Shell mineralogy of a foundational marine species, Mytilus californianus, over half a century in a changing ocean.

Anthropogenic warming and ocean acidification are predicted to negatively affect marine calcifiers. While negative effects of these stressors on physiology and shell calcification have been documented in many species, their effects on shell mineralogical composition remains poorly known, especially over longer time periods. Here, we quantify changes in the shell mineralogy of a foundation species, Mytilus californianus, under 60 y of ocean warming and acidification. Using historical data as a baseline and a resampling of present-day populations, we document a substantial increase in shell calcite and decrease in aragonite. These results indicate that ocean pH and saturation state, not temperature or salinity, play a strong role in mediating the shell mineralogy of this species and reveal long-term changes in this trait under ocean acidification.

Phase Stability and Miscibility in Ethanol/AOT/n-Heptane Systems: Evidence of Multilayered Cylindrical and Spherical Microemulsion Morphologies.

We describe the effects of ethanol on the phase behavior of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) in n-heptane. Using dynamic light scattering (DLS), molecular dynamics (MD) simulations, and nuclear magnetic resonance (1H NMR) spectroscopy, we investigate the aggregation behavior of AOT across a wide range of ethanol/AOT/n-heptane compositions. We conclude that reverse micelles do not form at any of the investigated concentrations. Instead, we observe the formation of other surfactant aggregate morphologies unique to this system, namely, multilayered cylindrical structures and spherical AOT-in-ethanol structures, which vary significantly with changes in ethanol concentration. We also identify mixed-solvent polarity as a driving factor for the surfactant behavior in the system. When the concentration of ethanol is 20 wt % or below, the system is inhomogeneous with varying sizes of AOT, ethanol, and AOT + ethanol aggregates, with the ethanol primarily exhibiting a cosurfactant behavior, almost exclusively binding at the surface of AOT aggregates. With increased ethanol concentration, the ethanol in the system also exhibits solvent-like behaviors in addition to the cosurfactant behaviors. Most significantly, when the ethanol concentration is raised above 35 wt %, the transition to solvent-like behavior allows AOT Na+ counterions to dissociate from the headgroups and they are dissolved in the ethanol. We use these results to construct a preliminary phase diagram for the ethanol/AOT/n-heptane system.

Deproteinization of Cortical Bone: Effects of Different Treatments.

Bone is a biological composite material having collagen and mineral as its main constituents. In order to better understand the arrangement of the mineral phase in bone, porcine cortical bone was deproteinized using different chemical treatments. This study aims to determine the best method to remove the protein constituent while preserving the mineral component. Chemicals used were H2O2, NaOCl, NaOH, and KOH, and the efficacy of deproteinization treatments was determined by thermogravimetric analysis and Raman spectroscopy. The structure of the residual mineral parts was examined using scanning electron microscopy. X-ray diffraction was used to confirm that the mineral component was not altered by the chemical treatments. NaOCl was found to be the most effective method for deproteinization and the mineral phase was self-standing, supporting the hypothesis that bone is an interpenetrating composite. Thermogravimetric analyses and Raman spectroscopy results showed the preservation of mineral crystallinity and presence of residual organic material after all chemical treatments. A defatting step, which has not previously been used in conjunction with deproteinization to isolate the mineral phase, was also used. Finally, Raman spectroscopy demonstrated that the inclusion of a defatting procedure resulted in the removal of some but not all residual protein in the bone.

Phase Stability and Mechanisms of Transformation of La-Doped γ-Alumina.

We report the phase stability of cubic γ-Al2O3 with respect to lanthanum dopant amount and describe a complete phase transition sequence up to a temperature of 1800 °C, which proceeds from La-doped γ-Al2O3 to LaAlO3/γ-Al2O3 to LaAl11O18. For this purpose, lanthanum contents from 0.81 to 10.0 atom % were incorporated into Al2O3 powders. X-ray diffraction analyses show that only γ-Al2O3 phase was present after heat treatment at 1000 °C for 2 h with 0.81, 1.68, 2.24, and 2.62 atom % lanthanum concentrations. The phase stabilization can be mainly attributed to the combined effects of small crystallite size of the Al2O3 powders and the presence of the lanthanum dopant, which occupies the Al2O3 octahedral sites. At compositions of 3.63, 5.00, 7.49, and 10.0 atom %, the amount of LaAlO3 phase formed by the solid phase reaction between Al2O3 and La3+ ions becomes detectable under X-ray diffraction.

Optimized Scintillator YAG:Pr Nanoparticles for X-ray Inducible Photodynamic Therapy.

