Behavior Of Aqueous Solutions Research Articles

Features of the rheological behavior of aqueous solutions of alumino-, aluminoboro- and aluminochromophosphates

Rheological studies carried out using rotational rheometer in the rotational and oscillatory modes at different temperatures and heating/cooling conditions revealed that the aqueous solutions of alumino-, aluminoboro- and aluminochromophosphates presented an unusual behavior. The largest increase in the viscosity of the studied systems was determined between 20 and 60 °C and was attributed to the formation of thermo-reversible inorganic gels in solutions of aluminophosphates due to interionic association. At the same time, the oscillation mode was found to be more sensitive to the process of polymer gel formation compared to the rotation mode. In addition, the process of polymer gel formation was more adequately studied from dynamic tests.

Modification of Single-Walled Carbon Nanotube Networks Anodes for Application in Aqueous Lithium-Ion Batteries

The changes in global energy trends and the high demand for secondary power sources, have led to a renewed interest in aqueous lithium-ion batteries. The selection of a suitable anode for aqueous media is a difficult task because many anode materials have poor cycling performance due to side reactions with water or dissolved oxygen. An effective method for improving the characteristics of anodes in aqueous electrolyte solutions is adding carbon nanotubes (CNTs) to the electrode materials. For a better comprehension of the mechanism of energy accumulation and the reasons for the loss of capacity during the cycling of chemical current sources, it is necessary to understand the behaviour of the constituent components of the anodes. Although CNTs are well studied theoretically and experimentally, there is no information about their behaviour in aqueous solutions during the intercalation/deintercalation of lithium ions. This work reveals the mechanism of operation of untreated and annealed single-walled carbon nanotubes (SWCNT) anodes during the intercalation/deintercalation of Li+ from an aqueous 5 M LiNO3 electrolyte. The presence of -COOH groups on the surface of untreated SWCNTs is the reason for the low discharge capacity of the SWCNT anode in 5 M LiNO3 (3 mAh g−1 after 100 cycles). Their performance was improved by annealing in a hydrogen atmosphere, which selectively removed the -COOH groups and increased the discharge capacity of SWCNT by a factor of 10 (33 mAh g−1 after 100 cycles).

Thermo- and pH-Sensitive Behavior of Copolymers of N-Vinylcaprolactam with N-Vinylimidazole

Free-radical copolymerization in bulk has afforded copolymers of N-vinylcaprolactam and N‑vinylimidazole (40–60 mol %). Thermosensitive behavior of aqueous solutions of the copolymers has been probed over wide pH range by means of dynamic and static light scattering as well as high-sensitivity differential scanning calorimetry. Three regions of thermally induced conformational behavior have been observed with the change in the medium pH from the alkaline to acidic: phase separation region (I), region of the conformational transition into the mesoglobules state (II), and region of stable molecular solution of the poly-electrolyte (III). Significant polyelectrolyte effects have been revealed for the salt-free solutions of the copolymers, reflected in the presence of fast and slow diffusion modes in the relaxation time distributions. Moderate increase in the ionic strength with the addition of the low-molecular salt has led to shielding of the polyelectrolyte effects, yet the pH-dependent regions of the conformational behavior have not been affected much. The existence of different types of the thermally induced conformational behavior depending on pH has been explained by the balance between hydrophobic interactions involving the N-vinylcaprolactam units and electrostatic interactions of the weakly basic N-vinylimidazole units.

Synthesis of poly(2-isopropyl-2-oxazoline)-b-poly(2-phenyl-2-oxazoline)-b-poly(2-isopropyl-2-oxazoline) and its self-assembly into polymersomes: Temperature-dependent aqueous solution behavior

This study reports on synthesis of poly(2-isopropyl-2-oxazoline)-b-poly(2-phenyl-2-oxazoline)-b-poly(2-isopropyl-2-oxazoline) (PiPOX-b-PPhOX-b-PiPOX) by a three-step sequential monomer addition through cationic ring opening polymerization (CROP). Self-assembly of PiPOX-b-PPhOX-b-PiPOX was triggered through solvent shifting or double emulsion methods, resulting in formation of polymersomes with hydrophilic and temperature-responsive PiPOX inner/outer coronae and hydrophobic PPhOX membrane. Double emulsion method provided smaller polymersomes with greater colloidal stability. Increasing the temperature of the polymersome solution led to formation of polymersome clusters and this transition was found to be irreversible. Glucose oxidase (GOx) encapsulated polymersomes were used as nanoreactors for GOx/horseradish peroxidase (HRP) cascade reactions. The increase in the rate of the enzymatic reaction with increasing temperature was found to be smaller for the encapsulated enzymes compared to free enzymes.

