• Restorative Dentistry and Endodontics
• /
• v.18 no.2
• /
• pp.423-430
• /
• 1993

The purpose of this study was to investigate the effect of ferric and ferric ions contained in phosphoric acid solution as a pretreatment solution on bonding of MMA/TBBO resin to dentin. Each of 1 % and 3 % ferric chloride. cupric chloride. cupric sulfate. and cupric nitrate was mixed into 10% phosphoric acid solution and pretreated dentin surface of bovine anterior teeth for 30 seconds followed- by water rinse and dry. Tensile bond strength was determined after bonding of pretreated dentin with MMA/TBBO resin by use of brush-on ;technique and storing for 24 hours in 3it distilled water. The amount of cupric ions adsorbed on pretreated dentin surface was detected by Wave-Dispersion X-ray microanalyzer for different groups of each pretreatment solution containing cupric salts. The pretreatment with cupric ions contained in 10% phosphoric acid solution was effective to increase bonding strength of MMA/TBBO resin to dentin but not in case of ferric ions. The pretreatment with 3 % cupric chloride and cupric nitrate both enhanced significant increase in bonding strength compared to the control group of 10% phosphoric acid solution(p<0.05). Cupric ions measured in pretreated dentin surface was higher in 3 % cupric chloride group than in 1% cupric chloride group, but couldn't find distinct relationship from the results of this experiment between the amount of adsorbed cupric ions according to the kind of cupric salts and the bonding strength value.

• Journal of Microbiology
• /
• v.37 no.4
• /
• pp.206-212
• /
• 1999

In order to isolate a Fe(III)-reducer from the natural environment, soil samples were collected from various patty fields and enriched with ferric citrate as a source of Fe(III) under anaerobic condition. Since the enrichment culture was serially performed, the Fe(III)-reduction activity was serially diluted and cultivated on an agar plate containing lactate and ferric citrate in an anaerobic glove box. A Gram negative, motile, rod-shaped and facultative anaerobic Fe(III)-reducer was isolated based on its highest Fe(III)-reduction activity, Bacterial growth was coupled with oxidation of lactate to Fe(III)-reduction, but the isolate fermented pyruvate without Fe(III), The isolate reduced an insoluble ferric iron (FeOOH) as well as a soluble ferric iron (ferric citrate). Using the BBL crystal enteric/non-fermentor identification kit and 16S rDNA sequence analysis, the isolate was identified as Shewanella putrefaciens IR-1.

• Textile Coloration and Finishing
• /
• v.9 no.6
• /
• pp.26-32
• /
• 1997

In order to remove the pollutants effectively in the dye-processing wastewater by chemical precipitation, coagulation and flocculation test was carried out using several coagulants on various reaction conditions. It was found that the Ferric sulfate was best coagulant for the treatment of mixed dye-processing wastewater. When the Ferric sulfate dosage was 1,100mg/$\ell$, the COD removal rate was very high(50%), and the color was removed very effectively. The COD was decreased relatively well up to 40%, when Alum was dosed as coagulant. But it was difficult to remove the color effectively. Test results about COD removal for the Ferrous sulfate and the Ferric chloride used were mostly same as those of the Alum used. However, the color removal by the Ferrous sulfate was much better than the case of the Alum or the Ferric chloride. It was found that the COD removal was increased and the sludge yield was decreased by pH control before polymer flocculant addition, during the jar test for the Ferrous sulfate and the Ferric sulfate as a coagulant.

• Resources Recycling
• /
• v.11 no.5
• /
• pp.21-23
• /
• 2002

A new process based on the co-precipitation method was developed fer removing harmful impurities during Mn-Zn ferrite production such as $SiO_2$ and P from waste pickle liquor. By this process a final result of less than 100 ppm of $SiO_2$ and less than 10 ppm of P content in the ferric oxide is easily attained. Though Ca cannot be removed by this process, water rinsing of the ferric oxide is effective fer reducing Ca content to less than 100 pm. For further purification, the origins of each impurity must be investigated and then taken away.

• Fisheries and Aquatic Sciences
• /
• v.17 no.2
• /
• pp.269-273
• /
• 2014

Coralline algae, the algal whitening phenomenon-causing seaweeds, are characterized by calcareous deposits in the cell wall. The viability of the coralline algae Lithophyllum yessoense and Corallina pilulifera was quantitated using a triphenyltetrazolium chloride assay and eight calcification inhibitors. Among these inhibitors, ferric citrate showed the strongest inhibition of coralline algae viability. The concentrations of ferric citrate conferring 50% inhibition were 1.7 and 3.8 mM for L. yessoense and C. pilulifera, respectively. Thus, at a specific concentration and in a localized area, ferric citrate may be used to prevent the blooming of coralline algae.

