Modeling of precipitation hardening in Mg-based alloys

This work deals with the development of Mg-based alloys with enhanced properties at elevated temperatures. This is achieved by precipitation of binary phases such as MgZn₂ and Mg₂Sn during the aging of these alloys. The aim of the present work is to develop and calibrate a model for precipitation hardening in Mg-based alloys, as different types of precipitates form simultaneously. The modified Langer-Schwartz approach, while taking into account nucleation, growth and coarsening of the new phase precipitations, was used for the analysis of precipitates’ evolution and precipitation hardening during aging of Mg-based alloys. Two strengthening mechanisms associated with particle-dislocation interaction (shearing and bypassing) were considered to be operating simultaneously due to particle size-distribution. Parameters of the model, R _N i and k _{σ i} , were found by fitting of calculated densities and average sizes of precipitates with ones estimated from experiments. The effective diffusion coefficients of phase formation processes, which determine the strengthening kinetics, were estimated from the hardness maximum positions on the aging curves.     

Straining phenomena of POY revealed by thermal retraction and other techniques

Partially oriented polyesters yarns (POY) were strained at different strain rates (0.03–12.00 min^?1) and temperatures above and below T_g (3–92°C). Thermal retraction, density, DSC, and WAXS techniques show that strain-induced crystallization takes place by straining at temperatures above as well as below T_g. Above T_g, depending upon the strain rate, two regimes are observed: Below the strain rate of 1.5 min^?1, the flow regime; the degree of crystallinity is reduced as the strain rate increases. Above the strain rate of 1.5 min^?1, the strain-induced crystallization regime; the degree of crystallinity increases as the strain rate increases. Thermal retraction, stress–relaxation, and sonic modulus techniques indicate that, upon cold straining, instead of the original T_g at 65–69°C, two glass transitions occur: an upper T_g (u) and a lower T_g (l). For POY strained at 3°C and at a strain rate of 10 min^?1, the values are 78°C and 37°C, respectively. The higher the strain rate and the lower the straining temperature, the large the difference between T_g (u) and T_g (l).     

Application of the CALPHAD approach to Mg-alloys design

The CALPHAD method can be applied as a tool for both alloy development and process guideline determination. In this study, two Mg alloys were designed, their process parameters derived and, using the CALPHAD method, the final results simulated. These results were later confirmed using tangible experimental methods. It was found that γ$\gamma$- Mg₁₇Al₁₂ precipitates along the grain boundaries (GB), Mg₂Sn forms both along the GB and as fine precipitates in the α$\alpha$-Mg matrix and the addition of Ce mishmetal (MM) leads to the formation of elongated Al- rare earth (RE) precipitates along the GB. The microstructural stability at 200 ^°C is high, showing no decrease in microhardness for 32 days. It is shown that the CALPHAD method considerably reduces the effort of alloy design and that the reliability of the results is high.     

Effects of supercooling and cooling rate on the microstructure of Cu–Co–Fe alloys

The effects of supercooling and cooling rate on the microstructure of ternary Cu–Fe–Co alloys were investigated. Electromagnetic levitation was used to supercool the liquids down by 180 K. Alloys with 11 at.% Cu and less than 19 at.% Fe contained fcc (Fe, Co) and fcc Cu phases; those with 19 to 23 at.% Fe contained bcc (Fe, Co), fcc (Fe, Co) and fcc Cu; those with more than 23 at.% Fe contained bcc (Fe, Co) and fcc Cu. The primary dendrites contained 10 to 20 at.% Cu, with Fe and Co contents depending on the alloy composition. Supercooling the melt below a certain temperature resulted in metastable separation of the melt into two liquids, one (Co + Fe)-rich, the other Cu-rich. The metastable phase separation temperatures and the two liquid compositions were determined experimentaly, and compared with calculated ones. Isothermal cross-sections at various temperatures were constructed for stable and metastable cases based on thermodynamic and experimental data of the Cu–Co, Cu–Fe, and Co–Fe systems. A peritectic reaction for the ternary alloys was found at approximately 1100°C.     

