Size distribution of CdS nanocrystal-doped silica xerogels

Pure and porous silica xerogels doped with CdS nanocrystals have been prepared by a sol-gel process. In order to determine parameters convenient for non-linear optical properties, particle size distributions were obtained by two complementary techniques: transmission electron microscopy (conventional, CTEM, and high resolution, HRTEM) and small angle X-ray scattering (SAXS). Monolithic samples having CdO concentrations varying from 5 to 20 wt% have been studied. Details are given of an image analysis technique used to study the CTEM micrographs.     

The Kinetic Inversion Problem in Ligand-Binding Heme Proteins

For a two-dimensional potential of intersecting parabolic bowls, we obtain an analytical approximation for the survival probability in the limit that the reactive mode is diffusive and the perpendicular protein mode frozen. The approximation is used in an automated computer algorithm for determining the parameters of the potential. Using this program, we are able to obtain a reasonably good fit to the low- temperature data of CO binding to horse myoglobin. We find, however, that features of the potential such as the saddle-point energy and the effective barrier, expected to dictate the high-temperature kinetics, are not uniquely determined for this potential from fitting the low-temperature data.     

A 100-MHz macropipelined VAX microprocessor

A macropipelined CISC microprocessor was implemented in a 0.75-μm CMOS 3.3-V technology. The 1.3-million-transistor custom chip measures 1.62×1.46 cm² and dissipates 16.3 W. The 100-MHz parts were benchmarked at 50 SPEC marks. The on-chip clocking system and several high-performance logic and circuit techniques are described. Macroinstruction handling, micropipeline management, and control store structures highlight the design architecture. The hierarchical array organization and fast tag comparison technique of the primary cache are discussed. Power estimation procedures are outlined, and the results are compared to measurements. Physical design and verification methods, and CAD tools are also described. After extensive functional verification efforts are described, chip and system test results are presented     

Encapsulation process development for flexible-circuit based chip scale packages

The ultimate driving forces for the development of small form-factor chip scale packages (CSPs) are the market demands for small, light and high performance products. The flex-based /spl mu/BGA technology has been a very successful package format, and tremendous efforts have been implemented in the process development for the technology. In this article, three flex-based chip scale packages (based on patented /spl mu/BGA technology) will be discussed. The focus will be on the encapsulation process development. Because of the unique package structures and material sets used in the flex-based CSPs, various encapsulation challenges were raised. The encapsulation solutions are compared and discussed for each type of flex-based /spl mu/BGA technologies, including the dispensing pump technologies, material characterization, process characterization and optimization. Based on the evaluation results, type C /spl mu/BGA technology is recommended for its simple assemble process flow, balanced protection on beam leads and solder ball joints and shorter manufacturing cycle time as well.     

Robust controller synthesis using the maximum entropy design equations

This note presents an application of the optimality conditions obtained in [1] for dynamic compensation in the presence of state-, control-, and measurement-dependent noise. By solving these equations, which represent a fundamental generalization of standard steady-state LQG theory, a series of increasingly robust control designs is obtained for the example considered in [2].     

Bacterial attachment to RO membranes surface-modified by concentration-polarization-enhanced graft polymerization

Concentration polarization-enhanced radical graft polymerization, a facile surface modification technique, was examined as an approach to reduce bacterial deposition onto RO membranes and thus contribute to mitigation of biofouling. For this purpose an RO membrane ESPA-1 was surface-grafted with a zwitterionic and negatively and positively charged monomers. The low monomer concentrations and low degrees of grafting employed in modifications moderately reduced flux (by 20-40%) and did not affect salt rejection, yet produced substantial changes in surface chemistry, charge and hydrophilicity. The propensity to bacterial attachment of original and modified membranes was assessed using bacterial deposition tests carried out in a parallel plate flow setup using a fluorescent strain of Pseudomonas fluorescens. Compared to unmodified ESPA-1 the deposition (mass transfer) coefficient was significantly increased for modification with the positively charged monomer. On the other hand, a substantial reduction in bacterial deposition rates was observed for membranes modified with zwitterionic monomer and, still more, with very hydrophilic negatively charged monomers. This trend is well explained by the effects of surface charge (as measured by ζ-potential) and hydrophilicity (contact angle). It also well correlated with force distance measurements by AFM using surrogate spherical probes with a negative surface charge mimicking the bacterial surface. The positively charged surface showed a strong hysteresis with a large adhesion force, which was weaker for unmodified ESPA-1 and still weaker for zwitterionic surface, while negatively charged surface showed a long-range repulsion and negligible hysteresis. These results demonstrate the potential of using the proposed surface- modification approach for varying surface characteristics, charge and hydrophilicity, and thus minimizing bacterial deposition and potentially reducing propensity biofouling.     

The effect of surface treatments on the adhesion of electrochemically deposited hydroxyapatite coating to titanium and on its interaction with cells and bacteria

The effect of different mechanical and chemical pre-treatments on the adhesion strength of hydroxyapatite (HAp) coating on a commercially pure titanium (CP-Ti) substrate was studied by means of a standard tensile test followed by microscopic and chemical analysis to determine the locus of fracture. In addition, the effects of either these pre-treatments or post-treatment by low-energy electron irradiation, which allowed tuning the wettability of the surface, on both osteoblast progenitor attachment and S. aureus bacteria attachment were investigated. A dedicated program was developed for unambiguous identification and count of stained cells. A single-phase HAp coating was formed by electrodeposition. A series of surface pre-treatments consisted of grinding down to P1000, etching in HNO₃/HF solution, grit blast, soaking in NaOH and subsequent heat treatment provided the highest adhesion strength to the HAp coating. Osteoblast progenitors derived from rats may be attached preferentially to a hydrophilic surface (post-treatment to θ = 30°), while the bacteria seemed to be less attached to hydrophobic surfaces (post-treatment to θ = 105°). However, the results were not statistically different. The bacteria seemed to be less attached to the smoother, uncoated surfaces.     

Compound-specific chlorine isotope analysis: a comparison of gas chromatography/isotope ratio mass spectrometry and gas chromatography/quadrupole mass spectrometry methods in an interlaboratory study

Chlorine isotope analysis of chlorinated hydrocarbons like trichloroethylene (TCE) is of emerging demand because these species are important environmental pollutants. Continuous flow analysis of noncombusted TCE molecules, either by gas chromatography/isotope ratio mass spectrometry (GC/IRMS) or by GC/quadrupole mass spectrometry (GC/qMS), was recently brought forward as innovative analytical solution. Despite early implementations, a benchmark for routine applications has been missing. This study systematically compared the performance of GC/qMS versus GC/IRMS in six laboratories involving eight different instruments (GC/IRMS, Isoprime and Thermo MAT-253; GC/qMS, Agilent 5973N, two Agilent 5975C, two Thermo DSQII, and one Thermo DSQI). Calibrations of (37)Cl/(35)Cl instrument data against the international SMOC scale (Standard Mean Ocean Chloride) deviated between instruments and over time. Therefore, at least two calibration standards are required to obtain true differences between samples. Amount dependency of δ(37)Cl was pronounced for some instruments, but could be eliminated by corrections, or by adjusting amplitudes of standards and samples. Precision decreased in the order GC/IRMS (1σ ≈ 0.1‰), to GC/qMS (1σ ≈ 0.2-0.5‰ for Agilent GC/qMS and 1σ ≈ 0.2-0.9‰ for Thermo GC/qMS). Nonetheless, δ(37)Cl values between laboratories showed good agreement when the same external standards were used. These results lend confidence to the methods and may serve as a benchmark for future applications.