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The synthesis of carbon-halloysite nanocomposites was carried out using aqueous sucrose solutions as a carbon precursor. Raw and calcined halloysite with different grain size classes were used as a carbon support. The influence of halloysite grain size and the calcination process on the carbon concentration in the composites and their adsorption characteristics towards the separation of naproxen from aqueous solutions was identified experimentally. The kinetic conditions of the process (pseudo-second-order kinetic model) indicate a favorable increase in the number of active sites formed after the deposition of the carbon layer on the surface of halloysite particles. Validation of the Langmuir multi-center isotherm adsorption model indicates a separation mechanism associated with the occurrence of multiple active centers on the nanocomposite adsorbent surface and the effect of separation without dissociation of naproxen particles. The obtained carbon-halloysite nanocomposite, due to the relatively cheap and simple, environmentally friendly production methodology and the required inexpensive raw materials, can be widely used in effective and common, economical treatment of wastewater streams from naproxen. The observed naproxen separation process effects are significant.

A new, innovative approach in the search for an effective and cheap carbon dioxide sorbent, in line with the circular economy and sustainable development principles, directs the attention of researchers to various types of waste ashes generated as a result of biomass combustion. In addition to the use of environmentally safe materials that have been experimentally identified, and that, in some way, have adjustable sorption capacity, it is also possible to rationally develop a widely applicable, simple, and inexpensive technology based on large amounts of this type of post-industrial waste, which is also an equally important issue for the natural environment (reducing the need for ash storage and accumulation). Even the lower sorption capacity can be successfully compensated for by their common availability and very low cost. Thus, the CO2 adsorption capability of the ashes from the combustion of straw biomass was experimentally investigated with the use of a high-pressure adsorption stand. The presented original technological concept has been positively verified on a laboratory scale, thus a functionalization-based approach to the combustion of substrate mixtures with nano-structural additives (raw, dried, calcined halloysite, kaolinite), introduced to improve the performance of straw biomass combustion and bottom ash formation in power boilers, clearly increased the CO2 adsorption capacity of the modified ashes. This allows for an advantageous synergy effect in the extra side-production of useful adsorbents in the closed-loop “cascade” scheme of the CE process. The addition of 4 wt.% kaolinite to straw biomass caused an over 2.5-fold increase in the CO2 adsorption capacity in relation to ash from the combustion of pure straw biomass (with a CO2 adsorption capacity of 0.132 mmol/g). In the case of addition of 4 wt.% nano-structured species to the straw combustion process, the best effects (ash adsorption capacity) were obtained in the following order: kaolinite (0.321 mmol/g), raw halloysite (0.310 mmol/g), calcined halloysite (0.298 mmol/g), and dried halloysite (0.288 mmol/g). Increasing the dose (in relation to all four tested substances) of the straw biomass additive from 2 to 4 wt.%, not only increase the adsorption capacity of the obtained ash, thus enriched with nano-structural additives, but also a showed a significant reduction in the differences between the maximum adsorption capacity of each ash is observed. The experimental results were analyzed using five models of adsorption isotherms: Freundlich, Langmuir, Jovanović, Temkin, and Hill. Moreover, selected samples of each ash were subjected to porosimetry tests and identification of the surface morphology (SEM). The obtained results can be used in the design of PSA processes or as permanent CO2 adsorbents, based on the environmentally beneficial option of using ashes from biomass combustion with appropriately selected additives.

Post-recycling sodium polyacrylate (SPA) derived from the selective recycling of personal hygiene products was tested as a potential key component of soil modifiers. Recycled SPA in combination with layered aluminosilicate (halloysite) with the sorption capacity of fertilizers allows for the creation of a fully functional, original system responsible for both water retention in soil and controlled dosing of fertilizers. The use of post-recycling SPA (possibly partially supplemented with virgin SPA) is advantageous for the natural environment. The results of different water types retention in post-recycling SPA (deionized water, rainwater, tap water) are discussed. The most beneficial effects of R-SPA swelling and water accumulation are achieved when it comes into contact with rainwater. The clear impact of Mg2+ ions on the sorption capacity of R-SPA introduces the need for a technological compromise between the solution composition (N, P, K or N, P, K, Mg) affecting its fertilization value and the possibility of obtaining maximum R-SPA swelling. The sorption capacity of R-SPA can be slightly increased by using R-SPA/V-SPA mixtures, but R-SPA still plays a decisive role in this system. The possibility of technological adjustment of the leaching rate of fertilizer components under dynamic conditions using different combinations of (R-SPA/V-SPA)/HAL was demonstrated by column tests.

