The antibacterial, antifungal and antioxidant effects of halloysite nanoclay, Cloisite 10A (C10A) and Cloisite 15A (C15A) organonanoclays were examined in this study. The antimicrobial action was assessed using the agar-well method and the disc diffusion method. The free radical-scavenging effects of the clays were determined using the 2,2-diphenyl-1-picrylhydrazyl method. Halloysite showed antimicrobial activity against Pseudomonas aeruginosa, Enterococcus faecalis and Staphylococcus aureus. C10A was effective against both Gram-positive bacteria (S. aureus, Listeria monocytogenes, Bacillus subtilis and E. faecalis) and Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae and P. aeruginosa). Additionally, only C10A was found to have an antimicrobial effect on Candida glabrata of 18 mm amongst the tested clays. C15A showed an antimicrobial effect on S. aureus and K. pneumoniae. It was determined that the antifungal properties of organoclays were higher than those of halloysite. The most effective clay type was determined to be C10A. The positively charged inner surface of the halloysite nanoclay can provide a large area to which negatively charged free radicals can attach. The modified C15A used in this study has two long-chain alkyl groups attached, whereas the modified C10A has a single long-chain alkyl group and a benzyl group attached. It is proposed that the differences in these antimicrobial effects are due to the structures of the molecules. According to these results, organoclays as green source materials could be used as additives and coatings in food processing, biomedical devices, filters and paints due to their antimicrobial and antioxidant properties.

Toxic pharmaceutical pollutants, such as nicotine, represent a significant threat to natural water sources due to their continuous discharge. To address this issue, clay minerals and their composites have demonstrated exceptional adsorptive and remedial capabilities for wastewater purification. This research focused on developing green clay-polymeric adsorbents for the efficient removal of pharmaceutical pollutants from industrial wastewater. The synthesis involves creating halloysite nanotube–polythiophene nanocomposites through a green and cost-effective method using vapour polymerization and a solvent-free, ball-milled technique for the adsorptive removal of nicotine from wastewater. The investigation evaluates the impacts of preparation, modification and environmental conditions on the adsorptive performance of these clay-based nanocomposites compared to pure polythiophene. The polymerization process was evaluated by varying the vapour polymerization holding time for a fixed amount of oxidant (FeCl3) and halloysite nanotube (HNT) to investigate the impacts of monomer vapour exposure time on the polymerization of nanocomposites. Following the characterization of the synthesized adsorbents using various methods, the study investigated the impacts of various parameters (e.g. adsorbent dosage, pH and contact time) on the adsorption capabilities of the materials on a laboratory scale. The results revealed that the incorporation of HNT improved the adsorbing performance of nanocomposites. The pH, absorbent concentration and contact time directly affect nicotine adsorption. Significantly, halloysite–polythiophene 3 with a 2 h polymerization duration demonstrated the maximum adsorption efficacy of 78.94% at pH 10 after a 24 h contact time. The environmentally friendly halloysite-based nanocomposite shows promising potential as an effective adsorbent for pharmaceutical pollutant (nicotine) removal from aquatic environments.

Montmorillonite (Mnt), belonging to the smectite group and representing a 2:1-type clay mineral with good cation-exchange and swelling capacities, is a common clay component of soils. It was observed that some Mnt preparations exhibit peroxidase-like (P-L) activity using N,N-diethyl-p-phenylenediamine sulfate salt as a substrate. Both native (non-swelling) and swelling Mnt exhibited similar P-L activity. Modification of Mnt with copper and iron influenced both P-L activity and phenol polymerization. Both free and textile-bound Cu-Mnt (Sigma-Aldrich) enabled phenol removal. Soil Mnt P-L activity is probably involved in lignin breakdown and decontamination of soils polluted with phenol-containing molecules.

