CO_(2)utilization in syngas conversion to dimethyl ether and aromatics:Roles and challenges of zeolites-based catalysts

Several studies have proven a strong correlation between global warming and CO_(2)emissions.Annually,38 billion tons of CO_(2)are approximately emitted into the atmosphere.Utilizing CO_(2)via chemical conversion to clean fuels and value-added aromatics can substantially contribute to controlling the problem.Considering the thermodynamic and environmental limitations of hydrogenation of CO_(2)alone to value-added aromatics and fuels,CO_(2)utilization has currently emerged as a promising and practical approach for the production of fuels and aromatics with simultaneous utilization of both CO and CO_(2)wastes.As such,the approach is economically preferable.CO_(2)could be converted directly to fuels by the hydrogenation process or as a part of a syngas mixture.Dimethyl ether(DME)is a clean fuel with a higher energy density,which could be used as a substituent for several fuels such as diesel.In the same vein,value-added aromatics such as benzene,toluene,and xylene(BTX)can be produced from a similar process.Herein,we report a review that collects the most recent studies for the conversion of CO_(2)to DME and aromatics via zeolite-based bifunctional catalysts.We highlighted the main routes for producing DME and aromatics,as well as thoroughly discussed the conducted studies on CO_(2)hydrogenation and CO_(2)-rich syngas utilized as feedstock for conversion to DME and aromatics.The CO_(2)hydrogenation mostly occurs through the methanol-mediated reaction route but is most often limited by low selectivity and catalyst deactivation,particularly in the utilization of CO_(2)alone for the reduction reaction.The review takes an overview of the progress made so far and concluded by identifying the roles and challenges of zeolite-based catalysts for CO_(2)utilization and conversion to DME and aromatics.Accordingly,despite the incredible growth the field received in the last couple of years,however,many research challenges and opportunities associated with this process are still abounded and required to be addressed.Special attention is required for the development of approaches to block diffusion of H2O through zeolite to suppress the excess formation of CO_(2)in CO_(2)-rich syngas hydrogenation to DME and aromatics,exceed the product distribution limits,and suppress catalysts deactivation.

Irrigation of Romaine Lettuce (Lactuca sativa)Using Wastewater Treated byNon-Conventional Technologies

The aim of this study was to assess the capacity for reuse of wastewater treated in stabilisation ponds and subsequently reclaimed by means of different filtration systems at pilot scale. An analysis of filtered water showed turbidity values of below 5 NTU, a total suspended solids (TSS) content of 7 mg/l, and Escherichia coli values of up to 1.6 log CFU/100 ml. These results fall within the parameters stipulated in RD 1620/2007 Spanish Water Reuse Regulations governing the reuse of reclaimed wastewater for agricultural purposes. The water reclaimed by means of filtration systems was used to irrigate Romainelettuce (Lactuca sativa longifolia), comparing growth with that of the same variety irrigated with water from the supply network. The results showed a mean difference in lettuce growth of up to 300% in favour of the crop irrigated with reclaimed water.

Simulation of the Traweling Wave Burning Regime on Epithermal Neutrons

New results of two computer experiments on modeling of superthermal neutron-nuclear combustion of natural uranium for two different flux densities of external neutron source and duration of half a year each are presented. The simulation results demonstrate the dependence of the autowave combustion modes on the parameters of the external source.

Volatile Solid and Bury Period Influence on Odorous Material Production in Simulating Landfill Treatment

Odor pollution in landfill area has attracted more social attention in China. It is very important to control the generation of odor pollutants in situ. Analyzing odorous materials production form buried waste, simulated columns of different volatile solid (VS) content and different buried period waste were designed. Gas compounds produced from the columns were collected and analyzed by comprehensive two-dimensional gas chromatography (GC × GC) method. It has remarkable relationship between VS content and concentrations of odorous material. When VS content more than 40%, the total amount of odorous compounds increases remarkably. It can be inferred that reduced VS content of original waste may effective decreasing odorous materials production in landfill area. The old rubbish produced more odorous compounds than that of fresh one in simulated columns.

