• 대한화학회지
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• 제61권3호
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• pp.97-103
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• 2017

In this study, the functional hydrogel ophthalmic lens containing tungsten oxide nanoparticles, 2,4-dihydroxy benzophenone and 2-hydroxy-4-(methacryloyloxy) benzophenone were manufactured. HEMA (2-hydroxyethyl methacrylate), MMA (methyl methacrylate), AA(acrylic acid), the cross-linker EGDMA (ethylene glycol dimethacrylate), the initiator AIBN (azobisisobutyronitrile) and the functional additives including tungsten oxide nanoparticles, 2,4-dihydroxy benzophenone, and 2-hydroxy-4-(methacryloyloxy) benzophenone were used respectively. The measurements of water content and refractive index of the sample was decreased and increased, respectively. And also, the UV transmittance of produced lens containing 2,4-dihydroxy benzophenone, 2-hydroxy-4-(methacryloyloxy) benzophenone and tungsten oxide nanoparticles was measured. Based on the results of this study, it is judged that the performance improvement increased over time when 2-hydroxy-4-(methacryloyloxy) benzophenone was used as an additive, while the use of tungsten oxide nanoparticles influenced on blue-ray-blocking effect of the hydrophilic lens.

• 한국염색가공학회지
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• 제10권4호
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• pp.53-61
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• 1998

The absorptions of ultraviolet rays of benzophenone derivatives were investigated in terms of the position of substituent, especially hydroxyl group. When the derivatives were added to the aqueous solution of Rhodamin B, which has very low light-fastness, all of them delayed the photofading of Rhodamin B solution. But on the fabrics, only the derivatives with the hydroxyl group at 2-position showed the good ability of ultraviolet rays absorption. The benzophenone derivatives absorb ultraviolet rays to form a hydrogen bond between hydroxyl group and carbonyl group, and return to their original structure by releasing heat energy. In solution, the derivatives can form a intermolecular hydrogen bond, and absorb the ultraviolet rays. But on the fabric, the intermolecular hydrogen bond is impossible, only hydroxyl group of 2-position forms a intramolecular hydrogen bond, and that makes the derivatives on the fabric absorb ultraviolet rays.

• 통합자연과학논문집
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• 제11권1호
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• pp.1-8
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• 2018

HEMA, AA, MMA, and EGDMA as crosslinking agent and AIBN as an initiator, and 2,4-dihydroxybenzophenone, 2-ethylhexyl-trans-4-methoxy-cinnamate, 2-hydroxy-4-(methacryloyloxy)benzophenone as additives at 0.1-1.0% ratios were used to manufacture hydrophilic ophthalmic lenses through thermal polymerization before their physical properties were measured. The results showed that the samples containing of 2,4-dihydroxybenzophenone and 2-ethylhexyl-trans-4-methoxy-cinnamate resulted in a decrease of the UV blocking performance after high-pressure sterilization whereas the sample containing 2-hydroxy-4-(methacryloyloxy)benzophenone showed no change in the UV blocking performance. It is judged that this is induced by presence or absence of an acyl functional group in benzophenone.

• 통합자연과학논문집
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• 제3권3호
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• pp.133-137
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• 2010

New synthetic route and characterization of alkyl-capped nanocrystalline silicon (R-n-Si) were achieved from the reaction of silicon tetrachloride with sodium/benzophenone ketal reducing agent followed by n-butyllithium. Surface of silicon nanoparticles was derivatized with butyl group. Effect of oxidation of silicon nanoparticle with benzophenone was investigated for their stabilization. Optical characteristics of silicon nanoparticles were characterized by fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible spectroscopy (UV-vis), and photoluminescence (PL) spectroscopy. Butyl-capped silicon nanoparticles exhibited an emission band at 410 nm with excitation wavelength of 360 nm. Average size of n-butyl-capped silicon nanoparticles was obtained by particle size analyzer (PSA) and transmission electron microscopy (TEM). Average size of n-butyl-capped Si nanoparticles was about 6.5 nm.

