Higher Alcohol Synthesis

It has been known for many years that it is possible to produce mixtures of methanol and higher alcohols from synthesis gas by alkali promotion of the methanol synthesis catalysts and by appropriate modification of the reaction conditions [l]. From 1927 to 1945 plants were in operation in the United States and Germany, that were dismantled with the coming of different feedstocks and the necessity of obtaining pure alcohols for chemical use. In the last decade the chemical and petroleum industry has shown a renewed and growing interest in the use of mixtures of methanol and higher aliphatic alcohols. The original goal in the late '70s was mainly to reduce oil dependence by producing synthetic components for gasoline blends. More recently the trend to lead phase-down due to environmental protection has focused the attention on the product performances of such alcohol mixtures as high octane blending stock for gasoline. It has been shown that the addition of higher alcohols to methanol increases the water tolerance in respect to phase separation, reduces the fuel volatility and the vapor lock tendency, and also results in higher volumetric heating values.     

Hydrodynamic transport parameters of wurtzite ZnO from analytic- and full-band Monte Carlo simulation

Analytic-band Monte Carlo simulation of electron transport in bulk wurtzite ZnO, validated against the results of a full-band code and available experimental data, is used to determine the main parameters required by drift-diffusion and hydrodynamic models. Steady-state drift velocity, carrier temperature, energy and momentum relaxation time, noise diffusivity, and electron thermal conductivity are calculated, and their dependence on temperature and electric field or average electron energy is approximated by means of a complete set of fitting models suitable for inclusion in commercial device simulation tools.     

The Association of Il28b Genotype with the Histological Features of Chronic Hepatitis C Is HCV Genotype Dependent

The interleukin 28B (IL28B) rs12979860 polymorphism is associated with treatment outcome in hepatitis C virus (HCV) genotype 1 and 4 patients. Its association with the histological features of chronic hepatitis C and disease severity needs further clarifications. To assess the correlation between IL28B genotype, HCV genotype and liver biopsy findings in untreated patients.

Materials and Methods

Pre-treatment liver biopsies from 335 HCV Caucasian patients (59% males, age 50 years) enrolled in the MIST study were staged for fibrosis and inflammation according to the METAVIR and the Ishak scoring systems; steatosis was dichotomized as <5% or ≥5%. IL28B was typed by Taqman Single Nucleotide Polymorphism (SNP) genotyping assay. HCV genotype was 1 in 151 (45%), 2 in 99 (30%), 3 in 50 (15%) and 4 in 35 (10%) patients. IL28B genotype was CC in 117 (34%), CT in 166 (49%) and TT in 52 (15%). At univariate analysis, the IL28B CC genotype was associated with severe portal inflammation in HCV-1 patients (CC vs. CT/TT: 86% vs. 63%, p = 0.005), severe lobular inflammation in HCV-2 patients (CC vs. CT/TT: 44% vs. 23%, p = 0.03), and less fatty infiltration in HCV-1 patients (CC vs. CT/TT: 72% vs. 51%, p = 0.02). Despite the lack of any association between IL28B and fibrosis stage, in HCV-3 patients IL28B CC correlated with METAVIR F3–F4 (CC vs. CT/TT: 74% vs. 26%, p = 0.05). At multivariate analysis, the genotype CC remained associated with severe portal inflammation in HCV-1, only (Odds Ratio (OR): 95% Confidence Interval (CI): 3.24 (1.23–8.51)). IL28B genotype is associated with the histological features of chronic hepatitis C in a HCV genotype dependent manner, with CC genotype being independently associated with severe portal inflammation.     

Evaluation of Quantum Efficiency,Crosstalk, and Surface Recombination in HgCdTe Photon-Trapping Structures

The quantum efficiency (QE) in HgCdTe photovoltaic pixel arrays employing a photon-trapping (PT) structure realized with a periodic array of pillars intended to provide broadband operation was investigated. It was found that the QE depends heavily on the passivation of the pillar surface. This is due to the presence of large fixed positive charge on the surface of pillars passivated with anodic oxide. A three-dimensional numerical simulation model was used to study the effect of the surface charge density and surface recombination velocity on the exterior of the pillars. Then, the QE of this structure was evaluated subject to different surface conditions. It was found that alone the surface charge density or surface recombination is detrimental to the QE but that the QE is recovered when both phenomena are present. Subsequently, the crosstalk was analyzed and the superior performance of the PT structure was demonstrated by evaluating the modulation transfer function.     

Defensive Disclosure of Patentable Inventions under Antitrust Enforcement

Why do large firms disclose patentable inventions defensively? We study IBM's disclosure and patenting activity and find that stronger antitrust enforcement and consent decrees limiting patent protection lead to more defensive disclosure. We extend our analysis to Xerox and show, using a differences-in-differences approach, a decline in patent propensity and an increase in patent scope in patent classes affected by the 1975 consent decree. We extend our analysis to include AT&;T, the other exceptionally large firm with defensive-disclosure activity, and show that their patenting propensity declined under increased antitrust enforcement relative to other firms in the industry. Overall, we show how these firms used defensive disclosure as a strategy to balance the benefits of patenting with the costs of uncertain antitrust enforcement. Our results are especially relevant in light of the defensive patent strategies many firms employ to preempt and cope with patent litigation.     

Tuning light emission of PbS nanocrystals from infrared to visible range by cation exchange

Colloidal semiconductor nanocrystals, with intense and sharp-line emission between red and near-infrared spectral regions, are of great interest for optoelectronic and bio-imaging applications. The growth of an inorganic passivation layer on nanocrystal surfaces is a common strategy to improve their chemical and optical stability and their photoluminescence quantum yield. In particular, cation exchange is a suitable approach for shell growth at the expense of the nanocrystal core size. Here, the cation exchange process is used to promote the formation of a CdS passivation layer on the surface of very small PbS nanocrystals (2.3 nm in diameter), blue shifting their optical spectra and yielding luminescent and stable nanostructures emitting in the range of 700–850 nm. Structural, morphological and compositional investigation confirms the nanocrystal size contraction after the cation-exchange process, while the PbS rock-salt crystalline phase is retained. Absorption and photoluminescence spectroscopy demonstrate the growth of a passivation layer with a decrease of the PbS core size, as inferred by the blue-shift of the excitonic peaks. The surface passivation strongly increases the photoluminescence intensity and the excited state lifetime. In addition, the nanocrystals reveal increased stability against oxidation over time. Thanks to their absorption and emission spectral range and the slow recombination dynamics, such highly luminescent nano-objects can find interesting applications in sensitized photovoltaic cells and light-emitting devices.