Clay minerals are effective adsorbents for the remediation of pesticides in wastewater due to their large superficial areas and excellent cation-exchange capabilities. However, this adsorption effect can be reduced by the accumulation of adsorbents on clay minerals, amongst other problems. Therefore, in this study, montmorillonite (Mnt) modified by layered double hydroxide (LDH) with different loading amounts was successfully prepared using an in situ method. The results from X-ray diffraction, Fourier-transform infrared spectrometry, Brunauer–Emmet–Teller (BET) and scanning electron microscopy analyses revealed that LDH structures were successfully combined with the Mnt layer and formed a porous structure. However, excess LDH still caused the aggregation and accumulation of layers. The adsorption performance of LDH@Mnt for atrazine (ATZ) and paraquat (PQ) was investigated, and the removal efficiency of the LDH@Mnt composite was higher than those of Mnt and LDH alone. The kinetic study revealed that the adsorption process fitted the pseudo-second-order model and internal diffusion model, and 3-LDH@Mnt had the greatest absorbability efficiency for both ATZ and PQ, indicating the adsorption process was controlled by the number of active sites of the adsorbent. The generalized Langmuir model accurately characterized the adsorption process of ATZ and PQ elimination in the adsorption isotherm investigation, indicating that the adsorption energies of the active sites on the adsorbents were different. 3-LDH@Mnt had better absorbability performance for ATZ/PQ, and the sorption capacities were 7.03 and 91.9 mg g–1, respectively. According to site energy distribution theory, the amount of sorption sites of the composite adsorbent was large and the average adsorption energy was high, both of which being beneficial for the adsorption of ATZ and PQ. The effects of pH, coexisting anions and reuse experiments were also tested, indicating that the LDH@Mnt composite possessed high adsorption stability. This excellent removal performance represents a promising strategy for the remediation and elimination of pesticide contaminations from the environment.

In this study, the effects of two different ammonium-exchange methods to improve the ammonia (NH3) gas adsorption of raw clinoptilolite (CLN) from Gördes (Türkiye) was investigated. The first method involved direct modification of CLN by 0.5 or 1.0 M NH4NO3 solutions at 80°C for 4 and 8 h followed by calcination. In the second method, CLN was converted to the Na+ form prior to modification with ammonium nitrate and calcination under the same conditions. Both methods yielded H+ forms of CLN through the removal of exchangeable cations without damaging the crystal structure. Ammonia adsorption isotherms were determined at 298 K for a total of eight different H+ forms synthetized using both methods. The Na-1.0-8h CLN sample with the highest NH3 adsorption capacity obtained using the second method was selected as the parent CLN. In addition, to determine the effects of doping different cations into the structure on the NH3 adsorption properties of the selected parent CLN sample, cation-exchange processes were carried out using 0.5 and 1.0 M NaNO3, KNO3, Ca(NO3)2 and Mg(NO3)2 solutions at 80°C for 4 h. The raw and modified CLNs were characterized using X-ray diffraction, X-ray fluorescence, scanning electron microscopy and N2 adsorption analyses. Cation-exchanged samples with a wide range of NH3 adsorption capacities (3.61–4.93 mmol g–1) were compared with other zeolites from the literature.

The objective of this research was to study the cellulose addition effect on the geopolymerization of heated clay. The clay, composed of illite, plagioclase and kaolinite, was heated at 700°C for 2 h and mixed with cellulose (up to 10 mass%). The mixtures were NaOH-activated, and shaped samples were aged at 83°C for 30 days. The cured samples were investigated by using X-ray diffraction, Fourier-transform infrared spectroscopy and scanning electron microscopy. The influence of the cellulose addition on the mechanical/physical properties was also evaluated. The results showed that zeolite ZK-14, hydrosodalite, sodium carbonate and a geopolymer composed of poly(sialate) units were formed in all cured samples. The relative amounts of zeolite and metakaolin evolved antagonistically, whereas that of illite slightly decreased with increasing cellulose content. Metakaolin and illite were involved in the geopolymerization process. Cellulose addition led to the improvement of the flexural strength of the samples and to porosity reduction. By contrast, water absorption was increased. The positive effect of cellulose on sample performance is explained on the basis of hydrogen bonding between the functional moieties of cellulose and the active sites of sample constituents, namely zeolites, metakaolin, illite and the geopolymer. As a filler, zeolite probably contributed to sample strengthening, and the detrimental impact of Na-carbonate was insignificant. Based on the results obtained, the composites could be used as binders for brick manufacturing or as lightweight mortars.