• 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.

• 폴리머
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• 제36권2호
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• pp.223-228
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• 2012

온도와 pH 민감성을 갖는 그래프트 공중합체[Pluronic-$g$-poly(NIPAAm-$co$-MMA), Polymer A]와 [Pluronic-$g$-poly(NIPAAm-$co$-MAA), Polymer C]는 $t$-butylperoxybenzoate를 이용하여 Pluronic 공중합체의 주사슬에 $N$-isopropylacrylamide (NIPAAm)/$N,N$-diethylaminoethylmethacrylate (DEAEMA)와 $N$-isopropylacrylamide(NIPAAm)/methacrylic acid (MAA)를 각각 합성하였다. 그래프트 공중합체는 $^1H$ NMR과 젤 투과 크로마토그래피를 통해 공중합체의 화학적 구조와 분자량을 측정하였다. 그래프트 공중합체의 수용액 상에서의 특성은 다른 온도와 pH 조건에서 자외 및 가시선 분광 분석법, 접촉각 측정과 동적 광산란으로 측정되었다. 그래프트 공중합체는 수용액상에서 온도와 pH에 따라 민감한 상 변화를 보인다. 이는 DEAEMA 단량체의 아민 그룹과 MAA 단량체의 카복실 그룹은 각각 Polymer A와 Polymer C에서 하한임계용액온도에 큰 영향을 미친다고 제시한다. 그래프트 공중합체는 온도와 pH 변화에 관련된 다양한 약물 전달과 분자 스위치 적용에 사용될 수 있다.

• Elastomers and Composites
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• 제37권1호
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• pp.21-30
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• 2002

개시제 ammonium persulfate(APS)와 유화제 sodium dodecyl benzene sulfonate(SDBS)를 이용하여 methyl methacrylate(MMA), styrene(St), ethyl acrylate(EA)등의 단량체를 core(내부)와 shell(외부)의 폴리머성분이 다른 core-shell 폴리머를 합성하고 각 core-shell 폴리머에 대한 구조를 연구하였다. 한 입자의 내부와 외부의 고분자 조성이 다른 composite 라텍스는 고분자 블렌딩과 공중합의 물성과는 달리 한 입자 내에서도 상반된 두 가지 물성을 동시에 나타내는 특성으로 인하여 여러 산업 분야에 응용이 가능하다. 그러나, core-shell 라텍스를 제조할 때 반응중입자가 성장하는 과정에서 입자의 응집과 중합율이 떨어지고, 라텍스의 응용시 기계적 안정성이 문제점으로 되고 있다. 따라서 shell 중합시에 새로운 입자의 생성이 적고 중합중 안정성이 우수한 라텍스를 제조하기 위해 유화제농도, 개시제농도, 중합온도가 PMMA/PSt과 PSt/PMMA의 core-shell 구조에 미치는 영향과 중합 후 입도분석기(particle size analyzer; PSA) 및 투과전자현미경(transmission electron microscope; TEM)을 이용하여 실제 입자측정과 입자형태 특성을 확인하였으며 시차주사열량계(differential scanning calorimeter, DSC)를 이용하여 유리전이온도($T_g$)의 측정, 최저성막온도(minimum film formation temperature; MFFT), NaOH 첨가에 의한 가수 분해에 따르는 pH를 측정하여 core-shell의 새로운 특성을 확인하였다.

• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.86-88
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• 2006

The novel linear- (V-LUM) and cross-type macromonomers (C-VUM) of vinyl-terminated bifunctional polyurethane were synthesized and applied to the dispersion polymerization of styrene and MMA in ethanol. The existence of the vinyl terminal groups and the grafted macromonomer with styrene and PMMA was verified using 1H NMR and 13C NMR. Monodisperse polystyrene (PS) microspheres were successfully obtained above 15 wt % of macromonomer relative to styrene. The macromonomer can efficiently stabilize higher surface area of the particles compared to a conventional stabilizer, PVP. The grafting ratio of the PS calculated from 1H NMR linearly increased up to 0.048 with 20 wt % of the macromonomer and the high molecular weights (501,300 g/mol) of PS with increased glass transition and enhanced thermal stability were obtained. Furthermore, the stable and monodisperse PMMA microspheres having a weight-average diameter of $5.09{\mu}m$ and a good uniformity of 1.01 were obtained with 20 wt% L-VUM. The molecular weight increased, but the size of the PMMA particles decreased with the macromonomer concentration due to the increased stabilizing effect. The molecular weight of the PMMA was approximately two fold higher than that by a conventional PVP. The L-VUM acts as a reactive stabilizer, which gives polyurethane-grafted PS or PMMA with a high molecular weight. In addition, the XPS result showed that the C-PS (PS using the C-VUM) was anchored with a larger amount of PEG than that of the L-PS (PS using the L-VUM) on the particle surface. Thus, the reaction and stabilizing mechanism of the macromonomers for the formation of PS particles is proposed.

