K. Chrissafis

Fabrication of alginate–gelatin crosslinked hydrogel microcapsules and evaluation of the microstructure and physico-chemical properties

Microencapsulation of cells by using biodegradable hydrogels offers numerous attractive features for a variety of biomedical applications including tissue engineering. This study highlights the fabrication of microcapsules from an alginate-gelatin crosslinked hydrogel (ADA-GEL) and presents the evaluation of the physico-chemical properties of the new microcapsules which are relevant for designing suitable microcapsules for tissue engineering. Alginate di-aldehyde (ADA) was synthesized by periodate oxidation of alginate which facilitates crosslinking with gelatin through Schiffs base formation between the free amino groups of gelatin and the available aldehyde groups of ADA. Formation of Schiffs base in ADA-GEL and aldehyde groups in ADA was confirmed by FTIR and NMR spectroscopy, respectively. Thermal degradation behavior of films and microcapsules fabricated from alginate, ADA and ADA-GEL was dependent on the hydrogel composition. The gelation time of ADA-GEL was found to decrease with increasing gelatin content. The swelling ratio of ADA-GEL microcapsules of all compositions was significantly decreased, whereas the degradability was found to increase with the increase of gelatin ratio. The surface morphology of the ADA-GEL microcapsules was totally different from that of alginate and ADA microcapsules, observed by SEM. Two different buffer solutions (with and without calcium salt) have an influence on the stability of microcapsules which had a significant effect on the gelatin release profile of ADA-GEL microcapsules in these two buffer solutions.

Microstructural changes of processed vitrified solid waste products

Abstract Toxic lead-rich solid industrial wastes were stabilized by the vitrification method. Vitrification was attained by the addition of SiO 2 and Na 2 O as vitrifying and melting agent, respectively. The non-toxic, homogeneous, vitreous products studied in the present work, contain 60 wt.% of solid waste. Products with such a high content of solid waste comprise an economically realistic suggestion, but are easily devitrified in conditions of large-scale production due to the difficulty to achieve rapid cooling conditions in the whole volume of a large piece of stabilized product. Thus, it must be ascertained that the loss of homogeneity is not accompanied with the loss of chemical stability. Differential Thermal Analysis (DTA) was applied in order to inspect the prospect to crystal phase separation. The separated crystal phases were characterized by X-ray diffraction and transmission electron microscopy. Possible devitrification processes are investigated in order to interconnect the microstructure with the chemical stability of the devitrified products.

Multiresponsive polymer conetworks capable of responding to changes in pH, temperature, and magnetic field: synthesis, characterization, and evaluation of their ability for controlled uptake and release of solutes.

This study deals with the preparation of novel multiresponsive (magnetoresponsive, thermoresponsive and pH-responsive) nanocomposite conetworks consisting of oleic acid-coated magnetite nanoparticles (OA·Fe(3)O(4)), hydrophilic/thermoresponsive hexa(ethylene glycol) methyl ether methacrylate (HEGMA), hydrophobic/metal binding 2-(acetoacetoxy)ethyl methacrylate (AEMA), and pH-responsive/thermoresponsive N-diethylaminoethyl methacrylate (DEAEMA) and 2-(dimethylamino)ethyl methacrylate (DMAEMA) moieties. Conventional free radical copolymerization was employed for the synthesis of random conetworks in the absence and presence of preformed OA·Fe(3)O(4). Further, in characterization of these materials in regards to their swelling behavior in organic and aqueous solvents, thermal/thermoresponsive properties, and composition, assessment of their magnetic characteristics disclosed tunable superparamagnetic behavior. These systems were also evaluated toward their ability to adsorb and release a solute (benzoic acid) in a controlled manner upon varying the pH.

Structural studies of MoS2 intercalated by lithium

Abstract Defects created by intercalation in MoS2 single crystals were studied by plane and cross-sectional electron microscopy. In the first stage of intercalation the effect is to create extensive dislocations. Further intercalation leads to a structural transformation of the type 2H → 1T , as is evident from the appearance of spots in the diffraction pattern belonging to the new phase. In addition, the transformation is accompanied by a 2a 0 × 2a 0 superstructure. This superstructure is unstable and disappears on heating, while the structural transformation is irreversible.

β-Nucleated Polypropylene: Processing, Properties and Nanocomposites

Polypropylene (PP) and its allotropic forms is one of the most important polymeric materials due to its wide commercial penetration and academic interest over the last decades. The current review deals with β-polypropylene, one of the most interesting crystalline forms of PP, due to its metastable nature and the various physical properties which it presents. The introduction of β-crystals into the PP structure can be either simple or more complex procedure and several strategies are discussed in the current manuscript. Also, the physical properties of the specific material including structure-property relationships, thermal properties, and supermolecular structure are presented in detail. Additionally, the presence of β-PP in polymeric blends is evaluated and the effect of each component and preparation method on the polymorphic composition is debated. Finally, β-PP has been used as a polymeric matrix in several polymer nanocomposites, therefore the performance, polymorphic composition, and preparation methods have been also discussed in terms of the β-crystalline structure and the ultimate physical properties of the nanocomposites.

Incineration of tannery sludge under oxic and anoxic conditions: study of chromium speciation.

