Chemical modification of rubber wood with styrene and glycidyl methacrylate

Rubber wood was impregnated with styrene and glycidyl methacrylate (GMA) as the crosslinking monomer. Polymerization was accomplished by catalyst heat treatment. Compressive strength both in parallel and perpendicular to fiber directions was measured and improvement was observed for wood polymer composites. Bending strength in terms of Modulus of Elasticity (MOE) and Modulus of Rupture (MOR) was measured and found improved on treatment over the untreated wood samples. Hardness for treated wood was also improved. Dynamic Mechanical Analysis (DMA) indicated an increase in interaction between wood, styrene, and GMA. Biodegradation of the treated and untreated wood samples was also determined and found to be improved on treatment. Scanning electron microscopy (SEM) study showed the wood polymer interaction. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Studies on dimensional stability and thermal properties of rubber wood chemically modified with styrene and glycidyl methacrylate

Rubber wood (Hevea brasiliensis) was impregnated with styrene and glycidyl methacrylate (GMA) as the crosslinking monomer. After impregnation, the polymerization was accomplished by catalyst heat treatment. Water uptake (%) and water vapor exclusion (%) of the rubber wood were found to be improved on treatment. Dimensional stability expressed in terms of volumetric swelling in water vapor (90% relative humidity) as well as in liquid water and water repellent effectiveness (WRE) of the treated samples were determined and also found to be improved. The wood–polymer interaction was confirmed by FTIR spectroscopy. Thermal properties of untreated and treated wood samples were evaluated by thermogravimetric analysis (TGA) and differential scanning calorimetery (DSC) and an improvement in thermal stability was observed for the wood–polymer composites. The improvement in properties observed as more with styrene–GMA (1:1) combination. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1938–1945, 2004     

Modification of rubber wood with styrene in combination with diethyl allyl phosphate as the flame‐retardant agent

Rubber wood (Hevea brasiliensis) polymer composite was prepared using styrene as the monomer in combination with diethyl allyl phosphate (DEAP) to improve flame‐retardant property. DEAP was synthesized, characterized and incorporated into wood with styrene. The polymerization was accomplished by catalyst heat treatment using AIBN as the catalyst. The properties of wood–polymer composites (WPC) like water absorption, swelling in water, hardness, modulus of elasticity (MOE), modulus of rupture (MOR) etc. were improved on treatment. The thermal degradation behavior of WPC was evaluated using thermogravimetric analysis (TGA) and the flammability of the WPC was evaluated using the limiting oxygen index (LOI) test. It was observed that fire retardancy of WPC improved on incorporation of DEAP. FTIR spectroscopy and SEM study showed the interaction between wood and the polymers. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Wood–polymer composites prepared by the in situ polymerization of monomers within wood

Wood–polymer composites (WPCs) were prepared from poplar wood (P. ussuriensis Komarov) in a two‐step procedure. Maleic anhydride (MAN) was first dissolved in acetone and impregnated into wood; this was followed by a heat process; and then, glycidyl methacrylate (GMA) and styrene (St) were further impregnated into the MAN‐treated wood, followed by a second thermal treatment. Finally, the novel WPC was fabricated. The reactions occurring in the WPC, the aggregation of the resulting polymers, and their interaction with the wood substrate were analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy, X‐ray diffraction, and dynamic mechanical analysis. The performance of WPC was also evaluated in terms of the mechanical properties and durability, which were then correlated with the structural analysis of the WPC. The test results show that MAN and GMA/St chemically reacted with the wood cell walls in sequence, and the quantity of hydroxyl groups in the wood cell walls was evidently reduced. Meanwhile, St copolymerized with GMA or MAN, and the resulting polymers mainly filled in the wood cell lumen in an amorphous form, tightly contacting the wood cell walls without noticeable gaps. As a result, the mechanical properties, decay resistance, and dimensional stability of the WPC were remarkably improved over those of the untreated wood, and its glass‐transition temperature also increased. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Rubberwood–polymer composites based on glycidyl methacrylate and diallyl phthalate

