Non-Aqueous Poly(dimethylsiloxane) Organogel Sponges for Controlled Solvent Release: Synthesis, Characterization, and Application in the Cleaning of Artworks.

Polydimethylsiloxane (PDMS) organogel sponges were prepared and studied in order to understand the role of pore size in an elastomeric network on the ability to uptake and release organic solvents. PDMS organogel sponges have been produced according to sugar leaching techniques by adding two sugar templates of different forms and grain sizes (a sugar cube template and a powdered sugar template), in order to obtain materials differing in porosity, pore size distribution, and solvent absorption and liquid retention capability. These materials were compared to PDMS organogel slabs that do not contain pores. The sponges were characterized by Fourier-transform infrared spectroscopy with attenuated total reflectance (FTIR-ATR) and compared with PDMS slabs that do not contain pores. Scanning electron microscopy (SEM) provided information about their morphology. X-ray micro-tomography (XMT) allowed us to ascertain how the form of the sugar templating agent influences the porosity of the systems: when templated with sugar cubes, the porosity was 77% and the mean size of the pores was ca. 300 µm; when templated with powdered sugar, the porosity decreased to ca. 10% and the mean pore size was reduced to ca. 75 µm. These materials, porous organic polymers (POPs), can absorb many solvents in different proportions as a function of their polarity. Absorption capacity, as measured by swelling with eight solvents covering a wide range of polarities, was investigated. Rheology data established that solvent absorption did not have an appreciable impact on the gel-like properties of the sponges, suggesting their potential for applications in cultural heritage conservation. Application tests were conducted on the surfaces of two different lab mock-ups that simulate real painted works of art. They demonstrated further that PDMS sponges are a potential innovative support for controlled and selective cleaning of works of art surfaces.

Sponge-like Cryogels from Liquid-Liquid Phase Separation: Structure, Porosity, and Diffusional Gel Properties.

Macroporous gels find application in several scientific fields, ranging from art restoration to wastewater filtration or cell entrapment. In this work, two-component sponge-like cryogels are challenged to assess their cleaning performances and to investigate how pores size and connectivity affect physico-chemical properties. The gels were obtained through a freeze-thaw process, exploiting a spontaneous polymer-polymer phase-separation occurring in the pre-gel solution. During the freezing step, a highly hydrolyzed polyvinyl alcohol (H-PVA) forms the hydrogel walls. The secondary components, namely a partially hydrolyzed polyvinyl alcohol (L-PVA) or polyvinyl pyrrolidone (PVP), act as modular porogens, being partially extracted during gel washing. H-PVA/L-PVA and H-PVA/PVP mixtures were studied by confocal laser scanning microscopy to unveil sols and gels morphology at the micron-scale, while small angle X-ray scattering was used to get insights about characteristic dimensions at the nanoscale. The gelation mechanism was investigated through rheology measurements, and the characteristic exponents were compared to De Gennes' scaling laws gathered from percolation. In the field of art conservation, these sponge-like gels are ideal systems for the cleaning of artistic painted surfaces. Their interconnected pores allow the diffusion of cleaning fluids at the painted interface, facilitating dirt uptake and/or detachment. This study uncovered a direct relationship linking a gel's cleaning performance to its apparent tortuosity. These findings can pave the way to fine-tuning systems with enhanced cleaning abilities, not restricted to the restoration of irreplaceable priceless works of art, but with possible application in diverse research fields.

Specific ion effects on copper electroplating.

The main goal of this work is to open new perspectives in the field of electrodeposition and provide green alternatives to the electroplating industry. The effect of different anions (SO42-, ClO3-, NO3-, ClO4-, BF4-, PF6-) in solution on the electrodeposition of copper was investigated. The solutions, containing only the copper precursor and the background electrolyte, were tailored to minimize the environmental impact and reduce the use of organic additives and surfactants. The study is based on electrochemical measurements carried out to verify that no metal complexation takes place. We assessed the nucleation and growth mechanism, we performed a morphological characterization through scanning electron microscopy and deposition efficiency by measuring the film thickness through X-ray fluorescence spectroscopy. Significant differences in the growth mechanism and in the morphology of the electrodeposited films, were observed as a function of the background electrolyte.

Recovery of structural extracellular polymeric substances (sEPS) from aerobic granular sludge: Insights on biopolymers characterization and hydrogel properties for potential applications.

