• 대한의용생체공학회:의공학회지
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• 제9권1호
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• pp.67-72
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• 1988

Poly (HPMA/NVP) hydrogel was synthesized according to the composition and the con- centration of the crosslinking agent. The swelling degree of the P(HPMA/NVP) hydrogel decreased with increasing of P(HPMA) composition and crosslinking agent. The glass transi- tion and softening temperatures of the P(HPMA/NVP) increased with increasing of P(HPMA) composition. The composition of P(HPMA/NVP) : 70/30 and the concentration of the crosslin- king agent of 0.5 wt % gave the optimum condition in the application to the contact lens. There were also adequate in the mechanical, refractive properties and in vivo test in the P(HPMA/ NVP): 70/30 system.

• 대한화학회지
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• 제60권3호
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• pp.181-186
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• 2016

친수성 안의료용 렌즈 재료에 하이드록시기를 가진 아크릴레이트계 모노머인 HEA(2-hydroxyethyl acrylate), HEMA(2-hydroxyethyl methacrylate), HPMA(hydroxypropyl methacrylate) 및 Ag nanoparticles가 첨가제로 사용되었으며, 교차결합제인 EGDMA(ethylene glycol dimethacrylate)와 개시제인 AIBN(azobisisobutyronitrile)을 사용하여 공중합하였다. 하이드로젤 친수성 렌즈는 100 ℃에서 1시간 동안 열 중합을 통해 제조되었다. 제조된 하이드로젤 친수성 렌즈의 함수율, 굴절률 그리고 광투과율을 측정함으로써 렌즈의 광·물리적 특성을 분석하였다. HEA, HEMA 그리고 HPMA의 평균 함수율은 82.12%, 37.06% 그리고 21.57%로 각각 측정되었으며, 굴절률의 경우 1.3540, 1.4330 그리고 1.4649로 각각 측정되었다. 제조된 하이드로젤 친수성 렌즈의 분광투과율을 측정한 결과, 근자외선 영역에서는 82.67%, 80.32% 그리고 79.83%로, 가시광선 투과율의 경우 89.72%, 88.24% 그리고 86.89%로 각각 측정되었다. 또한 은 나노입자를 포함한 시료의 광투과율은 근자외선 영역에서 10.59% 그리고 가시광선 투과율에서 43.74%로 각각 측정되었다. 이 결과로 볼 때 분자길이는 중합된 고분자 물질의 함수율 및 굴절률에 영향을 주는 것으로 판단된다.

• 대한화학회지
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• 제60권4호
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• pp.261-266
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• 2016

The major physical characteristics of macromolecules used in silicone hydrogel ophthalmic lenses include optical transmittance, oxygen permeability, water content, and refractive index. For the preparation of highly functional silicone hydrogel lens materials, two silicone monomers were used in the presence of 2-hydroxyethyl methacrylate (HEMA) and hydroxypropyl methacrylate (HPMA). The samples containing HEMA and HPMA had oxygen transmissibility (Dk) values in the range of 73.38–50.98 × 10^-11 (cm²/s) (mLO₂/mL×mmHg) and 71.94–42.80 × 10^-11 (cm²/s) (mLO₂/mL×mmHg), respectively. Furthermore, the water contents of samples containing HEMA and HPMA were in the range of 32.73–34.67% and 31.94–33.74%, respectively, and the refractive indices were in the range of 1.4348–1.4364 and 1.4385–1.4407, respectively. Thus, silicone monomers containing HEMA and HPMA are expected to be useful for fabricating high-oxygen-permeability silicon hydrogel ophthalmic lenses.

• 한국전기전자재료학회논문지
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• 제14권4호
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• pp.302-308
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• 2001

The polymers with various composition of 4-vinylpyridine (4-VP) with n-butyl acrylate (n-BA) and 2-hydroxypropyl methacrylate (HPMA) were synthesized as a humidity sensitive material and quaternized with 1.5-dibromopentane. Resistance versus relative humidity decreased with increase in the content of n-BA in the copolymer. The introduction of HPMA increased the resistance of the humidity sensor as well as enhanced the adherence to the alumina substrate. In the case of 4-VP/n-BA/HPMA=80/10.10, the hysteresis and temperature coefficient were $\pm$2%RH and -0.42∼0.46%RH/$\^{C}$. The average resistance at 30%RH, 60%RH and 90%RH are 3.1㏁, 155 ㏀ and 7.9 ㏀, respectively.

• Korean Chemical Engineering Research
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• 제55권5호
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• pp.586-592
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• 2017

본 연구에서는 n-butyl acrylate (BA), methyl methacrylate (MMA), 2-hydroxypropyl methacrylate (HPMA) 및 acetoacetoxyethyl methacrylate(AAEM) 단량체를 부가 중합시켜 고형분이 75%인 아크릴수지를 합성하였다. 이때, 아크릴수지의 유리전이온도($T_g$)를 20, 30, $40^{\circ}C$로, 수산기가(OH value)를 60, 90, 120으로 변화시켰다. 그 결과, 아크릴수지의 점성도는 $T_g$와 수산기가가 증가할수록 증가하였다. 합성된 아크릴수지는 높은 가교밀도를 갖도록 설계되어 고탄력성과 고내구성을 유지하였다. 가교된 아크릴수지는 블록이소시아네이트(Desmodur BL-3175)와 경화 반응시켜 아크릴 우레탄 투명 도료를 제조하는데 사용되었다. 도료에 대하여 점성도, 접착성, 연필경도 및 $60^{\circ}$ 경면광택도 등의 측정을 통해 물리적 특성을 분석하였고, 아크릴 우레탄 투명 도료는 코일코팅용 상도 도료로서 적용되기 위하여 시편으로 제조되어 다양한 특성이 평가되었다. 제조된 도료는 접착력이 뛰어났고, $60^{\circ}$ 경면광택도와 연필경도에서 우수한 특성을 나타내었으며, 환경 친화적이었다.