Immobilized reactor for rapid destruction of recalcitrant organics and inorganics in tannery wastewater

The wastewater discharged from tanneries lack biodegradability due to the presence of recalcitrant compounds at significant concentration. The focal theme of the present investigation was to use chemo-autotrophic activated carbon oxidation(CAACO) reactor, an immobilized cell reactor using chemoautotrophs for the treatment of tannery wastewater. The treatment scheme comprised of anaerobic treatment, sand filtration, and CAACO reactor, which remove COD, BOD, TOC, VFA and sulphides respectively by 86%, 95%, 81%, 71% and 100%. Rice bran mesoporous activated carbon prepared indigenously and was used for immobilization of chemoautotrophs. The degradation of xenobiotic compounds by CAACO was confirmed through HPLC and FT-IR techniques.

Preferential oxidation of CO in excess H_2 over CeO_2/CuO catalyst:Effect of calcination temperature

Different from the classical configuration CuO/CeO2 catalyst,the inverse configuration CeO2 /CuO catalyst (atomic ratio of Ce/Cu=10/100) was prepared by impregnation method.Five calcination temperatures were selected to investigate the interaction between CeO2 and CuO support.It is found that as calcination temperature increased from 500 to 900 C,sintering of CeO2 particles on the support occurred together with the diffusion of a portion of Ce 4+ ions into CuO crystals,forming solid solution.Formation of interface complex Ce-O-Cu was suggested by TPR measurements.The catalyst calcined at 700 C gives the highest activity for preferential oxidation of CO in excess H2 stream.

Study of reverse osmosis membranes fouling by inorganic salts and colloidal particles during seawater desalination

Fouling phenomenon is considered among the major reasons that cause significant increase of operating cost of desalination plants equipped with reverse osmosis(RO)membranes.This phenomenon is studied in the present work in the case of RO polyamide aromatic membranes using model seawater containing inorganic salts and colloidal compounds.Different solubility conditions of CaCO3 and CaSO4 were applied to study RO performances with and without colloid presence.During experiments,the membrane permeate fluxes were continuously monitored.Moreover,studies of chemical composition,structure,and morphology of the materials deposited on the membrane surface were conducted using energy dispersive microanalysis(EDS)X-ray diffraction and scanning electronic microscopy(SEM).Results show that in conditions of calcium carbonate oversaturation there is a reduction in the permeate flow of 11.2%due to fouling of the membrane by the precipitation of this compound.While in the same conditions of calcium sulphate oversaturation the reduction of the flow is 5%,so we can conclude that in conditions of oversaturation of both salts,calcium carbonate produces a greater fouling of the membrane that in its view causes greater decrease in the flow of permeate.All this based on the results of the test with both salts in oversaturated conditions.Resulting in the formation of calcite and gypsum crystals onto the membranes as XRD analyses stated.Additional presence of colloidal silica in those conditions intensifies strongly the fouling,leading until to 24.1%of permeate flux decrease.

Preferential oxidation of CO in excess H_2 over the CeO_2/CuO catalyst: Effect of initial support

Three series of CeO2/CuO samples were prepared by impregnation method and characterized by XRD, N2adsorption-desorption, temperatureprogrammed reduction(TPR), XPS and TEM techniques. In comparison with the samples prepared with CuO as initial support, the samples with Cu(OH)2as initial support have higher reducibilities and smaller relative TPR peak areas, and also larger specific surface areas at calcination temperatures of 400℃–600℃. As a result, Cu(OH)2is better than CuO as initial support for preferential oxidation of CO in excess H2(CO-PROX). The best catalytic performance was achieved on the sample calcined at 600℃ and with an atomic ratio of Ce/Cu at 40%. XPS analyses indicate that more interface linkages Ce-O-Cu could be formed when it was calcined at 600℃. And the atomic ratio of Ce/Cu at 40%led to a proper reducibility for the sample as illustrated by the TPR measurements.

Numerical Study of Flow and Gas Diffusion in the Near-Wake behind an Isolated Building

To assist validation of the experimental data of urban pollution dispersion,the effect of an isolated building on the flow and gaseous diffusion in the wake region have been investigated numerically in the neutrally stratified rough-walled turbulent boundary layer.Numerical studies were carried out using Computational Fluid Dynamics(CFD)models.The CFD models used for the simulation were based on the steady-state Reynolds-Average Navier-Stoke equations(RANS)withκ-εturbulence models;standardκ-ε and RNGκ-εmodels.Inlet conditions and boundary conditions were specified numerically to the best information available for each fluid modeling simulation.A gas pollutant was emitted from a point source within the recirculation cavity behind the building model.The accuracy of these simulations was examined by comparing the predicted results with wind tunnel experimental data.It was confirmed that simulation using the model accurately reproduces the velocity and concentration diffusion fields with a fine-mish resolution in the near wake region.Results indicated that there is a good agreement between the numerical simulation and the wind tunnel experiment for both wind flow and concentration diffusion.The results of this work can help to improve the understanding of mechanisms of and simulation of pollutant transport in an urban environment.