The research results and evaluation of the applicability of the original composition of hybrid paper based on silver nanowires (AgNWs), cellulose pulp (CP), and carbon nanotubes (CNTs) are presented and discussed. The material tested was used to manufacture sensors for mechanical deformation resulting from external influences or related to human activity interactions. The sensors were fabricated using an AgNWs + CP suspension and additives by the vacuum filtration method. The substrate obtained was machined and then laminated with a layer of poly(dimethylsiloxane) (PDMS). The recorded responses to selected types of imposed mechanical interactions in the form of changes in the relative resistance of the sensor throughout the tests showed a close cause-and-effect relationship. The response of the tested systems when applying an alternating magnetic field was also observed. The results indicate that the proposed solutions can find application in the monitoring of mechanical interactions resulting from the dynamic behavior of physical objects, as well as derived from selected human vital functions.

The article presents results of purification and comminution of raw halloysite from the Dunino deposit. The aim of the study was to clean halloysite from Dunino deposit with acid (H2SO4) leaching and to remove iron impurities in order to obtain fine grained fractions smaller than 20 μm, which can be used in future for manufacturing polymer-aluminosilicate composites. The proposed method, where nanotubes (HNT) and nanoplates (HNP) were separated, consisted of several simple stages including crushing, milling magnetic separation and sedimentation. A multi-stage process resulted in three products: heavy iron oxide fraction, HNP and HNT mixture (<20 um) and remaining intermediate product (mostly iron, titanium oxides and aluminosilicates >20μm).

The mining industry of Poland is based mostly on coal and copper ores. Strict carbon emissions and the depletion of deposits will slowly phase out coal. Therefore, metallic ores and other mineral raw materials will dominate the extractive industry of Poland. Current measured resources of the largest deposits of halloysite and diatomaceous earth in Poland are over 0.5 Mt and 10 Mt, respectively. Halloysite and diatomaceous earth samples from halloysite Dunino deposits and Jawornik diatomaceous earth deposits (composed mostly of diatomaceous skeletons (frustules)) were subjected to mineralogical analysis, scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM-EDS) nanostructural, chemical, elemental, and mineral content analysis. Both these minerals have similar properties, i.e., sorption capacity and cation exchange capacity, and are used mostly for the same purposes, e.g., adsorbents, filler material, and filtration. Samples of Dunino halloysite consist of minerals such as halloysite, kaolinite, hematite, magnetite, quartz, magnesioferrite, rutile, ilmenite, geikielite, goyazite, gorceixite, and crandallite, with little impurities in the form of iron oxides. Occasionally, halloysite nanoplates (HNP) nanotubes (HNT) were found. Diatomaceous earth is composed mainly of silica-containing phases (quartz, opal) and clay minerals (illite and kaolinite). The frustules of diatoms are mostly centric (discoid) and have radius values of approximately 50–60 μm. Large resources of these minerals could be used in the future either for manufacturing composite materials or highly advanced adsorbents.

The article presents comparative characteristics of the pore structure and sorption properties of raw halloysite (R-HAL) and after calcination (C-HAL) at the temperature of 873 K. Structural parameters were determined by optical scanning and transmission electron microscopy methods as well as by mercury porosimetry (MIP, Hg) and low-pressure nitrogen adsorption (LPNA, N2, 77 K). The surface area parameter (LPNA) of halloysite mesopores before calcination was 54–61 m2/g. Calcining caused the pore surface to develop to 70–73 m2/g. The porosity (MIP) of halloysite after calcination increased from 29% to 46%, while the surface area within macropores increased from 43 m2/g to 54 m2/g. The total pore volume within mesopores and macropores increased almost twice after calcination. The course of CH4 and CO2 sorption on the halloysite was examined and sorption isotherms (0–1.5 MPa, 313 K) were determined by gravimetric method. The values of equilibrium sorption capacities increased at higher pressures. The sorption capacity of CH4 in R-HAL was 0.18 mmol/g, while in C-HAL 0.21 mmol/g. CO2 sorption capacities were 0.54 mmol/g and 0.63 mmol/g, respectively. Halloysite had a very high rate of sorption equilibrium. The values of the effective diffusion coefficient for methane on the tested halloysite were higher than De > 4.2 × 10−7 cm2/s while for carbon dioxide De > 3.1 × 10−7 cm2/s.

