• Macromolecular Research
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• 제13권5호
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• pp.385-390
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• 2005

The electrospinning process is a fascinating method to fabricate small nanosized fibers of diameter several hundred nanometers. Surfactant-polymer solutions were prepared by adding poly(vinyl alcohol) (PVOH) to distilled water with cationic, anionic, amphoteric, and non-ionic surfactants. Average diameter of the electrospun PVOH fibers prepared from PVOH solution was over 300 nm, and was decreased to 150 nm for the mixture of PVOH/amphoteric surfactant. To explain the formation of ultra fine fiber, the characteristic properties in a mixture of PVOH/surfactant such as surface tension, viscosity, and conductivity were determined. In this paper, the effect of interactions between polymers with different classes of surfactants on the morphological and mechanical properties of electrospun PVOH nonwoven mats was broadly investigated.

• Elastomers and Composites
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• 제53권2호
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• pp.39-47
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• 2018

Styrene-butadiene rubber (SBR) is widely used in tire treads due to its excellent abrasion resistance, braking performance, and reasonable cost. Depending on the polymerization method, SBR is classified into solution-polymerized SBR (SSBR) and emulsion-polymerized SBR (ESBR). ESBR is less expensive and environmentally friendlier than SSBR because it uses water as a solvent. A higher molecular weight is also easier to obtain in ESBR, which has advantages in mechanical properties and tire performance. In ESBR polymerization, a surfactant is added to create an emulsion system with a hydrophobic monomer in the water phase. However, some amount of surfactant remains in the ESBR during coagulation, making the polymer chains in micelles clump together. As a result, it is well-known that residual surfactant adversely affects the physical properties of silica-filled ESBR compounds. However, researches about the effect of residual surfactant on the physical properties of ESBR are lacking. Therefore, in this study we compared the effects of remaining surfactant in ESBR on the mechanical properties of silica-filled and carbon black-filled compounds. The crosslinking density and filler-rubber interaction are also analyzed by using the Flory-Rehner theory and Kraus equation. In addition, the effects of surfactant on the mechanical properties and crosslinking density are compared with the effects of TDAE oil (a conventional processing aid).

• 한국응용과학기술학회지
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• 제24권2호
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• pp.160-166
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• 2007

The rheological properties and surface tensions of polymer solutions and polymer-surfactant mixed solutions were investigated. The polymers used in this study were a homopolymer of acrylic acid crosslinked with an allyl ether of pentaerythritol, an allyl ether of sucrose, or an allyl ether of propylene (CARBOMER), acylate/C10-30 alkyl acylate crosspolymer (AAAC), and ammonium acryloydimethyltaurate/VP copolymer (ADTV). A solubilizing agent PEG-40 hydrogenated castor oil (HCO-40) and an emulsifying agent polyoxyethylene (20) sorbitan monostearate (POLYSORBATE 60) made the micelles intervening between AAAC polymers, resulting in the increase of viscosity. However, HCO-40 made this behavior over the wider range of surfactant concentration than POLYSORBATE 60. From the view point of surface tensions in the same range of surfactant concentration, AAAC/HCO-40 solution showed the area of increasing surface tension with surfactant concentration in contrast to the AAAC/POLYSORBATE 60 solution showing no increasing area.

• Macromolecular Research
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• 제15권6호
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• pp.498-505
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• 2007

This study demonstrated the in-situ functionalization with polymers of multi-walled carbon nanotubes (MWNTs) via emulsion polymerization. Polystyrene-functionalized MWNTs were prepared in an aqueous solution containing styrene monomer, non-ionic surfactant and a cationic coupling agent ([2-(methacryloyloxy)ethyl]trime-thylammonium chloride (MATMAC)). This process produced an interesting morphology in which the MWNTs, consisting of bead-string shapes or MWNTs embedded in the beads, when polymer beads were sufficiently large, produced nanohybrid material. This morphology was attributed to the interaction between the cationic coupling agent and the nanotube surface which induced polymerization within the hemimicellar or hemicylindrical structures of surfactant micelles on the surface of the nanotubes. In a solution containing MATMAC alone without surfactant, carbon nanotubes (CNTs) were not well-dispersed, and in a solution containing only surfactant without MATMAC, polymeric beads were synthesized in isolation from CNTs and continued to exist separately. The incorporation of MATMAC and surfactant together enabled large amounts of CNTs (> 0.05 wt%) to be well-dispersed in water and very effectively encapsulated by polymer chains. This method could be applied to other well-dispersed CNT solutions containing amphiphilic molecules, regardless of the type (i.e., anionic, cationic or nonionic). In this way, the solubility and dispersion of nanotubes could be increased in a solvent or polymer matrix. By enhancing the interfacial adhesion, this method might also contribute to the improved dispersion of nanotubes in a polymer matrix and thus the creation of superior polymer nanocomposites.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2016년도 추계학술대회 논문집
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• pp.147-147
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• 2016

