• 한국전기전자재료학회논문지
• /
• 제16권12호
• /
• pp.1091-1096
• /
• 2003

Ion implantation in polymeric materials can induce dramatic chemical modifications, such as bond breaking, cross linking, formation of new chemical products, which have strong influences on the macroscopic properties of the materials. In this study ion implantation was performed onto polymer, PC(polycarbonate), in order to investigate change of the optical transmittance property focusing ultraviolet ray range(200-400nm). PC was irradiated with N, Ar, Kr, Xe ions at the ion energy of 50keV and the dose range of 5 ${\times}$ 10$\^$15/, 1 ${\times}$ 10$\^$16/, 7${\times}$10$\^$16/ ions/$\textrm{cm}^2$. FT-IR, XPS, UV/Vis transmittance spectroscopy measurement technologies were employed to obtain chemical. structural properties and optical transmittance of irradiated polymer. The original PC(unimplanted) is quite transparent that it has more than 88% transmittance in the range UV-A(320∼400nm), but after ion implantation, surface colors were changed to the dark brown and the transmittance of UV ray decreased for all implantation condition, and the absorption edge was shift to visible range with increasing mass of implanted ion species and dose.

• Korean Chemical Engineering Research
• /
• 제47권3호
• /
• pp.316-320
• /
• 2009

폴리카보네이트(polycarbonate)는 가볍고, 내충격성 및 가공성이 우수하여 광학기기의 렌즈 및 각종 건축물의 투명 소재 등에 유리의 대체품으로서 널리 이용되고 있으나 낮은 표면경도를 가지고 있어 유통 또는 사용시의 접촉으로 인하여 제품에 손상을 줄 염려가 있다. 따라서 본 연구에서는 폴리카보네이트 필름에 아크릴레이트 올리고머, 모노머, 용매, 염료, 실리콘 아크릴레이트, 그리고 광개시제 등을 다양한 함량비율에 따라 혼합한 코팅용액을 제조하고, 구성 성분의 비율에 따른 폴리카보네이트 필름의 표면 경도, 접착력, 그리고 투과율의 변화를 실험하였다. 그 결과 최대 연필 경도가 2H이고, 접착력과 가시광선 투과율이 우수한 코팅용액의 조성을 얻었다. 색상코팅 실험 결과, 기존 산화물 증착에 의해 구현하던 색상을 본 실험에서 제조한 코팅 용액을 사용하여 거의 대부분 구현할 수 있었으며, 이를 바탕으로 색상 윈도우 렌즈를 제작한 결과, 매우 깨끗하고 균일한 색상과 표면을 가졌다.

• 오토저널
• /
• 제12권1호
• /
• pp.26-32
• /
• 1990

This study investigated a method for the determination of the J-integral for a tough glassy polymer such as polycarbonate plates by using the method of caustics. Comparing the values of J-integral determined by a numerical analysis and by the method of caustics, the method of caustics was found to be an effective experimental technique for the determination of the J-integral. The ratio between two J-integrals determined by the method of caustics and by finite element method converged into 1 within the limit of low load. However, it was noticed that the greater the plastic zone at the crack tip was, the lower the J-integral obtained by the reflect method of caustics. This difference may be deduced from the damage at the crack tip such as craze appeared in the polycarbonate plate. It was confirmed that the ratio of longitudinal diameter( $D_{l}$ ) to transverse diameter ( $D_{t}$) of caustics generally converged into 1 at the low load. The transition of the state of stress at the vicinity of a crack tip from plane strain to plane stress was deduced by noticing that the longitudinal diameter( $D_{l}$ ) grew faster than the transverse diameter( $D_{t}$) of caustics within the higher load range.

• Macromolecular Research
• /
• 제10권3호
• /
• pp.135-139
• /
• 2002

Blends of the linear bisphenol-A polycarbonate (L-PC) and randomly branched bisphenol-A polycarbonate (Br-PC), prepared by co-rotating twin screw extrusion, were investigated using differential scanning calorimetry (DSC), sag resistance time tester, extensional rheometry, and advanced rheometric expansion system (ARES). From the DSC results, the glass transition temperature (T$_{g}$) of the L-PC/Br-PC blend was increased with the increase of Br-PC in the blend, and the blend showed a single T$_{g}$, which suggests a miscible blend. The sag resistance time of the L-PC/Br-PC blend was increased with the increase of Br-PC in the blends. From the results of rheological measurements of the L-PC/Br-PC blends, the extensional viscosity and the complex viscosity of the blends were found to increase with the increase of Br-PC in the blends. The increase of extensional viscosity and complex viscosity was related with the increase of sag resistance time with the Br-PC in the L-PC/Br-PC blends.nds.

• Macromolecular Research
• /
• 제15권7호
• /
• pp.640-645
• /
• 2007

The phase behavior of branched polycarbonate (BPC) blends with poly(ethylene terephthalate-co-1,4-dimethyl cyclohexane terephthalate) copolyesters (PECT), as well as their rheological properties, were assessed. Even though BPC blends with PECT prepared by solvent casting proved to be immiscible, BPC and PECT copolyesters containing 1,4-dimethyl cyclohexane (CHDM) from 32 to 80 mole% formed homogeneous mixtures upon heating. The homogenization temperatures of the blends decreased with increasing CHDM content in PECT. The interaction energies of the BPC-PECT pairs calculated from the phase boundary in accordance with the lattice-fluid theory were positive and also decreased with increasing CHDM content in PECT. It was shown that the phase homogenization of these blends occurs upon heating when the combinatorial entropy term, which is favorable for miscibility, overcomes unfavorable energetic terms at elevated temperatures. A novel product, which is not limited by the drawbacks of linear polycarbonate (PC) and evidences processability superior to that of the PC/PECT blends, can be developed via the blending of BPC and PECT.

