Influence of Polar Monomers on the Performance of Wood Fiber Reinforced Polystyrene Composites. I. Evaluation of Critical Conditions

Abstract

Wood fibers and nonpolar thermoplastics, e.g. polystyrene, are not the ideal partner for the preparation of composites because of a wide difference in their polarity. In the present study, polarity of the polystyrene was modified by the introduction of a—COOH group, through the reaction with maleic anhydride (MA) in the presence of an initiator (benzoyl peroxide: BPO) in a roll mill at the elevated temperatures. Optimum conditions for the preparation of polar polystyrene have been investigated. The temperature of the roll mill, i.e., the reaction temperature, and reaction time varied between 160–175°C and 10–15 min., respectively. The concentrations of the monomer, (MA) as well as the initiator (BPO), also varied: 0–10% and 0–2% (by weight of polymer), respectively. The mechanical properties of chemithermomechanical pulp (CTMP)-filled modified polystyrenes were evaluated. The effect of 3% coupling agent [e.g. poly(methylene (polyphenyl isocyanate))] (PMPPIC) on the mechanical properties of the same composites was also determined.

Generally, mechanical properties of the composite materials were enhanced when modified polymers were used as base polymers. Moreover, the extent of the improvement in mechanical properties depends on the reaction temperature and time, as well as on the concentrations of the monomer (maleic anhydride) and initiator. Maximum improvements in mechanical properties occur when the temperature was maintained at 175°C for 15 min. In addition, preferred concentrations of both the monomer and initiator were found to be 5% and 1% (by polymer weight), respectively. Once again, properties were further accelarated when coupling agent (e.g. PMPPIC) was used in addition to the modified polystyrene. The improvements in mechanical properties (over those of the original polymer and those of composites containing unmodified polymers) indicate that the compatibility between hydrophilic cellulosic fiber and hydrophobic polymer has increased.     

Performance of treated hybrid fiber reinforced-thermoplastic composites under extreme conditions. IV. Use of glass fiber and sawdust as hybrid fiber

The mechanical properties and dimensional stability of hardwood aspen in the form of sawdust and surface-treated glass fiber-polystyrene composites were evaluated under various extreme conditions, e.g., variation in the testing temperature (from +25° to ?20°C), exposure to boiling water and heat in an oven at +105°C. The compatibility of wood fiber with glass fiber and with polystyrene improved by precoating the wood fiber with a coupling agent, e.g., 8% isocyanate, 4% silane and polymer. The mechanical properties of the composites, in particular, treated sawdust/glass fiber-filled composites, increased under extreme conditions in comparison with those filled with nontreated sawdust/glass fiber. Under the same conditions, dimensional stability also supports this observation.     

Surface modification of wood fibers using maleic anhydride and isocyanate as coating components and their performance in polystyrene composites

The effect of surface modification of various wood fibers [e.g. woodflour and chemithermomechanical pulp (CTMP) of hardwood aspen, and woodflour of softwood spruce] by precoating with only maleic anhydride (MA) and/or poly[methylene (polyphenyl isocyanate)] (PMPPIC) in the presence of benzoyl peroxide (BPO) on the mechanical performance of modified fiber-filled polystyrene (PS 201 and PS 525) composites has been studied. The effects of the concentration of fiber, MA, PMPPIC, and BPO on the mechanical properties of the composites have also been evaluated. As opposed to unmodified fiber-filled composites, most of the mechanical properties of the modified fiber-filled composites increased with an increase in the concentration of BPO, MA, and/or PMPPIC up to a certain limit, and then either decreased or levelled off. The properties improved even more when both MA and PMPPIC were used as compared with the use of only one of them. The optimum concentrations of BPO, MA, PMPPIC, and fiber vary according to the wood species, the nature of the fiber, and the type of polystyrene. Compared with woodflour, CTMP is believed to be by far the best as far as the mechanical properties of the modified fiber-filled composites are concerned.     

