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Abstract In the last years, hydrogels from renewable biopolymers and low-cost row materials are a hot topic for biomedical applications. In this context, cellulose nanofibrils are considered suitable building blocks for the synthesis of many biocompatible products, with a variety of chemical-physical properties. Herein we report a multi-technique and multi-scale study, from the molecular to the nanometric length scale, of the sol–gel transition observed in aqueous solutions of TEMPO-oxidized nano-sized cellulose fibrils (TOCNFs), when in the presence of polyvalent cations (Mg2+ and Ca2+). We combine the data from Small Angle Neutron Scattering (SANS), which provide information about the inner structure of the nanofibril, with those from UV Resonant Raman (UVRR) spectroscopy, which is a sensitive probe of the intra- and inter-molecular interactions in the gel and the liquid state. The transition between the gel and the liquid phases is investigated as a function of the concentration of both TOCNFs and cations, the nature of the latter, and the pH at which the phenomenon is observed. SANS analysis reveals that ion concentration induces an anisotropic swelling in the nanofibrils which, at the same time, become more and more flexible. The nanofibrils flexibility is also dependent on TOCNF concentration and pH value. UVRR allows us to elucidate the structural organization and hydrogen-bonding properties of water in aqueous TOCNF dispersions and gels, showing how water molecules partially lose their typical bulk-like tetrahedral organization when ions are added, and the gel phase is formed. Graphical abstract

The food metabolic processes influence the gas composition of packaged products: by finely tuning the gas fluxes through the packaging, the aerobic and anaerobic respiration processes can be efficiently exploited to regulate the equilibrium gas concentrations. In this work, we present a generalised model able to predict the evolution of gases in micro-perforated equilibrium MAP, with a detailed evaluation of fluxes through the perforations by means of Computational Fluid Dynamics. It was found that the Sherwood number for the studied micro-perforations is 0.715 and it was confirmed via experiments on packaging with oxygen-depleted atmospheres. The kinetic model was experimentally validated on a smear short-ripened soft cheese (Taleggio) whose complex surface microbiota confer to the product a non-trivial respiration behaviour. Cheese slices were packed with three different micro-perforated solutions (one 120 μm diameter hole, two 90 μm diameter holes, and five 90 μm diameter holes) achieving three different equilibrium gas compositions with good model predictions. The model was applied to literature data with success, thus the model can be deemed general and applicable to many different systems.

The use of nanostructured materials has been recently proposed in the field of environmental nanoremediation. This approach consists in using nanomaterials not directly, but as building blocks for the design of nano‐porous micro‐dimensional systems, overcoming the eco‐ and health‐toxicology risks generally associated with the use of nano‐sized technologies. Herein we report the use of life cycle assessment (LCA) as an eco‐design tool for optimizing the production of cellulose nanosponges (CNS), nanostructured materials recently developed for water remediation purposes. LCA was applied from the acquisition of raw materials to the synthesis of CNS (from cradle‐to‐gate), considering three production systems, from the lab‐level to a modeled scale‐up system. The lab‐scale LCA identified the main environmental hotspots, namely the energy‐consuming steps and the final purification of the material (washing step). In a second lab‐scale production, an improvement action could be implemented, switching the washing solvent from methanol to water and decreasing the washing temperature. A second LCA showed a reduced contribution to the impacts from the materials, while the global impacts remained within the same order of magnitude. A simulated scale‐up of the process allowed to optimize the energy‐consuming steps and the water consumption, through internal recycling. A third LCA assessed the resulting benefits and a decrease in the global impacts by two orders of magnitude. Our study contributes to the discussion of LCA community, providing a focus on the importance of scaling‐up of emerging technologies, namely nanostructured porous materials, highlighting the benefits of a LCA based approach since the very beginning of product design (eco‐design).