Wood–polymer composites (WPC) of rubberwood (Hevea Brasiliensis) were prepared by impregnating the wood with glycidyl methacrylate (GMA), combinations of glycidyl methacrylate and diallyl phthalate (GMA–DAP), or diallyl phthalate (DAP) alone. Polymerization was carried out by catalyst-heat treatment. The results showed that WPC based on GMA exhibited greater dimensional stability (results of antishrink efficiency after six days of soaking) about five times than those based on DAP alone. Flexural [Modulus of Elasticity (MOE), Modulus of Rupture (MOR), and toughnes], compressive, and impact properties for all the samples tested are improved, especially for those with higher chemical loading. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 67:1221–1226, 1998     

Modification of some mechanical properties of spruce by radiation induced copolymerization of acrylonitrile and methyl methacrylate with allyl glycidyl ether

In this study, spruce samples were impregnated with acrylonitrile (AN), methyl methacrylate (MMA), allyl glycidyl ether (AGE), AGE/AN or AGE/MMA monomers and monomer mixtures. In situ polymerization (copolymerization) was achieved by gamma irradiation. The relationship between the mechanical properties of the wood‐polymer(copolymer) composites and the kind and quantity of polymers and copolymers, irradiation dose and artificial aging treatment of the wood was investigated. The fine structure of wood‐polymer(copolymer) composites was determined by Scanning Electron Microscopy. The presence of homopolymer and copolymers increased the mechanical properties of the wood. The compressive strength and Brinell Hardness Numbers, determined for untreated and treated wood samples, indicated that the mechanical strength of wood‐polymer (copolyrner) was significantly increased in the presence of P(AGE/MMA). At maximum percent conversion, the percentage increase in the compressive strength with regard to the applied force perpendicular to the fibers in spruce was 218%. After aging for 28 days, it was found that there were no significant changes in mechanical stability.     

Preparation and characterization of wood/styrene‐acrylonitrile copolymer/MMT nanocomposite

Wood polymer nanocomposite (WPNC) was prepared by impregnating Simul (Salmalia malabarica) wood with styrene‐acrylonitrile copolymer (SAN), glycidyl methacrylate(GMA), and a reactive polymerizable surfactant modified montmorillonite (MMT). The physical and mechanical properties of WPNC were investigated by using XRD, tensile tester, SEM, and FTIR. The polymer loading, dimensional stability, water uptake, mechanical property, and thermal stability were found to improve due to inclusion of MMT. SEM micrographs showed the presence of polymer and MMT into cell wall and cell lumen. FTIR analysis confirmed the presence of MMT and SAN in WPNC. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Elaboration of performance of tea dust–polypropylene composites

In this research work, dynamic, mechanical, and thermophysical properties of untreated and 5, 7, and 10 wt % styrene treated tea dust (TD):polypropylene (PP) composites prepared by injection‐molding machine were elaborated. There were distinctive and significant improvement observed in mechanical properties (tensile strength, tensile modulus, and elongation at break), physical analysis (water swelling), dynamic mechanical properties (storage modulus, loss modulus, and tan δ), and thermal behavior and surface morphological properties of styrene treated TD:PP (40:60) composites as compared to that of untreated one. The tensile strength (from 7.00 to 9.95 MPa), tensile modulus (from 350 to 715 MPa), storage modulus (from 8500 to ～10,500 MPa), and loss modulus (from ～150 to ～200 MPa) increased on 10 wt % styrene treatment of TD over the untreated TD:PP (40:60) composites. The styrene treated TD:PP (40:60) composites behaved as more elastic than their pure counterpart. Styrene treated TD:PP (40:60) composites were more thermally more stable (85 °C difference) as compared to virgin PP. Overall, this research also indicates the use of TD waste. An improvement in dispersion of styrene treated TD particles in PP was also observed in the preparation of the PP composites due to good compatibility of styrene with PP. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44750.     

Rubberwood–polymer composites based on diallyl phthalate and methyl methacrylate

Wood–polymer composites (WPC) of rubberwood (Hevea brasiliensis), were prepared by impregnating the wood with methyl methacrylate (MMA), and the combinations of MMA and diallyl phthalate (MMA/DAP). Polymerization was carried out by catalyst heat treatment. Impregnated samples showed significant improvements in compressive and impact strengths, hardness, and dimensional stability (toward water) over that the untreated rubberwood. © 1995 John Wiley & Sons, Inc.     