Betulin‐containing bioactive amphiphilic copolymers: Synthesis, characterization and self‐assembly

AbstractBetulin, a natural triterpene possessing a wide range of biological activities, has been modified via Steglich esterification to produce a methacrylate derivative capable of participating in radical polymerization. The modification is intended to increase the solubility of betulin, which is almost insoluble in water, by incorporating into the composition of an amphiphilic copolymer. The resulting solubility of betulin in water increased from 8·10−5 mg/mL to more than 10 mg/mL per betulin. For this, well‐defined biocompatible thermoresponsive copolymers with high betulin content have been synthesized through the conventional and RAFT copolymerizations of betulin methacrylate (BeMA) with methoxy oligo(ethylene glycol) methacrylate (MOEGMA). BeMA was more reactive in the BeMA‐MOEGMA pair; the resulting copolymers were slightly enriched with BeMA units (r1 = 1.70, r2 = 0.93). The copolymers exhibited LCST‐type behavior. LCST was tuned by balancing the hydrophobic betulin and hydrophilic OEG fragments. The molecular weight characteristics of polymers and their behavior in aqueous and organic solutions have been studied. Copolymers obtained by conventional polymerization had lower cloud points than RAFT copolymers of the same composition. The copolymers are characterized by low critical micelle concentrations that decrease as the BeMA fraction in the copolymers increases. RAFT copolymers were shown to form unimolecular micelles resistant to dissociation, which is promising for their use in targeted drug delivery.

Aggregation of magnetic nanoparticles functionalized with trans-resveratrol in aqueous solution

In the framework of a protein–ligand-fishing strategy to identify proteins that bind to trans-resveratrol, a natural phenolic compound with pharmacological benefits, we have developed magnetic nanoparticles covalently linked to trans-resveratrol through three different derivatives and examined their aggregation behavior in aqueous solution. The monodispersed magnetic core (18 nm diameter) with its mesoporous silica shell (93 nm diameter) exhibited a notable superparamagnetic behavior useful for magnetic bioseparation. The hydrodynamic diameter, deduced from dynamic light scattering analysis, of the nanoparticle increased from 100 to 800 nm when the aqueous buffer changed from pH 10.0–3.0. A size polydispersion occurred from pH 7.0–3.0. In parallel, the value of the extinction cross section increased according to a negative power law of the UV wavelength. This was mainly due to light scattering by mesoporous silica, whereas the absorbance cross section remained very low in the 230–400 nm domain. The three types of resveratrol-grafted magnetic nanoparticles exhibited similar scattering properties, but their absorbance spectrum was consistent with the presence of trans-resveratrol. Their functionalization increased their negative zeta potential when pH increased from 3.0 to 10.0. The mesoporous nanoparticles were monodispersed in alkaline conditions, where their anionic surface strongly repulsed each other but aggregated progressively under van der Waals forces and hydrogen bonding when negative zeta potential decreased. The characterized results of nanoparticle behavior in aqueous solution provide critical insight for further study of nanoparticles with proteins in biological environment.

Rapid wetting of shear-thinning fluids

By studying the spreading behavior of aqueous glycerol and polymer solutions on smooth surfaces, we found that shear-thinning solutions behave similarly to water in the initial spreading phase, while glycerol solutions show significantly slower spreading. For the glycerol solutions, an increase in glycerol concentration effectively increases the contact-line friction, resulting in increased resistance to wetting. For the polymeric solutions, however, an increase in polymer concentration does not modify contact-line friction. As a consequence, the energy dissipation at the contact line can not be controlled by varying the amount of additives for shear-thinning fluids.

Study of Genipin Behavior in Neutral and Acidic Aqueous Solutions at Elevated Temperatures

AbstractGenipin is known to polymerize under basic conditions, and the obtained genipin oligomers might have an impact on the chemical and physical properties of the crosslinked materials. In this study, we intend to mimic the experimental condition in which genipin is used as a chemical crosslinker. We focus on the degradation of genipin at neutral and slightly acidic conditions using NMR. We report genipin polymerization at neutral and acidic conditions. Unlike dialdehyde crosslinkers, genipin requires heating to promote its crosslinking activity. We found that elevated temperatures enhance the degradation of genipin and promote its polymerization.

