Relationships Between Number of Verbal Associations to Value Words and Subjective Ratings of Values

This study attempts to demonstrate whether or not there is a relationship between Ss\u27 rankings of statements descriptive of Spranger\u27s values and the number of verbal associations made by the same Ss to nouns referring to these values. Noble (2) has demonstrated that one may define the meaningfulness of a stimulus word in terms of the number of associations to this word written by Ss within a prescribed time. Bousfield and Samborski (1) using the written association method of Noble attempted to test the hypothesis that for individuals the relative strength of personal values should correlate positively with the extent of meaningfulness of words related to these values. To test this hypothesis they correlated two measures of the same values derived from the same group of Ss. These were (a) strengths of Spranger\u27s values based on the Study of Values Scale of Allport, Vernon and Lindzey and (b) meaningfulness of words related to the Spranger values obtained by Noble\u27s (2) method. Two of the six values investigated, religious and theoretical, showed significant correlations

Thermodynamic modeling and validation of the temperature influence in ternary phase polymer systems

The effect of the temperature, as a process variable in the fabrication of polymeric membranes by the non-solvent induced phase separation (NIPS) technique, has been scarcely studied. In the present work, we studied the influence of temperature, working at 293, 313 and 333 K, on the experimental binodal curves of four ternary systems composed of PVDF and PES as the polymers, DMAc and NMP as the solvents and water as the non-solvent. The increase of the temperature caused an increase on the solubility gap of the ternary system, as expected. The shift of the binodal curve with the temperature was more evident in PVDF systems than in PES systems indicating the influence of the rubbery or glassy state of the polymer on the thermodynamics of phase separation. As a novelty, the present work has introduced the temperature influence on the Flory–Huggins model to fit the experimental cloud points. Binary interaction parameters were calculated as a function of the temperature: (i) non-solvent/solvent (g12) expressions with UNIFAC-Dortmund methodology and (ii) non-solvent/polymer (c13) and solvent/polymer (c23) using Hansen solubility parameters. Additionally, the effect of the ternary interaction term was not negligible in the model. Estimated ternary interaction parameters (c123) presented a linear relation with temperature and negative values, indicating that the solubility of the polymers in mixtures of solvent/non-solvent was higher than expected for single binary interaction. Finally, PES ternary systems exhibited higher influence of the ternary interaction parameter than PVDF systems.This research was funded by the Spanish Ministry of Economy, Industry and Competitiveness (MINECO-FEDER) through project CTM2016-75509-R and by the Spanish Research Agency through the projects X-MEM (PCI2018-092929, project call APCIN 2018) and PID2019-105827RBI00/AEI/10.13039/501100011033

Fragility and compressibility at the glass transition

Isothermal compressibilities and Brillouin sound velocities from the literature allow to separate the compressibility at the glass transition into a high-frequency vibrational and a low-frequency relaxational part. Their ratio shows the linear fragility relation discovered by x-ray Brillouin scattering [1], though the data bend away from the line at higher fragilities. Using the concept of constrained degrees of freedom, one can show that the vibrational part follows the fragility-independent Lindemann criterion; the fragility dependence seems to stem from the relaxational part. The physical meaning of this finding is discussed. [1] T. Scopigno, G. Ruocco, F. Sette and G. Monaco, Science 302, 849 (2003)Comment: 4 pages, 2 figures, 2 tables, 33 references. Slightly changed after refereein

Thermomechanical properties and shape-memory behavior of bisphenol a diacrylate-based shape-memory polymers

A series of acrylate-based shape-memory materials are synthesized from bisphenol A diacrylate monomers as crosslinking agents. Networks are synthesized by keeping constant the content of bisphenol A-based crosslinking agent and systematically varying the content ratio of different monofunctional chain builder monomers. The implications of the structure of bisphenol A-based monomers and the chemical structure and content of monofunctional monomers on thermomechanical properties are discussed. Thermomechanical properties are analyzed using dynamic mechanical analyses and mechanical properties are studied at room temperature and at the onset of the glass transition temperature. Shape-memory performances under isothermal and transient temperature conditions are also carried out. Tensile tests show excellent values of stress at break up to 45 and 15 MPa at room and high temperature, respectively. The measurements show excellent shape recovery and shape fixity ratios, ˜95% and 97%, respectively. These materials also show very high recovery velocities under transient temperature conditions, up to 24% min-1, and very short recovery times, up to 1.5 s, under isothermal conditions in a water bath. The results confirm that networks synthesized from bisphenol A crosslinkers are promising shape-memory materials.Postprint (author's final draft

Comparing Laser Diffraction and Optical Microscopy for Characterizing Superabsorbent Polymer Particle Morphology, Size, and Swelling Capacity

