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Unit Operations Of Chemical Engineering

This review highlights recent developments in the synthesis of nanosized zeolites. The strategies available for their preparation (organic-template assisted, organic-template free, and alternative procedures) are discussed. Major breakthroughs achieved by the so-called zeolite crystal engineering and encompass items such as mastering and using the physicochemical properties of the precursor synthesis gel/suspension, optimizing the use of silicon and aluminium precursor sources, the rational use of organic templates and structure-directing inorganic cations, and careful adjustment of synthesis conditions (temperature, pressure, time, heating processes from conventional to microwave and sonication) are addressed. An on-going broad and deep fundamental understanding of the crystallization process, explaining the influence of all variables of this complex set of reactions, underpins an even more rational design of nanosized zeolites with exceptional properties. Finally, the advantages and limitations of these methods are addressed with particular attention to their industrial prospects and utilization in existing and advanced applications.

Advances in nanosized zeolites

Popularity of graphene oxide (GO) became ballistic in the last few years – in short, it almost seems that now everyone wants to work with graphene. However, as the number of electrochemical papers about graphene grows, so is the amount of misinterpretations. Our work was mostly focused on preparation of GO and its electrochemical properties, namely catalysis. Our results show, that chemical preparation of GO by strong oxidation is very tricky. Several approaches were tested, such as different sizes of graphite particles, oxidation mixtures, even repetitive preparations under the same conditions usually resulted in different products. Another big topic are impurities which are present due to natural occurrence in graphite and some of them might be also introduced during purification processes of GO. This could also lead to often observed catalytic activity of graphene. From our observations neither selectivity nor significant electrocatalytic abilities of the reduced graphene oxide modified electrodes towards H2O2 were observed. Moreover, our results suggest that GO does not need linking molecules in order to be deposited onto the surface of the electrodes, since it attaches spontaneously and keeps its electrochemical properties. Graphene is usually reported as a superior material, but its proper description and characterization should not be underestimated.

About graphene oxide

The subject of thermal transport at the mesoscopic scale and in low-dimensional systems is interesting for both fundamental research and practical applications. As the first example of truly two-dimensional materials, graphene has exceptionally high thermal conductivity, and thus provides an ideal platform for the research. Here we review recent studies on thermal and thermoelectric properties of graphene, with an emphasis on experimental progresses. A general physical picture based on the Landauer transport formalism is introduced to understand underlying mechanisms. We show that the superior thermal conductivity of graphene is contributed not only by large ballistic thermal conductance but also by very long phonon mean free path (MFP). The long phonon MFP, explained by the low-dimensional nature and high sample purity of graphene, results in important isotope effects and size effects on thermal conduction. In terms of various scattering mechanisms in graphene, several approaches are suggested to control thermal conductivity. Among them, introducing rough boundaries and weakly-coupled interfaces are promising ways to suppress thermal conduction effectively. We also discuss the Seebeck effect of graphene. Graphene itself might not be a good thermoelectric material. However, the concepts developed by graphene research might be applied to improve thermoelectric performance of other materials.

Thermal and Thermoelectric Properties of Graphene

Experimental optimization of engine performance of a dual-fuel compression-ignition engine operating on hydrogen-compressed natural gas and Moringa biodiesel

Effects of oxy-acetylation on performance, combustion and emission characteristics of Botryococcus braunii microalgae biodiesel-fuelled CI engines

Application of artificial intelligence in predicting the dynamics of bottom hole pressure for under-balanced drilling: Extra tree compared with feed forward neural network model

Optimization of natural gas treatment for the removal of CO2 and H2S in a novel alkaline-DEA hybrid scrubber

This study investigates the toxicological effects of heavy metals on lithofacies of the subsurface in a drilled hydrocarbon well as well as, to the drilling crew and people in an environment. The pollution levels of selected heavy metals were considered alongside their ecological effects during dry and wet seasons. The health hazard potential of human exposures to the metals, were estimated in terms of intensity and time using the USEPA recommended model. The heavy metal concentration for each layer decreased across the lithofacies as follows; Layer 5> Layer 4> Layer 3> Layer 2> Layer 1. The average concentrations of the heavy metals present in the samples obtained from the formation zone, varied significantly and decreased in the order of Al> Zn> Ni> Pb> Cr> Cu> Cd> As> Hg. The highest concentration of Al, Cu, and Zn in this present study were within the maximum allowable limits whereas, those of As, Cd, Hg and Ni were all above their maximum allowable limits. Among the transition metals analysed, the maximum mean daily dose of Pb (9.18 × 10−6 mg/kg/d) and Cr (1.42 × 10−6 mg/kg/d) were confirmed susceptible to human carcinogens and environmental toxins. The estimated hazard quotient shows that the dermal pathway is the most likely route via which the drilling crew and people in the environment can get contaminated. The cancer risk values for the Pb (7.72 × 10−4), Cd (1.35 × 10−1), Ni (9.97 × 10−3), As (1.50 × 10−1) and Cr (3.16 × 10−3) are all above the acceptable values. The cancer risk contribution for each metal was in the order of As> Cd> Ni> Cr> Pb. Layer 5 had the maximum Geo-accumulation index for the heavy metals considered. This higher Geo-accumulation index noted at the depth in Layer 5 may be attributed to the effect of water basin with turbidity currents, deltas, and shallow marine sediment deposits with storm impacted conditions. Also, the pollution from lead (Pb) in the dry season was maximum with an Igeo value> 5 for all the lithofacies considered because of the low background concentration of the metal. During the wet season, the heavy metal pollution rate was moderate for Zn whereas, it was extremely polluted with respect to Pb. The ecological risk potential of Pb shows that the associated ecological risks range from 536 – 664 in the wet season (i.e. extremely strong) and 2810 – 3480 in dry season (extremely strong). The high level of Pb pollution found in the area at such shallow depth may be due to the sedimentary folds possibly caused by the full spectrum of metamorphic rocks and primary flow structures at shallow depths. This was used to identify the environmental sensitivities of the heavy metals during the dry and wet seasons.

Samuel Eshorame Sanni

Papers

Experimental optimization of engine performance of a dual-fuel compression-ignition engine operating on hydrogen-compressed natural gas and Moringa biodiesel

Effects of oxy-acetylation on performance, combustion and emission characteristics of Botryococcus braunii microalgae biodiesel-fuelled CI engines

Application of artificial intelligence in predicting the dynamics of bottom hole pressure for under-balanced drilling: Extra tree compared with feed forward neural network model

Optimization of natural gas treatment for the removal of CO2 and H2S in a novel alkaline-DEA hybrid scrubber

Toxicology of Heavy Metals to Subsurface Lithofacies and Drillers during Drilling of Hydrocarbon Wells