• 제목/요약/키워드: water contact angle

검색결과 692건 처리시간 0.028초

The Influence of Hydrotalcite Intercalated with Benzoate on UV Stability of Acrylic Coating

  • Nguyen, Thuy Duong;Nguyen, Anh Son;Thai, Thu Thuy;Pham, Gia Vu;To, Thi Xuan Hang;Olivier, Marie-Georges
    • Corrosion Science and Technology
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    • 제19권1호
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    • pp.16-22
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    • 2020
  • It is important to realize that benzoate was intercalated into hydrotalcite (HTC-Bz) by the co-precipitation method. In this case, acrylic coating with 0.5 wt% HTC-Bz was deposited on carbon steel using the spin coating method. Next, the HTC-Bz structure was characterized by Field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). In fact, an ultraviolet vision spectroscopy (UV-Vis) was used to determine the benzoate content in HTC-Bz, and the UV absorption ability of HTC-Bz. Using electrochemical techniques, water contact angle measurement, and thermal-gravimetric analysis, we compared the protective properties before and after QUV test, hydrophobicity and the thermal stability of acrylic coating containing HTC-Bz. The obtained results showed that HTC-Bz with a plate-like structure was successfully synthesized; benzoate was intercalated into the interlayer of hydrotalcite with a concentration of 28 wt%. Additionally, it was noted that HTC-Bz has an UV absorption peak at 225 nm. In conclusion, the addition of HTC-Bz enhanced the UV stability, hydrophobicity and the thermal stability of acrylic coating.

두 용매에서의 폴리스타이렌의 용해도 차이를 이용한 초소수성 표면 제조 (Fabrication of Super-hydrophobic Surface using Solubility Difference of Polystyrene at Two Different Solvents)

  • 정진석;박광배;최호석
    • 청정기술
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    • 제14권1호
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    • pp.35-39
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    • 2008
  • 본 연구에서는 용매에 따른 고분자의 용해도 차이를 이용하여 슬라이드글라스 표면위에 초소수성 고분자막을 성공적으로 제조하였다. 폴리스타이렌 (PS)을 tetrahydrofuran (THF)에 녹인 후 다시 에탄올(EtOH)을 첨가하여 두 용매의 용해도 차이로 표면에 초소수성 성질을 갖게 제조하였다. 한편, EtOH 첨가, 코팅방법, 용액혼합 시간과 속도 및 다른 알콜들이 형성된 표면의 소수성에 미치는 영향들을 각각 조사하였다. 접촉 각 측정기를 사용하여 측정한 결과 $150^{\circ}$ 이상의 물 접촉각을 확인하였고, 광학현미경(optical microscopy)과 주사전자현미경(scanning electron microscope, SEM)으로 관찰한 표면 구조는 $5\;{\mu}m$ 이하의 입자들로 구성된 미세다공성 구조임이 확인되었다.

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Efficacy of various cleaning solutions on saliva-contaminated zirconia for improved resin bonding

  • Kim, Da-Hye;Son, Jun-Sik;Jeong, Seong-Hwa;Kim, Young-Kyung;Kim, Kyo-Han;Kwon, Tae-Yub
    • The Journal of Advanced Prosthodontics
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    • 제7권2호
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    • pp.85-92
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    • 2015
  • PURPOSE. This study aimed to investigate the efficacy of cleaning solutions on saliva-contaminated zirconia in comparison to air-abrasion in terms of resin bonding. MATERIALS AND METHODS. For saliva-contaminated air-abraded zirconia, seven cleaning methods)-no contamination (NC), water-spray rinsing (WS), additional air-abrasion (AA), and cleaning with four solutions (Ivoclean [IC]; 1.0 wt% sodium dodecyl sulfate [SDS], 1.0 wt% hydrogen peroxide [HP], and 1.0 wt% sodium hypochlorite [SHC])-were tested. The zirconia surfaces for each group were characterized using various analytical techniques. Three bonded resin (Panavia F 2.0) cylinders (bonding area: $4.5mm^2$) were made on one zirconia disk specimen using the Ultradent jig method [four disks (12 cylinders)/group; a total of 28 disks]. After 5,000 thermocycling, all specimens were subjected to a shear bond strength test with a crosshead speed of 1.0 mm/minute. The fractured surfaces were observed using an optical and scanning electron microscope (SEM). RESULTS. Contact angle measurements showed that groups NC, AA, IC, and SHC had hydrophilic surfaces. The X-ray photoelectron spectroscopy (XPS) analysis showed similar elemental distributions between group AA and groups IC and SHC. Groups IC and SHC showed statistically similar bond strengths to groups NC and AA (P>.05), but not groups SDS and HP (P<.05). For groups WS, SDS, and HP, blister-like bubble formations were observed on the surfaces under SEM. CONCLUSION. Within the limitations of this in vitro study, some of the cleaning solutions (IC or SHC) were effective in removing saliva contamination and enhancing the resin bond strength.