Surface functionalization of Si3N4 nanoparticles by graft polymerization of glycidyl methacrylate and styrene

To improve dispersibility and interfacial interaction of nano‐Si₃N₄ particles in epoxy‐based composites, graft of glycidyl methacrylate (GMA) and styrene (St)/GMA onto the nanoparticles' surface was carried out in terms of emulsion polymerization method. The grafting polymers proved to be chemically attached to the nanoparticles via the double bonds introduced during the coupling agent pretreatment. The factors affecting the graft parameters, such as monomer concentration, initiator consumption, reaction time, etc., were investigated. It was shown that higher concentrations of monomer and initiator are favorable for the graft polymerization. When St/GMA was employed as the grafting monomer, the nanoparticles were found to play the role of polymerization loci. The grafted nanoparticles exhibit greatly improved dispersibility in cured epoxy. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 992–999, 2006     

Effect of alkali and ultraviolet (UV) radiation pretreatment on physical and mechanical properties of 1,6‐hexanediol diacrylate–grafted jute yarn by UV radiation

To improve the physicomechanical properties of jute yarn, grafting with 1,6‐hexanediol diacrylate (HDDA) monomer was performed by a UV radiation technique. A series of HDDA solutions of various concentrations in methanol were prepared. A small quantity of photoinitiator (Darocur‐1664) was also added to HDDA solutions. To optimize the conditions for grafting, the effects of monomer concentration, soaking time, and radiation doses were studied by varying the number of soaking times along with variation of monomer concentrations and UV radiation intensities. The extent of polymer loading and the mechanical properties like tensile strength (TS), elongation at break (Eb), and tensile modulus of both treated and untreated jute were investigated. The highest tensile strength, polymer loading, and modulus were achieved with 5% HDDA concentration, 5 min soaking time, and the 4th pass of UV radiation. This set of conditions was selected as optimum and produced enhanced tensile strength (67%), modulus (108%), and polymer loading (11%) over those of virgin fiber. To further improve the mechanical properties the jute yarns were pretreated with alkali (5% NaOH) solution and after that the alkali‐treated yarn were treated under UV radiation of various intensities. The pretreated samples were grafted with optimized monomer concentration (5% HDDA). Increased properties of alkali + UV‐pretreated and grafted samples such as polymer loading (12%), tensile strength (103%), elongation at break (46%), and modulus (114%) were achieved over those of virgin jute yarn. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 18–24, 2004     

Functionalization of high‐density polyethylene in the molten state by glycidyl methacrylate grafting

:This study concerns the melt‐free radical grafting of glycidyl methacrylate (GMA) onto high‐density polyethylene (HDPE). We studied the effect of two initiators (tert‐butyl cumyl peroxide and di‐tert‐butyl peroxide) onto HDPE. Crosslinking of polymer was observed in the presence of 0.3 wt % tert‐butyl cumyl peroxide but not with 0.3 wt % di‐tert‐butyl peroxide. The grafting was carried out in a Brabender batch mixer at 190 °C. The grafting yield of GMA onto HDPE (determined by infrared spectrometry) is weak (<1 wt % for an initial concentration in monomer of 6 wt %). Moreover, it was noted that the degree of grafting did not vary with the concentration and the nature of peroxide used. To increase the grafting yield of GMA, we added to the HDPE/peroxide/GMA system an electron‐donating monomer, such as styrene. Adding this comonomer multiplied the rate of grafted GMA 3‐ or 4‐fold, resulting in a ratio [styrene]_i/[GMA]_i = 1 mol/mol with [GMA]_i = 6 wt %. So, the copolymerization is favored compared with the homopolymerization. This kind of copolymer presenting reactive functions is very attractive in the field of compatibilizing immiscible polymers. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 581–590, 2001     

Surface modification of henequen (Agave fourcroydes) fibers by ultraviolet curing with 2‐hydroxyethylacrylate and ethylacrylate: Effect of additives on degradable properties

