• Fibers and Polymers
• /
• 제7권1호
• /
• pp.36-41
• /
• 2006

PVC and SAN are often mixed to compensate for the disadvantages of each polymer. Miscibility and thermal stability of PVC/SAN blend were investigated in this study by blending SAN polymer having 20, 24, 28, 32 % of acrylonitrile contents. Two polymers were mixed using a melt blending method with a single screw extruder. DSC thermogram was used to evaluate miscibility of the two polymers. SAN having 24 % of acrylonitrile showed the best miscibility with PVC. In order to evaluate degradation behavior, blended polymer was heat treated in DSC furnace and glass transition temperature was measured consecutively. Glass transition temperature increased continuously with annealing time due to degradation and cross-linking of polymer chains. Melt index of blended polymer was always higher than that of PVC.

• Bulletin of the Korean Chemical Society
• /
• 제16권11호
• /
• pp.1109-1112
• /
• 1995

Bis(silyl)alkylbenzenes such as bis(1-sila-sec-butyl)benzene (1) and 2-phenyl-1,3-disilapropane (2) were prepared in high yields by reduction of the corresponding chlorosilanes with LiAlH4. The dehydropolymerization of 1 and 2 was carried out with group 4 metallocene complexes generated in situ from Cp2MCl2/Red-Al and Cp2MCl2/n-BuLi (M=Ti, Hf), producing two phases of polymers. The TGA residue yields of the insoluble polymers were in the range of 64-74%. The molecular weights of the soluble polymers produced ranged from 700 to 5000 (Mw vs polystyrene) and from 500 to 900 (Mn vs polystyrene). The dehydropolymerization of 1 and 2 seemed to initially produce a low-molecular-weight polymer, which then underwent an extensive cross-linking reaction of backbone Si-H bonds, leading to an insoluble polymer.

• Macromolecular Research
• /
• 제12권6호
• /
• pp.564-572
• /
• 2004

Modem applications could benefit from multifunctional materials having anisotropic optical, electrical, thermal, or mechanical properties, especially when coupled with locally controlled distribution of the directional response. Such materials are difficult to engineer by conventional methods, but the electric field-aided technology presented herein is able to locally tailor electroactive composites. Applying an electric field to a polymer in its liquid state allows the orientation of chain- or fiber-like inclusions or phases from what was originally an isotropic material. Such composites can be formed from liquid solutions, melts, or mixtures of pre-polymers and cross-linking agents. Upon curing, a 'created composite' results; it consists of these 'pseudofibers' embedded in a matrix. One can also create oriented composites from embedded spheres, flakes, or fiber-like shapes in a liquid plastic. Orientation of the externally applied electric field defines the orientation of the field-aided self-assembled composites. The strength and duration of exposure of the electric field control the degree of anisotropy created. Results of electromechanical testing of these modified materials, which are relevant to sensing and actuation applications, are presented. The materials' micro/nanostructures were analyzed using microscopy and X-ray diffraction techniques.

• Korea-Australia Rheology Journal
• /
• 제15권4호
• /
• pp.179-185
• /
• 2003

Associating polymers act as flocculants in colloidal suspensions, because the hydrophobic groups (hydrophobes) can adsorb onto particle surfaces and create intermolecular cross-linking. The steady-shear viscosity and dynamic viscoelasticity were measured for suspensions flocculated by multichain bridging of associating polymers. The effects of surfactant on the suspension rheology are studied in relation to the bridging conformation. The surfactant molecule behaves as a displacer and the polymer chains are forced to desorb from the particle surfaces. The overall effect of surfactant is the reduction of suspension viscosity. However, the additions of a small amount of surfactant to suspensions, in which the degree of bridging is low, cause a viscosity increase, although the number of chains forming one bridge is decreased by the forced desorption of associating polymer. Since the polymer chains desorbed from one bridge can form another bridge between bare particles, the bridging density over the system is increased. Therefore, the surfactant adsorption leads to a viscosity increase. The surfactant influences the viscosity in two opposing ways depending on the degree of bridging.

• 한국환경과학회지
• /
• 제13권3호
• /
• pp.319-325
• /
• 2004

An experimental study on the preparation of monolithic porous polymers by environmentally friend process in supercritical carbon dioxide has been carried out. Polymerization mixture composed of a cross-linking monomer, initiator and functional co-polymer was charged in the reactor with sapphire window. After the system was purged with a flow of $CO_2$ for 15 min, the reactor was pressurized with liquid $CO_2$ up to 100 bars. The reactor was isolated from and placed back to the system via quick connector for shaking until the mixture had become fully homogeneous. The reactor was then heated and pressurized to the required reaction conditions and left overnight. After cooling and $CO_2$ evacuation, the polymer was removed from the reactor as dry, white, continuous monoliths. The effect of experimental conditions on the physical properties of porous polymer was systematically examined, and it was found that monomer content had a major effect on the physical properties of the polymers.

• 멤브레인
• /
• 제30권6호
• /
• pp.395-408
• /
• 2020

고분자 전해질 막 연료전지(polymer electrolyte membrane fuel cell, PEMFC)는 환경오염물질 배출이 없는 친환경 에너지 변환 장치로 주목을 받고 있다. PEMFC의 구성요소 중 고분자 전해질 막(polymer electrolyte membrane, PEM)은 음극에서 발생되는 수소이온을 양극으로 전달하는 역할과 동시에 분리막으로써 연료의 투과를 차단하는 역할을 수행하는 핵심 소재이다. 대표적으로 Nafion®과 같은 과불소화계 고분자 전해질 막이 상용화 되어있지만 높은 단가 및 분해 시 환경오염물질이 배출되는 단점이 존재하여, 이를 대체할 탄화수소계 고분자를 활용한 전해질 막 개발에 관한 연구들이 수행되고 있다. 높은 수소이온 전도도를 가지며 동시에 우수한 물리·화학적 안정성을 갖는 탄화수소계 고분자 기반 전해질 막을 개발하기 위해 가교 구조가 도입된 전해질 막을 개발하는 연구들이 보고되고 있다. 본 총설은 가교 전해질 막을 제조하기 위해 이온교환 작용기가 도입된 탄화수소계 고분자를 활용하여 다양한 종류의 가교 전해질 막을 제조하는 방법에 대해 논하였다.

