Strain stiffening of non-colloidal hard sphere suspensions dispersed in Newtonian fluid near liquid-and-crystal coexistence region

Concentrated hard sphere suspensions often show an interesting nonlinear behavior, called strain stiffening, in which the viscosity or modulus starts to increase at critical strain amplitude. Sudden increase of rheological properties is similar to shear thickening; however, the particle dynamics in the strain stiffening under oscillatory shear flow does not necessarily coincide with the mechanism of shear thickening under step shear flow. In this study, we have systematically investigated the nonlinear rheology of non-colloidal (>1???m) hard sphere suspensions dispersed in Newtonian fluid near liquid-and-crystal coexistence region in order to better understand the strain stiffening behavior. The suspensions near liquid-and-crystal coexistence region are known to locally form the closed packing structure. The critical strain amplitude which is the onset of strain stiffening was different for the storage and loss modulus. But they converged to each other as the suspension forms a more crystalline structure. The critical strain amplitude was independent of medium viscosity, imposed angular frequency, and particle size, but was strongly dependent upon particle volume fraction. The onset of strain stiffening was explained in terms of shear-induced collision due to particle motion in the closed packing structure. Nonlinear stress wave-forms, which reflect the micro-structural change, were observed with the onset of strain stiffening. During the strain stiffening, enhanced elastic stress before and after flow reversal was observed which originates from changes in the suspension microstructure. Nonlinearity of the shear stress in terms of Fourier intensity was extremely increased up to 0.55. Beyond the strain stiffening, the suspension responded liquid-like and the nonlinearity decreased but the elastic shear stress was still indicating the microstructure rearrangement within a cycle.     

Anticancer Activity of 2-O-caffeoyl Alphitolic Acid Extracted from the Lichen,Usnea barbata 2017-KL-10

Colorectal cancer is one of the life-threatening ailments causing high mortality and morbidity worldwide. Despite the innovation in medical genetics, the prognosis for metastatic colorectal cancer in patients remains unsatisfactory. Recently, lichens have attracted the attention of researchers in the search for targets to fight against cancer. Lichens are considered mines of thousands of metabolites. Researchers have reported that lichen-derived metabolites demonstrated biological effects, such as anticancer, antiviral, anti-inflammatory, antibacterial, analgesic, antipyretic, antiproliferative, and cytotoxic, on various cell lines. However, the exploration of the biological activities of lichens’ metabolites is limited. Thus, the main objective of our study was to evaluate the anticancer effect of secondary metabolites isolated from lichen (Usnea barbata 2017-KL-10) on the human colorectal cancer cell line HCT116. In this study, 2OCAA exhibited concentration-dependent anticancer activities by suppressing antiapoptotic genes, such as MCL-1, and inducing apoptotic genes, such as BAX, TP53, and CDKN1A(p21). Moreover, 2OCAA inhibited the migration and invasion of colorectal cancer cells in a concentration-dependent manner. Taken together, these data suggest that 2OCAA is a better therapeutic candidate for colorectal cancer.     

On totally *-paranormal operators

In this paper we study some properties of a totally *-paranormal operator (defined below) on Hilbert space. In particular, we characterize a totally *-paranormal operator. Also we show that Weyl’s theorem and the spectral mapping theorem hold for totally *-paranormal operators through the local spectral theory. Finally, we show that every totally *-paranormal operator satisfies an analogue of the single valued extension property for W ²(D, H) and some of totally *-paranormal operators have scalar extensions.     

Phenothiazine‐S,S‐dioxide‐ and fluorene‐based light‐emitting polymers: Introduction of e−‐deficient S,S‐dioxide into e−‐rich phenothiazine

A novel series of poly(10‐hexyl‐phenothiazine‐S,S‐dioxide‐3,7‐diyl) and poly(9,9′‐dioctyl‐fluorene‐2,7‐diyl‐alt‐10‐hexyl‐3,7‐phenothiazine‐S,S‐dioxide) (PFPTZ‐SS) compounds were synthesized through Ni(0)‐mediated Yamamoto polymerization and Pd(II)‐catalyzed Suzuki polymerization. The synthesized polymers were characterized by ¹H NMR spectroscopy and elemental analysis and showed higher glass transition temperatures than that of pristine polyfluorene. In terms of photoluminescence (PL), the PFPTZ‐SS compounds were highly fluorescent with bright blue emissions in the solid state. Light‐emitting devices were fabricated with these polymers in an indium tin oxide/poly(3,4‐ethylene dioxythiophene):poly(styrene sulfonate)/polymer/Ca/Al configuration. The electroluminescence (EL) of the copolymers differed from the PL characteristics: the EL device exhibited a redshifted greenish‐blue emission in contrast to the blue emission observed in the PL. Additionally, this unique phenothiazine‐S,S‐dioxide property, triggered by the introduction of an electron‐deficient SO₂ unit into the electron‐rich phenothiazine, gave rise to improvements in the brightness, maximum luminescence intensity, and quantum efficiency of the EL devices fabricated with PFPTZ‐SS. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1236–1246, 2007     

