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A zeolitic sample, named MT-ZLSH, was synthesized using mining tailings (MT) as the precursor material, resulting in a structure comprising: Linde type A (LTA) and sodalite-hydroxysodalite (ZLSH). This naming convention reflects the material's origin and its structural characteristics. The material was further modified by incorporating lithium, producing MT-ZLSH-Li+. Physicochemical characterizations were performed, and the material was evaluated for its potential to remove methylene blue (MB) from synthetic wastewater through adsorption and photocatalysis. Efficient adsorption was observed under typical wastewater pH conditions, with a maximum adsorption capacity of 23.4 mg·g−1, which fit well with the Langmuir isotherm model. The key mechanisms governing MB adsorption were identified as ion exchange, electrostatic attraction, and hydrogen bonding. The adsorption process was exothermic, with kinetic data fitting both the pseudo-second order and intraparticle diffusion models, achieving 82% removal and a maximum adsorption capacity of 40 mg·g−1 over 12 h. MB adsorption followed a two-step process, initially involving film diffusion, followed by intraparticle diffusion. Additionally, photocatalytic degradation of MB achieved 77% degradation within 180 min. However, a decrease in reusability was observed during a second cycle of MB adsorption and photodegradation, highlighting the need for further optimization to enhance the material's long-term performance. [ABSTRACT FROM AUTHOR]

This study aimed to investigate the sustainable use of recycled plastics, specifically polypropylene (PP) and high-density polyethylene (HDPE), in the manufacture of geogrids for geotechnical and civil engineering applications. Plastics were collected from a recycling center, specifically targeting containers used for food, cleaning products, and other domestic packaging items. These plastics were sorted according to the Möbius triangle classification system, with HDPE (#2) and PP (#5) being the primary categories of interest. The research methodologically evaluates the mechanical properties of PP/HDPE (0/100, 25/75, 50/50, 75/25 and 100/0% w/w) composites through tensile and flexural tests, exploring various compositions and configurations of geogrids. The results highlight the superiority of pure recycled HDPE processed into 1.3 mm thick laminated yarns and hot air welded for 20 to 30 s, exhibiting a deformation exceeding 60% in comparison to the PP/HDPE composites. Through SolidWorks® Simulation, it was shown that the adoption of a trigonal geogrid geometry optimizes force distribution and tensile strength, significantly improving slope stabilization efficiency. Based on the results obtained, a laboratory-scale prototype geogrid was developed using an extrusion process. The results underscore the importance of careful composite design and yarn configuration selection to achieve the desired mechanical properties and performance in geogrid applications. It emphasizes the potential of recycled plastics as a viable and environmentally friendly solution for stabilizing slopes, contributing to the reduction in plastic waste and promoting sustainable construction practices. [ABSTRACT FROM AUTHOR]

The development of an efficient adsorbent is required in tertiary wastewater treatment stages to reduce the phosphate–phosphorous content within regulatory levels (1 mg L−1 total phosphorous). In this study, a natural muscovite was used for the preparation of muscovite/zeolite composites and the incorporation of Fe3+/Mn2+ (oxy)hydroxide nanoparticles for the recovery of phosphate from synthetic wastewater. The raw muscovite MC and the obtained muscovite/sodalite composite LMC were used in the powder form for the phosphate adsorption in batch mode. A muscovite/analcime composite was obtained in the pellets PLMCT3 and monolith SLMCT2 forms for the evaluation in fixed-bed mode for continuous operation. The effect of pH, equilibrium and kinetic parameters on phosphate adsorption and its further reuse in sorption–desorption cycles were determined. The characterization of the adsorbents determined the Fe3+ and Mn2+ incorporation into the muscovite/zeolite composite's structure followed the occupancy of the extra-framework octahedral and in the framework tetrahedral sites, precipitation and inner sphere complexation. The adsorbents used in this study (MC, LMC, PLMCT3 and SLMCT2) were effective for the phosphate recovery without pH adjustment requirements for real treated wastewater. Physical (e.g., electrostatic attraction) and chemical (complexation reactions) adsorption occurred between the protonated Fe3+/Mn2+ (oxy)hydroxy groups and phosphate anions. Higher ratios of adsorption capacities were obtained by powder materials (MC and LMC) than the pellets and monoliths forms (PLMCT3 and SLMCT2). The equilibrium adsorption of phosphate was reached within 30 min for powder forms (MC and LMC) and 150 min for pellets and monoliths forms (PLMCT3 and SLMCT2); because the phosphate adsorption was governed by the diffusion through the internal pores. The adsorbents used in this study can be applied for phosphate recovery from wastewater treatment plants in batch or fixed-bed mode with limited reusability. However, they have the edge of environmentally friendly final disposal being promissory materials for soil amendment applications. [ABSTRACT FROM AUTHOR]

