Development and effectiveness of a soluble manganese silicate compound in controlling manganese deficiency in plants

Summary A study was made of soluble manganese silicates prepared by adding a solution of manganese sulfate to different concentrations of sodium silicate in alkaline medium. The solubility of manganese increased with increasing amounts of sodium silicate and reached its maximum at a molar Na₂SiO₃/MnSO₄ ratio between 10 and 15. At molar Na₂SiO₃/MnSO₄ ratios of 5 and more a red-brown coloured manganese silicate is formed, which is stable in the pH range of 4 to 12. Gel chromatographic analysis indicated that this compound contains 1 molecule Mn per 15 molecules SiO₂. At a molar Na₂SiO₃/MnSO₄ ratio of 15 the yield of soluble manganese could be raised to 98.5% of the theoretical amount by preventing the rapid oxidation of the Mn²⁺-ions in the alkaline solution. A pot experiment with oats was conducted to evaluate the effectiveness of the red-brown manganese silicate in controlling manganese deficiency. The effect of the Mn-carrier on Mn-content and yield of grain and on the colour scores was compared with that of Mn-EDTA, Mn-DTPA and MnSO₄·4H₂O. The manganese silicate was found to be a more effective manganese source than Mn-EDTA, Mn-DTPA or MnSO₄·4H₂O.     

EFFECT OF AQUEOUS FLUORIDE SOLUTIONS ON RESPIRATION OF INTACT BUSH BEAN SEEDLINGS

Applegate , Howard G., Donald F. Adams , and Roy C. Carriker . (Washington State U., Pullman.) Effect of aqueous fluoride solutions on respiration of intact bush bean seedlings. I. Inhibition and stimulation of oxygen uptake. Amer. Jour. Bot. 47(5): 339—345. Illus. 1960.–Intact bush bean seedlings were infiltrated with 1 × 10^–1, 1 × 10^–2, 1 × 10^–3, and 1 × 10^–4 M fluoride. A linear relationship was found to exist between the fluoride concentrations of the infiltrating solutions and tissue fluoride. The higher fluoride concentrations inhibited oxygen uptake, whereas lower fluoride concentrations accelerated oxygen uptake. Both the inhibition and acceleration of oxygen uptake by fluoride were modified by light, CO₂, and presence or absence of chlorophyll.     

Red Blood Cell and Serum Magnesium Levels Among Children and Adolescents With Sickle Cell Anemia

This study investigated neurotoxicity of chronic fluorosis in the rat hippocampus. Newly weaning, male, Sprague-Dawley (SD) rats were administered 15, 30, and 60 mg/L sodium fluoride (NaF) solution (fluorine ion concentration 8.25, 16.50, and 33.00 mg/L, respectively), and tap water, for 18 months. The neurotoxicological mechanism was examined with a focus on intracellular calcium overload. Results showed that as the fluoride concentration increased, calcium ion concentration [Ca²⁺], the expression of calcium/calmodulin-dependent protein kinase II α (CaMKIIα), and the expression of catus proto-oncogene protein c-fos (c-fos) all tend to increase. Compared to the control group, Ca²⁺, CaMKIIα, and c-fos significantly increased (P < 0.05) in the moderate-fluoride and the high-fluoride groups. These results indicate that Ca²⁺/CaMKIIα/c-fos channel signal may be the molecular mechanism of central nervous system damage caused by chronic fluoride intoxication. Moreover, elevated Ca²⁺ concentration in the hippocampus may be the initiating factor of neuronal apoptosis induced by fluoride.     

Improvement of light emission of Mn-doped Zn(2) SiO(4) phosphors with sodium

Mn‐doped willemite (Zn₂SiO₄:Mn) green phosphor were synthesized by sol–gel technology. The effect of the addition of sodium, as in the composition Zn_{(1.92 – X)} Na_XMn_0.08SiO₄, on the emission behavior was studied. FT–IR and EPR results revealed that sodium ion is incorporated into the lattice and results in the formation of isolated Mn²⁺ and Mn–Mn pairs. The maximum emission intensity of the sample under ultraviolet (UV) excitation occurred at the sodium concentration of x = ~0.03. The green emission at about 525 nm is assigned to Mn²⁺–Mn²⁺ pair centres on nearest neighbour Zn sites. The highest intensity of the green emission for x = ~0.03 is well close to the highest concentration of the Mn²⁺–Mn²⁺ pair. Copyright © 2012 John Wiley & Sons, Ltd.     

