Sexuality and the Balance of Power in the Canterbury Tales

When examining ideas on the sexuality of Chaucer\u27s characters, one cannot help but come across the work of Alfred David. In his bookTheStrumpet Muse, David studies selected Canterbury tales from the perspective of New Criticism, analyzing various sexual attitudes expressed in the separate tales. In this paper I appropriate a basic concept of David\u27s and use it to my own feminist critical purposes, adding significantly to David\u27s core idea. Throughout the following study of sexuality and power in the Canterbury Tales, I use sexual natural to define a certain state of human sexuality. While the term is my own, the idea is drawn from David\u27s general argument on the comedy of innocence (95)

Band Formation during Gaseous Diffusion in Aerogels

We study experimentally how gaseous HCl and NH_3 diffuse from opposite sides of and react in silica aerogel rods with porosity of 92 % and average pore size of about 50 nm. The reaction leads to solid NH_4Cl, which is deposited in thin sheet-like structures. We present a numerical study of the phenomenon. Due to the difference in boundary conditions between this system and those usually studied, we find the sheet-like structures in the aerogel to differ significantly from older studies. The influence of random nucleation centers and inhomogeneities in the aerogel is studied numerically.Comment: 7 pages RevTex and 8 figures. Figs. 4-8 in Postscript, Figs. 1-3 on request from author

Assessment of combined scale/corrosion inhibitors - A combined jar test/bubble cell

The formation of calcium carbonate scale and the occurrence of CO corrosion are both widespread phenomena observed within pipework during oil and gas production. The most common form of treatment for both processes is the application of chemical inhibition through corrosion and/or scale inhibitors. Surface scaling of pipework rarely occurs in environments where no corrosion exists, yet techniques used to develop and assess the performance of scale inhibitors tend to focus on assessing and reducing solely bulk/surface scaling, without affording consideration towards corrosion, whilst corrosion inhibitors are frequently evaluated in non-scaling environments. Furthermore, both chemicals tend to be evaluated independently meaning that any potential antagonistic effects between the chemicals can go unrecognised. This paper addresses this very issue by presenting a unique setup and methodology to enable the occurrence of scale and corrosion to be monitored simultaneously in a CO-saturated environment in the presence and absence of combined scale and corrosion inhibitors. The test cell focuses on evaluating four key parameters which are quantified either throughout the duration of the test, or from the implementation of post-test surface analysis techniques. The multiple assessment of (i) bulk scale precipitation, (ii) surface scaling, (iii) general corrosion and (iv) localised corrosion permits a full assessment of the chemical blends propensity to mitigate both scaling and corrosion. Non-inhibited tests were initially conducted at 60 °C to form a baseline for comparison. Four combined scale/corrosion inhibitors were subsequently used at low concentrations in order to understand their mechanisms and highlight any competitive effect which existed in reducing either scale or corrosion. The results demonstrate that the methodology implemented is effective at assessing the efficiency of combined inhibitors in reducing both corrosion and scale in environments where both processes occur simultaneously. The limitations of conducting solely bulk scaling or corrosion tests in non-scaling environments are discussed relative to the results obtained in this work. The results of each individual inhibitor are discussed and markedly different behaviour is observed according to the concentration administered, as well as the particular blend of chemicals applied

B-spline parametrization of the dielectric function applied to spectroscopic ellipsometry on amorphous carbon

The remote plasma deposition of hydrogenated amorphous carbon (a-C:H) thin films is investigated by in situ spectroscopic ellipsometry (SE). The dielectric function of the a-C:H film is in this paper parametrized by means of B-splines. In contrast with the commonly used Tauc-Lorentz oscillator, B-splines are a purely mathematical description of the dielectric function. We will show that the B-spline parametrization, which requires no prior knowledge about the film or its interaction with light, is a fast and simple-to-apply method that accurately determines thickness, surface roughness, and the dielectric constants of hydrogenated amorphous carbon thin films. Analysis of the deposition process provides us with information about the high deposition rate, the nucleation stage, and the homogeneity in depth of the deposited film. Finally, we show that the B-spline parametrization can serve as a stepping stone to physics-based models, such as the Tauc-Lorentz oscillator. © 2009 American Institute of Physics. U7 - Export Date: 24 March 2010 U7 - Source: Scopus U7 - Art. No.: 12350

Aquatic Ecotoxicity Testing of Nanoparticles—The Quest To Disclose Nanoparticle Effects

