• 제목/요약/키워드: H-bonding

검색결과 895건 처리시간 0.029초

Modelling the Hydrogen-Bonding Interactions in a Copolymer/Biodegradable Homopolymer Blend through Excess Functions

  • Garcia-Lopera, Rosa;Monzo, Isidro S.;Campos, Agustin;Abad, Concepcion
    • Macromolecular Research
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    • 제16권5호
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    • pp.446-456
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    • 2008
  • A recent theoretical approach based on the coupling of both the Flory-Huggins (FH) and the Association Equilibria thermodynamic (AET) theories was modified and adapted to study the miscibility properties of a multi-component system formed by two polymers (a proton-donor and a proton-acceptor) and a proton-acceptor solvent, named copolymer(A)/solvent(B)/polymer(C). Compatibility between polymers was mainly attained by hydrogen-bonding between the hydroxyl group on the phenol unit of the poly(styrene-co-vinyl phenol) (PSVPh) and the carbonyl group of the biodegradable and environmentally friendly poly(3-hydroxybutyrate) (PHB). However, the self-association of PSVPh and specific interactions between the PSVPh and the H-acceptor group (an ether oxygen atom) of the epichlorohydrin (ECH) solvent were also established in a lower extension, which competed with the polymer-polymer association. All the binary specific interactions and their dependence with the system composition as well as with the copolymer content were evaluated and quantified by means of two excess functions of the Gibbs tree energy, ${\Delta}g_{AB}$ and ${\Delta}g_{AC}$. Experimental results from fluorescence spectroscopy were consistent with the theoretical simulations derived with the model, which could also be applied and extended to predict the miscibility in solution of any polymer blend with specific interactions.

폴리실라잔계 실란트를 이용한 정전척 실링특성 향상 연구 (Improvement of Sealing Property of Electrostatic Chuck by Applying Polysilazane Sealant)

  • 최재영;박현수;손민규;정창오;김우병
    • 한국표면공학회지
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    • 제49권6호
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    • pp.567-574
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    • 2016
  • We have analyzed chemical properties of polysiloxane and polysilazane films, respectively, as sealing materials for electrostatic chuck (ESC) and have investigated the possibility of polysilazane as an alternative sealant to polysiloxane. It has been revealed that Si-O with organic bonding ($Si-CH_3$) existed in polysiloxane films compared to only pure Si-O bonding in polysilazane films. The sealing property of polysilazane has been found outstanding even in a short time of application. In the polysiloxane films containing $H_2O$, pin holes have been found possibly due to $CO_2$ gas evolution, and low adhesion with Si substrate has been observed after heat stress test in connection with the existence of organic bonding. After acid resistance test in 0.5 vol.% HF, 68 wt.% $HNO_3$, and 37 wt.% HCl solution, polyilazane films have shown a longer survival times. Compared to the conventional polysiloxane sealant, polysilazane is expected as a new sealing material because of good thermal and chemical stability.

Fabrication of β-SiAlONs by a Reaction-Bonding Process Followed by Post-Sintering

  • Park, Young-Jo;Noh, Eun-Ah;Ko, Jae-Woong;Kim, Hai-Doo
    • 한국세라믹학회지
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    • 제46권5호
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    • pp.452-455
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    • 2009
  • A cost-effective route to synthesize $\beta$-SiAlONs from Si mixtures by reaction bonding followed by post-sintering was investigated. Three different z values, 0.45, 0.92 and 1.87, in $Si_{6-z}Al_zO_zN_{8-z}$ without excess liquid phase were selected to elucidate the mechanism of SiAlON formation and densification. For RBSN (reaction-bonded silicon nitride) specimens prior to post-sintering, nitridation rates of more than 90% were achieved by multistep heating to $1400^{\circ}C$ in flowing 5%$H_2$/95%$N_2$; residual Si was not detected by XRD analysis. An increase in density was acquired with increasing z values in post-sintered specimens, and this tendency was explained by the presence of higher amounts of transient liquid phase at larger z values. Measured z values from the synthesized $\beta$-SiAlONs were similar to the values calculated for the starting compositions. Slight deviations in z values between measurements and calculations were rationalized by a reasonable application of the characteristics of the nitriding and post-sintering processes.

α-Al2O3와 Ni 금속 접합을 위한 Ni 무전해 도금시 산처리의 영향 (The Effect of Acid Treatment Time for Ni Plating on the Joint of α-Al2O3 and Ni Metal)

  • 이은정;안용태;최병현;지미정;황해진
    • 한국수소및신에너지학회논문집
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    • 제27권3호
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    • pp.306-310
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    • 2016
  • In Na-base Battery for ESS, ${\alpha}-Al_2O_3$ and metal bonding was used to prevent direct reaction between electrolyte and electrode. The hard metal was metalized at $1600^{\circ}C$ in a flowing hydrogen gas for high bonding strength. In this study, instead of hard metal metalizing, Ni was plated on ${\alpha}-Al_2O_3$ by electroless Ni plating technique and then bonded with metal. To enhance the bonding strength, surface of ${\alpha}-Al_2O_3$ was treated with $H_3PO_4$. The effects of strength and leakage of joining as a function of acid treatment time on ${\alpha}-Al_2O_3$ are described.