Thermorheological Behavior of κ-Carrageenan Hydrogels Modified with Xanthan Gum

Hydrocolloids are long-chain biopolymers that can form viscous solutions or gels when dissolved in water. They are employed as rheological modifiers in various manufacturing processes or finished products. Due to its unique gelation properties, animal gelatin is one of the most widely used hydrocolloids, finding applications in several fields such as food, pharmaceutical, and photographic. Nowadays, the challenge of finding valid alternatives to animal products has become a crucial issue, for both ethical and environmental reasons. The aim of this work, is to propose a green hydrocolloidal network, able to reproduce the gelation features of animal gelatin gels. κ-carrageenan gels may be an interesting alternative to gelatin, due to their attractive gelling features. We investigate the thermorheological behavior of κ-carrageenan aqueous solutions at various concentrations, focusing on gel features such as transition temperature and gel strength. To improve the viscoelastic response of such gels, we add a viscosity-enhancing hydrocolloid, i.e., xanthan gum. The results show that the gel strength increases exponentially with xanthan concentration, thus suggesting a synergistic interaction between the two networks. We also study the effect of sucrose on the thermal and mechanical properties of modified gels, finding a marked increase in transition temperatures and gel elasticity. In recent years, three-dimensional (3D) food printing has been extensively studied in the food industry, due to its many advantages, such as customized food design, personalized nutrition, simplified supply chain, and the expansion of available food materials. In view of this growing interest for additive manufacturing, we also study the printability of the complete formulation composed of κ-carrageenan, xanthan gum and sucrose.

Thermoresponsive and co-nonsolvency behavior of poly(N-vinyl isobutyramide) and poly(N-isopropyl methacrylamide) as poly(N-isopropyl acrylamide) analogs in aqueous media

Sets of the nonionic polymers poly(N-vinyl isobutyramide) (pNVIBAm) and poly(N-isopropyl methacrylamide) (pNIPMAm) are synthesized by radical polymerization covering the molar mass range from about 20,000 to 150,000 kg mol−1, and their thermoresponsive and solvent-responsive behaviors in aqueous solution are studied. Both polymers feature a lower critical solution temperature (LCST) apparently of the rare so-called type II, as characteristic for their well-studied analogue poly(N-isopropyl acrylamide) (pNIPAm). Moreover, in analogy to pNIPAm, both polymers exhibit co-nonsolvency behavior in mixtures of water with several co-solvents, including short-chain alcohols as well as a range of polar aprotic solvents. While the cloud points of the aqueous solutions are a few degrees higher than those for pNIPAm and increase in the order pNIPAm < pNVIBAm < pNIPMAm, the co-nonsolvency behavior becomes less pronounced in the order pNIPAm > pNVIBAm > pNIPMAm. Exceptionally, pNIPMAm does not show co-nonsolvency in mixtures of water and N,N-dimethylformamide.Graphical

Preparation of an amphiphilic peptide (P13) with proton sponge effect and analysis of its antitumor activity

In order to prevent drugs from being captured and degraded by the acidic environment of organelles, such as lysosomes, after entering cells, this study designed and synthesized a novel carrier amphiphilic polypeptide (DGRHHHLLLAAAA), designated P13, for use as a tumor-targeting drug delivery vehicle. The P13 peptide was synthesized by the solid phase synthesis method, and its self-assembly behavior and drug-loading capacity in aqueous solution were studied and characterized in vitro. Doxorubicin (DOX) was loaded by dialysis method, and P13 and DOX were mixed at a mass ratio of 6:1 to form regular rounded globules. The acid–base buffering capacity of P13 was investigated determined by acid–base titration. The results revealed that P13 had excellent acid–base buffering capacity, a critical micelle concentration value of about 0.000 21 g l−1, and the particle size of P13-Dox nanospheres was 167 nm. The drug encapsulation efficiency and drug loading capacity of micelles were 20.40 ± 1.21% and 21.25 ± 2.79%, respectively. At the concentration of 50 μg ml−1 of P13-DOX , the inhibition rate was 73.35%. The results of the in vivo antitumor activity assay in mice showed that P13-DOX also exhibited excellent inhibitory effect on tumor growth, compared with the tumor weight of 1.1 g in the control group, the tumor weight in the P13-DOX-treated group was only 0.26 g. Additionally, the results of hematoxylin and eosin staining of the organs showed that P13-DOX had no damaging effect on normal tissues. The novel amphiphilic peptide P13 with proton sponge effect designed and prepared in this study is expected to be a promising tumor-targeting drug carrier with excellent application potential.