• Macromolecular Research
• /
• 제9권3호
• /
• pp.129-142
• /
• 2001

To efficiently demonstrate the molecular motion, physical properties, and mechanical properties of polycarbonates, we studied the differences between bisphenol-A polycarbonate(BPA-PC) and tetramethyl bisphenol-A-polycarbonate(TMBPA-PC) using molecular modeling techniques. To investigate the conformations of BPA-PC and TMBPA-PC and the effect of the conformation on mechanical properties, we performed conformational energy calculation, molecular dynamics calculation, and stress-strain curves based on molecular mechanics method. From the result obtained from conformational energy calculations of each segment, the molecular motions of the carbonate and the phenylene group in BPA-PC were seen to be more vigorous and have lower restriction to mobility than those in TMBPA-PC, respectively. In addition, from the results of radial distribution function, velocity autocorrelation function, and power spectrum, BPA-PC appeared to have higher diffusion constant than TMBPA-PC and is easier to have various conformations because of the less severe restrictions in molecular motion. The result of stress-strain calculation for TMBPA-PC seemed to be in accordance with the experimental value of strain-to-failure ∼4%. From these results of conformational energy calculations of segments, molecular dynamics, and mechanical properties, it can be concluded that TMBPA-PC has higher modulus and brittleness than BPA-PC because the former has no efficient relaxation mode against the external deformations.

• 접착 및 계면
• /
• 제9권3호
• /
• pp.1-6
• /
• 2008

자동차의 유리를 폴리카보네이트로 대체하기 위하여 폴리카보네이트 판 위에 하드 코팅을 시도하였다. 본 연구에서는 p-phenylene (PPH)과 m-phenylene (MPH)의 공중합체들을 합성하여 이것들을 이용하여 폴리카보네이트 판 위에 코팅을 시도하였다. 공중합체내의 PPH와 MPH의 비율에 따라서 다양한 강도를 나타내는 코팅이 형성되었다. PPH와 MPH의 비율이 20 : 80일 경우에 연필 경도 2H를 나타내었으며, 이 때 내마모성도 매우 우수하였다.

• 조명전기설비학회논문지
• /
• 제28권7호
• /
• pp.19-25
• /
• 2014

In the LED lighting applications, because LED packages are the origin of heat generation, there are thermal design problem on heat sinks. In the thermal design, it is important to consider the total volume and the total weight of heat sink simultaneously. In this study, an Al 6063 heat sink was optimized using Computational Fluid Dynamics(CFD) simulation tool for the cooling of 30W LED module, and then the cooling performance and the total weight of heat sinks with Al 6063 and Thermal Conductive Polycarbonate(TCP) were compared under the same conditions. As the result of simulation, an Al 6063 heat sink was optimized with 22 ea. of fins and 1.6 mm of fin thickness. LED Junction Temperature of the TCP Heat Sink was $5.6^{\circ}C$ higher, but total weight of it was 47 % less than the Al 6063.

• 폴리머
• /
• 제32권5호
• /
• pp.427-432
• /
• 2008

자동차의 유리를 폴리카보네이트로 대체하기 위하여 폴리카보네이트 판 위에 하드 코팅을 시도하였다. 본 연구에서는 polyphenylene 유도체들을 합성하여 이것들을 이용하여 폴리카보네이트 판 위에 코팅을 시도하였다. 합성한 polyphenylene 유도체는 poly(benzoylphenylene)과 그의 phenylene 공합체들이다. Poly (benzoylphenylene)을 이용한 코팅은 최고 연필 경도 1H를 나타내었으며, 이것의 공중합체를 이용한 코팅에서는 최고 연필 경도 2H를 나타내었다. 내마모성도 공중합체가 더 우수한 결과를 보여 주었다.

• 한국기계가공학회지
• /
• 제19권10호
• /
• pp.59-67
• /
• 2020

Polycarbonate thermoplastic composite materials are anisotropic and exhibit physical properties in the longitudinal direction. Therefore, the physical properties depend on the type and direction of reinforcements. The thermal conductivity, electrical conductivity, and resin impregnation can be controlled by adding carbon nanotubes to polycarbonate resin. However, the carbon fiber used as a reinforcing material is expensive, interfacial adhesion issues occur, and simulation values are different from actual values, making it difficult to perform mathematical analysis. However, carbon nanotubes have advantages such as light weight, rigidity, impact resistance, and reduced number of parts compared to metals. Due to these advantages, it has been applied to various products to reduce weight, improve corrosion resistance, and increase impact durability. As the content of carbon nanotubes or carbon fibers increases, the mechanical properties and antistatic and electromagnetic shielding performance improve. It is expected that the amount of carbon nanotubes or carbon fibers can be optimized and applied to various industrial products.