1,087 research outputs found
A Multivariate Homogeneously Weighted Moving Average Control Chart
This paper presents a multivariate homogeneously weighted moving average (MHWMA) control chart for monitoring a process mean vector. The MHWMA control chart statistic gives a specific weight to the current observation, and the remaining weight is evenly distributed among the previous observations. We present the design procedure and compare the average run length (ARL) performance of the proposed chart with multivariate Chi-square, multivariate EWMA, and multivariate cumulative sum control charts. The ARL comparison indicates superior performance of the MHWMA chart over its competitors, particularly for the detection of small shifts in the process mean vector. Examples are also provided to show the application of the proposed chart. - 2013 IEEE.Scopu
Low temperature expansion for the 3-d Ising Model
We compute the weak coupling expansion for the energy of the three
dimensional Ising model through 48 excited bonds. We also compute the
magnetization through 40 excited bonds. This was achieved via a recursive
enumeration of states of fixed energy on a set of finite lattices. We use a
linear combination of lattices with a generalization of helical boundary
conditions to eliminate finite volume effects.Comment: 10 pages, IASSNS-HEP-92/42, BNL-4767
Multi-interaction mean-field renormalization group
We present an extension of the previously proposed mean-field renormalization
method to model Hamiltonians which are characterized by more than just one type
of interaction. The method rests on scaling assumptions about the magnetization
of different sublattices of the given lattice and it generates as many flow
equations as coupling constants without arbitrary truncations on the
renormalized Hamiltonian. We obtain good results for the test case of Ising
systems with an additional second-neighbor coupling in two and three
dimensions. An application of the method is also done to a morphological model
of interacting surfaces introduced recenlty by Likos, Mecke and Wagner [J.
Chem. Phys. {\bf{102}}, 9350 (1995)].
PACS: 64.60.Ak, 64.60.Fr, 05.70.JkComment: Tex file and three macros appended at the end. Five figures available
upon request to: [email protected], Fax: [+]39-40-224-60
Tracking of fluorescently labeled polymer particles reveals surface effects during shear-controlled aggregation
Surface chemistry is believed to be the key parameter affecting the aggregation and breakage of colloidal suspensions when subjected to shear. To date, only a few works dealt with the understanding of the role of the physical and chemical properties of the particlesâ surface upon aggregation under shear. Previous studies suggested that surface modifications strongly affect polymer particlesâ adhesion, but it was very challenging to demonstrate this effect and monitor these alterations upon prolonged exposure to shear forces. More importantly, the mechanisms leading to these changes remain elusive. In this work, shear-induced aggregation experiments of polymer colloidal particles have been devised with the specific objective of highlighting material transfer and clarifying the role of the softness of the particleâs surface. To achieve this goal, polymer particles with a coreâshell structure comprising fluorescent groups have been prepared so that the surfaceâs softness could be tuned by the addition of monomer acting as a plasticizer and the percentage of fluorescent particles could be recorded over time via confocal microscopy to detect eventual material transfer among different particles. For the first time, material exchange occurring on the soft surface of coreâshell polymer microparticles upon aggregation under shear was observed and proved. More aptly, starting from a 50% labeled/nonlabeled mixture, an increase in the percentage of particles showing a fluorescent signature was recorded over time, reaching a fraction of 70% after 5 h
Molecular dynamics study of orientational order and rotational melting in clusters of TeF 6
Molecular dynamics simulations of the behavior of molecules in crystalline clusters of TeF 6 were carried out on systems of 100, 150, 250, and 350 molecules. Several diagnostic functions were applied to investigate whether rotational melting occurred before translational melting. These functions included the coefficient of rotational diffusion D Ξ ( T ), the âorientational Lindemann indexâ ÎŽ Ξ ( T ), the âorientational angular distribution functionâ Q (Ξ, T ), and the âorientational pair-correlation functionâ g Ξ ( r, T ). All indicators implied that rotational melting occurred before translational melting, that it began with the outermost molecules, and that its onset for smaller clusters was at lower temperatures than for larger clusters. Results also showed that the rotational transition coincided with the transition from a lower symmetry phase (monoclinic) to cubic, a phenomenon that had been noted by others to occur with some regularity for systems of globular molecules.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/43961/1/10053_2005_Article_BF01426586.pd
