• 한국균학회지
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• 제26권1호통권84호
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• pp.86-90
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• 1998

상황버섯 자실체, 액체배양 균사체 및 배양액으로부터 고분자물질(polymer)을 추출하여 면역활성을 anti-complementary assay 방법으로 측정하였다. 자연산과 인공재배 자실체로부터 생산된 polymer의 면역활성은 각각 65.77%와 63.94%로 나타나 큰 차이를 보이지 않았다. 자실체, 균사체 및 배양액으로부터 추출한 polymer의 면역활성 측정결과, 균사체는 41.95%, 배양액은 21.87%로 자실체 보다 낮게 나타났다.

• 폴리머
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• 제27권5호
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• pp.429-435
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• 2003

양이온η$^3$-알릴 팔라듐 촉매를 사용하여 환상형 올레핀 단량체인 노보넨 (NB)과 5-비닐-2-노보넨(VNB)을 조성별로 비닐 부가 공중합하였다. 공중합체는 고수율과 고분자량 (M$_{w}$ > 760000)으로 얻을 수 있었다. VNB 함량이 많아질수록 공중합체의 분자량과 수득율은 감소하였으며, 첨가한 공단량체의 양과 공중합한 후 함유된 단량체의 양이 비례함을 FT-IR 분광분석으로 확인하였다. $^1$H-NMR 분석 결과 VNB는 exo, endo 이성체 모두 중합에 참여하는 것을 알 수 있었다. NB-VNB 공중합체의 분해 개시 온도는 약 300 $^{\circ}C$이었고, 열안정성은 VNB 함량과 관계없이 유사한 거동을 나타내었다. 합성된 NB-VNB 공중합체의 곁사슬 비닐기는 m-CPBA를 이용하여 에폭시화 하였고, 또한 9-BBN을 이용하여 수산화기를 도입하였다. 조성별 공중합체에 각각의 치환기가 도입된 것은 FT-IR, $^1$H-NMR 분석으로 확인하였다..

• Macromolecular Research
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• 제16권7호
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• pp.651-658
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• 2008

Poly(butylene succiate) (PBS), poly(butylene succinate-co-L-lactate) (PBSL), and poly(butylene succinate-co-6-hydroxycaproate) (PBSCL) polymers were degraded by lipase $PS^{(R)}$, and the enzymatic degradation mechanism of PBS was analyzed in detail. The enzymatic degradation of PBS gave 4-hydroxybutyl succinate (4HBS) as the main product. An exo-type hydrolysis mechanism was proposed based on this observation. The terminal chain of PBS had conformational similarity to ordinary tri- and diglycerides and could be incorporated as a substrate in the active site of this lipase. The surface adsorption of the lipase was much larger on PBS and its copolymer films than on the other polyester films because the lipase adhered quite strongly to the polymer terminal through a specific adsorption mechanism. Kinetic analysis showed that the total number of surface adsorption points per unit area of PBSL and PBSCL copolymers was larger than that of the PBS homopolymer.

• Macromolecular Research
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• 제15권2호
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• pp.185-190
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• 2007

Poly(norbornene dimethyl dicarboxylate)s, (PNDMD)s, were prepared by addition polymerization with palladium(II) catalyst from pure exo-monomers, and their structure and properties were compared with those of poly(norbornene dicarboxylic acid dialkyl ester)s, (PNDADA)s. Both polymer series exhibited good solubility in general organic solvents and excellent thermal stability up to $330^{\circ}C$. Wide-angle X-ray scattering (WAXS) study indicated the presence of nano-scale layer-like order in amorphous PNDADAs, while PNDMDs showed random amorphous structure. The glass transition temperatures and dielectric constants of solid polymers were found to decrease as the alkyl side-chain length increases for both polymer series. However, PNDMDs showed lower glass transition temperatures and higher dielectric constants, as compared with those of PNDADAs containing the same alkyl substituents. This difference, caused by the higher side-group mobility of PNDMDs, may be closely related to the nano-scale order in amorphous PNDADAs and its absence in PNDMDs.

• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.222-222
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• 2006

New types of constrained geometry complexes comprising rigid silacycloalkyl group incorporated into the bridging position between cyclopentadienyl and amido functionalities were prepared. The catalytic activities of olefin polymerization were influenced by the change of exo-cyclic ring size on bridge-head silacycloalkyl unit. It has been noted that the activities of this unique series increase with increasing size of the silacycloalkyl bridge and reach the maximum in six-membered silacyclohexyl-bridged CGC complex. It is noteworthy that conformation of silacycloalkanes gives rise to enhanced catalytic activity of the titanium center although the cyclic ring and titanium center are far remoted from each other.

• Macromolecular Research
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• 제9권5호
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• pp.247-252
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• 2001

Tricyclic aliphatic dianhydride monomer, tricycle[4.2.2.0]dec-9-ene exo, endo-3,4: 7,8-tetra-carboxylicdianhydride (TCDDA), was synthesized by photochemical reaction and poly(amic acid)s from TCDDA and diamines such as 1,4-bis-(4-aminophenoxy)benzene (BAB), 2,2-bis(4-(4-aminophenoxy) phenyl) propane (BAPP), 2,2-bis(4-(4-aminophenoxy)phenyl)hexafluoropropane (BAPHF), bis(4-(4-ami-nophenoxy) phenyl)sulfone (BAPS), and 1,4-bis-(4-aminophenoxy)biphenyl (BABP) were prepared. The inherent viscosities of the poly(amic acid)s were between 0.39 and 0.50 dL/g. The poly(amic acid)s were converted to polyimide films by thermal imidization. The glass transition temperatures (T$\_$g/) of the polyimides were in the range of 201-263$\^{C}$. The thermogravimetric analysis (TGA) thermogram of these polyimides showed the temperatures of 5% weight losses between 375 and 393$\^{C}$ in nitrogen atmosphere. To show their utility for image generation, degradations of these polyimides in UV exposure were investigated by UV spectroscopy.

• 한국균학회지
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• 제27권4호통권91호
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• pp.304-311
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• 1999

영지버섯의 세포외 다당발효중 동력학적 특성을 기질(포도당, 전분), 기질농도$(1{\sim}7%)$ 및 계대배양(3회)의 함수로서 조사하였다. 영지버섯 균사체 증식은 logistic 모델이 Monod 모델 및 two- thirds power 모델과 비교하여 실험값에 잘 일치하였고, 기질 및 생성물은 Luedeking-Pirt 식에 의하여 잘 설명되었다. 또 다당 생성의 발효 기작은 증식연동형과 비증식 연동형이 함께 존재하는 혼합형이었으나 기질에 상관없이 비증식연동형 기작이 더 중요하였다. Glucose는 농도 증가에 따라 다당생성 및 기질소비의 기작이 증식연동형이 감소하고 비증식연동형이 증가하는 경향을 보였다. 그러나 starch를 사용하였을 경우는 glucose와는 달리, 기질소비의 증식연동형과 비증식연동형 기작이 모두 증가하여 높은 기질 이용성을 보였다. 아울러 starch배지에서는 glucose배지에서 보다 비증식속도의 증가와 계대배양시의 안정성을 보였다. 따라서 영지버섯의 배양시 starch배지는 비증식연동형에 의한 균체 생육 및 다당생성의 생합성 촉진에 의해 이들 생산성 및 계대배양시의 안정성을 증가시키는 것으로 생각되었다 최대의 균사체 생육 및 다당 생산은 각각 9.463 및 10.410 g/l로, 7% starch을 함유한 배지에서 $30^{\circ}C$로 7일간 진탕배양하였을 때 얻어졌다.

