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PubMed2005

Adsorption of phosphate from seawater on calcined MgMn-layered double hydroxides.

Adsorptive properties of MgMn-3-300 (MgMn-type layered double hydroxide with Mg/Mn mole ratio of 3, calcined at 300 degrees C) for phosphate were investigated in phosphate-enriched seawater with a concentration of 0.30 mg-P/dm3. It showed the highest phosphate uptake from the seawater among the inorganic adsorbents studied (hydrotalcite, calcined hydrotalcite, activated magnesia, hydrous aluminum oxide, manganese oxide (delta-MnO2)). The phosphate uptake by MgMn-3-300 reached 7.3 mg-P/g at an adsorbent/solution ratio of 0.05 g/2 dm3. The analyses of the uptakes of other constituents (Na+, K+, Ca(+, Cl-, and SO(2-)4) of seawater showed that the adsorbent had a markedly high selectivity for the adsorption of phosphate ions. Effects of initial phosphate concentration, temperature, pH, and salinity on phosphate uptake were investigated in detail by a batch method. The phosphate uptake increased slightly with an increase in the adsorption temperature. The adsorption isotherm followed Freundlich's equation with constants of logK(F)=1.25 and 1/n=0.65, indicating that it could effectively remove phosphate even from a solution of markedly low phosphate concentration as well as with large numbers of coexisting ions. The pH dependence showed a maximum phosphate uptake around pH 8.5. The pH dependence curve suggested that selective phosphate adsorption progresses mainly by the ion exchange of HPO(2-)4. The study on the effect of salinity suggested the presence of two kinds of adsorption sites in the adsorbent: one nonspecific site with weak interaction and one specific site with strong interaction. The effective desorption of phosphate could be achieved using a mixed solution of 5 M NaCl + 0.1 M NaOH (1 M = 1 mol/dm3), with negligible dissolution of adsorbent. The adsorbent had high chemical stability against the adsorption/desorption cycle; it kept a good phosphate uptake even after the repetition of the seventh cycle.

Adsorption↗
PubMed2005

Adsorption of NO on alumina-supported oxides and oxide-hydroxides of manganese.

The adsorption capacity for NO of alumina-supported oxides and oxide-hydroxides of manganese have been studied. Two series of samples have been prepared by precipitation on gamma-alumina and appropriate thermal treatment. The samples have been characterized by adsorption methods, magnetic methods, electronic paramagnetic resonance (EPR), transient response technique, and temperature-programmed desorption (TPD). The influence of the concentration of the initial manganese-containing solution has been investigated. The sample, prepared with a solution with Mn concentration of 4 g/100 ml, has been shown to be the best adsorbent for NO under the conditions of the experiment. It has been found that the presence mainly of Mn3+ ions on the surface of the support is probably responsible for the enhanced adsorption capacity.

Adsorption↗
PubMed2006

Preparation and characterization of surfactant-free polystyrene/layered double hydroxide exfoliated nanocomposite via soap-free emulsion polymerization.

The soap-free emulsion polymerization has been applied for preparing the surfactant-free polystyrene/layered double hydroxide exfoliated nanocomposite. The XRD and TEM determinations have been used to monitor the changes of interlayer spacing and morphology during polymerization. The results show that the obtained nanocomposite has the homogeneous structure of polymeric and inorganic components. Due to the absence of organic surfactant, the PS/LDH nanocomposite shows a remarked improvement on the onset decomposition temperature compared with virgin PS.

Emulsions↗
PubMed2005

Sorption of an anionic dye by uncalcined and calcined layered double hydroxides: a case study.

Layered double hydroxides (LDHs) with a Mg/Al molar ratio of 2:1 were synthesized by using a co-precipitation method and their calcined products (CLDHs) were obtained by heating Mg/Al-LDHs at 500 degrees C. Sorption of a weak acid dye, Brilliant Blue R (BBR), by LDHs and CLDHs indicated equilibrium time required for BBR sorption by CLDHs was less than 12h, regardless of initial concentration of BBR, whereas BBR sorption by LDHs was longer than 20 h. Sorption capacity of CLDHs was much larger than that of LDHs. Therefore, CLDHs could be used to remove anionic dyes of relatively high concentrations while LDHs may only be used to remove anionic dyes of low concentrations. Isotherms for BBR sorption by CLDHs and LDHs were well described using the Freundlich and Langmuir equations, respectively. When the initial pH of BBR solutions was lower than 8.0, the final pH of the solution after sorption was enhanced and stabilized at 10.6-10.8. The effect of initial pH (<8.0) on BBR removal was negligible, which would be environmentally important for precipitation/co-precipitation of co-existing metal cations. The effects of both Cl- and SO4(2-) on BBR sorption by CLDHs were minimal; but the presence of CO(3)2- markedly reduced BBR removal. Thermal regeneration for re-use of LDHs and CLDHs after BBR sorption was feasible only within the first two cycles, after which the regenerated materials suffered from a large loss in their sorption capacities.

