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1.
Xin-Rui Wang Hui-Min Cheng Xue-Wei Gao Wei Zhou Shu-Jing Li Xue-Li Cao Dongpeng Yan 《中国化学快报》2019,30(4):919-923
The inhibitor of melanin and the bacteriostatic agent kojic acid was inserted into Zn-Ti layered double hydroxide (LDH) by anion-exchange reaction. The structure, slow release, antibacterial and skin whitening activity were studied. 相似文献
2.
An organic ultraviolet (UV) ray absorbent, p-aminobenzoic acid (PABA) was intercalated into a Zn-Ti layered double hydroxide (LDH) precursor by an anion-exchange reaction to obtain ZnTi-PABA-LDH, a new organic-inorganic nanocomposite. The structure and the thermal stability of ZnTi-PABA-LDH were characterized by XRD, FT-IR and TG-DTA. The results indicate ZnTi-PABA-LDH, synthesized by this method, exhibit relatively high crystallinity, and markedly enhanced thermal stability of PABA after intercalation into ZnTi-LDH. The UV-vis-NIR spectrophotometric and ESR data show excellent UV ray resistance and greatly decreased photocatalytic activity when PABA is intercalated into the interlayers of the ZnTi-LDH. The studies suggest that ZnTi-PABA-LDH may have potential applications as safe sunscreen materials. 相似文献
3.
Sumio Aisawa 《Journal of solid state chemistry》2004,177(11):3987-3994
The intercalation of amino acids for the Zn-Al-layered double hydroxide (LDH) has been investigated by the calcination-rehydration reaction at 298 K using mainly phenylalanine (Phe) as a guest amino acid. The Zn-Al oxide precursor prepared by the calcination of Zn-Al-carbonated LDH at 773 K for 2 h was used as the host material. The amount of Phe intercalated by the rehydration was remarkably influenced by the initial solution pH and reached ca. 2.7 times for anion exchange capacity (AEC) of the LDH at neutral and weak alkaline solutions, suggesting that Phe was intercalated as amphoteric ion form into the LDH interlayer. As Phe is intercalated for the LDH as monovalent anion in alkaline solution, the amount of Phe intercalated at pH 10.5 corresponded with AEC of the LDH. The solid products were found to have the expanded LDH structure, which confirmed that Phe was intercalated into the LDH interlayer as amphoteric ion or anion form. The basal spacing, d003, of the Phe/LDH was 1.58 nm at pH 7.0 and 0.80 nm at pH 10.5; two kinds of expansion suggested for Phe in the interlayer space as vertical (pH 7.0) and horizontal (pH 10.5) orientations. The intercalation behavior of various amino acids for the LDH was also found to be greatly influenced by the feature of the amino acid side-chain, namely, its carbon-chain length, structure and physicochemical property. In particular, α-amino acids possessing a hydrophobic or negative-charged side-chain were preferentially intercalated for the LDH. 相似文献
4.
Gregorio Guadalupe Carbajal Arizaga Fernando Wypych Oscar Edel Contreras Lopez 《Journal of solid state chemistry》2010,183(10):2324-2328
A zinc/aluminum LDH was precipitated with recycled ammonia from a chemical vapor deposition reaction. The LDH presented a crystalline phase with basal distance of 8.9 Å, typical for nitrate-containing LDHs, and another phase with a basal distance of 13.9 Å. Thermal treatment at 150 °C eliminated the phase with the bigger basal distance leaving only the anhydrous nitrate-intercalated LDH structure with 8.9 Å. Intense N-H stretching modes in the FTIR spectra suggested that the expansion was due to intercalation of ammonia in the form of [NH4(NH3)n]+ species. When additional samples were precipitated with pure ammonia, the conventional LDH nitrate structure was obtained (8.9 Å basal distance) at pH=7, as well as a pure crystalline phase with 13.9 Å basal distance at pH=10 due to ammonia intercalation that can be removed by heating at 150 °C or by stirring in acetone, confirming a unusual sensu stricto intercalation process into a LDH without exchanging nitrate ions. 相似文献
5.
