• Macromolecular Research
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• 제14권5호
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• pp.504-509
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• 2006

Poly(vinyl phosphate-b-styrene) (PVPP-b-PS) block copolymers were synthesized successfully from poly(vinyl alcohol-b-styrene) (PVA-b-PS) by reaction with phosphorus oxychloride and subsequent hydrolysis. The obtained block copolymers were slightly crosslinked, and were characterized by various analytical techniques. The total phosphorus content and the ratio of the differently bound phosphorus were obtained by both solid-state $^{31}P$ NMR and pH titration, but the results differed slightly. Characterization by energy dispersion X-ray analysis (EDS) or Rutherford back scattering (RBS), on the other hand, determined the total phosphorus contents, but the results were quite different from those by solid-state $^{31}P$ NMR.

• Macromolecular Research
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• 제16권4호
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• pp.329-336
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• 2008

Core/shell ($\pm$)PS/(-)silica nanocomposite particles were synthesized by dispersion polymerization using an amphoteric initiator, 2,2'-azobis [N-(2-carboxyethyl)-2,2-methylpropionamidine] ($HOOC(CH_2)_2HN$(HN=) $C(CH_3)_2CN$=NC $(CH_3)_2C$(=NH)NH $(CH_2)_2COOH$), VA-057. Negatively charged (-6.9 mV) silica was used as the stabilizer. The effects of silica addition time and silica and initiator concentrations were investigated in terms of polymerization kinetics, ultimate particle morphology, and size/size distribution. Uniform hybrid microspheres with a well-defined, core-shell structure were obtained at the following conditions: silica content = 10-15 wt% to styrene, VA-057 content=above 2 wt% to styrene and silica addition time=0 min after initiation. The delay in silica addition time retarded the polymerization kinetics and broadened the particle size distribution. The rate of polymerization was strongly affected by the silica content: it increased up to 15 wt% silica but then decreased with further increase in silica content. However, the particle size was only marginally influenced by the silica content. The zeta potential of the composite particles slightly decreased with increasing silica content. With increasing VA-057 concentration, the PS microspheres were entirely coated with silica sol above 1.0 wt% initiator.

• 폴리머
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• 제28권2호
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• pp.162-169
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• 2004

0-0.3phr의 디큐밀 퍼옥사이드를 개시제로 사용하여 0-3.0 phr 말레산 무수물에 의해 폴리[스티렌-블록-(에틸렌-1-부텐)-블록-스티렌] 삼블록 공중합체 (SEBS)는 관능화되었다. 개질 SEBS의 젤 함량은 자일렌 추출에 의해 결정되었고, 폴리(옥시메틸렌)이 개질 SEBS와 혼합되었다. 혼합물의 충격, 인장, 굴곡강도 그리고 형태학적 특성을 조사하였다. 폴리(옥시메틸렌)의 충격강도는 개질 SEBS와의 블렌드를 통하여 향상되었다. 그러나 개질 SEBS가 5% 보다 더 많아지면 블렌드의 충격강도가 감소하였다. 충격강도에 대한 디큐밀퍼옥사이드 농도의 영향을 살펴보면, 폴리(옥시메틸렌)이 디큐밀 퍼옥사이드 0.1phr을 사용하여 제조된 개질 SEBS와 블렌드시 최대 충격강도를 나타내었다. 또한 주사전자 현미경 사진에 의하면 폴리(옥시메틸렌)/개질 SEBS블렌드의 개질 SEBS 입자크기가 폴리(옥시메틸렌)/SEBS블렌드의 SEBS 입자 크기보다 작게 나타났다.

• 폴리머
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• 제24권6호
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• pp.763-769
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• 2000

E-beam 전조사법을 이용하여 아크릴산과 스틸렌 단량체를 폴리프로필렌 섬유에 그라프트 반응시켜 PP-g-(AAc/Sty) 공중합체를 합성하고 술폰화 반응시켜 다관능성 섬유상 양이온 교환체를 합성하였다. 합성체의 그라프트율은 물과 메탄올 혼합비가 30 : 70 vol%인 혼합용매에서 아크릴산과 스틸렌, 단량체비가 30 : 70 vol%일 때 190%로 최대이었으며 혼합용매의 조성비가 일정할 때 아크릴산 단량체의 양이 증가할수록 그라프트율은 감소하였다. 또한 이온교환체의 이온교환용량은 4.6 meq/g이었으며, 술폰화 이온교환체와 아크릴산 이온교환체의 리튬이온에 대한 흡착량을 비교한 결과 본 연구에서 합성한 이온교환체의 흡착성이 우수한 것으로 나타났다.

