scholarly journals Simple Preparation of Polydimethylsiloxane and Polyurethane Blend Film for Marine Antibiofouling Application

Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2242
Author(s):  
Jirasuta Chungprempree ◽  
Sutep Charoenpongpool ◽  
Jitima Preechawong ◽  
Nithi Atthi ◽  
Manit Nithitanakul
Keyword(s):  
Contact Angle ◽  
Polymer Film ◽  
Water Contact Angle ◽  
Bonding Strength ◽  
Soft Lithography ◽  
Water Contact ◽  
Pdms Film ◽  
Lithography Process ◽  
Micro Patterning ◽  
Marine Industry

A key way to prevent undesirable fouling of any structure in the marine environment, without harming any microorganisms, is to use a polymer film with high hydrophobicity. The polymer film, which was simply prepared from a blend of hydrophobic polydimethylsiloxane elastomer and hydrophilic polyurethane, showed improved properties and economic viability for antifouling film for the marine industry. The field emission scanning electron microscope and energy dispersive X-ray spectrometer (FESEM and EDX) results from the polymer blend suggested a homogenous morphology and good distribution of the polyurethane disperse phase. The PDMS:PU blend (95:5) film gave a water contact angle of 103.4° ± 3.8° and the PDMS film gave a water contact angle of 109.5° ± 4.2°. Moreover, the PDMS:PU blend (95:5) film could also be modified with surface patterning by using soft lithography process to further increase the hydrophobicity. It was found that PDMS:PU blend (95:5) film with micro patterning from soft lithography process increased the contact angle to 128.8° ± 1.6°. The results from a field test in the Gulf of Thailand illustrated that the bonding strength between the barnacles and the PDMS:PU blend (95:5) film (0.07 MPa) were lower than the bonding strength between the barnacles and the carbon steel (1.16 MPa). The barnacles on the PDMS:PU blend (95:5) film were more easily removed from the surface. This indicated that the PDMS:PU blend (95:5) exhibited excellent antifouling properties and the results indicated that the PDMS:PU blend (95:5) film with micro patterning surface could be employed for antifouling application.

Research on the Formula of Polyaspartic Ester Polyurea Concrete Coating and its Application

2013 ◽  
Vol 423-426 ◽  
pp. 1159-1163 ◽  
Author(s):  
Jing Feng ◽  
Ling Min Liao ◽  
Liang Chen ◽  
Cheng Jing Xiao ◽  
Shan Feng Wang ◽  
...  
Keyword(s):  
Contact Angle ◽  
Crack Resistance ◽  
Water Contact Angle ◽  
Bonding Strength ◽  
Testing Machine ◽  
Weight Ratio ◽  
Hydrophobic Surface ◽  
Water Contact ◽  
North Water ◽  
Concrete Coating

Its of great importance to develop various outstanding protective concrete coating with favorable impermeability and crack-resistance properties. In this study, the polyaspartic ester polyurea was prepared, and its adhesion to concrete was evaluated by universal testing machine and SEM technology. The optimal formula of polyurea was obtained by investigating the effects of each component's content on the bonding strength to concrete and the water contact angle. Subsequently, the mechanical and surface properties of these polyurea coating were tested. The results showed that the polyurea was obtained by the following formula: the weight ratio of A1/A2/B was 0.612/ 0.408/ 1, and the fluoride filler content was 3%. The coating exhibited excellent mechanical properties, such as high bonding strength (4.5 MPa), sufficient tensile strength (16.4 MPa) and elongation at break (456%). Meanwhile, the coating showed a hydrophobic surface with its water contact angle of 105°. Hence, the polyurea coating is likely to improve the crack-resistance and impermeability properties of hydraulic concrete. Till now, the polyurea coating has been applied to the concrete repair and protection engineering in the South-to-North Water Transfers Project.