Luminescence enhancement of (Sr1–xMx)2SiO4:Eu2+ phosphors with M (Ca2+/Zn2+) partial substitution for white light‐emitting diodes

Eu²⁺‐doped Sr₂SiO₄ phosphor with Ca²⁺/Zn²⁺ substitution, (Sr_1–xM_x)₂SiO₄:Eu²⁺ (M = Ca, Zn), was prepared using a high‐temperature solid‐state reaction method. The structure and luminescence properties of Ca²⁺/Zn²⁺ partially substituted Sr₂SiO₄:Eu²⁺ phosphors were investigated in detail. With Ca²⁺ or Zn²⁺ added to the silicate host, the crystal phase could be transformed between the α‐form and the β‐form of the Sr₂SiO₄ structure. Under UV excitation at 367 nm, all samples exhibit a broad band emission from 420 to 680 nm due to the 4f⁶5d¹ → 4f⁷ transition of Eu²⁺ ions. The broad emission band consists of two peaks at 482 and 547 nm, which correspond to Eu²⁺ ions occupying the ten‐fold oxygen‐coordinated Sr.(I) site and the nine‐fold oxygen‐coordinated Sr.(II) site, respectively. The luminescence properties, including the intensity and lifetime of Sr₂SiO₄:Eu²⁺ phosphors, improved remarkably on Ca²⁺/Zn²⁺ addition, and promote its application in white light‐emitting diodes. Copyright © 2016 John Wiley & Sons, Ltd.     

Thermoluminescent properties of some phosphor glasses based on aluminum oxide

The transparent thermoluminescent aluminum oxide‐based glass of 15Al₂O₃–35P₂O₅–25CaO–25Na₂CO₃, abbreviated as APCN (all in mol%) doped with different concentrations of SiO₂ from 0.0–500 ppm was prepared using a conventional melt‐quenching technique. The TL sensitivities of the prepared glasses were investigated at 3 Gy γ‐dose using a ⁶⁰Co source and measured at a heating rate 10 C/sec. The highest TL intensity of the material doped with SiO₂ was found at a concentration of 500 ppm (APCNSi₅). Deconvolution of the glow curve from APCNSi₅ resulted in four peaks at about 161, 194, 237 and 293 C with a Figure Of Merit (FOM) of 1.28%. The APCNSi₅ specimen had the best dosimetric properties when compared with the other samples. Reproducibility, repeatability, dose–response curve and fading effect were checked for peak 3, which appeared at about 237 C. The results displayed that the APCNSi₅ glass system was a low‐Z material (Z_eff ≈ 10), and had good reproducibility and good repeatability. Peak 3 showed good linearity over a dose range up to 20 Gy (R² = 0.999) and sublinearity behaviour was found. The signal from APCNSi₅ faded by about 11% after 2 days post irradiation, therefore it showed almost no significant loss. Such properties make the newly prepared glasses suitable for and highly recommended for use in γ‐dosimeters. Copyright © 2016 John Wiley & Sons, Ltd.     

Sources of silicon influence photosystem and redox homeostasis-related proteins during the axillary shoot multiplication of Dianthus caryophyllus

