Effect of Cross-linking Agent on Tensile Properties of Chitosan/Corn Cob Biocomposite Films

2015 ◽  
Vol 54 (3) ◽  
pp. 270-275 ◽  
Author(s):  
Chan Ming Yeng ◽  
Salmah Husseinsyah ◽  
Sam Sung Ting
2013 ◽  
Vol 747 ◽  
pp. 649-652 ◽  
Author(s):  
Chan Ming Yeng ◽  
Husseinsyah Salmah ◽  
Sung Ting Sam

Recently, there has been renews interest in chitosan as materials in producing of biocomposite films. The chitosan (CS)/corn cob (CC) biocomposite films were prepared by solvent casting method. The effect of CC content on tensile properties of CS/CC biocomposite films was studied. The tensile strength and elongation at break of CS/CC biocomposite films decreased as increasing of CC content. However, the increasing of CC content was increased the tensile modulus of CS/CC biocomposite films. Scanning electron microscopy (SEM) was indicated that the deceasing of tensile properties was due to the poor interfacial adhesion between CC filler and CS matrix.


BioResources ◽  
2013 ◽  
Vol 8 (2) ◽  
Author(s):  
Ming Yeng Chan ◽  
Salmah Husseinsyah ◽  
Sung Ting Sam

Author(s):  
Ahmad Adlie Shamsuri ◽  
Khalina Abdan ◽  
Tatsuo Kaneko

In this prelude study, the gellan gum/kenaf core fiber (KCF) biocomposite films were fabricated with the addition of imidazolium-based ionic liquids such as 1-butyl-3-methylimidazolium chloride (Bmim Cl), 1,3-dimethylimidazolium methylsulphate (Dmim MeSO4), 1-ethyl-3-methylimidazolium acetate (Emim Ac), and 1-ethyl-3-methylimidazolium trifluoromethanesulfonate (Emim OTf). The fabrication of the biocomposite films was carried out by mixing KCF and the ionic liquids in an aqueous solution, followed by dissolution of gellan gum in the same solution at a temperature of 90°C. The mixed solution was gelled at room temperature, and the formed gel was dried in an oven at 40°C for 48 hours to obtain a freestanding biocomposite film. The fabricated films were characterized by using a universal testing machine to acquire tensile properties. The tensile test results indicated that the biocomposite film added with Emim Ac possesses a higher tensile extension at maximum (up to 24%) than the biocomposite film without ionic liquid (added with glycerol). In addition, the biocomposite film added with Emim OTf has a higher tensile modulus at maximum (up to 758%) compared to the biocomposite film without ionic liquid. In conclusion, the tensile properties of the gellan gum/KCF biocomposite films can be improved with the addition of Emim-based ionic liquids with different counter anions.


2009 ◽  
Vol 80 (12) ◽  
pp. 1131-1137 ◽  
Author(s):  
Naoya Katsuyama ◽  
Koji Shimizu ◽  
Shunya Sato ◽  
Jun Araki ◽  
Akira Teramoto ◽  
...  

2012 ◽  
Vol 441 ◽  
pp. 466-472
Author(s):  
Ming Hua Wu ◽  
Jian Peng Dong ◽  
Dong Ming Qi ◽  
Chong Qian ◽  
Xin Jiang

A series of acrylate latexes for pigment printing binder were prepared by semi-continuous pre-emulsifying emulsion polymerization, using lipophilic glycidyl meth-acrylate (GMA), ethylene glycol dimethyl acrylate (EGDMA) and hydrophilic HA (containing hydroxyl, acylamino), N-methylol acrylamide (NMA) as cross-linking monomer. The influences of cross-linker type on the particle size, viscosity and film-forming rate of latex, cross-linking degree and tensile properties of latex film were studied. It was found that the latex particle size, viscosity and film-forming rate were closely related with the hydrophile-lipophile property of cross linkers. The acrylate latex synthesized with hydrophilic cross-linkers always exhibits the characteristics of larger particle size, lower film-forming rate, higher viscosity and pseudoplastic fluid. The cross-linking degree and tensile properties of latex film generally depend on the crosslinking groups of cross-linkers and their reactivity.