In general, organic electrochromic (EC) materials have been known to be electrochemically unstable during the ionic exchange process. One effective method to realize stable EC materials is incorporating graphene derivatives in the polymer matrix, by using the strong interaction between graphene derivatives and polymer. However, previous studies are limited graphene derivatives. In this study, we developed a polymer-graphene derivative complex with the chemical assistance of a surfactant (octadecylamine, ODA). Surfactant-assisted graphene oxide (GO-ODA) was introduced as a protective layer on the electrochromic poly (3-hexyl thiophene) (P3HT) films by the Langmuir-Schaefer method. The deposition of GO-ODA protective layer with high coverage was confirmed by atomic force microscopy. The strong interactions between GO-ODA and P3HT were examined with UV-Vis spectrophotometry and X-ray photoelectron spectroscopy. Electrochemical and electrochromic investigations revealed that the GO-ODA layer greatly improved the long-term cyclability of the P3HT film. These findings imply that the GO-ODA complex has a significant role in creating stable EC cycling, due to its strong interaction with the P3HT film.

• 대한화장품학회지
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• 제33권1호
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• pp.7-10
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• 2007

수용성 폴리머와 계면활성제의 상호작용을 레올로지와 표면 장력을 측정하여 연구하였다. 본 연구에 사용된 폴리머는 acrylates/$C_{10-30}$ alkyl acrylate crosspolymer (AC), ammonium acryloyldimethyltaurate/VP copolymer (AV)이다. 계면활성제는 PEG-40 hydrogenated castor oil (HC), polysorbate 60 (P60)이다. HC와 P60은 AC 폴리머 주위에서 마이셀을 형성하여 점도를 증가하였다. 그러나, HC는 P60보다 보다 높은 농도 범위에서 점도 증가 거동을 보였다. 같은 농도 범위에서 계면활성제들의 표면장력을 비교해보면, 표면장력이 AC/HC의 농도 증가에 따라 증가한 반면, AC/P60의 농도증가에 대해서는 거의 증가하지 않았다. 이런 결과는 AC/HC 사이의 마이셀이 강하게 조직화된 구조를 형성하기 때문으로 추정된다.

• Bulletin of the Korean Chemical Society
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• 제26권4호
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• pp.548-552
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• 2005

The interaction between ionic surfactants and different nonionic molecules and polymers are studied using ion surfactant selective electrode. From the experimental data, critical concentrations of the interaction and binding process are evaluated. The interaction between hexadecyltrimethylammonium bromide (HTAB) with polyethylene glycol (PEG) in three molecular weights (1000, 10000 and 100000) and also schiff-bases, 2-[2-carboxyphenyl nitrilomethylidyne]-phenol (ortho CNP), 2-[3-carboxyphenyl nitrilomethylidyne]-phenol (meta CNP)and 2-[4-carboxyphenyl nitrilomethylidyne]-phenol (para CNP) with the potentiometric method were investigated using HTAB membrane selective electrode. In the case of PEG with increasing molecular weights more interaction to HTAB occurs. The electromotive force (EMF) data also showed that interaction between para CNP with HTAB is more than the other schiff-bases. It seems this case related to less space interference of COOH group for that compound. The onset of binding ($T_1$) of course is the same for three schiffbase molecules.