다공성 탄소전극기지상의 무전해 니켈도금에 관한 연구 (Electroless Nickel Plating on Porous Carbon Substrate)

  • 천소영;임영목;김두현;이재호
    • 마이크로전자및패키징학회지
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    • 제17권1호
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    • pp.75-80
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    • 2010
  • 다공성 탄소전극기지 위의 무전해 니켈도금에 관한 연구를 하였다. 다공성 탄소전극기지로는 다공도가 20 ${\mu}m$ 이상인 것과 16~20 ${\mu}m$ 인 것을 사용하였다. 소수성인 탄소 표면은 $60^{\circ}C$ 이상의 암모니아 용액에 침적함으로써 그 표면 성질이 친수성으로 변화 되었고, 40분 이상 침적 시 접촉각이 $20^{\circ}$ 이하까지 측정 되었다. 도금욕의 pH가 증가됨에 따라 탄소기지 위에 도금된 니켈 도금층의 인의 석출량은 감소하였으며 니켈 도금층이 결정질 구조를 갖는 현상이 관찰되었다. 도금층의 두께는 pH가 증가함에 따라 증가하였다. 활성화 처리를 위한 $PdCl_2$의 농도에 따른 도금층의 두께 변화는 없었으나, 도금에 필요한 $PdCl_2$의 최소농도는 5 ppm 이상인 것으로 나타났다.

양모.폴리에스터 혼방직물의 효소가공 시 활성제 복합사용의 효과 (Effects of Mixed Activators on Enzymatic Activation for Wool.polyester Blend Fabrics)

  • 송현주;송화순
    • 한국의류학회지
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    • 제32권9호
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    • pp.1461-1466
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    • 2008
  • This study provides effects of mixed activators on enzymatic activation and determines optimum mixture ratio for enzymatic treatment. Wool 80% and polyester 20% blend fabric and papain from carica papaya are used in this experiment. L-cysteine and sodium sulfite are used as activators for papain treatment process. The treatment condition is pH 7.5, $70^{\circ}$, papain concentration 10%(o.w.f), 60 minutes. L-cysteine and sodium sulfite are added in enzyme solution with various concentrations($0{\sim}50mM$). The optimum treatment condition is determined by measuring weight loss, tensile strength, whiteness, water contact angle(WCA), dyeability and surface micrographs. The results are as follow; The optimum mixture ratio of activators is L-cysteine 2mM and sodium sulfite 10mM. Mixed activators assists in improving the activation of papain. WCA of papain treated fabrics is decreased since papain treatment with activator mixture makes wool polyester blend fabrics more hydrophilic. Dyeing property of papain-treated fabrics more improves by the treatment with mixed activators than with single activator. It means that this method can save time and lower cost. After papain treatment in the presence of mixed activator, the surface of fabrics is modified. The surface of wool fiber shows to be descaled and hydrolyzed, and that of polyester fiber shows to be cracked.