Heterogeneous colorimetric sensors for fluoride ions were obtained by cross-linking TEMPO-oxidized cellulose nanofibers (TOCNF) with chemically modified branched polyethyleneimine 25 kDa (bPEI). Functionalization of bPEI primary amino groups with aromatic anhydrides led to the formation of the corresponding mono- and bis-imides on the grafted polymers (f-bPEI). A microwave-assisted procedure allowed the optimization of the synthetic protocol by reducing reaction time from 17 h to 30 minutes. Hydrogels obtained by mixing different ratios of TOCNF, bPEI and f-bPEI were lyophilized and thermally treated at about 100 °C to promote the formation of amide bonds between the amino groups of poly-cationic polymers and the carboxylic groups of cellulose nanofibers. This approach generated a series of cellulose nanosponges S1-S3 which were characterized by FT-IR and by solid state 13 C CPMAS NMR. These sponge materials can act as colorimetric sensors for the selective naked-eye recognition of fluoride ions over chloride, phosphate and acetate ions at concentrations of up to 0.05 M in DMSO. Moreover, when the sponges were functionalized with perylene tetracarboxylic diimide, successful naked-eye detection was achieved with only 0.02 % w/w of chromophore units per gram of material.

Cellulose nano-sponges (CNS), obtained by cross-linking TEMPO oxidized and ultra-sonicated cellulose nano-fibers (TOUS-CNFs) with branched polyethyleneimine (bPEI), underwent here a systematic small angle neutron scattering investigation, by varying the amount of cross-linker and the water content. The aim was to provide experimental evidence of nano-porosity in the TOUS-CNF network of these nano-sponges (CNSs) by investigating the water nano-confinement geometries in the adsorbent material. Moreover, we also verified how the breaking/reformation of specific intermolecular hydrogen bond interactions between water and the chemical groups present in the architecture of the CNSs could contribute to regulate the water adsorption process observed at macroscopic level. The analysis of the experimental data, performed in terms of the correlation length model, allowed us to extract the short-range correlation length ξ, interpreted as a very first indirect estimation of the effective nano-dimension of the cavities produced by the cross-linking of the reticulated cellulose nano-fibers. From the model, power-law (n) and Lorentzian (m) exponents have been also obtained, associated with the density of TOUS-CNFs at high (larger than hundreds of A) and low (~ 10–100 A) spatial scales, respectively. These parameters were all sensitive to the structural variations induced by the progressive uptake of water on the bPEI/TOUS-CNF sponges with different bPEI:TOUS-CNF (w/w) ratios. Finally, we investigated the effect of the addition of citric acid in the CNS formulation, confirming its role in increasing cross-linking density and sponge rigidity. The obtained results appear crucial in order to rationalize the design of these sponges and to track the changes in the ability of the final products as efficient nano-confinement systems for water.

Cellulose represents a low cost, abundant, and renewable polysaccharide with great versatility, it has a hierarchical structure composed of nanofibers with high aspect ratio (3–4 nm wide, hundreds of μm long). TEMPO-mediated oxidation represents one of the most diffused methods to obtain cellulose nanofibers (CNFs): It is possible to obtain physically crosslinked hydrogels by means of divalent cation addition. The presence of inorganic components, such as calcium phosphates (CaP), can improve not only their mechanical properties but also the bioactivity of the gels. The aim of this work is to design and characterize a TEMPO-oxidized cellulose nanofibers (TOCNFs) injectable hydrogel embedded with inorganic particles, CaP and CaP-GO, for bone tissue regeneration. Inorganic particles act as physical crosslinkers, as proven by rheological characterization, which reported an increase in mechanical properties. The average load value registered in injection tests was in the range of 1.5–4.4 N, far below 30 N, considered a reasonable injection force upper limit. Samples were stable for up to 28 days and both CaP and CaP-GO accelerate mineralization as suggested by SEM and XRD analysis. No cytotoxic effects were shown on SAOS-2 cells cultured with eluates. This work demonstrated that the physicochemical properties of TOCNFs-based dispersions could be enhanced and modulated through the addition of the inorganic phases, maintaining the injectability and bioactivity of the hydrogels.

Along with social and economic development, population growth and the increasing interests in exploitation of marine resources, a progressively increase of marine pollution is expected. Both marine communities populating coastal areas as well as the deep sea have been continuously threatened by various classes of chemical pollutants with associated environmental deterioration and reduction of ecosystem services. Since the sustainable development and ecological protection of the ocean means that of human beings, efficient solutions for pollution monitoring and hazards mitigation are mandatory. Here we propose innovative nano-based solutions developed in the framework of an ecologically based design strategy (eco-design) able to quick and efficient detect and remove chemical pollutants from marine waters with no further associated risk for humans and the environment.

