Selective adsorption mechanisms of iodinated trihalomethanes onto thiol-functionalized HKUST-1s in a mixed solute.

The selective adsorption mechanisms involved in the competitive adsorption of five iodinated trihalomethanes (I-THMs) onto dithiolglycol and (3-mercaptopropyl)-trimethoxy functionalized HKUST-1 (HK-SH and HK-MPTS, respectively) were investigated by single- and mixed-batch adsorption. HK-SH had the highest adsorption rates and capacities for the five I-THMs, followed by HK-MPTS and pristine HKUST-1, even though the porosity and surface area decreased after modification. The primary adsorptive mechanism of HK-SH consists of ion-dipole interactions of I-THMs with the protonated hydroxyl and thiol groups at the metal (Cu) node, which is supported by Lewis acid-base reactions via Cu-Cu complex and π-π interactions. In a mixed solute, bromodiiodomethane, which was the most hydrophobic and had the smallest molecular size, exhibited the most competitive adsorption on HK-SH. In contrast, the selective adsorption of I-THMs onto HK-MPTS was affected by their log Kow values, causing hydrophobic partitioning onto the alkyl chain of the mercaptopropyl group. Iodinated haloforms tend to achieve a higher adsorption rate and capacity than chlorinated and brominated haloforms via hydrophobic partitioning. Moreover, dithiolglycol grafted onto HK-SH can better promote the excellent selective adsorption performance of iodoacetamide than dichloroiodomethane and iodoacetic acid in both single- and mixed-solute solutions due to hydrogen bonding via the -NH2 group of diiodoacetamide.

Effects of electrolytes and fractionated dissolved organic matter on selective adsorption of pharmaceuticals on terephthalic acid-based metal-organic frameworks.

In this study, we investigated the synergetic effects of coexisting electrolytes and dissolved organic matter (DOM) on Carbamazepine (CBZ) and Ciprofloxacin (CIP) adsorption on the 1D flexible structure of MIL-53(Al) and 3D rigid structure of UiO-66(Zr). The effects of electrolytes on the adsorption of CBZ and CIP on 1D flexible framework of MIL-53(Al) were more significant than those observed from the 3D framework of UiO-66(Zr). The presence of sulfate, nitrate, and phosphate anions indicates high potential to promote the adsorption of CBZ and CIP onto MIL-53(Al) and UiO-66(Zr) because of the decrease of solubility and strengthening of electrostatic interactions by substitution of oxo-anions at the metal complex node via covalent bonding. The lower hydration energy of the potassium ion enhanced CBZ adsorption on MIL-53(Al), while the higher hydration energy of calcium and magnesium ions reduced the adsorption capacity of CBZ and CIP on MIL-53(Al) and UiO-66(Zr). CBZ interacted with fractionated humic acid better than CIP. High-density carboxylic and aromatic functional groups on humic acid ensured that only humic acid larger than 1KDa was adsorbed by MIL-53(Al). Tryptophan-like and humic acid-like DOM were both detected in real hospital effluent, and their effects on CIP and CBZ adsorption onto MIL-53(Al) were investigated. The presence of tryptophan did not affect CBZ adsorption on MIL-53(Al) (except when coexisting with calcium ions). Conversely, tryptophan interfered with CIP adsorption. The presence of humic acid lower than 1KDa promoted the adsorption of CBZ and CIP by increasing the breathing effect of MIL-53(Al)'s 1D flexible framework. The presence of humic acid with molecular size greater than 1KDa enhanced both CBZ and CIP adsorption via a multilayer adsorption mechanism.

Upcycling of post-consumer polyethylene terephthalate bottles into aluminum-based metal-organic framework adsorbents for efficient orthophosphate removal.

2-Phosphonobutane-1,2,4,-tricarboxylic acid (PBTC) is an orthophosphate compound widely used as an antiscalant chemical and corrosion inhibitor in manufacturing. However, PBTC poses persistent environmental concerns due to its stability and resistance to conventional water treatment. In addressing the issues of PBTC in aquatic systems, Al-based metal-organic frameworks (MOFs) have been developed and applied as sustainable adsorbents. The materials are synthesized from terephthalic acid (TPA) linkers derived from upcycling products of post-consumer polyethylene terephthalate (PET) bottles. The PET-derived linker was prepared using alkaline hydrolysis followed by acidification and employed in forming MIL-53 (Al), with a comparative assessment against the corresponding MOFs made from commercial-grade TPA. The structures and properties of the materials were characterized with microscopic and spectroscopic methods. The synthesized adsorbents achieved a phosphate adsorption capacity of 826 mg/g at pH 5, with kinetics fitting a pseudo-second-order model and isotherm patterns aligning with Langmuir, Freundlich, and Sips models, indicative of diverse adsorption on heterogeneous surfaces. The results highlight the role of electrostatic interactions and hydrogen bonding mechanisms in PBTC adsorption. The eco-friendly materials with high adsorption performance offer an innovative route for sustainable waste management and water purification.

