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团絮状双效催化聚苯硫醚滤料反应参数及机理
Reaction parameters and mechanism of flocculent multifunction polyphenylene sulfide filter
以N-油酰基多肽表面活化聚苯硫醚滤料,以酸性KMnO4在60~80℃操作温度下正向滴定,在氧化作用下实现活性组分氧化.实验研究了催化滤料的低温NO还原和Hg0氧化性能,并通过SEM、EDX及TPD表征手段对催化滤料物化结构进行分析.分别考察了(0.9)Mn-Ce-Fe-Co-Ox/PPS反应体系温度、气相O2浓度、初始NO浓度、氨氮比(NSR)、入口SO2浓度的最佳反应参数.结果表明,有效组分MnOx、CeOx、CoOx、Fe2O3以团絮状均匀分散在纤维表面;在反应温度170℃、O2≥5%、NO≤500×10-6、氨氮比1.0、SO2≤100 500×10-6条件下,催化滤料对NO还原及Hg0氧化效率基本达到80%左右;程序升温脱附实验Hg-TPD结果表明SO2的Hg0氧化促进作用机理于SO3与Hg0非均相反应优于SO2硫酸化反应,而NO-TPD结果则表明NO与O2在PPS表面相互作用类型以吸附态亚硝酸盐为主,吸附态NO2次之.
The in-situ generation method was proposed to prepare the catalytic functional polyphenylene sulfide (PPS) filter material. PPS would be activated with C21H40NNaO4S, and then treated in the metallic cations solution to adsorb Mn2+, Fe2+, Co2+, Ce3+ rapidly. After positive reaction with KMnO4, reactive metal oxides were produced in the PPS materials. The (0.9) Mn-Ce-Fe-Co-Ox/PPS composite filter materials were characterized by SEM, EDX and TPD. Catalytic performance in the low -temperature catalytic conversion of NO and Hg0 were then explored. The influences of reaction temperature, O2, NO, ammonia-nitrogen ratio and SO2 on the catalytic performance of catalytic PPS were investigated systematically. The results showed that MnOx, CeOx, CoOx, Fe2O3 were uniformly distributed on the PPS filter material in a flocculent structure; The catalytic PPS materials performed a synergistically NO and Hg0 removal efficiency of more than 80% in the conditions of T=170℃,O2≥5%, NO≤ 500×10-6, NSR=1.0, SO2≤100×10-6; The results of Hg-TPD desorption indicated that the mechanism of Hg0 oxidation promotion of SO2 was that the heterogeneous reaction between SO3 and Hg0 was faster than sulfation reaction of SO2, and the NO-TPD results also showed that NO mainly acted in the form of nitrite on the surface of PPS, and followed by the form of adsorbed NO2.
Hg0 / NO / TPD / 低温催化剂 / 化学氧化 / 聚苯硫醚 / 团絮状
flocculent / Hg0 / in-situ oxidation / low temperature catalyst / NO / polyphenylene sulfide / TPD
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国家重点研发计划(2016YFB0600604-02);江苏省科技成果转化专项资金(SBA2018020041)
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