New Materials Based on Polyvinylpyrrolidone-Containing Copolymers with Ferromagnetic Fillers

The article investigates the peculiarities of the effect of ferromagnetic fillers (FMFs) of various natures (Ni, Co, Fe, FeCo, SmCo₅) on the formation of the structure and properties of 2-hydroxyethylmethacrylate (HEMA) with polyvinylpyrrolidone (PVP) copolymers. The composites were characterized using FTIR-spectroscopy, SEM, DMTA, magnetometry of vibrating samples, specific electrical resistivity studies, and mechanical and thermophysical studies. The formation of a grafted spatially crosslinked copolymer (pHEMA-gr-PVP) was confirmed and it was established that the FMF introduction of only 10 wt.% into the copolymer formulation increased the degree of crosslinking of the polymer network by three times. The surface hardness of composites increased by 20–25%. However, the water content decreased by 16–18% and lay within 42–43 wt.%, which is a relatively high number. The heat resistance of dry composites was characterized by Vicat softening temperature, which was 39–42 °C higher compared to the unfilled material. It was established that the obtained composites were characterized by a coercive force of 200 kA × m⁻¹ and induction of a magnetic field at the poles of 4–5 mT and 10–15 mT, respectively. The introduction of FMF particles into pHEMA-gr-PVP copolymers, which, in the dry state, are dielectrics, provides them with electrical conductivity, which was evaluated by the specific volume resistance. Depending on the FMF nature and content, as well as their orientation in the magnetic field, the resistance of filled materials could be regulated within 10²–10⁶ Ohm·m. Therefore, the modification of HEMA with PVP copolymers by ferromagnetic fillers of various natures provides the possibility of obtaining materials with unique predicted properties and expands the fields of their use, for instance as magnetic sorbents for various applications, as well as the possibilities associated with their being electrically conductive materials that can respond by changing of electrical conductivity, depending on various factors.     

Combination of Pre- and Post-Mercerization Processes for Cotton Fabric

The dyeing process commonly deteriorates the luster of pre-mercerized cotton fabric, so post-mercerization processes are regularly applied to compensate for this. Herein, the influence of combining pre-mercerization with CS (caustic solution) or LA (liquid ammonia) and post-mercerization with CS or LA on the morphological structure, dyeing performance, tensile strength, and stiffness of woven cotton fabric was investigated. The crystallinity index values greatly decreased from 73.12 to 51.25, 58.73, 38.42, and 40.90% after the combined mercerization processes of LA–LA, CS–CS, LA–CS, and CS–LA, respectively. Additionally, the CS–LA- and LA–CS-treated samples exhibited a mixture of cellulose II and cellulose III allomorphs. The combined mercerization processing of cotton fabric resulted in slightly worse thermal stability. The LA and CS pre-mercerization processes increased the dye exhaustion, although the former decreased the dye fixation rate while the latter increased it by 4% for both dyes. The color strength of the dyed cotton fabric increased after both post-mercerization processes. Moreover, the fabric stiffness and mechanical properties showed an increasing trend due to the combined mercerization efforts.     

Impact of Washing Parameters on Thermal Characteristics and Appearance of Proban®—Flame Retardant Material

Proban^® is a multiphase treatment of cotton fabrics based on the formation of pre-condensates using the flame retardant (FR) agent tetrakis (hydroxymethyl) phosphonium salts (THPx). The assessment of the durability of a product demands a preliminary understanding of how relevant it is to extend its lifetime. It is therefore important to minimize the risk of agents impacting: (1) the protection level, (2) shape and dimensions, and (3) additional comfort characteristics of the fabric. This research focused on the impact of washing conditions on the durability of FR properties and appearance of Proban^® cotton fabrics, which was systematically arranged through the variation in the chemistry distribution in the Sinner’s circle. The chemical share was varied in laboratory conditions as a simulation of industrial washing based on component dosing, where the temperature, time and mechanical agitation were constant. The washing of cotton fabrics was performed through 10 cycles in four baths containing high alkali components, medium alkali components, high alkali reference detergent and water. The environmental acceptability of washing procedures through effluent analysis was assessed by physico–chemical and organic indicators. The limited oxygen index (LOI), calorimetric parameters (micro combustion calorimetry), thermal stability and evolved gases during thermal decomposition (thermogravimetric analyzer (TGA) coupled with an infrared spectrometer (TG–IR)), surface examination (FE-SEM), spectral characteristics and pH of the aqueous extract of the fabrics before and after 10 washing cycles were selected for proof of durability. The medium alkali bath was confirmed as a washing concept for Proban^® cotton fabric through the preservation of FR properties examined through LOI, TGA, TG–IR and MCC parameters and appearance color and low level of fibrillation.     