• 한국환경보건학회지
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• 제39권6호
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• pp.505-512
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• 2013

Objectives: Ultraviolet (UV) radiation may cause skin cancer, photo-ageing, erythema, and sunburn. Benzophenone (BP) is commonly used to protect skin from UV radiation. In Korea, sunscreen, sunblock, socalled 'blemish balm' (BB) and 'color correcting' (CC) creams, and foundation may contain from 0.5 to 5% benzophenone in order to protect skin from UV radiation. The purpose of this study is to understand the levels of benzophenone derivatives in urine among a group of university students and identify the contribution of cosmetics use. Methods: Forty volunteers (20 women and 20 men) were asked about skin type, frequency of use of cosmetics, and recognition of related health effects, etc. in a survey. Subjects were divided into several subgroups and were compared for concentration of benzophenone-1 (BP-1) and benzophenone-3 (BP-3). Their urine was pretreated with enzyme hydrolysis and solid phase extraction. Determinations of BP-1 and BP-3 in the urine were made with LC-MS/MS. Results: Among the study subjects, 82.5% used basic cosmetics at least once per day, and 77.5% used sunscreens at least once per day. The concentrations of BP-1 and BP-3 of the males were 4.36 ng/mL and 9.16 ng/mL, respectively. Those of the females were 3.98 ng/mL and 5.07 ng/mL, respectively. The use of cosmetics was positively related to urinary benzophenone levels. Conclusions: BP-1 and BP-3 were widely detected among the university students. Cosmetic use was identified as a potential source. Implications of such exposure deserve further investigation.

• 한국의류학회지
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• 제18권5호
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• pp.622-627
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• 1994

The purpose of this study is to investigate the adsorption rate, adsorption quantities and the UV-Cut effects of cotton fabrics treated with several UV absorbents. The result of this study were as follows: cotton fabric treated with 2,2'-dihydroxy-4- methoxy-benzophenone shows more efficient than ones treated with 4-aminobenzoic acid and 2·hydroxy-1, 4-naphthoquinone in UV absorption. This may be due to the absorption of UV light by formation of intra moleculaar hydrogen bond. The formation of hydrogen bonds between hydrogen atoms of two hydroxy groups and one oxygen atom of carboxyl group in 2, 2'-dihydroxy-4-methoxy-benzophenone would be easier than that of the other absorbents. The adsorption isotherms of 4-aminobenzoic acid and 2-hydroxy-1, 4-naphthoquinone were similar to Freundlich type, while that of 2, 2'-Dihydroxy-4-methoxy-benzophenone was Henry type. Cotton fabrics treated with Antifade MC-100 and W Cut I-2 were just alike in UV absorption, but Antifade 8001 was inferior to the others.

• 대한화학회지
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• 제55권1호
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• pp.98-103
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• 2011

본 연구는 자외선 흡수제로 사용되는 benzophenone계(group) 및 높은 굴절률과 화학적, 물리적으로 매우 안정한 물질로 알려진 $TiO_2$를 기존의 재료에 첨가하여 자외선 차단 기능을 가진 고분자 재료를 중합하였다. 중합 결과 생성된 고분자의 자외선 흡수 정도를 기존의 재료들과 비교하였으며, 제조된 콘택트렌즈의 함수율, 굴절률 및 광투과율등의 기본적인 물성을 측정하였다. 측정 결과, 자외선 흡수제를 첨가한 콘택트렌즈의 굴절률과 함수율은 각각 1.430~1.440, 35.0~45.0의 값들로 나타나 기존의 콘택트렌즈와 비슷한 결과를 나타내었다. 또한 각 파장대별 광투과율에서는 자외선 흡수제를 넣지 않은 콘택트렌즈에서는 UV-A, UV-B, 가시광선 투과율이 각각 89%, 88%, 89%로 나타나 자외선 투과율이 매우 높았으나, 2-hydroxy-4-methoxy-benzophenone와 2,4-dihydroxy-benzophenone을 첨가한 콘택트렌즈의 경우, 각각 UV-A 0%, UV-B 6%의 투과율을 나타내어 자외선 차단 효과가 있는 것으로 나타났다. 또한 $TiO_2$를 첨가한 콘택트렌즈의 경우, 각각 UV-A 6%, UV-B 51%의 투과율을 나타내어 자외선 차단 효과가 다소 있는 것으로 나타났다. 가시광선 투과율은 모두 77~89%로 콘택트렌즈의 가시광선 투과율의 조건에 만족함을 알 수 있었다.

