• 펄프종이기술
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• 제46권6호
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• pp.50-55
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• 2014

An oxidized starch was modified for surface sizing via etherification and esterification. Propylene oxide (PO), sodium monochloroacetate (SMCA), and acrylonitrile (AN) were used as etherification, and vinyl acetate monomer (VAM), maleic anhydride (MA), fumaric acid (FA), and itaconic acid (ITA) were used for esterification. Esterification and etherification of starch decreased both Brookfield viscosity and Brabender viscosity substantially even though the solids level was increased by 2% from 14 to 16%. Surface sizing performance of starches in tensile strength, stiffness and compressive strength was improved by esterification and etherification of the oxidized starch. Especially, SMCA etherification was found to be the most effective modification method.

• 약학회지
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• 제46권5호
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• pp.337-342
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• 2002

Propofol(2,6-diisopropyl phenol) is a phenol derivative that is chemically distinct from other intravenous sedative hypnotics. It has been extensively used as a short term anesthetic agent, because of the rapid onset and short duration of action. Propofol microemulsion system was prepared with different concentrations of ethyl oleate, $Solutol^{(R)}$ HS 15 and $Kollidon^{(R)}$ 17 PF. Propofol microemulsions were studied by transmittance, viscosity, particle size, in vitro release and pharmacokinetics. The range of transmittance of A group with 4% ethyl oleate and that of B group with 5% ethyl oleate were 92.6~95.1 and 91.3~94.2%, respectively. Transmittance 1~2% decreased as concentration of $Kollidon^{(R)}$ 17 PF was increased and increased 0.8~3.3% when 10 times diluted with normal saline. The viscosity of A and B group were in the range of 3.9~4.1 mPaㆍsec and 4.4~5.3 mPaㆍsec, respectively. The particle sizes of A and B group increased as amount of $Kollidon^{(R)}$ 17 PF. Also, release of propofol was slowly increased as the amount of $Kollidon^{(R)}$ 17 PF was increased. Propofol plasma concentration by i.v injection showed 2-compartment model. Pharmacokinetics of A-5 was similar to that of commercial emuision(POFOL).

• ETRI Journal
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• 제38권6호
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• pp.1179-1189
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• 2016

A chemorheological analysis of a no-flow underfill was conducted using curing kinetics through isothermal and dynamic differential scanning calorimetry, viscosity measurement, and solder (Sn/27In/54Bi, melting temperature of $86^{\circ}C$) wetting observations. The analysis used an epoxy system with an anhydride curing agent and carboxyl fluxing capability to remove oxide on the surface of a metal filler. A curing kinetic of the no-flow underfill with a processing temperature of $130^{\circ}C$ was successfully completed using phenomenological models such as autocatalytic and nth-order models. Temperature-dependent kinetic parameters were identified within a temperature range of $125^{\circ}C$ to $135^{\circ}C$. The phenomenon of solder wetting was visually observed using an optical microscope, and the conversion and viscosity at the moment of solder wetting were quantitatively investigated. It is expected that the curing kinetics and rheological property of a no-flow underfill can be adopted in arbitrary processing applications.

• Archives of Pharmacal Research
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• 제14권4호
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• pp.298-304
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• 1991

Isoprinosine, an antiviral agent with a bitter taste, has been clinically used up to a maximum of 4 g daily in 4-8 doses. In this investigation, isoprinosine was microencapsulated with ethylcellulose 22 cps, 50 cps and 100 cps by means of polymer deposition from cyclohexane through temperature change. Complete removal of cyclohexane from the microcapsules was necessary, since ethylcellulose-coated microcapsules obtained from cyclohexane medium were heavily solvated with cyclohexane and formed lumps even after drying. The displacement of cyclohexane by n-hexane during isolation of microcapsules (Method III) or the freezing of the anal-washed microcapsules before drying (Mothod II) provided the dried products which were more discrete microcapsules than those which were simply dried in the air overnight (Method I). Method III was especially the most effective procedure in preparing finer and more discrete microcapsules. The drug-release from microcapsules was influenced by the ratio of core to wall, the viscosity grade of ethylcellulose and the overall microcapsule size. The release rate was adequately fitted to both the first-order and the diffusion-controlled processes. It is therefore possible to design the release-controlled microcapsules with ethylcellulose of different viscosity along with various core to wall ratio.

