The role of elevated temperatures in the implantation of GaAs

The improvement in conductivity resulting from implanting n-type dopants into GaAs at elevated temperatures has been investigated. Measurement of the rate of introducing compensating defects at elevated temperatures shows only marginal reduction from the room temperature rate. The avoidance of lattice disorder buildup also has minimal effect on carrier recovery and the amount of residual compensation after annealing. It appears that compensation cannot account for the improved conductivity of heated implants and that alternatively a substantial fraction of the room temperature introduced ions, even with annealing, must fail to become substitutional in the first instance. For sulfur, the same temperature dependence consistent with the established behavior of selenium and tellurium is obtained. An increase in conductivity by a factor of 2·5 occurs ? 150°C to give up to 40 per cent utilization from 10¹⁴ S⁺ cm^?2 implants.     

Liquid phase epitaxial growth of InAs1-xSbx on GaSb

Reported here, for the first time, is the lattice matched growth of InAs_1-xSb_x on GaSb. The thermodynamic incompatibility of the system, i.e., the strong tendency for the In-As-Sb liquid to dissolve the GaSb substrate, was solved via a novel liquid phase epitaxial growth technique. Liquid compositions for lattice matching conditions have been determined in the 400-600°C range. Epitaxial growth has been examined for (100), (111)B and (111)A orientations. Dislocation etch pit densities for lattice matched, and near lattice matched conditions are shown to be less than 10⁴-cm⁻² and 10⁵-cm⁻⁴, respectively. The composition of the epitaxial layers are determined by the Gandolfi X-ray diffraction technique and compositional homogeneity has been confirmed by SEM X-ray analysis. Some material related device properties which demonstrate the reproducibility of the growth technique are presented.     

Design and validation of a high-throughput matrix-assisted laser desorption ionization time-of-flight mass spectrometry method for quantification of hepcidin in human plasma

Disorders of iron metabolism affect over a billion people worldwide. The circulating peptide hormone hepcidin, the central regulator of iron distribution in mammals, holds great diagnostic potential for an array of iron-associated disorders, including iron loading (β-thalassemia), iron overload (hereditary hemochromatosis), and iron deficiency diseases. We describe a novel high-throughput matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry assay for quantification of hepcidin in human plasma. This assay involves enrichment using a functionalized MALDI chip, a novel solvent-detergent precipitation buffer, and quantification using a stable isotope labeled internal standard. The linear range of hepcidin in plasma was 1-120 nM, with a low limit of quantification (LOQ) (1 nM), high accuracy (<15% relative error (RE)), and high precision (intraday average 5.52-18.48% coefficient of variation (CV) and interday 9.32-14.83% CV). The assay showed strong correlation with an established hepcidin immunoassay (Spearman; R(2) = 0.839 n = 93 ethylenediaminetetraacetic acid (EDTA) plasma). A collection of normal healthy pediatric samples (range 3.8-32.5 ng/mL; mean 12.9 ng/mL; n = 119) showed significant differences from an adult collection (range 1.8-48.7 ng/mL; mean 16.1 ng/mL; n = 95; P = 0.0096). We discuss these preliminary reference ranges and correlations with additional parameters in light of the utility and limitations of hepcidin measurements as a stand-alone diagnostic and as a tool for therapeutic intervention.     

Metal-ion-induced formation and stabilization of protein cages based on the cowpea chlorotic mottle virus

The cowpea chlorotic mottle virus (CCMV) is a versatile building block for the construction of nanoreactors and functional materials. Upon RNA removal, the capsid can be reversibly assembled and disassembed by adjusting the pH. At pH 5.0 the capsid is in the native assembled conformation, while at pH 7.5 it disassembles into 90 capsid protein dimers. This special property enables the encapsulation of various molecules, such as protein and enzymes, but only at low pH. It is possible to stabilize the capsid at pH 7.5 by addition of negatively charged polyelectrolytes or negatively charged particles, but these methods all fill the interior of the capsid, leaving little or no space for other cargo molecules. This pH restriction therefore severely limits the range of enzymes that can be encapsulated, and hampers the investigation of the CCMV capsid as a nanoreactor for the study of enzymes in confined spaces. Herein, the interaction of N-terminal histidine-tag-modified capsid proteins with several metal ions is reported. Depending on the conditions used, nanometer-sized protein particles or capsidlike architectures are formed that are stable at pH 7.5. This metal-mediated stabilization methodology is employed to form stable capsids containing multiple proteins at pH 7.5, thereby greatly expanding the scope of the CCMV capsid as a nanoreactor.     

Modeling Continuous Powder Mixing by Means of the Theory of Markov Chains

This article demonstrates the efficiency of the application of the theory of Markov chains as a tool to model and simulate continuous powder mixing to aid in better design of such equipment. Markov chain models allow calculating practically all parameters of the process necessary for its characterization, and in particular those related to particle residence time distribution (RTD). Some numerical examples from the model, which are important for better understanding the process, are also included. It is shown that the main factor defining the efficiency of continuous mixing, through the variance reduction ratio (VRR), is the ratio of the mean residence time and the period of inflows fluctuation, rather than the variance of the RTD. Also, the influence of the dimensions of the mixer outlet on the mean residence time, and in turn on the VRR, is examined as another way of improving the design.     

TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients

Clinical guidelines recommend concurrent treatment of anemia in end‐stage renal disease with erythropoiesis‐stimulating agents (ESAs) and iron. However, there are mixed data about optimal iron supplementation. To help address this gap, the relationship between iron markers and hemoglobin (Hb) response to ESA (Epoetin alfa) dose was examined. Electronic medical records of 1902 US chronic hemodialysis patients were analyzed over a 12‐month period between June 2009 and June 2010. The analysis included patients who had at least one Hb value during each 4‐week interval for four consecutive intervals (k ? 2, k ? 1, k, and k + 1; k is the index interval), received at least one ESA dose during intervals k ? 1 or k, had at least one transferrin saturation (TSAT) value at interval k, and at least one ferritin value during intervals k ? 2, k ? 1, or k. Effect modification by TSAT and ferritin on Hb response was evaluated using the generalized estimating equations approach. Patients had a mean (standard deviation) age of 62 (15) years; 41% were Caucasian, 34% African American, 65% had hypertension, and 39% diabetes. Transferrin saturation, but not ferritin, had a statistically significant (P < 0.05) modifying effect on Hb response. Maximum Hb response was achieved when TSAT was 34%, with minimal incremental effect beyond these levels. Of the two standard clinical iron markers, TSAT should be used as the primary marker of the modifying effect of iron on Hb response to ESA. Long‐term safety of iron use to improve Hb response to ESA warrants further study.     

Rapid decompression of pressurized aircraft fuselages

A methodology for determining compartment pressures at any point during a rapid decompression of a pressurized aircraft fuselage is presented. The approach takes into consideration the mass and mass moment of inertia of panels and doors through which pressurized air must pass. Failure to consider vent panel mass is shown to severely underestimate the pressure differential across partitions separating compartments during a rapid-decompression event.