Beyond Mechanical Recycling: Giving New Life to Plastic Waste.

Increasing the stream of recycled plastic necessitates an approach beyond the traditional recycling via melting and re-extrusion. Various chemical recycling processes have great potential to enhance recycling rates. In this Review, a summary of the various chemical recycling routes and assessment via life-cycle analysis is complemented by an extensive list of processes developed by companies active in chemical recycling.

One pot conversion of glucose to ethyl levulinate over a porous hydrothermal acid catalyst in green solvents.

The one-pot conversion of glucose to ethyl levulinate over an acid-functionalised hydrothermal catalyst (derived from glucose) provides high initial yields up to 37 mol%, comparable to the homogeneous HSO catalyst, whilst catalyst performance is strongly influenced by green solvent choice.

Towards a Sustainable Synthesis of Oxymethylene Dimethyl Ether by Homogeneous Catalysis and Uptake of Molecular Formaldehyde.

Oxymethylene dimethyl ethers (OME ; CH (-OCH -) O-CH , n=3-5) are a novel class of sustainable synthetic fuels, which are of increasing interest due to their soot-free combustion. Herein a novel anhydrous OME synthesis route is presented. Catalyzed by trimethyloxonium salts, dimethoxymethane takes up monomeric gaseous formaldehyde instantaneously and forms high purity OME at temperatures of 25-30 °C.

An Interesting Class of Porous Polymer--Revisiting the Structure of Mesoporous α-D-Polysaccharide Gels.

The processes involved in the transformation of non-porous, native polysaccharides to their highly porous equivalents introduce significant molecular complexity and are not yet fully understood. In this paper, we propose that distinct changes in polysaccharide local short-range ordering promotes and directs the formation of meso- and micro-pores, which are investigated here using N2 sorption, FTIR, and solid-state (13)C NMR. It is found that an increase in the overall double helical amylose content, and their local association structures, are responsible for formation of the porous polysaccharide gel phase.

Sustainable carbon materials.

Carbon-based structures are the most versatile materials used in the modern field of renewable energy (i.e., in both generation and storage) and environmental science (e.

Always look on the "light" side of life: sustainable carbon aerogels.

The production of carbon aerogels based on the conversion of inexpensive and abundant precursors using environmentally friendly processes is a highly attractive subject in materials chemistry today. This article reviews the latest developments regarding the rapidly developing field of carbonaceous aerogels prepared from biomass and biomass-derived precursors, highlighting exciting and innovative approaches to green, sustainable nanomaterial synthesis. A review of the state-of-the-art technologies will be provided with a specific focus on two complimentary synthetic approaches developed upon the principles of green chemistry.

A sustainable template for mesoporous zeolite synthesis.

A generalized synthesis of high-quality, mesoporous zeolite (e.g., MFI-type) nanocrystals is presented, based on a biomass-derived, monolithic N-doped carbonaceous template.

Molecular-level understanding of the carbonisation of polysaccharides.

Understanding of both the textural and functionality changes occurring during (mesoporous) polysaccharide carbonisation at the molecular level provides a deeper insight into the whole spectrum of material properties, from chemical activity to pore shape and surface energy, which is crucial for the successful application of carbonaceous materials in adsorption, catalysis and chromatography. Obtained information will help to identify the most appropriate applications of the carbonaceous material generated during torrefaction and different types of pyrolysis processes and therefore will be important for the development of cost- and energy-efficient zero-waste biorefineries. The presented approach is informative and semi-quantitative with the potential to be extended to the formation of other biomass-derived carbonaceous materials.

Direct methane oxidation over Pt-modified nitrogen-doped carbons.

Nitrogen-doped carbons derived from biomass precursors were modified with Pt(2+) and successfully tested as solid catalysts in the direct oxidation of methane in fuming sulfuric acid. Remarkably, the catalytic performance was found to be substantially better than the Pt-modified Covalent Triazine Framework (CTF) system previously reported, although deactivation is more pronounced for the biomass derived catalyst supports.

Carbohydrate-derived hydrothermal carbons: a thorough characterization study.

