1,278 research outputs found

    Carlos Drummond de Andrade, Jorge de Sena e Prêmios Internacionais: Uma Correspondência Pessoal

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    Tradução do inglês por Lúcia Regina de Sá e Benito Martinez Rodrigue

    Recommended Guanidine Suppressor for the Next-Generation Caustic-Side Solvent Extraction Process

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    The guanidine recommended for the Next-Generation Caustic-Side is N,N ,N -tris(3,7-dimethyloctyl)guanidine (TiDG). Systematic testing has shown that it is significantly more lipophilic than the previously recommended guanidine DCiTG, the active extractant in the commercial guanidine product LIX -79, while not otherwise changing the solvent performance. Previous testing indicated that the extent of partitioning of the DCiTG suppressor to the aqueous strip solution is significantly greater than expected, potentially leading to rapid depletion of the suppressor from the solvent and unwanted organic concentrations in process effluents. Five candidate guanidines were tested as potential replacements for DCiTG. The tests included batch extraction with simulated waste and flowsheet solutions, third-phase formation, emulsion formation, and partition ratios of the guanidine between the solvent and aqueous strip solution. Preliminary results of a thermal stability test of the TiDG solvent at one month duration indicated performance approximately equivalent to DCiTG. Two of the guanidines proved adequate in all respects, and the choice of TiDG was deemed slightly preferable vs the next best guanidine BiTABG

    Affinity chromatography in dynamic combinatorial libraries: one-pot amplification and isolation of a strongly binding receptor

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    We report the one-pot amplification and isolation of a nanomolar receptor in a multibuilding block aqueous dynamic combinatorial library using a polymer-bound template. By appropriate choice of a poly(N,N-dimethylacrylamide)-based support, unselective ion-exchange type behaviour between the oppositely charged cationic guest and polyanionic hosts was overcome, such that the selective molecular recognition arising in aqueous solution reactions is manifest also in the analogous templated solid phase DCL syntheses. The ability of a polymer bound template to identify and isolate a synthetic receptor via dynamic combinatorial chemistry was not compromised by the large size of the library, consisting of well over 140 theoretical members, demonstrating the practical advantages of a polymer-supported DCL methodology

    Dynamical chiral symmetry breaking and confinement with an infrared-vanishing gluon propagator?

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    We study a model Dyson-Schwinger equation for the quark propagator closed using an {\it Ansatz} for the gluon propagator of the form \mbox{D(q)∼q2/[(q2)2+b4]D(q) \sim q^2/[(q^2)^2 + b^4]} and two {\it Ans\"{a}tze} for the quark-gluon vertex: the minimal Ball-Chiu and the modified form suggested by Curtis and Pennington. Using the quark condensate as an order parameter, we find that there is a critical value of b=bcb=b_c such that the model does not support dynamical chiral symmetry breaking for b>bcb>b_c. We discuss and apply a confinement test which suggests that, for all values of bb, the quark propagator in the model {\bf is not} confining. Together these results suggest that this Ansatz for the gluon propagator is inadequate as a model since it does not yield the expected behaviour of QCD.Comment: 21 Pages including 4 PostScript figures uuencoded at the end of the file. Replacement: slight changes of wording and emphasis. ADP-93-215/T133, ANL-PHY-7599-TH-93, FSU-SCRI-93-108, REVTEX 3.

    Chiral Symmetry Breaking in Quenched Massive Strong-Coupling QED4_4

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    We present results from a study of subtractive renormalization of the fermion propagator Dyson-Schwinger equation (DSE) in massive strong-coupling quenched QED4_4. Results are compared for three different fermion-photon proper vertex {\it Ans\"{a}tze\/}: bare γμ\gamma^\mu, minimal Ball-Chiu, and Curtis-Pennington. The procedure is straightforward to implement and numerically stable. This is the first study in which this technique is used and it should prove useful in future DSE studies, whenever renormalization is required in numerical work.Comment: REVTEX 3.0, 15 pages plus 7 uuencoded PostScript figure