Viscosity Factor (VF) Complementary to the Statistical Indicators Associated with the Rheological Behavior of Aqueous Solutions of Polyvinyl Alcohol

The rheological behavior of aqueous solutions of polyvinyl alcohol at 4, 6, 8 and 10% by weight has been studied and evaluated at temperatures of 20, 25, 30 and 35 °C, using five non-Newtonian fluid models independent of time: Ferrys, Robertson-Stiff, Williamson, Sisko, and Ellis de Haven. The classical method consists in carrying out regression analysis. Using a comparative procedure of determination coefficients and variances, the model that most appropriately adjusts the experimental data to said model is selected. From the statistical point of view, the Sisko and Robertson-Stiff models present better regression parameters; to better specify the choice of the respective rheological model, a new factor has been proposed in the literature, the viscosity factor (VF), which expresses the relationship between apparent and dynamic viscosity. The analysis of this factor for the five models confirms the greater stability of the Ellis de Haven model in terms of the coefficient of variation of the VF. The value of VF fluctuates between 1 and 2 for all ranges of temperature and concentration experienced for vinyl alcohol solutions. As a consequence of the above, for the choice of the non-Newtonian fluid model associated with the rheology of the aqueous solution of polyvinyl alcohol, it is necessary to analyze the statistical parameters and the VF factor simultaneously.

Schwertmannite and akaganéite for adsorption removals of Cr(VI) from aqueous solutions

Iron hydroxides have received high attention in the treatment of chromium (Cr) polluted wastewater. In this study, the obtained chemical (or biological) pincushion-schwertmannite spheres had a diameter of 2 - 5μm (0.5-1μm), and akaganéite rods had a length of 300-500nm (100-150nm) at an axial ratio of about 3. The average diameters (μm) of their agglomerated particles in solutions were 20.6-32.5 (only 0.480 for Aka-Chem). Schwertmannites and akaganéites were used to investigate Cr(VI) adsorption behaviors in aqueous solutions by batch experiments, under various reaction times, initial Cr(VI) and adsorbent levels, pH values, temperature and anions of NO3-, Cl-, CO32-, SO42-, and H2PO4-. Adsorption data well fitted to pseudo-second-order rate model (R2 = 0.999), and Langmuir (R2 = 0.954-0.988) and Freundlich (R2 = 0.984-0.996) isothermal models at pH 7.0. Maximum Cr(VI) adsorption capacities were 119/133 for Sch-Chem/Sch-Bio, and 14.6/83.6 for Aka-Chem/Aka-Bio. The H2PO4- than SO42-/CO32- had a stronger effect on Cr(VI) adsorption. Adsorbents with pHZPC of near to 4.0 still had a good Cr(VI) removal ability at pH 3.0-8.0. The possible Cr(VI) adsorption mechanisms by FTIR and XPS results for schwertmannite and akaganéite were electrostatic attractions and ion exchanges between hydroxyl (or sulfate) and chromate ions. The Cr(VI) adsorption of optimal schwertmannite and bioakaganéite was a spontaneous, endothermic and random process at the temperatures of 288-318K. They had a good regeneration ability for Cr(VI) adsorption, and removal ratios could reach to about 80% of original values (60-70% in aqueous solution with 60mg/L Cr(VI) and pH7.0, and 35-50% in wastewater with 120mg/L Cr(VI) and about pH4.0), after three cycles. Herein, schwertmannite/bioakaganéite have a promising application in treatment of acidic/neutral wastewater with chromate.

Reactivity of non-organometallic ruthenium(II) polypyridyl complexes and their application as catalysts for hydride transfer reactions.