• 폴리머
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• 제28권2호
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• pp.111-120
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• 2004

반복 단위마다 양전하를 띄고 있는 폴리(디알릴디메틸암모늄 클로라이드) (PDADMAC)와 음이온 계면활성제인 도데실 황산 소듐 (SDS)와의 상호작용을 광산란법, 탁도법 및 형광법을 이용하여 조사하였다. 0.3 M NaCl 수용액에서의 PDADMAC는 마치 좋은 용매에서 팽창되어 있는 중성 고분자처럼 존재하나, SDS를 첨가함에 따라 이들 사이의 상호작용은 두 개의 임계 응집 농도로써 기술할 수 있었다. 첫 번째, 사슬 내 임계 응집 농도에서는 하나의 고분자 사슬 내에서 SDS의 마이셀화 과정으로써 [SDS]/[DADMAC] 0.06 정도에서 일어나며, 이 복합체 크기는 오히려 마이셀 형성되기 직전에 최대 값을 나타내고, 마이셀이 형성된 후부터는 일부 고분자 사슬도 마이셀 형성에 참여하기 때문에 SDS 첨가에 따라 점차로 수축되기 시작하였다. 두 번째, 사슬간 임계 응집 농도는 탁도 법에 의해 [SDS]/[DADMAC] 0.5에서 측정되었고, 이 두 번째 임계 응집농도 이상에서는 많은 마이셀들로 장식된 고분자 사슬들 사이의 응집화에 의한 거대한 응집체가 형성된다.

• 폴리머
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• 제25권5호
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• pp.736-743
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• 2001

N,N-Methylenebisacrylamide (MBAA)로 가교 결합된 electro-active 고분자(EAP) (poly(2-acrylamido-2-methylpropane sulfonic acid), PAMPS) 겔을 수용액 상에서 potassium persulfate를 개시제로 하여 라디칼 중합시켜 제조하였다. PAMPS 겔의 구동성을 부여하기 위하여 계면활성제로 팽윤하며 치환하였다. 계면활성제가 치환된 PAMPS 겔은 용액내의 인가된 전압하에서, 그 전기장 변화에 의해 큰 변위를 나타내는 구동특성을 보였다. PAMPS 겔은 빠른 응답속도와 가역적인 bending을 나타내었다. 겔의 구동원리는 양극과 PAMPS 겔 음이온간의 정전기 인력, 겔의 swelling-deswelling 효과 그리고 계면활성제의 소수성 반응의 협동적 과정으로 나타난다. PAMPS 겔의 응답속도는 인가된 전압 및 가교도가 증가할수록 증가하였으며, 구동이 반복적으로 진행됨에 따라 응답속도는 증가하였다. 겔의 두께가 증가하면 응답속도는 감소하였다.

• Korea-Australia Rheology Journal
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• 제14권4호
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• pp.189-201
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• 2002

The interaction between hydrophobically modified hydroxyethyl cellulose (hmHEC), containing approximately 1 wt% side-alkyl chains of $C_{16}$, and an anionic sodium dodecyl sulphate (SDS) surfactant was investigated. For a semi-dilute solution of 0.5 wt% hmHEC, the previously observed behaviour of a maximum in solution viscosity at intermediate SDS concentrations, followed by a drop at higher SDS concentrations, until above the cmc of surfactant when the solution resembles that of the unsubstituted polymer, was confirmed. Additionally, a two-phase region containing a hydrogel phase and a water-like supernatant was found at low SDS concentrations up to 0.2 wt%, a concentration which is akin to the critical association concentration, cac, of SDS in the presence of hmHEC. Above this concentration, SDS molecules bind strongly to form mixed micellar aggregates with the polymer alkyl side-chains, thus strengthening the network junctions, resulting in the observed increase in viscosity and elastic modulus of the solution. The shear behaviour of this polymer-surfactant complex during steady and step stress experiments was examined In great detail. Between SDS concentrations of 0.2 and 0.25 wt%, the shear viscosity of the hmHEC-polymer complex network undergoes shear-induced thickening, followed by a two-stage shear-induced fracture or break-up of the network. The thickening is thought to be due to structural rearrangement, causing the network of flexible polymers to expand, enabling some polymer hydrophobic groups to be converted from intra- to inter-chain associations. At higher applied stress, a partial local break-up of the network occurs, while at even higher stress, above the critical or network yield stress, a complete fracture of the network into small microgel-like units, Is believed to occur. This second network rupture is progressive with time of shear and no steady state in viscosity was observed even after 300 s. The structure which was reformed after the cessation of shear is found to be significantly different from the original state.