Hydrothermal carbonization (HTC) is an aqueous-phase route to produce carbon materials using biomass or biomass-derived precursors. In this paper, a comprehensive physicochemical and textural characterization of HTC materials obtained using four different precursors, namely, xylose, glucose, sucrose, and starch, is presented. The development of porosity in the prepared HTC materials as a function of thermal treatment (under an inert atmosphere) was specifically monitored using N(2) and CO(2) sorption analysis.

Renewable nitrogen-doped hydrothermal carbons derived from microalgae.

Nitrogen-doped carbon materials are synthesized via an effective, sustainable, and green one-step route based on the hydrothermal carbonization of microalgae with high nitrogen content (ca. 11 wt %). The addition of the monosaccharide glucose to the reaction mixture is found to be advantageous, enhancing the fixation of nitrogen in the synthesized carbons, resulting in materials possessing nitrogen content in excess of 7 wt %, and leading to promising reaction yields.

Carbon-based ionogels: tuning the properties of the ionic liquid via carbon-ionic liquid interaction.

The behavior of two ionic liquids (ILs), 1-ethyl-3-methylimidazolium dicyanamide [Emim][DCA] and 1-ethyl-3-methylimidazolium triflate [Emim][TfO], in (meso)porous carbonaceous hosts was investigated. Prior to IL incorporation into the host, the carbon matrix was thermally annealed between 180 and 900 °C to control carbon condensation and surface chemistry. The resulting materials have an increasing "graphitic" carbon character with increasing treatment temperature, reflected in a modified behavior of the ILs when impregnated into the carbon host.

A sweet killer: mesoporous polysaccharide confined silver nanoparticles for antibacterial applications.

Silver nanoparticles (AgNP) confined within porous starch have been prepared in a simple, green and efficient manner, utilising the nanoporous structure of predominantly mesoporous starch (MS) to act as nanoparticle stabiliser, support and reducing surface. MS/AgNP materials present high surface areas (S(BET) > 150 m(2) g(-1)) and mesopore volumes (V(meso) > 0.45 cm(3) g(-1)).

Functional hollow carbon nanospheres by latex templating.

A facile and sustainable synthesis of hollow carbonaceous nanospheres is presented, offering a scalable and multifunctional route to the generation of useful nanocontainers, which critically possess the stability not offered by polymeric equivalents and functionality not afforded by other nanocarbons. Carbonization temperature provides a subtle but elegant mechanism to control structure and thereby hydrophobicity, nanopartitioning, and permeation between the inner and outer space.

Tuneable porous carbonaceous materials from renewable resources.

Porous carbon materials are ubiquitous with a wide range of technologically important applications, including separation science, heterogeneous catalyst supports, water purification filters, stationary phase materials, as well as the developing future areas of energy generation and storage applications. Hard template routes to ordered mesoporous carbons are well established, but whilst offering different mesoscopic textural phases, the surface of the material is difficult to chemically post-modify and processing is energy, resource and step intensive. The production of carbon materials from biomass (i.

Pectin-derived porous materials.

Porous forms of pectin, a major industrial waste biomass polysaccharide, have been prepared by aqueous phase expansion routes (S(BET)>200 m(2) g(-1); V(pore)>0.80 cm(3) g(-1)). It was demonstrated that the aqueous phase acidity crucially influenced the properties of the porous pectin form.

Porous carbohydrate-based materials via hard templating.

Among various techniques, the hydrothermal carbonization (HTC) of biomass (either isolated carbohydrates or crude plants) is a promising candidate for the synthesis of novel carbon-based materials with a wide variety of potential applications. In this Minireview, we discuss various synthetic routes towards such porous carbon-based materials or composites through the HTC process, using the nanocasting procedure. We focus on the synthesis of carbon materials with different pore systems and morphologies directed by the presence of various nanostructured inorganic sacrificial templates.

Supported metal nanoparticles on porous materials. Methods and applications.

Nanoparticles are regarded as a major step forward to achieving the miniaturisation and nanoscaling effects and properties that have been utilised by nature for millions of years. The chemist is no longer observing and describing the behaviour of matter but is now able to manipulate and produce new types of materials with specific desired physicochemical characteristics. Such materials are receiving extensive attention across a broad range of research disciplines.