In this study, we determined the accuracy and practicality of using optical microscopy (OM) and laser diffraction (LD) to characterize hydrogel particle morphology, size, and swelling capacity (Q). Inverse-suspension-polymerized polyacrylamide particles were used as a model system. OM and LD showed that the average particle diameter varied with the mixing speed during synthesis for the dry (10–120 lm) and hydrated (34–240 lm) particles. The LD volume and number mean diameters showed that a few large particles were responsible for the majority of the water absorption. Excess water present in the gravimetric swelling measurements led to larger Qs (8.2 6 0.37 g/g), whereas the volumetric measurements with OM and LD resulted in reduced capacities (6.5 6 3.8 and 5.7 6 3.9 g/g, respectively). Results from the individual particle swelling measurements with OM (5.2 6 0.66 g/g) statistically confirmed that the volumetric methods resulted in a reduced and more accurate measurement of the Q than the gravimetric method

Deforming glassy polystyrene: Influence of pressure, thermal history, and deformation mode on yielding and hardening

The toughness of a polymer glass is determined by the interplay of yielding, strain softening, and strain hardening. Molecular-dynamics simulations of a typical polymer glass, atactic polystyrene, under the influence of active deformation have been carried out to enlighten these processes. It is observed that the dominant interaction for the yield peak is of interchain nature and for the strain hardening of intrachain nature. A connection is made with the microscopic cage-to-cage motion. It is found that the deformation does not lead to complete erasure of the thermal history but that differences persist at large length scales. Also we find that the strain-hardening modulus increases with increasing external pressure. This new observation cannot be explained by current theories such as the one based on the entanglement picture and the inclusion of this effect will lead to an improvement in constitutive modeling

Fatty Acid Methyl Esters as Biosolvents of Epoxy Resins: A Physicochemical Study

The C8 to C18 fatty acid methyl esters (FAME) have been compared as solvents for two epoxy resin pre-polymers, bisphenol A diglycidyl ether (DGEBA) and triglycidyl paminophenol ether (TGPA). It was found that the solubilization limits vary according to the ester and that methyl caprylate is the best solvent of both resins. To explain these solubility performances, physical and chemical properties of FAME were studied, such as the Hansen parameters, viscosity, binary diffusion coefficient and vaporization enthalpy. Determination of the physicochemical parameters of FAME was carried out by laboratory experimentations and by calculation from bibliographic data. The Hansen parameters of FAME and epoxy resins pre-polymers were theoretically and experimentally determined. The FAME chain length showed a long dependence on the binary diffusion parameters and kinematic viscosity, which are mass and momentum transport properties. Moreover, the vaporization enthalpy of these compounds was directly correlated with the solubilization limits

Gasification reactor engineering approach to understanding the formation of biochar properties

Operational reactor temperatures (spanning the reduction zone), pressure, and product gas composition measurements from a downdraft gasifier were compared against subsequent biochar elemental composition, surface morphology and PAH content. Pine feedstock moisture (FM), with values of 7% and 17% was the experimental variable. Moderately high steady-state temperatures were observed inside the reactor, with a ca. 50°C difference in how the gasifier operated between the two feedstock types. Both chars exhibited surface properties comparable to activated carbon, but the relatively small differences in temperature caused significant variations in biochar surface area and morphology: micropore area 584 m2.g-1 (FM7%) against 360 m2.g-1 (FM17%), and micropore volume 0.287 cm3.g-1 (FM7%) against 0.172 cm3.g-1 (FM17%). Differences in char extractable PAH content were also observed, with higher concentrations (187 μg.g-1 15 ± 18) when the gasifier was operated with FM7%, compared to 89 ± 19 μg.g-1 Σ16EPA PAH with FM17%. It is recommended that greater detail on operational conditions during biochar production should be incorporated as standard to future biochar characterisation research as a consequence of these results

On temperature- and space-dimension dependent matter agglomeration in a mature growing stage

Model matter agglomerations, with temperature as leading control parameter, have been considered, and some of their characteristics have been studied. The primary interest has been focused on the grain volume fluctuations, the magnitude of which readily differentiates between two commonly encountered types of matter agglomeration/aggregation processes, observed roughly for high- and low-density matter organizations. The two distinguished types of matter arrangements have been described through the (entropic) potential driving system. The impact of the potential type on the character of matter agglomeration has been studied, preferentially for (low density) matter agglomeration for which a logarithmic measure of its speed has been proposed. A common diffusion as well as mechanical relaxation picture, emerging during the mature growing stage, has been drawn using a phenomenological line of argumentation. Applications, mostly towards obtaining soft agglomerates of so-called jammed materials, have been mentioned

Heteroaromatic polyamides with Improved thermal and mechanical properties

We prepared high-performance aromatic copolyamides, containing bithiazole and thiazolo-thiazole groups in their main chain, from aromatic diamines and isophthaloyl chloride, to further improve the prominent thermal behavior and exceptional mechanical properties of commercial aramid fibers. The introduction of these groups leads to aramids with improved strength and moduli compared to commercial meta-oriented aromatic polyamides, together with an increase of their thermal performance. Moreover, their solubility, water uptake, and optical properties were evaluated in this work.Fondo Europeo de Desarrollo Regional and both the Spanish Ministerio de Economía, Industria y Competitividad (MAT2017-84501-R) and the Consejería de Educación, Junta de Castilla y León (BU306P18) is gratefully acknowledged. M.T.L. also thankfully acknowledges the Spanish Ministerio de Ciencia e Innovación (PID2019-108583RJ-I00/AEI/10.13039/501100011033