The interactions between zeolite and two cellulose derivatives: A comprehensive analysis of liquid and solid phase properties.

This study investigates the impact of cellulose-derived polymers, anionic carboxymethylcellulose (CMC), and cationic cellulose (CC) on the colloidal and thermal stability of zeolite Na-X materials. By exploring polymer adsorption onto Na-X surfaces and characterising the resultant materials, using FT-IR, XPS, SEM, PSD, CHN, and zeta potential, the research unveils how CMC and CC modify zeolite properties. This investigation elucidates the potential roles of these polymers in colloidal systems with zeolites, revealing their promise for crafting organic-inorganic materials. Additional insight was also provided by careful examination of the thermal stability (TGA-DSC) of the obtained cellulose/zeolite materials. Furthermore, the study distinguishes the different adsorption mechanisms of CMC and CC, with CMC relying on some weak interactions (H-bonding and van der Waals forces), while CC interacts mainly via electrostatic forces. Both CMC and CC can act as stabilizing agents, with CMC being more efficient and using both electrosteric and depletion stabilizations. Importantly, the concentration of CC plays a role in bridging flocculation, highlighting the concentration-dependent nature of the stabilization mechanism.

Green Synthesis of Iron Nanoparticles Using an Aqueous Extract of Strawberry (Fragaria × ananassa Duchesne) Leaf Waste.

In this study, we analysed the potential use of dried strawberry leaves and calyces for the production of nanoparticles using inorganic iron compounds. We used the following iron precursors FeCl3 × 6H2O, FeCl2 × 4H2O, Fe(NO3)3 × 9H2O, Fe2(SO4)3 × H2O, FeSO4 × 7H2O, FeCl3 anhydrous. It was discovered that the content of polyphenols and flavonoids in dried strawberries and their antioxidant activity in DPPH and FRAP were 346.81 µM TE/1 g and 331.71 µM TE/1 g, respectively, and were similar to these of green tea extracts. Microimages made using TEM techniques allowed for the isolation of a few nanoparticles with dimensions ranging from tens of nanometres to several micrometres. The value of the electrokinetic potential in all samples was negative and ranged from -21,300 mV to -11,183 mV. XRF analyses confirmed the presence of iron ranging from 0.13% to 0.92% in the samples with a concentration of 0.01 mol/dm3. FT-IR spectra analyses showed bands characteristic of nanoparticles. In calorimetric measurements, no increase in temperature was observed in any of the tests during exposure to the electromagnetic field. In summary, using the extract from dried strawberry leaves and calyxes as a reagent, we can obtain iron nanoparticles with sizes dependent on the concentration of the precursor.

Comparative Analysis of Laboratory-Made and Industrial-Made Sewage Sludge Ash: Implications for Effective Management Strategy Development.

In the pursuit of environmentally and economically sustainable sewage sludge ash (SSA) management methods, researchers often employ laboratory-made SSA (L-SSA) as a substitute for industrial-made SSA (I-SSA) produced in fluidized bed furnaces. To check whether L-SSA is a material that imitates I-SSA well, the fractionation of metals whose presence is a significant problem during SSA management was performed. In addition, the grain distribution, specific surface area, and textural properties of the tested materials were examined. Differences in total Pb and Hg content and mobility of Cu, Ni, Mn, and Zn were observed between I-SSA and L-SSA. Larger particle sizes of L-SSA compared to I-SSA were confirmed, while comparable textural properties and specific surface area of both types of materials were maintained. Based on the results, it was concluded that L-SSA is chemically different compared to I-SSA, and that L-SSA should not be used as a reference in research focused on the design of SSA management methods. Moreover, fractionation of metals was performed in disposed fluidized beds (FBs), which are diverted to non-hazardous waste landfills without prior analysis. It has been proven that studied metals are present in FBs as abundantly as in SSA, while Cu, Mn, and Ni may show higher mobility than in I-SSA.

Do You Know What You Drink? Comparative Research on the Contents of Radioisotopes and Heavy Metals in Different Types of Tea from Various Parts of the World.

The aim of this study was to assess the potential health risks of radioactive elements and heavy metals ingested through the consumption of various types of tea imported to the Polish market (black, green, red, oolong and white). The concentrations [Bq/kg] of radionuclides (40K, 137Cs, 226Ra, 210Pb and 228Th) in tea leaves before and after brewing were measured using γ-ray spectrometry with high-purity germanium (HPGe). The concentrations [mg/kg] of the studied elements (Fe, Cr, Cu, Mo, Al, Mn, Ni, P, V, Cd and Pb) were determined using a microwave-induced plasma optical emission spectrometer (MIP-OES). The results presented here will help to expand the database of heavy metals and radioactivity in teas. With regard to the potential health risk, the percentage of leaching of individual elements in different types of tea infusions was determined, and the assessment of the consumption risk was estimated. Since the calculated exposure factors, namely the HQ (Hazard Quotient) and THQ (Target Hazard Quotient), do not exceed critical levels, teas can still be considered health-beneficial products (most of the radionuclides as well as elements remain in the leaves (65-80%) after brewing).