Nowadays, wastewater treatment plants (WWTPs) are transforming into water resource recovery facilities (WRRFs) where the resource recovery from waste streams is pivotal. Aerobic granular sludge (AGS) is a novel technology applied for wastewater treatment. Extracellular polymeric substances (EPS) secreted by microorganisms promote the aggregation of bacterial cells into AGS and the structural fraction of EPS (sEPS) is responsible for the mechanical properties of AGS. sEPS can be extracted and recovered from waste AGS by physico-chemical methods and its characterization is to date of relevant concern to understand the properties in the perspective of potential applications. This study reports on: characterization of sEPS extracted and recovered from AGS; - formation and characterization of sEPS-based hydrogels. Briefly, sEPS were extracted by a thermo-alkaline process followed by an acidic precipitation. sEPS-based hydrogels were formed by a cross-linking process with a 2.5% w/w CaCl2 solution. The following key-findings can be drawn: i) hydrogels can be formed starting from 1% w/w sEPS on, by diffusion of Ca2+ into sEPS network; ii) the Ca/C molar ratio of hydrogels decreased with increasing concentration of sEPS from 1 to 10% w/w; iii) the thermogravimetric and spectroscopic behaviours of sEPS show that the cross-linking reaction mainly involves the polysaccharidic fraction of biopolymers; iv) water-holding capacity up to 99 gH2O/gsEPS was registered for 1% w/w sEPS-based hydrogels, suggesting applications in several industrial sectors (i.e. chemical, paper, textile, agronomic, etc.); v) rheological results highlighted a solid-like behaviour (G'≫G") of sEPS-based hydrogels. The power-law fitting of G' vs. sEPS concentration suggests that the expansion of the sEPS network during cross-linking occurs through a percolative mechanism involving the initial formation of sEPS oligomers clusters followed by their interconnection towards the formation of 3D network. These findings provide additional information about the mechanisms of sEPS-based hydrogel formation and reveal the peculiar physico-chemical characteristics of sEPS which nowadays are increasingly gaining interest in the context of resource recovery.

Performance of innovative nanomaterials for bone remains consolidation and effect on 14C dating and on palaeogenetic analysis.

An innovative protocol for the consolidation of ancient bone remains based on the use of nanometric HydroxyAPatite (HAP) was set up and tested through a multidisciplinary approach. A new protocol for the synthesis of HAP nanoparticles was developed, and the composition of the obtained nanomaterial was investigated through Fourier Transform Infrared Spectroscopy (FTIR) and X-Ray Diffraction (XRD); sizes, shape and morphology of the synthesized particles were studied by Scanning Electron Microscopy (SEM). The consolidation performance was evaluated by testing the new nanomaterial on degraded ancient bone findings. An increase of the mineral density and of the micro-hardness of the bone were observed. The new consolidation method was also tested to assess possible effects on the palaeogenetic analysis and radiocarbon dating on the treated bones. The consolidation treatment does not introduce any contaminations that could affect radiocarbon dating and has no general detrimental impact on the genetic characterization of the skeletal remains. This consolidation procedure represents a more compatible conservation tool with respect to traditional procedures: it has been shown that the treatment is effective, easily-applicable and compatible with post-consolidation analysis.

Lipid vesicular gels for topical administration of antioxidants.

The application of a formulation on the skin represents an effective way to deliver bio-active molecules for therapeutical purposes. Moreover, the outermost skin layer, the stratum corneum, can be overcome by employing chemical permeation enhancers and edge activators as components. Several lipids can be considered as permeation enhancers, such as the ubiquitous monoolein, one of the most used building blocks for the preparation of lipid liquid crystalline nanoparticles which are applied as drug carriers for nanomedicine applications. Recent papers highlighted how bile salts can affect the phase behavior of monoolein to obtain drug carriers suitable for topical administration, given their role as edge activators into the formulation. Herein, the encapsulation of natural antioxidants (caffeic acid and ferulic acid) into lipid vesicular gels (LVGs) made by monoolein and sodium taurocholate (TC) in water was studied to produce formulations suitable for topical application. TC induces a bicontinuous cubic to multilamellar phase transition for monoolein in water at the given concentrations, and by increasing its content into the formulations, unilamellar LVGs are formed. The encapsulation of the two antioxidants did not affect significantly the structure of the gels. The oscillating rheological studies showed that ferulic acid has a structuring effect on the lipid matrix, in comparison with the empty dispersion and the one containing caffeic acid. These gels were then tested in vitro on new-born pig skin to evaluate their efficacy as drug carriers for topical administration, showing that caffeic acid is mostly retained in the gel whereas ferulic acid is released at a higher degree. The data herein reported provide some further information on the effect of bile salts on the lipid self-assembly to evaluate useful compositions for topical administration of natural antioxidants.

