scholarly journals Hydrothermal liquefaction of microalgae over transition metal supported TiO2 catalyst

2018 ◽  
Vol 250 ◽  
pp. 474-480 ◽  
Author(s):  
Wenjia Wang ◽  
Youtong Xu ◽  
Xiaoxiao Wang ◽  
Bokun Zhang ◽  
Wenying Tian ◽  
...  
2018 ◽  
Vol 263 ◽  
pp. 569-575 ◽  
Author(s):  
Wenying Tian ◽  
Renlong Liu ◽  
Wenjia Wang ◽  
Zhaosen Yin ◽  
Xuewen Yi

2013 ◽  
Vol 205 ◽  
pp. 111-119 ◽  
Author(s):  
Mohamad El-Roz ◽  
Philipe Bazin ◽  
Frederic Thibault-Starzyk

Food Control ◽  
2019 ◽  
Vol 100 ◽  
pp. 183-188 ◽  
Author(s):  
Shumin Sun ◽  
Ran Zhao ◽  
Yanli Xie ◽  
Yong Liu

2011 ◽  
Vol 65 (3) ◽  
Author(s):  
Cornelia Ratiu ◽  
Florica Manea ◽  
Carmen Lazau ◽  
Corina Orha ◽  
Georgeta Burtica ◽  
...  

AbstractThis paper reports the results of an investigation into enhancement of the electrochemical oxidation of p-aminophenol (4-AP) in an aqueous solution with a boron-doped diamond (BDD) electrode, assisted by photocatalysis using a zeolite-supported TiO2 (Z-TiO2) catalyst. The BDD electrode was characterised in 0.1 M Na2SO4-supporting electrolyte and the presence of 4-AP by open-circuit potential behaviour (OCP) and cyclic voltammetry (CV). The electrode behaviour was investigated in the dark and following UV irradiation and in the absence/presence of the Z-TiO2 catalyst. The electro-oxidation process was carried out using chronoamperometry (CA) and multiple-pulsed amperometry (MPA) at the selected potential under potentiostatic conditions. The electrochemical degradation process of 4-AP on the BDD electrode was improved by the application of a pulsed potential, which allowed both in-situ electrochemical cleaning of the electrode and indirect oxidation of 4-AP by oxygen evolution. The application of photocatalysis using Z-TiO2 in the 4-AP electrochemical degradation exhibited an enhanced effect when the anodic potential was set at +1.25 V vs. Ag/AgCl in the water stability region, close to the oxygen evolution potential.


2021 ◽  
Vol 545 ◽  
pp. 149017
Author(s):  
Jimmy Nelson Appaturi ◽  
R. Jothi Ramalingam ◽  
Manickam Selvaraj ◽  
Stephen Chia ◽  
Soon Huat Tan ◽  
...  

2014 ◽  
Vol 26 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Kefayat Ullah ◽  
Shu Ye ◽  
Sourav Sarkar ◽  
Lei Zhu ◽  
Ze-Da Meng ◽  
...  

Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.


Author(s):  
Michel Fialin ◽  
Guy Rémond

Oxygen-bearing minerals are generally strong insulators (e.g. silicates), or if not (e.g. transition metal oxides), they are included within a rock matrix which electrically isolates them from the sample holder contacts. In this respect, a thin carbon layer (150 Å in our laboratory) is evaporated on the sections in order to restore the conductivity. For silicates, overestimated oxygen concentrations are usually noted when transition metal oxides are used as standards. These trends corroborate the results of Bastin and Heijligers on MgO, Al2O3 and SiO2. According to our experiments, these errors are independent of the accelerating voltage used (fig.l).Owing to the low density of preexisting defects within the Al2O3 single-crystal, no significant charge buildup occurs under irradiation at low accelerating voltage (< 10keV). As a consequence, neither beam instabilities, due to electrical discharges within the excited volume, nor losses of energy for beam electrons before striking the sample, due to the presence of the electrostatic charge-induced potential, are noted : measurements from both coated and uncoated samples give comparable results which demonstrates that the carbon coating is not the cause of the observed errors.


Author(s):  
G.A. Botton ◽  
C.J. Humphreys

Transition metal aluminides are of great potential interest for high temperature structural applications. Although these materials exhibit good mechanical properties at high temperature, their use in industrial applications is often limited by their intrinsic room temperature brittleness. Whilst this particular yield behaviour is directly related to the defect structure, the properties of the defects (in particular the mobility of dislocations and the slip system on which these dislocations move) are ultimately determined by the electronic structure and bonding in these materials. The lack of ductility has been attributed, at least in part, to the mixed bonding character (metallic and covalent) as inferred from ab-initio calculations. In this work, we analyse energy loss spectra and discuss the features of the near edge structure in terms of the relevant electronic states in order to compare the predictions on bonding directly with spectroscopic experiments. In this process, we compare spectra of late transition metal (TM) to early TM aluminides (FeAl and TiAl) to assess whether differences in bonding can also be detected. This information is then discussed in terms of bonding changes at grain boundaries in NiAl.


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