Neodymium adsorption from aqueous solution by ß-cyclodextrin nanosponges and a polymer valorized from potato peels waste: experiments and conventional and statistical physics interpretations.

Using organic waste and residue streams to be turned into valuable and greener materials for various applications has proven an efficient and suitable strategy. In this work, two green materials (nanosponges and a polymer) were synthesized using potato peels and applied for the first time to adsorb and recover Neodymium (Nd3+) from aqueous solutions. The recovery of Nd3+ that belongs to the rare earth elements has attracted important interest due to its/their importance in several industrial and technological applications. The fine potato peel waste (FPPW) polymer presented an irregular shape and porous surface. At the same time, the ß-cyclodextrin (ß-CD) nanosponges had uniform distribution with regular and smooth shapes. ß-CD nanosponges exhibited a much higher total carboxyl content (4.02 mmol g-1) than FPPW (2.50 mmol g-1), which could impact the Nd3+ adsorption performance because carboxyl groups can interact with cations. The adsorption capacity increased with the increase of the pH, reaching its maximum at pHs 6-7 for ß-CD nanosponges and 4-7 for FPPW polymer. The kinetic and equilibrium data were well-fitted by General order and Liu models. ß-CD nanosponges attained adsorption capacity near 100 mg Nd per gram of adsorbent. Thermodynamic and statistical physical results corroborated that the adsorption mechanism was due to electrostatic interaction/complexation and that the carboxyl groups were important in the interactions. ß-CD nanosponges (three cycles of use) were more effective than FPPW (one cycle of use) in the regeneration. Finally, ß-CD nanosponges could be considered an eco-friendly adsorbent to recover Nd3+ from aqueous matrices.

The Synthesis and Evaluation of Porous Carbon Material from Corozo Fruit (Bactris guineensis) for Efficient Propranolol Hydrochloride Adsorption.

This study explores the potential of the corozo fruit (Bactris guineensis) palm tree in the Colombian Caribbean as a source for porous carbon material. Its specific surface area, pore volume, and average pore size were obtained using N2 adsorption/desorption isotherms. The images of the precursor and adsorbent surface were obtained using scanning electron microscopy (SEM). Fourier transform infrared (FTIR) spectra were obtained to detect the main functional groups present and an X-ray diffraction analysis (XRD) was performed in order to analyze the structural organization of the materials. By carbonizing the fruit stone with zinc chloride, a porous carbon material was achieved with a substantial specific surface area (1125 m2 g⁻1) and pore volume (3.241 × 10-1 cm3 g⁻1). The material was tested for its adsorption capabilities of the drug propranolol. The optimal adsorption occurred under basic conditions and at a dosage of 0.7 g L⁻1. The Langmuir homogeneous surface model effectively described the equilibrium data and, as the temperature increased, the adsorption capacity improved, reaching a maximum of 134.7 mg g⁻1 at 328.15 K. The model constant was favorable to the temperature increase, increasing from 1.556 × 10-1 to 2.299 × 10-1 L mg-1. Thermodynamically, the adsorption of propranolol was found to be spontaneous and benefited from higher temperatures, indicating an endothermic nature (12.39 kJ mol⁻1). The negative ΔG0 values decreased from -26.28 to -29.99 kJ mol-1, with the more negative value occurring at 328 K. The adsorbent material exhibited rapid kinetics, with equilibrium times ranging from 30 to 120 min, depending on the initial concentration. The kinetics data were well-represented by the general order and linear driving force models. The rate constant of the general order model diminished from 1.124 × 10-3 to 9.458 × 10-14 with an increasing concentration. In summary, the leftover stone from the Bactris guineensis plant can be utilized to develop activated carbon, particularly when activated using zinc chloride. This material shows promise for efficiently adsorbing propranolol and potentially other emerging pollutants.

The production of activated biochar using Calophyllum inophyllum waste biomass and use as an adsorbent for removal of diuron from the water in batch and fixed bed column.

The Calophyllum inophyllum species annually produces a large volume of cylindrical fruits, which accumulate on the soil because they do not have nutritional value. This study sought to enable the use of this biomass by producing activated biochar with zinc chloride as an activating agent for further application as an adsorbent in batch and fixed bed columns. Different methodologies were used to characterize the precursor and the pyrolyzed material. Morphological changes were observed with the emergence of new spaces. The carbonaceous material had a surface area of 468 m2 g-1, Dp = 2.7 nm, and VT = 3.155 × 10-1 cm3 g-1. Scientific and isothermal studies of the adsorption of the diuron were conducted at the natural pH of the solution and adsorbent dosage of 0.75 g L-1. The kinetic curves showed a good fit to the Avrami fractional order model, with equilibrium reached after 150 min, regardless of the diuron concentration. The Liu heterogeneous surface model well represented the isothermal curves. By raising the temperature, adsorption was encouraged, and at 318 K, the Liu Qmax was reached at 250.1 mg g-1. Based on the Liu equilibrium constant, the nonlinear van't Hoff equation was employed, and the ΔG° were < 0 from 298 to 328 K; the process was exothermic nature (ΔH0 = -46.40 kJ mol-1). Finally, the carbonaceous adsorbent showed good removal performance (63.45%) compared to a mixture containing different herbicides used to control weeds. The stoichiometric column capacity (qeq) was 13.30 and 16.61 mg g-1 for concentrations of 100 and 200 mg L-1, respectively. The length of the mass transfer zone was 5.326 cm (100 mg L-1) and 4.946 cm (200 mg L-1). This makes employing the leftover fruits of the Calophyllum inophyllum species as biomass for creating highly porous adsorbents a very effective and promising option.

