Обнаружение и восстановление палладия, золота и кобальта металлов из рудника городской использующие новые Датчики / адсорбенты Места с наноразмерных Wagon колеса в форме порах

The overall goal of this method is to detect and recover metals from the urban mine using novel sensors absorbance designated with hierarchical cubic i a 3D wagon wheel shaped meso porous, and micrometric particle monoliths. This mist can help answer key question in the green environmental field, and at the same time create alternative source for the critical material in the industrial sector. The main advantage of this technique is overcoming the difficulty in recycling and reusing materials from urban mining, saving energy used in the mining process, conserving resources and reducing pollution.

The implication of this technique extend toward a sustainable use of scaled elements in industry. So this technique will not only apply to recycling, but also to develop a new extraction technique. First, add tri block copolymer onic, P 1 23 pentane and tetraethyl ortho silicate at a mass ratio of 1.6 to two to 1.2 to a 200 milliliter round bottom flask containing one molar hydrochloric acid and water.

Using a shaker thermostat, shake the mixture at 45 degrees Celsius until a homogeneous saw gel is formed. After concentrating the mixture using a rotary evaporator dry the as made monolith at 45 degrees Celsius for 24 hours to complete the drying process. Once the wagon wheel shaped monolith has been dried, calci it at 450 degrees Celsius for eight hours under normal atmospheric conditions.

Next, completely grind the calcine solid monolith by using a mortar and pestle. Store the ground material in a glass bottle for later use as a carrier platform in the fabrication of meso sensors, absorbent or MSAs. To fabricate solid meso porous sensor absorbent.

Add ethanol one five diphenyl thio carone di carboxylate, or two nitroso, one natal solutions to a round bottom flask containing the solid wagon wheel monoliths Mix for one minute to disperse the organic solution into the solid surfaces. After dispersing the one five diphenyl theo carone di carboxylate, or two nitroso, one naft all solutions into the solid monolith. Connect the flask containing this mixture to a rotary evaporator.

Evaporate the mixture at 50 degrees Celsius and at a starting pressure of 1023 Hector Pascal. To form solid MS A one or MSA three monoliths disperse one milligram of the MS A type sample in five milliliters of ethanol using an ultrasonic cleaner. When finished, add two droplets of the sample on a copper grid, perform high resolution transmission electron microscopy or H-R-T-E-M using a transmission electron microscope connected to a CCD camera.

Record the micrographs at an acceleration voltage of 200 kilovolts to obtain a lattice resolution of 0.1 nanometers. Following this pretreat the wagon wheel shaped samples at 100 degrees Celsius for eight hours under vacuum to e equate the pressure to tend to the minus three tor. Then measure the nitrogen absorption Desorption isotherms at 77 kelvin using a surface area and pore size analyzer as per the manufacturer’s instructions.

Next, measure the x-ray diffraction patterns by using an 18 kilowatt refractometer and monochromator copper K alpha radiation as per the manufacturer’s instructions record diffraction by using both a graphite monochrome and gal mirror detectors with two theta angles between 0.1 and 6.5 degrees corresponding to D spacings between 88.2 and 1.35 nanometers at this point, immerse 20 milligrams of the wagon wheel shaped MSAs in a mixture of palladium two, gold three, and cobalt two ions. Adjust the volume to 20 milliliters and the pH to two seven and 5.2 respectively using a proper acid based solution mechanically shake the mixtures in a temperature controlled water bath at 25 degrees Celsius for 45 minutes at a constant agitation speed of 300 RPM. Following this filter the MSAs through 25 millimeter filter paper after equilibration.

Use visual color assessment and reflectant spectrum measurements to determine ion concentrations that absorbed into the solid MSAs. Determine the ion concentrations by comparing the reflectance intensities of the MSAs at the appropriate lambda max during the addition of an unknown concentration of the target samples with those of standard concentration. Then conduct other experiments using target palladium two gold three and cobalt two ion concentrations at the optimum pH values of two seven and 5.2 respectively using UV vis spectroscopy.

After filtering the solid MSAs to remove the ions, analyze each filtrate by inductively coupled plasma mass spectroscopy or I-C-P-M-S. Next, determine the limits of detection of the MSAs using the following equation. Adjust the pH of extracted solution to two seven and 5.2 for the palladium two gold three and cobalt two ions respectively alter the concentrations of the interfering metal ions to less than or equal to five times greater than the concentrations of the target ions.

Then add two milliliters of a complex forming agent to the extracted solution prior to the addition of target ions to restrain actively reacting copper two ions for metal extraction from the urban mine. Dissolve the PCI board in strong acids at 90 degrees Celsius for six hours to get the metal ions in solution add 40 milligrams of the MSAs to a 150 milliliter solution containing the palladium two gold three and cobalt two ions to extract these ions into the solid MSAs. After filtering the solid MSAs, analyze the filtrate by I-C-P-M-S wagon and wheel shape pores.

Featured the cubic I A 3D structures of the MSAs as evidenced by TEM sixfold symmetric channels with different nano-sized interconnections. In wagon wheel pores are shown here. Organic moieties with potential functional active sites are strongly anchored onto the wagon wheel pores via hydrogen bonding with retention of the cubic IA 3D geometry as evidenced by the Bragg reflection planes.

The changes in reflectance intensity of the MSAs indicate metal to ligand binding events during the formation of the complexes. MSAs are effective in removing and monitoring palladium two gold three and cobalt two ions from the urban mine and lithium ion battery solutions over a wide range of concentrations and at very low metal quantities, the selectivity of the MSAs was evaluated. Significant changes in the reflectant spectra and visible color patterns were evident upon addition of one to 18 competing ions.

The reusability of the MSAs was assessed by examining the reflectant spectra of the target ion sensing capture assays and determining the uptake efficiency as a function of regeneration. Cycle results indicated that the MSA functionalities were maintained over eight regeneration cycles. One, Mr.The extraction technique.

A chemical effectively is if it is performed according to our method. While attending these procedures, it is important to remember it’s value in treating e-waste containing both hazards, materials and valuable elements. In a sense, this technique helps reduce high risk of environmental damage Forming December procedure.

A massive scale efficient, cost effective, and easy to use recovery system of metals from natural ore and e waste can be built for, for environmental protection in the industrial sector After its development. This technique paved a way for researchers in the material chemical analysis and engineering field to explore it as a power technology, not only in secondary metal sauce, but also in environmental operation. After watching this video, one should have a good understanding of how the hero VA well shaped nanomaterial can offer new approaches to chemical analysis and the recovery of metals from natural ore and industrial waste.

Don’t forget that recovering hazardous and the valuable resources from EWAS is a new venue in environmental and industrial applications.