The achievement of a homogeneous dispersion of nanoparticles is of paramount importance in supporting their technological application. In wet processing, stable dispersions were largely obtained via surfactant or surface functionalization: although effective, the use of dispersant can alter, or even impair, the functional properties of the resulting nanostructured systems. Herein, we report a novel integrated modeling and experimental approach to obtain stable ZrO2 nanoparticle (NP) dispersions at native dimensions (about 5 nm) in homogeneous ternary mixtures of solvents (i.e., water, ethanol, and 1,2-dichlorobenzene) without any further surface functionalization. A miscibility ternary diagram was computed exploiting the universal quasi-chemical functional-group activity coefficient (UNIFAC) model, which was then experimentally validated. Dynamic light scattering (DLS) on these mixtures highlights that nanometric structures, resembling nanoemulsion droplets, form close to the mixture two-phase boundary, with a size that depends on the ternary mixture composition. ZrO2-NPs were then synthesized following a classic sol-gel approach and characterized by XRD and Raman spectroscopy. ZrO2-NPs were dispersed in HCl and mixed with different mixtures of ethanol and 1,2-dichlorobenzene (DCB), obtaining homogeneous and stable dispersions. These dispersions were then studied by means of DLS as a function of DCB concentration, observing that the nanoparticles can be dispersed at their native dimensions when the mass fraction of DCB was lower than 60%, whereas the increase of the hydrophobic solvent leads to the NPs' agglomeration and sedimentation. The proposed approach not only offers specific guidelines for the design of ZrO2-NPs dispersions in a ternary solvent mixture but can also be extended to other complex solvent mixtures in order to achieve stable dispersions of nanoparticles with no functionalization.

Aerogels are commonly regarded as soft and versatile materials for multiple applications thanks to their features such as elastic behavior, swelling ability and responsive characteristics. In the last decades these qualities have ensured them multiple uses in biomedical field as controlled drug delivery systems and scaffolds for tissue engineering applications. Recently their employment as sensors has attracted great interest especially thanks to their tunability and the possibility to be used as soft material instead of conventional and many times unreliable sensors in multiple sensing applications. In this work we synthetized graphene oxide/polyaniline aerogels by in situ chemical polymerization of aniline monomer in aqueous dispersion of graphene oxide sheets. We characterized the system through chemical and mechanical analysis, and we its responsivity as gas sensing device was verified. Moreover, we investigated the influence of the encapsulation of graphene nanoplatelets on the responsive ability of the device. The addition of the graphene moieties improves the conductivity of the system, its compressive mechanical resistance and the applicability of these devices as gas sensors.

Fourier transform infrared spectroscopy in attenuated total reflectance geometry (FTIR-ATR), combined with a 2D correlation analysis, was here employed to investigate temperature-induced spectral changes occurring in a particular type of novel cellulosic-based nano-material prepared using 2,2,6,6-tetramethyl-piperidine-1-oxyl (TEMPO) oxidized and ultra-sonicated cellulose nano-fibers (TOUS-CNFs) as three-dimensional scaffolds, and branched polyethyleneimine (bPEI) as cross-linking agent. The aim was to highlight the complex sequential events involving the different functional groups of the polymeric network, as well as to gain insight into the interplay between the amount of bPEI and the resulting sponge-like material, upon increasing temperature. In this framework, synchronous and asynchronous 2D spectra were computed and analyzed in three wavenumber regions (900–1200 cm−1, 1500–1700 cm−1 and 2680–3780 cm−1), where specific vibrational modes of the cellulosic structure fall, and over a T-range between 250 K and 340 K. A step-by-step evolution of the different arrangements of the polymer functional groups was proposed, with particular regard to how the cooperativity degree of inter- and intramolecular hydrogen bonds (HBs) changes upon heating. Information acquired can be useful, in principle, in order to develop a next-generation, T-sensitive novel material to be used for water remediation applications or for drug-delivery nano-vectors.