The PEER Collaborative: Supporting Engineering Education Research Faculty with Near-peer Mentoring Unconference Workshops
The PEER Collaborative National Network is a national peer mentoring network for early career tenure-track or mid-career tenured faculty who conduct and are primarily evaluated based on their research related to engineering education. This paper discusses the development, logistics, and outcomes of two PEER workshops built around a community of practice framework. Data from internal and external evaluations are presented to provide insights into aspects that worked well and aspects that need further development. Additionally, by reflecting on the workshops, participants crafted vignettes describing the impact the PEER workshops had on their personal and professional lives. The paper concludes with a discussion on the future of PEER (and potential spin-off groups from the PEER cohorts), and the changes that will be made in future workshops. Recommendations are provided for other organizers interested in developing successful ânear peerâ groups to address specific community needs
Formulaic Language in Native and Second Language Speakers: Psycholinguistics, Corpus Linguistics, and TESOL
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/89473/1/j.1545-7249.2008.tb00137.x.pd
Embodied spatial practices and everyday organization: the work of tour guides and their audiences
This article introduces an interactional perspective to the analysis of organizational space. The study is based on the analysis of over 100 hours of video recordings of guided tours undertaken within two sites (an historic house and a world-famous museum), coupled with interviews and field observations. The analysis is informed by ethnomethodology and conversation analysis in order to focus on the everyday organization of these tours, and the lived experience of inhabiting museum spaces. We use an interactional lens to unpack the âembodied spatial practicesâ critical to the work of tour guides and their audiences, which reveals how the sense and significance of the workspace emerges moment to moment, and in relation to the ongoing work at hand. As a result, for those with an interest in organizational space, the article introduces a novel perspective, and methods, to highlight the dynamic and interactional production of workspaces. Additionally, for those with an interest in practice, the article demonstrates the fundamental import of taking spatial arrangements seriously when analysing the organization of work
Quantitation of Cellular Dynamics in Growing Arabidopsis Roots with Light Sheet Microscopy
To understand dynamic developmental processes, living tissues must be imaged
frequently and for extended periods of time. Root development is extensively
studied at cellular resolution to understand basic mechanisms underlying
pattern formation and maintenance in plants. Unfortunately, ensuring continuous
specimen access, while preserving physiological conditions and preventing
photo-damage, poses major barriers to measurements of cellular dynamics in
indeterminately growing organs such as plant roots. We present a system that
integrates optical sectioning through light sheet fluorescence microscopy with
hydroponic culture that enables us to image at cellular resolution a vertically
growing Arabidopsis root every few minutes and for several consecutive days. We
describe novel automated routines to track the root tip as it grows, track
cellular nuclei and identify cell divisions. We demonstrate the system's
capabilities by collecting data on divisions and nuclear dynamics.Comment: * The first two authors contributed equally to this wor
Rh-POP Pincer Xantphos Complexes for C-S and C-H Activation. Implications for Carbothiolation Catalysis
The neutral RhÂ(I)âXantphos
complex [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)ÂCl]<sub><i>n</i></sub>, <b>4</b>, and cationic RhÂ(III) [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(H)<sub>2</sub>]Â[BAr<sup>F</sup><sub>4</sub>], <b>2a</b>, and [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos-3,5-C<sub>6</sub>H<sub>3</sub>(CF<sub>3</sub>)<sub>2</sub>)Â(H)<sub>2</sub>]Â[BAr<sup>F</sup><sub>4</sub>], <b>2b</b>, are described [Ar<sup>F</sup> = 3,5-(CF<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>; Xantphos
= 4,5-bisÂ(diphenylphosphino)-9,9-dimethylxanthene; Xantphos-3,5-C<sub>6</sub>H<sub>3</sub>(CF<sub>3</sub>)<sub>2</sub> = 9,9-dimethylxanthene-4,5-bisÂ(bisÂ(3,5-bisÂ(trifluoromethyl)Âphenyl)Âphosphine].
