Comparison of decay resistance of wood and wood-polymer composite prepared by in-situ polymerization of monomers

2013 ◽  
Vol 84 ◽  
pp. 401-406 ◽  
Author(s):  
Yongfeng Li ◽  
Zhenbo Liu ◽  
Xiaoying Dong ◽  
Yunlin Fu ◽  
Yixing Liu
2011 ◽  
Vol 675-677 ◽  
pp. 491-494
Author(s):  
Yong Feng Li ◽  
Yi Xing Liu ◽  
Xiu Rong Li ◽  
Jian Li ◽  
Xiang Ming Wang

A novel biomass composite, wood-polymer composite with potential good mechanical properties, durability and environmental characteristic capable of applying in fields of construction and traffic as structural material, was prepared by generating high-performance polymer from in situ polymerization of styrene in wood porous structure. The vinyl monomer, styrene, combing with 1wt% AIBN as an initiation, was first impregnated into wood porous structure under a vacuum/pressure condition, and then in situ polymerized through a thermal treatment. The structure of the resultant composite was characterized by SEM, FTIR and XRD. Results show that styrene polymerized into polystyrene through free radical polymerization, and the resultant polymer fully filled in wood porous structure in a column form, partly contacting wood matrix. FTIR analysis indicates that polystyrene generated into wood pores, indicating weak interaction between them. XRD analysis suggests that the polystyrene generated into wood pores mainly existed in an amorphous form.


2012 ◽  
Vol 166-169 ◽  
pp. 2938-2941 ◽  
Author(s):  
Yong Feng Li ◽  
Ding Wang Gong ◽  
Xiao Ying Dong ◽  
Zhen Bo Liu

Fast-growing poplar wood, Populus ussuriensis Kom, was used to prepare novel wood-polymer composite by the in-situ polymerization of methyl methacrylate (MMA) and styrene (St). SEM observation and FTIR analysis indicated that the resulted polymer well filled up wood cell lumen and physically reinforce wood matrix. The test results also proved that the mechanical properties of wood including modulus of rupture, modulus of elasticity, compression strength and hardness of were improved by 68.28%, 110.27%, 62.43%, 357% over those of Untreated Wood, respectively. Such wood-based composite could be potentially used as reinforced material in construction fields.


2010 ◽  
Vol 26-28 ◽  
pp. 181-185 ◽  
Author(s):  
Yong Feng Li ◽  
Xin Meng ◽  
Jian Li ◽  
Yi Xing Liu

A new material was prepared by formation of polystyrene in situ wood porous structure from styrene monomer through thermal-catalyst treatment. And the performance of such wood-polymer composite, containing mechanical properties and durability, was also tested. The SEM results showed that polymer was generated inside wood, and filled in wood cellular structure. The mechanical properties of such wood-polystyrene composite including modulus of rupture (MOR), modulus of elasticity (MOE), compression strength and hardness, were respectively improved 38%, 77%, 21% and 97% over untreated wood. And the durability of the novel composite involving dimensional stability, decay resistance and stability against weather erosion were remarkably improved than those of untreated wood. Such composite can be widely used in fields of construction, traffic and interior decoration, which greatly enhanced the utilization of low-valued wood material instead of high-quality wood.


2011 ◽  
Vol 311-313 ◽  
pp. 177-180
Author(s):  
Yong Feng Li ◽  
Yun Lin Fu ◽  
Hua Wei Huang ◽  
Yi Xing Liu

Michelia macclurei wood with moderate strength is a fast-growing wood in South China. However, it has not been fully utilized. We first prepared it into wood-polymer composite with purpose of good performance by impregnating methyl methacrylate monomer (MMA) into wood pores and following in-situ polymerization. The micro structure of wood-polymer composite, and the morphology and reaction of polymer in wood were characterized by SEM, FTIR and XRD. The SEM observation showed that the MMA monomer polymerized into polymer under the employed conditions and filled up wood cell cavity. FTIR analysis indicated that the monomer rarely reacted with wood cell wall during its polymerization. XRD characterized that the polymer from MMA monomer mainly physically existed in wood pores and remained as an amorphous form.


