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Objective: Dental implants fabricated from titanium have several limitations and therefore, alternative materials that fulfil the criteria of successful dental implant (bioactivity and anti-bacterial activity) need to be considered. Polyether ether ketone (PEEK) has been suggested to replace titanium implants. However, this material needs surface modification to meet the appropriate criteria. A nano-sized zirconium phosphate/GO (nZrP/GO) composite coating was prepared to improve PEEK's biological qualities., Methods: Polished and cleaned PEEK discs were coated with the composite of nZrP doped with 1.25 wt% GO by the soft-template method. To analyze the composite coating, X-ray, atomic force microscopy, and field emission scanning electron microscopy-energy dispersive spectroscopy were used. The adhesion of the coating to PEEK was measured by adhesive tape test. By measuring the optical contact angle, the coated and non-coated samples' differences in wettability were evaluated. Antimicrobial activity was evaluated against S. aureus and E. coli and cytotoxicity tested employing gingival fibroblasts and osteoblast-like cells., Results: The nZrP/GO composite coating was 23.45 µm thick, was irregular and attached strongly to the PEEK surface. Following coating, the water contact angle dropped to 34° and surface roughness to 13 nm. The coating reduced the count of bacteria two-fold and was non-cytotoxic to mammalian osteoblast-like cells and fibroblasts. A precipitation of nano-calcium-deficient apatite was observed on the surface of the nZrP/GO coating following a 28-day immersion in SBF., Significance: PEEK-coated with nZr/GO coating is a good candidate as dental implant., Competing Interests: Declaration of Competing Interest None., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Polypropylene and ammonium phosphate (AP) composites were synthesized at a 25 wt% concentration. The changes in the morphological, thermal, and physical behavior of the composites were analyzed with the addition of lignosulfonate (LG) and zirconium phosphate (ZrP). Additionally, metallic zirconium was deposited onto lignosulfonate using the magnetron sputtering technique to develop polypropylene and zirconium-modified lignosulfonate (LGMod) composites. Thus, composites of PP/25AP, PP/25AP/8LG/5ZrP, and PP/25AP/8LGMod were synthesized. The synthesis involved mixing the materials in a Hake mixer, followed by compression molding. The composites were characterized by field emission scanning electron microscopy (SEM-EDS), a thermogravimetric analysis (TGA) with combustion parameters, a vertical burn test (UL-94), a thermal camera, and mechanical properties. All composites achieved a V2 rating according to UL-94 standards. The PP/25AP extinguishes flames more quickly compared to other materials, approximately 99.2% faster than PP and showed the lowest temperature variation and mass loss after burning. The PP/25AP/8LG/5ZrP composite exhibited a 7% higher rigidity and 84.5% better flame retardancy compared to pure PP. Additionally, substituting ZrP with LGMod led to a lower environmental impact and improved thermal properties, despite some mechanical disadvantages.

Background: Radioligand therapy using alpha emitters has gained more and more prominence in the last decade. Despite continued efforts to identify new appropriate radionuclides, the combination of 225 Ac/ 213 Bi remains among the most promising. Bismuth-213 has been employed in clinical trials in combination with appropriate vectors to treat patients with various forms of cancer, such as leukaemia, bladder cancer, neuroendocrine tumours, melanomas, gliomas, or lymphomas. However, the half-life of 213 Bi (T ½  = 46 min) implies that its availability for clinical use is limited to hospitals possessing a 225 Ac/ 213 Bi radionuclide generator, which is still predominantly scarce. We investigated a new Ac/Bi generator system based on using the composite sorbent α-ZrP-PAN (zirconium(IV) phosphate as active component and polyacrylonitrile as matrix). The developed 225 Ac/ 213 Bi generator was subjected to long-term testing after its development. The elution profile was determined and the elution yield, the contamination of the eluate with the parent 225 Ac and the contamination of the eluate with the column material were monitored over time., Results: The high activity (75 MBq of parent 225 Ac) generator with a length of 75 mm and a diameter of 4 mm containing the composite sorbent α-ZrP-PAN with a particle size of 0.8 to 1.0 mm as the stationary phase, eluted with a mixture of 10 mM DTPA in 5 mM nitric acid, provided 213 Bi with yields ranging from 77 % to 96 % in 2.8 mL of eluate, with parent 225 Ac contamination in the order of 10 -3  %, up to twenty days of use., Conclusion: All the results of the monitored parameters indicate that the composite sorbent α-ZrP-PAN based separation system for the elution of 213 Bi is a very promising and functional solution., Competing Interests: Declaration of competing interest The authors declare that they have no competing interests., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Composites of amorphous ZrP and N-doped carbon were prepared in a one-step pyrolysis process instead of general post-loading technique. Owing to their mesoporous structure (6-10 nm) and Zr content (up to 41 wt%), the amphoteric materials have potential use in the cycloaddition of CO 2 to epoxides, which is an acid‒base tandem process including the ring opening of epoxides and the addition of CO 2 . Substantial work has been done on how starting materials impact the structure and performance of composite materials. The coordination between metal and melamine has been confirmed, and it can be implanted in the melamine-polymer initiation of formation of porous metal-carbon materials. The composite catalysts exhibit amphoteric properties, present broad-spectrum adsorption, and finally produce carbonates via cycloaddition of CO 2 to epoxides. It is remarkable that the multiple characteristics of porous solids are stabilized, and no significant loss of catalytic performance is observed after four cycles., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2023 The Authors.)