Thermoplastic composties of polystyrene: Effect of different wood species on mechanical properties

Both softwood (spruce) and hardwood (aspen and birch) species in the form of different pulps (e.g., sawdust, chemithermomechanical pulp, explosion pulp and OPCO pulp) have been used (10–40 wt% composite) as reinforcing fillers for thermoplastic composites of polystyrene. Mechanical properties, are examined, e.g., tensile modulus, tensile strength at maximum point, and the corresponding elongation and energy as well as impact strength of compression molded composites. To improve the compatability of wood fibers which are hydrophilic and the polymer matrix which is hydrophobic, poly[methylene(polyphenyl isoeyanate)] (2 and 8 wt % of polymer) was used as a coupling agent. The mechanical properties of the treated composites are improved up to 30% in fiber content whereas a downward trend for untreated composites was observed when an increase in fiber content occurred. The overall improvements in mechanical properties due to the addition of isocyanate can be explained by the linkage of isocyanate molecules with fiber matrix through the chain of covalent bonds and the interaction of π-electrons of benzene rings of polystyrene as well as isocyanate. As a result, poly[methylene(polyphenyl isocyanate)] forms a bridge between fiber and polymer on the interfaces. This result is instrumental for efficient stress transfer between cellulose fibers and thermoplastics. The performance of different pulps of various wood species as reinforcing fillers for thermoplastic composites is also examined.     

Improving adhesion of wood fiber with polystyrene by the chemical treatment of fiber with a coupling agent and the influence on the mechanical properties of composites

—The mechanical properties of polystyrene filled with chemithermomechanical pulp and wood residues of softwood and hardwood species, which were precoated with phthalic anhydride and various polymers, e.g. polystyrene and PVC, have been investigated. The extent of improvement in the mechanical properties of the composite materials depends on the coating composition, the concentration of phthalic anhydride, the nature of the coated polymers, as well as the concentration of fiber, the nature of the wood species, and the nature of the pulps. Experimental results indicate that phthalic anhydride acts as a coupling agent, but when its performance was compared to that of poly[methylene (polyphenyl isocynate)], it seemed inferior to the latter.     

The Mechanical Properties of Wood Fiber-reinforced Polymethylmethacrylate

Abstract

The mechanical properties, e.g. tensile modulus (at 0.1% strain), tensile strength at maximum point and corresponding elongation and breaking energy, as well as impact strength, of compression molded PMMA and PMMA filled with wood fibers (10%-40% by weight of composite) have been investigated. Optimization of molding conditions, (e.g. temperature, time, pressure and mixing aids) was carried out. In optimum conditions of mixing and molding, the effect of different parameters, (e.g. nature and concentration of coupling agents (isocyanates), coating treatment, nature of wood species in the form of various pulps) on the mechanical properties of the resulting composites were evaluated. PMPPIC having 2%-4% (by weight of polymer) was found to behave as a true coupling agent because modulus as well as the tensile and impact strengths were improved. Moreover, PMPPIC acted as a coupling agent even when it was used for treatment of PMMA and fiber or to precoat the fiber. A distinct effect of the morphology of wood species and fiber-making techniques on the mechanical properties of wood fiber-filled composites was also observed.     

Effect of fiber treatment on the mechanical properties of hybrid fiber reinforced polystyrene composites. Part II. Use of glass fiber and wood pulp as hybrid fiber

The mechanical properties of polystyrene reinforced with a mixture of hardwood aspen chemithermomechanical pulp (CTMP) and surface-treated glass fiber have been studied. The adhesion of cellulose fiber to glass fiber as well as to thermoplastics improved thanks to various surface treatments of CTMP, e.g. coating with polymer+isocyanate or with silane, and grafting with polystyrene. In general, compared with non-treated CTMP-filled composites, the mechanical properties improved when surface-treated wood fiber was used as a filler. Experimental results indicate better compatibility between treated wood fiber and surface-treated glass fiber as well as polystyrene and, consequently, the mechanical properties were enhanced.     

Influence of modified wood fibers on the mechanical properties of wood fiber-reinforced polyethylene

Wood fiber of aspen was used as a reinforced filler in linear low-density polyethylene (LLDPE). To improve the compatibility between the wood fiber and the LLDPE matrix, the wood fiber was treated with titanate coupling agents (i.e., TC-PBT and TC-POT) or grafted by acrylonitrile. Both treatments resulted in an improvement in the mechanical properties of the resultant composites compared with the composites filled with the untreated wood fiber. Moreover, the grafting method displayed a more obvious benefit than that of titanate coupling methods to the mechanical property improvement. This was attributed to the crystalline structure of the wood fiber to be destroyed by grafting acrylonitrile, and the amorphous fiber was easily deformed to enhance fiber adhesion at the LLDPE matrix. In addition, the effect of the concentration of the filled wood fiber and the amount of coupling agent or grafting ratio on the mechanical properties of composites are discussed. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1561–1568, 1997     

