Constructing layer-by-layer self-assembly MoS2/C nanomaterials by a one-step hydrothermal method for catalytic hydrogenation of phenanthrene.

Layer-by-layer self-assembly MoS2/C nanomaterials are constructed through the electrostatic adsorption between MoS2 nuclei with positive charge and C nuclei with negative charge using a facile one-step hydrothermal method. The layer-by-layer self-assembly MoS2/C catalysts with high exposure of catalytic hydrogenation active sites exhibit enhanced catalytic performance in phenanthrene hydrogenation.

The Role of Slurry Reflux in a Corn Stalk Continuous Anaerobic Digestion System: Performance and Microbial Community.

Slurry reflux is a low-cost slurry reduction technology, which can solve the problem that a large amount of slurry cannot be completely consumed in a biogas plant. Anaerobic digestion (AD) of corn stalks with slurry reflux and non-reflux was compared and evaluated in continuous anaerobic digestion to clarify the effects of slurry reflux on AD with organic loading rate (OLR) variation. It was found that slurry reflux increased cumulative methane production and improved system stability. The average methane yield of the slurry reflux group was 224.19 mL/gVS, which was 41.35% higher than that of the non-reflux group. High-throughput sequencing results showed that slurry reflux increased the microbial community richness. The dominant microorganisms in the reflux group were in phylum Bacteroidetes, which have the capacity to degrade polymers, and Methanothrix, which is an aceticlastic methanogen. The relative abundances of Bacteroidetes and Methanothrix were 32.41% and 41.75%, respectively. Clostridium III and Saccharofermentans, which are related to syntrophic acetate oxidation and hydrolysis, were increased in relative abundance in the slurry reflux system. The increase of the OLR altered the main methane-producing pathway from the acetoclastic methanogenic pathway to the hydrogenotrophic methanogenic pathway in the AD system, and the slurry reflux can delay this trend. This study provided an effective way for the reduction and utilization of slurry in a biogas plant.

Highly Effective Pd/MgO/γ-Al2O3 Catalysts for CO Oxidative Coupling to Dimethyl Oxalate: The Effect of MgO Coating on γ-Al2O3.

The support of MgO/γ-Al2O3 was initially prepared by a multiple impregnation method and Pd was placed on the surface of the MgO/γ-Al2O3 support via incipient wetness impregnation. Pd/MgO/γ-Al2O3 (Pd/MAO) catalysts were systematically characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), CO2-temperature-programmed desorption (TPD), transmission electron microscopy (TEM), CO-Fourier transform infrared (CO-FTIR), and X-ray photoelectron spectroscopy (XPS) and tested in the CO oxidative coupling to dimethyl oxalate (DMO) reaction. Compared to Pd/γ-Al2O3, the catalytic activities of the Pd/MAO catalysts improved significantly. The Pd/MAO catalyst with a 30% mass ratio of Mg to γ-Al2O3 delivers 3 times higher STY of DMO than that of Pd/γ-Al2O3. It has been demonstrated that MgO covered γ-Al2O3 layer-by-layer forming MAO supports, which can increase surface basicity and the interaction between Pd particles and the MAO supports. Moreover, the relationship between metal and support interaction and catalytic performance was discussed.

Direct synthesis of shaped MgAPO-11 molecular sieves and the catalytic performance in n-dodecane hydroisomerization.