A parent Mg-Al-LDH was upgraded in its adsorption properties due to the incorporation of tri-metal species oxy(hydroxide) nanoparticles obtaining Mn2+/Zn2+/Fe3+/Mg-Al-LDH composite for the phosphate recovery from simulated urban treated wastewater. The physicochemical properties of the synthesized Mn2+/Zn2+/Fe3+/Mg-Al-LDH make promising for real application without being environmentally harmful. The performance of Mn2+/Zn2+/Fe3+/Mg-Al-LDH composite was evaluated through batch adsorption assays. The support of iron, manganese, and zinc (oxy)hydroxide nanoparticles onto the parent Mg-Al-LDH structure was performed by precipitation, isomorphic substitution, and complexation reactions. The main improvement of the Mn2+/Zn2+/Fe3+/Mg-Al-LDH composite was the highest phosphate adsorption capacity (82.3 mg∙g−1) in comparison to the parent Mg-Al-LDH (65.3 mg∙g−1), in a broad range of concentrations and the effective phosphate adsorption at neutral pH (7.5) near to the real wastewater effluents conditions in comparison to the conventional limitations of other adsorbents. The effectiveness of Mn2+/Zn2+/Fe3+/Mg-Al-LDH composite was higher than the conventional metal LDHs materials synthesized in a single co-precipitation step. The phosphate adsorption onto Mn2+/Zn2+/Fe3+/Mg-Al-LDH composite was described to be governed by both physical and chemical interactions. The support of Mn2+/Zn2+/Fe3+ oxy(hydroxide) nanoparticles over the parent Mg-Al-LDH was a determinant for the improvement of the phosphate adsorption that was governed by complexation, hydrogen bonding, precipitation, and anion exchange. The intra-particular diffusion also described well the phosphate adsorption onto the Mn2+/Zn2+/Fe3+/Mg-Al-LDH composite. Three specific stages of adsorption were determined during the phosphate immobilization with an initial fast rate, followed by the diffusion through the internal pores and the final equilibrium stage, reaching 80% of removal and the equilibrium within 1 h. The Mn2+/Zn2+/Fe3+/Mg-Al-LDH was strongly selective towards phosphate adsorption in presence of competing ions reducing the adsorption capacity at 20%. The Mn2+/Zn2+/Fe3+/Mg-Al-LDH has limited reusability, only 51% of the adsorbed phosphate could be recovered in the second cycle of the adsorption-desorption process. Around 14% of phosphate was loosely-bond to Mn2+/Zn2+/Fe3+/Mg-Al-LDH which brings the opportunity to be a new source of phosphorus. The use of eluted concentrates and the final disposal of the exhausted adsorbent for soil amendment applications can be an integral nutrient system (P, Mn, Zn, Fe) for agriculture purposes. [ABSTRACT FROM AUTHOR]

BACKGROUND The incorporation of Fe( III) was performed in a natural clinoptilolite (Z-N) for simultaneous phosphate and ammonium removal. RESULTS The existence of hydroxyl groups (≅Fe- OH) in the iron zeolite (Z-Fe) enhances the phosphate uptake from 0.6 ± 0.1 mg-P g−1 in Z-N to 3.4 ± 0.2 mg-P g−1 in Z-Fe. However, the ammonium sorption capacity slightly decreases from 33 ± 2 mg-N g−1 in Z-N to 27 ± 2 mg-N g−1 in Z-Fe. The equilibrium and kinetics sorption were well explained by the Langmuir isotherm and the intraparticle diffusion model, respectively. CONCLUSIONS Both the phosphate and ammonium uptake were slightly affected by the coexistence of competing ions. The phosphate sorption capacity of iron zeolite was decreased in the regeneration cycles. Desorption using a 1 mol L−1 NaOH solution under dynamic conditions provided higher enrichment factors for ammonium than phosphate. © 2015 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