Effect of recycling on the mechanical properties of wood fiber–polystyrene composites. Part I: Chemithermomechanical pulp as a reinforcing filler

The feasibility for recycling composites of polystyrene-hardwood aspen fiber (chemithermomechanical pulp or CTMP) was tested by evaluating the mechanical properties and dimensional stability of the original polymer and the recycled composites. The mechanical properties and dimensional stability of composites were investigated under extreme conditions (e.g., exposure to boiling water and at room temperature as well as exposure to +105°C and −20°C). The influence of coupling agent, e.g., 3% poly[methylene (polyphenyl isocyanate)] (PMPPIC), and various treatments, e.g., fiber coated with 10% polymer +8% PMPPIC and grafted with polystyrene 89.1% add-on, on the properties of the composites have also been studied. Compared with the original composites, the mechanical properties and dimensional stability of the recycled composites did not change significantly even after exposure to extreme conditions. Moreover, the treated composites offered improved properties compared with nontreated and original polymer under all experimental conditions.     

Moisture absorption properties of wood‐fiber‐reinforced recycled polypropylene matrix composites

To reduce the moisture absorption of wood‐fiber‐reinforced recycled plastic composites (WRPCs), a coupling agent (KH550), methyl methacrylate (MMA), and maleic anhydride (MA) were used to modify the wood fibers. The surface‐treated wood fibers were mixed with recycled polypropylene and processing agents to fabricate the WRPCs. The mechanical properties and moisture absorption behavior of the WRPCs were determined. The results showed that the three surface treatment methods could effectively reduce the moisture absorption and thickness swelling of WRPCs. In Comparison to the properties of untreated wood‐fiber‐reinforced WRPCs, the moisture absorption ratio of WRPCs with wood fibers treated by MMA, KH550, and MA was reduced by 31.4%, 49.8%, and 38.2%, respectively, and the tensile strength was increased by 22.1%, 26.3%, and 4.2%, respectively. The impact toughness of the WRPCs was increased by 36.2% KH550 treatment and 19.2% for MMA treatment but was decreased by 4.2% for MA treatment. Coupling treatment of the wood fibers was the best way to reduce the moisture absorption of WRPCs, and this kind of WRPC possessed the best comprehensive properties. J. VINYL ADDIT. TECHNOL., 2010. © 2009 Society of Plastics Engineers     

Comparative study of maleated polypropylene as a coupling agent for recycled low‐density polyethylene/wood flour composites

The effects of the type of coupling agent and virgin polypropylene (PP) content on the mechanical properties and water absorption behavior of recycled low‐density polyethylene/wood flour (WF) composites were investigated. The fractured surfaces of these recycled wood/plastic composites (rWPCs) were examined to gain insight into the distribution and dispersion of WF within the polymer matrix. The results indicate that the use of 100% recycled polymer led to inferior mechanical properties and to a greater degree of moisture absorption and swelling when compared to recycled polymer–virgin PP wood/plastic composites. This could have been related to the poor melt strength and inferior processability of the recycled polymer. The extent of improvement of the mechanical properties depended not only on the virgin PP content in the matrix but also on the presence of maleic anhydride (MA) modified PP as the coupling agent. Higher concentrations of MA group were beneficial; this improvement was attributed to increased chemical bonding (ester linkages) between hydroxyl moieties in WF and anhydride moieties in the coupling agent. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Development of basalt fiber‐reinforced thermoplastic composites and effect of PE‐g‐MA on composites

The thermoplastic matrix composites have gained great importance in last three decades. The chopped basalt fiber (mineral fiber) is considered to be a good fiber due to excellent properties as potential reinforcement of composite materials. In this work, composites of chopped basalt fiber (6 mm) with thermoplastic material Nylon‐6 (Polyamide‐6) were prepared and its mechanical and morphological properties were evaluated for automobile applications. The melt blending was carried out in corotating twin‐screw extruder and injection‐molded test samples were prepared for the analysis. The test samples of composite without coupling agent prepared by varying the loading of basalt fiber content of 5%, 10%, 15%, 20%, and 25% by weight and with coupling agent composite loading of Nylon‐6 and basalt fiber content were kept constant and the coupling agent (PE‐g‐MA) loading were changed as 1, 2, 3, 4, and 5 phr. The Mechanical and SEM properties were evaluated. From the test results, it was observed that the mechanical properties were improved with increasing coupling agent ratio. SEM images show good dispersion and adhesion of matrix and reinforcement. POLYM. COMPOS., 38:2798–2805, 2017. © 2015 Society of Plastics Engineers     