Adsorption↗
PubMed2005

Factors influencing the removal of fluoride from aqueous solution by calcined Mg-Al-CO3 layered double hydroxides.

Layered double hydroxides (LDH) calcined at different temperatures (denoted as CLDH) have been demonstrated to recover their original layered structure in the presence of appropriate anions. In the light of this so-called "memory effect", a study of removal of fluoride from aqueous solution by calcined Mg-Al-CO(3)-LDH has been carried out. The LDH calcined at 500 degrees C had the highest capacity of removal of fluoride ion, because of retention of its intrinsic structure. The CLDH with an Mg/Al ratio of 2 has a remarkable ability to adsorb anions. The adsorption loading is higher for the calcined Mg-Al-LDH than for calcined Zn-Al and Ni-Al-LDH. The influence of varying the conditions for removal of fluoride, such as the pH of aqueous solution, the initial fluoride concentration, the dosage of adsorbent, and temperature on removal of fluoride have been investigated. The influence of co-existing anions in fluoride aqueous solution indicates that the percentage of removal of fluoride increased in order PO(4)(3-) < Cl(-) approximately SO(4)(2-) < Br(-) << NO(3)(-). It was found that maximum removal of fluoride from aqueous solutions was obtained in 6h at pH 6.0 with an initial concentration of 50 mg/L, and that the retention of fluoride ions by the CLDH material was 98% or higher. The residual fluoride concentration was found to be 0.4 mg/L with an initial concentration of 20 mg/L, which meets the national standard for drinking water quality. The Freundlich isotherm and Langmuir isotherm were used to fit the data of equilibrium experiments. The results of X-ray diffraction, FT-IR and TG-MS demonstrate that the adsorption phenomenon is accompanied by rehydration with concomitant uptake of fluoride ions to rebuild the initial layered structure.

Adsorption↗
PubMed2006

Determination of trace metals by atomic absorption spectrometry after coprecipitation with europium hydroxide.

A procedure for the determination of trace amounts of chromium(III), iron(III), lead(II) and manganese(II) is described, that combines atomic absorption spectrometry-europium hydroxide coprecipitation. The influences of analytical parameters including amount of europium(III), amount of ammonia, sample volume, etc. were investigated on the recoveries of analyte ions. The effects of concomitant ions were also examined. The recoveries of the analyte ions were in the range of 95-104%. The detection limits (3 s) were in the range of 1.7-17.1 microg/L. The validation of the presented coprecipitation procedure was performed by the analysis of Bovine Liver 1577-b and BCR-144R Sewage Sludge (domestic origin) standard reference materials. The method was applied to the determination of analytes in real samples including natural waters and some food, soil and fertilizer samples, etc. and good results were obtained (relative standard deviations < 10%, recoveries > 95%).

Animals↗
PubMed2006

Dysprosium(III) hydroxide coprecipitation system for the separation and preconcentration of heavy metal contents of table salts and natural waters.

A procedure for the determination of trace amounts of Pb(II), Cu(II), Ni(II), Co(II), Cd(II) and Mn(II) is described, that combines atomic absorption spectrometry-dysprosium hydroxide coprecipitation. The influences of analytical parameters including amount of dysprosium(III), centrifugation time, sample volume, etc. were investigated on the recoveries of analyte ions. The effects of concomitant ions were also examined. The recoveries of the analyte ions were in the range of 95.00-104.00%. The detection limits corresponding to three times the standard deviation of the blank for the analytes were in the range of 14.1-25.3 microg/L. The method was applied to the determination of lead, copper, nickel, cobalt, cadmium and manganese ions in natural waters and table salts good results were obtained (relative standard deviations <10%, recoveries >95%).

Centrifugation↗
PubMed2006

Identification of cultivable microorganisms from root canals with apical periodontitis following two-visit endodontic treatment with antibiotics/steroid or calcium hydroxide dressings.