A solid-state structure of <b>2b</b> isolated from C<sub>6</sub>H<sub>5</sub>Cl solution shows a Îș<sup>1</sup>-chlorobenzene
adduct, [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos-3,5-C<sub>6</sub>H<sub>3</sub>(CF<sub>3</sub>)<sub>2</sub>)Â(H)<sub>2</sub>(Îș<sup>1</sup>-ClC<sub>6</sub>H<sub>5</sub>)]Â[BAr<sup>F</sup><sub>4</sub>], <b>3</b>. Addition of H<sub>2</sub> to <b>4</b> affords,
crystallographically characterized, [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(H)<sub>2</sub>Cl], <b>5</b>. Addition of diphenyl
acetylene to <b>2a</b> results in the formation of the CâH
activated metallacyclopentadiene [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(ClCH<sub>2</sub>Cl)Â(Ï,Ï-(C<sub>6</sub>H<sub>4</sub>)ÂCÂ(H)î»CPh)]Â[BAr<sup>F</sup><sub>4</sub>], <b>7</b>, a rare example of a crystallographically characterized Rhâdichloromethane
complex, alongside the RhÂ(I) complex <i>mer</i>-[RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(η<sup>2</sup>-PhCCPh)]Â[BAr<sup>F</sup><sub>4</sub>], <b>6</b>. Halide abstraction from [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)ÂCl]<sub><i>n</i></sub> in the presence of diphenylacetylene affords <b>6</b> as the
only product, which in the solid state shows that the alkyne binds
perpendicular to the Îș<sup>3</sup>-POP Xantphos ligand plane.
This complex acts as a latent source of the [RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)]<sup>+</sup> fragment and facilitates
<i>ortho</i>-directed CâS activation in a number
of 2-arylsulfides to give <i>mer</i>-[RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(Ï,Îș<sup>1</sup>-Ar)Â(SMe)]Â[BAr<sup>F</sup><sub>4</sub>] (Ar = C<sub>6</sub>H<sub>4</sub>COMe, <b>8</b>; C<sub>6</sub>H<sub>4</sub>(CO)ÂOMe, <b>9</b>; C<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>, <b>10</b>; C<sub>6</sub>H<sub>4</sub>CNCH<sub>2</sub>CH<sub>2</sub>O, <b>11</b>; C<sub>6</sub>H<sub>4</sub>C<sub>5</sub>H<sub>4</sub>N, <b>12</b>).
Similar CâS bond cleavage is observed with allyl sulfide,
to give <i>fac</i>-[RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(η<sup>3</sup>-C<sub>3</sub>H<sub>5</sub>)Â(SPh)]Â[BAr<sup>F</sup><sub>4</sub>], <b>13</b>. These products of CâS
activation have been crystallographically characterized. For <b>8</b> in situ monitoring of the reaction by NMR spectroscopy reveals
the initial formation of <i>fac</i>-Îș<sup>3</sup>-<b>8</b>, which then proceeds to isomerize to the <i>mer</i>-isomer. With the <i>para</i>-ketone aryl sulfide, 4-SMeC <sub>6</sub>H<sub>4</sub>COMe, CâH activation <i>ortho</i> to the ketone occurs to give <i>mer</i>-[RhÂ(Îș<sup>3</sup>-<sub>P,O,P</sub>-Xantphos)Â(Ï,Îș<sup>1</sup>-4-(COMe)ÂC<sub>6</sub>H<sub>3</sub>SMe)Â(H)]Â[BAr<sup>F</sup><sub>4</sub>], <b>14</b>. The temporal evolution of carbothiolation catalysis using <i>mer</i>-Îș<sup>3</sup>-<b>8</b>, and phenyl acetylene
and 2-(methylthio)Âacetophenone substrates shows initial fast catalysis
and then a considerably slower evolution of the product. We suggest
that the initially formed <i>fac</i>-isomer of the CâS
activation product is considerably more active than the <i>mer</i>-isomer (i.e., <i>mer</i>-<b>8</b>), the latter of
which is formed rapidly by isomerization, and this accounts for the
observed difference in rates. A likely mechanism is proposed based
upon these data
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