“Minisci reaction,” which is the nucleophilic substitution of protonated heteroaromatic bases by carbon-centered radicals under oxidative conditions, finds useful applications in organic synthesis. Over the last 50 years, Minisci reaction has reached its full consecration, finding application in several organic synthetic routes for a wide range of molecules of pharmaceutical and biological interest. This photocatalytic approach for the promotion of this chemo- and regioselective substitution of heteroarenes has appeared as a potential eco-friendly alternative to the classical thermal routes. In this context the sunlight-induced nucleophilic radical addition to protonated heteroaromatic bases catalyzed by TiO2-based semiconductors could be considered as the genesis of the photocatalytic approach. This protocol, which was successfully applied for the generation of a wide range of radical sources, has been widely analyzed in the first edition of this volume. Herein, after recalling some key aspects of the TiO2-photocatalysis, and our progress in the molecular dynamic studies finalized to the future design of ideal TiO2 crystals, we mainly focus on the recent advances in sun- and visible light–mediated Minisci reaction, outlining the progress behind the state-of-the-art to promote the regio- and even enantioselective functionalization of heteroaromatic bases under milder and more benign conditions.

Cellulose/polyethyleneimine composites have increasingly attracted the attention of scientific community, devoted to the design and development of new synthetic strategies and materials for different application fields. In this review, after introducing the main characteristics of the two polymeric components, we provide in the second section a critical overview on the main protocols for the synthesis of these composites, considering both the several cellulose sources and forms, and the different cross-linkers and cross-linking procedures developed for this purpose, outlining advantages and limits for the reported approaches. The last section analyses the principal results obtained in different application fields. A wide discussion is dedicated to the principal use of cellulose/polyethyleneimine composites as sorbents for water remediation from heavy metal ions and organic contaminants. Subsequently, we introduce the literature describing the use of these composites, functionalized appropriately, where necessary, as drug delivery systems, sensors, and heterogeneous catalysts for organic reactions. Finally, after a brief description of other random applications, we furnish a personal analysis of actual limits and potentialities for these systems.

To encourage the applicability of nano-adsorbent materials for heavy metal ion removal from seawater and limit any potential side effects for marine organisms, an ecotoxicological evaluation based on a biological effect-based approach is presented. ZnCl2 (10 mg L&minus, 1) contaminated artificial seawater (ASW) was treated with newly developed eco-friendly cellulose-based nanosponges (CNS) (1.25 g L&minus, 1 for 2 h), and the cellular and tissue responses of marine mussel Mytilus galloprovincialis were measured before and after CNS treatment. A control group (ASW only) and a negative control group (CNS in ASW) were also tested. Methods: A significant recovery of Zn-induced damages in circulating immune and gill cells and mantle edges was observed in mussels exposed after CNS treatment. Genetic and chromosomal damages reversed to control levels in mussels&rsquo, gill cells (DNA integrity level, nuclear abnormalities and apoptotic cells) and hemocytes (micronuclei), in which a recovery of lysosomal membrane stability (LMS) was also observed. Damage to syphons, loss of cilia by mantle edge epithelial cells and an increase in mucous cells in ZnCl2-exposed mussels were absent in specimens after CNS treatment, in which the mantle histology resembled that of the controls. No effects were observed in mussels exposed to CNS alone. As further proof of CNS&rsquo, ability to remove Zn(II) from ASW, a significant reduction of &gt, 90% of Zn levels in ASW after CNS treatment was observed (from 6.006 to 0.510 mg L&minus, 1). Ecotoxicological evaluation confirmed the ability of CNS to remove Zn from ASW by showing a full recovery of Zn-induced toxicological responses to the levels of mussels exposed to ASW only (controls). An effect-based approach was thus proven to be useful in order to further support the environmentally safe (ecosafety) application of CNS for heavy metal removal from seawater.

Stable hydrogels with tunable rheological properties were prepared by adding Ca2+ ions to aqueous dispersions of 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-oxidized and ultra-sonicated cellulose nanofibers (TOUS-CNFs). The gelation occurred by interaction among polyvalent cations and the carboxylic units introduced on TOUS-CNFs during the oxidation process. Both dynamic viscosity values and pseudoplastic rheological behaviour increased by increasing the Ca2+ concentration, confirming the cross-linking action of the bivalent cation. The hydrogels were proved to be suitable controlled release systems by measuring the diffusion coefficient of a drug model (ibuprofen, IB) by high-resolution magic angle spinning (HR-MAS) nuclear magnetic resonance (NMR) spectroscopy. IB was used both as free molecule and as a 1:1 pre-formed complex with &beta, cyclodextrin (IB/&beta, CD), showing in this latter case a lower diffusion coefficient. Finally, the cytocompatibility of the TOUS-CNFs/Ca2+ hydrogels was demonstrated in vitro by indirect and direct tests conducted on a L929 murine fibroblast cell line, achieving a percentage number of viable cells after 7 days higher than 70%.