Exfoliated nanocomposite, based on Zn, Al layered double hydroxide (LDH) and polystyrene (PS), has been achieved by in-situ
atom transfer radical polymerization reaction from initiator-modified LDH. The exfoliated structure is characterized by X-ray
diffraction and transmission electronic microscope. The results suggest that the exfoliated ZnAl(DS) LDH sheets with a thickness
of less than 1 nm disperse individually in the PS matrix, and the thermal stability of the nanocomposite shows a marked improvement.
When the 50 wt% weight loss is selected as a comparison point, the decomposition temperature of PS/LDH nanocomposite is about
45 °C higher than that of pure PS. 相似文献
6.
Rafael Marangoni Luiz Pereira Ramos Fernando Wypych 《Journal of colloid and interface science》2009,330(2):303-309
Different anionic blue and orange dyes have been immobilized on a zinc hydroxide nitrate (Zn5(OH)8(NO3)2nH2O — Zn–OH–NO3) by anion exchange with interlayer and/or outer surface nitrate ions of the layered matrix. Orange G (OG) was totally intercalated, orange II (OII) was partially intercalated, while Niagara blue 3B (NB) and Evans blue (EV) were only adsorbed at the outer surface. Several composite films of poly(vinyl alcohol) — PVA were prepared by casting through the dispersion of the hybrid material (Zn–OH–OG) into a PVA aqueous solution and evaporation of water in a vacuum oven. The obtained composite films were transparent, colored, and capable of absorbing UV radiation. Improved mechanical properties were also obtained in relation to the nonfilled PVA films. These results demonstrate the onset of a new range of potential applications for layered hydroxide salts in the preparation of polymer composite multifunctional materials. 相似文献
7.
Fabrice Leroux Julien Gachon Jean-Pierre Besse 《Journal of solid state chemistry》2004,177(1):245-250
Alginic acid, a biopolymer produced by brown seaweed, is incorporated between the sheets of a layered double hydroxide (LDH) via direct coprecipitation. The growth of the inorganic crystalline seeds over the polymer gives rise to a lamellar structure. The obtained nanocomposite presents a basal spacing in agreement with the ideal picture of the polymer lying perpendicularly to the inorganic sheets. A study using FTIR and 13C CP-MAS spectroscopies suggests that the interaction between the organic guest and the inorganic framework is weak. However, the polymer has a stabilizing effect in temperature, since ZnO is observed at 350°C, whereas it appears at 200°C for the chloride LDH pristine material. 相似文献
8.
A novel combination for an inorganic-organic nanocomposite material was demonstrated. Anthryl dendron, i.e., poly(amidoamine) dendron with an anthracene chromophore group at the focal point, was incorporated in the interlayer space of ZnAl-NO3 type layered double hydroxide (LDH) through an anion-exchange reaction. The photoabsorption and fluorescence properties of the resulting material were different from those of the bare anthryl dendron molecule. It was suggested that the change in photochemical properties was due to the organization and π-π interaction of anthracene chromophores within the interlayer of the LDH. 相似文献
9.
《Arabian Journal of Chemistry》2020,13(3):4513-4527
Bispyribac (BP) anions have been successfully intercalated in the interlayer region of zinc hydroxide nitrate (ZHN) in the presence of sodium dodecylsulphate (SDS) surfactant. The physicochemical properties of the intercalation compound ZHN–SDS–BP have been characterised herein with different instrumental techniques. The intercalation of BP and SDS is clearly reflected in the PXRD analysis, based on the appearance of symmetrical, sharp and intense intercalation peaks at lower 2θ with a basal spacing of 28.2–28.6 Å. The thermal studies show that the ZHN–SDS–BP nanocomposite has better thermal stability than the pristine BP. The intercalation of BP leads to significant changes in the surface area, porosity, and morphology. Nitrogen adsorption–desorption isotherms reveal that both ZHN–SDS and ZHN–SDS–BP are of Type IV. The release and kinetic studies were also carried out on the ZHN–SDS–BP, in aqueous solution of Na3PO4, Na2SO4 and NaCl as the release media. The releases of BP in both aqueous solutions of Na3PO4 and NaCl were found to follow the pseudo second order kinetic model, whereas the releases of BP in the aqueous solution of Na2SO4 obey the parabolic diffusion kinetic model. This study shows that ZHN has the potential to be used as a host material in slowing the release of BP herbicides in the paddy cultivation sector. 相似文献
10.