• Elastomers and Composites
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• 제29권5호
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• pp.444-452
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• 1994

Emulsion graft copolymerizations of vinyl monomers, butyl acrylate(BA), methyl methacrylate(MMA), 2-ethylhexyl acrylate (EHA), glycidyl methacrylate (GMA), 2-hydroxyethyl methacrylate(HEMA), methacrylonitrile(MAN), dimethylaminoethyl methacrylate(DAMA) or 2-vinyl pyridine(VP), onto carboxyl-terminated SBR latex were carried out under different experimental conditions. In case of synthesizing SBR-g-poly(butyl acrylate), the degree of grafting was increased with increasing the amount of emulsifier, polymerization temperature and the amount of initiator. Pull-out strength of resorcinol-formaldehyde-latex(RFL) adhesives formulated with modified latexes was very higher than that of RFL adhesive formulated with ungrafted latex. When the modified latexes with GMA, HEMA, MAN, DAMA or VP were used, the break occurred at cords. Peel strength of RFL adhesives formulated with SBR-g-poly(GMA), SBR-g-poly(HEMA) or SBR-g-poly(VP) was higher by about 1.3 times than that of RFL adhesives formulated with unmodified SBR against nylon cord and was higher by about 2.0 times against polyester cord.

• 한국재료학회지
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• 제28권8호
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• pp.452-458
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• 2018

This research is conducted to create a functional hydrogel ophthalmic lens containing nanoparticles. Carbon nanoparticles and PEGMEMA are used as additives for the basic combination of HEMA, MA, and MMA, and the materials are copolymerized with EGDMA as the cross-linking agent and AIBN as the thermal initiator. The hydrogel lens is produced using a cast-mold method, and the materials are thermally polymerized at $100^{\circ}C$ for an hour. The polymerized lens sample is hydrated in a 0.9 % saline solution for 24 hours before the optical and physical characteristics of the lens are measured. The refractive index, water content, contact angle, light transmittance, and tensile strength are measured to evaluate the physical and optical characteristics of the hydrogel lens. The refractive index, water content, contact angle, UV-B light transmittance, UV-A light transmittance, visible light transmittance, tensile strength and breaking strength of the hydrogel lens polymer are 1.4019~1.4281, 43.05~51.18 %, $31.95{\sim}68.61^{\circ}$, 21.69~58.11 %, 35.59~84.26 %, 45.85~88.06 %, 0.1075~0.1649 kgf and 0.1520~0.2250 kgf, respectively. The results demonstrate an increase in refractive index, tensile strength and breaking strength and a decrease in contact angle and light transmittance. Furthermore, the visible light transmissibility is significantly increased at PEG 10 %. It is clear that this material can be used for high-performance ophthalmic lenses with wettability, ultraviolet ray blocking effect, and tensile strength.

• 한국안전학회지
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• 제19권2호
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• pp.47-53
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• 2004

Emulsion polymerization ws carried out using Alkyl methacrylate(RMA) like MMA, EMA, BMA and Styrene Monomer(SM) for core-shell latex preparation. It was synthesized at $80^{\circ}C$ in the presence of anionic surfactant SLS(Sodium Lauryl Sulfate). FT-IR and DSC analysis are used to confirm the synthesized core-shell emulsion latexes. Moreover DSC and TGA were used to investigate the thermal characterisitcs of them. The differences of the decomposition rate and the activation energy from TGA and DSC analysis are not so big. It considers that the pendent group is not affect of the thermal characteristics and stability on core-shell latexes, which is synthesized with RMA and Styrene. For investigating combustion products, LC50 values were calculated by FED(Fractional Effective Dose)from the Pyrolyzer-Mass sepctrometer.

• 한국응용과학기술학회지
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• 제27권4호
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• pp.445-451
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• 2010

To prepare very stable acrylic type emulsion having a visible ray absorption property, in-situ preparation technique of $Cu_xS$ nanoparticle was adopted. Firstly, the acylic emulsions of methyl methacrylate(MMA), butyl acrylate(BA), and acrylonitrile(AN) were synthesized by pre-emulsion polymerization at $60^{\circ}C$ in the presence of anionic surfactant. Secondly, $Cu_xS$ nanocomposited emulsions were directly prepared in the prepolymerized acrylic emulsion with $CuSO_4$ at $50^{\circ}C$. The presnce of $Cu_xS$ nanoparticle in emulsion was confirmed by SEM and EDS. The final $Cu_xS$ nanocomposited emulsion showed an olive-green colour and good emulsion stability up to 1 month. In addition the PET films coated with our $Cu_xS$ nanocomposited emulsion absorbed effectively the visible ray.