Salt lake brine originating from Qinghai, China has abundant cesium resources and huge total reserves. The inorganic ion exchangers ammonium molybdophosphate (AMP) and zirconium phosphate (ZrP) have the significant advantages of separating and extracting Cs + as a special adsorbent. Nevertheless, their high solubility in water leads to a decrease in their ability to adsorb Cs + in aqueous solutions, causing problems such as difficulty with using adsorbents alone and a difficult recovery. In this work, an environmentally friendly polyurethane sponge (PU sponge) with a large specific surface area is employed as an adsorbent carrier by physically impregnating dopamine-coated AMP and ZrP onto a PU sponge, respectively. The experiment found that under the same conditions, the AMP/PU sponge performs better than the ZrP/PU sponge for Cs + adsorption. When the amount of adsorbent reaches 0.025 g, the adsorption capacity reaches saturation. The adsorption efficiency remains above 80% when the concentration of Cs + is 5-35 mg/L. The kinetic calculations show that adsorption is spontaneous, feasible, and has a higher driving force at high temperatures. In addition, the power and mechanism of the interaction between adsorbent and adsorbent are explained using the density functional theory calculation. This efficient, stable, and selective Cs + adsorbent provides design guidelines.

A supramolecular self-assembly method was used to prepare melamine cyanurate/α-ZrP nanosheets (MCA@α-ZrP) as a novel hybrid flame retardant for thermoplastic polyurethane (TPU). Microstructure characterization showed a uniform dispersion with strong interfacial strength of the MCA@α-ZrP hybrid within the TPU matrix, leading to simultaneous enhancements in both mechanical and fire-safety properties. The TPU/MCA@α-ZrP nanocomposite exhibited 43.1 and 47.0% increments in tensile strength and fracture energy, respectively. Thanks to the platelike structure of α-ZrP coupled with the dilution effect of MCA (releasing nonflammable gases), the hybrid MCA@α-ZrP reduced the peak heat release rate of TPU by 49.7% in comparison with 15.8 and 35.4% for TPU/MCA and TPU/ α-ZrP composites, respectively. The fire performance index of TPU is significantly promoted by 90% upon adding the MCA@α-ZrP hybrid. Additionally, LOI and UL-94 tests showed high flame-retarding characteristics for the MCA@α-ZrP hybrid. For example, LOI increased from 20.0% for neat TPU to 25.5% for the MCA@α-ZrP hybrid system, and it was rated V-1 from the UL-94 test. Furthermore, the smoke production and pyrolysis products were significantly suppressed by adding the MCA@α-ZrP hybrid into TPU. Interfacial hydrogen bonding, the dilution effect of MCA, forming a "labyrinth" layer, and catalytic action of α-ZrP nanosheets synergistically improved both the mechanical performance and flame retardancy of TPU nanocomposites. This work provides a new example of integrating traditional flame retardants with functional nanosheets to develop polymeric nanocomposites with high mechanical and fire-safety properties.

Different amounts of sodium-alendronate (ALN) were loaded into layered zirconium phosphates of alpha and gamma type (αZP and γZP) by means of topotactic exchange reactions of phosphate with ALN. In order to extend the exchange process to the less accessible interlayer regions, ALN solutions were contacted with colloidal dispersions of the layered solids previously exfoliated in single sheets by means of intercalation reaction of propylamine (for αZP) or acetone (for γZP). The ALN loading degree was determined by liquid P-nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP), and it was reported as ALN/Zr molar ratios (Rs). The maximum R obtained for γZP was 0.34, while αZP was able to load a higher amount of ALN, reaching Rs equal to 1. The synthesized compounds were characterized by X-ray powder diffractometry, scanning electron microscopy (SEM), solid-state NMR, and infrared spectroscopy. The way the grafted organo-phosphonate groups were bonded to the layers of the host structure was suggested. The effect of ZP derivatives was assessed on cell proliferation, and the results showed that after 7 days of incubation, none of the samples showed a decrease in cell proliferation.

The high mechanical strength, large specific surface area, favorable biocompatibility, and degradability of nanocellulose (CNC) enable it to be a potential alternative to petroleum-based materials. However, the traditional preparation of CNCs requires a large amount of strong acid, which poses a serious challenge to equipment maintenance, waste liquid recycling, and economics. In this study, a solid and easily recoverable zirconium phosphate (ZrP) was used to assist in the phosphoric acid co-catalyzed hydrolysis of lignocellulose for extracting CNCs. Due to the presence of acidic phosphate groups, ZrP has a strong active center with a high catalytic activity. With the assistance of ZrP, the amount of phosphoric acid used in the reaction is significantly reduced, improving the equipment's durability and economic efficiency. The effects of the process conditions investigated were the phosphate acid concentration, reaction temperature, and reaction time on the yield of CNCs. The Box-Behnken design (BBD) method from the response surface methodology (RSM) was applied to investigate and optimize the preparation conditions. The optimized pre-treatment conditions were 49.27% phosphoric acid concentration, 65.38 °C reaction temperature, and 5 h reaction time with a maximal cellulose yield (48.33%). The obtained CNCs show a granular shape with a length of 40~50 nm and a diameter of 20~30 nm, while its high zeta potential (-24.5 mV) make CNCs present a stable dispersion in aqueous media. Moreover, CNCs have a high crystallinity of 78.70% within the crystal type of cellulose Ⅰ. As such, this study may pioneer the horizon for developing a green method for the efficient preparation of CNC, and it is of great significance for CNCs practical production process.