• Elastomers and Composites
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• 제53권2호
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• pp.57-66
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• 2018

Styrene-butadiene rubber (SBR), reinforced with different contents of silica (with or without modification using silane coupling agents), was prepared by a modified sol-gel method involving hydrolyzation of tetraethoxysilane over an acid catalyst. The structures of the as-prepared samples were characterized using various techniques, such as scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, and thermogravimetric analysis. The mechanical properties of the as-prepared samples were discussed in detail. The results revealed an increasing of the storage modulus (G') with increase in the silica content without modification. In contrast, G' decreased after modification using silane coupling agents, indicating a reduction in the silica-silica interaction and improved dispersion of silica in the SBR matrix. Both tensile stress and hardness increased with increase in the silica content (with modification) in the SBR matrix, albeit with low values compared to the samples with un-modified silica, except for the case of silica modified using (3-glycidyloxypropyl) trimethoxysilane (GPTS). The latter observation can be attributed to the special structure of GPTS and the effort of oxygen atom lone-pair.

• 콘크리트학회논문집
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• 제14권3호
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• pp.315-320
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• 2002

본 연구에서는 고로슬래그 미분말을 이용한 SBR혼입 폴리머 시멘트 콘크리트의 강도 성상에 미치는 고로슬래그 치환율 및 폴리머 결합재비의 영향에 대하여 구명하였다. 그 결과, 고로슬래그 미분말을 이용한 SBR혼입 폴리머 시멘트 콘크리트의 압축, 인장 및 휨강도는 폴리머-결합재비 및 고로슬래그 치환율의 증가에 따라 증가하였으며, 고로슬래그 치환율 40%에서 가장 높은 강도를 나타내었다. 특히 고로슬래그 치환율 40%의 SBR혼입 폴리머 시멘트 콘크리트의 인장 및 휨강도는 폴리머 미혼입의 강도보다 약 2배 이상의 높은 강도를 보였다. 이와 같이 높은 강도의 발현은 SBR 폴리머의 높은 인장강도와 SBR라텍스의 혼입에 의한 시멘트 수화물과 골재간의 접착성이 개선되었기 때문이라 판단된다.

• Macromolecular Research
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• 제9권3호
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• pp.157-163
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• 2001

The influences of carbon black loading and cure type on the cure characteristics including kinetics and dynamic mechanical properties were investigated for a styrene-butadiene rubber (SBR). The rate constants of accelerated sulfur vulcanization reaction at three different temperatures were determined using a cure rheometer, and they were compared with those from the direct measurement of sulfur concentration. The strain softening behavior under dynamic deformation, known as the Payne effect was also discussed depending on the carbon black loading and cure type.

• 공업화학
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• 제9권5호
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• pp.758-762
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• 1998

유화중합을 이용하여 중량 평균입자크기가 $0.3{\mu}m{\sim}1.5{\mu}m$인 중공 라텍스 입자를 제조함에 있어 평균입자크기와 고형분 함량에 영향을 미치는 반응 인자를 조사하였다. 실험결과 유화제 (SDS)의 농도가 증가함에 따라 친수성 코어 폴리머의 크기가 작아졌으며, 친유성 스티렌 단량체 (styrene monomer)와 개시제 (SPS)의 첨가량이 증가함에 따라 중공입자의 크기가 커졌다. 한편, 친수성 아크릴산의 첨가속도가 증가함에 따라 중공입자의 크기가 작아졌다. 또한, 스틸렌 단량체의 첨가량이 증가함에 따라 에멀젼 폴리머의 고형분 함량이 선형적으로 증가하였다.

• 통합자연과학논문집
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• 제6권3호
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• pp.151-157
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• 2013

The ion exchange resins were synthesized from 1-aza-18-crown-6 macrocyclic ligand attached to styrene (2th petroleum in 4th class hazardous material) divinylbenzene (DVB) copolymer with crosslinks of 1%, 6%, and 15% by substitution reaction. These synthetic resins were confirmed by chlorine content, elementary analysis, surface area, and IR-spectrum. The object of this study was to seperate the metal ion absorbed in reinforcement water fire extinguishing agent. As the results of the effects of pH, equilibrium arrival time, and crosslink of synthetic resin on metal ion adsorption for resin adsorbent, the metal ions were showed high adsorption at pH 3 or over and adsorption equilibrium of metal ions was about 2 hours. In addition, adsorption selectivity for the resin in water was the order of Al (III) > Ni (II) > Sm (III) ions, adsorbability of the metal ions was in the crosslinks order of 1%, 6%, and 15%.

• 약학회지
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• 제34권6호
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• pp.429-433
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• 1990

Transdermal patches and polymer membrane were prepared and evaluated for their ability to antiviral agent in vitro. The membrane perpared with styrene and HEMA by 0.5 and 10% of styrene composition. And the transdermal patches were fabricated with this membrane and silastic silicone sheeting. The antiviral agents used were ACV, BVDU and FEAU. The higher HEMA content membranes exhibited relatively high release rate of each drug. Permeation was enhanced by increasing of drug concentration. The parameters of each drug in diffusion experiment with styrene-HEMA membrane were investigated.