Efficient Removal of Methylene Blue from Aqueous Solutions Using a High Specific Surface Area Porous Carbon Derived from Soybean Dreg

Porous carbon material with high specific surface area was prepared from soybean dreg by a simple and effective two-step method (high temperature pyrolysis and activation). The structural characteristics of the synthesized carbon were evaluated by Brunauer–Emmett–Teller (BET), N₂ adsorption/desorption measurements/techniques, an elemental analyzer (EA), scanning electron microscopy equipped with energy dispersive X-ray spectroscopy (SEM-EDS), transmission electron microscopy (TEM), an X-ray diffractometer (XRD), Raman spectroscopy (Raman), a Fourier transform infrared spectrometer (FTIR), and X-ray photoelectron spectroscopy (XPS). The specific surface area of SDB-6-K was 2786 m² g⁻¹, the pore volume was 2.316 cm³ g⁻¹, and the average pore size was 3.326 nm. The high specific surface area and effective functional groups of carbon material promoted the adsorption of methylene blue. The maximum adsorption capacity of SDB-6-K to methylene blue was 2636 mg g⁻¹ at 318 K. The adsorption kinetic and isotherm data were most suitable for pseudo-second-order and Langmuir equations. The results showed that the adsorbent had excellent adsorptive ability and had good practical application potential in the field of dye wastewater treatment in the future.     

Assessment of Coating Quality Obtained on Flame-Retardant Fabrics by a Magnetron Sputtering Method

Innovative textile materials can be obtained by depositing different coatings. To improve the thermal properties of textiles, aluminum and zirconium (IV) oxides were deposited on the Nomex^® fabric, basalt fabric, and cotton fabric with flame-retardant finishing using the magnetron sputtering method. An assessment of coating quality was conducted. Evenly coated fabric ensures that there are no places on the sample surface where the values of thermal parameters such as resistance to contact heat and radiant heat deviate significantly from the specified ones. Energy-dispersive spectroscopy was used for the analysis of modified fabric surfaces. Non-contact digital color imaging system DigiEye was also used. The criterion allowing one to compare surfaces and find which surface is more evenly coated was proposed. The best fabrics from the point of view of coating quality were basalt and cotton fabrics coated with aluminum as well as basalt fabric coated with zirconia. The probability of occurrence of places on the indicated sample surfaces where the values of thermal parameters (i.e., resistance to contact heat and radiant heat) deviated significantly from the specified ones was smaller for Nomex^® and cotton fabrics coated with zirconia and Nomex^® fabric coated with aluminum.     

Laser Treatment of Cotton Fabric for Durable Antibacterial Properties of Silver Nanoparticles

In the present study, cotton fabric was exposed to laser exposure at different energy levels and then the silver nanoparticles were coated on untreated and laser treated cotton fabrics. Methylene blue dye was used to detect the presence of carboxylic acid groups (-COO⁻) on laser treated cotton and the dye absorption results were determined spectrophotometrically. ICP-OES (Inductively Coupled Plasma Optical Emission Spectroscopy) analysis and antibacterial tests were carried out to investigate the silver ion content and bactericidal properties of silver nanoparticles on cotton fabrics. Infrared spectroscopy (FTIR/ATR) analysis and scanning electron microscopy (SEM) were used to identify chemical changes and to study the morphology of the surface of the fibers. EDAX (Energy Dispersive X-ray Spectroscopy) analysis was calculated for SEM micrographs. The results showed according to the higher uptake of methylene blue dye that the negative charge of the carboxylic acid groups had been created by laser treatment. Although the FTIR spectroscopy results did not show an increase in carboxylic acid groups, the cationic dye absorption increased. The durability of the Ag⁺ ion particles on repeated laundered laser treated cotton was proven by antibacterial and ICP tests, particularly when the laser energy was increased.     