Heavy metal biosorption by Extracellular Polymeric Substances (EPS) recovered from anammox granular sludge.

The recovery and conversion of Extracellular Polymeric Substances (EPS) from sewage sludge into bio-based commodities might improve the economics and environmental sustainability of wastewater treatment. This contribution explores the application of EPS from anammox granular waste sludge as biosorbent for the removal of heavy metals, specifically lead, copper, nickel, and zinc. Adsorption capacities equivalent or higher than well-established adsorbent media emerged from single-metal biosorption studies (up to 84.9, 52.8, 21.7 and 7.4 mg/gTSEPS for Pb2+, Cu2+, Ni2+ and Zn2+, respectively). Combining spectroscopic techniques, a mechanistic hypothesis for metal biosorption, based on a combination of electrostatic interaction, ion exchange, complexation, and precipitation, was proposed. The adsorption mechanisms of extracted EPS and non-extracted EPS in the native biomass were indirectly compared by means of single-metal biosorption studies performed with pristine granules (adsorbing up to 103.7, 36.1, 48.2 and 49.8 mg/gTSgranules of Pb2+, Cu2+, Ni2+, and Zn2+, respectively). In comparison with pristine anammox granules, EPS showed lower adsorption capacities except for copper and different adsorption pathways as postulated based on the adsorption data interpretation via theoretical models. The multi-metal biosorption tests excluded significant competitions among different heavy metals for the EPS binding sites, thus opening further scenarios for the treatment of complex wastewaters.

Rigid and film bioplastics degradation under suboptimal composting conditions: A kinetic study.

The present research investigates the degradation rate of bioplastics under various composting conditions, including suboptimal ones. Lab-scale tests were carried out setting three variables: temperature (37°C-58°C), humidity (30%-60%) and duration of the thermophilic and the maturation phases (15-60 days). The composting tests were carried out following modified guideline ISO 20200:2015 and lasted for 60 days. Bioplastics in the synthetic waste matrix consisted of Mater-Bi® film biobags and PLA rigid teaspoons. A kinetic study was performed, resulting in faster degradation rates for film bioplastics (first-order kinetics with k = 0.0850-0.1663 d-1) than for rigid (0.0018-0.0136 d-1). Moreover, film bioplastics reached a complete degradation within the 60 days of the test. Concerning the rigid products, 90% degradation would be achieved in 2-3 years for mesophilic conditions. Finally, in the undersieve of 0.5 mm some microplastics were identified with the ImageJ software, mainly relatable to rigid (PLA) bioplastics. Overall, the results disclosed that the combination of mesophilic temperatures and absence of moistening slowed down both the degradation and the disintegration process of bioplastics.

Physicochemical characterization of green sodium oleate-based formulations. Part 1. Structure and rheology.

HYPOTHESIS: The structure, rheology and other physicochemical properties of dilute aqueous dispersions of sodium oleate (NaOL) are well known. This paper is the first report in which a moderately concentrated (13% w/w) dispersion of NaOL in water is investigated. In fact, at this concentration the phase and rheology behavior of the surfactant remarkably deviates from those of its dilute solutions in water and a significant effect is imparted by the addition of potassium chloride. EXPERIMENTAL: The structural, thermal and rheological properties of a 13% w/w dispersion of NaOL in water were investigated by cryo-TEM, rheology, and DSC experiments with and without the addition of potassium chloride. The system is comprised of elongated wormlike micelles that turn into a gel-like more disordered viscous material upon addition of small amounts of KCl (4% w/w). FINDINGS: This paper illustrates the multifaceted behavior of sodium oleate dispersions at intermediate concentrations that depends on the presence of other cosolutes (such as KCl). The results show that viscoelastic aqueous dispersions of NaOL are excellent candidates for the preparation of stimuli-responsive green materials to be used in a number of different applications. We also discuss the genesis of wormlike micelles (WLMs) in terms of the general theory of self-assembly.

