• Journal of the Korean Society of Safety
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• v.31 no.4
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• pp.42-47
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• 2016

The combustible properties(flash point, explosion limit and autoignition temperature) are the important safety items which are considered in the typical MSDS(material safety data sheet). In this study, for the safe handling of n-butyl methacrylate(n-BMA) being used in various ways in the chemical industry, the flash point and the autoignition temperature(AIT) of n-butyl methacrylate was experimented. And, the lower explosion limit of n-butyl methacrylate was calculated by using the lower flash point obtained in the experiment. The flash points of n-butyl methacrylate by using the Setaflash and Pensky-Martens closed-cup testers measured $44^{\circ}C$ and $51^{\circ}C$, respectively. The flash points of n-butyl methacrylate by using the Tag and Cleveland open cup testers are measured $53^{\circ}C$. The AIT of n-butyl methacrylate by ASTM 659E tester was measured as $295^{\circ}C$. The lower explosion limit by the measured flash point $44^{\circ}C$ was calculated as 0.85 vol.%. It was possible to predict lower explosion limit by using the experimental flash point or flash point in the literature.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.14 no.10
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• pp.5299-5303
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• 2013

Poly(butyl methacrylate-co-polyethyleneglycol methacrylate) (Poly(BMA-co-PEGMA)) microsphere was prepared by precipitation copolymerization of PEGMA and butyl methacrylate in ethanol solution. Microspheres were controlled by experimantal conditions 140nm to 210nm. The particle size of Poly(BMA-co-PEGMA) microspheres was decreased with increasing the concentration of PEGMA and increased with BMA of monomer.

• Membrane Journal
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• v.2 no.2
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• pp.129-134
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• 1992

The solubility of methane in poly(n-butyl methacrylate)(PnBMA) was determined at pressures up to 35 atm. These measurements were made by volumetric technique in the temperature range from -10 to 30$^{\circ}$C. The solubility was found to be a nonlinear function of the applied pressure and could be satisfactorily described by dual-mode sorption model at temperatures below the glass txansition temperature($T_g$) of the polymer. The Langmuir capacity constant decreased with increasing temperature and vanished near the glass transition temperature of PnBMA. The solubility isotherm became linear at temperatures above the glass transition temperature of PnBMA. The temperature dependence of the dual-mode sorption parameters was also discussed.

• Journal of Korean Ophthalmic Optics Society
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• v.13 no.3
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• pp.29-34
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• 2008

Purpose: In this study, we compared the physical properties of the compositions that were mixed with basic materials of HEMA (2-Hydroxyethyl methacrylate)/Silicone and BMA (Butyl methacrylate), MMA (Methyl methacrylate) by making the silicone contact lens. Method: Each sample of contact lenses was fabricated by cast mould method. We analyzed results by using average values of physical property of each sample. Results: In the composition of HEMA/Silicone/BMA, water contents of samples showed the value from 24.69% to 29.26%. Ultimate strength of samples showed the value from 0.109 kgf to 0.263 kgf. In the composition of HEMA/Silicone/MMA, swelling ratio of samples showed the value from 13.56% to 14.83%. Water contents of samples showed the value from 25.61% to 29.33%. Ultimate strength of samples showed the value from 0.107 kgf to 0.286 kgf. Conclusions: The compositions of percents of silicone were ranged from 0.20% to 11.50% and the composition percent of BMA and MMA was 5.15% in total. Swelling ratio and water contents increased with decreasing of BMA (Butyl methacrylate) and MMA (Methyl methacrylate) percent. In the composition of HEMA/Silicone/MMA, the values of ultimate strength increased with increasing of silicone percent to 4-MMA sample. In the composition of HEMA/Silicone/BMA, the values of ultimate strength decreased with increasing of silicone percent.

• Bulletin of the Korean Chemical Society
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• v.26 no.12
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• pp.2027-2032
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• 2005

This paper demonstrates details of thermal behavior of Langmuir-Blodgett (LB) film of poly(tert-butyl methacrylate) (PtBMA) by using the principal component analysis based two-dimensional correlation spectroscopy (PCA2D) through eigenvalue manipulating transformation (EMT). By uniformly lowering the power of a set of eigenvalues associated with the original data, the smaller eigenvalues becomes more prominent and the subtle contribution from minor components is now highlighted much more strongly than the original data. Thus, the subtle difference of thermal behavior of LB film of PtBMA from minor components, which is not readily detectable in the conventional 2D correlation analysis, is much more noticeable than the original data. PCA2D correlation spectra with EMT operation for the temperature-dependent IR spectra of LB film of PtBMA reveal the hidden property of phase transition processes during heating.