Designing block copolymer architectures for targeted membrane performance

Using a combination of block copolymer self-assembly and non-solvent induced phase separation, isoporous ultrafiltration membranes were fabricated from four poly(isoprene-b-styrene-b-4-vinylpyridine) triblock terpolymers with similar block volume fractions but varying in total molar mass from 43 kg/mol to 115 kg/mol to systematically study the effect of polymer size on membrane structure. Small-angle X-ray scattering was used to probe terpolymer solution structure in the dope. All four triblocks displayed solution scattering patterns consistent with a body-centered cubic morphology. After membrane formation, structures were characterized using a combination of scanning electron microscopy and filtration performance tests. Membrane pore densities that ranged from 4.53 × 10¹⁴ to 1.48 × 10¹⁵ pores/m² were observed, which are the highest pore densities yet reported for membranes using self-assembly and non-solvent induced phase separation. Hydraulic permeabilities ranging from 24 to 850 L m⁻² h⁻¹ bar⁻¹ and pore diameters ranging from 7 to 36 nm were determined from permeation and rejection experiments. Both the hydraulic permeability and pore size increased with increasing molar mass of the parent terpolymer. The combination of polymer characterization and membrane transport tests described here demonstrates the ability to rationally design macromolecular structures to target specific performance characteristics in block copolymer derived ultrafiltration membranes.     

Relating organic fouling of reverse osmosis membranes to intermolecular adhesion forces

Organic fouling of reverse osmosis (RO) membranes and its relation to foulant--foulant intermolecular adhesion forces has been investigated. Alginate and Suwannee River natural organic matter were used as model organic foulants. Atomic force microscopy was utilized to determine the adhesion force between bulk organic foulants and foulants deposited on the membrane surface under various solution chemistries. The measured adhesion force was related to the RO fouling rate determined from fouling experiments under solution chemistries similar to those used in the AFM measurements. A remarkable correlation was obtained between the measured adhesion force and the fouling rate under the solution chemistries investigated. Fouling was more severe at solution chemistries that resulted in larger adhesion forces, namely, lower pH, higher ionic strength, presence of calcium ions (but not magnesium ions), and higher mass ratio of alginate to Suwannee River natural organic matter. The significant adhesion force measured with alginate in the presence of calcium ions indicated the formation of a crossed-linked alginate gel layer during fouling through intermolecular bridging among alginate molecules.     

Solid Solutions within Selected SrO-LnO1.5-TiO2 Systems

A region of selected SrO-LnO_1.5-TiO₂ (Ln = La, Ce, Pr, or Nd) systems was studied experimentally using X-ray diffractometry (XRD). A series of solid solutions with composition Sr_{4 x} Ln_{2 x/ 3}Ti₄O₁₂ having tetragonally distorted per-ovskite structures was found to exist along the tie line connecting SrTiO₃ and Ln₂Ti₃O₉. Reactions of SrLn₂Ti₄O₁₂, representative compounds of the series, with SrO were also studied. Additionally, the solubility of TiO₂ in Ln₂O₃-(3TiO_{2- m} (Ln = La, Pr, or Nd) at 1300°C was investigated using XRD.     

Air Pollution Emission Inventory Survey for Israel

High ozone levels are regularly measured during summer months over the inland and mountainous regions of Israel. Studies analyzing the back trajectories of air masses responsible for the high ozone levels showed that the precursors originated from the densely populated Israeli coastline. In order to better understand the contribution of those emission sources to ozone production, it is essential to have an accurate emission inventory that can be inputted into a photochemical model. The present paper describes the methods used in preparing an emission inventory for Israel based on information available and published until 1998. The source and accuracy of the data available are described. The calculations performed and the assumptions taken in order to obtain data not directly available are clarified. The sources reported in the inventory were the major polluters (power plants, oil refineries, and cement industries); industry; transportation; and biogenic sources. The pollutants studied were SO₂, NO_x, CO, saturated and unsaturated hydrocarbons, ethylene, isoprene, toluene, xylene, formaldehyde, and aldehydes. The inventory showed that transportation is responsible for almost the entire CO and 30% of the volatile organic compounds emitted, although transportation itself accounts for only a fifth of total fuel consumption. About 75% of the NO_x emitted can be attributed to industrial sources and the remaining 25% to transportation. Model simulations using the emission inventory were performed and compared to data available from a monitoring station situated 30 km east of Tel Aviv. The results showed good agreement, validating the accuracy of the emission inventory. The present emission inventory provides an important database as input to photochemical models used in forecasting ozone levels over Israel.     

Basic chemistry of a new cycle, based on reactions of Ce(III) titanate, for splitting water

The chemistry of a new thermochemical cycle for splitting water is described. It consists essentially of three reactions: (a) Ce(IV), as CeO₂, is reduced to Ce(III) by reaction with TiO₂, evolving oxygen and forming one or more Ce(III) titanates; (b) the Ce(III) titanates react with molten NaOH to evolve hydrogen, and form CeO₂ and Na-titanate; and (c) the sodium titanate is hydrolyzed by boiling water into a hydrous titanium dioxide and a sodium hydroxide solution. The cycle has been demonstrated with regenerated materials.