The emergence of antibiotics in water has been globally recognized as a critical pollution issue. Antibiotics (such as Ciprofloxacin (CPFX) pose a serious threat to humans and to the ecosystem due to its accumulation in water sources which can lead to chronic health problems and endanger aquatic life. It is therefore crucial to properly remove them from water. In this work, a nano-composite adsorptive membrane based on Zirconium Phosphate (ZrP) adsorbent supported on Polyethersulfone (PES) was synthesized and evaluated for the removal of CPFX from synthetic aqueous solutions. The membranes described here showed a very high antibiotic removal rate. The effect of various parameters such as the initial concentration of the antibiotic, the adsorbent dosage, contact time, pH, and temperature was studied. The equilibrium data were found to reasonably best fit with the Temkin isotherm model. The membranes showed a high ciprofloxacin removal (99.7%) as opposed to (68%) when PES membrane alone was used. Moreover, a significant improvement in the membrane's water flux (100.84 L/m 2 .h) and permeability (97.62 L/m 2 .hr.bar) were noticed as opposed to pure PES membrane's flux and permeability. The adsorptive membranes were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Brunauer-Emmett-Teller (BET). The results confirmed the successful formation of ZrP nanoparticles adsorbent within the membrane matrix, and with enhanced hydrophilic properties. The membrane was successfully regenerated and reused up to 5 times. The results of this work showed the potential of such membranes for the removal of ciprofloxacin and at a high efficiency., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Effective and efficient disposal of radioactive pollution has been crucial for responding to unexpected nuclear accidents and guaranteeing the sustainable development of nuclear energy. In this study, a kind of porous zirconium phosphate was synthesized with a sol-gel process followed by a post-synthesis modification to remove the radioactive Sr 2+ from wastewater. The prepared materials were characterized by different technologies including FT-IR, SEM-EDS, XRD and XPS, and then the adsorption performance was evaluated in batch and column modes. Experimental results suggested that the porous zirconium phosphate adsorbent was successfully prepared with Na + dispersed in the channels for exchange. It inherited the excellent properties of zirconium dioxide aerogel and exhibited mesoporous structure and large specific surface area. Compared with traditional zirconium phosphate, the adsorption kinetics and the adsorption capacity were improved simultaneously. Especially, it showed excellent selectivity towards Sr 2+ among different cations, and even could remove the low-level Sr 2+ from natural seawater efficiently, which powerfully demonstrated that the prepared material could be applied in the treatment of practical wastewater. Spectra studies uncovered that the adsorption activities were dominated by the ion exchange mechanism between external Sr 2+ and interlaminar Na + or H + . In conclusion, this paper not only reports a novel synthesis strategy for the acquisition of porous zirconium phosphate, but also presents a promising adsorbent for the Sr 2+ removal., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The nanofiller zirconium phosphate (ZrP) was mixed into poly(lactic acid) (PLA) to ameliorate its thermal stability. The elastomer ethylene-methyl acrylate-glycidyl methacrylate copolymer (E-MA-GMA) was introduced into the PLA/ZrP nanocomposite through melt-mixing to improve its toughness and obtain a super-tough PLA/ZrP/E-MA-GMA nanocomposite. The impact strength of the PLA/ZrP/E-MA-GMA nanocomposite, with a composition ratio of 72/3/25, was improved to 71.5 kJ/m 2 , about 25 times greater than the impact strength of pure PLA. The dynamic mechanical analysis (DMA) confirmed that E-MA-GMA has excellent compatibility with the matrix of PLA. A typical core-shell structure that can cause massive shear-yielding deformation was characterized by transmission electron microscopy (TEM), which gave the nanocomposite excellent toughness.

The paper presented the mechanical (MChT), microwave (MWT), and hydrothermal (HTT) methods of zirconium phosphate samples modification in order to improve its adsorption affinity for the Ag (I) ions. The FTIR studies proved that the modification of both gel and xerogel samples with the ultrasonic microwaves causes an increase in the concentration of phosphate groups on the surface of MWT-modified zirconium phosphate: the isoelectric point pHiep = 2.2-2.9 for these samples against 3.9 for the initial sample and pKa2 values were 4.7-5.6 and 6.3, respectively. As resulting from the Ag + ion adsorption studies, the MWT treatment of zirconium phosphate samples caused the greatest affinity of Ag + ions for the surface of MWT zirconium phosphate. Compared with the initial ZrP sample, the shift of the Ag (I) ion adsorption edge towards lower pH values was observed, e.g., with adsorption of Ag (I) ions from the solution with the initial concentration of 1 µmol/dm 3 for the initial ZrP sample pH50% = 3.2, while for the sample MWT ZrPxero pH50% = 2.6.

Nanotechnology has provided a new opportunity for water decontamination from trace heavy metals, yet the relatively poor acidic stability remains a major obstacle for the nano-adsorbents, given that acidic treatment is frequently used to regenerate the heavy metal-saturated adsorbents. Zirconium phosphate (ZrP) is very promising for water treatment due to its absolute insoluble nature, though it interacts with heavy metals mainly through the non-specific electrostatic attraction. Herein, we prepared the ultrafine ZrP (~3.9 nm) inside the commercially available gel-type cation exchanger (N001), i.e., the sulfonated poly(styrene-co-divinylbenzene) bead. The resultant nanocomposite ZrP@N001 contained the amorphous nanoparticles (NPs) with metastable γ-ZrP structure as the main phase, unlike the layered α-ZrP formed inside the macroporous cation exchanger D001 (referred to as ZrP@D001). As a result, ZrP@N001 could selectively adsorb heavy metals through inner-sphere coordination, possessing a much stronger adsorption affinity than ZrP@D001, as confirmed by XPS analysis. In both batch and column assays on the Pb(II)-polluted water, ZrP@N001 exhibited superior adsorption performance over ZrP@D001. After adsorption, the exhausted ZrP@N001 was fully refreshed by acidic treatment for a 5-cyclic adsorption-regeneration run with constant removal efficiencies. This study may open a door for the rational design of highly efficient water purifiers for heavy metal control., (Copyright © 2021 Elsevier B.V. All rights reserved.)

A Zr-loaded P-containing biomass-derived activated carbon (ACPZr) has been tested for methanol dehydration between 450 and 550 °C. At earlier stages, methanol conversion was complete, and the reaction product was mainly dimethyl ether (DME), although coke, methane, hydrogen and CO were also observed to a lesser extent. The catalyst was slowly deactivated with time-on-stream (TOS), but maintained a high selectivity to DME (>80%), with a higher yield to this product than 20% for more than 24 h at 500 °C. A kinetic model was developed for methanol dehydration reaction, which included the effect of the inhibition of water and the deactivation of the catalyst by coke. The study of stoichiometric rates pointed out that coke could be produced through a formaldehyde intermediate, which might, alternatively, decompose into CO and H 2 . On the other hand, the presence of 10% water in the feed did not affect the rate of coke formation, but produced a reduction of 50% in the DME yield, suggesting a reversible competitive adsorption of water. A Langmuir-Hinshelwood reaction mechanism was used to develop a kinetic model that considered the deactivation of the catalyst. Activation energy values of 65 and 51 kJ/mol were obtained for DME and methane production in the temperature range from 450 °C to 550 °C. On the other hand, coke formation as a function of time on stream (TOS) was also modelled and used as the input for the deactivation function of the model, which allowed for the successful prediction of the DME, CH 4 and CO yields in the whole evaluated TOS interval.