• Macromolecular Research
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• 제17권12호
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• pp.1003-1009
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• 2009

Copolymers of N-vinylpyrrolidone (NVP) comonomer with styrene (St), hydroxypropyl methacrylate (HPMA) and carboxyphenyl maleimide (CPMI) were synthesized by free radical polymerization using 2,2'-azobisisobutyronitrile (AIBN) initiator in 1,4-dioxane solvent. The copolymers formed were characterized by FTIR, $^1H$ NMR and $^{13}C$ NMR techniques and their thermal properties were studied by DSC and TGA. Copolymer composition was determined by $^1H$ NMR and/or by elemental analysis and monomer reactivity ratios (MRR) were estimated by the linear methods of Kelen-Tudos (K-T) and extended Kelen-Tudos (EK-T) and the non-linear approach. Copolymers of St and HPMA with NVP formed blocks of one of the monomer units, whereas alternating copolymers were obtained in CPMI-NVP, depending upon the side chain substitution. The MRR values are discussed in terms of monomer structural properties such as electronegativity and electron delocalization. The sequence distribution of monomers in the copolymers was studied by statistical method based on the average reactivity ratios obtained by EK-T method.

• 한국응용과학기술학회지
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• 제20권1호
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• pp.8-19
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• 2003

Environmental friendly acrylics/urea high-solid paints (BEHCU) were prepared through the curing reaction of acrylics resin(BEHC) containing 70wt% of solids content and butylated urea curing agent. BEHC was synthesized by addition copolymerization of caprolactone acrylate(CLA), 2-hydroxypropyl methacrylate(2-HPMA), ethyl methacrylate, and n-butyl acrylate. The addition polymerization of these monomers, especially including flexible CLA monomer and 2-HPMA monomer with OH funtional group, under appropriate reaction conditions resulted in polymers with controlled glass transition temperature($T_g$) and crosslinking density. The molecular weight($M_w$) of these polymers(BEHCs) was 2940${\sim}$3240 and polydispersity ($M_w/M_n$) was in the range of 1.61${\sim}$1.72. The viscosity and the molecular weight of these acrylic resins increased with increasing $T_g$. The coated films were prepared using curing reaction between BEHC resin and butylated urea curing agent at 100$^{\circ}C$ for 30 minutes. Our experimental resulted showed that enhancement of the coating properties such as adhesion, flexibility, impact resistance, water resistance, and abrasion resistance could be expected through introducing CLA component in acrylic resin for the high-solid content acrylics/urea coatings.

• 대한화학회지
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• 제61권6호
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• pp.346-351
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• 2017

This study was planned considering the chain length, hydrophilicity, and hydrophobicity of the additives to be used in the polymerization, while various ophthalmic lenses that use various additives with similar water contents were manufactured before their optical and physical properties were compared and analyzed. With regard to the additives required for manufacturing high-, medium-, and low-water content lens groups, HEA (hydroxyethyl acrylate), PVP (polyvinylpyrrolidone), and NMV(N-methyl-N-vinylacetamide) were used as additives for preparing the high-water content lens group, HEMA(2-hydroxyethyl methacrylate), HPMA(hydroxypropyl methacrylate) and BD(1,4-butanediol) were used for the medium-water content lens group. For the low-water content lens group, BMA(buthyl methacrylate), BDDA(1,4-butanediol diacrylate), and Bis-GMA(bisphenol A glycerolate diacrylate) were used, respectively. The average water content of HEA was 40.14%; that of PVP, 39.63%; and that of NMV, 40.52%. The mean of water content was 35.92% for HEMA, 35.74% for BD, and 34.62% for HPMA. For the low-water content lens group, the mean of water content was 26.69% for BMA, 27.76% for BDDA, and 26.14% for Bis-GMA. With regard to the results of the water content measurement using a moisture analyzer, the average water content of the high-water content lens group was 41.34% for HEA, 42.62% for PVP, and 42.73% for NMV. Finally, for the low-water content lens group, the average water content was 28.62% for BMA, 28.82% for BDDA, and 28.32% for Bis-GMA. The measurements of the water contents of the lenses using the two methods showed that the water content and refractive index of the lenses were similar in all the lens groups. The measurements of the contact angles, however, showed a different wettability value for each lens with a similar water content. Also, the change tendency of the lens curvature according to the change of time showed that the change amount became larger and the recovery time became longer from the lens samples with a lower water content to those with a higher water content. Based on these results that will be helpful for the study of ophthalmic lenses.