The catechol functional group of dopamine (3,4‐dihydroxyphenethylamine) has the ability to form strong adhesive bonds to inorganic and organic surfaces in aqueous environments. In this study, novel adhesive polyaspartamides containing catechol pendant groups were synthesized from polysuccinimide through successive aminolysis reactions with quantitative dopamine and ethylenediamine. The adhesion and crosslinking of dopamine‐modified polyaspartamide in aqueous alkaline media was used successfully to modify the surface of various materials (including synthetic polymers, metals, metal oxides, ceramics) using a simple immersion method. Contact angle measurements, SEM and X‐ray photoelectron spectroscopy of the modified surfaces were used to verify the surface coating on a variety of materials with very different inherent wetting properties. These novel biocompatible polymers have potential industrial and biomedical applications as adhesives or coating materials for functional surface modification. Copyright © 2011 Society of Chemical Industry

Lately, copper‐assisted azide–alkyne cycloaddition (CuAAC) has become a very interesting tool for synthesizing biocompatible polymer‐based materials such as hydrogels or microgels, which can be used as biomaterials for tissue engineering and drug delivery. Novel poly(2‐hydroxyethyl aspartamide)s (PHEAs) functionalized with pendent acetylene or azide groups were prepared from polysuccinimide, which is the thermal polycondensation product of aspartic acid, through successful ring‐opening reactions using propargylamine, 1‐azido‐2‐aminoethane and ethanolamine. The composition of the prepared copolymers was analyzed using 1H NMR spectroscopy. Clickable PHEA derivatives were crosslinked by mixing together in water with a catalyst system of Cu(I) and N, N, N′, N′, N″‐pentamethyldiethylenetriamine, a type of Huisgen's 1,3‐dipolar azide‐alkyne cycloaddition. The reaction of the polymers resulted in a chemoselective coupling between alkynyl and azido functional groups with multiple formation of triazole crosslinks to give hydrogels. The triazole linkages in the hydrogels are highly stable and may also play a role in swelling behavior. PHEA‐based hydrogels were also obtained by the crosslinking of azide‐ or alkyne‐modified PHEA with a small‐molecule crosslinker. The hydrogels prepared using these two methods were characterized by their degree of swelling and the morphology of the hydrogels was confirmed using scanning electron microscopy. The approach we describe here presents a promising alternative to common chemical hydrogel preparation techniques, and these hydrogels seem to possess structures having potential for a variety of industrial and biomedical applications. © 2012 Society of Chemical Industry

Phosphate glasses have several advantages over traditional silicate-based bioglasses but are inferior in the crucial step of cell attachment to their surface. Here, as a proof of concept, we analyze fibroblast attachment to the phosphate glass surface subjected to basic treatment and silanization. Silicate (S53P4)-and phosphate (Sr50)-based bioactive glasses were either untreated or surface-treated with basic buffer and functionalized with silane. The surface-treated samples were studied as such and after fibronectin was adsorbed on to their surface. With both glass types, surface treatment enhanced fibroblast adhesion and spreading in comparison to the untreated glass. The surface-treated Sr50 glass allowed for cell adhesion, proliferation, and spreading to a similar extent as seen with S53P4 and borosilicate control glasses. Here, we show that surface treatment of bioactive glass can be used to attract cell adhesion factors found in the serum and promote cell−material adhesion, both important for efficient tissue integration.

Membrane contactor technology affords great opportunities for nitrogen recovery from waste streams. This study presents a performance comparison between lab- and pilot-scale membrane contactors using landfill leachate samples. Polypropylene (PP) and polytetrafluoroethylene (PTFE) fibers in different dimensions were compared in terms of ammonia (NH3) recovery on a lab scale using a synthetic ammonium solution. The effect of pre-treating the leachate with tannin coagulation on nitrogen recovery was also evaluated. An ammonia transfer on the lab and pilot scale was scrutinized using landfill leachate as a feed solution. It was found that PTFE fibers performed better than PP fibers. Among PTFE fibers, the most porous one (denoted as M1) had the highest NH3 flux of 19.2 g/m2.h. Tannin pre-treatment reduced fouling and increased NH3, which in turn improved nitrogen recovery. The mass transfer coefficient of the lab-scale reactor was more than double that of the pilot reactor (1.80 × 10−7 m/s vs. 4.45 × 10−7 m/s). This was likely attributed to the difference in reactor design. An analysis of the membrane surface showed that the landfill leachate caused a combination of inorganic and organic fouling. Cleaning with UV and 0.01 M H2O2 was capable of removing the fouling completely and restoring the membrane characteristics.

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Lignocellulosics, microalgae, and SDS were used to generate stable and colored wet foams intended for camouflage use. It was found that the addition of microalgae increased the foam stability. The hyperspectral and thermal properties were studied.

In this work, MXene as a hydrophilic 2D nanosheet has been suggested to tailor the polyphenylsulfone (PPSU) flat sheet membrane characteristics via bulk modification. The amount of MXene varied in the PPSU casting solution from 0–1.5 wt.%, while a series of characterization tools have been employed to detect the surface characteristics changes. This included atomic force microscopy (AFM), scanning electron microscopy (SEM), contact angle, pore size and porosity, and Fourier-transform infrared spectroscopy (FTIR). Results disclosed that the MXene content could significantly influence some of the membranes’ surface characteristics while no effect was seen on others. The optimal MXene content was found to be 0.6 wt.%, as revealed by the experimental work. The roughness parameters of the 0.6 wt.% nanocomposite membrane were notably enhanced, while greater hydrophilicity has been imparted compared to the nascent PPSU membrane. This witnessed enhancement in the surface characteristics of the nanocomposite was indeed reflected in their performance. A triple enhancement in the pure water flux was witnessed without compromising the retention of the membranes against the Cu2+, Cd2+ and Pd2+ feed. In parallel, high, and comparable separation rates (>92%) were achieved by all membranes regardless of the MXene content. In addition, promising antifouling features were observed with the nanocomposite membranes, disclosing that these nanocomposite membranes could offer a promising potential to treat heavy metals-containing wastewater for various applications.