The Study on the Synthesis of Polyfluoroacrylate

2013 ◽  
Vol 395-396 ◽  
pp. 351-354
Author(s):  
Qin Huan Yang
Keyword(s):  
Contact Angle ◽  
Particle Size ◽  
Polymer Film ◽  
Water Contact Angle ◽  
Film Surface ◽  
Contact Angles ◽  
Fluoride Content ◽  
Water Contact ◽  
Copolymer Films ◽  
High Fluoride

Cationic polyfluoroacrylate has been synthesized in the dual presence of cationic and non-ionic emulsifiers. Optimization studies indicated that the optimal proportions of cationic emulsifier 1631 and non-ionic emulsifiers FSA and AEO-9 were 1.75%, 1.25%, and 0.08%, respectively. Under these conditions, the conversion to the polymer was 92.5%, the particle size was 142 nm, and the water contact angle on a polymer film surface was 94.0°. With increasing dosage of hydrocarbon emulsifier, the water contact angles of copolymer films decreased dramatically. The magnitude of this decrease for a polymer with low fluoride content was greater than that for a polymer with high fluoride content. The fluorinated emulsifier FSA behaved similarly to the hydrocarbon emulsifier.

An Effect of Viscosity of Coating Materials on Silicon Micro-Patterning Arrays for Superhydrophobic Surface

2010 ◽  
Vol 93-94 ◽  
pp. 447-450 ◽  
Author(s):  
N. Atthi ◽  
O. Nimittrakoolchai ◽  
Sitthisuntorn Supothina ◽  
J. Supadech ◽  
W. Jeamsaksiri ◽  
...  
Keyword(s):  
Contact Angle ◽  
Water Contact Angle ◽  
Surface Property ◽  
Superhydrophobic Surface ◽  
Rough Surfaces ◽  
Coating Materials ◽  
Water Contact ◽  
Viscous Material ◽  
Micro Patterning

Two different viscous coating materials, which are Polydimethylsiloxane (PDMS) mixed with 10%wt of Dicumylperoxide (DCP), and Semifluorinate Silane (SFS), were applied to silicon micro-asperity. The cosine’s Young and viscosity of those coating materials are -0.3584,-0.3496 and 3.176x10-3, 1.339 x10-3 Pas, respectively. The rough surfaces with nine asperity shapes were studied. The results shown that, pillar shape has an effect on water contact angle (WCA): Stripe asperity cannot make the average WCA greater than 150. When consider the pillar asperity, the WCA falls between 152 and 157, which exhibits a superhydrophobic surface property. However, actual WCA of the micro-asperity coated with PDMS+10%wt of DCP is lower than that coated with SFS around 1 to 7. High viscous material makes the asperity size bigger than the design and decreases the WCA: the low viscous material is more suitable for coating on the asperities.

Long-Term Stable Metal Organic Framework (MOF) Based Mixed Matrix Membranes for Ultrafiltration

2020 ◽  
Author(s):  
Muayad Al-shaeli ◽  
Stefan J. D. Smith ◽  
Shanxue Jiang ◽  
Huanting Wang ◽  
Kaisong Zhang ◽  
...  
Keyword(s):  
Contact Angle ◽  
Water Contact Angle ◽  
Mixed Matrix Membranes ◽  
Recovery Ratio ◽  
Mixed Matrix ◽  
Water Contact ◽  
Membrane Performance ◽  
Metal Organic ◽  
Matrix Membranes

<p>In this study, novel <a>mixed matrix polyethersulfone (PES) membranes</a> were synthesized by using two different kinds of metal organic frameworks (MOFs), namely UiO-66 and UiO-66-NH<sub>2</sub>. The composite membranes were characterised by SEM, EDX, FTIR, PXRD, water contact angle, porosity, pore size, etc. Membrane performance was investigated by water permeation flux, flux recovery ratio, fouling resistance and anti-fouling performance. The stability test was also conducted for the prepared mixed matrix membranes. A higher reduction in the water contact angle was observed after adding both MOFs to the PES and sulfonated PES membranes compared to pristine PES membranes. An enhancement in membrane performance was observed by embedding the MOF into PES membrane matrix, which may be attributed to the super-hydrophilic porous structure of UiO-66-NH<sub>2</sub> nanoparticles and hydrophilic structure of UiO-66 nanoparticles that could accelerate the exchange rate between solvent and non-solvent during the phase inversion process. By adding the MOFs into PES matrix, the flux recovery ratio was increased greatly (more than 99% for most mixed matrix membranes). The mixed matrix membranes showed higher resistance to protein adsorption compared to pristine PES membranes. After immersing the membranes in water for 3 months, 6 months and 12 months, both MOFs were stable and retained their structure. This study indicates that UiO-66 and UiO-66-NH<sub>2</sub> are great candidates for designing long-term stable mixed matrix membranes with higher anti-fouling performance.</p>