We describe a sol-gel synthetic method for the production of praseodymium-doped yttrium aluminum garnet (YAG) nanoparticles suitable for X-ray inducible photodynamic therapy (X-PDT). Our sol-gel based approach was optimized by varying temperature and time of calcination, resulting in nanoparticles that were smooth, spherical, and 50-200 nm in crystallite size. The powders were uniformly coated with a thin (10 nm) layer of silica to facilitate surface conjugation with functional moieties. Measurements of photon flux revealed that coated and uncoated powders emitted a similar photon emission spectrum in response to 50 keVp X-rays. We also determined that the presence of silica did not significantly reduce flux and the emission peak had a maximum at approximately 320 nm. Thus, these YAG:Pr powders are suitable candidates for future in vivo X-PDT studies.

Development of mesoporosity in scandia-stabilized zirconia: particle size, solvent, and calcination effects.

We present the mechanisms of formation of mesoporous scandia-stabilized zirconia using a surfactant-assisted process and the effects of solvent and thermal treatments on the resulting particle size of the powders. We determined that cleaning the powders with water resulted in better formation of a mesoporous structure because higher amounts of surfactant were preserved on the powders after washing. Nonetheless, this resulted in agglomerate sizes that were larger. The water-washed powders had particle sizes of >5 µm in the as-synthesized state. Calcination at 450 and 600 °C reduced the particle size to ∼1-2 and 0.5 µm, respectively. Cleaning with ethanol resulted in a mesoporous morphology that was less well-defined compared to the water-washed powders, but the agglomerate size was smaller and had an average size of ∼250 nm that did not vary with calcination temperature. Our analysis showed that surfactant-assisted formation of mesoporous structures can be a compromise between achieving a stable mesoporous architecture and material purity. We contend that removal of the surfactant in many mesoporous materials presented in the literature is not completely achieved, and the presence of these organics has to be considered during subsequent processing of the powders and/or for their use in industrial applications. The issue of material purity in mesoporous materials is one that has not been fully explored. In addition, knowledge of the particle (agglomerate) size is essential for powder handling during a variety of manufacturing techniques. Thus, the use of dynamic light scattering or any other technique that can elucidate particle size is essential if a full characterization of the powders is needed for achieving postprocessing effectiveness.

Decomposition of Luminescent Hydroxyapatite Scaffolds in Simulated Body Fluid.

We present a luminescence study investigating the dissolution of rare-earth-doped hydroxyapatite scaffolds in simulated body fluid (SBF), aiming to assess the luminescence stability of Tb-, Ce-, and Eu-doped scaffolds over time. Our findings reveal a consistent decrease in luminescence emission intensity across all samples over a four-week period in which the scaffolds were immersed in the SBF. In addition, energy-dispersive spectroscopy confirms a decrease in rare-earth ion concentration in the scaffolds with respect to time, whereas fluorescence spectroscopy shows the presence of rare-earth ions in the SBF, indicating the partial dissolution of the scaffolds over time. The use of rare-earth ions as luminescence markers provides insights into the mechanisms of apatite formation in hydroxyapatites. Thus, these scaffolds may find wider use in regenerative medicine, particularly in targeted drug delivery systems, where their luminescent properties have the potential to noninvasively track drug release.

Ionic concentration effects on reverse micelle size and stability: implications for the synthesis of nanoparticles.

We present a systematic investigation and analysis of the structure and stability of reverse micelle systems with the addition of NH(4)OH, ZrOCl(2), and Al(NO(3))(3) salts. We demonstrate that the reverse micelle size decreases with increasing salt additions until one reaches a critical concentration, which characterizes the onset of system destabilization. The concept of an electrical double layer, as it applies to reverse micelles, is considered for explaining features of destabilization, including the initial decrease in reverse micelle size, the destabilization concentration, and the effect of cation valence. We propose that the reduction in size prior to instability is caused by compression of the reverse micelle electrical double layers, as higher concentrations of salts are present. The reduced thickness of the electrical double layers allows the decaying potentials to move into closer proximity to each other before generating enough repulsion to balance the forces for reverse micelle formation and form a new equilibrium average reverse micelle size. The point of reverse micelle instability has been related to the formation of a two-phase system as a result of the inability to further compress the salt co-ions in the core of the reverse micelles, which would cause an excessive repulsive force between the overlapping potentials. We have extracted a critical potential of -89 nV between the two overlapping potentials for the AOT/water/isooctane (ω(0) = 10) systems studied. All these effects have important implications for the preparation of nanopowders by reverse micelle synthesis. If the reverse micelles are unstable before the precipitates are formed, then the advantage of reverse micelle synthesis is immediately lost.

