• Journal of Applied and Pure Mathematics
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• 제5권3_4호
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• pp.165-186
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• 2023

In this paper we give some prperties of the (p, q)-poly-cosine tangent polynomials and (p, q)-poly-sine tangent polynomials.

• 폴리머
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• 제24권6호
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• pp.854-859
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• 2000

N,N-dimethylamino ethyl methacrylate(DMAEMA)와 poly(ethylene glycol) (PEG)로 이루어진 블록 공중합체를 합성하였고, 그 구조를 FT-IR, DSC, 및 $^1$H-NMR로 확인하였다. 준비된 poly(DMAEMA))-PEG 블록 공중합체 수용액에 poly(ethyl acrylamide)(PEAAm)를 첨가하면 블록 공중합체의 DMAEMA와 poly(EAAm) 사이에서 일어나는 수소결합에 의해 나노복합체가 형성되었다. 나노복합체는 임계미셀농도 이상의 농도에서 이루어졌다.

• Bulletin of the Korean Chemical Society
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• 제3권2호
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• pp.60-66
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• 1982

In relation to denaturation of proteins, thermally induced conformational change of poly(D-glutamic acid) was studied in the presence of poly(vinyl alcohol) at low pH, where poly(D-glutamic acid) undergoes a helix-to-${\beta}$ transition without any other polymer. In a dilute solution, poly(vinyl alcohol) enhanced the ${\alpah}-to-{\beta}_1$ transition of poly(D-glutamic acid) due to intermolecular interaction between the two polymers. On the other hand, this conformational change was interrupted to a large extent in a concentrated solution, due to the interpenetration of poly(vinyl alcohol) chain into poly(D-glutamic acid) chain which prevented the intramolecular association of poly(D-glutamic acid) chain. A conformational change from ${\beta}_1\;to\;{\beta}_2$ of poly(D-glutamic acid) was observed for the films obtained by casting during annealing the mixture solutions. The ${\beta}_2$ content in the cast film increased with increasing poly(vinyl alcohol) content in the mixture.

• Asian-Australasian Journal of Animal Sciences
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• 제33권1호
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• pp.127-131
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• 2020

Objective: This study was conducted to determine catalytic properties of wheat phytase with exopolyphosphatase activity toward medium-chain and long-chain inorganic polyphosphate (polyP) substrates for comparative purpose. Methods: Exopolyphosphatase assay of wheat phytase toward polyP75 (medium-chain polyP with average 75 phosphate residues) and polyP1150 (long-chain polyP with average 1150 phosphate residues) was performed at pH 5.2 and pH 7.5. Its activity toward these substrates was investigated in the presence of Mg²⁺, Ni²⁺, Co²⁺, Mn²⁺, or ethylenediaminetetraacetic acid (EDTA). Michaelis constant (K_m) and maximum reaction velocity (V_max) were determined from Lineweaver-Burk plot with polyP75 or polyP1150. Monophosphate esterase activity toward p-nitrophenyl phosphate (pNPP) was assayed in the presence of polyP75 or polyP1150. Results: Wheat phytase dephosphorylated polyP75 and polyP1150 at pH 7.5 more effectively than that at pH 5.2. Its exopolyphosphatase activity toward polyP75 at pH 5.2 was 1.4-fold higher than that toward polyP1150 whereas its activity toward polyP75 at pH 7.5 was 1.4-fold lower than that toward polyP1150. Regarding enzyme kinetics, K_m for polyP75 was 1.4-fold lower than that for polyP1150 while V_max for polyP1150 was 2-fold higher than that for polyP75. The presence of Mg²⁺, Ni²⁺, Co²⁺, Mn²⁺, or EDTA (1 or 5 mM) exhibited no inhibitory effect on its activity toward polyP75. Its activity toward polyP1150 was inhibited by 1 mM of Ni²⁺ or Co²⁺ and 5 mM of Ni²⁺, Co²⁺, or Mg²⁺. Ni²⁺ inhibited its activity toward polyP1150 the most strongly among tested additives. Both polyP75 and polyP1150 inhibited the monophosphate esterase activity of wheat phytase toward pNPP in a dose-dependent manner. Conclusion: Wheat phytase with an unexpected exopolyphosphatase activity has potential as a therapeutic tool and a next-generational feed additive for controlling long-chain polyP-induced inappropriate inflammation from Campylobacter jejuni and Salmonella typhimurium infection in public health and animal husbandry.