Min Wei 《Journal of solid state chemistry》2004,177(7):2534-2541
Layered double hydroxides, novel anionic clay, meet the first requirement as inorganic matrices for encapsulating functional drugs or biomolecules with negative charge in aqueous media. In this study, naproxen has been intercalated into Mg-Al layered double hydroxide by the methods of ion exchange. The structure and composition of the intercalated material have been studied by X-ray diffraction (XRD), UV-vis spectroscopy and inductively coupled plasma emission spectroscopy. A schematic model has been proposed. Furthermore, in situ Fourier transform infrared spectroscopy, in situ high-temperature XRD, and thermogravimetry (TG) have been used to characterize the thermal decomposition of the hybrid material. It has been found that the thermal stability of the intercalated naproxen is significantly enhanced compared with the pure form before intercalation, which suggests that this drug-inorganic layered material may have prospective application as the basis of a novel drug delivery system. 相似文献
11.
A novel optical chemosensor was fabricated based on 1-amino-8-naphthol-3,6-disulfonic acid sodium (H-acid) intercalated layered double hydroxide (LDH) film via the electrophoretic deposition (EPD) method. The film of H-acid/LDH with the thickness of 1 μm possesses a well c-orientation of the LDH microcrystals confirmed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The fluorescence detection for Hg(II) in aqueous solution was performed by using the H-acid/LDH film sensor at pH 7.0, with a linear response range in 1.0 × 10−7 to 1.0 × 10−5 mol L−1 and a detection limit of 6.3 × 10−8 mol L−1. Furthermore, it exhibits excellent selectivity for Hg(II) over a large number of competitive cations including alkali, alkaline earth, heavy metal and transitional metals. The specific fluorescence response of the optical sensor is attributed to the coordination between Hg(II) and sulfonic group in the H-acid immobilized in the LDH matrix, which was verified by NMR spectroscopy and UV–vis spectra. In addition, density functional theory (DFT) calculation further confirms that the coordination occurs between one Hg2+ and two O atoms in the sulfonic group, which is responsible for the significant fluorescence quenching of the H-acid/LDH film. The results indicate that the H-acid/LDH composite film can be potentially used as a chemosensor for the detection of Hg2+ in the environmental and biomedical field. 相似文献
12.
Bettina Lotsch Franck Millange Richard I. Walton Dermot O'Hare 《Solid State Sciences》2001,3(8):883-886
We report the first example of selective intercalation of nucleoside monophosphates in a layered host material. The intercalated nucleoside monophosphates can then be quantitatively recovered from the inorganic host and so this opens up the possibility of using simple layered inorganic hosts as rapid, cost effective and recyclable materials for the purification and separation of complex biomolecules. 相似文献
13.
Surface-charging behavior of Zn-Cr layered double hydroxide 总被引:1,自引:0,他引:1
Rojas Delgado R Arandigoyen Vidaurre M De Pauli CP Ulibarri MA Avena MJ 《Journal of colloid and interface science》2004,280(2):136-441
A Zn-Cr layered double hydroxide (LDH) having the formula Zn(2)Cr(OH)(6)Cl(0.7)(CO(3))(0.15)2.1H(2)O was synthesized and characterized by powder X-ray diffraction, infrared spectroscopy, acid-base potentiometric titration, mass titration, electrophoretic mobility, and modeling of the electrical double layer. Adsorption of alizarin was also performed in order to show some particular features of the HDL. Net hydroxyl adsorption, which increases with increasing pH and decreasing supporting electrolyte concentration, takes place above pH 5. The electrophoretic mobility of the particles was always positive and it decreased when the pH was higher than 9. An isoelectric point of 12 could be estimated by extrapolating the data. The modified MUSIC model was used to estimate deprotonation constants of surface groups and different adsorption models were compared. Good fit of hydroxyl adsorption and electrophoresis could be achieved by considering both OH(-)/Cl(-) exchange at structural sites and proton desorption from surface hydroxyl groups. The modeling, in agreement with alizarin adsorption, indicates that most of the structural positive charge of the LDH is screened at the surface by exchanged anions and negatively charged surface groups. It also suggests that only structural charge sites initially neutralized by chloride ions are active for anion exchange. The remaining sites are blocked by carbonate and do not participate in the exchange. 相似文献
14.