The present endeavor has demonstrated the impacts of different sources of silicon (Si) such as potassium silicate (K₂SiO₃) and calcium silicate (CaSiO₃) during the in vitro axillary shoot multiplication of carnation. For the Si treatments, nodal explants were cultured onto the Murashige and Skoog’s medium fortified with 1.0 mg L^?1 of 6-benzyladenine and 0.5 mg L^?1 indole-3-acetic acid with or without K₂SiO₃ and CaSiO₃ in three different concentrations (0, 1.8, or 3.6 mM). After six weeks, the shoot induction ratio, number of shoots produced per explant, expression of photosystem (PS) I and II core proteins, and activities of antioxidant enzymes were examined. Among the Si sources, K₂SiO₃ application enhanced the axillary shoot multiplication and the uptake of Si on comparison with CaSiO₃. Both forms of Si resulted in the enhancement of stomatal density, and PS-related protein such as PsaA and PsbA illustrating the apparent involvement of Si on the photosynthetic process. Nevertheless, addition of Si improved the antioxidant capacity during the in vitro shoot multiplication. Overall, the outcomes of the present study suggested that Si can be utilized as a supplementary source during the in vitro propagation of carnation.     

Perovskite Oxyfluoride Electrode Enabling Direct Electrolyzing Carbon Dioxide with Excellent Electrochemical Performances

Solid oxide electrolysis cells (SOECs) can efficiently convert the greenhouse‐gas CO₂ to valuable fuel CO at the cathodes. Herein, fluorine is doped into mixed ionic–electronic conducting Sr₂Fe_1.5Mo_0.5O_6‐δ (SFM), to evaluate its potential use as a cathode for CO₂ reduction reaction (CO₂‐RR). SFM retains its cubic structure after doped with fluorine, forming perovskite oxyfluoride Sr₂Fe_1.5Mo_0.5O_6‐δF_0.1 (F‐SFM). The substitution of oxygen by fluorine increases CO₂ adsorption by a factor of ≈2, bulk oxygen vacancy concentration by 35–37% at 800 °C, and consequently enhances the surface reaction rate constant for CO₂‐RR and chemical bulk diffusion coefficient by factors of 2–3. The faster kinetics are also reflected by a lower polarization resistance of 0.656 Ω cm² for F‐SFM than 1.130 Ω cm² for SFM at 800 °C in symmetrical cells. Furthermore, the single cell with F‐SFM cathode exhibits the best CO₂ electrolysis performance among the reported perovskite electrodes, achieving current density of 1.36 A cm^?2 at 1.5 V and excellent stability over 120 h at 800 °C under harsh conditions. The theoretical computations confirm that fluorine doping is energetically favorable to CO₂ adsorption and dissociation. The present work provides a promising strategy for the design of robust cathodes for direct CO₂ electrolysis in SOECs.     

Fluoride-containing bioactive glasses inhibit pentose phosphate oxidative pathway and glucose 6-phosphate dehydrogenase activity in human osteoblasts

Bioactive glasses such as Hench's 45S5 (Bioglass^®) have applications to tissue engineering as well as bone repair, and the insertion of fluoride in their composition has been proposed to enhance their bioactivity. In view of a potential clinical application, we investigated whether fluoride-containing glasses exert toxic effects on human MG-63 osteoblasts, and whether and how fluoride, which is released in the cell culture medium, might play a role in such cytotoxicity. A 24 h incubation with 50 μg/ml (12.5 μg/cm²) of fluoride-containing bioactive glasses termed HCaCaF₂ (F content: 5, 10 and 15 mol.%) caused the release of lactate dehydrogenase in the extracellular medium (index of cytotoxicity), the accumulation of intracellular malonyldialdehyde (index of lipoperoxidation), and the increase of glutathione consumption. Furthermore, fluoride-containing glasses inhibited the pentose phosphate oxidative pathway and the glucose 6-phosphate dehydrogenase activity. These effects are ascribable to the fluoride content/release of glass powders, since they were mimicked by NaF solutions and were prevented by dimethyl sulfoxide and tempol (two radical scavengers), by superoxide dismutase (a superoxide scavenger), and by glutathione (the most important intracellular antioxidant molecule), but not by apocynin (an inhibitor of NADPH oxidase). The presence of fluoride-containing glasses and NaF caused also the generation of reactive oxygen species, which was prevented by superoxide dismutase and catalase. The data suggest that fluoride released from glasses is the cause of MG-63 cell oxidative damage and is independent of NADPH oxidase activation. Our data provide a new mechanism to explain F^? ions toxicity: fluoride could trigger, at least in part, an oxidative stress via inhibition of the pentose phosphate oxidative pathway and, in particular, through the oxidative inhibition of glucose 6-phosphate dehydrogenase.     