Sorption of Aromatic Compounds with Copolymer Sorbent Materials Containing β-Cyclodextrin

Urethane copolymer sorbent materials that incorporate β-cyclodextrin (CD) have been prepared and their sorption properties with chlorinated aromatic compounds (i.e., pentachlorophenol, 2,4-dichlorophenol and 2,4-dichlorophenoxy acetic acid) have been evaluated. The sorption properties of granular activated carbon (GAC) were similarly compared in aqueous solution at variable pH conditions. The sorbents displayed variable BET surface areas as follows: MDI-X copolymers (< 10¹ m²/g), CDI-X copolymers (< 10¹ m²/g), and granular activated carbon (GAC ~10³ m²/g). The sorption capacities for the copolymers sorbents are listed in descending order, as follows: GAC > CDI-3 copolymer ≈ MDI-3 copolymer. The sorption capacity for the aromatic adsorbates with each sorbent are listed in descending order, as follows: 2,4-dichlorophenol > 2,4-dichlorophenoxy acetic acid > pentachlorophenol. In general, the differences in the sorption properties of the copolymer sorbents with the chlorinated organics were related to the following factors: (i) surface area of the sorbent; (ii) CD content and accessibility; and (iii) and the chemical nature of the sorbent material.     

Synthesis and Characterization of Nanoporous Carbon Carriers for Losartan Potassium Delivery

Losartan potassium is most commonly used for the treatment of hypertension. In recent years, new applications of this drug have emerged, encouraging the design of novel nanoporous carriers for its adsorption and release. The purpose of this study was to synthesize ordered mesoporous carbon vehicles via a soft-templating method altered with the use of nitrogen precursors and via a hard-templating method followed by chitosan functionalization. As a result, the materials obtained differed in nitrogen content as well as in the number of total surface functional groups. The impact of the modification on the physicochemical properties of carbon carriers and their interaction with losartan potassium during adsorption and release processes was examined. The materials were characterized by various morphologies, specific surface areas (101–1180 m² g⁻¹), and the amount of acidic/basic oxygen-containing functional groups (1.26–4.27 mmol g⁻¹). These features, along with pore sizes and volumes, had a key effect on the sorption capacity of carbon carriers towards losartan potassium (59–161 mg g⁻¹). Moreover, they contributed to the differential release of the drug (18.56–90.46%). Losartan potassium adsorption onto the surface of carbonaceous materials was mainly based on the formation of hydrogen bonds and π–π interactions and followed the Langmuir type isotherm. It has been shown that the choice of the method of carbon carriers’ synthesis and their modification allows for the precise control of the kinetics of the losartan potassium release from their surface, resulting in rapid or sustained drug liberation.     

Preparation of a Novel Millet Straw Biochar-Bentonite Composite and Its Adsorption Property of Hg2+ in Aqueous Solution

The remediation of mercury (Hg) contaminated soil and water requires the continuous development of efficient pollutant removal technologies. To solve this problem, a biochar–bentonite composite (CB) was prepared from local millet straw and bentonite using the solution intercalation-composite heating method, and its physical and chemical properties and micromorphology were then studied. The prepared CB and MB (modified biochar) had a maximum adsorption capacity for Hg²⁺ of 11.722 and 9.152 mg·g⁻¹, respectively, far exceeding the corresponding adsorption value of biochar and bentonite (6.541 and 2.013 mg·g⁻¹, respectively).The adsorption of Hg²⁺ on the CB was characterized using a kinetic model and an isothermal adsorption line, which revealed that the pseudo-second-order kinetic model and Langmuir isothermal model well represented the adsorption of Hg²⁺ on the CB, indicating that the adsorption was mainly chemical adsorption of the monolayer. Thermodynamic experiments confirmed that the adsorption process of Hg²⁺ by the CB was spontaneous and endothermic. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and a thermogravimetric analysis (TGA) showed that after Hg²⁺ was adsorbed by CB, functional groups, such as the –OH group (or C=O, COO–, C=C) on the CB, induced complexation between Hg and –O–, and part of Hg (ii) was reduced Hg (i), resulting in the formation of single or double tooth complexes of Hg–O– (or Hg–O–Hg). Therefore, the prepared composite (CB) showed potential application as an excellent adsorbent for removing heavy metal Hg²⁺ from polluted water compared with using any one material alone.     