This chapter reports a single-step preparation of nanoarmored bi-enzyme systems assembled on 1-D and 2-D nanomaterials, with glucose oxidase and peroxidase enzymes as model systems for cascade bio-catalysis. This is a simple and facile method to both exfoliate the bulk 1D (carbon nanotubes, CNT) and 2D nanomaterials (α-Zirconium phosphate, α-ZrP) and bind the enzymes in a single step. Exfoliation of the bulk material enhances the accessible surface area of the materials for the enzyme binding, and it also boosts the diffusion of reagents from the bulk phase to the active sites of the bio-catalysts. For example, a mixture of horseradish peroxidase, glucose oxidase, and bovine serum albumin (BSA) were adsorbed on the surfaces of the α-ZrP nanoplates or carbon nanotubes (CNT) as the bulk materials are exfoliated simultaneously, in a one-step process. The resulting bio-catalysts were thoroughly characterized by powder X-ray diffraction, electron microscopy, biochemical and biophysical methods, while enzyme activity studies proved successful binding of enzymes with retention of activities or even enhancements in their specific activities. For example, GOx/HRP/BSA/CNT displayed 6 times the activity of a mixture of GOx/HRP/BSA, under otherwise identical conditions. Similarly, GOx/HRP/BSA/ZrP had 3.5 times the activity of the corresponding mixture of GOx/HRP/BSA, in the absence of the nanoplates. These robust nano-dispersions worked extraordinarily well as active bio-catalysts. These two kinds of fabricated biocatalyst dispersions are also highly stable., (© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)

We report the rational design of nanocomposite with zirconium phosphate encapsulated on graphene oxide (ZrP/GO) for the highly sensitive and selective analysis of fenitrothion (FT). The characteristics of ZrP/GO nanocomposite are systematically analyzed by various in-depth electron microscopic, spectroscopic and analytical techniques. The ZrP/GO nanocomposite modified electrodes show better electrochemical response towards FT than other electrodes. The improved electrochemical activity of nanocomposite is attributed to large surface area, high conductivity, numerous active surface sites, GO nanosheets served as the conductivity matrix while preventing ZrP from agglomeration and the synergistic effect of ZrP and GO. Benefitting from the unique features, our fabricated sensor exhibits the superior performance in terms of wide working range (0.008-26 μM), appropriate peak potential (-0.61 V), low limit of detection (0.001 µM), high sensitivity (6 µA µM -1 cm -2 ) with the regression coefficient of 0.999. Additionally, the electrochemical sensor also displays good selectivity, excellent stability (99.6%), reproducibility (4.9%) and reusability (6.1%). The practical applicability of ZrP/GO sensor is shown by performing the detection of FT in water samples. These results clearly suggest that the ZrP/GO nanocomposite is an efficient electrode material for the future real-time environmental monitoring of FT., (Copyright © 2021. Published by Elsevier B.V.)

Layered zirconium phosphate (ZrP) is a versatile material with phosphate (POH ) groups able to exchange inorganic and organic cations or to intercalate basic molecules. The present review deals with the use of this material as a sorbent for heavy metal cations or dye molecules in wastewater treatments. The possibility to combine ZrP with polymers or other inorganic materials, in order to have suitable systems for real and large scale applications, was investigated, as well as the combination with photocatalytic materials to obtain hetrogeneous photocatalysts for the capture and photodegradation of organic dye molecules.

There is an increasing demand on synthesizing pharmaceuticals and biomaterials that possess antimicrobial and/or antiviral activities. In this respective silver nanoparticles are known for their excellent antimicrobial activity. Nevertheless, their uncontrolled release in a biological medium can induce a cytotoxic effect. For this, we explored the use of nanolayered metal phosphates based on titanium and zirconium as materials that can be enriched with silver nanoparticles. Employing the hydrothermal route, crystalline α-phases of zirconium and titanium phosphates (α-ZrP, α-TiP) were synthesized and there after surface-enriched with silver nanoparticles. The structural assessment confirmed the stability of the structures and their sizes are in the nanoscale at least in one dimension. The cytocompatibility assays confirmed the biocompatibility of the pristine phases and the antimicrobial assay confirmed that both silver-enriched nanolayered structures maintain an antibacterial effect at reasonably low concentrations.

Polymeric composites, where bioactive species are immobilized on inorganic nanostructured matrix, have received considerable attention as surfaces able to reduce bacterial adherence, colonization, and biofilm formation in implanted medical devices. In this work, potent in-house S. aureus NorA efflux pump inhibitors (EPIs), belonging to the 2-phenylquinoline class, were immobilized on nanometric alpha-zirconium phosphate (ZrP) taking into advantage of acid-base or intercalation reactions. The ZrP/EPI were used as filler of poly(lactide- co -glycolic acid) (PLGA) to obtain film composites with a homogeneous distribution of the ZrP/EPI fillers. As reference, PLGA films loaded with ZrP intercalated with thioridazine (TZ), that is recognized as both a NorA and biofilm inhibitor, and with the antibiotic ciprofloxacin (CPX) were prepared. Composite films were characterized by X-ray diffraction, scanning electron microscopy, and thermogravimetric analysis. The ability of the composite films, containing ZrP/EPI, to inhibit biofilm formation was tested on Staphylococcus aureus ATCC 29213 and Staphylococcus epidermidis ATCC 12228, and it was compared with that of the composite loaded with ZrP/TZ. Finally, the antibacterial activity of CPX intercalated in ZrP was evaluated when used in combination with ZrP/EPI in the PLGA films.