Effects of Chemical Cleaning on the Ageing of Polyvinylidene Fluoride Microfiltration and Ultrafiltration Membranes Fouled with Organic and Inorganic Matter.

Herein, the effects of cleaning with sodium hydroxide and citric acid solutions as cleaning reagents on the changes in the properties of two hollow-fiber PVDF microfiltration (MF) and ultrafiltration (UF) membranes fouled with organic and inorganic matter were investigated. Accelerated membrane ageing was induced by use of high concentrations of tannic acid and iron oxide (Fe2O3) particles in the feed water; these conditions were kept with different membrane soaking times to observe temporal effects. It was found that tannic acid molecules adsorb onto the membrane surface that results in changes in surface characteristics, particularly surface functional groups that are responsible for enhancing membrane's hydrophilicity. Experimental results demonstrate that NaOH had a stronger effect on the tensile strength and surface chemistry of the fouled MF and UF membranes than citric acid. Prediction of lifetime by an exponential (decay) model confirmed that the UF membrane cleaned with NaOH would be aged within about 1.8 years and the MF membrane after about 5 years, at cleaning every 15 days, downtime 2 h per cleaning, when a 10% tensile strength decrease against the original membrane is allowed.

Transparent Anti-SARS COV-2 Film from Copper(I) Oxide Incorporated in Zeolite Nanoparticles.

The high antibacterial and antiviral performance of synthesized copper(I) oxide (Cu2O) incorporated in zeolite nanoparticles (Cu-Z) was determined. Various Cu contents (1-9 wt %) in solutions were loaded in the zeolite matrix under neutral conditions at room temperature. All synthesized Cu-Z nanoparticles showed high selectivity of the cuprous oxide, as confirmed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analysis. An advantage of the prepared Cu-Z over the pristine Cu2O nanoparticles was its high thermal stability. The 7 and 9 wt % Cu contents (07Cu-Z and 09Cu-Z) exhibited the best activities to deactivate Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus bacteria. The film coated with 07Cu-Z nanoparticles also had high antiviral activities against porcine coronavirus (porcine epidemic diarrhea virus, PEDV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Specifically, the 07Cu-Z-coated film could reduce 99.93% of PEDV and 99.94% of SARS-CoV-2 viruses in 5 min of contact time, which were higher efficacies and faster than those of any previously reported works. The anti-SARS-CoV-2 virus film was coated on a low-cost PET or PVC film. A very small amount of cuprous oxide in zeolite was used to fabricate the antivirus film; therefore, the film was more transparent (79.4% transparency) than the cuprous oxide film or other commercial products. The toxicity of 07Cu-Z nanoparticles was determined by a toxicity test on zebrafish embryo and a skin irritation test to reconstruct a human epidermis (RhE) model. It was found that the impact on the aquatic environment and human skin was lower than that of the pristine Cu2O.

S-nitrosocysteine-decorated PbS QDs/TiO2 nanotubes for enhanced production of singlet oxygen.

Nitric oxide (NO) is an endogenous diatomic molecule important in regulation of numerous physiological functions. The photorelease of NO in a controlled manner can potentially be used in photodynamic therapy (PDT). We present here a method to combine S-nitrosocysteine with TiO(2) nanotube-doped PbS quantum dots (PbS QDs) as a nitric oxide-releasing vehicle to promote production of singlet oxygen. The PbS QDs with a diameter ∼3.6 nm (PbS/TNTs) were attached to the TiO(2) nanotube by using a thiolactic acid linker. S-nitrosocysteine-decorated PbS/TiO(2) nanotubes were prepared by dipping PbS/TNTs in a cysteine solution followed by nitrosylation. The results suggest that this hybrid nanomaterial is capable of photoreleasing nitric oxide and producing singlet oxygen using near-IR light.

Synthesis of gold nanoclusters: a fluorescent marker for water-soluble TiO2 nanotubes.

The first example of a water-soluble wrapped titania nanotube (TNT) decorated with fluorescent gold nanoparticles has been prepared. Gold nanoparticles ∼ 1.6 nm in diameter were grown on the TiO(2) nanotubes using a thiolactic acid linker to control the size. The gold clusters emit at 660 nm in water and were imaged using confocal microscopy. The gold decorated TNTs were suspended in water by wrapping the nanotubes with poly-L-arginine.

Adsorption of iodinated trihalomethanes onto thiol functionalized ZIF-8s: Active adsorption sites, adsorptive mechanisms, and dehalogenation by-products.