Controllable fabrication of carbon aerogels

Nano-pore carbon aerogels were prepared by the sol-gel polymerization of resorcinol (1,3-dihydroxybenzene)(C6H4(OH)2) with formaldehyde (HCHO) in a slightly basic aqueous solution, followed by super-critical drying under liquid carbon dioxide as super-critical media and carbonization at 700 ℃ under N2 gas atmosphere. The key of the work is to fabricate carbon aerogels with controllable nano-pore structure, which means extremely high surface area and sharp pore size distribution. Aiming to investigate the effects of preparation conditions on the gelation process, the bulk density, and the physical and chemical structure of the resultant carbon aerogels, the molar ratio of R/C (resorcinol to catalyst) and the amount of distilled water were varied, consequently two different sets of samples, with series of R/C ratio and RF/W (Resorcinol-Formaldehyde to water, or the content of reactant) ratio, were prepared. The result of N2 adsorption/desorption experiment at 77 K shows that the pore sizes decreasing from 11.4 down to 2.2 nm with the increasing of the molar ratio of R/C from 100 to 400, and/or, the pore sizes decreasing from 3.8 down to 1.6 nm with the increasing of reactant content from 0.4 to 0.6.

Sorption of biodegradation end products of nonylphenol polyethoxylates onto activated sludge

Nonylphenol(NP), nonylphenoxy acetic acid(NP1EC), nonylphenol monoethoxy acetic acid(NP2EC), nonylphenol monoethoxylate(NP1EO) and nonylphenol diethoxylate(NP2EO) are biodegradation end products(BEPs) of nonionic surfactant nonylphenolpolyethoxylates (NPnEO). In this research, sorption of these compounds onto model activated sludge was characterized. Sorption equilibrium experiments showed that NP, NP1EO and NP2EO reached equilibrium in about 12 h, while equilibrium of NP1EC and NP2EC were reached earlier, in about 4 h. In sorption isotherm experiments, obtained equilibrium data at 28℃ fitted well to Freundlich sorption model for all investigated compounds. For NP1EC, in addition to Freundlich, equilibrium data also fitted well to Langmuir model. Linear sorption model was also tried, and equilibrium data of all NP, NP1EO, NP2EO and NP2EC except NP1EC fitted well to this model. Calculated Freundlich coefficient(K F) and linear sorption coefficient(K D) showed that sorption capacity of the investigated compounds were in order NP>NP2EO>NP1EO>NP1EC≈NP2EC. For NP, NP1EO and NP2EO, high values of calculated K F and K D indicated an easy uptake of these compounds from aqueous phase onto activated sludge. Whereas, NP1EC and NP2EC with low values of K F and K D absorbed weakly to activated sludge and tended to preferably remain in aqueous phase.

Effect of Arbuscular Mycorrhizal (AM) Fungi on the Physiological Performance of Phaseolus vulgaris Grown under Crude Oil Contaminated Soil

An experiment was conducted to assess the influence of arbuscular mycorrhizal (AM) fungi on the performance of Phaseolus vulgaris under crude oil contaminated soil. P. vulgaris was grown on soil under 2%, 4% and 8% (v/w) crude oil contamination. The experimental units were biostimulated with 2 g NPK fertilizer pot-1 and were inoculated with 12 g AM inoculum pot-1. Non inoculated pots served as control. The results showed that AM inoculated pots recorded higher and significantly (P < 0.05) different dry matter yields and chlorophyll content than non AM inoculated pots. Residual total petroleum hydrocarbon (TPH) increased as percent crude oil contamination increased. Total petroleum hydrocarbon decomposition and removal was higher on pots inoculated with AM than non inoculated pots. With AM colonization, physiological characteristics of P. vulgaris and TPH decomposition improved. This is evinced by the linear regression analysis between colonization and TPH (R2 = 0.77).