A tannery sludge, produced from physico-chemical treatment of tannery wastewaters, was incinerated without any pre-treatment process under oxic and anoxic conditions, by controlling the abundance of oxygen. Incineration in oxic conditions was performed at the temperature range from 300°C to 1200°C for duration of 2h, while in anoxic conditions at the temperature range from 400°C to 600°C and varying durations. Incineration under oxic conditions at 500°C resulted in almost total oxidation of Cr(III) to Cr(VI), with CaCrO4 to be the crystalline phase containing Cr(VI). At higher temperatures a part of Cr(VI) was reduced, mainly due to the formation of MgCr2O4. At 1200°C approximately 30% of Cr(VI) was reduced to Cr(III). Incineration under anoxic conditions substantially reduced the extent of oxidation of Cr(III) to Cr(VI). Increase of temperature and duration of incineration lead to increase of Cr(VI) content, while no chromium containing crystalline phase was detected.

Hybrid hydrogels based on keratin and alginate for tissue engineering

Novel hybrid hydrogels based on alginate and keratin were successfully produced for the first time. The self-assembly properties of keratin, and its ability to mimic the extracellular matrix were combined with the excellent chemical and mechanical stability and biocompatibility of alginate to produce 2D and 3D hybrid hydrogels. These hybrid hydrogels were prepared using two different approaches: sonication, to obtain 2D hydrogels, and a pressure-driven extrusion technique to produce 3D hydrogels. All results indicated that the composition of the hydrogels had a significant effect on their physical properties, and that they can easily be tuned to obtain materials suitable for biological applications. The cell-material interaction was assessed through the use of human umbilical vein endothelial cells, and the results demonstrated that the alginate/keratin hybrid biomaterials supported cell attachment, spreading and proliferation. The results proved that such novel hybrid hydrogels might find applications as scaffolds for soft tissue regeneration.

Competitive crystallization of a propylene/ethylene random copolymer filled with a β-nucleating agent and multi-walled carbon nanotubes. Conventional and ultrafast DSC study.

A propylene/ethylene polymeric matrix was reinforced by the simultaneous addition of a β-nucleating agent (calcium pimelate) and multi-walled carbon nanotubes (MWCNTs) in various concentrations. The present manuscript explores the competitive crystallization tendency that is caused by the presence of the two fillers. On the one hand, calcium pimelate forces the material to crystallize predominantly in the β-crystalline form, while, on the other, the strong α-nucleating ability of MWCNTs compels the material to develop higher α-crystalline content. An in-depth study has been performed on the nanocomposite samples by means of conventional, temperature-modulated, and differential fast scanning calorimetry (DFSC) under various dynamic and isothermal conditions. The results showed that β-crystals are predominant at low MWCNT content (<2.5 wt %), while, at high MWCNT content, the material crystallizes mainly in the α-form. The recrystallization phenomenon during melting was confirmed with step-scan DSC, and the use of very high cooling rates by UFDSC made it possible to achieve and study the nucleation of the samples. The presence of MWCNTs enabled the nanocomposites to crystallize faster under both isothermal and dynamic conditions. The activation energy of the samples was also calculated according to Friedmans theory.

Factors controlling the enhanced mechanical and thermal properties of nanodiamond-reinforced cross-linked high density polyethylene.

A systematic investigation of the factors influencing the notable enhancement of the mechanical and thermal properties of nanodiamonds (NDs)-reinforced cross-linked high density polyethylene (PEX) is presented in this work. The effects of crystal structure and molecular conformation as well as filler dispersion and adhesion with the matrix were found to govern the mechanical properties of the final composites. A considerable increase in the strength, toughness, and elastic modulus of the materials was found for the composites with filler content below 1 wt %. For higher NDs concentrations, the properties degraded. When filler concentration does not exceed 1 wt %, enhanced adhesion with the matrix is achieved, allowing a more successful load transfer between the filler and the matrix, thus enabling an effective reinforcement of the composites. The higher degree of crystallinity along with larger crystal size are also positively influencing the mechanical properties of PEX. Higher filler concentrations, on the other hand, lead to the formation of larger aggregates, which lead to lower adhesion with the matrix, while they also constitute stress concentrators and therefore reduce the positive reinforcement of the matrix. The thermal conductivity of the composites was also found to be significantly increased for low-filler concentrations. This enhancement was less significant for higher NDs concentrations. It is concluded that this reinforcement is due to the heat capacity increase that NDs incorporation causes in PEX. Additionally, a thermal stability enhancement was found for the composite with minimum filler content.

Soft-matrices based on silk fibroin and alginate for tissue engineering

Soft tissue regeneration requires the use of matrices that exhibit adequate mechanical properties as well as the ability to supply nutrients and oxygen, and to remove metabolic bio-products. In this work, we describe the development of hydrogels based on the blend between alginate (Alg) and silk fibroin (SF). Herein, we report two main strategies to combine cells with biomaterials: cells are either seeded onto prefabricated hydrogels films (2D), or encapsulated during hydrogel microcapsules formation (3D). Both geometries were successfully produced and characterized. FTIR results indicated a change of conformation of SF from random coil to β-sheet after hydrogel formation. The thermal degradation behavior of films and microcapsules fabricated from Alg, and Alg/SF was dependent on the hydrogel composition and on the geometry of the samples. The presence of SF caused decreased water uptake ability and affected the degradation behavior. Mechanical tests showed that addition of SF promotes an increase in storage modulus, leading to a stiffer material as compared with pure Alg (6 times higher stiffness). Moreover, the in vitro cell-material interaction on Alg/SF hydrogels of different geometries was investigated using human umbilical vein endothelial cells (HUVECs). Viability, attachment, spreading and proliferation of HUVECs were significantly increased on Alg/SF hydrogels compared to neat Alg. These findings indicate that Alg/SF hydrogel is a promising material for the biomedical applications in tissue-engineering and regeneration.