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1.
Let H x a regular Hausdorff method and P(w)=∑ ak wk a power series with positive radius of convergence. A theorem of Okada states that P(w) is summable (H x ) for w in a certain starshaped region G(H x ,P). We call G=G(H x ,P) the exact region of summability for P if summability cannot hold for any w \( \in \bar G\) Okada's theorem is said to be sharp for Hx if G(Hx,P) is the exact region of summability for any P. Three items are treated: 1. Criteria for Okada's theorem to be sharp are given in terms of the distribution function X (t) and the Mellin transform \(D(z) = \int\limits_0^1 {t^z d\chi (t)} \) . 2. When is Okada's theorem sharp for product methods? 3. Special classes of functions P(w) are indicated such that G(Hx, P) is the exact region of summability for any Hx. We use the notations of “Hausdorff-Summability of Power Series I” referred as “I”.  相似文献   
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3.
A finite-difference approach has been developed for precisely determining diffusion coefficient and T1 relaxation time in fluid samples analyzed by magnetization-grating rotating-frame imaging (MAGROFI) with either a surface coil or a toroid cavity detector (TCD). This approach avoids shortcomings of phenomenologically based approximations, such as neglect of sample geometries with singularities at the confines of the sample volume, and accounts for the diffusive edge enhancement observed in fluid imaging. Error limits are discussed. The new method has been applied to the determination of the self-diffusion coefficient for MAGROFI experiments using TCDs filled with acetone.  相似文献   
4.
The effect of the “stir” of a structure (small deviations from strict periodicity) on effective conductivity is considered. For determinate and random deviations, concentration and field dependences of the effective conductivity are found. Numerical experiments with determinate deviations are carried out for the cases of linear (with respect to the field) inclusions embedded in both a linear and nonlinear matrix. The numerical results are compared with the effective conductivity calculated analytically.  相似文献   
5.
In this paper we are concerned with the summability of the geometric series by matrix methods. We prove the following theorem: Suppose Mo:={z:|z|<1}, M1, M2, is a collection of countably many Lebesgue measureable, disjoint sets. For k=1,2, let fk be a prescribed function, analytic on . Then there exists a triangular matrix , such that the V-transform {n(z)} of the geometric series has the following properties: {n(z)} converges compactly to on Mo; for k=1,2, there are sets Bk, such that has Lebesgue-measure zero and n(z)fk(z) for zBk; if there is a set B*, such that B*M* has Lebesgue-measure zero and {n(z)} diverges for zB*.  相似文献   
6.
The Komlós-Révész theorem states: For r.v.s.X n with X n 1M there exists a subsequenceX k n and a r.v.X with X1M such that
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7.
Fast chemical-shiftT 1 imaging in toroid cavity cells (TCCs) is introduced and applications to diagnostic ultrasound gel and skin-care ointment are presented. TCCs are an advancement over previously used toroid cavity detectors because they combine resonator and sample container into one part. Additionally, they are removable from the top of the probe and facilitate convenient probe and sample handling. Radially resolvedT 1 relaxation times in TCCs are obtained through combination of SR (saturation recovery) experiments with the RIPT (rapid imaging with a pulse train) technique. Because of the strong radialB 1 gradient in TCCs, only pulse-burst saturation was found satisfactory to generate the most even starting condition for SR experiments. Because RIPT does not resolve chemical-shift information, magnetization andT 1 profiles of individual components in mixed samples are monitored by double-transient experiments with selective on-resonance saturation, which is achieved by converging trains of sinc pulses. The new techniques were applied to cellulose hydrogel and oil-in-water emulsion both exposed to significant shear stress deformation during the charging of the TCC. In both cases,T 1 profiles as a function of time reveal structural recovery (thixotropy) that slowly progresses from one or more sample interfaces into the bulk.  相似文献   
8.