Effects of processing variables on the mechanical properties of compression molded polystyrene-wood fiber composites

Optimization of mixing and molding conditions (e.g. temperature, time and pressure) of aspen chemithermomechanical pulp (CTMP)-polystyrene composites was carried out. Compounding conditions showed a substantial effect on the mechanical properties of the composites. The effect of fiber encapsulation with polystyrene on the mechanical properties of the composites was also evaluated. Compared to non-encapsulated ones, the mechanical properties of composites showed superior results when encapsulated CTMP fibers were used. After encapsulation of wood fibers, and optimization of mixing and molding conditions, composites with up to 36% of fiber volume fraction could be incorporated in polystyrene with improved mechanical properties.     

Wood‐fiber‐reinforced poly(lactic acid) composites: Evaluation of the physicomechanical and morphological properties

This article presents the results of a study of the processing and physicomechanical properties of environmentally friendly wood‐fiber‐reinforced poly(lactic acid) composites that were produced with a microcompounding molding system. Wood‐fiber‐reinforced polypropylene composites were also processed under similar conditions and were compared to wood‐fiber‐reinforced poly(lactic acid) composites. The mechanical, thermomechanical, and morphological properties of these composites were studied. In terms of the mechanical properties, the wood‐fiber‐reinforced poly(lactic acid) composites were comparable to conventional polypropylene‐based thermoplastic composites. The mechanical properties of the wood‐fiber‐reinforced poly(lactic acid) composites were significantly higher than those of the virgin resin. The flexural modulus (8.9 GPa) of the wood‐fiber‐reinforced poly(lactic acid) composite (30 wt % fiber) was comparable to that of traditional (i.e., wood‐fiber‐reinforced polypropylene) composites (3.4 GPa). The incorporation of the wood fibers into poly(lactic acid) resulted in a considerable increase in the storage modulus (stiffness) of the resin. The addition of the maleated polypropylene coupling agent improved the mechanical properties of the composites. Microstructure studies using scanning electron microscopy indicated significant interfacial bonding between the matrix and the wood fibers. The specific performance evidenced by the wood‐fiber‐reinforced poly(lactic acid) composites may hint at potential applications in, for example, the automotive and packaging industries. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4856–4869, 2006     

Effect of fiber pretreatment condition on the interfacial strength and mechanical properties of wood fiber/PP composites

The effect of fiber surface pretreatment on the interfacial strength and mechanical properties of wood fiber/polypropylene (WF/PP) composites are investigated. The results demonstrate that fiber surface conditions significantly influence the fiber–matrix interfacial bond, which, in turn, determines the mechanical properties of the composites. The WF/PP composite containing fibers pretreated with an acid–silane aqueous solution exhibits the highest tensile properties among the materials studied. This observation is a direct result of the strong interfacial bond caused by the acid/water condition used in the fiber pretreatment. Evidence from coupling chemistry, rheological and electron microscopic studies support the above conclusion. When SEBS‐g‐MA copolymer is used, a synergistic toughening effect between the wood fiber and the copolymer is observed. The V‐notch Charpy impact strength of the WF/PP/SEBS‐g‐MA composite is substantially higher than that of the WF/PP composite. The synergistic toughening mechanisms are discussed with respect to the interfacial bond strength, fiber‐matrix debonding, and matrix plastic deformation. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 1000–1010, 2000     

Effect of Coupling Agent Concentration,Fiber Content,and Size on Mechanical Properties of Wood/HDPE Composites

In this study, the influence of coupling agent concentration (0 and 3 wt%), wood fiber content (50, 60, 70, and 80 wt%), and size (40–60, 80–100, and 160–180 mesh) on the mechanical properties of wood/high-density-polyethylene (HDPE) composites (WPCs) was investigated. WPC samples were prepared with poplar wood-flour, HDPE, and polyethylene maleic anhydride copolymer (MAPE) as coupling agent. It was found that the tensile properties and the flexural properties of the composites were improved by the addition of 3 wt% MAPE, and the improved interfacial adhesion was well confirmed by SEM micrographs. It was also observed that the best mechanical properties of wood/HDPE composites can be reached with larger particle size in the range studied, while too-small particle size was adverse for the mechanical properties of wood/HDPE composites. Moreover, the tensile modulus, tensile strength, and flexural strength of WPCs decreased with the increase in fiber content from 50 to 80 wt%; the flexural modulus of WPCs increased with the increase in fiber content from 50 to 70 wt% and then decreased as the fiber content reached 80 wt%. The variances in property performance are helpful for the end-user to choose an appropriate coupling agent (MAPE) concentration, wood fiber content, and particle size based on performance needs and cost considerations.     

