Operator trigonometry of Hotelling correlation, Frobenius condition, Penrose twistor

Three new applications of the author’s operator trigonometry are presented. These take place in three diverse mathematical domains: matrix statistics, numerical analysis, and theoretical physics. The goal is to continue to develop and expand the scope of the operator trigonometry.     

Compact operators which factor through subspaces of lp

Let 1 ≤ p ≤ ∞. A subset K of a Banach space X is said to be relatively p ‐compact if there is an 〈x_n 〉 ∈ l^s _p (X) such that for every k ∈ K there is an 〈α_n 〉 ∈ l_{p ′} such that k = σ^∞_n=1 α_n x_n . A linear operator T: X → Y is said to be p ‐compact if T (Ball (X)) is relatively p ‐compact in Y. The set of all p ‐compact operators K_p (X, Y) from X to Y is a Banach space with a suitable factorization norm κ_p and (K_p , κ_p ) is a Banach operator ideal. In this paper we investigate the dual operator ideal (K^d _p , κ^d _p ). It is shown that κ^d _p (T) = π_p (T) for all T ∈ B (X, Y) if either X or Y is finite‐dimensional. As a consequence it is proved that the adjoint ideal of K^d _p is I_{p ′}, the ideal of p ′‐integral operators. Further, a composition/decomposition theorem K^d _p = Π_p K is proved which also yields that (Π^min _p )^inj = K^d _p . Finally, we discuss the density of finite rank operators in K^d _p and give some examples for different values of p in this respect. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

混合型表达式及其应用

混合型表达式的定义及其应用     

Binding of a surfactant counterion to low-charge-density poly(acrylic acid) and poly(methacrylic acid)

The binding of a cationic surfactant, dodecylpyridinium (C12Py) chloride, with a low-charge-density poly (methacrylic acid) (PMA) was investigated in buffer solutions under the condition of constant pH. The binding isotherms with PMA consisted of two and three steps at a pH lower and higher than 3.2, respectively. Bindings in the first step were independent of pH and this step was considered to correspond to the solubilization of the hydrocarbon chains of C12Py into the nonpolar region of the compact form of PMA. This is the indication of the compact form from the binding isotherm. At pH higher than 3.2, the second step was discriminated and it depended on the pH. In the third step, a sharp rise in the degree of binding (β) was observed accompanying the solubilization of the precipitates of the PMA–C12Py complex. The binding with poly(acrylic acid) (PAA) and PMA in conventional unbuffered NaCl solutions was also examined and the pH profile of the solution during the binding process was determined. In the case of unbuffered NaCl solutions, the binding with PAA took place cooperatively at the critical association concentration (cac). The binding isotherm consisted of two steps and the pH decreased with the increase in β. The binding isotherm of PMA, on the other hand, consisted of three steps: the pH decreased slightly in the first step and considerably in the second step with the increase in β but it increased with β in the third step, exhibiting a pH minimum around 3.2. The binding in the first step coincided with that obtained in the buffered solutions. Linear relationships between β and the pH were found for both polymers. In the case of PMA, no cac was observed in both buffered and unbuffered NaCl solutions. Received: 24 January 2001 Accepted: 23 May 2001     

Error analysis of the numerical solution of split differential equations

The operator splitting method is a widely used approach for solving partial differential equations describing physical processes. Its application usually requires the use of certain numerical methods in order to solve the different split sub-problems. The error analysis of such a numerical approach is a complex task. In the present paper we show that an interaction error appears in the numerical solution when an operator splitting procedure is applied together with a lower-order numerical method. The effect of the interaction error is investigated by an analytical study and by numerical experiments made for a test problem.     

Convergence Results of the ERM Method for Nonlinear Stochastic Variational Inequality Problems

This paper considers the expected residual minimization (ERM) method proposed by Luo and Lin (J. Optim. Theory Appl. 140:103–116, 2009) for a class of stochastic variational inequality problems. Different from the work mentioned above, the function involved is assumed to be nonlinear in this paper. We first consider a quasi-Monte Carlo method for the case where the underlying sample space is compact and show that the ERM method is convergent under very mild conditions. Then, we suggest a compact approximation approach for the case where the sample space is noncompact. This work was supported in part by Project 10771025 supported by NSFC and SRFDP 20070141063 of China.     

无限秩仿射李代数的紧致实形

给出了无限秩仿射李代数的实形和某种类型的紧效实形的定义，并证明了这种紧致实形在自同构下的唯一性.     

Single machine unbounded parallel-batch scheduling with forbidden intervals

In this paper we consider the single machine parallel-batch scheduling with forbidden intervals. There are some forbidden intervals in which the machine cannot be available. The jobs are processed in batches form in the remaining free time-slots without preemption, where the processing time of a batch is defined to be the maximum processing time of the jobs in this batch. We show that, when the objective is bottleneck form, maximum lateness, or makespan with release dates of jobs, the considered problem can be solved in polynomial time.     

空间中混合均衡问题和相对拟非扩张半群公共解的一种逼近方法

在Banach空间中,通过广义投影算子,建立一种求解混合均衡问题和相对拟非扩张半群的公共解的迭代算法,并证明迭代序列的强收敛性.     

Determination of Hg and Pb in compact fluorescent lamp by slurry sampling inductively coupled plasma optical emission spectrometry

Mercury and lead were determined in an extraction solution applied to compact fluorescent lamps by axial view inductively coupled plasma optical emission spectrometry (ICP OES). The solution contained 50% v/v HNO₃ and 10% v/v H₂O₂. The compact fluorescent lamps were treated by removing the socket and breaking the rest of the lamp inside the solution, followed by placing the mixture in an ultrasonic bath for 1 h. The mixture was filtrated in a coarse paper filter and the resulting extraction slurry was analyzed. The determination of Pb in the slurry required calibration by the analyte addition technique, while for Hg, external calibration was adequate. The quantification limits (10 s, n = 7), for Hg (194.164 nm) and Pb (220.353 nm) were, respectively, 10 and 30 µg per lamp. Analysis of spiked samples demonstrated reasonable accuracy of the method, with recoveries in the range from 99 to 120% for Hg and from 91 to 107% for Pb. Fifteen analyzed samples showed Hg masses per lamp in the range from 1.6 to 27 mg, and six samples were above the limit allowed by the European Community that is 5 mg per compact lamp. The values for Pb were between 0.07 and 0.75 mg per lamp. By filtrating the slurry in a membrane filter, and analyzing the resulting solution, it was found that all Hg was extracted to the liquid phase of the slurry, while a fraction of about 40% m/v of Pb is retained in the solid particles. The lamp cover glass, after extraction of the phosphor layer, was also analyzed for Hg and Pb. The concentration of Hg in the glass is quite low; however, the Pb content is high.