Рассматриваются слу чайная величина \(\mathfrak{X} = (X_n (\omega ))\) , удовлетворяющая усл овиюE(X n 4 )≦M, и соответствующ ий случайный степенн ой ряд \(f_x (z;\omega ) = \mathop \sum \limits_{n = 0}^\infty a_n X_n (\omega )z^n\) . Устанавливаются тео ремы непродолжимост и почти наверное:
  1. дляf x при условиях с лабой мультипликати вности на \(\mathfrak{X}\) ,
  2. для \(f_{\tilde x}\) , где \(\mathop \mathfrak{X}\limits^ \sim = (\mathop X\limits^ \sim _n )\) есть подп оследовательность в \(\mathfrak{X}\) ,
  3. для по крайней мере од ного из рядовf x′ илиf x″ , где \(\mathfrak{X}'\) и \(\mathfrak{X}''\) — некоторые п ерестановки \(\mathfrak{X}\) , выбираемые универс ально, т. е. независимо от коэффициентовa n .
  相似文献   
9.
The molecular structure and conformational properties of O=C(N=S(O)F2)2 (carbonylbisimidosulfuryl fluoride) were determined by gas electron diffraction (GED) and quantumchemical calculations (HF/3-21G* and B3LYP/6-31G*). The analysis of the GED intensities resulted in a mixture of 76(12)% synsyn and 24(12)% synanti conformer (ΔH0=H0(synanti)−H0(synsyn)=1.11(32) kcal mol−1) which is in agreement with the interpretation of the IR spectra (68(5)% synsyn and 32(5)% synanti, ΔH0=0.87(11) kcal mol−1). syn and anti describe the orientation of the S=N bonds relative to the C=O bond. In both conformers the S=O bonds of the two N=S(O)F2 groups are trans to the C–N bonds. According to the theoretical calculations, structures with cis orientation of an S=O bond with respect to a C–N bond do not correspond to minima on the energy hyperface. The HF/3-21G* approximation predicts preference of the synanti structure (ΔE=−0.11 kcal mol−1) and the B3LYP/6-31G* method results in an energy difference (ΔE=1.85 kcal mol−1) which is slightly larger than the experimental values. The following geometric parameters for the O=C(N=S)2 skeleton were derived (ra values with 3σ uncertainties): C=O 1.193 (9) Å, C–N 1.365 (9) Å, S=N 1.466 (5) Å, O=C–N 125.1 (6)° and C–N=S 125.3 (10)°. The geometric parameters are reproduced satisfactorily by the HF/3-21G* approximation, except for the C–N=S angle which is too large by ca. 6°. The B3LYP method predicts all bonds to be too long by 0.02–0.05 Å and the C–N=S angle to be too small by ca. 4°.  相似文献   
10.
По определению после довательность {μ n пр инадлежит классуG s , если звезда М иттагЛеффлера произвольного степе нного ряда (1) $$\mathop \sum \limits_0^\infty a_n z^n , \mathop {lim sup}\limits_{n \to \infty } \left| {a_n } \right|^{1/n}< \infty $$ , совпадает со звёздам и Миттаг-Леффлера сте пенных рядов $$\mathop \sum \limits_0^\infty \mu _n a_n z^n ,\mathop \sum \limits_0^\infty \mu _n^{ - 1} a_n z^n $$ . В работе установлены следующие утвержден ия Теорема 1.Для произво льной последователь ности ? n с условиями $$0< \varphi _n< 1,\mathop {lim}\limits_{n \to \infty } \varphi _n = 0,\mathop {lim}\limits_{n \to \infty } \varphi _n^{1/n} = 1$$ существует неубываю щая функция χ(t) такая, ч то моменты \(\mu _n = \int\limits_0^1 {t^n d\chi (t)} \) удовлетворяют условию 0<μnn звезда М иттаг-Леффлера любог о ряда (1) совпадает со звездой МиттагЛеффлера степенных рядов . Теорема 2. Для произвол ьной неотрицательно й последовательности {аn} с условием {a n } и для любой последов ательности {?n} для к оторой 0n<1, \(\mathop {\lim }\limits_{n \to \infty } \varepsilon _n = 0\) сущест вуютπ={π n }∈G s и последовательнос ть {пi} такие, что anμn≦1 (n≧n0), \(a_{n_i } \mu _{\mu _i } \geqq exp( - \varepsilon _{n_i } )\) (i=1, 2, ...) и при эmom звезда Миттаг-Леффлера ряда (1) совпа дает со звездой Миттаг- Леффлера степенных р ядов .  相似文献   
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