HA 코팅된 스테인레스강과 뼈의 계면에서의 경조직 성장 및 결합력 향상 (Bone Ingrowth and Enhancement of Bone Bonding Strength at Interface between Bone and HA Coated Stainless Steel)

  • 김철생;김상윤;김동헌;강곤
    • 대한의용생체공학회:학술대회논문집
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    • 대한의용생체공학회 1996년도 춘계학술대회
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    • pp.133-136
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    • 1996
  • We investigated how hydroxyapatite (HA) coating onto a porous super stainless steel (S.S.S, 22Cr-20Ni-6Mo-0.25N) affects bone ingrowth in a dog transcortical femoral model. Implants were histologically evaluated after 4 and 48 weeks of implantation, and the bone bonding strength at the bone/implant interface was examined by employing the pull-out test. The direct osseous tissue bonding onto the HA-coated S.S.S was observed, but the uncoated stainless steels had thin fibrous tissue layers. The mean interface strength of the HA-coated S.S.S was 1.5 and 2.5 times greater than those of the S.S.S and the 316L SS after one year of implantation, respectively. In preliminary studies, no toxic responce was observed from a cytotoxicity test of the S.S.S, having similar corrosion resistance to titanium. Our results suggest that early osteoconductive nature of HA coating may induce long term osteointegration for a bioinert substrate.

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접합유리와 반응된 Fe-Hf-N 박막의 연자기 특성 (Soft Magnetic Properties of Fe-Hf-N Films Reacted with Bonding Glass)

  • 김경남;김병호;제해준
    • 한국자기학회지
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    • 제13권1호
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    • pp.6-14
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    • 2003
  • 열처리 온도에 따라 접합유리와의 화학적 반응이 Fe-Hf-N/SiO$_2$, 및 Fe-Hf-N/Cr/SiO$_2$ 박막의 물리적, 자기적 특성에 미치는 영향을 고찰하였다. 접합유리와 반응된 Fe-Hf-N/SiO$_2$ 박막의 연자기 특설은 온도가 증가함에 따라 크게 떨어졌으며, $600^{\circ}C$에서 포화자화값은 1 kG, 보자력이 27 Oe, 10MHz에서의 유효투자율이 70로 자기적 특성이 급격히 열화되었다. 이는 접합유리와의 화학적 반응에 의해 Fe-Hf-N 박막이 H$_{f}$ O$_2$, Fe$_3$O$_4$ 등으로 산화되기 때문인 것으로 나타났다. Fe-Hf-N/Cr/SiO$_2$ 박막의 경우, $600^{\circ}C$에서 포화자화값 13.5kG, 보자력은 4Oe, 10 MHz에서의 유효 투자율이 700으로 Fe-Hf-N/SiO$_2$ 박막보다 연자기 특성 열화가 덜 일어났다. 이는 Fe-Hf-N/Cr/SiO$_2$ 박막의 Cr 층이 Fe-Hf-N 박막의 산화를 억제하여. 일부에서만 HfO$_2$가 생성되고 나머지는 원래의 $\alpha$-Fe상을 유지하기 때문인 것으로 나타났다.

사염화탄소 중에서 Thiopropionamide와 N,N-Dimethylalkylamide사이의 수소결합에 관한 분광학적 연구 (Near-IR Spectroscopic Studies of the Hydrogen Bonding Between Thiopropionamide and N,N-Dimethylalkylamide in Carbon Tetrachloride)

  • 김병철;윤창주;송규석;최영상
    • 대한화학회지
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    • 제33권2호
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    • pp.156-163
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    • 1989
  • 사염화탄소 용액중에서 thiopropionamide(TPA)와 N,N-dimethylalkylamides(DMF, DMA, DMP)간의 수소결합에 관한 열역학적 상수를 구하기 위하여 TPA의 근적외선 영역의 흡수띠 중에서 $ν_a+amide II$조합띠를 사용하여 5${\sim}$55$^{\circ}C$ 범위에서 실험하였다. TPA 단위체와 수소결합을 하고 있는 TPA의 혼합 흡수띠를 Lorentzian-Gaussian product function을 사용하여 개개의 띠로 분리하였다. 컴퓨터로 분해하여 얻은 개개의 흡수띠의 면적을 사용하여 단위체 및 1 : 1 복합체의 농도를 계산하였고 이로부터 평형상수를 구하였다. 열역학적 상수들은 온도의존 흡수띠를 분석하여 구하였다. TPA와 DMF, DMA 및 DMP간의 1 : 1 복합체의 ${\Delta}$$H^{\circ}$는 각각 -12.5, -13.5, -14.1kJ/mol이었고.${\Delta}$$S^{\circ}$는 각각 -15.2, -17.9, -22.3kJ/mol${\cdot}$deg이었다.

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$CCl_4$속에서 Thioamides 와 Dimethyl Sulfoxide (DMSO) 사이의 수소 결합에 대한 연구 (Hydrogen Bonding between Thioamides and Dimethylsulfoxide (DMSO) in $CCl_4$)

  • 도영락;김선진;윤창주;최영상
    • 대한화학회지
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    • 제36권2호
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    • pp.185-190
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    • 1992
  • 사염화탄소 속에서 대단히 묽은 티오아미드 및 티오아미드-DMSO 용액의 $ν_{\alpha}$ + Amide II 조합띠에 대한 근적외선 스펙트럼을 $5^{\circ}C$$55^{\circ}C$ 사이에서 얻었다. 이 조합띠는 두 개의 Lorentzian-Gaussian product 함수로 분해되며, 각각은 단체 티오아미드 및 1 : 1 티오아미드-DMSO 복합체로 확인되었다. 티오아세트아미드(TA)와 DMSO 사이의 수소결합은 티오프로피온 아미드(TPA)와 DMSO 사이의 수소결합보다 약간 강하며 $CCl_4$ 속에서 TA-DMSO와 TPA-DMSO 1: 1 복합체에 대한 ${\Delta}H^{\circ}$는 각각 -15.3 kJ${\cdot}$$mol^{-1}$ 및 -14.2 kj${\cdot}$$mol^{-1}$이었다.

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