Construction of Cu-BTC by carboxylic acid organic ligand and its application in low temperature SCR denitration
Shu Hao1, Liu Yuling1, Jia Yang1
1Institute of Water Resources and Hydro-electric Engineering, Xi'an University of Technology, Xi'an 710048, China.
Abstract:
The removal of NO has always been a hot issue in the treatment of coal-fired flue gas. In this paper, a hydrothermal synthesis method was used to prepare porous denitration catalysts with polycarboxyl organic isomers (trimellitic acid, phthalic acid, and benzoic acid). And then developed as the NO removing catalysts for low temperature selective catalytic reduction (SCR) with NH3. XRD, BET, SEM, FTIR, XPS, Raman, H2-TPR, NH3-TPD and TG were used to analyze the crystallinity, microscopic morphology, surface functional groups and metal content. The results showed that: (1) From the crystal structure analysis, the catalyst prepared with 1,3,5 and 1,2,4-benzenetricarboxylic acid as ligands (1,3,5-A and 1,2,4-B) was Cu-BTC. (2) 1,3,5-A catalyst had a huge specific surface area, up to 1421.32 m2/g, and a pore volume up to 0.5798 cm3/g. (3) The prepared catalysts were applied to NH3-SCR denitration, and the catalyst with Cu-BTC structure had relatively high catalytic performance, and the overall catalytic capacity showed an increasing trend with the temperature. (4) 1,3,5-A catalyst had stability and catalytic activity. When the temperature was 270 °C, the denitration efficiency reached 83.87%. And within 8 h, the denitration efficiency was stable up to 82%.
Related Concept Videos
Acid Halides to Ketones: Gilman Reagent
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
Extraction: Advanced Methods
Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids
Reducing carboxylic acid derivatives like acyl chlorides (RCOCl), esters (RCO2R′), and nitriles (RCN) using milder aluminum hydride agents like lithium tri-tert-butoxyaluminum hydride [LiAlH(O-t-Bu)3] and diisobutylaluminum hydride [DIBAL-H]...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Preparation of Carboxylic Acids: Hydrolysis of Nitriles
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...


