• Title/Summary/Keyword: MCS/CTF

Search Result 2, Processing Time 0.014 seconds

Simulations of BEAVRS benchmark cycle 2 depletion with MCS/CTF coupling system

  • Yu, Jiankai;Lee, Hyunsuk;Kim, Hanjoo;Zhang, Peng;Lee, Deokjung
    • Nuclear Engineering and Technology
    • /
    • v.52 no.4
    • /
    • pp.661-673
    • /
    • 2020
  • The quarter-core simulation of BEAVRS Cycle 2 depletion benchmark has been conducted using the MCS/CTF coupling system. MCS/CTF is a cycle-wise Picard iteration based inner-coupling code system, which couples sub-channel T/H (thermal/hydraulic) code CTF as a T/H solver in Monte Carlo neutron transport code MCS. This coupling code system has been previously applied in the BEAVRS benchmark Cycle 1 full-core simulation. The Cycle 2 depletion has been performed with T/H feedback based on the spent fuel materials composition pre-generated by the Cycle 1 depletion simulation using refueling capability of MCS code. Meanwhile, the MCS internal one-dimension T/H solver (MCS/TH1D) has been also applied in the simulation as the reference. In this paper, an analysis of the detailed criticality boron concentration and the axially integrated assembly-wise detector signals will be presented and compared with measured data based on the real operating physical conditions. Moreover, the MCS/CTF simulated results for neutronics and T/H parameters will be also compared to MCS/TH1D to figure out their difference, which proves the practical application of MCS into the BEAVRS benchmark two-cycle depletion simulations.

A New Shuttle Plasmid That Stably Replicates in Clostridium acetobutylicum

  • Lee, Sang-Hyun;Kwon, Min-A;Choi, Sunhwa;Kim, Sooah;Kim, Jungyeon;Shin, Yong-An;Kim, Kyoung Heon
    • Journal of Microbiology and Biotechnology
    • /
    • v.25 no.10
    • /
    • pp.1702-1708
    • /
    • 2015
  • We have developed a new shuttle plasmid, designated as pLK1-MCS that can replicate in both Clostridium acetobutylicum and Escherichia coli, by combining the pUB110 and pUC19 plasmids. Plasmid pLK1-MCS replicated more stably than previously reported plasmids containing either the pIM13 or the pAMβ1 replicon in the absence of antibiotic selective pressure. The transfer frequency of pLK1-MCS into C. acetobutylicum was similar to the transfer frequency of other shuttle plasmids. We complemented C. acetobutylicum ML1 (that does not produce solvents such as acetone, butanol, and ethanol owing to loss of the megaplasmid pSOL1 harboring the adhE1-ctfAB-adc operon) by introducing pLK1-MCS carrying the adhE1-ctfAB-adc operon into C. acetobutylicum ML1. The transformed cells were able to resume anaerobic solvent production, indicating that the new shuttle plasmid has the potential for practical use in microbial biotechnology.