2020 ◽  
Vol 142 (6) ◽  
pp. 2371-2383
Author(s):  
Sebestyén Nagy ◽  
Erika Fekete ◽  
János Móczó ◽  
Krisztina Koczka ◽  
Emília Csiszár

AbstractCellulose nanocrystals (CNCs) were extracted from natural cellulosic fibres such as bleached cotton and flax with a controlled multi-step sulphuric acid hydrolysis. From the aqueous suspensions of CNCs, the biocomposite films were prepared by casting and evaporation, with an amino-aldehyde (AA) compound in a wide concentration range from 0 to 30%. The AA compound (dimethylol dihydroxy ethylene urea) was considered both as a cross-linker of the CNC and as a matrix polymer for the CNC-reinforced composite system. Two series of films were prepared using different polyols such as sorbitol and glycerol as plasticizers to improve tractability. Heat treatment of the films was performed at elevated temperatures ranging from 140 to 200 °C for 10 min. Results clearly proved that besides temperature, the factors affecting the response of CNC-based nanocomposites to heat treatment were the source of cellulose, the type of plasticizer and the amount of cross-linking agent. Films based on flax–CNC and plasticized with glycerol showed a higher increase in yellowness and a more significant decrease in haze than those derived from cotton–CNC and plasticized with sorbitol, respectively. The cross-linking agent (AA) had a moderating effect on the heat-induced changes of properties. Furthermore, thermal gravimetric analysis (TG) of films revealed that thermal stability of the CNC films improved considerably when AA was added and cross-linking occurred. The increase in Tmax was more significant for the flax–CNC films (from about 230 to 290 °C) than for the cotton–CNC ones (from about 250 to 280 °C).


1948 ◽  
Vol 21 (2) ◽  
pp. 301-313 ◽  
Author(s):  
Geoffrey Gee

Abstract The tensile properties of a range of pure-gum natural rubbers have been reviewed, and it has been shown that their principal features can be understood on the assumption that the tensile strength measured in a given test depends directly on the amount of crystallization at break. The most important single factor in determining tensile strength is the degree of cross-linking. Cross-linking is only needed in order to prevent plastic flow, thus making it possible for the molecules to align themselves by stretching, and hence to crystallize. A very highly cross-linked rubber is weak because the load required to stretch it is so high that the rubber is broken before the elongation becomes large enough to produce crystallization. In general, vulcanization also involves reactions, e.g., the combination of sulfur with the rubber, which inhibit crystallization by producing structural modifications of the rubber. These reduce the tensile strength, especially when the degree of cross-linking is large. These ideas readily explain the effects of swelling and of the temperature of test. They are also used in a brief discussion of the phenomena of overcure, reversion, and aging.


1982 ◽  
Vol 55 (5) ◽  
pp. 1328-1340 ◽  
Author(s):  
L. F. Ramos-DeValle ◽  
R. R. Ramírez

Abstract An experimental study of the mixing and final mechanical properties of blends of guayule rubber with polyolefins was carried out. It was found that (1) variation in total mixing time during blend preparation produced only minor differences in maximum tensile properties; (2) tensile properties of the blends approach those of the plastic at GR concentrations of 50% and lower, those of the rubber at GR concentrations of 70% and higher; (3) tensile properties of partially crosslinked blends improve if the addition of DCP is effected after partial mixing of the pure homopolymers; (4) the partial cross-linking of the blend exerts a strong beneficial influence on the mechanical properties; (5) the addition of carbon black exerts little influence on the mechanical properties of the blend. It can be suggested that, at 60% GR, both polymers (GR and HDPE) show the same tendency to form the continuous or dominant phase. Above 60%, the rubber tends to be the dominant phase, and below 60% the plastic tends to be the dominant phase. The mechanical properties of partially crosslinked GR-HDPE blends are comparable with those of similar commercially available products. This suggests a further alternative in the commercialization of natural guayule rubber, namely, thermoplastic rubbers.


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