锆合金初始氧化行为的原位近常压XPS研究

引用本文: 戴久翔, 龚忠苗, 徐诗彤, 崔义, 姚美意. 锆合金初始氧化行为的原位近常压XPS研究[J]. 物理化学学报, 2022, 38(3): 200302. doi: 10.3866/PKU.WHXB202003026 shu

Citation: Jiuxiang Dai, Zhongmiao Gong, Shitong Xu, Yi Cui, Meiyi Yao. In Situ Study on the Initial Oxidation Behavior of Zirconium Alloys with Near-Ambient Pressure XPS[J]. Acta Physico-Chimica Sinica, 2022, 38(3): 200302. doi: 10.3866/PKU.WHXB202003026 shu

锆合金初始氧化行为的原位近常压XPS研究

戴久翔 ^{1, 2,} ,
龚忠苗 ^2, ,
徐诗彤 ^1, ,
崔义 ^{2,
,} ,
姚美意 ^{1,
,}

1.
上海大学材料研究所，上海 200072
2.
中国科学院苏州纳米技术与纳米仿生研究所，纳米真空互联实验站，江苏苏州 215123

通讯作者: 崔义, ycui2015@sinano.ac.cn; 姚美意, yaomeiyi@shu.edu.cn

基金项目:
国家自然科学基金 51871141

111引智项目 D17002

表面物理与化学重点实验室学科发展基金 XKFZ201711

摘要: 锆基合金由于具有低的热中子吸收截面、良好的耐腐蚀性能和力学性能等优点，通常被用于水冷核反应堆中的核燃料包壳和其他结构材料。通过在合金中添加适量的Nb元素可以有效地降低锆合金的氧化速率和吸氢分数，从而改善锆合金的耐腐蚀性能。尽管对锆合金的耐腐蚀性能得到了广泛的认识，但关于其在接近真实氧化腐蚀条件下的原位研究一直是具有挑战性的课题。本工作中利用近常压X射线光电子能谱(NAP-XPS)原位研究了1.3 × 10^-8 - 1.3 × 10^-1 mbar (1 mbar = 100 Pa)连续分压下室温到623 K温度时两种锆基合金表面在水，氧中的初始氧化腐蚀行为。结果表明，未添加Nb和添加1%Nb的锆合金表面在初始氧化过程中锆元素都会由金属态向多种氧化态过渡。水蒸气环境下两种合金的氧化速率都要低于氧气环境。室温下无论水蒸气还是氧气环境两种合金的氧化速率都要比623 K高温情况下的慢。在623 K的氧气气氛下，未添加Nb的锆合金相较于添加1%Nb的锆合金更容易被氧化，Nb的添加一定程度上会降低氧物种的吸附能力。在室温下和623 K低水蒸气压力下，1%Nb锆合金氧化速率更快，Nb促进OH^-在表面生成。而在623 K高水蒸气压力下，未添加Nb的锆合金有更易于被氧化的倾向，Nb在高温下向表面扩散并抑制OH^-键的断裂，但两种样品表面短时间内都无法被完全氧化。

关键词:

English

In Situ Study on the Initial Oxidation Behavior of Zirconium Alloys with Near-Ambient Pressure XPS

Jiuxiang Dai ^{1, 2,} ,
Zhongmiao Gong ^2, ,
Shitong Xu ^1, ,
Yi Cui ^{2,
,} ,
Meiyi Yao ^{1,
,}

1.
Institute of Materials, Shanghai University, Shanghai 200072, China
2.
Vacuum Interconnected Nanotech Workstation, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, Jiangsu Province, China

Corresponding author: Email: ycui2015@sinano.ac.cn (Y.C.); Tel.: +86-13913595977 (Y.C.); Email: yaomeiyi@shu.edu.cn (M.Y.); +86-21-56338586 (M.Y.)