Silver nanoparticles (AgNPs) are widely used as engineered nanomaterials (ENMs) in many advanced nanotechnologies, due to their versatile, easy and cheap preparations combined with peculiar chemical-physical properties. Their increased production and integration in environmental applications including water treatment raise concerns for their impact on humans and the environment. An eco-design strategy that makes it possible to combine the best material performances with no risk for the natural ecosystems and living beings has been recently proposed. This review envisages potential hybrid solutions of AgNPs for water pollution monitoring and remediation to satisfy their successful, environmentally safe (ecosafe) application. Being extremely efficient in pollutants sensing and degradation, their ecosafe application can be achieved in combination with polymeric-based materials, especially with cellulose, by following an eco-design approach. In fact, (AgNPs)–cellulose hybrids have the double advantage of being easily produced using recycled material, with low costs and possible reuse, and of being ecosafe, if properly designed. An updated view of the use and prospects of these advanced hybrids AgNP-based materials is provided, which will surely speed their environmental application with consequent significant economic and environmental impact.

The contamination of freshwaters by heavy metals represents a great problem, posing a threat for human and environmental health. Cadmium is classified as carcinogen to humans and its mechanism of carcinogenicity includes genotoxic events. In this study a recently developed eco-friendly cellulose-based nanosponge (CNS) was investigated as a candidate in freshwater nano-remediation process. For this purpose, CdCl2 (0.05 mg L&minus, 1) contaminated artificial freshwater (AFW) was treated with CNS (1.25 g L&minus, 1 for 2 h), and cellular responses were analyzed before and after CNS treatment in Dreissena polymorpha hemocytes. A control group (AFW) and a negative control group (CNS in AFW) were also tested. DNA primary damage was evaluated by Comet assay while chromosomal damage and cell proliferation were assessed by Cytome assay. AFW exposed to CNS did not cause any genotoxic effect in zebra mussel hemocytes. Moreover, DNA damage and cell proliferation induced by Cd(II) turned down to control level after 2 days when CNS were used. A reduction of Cd(II)-induced micronuclei and nuclear abnormalities was also observed. CNS was thus found to be a safe and effective candidate in cadmium remediation process being efficient in metal sequestering, restoring cellular damage exerted by Cd(II) exposure, without altering cellular physiological activity.

The growing human activity on the sea coasts is more and more associated to a progressively increasing of seawater pollution. Ship operational discharges (such as bilge water), together with local accidents or illegal activities, often lead to detect ppm concentrations of heavy metal ions in marine waters. For this reason, highly efficient remediation technologies are required to guarantee the abatement of these contaminants. The use of engineered nanomaterials (ENMs) is emerging as a valuable alternative for environmental remediation. However, the concerns related to ENMs potential ecotoxicity still limit their use in real scenarios, in spite of the good to excellent remediation performances. The correct choice of the starting material and of the synthetic protocol could provide new safe-by-design solutions for this purpose. Following this approach, we herein report the eco-design strategy used for the development of eco-friendly cellulose-based nanostructured sponges (CNS). The latter resulted to be effective sorbent units for heavy metals removal from seawater. The materials were obtained following a two-step protocol, consisting first in the production of TEMPO-oxidized cellulose nanofibers, followed by their cross-linking in the presence of branched polyethyleneimine. CNSs herein described exhibit high performances in removing a wide range of heavy metal ions (Zn(II), Cd(II), Cr(III), Hg(II), Ni(II), and Cu(II)) from artificial sea water (ASW) in a concentration range of 1–250 ppm. Environmental safety of materials (ecosafety) was investigated by using a standardized ecotoxicity bioassay as algal growth inhibition test (OECD 201) coupled with an in vivo exposure study using a filter-feeder marine bivalve species in which immune cells viability (neutral red retention time) and genotoxicity (micronucleus test) were investigated. The results in terms of eco-safety evaluation led to the optimization of the material synthetic strategy (eco-design) and allow to combine the best decontamination efficiency with no risk for aquatic biota.

