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1.忻州师范学院化学系, 山西 忻州 034000
2.山西大学精细化学品研究中心, 山西 太原 030000
Received:23 June 2026,
Revised:2026-08-27,
Accepted:28 August 2026,
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BAN Lijun, HU Xiaobo, FEN Linyan, et al. Nitrogen-tunable carbon nitride-supported CuO for efficient formaldehyde ethynylation[J/OL]. CIESC Journal, 2026.
BAN Lijun, HU Xiaobo, FEN Linyan, et al. Nitrogen-tunable carbon nitride-supported CuO for efficient formaldehyde ethynylation[J/OL]. CIESC Journal, 2026. DOI: 10.11949/0438-1157.20260868.
甲醛乙炔化制备1
4-丁炔二醇是煤制高附加值产品生产的关键环节,可进一步延伸合成1
4-丁二醇、聚氨酯、生物降解塑料等高值化学品,在药物合成与材料科学等领域具有重要应用价值。但传统用于甲醛乙炔化合成1
4-丁炔二醇催化剂存在效率低、活性相流失严重等局限性,开发新型高效、稳定的催化剂成为研究重点。本工作聚焦可调氮的碳氮化物负载CuO纳米颗粒催化剂,探究其在甲醛乙炔化反应中的应用。结果表明,CuO/C
3
N
5.76
催化剂的催化性能要优于CuO/C
3
N
5.22
和CuO/C
3
N
6.51
催化剂,在90 ℃下实现了甲醛转化率为55.4%,1
4-丁炔二醇收率为50.1%。X射线光电子能谱(XPS)和CO
2
-程序升温脱附(CO
2
-TPD)表征发现,CuO/C
3
N
5.76
中的碱性位点含量明显高于其它催化剂,而碱性位点可吸附、活化反应物促进甲醛乙炔化反应。本工作为甲醛乙炔化反应中碱性位点结构设计和调控提供了新路径。
The formaldehyde ethynylation for the synthesis of 1
4-butynediol is a key step in the production of high value-added products from coal
which can be further extended to synthesize high-value chemicals such as 1
4-butanediol
polyurethanes
and biodegradable plastics
with important application value in pharmaceutical synthesis
materials science and other fields. However
traditional catalysts have limitations including low efficiency and severe leaching of active phases
making the development of novel
highly efficient and stable catalysts a research focus. In this work
we synthesized CuO nanoparticles supported on nitrogen-modulated carbon nitrides and systematically investigated their catalytic performance toward formaldehyde ethynylation. The results showed that the catalytic performance of the CuO/C
3
N
5.76
catalyst is superior to that of CuO/C
3
N
5.22
and CuO/C
3
N
6.51
achieving a formaldehyde conversion of 55.4% and a 1
4-butynediol yield of 50.1% at 90 °C. X-ray photoelectron spectroscopy (XPS) and CO
2
temperature-programmed desorption (CO
2
-TPD) characterizations indicated that the content of basic sites in CuO/C
3
N
5.76
is significantly higher than that in other catalysts
and these basic sites can adsorb and activate reactants to promote formaldehyde ethynylation. This work provides a new pathway for the structural design and regulation of basic sites in formaldehyde ethynylation.
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