Production of Hydroxypyruvic Acid by Glycerol Oxidation over Pt/CeO2-ZrO2-Bi2O3-PbO/SBA-16 Catalysts

Pt/CeO2-ZrO2-Bi2O3-PbO/SBA-16 (SBA-16: Santa Barbara Amorphous No. 16) catalysts were synthesized to produce hydroxypyruvic acid by glycerol oxidation. In the catalysts, the introduction of PbO into CeO2-ZrO2-Bi2O3 improved the oxygen release and storage abilities owing to the synergistic redox reaction of Pb2+/4+ and Ce3+/4+, which facilitated the oxidation ability of Pt. In addition, the oxidation of the secondary OH group in glycerol might be accelerated by the geometric effects of glycerol, Pt, and Bi3+ or Pb2+/4+. Furthermore, the moderate reaction conditions such as room temperature and open-air atmosphere enabled the suppression of further oxidation of hydroxypyruvic acid. The highest catalytic activity was obtained for 7 wt% Pt/16 wt% Ce0.60Zr0.15Bi0.20Pb0.05O2−δ/SBA-16, which provided a hydroxypyruvic acid yield maximum of 24.6%, after the reaction for 6 h at 30 °C in atmospheric air.

Chemoenzymatic synthesis of 3-ethyl-2,5-dimethylpyrazine by L-threonine 3-dehydrogenase and 2-amino-3-ketobutyrate CoA ligase/L-threonine aldolase

Pyrazines are typically formed from amino acids and sugars in chemical reactions such as the Maillard reaction. In this study, we demonstrate that 3-ethyl-2,5-dimethylpyrazine can be produced from L-Thr by a simple bacterial operon. We conclude that EDMP is synthesized chemoenzymatically from L-Thr via the condensation reaction of two molecules of aminoacetone and one molecule of acetaldehyde. Aminoacetone is supplied by L-threonine 3-dehydrogenase using L-Thr as a substrate via 2-amino-3-ketobutyrate. Acetaldehyde is supplied by 2-amino-3-ketobutyrate CoA ligase bearing threonine aldolase activity from L-Thr when CoA was at low concentrations. Considering the rate of EDMP production, the reaction intermediate is stable for a certain time, and moderate reaction temperature is important for the synthesis of EDMP. When the precursor was supplied from L-Thr by these enzymes, the yield of EDMP was increased up to 20.2%. Furthermore, we demonstrate that this reaction is useful for synthesizing various alkylpyrazines.

Histochemical Distribution of Acetylcholinesterase in the Forebrain Nuclei of an Indian Non Catfish Channa punctatus

Background: Acetylcholinesterase (AChE) is an enzyme belonging to hydrolase group which splits the acetylcholine in to choline and acetate. It is supposed to be a marker of cholinergic and cholinoceptive neurons. Acetylcholinesterase histochemisry has been done in a number of vertebrates but it is still obscure and scattered in fishes, particularly in Indian fishes. Methods: In the present study a modified histochemical technique has been employed to histochemically map the acetylcholinesterase containing neurons in the telencephalic and diencephalic nuclei of C. punctatus described by Hedreen, et al (1985).Result: Acetylchoinesterase is differentially expressed in the various prosencephalic centres and nuclei of the brain, thus its staining clearly demarcates these centres and nuclei based on varying enzyme intensity. Among the pallial nuclei of the forebrain, medial and dorsolateral nuclei showed intense enzyme activity while ventral dorsolateral nucleus and central nucleus showed moderate reaction. In contrast, most of the subpallial nuclei of the forebrain showed high intensity. Diencephalic nuclei of the forebrain exhibited mosaic pattern of enzyme distribution.