BACKGROUND: This study evaluated a polymeric ion exchanger impregnated with nanoparticles of hydrated ferric oxide as a selective sorbent for anionic P(V) species. The hybrid impregnated anion exchanger (HAIX) employed as sorbent combines the durability and mechanical strength of a polymeric weak base anion exchange resin with the high sorption affinity of hydrated ferric oxide towards P(V) species. RESULTS: The P(V) loading capacity of the sorbent at a pH simulating the expected conditions in treated wastewaters was 92±3mg P-PO4 g-1 in single component solutions. The sorption of P(V) is affected slightly by the common ions typically present in these effluents such as Cl-, SO4 2- and NO3-, and a reduction of only 5% was observed (89±2mg P-PO4 g-1) in multicomponent solutions. The sorbent can be regenerated (95±3%) using 4% (w/w) sodium hydroxide solution. CONCLUSIONS: HAIX displays high selectivity for phosphate and small affinity for SO4 2-, NO3- and Cl- ions, which provides excellent conditions for its application at pH values typical of secondary wastewater effluents. HAIX exhibits higher and competitive phosphate removal capacity compared with data reported in the literature for materials based on HFO and for adsorbents prepared by impregnation of HFO onto polymeric supports. [ABSTRACT FROM AUTHOR]

The essential oil of aerial parts from Baccharis obtusifolia (Asteraceae) growing wild in Ecuador was obtained by hydrodistillation and examined by gas chromatography–mass spectrometry (GC–MS and GC–flame ionization detector (GC–FID) analysis. Thirty-one individual compounds were identified and constitute 96.1% of the total composition of the oil. The main constituents of the oil were limonene (28.3%), germacrene-D (9.8%), α-pinene (9.0%), β-pinene (8.2%), bicyclogermacrene (6.2%) and δ-cadinene (5.7%). The essential oil showed significant antibacterial and antifungal activity. Baccharis obtusifolia oil exhibited a moderate antibacterial effect against Klebsiella pneumoniae (ATCC 9997) and Enterococcus faecalis (ATCC 29212), and good antifungal activity against Trichophyton rubrum (ATCC 28188) and Trichophyton mentagrophytes (ATCC 28185). In this study, the chemical composition and biological activity of the essential oil of B. obtusifolia (Asteraceae) are reported for the first time. [ABSTRACT FROM AUTHOR]

Scutellaria volubilis and Lepechinia paniculata belong to the Lamiaceae family of species. They are used widely in traditional medicine in Ecuador. The physical properties and chemical composition of the essential oils from the aerial part of Scutellaria volubilis in its foliation -- flowering stage and Lepechinia paniculata in its flowering phase have been studied after their hydrodistillation. The components of these essential oils were investigated by means of gas chromatography/mass spectrometry (GC/MS) and gas chromatography/flame ionization detection (GC/FID) techniques. Thirty-seven components were determined in the essential oil of 5. volubilis. The principal constituents were found to be sesquiterpene hydrocarbons: germacrene D (20.4%), β-caryophyllene (17.5%), α-humulene (14.7%) and β-bisabolene (5.8%). Thirty-four components were identified in the essential oil of L. paniculata, the principal groups were sesquiterpene hydrocarbons such as aromadendrene (24.6%), viridiflorene (12.4%), β-selinene (7.4%) and valencene (6.7%). The monoterpene hydrocarbons were present in lower amounts as well as β-phellandrene (6.9%) and (7.7%). Oxygenated monoteipenes and sesquiterpenes contribute below 5% in both species. This is the first report on the chemical composition of this species. [ABSTRACT FROM AUTHOR]

The essential oil (EO) was obtained by hydrodistillation from the aerial parts of Lepechinia radula Benth Epling (Lamiaceae) from Ecuador. Thirty-four compounds accounting to 93.4% of the total oil were identified. The main constituents of the essential oil were δ-3-carene (19.9%), β-pinene (17.0%), (E)-β- caryophyllene (9.7%) and (E-E)-α-farnesene (9.4%). The essential oil of L. radula possessed strong antifungal activity against Trichophyton rubrum (ATCC® 28188) and Trichophyton mentagrophytes (ATCC® 28185). [ABSTRACT FROM AUTHOR]