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1.
Louis Block James Keesling Shihai Li Kevin Peterson 《Journal of statistical physics》1989,55(5-6):929-939
A new algorithm is presented for computing the topological entropy of a unimodal map of the interval. The accuracy of the algorithm is discussed and some graphs of the topological entropy which are obtained using the algorithm are displayed. 相似文献
2.
Backman Ulrika Jokiniemi Jorma K. Auvinen Ari Lehtinen Kari E.J. 《Journal of nanoparticle research》2002,4(4):325-335
We have prepared spherical non-agglomerated silver nanoparticles by an evaporation–condensation–dilution/cooling technique. Silver was evaporated from a crucible in a tubular flow reactor. A porous tube diluter was used to quench the carrier gas at the outlet of the reactor to enhance the formation of small particles and to suppress agglomeration and other particle growth mechanisms. The number size distribution of the prepared particles was measured with a differential mobility analyser–condensation nucleus counter combination and the size and the shape of the particles were analysed with transmission electron microscope. The system was modelled using a sectional aerosol dynamics computer code to estimate the importance of different aerosol processes. In all conditions the particles obtained were non-agglomerated and spherical. The mean particle diameter varied from 4 to 10-nm depending on boundary conditions. From the modelling studies it can be concluded that the nucleation rate is the most important parameter controlling the final particle size. 相似文献
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4.
Gary L. Peterson 《Monatshefte für Mathematik》1996,121(3):275-290
AnI-E group is a group in which the endomorphism near-ring generated by the group's inner automorphisms equals the endomorphism near-ring generated by its endomorphisms. In this paper we shall completely determine the finite groups that are semidirect products of cyclic groups and areI-E groups. 相似文献
5.
John R. Peterson Tamara J. Winter Hoang D. Do Robin D. Rogers 《Journal of chemical crystallography》1989,19(1):135-145
Structural and conformational information obtained from the crystal structure and solution1H nmr investigations of the title compound are compared. The 4-aryltetralone, C24H24O10, crystallizes as a chloroform solvate in the monoclinic space group, P21/n, witha=12.519(4),b=17.938(6),c=12.534(9)Å,=111.90(5)°, and Dcalc=1.51 g cm–3 forZ=4. The data for this compound were collected at –150°C. Least-squares refinement of 2796 observed [F
o5(F
o)] reflections led to the final agreement index ofR=0.062. A threefold static disorder was observed for one of the carboxyl groups. The second carboxyl group participates in an intramolecular hydrogen bond and is thus ordered. The1H nmr spectrum revealed the title compound to exist as a keto-enol tautomeric mixture in solution. Vicinal hydrogen coupling constant analysis proved reliable in ascertaining B-ring stereochemistry of 2,3-disubstituted-4-aryltetralones. 相似文献
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8.
Bortoletto D Goldberg M Horwitz N Mestayer MD Moneti GC Sharma V Shipsey IP Skwarnicki T Csorna SE Letson T Brock IC Ferguson T Artuso M Bebek C Berkelman K Blucher E Byrd J Cassel DG Cheu E Coffman DM Crawford G DeSalvo R DeWire JW Drell PS Ehrlich R Galik RS Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Kandaswamy J Kowalewski R Kreinick DL Kubota Y Lewis JD Mistry NB Mueller J Namjoshi R Nandi S Nordberg E O'Grady C Peterson D Pisharody M Riley D Sapper M Silverman A Stone S Worden H 《Physical review letters》1989,62(21):2436-2439
9.
Alam MS Katayama N Kim IJ Li WC Lou XC Sun CR Bortoletto D Goldberg M Horwitz N Mestayer MD Moneti GC Sharma V Shipsey IP Skwarnicki T Csorna SE Letson T Brock IC Ferguson T Artuso M Bebek C Berkelman K Blucher E Byrd J Cassel DG Cheu E Coffman DM Crawford G DeSalvo R DeWire JW Drell PS Ehrlich R Galik RS Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Kandaswamy J Kowalewski R Kreinick DL Kubota Y Lewis JD Mistry NB Mueller J Namjoshi R Nandi S Nordberg E O'Grady C Peterson D Pisharody M 《Physical review D: Particles and fields》1989,40(11):3790
10.
E. R. Peterson 《Research on Chemical Intermediates》1994,20(1):93-96
The chemical industry admits to minimal use of microwave power because of its high capital and operating costs relative to
steam, combustion, electrical, and other traditional sources of energy. Other valid historical and persistent reasons for
their lack of proper use include: a poor conceptual understanding of microwaves by chemical professionals, their unwillingness
to replace existing adequate methods with radically new technology, the infancy of the microwave industrial power supply,
and unfamiliarity of microwave power systems manufacturers with the chemical industry. In years past, the North American chemical
industry had few competitors and profits were generally large. Environmental regulations were few and product quality was
less a concern than production volume. The microwave power industry relied on the government and communications for lucrative
sales. Those days appear over.
Chemical manufacturers must probe every technology to achieve the edge necessary to stay competitive while meeting environmental
stewardship demands. Microwave power has always offered unique advantages in heating materials selectively and/or quickly
to high or preselected temperatures with fast control response. In the cases discussed in this paper, novel applications of
microwave power afford: faster production, a reduction in product contaminants, reduced downtime, reduced waste, product quality
improvements, and better pollution control. 相似文献