The study was aimed at comparing the efficacy of disinfection of root canals with periapical radiolucencies when treated with either antibiotics/steroid medicaments (Ledermix or Septomixine) or a calcium hydroxide paste (Calasept). Microbiological samples were taken before and after two-visit endodontic treatment from 88 canals with apical periodontitis. All of the canals but one (87 of 88) had cultivable growth before treatment. After dressing with Ledermix, Septomixine, or Calasept, the percentages of canals remained with positive growth were 48% (13 of 27), 31% (8 of 26), and 31% (11 of 35), respectively. The chi(2) tests showed there were no significant differences in the number of canals with positive growth or mean colony forming units counts after instrumentation, irrigation and dressing. In the Ledermix group, 38 strains of bacteria were recovered. The Septomixine group had 25 strains, and the Calasept group had 25 strains. Gram-positive facultative anaerobic cocci (including staphylococci and streptococci) were more prevalent than the Gram-negative obligate anaerobic rods after treatment in all three groups. Similarities in the reduced number of canals with residual growth, and the prevalence of Gram-positive facultative anaerobic cocci suggest that the use of different inter-appointment dressings produced similar microbiological outcomes. However, factors other than the antimicrobial effectiveness of intracanal medicaments may also be responsible for the results observed.

Anti-Bacterial Agents↗
PubMed2006

A quantitative assessment of efficacy of various calcium hydroxide removal techniques.

This study evaluated the amount of calcium hydroxide [Ca(OH)(2))] remaining in canals after removal with various techniques including combinations of NaOCl with EDTA irrigation, hand filing, rotary instrumentation, or ultrasonics. The mesial canals of 12 mandibular molars were uniformly instrumented. Teeth were sectioned longitudinally along the length of the instrumented canals. Acrylic jigs were fabricated, allowing reapproximation of the opposing segments. After Ca(OH)2 placement into the canals, four techniques were used for its removal. In the first method, the master apical file was placed to working length in between two 5-ml rinses of NaOCl. The other three techniques combined with the first method either a 2.5-ml EDTA rinse, a rotary file (MAF size) to working length, or passive ultrasonication. Results showed that no technique removed all Ca(OH)2. Rotary and ultrasonic techniques, while not different from each other, removed significantly more Ca(OH)2 than irrigant only techniques. The irrigant only techniques were not different from each other.

Calcium Hydroxide↗
PubMed2006

Effect of calcium hydroxide-treated Prevotella nigrescens on the gene expression of matrix metalloproteinase and its inhibitor in MG63 cells.

The purpose of this study was to monitor the expression of matrix metalloproteinase-1 (MMP-1) and tissue inhibitor of metalloproteinase-1 (TIMP-1) produced by an osteoblastic cell line MG63 stimulated with Prevotella nigrescens lipopolysaccharides (LPS), and to compare the level of secretion before and after the P. nigrescens LPS was treated with calcium hydroxide [Ca(OH)2]. The underlying hypothesis is that the balance between MMP and TIMP secretion is the key to an understanding of the host degradative pathways involved in the pathogenesis of bacterial derived pulpal and periapical diseases. Confluent monolayers of MG63 human osteosarcoma cells were exposed to varying concentrations of P. nigrescens or Escherichia coli LPS. Alternately, confluent cultures were exposed to 10 microg/ml of bacterial LPS pretreated with Ca(OH)2 (12.5 mg/ml) for 72 hours. At the end of the experimental period, total RNA was extracted and real-time quantitative polymerase chain reaction (PCR) was performed for MMP-1, TIMP-1, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The results showed that the expression of MMP-1 mRNA was low and invariant for the experimental period in the negative controls. However, exposure to P. nigrescens LPS increased expression after 48 hours. Expression of TIMP-1 mRNA was highly increased at 24 and 48 hours with lower concentrations of LPS in contrast to a suppression with a concentration of 10 microg/ml. Treatment of P. nigrescens LPS with Ca(OH)2 resulted in a down-regulation of MMP-1, whereas pretreated E. coli LPS demonstrated no stimulatory activity for MMP-1 gene expression. Both types of LPS when pretreated with Ca(OH)2 induced slightly up-regulated expression of TIMP-1.

Calcium Hydroxide↗
PubMed2004

Solid state and solution 43Ca NMR of calcium peroxides involved in the disproportionation of hydrogen peroxide by calcium hydroxide.