    ?2-Microglobulin Amyloid Fibril-Induced Membrane Disruption Is Enhanced by Endosomal Lipids and Acidic pH

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    Although the molecular mechanisms underlying the pathology of amyloidoses are not well understood, the interaction between amyloid proteins and cell membranes is thought to play a role in several amyloid diseases. Amyloid fibrils of ?2-microglobulin (?2m), associated with dialysis-related amyloidosis (DRA), have been shown to cause disruption of anionic lipid bilayers in vitro. However, the effect of lipid composition and the chemical environment in which ?2m-lipid interactions occur have not been investigated previously. Here we examine membrane damage resulting from the interaction of ?2m monomers and fibrils with lipid bilayers. Using dye release, tryptophan fluorescence quenching and fluorescence confocal microscopy assays we investigate the effect of anionic lipid composition and pH on the susceptibility of liposomes to fibril-induced membrane damage. We show that ?2m fibril-induced membrane disruption is modulated by anionic lipid composition and is enhanced by acidic pH. Most strikingly, the greatest degree of membrane disruption is observed for liposomes containing bis(monoacylglycero)phosphate (BMP) at acidic pH, conditions likely to reflect those encountered in the endocytic pathway. The results suggest that the interaction between ?2m fibrils and membranes of endosomal origin may play a role in the molecular mechanism of ?2m amyloid-associated osteoarticular tissue destruction in DRA

    On Renormalized Strong-Coupling Quenched QED in Four Dimensions

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    We study renormalized quenched strong-coupling QED in four dimensions in arbitrary covariant gauge. Above the critical coupling leading to dynamical chiral symmetry breaking, we show that there is no finite chiral limit. This behaviour is found to be independent of the detailed choice of photon-fermion proper vertex in the Dyson-Schwinger equation formalism, provided that the vertex is consistent with the Ward-Takahashi identity and multiplicative renormalizability. We show that the finite solutions previously reported lie in an unphysical regime of the theory with multiple solutions and ultraviolet oscillations in the mass functions. This study supports the assertion that in four dimensions strong coupling QED does not have a continuum limit in the conventional sense.Comment: REVTEX 3.0, 15 pages,including 4 eps files comprising 3 figures. Submitted to Phys. Rev.

    Book reviews

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/45784/1/11153_2004_Article_BF00140614.pd

    The Future of Fundamental Science Led by Generative Closed-Loop Artificial Intelligence

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    Recent advances in machine learning and AI, including Generative AI and LLMs, are disrupting technological innovation, product development, and society as a whole. AI's contribution to technology can come from multiple approaches that require access to large training data sets and clear performance evaluation criteria, ranging from pattern recognition and classification to generative models. Yet, AI has contributed less to fundamental science in part because large data sets of high-quality data for scientific practice and model discovery are more difficult to access. Generative AI, in general, and Large Language Models in particular, may represent an opportunity to augment and accelerate the scientific discovery of fundamental deep science with quantitative models. Here we explore and investigate aspects of an AI-driven, automated, closed-loop approach to scientific discovery, including self-driven hypothesis generation and open-ended autonomous exploration of the hypothesis space. Integrating AI-driven automation into the practice of science would mitigate current problems, including the replication of findings, systematic production of data, and ultimately democratisation of the scientific process. Realising these possibilities requires a vision for augmented AI coupled with a diversity of AI approaches able to deal with fundamental aspects of causality analysis and model discovery while enabling unbiased search across the space of putative explanations. These advances hold the promise to unleash AI's potential for searching and discovering the fundamental structure of our world beyond what human scientists have been able to achieve. Such a vision would push the boundaries of new fundamental science rather than automatize current workflows and instead open doors for technological innovation to tackle some of the greatest challenges facing humanity today.Comment: 35 pages, first draft of the final report from the Alan Turing Institute on AI for Scientific Discover
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