• Journal of Korean Society for Atmospheric Environment
• /
• v.31 no.2
• /
• pp.173-180
• /
• 2015

The purpose of this study was to fabricate a ferric nitrate impregnated activated carbon, and the performance for hydrogen sulfide by adsorption was evaluated. Sodium hydroxide was utilized to control pH in the process during generation of ferric hydroxide on the surface of the carbon. Critical mixing duration for generation of ferric hydroxide on the carbon was 48 hrs at pH 1 of the solution, in which the chemical adsorption of hydrogen sulfide was enhanced. The adsorption capacity of the impregnated carbon increased up to 0.10 g hydrogen sulfide/g carbon, which was 4.3 times higher than that of the raw carbon. Presence of FeOOH on the surface of the impregnated carbon was examined by X-ray diffraction.

• Journal of Microbiology and Biotechnology
• /
• v.21 no.5
• /
• pp.464-469
• /
• 2011

The arsH gene is one of the arsenic resistance system in bacteria and eukaryotes. The ArsH protein was annotated as a NADPH-dependent flavin mononucleotide (FMN) reductase with unknown biological function. Here we report for the first time that the ArsH protein showed high ferric reductase activity. Glu104 was an essential residue for maintaining the stability of the FMN cofactor. The ArsH protein may perform an important role for cytosolic ferric iron assimilation in vivo.

• Journal of Sasang Constitutional Medicine
• /
• v.3 no.1
• /
• pp.173-183
• /
• 1991

These studies were conducted about the effects of Ferric oxide in the aspect of the basic pharmacology through experimental animals with the investigation of its clinical effects on oriental medical literatures of Ferric oxide. The results were as follows: 1. The analgenic effects induced by acetic acid were significant. 2. The anticonvulsive effects induced by ECT unit were significant. 3. The sedative effects in Rotor rod method were significant. 4. The number of platelets was increased but not significantly. 5. Prothrombin time was decreased significantly. 6. Fibrinogen was increased but not significantly. 7. The degree of concentration of FDP was decreased significantly. According to the above results, it is considered that Ferric oxide retains effectiveness on the treatment of cerebral stroke.

• Journal of the Korean Ceramic Society
• /
• v.35 no.3
• /
• pp.239-244
• /
• 1998

Iron complexes were prepared using ferric nitrate and ethylene glycol as starting materials and the ul-trafine ${\alpha}-Fe_2O_3$ particles with the sizes smaller than 200nm were obtained by the pyrolysis of iron com-plexes at over $350^{\circ}C$ In addition the decomposition mechanism of the synthesized iron complexes was in-vestigated by differential scanning calorimeter X-ray diffractometer and IR spectrometer. Transmission electron microscopy and BET method were performed to analyze the effects of ferric nitrate contents and reaction temperatures on the size and shape of the particles.

• Korean Journal of Materials Research
• /
• v.20 no.6
• /
• pp.301-306
• /
• 2010

The chemical formula of magnetite ($Fe_3O_4$) is $FeO{\cdot}Fe_2O_3$, t magnetite being composed of divalent ferrous ion and trivalent ferric ion. In this study, the influence of the coexistence of ferrous and ferric ion on the formation of iron oxide was investigated. The effect of the co-precipitation parameters (equivalent ratio and reaction temperature) on the formation of iron oxide was investigated using ferric sulfate, ferrous sulfate and ammonia. The equivalent ratio was varied from 0.1 to 3.0 and the reaction temperature was varied from 25 to 75. The concentration of the three starting solutions was 0.01mole. Jarosite was formed when equivalent ratios were 0.1-0.25 and jarosite, goethite, magnetite were formed when equivalent ratios were 0.25-0.6. Single-phase magnetite was formed when the equivalent ratio was above 0.65. The crystallite size and median particle size of the magnetite decreased when the equivalent ratio was increased from 0.65 to 3.0. However, the crystallite size and median particle size of the magnetite increased when the reaction temperature was increased from $25^{\circ}C$ to $75^{\circ}C$. When ferric and ferrous sulfates were used together, the synthetic conditions to get single phase magnetite became simpler than when ferrous sulfate was used alone because of the co-existence of $Fe^{2+}$ and $Fe^{3+}$ in the solution.