Received Date: 11 March 2020
Accepted Date: 10 April 2020
Revised Date: 09 April 2020
Available Online: 15 March 2022
Fund Project:
the National Natural Science Foundation of China

the National 111 Project

ZDXKFZ

Abstract: Zirconium alloys are often used to fabricate nuclear fuel cladding and other structural materials because of their low thermal neutron absorption cross section, satisfactory corrosion resistance, and decent mechanical properties. The oxidation rate and hydrogen-absorption fraction of zirconium alloys can be reduced by adding moderate amount of Nb to them, and the corrosion resistance of zirconium alloys can be improved as well. Although the corrosion resistance of zirconium alloys has been widely recognized, the in situ study of zirconium alloys in conditions that resemble real oxidative-corrosion environments has still been a challenging subject. The initial oxidation behavior of zirconium alloys might affect the subsequent generation of oxides in the form of the element valence and type of surface oxides changes, resulting in the long-term corrosion-behavior changes. In addition, the reaction mechanism of Nb in zirconium alloys is still controversial. To investigate the influence of the alloy composition and environmental conditions on the initial oxidation behavior of zirconium alloys, in situ initial oxidation experiments were performed on two different Zr alloys in a near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) chamber. The samples were cut to the size of 12 mm × 3 mm, and the primary oxide film was removed via pickling, argon etching and annealing. Oxygen or water vapors with the pressure in the range of 1.3 × 10^-8-1.3 × 10^-1 mbar (1 mbar = 100 Pa) were gradually introduced into the NAP-XPS chamber after sample-surface cleaning. The experiment was repeated at room temperature (300 K) and 623 K. The results showed that both Nb-containing and Nb-free zirconium-alloy surfaces transitioned from a metallic state to various oxidation states during the initial oxidation process. The oxidation rates of both the alloys were lower in water vapors than those in oxygen. In the presence of water vapors or oxygen, both the alloys oxidized more slowly at room temperature than at 623 K. Compared with 1%Nb zirconium alloys, the Nb-free zirconium alloys were more easily oxidized and had a denser oxide layer, in the oxygen atmosphere at 623 K. To some extent, the presence of Nb would reduce the adsorption capacity of oxygen atoms. The oxidation rate of 1%Nb zirconium alloy was quick at room temperature and also at low water vapor pressures at 623 K; Nb promoted the formation of OH^- at the surface. Under the high pressure vapor atmosphere at 623 K, the Nb-free zirconium alloys were more prone to be oxidized; Nb diffused to the surface at high temperatures and inhibited the breaking of the OH^- bond; however, the surfaces of both the samples could not be completely oxidized in a short time.

Key words:

1. [1]
  Zinkle, S. J.; Was, G. S. Acta Mater. 2013, 61 (3), 735. doi: 10.1016/j.actamat.2012.11.004
2. [2]
  Motta, A. T.; Couet, A.; Comstock, R. J. Annu. Rev. Mater. Res. 2015, 45 (1), 311. doi: 10.1146/annurev-matsci-070214-020951
3. [3]
  Chen, L. Y.; Li, J. X.; Zhang, Y.; Zhang, L. C.; Lu, W. J.; Wang, L. Q.; Zhang, L. F.; Zhang, D. Corros. Sci. 2015, 100, 332. doi: 10.1016/j.corsci.2015.08.005
4. [4]
  Yang, H. L.; Shen, J. J.; Matsukawa, Y.; Satoh, Y.; Kano, S.; Zhao, Z. S.; Li, Y. F.; Li, F.; Abe, H. J. Nucl. Sci. Technol. 2015, 52 (9), 1162. doi: 10.1080/00223131.2014.996622
5. [5]
  Hong, H. S.; Moon, J. S.; Kim, S. J.; Lee, K. S. J. Nucl. Mater. 2001, 297 (2), 113. doi: 10.1016/S0022-3115(01)00601-8
6. [6]
  Sabol, G. P.; Comstock, R. J.; Nayak, U. P. Effect of Dilute Alloy Additions of Molybdenum, Niobium, and Vanadium on Zirconium Corrosion. In Zirconium in the Nuclear Industry: Twelfth International Symposium; Sabol, G. P., Moan, G. D., Eds.; ASTM International: West Conshohocken, PA, USA, 2000; pp. 525-544.
7. [7]
  Bell, B. D. C.; Murphy, S. T.; Grimes, R. W.; Wenman, M. R. Acta Mater. 2017, 132, 425. doi: 10.1016/j.actamat.2017.04.063
8. [8]
  Bell, B. D. C.; Murphy, S. T.; Burr, P. A.; Comstock, R. J.; Partezana, J. M.; Grimes, R. W.; Wenman, M. R. Corros. Sci. 2016, 105, 36. doi: 10.1016/j.corsci.2015.12.022
9. [9]
  Shibata, A.; Kato, Y.; Taguchi, T.; Futakawa, M.; Maekawa, K. Nucl. Technol. 2016, 196 (1), 89. doi: 10.13182/NT16-54
10. [10]
  Steinbrück, M.; Böttcher, M. J. Nucl. Mater. 2011, 414 (2), 276. doi: 10.1016/j.jnucmat.2011.04.012
11. [11]
  Wang, Z.; Zhou, B. X.; Chen, B.; Zhu, W.; Wen, B.; Wu, L.; Tang, H. K.; Fang, Z. Q.; Li, Q.; Yao, M. Y. Corros. Sci. 2017, 122, 26. doi: 10.1016/j.corsci.2017.03.017
12. [12]
  Wang, Z.; Zhou, B. X.; Wang, B. Y.; Yao, M. Y.; Li, Q.; Huang, J. Corros. Sci. 2016, 105, 141. doi: 10.1016/j.corsci.2016.01.011
13. [13]
  Azdad, Z.; Marot, L.; Moser, L.; Steiner, R.; Meyer, E. Sci. Rep. -UK 2018, 8 (1), 16251. doi: 10.1038/s41598-018-34570-w
14. [14]
  Harlow, W.; Ghassemi, H.; Taheri, M. L. J. Nucl. Mater. 2016, 474, 126. doi: 10.1016/j.jnucmat.2016.03.009
15. [15]
  Yoshitaka, N.; Krauss, A. R.; Yuping, L.; Gruen, D. M. J. Nucl. Mater. 1996, 228 (3), 346. doi: 10.1016/0022-3115(95)00194-8
16. [16]
  Bakradze, G.; Jeurgens, L. P. H.; Mittemeijer, E. J. J. Phys. Chem. C 2011, 115 (40), 19841. doi: 10.1021/jp206896m
17. [17]
  Lyapin, A.; Jeurgens, L. P. H.; Mittemeijer, E. J. Acta Mater. 2005, 53 (10), 2925. doi: 10.1016/j.actamat.2005.03.009
18. [18]
  Zhang, H. B.; Liu, G. G.; Shi, L.; Ye, J. H. Adv. Energy Mater. 2018, 8 (1), 1701343. doi: 10.1002/aenm.201701343
19. [19]
  Toyoshima, R.; Yoshida, M.; Monya, Y.; Suzuki, K.; Amemiya, K.; Mase, K.; Mun, B. S.; Kondoh, H. Phys. Chem. Chem. Phys. 2014, 16 (43), 23564. doi: 10.1039/C4CP04318A
20. [20]
