EFFECT OF THE EXISTING STATES OF CHROMIUM ION ON THE COLOR CHARACTERISTICS OF DOPED β-C_2S

According to the theory of crystal field, the existing state of chromium ions in β-C_2S was studied with optical spectra and EPR. The energy levels of chromium ions were calculated. Chromium ions exist in form of Cr^(4+) and Cr^(5+) coordinated with distorted octahedra. The reason of fading of β-C_2S hydrate is that the strength of light absorption declines be- cause of the valence change of chromium ions and chroninm dissolves out and loses in water.

Spectrophotometric Method for Determination of Chromium Ion in Aqueous Solution Using Ninhydrin

A simple, precise, inexpensive and reproducible spectrophotometric method was investigated for the determination of chromium ion (III) in aqueous media, this method based on the formation of a complex between chromium ion (III) and ninhydrin, a deep greenish-violet colored product in the presence of potassium hydroxide was obtained. The absorption of this product was measured at λmax = 375 nm. The reaction proceeds quantitatively at room temperature. The linear calibration curve was constructed over range of (4.8 × 10-4 - 1.6 × 10-2) mol/L of chromium ions with molar absorptivity of 2.90 × 102 and correlation coefficient R2 = 0.9989. The calculated Sandell’s sensitivity value is 0.179 μg/cm2, the limits of detection (LOD) and the limit of quantification (LOQ) are found to be 3.74 × 10-5 and 1.24 × 10-4 mol/L, respectively. The method was successfully applied for determination of the chromium ion in aqueous solution. The stoichiometry of the reactions was determined molar combining ratio of 1:2 between chromium and ninhydrin.

Highly Selective Fluorescence Turn-on Chemosensor Based on Naphthalimide Derivatives for Detection of Trivalent Chromium Ions

A new fluorescent probe, NPQ-C, was synthesized. NPQ-C was based on the naphthalimide derivatives and exhibited high selectivity and sensitivity for Cr3＋ ions. As a Cr3＋-amplified fluorescent probe, Its fluorescence spectrum showed 5.5-fold enhancement in the intensity of the signal at 500 nm on binding with the Cr3＋. Based on the fluorescence titration spectra and Job＇s-plot analysis, binding mode of NPQ-C with Cr3＋ was proposed. Fluorescence intensity was linear with concentration of Cr3＋ cation in a range from 0 to 10 μmol·L-1. NPQ-C was also sensitive for Cr3＋. The detection limit was calculated to be 0.20 pmol.L-1 which indicated that NPQ-C was sensitive to Cr3＋.

Effect of partial pressure of reactive gas on chromium nitride and chromium oxide deposited by arc ion plating

The effects of reactive gas partial pressure on droplet formation, deposition rate and change of preferred orientation of CrN and Cr2O3 coatings were studied. For CrN coatings, as nitrogen partial pressure increases, the number and size of droplets increases, the deposition rate initially increases obviously and then slowly, and the preferred orientation of CrN changes from high-index plane to low-index one. For Cr2O3 coatings, with the increase of oxygen partial pressure, the number and size of droplets decreases, the deposition rate decreases and the (300) becomes the preferred orientation. These differences are ascribed to the formation of CrN (with a lower melting point) and Cr2O3 (with a higher melting point) on the surface of Cr target during the deposition of CrN and Cr2O3. Complete coatings CrN or Cr2O3 film can be formed when reactive gas partial pressure gets up to 0.1 Pa. The optimized N2 partial pressure for CrN deposition is about 0.1?0.2 Pa in order to suppress the formation of droplets and the suitable O2 partial pressure for Cr2O3 deposition is approximately 0.1 Pa for the attempt to prevent the peel of the coating.