γ-Zirconium phosphate (γ-ZrP) has potential as a very useful inorganic ion-exchanger due to its stability under thermal and acidic conditions. We recently reported its facile synthesis using a modified solventless method, which could make the exploitation of its ion-exchange properties for cleanup of radioactive materials and extraction of valuable ions feasible. The adsorption isotherms of Rb + and Sr 2+ over γ-ZrP are described well with the Langmuir model, with maximum adsorption capacity of 1.52 and 1.31 mmol/g, respectively. Both ions adsorb on γ-ZrP following pseudo-second order kinetics with a much faster uptake of Rb + than of Sr 2+ . γ-Zirconium phosphate shows very high affinity for Rb + , allowing its enrichment from low-concentration solutions. Notably, Rb + is selectively removed from complex solutions containing large amounts of Na + , Mg 2+ , Ca 2+ , or transition metals such as Cu 2+ , Ni 2+ , Fe 2+ , Fe 3+ , Co 2+ and Zn 2+ . The used sorbent can be fully regenerated by nitric acid, enabling the recovery of Rb + ., (© 2020 Wiley-VCH GmbH.)

Selective transformation of glycerol to propanal (PA) provides a feasible route towards the sustainable synthesis of high value-added chemicals. In this work, zirconium phosphate (ZrP) was studied as support and Ru and Co as metal sites for glycerol hydrogenolysis in a continuous-flow reactor. It was found that ZrP-supported Co-O species had a moderate selectivity to PA (49.5 %) in glycerol hydrogenolysis. Notably, once Ru species were doped into CoO/ZrP, the resulting catalyst exhibited not only an outstanding catalytic performance for glycerol hydrogenolysis to PA (a selectivity of 80.2 % at full conversion), but also a high stability at least a 50 h long-term performance. The spent catalyst could be regenerated by calcining in air to remove carbonaceous deposits. Characterization indicated that the acid sites on ZrP played a very critical role in the dehydration of glycerol into acrolein (AE), that the distribution of Co was uniform, basically consistent with that of Zr, P and Ru, and that an especially close contact between Co-O and Ru species was formed on Ru/CoO/ZrP catalyst. The further activity tests and characterizations confirmed that there was a strong interaction between the dispersed Co-O species and Ru 0 nanoparticles, which endowed Ru sites with high electronic density. This effect could play a role in facilitating the dissociation of H 2 , and thus in promoting the hydrogenation reaction. Besides, DFT calculations suggested that the Co-O species can adsorb more strongly the C=C bond of the intermediate AE on a highly coordinatively unsaturated Co (Co cus ) site and thus lead to preferential hydrogenation at the C=C bond of AE to PA., (© 2020 Wiley-VCH GmbH.)

In this work, we have studied sorption of 137 Сs and 90 Sr radionuclides from seawater under batch conditions by ferrocyanide sorbents based on hydrated titanium and zirconium dioxides (Т-35, NPF-HTD), clinoptilolite and glauconite (NPF-GL, NPF-CL) natural aluminosilicates, zirconium phosphate (T-3A), modified hydrated titanium dioxide (T-3K) as well as by manganese dioxide based on hydrated titanium dioxide (MD-HTD). Isotherms of sorption and dependences of cesium distribution coefficients on salt content and calcium concentration were obtained. Distribution coefficients of cesium and strontium were calculated. Stability of spent sorbents against radionuclides leaching was studied in from the point of view of their further treatment. The NPF-GL and NPF-HTD sorbents are recommended for treatment of seawater-based liquid radioactive waste with various salinity; these sorbents possess high distribution coefficients of cesium 10 4 and 10 5  ml/g even at the salinity of waste as high as 100 g L -1 . Distribution coefficients of strontium from seawater were (1.0-1.9)·10 2  ml/g for all sorbents that is conditioned by the presence of colloidal species of strontium (34 ± 7%) in the simulated seawater. Capacities of the sorbents for strontium varied within 200-310 mg/g. The sorbents strongly retain adsorbed radionuclides: the total percentage of leaching for 28 days was 4.4%, 2.2% and 3.1% for 137 Cs leaching from the NPF-HTD, T-35 and T-3A sorbents respectively and 10.7% for 90 Sr leaching from the NPF-CL sorbent., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020. Published by Elsevier Ltd.)

Zirconium phosphate (ZrP) nanomaterials have been studied extensively ever since the preparation of the first crystalline form was reported in 1964. ZrP and its derivatives, because of their versatility, have found applications in several fields. Herein, we provide an overview of some advancements made in the preparation of ZrP nanomaterials, including exfoliation and morphology control of the nanoparticles. We also provide an overview of the advancements made with ZrP as an inorganic support for the electrocatalysis of the oxygen evolution reaction (OER). Emphasis is made on how the preparation of the ZrP electrocatalysts affects the activity of the OER., Competing Interests: The authors declare no conflict of interest.

Layered molecular sieve membranes containing uniform interlayer galleries have offered unprecedented opportunities to reach a performance far beyond the Robeson upper bound line. In this study, we took the initiative to prepare layered zirconium phenylphosphonate (ZrPP) molecular sieve membranes with optimized microstructure on tetragonal zirconia ( t -ZrO 2 ) buffer layer-modified porous α-Al 2 O 3 substrates by facile in situ hydrothermal growth. Relying on the 3.2 Å-sized gallery height and preferential CO 2 adsorption behavior, prepared ZrPP membranes showed exceptional H 2 /CO 2 selectivity (>100) as well as considerable H 2 permeability. Furthermore, extraordinary thermal, mechanical, and chemical stability of ZrPP membranes made them potentially attractive for long-term operations under harsh conditions.