Experimental Study of Tensile Properties of Styrene–Butadiene–Styrene Modified Asphalt Binders

The requirements imposed on road pavements are ever increasing nowadays, necessitating the improvement of the properties of paving materials. The most commonly used paving materials include bituminous mixtures that are composed of aggregate grains bound by a bituminous binder. The properties of bitumens can be improved by modification with polymers. Among the copolymers used for modifying bitumens, styrene–butadiene–styrene, a thermoplastic elastomer, is the most commonly used. This article presents the results of tests conducted on bitumens modified with two types of styrene–butadiene–styrene copolymer (linear and radial). Two bitumen types of different penetration grades (35/50 and 160/220) were used in the experiments. The content of styrene–butadiene–styrene added to the bitumen varied between 1% and 6%. The results of the force ductility test showed that cohesion energy can be used for qualitative evaluation of the efficiency of modification of bitumen with styrene–butadiene–styrene copolymer. The determined values of the cohesion energy were subjected to the original analysis taking into account the three characteristic elongation zones of the tested binders. The performed analyses made it possible to find a parameter whose values correlate significantly with the content of styrene–butadiene–styrene copolymer in the modified bitumen. With smaller amounts of added modifier (approximately 2%), slightly better effects were obtained in the case of linear copolymer styrene–butadiene–styrene and for larger amounts of modifier (5–6%) radial copolymer styrene–butadiene–styrene was found to be more effective. This is confirmed by the changes in the binder structure, as indicated by the penetration index (PI).     

Thermo-Physiological Comfort Properties of Sportswear with Different Combination of Inner and Outer Layers

Consumers expect high-performance functionality from sportswear. To meet athletic and leisure-time activity requirements, further research needs to be carried out. Sportswear layers and their specific thermal qualities, as well as the set and air layer between materials, are all important factors in sports clothing. This research aims to examine the thermal properties of sports fabrics, and how they are affected by structure parameters and maintained with different layers. Three inner and four outer layers of fabric were used to make 12 sets of sportswear in this study. Before the combination of outer and inner layers, thermal properties were measured for each individual layer. Finally, the thermal resistance, thermal conductivity, thermal absorptivity, peak heat flow density ratio, stationary heat flow density, and water vapor permeability of bi-layered sportswear were evaluated and analyzed. The findings show that sportswear made from a 60% cotton/30% polyester/10% elastane inner layer and a 100% polyester outer layer had the maximum thermal resistance of 61.16 (×10³ K·m² W⁻¹). This performance was followed by the sample made from a 90% polyester/10% elastane inner layer and a 100% polyester outer layer, and the sample composed of a 100% elastane inner layer and a 100% polyester outer layer, which achieved a thermal resistance value of 60.41 and 59.41 (×10³ K·m² W⁻¹), respectively. These results can be explained by the fact that thicker textiles have a higher thermal resistance. This high-thermal-resistance sportswear fabric is appropriate for the winter season. Sportswear with a 90% polyester/10% elastane inner layer had worse water vapor resistance than sportswear with a 60% cotton/30% polyester/10% elastane and a 100% elastane layer. Therefore, these sports clothes have a higher breathability and can provide the wearers with very good comfort. According to the findings, water vapor permeability of bi-layered sportswear is influenced by geometric characteristics and material properties.     

