Summary The finite element method with non-uniform mesh sizes is employed to approximately solve Helmholtz type equations in unbounded domains. The given problem on an unbounded domain is replaced by an approximate problem on a bounded domain with the radiation condition replaced by an approximate radiation boundary condition on the artificial boundary. This approximate problem is then solved using the finite element method with the mesh graded systematically in such a way that the element mesh sizes are increased as the distance from the origin increases. This results in a great reduction in the number of equations to be solved. It is proved that optimal error estimates hold inL2,H1 andL, provided that certain relationships hold between the frequency, mesh size and outer radius. 相似文献
A necessary and sufficient condition for the group of isomorphisms involved in a factorization of a complete graph into isomorphic factors is established. 相似文献
We consider the following problem: Let (G, +) be an abelian group,B a complex Banach space,a, bB,b0,M a positive integer; find all functionsf:GB such that for every (x, y) G ×G the Cauchy differencef(x+y)–f(x)–f(y) belongs to the set {a, a+b, a+2b, ...,a+Mb}. We prove that all solutions of the above problem can be obtained by means of the injective homomorphisms fromG/H intoR/Z, whereH is a suitable proper subgroup ofG. 相似文献
We report on the operation of a thallium photodissociation laser with an active medium in the form of a thin layer on a quartz wall. Laser emission has been obtained with layer thicknesses below 100 m. This gas laser seems to be feasible with an active volume as small as 10–1 to 10–2 mm3. 相似文献
The photochemistry of some members of the two series of γ-phenyl substituted acyclic β, γ-unsaturated ketones 1 and 2 upon direct irradiation with γ 310nm has been investigated, viz 1c–1h and 2b+2c.The alkyl substituted (E)-5-phenyl-4-penten-2-ones 1c–1h yield the corresponding 1,3-acyl shift products and (Z)-isomers, and 1g and 1h in addition two decarbonylated products. 2b only yields the (Z)-isomer and some benzaldehyde, but 2c yields the 1,3-acyl shift product, the ODPM product, three hydrocarbons formed by disproportionation of the allyl radical, and some benzaldehyde. The β-phenyl β, γ-UK 3a proved to be photostable. The 1,3-acyl shift products of 1c–1h result mainly from the singlet excited state in a cage radical process. The exclusive formation of the (E)-configuration of the 1,3-acyl shift product is explained in terms of conformational preference of the intermediate allyl radical. It is proposed that the formation of the (Z)-isomer proceeds from 1T(π -π*) which is populated according to . Evidence is presented which supports the proposed mechanism.The β,γ-UK 2b containing a benzoyl moiety leads to a higher degree of (E)-(Z) isomerization than the corresponding 1d which has an acetyl moiety.The triplet energies of (E)- and (Z)-1h are 56 and ca 70 kcal/mol respectively. 相似文献
The thermal behaviour of complexes [Li+-EC](AlH4)– withEC=12-C-4, 15-C-5, DC 18-C-6 (cis-anti-cis andcis-syn-cis isomers) was investigated by Differential Scanning Calorimetry (DSC). These complexes were prepared as solids from benzene solutions. Pure EC and several solvated species [Li+-EC](AlH4)–·nC6H6 (EC=15-C-5, DC 18-C-6syn) were also studied. DSC has revealed various phenomena. Solid-solid transitions were observed before melting for [Li+-EC](AlH4)– withEC=12-C-4 and 15-C-5. They are probably explained by small molecular modifications strongly dependent on the thermal history of the sample. A glass-transition was found for the pure crown-ether DC 18-C-6anti, the complex [Li+-EC](A1H4)– withEC=DC-18-C-6anti and the two solvates mentioned above. 相似文献