• Proceedings of the Korean Fiber Society Conference
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• 2002.04a
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• pp.301-304
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• 2002

In the prior work,$\^$l)/ we introduced several chemical cross-linking agents in order to improve elastic recovery of copolyetheresters, but we are confronted by two difficulties. The first is that cross-linking agents interfere with crystal growth which acts as a physical interlocking. The second is that strain at breaking decreases with the amount of cross-linking agent. It is considered that the chemical interlocking parts couldn't be deformed like crystalline phase. (omitted)

• Journal of Fashion Business
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• v.13 no.1
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• pp.102-114
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• 2009

Chitosan is a polysaccharide with cationic amino groups in its structure and has useful properties as functional materials. Various end-use developments of chitosan are in progress. When the cotton fabric is pretreated with chitosan, the hand property of cotton fabric may be improved expecially for the summer apparel. In this study, as a cross-linking agent to introduce chitosan into cotton, BTCA(butane-1,2,3,4-tetracarboxylic acid) or CA(citric acid) was added in order to prevent detachment of chitosan by the cross-linking. During the cross-linking procedure, via the padding-drying-heat setting, amino groups of chitosan and hydroxyl groups of cotton, carboxyl groups of BTCA/CA are cross-linked by forming anhydrous cyclic rings. Since BTCA has four carboxyl groups, cross-linking by thermal treatment is easy, leading to the trials in wrinkle-recovery treatment of cotton fabrics. However, the high price of the BTCA reagent has been a shortcoming in the actual application for industrial use. Therefore, in this study, we tried the application of CA having three carboxyl groups, which is relatively low priced, as the substituting cross-linking agent. The hand of the treated fabrics were evaluated by measuring physical properties. In addition, based on the physical properties, three-dimensional images were introduced by using 3D CAD systems and results were compared.

• Journal of Adhesion and Interface
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• v.10 no.3
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• pp.134-140
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• 2009

The acrylic copolymers with variation in side chain were synthesized based on molecular design. Wettability and adhesion properties on the wafer surface were investigated for these acrylic copolymer pressure sensitive adhesives. Three-dimensional networks of linear acrylic copolymers were produced with epoxy-type Tetra-DX cross-linking agent. The effect of cross-linking on adhesion characteristics was investigated. The side chain of acrylic copolymer played more important role in wettability than the interfacial interaction. As the degree of cross-linking increased, both probe tack and peel strength decreased. Also, heat resistance measured by SAFT increased with cross-linking; however, it showed the deterioration when excess cross-linking agent was added.

• Proceedings of the Korean Fiber Society Conference
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• 1999.10a
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• pp.509-512
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• 1999

• Journal of the Korean Chemical Society
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• v.57 no.4
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• pp.439-446
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• 2013

Chitosan (CS) and hydroxypropylmethyl cellulose (HPMC) blend microspheres were prepared by water-in-oil emulsion technique and were loaded with an anti-cancer drug 5-fluorouracil (5-FU). CS-HPMC microspheres were characterized by Fourier transform infrared spectroscopy to confirm the cross-linking reaction. Scanning electron microscopy (SEM) was also used to assess the surface morphology of particles prepared. The quantity of release of 5-FU from the microspheres have been studied in terms of blend composition and amount of cross-linking agent. Differential scanning calorimetry and X-ray diffraction techniques indicated a uniform distribution of 5-FU particles in microspheres, whereas SEM suggested the spherical structure of the microspheres with slight rough surface. The in vitro drug release indicated that the particle size and release kinetics depend upon blend composition, amount of cross-linking agent used and amount of 5-FU present in the microspheres.

• Microbiology and Biotechnology Letters
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• v.16 no.2
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• pp.79-84
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• 1988

Dye materials and cross linking agents were used for the determination of $\beta$-glucanase activities. The objective of this study was to prepare the blue coloured substrates which are sensitive, specific and simple for the determination of $\beta$-glucanase in malt and Bacillus subtilis K-4-3 enzymes. This method is based on the principle of measuring colorimetrically the split product of coloured and cross linked substrate. The best coupling of dye stuff of $\beta$-glucan was cibacron blue 3G-A and the colour released can suitably be measured at 623nm. Optimal concentration of dye and cross linking agents was 1.5g and 1.25$m\ell$ under 0.1N NaOH. The sensitivity comparison proved that the stained $\beta$-glucan method is much more sensitive than the DNS method to determine reducing sugar released by the enzyme.

