• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2008년도 제39차 학술발표회
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• pp.11-12
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• 2008

Poly(ethylene oxide)(PEO) of molecular weight of 300,000 was crosslinked by UV irradiation in the presence of crosslinker. The photochemical crosslinking of PEO was enhanced by the addition of dimethacrylate crosslinkers in the film. Percent conversion of the polymer into gel as well as water absorbency were investigated gravimetrically. Gel fraction of PEO films increased with increasing crosslinker concentration. In the case of photocrosslinked PEO films with benzophenone, gel fraction reached about 95%. The thermal behavior of crosslinked PEO films was characterized by thermogravimetric analysis. The maximum decomposition temperature increased with increasing crosslinker concentration.

• 자연과학논문집
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• 제9권1호
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• pp.89-93
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• 1997

여러 가지의 친수성기와 소수성기를 함유하는 폴리포스파진을 합성하고 이들 고분자의 가교 반응을 수행하였다. 사용한 치환기는 (2-메톡시에톡시)에톡시기와 2,2,2-트라이플로로에톡시, 페닐옥시, 알라닌 등이었다. 합성된 고분자의 가교는 감마선 조사, 자외선 조사 및 가교제와 감광제를 사용한 자외선 조사 등의 방법을 사용하여 가교시켰다. 세가지 방법 중에서 가교제와 감광제를 사용한 자외선 조사가 가장 좋은 결과를 주었다. 얻어진 고분자를 물에 담궈 하이드로젤을 얻어내었으며 이들의 성질을 간략히 조사한 결과 모든 경우 최저 임계온도를 나타내는 행동을 하였다.

• Elastomers and Composites
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• 제49권3호
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• pp.199-203
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• 2014

아크릴 단량체인 2-ethylhexyl acrylate (2-EHA), 2-hydroxyethyl acrylate (2-HEA), isobornyl acrylate (IBOA)를 광중합을 통하여 3원 공중합체 시럽을 합성하였다. 이관능기 아크릴 단량체인 1,6-hexanediol diacrylate (HDDA), poly(ethylene glycol) diacrylate (PEGDA, Mn = 250, 575, 700)를 가교제로 사용하여 semi-IPN형 감압성 점착제 (Pressure sensitive adhesives; PSAs)를 UV-광가교 시켜 제조하였다. 가교제 변화에 따른 감압성 점착제의 점착특성, 저장탄성율, 그리고 광학특성을 고찰하였으며, 점착특성과 저장탄성율은 가교제의 화학구조와 분자량에 의존하였다. 광학특성은 모든 감압성 점착제에서 92.5 % 이상의 광투과도 (at 550 nm), 1.0 % 이하의 haze값, 0.3 이하의 색차계값을 보임을 확인하였다. 결과적으로 가교제의 종류에 영향을 받지 않음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제19권11호
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• pp.1168-1171
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• 1998

Two kinds of second-order nonlinear optical copolymers were prepared by the copolymerization of the vinyl monomers containing NLO chromophore, methacrylic acid, and methyl methacrylate or butyl methacrylate. Glass transition temperatures (Tg of copolymers were around 130 ℃. The copolymers were soluble in common organic solvents such as tetrahydrofuran (THF), cyclohexanone, and N,N-dimethylformamide (DMF). The crosslinked copolymer was obtained by thermal treatment using pentaerythritol tetrakis(2-mercaptoacetate) as a crosslinker and became insoluble in tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). Poling was carried out at 120 ℃ for 20 min and identified with UV-Vis spectroscopy. Electro-optic coefficient (r33) measurement showed a value of 35 pm/V for polymer 2 at 633 nm. Temporal stability of copolymers was improved owing to the crosslinked network, which was successfully obtained at 170 ℃ for 30 min after poling.

• Elastomers and Composites
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• 제34권1호
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• pp.3-10
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• 1999

아크릴로니트릴(AN) 단일중합체를 항온장치가 부착된 광중합반응기내에서 합성하여 최적반응조건하에서 중합속도모델식을 구하였다. AN의 농도($1.8{\sim}7.58mo1/1$), 증감제의 종류($NaSCN,\;KSCN,\;Ba(SCN)_2,\;NH_4SCN,\;ZnCl_2,\;Na_2SeO_3$) 및 농도($10{\sim}60%$), 반응온도($10{\sim}70^{\circ}C$), 에너지 세기($1,000{\sim}9,900{\mu}J/cm^2$)를 변화시켰다. 광증감제의 농도에 관계없이 반응온도 $50^{\circ}C$, 반응시간 3시간에서 균일한 분자량분포를 얻고, 이중 광증감제로 50%의 NaSCN의 경우 다음과 같은 중합속도 모델식을 구하였다. $R_p=0.0142[M]^{0.82}[I]^{0.49}[S]^{0.52}$ exp(-1.33/RT).

• 한국염색가공학회지
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• 제33권2호
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• pp.64-71
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• 2021

Large amount of formaldehyde could be released inevitably during the flame-retardant (FR) treatments or from the finished fabrics using Provatex reagent and Proban polymers which have been used as durable FRs for cotton. A water-soluble cyclophosphazene derivative was synthesized as an ecofriendly phosphorus-based FR for cotton fibers. Dichloro tetrakis{N-[3-(Dimethylamino)propyl]methacrylamido} cyclcophosphazene (DCTDCP) was synthesized through the substiutution reaction of Hexachloro cyclophosphazene and N-[3-(Dimethylamino)propyl] methacrylamide at a mole ratio of 1 : 4, which can be cured dually by both alkaline treatment and UV irradiation. More crosslinked networks were produced through the addition of Triacryloyl hexahydrotriazine and Acrylamide as a UV-curable crosslinker and a comonomer respectively. Both flame retardancy and washing durability of the FR cotton were improved synergistically. The durability improvement may be caused by the covalent bond formation of the FR with cellulose and the high degree of polymerization of DCTDCP, which can be verified by the pyrolysis and combustion behaviors analyzed by LOI, TGA, and microcalorimeter.