Using Ferrous Ion for the Reductive Degradation of Hexavalent Chromium

This paper discusses the toxicity and mobility of chromium species. And it presents the extent and kinetics of reductive remediation of hexavalent chromium, Cr+ using ferrous ion, Fe2+. Molar ratios of 1:3 and 1:6 of Cr (VI) to Fe (II) were used. Integral method of data analysis showed reaction followed second-order kinetics with R square values near unity. Reaction was initially fast but with a rapid precipitation attributed to Cr (III)-Fe (III) in previous studies. This colloidal precipitate ultimately stops the reaction, which explains while conversion efficiency increases with increased molar ratio of Cr (VI) to Fe (II). The impact of pH was investigated by adjusting the Cr (VI)-Fe (II) medium to pH 2.78, 5.24, 7.00, 9.00 and 11.96 using predetermined drops of acid or base. Reaction was more rapid under alkaline conditions with higher extent of degradation consistent with previous research. In soil system, mass transfer limitation was hardly noticed as high extent of reduction was recorded relative to aqueous phase. The high solubility of Cr (VI) aided the release into the aqueous media for reduction by ferrous sulfate.

The Electrode for Potentiometric Determinаtion of Chromium (III, VI) in Wаter Solutions

The possibility of determining of chromium (III, VI) ions was investigated in this paper. It is shown that the electrode on а basis of heаzlewoodite has high selectivity to chromium (III) ions. Also the stability constants of complexes, forming in system “Cr3+-Mohr’s salt-Ca(OH)2-PVA ÷ PAA” were determined by potentiometric titration with ion-selective electrode.

Removal of Chromium(III) from the Waste Solution of an Indian Tannery by Amberlite IR 120 Resin

The extraction of chromium(III) from a model waste solution and also from a waste solution of an Indian tannery with Amberlite IR 120 resin is described, and the performance of this resin is compared with other similar resins. The parameters that were optimized include effect of mixing time, pH, loading and elution behaviours of chromium(III) for this resin. Sorption of chromium(III) on Amberlite IR 120 followed Freundlich isotherm and Langmuir isotherm model, and the maximum sorption capacity was determined to be 142.86 mg Cr(III)/g of the resin. Higher Freundlich constant (Kf) values (6.30 and 13.46 for aqueous feed of 500 and 1000 ppm Cr(III)) indicated strong chemical interaction through ion exchange mechanism of the metal ion with the resin. The kinetic data showed good fit to the Lagergren first order model for extraction of chromium(III). Desorption of chromium(III) from the loaded resin increased with the increase in concentration of eluent (5-20% H2SO4). With 20% (v/v) sulphuric acid solution 94% chromium(III) was eluted in three stages. Elution of the Cr(III) in the column experiments was however, found to be lower (82%) than that of the shake flask data. In case of Indian tannery’s waste solution, it was observed that almost total chromium was extracted in four stages with Amberlite IR 120.

Deposition of chromium aluminum nitride coatings by arc ion plating

Cr-Al-N ternary coatings were deposited by arc ion plating method using isolated Cr target and Al target. The influence of AlN content on the phase change was studied by synthesizing Cr1-xAlxN coatings with different x values. The effects of substrate negative bias on the surface morphology,deposition rate and phase structure were investigated. As the aluminum content increases,the structure of(Cr1-xAlx)N changes from B1(NaCl) phase to B4(wurtzite) phase. The critical content of AlN solubilized in B1(NaCl) lattice is close to 0.7. With the increasing pulse negative bias,the deposition rate decreases constantly,the droplet contamination is more serious,the ion-etching effect on coating surface is more obvious,and the change of preferred orientation and the shift of XRD peak take place.

Potential of <i>Artocarpus heterophyllus</i>Seed Powder in the Adsorption of Chromium(VI) from Aqueous Solution

The potential of Artocarpus heterophyllus (Jackfruit) seed powder in adsorption of chromium(VI) from aqueous solution was studied using batch technique. The performance of the adsorption process was evaluated against contact time, pH, adsorbent dose, temperature and initial chromium(VI) ion concentration. The influence of the presence of interfering anionic species including chlorides, nitrates and sulphates on the adsorption process was also evaluated. The adsorption of chromium(VI) by Jackfruit seed powder reached equilibrium after 60 minutes. Higher chromium(VI) adsorption was observed at lower pH values with maximum removal (96.05%) occurring at pH 2. A great deal of adsorption (92.53%) was observed at the adsorbent dosage level of 1.0 g/100 ml solution. There was an improvement in the adsorption process when the temperature was increased from 25&#176C (95.35%) to 60&#176C (99.56%) followed by a decrease to 98.76% at 70&#176C. Adsorption decreased with increasing initial chromium(VI) ion concentration. The adsorption followed both Freundlich and Langmuir adsorption models with correlation coefficients of 0.998 and 0.994 respectively, and Qm of 0.57 mg/g. The presence of nitrate and chloride ions significantly lowered the adsorption, with all the p values 0.05. From the obtained Qm, Jackfruit Seed Powder is a good adsorbent for the aqueous solutions of Cr(VI). The adsorption process is slowed by the presence of the interfering anionic species.