Evaluation of Carbon Sequestration Potential of Soils―What Is Missing?

It is no doubt that soils are among the Earth’s largest terrestrial reservoirs of carbon pool and hold potential for its sequestration and thus, soils can serve as potential way of mitigating the ever-increasing atmospheric CO2 concentration. However, the stability and flux of soil organic carbon are affected in response to changes that are being driven by forms of environmental and anthropogenic factors. Therefore, to establish carbon sequestration potential of soils, an in-depth scientific evaluation that would provide mapping of and speciation of carbon chemical forms, as well as factors influencing the persistence of carbon in soils are key to the process which are beyond quantitative measurements that are conventionally implemented under different land use and/or soil management. This involves soil chemistry, physics, biology, and microbiology. Hence, this short review communication highlights portions of soil chemistry and physics as well as soil biology and microbiology that have not been given attention in determining and/or underpinning decisions on carbon sequestration potential of soils.

Effect of Fe_(3)O_(4) nanoparticles on magnetic xerogel composites for enhanced removal of fluoride and arsenic from aqueous solution

Fe_(3)O_(4)magnetic xerogel composites were prepared by polycondensation of resorcinol(R)-formaldehyde reaction via a sol-gel process in an aqueous solution through varying the molar ratio of Fe_(3)O_(4)nanoparticles(MNPs),catalyst(C),and water(W)content.MNPs were obtained by co-precipitation(MC),oxidation of iron salts(MO),or solvothermal synthesis(MS).Both MNPs and magnetic xerogels were examined regarding the performance of arsenic and fluoride removal in a batch system.The MC-based MNPs had higher adsorption capacities for both fluoride(202.9 mg/g)and arsenic(3.2 mg/g)than other MNPs in optimum conditions.The X-ray diffraction,Fourier transform infrared spectroscopy,and energy-dispersive X-ray spectroscopy confirmed that Fe was composed into the polymeric matrix of magnetic xerogels that contained 0.59%-4.42%of Fe with a molar ratio of MNPs(M)to R between 0.01 and 0.10.With low R/C and optimum M/R ratios,an increase in the surface area of magnetic xerogels affected the fluoride and arsenic adsorption capacities.The magnetic xerogel composites with the MC-based MNPs prepared at a fixed R/C ratio(100)and at different R/W(0.05-0.06)and M/R(0.07-0.10)ratios had a high arsenic removal efficiency of 100%at an As(V)concentration of 0.1 mg/L and pH of 3.0.The maximum adsorption capacities of magnetic xerogels were approximately five times higher than those of the xerogels without MNP composites.Therefore,Fe_(3)O_(4)nanoparticles enhanced the adsorption of arsenate and fluoride.The variations of alkaline catalyst and water content significantly affected the resulting properties of textural and surface chemistry of magnetic xerogel composites.

Investigating Temperature and Nutrients as Drivers of Primary Productivity in Aquatic Environment

An investigation into the relationship between temperature and the nutrients (,, and ) in pelagial primary productivity of the middle reaches of Otamiri River in Owerri, Southeastern Nigeria was carried out between October and November, 2018 at ten sampling points (OTP 1-OTP 10). The estimation of productivity was made with the light and dark bottle technique. Maximum yields in Gross Primary Productivity (GPP) (0.8738 mgCL-1d-1), Net Primary Productivity (NPP) (0.8513 mgCL-1d-1), as well as Community Respiration (CR) (0.1613 mgCL-1d-1) were recorded at OTP 3, OTP 3 and OTP 8 respectively that had more vegetation covers than in segments without cover. GPP is correlated withions (r = 0.400),ions (r = 0.418), and water temperature (r = 0.379) (p 0.05), while CR is correlated with ions (r = 0.500) (p 0.01). The variability of GPP increased mildly with increasing temperature and the nutrients;with predicted regression model productivities of 0.1388, 0.5621, and 0.6066 mgCL-1d-1, corresponding with mean values of 28.41℃, 0.33 mg/L, 1.04 mg/L and 10.25 mg/L recorded for temperature,,, and ions concentrations. Mean GPP was estimated to result in a comparatively low annual productivity of 188.75 mgCL-1yr-1. Conservation and restoration of riparian vegetation covers in watershed corridors of the river for optimal driver roles were recommended.