• Applied Chemistry for Engineering
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• v.8 no.5
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• pp.866-871
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• 1997

The com starch was treated with propylene oxide, 1,2-epoxybutane, glycidyl methacrylate, maleic anhydride, caprolactone, respectively, in order to alter the hydrophilicity and the reactivity of starch. When the starch was not dried, poor reaction was observed except the reaction with propylene oxide or maleic anhydride. The treated starches were grafted with styrene by several different polymerization methods. Solution polymerization and redox polymerization using cerium(IV) ion show poor grafting efficiency and poor yield. Encapsulation of starch with polystyrene by suspension polymerization was difficult due to the hydrophilicity of the starch. Among the examined methods, emulsion polymerization was found to be the suitable way to graft styrene onto starch.

• Applied Chemistry for Engineering
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• v.1 no.1
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• pp.73-82
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• 1990

Rosin-maleic anhydride adduct (RMA) was synthesized from rosin and maleic anhydride. The polyamideimides were obtained by reacting the adduct with two aromatic diisocyanates using sodium methoxide as catalyst. The yield and the inherent viscosity of polymers obtained by the reaction in NMP solvent were low because of the possible reaction of NMP solvent with diisocyanate monomer. The polymers were synthesized in solvent mixture of NMP and cosolvents such as xylene, acetophenone, benzonitrile, and nitrobenzene in order to minimize the side reaction of NMP with diisocyanates. The yield of polymer obtained by the reaction in NMP-nonpolar cosolvent mixtures was about 70% and that obtained by the reaction in NMP-polar cosolvent mixtures was over 90%, respectively. The polymers were either amorphous or poorly cystalline, and soluble only in highly polar solvents. The inherent viscosity of polymers ranges from 0.12-0.26dl/g. The results of thermal analysis showed that the polymer had good thermal stability with initial decomposition temperature over $330^{\circ}C$.

• Applied Chemistry for Engineering
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• v.24 no.6
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• pp.650-655
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• 2013

In this study, the synthesis of succinic acid from hydrogenation of maleic anhydride over Pd/C were performed in aqueous solution at various reaction conditions. We confirmed that the distribution of product was different according to process parameters. When increasing the reaction pressure and agitation speed, the by-product decreased and the purity of succinic acid increased. From the result, we may conclude that the reaction pressure and agitation speed are important factors for promoting the mass transfer rate of gas-liquid interface by increasing gas-liquid solubility in liquid hydrogenation. When the reaction pressure increased from 5 bar to 10 bar, the reaction rate increased 2.14 times. When the agitation speed increased from 300 rpm to 700 rpm, the reaction rate increased 2.75 times.

• Elastomers and Composites
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• v.49 no.4
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• pp.267-274
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• 2014

Self vulcanizable blend system for magnetorheological elastomer (MRE) has been studied by dispersing magneto responsible particle (MRP) on elastomeric matrix. Chloroprene rubber was modified with maleic anhydride (MAH) using heat and pressure which is called dynamic maleation process. The optimum graft ratio of MAH was found at 10 phr contents and reaction temperature of $100^{\circ}C$. This could be confirmed by FT-IR analysis. Epoxided natural rubber (ENR) was blended with modified CR-g-MAH for self vulcanization. The optimum amounts of ENR was 30 wt% in terms of scorch time and curing rate. MRE was manufactured by electromagnetic equipment and orientation of MRE was confirmed by SEM. Finally, it was found that the tensile strength of anisotropic-MRE was higher than that of isotropic-MRE and the hardness was reverse.

• Polymer(Korea)
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• v.37 no.6
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• pp.770-776
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• 2013

The ENR 50 having the lowest gas permeability was blended with Nylon 6 which exhibits superior gas permeability, excellent wear resistance by using a twin-screw extruder. The blended materials showed the increased gas barrier property and physical properties, but did not yield a great synergistic effect due to low dispersion of Nylon 6 to ENR 50. To improve dispersion of Nylon 6 in the rubber matrix, maleic anhydride (MAH) was grafted to ENR 50. The grafting reaction between MAH and ENR 50 was evidenced using IR spectroscopy. The grafted and blended materials, ENR 50- g-MAH/Nylon 6 compounds, resulted in an enhanced gas barrier property and physical properties compared with compounds without MAH. The compound at 5 phr of MAH showed the highest crosslinking density and the best performances.

