• Title/Summary/Keyword: Odd number

Search Result 186, Processing Time 0.019 seconds

A comparative study of three collocation point methods for odd order stochastic response surface method

  • Li, Dian-Qing;Jiang, Shui-Hua;Cheng, Yong-Gang;Zhou, Chuang-Bing
    • Structural Engineering and Mechanics
    • /
    • v.45 no.5
    • /
    • pp.595-611
    • /
    • 2013
  • This paper aims to compare three collocation point methods associated with the odd order stochastic response surface method (SRSM) in a systematical and quantitative way. The SRSM with the Hermite polynomial chaos is briefly introduced first. Then, three collocation point methods, namely the point method, the root method and the without origin method underlying the odd order SRSMs are highlighted. Three examples are presented to demonstrate the accuracy and efficiency of the three methods. The results indicate that the condition that the Hermite polynomial information matrix evaluated at the collocation points has a full rank should be satisfied to yield reliability results with a sufficient accuracy. The point method and the without origin method are much more efficient than the root method, especially for the reliability problems involving a large number of random variables or requiring complex finite element analysis. The without origin method can also produce sufficiently accurate reliability results in comparison with the point and root methods. Therefore, the origin often used as a collocation point is not absolutely necessary. The odd order SRSMs with the point method and the without origin method are recommended for the reliability analysis due to their computational accuracy and efficiency. The order of SRSM has a significant influence on the results associated with the three collocation point methods. For normal random variables, the SRSM with an order equaling or exceeding the order of a performance function can produce reliability results with a sufficient accuracy. The order of SRSM should significantly exceed the order of the performance function involving strongly non-normal random variables.

ON THE MINKOWSKI UNITS OF 2-PERIODIC KNOTS

  • Lee, Sang-Youl
    • Bulletin of the Korean Mathematical Society
    • /
    • v.38 no.3
    • /
    • pp.475-486
    • /
    • 2001
  • In this paper we give a relationship among the Minkowski units, for all odd prime number including $\infty$, of 2-periodic knot is $S^3$, its factor knot, and the 2-component link consisting of the factor knot and the set of fixed points of the periodic action.

  • PDF

Electronic Absorption and Raman Spectroscopic Studies of ${\alpha},{\omega}$-Diphenylpolyenyl Anions with Odd Number of Polyene Carbons

  • Kim, Jin Yeol;Kim, Eung Ryeol;Ju, Jae Beom
    • Bulletin of the Korean Chemical Society
    • /
    • v.22 no.8
    • /
    • pp.837-841
    • /
    • 2001
  • The electronic absorption and Raman spectra of $\alpha\omega-diphenylpolyenyl$, anions Ph(CH)nPh- (DPn- , n = 3, 5, 7, 9, and 13), with odd number of carbons at the polyene part, have been studied in the tetrahydrofuran (THF) solutions and in their solid film states, respectively. In the case of Raman spectra for DPn- , the frequencies and relative intensities of some Raman peaks regularly change with the increase of polyene chain length. The spectral patterns of anions (DPn- ) are very similar with those of radical anion (DPn${\cdot}$- ). However, the C=C stretching peaks of DPn- anions are observed in the 25-35 cm-1 higher frequency region than those of DPn${\cdot}$- radical anions. In the case of long chain models such as DP9- and DP13- , the C=C stretching peaks are observed in even higher frequency region than those of the corresponding neutral polyenes such as DP8, DP10, and DP12. The Raman patterns of DPn- anions in the THF solutions are similar with those in their solid film states. On the other hand, their electronic absorption spectra show a considerable difference each other. The n- ${\pi}*$ electronic absorption bands of DPn- anions in the THF solutions have been observed in the 0.27-0.39 eV lower energy region than those in their solid film states due to the solvent effects on polyene anions.