• Journal of the Korean Chemical Society
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• v.53 no.3
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• pp.335-339
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• 2009

Polydimethylsiloxane (PDMS) with methacrylate endgroup is used as contact lens material with elasticity and high oxygen permeability. PDMS prepolymer with methacrylate endgroup was prepared by reacting PDMS (polydimethylsiloxane) with HEMA (2-hydroxyethyl methacrylate). The HEMA-substituted PDMS prepolymer was then copolymerized using AIBN (azobisisobutyronitrile) with BMA (butyl methacrylate; to increase elasticity and flexibility). The water content, oxygen permeability, and visible-ray transmissibility of the resulting polymer were measured to be 23%, 83% and Dk/t > 50, indicating that the copolymer can be used as a good contact lens material.

• Polymer(Korea)
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• v.35 no.1
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• pp.23-29
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• 2011

We measured shear viscosity of polymeric particles, prepared by suspension polymerization with hydrophobic silica as a stabilizer at $75^{\circ}C$, by a capillary rheometer. Shear viscosity displayed a non-Newtonian behavior with an increase in weight average molecular weight. Measurement of shear viscosity at 170 and $190^{\circ}C$ with copoly(styrene/butyl methacrylate) (co-PSB) particles by varying the ratio between styrene (St) and butyl methacrylate (BMA) showed that shear viscosity was a function of molecular weight, temperature and compositional ratio. When the ratio was 7/3, 5/5 and 3/7, shear viscosity slightly reduced with an increase in BMA concentration despite similar weight average molecular weights. We found that shear viscosity of copolymers with BMA concentrations exceeding 70% displayed a sharp reduction at high shear rates. It is speculated that increased PBMA chain length contributes to enhanced flowability of copolymers. When carbon black was incorporated into co-PSB, shear viscosity progressively increased with increasing carbon black concentration. The increase in shear viscosity, however, was less pronounced compared to the cases of molecular weight increase.

• Korean Chemical Engineering Research
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• v.55 no.5
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• pp.579-585
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• 2017

Acrylic resins containing tertiary amine were synthesized by a radical polymerization of monomers including n-butyl acrylate (BA), methyl methacrylate (MMA), n-butyl methacrylate (BMA) and dimethylaminoethyl methacrylate (DMAEMA), and diethylaminoethyl methacrylate (DEAEMA) containing tertiary amine. Synthesized acrylic resins were applied to develope coatings of acrylic resins containing tertiary amine. And ${\gamma}$-glycidoxypropyl trimethoxysilane (GPTMS) or ${\gamma}$-glycidoxypropyl triethoxysilane (GPTES) was used as hardener. Developed coatings were white colored ones to use titanium dioxide and were hardened with hardener for measuring their physical properties. Measured physical properties were basic properties, adhesivity and weatherability. As a result, developed acrylic resins coatings containing tertiary amine showed excellent adhesivity on various substrates and also showed the same result on weatherability on dry weather condition.

• Journal of the Korean Applied Science and Technology
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• v.19 no.4
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• pp.273-280
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• 2002

Thermal decomposition of the copolymer of butyl methacylate(BMA) with styrene(St) was investigated. The copolymer Was obtained at 80 $^{\circ}C$ in a continuous stirred tank reactor(CSTR) using toluene and benzoyl peroxide(BPO), as solvent and initiator, respectively. The reactor volume was 0.3 liters and residence time was 3 hours. The thermal decomposition followed the second order kinetics for BMA/St copolymer. The activation energies of thermal decompositon were in the ranges of 38 ${\sim}43$ kcal/mol for BMA with St copolymer and a good additivity rule was observed with the composition of copolymer. The thermogravimetric trace curve agreed well with the theoretical calculation.

• Elastomers and Composites
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• v.23 no.3
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• pp.213-222
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• 1988

The thermal decomposition of poly(n-butyl methacrylate)(Pn-BMA) was studied using a dynamic and isothermal thermogravimetry in nitrogen gas with 50ml/min at several heating rates from 1 to $20^{\circ}C/min$, and at several heating temperature from 320 to $370^{\circ}C$. The mathematical techniques used for calculation of activation energy were Kissinger, Anderson, Chatterjee-Conrad, Friedman, Fuoss, Ozawa and isolthermal method. The range of activation energies obtained using the several techniques was between 43 and 51Kcal/mol except Chatterjee-Conrad and this range agreed with each other very well. The thermal degradation of Pn-BMA was considered to be carried out by main chain scission.