In order to get some insight into the mechanism of the disproportionation of hydrogen peroxide catalyzed by calcium hydroxide, 43Ca NMR spectra of enriched samples of calcium peroxides and of their precursors have been studied in both solution and solid state. This study demonstrates that no well-defined peroxidized calcium species are formed in solution, showing that the catalytic role of calcium is likely restricted to the solid state. Most of the calcium compounds that could be involved in the catalytic process have been investigated with solid state NMR. The shift and quadrupolar parameters of Ca(OH)2, CaO2.8H2O and CaO2.2H2O2 are reported for the first time. These parameters are different enough to allow the quantitative analysis of a complex mixture of these compounds by NMR.

Calcium Hydroxide↗
PubMed2006

Immunohistochemical expression of fibronectin and tenascin after direct pulp capping with calcium hydroxide.

The aim of this study was to investigate the expression of 2 extracellullar matrix glycoproteins, fibronectin (FNC) and tenascin (TNC), following direct pulp capping with calcium hydroxide (CH). Third molars scheduled for extraction were used. Standardized class I cavities with pulp exposures were prepared. After control of bleeding, CH powder was applied in the exposure sites, which were covered with CH cement (Dycal; Dentsply) and the cavities were filled with zinc oxide-eugenol cement. Three teeth were extracted at each post-treatment period (1, 7, 14, and 30 days). Demineralized and paraffin-embedded specimens were stained for histologic technique (hematoxylin-eosin) and for immunohistochemical analysis. Anti-TNC and anti-FNC monoclonal antibodies were used with the streptavidin-biotin complex method. Generally, similar patterns of immunohistochemical expression were observed for TNC and FNC in the pulp tissue as a whole. In the exposure site, TNC immunostaining increased over time, exhibiting a thicker immunostaining pattern within 30 days. The imunohistochemical technique showed expression of both glycoproteins during pulp healing process.

Calcium Hydroxide↗
PubMed2006

Histologic evaluation of direct pulp capping with a self-etching adhesive and calcium hydroxide in beagles.

OBJECTIVE: To evaluate the pulpal response of beagles following direct pulp capping with Clearfil SE Bond (SB), a self-etching adhesive. STUDY DESIGN: One hundred thirty sound teeth from 6 male beagles were used. One hundred twenty teeth had their pulp mechanically exposed at the bottom of the class V cavities and were divided into 2 groups. In group 1, teeth were capped with SB; group 2 teeth were capped with calcium hydroxide cement (CH). Ten teeth were kept intact as an untreated control group. After 7, 30, and 90 days, 40 teeth from 2 beagles were extracted and processed for light microscopic examination. RESULTS: After the 7-day observation period, inflammatory reaction in the SB group was similar to that of the CH group (P > .05). After the 30-day and 90-day observation periods, inflammatory reaction was slight in both groups, but less dentin bridge formation was observed in specimens from the SB group than in those from the CH group (P < .05). CONCLUSION: SB showed good biocompatibility with pulp, but its ability to induce reparative dentin was lower than that of CH.

Animals↗
PubMed2006

In vitro evaluation of the antimicrobial activity of calcium hydroxide combined with chlorhexidine gel used as intracanal medicament.

The aim of this study was to investigate the antimicrobial activity of calcium hydroxide (Ca(OH)2) combined with 2% chlorhexidine gluconate (CHX) gel against endodontic pathogens and to compare the results with the ones achieved by Ca(OH)2 mixed with sterile water and by CHX gel alone. Two methods were used: the agar diffusion test and the direct contact test. Ca(OH)2 + 2% CHX gel produced inhibitory zones ranging from 2.84 to 6.5 mm, and required from 30 seconds to 6 hours to eliminate all tested microorganisms. However, 2% CHX gel showed the largest microbial growth zones from 4.33 to 21.67 mm, and required 1 minute or less to inhibit all tested microorganisms. A paste of Ca(OH)2 plus sterile water inhibited only the microorganisms with which it was in direct contact and required from 30 seconds to 24 hours to kill all tested microorganisms. In conclusion, 2% CHX gel + Ca(OH)2 showed better antimicrobial activity than Ca(OH)2 manipulated with sterile water.

Anti-Infective Agents, Local↗
PubMed2005

Removal of the herbicide 2,4-dichlorophenoxyacetate from water to zinc-aluminium-chloride layered double hydroxides.