PAIR DIFFERENCE CORDIAL LABELING OF PETERSEN GRAPHS P(n, k)

  • R. PONRAJ;A. GAYATHRI;S. SOMASUNDARAM
    • Journal of Applied and Pure Mathematics
    • /
    • v.5 no.1_2
    • /
    • pp.41-53
    • /
    • 2023
  • Let G = (V, E) be a (p, q) graph. Define $${\rho}=\{{\frac{2}{p}},\;{\text{{\qquad} if p is even}}\\{\frac{2}{p-1}},\;{{\text{if p is odd}}$$ and L = {±1, ±2, ±3, … , ±ρ} called the set of labels. Consider a mapping f : V ⟶ L by assigning different labels in L to the different elements of V when p is even and different labels in L to p-1 elements of V and repeating a label for the remaining one vertex when p is odd.The labeling as defined above is said to be a pair difference cordial labeling if for each edge uv of G there exists a labeling |f(u) - f(v)| such that ${\mid}{\Delta}_{f_1}-{\Delta}_{f^c_1}{\mid}{\leq}1$, where ${\Delta}_{f_1}$ and ${\Delta}_{f^c_1}$ respectively denote the number of edges labeled with 1 and number of edges not labeled with 1. A graph G for which there exists a pair difference cordial labeling is called a pair difference cordial graph. In this paper we investigate pair difference cordial labeling behaviour of Petersen graphs P(n, k) like P(n, 2), P(n, 3), P(n, 4).

PAIR DIFFERENCE CORDIALITY OF CERTAIN SUBDIVISION GRAPHS

  • R. PONRAJ;A. GAYATHRI;S. SOMASUNDARAM
    • Journal of applied mathematics & informatics
    • /
    • v.42 no.1
    • /
    • pp.1-14
    • /
    • 2024
  • Let G = (V, E) be a (p, q) graph. Define $$\begin{cases}\frac{p}{2},\:if\:p\:is\:even\\\frac{p-1}{2},\:if\:p\:is\:odd\end{cases}$$ and L = {±1, ±2, ±3, ···, ±ρ} called the set of labels. Consider a mapping f : V → L by assigning different labels in L to the different elements of V when p is even and different labels in L to p - 1 elements of V and repeating a label for the remaining one vertex when p is odd.The labeling as defined above is said to be a pair difference cordial labeling if for each edge uv of G there exists a labeling |f(u) - f(v)| such that |Δf1 - Δfc1| ≤ 1, where Δf1 and Δfc1 respectively denote the number of edges labeled with 1 and number of edges not labeled with 1. A graph G for which there exists a pair difference cordial labeling is called a pair difference cordial graph. In this paper we investigate the pair difference cordial labeling behavior of subdivision of some graphs.

COHOMOLOGY GROUPS OF CIRCULAR UNITS

  • Kim, Jae-Moon;Oh, Seung-Ik
    • Journal of the Korean Mathematical Society
    • /
    • v.38 no.3
    • /
    • pp.623-631
    • /
    • 2001
  • Let $\kappa$ be a real abelian field of conductor f and $\kappa$(sub)$\infty$ = ∪(sub)n$\geq$0$\kappa$(sub)n be its Z(sub)p-extension for an odd prime p such that płf$\phi$(f). he aim of this paper is ot compute the cohomology groups of circular units. For m>n$\geq$0, let G(sub)m,n be the Galois group Gal($\kappa$(sub)m/$\kappa$(sub)n) and C(sub)m be the group of circular units of $\kappa$(sub)m. Let l be the number of prime ideals of $\kappa$ above p. Then, for mm>n$\geq$0, we have (1) C(sub)m(sup)G(sub)m,n = C(sub)n, (2) H(sup)i(G(sub)m,n, C(sub)m) = (Z/p(sup)m-n Z)(sup)l-1 if i is even, (3) H(sup)i(G(sub)m,n, C(sub)m) = (Z/P(sup)m-n Z)(sup l) if i is odd (※Equations, See Full-text).

  • PDF

TANGENTIAL REPRESENTATIONS AT ISOLATED FIXED POINTS OF ODD-DIMENSIONAL G-MANIFOLDS

  • Komiya, Katsuhiro
    • Bulletin of the Korean Mathematical Society
    • /
    • v.45 no.1
    • /
    • pp.33-37
    • /
    • 2008
  • Let G be a compact abelian Lie group, and M an odd-dimensional closed smooth G-manifold. If the fixed point set $M^G\neq\emptyset$ and dim $M^G=0$, then G has a subgroup H with $G/H{\cong}\mathbb{Z}_2$, the cyclic group of order 2. The tangential representation $\tau_x$(M) of G at $x{\in}M^G$ is also regarded as a representation of H by restricted action. We show that the number of fixed points is even, and that the tangential representations at fixed points are pairwise isomorphic as representations of H.