Resurgent Powers and the Failure of Conceptual Analysis

Jennifer McKitrick examines the causes moving many philosophers to pull Aristotelian powers out of history’s dustbin, the failure to reduce or eliminate dispositional ascriptions from philosophical and scientific discourses. Although many see this failure as grounds for rejecting Humeanism and return to Aristotelianism, McKitrick argues that only a more moderate reaction is warranted. She argues that restricting analysis to fundamental dispositions and adding a condition requiring the power ascription be grounded in or made true by the fact that the object possesses that fundamental disposition is the better reaction. McKitrick canvasses the main twentieth-century attempts to reduce or eliminate dispositional talk. She begins with the logical positivists’ attempt to replace dispositional talk with material conditionals. Then, after briefly considering Ryle’s version, she turns to Goodman and the move to replace material conditional analyses with stronger-than-material conditionals, such as causal implication or counterfactual conditionals backed up by natural kinds and laws of nature. Next, she turns to Lewis’s possible worlds semantics and concludes with a presentation of the ‘Simple Counterfactual Analysis’. Despite these problems with providing analyses of dispositional ascriptions in terms of counterfactuals, McKitrick recognizes that there is still an important connection between dispositions and counterfactuals. A thing’s disposition is its property of having a certain kind of counterfactual hold of it. But she advocates restricting counterfactual analyses to fundamental dispositions and powers and requiring that they be made true, or grounded by, the fact that the object has that power.

Enhanced one-pot selective conversion of cellulose to ethylene glycol over NaZSM-5 supported metal catalysts

The mesopores/micropores NaZSM-5 was synthesised by sol–gel method. The 5%Al–8%Ni–25%W/NaZSM-5 catalyst exhibited the highest cellulose conversion of 100% with EG yield as high as 89% (C mol%) at moderate reaction conditions which is highly applicable in polymer Industry.

Improved ethanol dehydration catalysis by superior acid properties of Cs-impregnated silicotungstic acid supported on silica

We herein investigate the selective dehydration of ethanol at high conversions (>99.5%) at a moderate reaction temperature of only 493 K over a catalyst of silicotungstic acid (STA) supported on...

Polyethylene upcycling to long-chain alkylaromatics by tandem hydrogenolysis/aromatization

The current scale of plastics production and the accompanying waste disposal problems represent a largely untapped opportunity for chemical upcycling. Tandem catalytic conversion by platinum supported on γ-alumina converts various polyethylene grades in high yields (up to 80 weight percent) to low-molecular-weight liquid/wax products, in the absence of added solvent or molecular hydrogen, with little production of light gases. The major components are valuable long-chain alkylaromatics and alkylnaphthenes (average ~C30, dispersity Ð = 1.1). Coupling exothermic hydrogenolysis with endothermic aromatization renders the overall transformation thermodynamically accessible despite the moderate reaction temperature of 280°C. This approach demonstrates how waste polyolefins can be a viable feedstock for the generation of molecular hydrocarbon products.

Microwave-assisted direct transformation of lignocellulose into methyl glycopyranoside in ionic liquid

Recently, conversion of lignocellulose into useful substances has attracted increasing attention. In our previous investigations, microcrystalline cellulose was successfully converted to methyl glucopyranosides (MeGlc) by the combined use of ionic liquid (IL) and microwave irradiation under moderate reaction conditions. In this study, lignocelluloses, including softwood, hardwood, and rice straw, were directly converted to methyl glycopyranosides (MG), including MeGlc, methyl mannopyranosides (MeMan), and methyl xylopyranosides (MeXyl) using acid-catalyzed methanolysis under microwave irradiation in ILs. Lignocellulose ball-milling was quite effective as a crucial process of increasing the yield of MG. Under the optimized reaction conditions, the molar yield of MeGlc reached 40% from softwood, which was a comparable yield from microcrystalline cellulose. MeXyl was also obtained in a 48% yield. These results showed that the combination of the dissolution of ball-milled lignocellulose in IL and the microwave-assisted methanolysis was an effective method of converting lignocellulose into a high-value-added substance.

Green biorefinery — the ultra-high hydrolysis rate and behavior of Populus tomentosa hemicellulose autohydrolysis under moderate subcritical water conditions

A high monosaccharide conversion rate of hemicellulose in a green solvent and under moderate reaction conditions for industrialization is one of the most important keys in a lignocellulosic biorefinery.