• 폴리머
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• 제32권2호
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• pp.138-142
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• 2008

분자 날인 기술은 표적 분자에 대해 높은 선택도를 갖는 합성 재료를 제조하기 위한 효과적인 방법이다. 본 연구에서는 주형 분자로 테오필린(theophylline)을, 가교제로 폴리에스터-아크릴레이트 수지를 사용하여 UV 중합을 통해 분자 날인 고분자(MIP)를 합성하였다. 기능성 단량체 종류가 MIP의 성능에 미치는 영향을 알아보기 위해, 메타크릴산(mathacrylic acid), 아크릴산(acrylic acid), 그리고 아크릴 아미드(acrylic amide)를 기능성 단량체로 각각 사용하여 MIP를 합성하였다. MIP는 비날인 고분자(NIP)보다 테오필린에 대해 훨씬 더 높은 재결합 능력을 보였다. 메타크릴산을 사용하여 합성한 MIP는 가장 높은 재결합 능력을 보였다. MIP의 선택도는 테오필린과 분자구조가 유사한 카페인(caffeine) 용액을 사용하여 조사하였다. 클로로포름보다 극성인 증류수를 용매로 사용하였을 경우 MIP의 테오필린 재결합 성능은 감소하였다.

• Journal of Pharmaceutical Investigation
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• 제31권2호
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• pp.101-106
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• 2001

Alginate-chitosan (anion-cationic polymeric complex) was prepared to control the release rate of silver sulfadiazine (AgSD). Na-alginate (2%) solution containing AgSD was gelled in $CaCl_2$ solution. The gel beads formed were immediately encapsulated with chitosan (CS). The gel matrix and membrane were then reinforced with chondroitin-6-sulfate (Ch6S). Release rate of AgSD from the gel matrix was investigated by placing alginate beads in the sac of cellulose membrane simmered in HEPES-buffer solution. The concentration of AgSD released was analyzed by UV at 264 nm. Incorporation capacity of AgSD in Ca-alginate gel was more than 90%. Alginate-Ch6S-CS could control the release rate of AgSD. The amount of AgSD release was dependent on the AgSD loading dose. Incorporation of tripolyphosphate (polyanionic crosslinker) onto the alginate-Ch6S-CS bead increased the release rate of AgSD. Collagen-coating had no influence on the AgSD release rate. Alginate-Ch6S-CS beads with a sufficiently high AgSD encapsulation were capable of controlling the release of the drug over 10 days. In summary, alginate-Ch6S-CS beads could be used as a sustained delivery for AgSD and provide local targeting with low silver toxicity and patient discomfort.

• Bulletin of the Korean Chemical Society
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• 제25권3호
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• pp.357-360
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• 2004

We developed in the present study molecular imprinted polymers (MIPs), using single templates (pentoxifylline, caffeine and theophylline) and mixed-templates (pentoxifylline-caffeine, pentoxifylline-theophylline and caffeine-theophylline). The MIPs were prepared with methacrylic acid (MAA) as the monomer, ethylene glycol dimetharylate (EGDMA) as the crosslinker and 2,2'-azobis(isobutyronitrile) (AIBN) as the initiator. The obtained polymer particles (particle size after grinding was about 25-35 ${\mu}$m) were packed into a HPLC column (3.9 mm i.d. ${\times}$ 150 mm). The selectivity and chromatographic characteristics of the MIPs were studied using acetonitrile as the mobile phase at a flow rate of 0.8 mL/min. UV detector wavelength was set at 270 nm. Different single template MIPs showed different molecular recognitions to the templates and the structurally analogues, according to the rigidity and steric hindrance of the compounds. Recognition was improved on the mixed-template MIPs as a result of the cooperation or sum effect of the templates, whereas on the pentoxifylline-theophylline imprinted polymer, the highest selectivity and affinity were obtained. Separations of the test compounds on different polymers were also investigated.

• 한국염색가공학회지
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• 제33권4호
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• pp.230-237
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• 2021

The flame-retardant (FR) treatments of wool fibers using Hexafluorozirconate/titanate salts and tetrabromophthalic anhydride can cause skin irritation and gas toxicity due to Zr and Br compounds respectively. A water-soluble polyfunctional cyclophosphazene derivative, synthesized through substitution reaction of Hexachloro cyclophosphazene and N-[3-(Dimethylamino)propyl] metacrylamide, was applied as a durable flame-retardant for wool fabrics. Also, a crosslinked structure was introduced to improve washing durability of the FR-wool, up to 10 laundering cycles, using Acrylamide(AAm) and Triacryloylhexahydrotriazine (TAHT) as a comonomer and a crosslinker respectively. The mole ratios of the TAHT and AAm concentrations compared to the Dichloro tetrakis{N-[3-(Dimethylamino)propyl]methacrylamido} cyclcophosphazene (DCTDCP) were optimized to 1.33 and 7.5 respectively. In addition, the pyrolysis and combustion properties of the FR wool were assessed using LOI, TGA and microcalorimetry suggesting a solid-phase FR mechanism.