Summary.
The functions
are
refinable if they are
combinations of the rescaled and translated functions
.
This is very common in scientific computing on a regular mesh.
The space of approximating functions with meshwidth
is a
subspace of with meshwidth
.
These refinable spaces have refinable basis functions.
The accuracy of the computations
depends on , the
order of approximation, which is determined by the degree of
polynomials
that lie in .
Most refinable functions (such as scaling functions in the theory
of wavelets) have no simple formulas.
The functions
are known only through the coefficients
in the refinement equation – scalars in the traditional case,
matrices for multiwavelets.
The scalar "sum rules" that determine
are well known.
We find the conditions on the matrices
that
yield approximation of order
from .
These are equivalent to the Strang–Fix conditions on the Fourier
transforms
, but for refinable
functions they can be explicitly verified from
the .
Received
August 31, 1994 / Revised version received May 2, 1995 相似文献
The syntheses, structure solutions, and physicochemical and catalytic characterizations of the novel zeolites SSZ-53 and SSZ-59 are described. SSZ-53 and SSZ-59 were synthesized under hydrothermal conditions with the [1-(4-fluorophenyl)cyclopentylmethyl]trimethyl ammonium cation and 1-[1-(4-chlorophenyl)cyclopentylmethyl]-1-methyl azocanium cation, respectively, as structure-directing agents. The framework topology of SSZ-53 was solved with the FOCUS method, and the structure of SSZ-59 was determined by model building. Rietveld refinement of synchrotron X-ray powder diffraction data confirms each proposed model. SSZ-53 and SSZ-59 each possess a one-dimensional channel system delimited by 14-membered rings. Results from transmission electron microscopy, electron diffraction, catalytic experiments (spaciousness index and constraint index tests), and argon and hydrocarbon adsorption experiments are consistent with the proposed structures. 相似文献
Data are presented on the time evolution of particle-size distributions (PSDs) in seeded and ab initio styrene emulsion polymerization systems. Initiation was by chemical reagent (potassium persulfate) or γ-radiation. The unswollen PSDs at various times during interval II of the polymerization were obtained by direct measurement of calibrated electron micrographs. Experimental results were fitted with the equations that describe the time evolution of an initial PSD. Analytic solutions to these equations that allow for entry, exit, and propagation of free radicals were obtained. The values of the rate coefficients for these processes used to fit the experimental data were in excellent agreement with those obtained from dilatometric kinetics experiments. 相似文献
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The mass spectrometric study of acetylenic dialkylphosphonates (I) and of γ, δ-éthylenic-β-ketophosphonates (II) is characterised by rearrangement processes of the phosphorylated group and cleavage of the phosphorus-carbon bond. The fragmentation patterns of compounds II were identical to those found for I by loss of water. 相似文献