• 적정기술학회지
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• 제6권2호
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• pp.219-225
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• 2020

터치 장비와 스마트 러닝의 중요성이 높아짐에 따라 공공 기관 및 교육시설에서는 스마트 디바이스(smart device)를 업무 및 교육 환경에 적용하는 추세이다. 그러나 공공 스마트 디바이스 사용자들은 직·간접적 감염병 확산에 노출될 위험이 있다. 본 연구는 스마트 디바이스 사용자를 위해 손가락 끝을 감싸는 외골격 장치(Exo-finger)를 개발하였으며, 공용 장비에 활용 시 질병 예방 효과를 가지고자 한다. 활성화 재료인 카본 블랙(Carbon Black, CB)과 고분자 탄성중합체(elastomer)를 혼합한 2차 재료를 금형에 넣어 외골격 장치를 제작하였다. 이 장치는 CB 함량이 0.030 wt.% 이상일 때, 터치 기능이 있는 것으로 확인되었으며 탄성중합체의 함량을 변화시켜 사람이 스마트 디바이스를 터치할 때와 유사한 마찰력(마찰계수 2.5)를 가질 수 있도록 하였다. 실험을 통하여 CB의 함유량은 마찰 계수에 주는 영향이 거의 없음을 확인하였다. 완성된 시제품을 스마트 디바이스에 테스트한 결과, 개발된 외골격 장치는 보호 장구를 착용하여 터치가 불가능한 경우 또는 감염병 확산을 막기 위해 장갑 등의 장비를 사용하는 경우에 유용하게 활용할 수 있음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제35권12호
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• pp.3459-3464
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• 2014

Synthesis and structural characterization of mercury(II) halides and perchlorate complexes (1-4) of bis-$OS_2$-macrocycle (L) are reported. L reacts with mercury(II) chloride and bromide to yield an isostructural 2D coordination polymers with type $[Hg(L)X_2]_n$ (1: X = Cl and 2: X = Br). In 1, each Hg atom which lies outside the cavity is six-coordinate with a distorted octahedral geometry, being bound to four adjacent ligands via monodentate Hg-S bonds and two remaining sites are occupied by two terminal chlorido ligands to form a fishnet-like 2D structure. When reacting with mercury(II) iodide, L afforded a 1D coordination polymer $\{[Hg_2(L)I_4]{\cdot}CHCl_3\}_n$ (3) in which each exocyclic Hg atom is four-coordinate, being bound to two sulfur donors from different ligands doubly bridging the ligand molecules in a head-to-tail mode. The coordination sphere in 3 is completed by two iodo terminal ligands, adopting a distorted tetrahedral geometry. On reacting with mercury(II) perchlorate, L forms solvent-coordinated 1D coordination polymer $\{[Hg_2(L)(DMF)_6](ClO_4)_4{\cdot}2DMF\}_n$ (4) instead of the anion-coordination. In 4, the Hg atom is five-coordinate, being bound to two sulfur donors from two different ligands doubly bridging the ligand molecules in a side-by-side mode to form a ribbon-like 1D structure. The three remaining coordination sites in 4 are completed by three DMF molecules in a monodentate manner. Consequently, the different structures and connectivity patterns for the observed exocyclic coordination polymers depending on the anions used are influenced not only by the coordination ability of the anions but also by anion sizes.

• 한국물환경학회지
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• 제27권1호
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• pp.44-53
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• 2011

Membrane bio-reactor (MBR) has several advantages over the conventional activated sludge process, including a high biomass, low sludge production, and better permeate quality. Therefore, the MBR have gained popularity for municipal and industrial wastewater treatment. However the MBR usually were used for sewage and low streng th wastewater treatment because of membrane fouling problem and limitation of oxygen transfer into biomass. In this study, the hybrid process combining MBR and pure oxygen was tested for high strength organic wastewater treatment in the COD loading range from 2 to $10kgCOD/m^3{\cdot}day$. The hybrid process, membrane coupled pure oxygen high compact reactor (MPHCR), had been operated for one year and operation parameters, the effect of COD loading, MLSS concentration and the location of membrane module were studied for membrane fouling characteristic. Also membrane resistance test and the component of foulant was analyzed to investigate what is specific foulant in the MBR.