The environmental pollution caused by cemeteries and cremations: A review.

In recent years the funeral industry has drawn attention from the scientific community concerning the potential pollution of the environment and the urban environment. In this review, the pollution caused by the cemeteries and crematoria around the world was addressed. The traditional burial leads to the production of ions, in the form of organic and heavy metals, bacteria, fungi, and viruses, that spread along with the soil and underwater. The crematoria produce small particles, trace gases (SOx, NOx, CO), and toxic organic volatiles. The effluent generated by both methods can lead to several environmental problems and further threaten human health. The current solution for the cemeteries in the development of a system in which effluent generated by the traditional burials are collected and treated before realizing in the environment. In addition to that, the green burial should be an alternative, since the corpse does not go through the embalming process, thus eliminating the presence of any undesired chemicals, that are further leached onto the environment. The crematoria should be employed as it is, however, the gas treatment station should be employed, to ensure the minimization of the impact on the environment. Last, future researches regarding the treatment of the cemeteries leached still need to be explored as well as the optimization and further development of the crematoria gas treatment process.

Pharmaceuticals as emerging pollutants: Case naproxen an overview.

Nonsteroidal anti-inflammatory drugs (NSAIDs), including naproxen (NP), diclofenac, ibuprofen, etc., are widely used for fever and pain relief. NP is one of the most widely consumed drugs in the world, because it is available over the counter in many countries. Many studies have proven that NP is not eliminated in conventional water treatment processes and its biodegradation in the environment is also difficult compared to other drugs. Along these lines, we are aware that both the original compound and its metabolites can be found in different destinations in the environment. To assess the environmental exposure and the risks associated with NP, it is important to understand better the environment where they finally reach, the behavior of its original compounds, its metabolites, and its transformation products. In this sense, the purpose of this review is to summarize the current state of knowledge about the introduction and behavior of NP in the environments they reach and highlight research needs and gaps. Likewise, we present the sources, environmental destinations, toxicology, environmental effects, and quantification methodologies.

Understanding the mobility of potential nutrients in rock mining by-products: An opportunity for more sustainable agriculture and mining.

The increase in demand for highly soluble fertilizers brings a global sustainability concern. Alternative sources for traditional fertilization are therefore needed. Rock powder use has been proposed as an alternative approach to soil remineralization. However, research on the agricultural potential of minerals and rocks as alternative sources of nutrients is limited to changes in soil chemical attributes or effects on crop yield. In this work, we report an experimental study addressing the dissolution of two silicate rock-derived powders (andesite and dacite) that were produced during mining activities in Southern Brazil. The rock powders were exposed to Milli-Q water at pH (7.4-8.8) range, in solutions of 0.1 mol L-1 citric acid at pH range 2.1-3.3, and Milli-Q water acidified with 0.5 mol l-1 acetic acid (pH 5-5.8), in a continuous mechanical rotatory shaker at room temperature. Dissolution kinetics were determined as a function of reaction times at 24 to 5760 h, and solution pH. Based on this kinetics, dissolution rates were determined for the individual powders and compared to expected values for aluminosilicates. Based on this comparison, it was shown that the application of andesite and dacite rock-derived powder to replace high soluble fertilizers is feasible due to high dissolution rates of their minerals. The average andesite dissolution rates in Milli-Q water, in citric acid solution, and in Milli-Q water acidified with acetic acid were 2.1 × 10-5, 1.92 × 10-1 and 6.3 × 10-4 mmol cm-2 s-1, respectively for Ca, being 183%, 22.6%, and 69.2% higher than for the dacite rock. This make andesite rock a potential substitute for carbonate-based liming. In contrast, the average dacite dissolution rates in Milli-Q water, in citric acid solution, and in Milli-Q water acidified with acetic acid were 1.05 × 10-5, 7.22 × 10-5, and 3.72 × 10-5 mmol cm-2 s-1, respectively for K, being 72.0%, 61.4%, and 73.6% higher than the andesite rock. This highlights its potential use as a K source for agriculture to replace highly soluble K-fertilizers.