Dual-Drug Delivery via the Self-Assembled Conjugates of Choline-Functionalized Graft Copolymers

Graft copolymers based on a choline ionic liquid (IL), [2-(methacryloyloxy)ethyl]-trimethylammonium chloride (TMAMA), were obtained by atom transfer radical polymerization. The presence of chloride counterions in the trimethylammonium groups promoted anion exchange to introduce fusidate anions (FUS, 32–55 mol.%) as the pharmaceutical anions. Both the choline-based IL copolymers and their ionic drug-carrier conjugates (FUS systems as the first type, 26–208 nm) formed micellar structures (CMC = 0.011–0.025 mg/mL). The amphiphilic systems were advantageous for the encapsulation of rifampicin (RIF, 40–67 mol.%), a well-known antibiotic, resulting in single-drug (RIF systems as the second type, 40–95 nm) and dual-drug systems (FUS/RIF as the third type, 31–65 nm). The obtained systems released significant amounts of drugs (FUS > RIF), which could be adjusted by the content of ionic units and the length of the copolymer side chains. The dual-drug systems released 31–55% FUS (4.3–5.6 μg/mL) and 19–31% RIF (3.3–4.0 μg/mL), and these results were slightly lower than those for the single-drug systems, reaching 45–81% for FUS (3.8–8.2 μg/mL) and 20–37% for RIF (3.4–4.0 μg/mL). The designed polymer systems show potential as co-delivery systems for combined therapy against drug-resistant strains using two drugs in one formula instead of the separate delivery of two drugs.     

Biological Cloth Face Coverings—The Reduction of SARS-CoV-2 and Influenza (H1N1) Infectivity by Viruferrin™ Treatment

In an attempt to create novel methods to reduce the transmission of SARS-CoV-2 and influenza viruses, fabric material was treated with Viruferrin™ and tested for its inactivating properties against the pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza A viruses. Inactivating properties were evaluated by comparing Viruferrin-treated and cotton control fabric material with and without the application of saliva at various time points after virus exposure. A statistically significant (p < 0.0001) decrease in the number of infectious virus particles exposed to Viruferrin-treated fabric when compared with the cotton control for both SARS-CoV-2 and influenza A viruses was observed. For both SARS-CoV-2 and influenza A, Viruferrin-treated fabrics experienced a >99% virus reduction without saliva after five minutes of contact when compared to the positive control at time point 0. Furthermore, the reusability of the Viruferrin treated fabric was demonstrated by stability for up to 10 washes. The level of anti-viral (SARS-CoV-2) activity remained constant from 5 to 10 washes and demonstrated a significant difference (p < 0.0001) from the unwashed untreated material. Applications for this treated fabric are far reaching, as a biological face covering offers not only a unique 2-way protection but also is unlikely to cause onward touch transmission.     

Evaluation of Cocoa Beans Shell Powder as a Bioadsorbent of Congo Red Dye Aqueous Solutions

The use of synthetic dyes in the textile, leather, and paper industries is a source of groundwater pollution around the world. There are different methods for the treatment of wastewater that has been contaminated with dyes, among which adsorption with agro-industrial wastes is gaining relevance. In the present study, the adsorption capacity of cocoa bean shell powder was evaluated when it was used as a bioadsorbent for Congo red dye in an aqueous medium. A 2⁴ central factorial design with central and axial points was proposed to determine the adsorption capacity. The factors that were studied were the adsorbent (0.06–0.15 g), Congo red (40–120 mg L⁻¹), pH (3–11), and time (4–36 h). The bioadsorbent was characterized through scanning electron microscopy and Fourier-transform infrared spectroscopy. The effects of the factors on the adsorption capacity for Congo red using cocoa bean shell were nonlinear, and they were modeled with a second-order polynomial (p < 0.05) and with an R² of 0.84. The bioadsorbent obtained a maximum adsorption of 89.96% in runs. The process of optimization by using the surface response allowed the maximization of the adsorption, and the validation showed that 95.79% adsorption of the dye was obtained.     

