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High internal phase emulsions (HIPEs) have templated self-standing porous carbonaceous materials (carboHIPEs) while employing Kraft Black Liquor, a paper milling industry byproduct, as a carbon precursor source. As such, the starting emulsion has been prepared through a laboratory-made homogenizer, while native materials have been characterized at various length scales either with Raman spectrometry, X-ray diffraction (XRD), mercury intrusion porosimetry, and nitrogen absorption. After thermal carbonization, specific surface areas ranging from ∼600 m 2 g -1 to 1500 m 2 g -1 have been reached while maintaining a monolithic character. Despite a poor graphitization yield, the carbonaceous materials offer good electronic transport properties, reaching 31 S m -1 . When tested toward energy storage applications, the native unwashed materials revealed a hydrogen storage of 0.07 wt % at 40 bar and room temperature (RT), while hydrogen retention is reaching 0.37 wt % at 40 bar and RT for the washed sample. When employed as supercapacitor electrodes, these carbonaceous foams are able to deliver high capacities of ∼140 F/g at 1 A/g, thereby matching the ones obtained from a commercial carbon reference, while additionally providing a restored remnant capacity of 120 F/g at 2 A/g over 5000 cycle numbers.

Hybrid materials consisting of metallic nanoparticles (NPs) adsorbed on porous polymeric supports have been the subject of intense research for many years. Such materials indeed gain from intrinsic properties, e.g., high specific surface area, catalytic properties, porous features, etc., of both components. Rational design of such materials is fundamental regarding the functionalization of the support surface and thus the interactions required for the metallic NPs to be strongly immobilized at the pore surface. Herein are presented some significant scientific contributions to this rapidly expanding research field. This contribution will notably focus on various examples of such hybrid systems prepared from porous polymers, whatever the morphology and size of the pores. Such porous polymeric supports can display pores with sizes ranging from a few nanometers to hundreds of microns while pore morphologies, such as spherical, tubular, etc., and/or open or closed, can be obtained. These systems have allowed some catalytic molecular reactions to be successfully undertaken, such as the reduction of nitroaromatic compounds or dyes, e.g., methylene blue and Eosin Y, boronic acid-based C-C homocoupling reactions, but also cascade reactions consisting of two catalytic reactions achieved in a row.

A simple and easy way is proposed for the fabrication of a highly attenuating composite material for underwater acoustics. The approach involves the introduction of porous polymer beads into a polyurethane matrix. The porous beads are prepared through an emulsion-templating approach, and two different processes are used. The first one uses microfluidics to synthesize beads of controlled diameter and porosity. The control over the bead size allows the selection of the frequency range where the material exhibits the highest acoustic attenuation. The second one uses a double emulsion approach and allows for the production of much larger quantities of beads. Both approaches yield materials exhibiting much higher acoustic absorption than the one obtained using the most commonly used micro-balloon inclusion. We present both the synthesis procedures and the structural and acoustic characterizations of the beads and the final acoustic materials., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Photocatalysis is one of the most promising processes for treating air and water pollution. Innovative civil engineering materials for environmental depollution by photocatalysis have already been synthesized by incorporating TiO 2 or ZnO nanoparticles in cement. This method suffers from two flaws: first, most of the NPs are incorporated into the cement and useless for photocatalysis; second, rain and wind could spread the potentially carcinogenic nanoparticles from the cement surface into nature. Thus, we propose the efficient synthesis of nontoxic and biocompatible ZnO nanostructures solely onto the surface of commercially available concrete and tiling pavements by a low-cost and low-temperature hydrothermal method. Our samples exhibited enhanced photocatalytic activity for degrading organic dyes in aqueous media, and dye molecules are commonly used in the pharmaceutical, food, and textile industries. Durability studies showed no loss of efficiency after four photocatalysis experiments. Such supported structures, which are easy to implement onto the varying surfaces of commercially available materials, are promising for integration into civil engineering surfaces for environmental depollution in our daily life., Competing Interests: Conflict of interestThe authors declare that they have no conflict of interest., (© The Author(s) 2019.)

Original porous catalytic supports can be engineered via an effective and straightforward synthetic route to polystyrene-block-poly(d,l-lactide) diblock copolymer precursors displaying an acid-cleavable acetal junction between both blocks. To this purpose, we synthesized an acetal-containing heterodifunctional initiator, thus enabling to combine two different polymerization methods, i.e., first atom transfer radical polymerization (ATRP) of styrene, and then ring-opening polymerization (ROP) of d,l-lactide. Thanks to the labile nature of the acetal junction, oriented porous frameworks could be obtained upon trifluoroacetic acid-mediated cleavage of the latter, after orientation of the block copolymer nanodomains by solvent vapor annealing. The resulting porous materials bearing a reactive aldehyde function at the pore surface allowed for further chemical modification via reductive amination with amino-containing compounds, such as tetraethylenepentamine, thus leading to amine-functionalized porous polystyrene. In situ generated gold nanoparticles could then be immobilized within such functionalized porous nanoreactors, and these hybrid materials could find interesting applications in heterogeneous supported catalysis. In this regard, model catalytic reactions, including C-C homocoupling of benzeneboronic acid derivatives, hydride-mediated reduction of nitroaromatic compounds, and especially unprecedented "one-pot" cascade reactions consisting of the latter consecutive reactions from 3-nitrobenzeneboronic acid, were successfully monitored by different chromatographic and spectroscopic techniques.