Henequen fibers were grafted with a double impregnating monomer 2‐hydroxyethylacrylate (HEA) and ethylacrylate (EA) to improve the physicomechanical properties. The fibers soaked in different concentration (1–10%) of monomer + MeOH solution along with photoinitiator Irgacure 907 [2%] were cured under ultraviolet (UV) lamp at different UV radiation intensities (2–14 passes). Concentration of monomer at different radiation intensities was optimized with extent of mechanical properties such as polymer loading, tensile strength, and elongation at break. Enhanced tensile strength (268%) and elongation at break (110%) were achieved by the polymer treated fibers than untreated virgin fibers. We observed that, henequen fibers treated by 3% EA showed better physico‐mechanical properties than those treated by 5% HEA. The tensile properties of henequen fibers treated by 3% EA can be enhanced by adding aloxysilane; 3‐(trimethoxysilyl) propylmethacrylate additives with bulk monomer EA (3%). The degradability of the treated and untreated fibers due to accelerated weathering were also studied and it has been found that surface modified henequen fibers produced more resistivity towards different weathering conditions than untreated fibers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4000–4006, 2006     

Improvement of mechanical stability of beechwood by radiation‐induced in situ copolymerization of allyl glycidyl ether with acrylonitrile and methyl methacrylate

Acrylonitrile (AN), methyl methacrylate (MMA), allyl glycidyl ether (AGE), AGE + AN monomer, AGE + MMA monomer, and monomer mixtures were used to conserve and consolidate beechwood. After the impregnation of these monomer mixtures in the wood, polymerization was accomplished by gamma irradiation. The fine structures of wood + polymer(copolymer) composites were investigated by scanning electron microscopy (SEM). The copolymer obtained from AGE + MMA monomer mixtures showed the optimum compatibility with the wood. The compressive strength and Brinell hardness numbers determined for untreated and treated wood samples indicated that the mechanical strength was greater in wood + polymer(copolymer) composites than in untreated wood and was greatest in the samples containing AGE + AN and AGE + MMA copolymers. All monomer couples used in this study increased the mechanical strength of the wood and protected the samples against aging. AGE + MMA copolymers were the most effective in protecting the wood against various environmental attacks. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1515–1523, 1999     

New wood-polymer composites containing ethyl α-hydroxymethyl acrylate polymers

Ethyl α-hydroxymethyl acrylate (EHMA) was synthesized and evaluated as a candidate for wood impregnation and in-situ polymerization. Southern Pine softwood was impregnated under a variety of conditions with EHMA alone and with various comonomers plus free radical initiator. Following thermal polymerization, the wood-polymer composites were tested for increased dimensional stability (water soaking swell resistance) and mechanical properties over untreated wood. The greatest increase in dimensional stability was attained using EHMA alone, while the maximum compression modulus was achieved by impregnating with 1:1 EHMA-styrene and styrene alone. The composites were further characterized by ¹³C CP/MAS solid state NMR and scanning electron microscopy.     

Evaluation of dimensional stability,weathering and decay resistance of modified pine wood by in-situ polymerization of styrene

Abstract

In this study, polystyrene modified Scots pine (Pinus sylvestris L.) wood was investigated upon artificial weathering, decay resistance, dimensional stability and water uptake properties. Polystyrene modification was carried out on pretreated wood by immersion of wood into styrene monomer and further polymerization. The resistance of modified wood against cycles of UV and water exposures was examined by artificial weathering test for 672?hours, and decay resistance was evaluated by attacks of Coniophora puteana and Trametes versicolor on the samples. During the artificial weathering, color and surface roughness of the samples, and macroscopic changes were determined periodically. Changes in the surface chemistry and morphology of the weathered samples were investigated by ATR-FTIR and SEM, respectively. It was proven that polystyrene effectively protected pine samples from both fungi even after leaching procedure, but it was more effective in preventing C. puteana attacks than T. versicolor attacks. As a result of artificial weathering, the surface of all samples was darkened. However, changes in color and roughness as well as crack formations of the modified sample surfaces were found less than those of the untreated samples. Polystyrene also provided considerable improvement on dimensional stability, as well as water repellence of wood.     