The number of products on the market containing engineered nanoparticles (ENPs) has increased significantly, and concerns have been raised regarding their ecotoxicological effects. Environmental safety assessments as well as relevant and reliable ecotoxicological data are required for the safe and sustainable use of ENPs. Although the number of publications on the ecotoxicological effects and uptake of ENPs is rapidly expanding, the applicability of the reported data for hazard assessment is questionable. A major knowledge gap is whether nanoparticle effects occur when test organisms are exposed to ENPs in aquatic test systems. Filling this gap is not straightforward, because of the broad range of ENPs and the different behavior of ENPs compared to “ordinary” (dissolved) chemicals in the ecotoxicity test systems. The risk of generating false negatives, and false positives, in the currently used tests is high, and in most cases difficult to assess. This Review outlines some of the pitfalls in the aquatic toxicity testing of ENPs which may lead to misinterpretation of test results. Response types are also proposed to reveal potential nanoparticle effects in the aquatic test organisms

Teaching the electrical origins of the electrocardiogram: An introductory physics laboratory for life science students

We present the design, pedagogical logic, and assessment of a laboratory and supporting materials that integrate a clinical academic cardiologist\u27s understanding of the origins of the electrocardiogram (ECG) with a physics educator\u27s insights into how to teach the underlying physics at the introductory level to life science students. In this article, we explain the choices made throughout the design process, connect a more advanced treatment of the physics to our approach, and present our assessment of the curriculum. Before the laboratory, students learn the cellular origins of the electric dipole potential produced by the heart on the body\u27s surface, including a simple physical model for the electrical activity of excitable cells, and learn to interpret the measured voltages of an ECG as probing components of the heart\u27s time-varying electric dipole moment. In the laboratory, students measure their own ECGs and analyze the data accordingly; they animate their data to display their own heart\u27s dipole moment for a single heartbeat. Our results from the assessment of student understanding and attitudes indicate that although students find the content challenging, nearly all students find it at least moderately interesting, and for about a quarter of the students in the course, this lab plays a highly meaningful part in connecting physics to medicine

In quest of a systematic framework for unifying and defining nanoscience

This article proposes a systematic framework for unifying and defining nanoscience based on historic first principles and step logic that led to a “central paradigm” (i.e., unifying framework) for traditional elemental/small-molecule chemistry. As such, a Nanomaterials classification roadmap is proposed, which divides all nanomatter into Category I: discrete, well-defined and Category II: statistical, undefined nanoparticles. We consider only Category I, well-defined nanoparticles which are >90% monodisperse as a function of Critical Nanoscale Design Parameters (CNDPs) defined according to: (a) size, (b) shape, (c) surface chemistry, (d) flexibility, and (e) elemental composition. Classified as either hard (H) (i.e., inorganic-based) or soft (S) (i.e., organic-based) categories, these nanoparticles were found to manifest pervasive atom mimicry features that included: (1) a dominance of zero-dimensional (0D) core–shell nanoarchitectures, (2) the ability to self-assemble or chemically bond as discrete, quantized nanounits, and (3) exhibited well-defined nanoscale valencies and stoichiometries reminiscent of atom-based elements. These discrete nanoparticle categories are referred to as hard or soft particle nanoelements. Many examples describing chemical bonding/assembly of these nanoelements have been reported in the literature. We refer to these hard:hard (H-n:H-n), soft:soft (S-n:S-n), or hard:soft (H-n:S-n) nanoelement combinations as nanocompounds. Due to their quantized features, many nanoelement and nanocompound categories are reported to exhibit well-defined nanoperiodic property patterns. These periodic property patterns are dependent on their quantized nanofeatures (CNDPs) and dramatically influence intrinsic physicochemical properties (i.e., melting points, reactivity/self-assembly, sterics, and nanoencapsulation), as well as important functional/performance properties (i.e., magnetic, photonic, electronic, and toxicologic properties). We propose this perspective as a modest first step toward more clearly defining synthetic nanochemistry as well as providing a systematic framework for unifying nanoscience. With further progress, one should anticipate the evolution of future nanoperiodic table(s) suitable for predicting important risk/benefit boundaries in the field of nanoscience

Synthesis of 1,3-Bis(hydroxy-halogenophenyl)propane-1,3-diamines and their Pt(II) Complexes, Preparation of the Pt(II) Complexes

The preparation of the Pt(II) complexes of the diamines described in Part A with CI- I-, S04 2-, and water as additional ligands is reported. Über die Herstellung der Pt(II) Komplexe der in Teil A beschriebenen Diamine mit CI- I-, S042- und Wasser als zusätzlichen Liganden wird berichtet