Trace-Level Analysis of Hexavalent Chromium in Lake Sediment Samples Using Ion Chromatography Tandem Mass Spectrometry

The analysis of hexavalent chromium, Cr(VI), in soil and sediment samples has been predominantly carried out in materials containing elevated levels. Reliable analysis of trace-level of Cr(VI) in sediment samples remains challenging. Cr(VI) analyses with multipoint calibration and speciated isotope dilution (SID) adapted from U.S. EPA method 6800 were used to measure lower-level Cr(VI) on an ion chromatograph coupled with a tandem mass spectrometer (IC-MS/MS). Lake sediment samples were collected from various locations in Northern Ontario and Cr(VI) was extracted using both alkaline digestion and ethylene diaminetetraacetic acid (EDTA) extraction. Certified reference materials were extracted and analyzed by IC-MS/MS and UV-VIS detection. The SID-MS approach allowed for the quantification of Cr(VI) in samples with concentration levels below 0.5 μg.g-1 wet weight.

Thickness Dependence of Structural and Optical Properties of Chromium Thin Films as an Infrared Reflector for Solar-thermal Conversion Applications

The thermal emittance of Cr film, as an IR reflector, was investigated for the use in SSAC. The Cr thin films with different thicknesses were deposited on silicon wafers, optical quartz and stainless steel substrates by cathodic arc ion plating technology as a metallic IR reflector layer in SSAC. The thickness of Cr thin films was optimized to achieve the minimum thermal emittance. The effects of structural, microstructural, optical, surface and cross-sectional morphological properties of Cr thin films were investigated on the emittance. An optimal thickness about 450 nm of the Cr thin film for the lowest total thermal emittance of 0.05 was obtained. The experimental results suggested that the Cr metallic thin film with optimal thickness could be used as an effective infrared reflector for the development of SSAC structure.

Novel Cr^(3+)-activated far-red emitting phosphors withβ-Ca_(3)(PO_(4))_(2)-type structure for indoor plant cultivation

Cr^(3+)-activated far-red and near-infrared phosphors have drawn considerable attention owing to their adjustable emission wavelengths and wide applications.Herein,we reported a series of Cr^(3+)-doped phosphors withβ-Ca_(3)(PO_(4))_(2)-type structure,of which Ca_(9)Ga(PO_(4))_(7):Cr^(3+) possessed the highest far-red emission intensity.At an excitation of 440 nm,the Ca_(9)Ga(PO_(4))_(7):Cr^(3+) phosphors exhibited a broad emission band ranging from 650 to 850 nm and peaking at 735 nm,and the broadband superimposed two sharp lines centering at 690 and 698 nm.The optimal sample Ca_(9)Ga_(0.97)(PO_(4))_(7):0.03 Cr^(3+) had an internal quantum efficiency of 55.7%.The luminescence intensity of the Ca_(9)Ga_(0.97)(PO_(4))_(7):0.03 Cr^(3+) phosphor obtained at 423 K could maintain 68.5%of that at room temperature,demonstrating its outstanding luminescence thermal stability.A phosphor-conversion light-emitting diode was fabricated,indicating that the Ca_(9)Ga(PO_(4))_(7):Cr^(3+) phosphor has potential applications in indoor plant cultivation.