• Elastomers and Composites
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• v.57 no.2
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• pp.29-39
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• 2022

In this research, the relationships between the chemical structures of 10 different acrylate monomers with 3 different cross-linking monomers were evaluated. The thermal stabilities of the prepared copolymers were evaluated by their weight-loss percentage through thermogravimetric analysis, and their glass-transition temperatures were analyzed using differential scanning calorimetry. Based on the results, some relationships between the chemical structures of the monomers and their properties were derived and are discussed herein.

• Fibers and Polymers
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• v.4 no.4
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• pp.182-187
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• 2003

Low molecular weight copolymers of maleic anhydride and vinyl acetate were prepared to develop formaldehyde free cross-linking agents. Since lower molecular weight is favorable for efficient penetration of the finishing agent into the cotton fibers in the padding process, the concentration of the initiator, chain transfer agent and the monomer ratios were varied to obtain copolymers of low molecular weights. The prepared polymers were characterized by GPC, $^1{H-NMR}$, FTIR, DSC and TGA. Copolymers of molecular weights of 2 000 to 10 000 were obtained and it was found that the most efficient method of controlling the molecular weight was by varying the monomer ratios. Poly(maleic anhydride-co-vinyl acetate) did not dissolve in water, but the maleic anhydride residue hydrolyzed within a few minutes to form poly(maleic acid-co-vinyl acetate) and dissolved in water. However, the maleic acid units undergo dehydration to form anhydride groups on heating above ${160}^{\circ}C$ to some extent even in the absence of catalysts. The possibility of using the copolymers as durable press finishing agent for cotton fabric was investigated. Lower molecular weight poly(maleic anhydride-co-vinyl acetate) copolymers were more efficient in introducing crease resistance, which appears to be due to the more efficient penetration of the cross-linking agent into cotton fabrics. The wrinkle recovery angles of cotton fabrics treated with poly(maleic anhydride-co-vinyl acetate) copolymers were slightly lower than those treated with DMDHEU and were higher when higher curing temperatures or higher concentrations of copolymer were used, and when catalyst, $NaH_2$$PO_2$, was added. The strength retention of the poly(maleic anhydride-co-vinyl acetate) treated cotton fabrics was excellent.

• Membrane Journal
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• v.27 no.5
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• pp.441-448
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• 2017

In this study, the effects of membrane characteristics on the power generation performance in reverse electrodialysis (RED) have been investigated with pore-filled ion-exchange membranes (PFIEMs) prepared by employing a porous polyethylene substrate and the mixtures of three cross-linking agents. As a result, it was confirmed through the correlation analyses that the cross-linking degree and free volume of the PFIEMs were effectively controlled by mixing the cross-linking agents having different molecular sizes, influencing complexly the electrochemical characteristics of the membranes and the power generation performance in RED. In particular, the pore-filled cation-exchange membranes at the optimum cross-linking conditions exhibited the power generation performance superior to that of the commercial membranes and the pore-filled anion-exchange membranes also showed the excellent performance close to that of the commercial membrane.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.13 no.5
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• pp.2408-2413
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• 2012

Effects of stanous catalyst on the cross-linking reaction characteristics of multi-functional fluoropolymer with blocked-hexamethylene diisocyanate(HMDI) were studied by dynamic DSC and non-isothermal thermogravimetric analysis (TGA). Results showed that cross-linking reaction occurred around $230-250^{\circ}C$ aftr the solvent and phenol, blocking agent, were removed upto the $150^{\circ}C$. It was considered that the reaction mechanism of the multi-functional fluoropolymer with HMDI might not be changed by the catalyst, however, the reaction rate became extremely faster upto to 100 times, showing the change of activation energy 81.8 kJ/mol for non-catalytic system to 61.7 kJ/mol for 1 phr catalytic system.