Fabrication of Robust and Effective Oil/Water Separating Superhydrophobic Textile Coatings.

A superhydrophobic (SH) surface is typically constructed by combining a low-surface-energy substance and a high-roughness microstructure. Although these surfaces have attracted considerable attention for their potential applications in oil/water separation, self-cleaning, and anti-icing devices, fabricating an environmentally friendly superhydrophobic surface that is durable, highly transparent, and mechanically robust is still challenging. Herein, we report a facile painting method to fabricate a new micro/nanostructure containing ethylenediaminetetraacetic acid/poly(dimethylsiloxane)/fluorinated SiO2 (EDTA/PDMS/F-SiO2) coatings on the surface of a textile with two different sizes of SiO2 particles, which have high transmittance (>90%) and mechanical robustness. The different-sized SiO2 particles were employed to construct the rough micro/nanostructure, fluorinated alkyl silanes were employed as low-surface-energy materials, PDMS was used for its heat-durability and wear resistance, and ETDA was used to strengthen the adhesion between the coating and textile. The obtained surfaces showed excellent water repellency, with a water contact angle (WCA) greater than 175° and a sliding angle (SA) of 4°. Furthermore, the coating retained excellent durability and remarkable superhydrophobicity for oil/water separation, abrasion resistance, ultraviolet (UV) light irradiation stability, chemical stability, self-cleaning, and antifouling under various harsh environments.

Biobased Copolyamides 56/66: Synthesis, Characterization and Crystallization Kinetics.

This study synthesized a series of new biobased copolyamides (co-PAs), namely PA56/PA66 with various comonomer ratios, by using in situ polycondensation. The structures, compositions, behaviors, and crystallization kinetics of the co-PAs were investigated through proton nuclear magnetic resonance (1H NMR) spectroscopy, gel permeation chromatography (GPC), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), polarized optical microscopy (POM), and X-ray diffraction (XRD). The influence of the composition of co-PAs on their mechanical properties and thermal stability was investigated. The co-PAs exhibited a eutectic melting point when the PA56 content was 50 mol%, with the crystallization temperature decreasing from 229 to a minimum 188 °C and the melting temperature from 253 to a minimum 218 °C. The results indicated that the tensile strength and flexural modulus first decreased and then increased as the PA66 content increased. The nonisothermal crystallization kinetics of the PA56/PA66 co-PAs were analyzed using both the Avrami equation modifications presented by Jeziorny and Mo. The results also indicated that the crystallization rate of the PA56/PA66 co-PAs was higher than that of PA56.

The Isothermal and Nonisothermal Crystallization Kinetics and Morphology of Solvent-Precipitated Nylon 66.

Solvent-precipitated nylon 66 (SP PA66) is a key material used to fabricate microfiltration membranes. The crystallization kinetics and behavior of SP PA66 were investigated through differential scanning calorimetry (DSC), polarized optical microscopy (POM) and X-ray diffraction (XRD). The Avrami equation was used to describe the isothermal crystallization of SP PA66. Nonisothermal crystallization behaviors were analyzed using Avrami equations modified by Jeziorny, Ozawa and Mo. The Avrami analysis demonstrated that the k values of SP PA66 were higher than those of neat PA66. The  n was between 2 and 3 indicating the presence of two- and three-dimensional mode with thermal nucleation. With an increasing cooling rate, the Jeziorny crystallization rate constant increased for SP PA66; however, the Ozawa model was not satisfactory for all SP PA66 samples. The Mo method suggested that SP PA66 had a faster crystallization rate than neat PA66 during the nonisothermal crystallization process. The solvents dissolved nylon 66, rearranged it and formed a regular hydrogen-bonded region. These regions served as nucleation sites and increased the crystallization rate constant in the subsequent melting process. The crystal morphology of the SP PA66 under the POM investigation exhibited Maltese cross spherulites. The sizes of the spherulites of SP PA66 were significantly smaller than those of neat PA66. Wide-angle XRD revealed that SP PA66 had the same crystal structure and a higher crystal perfection than neat PA66.

Synthesis and characterization of CdS x Se1-x alloy quantum dots with composition-dependent band gaps and paramagnetic properties.