Fluorescence sensor based on glutathione capped CdTe QDs for detection of Cr^3+ ions in vitamins

In this work,glutathione capped CdTe QDs(GSH-QDs)were prepared through a one-pot process and found to be quenched by Cr^3+,Ag^+and Cu^2+ions.Cr^3+and chromium(III)picolinate could be quantitatively measured after masking Cu^2+and Ag+ions by sulfide.Under optimal conditions,linear quenching was observed for Cr^3+in the ranges of 0–2.0M and the limit of detection was 3.0 nM.The recoveries for Cr^3+in vitamin supplements obtained were from 92.5%to 106%.The determination results of chromium(III)picolinate in vitamin supplement samples were compared to that obtained using flame atomic absorption spectrometry(FAAS)method,and the result showed good reliability.

Adsorption of Cr(III) from an Aqueous Solution by Chitosan Beads Modified with Sodium Dodecyl Sulfate (SDS)

This study is to prepare chitosan beads modified with sodium dodecyl sulfate (SDS) to effectively remove Cr(III) from an aqueous solution. The characterizations of SDS-chitosan by scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), Fourier transform-infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) proved the successful synthesis of the adsorbent. The adsorption of Cr(III) on the SDS material was investigated by varying experimental conditions such as pH, contact time and adsorbent dosage. The maximum adsorption capacity of SDS-chitosan for Cr(III) was estimated to be 3.42 mg?g-1. The results of adsorption kinetics and isothermal models show that the adsorption process conforms to the pseudo-second-order and Langmuir isotherm models, indicating that the adsorption is single-layer chemical adsorption. Thermodynamic analyses indicate that the adsorption of Cr(III) is an endothermic reaction. These results show that the new adsorbent has obvious application prospect to eliminate Cr(III).

Optimal Sample Preservation and Analysis of Cr(VI) in Drinking Water Samples by High Resolution Ion Chromatography Followed by Post Column Reaction and UV/Vis Detection

A recent study by the Environmental Working Group reported the detection of hexavalent chromium (Cr(VI)) in tap water at 31 out of 35 states investigated in the United States. Even though Cr(III) is an essential element for human diet, Cr(VI) is a potential carcinogen. Previous work has clearly identified a linear trend of increasing risk of lung cancer mortality with increasing cumulative exposure to water soluble Cr(VI). Regardless, Cr(VI) is still not regulated or monitored in drinking water in the U.S. There is an existing method (EPA 218.6) for the analysis of Cr(VI), however, this analytical method does not addresses detailed sample preservation techniques and optimization process to achieve lowest detection limit possible. In this study, five buffer solutions with pH of 9 and above were compared to determine the most suitable buffer to preserve Cr(VI) in drinking water samples for an extended period of time. Results showed that the five buffers responded very differently to Cr(VI)-fortified drinking water. The best preserving reagent was found to be Ammonium Hydroxide + Ammonium Sulfate (pH 9.2) and Sodium Carbonate + Sodium Bicarbonate+ Ammonium Sulfate (pH 9.7), whereas a buffer solution with Sodium Hydroxide + Sodium Carbonate (pH 11.5+) resulted in a poor chromatographic resolution. A controlled study with a fortified Cr(III) at 1 ppb was also conducted to ensure no false positive detection of Cr(VI) due to the potential oxidation of Cr(III) during sample storage. The optimal preserving reagent identified from this study was compatible with the existing EPA method 218.6 using ion chroma-tography followed by post column reaction, with a method quantitation limit of 0.020 ppb and matrix spike recovery of ± 10%.

Effects of lanthanum ion-implantation on microstructure of oxide film formed on Co-Cr alloy

Isothermal and cyclic oxidizing behavior of Co-40Cr alloy and its lanthanum ion-implanted samples were studied at 1000 ℃ in the air by thermal-gravimetric analysis （TGA）. Scanning electronic microscopy （SEM） and transmission electronic microscopy （TEM） were used to examine the morphology and structure of oxide film after oxidation. Secondary ion mass spectrum （SIMS） method was used to examine the binding energy change of chromium caused by La-doping and its influence on the formation of Cr2O3 film. laser Raman spectrum was used to examine the stress changes within the oxide film. It was found that lanthanum implantation remarkably reduced isothermal oxidizing rate of Co-40Cr and improved anti-cracking and anti-spalling properties of Cr2O3 oxide film. The reasons for the improvement were mainly that the implanted lanthanum reduced the grain size and internal stress of Cr2O3 oxide and increased high temperature plasticity of the oxide film. Lanthanum mainly existed on the outer surface of Cr2O3 oxide film in the form of fine La2O3 and LaCrO3 spinel particles.