A highly efficient multi-step methodology for the quantification of micro-(bio)plastics in sludge.

The present study develops a multi-step methodology for identification and quantification of microplastics and micro-bioplastics (together called in the current work micro-(bio)plastics) in sludge. In previous studies, different methods for the extraction of microplastics were devised for traditional plastics, while the current research tested the methodology on starch-based micro-bioplastics of 0.1-2 mm size. Compostable bioplastics are expected to enter the anaerobic or aerobic biological treatments that lead to end-products applicable in agriculture; some critical conditions of treatments (e.g. low temperature and moisture) can slow down the degradation process and be responsible for the presence of microplastics in the end-product. The methodology consists of an initial oxidation step, with hydrogen peroxide 35% concentrated to clear the sludge and remove the organic fraction, followed by a combination of flotation with sodium chloride and observation of the residues under a fluorescence microscope using a green filter. The workflow revealed an efficacy of removal from 94% to 100% and from 92% to 96% for plastic fragments, 0.5-2 mm and 0.1-0.5 mm size, respectively. The methodology was then applied to samples of food waste pulp harvested after a shredding pre-treatment in an anaerobic digestion (AD) plant in Italy, where polyethylene, starch-based Mater-Bi® and cellophane microplastics were recovered in amounts of 9 ± 1.3/10 g <2 mm and 4.8 ± 1.2/10 g ⩾2 mm. The study highlights the need to lower the threshold size for the quantification of plastics in organic fertilizers, which is currently set by legislations at 2 mm, by improving the background knowledge about the fate of the micro-(bio)plastics in biological treatments for the organic waste.

Indoor levels of volatile organic compounds at Florentine museum environments in Italy.

Indoor Air Quality monitoring in cultural institutions is of particular concern to protect these places and the cultural heritage content. An indoor monitoring campaign was performed in three museums in Florence (Italy) to determine the occurrence and levels of volatile organic compounds (VOCs). VOCs of interest included BTEX (benzene, toluene, ethylbenzene, xylenes), terpenes, aldehydes, organic acids, and cyclic volatile methyl siloxanes (cVMS). The most abundant VOCs in all samples analyzed were BTEX, which were strictly related to the traffic source, followed by siloxanes and terpenes. Among BTEX, toluene was always the most abundant followed by xylenes, ethylbenzene, and benzene. cVMS in exhibition rooms with the presence of visitors showed higher values compared to samples collected when the museums were closed. Terpenes showed not only the influence of vegetation-biogenic sources surrounding a museum but could also be related to the wood used for the construction of showcases and furniture and the use of cleaning products. Data obtained also showed the presence of organic acids and aldehydes whose source can be traced back to exhibits themselves and wood-based furniture. Assessing the levels of organic acids in museums is important because, over time, it can cause deterioration of the artifacts.

Monitoring of degradation of starch-based biopolymer film under different composting conditions, using TGA, FTIR and SEM analysis.

This paper presents the results of a composting lab-scale test carried out on Mater-Bi® film, a starch-based biopolymer. The test material is composed by starch, additives and polybutylene adipate terephthalate (PBAT). The test lasted for 45 days and was developed in three replicates under different temperature and moisture conditions, with the aim to assess the influence on Mater-Bi® degradation of less favourable composting conditions as short thermophilic phase, absence of moistening, and a combination of the two factors. The chemical nature and the morphology of the material and of its single components have been investigated before, during and at the end of the composting process, by means of different analytical techniques. ThermoGravimetric Analysis (TGA) allowed to obtain activation energy and weight loss; Fourier Transform InfraRed spectroscopy (FTIR) and Scanning Electron Microscopy (SEM) were used to study changes in the polymeric and morphological structure, and visual analysis provided information on the size of the Mater-Bi® particles. The results show that the biodegradation of PBAT is strongly influenced by the environmental conditions (temperature and moisture); on the contrary, in all the three replicates, both starch and additives are completely biodegraded within the first days of the process.

Hydrogels formed by anammox extracellular polymeric substances: structural and mechanical insights.