Although lithium-sulfur batteries are promising environmentally friendly and low-cost energy storage devices with high energy densities, many obstacles such as poor conductivity, volume expansion and the "shuttle effect" still limit their large-scale commercialization. In this work, a 2D sandwich-like α-ZrP/polypyrrole (α-ZrP/PPy) material with a nanosheet structure was designed as a sulfur host. The material can provide unique ion transfer channels for the rapid transfer of Li + ions and catalytically promote the conversion of lithium polysulfides (LiPSs). Moreover, the α-ZrP nanosheets provides a true covalent anchor for sulfur species, whereas the PPy builds a physical barrier and forms a conductive network for accelerating the electron transport and promoting the electrochemical performance. In addition, the moderate catalytic activity and true sulfur confinement effect of α-ZrP were confirmed by experiments and theoretical calculations. The α-ZrP/PPy@S cathode exhibits a highly reversible capacity of 727.2 mAh g -1 even at a high current density of 5 C, offering a novel cathode material for high performance Li-S batteries., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

In this study, commercial cellulose membranes were surface coated with alpha‑zirconium phosphate nanoparticles (α-ZrP-n) to study their impact on the overall removal efficiency of heavy metals from synthetic metal mixture wastewater solution. A total of four homogeneous solutions (0.25, 0.50, 0.75, and 1.00 wt%) of α-ZrP-n were prepared by sonicating the nanoparticles in deionized water. These solutions were used to surface coat the commercial cellulose membranes. The Scanning Electron Microscopy (SEM) along with Energy Dispersive Spectroscopy (EDS) were used to confirm the attachment of α-ZrP-n on the cellulose membrane surface. Furthermore, the structural characteristics of the α-ZrP-n modified cellulose membranes were also studied. The water contact angle results showed that all coated membranes remained super-hydrophilic. The porosity of the membranes decreased to 48% with the addition of 1.00 wt% α-ZrP-n compared to 65% for the pristine membrane. The mechanical strength has improved from 3.4 MPa for the pristine membrane to about 4 MPa for the 1.00 wt% α-ZrP-n membrane. Similarly, the thermal stability was found to be slightly enhanced as evidenced by the increase in decomposition temperature to 280 and 285 °C in the 0.75 and 1.00 wt% α-ZrP-n membranes, respectively. Furthermore, a removal efficiency of 97.0 ± 0.6, 98.0 ± 0.5, 99.5 ± 0.2, and 91.5 ± 2.0% for Cu (II), Zn (II), Ni (II), and Pb (II), respectively, was observed with the 0.50 wt% α-ZrP-n membrane. This removal was achieved at a flux of 41.85 ± 0.87 × 10 3 LMH. Increasing the α-ZrP-n concentration further did not show any improvement in the overall removal efficiency. However, it led to 46% flux reduction in the 1.00 wt% α-ZrP-n membrane. The mechanism of removal of the heavy metal ions was postulated to be a combination of ion exchange and electrostatic attraction of the strong negatively charged α-ZrP-n membranes and the free metal ions in the wastewater solution., (Copyright © 2019 Elsevier B.V. All rights reserved.)

This study investigated the position of ultrasonic irradiation source and reactor geometry on fragmentation rate of a layered compound, α-zirconium phosphate (α-ZrP). By numerically solving the acoustic pressure distribution using COMSOL Multiphysics®, it is clarified the mechanism whereby the operating factors influenced the α-ZrP dispersion to make a suggestion of guideline of the process design method. Two vessels made of glass with a flat-bottom and a spherical-bottom, respectively, were used. Although the flat-bottom vessel at lower horn position showed the best performance of fragmentation, the region of high acoustic pressure field in the flat bottom vessel sharply narrowed and the transmittance became prominently low. On the other hand, no significant difference of the transmittance value in the spherical bottom vessel between the cases of low and high horn positions could be observed and the spherical bottom vessel was robust for the horn position. These results suggest that not only the magnitude of acoustic pressure but also the size of high acoustic pressure region is also an important factor and a spherical bottom vessel is one of suitable shape which gives large size of high acoustic pressure region regardless of the horn position., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Polypropylene (PP) is currently widely used in areas requiring lightweight materials because of its low density. Due to the intrinsic flammability, the application of PP is restricted in many conditions. Aluminum trihydroxide (ATH) is reported as a practical flame retardant for PP, but the addition of ATH often diminishes the lightweight advantage of PP. Therefore, in this work, glass bubbles (GB) and octacedylamine-modified zirconium phosphate (mZrP) are introduced into the PP/ATH composite in order to lower the material density and simultaneously maintain/enhance the flame retardancy. A series of PP composites have been prepared to explore the formulation which can endow the composite with balanced flame retardancy, good mechanical properties, and low density. The morphology, thermal stability, flame retardancy, and mechanical properties of the composites were characterized. The results indicated the addition of GB could reduce the density, but decreased the flame retardancy of PP composites at the same time. To overcome this defect, ATH and mZrP with synergetic effect of flame retardancy were added into the composite. The dosage of each additive was optimized for achieving a balance of flame retardancy, good mechanical properties, and density. With 47 wt % ATH, 10 wt % GB, and 3 wt % mZrP, the peak heat release rate (pHRR) and total smoke production (TSP) of the composite PP-4 were reduced by 91% and 78%, respectively. At the same time, increased impact strength was achieved compared with neat PP and the composite with ATH only. Maintaining the flame retardancy and mechanical properties, the density of composite PP-4 (1.27 g·cm -3 ) is lower than that with ATH only ( PP-1 , 1.46 g·cm -3 ). Through this research, we hope to provide an efficient approach to designing flame retardant polypropylene (PP) composites with low density.

Zirconium phosphate (ZrP) was prepared and employed to separate strictinin-rich tea polyphenol from Chinese green tea extracts. The influences of ZrP calcination temperatures, green tea extraction conditions, and the amounts of ZrP on the isolation of strictinin-rich tea polyphenol were evaluated; the absorption and desorption dynamics of strictinin on ZrP were also determined. Our results revealed that the HPLC content of strictinin increased from 4.96% in 70% ethanol extract of green tea to 58.2% in isolated strictinin-rich tea polyphenol obtained by ZrP-900 (ZrP calcined at 900°C). Furthermore, the suitable time for both strictinin absorption and desorption was 4 hours at 37°C. The method developed here consisted of easy steps such as ZrP absorption, water washing, and 0.4% phosphoric acid solution desorption, which may facilitate the detection and isolation of strictinin from different samples., (Copyright © 2017. Published by Elsevier B.V.)