Ternary CdS x Se1-x alloy quantum dots (QDs) and CdS x Se1-x /ZnS core/shell nanocrystals exhibiting composition dependent band gaps have been successfully synthesized. The ZnS shell was doped with 0.1% and 5% of paramagnetic manganese ions so as to be used as a fluorescent/paramagnetic bi-functional probe. Energy-dispersive X-ray spectroscopy (EDS) measurements confirmed the presence of Cd, S, and Se in CdS x Se1-x nanocrystals with the atomic ratios of Cd, S, and Se which are well consistent with our synthetic ratios. Wide angle X-ray diffraction (WAXD) indicated that the crystal structures of the CdS x Se1-x core QDs and CdS x Se1-x /ZnS core/shell QDs were zinc blende phases. Both dynamic light scattering (DLS) and transmission electron microscopy (TEM) revealed that the as-synthesized nanocrystals had a narrow size distribution and high crystallinity. The band gaps of CdS x Se1-x nanocrystals were adjustable by varying the ratio of S:Se in the CdS x Se1-x core and were in the range of 1.96 eV to 2.32 eV. Hence, when composition x was changed from 0 to 1, the fluorescence color of the nanocrystals varied from red to green. After shell coverage, the ternary alloy QDs exhibited a superior photoluminescence (PL) quantum yield up to 57%. In comparison with the alloy core QDs, the PL emission peaks of the CdS x Se1-x /ZnS core/shell QDs displayed a small redshift. Electron paramagnetic resonance (EPR) measurements for manganese-doped CdS x Se1-x /ZnS nanocrystals revealed paramagnetic properties for both low and high Mn2+ doping levels.

Hierarchically structured superhydrophobic coatings fabricated by successive Langmuir-Blodgett deposition of micro-/nano-sized particles and surface silanization.

The present study demonstrates the creation of a stable, superhydrophobic surface by coupling of successive Langmuir-Blodgett (LB) depositions of micro- and nano-sized (1.5 µm/50 nm, 1.0 µm/50 nm, and 0.5 µm/50 nm) silica particles on a glass substrate with the formation of a self-assembled monolayer of dodecyltrichlorosilane on the surface of the particulate film. Particulate films, in which one layer of 50 nm particles was deposited over one to five sublayers of larger micro-sized particles, with hierarchical surface roughness and superhydrophobicity, were successfully fabricated. Furthermore, the present 'two-scale' (micro- and nano-sized particles) approach is superior to the previous 'one-scale' (micro-sized particles) approach in that both higher advancing contact angle and lower contact angle hysteresis can be realized. Experimental results revealed that the superhydrophobicity exhibited by as-fabricated particulate films with different sublayer particle diameters increases in the order of 0.5 µm>1.0 µm>1.5 µm. However, no clear trend between sublayer number and surface superhydrophobicity could be discerned. An explanation of superhydrophobicity based on the surface roughness introduced by two-scale particles is also proposed.

Fabrication of hydrophobic surfaces by coupling of Langmuir-Blodgett deposition and a self-assembled monolayer.

A novel method coupling the Langmuir-Blodgett (LB) deposition of silica particles and the formation of a self-assembled monolayer (SAM) of alkylsilane is proposed for fabricating hydrophobic surfaces. The LB deposition and the SAM are supposed to confer the substrate surface roughness and low surface energy, respectively. By controlling the hydrophobic-hydrophilic balance of the silica particle surface through the adsorption of surfactant molecules, deposition of monolayers consisting of hexagonally close-packed arrays of particles on a glass substrate can then be successfully conducted in a Langmuir trough. LB particulate films with a particle layer number up to 5 were thereby prepared. A sintered and hydrophobically finished particulate film with roughness factor of 1.9 was finally fabricated by sintering and surface silanization. Effects of particle size and particle layer number on the wetting behavior of the particulate films were systematically studied by measuring static and dynamic water contact angles. The experimental results revealed that a static contact angle of about 130 degrees resulted from the particulate films regardless of the particle size and particle layer number. This is consistent with the predictions of both the Wenzel model and the Cassie and Baxter model in that roughness of a hydrophobic surface can increase its hydrophobicity and a switching of the dominant mode from Wenzel's to Cassie and Baxter's. In general, an advancing contact angle of about 150 degrees , a receding contact angle of about 110 degrees , and a contact angle hysteresis of about 40 degrees were exhibited by the particulate films fabricated.