CO DIFFUSION INTO AMORPHOUS H2O ICES

被引:64
|
作者
Lauck, Trish [1 ]
Karssemeijer, Leendertjan [2 ]
Shulenberger, Katherine [3 ]
Rajappan, Mahesh [4 ]
Oeberg, Karin I. [4 ]
Cuppen, Herma M. [2 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
[2] Radboud Univ Nijmegen, Inst Mol & Mat, Theoret Chem, NL-6525 AJ Nijmegen, Netherlands
[3] Wellesley Coll, Dept Chem, Wellesley, MA 02481 USA
[4] Harvard Smithsonian Ctr Astrophys, Cambridge, MA 02138 USA
来源
ASTROPHYSICAL JOURNAL | 2015年 / 801卷 / 02期
基金
欧洲研究理事会;
关键词
astrochemistry; ISM: molecules; methods: laboratory: molecular; molecular processes; GAS-GRAIN CHEMISTRY; BAND STRENGTHS; WATER-ICE; BULK DIFFUSION; INTERSTELLAR; MODEL; SIMULATIONS; ADSORPTION; PROFILES; DYNAMICS;
D O I
10.1088/0004-637X/801/2/118
中图分类号
P1 [天文学];
学科分类号
0704 ;
摘要
The mobility of atoms, molecules, and radicals in icy grain mantles regulates ice restructuring, desorption, and chemistry in astrophysical environments. Interstellar ices are dominated by H2O, and diffusion on external and internal (pore) surfaces of H2O-rich ices is therefore a key process to constrain. This study aims to quantify the diffusion kinetics and barrier of the abundant ice constituent CO into H2O-dominated ices at low temperatures (15-23 K), by measuring the mixing rate of initially layered H2O(:CO2)/CO ices. The mixed fraction of CO as a function of time is determined by monitoring the shape of the infrared CO stretching band. Mixing is observed at all investigated temperatures on minute timescales. and can be ascribed to CO diffusion in H2O ice pores. The diffusion coefficient and final mixed fraction depend on ice temperature, porosity, thickness, and composition. The experiments are analyzed by applying Fick's diffusion equation under the assumption that mixing is due to CO diffusion into an immobile H2O ice. The extracted energy barrier for CO diffusion into amorphous H2O ice is similar to 160 K. This is effectively a surface diffusion barrier. The derived barrier is low compared to current surface diffusion barriers in use in astrochemical models. Its adoption may significantly change the expected timescales for different ice processes in interstellar environments.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] DIFFERENCE IN THE SPATIAL DISTRIBUTION BETWEEN H2O AND CO2 ICES IN M 82 FOUND WITH AKARI
    Yamagishi, Mitsuyoshi
    Kaneda, Hidehiro
    Ishihara, Daisuke
    Oyabu, Shinki
    Onaka, Takashi
    Shimonishi, Takashi
    Suzuki, Toyoaki
    Minh, Young Chol
    ASTROPHYSICAL JOURNAL LETTERS, 2013, 773 (02)
  • [32] CRYSTAL AND MOLECULAR-STRUCTURE STUDIES OF [CO(H2O)6[2+[CO(H2O)HEDTA](2)-.2H2O AND [CO(H2O)HEDTA].2H2O
    LOTT, S
    ZUBKOWSKI, JD
    VALENTE, EJ
    PERRY, DL
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1993, 206 : 139 - INOR
  • [33] SPECTROSCOPY AND PHYSICO-CHEMISTRY OF CO-H2O AND CO2-H2O ICES
    SCHMITT, B
    GRIM, R
    GREENBERG, M
    INFRARED SPECTROSCOPY IN ASTRONOMY, 1989, 290 : 213 - 219
  • [34] Role of H2O andCO2 ices in martian climate changes
    Yokohata, T
    Odaka, M
    Kuramoto, K
    ICARUS, 2002, 159 (02) : 439 - 448
  • [35] Rigid H2O molecule model of anomalous thermal expansion of ices
    Katrusiak, A
    PHYSICAL REVIEW LETTERS, 1996, 77 (21) : 4366 - 4369
  • [36] H2O diffusion in dacitic melts
    Liu, Y
    Zhang, YX
    Behrens, H
    CHEMICAL GEOLOGY, 2004, 209 (3-4) : 327 - 340
  • [37] EFFECTS OF H2O ON DIFFUSION IN GLASS
    MCVAY, GL
    BAUGHMAN, RJ
    AMERICAN CERAMIC SOCIETY BULLETIN, 1974, 53 (04): : 354 - 354
  • [38] Laboratory submillimeter spectrscopic analysis of desorbed H2O and D2O ices
    Yocum, Katarina
    Jones, Ayanna
    Todd, Ethan
    Weaver, Susanna Widicus
    Gerakines, Perry
    Milam, Stefanie
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2019, 258
  • [39] Diffusion of H2O in smectite gels: Obstruction effects of bound H2O layers
    Yoshito Nakashima
    Clays and Clay Minerals, 2003, 51 : 9 - 22
  • [40] Diffusion of H2O in smectite gels:: Obstruction effects of bound H2O layers
    Nakashima, Y
    CLAYS AND CLAY MINERALS, 2003, 51 (01) : 9 - 22