The present paper reports a detailed experimental vibrational analysis, performed by Fourier transform infrared spectroscopy in attenuated total reflectance geometry (FTIR-ATR), of water confined in the pores of cellulose nano-sponges (CNSs), prepared using TEMPO oxidized and ultra-sonicated cellulose nano-fibers (TOUS-CNFs) as three-dimensional scaffolds, and branched polyethyleneimine (bPEI) as the cross-linking agent. The analysis was carried out by varying hydration and cross-linker amount, with the aim of achieving a deep understanding of how the hydrogen bond (H-bond) scheme developed by engaged water molecules can play a role in the water adsorption process already observed at macroscopic level, furnishing at the same time evidence of a nano-porous network for CNSs. In particular, the combined investigation of the FTIR-ATR spectra of CNSs hydrated with H2O and D2O allowed for the selective analysis of vibrational modes of entrapped water molecules, namely O–H stretching and HOH bending modes. As main result, a destructuring effect of hydration on the H-bond pattern of interfacial water molecules is revealed, associated to structural modifications of the bPEI/TOUS-CNFs network previously detected by small angle neutron scattering (SANS) technique. It turned out to be more relevant for low bPEI amounts. In addition, a supercooled behavior of entrapped water molecules is detected, supporting the idea of a nano-confinement for water in these systems. The obtained information can be very helpful in view of all the possible applications of bPEI-TOCNF sponges as efficient adsorbent materials, especially for water remediation.

The use of engineered nanomaterials (ENMs) for environmental remediation, known as nanoremediation, represents a challenging and innovative solution; however, their environmental application still poses many questions in terms of ecological impact, as their benefits could be overcome by environmental costs. The documented hazard of ENMs for aquatic species raises regulatory concerns and public awareness in terms of risk–benefit and calls for a more ecologically safe predictive assessment approach in order to support their safe application in the field (ecosafety). The need of efficient and sustainable technologies for environmental remediation is now moving the research interest toward new eco-friendly materials, abundant in nature, that require little processing and biodegradable. Biomass waste is a priceless source of building blocks for the design of ecosafe solutions.

Stable hydrogels with tunable rheological properties were prepared by adding Ca2+ ions to aqueous dispersions of 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-oxidized and ultra-sonicated cellulose nanofibers (TOUS-CNFs). The gelation occurred by interaction among polyvalent cations and the carboxylic units introduced on TOUS-CNFs during the oxidation process. Both dynamic viscosity values and pseudoplastic rheological behaviour increased by increasing the Ca2+ concentration, confirming the cross-linking action of the bivalent cation. The hydrogels were proved to be suitable controlled release systems by measuring the diffusion coefficient of a drug model (ibuprofen, IB) by high-resolution magic angle spinning (HR-MAS) nuclear magnetic resonance (NMR) spectroscopy. IB was used both as free molecule and as a 1:1 pre-formed complex with β-cyclodextrin (IB/β-CD), showing in this latter case a lower diffusion coefficient. Finally, the cytocompatibility of the TOUS-CNFs/Ca2+ hydrogels was demonstrated in vitro by indirect and direct tests conducted on a L929 murine fibroblast cell line, achieving a percentage number of viable cells after 7 days higher than 70%.

The challenging bioamination of hydrophobic substrates has been attained through the employment of a disperse system consisting in a combination of a low polarity solvent (e.g. isooctane or MTBE), a non-ionic surfactant and a minimal amount of water. In these conditions, good conversions are achieved, often coupled with a superior stereoselectivity if compared with the corresponding chemical reductive amination. An array of synthetically useful 4-substituted aminocyclohexanes was consequentially synthesized and stereochemically characterized.

Co-author Andrea Fiorati’s status as one of the two corresponding authors was not originally indicated on the published version. This Correction remedies that omission.