Recently, we investigated the substitution behavior of a series of ruthenium(II) complexes of the general formula [RuII(terpy)(N∧N)Cl]Cl, where terpy = 2,2':6',2″-terpyridine, N∧N = bidentate ligand, in aqueous solutions. We have shown that the most and least reactive complexes of the series are [RuII(terpy)(en)Cl]Cl (en = ethylenediamine) and [RuII(terpy)(phen)Cl]Cl (phen = 1, 10-phenantroline), respectively, as a result of different electronic effects provided by the bidentate spectator chelates. Polypyridyl amine Ru(II) complex, viz. [Ru(terpy)(en)Cl]Cl and [Ru(terpy)(ampy)Cl]Cl (where ampy = 2-(aminomethyl)pyridine), in which the terpy chelate labilizes the metal center, are able to catalyze the conversion of NAD+ to 1,4-NADH using sodium formate as a source of hydride. We showed that this complex can control the [NAD+]/[NADH] ratio and potentially induce reductive stress in living cells, which is accepted as an effective method to kill cancer cells. Polypyridyl Ru(II) complexes, characterized in terms of the behavior in aqueous solutions, can be used as model systems to monitor heterogeneous multiphase ligand substitution reactions at the solid-liquid interface. Colloidal coordination compounds in the submicron range were synthesized from Ru(II)-aqua derivatives of starting chlorido complexes via the anti-solvent procedure and stabilized by a surfactant shell layer.

Rheological and physico-mechanical investigations on the destabilization of unfired clay bricks with almond husk additive by salt

In the aim of enhancing unfired clay bricks’ strength, waste materials incorporation gains huge interest among researchers. In this context, various methodologies are extensively used. However, the salt concentration’s effect is poorly known. In this paper, we study, through rheological and physicomechanical investigations the influence of different salt concentrations on unfired clay bricks incorporating 0%, 2%, 5%, 10%, and 20% almond husk powder by weight. We report comprehensive measurements, under dynamic conditions, of the viscoelastic behavior of aqueous solutions at high colloidal clay minerals concentrations, allowing us to derive the storage modulus which expresses the elasticity potential of the material. The same materials are used to manufacture corresponding bricks. Their strengths and water absorptions are determined and reported. In all studied suspensions, the oscillatory test showed a plateau-like with solid-like characteristic. It was indicated that the storage modulus highly depends on the amount of the additive in the clay. It increases with the incorporation of almond husk powder, and it decreases with higher salt concentration. This is explained by interparticle phenomena involving cation exchange, and hydrophilic and hydrophobic effects. Compared to old works that used the raw soil without any kind of treatment, the utilization of washed clay enabled the production of stronger bricks by up to 10,85 %. The gain, when using washed clay and incorporating 2 wt% almond husk, reached 18.88% compared to the brick with pure raw clay. The corresponding brick recorded 23.17 MPa in strength which conformed to ASTM C62 – severe weathering grade. A decrease in strength with the incorporation of almond husk is reported due to the constitution of flocculating particles that generated a porous network. To improve unfired clay bricks’ strength quality, this research comes with the recommendation of washing the soil used in unfired bricks down to reach a specific value of conductivity which can be determined facilely by rheological measurements (13 µS/cm in the case of this article)..

Development of Sustainable Magnetic Biosorbent Using Aqueous Leaf Extract of Vallesia glabra for Methylene Blue Removal from Wastewater

Vallesia glabra (Vg) is a species that has been used in traditional medicine due to its secondary metabolites (alkaloids, saponins, flavonoids, phenols, and cardiac glucosides) for the treatment of measles, rheumatism, muscle aches, and eye inflammation. The biosynthesis of magnetite nanoparticles (Fe3O4 NPs) was carried out using an aqueous leaf extract of Vg and was characterized using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Afterward, the magnetic adsorbent was tested for its potential to remove cationic dye from aqueous solutions at different pH and adsorbent mass and its reusability after several adsorption/desorption cycles. The XRD pattern and SEM micrographs resulted in an average size of NPs of 12.2 nm. Regarding the removal of MB from an aqueous solution, the kinetic and isotherm adsorption behavior is governed by the pseudo-second-order model and a Langmuir isotherm which describes an ionic exchange and chemisorption process between the positive partial charges of MB and Vg compounds stabilizing Fe3O4 NPs following a thermodynamically favorable process. Therefore, the green synthesis of NPs from Vg leaf extract is considered a sustainable alternative to removing dyes from aqueous solutions.

Shear-induced phase transition in the aqueous solution of an imidazolium-based ionic liquid.

