Page 31 - 《精细化工》2023年第5期

第 5 期 张呈平，等: 氯氟烃替代物的过去、现在和未来 ·951·

[5] MCELROY M B, WOFSY S C, PENNER J E, et al. Atmospheric [29] ISHIKAWA T, TERADA J. Process for producing
ozone: Possible impact of stratospheric aviation[J]. Journal of 2,3,3,3-tetrafluoropropene: WO200935130A2[P]. 2009-03-19.
Atmospheric Science, 1974, 31(1): 287-304. [30] KANDA M, KAWAGUCHI S, TERAZONO S. Process for
[6] FARMAN J C, GARDINER B G, SHANKLIN J D. Large losses of producing hydrofluoroolefin: US2017158587A1[P]. 2017-06-08.
ozone in Antarctica reveal seasonal ClO x/NO x interaction[J]. Nature, [31] BOIKO V N, FILATO V A A, NAPPA M J, et al. Synthesis of
1985, 315: 207-210. hydrofluoroalkanols and hydrofluoroalkenes: US2009143604A1[P].
[7] RAMANATHAN V. Greenhouse effect due to chlorofluorocarbons- 2009-06-04.
Climatic implications[J]. Science, 1975, 190(4209): 50-51. [32] NOSE M, SUGIYAMA A, SUZUKI A. Process for preparing
[8] WANG W C, YUNG Y L, LACIS A A, et al. Greenhouse effects due fluorine-containing propene by gas phase: WO2010013577A1[P].
to man-made perturbations of trace gases[J]. Science, 1976, 194(4266): 2010-02-04.
685-690. [33] MCGUINESS C, SHARRATT A P, SMITH J W. Process:
[9] RAMANATHAN V, CICERONE R J, SINGH H B, et al. Trace gas WO2009125201A2[P]. 2009-10-15.
trends and their potential role in climate change[J]. Journal of [34] KOMATSU Y, NOSE M, SHIBANUMA T. Process for preparing
Geophysical Research, 1985, 90: 5547-5566. 2,3,3,3-tetrafluoropropene: WO2010050373A2[P]. 2010-05-06.
[10] RAMANATHAN V. Climate-chemical interactions and effects of [35] KOMATSU Y, SHIBANUMA T, SUGIYAMA A. Process for
changing atmospheric trace gases[J]. Reviews of Geophysics, 1987, producing fluorine-containing propene compounds:
25(7): 1441-1482. WO2010001768A1[P]. 2010-01-07.
[11] HANSEN J, LACIS A, PRATHER M. Greenhouse effect of [36] VAN D P M. Process for preparation of 2,3,3,3-tetrafluoropropene
chlorofluorocarbons and other trace gases[J]. Journal of Geophysical (HFO-1234yf): US2009253946A1[P]. 2009-10-08.
Research, 1989, 94(D13): 16417-16421. [37] GENG W L (耿为利), WANG Z L (王宗令), WU Q (吴庆), et al. A
[12] HANSEN J, SATO M, RUEDY R, et al. Efficacy of climate method of synthesizing 2,3,3,3-tetrafluoropropene: CN106380369[P].
forcing[J]. Journal of Geophysical Research, 2005, 110: D18104. 2017-02-08.
[13] FUGLESTVEDT J S, SHINE K P, BERNTSEN T, et al. Transport [38] CHAKI T, KARUBE D. Method for producing 2,3,3,3-tetrafluoropropene:
impacts on atmosphere and climate: Metrics[J]. Atmospheric US2017233315A1[P]. 2017-08-17.
Environment, 2010, 44(37): 4648-4677. [39] HU R Z (胡儒柱). Research and development of a next generation
[14] PINNOCK S, HURLEY M D, SHINE K P, et al. Radiative forcing of environment-friendly refrigerant 2,3,3,3-tetrafluoropropene with zero
climate by hydrochlorofluorocarbons and hydrofluorocarbons[J]. ODP value and low GWP value[D]. Beijing: Beijing Institute of
Journal of Geophysical Research, 1995, 100(D11): 23227-23238. Technology (北京理工大学), 2016.
[15] ENGLE A, RIGBY M, BURKHOLDER J B, et al. WMO (World [40] HU R Z, ZHANG C P, QING F Y, et al. Synthesis of 2, 3, 3,
Meteorological Organization), scientific assessment of ozone 3-tetrafluoropropene via vapor-phase catalytic fluorination in the
depletion: 2018, global ozone research and monitoring project-report presence of Cr-based catalyst[J]. Journal of Fluorine Chemistry,
No.58, 588 pp[R]. Geneva, Switzerland, 2018. 2016, 185: 187-190.
[16] WANG D F (王大枋). Present status and development of ODS [41] CERRI G, CHIU Y, COTTRELL S A. Process for the manufacture of
substitutes at home and abroad[J]. Chemical Production and fluorinated olefins: US2009234165A1[P]. 2009-09-17.