다공성 탄소전극상 무전해 니켈도금의 산성과 알칼리용액 비교 연구 (Comparison of Acidic and Alkaline Bath in Electroless Nickel Plating on Porous Carbon Substrate)

  • 천소영;강인석;임영목;김두현;이재호
    • 한국표면공학회지
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    • 제43권2호
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    • pp.105-110
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    • 2010
  • Electroless nickel plating on porous carbon substrate for the application of MCFC electrodes was investigated. Acidic and alkaline bath were used for the electroless nickel plating. The pore sizes of carbon substrates were 16-20 ${\mu}m$ and over 20 ${\mu}m$. The carbon surface was changed from hydrophobic to hydrophilic after immersing the substrate in an ammonia solution for 40 min at $60^{\circ}C$. The contact angle of water was decreased from $85^{\circ}C$ to less than $20^{\circ}$ after ammonia pretreatment. The deposition rate in the alkaline bath was higher than that in the acidic bath. The deposition rate was increased with increasing pH in both acidic and alkaline bath. The content of phosphorous in nickel deposit was decreased with increasing pH in both acidic and alkaline bath. The contents of phosphorous is low in alkaline bath. The minimum concentration of $PdCl_2$ for the electroless nickel plating was 10 ppm in alkaline bath and 5 ppm in acidic bath. The thickness of nickel was not affected by the concentration of $PdCl_2$.

시스틴으로 화학흡착된 금 코팅 니티놀 표면에 앙쪽성 이온 폴리에틸렌글리콜의 그래프트 및 특성 평가 (Grafting and Characterization of Zwitter Ionic Poly(ethylene glycol) on Gold-Coated Nitinol Surface Chemisorbed with L-Cysteine)

  • 신홍섭;박귀덕;김재진;김지흥;한동근
    • 폴리머
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    • 제33권1호
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    • pp.84-90
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    • 2009
  • 니티놀(Nitinol) 합금(TiNi)은 혈관 스텐트로서 널리 사용되고 있다. 본 연구에서는 니티놀 합금의 혈액적 합성을 개선시키기 위해서 화학적인 표면개질을 행하였다. 먼저 니티놀의 표면을 금으로 코팅한 다음 시스턴(L-cysteine, C/N)을 화학흡착한 후 신규 합성한 양쪽성 이온 폴리에틸렌글리콜(PEG) (PEG-$N^+-SO_3{^-}$)을 그래프트 시켜서 TiNi-C/N-PEG-N-S를 제조하였다. 양쪽성 이온 PEG가 그래프트된 니티놀의 표면은 ATR-FTIR, ESCA 및 SEM을 통해서 확인하였고 친수성 표면은 물 접촉각의 감소를 통해서 입증하였다. 또한, 단백질 흡착 및 혈소판 점착과 혈액응고시간 측정과 같은 혈액적합성 평가 결과로부터 미처리 니티놀 합금에 비해서 표면개질된 니티놀 합금이 상대적으로 훨씬 우수한 혈액적합성을 나타내었다. 이는 그래프트된 친수성 PEG와 항응혈성 양쪽성 이온의 상승효과에 의해서 혈액적합성을 대폭 개선시킨 것으로 사료된다.

다공성 고분자 분리막의 임계투과압력 (Critical Breakthrough Pressure through Porous Polymer Membrane)

  • 이용택;전현수;안효성;이영진;송인호;이형근
    • 멤브레인
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    • 제16권4호
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    • pp.259-267
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    • 2006
  • 다공성 폴리비닐리덴플루오라이드(PVDF, polyvinylidenefluoride) 그리고 폴리테트라플루오르에틸렌(PTFE, Polytetrafluoroethylene)에 대하여 순수한 물, $0.1M{\sim}4.0M$ NaOH 수용액, 그리고 $0.1M{\sim}3.0M\;NaHSO_3$ 수용액을 사용하여 임계투과압력을 측정하였다. 임계투과압력은 동일한 평균 기공 크기의 PVDF보다 PTFE가 크게 나타남을 관찰할 수 있었다. NaOH 수용액의 경우 NaOH의 농도 증가에 따라 임계투과압력은 감소하였으며 1.0 M 농도에서 최소값을 나타낸 후 다시 증가함을 확인하였다. 그러나 NaOH이 아닌 다른 염을 용해한 수용액인 $NaHSO_3$ 수용액의 경우 농도를 3.0 M까지 증가하여도 임계투과압력이 계속 감소함을 알 수 있었다. 이와 같은 현상을 이론적인 Cantor식으로 해석할 수 있었다.