Nonlinear charge regulation for the deposition of silica nanoparticles on polystyrene spherical surfaces.

HYPOTHESIS: We describe the deposition behavior of monodispersed silica nanoparticles on polystyrene spherical particles by using modified pairwise DLVO (Derjaguin-Landau-Verwey-Overbeek) interaction force profiles at pH values between two and twelve. Our modified model contains a new nonlinear charge regulation parameter that considers redistribution of ions, which allows us to realistically express the electrical double layer (EDL) interaction forces. EXPERIMENTS: Silanol-terminated silica nanoparticles (7.6 ± 0.4 nm), l-lysine-covered silica nanoparticles (7.8 ± 0.4 nm), and polyallylamine hydrochloride-covered polystyrene (PAH/PS) particles (348 ± 1 nm) were synthesized. Then, each type of silica nanoparticle was deposited on the PAH/PS particles at a range of pH values. FINDINGS: Our new regulation parameter describes the realistic redistribution of charges governed by pH, total salt concentration, ionic strength of solution, and separation distance of particles. We find that this regulation parameter can be roughly approximated from the absolute values of theoretically calculated surface charge density and potential distributions, as well as experimentally measured ζ-potentials. Morphological analysis using electron microscopy of the experimental systems shows that the modified pairwise DLVO interaction forces exceptionally describe the deposition behavior of the silica nanoparticles physically adsorbed on the PAH/PS particle substrates.

Building Compassion and Human Bridges through Research Collaborations.

Our ENLACE binational summer research program was established with the aim of encouraging the participation of high school and college students in research in the sciences and engineering, while promoting cross-border friendships between the United States and Mexico. The program unites students around science and engineering questions and concurrently engages them in a rich curriculum that promotes understanding of broader societal issues of equity, inclusion, tolerance, and social justice. Because we built our program around hope and cooperation, it is our aspiration and promise that walls and borders-all kinds of walls and borders-can be eradicated through kindness, compassion, and respect for others. ENLACE is not just a program we organize every summer, it is also a program that defines who we are as people and the kind of contribution we want to make in the world.

Predicting the size of salt-containing aqueous Na-AOT reverse micellar water-in-oil microemulsions with consideration for specific ion effects.

HYPOTHESIS: Reverse micellar solutions are thermodynamically stable systems in which surfactant molecules surround water droplets within a continuous organic phase. Among their many applications, they can be used for the synthesis of nanoparticles of controlled agglomeration. Here, we consider the role specific ion effects play in reverse micelle size reduction. EXPERIMENTS: Dynamic light scattering measurements and the Gouy-Chapman electrical double layer model were combined to study water/AOT/isooctane reverse micellar systems (wo = 10). Linear relationships between the solvodynamic diameter (D) of reverse micelles containing various concentrations of FeSO4, Mg(NO3)2, CuCl2, Al(NO3)3, Fe(NO3)3, Y(NO3)3, NaBH4, ZrOCl2, and NH4OH, and their calculated Debye screening lengths, κ-1, were observed with decreasing D and increasing salt concentration (c). FINDINGS: By comparing the linear fits for reverse micelle size as a function of c-1/2, we determined the size can be described as a function of the Debye screening length, cation valency (z), and specific anion hydrated radius (ran), where D = 3.1z κ-1 + bi, and bi is linearly related to ran. Our model accurately predicts reverse micelle sizes with the addition of monovalent, divalent, and trivalent salts for which the primary hydrolyzed cation species has a charge that is equal to the cation valency.

A method to quantify crystallinity in amorphous metal alloys: A differential scanning calorimetry study.

We developed and describe a differential scanning calorimetry method for calculating the initial crystallinity, change of crystallinity and crystallinity percentage of amorphous metal alloys as a function of temperature. Using thermodynamic enthalpies of amorphous, crystalline and partially devitrified specimens, our methodology is capable of determining crystallinity percentages as low as a few percent. Moreover, the linear relationship between the set (pre-determined) and calculated crystallinities of experimental samples indicates that there is no need to prepare calibration samples before measuring the crystallinity percentage of target samples. This technique also eliminates the need for expensive in situ accessories, such as those required in electron microscopy. Thus, the technique is highly relevant as a primary technique for characterization of devitrification behavior in amorphous materials.

Mechanical Optimization of Diatomite Monoliths from Freeze Casting for High-Throughput Applications.

