无机材料学报

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单钯三效催化剂在梯度温度老化下的失活机制

刘栩孜1, 宋兆华1, 曾路1, 屈丽2, 焦毅1, 蒋发军3, 李大成3, 严会成4, 王健礼2, 陈耀强2   

  1. 1.四川大学 新能源与低碳技术研究院,成都 610064;
    2.四川大学 化学学院,成都 610064;
    3.中自环保科技股份有限公司,成都 611731;
    4.四川蜀泰化工科技有限公司,遂宁 629300
  • 收稿日期:2025-10-10 修回日期:2025-12-24
  • 通讯作者: 焦 毅, 副研究员. E-mail: jiaoyiscu@163.com
  • 作者简介:刘栩孜(2000-), 女, 硕士研究生. E-mail: lxz@stu.scu.edu.cn
  • 基金资助:
    国家科技重大专项(2024ZD0606500); 国家自然科学基金(22472108)

Deactivation Mechanism of Pd Only Three-way Catalysts under Aging Temperature Gradient

LIU Xuzi1, SONG Zhaohua1, ZENG Lu1, QU Li2, JIAO Yi1, JIANG Fajun3, LI Dacheng3, YAN Huicheng4, WANG Jianli2, CHEN Yaoqiang2   

  1. 1. Institute of New Energy and Low-Carbon Technology, Sichuan University, Chengdu 610064, China;
    2. College of Chemistry, Sichuan University, Chengdu 610064, China;
    3. SINOTECH Company Limited, Chengdu 611731, China;
    4. Sichuan Shutai Chemical Technology Co., Ltd., Suining 629300, China
  • Received:2025-10-10 Revised:2025-12-24
  • Contact: JIAO Yi, associate professor. E-mail: jiaoyiscu@163.com
  • About author:LIU Xuzi (2000-), female, Master candidate. E-mail: lxz@stu.scu.edu.cn
  • Supported by:
    Advanced Materials-National Science and Technology Major Project (2024ZD0606500); National Natural Science of China (22472108)

摘要: 单Pd/CZA催化剂由第三代储氧材料CeO2-ZrO2-Al2O3(CZA)与钯(Pd)构成,因其优异的污染物转化效率和抗烧结性能,成为一种更具实用性的汽油车三效催化剂(TWC)。尽管已有研究证实,Pd基TWC的热失活机制与Pd颗粒烧结以及金属-载体相互作用(MSI)减弱密切相关,但其在极端高温条件下的热老化行为仍缺乏系统研究。本研究通过制备800~1000 ℃温度老化的Pd/CZA催化剂,系统分析了其热失活过程,揭示了Pd微观化学状态随梯度老化温度的演变规律。利用一系列表征手段,评估了Pd微观化学状态及MSI与抗老化性能的关系。研究发现三效催化活性随老化温度的升高呈现出非线性衰减的趋势。在850~900 ℃温度区间内,催化剂活性显著下降,一氧化碳(CO)、一氧化氮(NO)和碳氢化合物(HCs)的T50T90(污染物转化率达到50%和90%时的温度)分别升高了26~40 ℃和39~67 ℃; 而在900~1000 ℃温度区间内, 催化活性变化不大。这种活性急剧下降的本质是Pd的微观化学状态发生了突变, 当老化温度升高至900 ℃时,Pd-O-Ce键变弱,导致MSI被削弱,Pd颗粒失去对Pd-O-Ce的有效锚定,发生快速烧结和晶粒生长,从而明显阻碍反应物和氧气的吸附与活化过程。

关键词: 温度梯度, 热老化, Pd-O-Ce键, 金属-载体相互作用, 三效催化剂

Abstract: Pd/CZA catalyst composed of third-generation oxygen storage material CeO2-ZrO2-Al2O3 (CZA) loaded only with Pd represents a practical three-way catalyst (TWC) owing to its exceptional pollutant conversion efficiency and sintering resistance. Although the thermal degradation mechanism of Pd-based TWC has been confirmed to be closely associated with Pd sintering and the weakening of metal-support interaction (MSI), a systematic investigation into its thermal aging behavior under an extreme high temperature gradient remains necessary. A series of Pd/CZA catalysts aged at 800-1000 ℃ were prepared in this study and their thermal degradation was systematically explored, presenting a pioneering investigation into the evolution pattern of the microchemical state of Pd with aging temperature gradient. The correlation among the microchemical state of Pd, MSI and aging resistance was evaluated through different characterization techniques. The results showed that catalytic activity exhibited a nonlinear decay with increasing aging temperature. Catalytic performance declined sharply in the range of 850-900 ℃, with increases of 26-40 ℃ and 39-67 ℃ for T50 and T90 (the temperatures at which the pollutant conversions are 50% and 90%, respectively) of carbon monoxide (CO), nitric oxide (NO) and hydrocarbon (HCs), while showed little variation within the range of 900-1000 °C. The underlying reason for this sharp decline in activity is an abrupt transformation in the microchemical state of Pd. When the aging temperature increases to 900 °C, the Pd-O-Ce bond is weakened, which compromises the MSI. Consequently, Pd particles become unanchored, undergo rapid sintering and growth, and exhibit diminished capabilities for adsorbing and activating both reactants and oxygen.

Key words: temperature gradient, thermal aging, Pd-O-Ce bond, metal-support interaction, three-way catalyst

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