Solving the Dym initial value problem in reproducing kernel space

We consider two numerical solution approaches for the Dym initial value problem using the reproducing kernel Hilbert space method. For each solution approach, the solution is represented in the form of a series contained in the reproducing kernel space, and a truncated approximate solution is obtained. This approximation converges to the exact solution of the Dym problem when a sufficient number of terms are included. In the first approach, we avoid to perform the Gram-Schmidt orthogonalization process on the basis functions, and this will decrease the computational time. Meanwhile, in the second approach, working with orthonormal basis elements gives some numerical advantages, despite the increased computational time. The latter approach also permits a more straightforward convergence analysis. Therefore, there are benefits to both approaches. After developing the reproducing kernel Hilbert space method for the numerical solution of the Dym equation, we present several numerical experiments in order to show that the method is efficient and can provide accurate approximations to the Dym initial value problem for sufficiently regular initial data after relatively few iterations. We present the absolute error of the results when exact solutions are known and residual errors for other cases. The results suggest that numerically solving the Dym initial value problem in reproducing kernel space is a useful approach for obtaining accurate solutions in an efficient manner.     

Clustering Categorical Data via Ensembling Dissimilarity Matrices

We present a technique for clustering categorical data by generating many dissimilarity matrices and combining them. We begin by demonstrating our technique on low-dimensional categorical data and comparing it to several other techniques that have been proposed. We show through simulations and examples that our method is both more accurate and more stable. Then we give conditions under which our method should yield good results in general. Our method extends to high-dimensional categorical data of equal lengths by ensembling over many choices of explanatory variables. In this context, we compare our method with two other methods. Finally, we extend our method to high-dimensional categorical data vectors of unequal length by using alignment techniques to equalize the lengths. We give an example to show that our method continues to provide useful results, in particular, providing a comparison with phylogenetic trees. Supplementary material for this article is available online.     

Modeling elongational viscosity of blends of linear and long-chain branched polypropylenes

To enhance the melt strength of a conventional linear polypropylene (L-PP), blends with a long-chain branched polypropylene (LCB-PP) were produced by adding 2, 5, 10, 25, 50, and 75 wt% of LCB-PP to L-PP and mixing in a twin screw extruder. It was found that, already, an addition of 10% or less of LCB-PP to L-PP leads to significant strain hardening. Elongational viscosity data of L-PP and LCB-PP and those of their blends were analyzed by the use of the molecular stress function (MSF) theory. While L-PP is characterized by the MSF parameter, β=1 (typical for linear melts), and shows very little chain stretch (), melt elongational behavior of LCB-PP is characterized by the MSF parameters, β=2 (typical of LCB melts), and (which corresponds to a maximum stretch of molecular chains by a factor of 15). By extruding LCB-PP, a refining effect is observed similar to the refining effects seen in low density polyethylene (LDPE), which reduces the steady-state elongational viscosity and reduces to 121. A second-order mixing rule for the fractional relaxation moduli, g _i , was found to show good agreement with the linear-viscoelastic data of the blends. To simulate the elongational viscosities of the L-PP/LCB-PP blends, a similar second-order mixing rule was used for the MSF parameter, β, while a first-order mixing rule was found to be appropriate for . This allows for a quantitative prediction of the time-dependent elongational viscosities of all L-PP/LCB-PP blends on the basis of the linear and nonlinear parameters of the mixing components L-PP and LCB-PP only. Comparison between the steady-state elongational viscosities as obtained from creep experiments shows good agreement with predictions.     

Homotopy analysis method for multiple solutions of the fractional Sturm-Liouville problems

In this paper, Homotopy Analysis Method (HAM) is applied to numerically approximate the eigenvalues of the fractional Sturm-Liouville problems. The eigenvalues are not unique. These multiple solutions, i.e., eigenvalues, can be calculated by starting the HAM algorithm with one and the same initial guess and linear operator L\mathcal{L}. It can be seen in this paper that the auxiliary parameter (^h/_2p),\hbar, which controls the convergence of the HAM approximate series solutions, has another important application. This important application is predicting and calculating multiple solutions.     

Certain strict topologies on the space of regular Borel measures on locally compact groups

Let G   denote a locally compact Hausdorff group and M(G)$M(G)$ be the space of all bounded complex-valued regular Borel measures on G  . In this paper, we define two strict topologies on M(G)$M(G)$ and study various properties of these topologies such as metrizability, barrelledness and completeness. We also determine the dual space of M(G)$M(G)$ and consider various continuity properties for the convolution product on M(G)$M(G)$ under these topologies.     