The silica cell walls of diatoms, the abundant microalga 1-100 µm in size, show a highly ordered hierarchical porosity and are widely available through their fossilized form known as diatomite. The goal of this research was to use this cost-effective source of porous silica in a unidirectional freezing process called ice-templating, or freeze casting, to create a ceramic membrane with unidirectional lamellar walls of ∼15 µm channels, which allows for an efficient mass transport of fluids (i.e., low pressure drop), while maintaining the optimal mechanical properties. Control over the monoliths was explored by varying the mass ratio of diatomite and sodium carbonate and the solid ratio in the initial slurry before freeze casting. The resultant monolith properties were assessed using scanning electron microscopy, mercury intrusion porosimetry, and mechanical testing. The membranes then underwent an in-line vacuum filtration of methylene blue dye and monodisperse latex beads to quantify the membrane filtration performance through chemical adsorption and depth filtration capabilities, respectively. Control over the material properties of the biosourced ceramic monoliths allows for a cost-efficient and hierarchically porous ceramic template with efficient mass transfer capabilities that can be potentially functionalized with a variety of sophisticated nanomaterials for various adsorbent, filter, catalysis, and sensor applications.

Interaction of Hydrogen with MB6 (M = Ba, Ca, La, and Sr) Surfaces from First Principles.

We show results of basic energetics and interacting behavior of hydrogen with metal hexaboride surfaces using a combination of self-consistent density functional calculations and dynamics based on the Car-Parrinello method. Our results show that hydrogen is strongly attracted to localized exposed boron atoms and interactions with the terminal cations are strictly repulsive. From these, preliminary local adsorption energy calculations suggest that a single hydrogen molecule per surface unit-cell is possible (one ML). Strongest bonds are found when hydrogen is above the terminal boron atoms affected by reduced coordination and dangling bonds. This location serves to restore the hexaboride unit to a more stable structure by providing electronic density to the deficient surface octahedra. Additionally, trajectories from dynamic simulations provide insight into how hydrogen recombination reactions occur on the surface through dissociative adsorption and the method of travel prior to recombination to be along the octahedral face and bridging sites connecting separate unit cells on the surface. Upon adsorption, a single hydrogen atom becomes localized at the dangling bond site while the second interacts with the surface along a weaker potential energy path. Desorption at lower temperatures occurs when migrating atoms from separate adsorption sites intersect to form a new pair.

No compromise between metabolism and behavior of decorator crabs in reduced pH conditions.

Many marine calcifiers experience metabolic costs when exposed to experimental ocean acidification conditions, potentially limiting the energy available to support regulatory processes and behaviors. Decorator crabs expend energy on decoration camouflage and may face acute trade-offs under environmental stress. We hypothesized that under reduced pH conditions, decorator crabs will be energy limited and allocate energy towards growth and calcification at the expense of decoration behavior. Decorator crabs, Pelia tumida, were exposed to ambient (8.01) and reduced (7.74) pH conditions for five weeks. Half of the animals in each treatment were given sponge to decorate with. Animals were analyzed for changes in body mass, exoskeleton mineral content (Ca and Mg), organic content (a proxy for metabolism), and decoration behavior (sponge mass and percent cover). Overall, decorator crabs showed no signs of energy limitation under reduced pH conditions. Exoskeleton mineral content, body mass, and organic content of crabs remained the same across pH and decoration treatments, with no effect of reduced pH on decoration behavior. Despite being a relatively inactive, osmoconforming species, Pelia tumida is able to maintain multiple regulatory processes and behavior when exposed to environmental pH stress, which underscores the complexity of responses within Crustacea to ocean acidification conditions.

Improved high temperature radiation damage tolerance in a three-phase ceramic with heterointerfaces.

Radiation damage tolerance for a variety of ceramics at high temperatures depends on the material's resistance to nucleation and growth of extended defects. Such processes are prevalent in ceramics employed for space, nuclear fission/fusion and nuclear waste environments. This report shows that random heterointerfaces in materials with sub-micron grains can act as highly efficient sinks for point defects compared to grain boundaries in single-phase materials. The concentration of dislocation loops in a radiation damage-prone phase (Al2O3) is significantly reduced when Al2O3 is a component of a composite system as opposed to a single-phase system. These results present a novel method for designing exceptionally radiation damage tolerant ceramics at high temperatures with a stable grain size, without requiring extensive interfacial engineering or production of nanocrystalline materials.

Effect of Current on Diffusivity in Metal Hexaborides: A Spark Plasma Sintering Study.