• Korean Chemical Engineering Research
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• 제40권6호
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• pp.703-708
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• 2002

본 연구는 초임계 용매인 $CO_2$, 에틸렌, 프로판, 부탄, 프로필렌, 1-부텐, 디메틸에테르 및 $CHClF_2$내에서 poly(propyl acrylate)와 poly(propyl methacrylate) 용액과의 고압 상거동을 측정하였다. 초임계 용매들과 poly(propyl acrylate) 및 poly(propyl methacrylate)간의 상거동 측정 범위는 온도 $23-186^{\circ}C$와 압력 2,400 bar까지 실험하여 나타내었다. poly(propyl acrylate)-$CO_2$ 혼합물은 약 2,070 bar 이내에서, poly(propyl acrylate)-에틸렌계는 1,400 bar 이하에서, poly(propyl acrylate)-프로판계는 1,880 bar 이하에서, poly(propyl acrylate)-프로필렌계는 450 bar 이하에서, poly(propyl acrylate)-부탄계는 2,200 bar이하에서, poly(propyl acrylate)-1-부텐계는 250 bar 이하에서, poly(propyl acrylate)-디메틸에테르계는 150 bar 이하에서 각각 용해되었으며, 이때 온도범위는 $23-175^{\circ}C$이였다. poly(propyl methacrylate)-$CO_2$ 혼합물은 2,900 bar 및 온도 $240^{\circ}C$에서도 용해되지 않았다. poly(propyl methacrylate)-프로판계는 약 2,390 bar이하에서, poly(propyl methacrylate)-부탄계에 대해서는 2,100 bar이하에서, poly(propyl methacrylate)-프로필렌계에 대해서는 570 bar 이하에서 poly(propyl methacrylate)-1-부텐계는 310 bar 이하에서, poly(propyl methacrylate)-$CHClF_2$계에 대해서는 300 bar 이하에서, 그리고 poly(propyl methacrylate)-디메틸에테르계에 대해서는 170 bar 이하에서 각각 용해되었으며, 이때 온도범위는 $40-186^{\circ}C$ 사이였다. 또한 이성분 poly(propyl acrylate)-$CO_2$와 poly(propyl acrylate)-디메틸에테르계의 상거동 사이에 디메틸에테르를 공용매로 사용하여 5, 15 및 50 wt% 첨가하여 구름점의 거동을 상임계용액온도 영역에서 하임계용액온도 영역까지 나타내었다.

• 폴리머
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• 제37권2호
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• pp.135-140
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• 2013

Poly(methyl acrylate)-poly(acrylonitrile) 공중합체의 응력완화 실험은 용매기를 부착한 인장 시험기를 사용하여 여러 온도의 공기 중, 증류수, pH 3, 7, 11 용액에서 실행하였다. Ree-Eyring and Maxwell 모델로부터 얻은 완화스펙트럼 식에 실험적인 응력완화 곡선을 대입하여 poly(methyl acrylate)-poly(acrylonitrile) 공중합체의 완화스펙트럼을 얻었다. 완화스펙트럼의 계산은 Laplace 변환법을 사용한 컴퓨터 프로그램을 이용하였다. 이들 시료의 완화스펙트럼은 유동단위의 분자량과 자체확산 분포와 밀접한 관계가 있음을 알 수 있었다.

