17 research outputs found

    S-band electron linac with beam energy of 30…100 MeV

    No full text
    The S-band electron linac has been designed at NSC KIPT to cover an energy range from 30 to 100 MeV. The linac consists of the injector based on evanescent oscillations and the two four-meter long piecewise homogeneous accelerating sections. Each section is supplied with RF power from the KIU-12AM klystron. Variation of mean energy of the beam over a wide range is produced by placing bunches out of the wave crest in the second accelerating section. The report presents layout of the linac as well as simulation results of self-consistent particle dynamics in the linac and its present status.Π›Ρ–Π½Ρ–ΠΉΠ½ΠΈΠΉ ΠΏΡ€ΠΈΡΠΊΠΎΡ€ΡŽΠ²Π°Ρ‡ Π΅Π»Π΅ΠΊΡ‚Ρ€ΠΎΠ½Ρ–Π² 10 см - Π΄Ρ–Π°ΠΏΠ°Π·ΠΎΠ½Ρƒ Π±ΡƒΠ»ΠΎ Ρ€ΠΎΠ·Ρ€ΠΎΠ±Π»Π΅Π½ΠΎ Π² ННЦ Π₯Π€Π’Π† Π· ΠΌΠ΅Ρ‚ΠΎΡŽ ΠΏΠ΅Ρ€Π΅ΠΊΡ€ΠΈΡ‚ΠΈ Π΄Ρ–Π°ΠΏΠ°Π·ΠΎΠ½ Π΅Π½Π΅Ρ€Π³Ρ–ΠΉ 30…100 MeΠ’. ΠŸΡ€ΠΈΡΠΊΠΎΡ€ΡŽΠ²Π°Ρ‡ ΡΠΊΠ»Π°Π΄Π°Ρ”Ρ‚ΡŒΡΡ Π· Ρ–Π½ΠΆΠ΅ΠΊΡ‚ΠΎΡ€Π°, основаного Π½Π° коливаннях, Ρ‰ΠΎ Π½Π΅ Ρ€ΠΎΠ·ΠΏΠΎΠ²ΡΡŽΠ΄ΠΆΡƒΡŽΡ‚ΡŒΡΡ, Ρ– Π΄Π²ΠΎΡ… ΡˆΠΌΠ°Ρ‚ΠΊΠΎΠ²ΠΎ-ΠΎΠ΄Π½ΠΎΡ€Ρ–Π΄Π½ΠΈΡ… Ρ‡ΠΎΡ‚ΠΈΡ€ΠΈΠΌΠ΅Ρ‚Ρ€ΠΎΠ²ΠΈΡ… ΠΏΡ€ΠΈΡΠΊΠΎΡ€ΡŽΠ²Π°Π»ΡŒΠ½ΠΈΡ… сСкцій. КоТна сСкція Π·Π°Π±Π΅Π·ΠΏΠ΅Ρ‡ΡƒΡ”Ρ‚ΡŒΡΡ НВЧ-ΠΏΠΎΡ‚ΡƒΠΆΠ½Ρ–ΡΡ‚ΡŽ Π²Ρ–Π΄ клістрона KΠ†Π£-12AM. Π—ΠΌΡ–Π½Π° ΡΠ΅Ρ€Π΅Π΄Π½ΡŒΠΎΡ— Π΅Π½Π΅Ρ€Π³Ρ–Ρ— ΠΏΡƒΡ‡ΠΊΠ° Π² ΡˆΠΈΡ€ΠΎΠΊΠΈΡ… ΠΌΠ΅ΠΆΠ°Ρ… Π·Π°Π±Π΅Π·ΠΏΠ΅Ρ‡ΡƒΡ”Ρ‚ΡŒΡΡ прискорСнням згустків Π½Π΅ Π½Π° Π³Ρ€Π΅Π±Π΅Π½Ρ– Ρ…Π²ΠΈΠ»Ρ– Π² Π΄Ρ€ΡƒΠ³Ρ–ΠΉ ΠΏΡ€ΠΈΡΠΊΠΎΡ€ΡŽΠ²Π°Π»ΡŒΠ½Ρ–ΠΉ сСкції. ΠŸΡ€Π΅Π΄ΡΡ‚Π°Π²Π»Π΅Π½ΠΎ структурну схСму ΠΏΡ€ΠΈΡΠΊΠΎΡ€ΡŽΠ²Π°Ρ‡Π°, Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚ΠΈ модСлювання Π΄ΠΈΠ½Π°ΠΌΡ–ΠΊΠΈ частинок Π² ΠΏΡ€ΠΈΡΠΊΠΎΡ€ΡŽΠ²Π°Ρ‡Ρ– Ρ– ΠΉΠΎΠ³ΠΎ ΠΏΠΎΡ‚ΠΎΡ‡Π½ΠΈΠΉ стан.Π›ΠΈΠ½Π΅ΠΉΠ½Ρ‹ΠΉ ΡƒΡΠΊΠΎΡ€ΠΈΡ‚Π΅Π»ΡŒ элСктронов 10 см - Π΄ΠΈΠ°ΠΏΠ°Π·ΠΎΠ½Π° Π±Ρ‹Π» Ρ€Π°Π·Ρ€Π°Π±ΠΎΡ‚Π°Π½ Π² ННЦ Π₯ЀВИ с Ρ†Π΅Π»ΡŒΡŽ пСрСкрытия Π΄ΠΈΠ°ΠΏΠ°Π·ΠΎΠ½Π° энСргий 30…100 MэВ. Π£ΡΠΊΠΎΡ€ΠΈΡ‚Π΅Π»ΡŒ состоит ΠΈΠ· ΠΈΠ½ΠΆΠ΅ΠΊΡ‚ΠΎΡ€Π°, основанного Π½Π° Π½Π΅ Ρ€Π°ΡΠΏΡ€ΠΎΡΡ‚Ρ€Π°Π½ΡΡŽΡ‰ΠΈΡ…ΡΡ колСбаниях ΠΈ Π΄Π²ΡƒΡ… кусочно-ΠΎΠ΄Π½ΠΎΡ€ΠΎΠ΄Π½Ρ‹Ρ… Ρ‡Π΅Ρ‚Ρ‹Ρ€Π΅Ρ…ΠΌΠ΅Ρ‚Ρ€ΠΎΠ²Ρ‹Ρ… ΡƒΡΠΊΠΎΡ€ΡΡŽΡ‰ΠΈΡ… сСкций. КаТдая сСкция питаСтся Π‘Π’Π§-ΠΌΠΎΡ‰Π½ΠΎΡΡ‚ΡŒΡŽ ΠΎΡ‚ клистрона KИУ-12AM. ИзмСнСниС срСднСй энСргии ΠΏΡƒΡ‡ΠΊΠ° Π² ΡˆΠΈΡ€ΠΎΠΊΠΈΡ… ΠΏΡ€Π΅Π΄Π΅Π»Π°Ρ… обСспСчиваСтся ускорСниСм сгустков Π½Π΅ Π½Π° Π³Ρ€Π΅Π±Π½Π΅ Π²ΠΎΠ»Π½Ρ‹ Π²ΠΎ Π²Ρ‚ΠΎΡ€ΠΎΠΉ ΡƒΡΠΊΠΎΡ€ΡΡŽΡ‰Π΅ΠΉ сСкции. ΠŸΡ€Π΅Π΄ΡΡ‚Π°Π²Π»Π΅Π½Ρ‹ структурная схСма ускоритСля, Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹ модСлирования Π΄ΠΈΠ½Π°ΠΌΠΈΠΊΠΈ частиц Π² ускоритСлС ΠΈ Π΅Π³ΠΎ Ρ‚Π΅ΠΊΡƒΡ‰Π΅Π΅ состояниС