• 한국건축시공학회:학술대회논문집
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• 한국건축시공학회 2009년도 춘계 학술논문 발표대회 학계
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• pp.213-217
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• 2009

Underground structures are built into concrete like a architecture and public works. Concrete has watertightness as such, But buildings are leaking from the cracks. Recently, construction method do a lot of close construction in the downtown area. So architects are using the method for the outer layer of a two-layer wall to save spaces. They have been using Top-down method and waterproof agent method and others to outer layer of a two-layer wall method. But, There are many leakage in underground structure from lack on requirements performance of materials. Therefore, I hope to test the outside Waterproof Method of Ground using Wire-mesh and Non-hardening Viscosity Waterproof. In addition to, I wish to apply as outside waterproof method for the section for the outer layer of a two-layer wall in underground structure.

• 한국세라믹학회지
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• 제37권7호
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• pp.693-699
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• 2000

Casting behavior of Zr(Y,Ce)O2 TZP/Mullite suspension during pressure filtration was investigated to prepare multi-layered Functionally Gradient Materials(FGM). The dispersion stabilities of each layer suspension were investigated by examination of zeta potential and viscosity. The each suspensions with 20 vol.% solid loading and 100 첸 of viscosity was prepared after fix of the dispersing agent (Sodium hexa-meta phosphate) and the binder (Hydroxyethyl cellulose), and then the cakes were formed at the 2.5 MPa~10.0MPa pressure range. The cake thickness of all suspensions was increased with the square root of time at the constant pressure, and the relations between filtration pressure(P)a nd dehydration rate (Q=dh/dt) showed that the flows of filtrates in the consolidated layers were laminar. The permeabilities were nearly constant during filtration, and kozeny constants(Kc) of the suspensions were 4.8~6.7. These valumes were seen as close to 5, which might be homogeneous particle packing during filtration. On the basis of those data, the multi layered compaction with 9 mm thickness and 52.5% green density was prepared by continuous pressure filtration.

• 폴리머
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• 제24권3호
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• pp.342-349
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• 2000

아이소탁틱 폴리프로필렌과 대두유 시스템으로부터 열유도 상분리 및 연신공정에 의하여 중공사막을 제조하였다. 막의 구조와 성능에 관계되는 각종 조업변수들의 영향을 조사하였고 이들을 최적화하였다. 폴리프로필렌/대두유의 용융점도가 microfibril 형성에 영향을 미침을 확인하였고 기핵제를 첨가함에 따라 핵생성 밀도가 증가하여 연신에 의한 구정 간의 기공형성이 향상되었다. 막을 열처리함으로써 연신 시 유도되었던 stress를 이완시켜 막의 수축현상을 방지하여 다공도를 유지할 수 있었다. 기핵제를 첨가한 경우 고-액 상분리에 의하여 구조가 형성되며 응고조의 온도 변화에 따라 핵 생성 밀도가 변화하게 되고 이에 따라 연신에 의한 기공 형성이 영향을 받게 되었다. 기핵제를 첨가하지 않은 경우 핵 생성이 활발하지 않아서 주로 액-액 상분리 거동이 구조 형성에 영향을 미치게 되며 응고조 온도 변화에 따른 효과가 기핵제를 넣은 경우와는 반대의 경향을 나타내었다.

• 폴리머
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• 제36권1호
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• pp.29-33
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• 2012

관능성 단량체로서 acrylic acid(AA)를 사용하였고, 기본 단량체로서는 2-ethylhexyl acrylate(2-EHA)를 사용하여 용액중합의 방법으로 점착제를 합성하였다. 점착제의 점착물성 중에 AA와 경화제 함량에 따른 점착제의 표면에너지와 물성변화 연구를 조사하였다. 합성된 점착제의 구조는 FTIR을 통하여 확인하였고 점도와 분자량은 Brookfield 점도계와 GPC를 사용하여 각각 측정하였다. 분자량과 점도는 AA가 6 wt%까지는 함량증가에 따라 증가하였으며 6 wt% 이상에서는 감소하였다. 이러한 경향은 표면에너지 역시 AA 함량증가에 따라 COOH 그룹에 의한 극성 강화로 표면에너지는 증가하였다. 반면, 점착력은 분자량과 반비례 관계를 보였으며 AA 함량과 경화제 함량 증가에 따라 감소하는 경향을 나타내었다.

