One-Step Synthesis of Lemonile from Citral by Liquid Phase Catalytic Ammoxidation

2013 ◽  
Vol 641-642 ◽  
pp. 959-961
Author(s):  
Ye Wang ◽  
Shao Feng Pi ◽  
Jin Hua Zhou ◽  
Hai Li Gao ◽  
Ji Lie Li ◽  
...  

Lemonile is a new kind of spice. The new technology for synthesis of lemonile from citral by catalytic ammoxidation has been investigated. Experimental results showed the optimal synthetic conditions are as follows. The molar material ratio n(H2O2):n(Citral) is 3:1, solvent for the reaction is isopropanol, dosage of the catalyst CuCl is 3% (wt, calculated by citral), the drop-feeding temperature and time for hydrogen peroxide are 10 °C-14 °C and 3 hrs, respectively; after hydrogen peroxide being drop-fed into the reaction system, the reaction should be continued for 4 hrs. Lemonile yield is 91.2% and purity is 98.5% (detected by GC) under the optimal conditions. This new one-step liquid phase catalytic ammoxidation technology is a green synthesis way for lemonile. The structure of the product has been confirmed by GC-MS.

BioResources ◽  
2019 ◽  
Vol 14 (3) ◽  
pp. 5025-5044 ◽  
Author(s):  
Tao Yang ◽  
Wenzhi Li ◽  
Qinchuan Liu ◽  
Mingxue Su ◽  
Tingwei Zhang ◽  
...  

A one-step, liquid-phase hydrogen peroxide reaction system, which was heterogeneously catalyzed by KBr-doped graphitic carbon nitride (KBr/g-C3N4), was developed for the conversion of furfural to maleic acid (MA). At first, a 68.0% MA yield was achieved in a homogeneous reaction system catalyzed by KBr-KOH. Next, a series of K-doped g-C3N4 catalysts with various potassium salts (KBr, KCl, KNO3, and KOH) was synthesized and tested for the conversion of furfural to MA, 2-buten-1,4-olide (FRO), and succinic acid (SA). When comparing the various K-doped g-C3N4 catalysts, KBr/g-C3N4 enhanced MA selectivity, which resulted in complete furfural conversion and a 70.4% MA yield (at 100 °C for 180 min). Furthermore, a synergistic interaction was observed between KBr and the g-C3N4 support, which could explain why KBr/g-C3N4 had the highest MA selectivity.


RSC Advances ◽  
2015 ◽  
Vol 5 (116) ◽  
pp. 95744-95749 ◽  
Author(s):  
Jiangling He ◽  
Bingfu Lei ◽  
Haoran Zhang ◽  
Mingtao Zheng ◽  
Hanwu Dong ◽  
...  

The strategy for the formation mechanism of N-CDs under high temperature and high pressure can be summarized as consisting of two parts including top-down and bottom-up. It can serve as an efficient way to express the detailed formation process of N-CDs.


2015 ◽  
Vol 49 (5) ◽  
pp. 837-840 ◽  
Author(s):  
Sze Shin Low ◽  
Michelle T.T. Tan ◽  
Poi Sim Khiew ...

2015 ◽  
Vol 19 (0) ◽  
pp. 55-58
Author(s):  
Zhen-xue Liu ◽  
◽  
Zhong-xue Gan ◽  
Jun-jie Gu ◽  
Qing-feng Song

1987 ◽  
Vol 19 (12) ◽  
pp. 79-83
Author(s):  
K. Bartoszewski ◽  
A. Bilyk

Rettery wastewaters were treated in anaerobic and aerobic ponds. Anaerobic treatment yielded efficiencies of BOD5 and COD removal as low as 20%. The treatment process conducted under aerobic conditions in aerated and stabilizing ponds arranged in series took from 18 to 20 days and gave efficiencies of BOD5 and COD removal amounting to 90%. The experimental results were interpreted by virtue of the Eckenfelder equation. Excess activated sludge was subjected to aerobic stabilization in a separate tank. A new technology was suggested for the existing obsolete industrial treatment plant.


Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 283
Author(s):  
Oxana Kholdeeva ◽  
Nataliya Maksimchuk

In recent years, metal–organic frameworks (MOFs) have received increasing attention as selective oxidation catalysts and supports for their construction. In this short review paper, we survey recent findings concerning use of MOFs in heterogeneous liquid-phase selective oxidation catalysis with the green oxidant–aqueous hydrogen peroxide. MOFs having outstanding thermal and chemical stability, such as Cr(III)-based MIL-101, Ti(IV)-based MIL-125, Zr(IV)-based UiO-66(67), Zn(II)-based ZIF-8, and some others, will be in the main focus of this work. The effects of the metal nature and MOF structure on catalytic activity and oxidation selectivity are analyzed and the mechanisms of hydrogen peroxide activation are discussed. In some cases, we also make an attempt to analyze relationships between liquid-phase adsorption properties of MOFs and peculiarities of their catalytic performance. Attempts of using MOFs as supports for construction of single-site catalysts through their modification with heterometals will be also addressed in relation to the use of such catalysts for activation of H2O2. Special attention is given to the critical issues of catalyst stability and reusability. The scope and limitations of MOF catalysts in H2O2-based selective oxidation are discussed.


Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3844
Author(s):  
Lijuan Li ◽  
Bingdong Li ◽  
Liwei Feng ◽  
Xiaoqiu Zhang ◽  
Yuqian Zhang ◽  
...  

In this work, Au-modified F-TiO2 is developed as a simple and efficient photocatalyst for H2O2 production under ultraviolet light. The Au/F-TiO2 photocatalyst avoids the necessity of adding fluoride into the reaction medium for enhancing H2O2 synthesis, as in a pure TiO2 reaction system. The F− modification inhibits the H2O2 decomposition through the formation of the ≡Ti–F complex. Au is an active cocatalyst for photocatalytic H2O2 production. We compared the activity of TiO2 with F− modification and without F− modification in the presence of Au, and found that the H2O2 production rate over Au/F-TiO2 reaches four times that of Au/TiO2. In situ electron spin resonance studies have shown that H2O2 is produced by stepwise single-electron oxygen reduction on the Au/F-TiO2 photocatalyst.


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