Functionalized Biomass Carbon-Based Adsorbent for Simultaneous Removal of Pb2+ and MB in Wastewater

It is of great significance to realize the sustainable development of the environment to synthesize functional materials by value-added utilization of waste resources. Herein, a composite material of polyacrylic acid/lignosulfonate sodium/cotton biochar (PAA/LS/BC) was successfully prepared by grafting polyacrylic acid with functionalized waste cotton biochar and lignosulfonate sodium. The obtained absorbent showed prominent capture ability toward Pb²⁺ and methylene blue (MB) with capture characteristics of the pseudo-second-order model and Langmuir isotherm model. This experiment explored the adsorption performance of the adsorbent for pollutants at different conditions, and further revealed the selective adsorption of Pb²⁺ and MB in the mixed system. Analysis confirmed that electrostatic attraction and complexation are the most critical methods to remove contaminants. Additionally, the regeneration and stability experiment showed that the adsorption capacity of PAA/LS/BC for pollutants did not significantly decrease after five runs of adsorption–desorption. Various results can demonstrate that the adsorbent has excellent performance for removing pollutants and can be used as a material with development potential in the field of adsorption.     

Facile Fabrication of Novel NiFe2O4@Carbon Composites for Enhanced Adsorption of Emergent Antibiotics

Water purification is becoming one of the most pertinent environmental issues throughout the world. Among common types of water pollution involving heavy metals, pharmaceutical drugs, textile dyes, personal care products, and other persistent organic pollutants, the pollution of antibiotic drugs is increasingly emerging due to their adverse effects on microorganisms, aquatic animals, and human health. Therefore, the treatment of such contaminants is very necessary to reduce the concentration of antibiotic pollutants to permissible levels prior to discharge. Herein, we report the use of NiFe₂O₄@C composites from a bimetallic-based metal-organic framework Ni-MIL-88B(Fe) for removal of ciprofloxacin (CFX) and tetracycline (TCC). The effect of production temperatures (600–900 °C), solution pH (2–10), NiFe₂O₄@C dose (0.05–0.2 g/L), concentration of antibiotics (10–60 mg/L), and uptake time (0–480 min) was investigated systematically. Response surface methodology and central composite design were applied for quadratic models to discover optimum conditions of antibiotic adsorption. With high coefficients of determination (R² = 0.9640–0.9713), the proposed models were significant statistically. Under proposed optimum conditions, the adsorption capacity for CFX and TCC were found at 256.244, and 105.38 mg/g, respectively. Recyclability study was employed and found that NiFe₂O₄@C-900 could be reused for up to three cycles, offering the potential of this composite as a good adsorbent for removal of emergent antibiotics.     

Regular Polymeric Microspheres with Highly Developed Internal Structure and Remarkable Thermal Stability

In this study, the synthesis and characterization of permanently porous polymeric microspheres was presented. The microspheres were obtained via suspension polymerization using diverse functional monomers, such as 4,4′-bis(methacryloyloxymethylphenyl)sulphone, 1,4-bis(methacryloyloxymethyl)benzene, 4,4′-bis(methacryloyloxymethylphenyl)methane, N-vinylpyrrolidone, ethylene glycol dimethacrylate, and divinylbenzene as a co-monomer. As porogenic solvents, toluene and chlorobenzene were applied. The main aim of the research was to synthesize polymers having a highly developed internal structure and a good thermal stability. The synthesized materials were characterized by ATR-FTIR, scanning electron microscopy, a size distribution analysis, a low-temperature nitrogen adsorption–desorption method, differential scanning calorimetry, and thermogravimetry coupled with FTIR and inverse gas chromatography. It was found that, depending on the functional monomer, regular microspheres with a specific surface area in the range of 418–746 m²/g can be successfully synthesized. Moreover, all the synthesized copolymers showed a good thermal stability. In helium, they exhibited 5% mass losses at temperatures over 300 °C, whereas in air these values were only slightly lower. In addition, the presence of miscellaneous functional groups promoted diverse kinds of interactions. Therefore, the microspheres can be possibly use in many adsorption techniques including high temperature processes.     