2012 ◽  
Vol 174-177 ◽  
pp. 826-829
Author(s):  
Yong Feng Li ◽  
Xiao Ying Dong ◽  
Yi Xing Liu

The fast-growing poplar wood, Populus ussuriensis Kom, was prepared into wood-polymer composite by the in-situ polymerization of methyl methacrylate (MMA) and styrene (St) under vacuum/pressure and subsequent catalyst-thermal conditions. SEM observation, FTIR, XRD and DMA analysis indicated that the resulted polymer well filled up wood cell lumen in an amorphous form and physically reinforce wood matrix, which resulted in the improvement of glass transition temperature and storage modulus of wood. Such method could endow low-quality wood with potential value-added applications.


2012 ◽  
Vol 571 ◽  
pp. 69-72
Author(s):  
Ding Wang Gong ◽  
Zhen Bo Liu ◽  
Hua Wei Huang ◽  
Chang Qing Zhang ◽  
Chen Liang

Fast-growing plant wood, Micheliamacclurel wood, was modified by formation of wood-polymer composite to improve its decay resistance. Two functional monomers, glycidyl methacrylate and ethylene glycol dimethacrylate, added with a few Azo-bis-isobutryonitrile as initiator, and maleic anhydride as catalyst, were first impregnated into wood cell lumen under a vacuum-pressure condition, and then in-situ polymerized into copolymers through a catalyst-thermal treatment. The decay resistances of untreated wood and wood-polymer composites were assessed by weight loss and compared by SEM observations. SEM and FTIR analysis indicated that the in-situ polymerized copolymers fully filled up wood cell lumen and also grafted onto wood cell walls, resulting in the blockage of passages for microorganisms and moisture to wood cell walls. Thus, the decay resistance of the wood-polymer composite against brown rot fungus and white rot fungus in terms of weight loss achieved 1.04%~1.33%, improved 95.10%~95.35% than those of untreated Micheliamacclurel wood; and also higher than that of boron-treated wood. The SEM observations presented the remarkable improvement of decay resistance of wood after such treatment, which effectively protected wood from degradation by fungi.


2010 ◽  
Vol 150-151 ◽  
pp. 1-5
Author(s):  
Yong Feng Li ◽  
Chi Jiang ◽  
Duo Jun Lv ◽  
Xiao Ying Dong ◽  
Yi Xing Liu

In order to improve the value-added applications of low-quality wood, a novel Wood-Polymer Composite was fabricated by in-situ synthesis of copolymer from monomers within wood porous structure. The structure was characterized with SEM and FTIR, and its dimensional stability was also tested. The SEM observations showed that copolymer filled up wood pores and contact tightly with wood matrix, indicating strong interactions between them. FTIR analysis indicated that when the monomers copolymerized in situ wood porous structure, they also reacted with wood matrix by reaction of hydroxyl groups and ester groups, indicating chemical bond between the two phases, which is agreement with SEM observations. The volume swelling efficiency and contact angle of such composite were higher than those of wood, respectively, indicating good dimensional stability involving volume swelling efficiency and contact angle. Such composite could be potentially applied in fields of construction, traffic and indoor decoration.


2010 ◽  
Vol 34-35 ◽  
pp. 1165-1169 ◽  
Author(s):  
Yong Feng Li ◽  
Bao Gang Wang ◽  
Qi Liang Fu ◽  
Yi Xing Liu ◽  
Xiao Ying Dong

In order to improve the value-added applications of low-quality wood, a novel composite, wood-polymer composite, was fabricated by in-situ terpolymerization of MMA, VAc and St within wood porous structure. The structure of the composite and the reaction of monomers within wood were both analyzed by SEM and FTIR, and the mechanical properties were also evaluated. The SEM observation showed that the polymer mainly filled up wood pores, suggesting good polymerizating crafts. The FTIR results indicated that under the employed crafts, three monomers terpolymerized in wood porous structure, and grafted onto wood matrix through reaction of ester group from monomers and hydroxyl group from wood components, suggesting chemical combination between the two phases. The mechanical properties of the wood-polymer composite involving modulus of rupture, compressive strength, wearability and hardness were improved 69%, 68%, 36% and 210% over those of untreated wood, respectively. Such method seems to be an effective way to converting low-quality wood to high-quality wood.


Sign in / Sign up

Export Citation Format

Share Document