Composite membranes were obtained by modification of heterogeneous polymer cation and anion-exchange membranes with nanoparticles of zirconium hydrophosphate and hydrated zirconium dioxide, respectively. The ion-exchange materials were investigated with the methods of electron microscopy, potentiometry, voltammetry, and impedance spectroscopy. Single nanoparticles, which were precipitated in aqueous media, form aggregates, when the composites are in a contact with polar organic solvent. Both single nanoparticles (up to 10 nm) and their aggregates (up to 200 nm) were precipitated in ion-exchange polymers in glycerol media. Non-aggregated nanoparticles improve electrical conductivity of the ion-exchange materials, the aggregates are barriers against fouling. The membranes were applied to NaCl removal from highly concentrated glycerine-water mixture containing organic additives (byproduct of biodiesel production). As opposite to pristine materials, the composites demonstrate stability against fouling.

Two-dimensional (2D) inorganic layered nanoplatelets exhibit superior lubricating properties in both solid states and oil dispersions. In this paper, we have systematically investigated the effects of surface and interlayer modifications on the tribological performance of layered α-zirconium phosphate (ZrP) nanoplatelets in mineral oil. The pristine layered ZrP nanoplatelets were first reacted with silanes of different alkyl chains to achieve outer surface modifications, followed by intercalation with different alkyl amines to alter the interlayer spacing. Friction and anti-wear studies on ZrP nanoplatelets with various modifications in mineral oils suggest that a longer alkyl chain on the outer surfaces along with a small increase in interlayer spacing would lead to a better tribological behavior especially under a relatively heavy load condition. Our results illustrate the ability of tuning the tribological properties of 2D layered nanoplatelets in oils by varying their surface and interlayer functionalities and would be helpful for understanding the underlying tribological mechanisms of nanolubricating oils containing 2D layered nanoplatelets. Graphical abstract ᅟ.

In this work, a series of composites of insulin (Ins)/zirconium phosphate (ZrP) were synthesized by intercalation method, then, these composites were coated with TiO 2 by sol-gel method to prepare Ins/ZrP@TiO 2 hybrid composites and the drug release of the composites was investigated by using UV-Vis spectroscopy. Ins/ZrP (10, 30, 60 wt%) composites were prepared by intercalation of insulin into the ZrP layers in water. Then Ins/ZrP composites were coated with different amounts of TiO 2 (30, 50, 100 wt %) by using titanium tetra n-butoxide, as precursor. Formation of intercalated Ins/ZrP and Ins/ZrP@TiO 2 hybrid composites was characterized by FT-IR, FE-SEM, BET and XRD analysis. Zeta potential of the optimized Ins/ZrP@TiO 2 hybrid composite was determined -27.2 mV. Cytotoxic effects of the optimized Ins/ZrP@TiO 2 hybrid composite against HeLa and Hek293T cell lines were evaluated using MTT assay and the results showed that designed drug delivery system was not toxic in biological environment. Compared to the Ins/ZrP composites, incorporation of TiO 2 coating enhanced the drug entrapment considerably, and reduced the drug release. The Ins/ZrP composites without TiO 2 coating released the whole drug after 30 min in pH 7.4 (phosphate buffer solution) while the TiO 2 -coated composites released the entrapped drug after 20 h. In addition to increasing the shelf life of hormone, this nanoencapsulation and nanocoating method can convert the insulin utilization from injection to oral and present a painless and more comfortable treatment for diabetics.

The 68 Ge/ 68 Ga generator system is an excellent source for producing ready-to-use Ga-68 in clinical Positron Emission Tomography (PET) applications. The column adsorbent is the key component for the 68 Ge/ 68 Ga generator system. Therefore, several studies have been conducted to identify column materials with a stable and superior elution yield in an acidic eluent (0.1 N HCl solution). In this study, four different zirconium phosphates were synthesized with a particle size of 200-800nm, pore-size of 55∼190Å and surface area of 0.72-268m 2 g -1 . Synthesized and studied amorphous zirconium phosphate (ZrP-1) exhibited excellent acid resistant properties for the 0.1 N HCl eluent and a large surface area of 268m 2 g -1 . Amorphous ZrP-1 showed a good Ga-68 elution yield of 74% in 0.1 N HCl eluent accompanying extraordinary low breakthrough of Ge-68 (0.007%)., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Lead contamination is one of the most serious problems in drinking water facing humans. In this study, a novel zirconium phosphate modified polyvinyl alcohol (PVA)-PVDF membrane was developed for lead removal. The zirconium ions and PVA were firstly coated onto a PVDF membrane through crosslinking reactions with glutaraldehyde, which was then modified by phosphate. The adsorption kinetics study showed that most of ultimate uptake occurred in 5 h. The adsorption increased with an increase in pH; the optimal adsorption was achieved at pH 5.5. The experimental data were better described by Langmuir equation than Freundlich equation; the maximum adsorption capacity was 121.2 mg-Pb/g at pH 5.5, much higher than other reported adsorptive membranes. The membrane exhibited a higher selectivity for lead over zinc with a relative selectivity coefficient (Pb(2+)/Zn(2+)) of 9.92. The filtration study showed that the membrane with an area of 12.56 cm(2) could treat 13.9 L (equivalent to 73,000 bed volumes) of lead containing wastewater with an influent concentration of 224.5 μ g/L to meet the maximum contaminant level of 15 μ g/L. It was demonstrated that the membrane did well in the removal of lead in both simulated wastewater and lead-spiked reservoir water and had a good reusability in its applications. The XPS studies revealed that the lead uptake was mainly due to cation exchange between hydrogen ions and lead ions., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Introduction: 5-O-Galloylquinic acid from green tea and other plants is attracting increasing attention for its antioxidant and antileishmanial bioactivities. It is always isolated using a silica column, a Sephadex column and high-performance liquid chromatography (HPLC) methods, which are either laborious or instrument dependent., Objective: To develop a new method to easily separate 5-O-galloylquinic acid., Methodology: Mesoporous zirconium phosphate (m-ZrP) was prepared to conveniently separate 5-O-galloylquinic acid from Chinese green tea extract, and the target compound was easily obtained by simple steps of adsorption, washing and desorption. The effects of the green tea extraction conditions, extract concentrations, and m-ZrP adsorption/desorption dynamics on the 5-O-galloylquinic acid separation were evaluated., Results: 5-O-Galloylquinic acid that was separated from a 70% ethanol extract of green tea was of moderate HPLC purity (92%) and recovery (88%), and an increased non-specific binding of epigallocatechin gallate (EGCG) on m-ZrP was observed in the diluted tea extract. The times for maximal adsorption of 5-O-galloylquinic acid in 70% ethanol extract and maximal desorption of 5-O-galloylquinic acid in 0.4% phosphoric acid solution were confirmed as 7 h and 5 h, respectively., Conclusion: A facile method to separate 5-O-galloylquinic acid from Chinese green tea extract using m-ZrP was established. Copyright © 2016 John Wiley & Sons, Ltd., (Copyright © 2016 John Wiley & Sons, Ltd.)