The recovery of biopolymers from the waste sludge produced in wastewater treatments and their application in other industrial sectors, would substantially increase the environmental and economical sustainability of the process, promoting the development of a circular economy. In this study, extracellular polymeric substances (EPS) extracted from anammox granular waste sludge, were investigated and characterized. Rheological and differential scanning calorimetry measurements on EPS aqueous dispersions indicate the formation of an extended 3-D network above a threshold concentration, with a clear dependence of the mechanical and water retention properties on EPS content. The structural characterization, performed with transmission electron microscopy and small angle X-ray scattering, reveals the presence of functional amyloids as putative structural units, observed for the first time in an EPS-based hydrogel. As a proof of concept of the applicative potential, we explored the water and grease resistance provided to paper by an EPS coating. These results shed light on the structural details of EPS-based hydrogels, and pave the way for the possible use of EPS-based materials as a cheap, eco-friendly alternative to commonly adopted paper coatings, in line with a circular economy pattern for wastewater treatment.

Associative properties of poly(ethylene glycol)-poly(vinyl acetate) comb-like graft copolymers in water.

The self-assembly of amphiphilic graft copolymers is generally reported for polymer melts or polymers deposited onto surfaces, while a small number of cases deal with binary mixtures with water. We report on the associative properties of poly(ethylene glycol)-graft-poly(vinyl acetate) (PEG-g-PVAc) comb-like copolymers in water, demonstrating the existence of a percolative behaviour when increasing the PEG-g-PVAc content. Rheology, light- and small-angle X-ray scattering experiments, together with dissipative particle dynamics simulations, reveal a progressive transition from spherical polymer single-chain nanoparticles (SCNPs) towards hierarchically complex structures as the weight fraction of the polymer in water increases. The ability of PEG-g-PVAc to attain different nano- and microstructures is of great importance in numerous applications such as in the fields of cosmetics, detergency and drug delivery.

Inorganic nanoparticles modify the phase behavior and viscoelastic properties of non-lamellar lipid mesophases.

The inclusion of inorganic nanoparticles (NPs) within organized lipid assemblies combines the rich polymorphism of lipid phases with advanced functional properties provided by the NPs, expanding the applicative spectrum of these materials. In spite of the relevance of these hybrid systems, fundamental knowledge on the effects of NPs on the structure and physicochemical properties of lipid mesophases is still limited. This contribution combines Small-Angle X-ray Scattering (SAXS) and Rheology to connect the structural properties with the viscoelastic behavior of liquid crystalline mesophases of Phytantriol (Phyt) containing two kinds of hydrophobic NPs of similar size, i.e., gold NPs (AuNPs) and Superparamagnetic Iron Oxide NPs (SPIONs). Both types of NPs spontaneously embed in the hydrophobic domains of the liquid crystalline mesophase, deeply affecting its phase behavior, as SAXS results disclose. We propose a general model to interpret and predict the structure of cubic mesophases doped with hydrophobic NPs, where the effects on lipid phase behavior depend only on NPs' size and volume fraction but not on chemical identity. The rheological measurements reveal that NPs increase the solid-like behavior of the hybrid and, surprisingly, this effect depends on the chemical nature of the NPs. We interpret these results by suggesting that the long-range dipolar interactions of SPIONs affect the viscoelastic response of the material and provide an additional control parameter on mechanical properties. Overall, this study discloses new fundamental insights into hybrid liquid crystalline mesophases doped with hydrophobic NPs, highly relevant for future applications, e.g. in the biomedical field as smart materials for drug delivery.

Extraction, recovery and characterization of structural extracellular polymeric substances from anammox granular sludge.

The composition and colloidal properties of extracellular polymeric substances (EPS) from anammox granular sludge were investigated through a complete set of spectroscopic and scattering techniques. To fully characterize EPS, we developed a robust and reproducible extraction/recovery protocol specific for anammox biofilms, based on the change of water affinity under alternated alkaline and acidic conditions, each monitored with Z-potential and dynamic light scattering analysis. This method enabled both extraction as a colloidal suspension and recovery as a solid of large amounts of EPS (0.38 ±â€¯0.04 and 0.21 ±â€¯0.02 g/g, respectively), including for the first time its structural components. The dominance of the proteinaceous fraction was revealed by all methods tested, resulting in the highest protein/carbohydrates ratio reported for biofilms applied in the wastewater sector. The abundance of proteinaceous ordered structures and in particular of cross-ß motifs was detected, indicating for the first time the presence of amyloid-like aggregates in anammox EPS, and suggesting the key role of the protein fraction in determining the mechanical properties of the parent biofilm. The robustness and reproducibility of the proposed method fill the current gap towards a reliable full-scale recovery as well as towards an accurate and meaningful investigation of anammox EPS and pave the way for further exploration of their applicative potential thus stimulating the desirable shift from the current wastewater treatment perspective towards biorefinery in a circular economy context.