• 공업화학
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• 제10권8호
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• pp.1169-1174
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• 1999

본 연구에서는 sodium 2-diazo-1-naphthoquinone-5-sulfonate를 chlorination하여 2-diazo-naphthoquinone-5-sulfonyl chloride(NQD-Cl)를 합성하였다. NQD-Cl을 여러 종류의 hydroxybenzophenone 유도체와 esterification하여 hydroxy group이 2-diazo-naphthoquinone-5-sulfonyl(NQD) group으로 치환된 여러 종류의 1,2-naphthoquinone-(1,2)-diazide-5-sulfonic acid esters(NQD0ester) 유도체를 합성하였다. NQD-ester 유도체의 용해도를 증가시키기 위해 methoxy group이 도입된 유도체와 이와 비교를 위해 hydroxy group만을 가지는 benzophenone 유도체를 사용하여 비교하였다. 각각의 NQD-ester 유도체의 용해특성을 조사하였으며, novolac수지와 혼용(formulation)하여 감광액을 제조하여 알루미늄판에 도포, 건조하여 PS판을 제조하였다. PS판의 감광특성과 광퇴색도와 화상형성에 적합한 노광시간을 조사하였으며, 상대감도를 gray scale(GS)법으로 조사하였다. 치환된 NQD group 의 수에 따라 GS법에 의한 상대감도가 다르게 나타나는 것을 알 수 있었다. Methoxy group이 도입된 NQD-ester유도체는 좋은 용해특성을 보여주었으며 시판되는 PS판과 동일한 노광조건에서 비교해 본 결과 보다 우수한 감도를 보였다.

• 공업화학
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• 제17권2호
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• pp.217-222
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• 2006

폴리이미드는 높은 열안정성, 우수한 기계적, 전기적 성질을 가지고 있어 많은 연구가 진행되어 왔지만, 대부분의 유기용매에 불용인 관계로 그 용도가 제한되어 있다. 본 연구에서는 방향족 디아민인 2,2,-bis(3-amino-4-hydroxyphenyl) hexafluoropropane (BAPAF)와 3,3,-diamino-4,4- dihydroxybyphenyl (HAB)를 사용하고 방향족 디안하이드라이드인 4,4-(hexafluoroisopropylidene)diphthalic dianhydride (6FDA), pyromellitic dianhydride (PMDA), 4,4-oxydiphthalic dianhydride (OPDA), 3,3,4,4-benzophenone tetracarboxylic dianhydride (BTDA) 및 3,3,4,4-diphenylsulfone tetracarboxylic dianhydride (DSDA)를 사용하여 가용성 폴리이미드를 합성하였다. 폴리이미드의 성질은 NMR, FR-IR 및 TGA를 이용하여 조사하였으며, 유전상수는 축전용량을 측정하여 계산하였다. 히드록시기를 포함한 폴리이미드와 methacryloyl chloride를 반응시켜 감광성 폴리이미드를 합성하고, photolithography기술을 이용하여 micro-패턴을 형성하였다.

• The Journal of Advanced Prosthodontics
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• 제7권5호
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• pp.386-391
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• 2015

PURPOSE. The purpose of this preliminary study was to investigate the effects of adding 4,4'-bis(N,N-diethylamino) benzophenone (DEABP) as a co-initiator to a binary photoinitiating system (camphorquinone-amine) to analyze on the degree of conversion (DC) of a light-cured resin for dental 3D printing. MATERIALS AND METHODS. Cylindrical specimens (N=60, n=30 per group, ${\phi}5mm{\times}1mm$) were fabricated using bisphenol A glycerolate dimethacrylate (BisGMA) both with and without DEABP. The freshly mixed resins were exposed to light in a custom-made closed chamber with nine light-emitting diode lamps (wavelength: 405 nm; power: $840mW/cm^2$) for polymerization at each incidence of light-irradiation at 10, 30, 60, 180, and 300 seconds, while five specimens at a time were evaluated at each given irradiation point. Fourier-transform infrared (FTIR) spectroscopy was used to measure the DC values of the resins. Two-way analysis of variance and the Duncan post hoc test were used to analyze statistically significant differences between the groups and given times (${\alpha}$=.05). RESULTS. In the DEABP-containing resin, the DC values were significantly higher at all points in time (P<.001), and also the initial polymerization velocity was faster than in the DEABP-free resin. CONCLUSION. The addition of DEABP significantly enhanced the DC values and, thus, could potentially become an efficient photoinitiator when combined with a camphorquinone-amine system and may be utilized as a more advanced photopolymerization system for dental 3D printing.