The application of Py-GC/MS for the catalytic upgrading of oil separated from summer food waste leachate

The catalytic cracking of oil fractions separated from summer food waste leachate was investigated over BEA zeolite and Al-SBA-15 catalysts. In this study, a mixture of food waste oil fractions and catalyst was directly introduced to pyrolysis gas chromatography/mass spectrometry (Py-GC/MS), with the resulting vapor phase products being simultaneously analyzed. Various acid compounds, including oleic acid, produced by the non-catalytic pyrolysis of food waste leachate were reformed into valuable compounds, such as oxygenates, hydrocarbons, and aromatics. The BEA zeolite catalyst showed higher selectivity for hydrocarbon compounds, especially aromatics, within the gasoline range due to its superior cracking ability originating from its highly acidic sites. Conversely, the cracking performance of the Al-SBA-15 catalyst, possessing mild acidic sites, was lower than that of the BEA zeolite. Increasing the amount of Al-SBA-15 catalyst enhanced the cracking activity and resulted in higher selectivity for hydrocarbons.     

Multiresidue analysis of pesticides with hydrolyzable functionality in cooked vegetables by liquid chromatography tandem mass spectrometry

It would be preferable for pesticide residues substituted by hydrolyzable functionality to be analyzed after cooking because their structures are apt to degrade during boiling and/or heating. A liquid chromatography–tandem mass spectrometry (LC‐MS/MS) method for the quantitative determination of 44 pesticide residues with hydrolyzable functional group in five typical vegetable widely consumed in Republic of Korea is described. The sample clean‐up was carried out according to the method of Food Code No. 83 established by the Korea Food and Drug Administration (KFDA). Zorbox XDB‐C₁₈ column was selected for the analysis because of the best peak separation. The LC mobile phase consisted of water and 5 mm methanolic ammonium formate, which resulted in a peak shape with good symmetry at each run. Tandem mass spectroscopic (MS/MS) experiments were performed in ESI positive mode and the multiple reaction monitoring modes. A conventional matrix effect was modified to more comprehensive form 100γ_ij (%). A high matrix effect (相似文献   

Fast and low error color encrypted computer-generated hologram based on amplitude-phase modulation with a random mask for an identification tag application

A new APM computer-generated hologram algorithm for minimizing DC components and more effective data recovery is presented for the purpose of an ID tag application. In this method, a technique of randomization of the input data is introduced prior to the Fourier transform. As a result, DC components are localized at the center region, which is only 1 data cell, regardless of input data. The size of the tag pattern is reduced 2.25 times using a color encryption technique. Our experimental result through the image captured by a camera also shows that approximately 50% damaged APM-CGH tags can be reconstructed at a low error rate of about 1.8%.     

2‐[(Diphenylphosphino)methyl]pyridine as ligand for iron‐based atom transfer radical polymerization

2‐[(Diphenylphosphino)methyl]pyridine (DPPMP) was successfully used as a bidentate ligand in the iron‐mediated atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) with various initiators and solvents. The effect of the catalytic system on ATRP was studied systematically. Most of the polymerizations with DPPMP ligand were well controlled with a linear increase in the number‐average molecular weights (M_n) versus conversion and relatively low molecular weight distributions (M_w/M_n = 1.10–1.3) being observed throughout the reactions, and the measured molecular weights matched the predicted values. Initially added iron(III) bromide improved the controllability of the polymerization reactions in terms of molecular weight control. The ratio of ligand to metal influenced the controllability of ATRP system, and the optimum ratio was found to be 2:1. It was shown that ATRP of MMA with FeX₂/DPPMP catalytic system (X = Cl, Br) initiated by 2‐bromopropionitrile (BPN) was controlled more effectively in toluene than in polar solvents. The rate of polymerization increased with increasing the polymerization temperature and the apparent activation energy was calculated to be 56.7 KJ mol^?1. In addition, reverse ATRP of MMA was able to be successfully carried out using AIBN in toluene at 80 °C. Polymerization of styrene (St) was found to be controlled well by using the PEBr/FeBr₂/DPPMP system in DMF at 110 °C. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2922–2935, 2008     

Application of a new projection technique to the 2D Heisenberg Hamiltonian

A recently developed new form of projection technique is applied to the computation of the ground-state energyE ₀ of the antiferromagnetic Heisenberg Hamiltonian on a square lattice, demonstrating its usufulness. The calculations are done analytically and do neither require the use of time-dependent operators nor Wick's theorem. A value ofE ₀=–2NJ0.3337 is found whereN is the number of sites in good agreement with series expansions.     

Quasi-persistent photocurrent in the UV-irradiated MEH-PPV conjugated polymer

We report the quasi-persistent photocurrent in the MEH-PPV conjugated polymer, induced by UV-irradiation in air. It is attributed to the irradiation-induced defects, which also act to accelerate its decay.     

Palladium-Catalyzed Regioselective Synthesis of 3-Arylindoles from N-Ts-Anilines and Styrenes

A Pd-catalyzed intermolecular oxidative annulation between N-Ts-anilines and styrenes was developed. This method offers a straightforward and robust approach to a wide range of 3-arylindoles using readily available starting materials with good functional-group tolerance and high regioselectivity and efficiency. Further elaboration of the products obtained from this process provided access to highly functionalized and structurally diverse indoles, for example, 3-(indol-3-yl)carbazoles, 1,9-dihydropyrrolo-[2,3-b]carbazoles, and 3′-aryl-3,5′-biindoles.     

Preparation of silica/perfluoroalkyl methacrylate polymer inorganic/organic particles in supercritical carbon dioxide

Silica/perfluoroalkyl methacrylate polymer (PHDFDMA) particles were prepared using various types of silica by polymerization in supercritical carbon dioxide. There are three steps in the fabrication of inorganic/organic hybrid composites: silane treatment, polymerization, and soxhlet extraction. After these steps, we observed the morphology of silica/PHDFDMA particles using field emission scanning electron microscope and transmission electron microscope. From these analyses, we can confirm that the silica/PHDFDMA core/shell particles were obtained when we used Ludox and silica gel as a silica template. On the other hand, core/shell particles were not formed when using fused silica and precipitated silica. In addition, to confirm the amount of polymer on silica, we performed an analysis using thermogravimetric analysis and electron probe micro-analyzer. In this case, PHDFDMA was approximately 20 wt.% on the silica gel and 40 wt.% on the Ludox, respectively. When using fused silica and precipitated silica as a template, amount of PHDFDMA on silica was maximum 5 wt.% and over 40 wt.%, respectively. From these results, to obtain enough PHDFDMA encapsulated silica particle, colloidal silica, Ludox is the best template in four different types of silica.