    Reaction of pyrido[1,2-a]benzimidazole and tetrahydropyrido[1,2-a]benzimidazole with acetylenedicarboxylic ester

    No full text
    Previously unknown polynuclear condensed systems with bridgehead nitrogen atoms have been obtained by treating acetylenedicarboxylic ester with pyrido[1,2-a]-benzimidazole and tetrahydropyrido[1,2-a]benzimidazole. Β© 1986 Plenum Publishing Corporation

    CONDENSATION OF PYRIDO[1,2-A]BENZIMIDAZOLE AND TETRAHYDROPYRIDOL[1,2-A]BENZIMIDAZOLE WITH DIMETHYLACETYLENEDICARBOXYLATE

    No full text

    SPLITTING OF PYRIDO[1,2-A]BENZIMIDAZOLE UNDER ACTION OF PHENYLLITHIUM

    No full text

    Reaction of pyrido[1,2-a]benzimidazole and tetrahydropyrido[1,2-a]benzimidazole with acetylenedicarboxylic ester

    No full text
    Previously unknown polynuclear condensed systems with bridgehead nitrogen atoms have been obtained by treating acetylenedicarboxylic ester with pyrido[1,2-a]-benzimidazole and tetrahydropyrido[1,2-a]benzimidazole. Β© 1986 Plenum Publishing Corporation

    SPLITTING OF PYRIDO[1,2-A]BENZIMIDAZOLE UNDER ACTION OF PHENYLLITHIUM

    No full text

    CONDENSATION OF PYRIDO[1,2-A]BENZIMIDAZOLE AND TETRAHYDROPYRIDOL[1,2-A]BENZIMIDAZOLE WITH DIMETHYLACETYLENEDICARBOXYLATE

    No full text

    N-OXIDES OF 2-AZAFLUORENONES AND 4-AZAFLUORENONES AND NITRODERIVATIVES OF 2-AZAFLUORENES AND 4-AZAFLUORENES

    No full text

    N-oxides of 2- and 4-azafluorenones and nitro derivatives of 2- and 4-azafluorenes

    No full text
    It was demonstrated by PMR spectroscopy that mixtures of N-oxides of 6- and 7-nitro derivatives are formed in the nitration of the N-oxides of 3-methyl-2- and 4-azafluorenes. The products were deoxygenated to give nitro derivatives of 2- and 4-azafluorenes. The N-oxides of nitro-substituted azafluorenes were converted to salts of the aci forms by the action of alkali. Β© 1983 Plenum Publishing Corporation

    N-OXIDES OF 2-AZAFLUORENONES AND 4-AZAFLUORENONES AND NITRODERIVATIVES OF 2-AZAFLUORENES AND 4-AZAFLUORENES

    No full text
    corecore