Zn-Al layered double hydroxide(LDH) was used as precursor to produce ZnO nanostructures through dissolution of aluminum hydroxide in caustic soda.The Zn-Al LDH could transform into different nanostructures of ZnO on LDH nanosheets and even pure ZnO nanorods under various NaOH concentration.The formed ZnO nanorods vertically aligned on both LDH sides.UV-vis diverse reflectance spectra show that the obtained ZnO nanorods have a band gap of approximately 3.05 eV.Such ZnO/LDH nanostructures might be used as photocatalyst in the organic pollutant decomposition. 相似文献
15.
Layered double hydroxides (LDHs) are new nanofillers which exhibit improved thermal and flammability properties in various kinds of polymer matrices. These materials have certain advantages over conventional metal hydroxides and also layered silicates so far as the flame retardancy is concerned. In this article, flammability and thermal properties of the nanocomposite based on low density polyethylene (LDPE) and Mg-Al based layered double hydroxide (Mg-Al LDH) are reported in detail. The nanocomposites containing different LDH concentrations were prepared by melt-compounding using a tightly intermeshing co-rotating twin-screw extruder. The morphological analysis reveals an exfoliated/intercalated type LDH particle morphology in these nanocomposites. The thermogravimetric analysis (TGA) shows that even a small amount of LDH improves the thermal stability and onset decomposition temperature in comparison with the unfilled LDPE. The heat release rate (HRR) and its maximum (PHRR) during cone-calorimeter investigation are found to be reduced significantly with increasing LDH concentration. The nanocomposites not only exhibit reduced total heat released (measure of propensity to produce long duration fire), but also lower tendency to fast fire growth (measured by the ratio of PHRR and time of ignition). The limited oxygen index (LOI) and the dripping behavior are also improved with increasing LDH concentration. 相似文献
16.
Hydrotalcite-like compounds are often used as host structures for intercalation of various anionic species. The product intercalated with the nonionic, water-soluble pharmaceuticals paracetamol, N-(4-hydroxyphenyl)acetamide, was prepared by rehydration of the Mg-Al mixed oxide obtained by calcination of hydrotalcite-like precursor at 500 °C. The successful intercalation of paracetamol molecules into the interlayer space was confirmed by powder X-ray diffraction and infrared spectroscopy measurements. Molecular simulations showed that the phenolic hydroxyl groups of paracetamol interact with hydroxide sheets of the host via the hydroxyl groups of the positively charged sites of Al-containing octahedra; the interlayer water molecules are located mostly near the hydroxide sheets. The arrangement of paracetamol molecules in the interlayer is rather disordered and interactions between neighboring molecules cause their tilting towards the hydroxide sheets. Dissolution tests in various media showed slower release of paracetamol intercalated in the hydrotalcite-like host in comparison with tablets containing the powdered pharmaceuticals. 相似文献
17.