Colloidal and Thermal Stability of Three-Component Hybrid Materials Containing Clay Mineral, Polysaccharide and Surfactant.

The paper presents the colloidal and thermal stability of the three-component hybrid materials containing halloysite, polysaccharides (alginic acid, cationic cellulose and hydroxyethyl cellulose) and Tritons. TX-100, TX-165 and TX-405 were used as non-ionic surfactants. Stability and other properties of the hybrid materials were tested by the following methods: UV-Vis, TGA (thermogravimetric analysis) and DSC (differential scanning calorimetry), CHN (elemental analysis), SEM-EDX (scanning electron microscopy with energy dispersive X-ray spectroscopy) and tensiometry. According to the results with the increasing polymer concentration the colloidal stability of the tested systems also increases. Moreover, the addition of the surfactants causes the increase of polysaccharide adsorption but the colloidal stability of the tested systems decreases due to large weights of formed aggregates. As follows from the thermal analysis, the comparison of the TG/DTG-DSC curves obtained for the investigated polymers confirms that their thermal decomposition courses have some common features. The obtained results have the application potential in the formation of the materials for the pollutants removal from water and sewages.

Interactions between Nanoclay, CTAB and Linear/Star Shaped Polymers.

The influence of star-shaped (PAA-SS) and linear polyacrylic acid (PAA) with different molecular weights (high-PAA-HMW and low-PAA-LMW) on the structure of the adsorption layer, adsorption amount, electrokinetic and stabilizing properties of the PAA/CTAB/nanoclay suspensions was studied. The properties of the systems containing one of these polymers, the cationic surfactant-hexadecyltrimethylammonium bromide (CTAB) and the surface-modified nanoclay (N-SM) were analyzed using the following techniques: BET, CHN, FT-IR, ED-XRF, XRD, HRTEM, UV-Vis, tensiometry and zeta potential measurements. It was proved that PAA could be used as an effective stabilizer of N-SM. Moreover, the addition of CTAB caused a significant increase in the stability of the systems but decreased the adsorption of PAA on the N-SM surface and changed the structure of the adsorption layers. The largest stability was observed in the PAA-HMW/CTAB system. The PAA polymers and PAA/CTAB complexes adsorbed, especially on the clay surface, influenced the primary distribution of the layered sheets but kept the same basal d-spacing. The adsorption of PAA and the PAA/CTAB complexes took place mainly at the plate edges and on the contact space between the sheets. The obtained results will be used for the preparation of the PAA/CTAB/nanoclay composite for water purification.

Textural and Thermal Properties of the Novel Fucoidan/Nano-Oxides Hybrid Materials with Cosmetic, Pharmaceutical and Environmental Potential.

The main purpose of the research was to obtain and study hybrid materials based on three different nano-oxides commonly used in the cosmetic and pharmaceutical industries: Al2O3, TiO2, and ZnO, with the natural bioactive polysaccharide fucoidan. Since the mentioned oxides are largely utilized by industry, there is no doubt that the presented studies are important from an environmental point of view. On the basis of the textural studies (dynamic light scattering DLS, low temperature nitrogen adsorption, X-ray diffraction analysis XRD, scanning electron microscopy SEM) it was proved that the properties of the hybrid materials differ from the pure components of the system. Moreover, the advanced thermal analysis (TG-DTG-DSC) combined with the evolved gas analysis using Fourier transformed infrared spectroscopy (FTIR) and mass spectrometry were applied to describe the thermal decomposition of fucoidan, oxides and hybrid materials. It was found that the interactions between the polymer and the oxides results in the formation of the hybrid materials due to the functionalization of the nanoparticles surface, and that their thermal stability increased when compared to the pure substrates. Such findings definitely fill the literature void regarding the fucoidan based hybrid materials and help the industrial formulators in the preparation of new products.

Accumulation of radioisotopes and heavy metals in selected species of mushrooms.

Seven species of forest mushrooms from different regions of Poland (edible: Imleria badia, Cantharellus cibarius, Xerocomus subtomentosus, Suillus luteus and inedible by humans but being food for animals: Paxillus involutus, Tylopilus felleus and Russula emetica) were analyzed for radioisotope activity (Cs-137, K-40, Bi-214 and Pb-210) as well as concentrations of heavy metals (aluminum, chromium, cadmium, manganese, iron, lead, zinc, copper, nickel and mercury). The activity of radioisotopes was measured with a gamma spectrometer, while the concentrations of heavy metals were examined by microwave plasma - atomic emission spectrometry. The obtained results of the analyses were compared with the recommendations of the European Food Safety Authority concerning the consumption of the determined heavy metals and the European standards concerning the content of radioisotopes in food. The obtained results proved that the consumption of mushrooms may result in a significant exceeding of the consumption limits of cadmium, copper and Cs-137.