scholarly journals Surface modification of PMMA polymer and its composites with PC61BM fullerene derivative using an atmospheric pressure microwave argon plasma sheet

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Andrzej Sikora ◽  
Dariusz Czylkowski ◽  
Bartosz Hrycak ◽  
Magdalena Moczała-Dusanowska ◽  
Marcin Łapiński ◽  
...  
Keyword(s):  
Contact Angle ◽  
Surface Modification ◽  
Chemical Composition ◽  
Water Contact Angle ◽  
Plasma Sheet ◽  
Atmospheric Pressure ◽  
Argon Plasma ◽  
Fullerene Derivative ◽  
Water Contact ◽  
Pmma Polymer

AbstractThis paper presents the results of experimental investigations of the plasma surface modification of a poly(methyl methacrylate) (PMMA) polymer and PMMA composites with a [6,6]-phenyl-C61-butyric acid methyl ester fullerene derivative (PC61BM). An atmospheric pressure microwave (2.45 GHz) argon plasma sheet was used. The experimental parameters were: an argon (Ar) flow rate (up to 20 NL/min), microwave power (up to 530 W), number of plasma scans (up to 3) and, the kind of treated material. In order to assess the plasma effect, the possible changes in the wettability, roughness, chemical composition, and mechanical properties of the plasma-treated samples’ surfaces were evaluated by water contact angle goniometry (WCA), atomic force microscopy (AFM), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS). The best result concerning the water contact angle reduction was from 83° to 29.7° for the PMMA material. The ageing studies of the PMMA plasma-modified surface showed long term (100 h) improved wettability. As a result of plasma treating, changes in the samples surface roughness parameters were observed, however their dependence on the number of plasma scans is irregular. The ATR-FTIR spectra of the PMMA plasma-treated surfaces showed only slight changes in comparison with the spectra of an untreated sample. The more significant differences were demonstrated by XPS measurements indicating the surface chemical composition changes after plasma treatment and revealing the oxygen to carbon ratio increase from 0.1 to 0.4.

scholarly journals Physicochemical Properties and Biocompatibility of Electrospun Polycaprolactone/Gelatin Nanofibers

2021 ◽  
Vol 18 (9) ◽  
pp. 4764
Author(s):  
Wei Lee Lim ◽  
Shiplu Roy Chowdhury ◽  
Min Hwei Ng ◽  
Jia Xian Law
Keyword(s):  
Contact Angle ◽  
Physicochemical Properties ◽  
Water Contact Angle ◽  
Ligament Injury ◽  
Great Promise ◽  
Composition Analysis ◽  
Water Contact ◽  
Tenogenic Differentiation ◽  
Good Biocompatibility ◽  
Tissue Grafts