Antiferromagnetic half-metallicity of transition metal nitrides under volume expansion

The transition metal pnictides ABX₂ have been recently proposed as half-metallic fully compensated ferrimagnets, also briefly referred to as half-metallic “antiferromagnets” [N. Long, M.Ogura, H. Akai, J. Phys.: Condens. Matter 21, 064241 (2009)]. In this work we carry out a systematic study of the more promising cases of the transition metal nitrides MnCoN₂ and NiCrN₂ on the basis of density functional theory in the framework of full-potential linearized augmented plane wave method. The electronic structures and the magnetic properties of the above hypothetical compounds in Zinc-blende-type, NaCl-type, and Wurtzite-type structure are calculated within generalized gradient approximation. The results reveal that, although these compounds are metallic in their bulk equilibrium in all three structures, they exhibit antiferromagnetic half-metallicity under negative stress or volume expansion in a limited range of lattice parameters, which is significantly larger than the equilibrium values. This suggests that a situation in which half-metallicity may arise, is when these compounds are coated on semiconducting layers of larger lattice constant.     

A presentation for reduced extended affine weyl groups

In 1985 K. Saito [Sal] introduced the concept of an extended affine Weyl group (EAWG), the Weyl group of an extended affine root system (EARS). In [A2, Section 5J, we gave a presentation called “a presentation by conjugation” for the class of EAWGs of index zero, a subclass of EAWGs. In this paper we will give a presentation wh.ich we call a “generalized present.ation by conjugation” for the class of reduced EAWGs. If the extended affine Weyl group is of index zero this presentation reduces to “a presentation by conjugation”. Our main result states that when the nullity of the EARS is 2, these two presentations coincide that is, EAWGs of nullity 2 have “a presentation by conjugation”. In [ST] another presentation for EAWGs of nullity 2 is given.     

Evaluation of new 99mTc-labeled HYNIC-bombesin analogue for prostate cancer imaging

Journal of Radioanalytical and Nuclear Chemistry - In this study, we introduce a new 99mTc-radiolabeled bombesin derivative for imaging of prostate cancer (PC). We used 6-hydrazinonicotinamide...     

Lectin-based electrophoretic analysis of the expression of the 35 kDa inter-alpha-trypsin inhibitor heavy chain H4 fragment in sera of patients with five different malignancies

A 35 kDa glycoprotein whose abundance was previously demonstrated to be enhanced in sera of patients with endometrial adenocarcinoma (n = 12), was isolated from pooled sera of three of the cancer patients using champedak galactose-binding lectin affinity chromatography in the present study. Subjecting it to 2-DE and MS/MS, the glycoprotein was identified as the O-glycosylated fragment of inter-alpha-trypsin inhibitor heavy chain H4 (ITIH4). When compared to control sera (n = 17), expression of the 35 kDa ITIH4 cleavage fragment was demonstrated to be significantly enhanced in sera of patients with breast carcinoma (n = 10), epithelial ovarian carcinoma (n = 10), and germ cell ovarian carcinoma (n = 10) but not in patients with nasopharyngeal carcinoma (n = 13) and osteosarcoma (n = 7). The lectin-based electrophoretic bioanalytical method adopted in the present study may be used to assess the physiological relevance of ITIH4 fragmentation and its correlation with different malignancies, their stages and progression.     

Adsorption kinetics at the solid/solution interface: statistical rate theory at initial times of adsorption and close to equilibrium

The kinetics of solute adsorption at the solid/solution interface has been studied by statistical rate theory (SRT) at two limiting conditions, one at initial times of adsorption and the other close to equilibrium. A new kinetic equation has been derived for initial times of adsorption on the basis of SRT. For the first time a theoretical interpretation based on SRT has been provided for the modified pseudo-first-order (MPFO) kinetic equation which was proposed empirically by Yang and Al-Duri. It has been shown that the MPFO kinetic equation can be derived from the SRT equation when the system is close to equilibrium. On the basis of numerically generated points ( t, q) by the SRT equation, it has been shown that we can apply the new equation for initial times of adsorption in a larger time range in comparison to the previous q vs radical t linear equation. Also by numerical analysis of the generated kinetic data points, it is shown that application of the MPFO equation for modeling of whole kinetic data causes a large error for the data at initial times of adsorption. The results of numerical analysis are in perfect agreement with our theoretical derivation of the MPFO kinetic equation from the SRT equation. Finally, the results of the present theoretical study were confirmed by analysis of an experimental system.