Wood fiber surface treatment level effects on selected mechanical properties of wood fiber-cement composites

The objective of this study was to determine the effects of sodium (N) silicate, potassium (K) silicate, and silane (Si) treatment levels on newspaper and unbleached kraft fibers for enhancing selected mechanical properties of wood fiber-cement composites compared to untreated wood fiber-cement composites. Both wood fiber types were treated with selected aqueous solution strengths, air dried, and mixed with water and cement. The bending and compression properties of the specimens were determined after 28 days of hydration. Results of this study indicated that the aqueous chemical treatments of the wood fibers enhanced some of the mechanical properties of wood fiber-cement composites compared to the untreated wood fiber-cement composites. The enhancement depended on chemical treatment and wood fiber type. All three chemical treatments of newspaper fiber enhanced the normalized toughness values compared to the untreated newspaper fiber-cement composites. In addition, higher treatment levels using N silicate with newspaper fiber improved the compressive strength and bending modulus of the composites compared to the untreated newspaper fiber-cement composites. Kraft fiber treated with all three chemicals enhanced the compressive strength, bending modulus and bending strength compared to the untreated kraft fiber-cement composites. However, only silane-treated kraft fiber improved the normalized toughness values compared to the untreated kraft fiber-cement composites. The results of the study indicated that certain chemical treatments react better with different wood fiber types resulting in selected mechanical property enhancements.     

Effect of polymer in situ synthesized from methyl methacrylate and styrene on the morphology,thermal behavior,and durability of wood

A novel fast‐growing poplar wood, Populus ussuriensis Kom, was prepared into wood‐polymer composite by the in situ polymerization of methyl methacrylate and styrene through a vacuum/pressure and subsequent catalyst‐thermal process. scanning electron microscopy observation, FTIR, X‐ray diffraction, dynamic mechanical analysis, and thermogravimetric/derivative thermogravimetric analysis indicated that the resulted polymer well filled up wood cell lumen in an amorphous form and reinforced wood matrix, which resulted in the improvement of glass transition temperature, storage modulus, and thermal stability of wood. The decay resistance and dimensional stability of wood were also improved. Such wood‐based composite could be potentially used as reinforced material in construction fields. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Mechanical characterization of polypropylene–wood flour composites

The mechanical performance of different wood flour/polypropylene (PP) composites with interface modifications was compared. Wood flour was incorporated into the matrix after esterification with maleic anhydride (MAN) or without any modification but with the addition of a compatibilizing agent [maleic anhydride–polypropylene copolymer (PPMAN)] to modify the polymer–filler interaction. Composites were prepared by injection molding with different concentrations of wood flour. Mechanical properties (except Young's modulus) were not improved either by the wood flour chemical modification or by the use of PPMAN. However, both compatibilization methods were successful in improving the dispersion of the wood flour in the PP matrix. Creep behavior of composite samples was improved by the addition of PPMAN, whereas the composites prepared from MAN‐treated wood flour showed larger deformations than composites made with untreated particles. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1420–1428, 2003     

Reconsideration on the mechanism of free-radical melt grafting of glycidyl methacrylate on polyolefin

The styrene (St) assisted melt grafting of glycidyl methacrylate (GMA) on polyolefin was carried out by Haake mixer, and the grafting mechanism was investigated and reconsidered. It was revealed that there is equilibrium of grafting of GMA and depolymerization of grafted PGMA chains in the GMA/polyolefin grafting process, which was affected by both of the temperature and GMA concentration. It was found that the depolymerization of PGMA grafted on polyolefin occurred at the temperature above ceiling temperature of PGMA and dominated the grafting process before the addition of styrene monomer, which induced the decrease in grafting ratio of GMA. Adding styrene as co-monomer could promote the equilibrium moving forward to form the St-GMA chains so that the grafting ratio was greatly improved. It is proved that either controlling the reacting temperature below the ceiling temperature or changing the feeding order of styrene and GMA is effective to attain high grafting ratio of GMA on polyolefin.