Tissue-engineered substitutes have shown great promise as a potential replacement for current tissue grafts to treat tendon/ligament injury. Herein, we have fabricated aligned polycaprolactone (PCL) and gelatin (GT) nanofibers and further evaluated their physicochemical properties and biocompatibility. PCL and GT were mixed at a ratio of 100:0, 70:30, 50:50, 30:70, 0:100, and electrospun to generate aligned nanofibers. The PCL/GT nanofibers were assessed to determine the diameter, alignment, water contact angle, degradation, and surface chemical analysis. The effects on cells were evaluated through Wharton’s jelly-derived mesenchymal stem cell (WJ-MSC) viability, alignment and tenogenic differentiation. The PCL/GT nanofibers were aligned and had a mean fiber diameter within 200–800 nm. Increasing the GT concentration reduced the water contact angle of the nanofibers. GT nanofibers alone degraded fastest, observed only within 2 days. Chemical composition analysis confirmed the presence of PCL and GT in the nanofibers. The WJ-MSCs were aligned and remained viable after 7 days with the PCL/GT nanofibers. Additionally, the PCL/GT nanofibers supported tenogenic differentiation of WJ-MSCs. The fabricated PCL/GT nanofibers have a diameter that closely resembles the native tissue’s collagen fibrils and have good biocompatibility. Thus, our study demonstrated the suitability of PCL/GT nanofibers for tendon/ligament tissue engineering applications.

Osteoconductivity of Superhydrophilic Ti- and Zr-Alloy for Biomedical Application

2016 ◽  
Vol 879 ◽  
pp. 2524-2527
Author(s):  
Masazumi Okido ◽  
Kensuke Kuroda
Keyword(s):  
Contact Angle ◽  
Water Contact Angle ◽  
Strong Influence ◽  
Biomedical Application ◽  
Hydrophobic Surface ◽  
Hydrophilic Surface ◽  
Water Contact ◽  
Zr Alloy ◽  
Zr Alloys

Surface hydrophilicity is considered to have a strong influence on the biological reactions of bone-substituting materials. However, the influence of a hydrophilic or hydrophobic surface on the osteoconductivity is not completely clear. In this study, we produced super-hydrophilic and hydrophobic surface on Ti-and Zr-alloys. Hydrothermal treatment at 180 oC for 180 min. in the distilled water and immersion in x5 PBS(-) brought the super-hydrophilic surface (water contact angle < 10 (deg.)) and heat treatment of as-hydrothermaled the hydrophobic surface. The osteoconductivity of the surface treated samples with several water contact angle was evaluated by in vivo testing. The surface properties, especially water contact angle, strongly affected the osteoconductivity and protein adsorbability, and not the surface substance.

scholarly journals Vertical Orientation of Liquid Crystal on Polystyrene Substituted with n-Alkylbenzoate-p-oxymethyl Pendant Group as a Liquid Crystal Precursor

Polymers ◽  
2021 ◽  
Vol 13 (13) ◽  
pp. 2058
Author(s):  
Kyutae Seo ◽  
Hyo Kang
Keyword(s):  
Contact Angle ◽  
Liquid Crystal ◽  
Water Contact Angle ◽  
Polymer Films ◽  
Molar Fraction ◽  
Side Chain ◽  
Pendant Group ◽  
Polymer Modification ◽  
Vertical Orientation ◽  
Water Contact

We synthesized a series of polystyrene derivatives modified with precursors of liquid crystal (LC) molecules via polymer modification reactions. Thereafter, the orientation of the LC molecules on the polymer films, which possess part of the corresponding LC molecular structure, was investigated systematically. The precursors and the corresponding derivatives used in this study include ethyl-p-hydroxybenzoate (homopolymer P2BO and copolymer P2BO#, where # indicates the molar fraction of ethylbenzoate-p-oxymethyl in the side chain (# = 20, 40, 60, and 80)), n-butyl-p-hydroxybenzoate (P4BO), n-hexyl-p-hydroxybenzoate (P6BO), and n-octyl-p-hydroxybenzoate (P8BO). A stable and uniform vertical orientation of LC molecules was observed in LC cells fabricated with P2BO#, with 40 mol% or more ethylbenzoate-p-oxymethyl side groups. In addition, the LC molecules were oriented vertically in LC cells fabricated with homopolymers of P2BO, P4BO, P6BO, and P8BO. The water contact angle on the polymer films can be associated with the vertical orientation of the LC molecules in the LC cells fabricated with the polymer films. For example, vertical LC orientation was observed when the water contact angle of the polymer films was greater than ~86°. Good orientation stability was observed at 150 °C and with 20 J/cm2 of UV irradiation for LC cells fabricated with the P2BO film.

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