• 한국안전학회지
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• 제16권3호
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• pp.68-75
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• 2001

Photopolymerization, the utilization of electromagnetic radiation(or light) as the energy source for polymerization of functional monomers, oligomers is the basis of important commercial processes with broad applicability, including photoimaging and RV curing of coatings and inks. The objective of this study is to investigate the characteristics of environmental fraternitive photopolymerization of methyl methacrylate(MMA). This work is the first step to continue further research about alkyl methacrylate. The experiment was done in aqueous solution under the influence of photo-initiator concentration(0.05-0.25mol/l), light intensity (5000-9000 ${\mu}J/cm^2$) and monomer concentration(2-6mol/l). Methyl methacrylate was polymerized to high conversion ratio using hydrogen peroxide($H_2O_2$) and the kinetics model we have obtained is as follows. $R_p=k_p[S]^{0.41}[M]^{0.62}[L]^{2.45} exp(53.64/RT$). The differential method of thermogravimetric analysis(Friedman method) was used to obtain value of activation energy on decomposition reaction. The average value of it res 45.4Kca1/mol.

• Journal of the Korean Wood Science and Technology
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• 제13권2호
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• pp.14-34
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• 1985

본(本) 연구(硏究)에서는 국내산(國內産) 미이용(未利用) 활엽수재(闊葉樹材)인 현사시나무의 재질개량(材質改良)을 위한 방안(方案)으로 비닐계 단량체(單量體)인 methylmethacrylate (MMA) 용액(溶液)을 목재내(木材內)로 주입(注入)한 후(後) 가압(加壓) 가열(加熱) 촉매중합법(觸媒重合法)에 의하여 제조(製造)한 목재(木材)-고분자(高分子) 복합체(複合體)(WPC ; wood-polymer composites)와 열압축목재(熱壓縮木材) (Staypak ; heat-stabilized compressed wood)의 물리적(物理的), 기계적(機械的) 성질(性質)과 치수 안정성(安定性)을 조사(調査)하였다. WPC 제조시(製造時) 단량체(單量體)의 주입량(注入量)을 비교(比較)하기 위하여 침지법(浸漬法)과 진공감압법(眞空減壓法)을 실시(實施)하였다. 본(本) 연구(硏究)에서 얻어진 결과(結果)는 다음과 같다. 1. 목재내(木材內) 단량체(單量體)의 주입량(注入量)은 진공감압법(眞空減壓法)이 침지법(浸漬法)에 비(比)해 약(約) 2배(培)의 효과(效果)가 있었다. 2. 목재내(木材內)로 주입(注入)된 단량체(單量體)는 WPC 제조시(製造時) 약(約) 절반가량 중합(重合)되었다. 3. 제조(製造)된 WPC의 치수 안정효과(安定效果)의 측정결과(測定結果), 반경방향(半徑方向)에서의 항수축율(抗收縮率) 12.5~13.6%, 접선방향(接線方向)에서의 항수축율(抗收縮率)은 12.5~13.6%, 접선방향(接線方向)이 17.18~40.14%였다. 흡수감소율(吸收減少率)은 8.19~15.5%로 진공감압법(眞空減壓法)이 침지법(浸漬法)에 의(依)한 WPC보다 효과(效果)가 좋았다. 4. 휨강도(强度) 시험시(試險時) 하중(荷重)을 가(加)하는 방향(方向)을 달리하였을 때 반경방향(半徑方向)으로 하중(荷重)을 가(加)한 경우(境遇)가 접선방향(接線方向)에 비(比)해 높은 강도치(强度値)를 나타내었다. 5. Staypak 및 WPC는 소재(素材)에 비(比)해 횡압축강도(橫壓縮强度)가 70~90% 향상(向上)되었으며, 종압축강도(從壓縮强度)는 10~30% 증가(增加)되었다. 6. Staypak의 비중(比重)은 0.66, 침지법(浸漬法)에 의(依)한 WPC는 0.61, 진공감압법(眞空減壓法)에 의(依)한 WPC의 비중(比重)은 0.62, 소재(素材)는 0.44였다.