White electroluminescence from a single polyfluorene containing bis‐DCM units

A series of fluorene‐based copolymers composed of blue‐ and orange‐light‐emitting comonomers were synthesized through palladium‐catalyzed Suzuki coupling reactions. 9,9‐Dihexylfluorene and 2‐(2,6‐bis‐{2‐[1‐(9,9‐dihexyl‐9H‐fluoren‐2‐yl)‐1,2,3,4‐tetrahydroquinolin‐6‐yl]‐vinyl}‐pyran‐4‐ylidene)‐malononitrile (DCMF) were used as the blue‐ and orange‐light‐emitting chromophores, respectively. The resulting single polymers exhibited simultaneous blue (423/450 nm) and orange (580–600 nm) emissions from these two chromophores. By adjusting the fluorene and DCMF contents, white light emission could be obtained from a single polymer; a device with an ITO/PEDOT:PSS/polymer/Ca/Al configuration was found to exhibit pure white electroluminescence with Commission Internationale de L'Eclairage (CIE) coordinates of (0.33, 0.31), a maximum brightness of 1180 cd/m², and a current efficiency of 0.60 cd/A. Furthermore, the white light emission of this device was found to be very stable with respect to variation of the driving voltage. The CIE coordinates of the device were (0.32, 0.29), (0.32, 0.29), and (0.33, 0.31) for driving voltages of 7, 8, and 10 V, respectively. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3380–3390, 2007     

Students' Retention of Mathematical Knowledge and Skills in Differential Equations

This study investigates students' retention of mathematical knowledge and skills in two differential equations classes. Posttests and delayed posttests after 1 year were administered to students in inquiry‐oriented and traditional classes. The results show that students in the inquiry‐oriented class retained conceptual knowledge, as seen by their performance on modeling problems, and retained equal proficiency in procedural problems, when compared with students in the traditionally taught classes. The results of this study add additional support to the claim that teaching for conceptual understanding can lead to longer retention of mathematical knowledge.     

Optically detected electrophonon resonance effects in quantum wells

Optical detected electrophonon resonance (ODEPR) effects in quantum wells of n-GaAs materials are investigated for square potential and parabolic potential, respectively. We also obtain the ODEPR conditions as functions of confinement frequency in parabolic potential and well-width in square potential for the various photon frequencies, respectively. In particular, anomalous behaviors of the ODEPR lineshape such as the splitting of ODEPR peaks for incident photon frequency are discussed. Furthermore, we obtain the selection rules for transition in quantum wells of two different potentials, respectively.     

Energy Dispersive X-Ray Spectrometry by Microcalorimetry for the SEM

 Analytical X-ray spectrometry for electron beam instruments has advanced significantly with the development of the microcalorimeter energy dispersive X-ray spectrometer (μcal EDS). The μcal EDS operates by measuring the temperature rise when a single photon is absorbed in a metal target. A cryoelectronic circuit with electrothermal feedback and a superconducting transition edge sensor serves as the thermometer. Spectral resolution approaching 4.5 eV for high energy photons (6000 eV) and 2 eV for low energy photons below 2000 eV has been demonstrated in energy dispersive operation across a photon energy range from 250 eV to 8 keV. Spectra of a variety of materials demonstrate the power of the μcal EDS to solve practical problems while operating on a scanning electron microscope platform.     

Extensions of zip rings

A ring R is called right zip provided that if the right annihilator r_R(X) of a subset X of R is zero, r_R(Y)=0 for a finite subset Y⊆X. Faith [5] raised the following questions: When does R being a right zip ring imply R[x] being right zip?; Characterize a ring R such that Mat_n(R) is right zip; When does R being a right zip ring imply R[G] being right zip when G is a finite group? In this note, we continue the study of the extensions of noncommutative zip rings based on Faith's questions.