In industrial application, molecular sieves are usually used in a certain shape. This requires the addition of binder and causes the reduction of both the molecular sieve content and catalytic performance. Herein, pseudo-boemite was mixed with deionized water at room temperature, followed by the drop-wise addition of phosphoric acid, magnesium acetate solution, hydrofluoric acid, di-n-propylamine and 1-ethyl-3-methyl imidazolium bromide with vigorous stirring. The molar ratio of Al2O3 : P2O5 : MgO : HF : DPA : [EMIm]Br : H2O in the gel was 1 : 1 : 0.03 : 0.18 : 0.4 : 1 : 45. Then the gel was dried, extruded and directly crystallized to form a shaped MgAPO-11 molecular sieve. X-ray diffraction, scanning electron microscopy, N2 adsorption, ammonia temperature programmed desorption, pyridine adsorption infrared spectroscopy and nuclear magnetic resonance spectroscopy were used to investigate the physicochemical properties of the samples. X-ray diffraction, scanning electron microscopy and N2 adsorption tests show that the shaped MgAPO-11 molecular sieve is fully crystallized and possesses hierarchical porosity. Mg is incorporated into the molecular sieve framework and the Pt catalyst supported by the obtained shaped MgAPO-11 exhibits excellent catalytic performance with n-dodecane conversion of 94% and isomer selectivity of 95% at 280 °C. Such a method for the direct synthesis of shaped molecular sieves shows potential for the green synthesis of molecular sieves in industry.

Biomass-Derived Graphene-like Carbon: Efficient Metal-Free Carbocatalysts for Epoxidation.

N-doped graphene-like layered carbon (NG) could be synthesized via a metal-free pyrolysis route from glucose, fructose, and 5-hydroxymethylfurfural (5-HMF), which are cheap and widely available biomass or biomass derivatives. A well-developed thin-layer structure with large lateral dimensions could be obtained when 5-HMF was used as the precursor. More importantly, the 5-HMF-derived NG gave superior performance in epoxidation reactions compared with the conventional carbon catalysts and the performance of 5-HMF derived NG was even similar to that of a cobalt catalyst. Characterizations by TEM and XPS accompanied by EPR analysis revealed that the enhanced catalytic properties for NG arise from its high activation ability for both alkenes and O2 , which are attributed to the graphitic layered structure and graphitic N species, respectively.

Hydrothermal Carbon Enriched with Oxygenated Groups from Biomass Glucose as an Efficient Carbocatalyst.

Metal-free carbocatalysts enriched with specific oxygenated groups with different morphology and size were synthesized from glucose by hydrothermal carbonization, in which cheap and widely available biomass could be converted into functionalized carbon using an environmentally benign process. The hydroxy- and carbonyl-enriched hydrothermal carbon (HTC) could be used in nitrobenzene reduction, and higher conversion was obtained on the sphere morphology with smaller size. In the Beckmann rearrangement of cyclohexanone oxime, carboxyl-enriched HTC exhibited superior performance compared with conventional solid acid (such as HY and HZSM-5), on which the strong acid sites and weak Lewis acid sites lead to high selectivity for the side product. Although the intrinsic acidity of carbon is weak, the carboxyl-enriched carbon was used in weak Brønsted acid-catalyzed reactions, such as the Beckmann rearrangement.

One-step hydrotreatment of vegetable oil to produce high quality diesel-range alkanes.

A one-step hydrotreatment of vegetable oil combining deoxygenation and isomerization to directly produce low cloud point, high quality diesel is devised. The Pt/zeolite bifunctional catalysts prepared by using SAPO-11 and ZSM-22 zeolites as supports are used in this process. Catalytic reactions are conducted in a fixed-bed reactor under a hydrogen atmosphere. Over the bifunctional catalyst, 100 % conversion of soybean oil is obtained at 357 °C, 4 MPa, and 1 h(-1), and 80 % organic liquid yield is achieved, which is close to the maximum theoretical liquid yield. In the organic products, the alkanes selectivity is 100 % with an i-alkanes selectivity above 63 %. NH(3)-temperature programmed desorption (TPD), pyridine IR spectroscopy, and other characterization techniques are used to study the effect of the support acidity on the reaction pathway. Over the Pt/zeolite bifunctional catalyst with less strong Lewis acid sites, the reaction proceeds via the decarboxylation plus decarbonylation pathway. This one-step method provides a new strategy to produce low cloud point, high quality diesel from biomass feedstock in a more economic and attractive way.