Study of the d-f Emission,and f-d Ground-State and Excited-State Absorption of Nd3+ in Crystals Using the Simple Model

The simplified model for 4f-5d transitions is applied to obtain the line strengths for emission, ground-state absorption and excited states absorption involving 4f-5d transitions of Nd³⁺ in crystals. The results are host independent for the usual case where 5d crystal-field interaction can be considered as strong, in the sense that the calculated 5d-4f emission relative line strengths will be the same for Nd³⁺ in any host. Also the calculated 4f-5d absorption line strengths can be grouped by the 5d crystal-field components. For each 5d crystal-field component, the group of absorption line strengths for different 4f²5d transition final states forms a pattern independent of the 5d crystal-field component and the host. For practical cases, due to strong but still limited 5d crystal-field splitting, the transitions to different 5d crystal-field components may overlap each other. The theoretical results are used to interpret available experimental data.     

SPECTROSCOPIC PROPERTIES AND ELECTRONIC STRUCTURE OF [CuCl(L-PROLINATO)(H2O)]

ABSTRACT

[CuCl(L-Prolinato)(H₂O)] was prepared. Its electronic absorption spectrum and photoacoustic spectrum were recorded at the room temperature. A semi-empirical method of ligand-field-theory PLFT was utilized to calculate the d-d transition energy. According to the results, the spectrum was explained satisfactorily.     

Spectral Characterization of Nitrogen in Farmland Soil by Laser-Induced Breakdown Spectroscopy

Nitrogen is one of the most important elements in farmland soil, and nitrogen content is one of the evaluation indicators of fertilizers. It is difficult to measure the nitrogen content in farmland soil because the chemical and physical properties of farmland soil are complex. Through the adoption of buffer gases to remove the influence of the nitrogen in air, this paper studied the laser-induced breakdown spectroscopy (LIBS) characteristics of nitrogen in soil to establish a foundation for in situ measurement of nitrogen in farmland soil. Three characteristic spectral lines have been found. Based on the precise controlling of laser power and triggering of delay time between laser generation and spectra collection, we have studied the effects of laser energy on LIBS spectral characteristics and the time evolution characteristics to supply the basis of parameter optimization for the measurement. In addition, we have studied the relationship between nitrogen concentration and LIBS spectral intensity. The results demonstrated that LIBS was an effective measurement method of nitrogen content in farmland soil with simple hardware structure, fast detection, and high precision.     

Spectroscopic Properties and Electronic Structure of (L-Glutamato)(2, 2′-Bipyridine) copper(II)

Cu(L-glu)(bpy)(L-glu = L-glutamato; bpy = 2, 2′-bipyridine) was prepared. Its electronic absorption spectrum and photoacoustic spectrum were recorded at room temperature. They were compared with each other and compared quantitatively with ligand field theory(LFT) and the radical wave function of non-free ions^[1–3]. Therefore, the electronic structure was also investigated with its spectrum behaviors and PLFT^[1–3].     

The Significance of Thermally-Assisted Processes in Atomic Absorption

The use of non-resonance lines in atomic absorption spectroscopy has been included in the theoretical treatment of the selection of lines for A.A.S.^1,2, and such lines are not infrequently used on an empirical basis in practical analyses. This aspect of the technique is invariably ignored in reviews and text-books on atomic absorption, however, and has only been given serious consideration in isolated cases^3,4. The object of this publication is to illustrate the significance of thermally-assisted absorption, and the difference between the use of thermally-assisted and resonance absorption lines.     

The Mineral Content of Rhizona cyperi after Microwave-Assisted Digestion and Determination by AAS

ABSTRACT

Rhizoma cyperi (tuberal part of Cyperus rotundus Linn) obtained from 15 different zones of China was studied to determine the contents of 16 trace elements such as 4 minor (Ca, K, Mg, and Na), 9 trace (Co, Cr, Cu, Fe, Mn, Mo, Ni, V, and Zn), and 3 toxic (Ag, Cd, and Pb) elements. The concentration determination of 16 elements was performed by atomic absorption spectrophotometry (AAS) after microwave-assisted digestion. A microwave-assisted digestion procedure based on the mixture nitric acid–hydrogen peroxide was evaluated. The method was successfully validated with the good recoveries (97–105%) against CRM GBW07603 (bush twigs and leaves). The calibration curve furnished good linear correlation coefficients (r = 0.9956–0.9999), excellent recoveries (99.35–103.7%), and limits of detection (LOD = 1–50 ng·mL^?1) suitable to determine in Rhizoma cyperi. The results showed that K, Ca, Mg, and Na were the most abundant of the major elements in Rhizoma cyperi with average concentrations of K, 26,221 µg·g^?1; Ca, 1097 µg·g^?1; Mg, 714 µg·g^?1, and Na, 293 µg·g^?1, respectively. K element was determined for the first time in this plant.     

Atomic Absorption Spectrometry of Silver with Absorption Tube Having Nebulization Chamber

In the atomic absorption spectrometry with the long absorption tube using a hydrogen-air flame, only the total consumption type of the burners, e.g., Beckman¹ or ring burners², have been used for the input of a sample solution to the flame. The use of the indirect input method with nebulization chamber has never been attempted, though, by use of a commercially available apparatus with nebulization chamber, the large increase of the sensitivity has been easily obtained by heating the chamber and nebulizing air^3–5.     

An Improved Double Stage Furnace for Speciatton and Quantitative Atomic Absorption Spectrometry

Atomic absorption using furnace atomization suffers from three major problems. First, the matrix causes a change in absorption signal, second, the decomposition products cause a very high, variable background, and third, volatile elements are often lost during the evaporation and ashing steps. These problems are significantly reduced using the double stage system described below.

It consists of a separately heated atomization section, and vaporization section; and a light path which does not pass through the atomization section. This reduces background. The system operates in three modes. With the atomization section hot and the sample placed in the vaporization section, the latter is heated rapidly. This gives a fast quantitative signal with reduced background. With the atomization section cold, the sample is heated leisurely. The metal     

Effect of Ethanol on the Partition Coefficient Of Cyclohexylacetate Between Bulk and Cetyltrjmethylammonium Bromide Micellar Pseudophases

Variation of the partition coefficient of cyclohexylacetate (CA) was studied by a differential absorption spectroscopic method as a function of ethanol and (CTAB) cetyltrimethylammoniumbromide concentrations. Approach used was based upon the pseudo-two phase model, including effect of ethanol concentrations on the critical micelle concentration (CMC) of CTAB. Ethanol enhanced micelle formation of CTAB at concentrations below 1% by volume, had a slight inhibitory effect at higher concentrations and totally inhibited at a concentration above 15% by volume.

Various amounts of ethanol were used with a purpose of changing the solubility of CA in water. The differential absorbance (AA), was almost zero at low concentrations of CTAB, however an increase in AA began at a certain concentration of CTAB which can accordingly be assumed to be consistent with CMC of CTAB in the presence of ethanol. As CTAB concentration increased above CMC, ΔA reached a plateau. In this plateau, ΔA can reasonably be interpreted as the saturation of CA in micellar phase.

Plateau values of ΔA decreased with increasing ethanol concentration. This showed that the fraction of CA in the micellar phase depended on the ethanol concentration in terms of changing the solubility. Partition coefficients, K_c, were obtained from the plots of 1/ΔA against 1/[C_CA] +[C³ _m], which were linear in high CTAB concentrations. It was also seen that as ΔA, K_c decreased when the ethanol percentage were increased. In other words, the lower the solubility of CA in the bulk, the higher the partition coefficient.