The aim of this work was to characterize the structure and corrosion properties of the MgCa4.5(Gd0.5) alloys surface treated by the micro-arc oxidation (MAO) process. The MgCa4.5 and MgCa4.5Gd0.5 alloy samples were processed by MAO in an electrolyte composed of NaOH (10 g/dm3), NaF (10 g/dm3), NaH2PO4 (5 g/dm3), Na2SiO2·5H2O (10 g/dm3) and water. Two different voltages (120 V and 140 V) were used in the MAO process. The alloys protected by an oxide layer formed in the MAO were then the subject of corrosion resistance tests in an environment simulating the human body (Ringer’s solution). After the experiments, the resulting samples were investigated using SEM, XPS and EDS techniques. The addition of Gd affected the fragmentation of the coating structure, thereby increasing the specific surface; higher voltages during the MAO process increased the number and size of surface pores. Corrosion tests showed that the MgCa4.5Gd0.5 alloys were characterized by low polarization resistances and high corrosion current densities. The studies indicated the disadvantageous influence of gadolinium on the corrosion resistance of MgCa4.5 alloys. The immersion tests confirmed lower corrosion resistance of MgCa4.5Gd0.5 alloys compared to the referenced MgCa4.5 ones. The MgCa4.5 alloy with the MAO coating established at voltage 140 V demonstrated the best anticorrosion properties.

The article presents comparative characteristics of the pore structure and sorption properties of raw halloysite (R-HAL) and after calcination (C-HAL) at the temperature of 873 K. Structural parameters were determined by optical scanning and transmission electron microscopy methods as well as by mercury porosimetry (MIP, Hg) and low-pressure nitrogen adsorption (LPNA, N , 77 K). The surface area parameter (LPNA) of halloysite mesopores before calcination was 54-61 m /g. Calcining caused the pore surface to develop to 70-73 m /g. The porosity (MIP) of halloysite after calcination increased from 29% to 46%, while the surface area within macropores increased from 43 m /g to 54 m /g. The total pore volume within mesopores and macropores increased almost twice after calcination. The course of CH and CO sorption on the halloysite was examined and sorption isotherms (0-1.5 MPa, 313 K) were determined by gravimetric method. The values of equilibrium sorption capacities increased at higher pressures. The sorption capacity of CH in R-HAL was 0.18 mmol/g, while in C-HAL 0.21 mmol/g. CO sorption capacities were 0.54 mmol/g and 0.63 mmol/g, respectively. Halloysite had a very high rate of sorption equilibrium. The values of the effective diffusion coefficient for methane on the tested halloysite were higher than > 4.2 × 10 cm /s while for carbon dioxide > 3.1 × 10 cm /s.

This paper presents a new, innovative technological approach, in line with Circular Economy principles, to the effective management of sludge generated during municipal wastewater treatment processes and subsequently used for biogas production. This approach allows for optimal, functional, and controlled cascade-type biotechnological thermal conversion of carbon compounds present in sewage sludge, later in solid digestate residues (after biogas production), and finally in the ash structure (after incineration, purposefully dosed nanostructural additives make the production of a useful solid product possible, especially for cyclic adsorption and slow release of nutrients (N, P, K) in the soil). The idea is generally targeted at achieving an innovative conversion cycle under a Circular Economy framework. In particular, it is based on an energy carrier (methane biogas) and direct energy production. The functionalized combustion by-products can be advantageous in agriculture. The use of ashes with nanostructural additives (halloysite, kaolinite) from combustion of sewage sludge after the anaerobic fermentation as an adsorbent of selected nutrients important in agriculture (Na+, K+, NO3−, SO42−, PO43−, Cl−) was verified at laboratory scale. The tests were carried out both for pure ash and for the ash derived from combustion with the purposeful addition of kaolinite or halloysite. The equilibrium conditions for nitrate, potassium, sodium, phosphate(V), sulphate(VI), and chloride ions from aqueous solutions with the use of the three adsorbent structures were determined. The obtained innovative results were interpreted theoretically with adsorption isotherm models (Langmuir, Freundlich, Temkin, Jovanović). The most spectacular and clearly favorable results related to the influence of nanostructural additives in the process of sludge combustion, and formation of sorption surfaces under high temperature conditions were identified in the case of sorption-based separation of phosphate(V) ions (an increase from 1.13% to 61.24% with the addition of kaolinite, and even up to 76.19% with addition of halloysite).