Synthesis and characterization of glycine copolymers of nylons 6 and 12

Copolymers of glycine and 6-aminohexanoic or 12-aminododecanoic acid within a range of molar compositions from 80/20 to 5/95 were prepared by solution polycondensation of the adequate proportion of the respective pentachlorophenyl ester hydrobromides. Despite their random composition, the copolymers obtained were found to be highly crystalline. Intrinsic viscosities of 2/6 and 2/12 copolyamides were similar and rather low (M_n, ca. 3000-5000). Thermal post-polycondensation allowed to increase the molecular weight of 2/12 copolyamides, so that fibers could be prepared. The composition and sequence distributions were evaluated by means of ¹H- and ¹³C-NMR spectroscopies. Copolyamides were also characterized in terms of thermal properties. Melting and glass transition temperatures are reported. Crystallinity was evaluated from heats of fusion. Crystalline structure was examined by infrared spectroscopy and wide-angle x-ray diffraction. The presence of structures related to the polyglycine I and to α/γ-nylons was confirmed depending on the molar composition. Highly oriented fibers with good tensile properties were obtained from the nylon 2/12 (10 : 90) copolymer. © 1995 John Wiley & Sons, Inc.     

Relative permeability relations: A key factor for a drying model

In the modelling of heat, mass and momentum transfer phenomena which occur in a capillary porous medium during drying, the liquid and gas flows are usually described by the generalised Darcy laws. Nevertheless, the question of how to determine experimentally the relative permeability relations remains unanswered for most materials that consist of water and humid air, and as a result, arbitrary functions are used in the drying codes. In this paper, the emphasis is on deducing from both numerical and experimental studies a method for estimating pertinent relations for these key parameters. In the first part, the sensitivity of liquid velocity and, consequently, of drying kinetics in the variation of the relative permeabilities is investigated numerically by testing various forms. It is concluded that in order to predict a realistic liquid velocity behaviour, relative permeabilities can be linked to a measurable quantity: the capillary pressure. An estimation technique, based on simulations coupled with experimental measurements of capillary pressure, together with moisture content kinetics obtained for low or middle temperature convective drying, is deduced. In the second part, the proposed methodology is applied to pine wood. It is shown that the obtained relations provide closer representation of physical reality than those commonly used.     

Schiff-Basen aus 1,3-Dicarbonylverbindungen und Triaminen und ihre Fe (III)-, Co (III)-, Ni(II)- und Cu(II)-Komplexe

Schiff bases of 1,3-dicarbonyl compounds with triamines and their Fe(III), Co(III), Ni(II) and Cu(II) complexes The preparation of new hexadentate ligands obtained by the reaction of cis, cis-1,3,5-triaminocyclohexane (tach) or 1,1,1-tris (aminomethyl)ethane (tame) with an 2-ethoxymethylidene-1,3-dicarbonyl compound as well as their Fe(III), Co(III), Ni(II) and Cu(II) complexes is reported. Fe(III) and Co(III) yield neutral complexes with an octahedral N₃O₃-coordination sphere, Ni(II) and Cu(II) complexes with a square-planar coordination-sphere. In the later complexes one of the bidentate branches of the ligand is not deprotonated and stays uncoordinated.     

Structural data on the packing of poly(ester amide)s derived from glycine,hexanediol, and odd‐numbered dicarboxylic acids

The crystalline structure of a series of Poly(ester amide)s derived from glycine, hexanediol, and odd‐numbered dicarboxylic acids has been studied using transmission electron microscopy and X‐ray diffraction. Polymers crystallize in an orthorhombic lattice with parameters a = 4.80 Å, b = 22.68 Å, and c in the 45–55 Å interval, depending on the number of methylenes of the chemical repeat unit. The structure of the glutaric derivative can be interpreted as a singular packing of six hydrogen‐bonded sheets. Amide and ester interactions between neighboring layers favor two different sheet arrangements that give rise to the observed superstructure. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2521–2533, 1999