Surface reactivity and in vitro biological evaluation of sol gel derived silver/calcium silicophosphate bioactive glass

Ag ions are known for their antibacterial effects. Ag containing silicate glasses have been extended to create bioactive glasses that exhibit inhibitory effects on bacterial growth using different techniques. In this work, calcium and calcium/silver silicophosphate glasses were synthesized from the sol-gel process and their physicochemical and in vitro biological properties were studied and compared. The effect of silver concentration on in vitro bioactivity and antibacterial properties of the glasses was investigated. Ag₂O was substituted for CaO in the glass formula up to 2 mol% and in vitro bioactivity of the samples was evaluated by soaking them in simulated body fluid followed by structural characterization using XRD, FTIR and SEM techniques. The results showed that both glasses favored precipitation of the calcium phosphate layer when they were soaked in simulated body fluid; however, the morphology of apatite crystals changed for the 2% mol silver containing sample. Substitution of 2% mol Ag₂O for CaO seemed to slightly stimulate the rate of precipitation. The in vitro biodegradation rate of the silver/ calcium silicophosphate glasses was lower than that of the silver-free one (control). Also, the antibacterial properties of the samples indicated that these effects were improved by increasing silver concentration in bioactive glass composition.     

New coordination polymer based on salpn Schiff base and azide bridging ligands: Synthesis and structural characterization of {Na[Co(μ-salpn)(μ1,1-N3)2]}n (H2salpn = N,N′-bis(salicylidene)-1,3-diaminopropane)

One-pot reaction of cobalt(II) nitrate hexahydrate Co(NO₃)₂ · 6H₂O with H₂salpn (N,N′-bis(salicylidene)-1,3-diaminopropane) in presence of a large excess of sodium azide (NaN₃) gives the new Co(III) compound {Na[Co^III(μ-salpn)(μ_1,1-N₃)₂]}_n (1), which was characterized by single crystal X-ray diffraction analysis. The crystal structure shows polymeric 1D complex generated by the hexadentate Schiff base salpn²⁻ and two crystallographically different azide ligands. The two nitrogen atoms of the salpn ligand are bonded to the cobalt(III) ion while each phenoxo oxygen atom is bonded to the same Co(III) ion and to two equivalent sodium ions. Each azide ligand acts with the end-on bridging coordination mode between Co(III) and Na(I) ions. The Co(III) ion adopts a distorted octahedral geometry arising from two oxygen and two nitrogen atoms of the salpn ligand and from two nitrogen atoms of the two crystallographically different azide ligands in trans positions. Such [Co(salpn)(N₃)₂] entities are connected each other by sodium ions through four oxygen atoms of two equivalent Schiff base ligands and two nitrogen atom of the two different azide ligands to generate the 1D structure of 1.     

Highly luminescent hybrid SiO2‐coated CdTe quantum dots: synthesis and properties

Novel hybrid SiO₂‐coated CdTe quantum dots (QDs) were created using CdTe QDs coated with a hybrid SiO₂ shell containing Cd²⁺ ions and a sulfur source via a sol–gel process in aqueous solution. Aqueous CdTe QDs with tunable emitting color created through a reaction between cadmium chloride and sodium hydrogen telluride was used as cores for the preparation of hybrid SiO₂‐coated CdTe QDs. In our experiments we found that the surface state of the cores and preparation conditions that affect the formation of the hybrid SiO₂ shell also greatly affect photoluminescence of the hybrid SiO₂‐coated CdTe QDs. The generation of CdS‐like clusters in the vicinity of the CdTe QDs, caused the quantum size effect of the QDs to be greatly reduced, which changes photoluminescence properties of the hybrid QDs fundamentally. Namely, the novel hybrid SiO₂ shell played an important role in generating a series of specific optical properties. In addition, the novel hybrid SiO₂ shell can be created if no CdTe QD is added. In order to gain an insight into the inter structure of the hybrid shell, we characterized the hybrid SiO₂‐coated CdTe QDs using X‐ray diffraction analysis and discuss the formation mechanism of such a hybrid structure. This work is significant because the novel hybrid SiO₂‐coated CdTe QDs with its excellent properties can be used in many applications, such as biolabeling and optoelectronic devices. Copyright © 2013 John Wiley & Sons, Ltd.     