Natasja Schouten Louis G. J. van der Ham Gert-Jan W. Euverink André B. de Haan 《Adsorption》2007,13(5-6):523-532
Low cost adsorption technology offers high potential to clean up laundry rinsing water. From an earlier selection of adsorbents
(Schouten et al. 2007), layered double hydroxide (LDH) proved to be an interesting material for the removal of anionic surfactant, linear alkyl
benzene sulfonate (LAS) which is the main contaminant in rinsing water. The main research question was to identify the effect
of process parameters of the LDH synthesis on the stability of the LDH structure and the adsorption capacity of LAS. LDH was
synthesized with the co-precipitation method of Reichle (1986); a solution of M2+(NO3)2 and M3+(NO3)3 and a second solution of NaOH and Na2CO3 were pumped in a beaker and mixed. The precipitate that was formed was allowed to age and was subsequently washed, dried
and calcined. The process parameters that were investigated are the concentration of the initial solutions, M2+/M3+ ratio and type of cations. The crystallinity can be improved by decreasing the concentration of the initial solutions; this
also decreases the leaching of M3+ from the brucite-like structure into the water. The highest adsorption capacity is obtained for Mg2+/Al3+ with a ratio 1 and 2 because of the higher charge density compared to ratio 3. Storing the LDH samples in water resulted
in a reduction of adsorption capacity and a decrease in surface area and pore volume. Therefore, LDH is not applicable in
a small device for long term use in aqueous surroundings. The adsorption capacity can be maintained during storage in a dry
N2 atmosphere. 相似文献
18.
Thermal, solution and reductive decomposition of Cu-Al layered double hydroxides into oxide products
Sylvia Britto 《Journal of solid state chemistry》2009,182(5):1193-1199
Cu-Al layered double hydroxides (LDHs) with [Cu]/[Al] ratio 2 adopt a structure with monoclinic symmetry while that with the ratio 0.25 adopt a structure with orthorhombic symmetry. The poor thermodynamic stability of the Cu-Al LDHs is due in part to the low enthalpies of formation of Cu(OH)2 and CuCO3 and in part to the higher solubility of the LDH. Consequently, the Cu-Al LDH can be decomposed thermally (150 °C), hydrothermally (150 °C) and reductively (ascorbic acid, ambient temperature) to yield a variety of oxide products. Thermal decomposition at low (400 °C) temperature yields an X-ray amorphous residue, which reconstructs back to the LDH on soaking in water or standing in the ambient. Solution decomposition under hydrothermal conditions yields tenorite at 150 °C itself. Reductive decomposition yields a composite of Cu2O and Al(OH)3, which on alkali-leaching of the latter, leads to the formation of fine particles of Cu2O (<1 μm). 相似文献
19.
T. Kuwahara O. Onitsuka H. Tagaya J. Kadokawa K. Chiba 《Journal of inclusion phenomena and macrocyclic chemistry》1994,18(1):59-68
On intercalation ofp-toluenesulfonate (PTS) into Mg/Al (0.73/0.27) layered double hydroxide (LDH), the layer expanded from 4.77 Å to 17.7 Å, indicating that the plane of PTS was perpendicular to the plane of the LDH layers. Thermal treatment of the PTS intercalate resulted in 82% of the included PTS being evolved as decomposition products. This value was higher than the value of 32.5% obtained with sodium PTS and 43.8% with a mixed sample of PTS and Mg/Al (0.73/0.27) LDH. It was considered that the intercalated PTS in Mg/Al (0.73/0.27) LDH was easy to decompose because interaction between intercalated PTS and Mg/Al (0.73/0.27) LDH was smaller than that between sodium and PTS in sodium PTS. 相似文献
20.
Potential flame retardants, MgAl-LDH and ammonium polyphosphate (APP), were added to neat polystyrene (PS) individually or in combinations at weight fractions no greater than 10%. Structural morphologies of MgAl-LDH and the corresponding PS nanocomposites were established via X-ray diffraction (XRD) and transmission electron microscopy (TEM). Thermogravimetric analysis (TGA) and cone calorimetry were used to study the thermal stability and fire performance of the composites. Time to ignition is greatly reduced for PS composites when compared to the virgin polymer. Synergistic effects were observed in both TGA and cone calorimetry for formulations containing both MgAl-LDH and APP. Physical and chemical interactions between MgAl-LDH and APP are responsible for the observed synergy in thermal stability and fire performance. 相似文献