Biomedical subjects

Paul Bowen

Publications and source records attributed to Paul Bowen.

5 recordsLinked to original sources

PubMed2006

Precipitation of nanostructured copper oxalate: substructure and growth mechanism.

The possibility of controlling materials properties by tailoring their substructure at the nanometer scale is a current topic of great interest. To do so, a fundamental understanding of the growth mechanism is of key importance and an analytical challenge as nanostructured materials are often produced by precipitation methods at high supersaturations where formation kinetics are fast. The current study focuses on the precipitation of copper oxalate, which has been previously shown to produce self-assembled ordered nanostructured particles with the promise of being able to tailor this nanometer substructure. In the current study we investigate in detail the growth mechanism and kinetics of precipitation by using in-situ particle size measurement or by stopping the reaction at various stages and using ex-situ methods. Combining the ex-situ methods of high-resolution scanning electron microscopy, transmission electron microscopy, and X-ray powder diffraction along with the in-situ methods, we were able to follow the growth process from 2 min to 2 weeks. The results in the 2-30 min period lead to the proposal of a core-shell growth model with a poorly ordered core and a well-structured shell of nanosized crystallites (50-70 nm), adding support to the brick-by-brick model previously proposed for this phase of particle growth. Particle evolution over long periods up to 2 weeks show a ripening which produces lens-shaped particles that eliminate the "high" surface energy faces observed in the earlier stages of growth. A more complete growth mechanism for copper oxalate precipitation at moderate supersaturations is proposed similar to recent findings for other self-assembled nanostructured particles.

Chemical Precipitation↗

PubMed2006

Graphical comparison of image analysis and laser diffraction particle size analysis data obtained from the measurements of nonspherical particle systems.

The purpose of this paper is to describe results from the use of a set of Excel macros written to facilitate the comparison of image analysis (IA) and laser diffraction (LD) particle size analysis (psa) data. Measurements were made on particle systems of differing morphological characteristics including differing average aspect ratios, particle size distribution widths and modalities. The IA and LD psa data were plotted on the same graph treating both the weighting and the size unit of the LD psa data as unknowns. Congruency of the IA and LD plots was considered to indicate successful experimental determination of the weighting and size unit .The weighting of the resulting LD psa data (so-called volume-weighted) is shown to be better correlated with IA area-weighted data. The size unit of LD psa data is shown to be a function of particle shape. In the case of high aspect ratio particles characterized by approximately rectangular faces the LD psa data is shown to be a function of multiple particle dimensions being related to IA size descriptors through a simple variation of the law of mixtures. The results demonstrate that successful correlations between IA and LD psa data can be realized in the case of non-spherical particle systems even in the case of high aspect ratio particles; however, the inappropriateness of the application of the Equivalent Spherical Volume Diameter and the Random Particle Orientation assumptions to the interpretation of the LD psa results must first be acknowledged. Correlation permits cross validation of IA and LD psa results increasing confidence in the accuracy of the data from each orthogonal technique.

Humans↗

PubMed2006

Formation and drying of colloidal crystals using nanosized silica particles.

Much interest has been generated in the fabrication of colloidal crystals from suspensions because of the promise of photonic band gap applications. However, since the case of small, nonsedimenting colloidal particles indeed remains rather rarely treated, spherical silica particles with diameters varying from 75 down to 20 nm have been used in the present work to fabricate colloidal crystals by drying the suspending liquid. Typical events that take place during the drying process of a particulate film, such as cracking, compaction and penetration of air into a porous network, have been evaluated using existing theories, and the maximum stress in the drying film could be approximated. Investigation on the dry film structure by scanning electron microscopy showed the arrangement of particles in a close-packed system. To interpret the formation of such crystals, the amplitudes of the interparticle and capillary forces have been estimated from existing models. The repulsive interparticle forces allow the particles to remain stable and thus rearrange up to fairly high particle concentration. These modeling results showed the dominance of the capillary contribution at the end of the drying process. Nitrogen adsorption/desorption measurements gave very coherent results regarding both pore volume and pore size of the dry particulate films when compared to the expected ordered packing arrangements.

Journal Article↗

PubMed2005

Aggregation and charging of colloidal silica particles: effect of particle size.

We studied systematically aqueous suspensions of amorphous well-characterized silica particles by potentiometric titration, electrophoretic mobility, and time-resolved light scattering. Their charging behavior and aggregation rate constants were measured as a function of pH and ionic strength in KCl electrolytes for three types of particles of approximately 30, 50, and 80 nm in diameter. The charging behavior was consistent with the basic Stern model; the silica particles carry a negative charge, and its magnitude gradually increases with increasing pH and ionic strength. On the other hand, their early-stage aggregation (or coagulation) behavior is complex. The aggregation of the largest particles shows features resembling predictions of the Derjaguin, Landau, Verwey, and Overbeek (DLVO) theory. On one hand, the rate constant decreases sharply with increasing pH at low ionic strengths and attains fast aggregation conditions at high ionic strengths. On the other hand, we observe a characteristic slowing down of the aggregation at low pH and high ionic strengths. This feature becomes very pronounced for the medium and the small particles, leading to a complete stabilization at low pH for the latter. Stabilization is also observed at higher pH for the medium and the small particles. From these aggregation measurements we infer the existence of an additional repulsive force. Its origin is tentatively explained by postulating hairy layers of consisting of poly(silicilic acid) chains on the particle surface.

Journal Article↗

PubMed2005

Use of seeds to control precipitation of calcium carbonate and determination of seed nature.

Understanding and controlling precipitation reactions is a major challenge for industrial crystallization. Calcium carbonate is a widely studied system: more than 3000 papers have been devoted to the subject over the past 10 years. The first step of the precipitation of calcium carbonate, from relatively concentrated solutions (0.01 mol/L), involves the formation of an initial gel phase which later transforms into calcite, vaterite, or a mixture of both phases. Our work aimed at controlling this first step. Nanosized seeds (8 nm), formed in situ, were used in order to control the often chaotic nucleation step which normally leads to poor phase selection and broad particle size distributions. Seeding has often been used to avoid spontaneous nucleation in metastable solutions for growth mechanism investigations of single-crystal calcium carbonate. Here the ability of a seeding method to control the precipitation reaction evolution even in the case of high supersaturation is demonstrated. The seeds and the presence of a polymeric additive (poly(acrylic acid)) allow the control of the precipitated polymorph and the specific surface area, while maintaining a narrow particle size distribution in the submicron range. Direct characterization methods did not succeed in identifying these nanoseeds; indirect methods using solubility calculations are used to demonstrate their existence and quantify size and number density of the nanosized seeds.

Calcium Carbonate↗