The present work reports the synthesis of biocompatible zirconium phosphate (ZP) nanoparticles as nanocarrier for drug delivery application. The ZP nanoparticles were synthesized via a simple sonochemical method in the presence of cetyltrimethylammonium bromide and their efficacy for the delivery of drugs has been tested through various in-vitro experiments. The particle size and BET surface area of the nanoparticles were found to be ~48 nm and 206.51 m(2)/g respectively. The conventional MTT assay and cellular localization studies of the particles, performed on MDA-MB-231 cell lines, demonstrate their excellent biocompatibility and cellular internalization behavior. The loading of curcumin, an antitumor drug, onto the ZP nanoparticles shows the rapid drug uptake ability of the particles, while the drug release study, performed at two different pH values (at 7.4 and 5) depicts pH sensitive release-profile. The MTT assay and cellular localization studies revealed higher cellular inhibition and better bioavailability of the nanoformulated curcumin compared to free curcumin., (Copyright © 2015 Elsevier B.V. All rights reserved.)

A novel thermochemical conversion route has been developed that yields 5-hydroxymethylfurfural (HMF) from food waste biomass (FWB) in the presence of a heterogeneous catalysts (zirconium phosphate (ZrP)). The ZrP catalyst was prepared by precipitation followed by calcination at 400 (ZrP-400) and 600 °C (ZrP-600) and was characterized by SEM, XRD, XPS, N2 sorption and NH3-TPD. The optimized reaction conditions were identified to maximize HMF yield by varying the type of catalyst, the catalyst loading and the reaction time. The highest HMF yield achieved was 4.3%. On average 33% higher yield for ZrP-600 was obtained compared to that for ZrP-400, which might be due to higher number of acid sites on ZrP-600. The ZrP catalyst was easily regenerated by thermal treatment and showed stable activity upon its reuse. Preliminary calculations of the "minimum selling price" of HMF suggest that it is economically attractive to make this industrially-relevant chemical from FWB., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Layered zirconium phosphate (ZP) that bears fluorinated alkyl chains bonded covalently to the layers (ZPR) was used as a nanofiller in membranes based on a short-side-chain perfluorosulfonic acid (PFSA) to mechanically reinforce the PFSA hydrophobic component. Compared to the pristine PFSA, membranes with a ZPR loading up to 30 wt% show enhanced mechanical properties, and the largest improvement of elastic modulus (E) and yield stress (σY ) are observed for the 10 wt% ZPR membrane: ΔE/E up to 90% and ΔσY /σY up 70% at 70°C and 80% relative humidity (RH). In the RH range 50-95%, the in-plane conductivity of the composite membranes reaches 0.43 S cm(-1) for 10 wt% ZPR at 110°C and is on average 30% higher than the conductivity of the pristine PFSA. The 10 wt % ZPR membrane is as hydrated as the neat PFSA membrane at 50% RH but becomes progressively less hydrated with increasing RH both at 80 and 110°C. The fuel cell performance of this membrane, at 80°C and 30% RH, is better than that of the unmodified PFSA., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

This paper presented a simple and effective solid-phase extraction method using α-zirconium phosphate intercalated by hexadecyl trimethyl ammonium bromide (α-ZrP-CTMAB) as a novel adsorbent. Surfactant-assisted method was applied to prepare α-ZrP-CTMAB whose sorbent properties and extraction efficiency were investigated. Four sulfonamides (SAs) in honey were selected as analytical models and finally determined by liquid chromatography-tandem mass spectrometry. The recoveries of SAs at three spiked levels (10, 100, 1000ngg(-1)) were in the range of 58.7-99.3% and the relative standard deviations ranged from 2.69% to 7.48%. The detection limits obtained were 0.25-0.5ngg(-1). Compared with other methods in the literatures, the proposed method reduced the consumption of organic solvents and simplified the sample preparation procedure for the analysis of SAs in honey. Therefore, modified α-ZrP showed great potential in the analysis of pollutants in complex samples., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Ammonium molybdophosphate and Phozir (alone or in combination) have been encapsulated in alginate beads for the synthesis of rubidium sorbents. SEM and SEM-EDX analyses confirm the homogeneity of the sorbents in terms of composition and metal binding. AMP sorbent is less sensitive to pH than Phozir, and optimum pH is close to pH 3 for the binding of Rb(I). The Langmuir equation fitted well sorption isotherms and the maximum sorption capacities were in the range 0.65-0.74 mmol Rb g(-1). The resistance to intraparticle diffusion contributes to control uptake kinetics (effect of particle size) though the presence of solid inorganic particles reduces the impact of drying alginate capsules (preventing the collapse of the porous structure during the drying step). Breakthrough curves demonstrate the potential of these sorbents for the dynamic sorption of Rb(I) while using ammonium chloride (combined to nitric acid) allows recovering Rb(I) from loaded sorbents., (Copyright © 2013 Elsevier Inc. All rights reserved.)