Summary: A new method for the preparation of poly(ester amide)s derived from glycolic acid units has been developed. Glycolic acid units can be incorporated with a high yield into a nylon‐n or a nylon‐n,m. The synthesis is based on a final thermal polycondensation with the formation of a metal halide salt as a driving force. New poly(ester amide)s have high molecular weights, good mechanical behaviour, and variable thermal properties, giving rise to a group of materials with potential interest as biodegradable materials in applications like surgical sutures.Results of the differential scanning calorimeter heating runs for the sodium (a) and potassium (b) salts of N‐chloroacetyl‐6‐aminohexanoic acid.magnified imageResults of the differential scanning calorimeter heating runs for the sodium (a) and potassium (b) salts of N‐chloroacetyl‐6‐aminohexanoic acid.

The scaled skin of fish is a high-performance natural armor that represents a source of inspiration for novel engineering designs. In this paper, we present a biomimetic fish skin material, fabricated with a design and components that are simple, that achieves many of the advantageous attributes of natural materials, including the unique combination of flexibility and mechanical robustness. The bioinspired fish skin material is designed to replicate the structural, mechanical, and functional aspects of a natural teleost fish skin comprised of leptoid-like scales, similar to that of the striped red mullet Mullus surmuletus. The man-made fish skin material consists of a low-modulus elastic mesh or "dermis" layer that holds rigid, plastic scales. The mechanics of the synthetic material is characterized under in-plane, bending, and indentation modes of deformation and is successfully described by theoretical deformation models that have been developed. This combined experimental and modeling approach elucidates the critical mechanisms by which the composite material achieves its unique properties and provides design rules that allow for the engineering of scaled skins. Such artificial scaled skins that are flexible, lightweight, transparent, and robust under mechanical deformation may thus have potential as thin protective coatings for soft materials.

Summary: Poly(ester amide)s derived from glycolic acid and ω‐amino acid units, such as aminohexanoic or aminoundecanoic acids, are synthesized by a thermal polycondensation reaction that involves the formation of metal halide salts. Polymerization kinetics of different metal salts are studied by isothermal and nonisothermal methods and the corresponding parameters compared. The condensation reaction begins in the solid state for the aminohexanoic derivatives, although a rapid liquefaction is observed. On the other hand, the melting temperatures of the sodium and the potassium chloroacetylaminoundecanoate salts are lower than the reaction temperatures, and consequently polycondensation proceeds fully in the liquefied state. These polymers are characterized by an alternate disposition of ester and amide groups and can be obtained with high molecular weights and short polymerization times. Thermal properties (glass transition and melting temperatures) of the two new polymers are determined and compared. Thermal stability is also investigated; the results indicated that decomposition temperatures were always far from both reaction and polymer fusion temperatures.DSC heating scans performed at different rates for potassium chloroacetylaminoundecanote.magnified imageDSC heating scans performed at different rates for potassium chloroacetylaminoundecanote.

An alternating poly(ester amide) constituted by 6-amino-1-hexanol and glutaric units has been synthesized by different ways involving solution or thermal polycondensation. Results of the synthesis are compared, and the occurrence of a thermal degradation through imide ring formation is demonstrated. Hydrolytic and enzymatic degradation of the new polymer has been evaluated by means of weight loss measures and changes in intrinsic viscosity or by analysis of NMR spectra. Thermal properties and crystallization kinetics have also been studied. Crystalline structure has been investigated by X-ray fiber diffraction and electron microscopy of lamellar single crystals. Results indicate that polymorphism exists involving packing modes similar to those found on aliphatic polyamides.

A series of biodegradable poly (ester amide)s composed of sebacic acid, dodecanediol and different ratios of the stereoisomers of L- and D-alanine were synthesized for applications in drug delivery systems. Microspheres loaded with diclofenac sodium salt, triclosan and clofazimine were prepared with the solvent evaporation technique. No influence of polymer constitution in the drug release rate was found in vitro and no degradation occurred during the period of drug release. It was shown that a sustained delivery of the hydrophilic diclofenac sodium salt in Sörensen media occurred and it was controlled by diffusion. However, exhaustion of microspheres was feasible only from the most porous matrices where channelling had an important contribution.

The polymerization of metal salts of N‐chloroacetyl‐β‐alanine and N‐chloroacetyl‐4‐aminobutyric acid was investigated. The former gives a mixture of polymer and a seven‐membered cyclic compound constituted of glycolic and β‐alanine units, and its reaction proceeds in the solid state. However, liquefaction is observed in the second case giving rise to a polymer with a moderate molecular weight. Condensation kinetics of both sodium and silver salts of N‐chloroacetyl‐β‐alanine have been studied by differential scanning calorimetry. Copolymers of glycolic acid and β‐alanine with a molar ratio of glycolic acid/β‐alanine varying from 0.5 to 1.0 have been synthesized by thermal reaction of co‐precipitated crystals of the sodium salts of chloroacetic acid and N‐chloroacetyl‐β‐alanine. NMR spectroscopy indicates that copolymers tend to have a random distribution. The resulting new poly(ester amide)s have been characterized by spectroscopy and thermal analysis.DSC heating runs corresponding to different mixtures of the sodium salts of chloroacetic acid and chloroacetyl‐β‐alanine.magnified imageDSC heating runs corresponding to different mixtures of the sodium salts of chloroacetic acid and chloroacetyl‐β‐alanine.

Fluorescence excitation emission matrix (FEEM) spectroscopy was used to evaluate its applicability as a tool to track dissolved organic matter (DOM) in a drinking water treatment plant (DWTP) that incorporates a conventional line (consisting in ozonation and GAC filtration) and a membrane-based line (consisting in ultrafiltration, reverse osmosis and mineralization) working in parallel. Seven sampling points within the different process stages were characterized monthly during 2014. A global Parallel Factor Analysis (PARAFAC) was used to pull out underlying organic fractions from the fluorescence spectra. Accordingly a five components model was selected to describe the system and the pros and cons of the model were discussed by analysis of the residuals. Among the five fluorescent components, those associated to humic-like matter (C1, C3 and C4) showed a similar season variability in the river water feeding the DWTP (which resembled that of UV and TOC), whereas the two components associated to protein-like matter (C2 and C5) exhibited a different behavior. The maximum fluorescence intensity values (Fmax) were used to quantify DOM removals across the plant. Compared to the conventional line, water from the UF/RO membrane-based line showed between 6 and 14 times lower fluorescence intensity signal for the humic-like components and between 1 and 3 for the protein-like components as compared to the conventional line. The differences in DOM composition due to seasonal variations and along the treatment trains point out the suitability of using fluorescence measurements over other parameters such as UV as a monitoring tool to help optimize operation conditions of each treatment stage and improve produced water quality in a DWTP.

No abstract