Batch sorption studies were conducted to investigate the potential of [Zn-Al-Cl] layered double hydroxides (LDHs) for the removal of the herbicide 2,4-dichlorophenoxyacetate (2,4-D) from contaminated aqueous solutions. Experiments were performed at different pH values, initial pesticide concentration, solid/pesticide ratio and anion exchange capacity of LDHs. The LDH samples evaluated had very high retention capacity for 2,4-D whose removal was a rapid process, as a quasi-equilibrium state was reached after 1-h reaction time. The adsorption can be described by Langmuir-type isotherms, with an average affinity constant of 12.5 L mmol(-1). At initial 2,4-D concentrations between 0.08 and 4 m molL(-1), the solids removed up to 98% of the pesticide. Physicochemical characterization of the LDH solids, both fresh and after removal of 2,4-D, by X-ray diffraction, infrared spectroscopy and thermogravimetry, indicates that the retention of 2,4-D is done by adsorption on the surface of the solid for low 2,4-D concentrations. However, a combination of surface adsorption and interlayer ion exchange takes place when the 2,4-D concentration is high.

2,4-Dichlorophenoxyacetic Acid↗
PubMed2006

Uptake of chloride ion from aqueous solution by calcined layered double hydroxides: equilibrium and kinetic studies.

Layered double hydroxides (LDH) calcined within a certain temperature range (denoted as CLDH) have been shown to recover their original layered structure in the presence of appropriate anions. In the light of this so-called "memory effect", uptake of chloride ion from aqueous solution by calcined MgAl-CO3 LDH was investigated in batch mode. The equilibrium isotherm showed that the uptake of chloride ion by CLDH was consistent with the Langmuir and Freundlich equations and that the Langmuir model gave a better fit to the experimental data than the Freundlich model. The maximum uptake capacity of CLDH for chloride ion was 149.5 mg/g, close to the stoichiometric uptake (168 mg/g). The influence of varying pH of solution, initial chloride concentration, adsorbent quantity, and temperature on the kinetics of chloride removal has also been explored. Four kinetic models were used to fit the experimental data, and it was found that the pseudo-second-order kinetics model could be used to describe the uptake process satisfactorily. The calculated value of Ea was found to be 56.8 kJ/mol, which suggests that the process of uptake of chloride ion is controlled by the rate of reaction of chloride ion with the CLDH rather than diffusion. A mechanism for removal of chloride ion has been confirmed by X-ray diffraction, FT-IR spectroscopy and TG-MS measurements.

Adsorption↗
PubMed1997

Inorganic species in geologic fluids: correlations among standard molal thermodynamic properties of aqueous ions and hydroxide complexes.

Correlations among experimentally determined standard partial molal thermodynamic properties of inorganic aqueous species at 25 degrees C and 1 bar allow estimates of these properties for numerous monatomic cations and anions, polyatomic anions, oxyanions, acid oxyanions, neutral oxy-acid species, dissolved gases, and hydroxide complexes of metal cations. Combined with correlations among parameters in the revised Helgeson-Kirkham-Flowers (HKF) equation of state (Shock et al., 1992), these estimates permit predictions of standard partial molal volumes, heat capacities, and entropies, as well as apparent standard partial molal enthalpies and Gibbs free energies of formation to 1000 degrees C and 5 kb for hundreds of inorganic aqueous species of interest in geochemistry. Data and parameters for more than 300 inorganic aqueous species are presented. Close agreement between calculated and experimentally determined equilibrium constants for acid dissociation reactions and cation hydrolysis reactions supports the generality and validity of these predictive methods. These data facilitate the calculation of the speciation of major, minor, and trace elements in hydrothermal and metamorphic fluids throughout most of the crust of the Earth.

Algorithms↗
PubMedDate not supplied

Suppression or exacerbation of experimental autoimmune uveoretinitis in Lewis rats by pretreatment with or without an autoantigenic peptide in aluminum hydroxide.

PURPOSE: Aluminum hydroxide (Al) is an adjuvant to induce Th2 immune responses. The aim of this study is to investigate the effects of pretreatment with Al on experimental autoimmune uveoretinitis (EAU), a Th1 disease model. METHODS: Lewis rats were pretreated with an uveitogenic peptide (#29)/Al, phosphate-buffered saline (PBS)/Al or PBS. EAU was then induced by immunization of #29 in complete Freund's adjuvant (CFA) with intravenous injection of Bordetella pertussis. Three weeks later, EAU was evaluated histologically and antigen-specific cellular immune responses were assessed. RESULTS: EAU was exacerbated in the PBS/Al group and attenuated in the #29/Al group, compared to the control PBS group. Antigen-specific cellular proliferation and interferon-gamma production were augmented in the PBS/Al group and suppressed in the #29/Al group. CONCLUSIONS: Suppression or exacerbation of EAU by the pretreatment in this study is related to inhibition or augmentation of antigen-specific Th1 immunity.

Adjuvants, Immunologic↗