The response to pH variation of polymeric cyclodextrin-based hydrogels has been investigated by a multi-technique approach based on UV Raman and Brillouin light scattering (BLS) together with Small Angle Neutron Scattering (SANS). By exploiting the complementary information of these three investigation methods, the structural, viscoelastic and molecular modifications of the polymer brought about by the pH changes have been examined, over a spatial range going from mesoscopic to nanoscopic length-scale. The data provide a picture where an increase of pH promotes the change of the characteristic size of the hydrophilic pores when the cross-linker has the suitable structural and acid-base properties, and leads to the reinforcement of the polymer domains interconnections, providing a stiffer gel network on the length-scale probed by BLS. Raman signals are sensitive both to structural changes of the polymer network and to changes of the intermolecular ordering of water due to solvent-polymer interactions. The destructuring effect on the tetrahedral ice-like configurations of water is especially evident at high pH, and might be ascribed to an increased exposition to the solvent of the ionic portions of the polymer surface.

All-organic porous sponges were obtained throughout the direct and solvent-free (oven 105 °C, time>6 h) crosslinking of TEMPO-oxidized cellulose nanofibers (TOCNF) with 25 kDa branched polyethyleneimine (bPEI) in the presence of different amounts of citric acid (CA) as co-crosslinker. The chemical and mechanical stability of these materials was provided by the formation of amide bonds between the carboxylic moieties of TOCNF and CA with the primary amines of bPEI. The mechanical properties were investigated under static and dynamic loads with both dry and wet samples. The materials had the interesting capability to recover their shape with reduced losses in mechanical resistance, while their Young's modulus progressively increased with the content of CA. In work toward developing possible applications of bPEI-TOCNF sponges in drug delivery, amoxicillin (AM) and ibuprofen (IB) were considered as model drugs. All materials showed very good performance in adsorbing both AM and IB (ca. 200 mg g-1 ) from methanol solution. In particular, an increased adsorption of IB was observed in parallel to the increase of citrate moieties in the samples. Moreover, samples crosslinked in presence of CA showed slower kinetic release in aqueous environments than materials obtained without CA.

International audience; The oxidation of natural polysaccharides by TEMPO has become by now an “old chemical reaction” which led to numerous studies mainly conducted on cellulose. This regioselective oxidation of primary alcohol groups of neutral polysaccharides has generated a new class of polyuronides not identified before in nature, even if the discovery of enzymes promoting an analogous oxidation has been more recently reported. Around the same time, the scientific community discovered the surprising biological and techno-functional properties of these anionic macromolecules with a high potential of application in numerous industrial fields. The objective of this review is to establish the state of the art of TEMPO chemistry applied to polysaccharide oxidation, its history, the resulting products, their applications and the associated modifying enzymes.

Nanoremediation, which is the use of nanoparticles and nanomaterials for environmental remediation, is widely explored and proposed for preservation of ecosystems that suffer from the increase in human population, pollution, and urbanization. We herein report a critical analysis of nanotechnologies for water remediation by assessing their sustainability in terms of efficient removal of pollutants, appropriate methods for monitoring their effectiveness, and protocols for the evaluation of any potential environmental risks. Our purpose is to furnish fruitful guidelines for sustainable water management, able to promote nanoremediation also at European level. In this context, we describe new nanostructured polysaccharide-based materials obtained from renewable resources as alternative efficient and ecosafe solutions for water nano-treatment. We also provide eco-design indications to improve the sustainability of the production of these materials, based on life-cycle assessment methodology.

L-Aspartate oxidase from the thermophilic archaebacterium Sulfolobus tokodaii (StLASPO) catalyzes the stereoselective oxidative deamination of L-aspartate to yield oxaloacetate, ammonia and hydrogen peroxide. The recombinant flavoenzyme shows distinctive features that make it attractive for biotechnological applications (it is highly thermostable, it is stable in a broad pH range, it tightly binds the FAD cofactor and it shows a low K-m for dioxygen). In order to set up an efficient and economically feasible bioconversion process, in this work, we investigated the immobilization of this novel biocatalyst. The best results in terms of immobilization yield have been obtained when StLASPO was immobilized on the amino support Relizyme (TM) HA403/S R after activation with glutaraldehyde and on the epoxy support SEPABEADS (R) EC-EP/S (in both cases, through the free amino groups of the enzyme), as well as prepared as cross-linked enzyme aggregates (CLEA). By using the Relizyme (TM) HA403/S R support, as well as by the CLEA preparation procedure, full immobilization in terms of enzymatic activity was obtained. Immobilized StLASPO was used for the resolution of racemic solutions of 50 mM D, L-aspartate achieving full resolution in