  段园, 陈明树, 万惠霖. 物理化学学报, 2018, 34 (12), 1358. doi: 10.3866/PKU.WHXB201803071Duan, Y.; Chen, M. S.; Wan, H. L. Acta Phys. -Chim. Sin. 2018, 34 (12), 1358. doi: 10.3866/PKU.WHXB201803071
21. [21]
  Bespalov, I.; Datler, M.; Buhr, S.; Drachsel, W.; Rupprechter, G.; Suchorski, Y. Ultramicroscopy 2015, 159, 147. doi: 10.1016/j.ultramic.2015.02.016
22. [22]
  Lyapin, A.; Jeurgens, L. P. H.; Graat, P. C. J.; Mittemeijer, E. J. J. Appl. Phys. 2004, 96 (12), 7126. doi: 10.1063/1.1809773
23. [23]
  Roustila, A.; Chêne, J.; Séverac, C. J. Alloy. Compd. 2003, 356-357, 330. doi: 10.1016/S0925-8388(03)00356-6
24. [24]
  张海辉, 李晓娣, 谢耀平, 胡丽娟, 姚美意. 物理学报, 2016, 65 (9), 96802. doi: 10.7498/aps.65.096802Zhang, H. H.; Li, X. D.; Xie, Y. P.; Hu, L. J.; Yao, M. Y. Acta Phys. Sin. 2016, 65 (9), 96802. doi: 10.7498/aps.65.096802
25. [25]
  Kim, H.; Park, J.; Jeong, Y. J. Nucl. Mater. 2005, 345 (1), 1. doi: 10.1016/j.jnucmat.2005.04.061
26. [26]
  Jeong, Y. H.; Kim, H. G.; Kim, D. J.; Choi, B. K.; Kim, J. H. J. Nucl. Mater. 2003, 323 (1), 72. doi: 10.1016/j.jnucmat.2003.08.031
27. [27]
  孙国成, 周邦新, 姚美意, 谢世敬, 李强. 金属学报, 2012, 48 (7), 1103. doi: 10.3724/SP.J.1037.2012.00329Sun, G. C.; Zhou, B. X.; Yao, M. Y.; Xie, S. J.; Li, Q. B. Acta Metall Sin. 2012, 48 (7), 1103. doi: 10.3724/SP.J.1037.2012.00329
28. [28]
  Luo, L. L.; Su, M.; Yan, P. F.; Zou, L. F.; Schreiber, D. K.; Baer, D. R.; Zhu, Z. H.; Zhou, G. W.; Wang, Y. T.; Bruemmer, S. M.; et al. Nat. Mater. 2018, 17 (6), 514. doi: 10.1038/s41563-018-0078-5
29. [29]
  杨忠波, 赵文金, 程竹青, 邱军, 张海, 卓洪. 金属学报, 2017, 53 (1), 47. doi: 10.11900/0412.1961.2016.00136Yang, Z. B.; Zhao, W. J.; Cheng, Z. Q.; Qiu, J.; Zhang, H.; Zhuo, H. Acta Metall Sin. 2017, 53 (1), 47. doi: 10.11900/0412.1961.2016.00136
30. [30]
  王波阳, 周邦新, 王桢, 黄娇, 姚美意, 周军. 金属学报, 2015, 51 (12), 1545. doi: 10.11900/0412.1961.2015.00254Wang, B. Y.; Zhou, B. X.; Wang, Z.; Huang, J.; Yao, M. Y.; Zhou, J. Acta Metall Sin. 2015, 51 (12), 1545. doi: 10.11900/0412.1961.2015.00254

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通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

锆合金初始氧化行为的原位近常压XPS研究

通讯作者: 崔义, ycui2015@sinano.ac.cn; 姚美意, yaomeiyi@shu.edu.cn

English

In Situ Study on the Initial Oxidation Behavior of Zirconium Alloys with Near-Ambient Pressure XPS

Corresponding author: Email: ycui2015@sinano.ac.cn (Y.C.); Tel.: +86-13913595977 (Y.C.); Email: yaomeiyi@shu.edu.cn (M.Y.); +86-21-56338586 (M.Y.)

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通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

锆合金初始氧化行为的原位近常压XPS研究

通讯作者: 崔义, ycui2015@sinano.ac.cn; 姚美意, yaomeiyi@shu.edu.cn

English

In Situ Study on the Initial Oxidation Behavior of Zirconium Alloys with Near-Ambient Pressure XPS

Corresponding author: Email: ycui2015@sinano.ac.cn (Y.C.); Tel.: +86-13913595977 (Y.C.); Email: yaomeiyi@shu.edu.cn (M.Y.); +86-21-56338586 (M.Y.)

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南： 你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

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