Impact of soil environmental factors on rates of N2-fixation associated with roots of intact maize and sorghum plants

We have evaluated the effects of oxygen partial pressure (pO₂), combined nitrogen, and the availability of organic substrates on nitrogen fixation (acetylene reduction) by bacteria associated with the roots of intact maize and sorghum plants. We also investigated the possibility of enhancing associative nitrogen-fixation by inoculating the soil in which the plants were grown withAzospirillum. Acetylene reduction (AR) activity was greatest when roots of intact plants were exposed to pO₂ between 1.3 and 2.1 kPa. Field-grown and greenhouse-grown plants supported similar levels of activity. Respiration inhibitors (2,4-dinitrophenol and sodium azide) eliminated AR activity at 2 kPa O₂, whereas a fermentation inhibitor (sodium fluoride) only partially reduced the activity. Acetylene reduction activity was rapidly (1–3 h) inhibited by NH ₄ ⁺ , NO ₃ ^– , and NO ₂ ^– at concentrations of 4–20 mg Nl^–1. Rates of AR varied substantially among individual plants in each experiment and between experiments. Amendment with any of several organic substrates greatly increased AR activity when rates were low, suggesting that the lack of activity was caused by a shortage of available carbon in the rhizosphere. Inoculation withAzospirillum failed to increase rates of AR associated with maize plants. In several experiments the indigenous bacteria associated with uninoculated plants exhibited greater activity than the bacteria associated with inoculated plants.     

The structure and luminescence properties of Mn2+/Eu2+/Er3+‐doped MgO‐Ga2O3‐SiO2 glasses and glass‐ceramics

The MgO–Ga₂O₃–SiO₂ glasses and glass‐ceramics samples doped with Eu²⁺/Mn²⁺/Er³⁺ and heated in reductive atmosphere were prepared by the sol–gel method. The structure, morphology and the luminescence properties were studied using X‐ray diffraction, high‐resolution transmission electron microscope, fluorescence spectra, and up‐conversion emission. The luminescence characteristics of doped ions could be influenced by temperature and matrix component. The characteristic emission of Mn²⁺, Eu²⁺ and Er³⁺ were seen and the energy transfer efficiency from Eu²⁺ to Mn²⁺ was enhanced as Mn²⁺ concentration was increased. In addition, the two‐photon process was determined for the Er³⁺‐doped samples.     

Spectroscopic investigations of Er(3+) :CdO-Bi(2) O(3) -B(2) O(3) glasses

This article reports on the optical properties of Er³⁺ ions doped CdO–Bi₂O₃–B₂O₃ (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ω_λ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er³⁺:CdBiB glasses. The concentration quenching and energy transfer from Yb³⁺–Er³⁺ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er³⁺:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd.     

Effects of adenosine and adenosine-analogs on adenylate cyclase activity in the rat adipocyte plasma membrane: comparison of the properties of the enzyme with Mn2+ and Mg2+ as divalent cations