Preparation of Poly(acrylic acid-acrylamide/starch) Composite and Its Adsorption Properties for Mercury (II)

The poly(acrylic acid-acrylamide/starch) composite was synthesized by solution polymerization, aiming to adsorb mercury (II) in water. The resulted copolymer was characterized by particle size exclusion chromatography (SEC), Fourier transform infrared spectroscopy (FTIR), thermogravimetry (TG), scanning electron microscopy (SEM) and dynamic light scattering particle size analyzer (DLS). It turned out that starch was successfully incorporated with the macromolecular polymer matrix and played a key role for improving the performance of the composites. These characterization results showed that the graft copolymer exhibited narrow molecular weight distribution, rough but uniform morphology, good thermal stability and narrow particle size distribution. The graft copolymer was used to remove Hg(II) ions from aqueous solution. The effects of contact time, pH value, initial mercury (II) concentration and temperature on the adsorption capacity of Hg(II) ions were researched. It was found that after 120 min of interaction, poly(acrylic acid-acrylamide/starch) composite achieved the maximum adsorption capacity of 19.23 mg·g⁻¹ to Hg(II) ions with initial concentration of 15 mg·L⁻¹, pH of 5.5 at 45 °C. Compared with other studies with the same purpose, the composites synthesized in this study present high adsorption properties for Hg(II) ion in dilute solution. The adsorption kinetics of Hg(II) on the poly(acrylic acid-acrylamide/starch) composite fits well with the pseudo second order model.     

Toughness Behavior of SBR Acrylate Copolymer-Modified Pervious Concrete with Single-Sized Aggregates

Pervious concrete is an eco-efficient concrete but has problems regarding its mechanical performance and permeability balance. This research investigated the feasibility of using a combination of styrene–butadiene rubber (SBR) and acrylate polymer to improve the toughness of pervious concrete while keeping its permeability. Single-sized aggregate and no sand were considered in the concrete mixture. Acrylate polymers with different solid content, PH, density, and viscosity were emulsion copolymerized with an SBR polymer. Eleven scenarios with different mix proportions and 220 specimens for compressive strength, flexural strength, flexural stiffness, impact resistance, and fracture toughness tests were selected to evaluate the effects of the copolymer on the toughness of copolymer-modified pervious concrete (CMPC). The studies showed that (1) the influence trend of the copolymers generally varied according to different mechanical indexes; (2) XG–6001 acrylate polymer mainly and comprehensively enhanced the toughness of the CMPC; (3) it was difficult to increase the enhancing property of the XG–6001 acrylate polymer with the growth of its mix proportion; (4) the zero-sand pervious concrete with 90% SBR and 10% XG–6001 acrylate emulsion copolymerization proved to have relatively high toughness. The proposed CMPC holds promising application value in sustainability traffic road construction.     

Carbon Derived from Jatropha Seed Hull as a Potential Green Adsorbent for Cadmium (II) Removal from Wastewater

Carbon from jatropha seed hull (JC) was prepared to study the adsorption of cadmium ions (Cd²⁺) from aqueous solutions under various experimental conditions. Batch equilibrium methods have been used to study the influences of the initial metal ion concentration (0.5–50 ppm), dosage (0.2–1 g), contact time (0–300 min), pH (2–7), and temperature (26–60 °C) on adsorption behavior. It has been found that the amount of cadmium adsorbed increases with the initial metal ion concentration, temperature, pH, contact time, and amount of adsorbent. A kinetic study proved that the mechanism of Cd²⁺ adsorption on JC followed a three steps process, confirmed by an intraparticle diffusion model: rapid adsorption of metal ions, a transition phase, and nearly flat plateau section. The experimental results also showed that the Cd²⁺ adsorption process followed pseudo-second-order kinetics. The Langmuir and Freundlich adsorption isotherm models were used to describe the experimental data, with the former exhibiting a better correlation coefficient than the latter (R² = 0.999). The monolayer adsorption capacity of JC has been compared with the capacities of the other reported agriculturally-based adsorbents. It has been clearly demonstrated that this agricultural waste generated by the biofuel industry can be considered a potential low-cost adsorbent for the removal of Cd²⁺ from industrial effluents.