• 한국수소및신에너지학회논문집
• /
• 제17권2호
• /
• pp.149-157
• /
• 2006

Hydrogen as new energy sources is highly efficient and have very low environmental emissions. The proton exchange membrane fuel cell (PEMFC) is an emerging technology that can meet these demands. Therefore, the preparation of stable polymeric membranes with good proton conductivity and durability are very important for hydrogen production via water electrolysis with PEM at medium temperature above $80^{\circ}C$. Currently Nafion of Dupont and Aciflex of Asahi, etc., solid polymer electrolytes of perfluorosulfonic acid membrane, are the best performing commercially available polymer electrolytes. However, these membrane have several flaws including its high cost, and its limited operational temperature above $80^{\circ}C$. Because of this, significant research efforts have been devoted to the development of newer and cheaper membranes. In order to make up for the weak points and to improve the mechanical characteristics with cross -linking, acid-base complexes were prepared by the combination PSf-co-PPSS-$NH_2$ with PEEK-$SO_3H$. The results showed that the proton conductivity decreased in 17.6% and 40% but tensile strength increased in 78% and 98%, about $20.65\;{\times}\;10^6N/m^2$, in comparison with SBPSf/HPA and SPEEK/HPA complex membrane.

• 펄프종이기술
• /
• 제43권4호
• /
• pp.49-58
• /
• 2011

The maximum drying shrinkage velocity was proposed to verify bulk and stiffness improvement mechanism during drying according to papermaking parameters. It was based on the wet-web shrinkage behavior without the restraint of wet-web during drying, so intact drying impact could be measured. Bulking agent reduced the drying shrinkage and the maximum drying shrinkage velocity, so paper bulk increased and paper strength decreased. When adding cationic starch to stock with the bulking agent for strengthening, the bulk was increased further with additional decreasing of the drying shrinkage and the maximum drying shrinkage velocity. Paper strength also increased except tensile stiffness index with decreasing the drying shrinkage and the maximum drying shrinkage velocity. When using additional strength additives for strengthening of fiber interfaces extended by bulking agent and cationic starch, amphoteric strength additive increased paper stiffness without loss of paper bulk. It was considered that the added amphoteric strength additives were cross-linked to the stretched cationic starch and this cross-linking increased elasticity of fiber-polymer-fiber interfaces without changing the drying behavior. Paper bulk could be increased with decreasing the maximum drying shrinkage velocity. The drying shrinkage of paper also could be controlled by fiber-to-fiber bonding interfaces by the bulking agent. In this case, paper strength including stiffness was decreased by reducing fiber-to-fiber bonding but it could be improved by strengthening fiber-to-fiber interfaces with polymer complex without loss of bulk.

• 멤브레인
• /
• 제33권2호
• /
• pp.77-86
• /
• 2023

본 연구에서는 낮은 막 저항과 높은 수산화 이온 전도성을 가지는 세공 충진 이온교환막 제조법으로 연구하였다. 알칼리 내구성을 향상하기 위해 폴리 테트라 플로오 에틸렌 소재인 다공성 지지체를 사용하였고 세공에는 단량체 2-(dimethylamino)ethyl methacrylate (DMAEMA), vinylbenzyl chloride (VBC)를 이용하여 copolymer를 제조했다. 가교제는 divinylbenzene (DVB)를 사용하였고 가교제 함량별로 이온교환막을 제조하여 DMAEMA-DVB와 VBC-DMAEMA-DVB copolymer에서 가교제 함량이 미치는 영향에 관해 연구하였다. 그 결과, PTFE 소재 지지체를 이용하여 화학적 안정성이 향상했고 저압 UV 램프를 사용하여 낮은 온도에서 빠른 광중합이 가능하여 생산성을 높일 수 있는 장점이 있다. 음이온교환 막 연료전지에 요구되는 이온교환막의 물리적 및 화학적 안정성을 확인하기 위해서 인장강도와 내알칼리성 테스트를 진행하였다. 그 결과, 가교도가 증가할수록 인장강도 대략 40 MPa가 증가하였고, 최종적으로 이온전도도와 내알칼리성 테스트를 통해 가교제 함량이 증가할수록 알칼리 안정성이 증가하는 것을 확인하였다.

• Macromolecular Research
• /
• 제11권5호
• /
• pp.322-327
• /
• 2003

Two kinds of mutually cross-linkable copolymers were prepared to be used as humidity-sensing materials. The humidity-sensitive thin films consist of cross-linked polyelectrolytes of the following component: 4-vinylbenzyl dimethyl 2-(dimethylphosphino)ethyl phosphonium chloride (1)/ bis(2-methoxyethyl)itaconate (2)= 3/l, 2/l, 1/1 and 1/2 and 4-vinylbenzyl chloride (3)/ vinylbenzyl tributyl phosphonium chloride (4)= 3/l, 2/l, 1/1 and 1/2. The humidity sensor prepared from the reaction of 1/2= 2/l with 3/4= 2/l showed an average resistance of 723,36.2 and 2.42 ㏀ at 30, 60 and 90%RH, respectively. Temperature dependence, frequency dependence, and response time were measured and the reliability test such as water durability and long-term stability were also estimated.