Molecular self-assembly is the spontaneous association of molecules under equilibrium conditions into stable, structurally well-defined aggregates joined by noncovalent bonds. Molecular self-assembly is ubiquitous in biological systems and underlies the formation of a wide variety of complex biological structures. Understanding self-assembly and the associated noncovalent interactions that connect complementary interacting molecular surfaces in biological aggregates is a central concern in structural biochemistry. Self-assembly is also emerging as a new strategy in chemical synthesis, with the potential of generating nonbiological structures with dimensions of 1 to 10(2) nanometers (with molecular weights of 10(4) to 10(10) daltons). Structures in the upper part of this range of sizes are presently inaccessible through chemical synthesis, and the ability to prepare them would open a route to structures comparable in size (and perhaps complementary in function) to those that can be prepared by microlithography and other techniques of microfabrication.

Molecular self-assembly and nanochemistry: A chemical strategy for the synthesis of nanostructures

Renewable resources are used increasingly in the production of polymers. In particular, monomers such as carbon dioxide, terpenes, vegetable oils and carbohydrates can be used as feedstocks for the manufacture of a variety of sustainable materials and products, including elastomers, plastics, hydrogels, flexible electronics, resins, engineering polymers and composites. Efficient catalysis is required to produce monomers, to facilitate selective polymerizations and to enable recycling or upcycling of waste materials. There are opportunities to use such sustainable polymers in both high-value areas and in basic applications such as packaging. Life-cycle assessment can be used to quantify the environmental benefits of sustainable polymers.

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Sustainable polymers from renewable resources

Chemical modification of lignins: Towards biobased polymers

Synthesis, properties, and applications of magnetic iron oxide nanoparticles

A review on pyrolysis of plastic wastes

Polyvinyl alcohol (PVA) and chitosan (CS) based hydrogels are often chosen to obtain hydrogels as being considered non-toxic for human body. The present study aims the preparation and physical chemical characterisation of hydrogels based PVA and CS by using an environmental friendly method i.e. freeze/thaw. In this method the only parameters affecting the hydrogels’ properties is the PVA concentration in solution, time and number of cycles of freezing / thawing. Repeated freezing and thawing cycles resulted in production of a highly elastic polyvinyl alcohol hydrogel with higher degree of crystallization. Adding chitosan in polyvinyl alcohol hydrogel is giving to the newly formed material, biocompatibility and antibacterial properties due to the free amino groups of chitosan. Higher mechanical and thermal characteristics of PVA/CS based hydrogels were obtained by addition of a small amount of inorganic nanoparticles (montmorillonite clay, C30B) into the matrix (i.e. 1%). Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), near-infrared chemical imaging spectroscopy (NI-CI), X-ray diffraction (XRD), * Cornelia, Vasile, e-mail: cvasile@icmpp.ro 10.2478/achi-2014-0008 Downloaded from PubFactory at 09/03/2016 06:11:00AM via free access 76 E. Parpariţa et al. thermogravimetric analysis (TG), swelling and rheological measurements were used to characterize the polyvinyl alcohol/chitosan/montmorillonite properties. The swelling degree increased with decreasing chitosan content in hydrogels and the variation is opposite in nanocomposites, decreasing after introducing the nanoclay. The swelling behaviour was influenced by the presence of the nanoparticles. The plasticizer effect of the nanoparticles was reflected by obtaining a more compact hydrogel network with higher mechanical and thermal properties. The proposed materials can be a promising alternative in biomedical applications.

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Polyvinyl alcohol/chitosan/montmorillonite nanocomposites preparation by freeze/thaw cycles and characterization

The effect of the nanoclay content on the thermal decomposition of nanocomposites based on poly(vinyl alcohol)/thermoplastic starch, as intercalated hybrids, has been established. The changes in the decomposition products distribution and their evolution have been investigated by coupled thermogravimetric analysis, Fourier transform infrared spectroscopy, and mass spectrometry. Detailed analysis of the in situ vapor phase showed that the poly(vinyl alcohol)/starch/clay nanocomposites display a completely different distribution pattern of degradation product, depending on nanoclay content. By in situ vapor phase FTIR and MS spectroscopic techniques, both decomposition compounds of the constituent polymers and some new ones, depending on the nanoparticles content, are identified. The effect of the increase in nanoparticles content consists mainly in variation of some volatile compounds evolution, such as formic acid, water, formaldehyde, propionic acid, methanol, acetic acid carbon dioxide, benzene, etc., which in the case of nanocomposites is very complex. Thus, a content of 2–4 wt% organically-modified montmorillonite hinders the decomposition of the poly(vinyl alcohol)/starch blend. Both characteristic temperature of evolution of the main compounds increases by increasing its content and evolution starting time is delayed; while the untreated nanoclay acts like a catalyst, which decreases characteristic temperatures and evolution time with increasing its content. The temperature dependence of the maximum evolution rate of various compounds on the nanoclay content is very complex as, in the case of nanocomposites, of both primary and secondary reactions and transport phenomena occur simultaneously. Generally, this behavior is related to the dispersion of nanoclays in the polymeric matrix.

TG/FTIR/MS study on the influence of nanoparticles content upon the thermal decomposition of starch/poly(vinyl alcohol) montmorillonite nanocomposites

Over the past few decades, a considerable interest was shown in developing nanogels (NGs) based on natural polymers or their derivatives to serve as generally regarded as safe (GRAS) biomedical devices that fuse the properties of both hydrogels and nanoparticles This chapter presents different strategies to synthesize NGs via physical self-assembly or covalent crosslinking and their applications in therapeutic/biomedical fields, such as drug delivery systems, tissue engineering, artificial chaperone, imaging probes

Nanogels of Natural Polymers

The hydrogen bonding-interpolymer association of hydroxypropyl cellulose (HPC) with maleic acid-styrene (MAc-S) copolymer has been investigated in dilute aqueous solution by viscometry, turbidimetry and potentiometry. At a mixing ration between MAc-S and HPC of 10:90, the solution exhibits a phase separation upon heating, while for other mixing ration no phase separation could be detected. The stability of the interpolymer complex (IPC) increases as the temperatures rises. The stoichiometry of the IPC, in mole units, was estimated as being MAc-S:HPC=5:2. The thermodynamic functions (enthalpy and entropy) of the complexation process have been determined.

Investigation of the Interpolymer Complex between Hydroxypropyl Cellulose and Maleic Acid‐Styrene Copolymer, 1

Polyurethane–extracellular matrix membranes with bionanocomposites or coatings containing a small amount of biocompatible polymers such as hydrolyzed collagen, elastin, hyaluronic acid or chondroit...

Cornelia Vasile

Papers

Polyvinyl alcohol/chitosan/montmorillonite nanocomposites preparation by freeze/thaw cycles and characterization

TG/FTIR/MS study on the influence of nanoparticles content upon the thermal decomposition of starch/poly(vinyl alcohol) montmorillonite nanocomposites

Nanogels of Natural Polymers

Investigation of the Interpolymer Complex between Hydroxypropyl Cellulose and Maleic Acid‐Styrene Copolymer, 1

Polyurethane–extracellular matrix/silver bionanocomposites for urinary catheters