We present the effect of pulsed direct current on metal ion diffusion in CaB6-SrB6 diffusion couples, showing that the diffusivity of Ca2+ and Sr2+ across the diffusion couple interface is higher toward the positive electrode when subjected to a current flow of 2.2 kA at a temperature of 2007 K. We attribute this enhanced mobility to the movement of negatively charged metal vacancies toward the positive electrode in the system. Energy-dispersive spectroscopy is used to map the concentration of Ca2+ and Sr2+ in the region near the interface, and diffusion profiles are fitted with error functions. The concentration curves display concentration-dependent Boltzmann-Matano diffusivity. Total dopant values (Q) have been used to numerically compare the differences between Ca2+ diffusion in SrB6 and Sr2+ diffusion in CaB6. We determine an enhancement of 3.8× for Ca2+ into SrB6 versus an enhancement of 1.8× for Sr2+ into CaB6. No new phases are formed at the interface between CaB6 and SrB6, since hexaboride compounds readily form solid solutions. The results elucidate the role of pulsed direct current on the diffusion of metal ions in hexaboride compounds.

Spines of the porcupine fish: Structure, composition, and mechanical properties.

This paper explores the structure, composition, and mechanical properties of porcupine fish spines for the first time. The spine was found to be composed of nanocrystalline hydroxyapatite, protein (collagen), and water using X-ray diffraction, energy-dispersive X-ray spectroscopy, and thermogravimetric analysis. Microstructures have mineralized fibrillar sheets in the longitudinal direction and in a radial orientation in the transverse direction that were observed using light and electron microscopy. Based on the images, the hierarchical structure of the spine shows both concentric and radial reinforcement. Mechanical properties were obtained using cantilever beam and nanoindentation tests. A tapered cantilever beam model was developed and compared to that of a uniform cantilever beam. The tapered beam model showed that while the stresses experienced were similar to those of the uniform beam, the location of the maximum stress was near the distal region of the beam rather than at the base, which allows the porcupine fish to conserve energy and resources if the spine is fractured.

Synergistic structures from magnetic freeze casting with surface magnetized alumina particles and platelets.

Magnetic freeze casting utilizes the freezing of water, a low magnetic field and surface magnetized materials to make multi-axis strengthened porous scaffolds. A much greater magnetic moment was measured for larger magnetized alumina platelets compared with smaller particles, which indicated that more platelet aggregation occurred within slurries. This led to more lamellar wall alignment along the magnetic field direction during magnetic freeze casting at 75 mT. Slurries with varying ratios of magnetized particles to platelets (0:1, 1:3, 1:1, 3:1, 7:1, 1:0) produced porous scaffolds with different structural features and degrees of lamellar wall alignment. The greatest mechanical enhancement in the magnetic field direction was identified in the synergistic condition with the highest particle to platelet ratio (7:1). Magnetic freeze casting with varying ratios of magnetized anisotropic and isotropic alumina provided insights about how heterogeneous morphologies aggregate within lamellar walls that impact mechanical properties. Fabrication of strengthened scaffolds with multi-axis aligned porosity was achieved without introducing different solid materials, freezing agents or additives. Resemblance of 7:1 particle to platelet scaffold microstructure to wood light-frame house construction is framed in the context of assembly inspiration being derived from both natural and synthetic sources.

Stiff, porous scaffolds from magnetized alumina particles aligned by magnetic freeze casting.

Bone consists of a hard mineral phase and a compliant biopolymer phase resulting in a composite material that is both lightweight and strong. Osteoporosis that degrades spongy bone preferentially over time leads to bone brittleness in the elderly. A porous ceramic material that can mimic spongy bone for a one-time implant provides a potential solution for the future needs of an aging population. Scaffolds made by magnetic freeze casting resemble the aligned porosity of spongy bone. A magnetic field applied throughout freezing induces particle chaining and alignment of lamellae structures between growing ice crystals. After freeze drying to extract the ice and sintering to strengthen the scaffold, cubes from the scaffold center are mechanically compressed along longitudinal (z-axis, ice growth direction) and transverse (y-axis, magnetic field direction) axes. The best alignment of lamellar walls in the scaffold center occurs when applying magnetic freeze casting with the largest particles (350nm) at an intermediate magnetic field strength (75mT), which also agrees with stiffness enhancement results in both z and y-axes. Magnetic moments of different sized magnetized alumina particles help determine the ideal magnetic field strength needed to induce alignment in the scaffold center rather than just at the poles.