• 한국식품영양학회지
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• 제11권1호
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• pp.99-106
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• 1998

Russia 연안에서 채취한 홍조류인 Tichocarpus crinitus로부터 열수 추출한 KC1-insoluble carrageenan의 수율은 17.1%, KC1-soluble carrageenan의 수율은 3.52%였다. KC1-insoluble carrageenan의 경우 total sulfate 18.06%, protein 5.61%, K+ 3.51%, Na+0.49%, Ca2+ 1.66%, galactose 54.26%, xylose 4.68%, glucose, mannose가 소량(0.1%미만) 검출되었다. FT-IR spectroscopy 측정 결과 KC1-insoluble carrageenan은 $ extsc{k}$-carrageenan으로, KC1-soluble carrageenan은 λ-carrageenan이 주를 이루는 λ,$ au$ 혼합형 carrageenan으로 나타났다. KC1-insoluble carrageenan과 KC1-soluble carrageenan 수용액의 점도는 열 안정성 측정 결과 두 가지 획분 모두 9$0^{\circ}C$에서 1시간 정도까지도 안정한 것으로 나타났다. KC1-insoluble carrageenan의 경우는 K+ 첨가에 의하여 두 배 정도까지의 점도 증가를 나타내었으나 Ca2+ 첨가에 의한 경우와 KC1-soluble carrageenan에 대하여 K+ 및 Ca2+을 첨가한 경우 모두 점도에 영향을 미치지 않았다. 산, 알칼리에 대한 안정성을 조사한 결과 두 가지 시료 모두 알칼리 존재에서는 안정하나 산의 존재에서는 급격한 안정성의 저하를 나타내었다. 이와 같은 결과로 볼 때 Tichocarpus crinitus로부터 열수 추출한 $textsc{k}$-carrageenan으로 판단되는 KC1-insoluble carrageenan은 KC1-soluble carrageenan과 함께 식품첨가물로 이용시 겔화제보다는 점도 증진제로의 이용이 기대된다.

• 대한소아치과학회지
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• 제24권2호
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• pp.460-474
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• 1997

The purpose of this study was to evaluate and compare the effectiveness of various low-viscosity resin systems used as rebonding agents to prevent microleakage at the margins of class I composite resin restorations. Seventy sound human premolars were selected for experiment. Class I cavities were prepared and each cavity was conditioned with a 37% phosphoric acid for 15 sec, rinsed with water for 15 sec, and dried with compressed air. Bonding agent(Scotchbond Multipurpose, 3M Co.) was applied and a hybrid composite resin (Z-100, 3M Co.) was placed using an incremental technic. The excess cured composite resin was carefully removed with Sof-Lex discs(3M Co.) to expose the original margins of the cavity. The following seven groups were established : group 1 was not rebonded and used as control group ; group 2 was rebonded with a Scotchbond Multipurpose(3M Co.) and finished ; group 3 was rebonded with a Fortify(BISCO) and finished ; group 4 was rebonded with a Concise white sealant(3M Co.) and finished ; group 5 was rebonded with a Concise white sealant(3M Co.) and not finished ; group 6 was rebonded with a P&F sealant(BISCO) and finished; group 7 was rebonded with a P&F sealant(BISCO) and not finished. The specimens were then subjected to 500 thermocycles between 5 & 65 with a 10 see dwell time and immersed in 2% methylene blue dye solution for 24 hours and sectioned with low-speed diamond cutter into two part under water condition. The extent of microleakage at rebonded margins was evaluated microscopically and scored for dye penetration according to the following scale : 0=no dye penetration ; 1=dye penetration to half-way along axial wall between enamel surface and DEJ ; 2=dye penetration beyond halfway along axial wall between enamel surface and DEJ ; 3=dye penetration to the full depth of DEJ or beyond DEJ. Selected samples were prepared for SEM observation to determine the depth of penetration of the rebonding agent into the marginal interface. The obtained results were as follows: 1. In the group 2 and 3, which is rebonded with a Scotchbond Multipupose and Fortify, dye penetration score were decreased significantly than that of group 1 (P<0.05), but group 4 and 6 were not statistically different from group 1(P>0.05). 2. There were significant differences between group 4, 6 and group 5, 7 when compared by dye penetration score (P<0.05). 3. In the SEM observation, Scotchbond Multipurpose and Fortify were penetrated within $30-40{\mu}m$ depth of the outermost surface. However, both sealants were failed to penetrate into the debonded interface.