An ionic liquid (IL) is a salt in the liquid state that consists of a cation and an anion, one of which possesses an organic component. Because of their non-volatile property, these solvents have a high recovery rate, and, hence, they are considered as environment-friendly green solvents. It is necessary to study the detailed physicochemical properties of these liquids for designing and processing techniques and find suitable operating conditions for IL-based systems. In the present work, the flow behavior of aqueous solutions of an imidazolium-based IL, 1-methyl-3-octylimidazolium chloride, is investigated, where the dynamic viscosity measurements indicate non-Newtonian shear thickening behavior in the solutions. Polarizing optical microscopy shows that the pristine samples are isotropic and transform into anisotropic after shear. These shear thickened liquid crystalline samples change into an isotropic phase upon heating, which is quantified by the differential scanning calorimetry. The small angle x-ray scattering study revealed that the pristine isotropic cubic phase of spherical micelles distort into non-spherical micelles. This has provided the detailed structural evolution of mesoscopic aggregates of the IL in an aqueous solution and the corresponding viscoelastic property of the solution.

Amphiphilic Block-Random Copolymers: Shedding Light on Aqueous Self-Assembly Behavior

The aqueous solution and aggregation behavior of polystyrene-b-poly[styrene-r-(acrylic acid)] block-random copolymers have been examined. Previous work conducted by our group showed that these materials exhibit an unanticipated ease of dispersion in water compared to polystyrene-b-poly(acrylic acid) block copolymers of similar molecular weight and composition. Herein, fluorescence labeling experiments and the presence of a critical aggregation concentration suggest the self-assembly of these materials into multichain aggregates as opposed to the self-folding behavior that was previously hypothesized. In our analysis, we demonstrate that caution must be used when interpreting particle size data from dynamic light scattering with polyelectrolyte solutions and that other characterization methods should be used to confirm findings. The fundamental understanding of block-random copolymer solution properties enables the widespread application of these easily dispersible materials in fields where amphiphilic copolymers are of interest, including biomedicine, catalysis, and stabilizers in emulsion polymerization.

Isotropic conductive paste for bioresorbable electronics.

Bioresorbable implantable medical devices can be employed in versatile clinical scenarios that burden patients with complications and surgical removal of conventional devices. However, a shortage of suitable electricalinterconnection materials limits the development of bioresorbable electronic systems. Therefore, this study highlights a highly conductive, naturally resorbable paste exhibiting enhanced electrical conductivity and mechanical stability that can solve the existing problems of bioresorbable interconnections. Multifaceted experiments on electrical and physical properties were used to optimize the composition of pastes containing beeswax, submicron tungstenparticles, and glycofurol. These pastes embody isotropic conductive paths for three-dimensional interconnects and function as antennas, sensors, and contact pads for bioresorbable electronic devices. The degradation behavior in aqueous solutions was used to assess its stability and ability to retain electrical conductance (∼7​kS/m) and structural form over the requisite dissolution period. In vitro and in vivo biocompatibility tests clarified the safety of the paste as an implantable material.

In situ growth of UiO-66-NH2 in wood-derived cellulose for iodine adsorption.

The capture of radioactive iodine is an inevitable requirement in nuclear industry for environmental protection. Metal-organic frameworks (MOFs) are a new generation of sorbents that have wide applications for iodine adsorption and recovery. Although the loading of MOFs on wood can avoid the drawbacks of the powder form of MOFs in implementation, the dense structure of wood results in the lower loading, even after delignification, which limits the adsorption capacity. Herein, a hierarchically porous UiO-66-NH2 @WCA composite was fabricated by in-situ synthesis of UiO-66-NH2 in wood-derived cellulose aerogel (WCA) that was further removed hemicellulose from delignified wood. UiO-66-NH2 @WCA exhibited a high loading (36wt%) of UiO-66-NH2 crystals and a high adsorption capacity of 704mg/g for iodine vapor and 248mg/g for iodine aqueous solution. The adsorption behavior in iodine aqueous solution was well predicted by the Freundlich isotherm and pseudo-second-order kinetic model. The adsorption capacity of UiO-66-NH2 @WCA was highest in solution when the pH was 6, while the ionic strength had little effect. The hydroxyl groups on the WCA matrix had a charge transfer effect with iodine, providing additional sites for iodine capture. Furthermore, a packed column system was applied to demonstrate the excellent recyclability and potential for practical application.