A low‐cost,low‐fiber‐breakage,injection molding process for long sisal fiber reinforced polypropylene

Composites of polypropylene (PP) and non‐treated sisal fiber (SF) were prepared in a non‐conventional two‐step process that offers significant advantages. Maleic anhydride–grafted polypropylene (MA‐g‐PP) was used as a coupling agent, to improve adhesion between the polar sisal fiber and the non‐polar polypropylene continuous matrix. At a first step, SF/MA‐g‐PP pellets with large aspect ratio and very high fiber content are prepared by extrusion impregnation and coating of a continuous SF yarn, followed by cooling and cutting. The composite pellets are thus dry blended with regular PP pellets in the injection machine hopper, and injected to obtain composite tensile specimens with a minimum quantity of expensive MA‐g‐PP, minimum fiber breakage and thermal degradation, and excellent mechanical properties. The SF/MA‐g‐PP pellets have a fiber content of 70% (w/w). The composite tensile specimens have final fiber contents ranging from about 3.5% to 24.5% (w/w). The PP tensile strength rises by about 44%. The tensile modulus increases by 126%, and the heat distortion temperature (HDT) is raised by about 35 K. FT‐IR spectroscopy and SEM micrographic observation show that the MA‐g‐PP is covalently bonded to SF through esterification. Besides the improvement in mechanical and thermal properties, costs are reduced because of the lower content of very expensive MA‐g‐PP, and the use of a single‐screw extruder at high production rates. Polym. Eng. Sci. 44:1766–1772, 2004. © 2004 Society of Plastics Engineers.     

硅烷偶联剂对HDPE/木粉复合材料性能的影响

使用经硅烷偶联剂HP-172和HP-174改性的木粉制备了HDPE/木粉复合材料,研究了偶联剂用量对其性能的影响。实验结果表明:当使用1.5%的HP-172处理木粉后,可使复合材料的各项力学性能提高30%以上;HP-174的用量为1%~1.5%也得到了较好的改性效果。通过FIR和SEM分析发现,硅烷偶联剂可与木粉表面发生化学反应,从而提高了HDPE与木粉的界面粘合强度,使复合材料的力学性能得以提高     

Effects of wood flour and chitosan on mechanical,chemical, and thermal properties of polylactide

Composites of polylactide (PLA, 100–60 wt%) and wood flour (0–40 wt%) were prepared to assess the effects of wood filler content on the mechanical, chemical, thermal, and morphological properties of the composites. The polysaccharide chitosan (0–10 wt%) was added as a potential coupling agent for the PLA‐wood flour composites. Addition of wood flour significantly increased the flexural modulus and the storage modulus of PLA‐wood flour composite, but neither the wood flour nor chitosan had an effect on the glass transition temperature (T_g). Fourier transform infrared spectra did not show any evidence of covalent bonding, but chitosan at the interface between wood and PLA is thought to have formed hydrogen bonds to PLA‐carbonyl groups. SEM images of fracture surfaces showed that fiber breakage was far more common than fiber pullout in the composites. No evidence of discrete chitosan domains was seen in SEM micrographs. When added at up to 10 wt% (based on wood flour mass), chitosan showed no significant effect on the mechanical, chemical, or thermal properties of the composites, with property changes depending on wood flour content only. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers.     

Some studies on mechanical properties of wood flour/continuous glass mat/polypropylene composite

The mechanical properties and the surface property of wood flour/continuous glass mat/polypropylene composites have been investigated. The suitability of wood flour as a filler for continuous glass mat–reinforced polypropylene has been tested using different mesh sizes (e.g., 20 and 40 mesh), as well as by varying the weight percentage of wood flour from 0%– 30%. Moreover, different treatments such as coupling agent A‐1100 and functionalized polypropylene grafting with maleic anhydride, and so forth, have also been used to improve the compatibility of wood flour and glass fiber with the polymer resin. In addition, the effects of the surface weight of glass mat and matrix resin have been studied. The extent of the improvement in mechanical properties depends on the wood flour content and size, the surface weight of the glass mat, the matrix resin, and the surface treatment of wood flour. After adding wood flour, the contact angle of distilled water on the composite surface decreases and the polar component of surface tension increases. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 536–544, 2002