile strength of these nanofibers is supposed to be well above 2 GPa, based on the strength of pulp single fibers [2]. However the extraction of nanofibers from plant fibers has been the bottleneck in terms of cost since nanofibrillation is highly time and energy demanding, significantly raising the cost of originally low cost raw materials. Here we present a new approach to nanofibrillate pulp that significantly reduces the energy input and increases yield, by the application of shear forces in a twin-screw extruder. MATERIALS AND METHODS The raw materials from which the cellulose nanofibers were obtained consisted of needle-leaf unbleached pulp (NUKP). The resin was unsaturated polyester dissolved in styrene and benzoyl peroxide was used as the free radical initiator. Pulp fibers were fibrillated by an intermeshing co-rotating twin-screw extruder equipped with a screw pattern optimized to apply shear force to the fibers. The pulp fibers had the moisture content adjusted to approximately 3 wt% before feeding and the extruder s barrel was cooled to prevent the temperature to exceed the boiling point of water. The screw rotation speed was set to 4 rpm. Hand sheets were obtained by a papermaking process according to TAPPI T 25 sp-2. The sheets were cut into 4 mm by 3 mm rectangles and dried in a convection oven at 15 C for 1 hour. Unsaturated polyester (UP) was mixed with 1 wt% benzoyl

peroxide and the sheets were dipped in the UP solution and maintained at reduced pressure for 3 minutes. The impregnated sheets consisting of about 2 layers were stacked inside a metal mold and compressed at 1.5 MPa and 9 C for 3 minutes. RESULTS AND DISCUSSION The fabrication of cellulose nanofiber-reinforced UP composites required relatively low compressing pressures. Differently from nanocomposites fabricated with another thermoset resin, phenol formaldehyde, which demanded pressures in the order of 5 MPa [3], UP-based nanocomposites required pressures less than 1 times lower. Higher pressures tend to squeeze out the impregnated UP resin from the sheets and the composites fail by delamination. As shown in Table I the flexural modulus and strength of the composites were significantly improved over the neat resin UP, however the impact strength was not striking (up to 38 kj/m 2 ). Interface modification is still needed to enhance this property. The refining pre-treatment prior to extrusion fibrillation seems not to affect the performance of the composites, nevertheless nanofibrillation by extrusion significantly enhances the mechanical properties of the composites relative to the solely refined pulp fiber-based composites. Table I. Flexural properties of neat UP and NUKP nanofiber-reinforced UP composites. Reinforcing fiber Compres. pres. (MPa) Resin cont. (wt%) E (GPa) σ b (MPa) Neat UP, no reinforcement - 1 3.7±.9 126±6 NUKP 4 passes refiner 1.5 2.7 9.5±.3 136±3 NUKP pass refiner, extruded 1.5 15.5 12.2±.2 254±2 NUKP 4 passes refiner, extruded 1.5 13.9 13.6±.2 26±4 ACKNOWLEDGEMENTS The authors are indebted to the New Energy and Industrial Technology Development Organization (NEDO) for funding the project that made this study possible. References 1. Nishino, T., Takano K., Nakamae, K., Elastic Modulus of the Crystalline Regions of Cellulose Polymorphs, J. Polym. Sci., Part B: Polym. Phys., 33, pp. 1647-1651 (1995). 2. Page, D. H., El-Hosseiny, F., The Mechanical Properties of Single Wood Pulp Fibres. Part VI. Fibril Angle and the Shape of the Stress-Strain Curve, J. Pulp Pap. Sci. 84, pp. 99-1 (1983). 3. Nakagaito, A. N., Yano, H., Novel high-strength biocomposites based on microfibrillated cellulose having nano-order-unit web-like network structure, Appl. Phys. A, 8, pp. 155-159 (25).

Cellulose Nanofiber-reinforced Unsaturated Polyester as a Potential Substitute for Glass Fiber-reinforced Plastics A. N. Nakagaito a,b, S. Sato a,c, A. Sato a,d and H. Yano a a Research Institute for Sustainable Humanosphere, Kyoto University, Japan b Department of Chemistry and Biotechnology, Tottori University, Japan c NIPPON PAPER Chemicals CO., LTD., Japan d SEIKO PMC Corp., Japan

Problem and proposed Disposal of GFRP; solution Make composites with cellulose and UP with mechanical properties comparable to GFRP; Bio-based nanofiber as substitute for glass fiber; Low cost nanofibrillation by extrusion.

Intermeshing co-rotating twinscrew extruder Screw pattern: continuous version of a kneader

SEM of nanofibers obtained by twin-screw extruder

Experimental Sheets obtained according to TAPPI T 25 sp-2

Experimental Nanofiber sheets UP + benzoyl peroxide 3 min., vacuum Metal mold 9 C, 3 min., 5 MPa Composite RC 1~2%

E (GPa) 2 16 12 8 4 Effect of compressing pressure (E) 1.5 5 1 Compressing pressure (MPa) UP PF

σb (MPa) 4 3 2 1 Effect of compressing pressure (σ b ) UP PF 1.5 5 1 Compressing pressure (MPa)

Effect of impregnation time 16 (E) E (GPa) 12 8 4 NUKP.5 1 2 Impreg. time (h)

Effect of impregnation time (σ b ) σb (MPa) 25 2 15 1 5.5 1 2 Impreg. time (h) NUKP

Effect of nanofibrillation by 16 extrusion (E) E (GPa) 12 8 4 NUKP NBKP NO YES Extrusion

Effect of nanofibrillation by extrusion (σ b ) σb (MPa) 25 2 15 1 5 NO YES NUKP NBKP Extrusion

Effect of refining pretreatment (E) E (GPa) 16 12 8 4 NUKP 1 4 Refiner passes

Effect of refining pretreatment (σ b ) σb (MPa) 3 25 2 15 1 5 1 4 Refiner passes NUKP

Neat UP vs. NUKP/UP nanocomposites (E) E (GPa) 16 14 12 1 8 6 4 2 ~4 x neat UP NUKP/UP neat UP NUKP/UP

Neat UP vs. NUKP/UP nanocomposites (σ b ) 3 σb (MPa) 25 2 15 1 ~2 x neat UP NUKP/UP 5 neat UP NUKP/UP

5 4 Neat UP vs. NUKP/UP nanocomposites (Izod) kj/m 2 3 2 ~6 x neat UP NUKP/UP 1 neat UP NUKP/UP

Conclusions Nanofibrillation by twin-screw extruder; Refiner pre-treatment unnecessary; Compressing pressure 5 MPa; Pulp nanofiber/up composites: E = 13.6 GPa σ b = 26 MPa Unnotched Izod impact strength = 38kJ/m 2 Expected water absorbance.

Acknowledgement New Energy and Industrial Technology Development Organization (NEDO), Japan