Influence of Zwitterionic CAPB on Flocculation of the Aqueous Cationic Guar Gum/Glauconite Suspensions at Various pH.

The influence of the pseudoamphoteric zwitterionic surfactant cocamidopropylbetaine (CAPB) on the stabilizing flocculating properties of the aqueous suspensions of glauconite (GT) with cationic guar gum (CGG) at various pH values was investigated. The following techniques were used: turbidimetry, UV-VIS spectrophotometry, tensiometry, electrophoretic mobility measurements, SEM, CHN, XRD, and FT-IR. It was established that CGG is an effective glauconite flocculant. Moreover, the most probable mechanism that is responsible for flocculation is bridge flocculation resulting from polymer adsorption on the glauconite surface. The adsorption process is caused by electrostatic interactions between the negatively charged glauconite surface and the positively charged polymer. The amount of CGG adsorption increases with the increase of the pH, which was confirmed by the adsorption and zeta potential measurements. The addition of CAPB increases the amount of the polymer adsorption due to the formation of intermolecular polymer-surfactant complexes; however, it reduces flocculation effectiveness.

Stabilizing properties of fucoidan for the alumina suspension containing the cationic surfactant.

The paper presents the influence of fucoidan (FD) on stability of alumina suspensions in the presence of cationic surfactant hexadecyltrimethylammonium bromide (CTAB). The research results show that fucoidan adsorbs on the alumina surface and that the adsorption decreases in the CTAB presence. This is due to formation of the polymer-surfactant complexes characterized by lower affinity for the alumina surface than pure fucoidan. The complex formation was confirmed by the tensiometric studies where the increase of the CTAB/FD surface tension in comparison to pure CTAB was observed. It was established that fucoidan possesses great stabilizing efficiency regardless of pH. Furthermore, stability of the fucoidan/alumina system increased after CTAB addition due to the presence of non-adsorbed complexes between the alumina particles. The results indicate that fucoidan could be successfully used as a stabilizer of colloidal suspensions where the presence of surfactant is required, that is in cosmetic and pharmaceutical industries.

Comparison of adsorption affinity of polyacrylic acid for surfaces of mixed silica-alumina.

The influence of solution pH (in the range 3-9) on the adsorption of polyacrylic acid (PAA) on the mixed silica-alumina surface (SA-3: SiO2 97 %-Al2O3 3 % and SA-96: SiO2 4 %-Al2O3 96 %) was investigated. The following methods were applied in experiments: spectrophotometry, viscosimetry, potentiometric titration, and microelectrophoresis, which enable determination of adsorbed amount of the polymer, thickness of its adsorption layers, surface charge density, and zeta potential of solid particles in the presence and absence of PAA, respectively. The obtained results indicate that rise of solution pH causes the decrease of PAA adsorption and the increase of its adsorption layer thickness on surfaces of both solids. Moreover, significantly higher adsorption of polyacrylic acid was obtained on the SA-96 surface. This is a result of more favorable electrostatic interactions occurring between the adsorbing polymer chains and the SA-96 surface and formation of a greater number of adsorbate-adsorbent connections through hydrogen bridges.

The Adsorption Layer in the System: Carboxymethylcellulose/Surfactants/NaCl/MnO(2).

The influence of surfactants (anionic sodium dodecyl sulfate, and nonionic tert-octylphenol ethoxylate with 9.5EO) and their mixtures on the adsorption of carboxymethylcellulose (CMC) in the presence of 0.001 M NaCl on the manganese dioxide surface (MnO(2)) was studied. The increase in CMC adsorption was observed in all measured systems in the presence of surfactants. The reason for this is the formation of complexes between polymer macromolecules and surfactants. Moreover, the dependence between the amount of surfactants adsorption and the CMC initial concentration was also studied. It proves that surfactant adsorption does not depend on the initial concentration of CMC. Another observation is that the increase in pH caused the decrease in CMC adsorption. The explanation of this phenomenon is connected with the influence of pH on the dissociation degree of the polyelectrolyte, kind and concentration of the surface active groups of the adsorbent. To characterize the compact and diffuse adsorption layer the surface charge density and the zeta potential of MnO(2) in the presence of CMC and surfactants were measured. The surface charge density of MnO(2) decreases in the presence of CMC or CMC/surfactant complexes. This is due to the presence of negatively charged groups in the compact part of the electric double layer. The zeta potential of MnO(2) is also lower in the presence of CMC and the CMC/surfactants complexes. The main reason for that is the shift of the slipping plane towards the bulk solution.