• Macromolecular Research
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• 제10권6호
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• pp.339-344
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• 2002

Poly(vinyl alcohol-b-styrene) (poly(VA-b-St)) diblock copolymer containing high syndiotactic poly (vinyl alcohol) (PVA) was synthesized by the saponification of poly(vinyl pivalate-b-styrene) (poly(VPi-b-St)). For the block copolymer, poly(vinyl pivalate) (PVPi) with trichloromethyl end group was obtained via telomerization of vinyl pivalate with carbon tetrachloride as a telogen and 2,2-azobisisobutyronitrile (AIBN) as an initiator. Then resulting poly(vinyl pivalate) with trichloromethyl end group was used as an effient macroinitiator for the synthesis of poly(VPi-b-St) using atom transfer radical polymerization (ATRP) in the presence of CuCl/2,2'-bipyridine at 130 $^{\circ}C$. The poly(vinyl pivalate) macroinitiator, poly(VPi-b-St), poly(VA-b-St) were characterized by GPC, FT-IR and $^1$H-NMR. And the analysis showed that integrity of the block copolymer was maintained during saponification reaction.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2000년도 춘계학술대회 논문집 전자세라믹스 센서 및 박막재료 반도체재료 일렉트렛트 및 응용기술
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• pp.143-146
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• 2000

We studied effects of alkyl($C_nH_{2n+1}$) chain length on characteristics of poly(3-alkylthiophene) electroluminescent diodes. Among the poly(3-alkylthiophene), poly(3-hexylthiophene)(n=6) and poly(3- octyIthiophene)(n=8) were mainly used for the emitting layer of the diode. The result of experiment, the emission intensity of poly(3-alkylthiophene) electroluminescent diodes depends on the alkyl chain length. Strong emission is obtained from a poly(3-alkylthiophene) diodes of long alkyl side chain length. Emission intensities are enhanced by a confinement of carriers on a main chain with a long interchain distance caused by a long alkyl side chain.

• Journal of Pharmaceutical Investigation
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• 제22권4호
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• pp.323-326
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• 1992

$Poly({\varepsilon}-carbobenzoxy\;L-lysine)/poly(ethylene oxide)/poly({\varepsilon}-carbobenzoxy\;L-lysine)$ (LEL) block copolymers containing $poly({\varepsilon}-carbobenzoxy\;L-lysine)$ (PCLL) as the A component and poly(ethylene oxide) (PEO) as the B component were investigated as drug delivery matrix. PCLL homopolymer and LEL block copolymer microspheres containing anticancer drug, cytarabine, were prepared by a solvent evaporation process and the release patterns of cytarabine from the microspheres were investigated in vitro. The size of PCLL homopolymer and LEL block copolymer microspheres was ranged from $0.2\;{\mu}m$ to $1\;{\mu}m$ in diameter and the shape of the microspheres was almost round. The release pattern of cytarabine from the block copolymer microspheres was dependent on the mole % of PEO of the block copolymers.

• 공업화학
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• 제19권2호
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• pp.205-208
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• 2008

저가인 aromatic elastomer polymer인 polySEBS와 PS의 방향족 작용기에 술폰기를 도입시킴으로써 sulfonated polySEBS과 sulfonated PS를 얻었다. 이 술폰화된 고분자를 활용하여 고분자 전해질 연료전지의 이온 교환막으로 사용될 수 있는 새로운 sulfonated polySEBS/sulfonated PS blending films를 제조하였다. 이 필름들의 수소이온 전도도는 sulfonated polySEBS와 sulfonated PS의 혼합비에 따라 $10^{-2}{\sim}10^{-3}S/cm$로 다양하게 나타났다. 특히, sulfonated polySEBS 10.0 g에 sulfonated PS를 0.5 g 첨가하여 제조한 film이 0.75 meq/g의 이온교환용량 및 25%의 함수율과 함께 가장 우수한 0.07 S/cm의 이온전도도를 나타냈다.