Technology (化工生产与技术), 2006, 13(4): 1-3. [42] NAPPA M J, RAO M V N, SIEVERT A C. Process to manufacture
[17] BURKHOLDER J B, COX R A, RAVISHANKARA A R. Atmospheric 2,3,3,3-tetrafluoropropene: WO2008030440A2[P]. 2008-03-13.
degradation of ozone depletion substances, their substitutes, and [43] LIM S, KIM M S, CHOI J W, et al. Catalytic dehydrofluorination of
related species [J]. Chemical Review, 2015, 115: 3704-3759. 1,1,1,2,3-pentafluoropropane (HFC-245eb) to 2,3,3,3-tetrafluoropropene
[18] YAMABE (山边正显), MATSUO H (松尾仁). Research and (HFO-1234yf) using in-situ fluorinated chromium oxyfluoride
development of fluorine-containing materials[M]. WEN J X (闻建 catalyst[J]. Catalysis Today, 2017, 293-294: 42-48.
勋), WEN Y Q(闻宇清). 译. Shanghai: East China University of [44] KERVAREC M C, BRAUN T, AHRENS M, et al. Activation of
Science and Technology Press (华东理工大学出版社), 2003: 6-54. pentafluoropropane isomers at a nanoscopic aluminum chlorofluoride:
[19] CALVER J G, DERWENT R G, ORLANDO J J, et al. Mechanisms Hydrodefluorination versus dehydrofluorination[J]. Beilstein Journal
of atmospheric oxidation of the alkanes[M]. New York: Oxford of Organic Chemistry, 2020, 16: 2623-2635.
University Press, 2008:15-62. [45] BORTZ C, CANTLON C L, JOHNSON R C, et al. Process for
[20] HU W (胡伟). Fluorine chemical production technology[M]. Beijing: synthesis of fluorinated olefins: US2009099396A1[P]. 2009-04-16.
Science Press (科学出版社), 2009: 225-254. [46] GRANDBOIS M L, MURDOCH B, MEYER M M. Process for the
[21] ATKINSON R. Gas-phase tropospheric chemistry of volatile organic production of chlorinated propenes: US2016009615A1[P]. 2016-01-14.
compounds: 1. Alkanes and alkenes[J]. Journal of Physical and [47] KRUPER J W, TIRTOWIDJOJO M M, HIRSEKORN K F, et al.
Chemical Reference Data, 1997, 26: 215-290. Process for the production of chlorinated and/or fluorinated
[22] ATKINSON R, AREY J. Atmospheric degradation of volatile organic propenes: US2011178343A1[P]. 2011-07-21.
compounds[J]. Chemical Review, 2003, 103: 4605-4638. [48] NOSE M, SUZUKI A, YAMASHITA T. Process for preparation of
[23] KONSTANTINOS K. HFO-1336mzz-Z: High temperature chemical 2,3,3,3-tetrafluoropropene: WO2010123154 A2[P]. 2010-10-28.
stability and use as a working fluid in organic rankine cycles[R]. [49] NOSE M, SUZUKI A, YAMASHITA T, et al. Process for preparing
Wilmington: DuPont Fluorochemicals R&D, 2014. 2-chloro-3,3,3-trifluoropropene: US2012022303A1[P]. 2012-01-26.
[24] ZHANG N, CHEN L, MIZUKADO J, et al. Rate constants for the [50] JOHNSON R C, MERKEL D C, TUNG H S. Method for producing
gas-phase reactions of (Z)-CF 3CH==CHF and (E)-CF 3CH==CHF fluorinated organic compounds: US2009030247A1[P]. 2009-01-29.
with OH radicals at 253-328 K[J]. Chemical Physics Letters, 2015, [51] BEKTESEVIC S, JOHNSON R C, MERKEL D C, et al. Integrated
621: 78-84. process to produce 2,3,3,3-tetrafluoropropene: EP2103587A2[P].
[25] ØSTERSTRØM F F, ANDERSON S T, SØLLING T I, et al. 2009-09-23.
Atmospheric chemistry of Z- and E-CF 3CH==CHCF 3[J]. Physical [52] KERVARECA M C, MARSHALL C P, BRAUN T. Selective
Chemistry Chemical Physics, 2017, 19: 735-750. dehydrofluorination of 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb)
[26] RAUSCH D A. Preparation of 2,3,3,3-tetrafluoropropene: to 2-chloro-3,3,3-trifluoropropene (HFO-1233xf) using nanoscopic
US2996555A[P]. 1961-08-15. aluminium fluoride catalysts at mild conditions[J]. Journal of
[27] NAPPA M J, RAO M V N, SIEVERT A C. Process for producing and Fluorine Chemistry, 2019, 221: 61-65.
compositions comprising 2,3,3,3-tetrafluoropropene and/or 1,2,3,3- [53] TEINZ K, MANUEL S R, CHEN B B, et al. Catalytic formation of
tetrafluoropropene: WO2008054780A2[P]. 2008-05-08. 2,3,3,3-tetrafluoropropene from 2-chloro-3,3,3-trifluoropropene at
[28] RAO M V N, SIEVERT A C. Process for producing fluorinated chromia: A study of reaction pathways[J]. Applied
2,3,3,3-tetrafluoropropene: WO2008060614A2[P]. 2008-05-22. Catalysis B: Environmental, 2015, 165: 200-208.