Complex Fluids Confined into Semi-interpenetrated Chemical Hydrogels for the Cleaning of Classic Art: A Rheological and SAXS Study.

The removal of aged varnishes from the surface of easel paintings using the common conservation practice (i.e., by means of organic solvents) often causes pigment leaching, paint loss, and varnish redeposition. Recently, we proposed an innovative cleaning system based on semi-interpenetrated polymer networks (SIPNs), where a covalently cross-linked poly(hydroxyethyl methacrylate), pHEMA, network is interpenetrated by linear chains of poly(vinylpyrrolidone), PVP. This chemical gel, simply loaded with water, was designed to safely remove surface dirt from water-sensitive artifacts. Here, we modified the SIPN to confine complex cleaning fluids, able to remove aged varnishes. These complex fluids are 5-component water-based nanostructured systems, where organic solvents are partially dispersed as nanosized droplets in a continuous aqueous phase, using surfactants. The rheological behavior of the SIPN and the nanostructure of the fluids loaded into the gel were investigated, and the mechanical behavior of the gel was optimized by varying both the cross-linking density and the polymer concentration. Once loaded with the complex fluids, the hydrogels maintained their structural and mechanical features, while the complex fluids showed a decrease in the size of the dispersed solvent droplets. Two challenging case studies have been selected to evaluate the applicability of the SIPN hydrogels loaded with the complex fluids. The first case study concerns the removal of a surface layer composed by an aged brown resinous patina from a wood panel, the second case study concerns the removal of a homogeneous layer of yellowed varnish from a watercolor on paper. The results show that the confinement of complex fluids into gels allowed unprecedented removal of varnishes from artifacts overcoming the limitations of traditional cleaning methods.

Structural, rheological and dynamics insights of hydroxypropyl guar gel-like systems.

A dynamic, rheological, and structural characterization of aqueous gel-like systems containing hydroxypropyl guar gum (HPG), borax and glycerol is presented in this paper. The role of glycerol, which is introduced as a plasticizer in the formulation, is investigated by means of 11B NMR and 1H NMR PGSTE measurements in order to clarify its contribution to the gel network formation and its interaction with borax, with whom it forms a complex. The effect of gels components on the rheological behaviour and on the activation energy related to the relaxation process of the system was assessed by means of rheology. The results obtained suggest that the mechanical properties of these gels can be tuned and controlled by modulating the formulation in a wide range of compositions. Moreover, a structural characterisation has been also carried out by means of Small Angle X-ray Scattering (SAXS) to highlight the role of the various components on the mesh size of the network. The structural and mechanical characteristics of these systems suggest their potential use for applicative purposes. In this regard, one of the gel set up has been successfully tested as cleaning agent on the surface of a XIX stucco fragment coming from the La Fenice theatre (Venice, Italy) for the removal of a dirt layer composed by dust and particulated matter originated during a fire in 1996.

Specific ion effects in polysaccharide dispersions.

The specific effects induced by some strong electrolytes or neutral co-solutes on aqueous mixtures of guar gum (GG), sodium alginate (SA) and sodium hyaluronate (SH) were studied through rheology and DSC experiments. The results are discussed in terms of changes in the polymer conformation, structure of the network and hydration properties. This study is also aimed at controlling the viscosity of the aqueous mixtures for application in green formulations to be used as fracturing fluids for shale gas extraction plants.

Injectable composites via functionalization of 1D nanoclays and biodegradable coupling with a polysaccharide hydrogel.

The use of injectable materials in minimally invasive surgical procedures could help in facing the bone diseases connected to the ageing of world population. To this aim, materials integrating the rheological properties of biocompatible polymers with the mechanical properties of 1D inorganic nanostructures represent promising scaffolds. Here we describe the preparation of hydrogel composites made of carboxymethyl cellulose (CMC) and halloysite nanotubes (HNT) as injectable materials for the local treatment of bone defects. The rheology and injectability of the materials reflects their structural properties, showing the possibility of successfully injecting the prepared composites over a large range of operative conditions.