Preparation of spherical spinel LiCr_(0.04)Mn_(1.96)O_4 cathode materials based on the slurry spray drying method

Regular spherical chromium doped spinel lithium manganese oxides （LiCr0.04Mn1.96O4） with an average particle size of about 20μm were prepared by the slurry spray drying process. The materials were compared with non-spherical LiCr0.04Mnl.96O4 materials prepared by the common drying process, and all materials were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, laser particle analyzer and Brunaner-Emmett-Teller （BET） specific surface area test. Electrochemical performances of these cathode materials were studied by cyclic voltammetry （CV）, electrochemical impedance spectroscopy （EIS） and Li/LiCr0.04Mn1.9604 battery test. The results show that the spherical active material is single spinel structure, compact, and with narrow particle size distribution and low BET specific surface area. Compared with the non-spherical material, the spherical material prepared by the spray drying process shows a lower electrochemical impedance, a fewer electrochemical polarization and a better charge/discharge rate capability and capacity retention at elevated temperatures.

Mid-Term Review of ADEPT Metal-On-Metal Hip Prosthesis. Functional, Radiological and Metal Ion Analysis

Background: There is much interest regarding metal-on-metal implants in medical and general media. Much of this has been regarding failure of specific implant systems and metal ion toxicity. We present our early mid-term experience of the ADEPT metal-on-metal system which has both modular and non-modular hip options. Methods: Functional assessment, blood metal ion quantification, and radiographic analysis were performed for the modular and non-modular ADEPT variants. Fifty implants were implanted with a mean follow up time of 28 months. Unpaired t-tests were used to compare modular and resurfacing groups, standardised hip scores were used to compare function to conventional total hip arthroplasty. Results: Metal ion levels were significantly higher in modular prostheses compared to resurfacing implants, but not at “harmful” levels (as determined by a previous metal-on-metal implant recall). Functional outcomes were excellent and revision rates were lower than expected. Conclusions: At our institution we have good outcomes with the ADEPT hip prosthesis. Though patient selection and implant position are crucial, poor performance of metal-on-metal hip replacements is implant specific.

Improvement of Pretreatment for Environmental Analysis of Cr （VI） Ion for Sediment Soil in Tama River

Compounds containing Cr （VI） ion are widely used for chemical industry, paints, dyes, and other applications. Because of commonly known toxicity of Cr （VI） ion, Cr （VI） is one of the important check items for quality of water in natural river or industrial waste water. Although the only method for selective detection for Cr （VI） ion is diphenylcarbazide, of which pretreatment spends long time according to the regulat^ons by the Ministry of Environment, Japan. Herein we develop a new and simple pretreatment for the job site and suitable for education and attempt to apply for analysis of the soil in Tama River actually.

Removal of Some Toxic Ions from Seawater and Wastewater by Sorption onto Natural, Synthetic Hydroxyapatite and Alginate-Hydroxyapatite Composite Nanoparticles: A Comparative Study

The main objective of this paper is to study the removal of Cadmium(II), Lead(II), Chromium(VI), and Mercury(II) ions by sorption onto different natural and synthetic nanoparticles. Special attention has been given to the application of fish bone in nanoform as a useful, inexpensive and eco-friendly alternative material. A comparison between natural hydroxyapatite (fish bone), synthetic hydroxyapatite nanoparticles (HAP) and alginate-hydroxyapatite composite (Alg/Hap) to assess their removal efficiencies to remediate the selected heavy metals has been done. Surface characterization by using different techniques has also been performed to understand the influence of surface characteristics of the adsorbent materials in the removal process. Different parameters (pH, contact time, mass dose and metal ion concentration) have been examined to identify the optimum conditions for remediation of different metals from polluted water. The potential applications of the biosorbents for removal and sorption of these metal ions from seawater and wastewater samples were also investigated and evaluated.