Polyetherimide 접착제의 표면 처리에 따른 MCM-D 계면 접착력 및 고온고습 신뢰성 변화에 관한 연구 (A Study on the Effect of Polyetherimide Surface Treatment on the Adhesion and High Temperature/High Humidity Reliability of MCM-D Interface)

  • 윤현국;고형수;백경욱
    • 한국재료학회지
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    • 제9권12호
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    • pp.1176-1180
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    • 1999
  • Polyetherimide와 실리콘 사이의 RIE 처리 및 알루미늄 킬레이트 계열의 adhesion promoter 처리에 따른 접착력과 고온고습환경에서의 신뢰성 변화를 연구하였다. 실험 방법으로는 180$^{\circ}$ 필 테스트 및 <85$^{\circ}C$ 85%> 테스트, SEM, AFM, 증류수 접촉각 실험이 수행되었다. $^O_2$ RIE 실험 결과 초기 접착력은 RIE 처리시간에 따라 약간의 변화를 가져왔으나 고온고습 환경에서의 저항성은 급격히 떨어지는 것이 관찰되었고 이것은 표면 거칠기의 영향이 아닌 표면의 친수성 정도에 따른 것으로 나타났다. Al-chelate adhesion promoter의 경우 초기 접착력에는 변화가 없으나 고온 고습환경에서의 저항성이 크게 증가하였는데 이것은 표면이 소수성으로 변한 데 따른 것으로 나타났다.

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Surface Modification and Fibrovascular Ingrowth of Porous Polyethylene Anophthalmic Implants

  • Yang, Hee-Seok;Park, Kwi-Deok;Son, Jun-Sik;Kim, Jae-Jin;Han, Dong-Keun;Park, Byung-Woo;Baek, Se-Hyun
    • Macromolecular Research
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    • 제15권3호
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    • pp.256-262
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    • 2007
  • The purpose of this study was to determine the effect of surface modification on the fibrovascular ingrowth into porous polyethylene (PE) spheres ($Medpor^{(R)}$), which are used as an anophthalmic socket implant material. To make the inert, hydrophobic PE surface hydrophilic, nonporous PE film and porous PE spheres were subjected to plasma treatment and in situ acrylic acid (AA) grafting followed by the immobilization of arginine-glycine-aspartic acid (RGD) peptide. The surface-modified PE was evaluated by performing surface analyses and tested for fibroblast adhesion and proliferation in vitro. In addition, the porous PE implants were inserted for up to 3 weeks in the abdominal area of rabbits and, after their retrieval, the level of fibrovascular ingrowth within the implants was assessed in vivo. As compared to the unmodified PE control, a significant increase in the hydrophilicity of both the AA-grafted (PE-g-PAA) and RGD-immobilized PE (PE-g-RGD) was observed by the measurement of the water contact angle. The cell adhesion at 72 h was most notable in the PE-g-RGD, followed by the PE-g-PAA and PE control. There was no significant difference between the two modified surfaces. When the cross-sectional area of tissue ingrowth in vivo was evaluated, the area of fibrovascularization was the largest with PE-g-RGD. The results of immunostaining of CD31, which is indicative of the degree of vascularization, showed that the RGD-immobilized surface could elicit more widespread fibrovascularization within the porous PE implants. This work demonstrates that the present surface modifications, viz. hydrophilic AA grafting and RGD peptide immobilization, can be very effective in inducing fibrovascular ingrowth into porous PE implants.