The adsorptive mechanisms operating in, and the effect of two different thiol modification methods on, the removal of five iodinated trihalomethanes (I-THMs) by the zeolite imidazolate framework (ZIF-8) were investigated in single and mixed solutions. The direct postgrafting of dithioglycol to the zinc complex node of ZIF-8 (ZF-SH) can increase the mesopore structures that enhance inner pore accessibility; this increase is a critical property required for excellent adsorption of I-THMs. The synergetic adsorptive interactions consist of Lewis acid-base interactions via the Zn-Zn complex, ion-dipole interactions involving the protonated hydroxyl and thiol groups, and hydrophobic interactions at the imidazole ring. In contrast to ZF-SH, the (3-mercaptopropyl)-trimethoxy functionalized silica coating on ZIF-8 (ZF-Si-SH) causes a lower thiol moiety and a steric effect that is reflected in its lower adsorption capacity. In both single and mixed solutions, the small molecular size and hydrophobic nature of I-THMs can promote better adsorption capacity on all thiol-modified ZIF-8, while the minus dipole charge distribution of the I-THMs structure plays a more critical role in selective adsorption on pristine ZIF-8. Interestingly, the dehalogenation of triiodomethane to diiodomethane due to a nucleophilic substitution (SN2) reaction can be accelerated by the thiol functionalized silica layer on ZIF-8.

Flexible and Hydrophilic Copolyamide Thin-Film Composites on Hollow Fiber Membranes for Enhanced Nanofiltration Performance.

Flexible and hydrophilic copolyamide (Co-PA) thin-film composite (TFC) membranes were fabricated as a selective layer on the outer surface of the polyvinylidene fluoride hollow fiber membrane substrate. The fabrication process was carried out by the dip-coating method to create three TFC membranes. The first layer is tannic acid and the second layer is (3-aminopropyl)triethoxysilane, which is followed by Co-PA as a final selective layer. The Co-PA TFC membrane was prepared through interfacial polymerization via the combination of various short-chain aliphatic diamines and conventional aromatic diamines with trimesoyl chloride. The influence of coating layers and total diamine concentration on the Co-PA TFC membrane was investigated in terms of the membrane's physicochemical and mechanical properties, morphology, surface thickness and roughness, water contact angle, surface charge, and nanofiltration (NF) performance. The obtained Co-PA TFC membrane system was operated under low pressure (2 bar) with pure water flux in the range of 23.8-83.9 L m-2 h-1 and exhibited better hydrophilicity, flexibility, molecular weight cutoff, and NF performance compared to the conventional PA TFC membrane. The superior properties of Co-PA are due to the increased chain mobilities provided by short-chain aliphatic diamines in its structure. The best Co-PA TFC membranes, which were synthesized using diamines containing four carbon atoms, achieved a significant improvement in NF membrane performance and selectivity (pure water flux = 56.9 L m-2 h-1 and salt and dye rejection in the range of 46.2-99.2%). This Co-PA TFC membrane is a promising membrane for its high flexibility, hydrophilicity, and selectivity of the NF membrane.

Selective adsorption mechanisms of pharmaceuticals on benzene-1,4-dicarboxylic acid-based MOFs: Effects of a flexible framework, adsorptive interactions and the DFT study.

The synergetic effects of benzene-1,4-dicarboxylic acid (BDC) linker structure and the metal cluster of MOFs on adsorption mechanisms of carbamazepine, ciprofloxacin and mefenamic acid were investigated in single and mixed solutions. A 1D flexible framework MIL-53(Al), 3D rigid framework UiO-66(Zr) and 3D flexible framework MIL-88B(Fe) were applied as adsorbents. The breathing effect of MIL-53(Al) caused by its flexible structure can enhance intraparticle diffusion for all pharmaceuticals and perform a critical role in excellent adsorption performances. The 3D rigid BDC structure of UiO-66(Zr) caused a steric effect that reflected low or negligible adsorption. Unless concerning accessibility through the internal structure of the MOFs, the binding strengths calculated by the DFT study were in the following order: MIL-88B(Fe) > MIL-53(Al) > UiO-66(Zr). The Fe cluster in MIL-88B(Fe) seems to have the highest affinity for the carboxylic group of pharmaceuticals compared with Al and Zr; however, the lower porosity of MIL-88B(Fe) might limit the adsorption capacity. Moreover, in mixed solutions, the higher acidity of mefenamic acid can enhance competitive performance in interactions with the metal cation cluster of each MOF. Together with the breathing effect, H-bonding and π-π interaction were shown to be the alternative interactions of synergetic adsorption mechanisms.

Fabrication of PbS quantum dot doped TiO2 nanotubes.

PbS quantum dots (PbS QDs) were prepared on the inside and outside surfaces of TiO(2) nanotubes by using thiolactic acid as an organic linker. The sizes of PbS QDs were controlled by employing a dip coating process to anchor the PbS QDs onto the TiO(2) nanotubes. The PbS QDs with diameters of 2-10 nm were obtained by adjusting the concentration of thiolactic acid. TiO(2) nanotubes with PbS QDs located only inside the nanotubes were prepared by first coating the tubes with the double-chain cationic surfactant DDAB. The PbS QDs supported on TiO(2) nanotubes were characterized by TEM, as well as Raman, FT-IR, and UV-vis spectroscopy.