• Journal of Adhesion and Interface
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• v.19 no.4
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• pp.145-153
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• 2018

In this study, adhesion promoters with acrylate and carboxylic acid moiety were synthesized from malenized polybutadiene and 2-hydroxyethyl acrylate for producing adhesive film with low water absorption and high adhesion. The surface properties, adhesion strength, mechanical properties and water absorption of adhesive films were characterized according to the amount of acrylate and carboxylic acid in the synthesized adhesion promoters. As the carboxylic acid in the adhesion promoters increased, the adhesion strength showed a tendency to increase and the mechanical properties also improved compared to the commercial adhesion promoter. The compatibility of adhesion promoters improved remarkably due to the presence of polybutadiene (hydrophobic nature), maleic anhydride (hydrophilic nature) and carboxylic acid (hydrophilic nature).

• Journal of the Korean Ceramic Society
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• v.53 no.1
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• pp.24-33
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• 2016

The grafting reaction for maleic anhydride (MA) onto high density polyethylene (HDPE) was investigated from solution process with initiators. The chemical modification of neat HDPE was carried out with various contents of MA (3-21 wt.%) and initiator (0.2-1 wt.%) at different temperature ($80-130^{\circ}C$). The grafting degree was obtained from the titration and the highest grafting degree was 3.1%. The grafting degree increased as the content of MA and initiator increased, however, the highest grafting degree was demonstrated for a particular content of MA and initiator. In the non-isothermal crystallization kinetics, the Ozawa model was unsuitable method to investigate the crystallization behavior of MA onto HDPE, whereas the Avrami and Liu models found effective. The crystallization rate was accelerated as the cooling rate increased, but postponed by combination of MA onto neat HDPE backbone.

• Clean Technology
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• v.17 no.3
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• pp.238-243
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• 2011

We investigate new polyols based on castor oil for polyurethane. In order to introduce primary alcohol groups, which exhibit higher reactivity with isocyanate than secondary alcohol groups, the secondary alcohol groups on castor oil were modified with maleic anhydride and aminoalcohol derivatives ($H_2N$-R-OH). The reactions with various molar ratio of castor oil and maleic anhydride were done at relatively low reaction temperature in the absence of catalyst. The polyols based on castor oil with flexible side-chains exhibit better miscibility with conventional synthetic polyols.

• Journal of the Korean Chemical Society
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• v.9 no.2
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• pp.88-95
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• 1965

The exo adduct between furfuryl derivatives (furan, furfuryl acetate and furfuryl alcohol) and maleic anhydride were prepared in the presence of ethyl ether. The bromination of the exo adduct of each derivatives gave a monobromolactone and dibromoacid when the reaction was done in the presence of water. The formation of the bromolactone was proved to be dependent to the carboxylic participation to the incipient rearranged carbonium ion of a classical type, and the participation was sterically hindered by the steric structure of the substituents. The bromination of the furan-maleic anhydride adduct in the presence of organic solvent $(CCl_4,\;CH_2Cl_2)$ gave the dibromide, whereas the photochlorination of the same adduct in the presence of carbon tetrachloride gave the tetrachloride. The procedure of the preparation and the reaction path of the halogenation were described.

• Journal of Adhesion and Interface
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• v.25 no.1
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• pp.152-156
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• 2024

We conducted research on a two-component epoxy adhesive material based on acid graft polyolefin using maleic anhydride to address the lack of formability due to epoxy adhesives' hard segments. To understand the graft efficiency according to reaction conditions, we conducted studies based on polyolefin molecular weight, initiator half-life, and initiator concentration for each process. The maleic anhydride grafted polyolefin produced was used as an adhesive material for aluminum and CPP film lamination after mixing with epoxy hardener. The graft efficiency in the solution process was approximately 30% superior to that in the melt process, and an increase in graft ratio confirmed an increase in peel strength.