Summary We investigated the influence of Mg²⁺ and Mn²⁺ on the effects of adenosine and some derivatives on basal adenylate cyclase activity in rat fat cell membranes as well as on enzyme activity stimulated by isoprenaline or sodium fluoride. Adenosine and derivatives modified in the ribose function were inhibitory, irrespective of the stimulant used, both in the presence of MgCl₂ or MnCl₂. Inhibition of basal and sodium fluoride stimulated adenylate cyclase activity was more pronounced in the presence of MnCl₂ than in the presence of MgCl₂. N⁶-substituted adenosine analogs proved to be inhibitory in the presence of 5 MM MgCl₂, but in the presence of 1 mM MnCl₂ the fluoride stimulated adenylate cyclase activity was potentiated, while basal and isoprenaline stimulated activity were not significantly inhibited. These effects of adenosine and derivatives could not be blocked by theophylline with or without guanyl nucleotides.The potentiating effect of N⁶-substituted adenosine derivatives on sodium fluoride activated adenylate cyclase is dependent on the structure of the N₆-substitutent and consists of an enhancement of Vrnax in combination with a small decrease of the K_m for MnATP^2–, indicative of an allosteric effect on adenylate cyclase. No potentiation by N⁶-phenylisopropyladeno sine of sodium fluoride stimulated cyclase was found on digitonin solubilized cyclase, while the inhibitory effect of adenosine was retained. The relevance of these findings is discussed in connection with the current hypothesis concerning the presence of two adenosinesensitive sites on rat fat cell membranes.     

Optical analysis of RE3+ (RE = Nd or Er):B2O3–P2O5–CaF2–ZnO–(Li2O/Na2O/K2O) glasses

Calcium boro fluoro zinc phosphate glasses modified using alkali oxide and doped with Nd³⁺ and Er³⁺ ions with the chemical composition of 69.5 (B₂O₃) + 10 (P₂O₅) + 10 (CaF₂) + 5 (ZnO) + 5 (Na₂O/Li₂O/K₂O) + 0.5 (Er₂O₃/Nd₂O₃) were prepared using a conventional melt quenching technique. The results of X-ray diffraction patterns indicated the amorphous nature of all the prepared glasses. The visible–near-infrared red (NIR) absorption spectra of these glasses were analyzed systematically. The NIR emission spectra of Er³⁺ and Nd³⁺:calcium boro fluoro zinc phosphate glasses showed prominent emission bands at 1536 nm (⁴I_13/2→⁴I_15/2) and 1069 nm (⁴F_3/2→⁴I_11/2) respectively with λ_exci = 514.5 nm (Ar⁺ laser) as the excitation source.     

Improved Cycling Performance of Li‐Excess Cation‐Disordered Cathode Materials upon Fluorine Substitution

The recent discovery of Li‐excess cation‐disordered rock salt cathodes has greatly enlarged the design space of Li‐ion cathode materials. Evidence of facile lattice fluorine substitution for oxygen has further provided an important strategy to enhance the cycling performance of this class of materials. Here, a group of Mn³⁺–Nb⁵⁺‐based cation‐disordered oxyfluorides, Li_1.2Mn³⁺_0.6+0.5xNb⁵⁺_0.2?0.5xO_2?xF_x (x = 0, 0.05, 0.1, 0.15, 0.2) is investigated and it is found that fluorination improves capacity retention in a very significant way. Combining spectroscopic methods and ab initio calculations, it is demonstrated that the increased transition‐metal redox (Mn³⁺/Mn⁴⁺) capacity that can be accommodated upon fluorination reduces reliance on oxygen redox and leads to less oxygen loss, as evidenced by differential electrochemical mass spectroscopy measurements. Furthermore, it is found that fluorine substitution also decreases the Mn³⁺‐induced Jahn–Teller distortion, leading to an orbital rearrangement that further increases the contribution of Mn‐redox capacity to the overall capacity.     

The interrelationships between sodium ion,calcium transport and oxygen utilization in the isolated chick chorioallantoic membrane

Summary The interrelationships between sodium ion, calcium transport and oxygen utilization have been investigated in the chick chorioallantoic membrane. The oxygen uptakes of the two surface layers of the tissue, the ectoderm and the endoderm, were separated into their basal, Na⁺ dependent and Ca⁺⁺ dependent components. The endoderm has a basal rate of respiration of 3.6 liters O₂/cm²/hr and a Na⁺ dependent component of 1.4 liters O₂/cm²/hr. The ectoderm has a basal rate of respiration of about 3.5 liters O₂/cm²/hr, and Na⁺ and Ca⁺⁺ dependent components of 1.1 and 3.6 liters O₂/cm²/hr, respectively. The rate of ectodermal calcium transport and calcium-stimulated oxygen uptake is strictly dependent on the presence of sodium in the bathing medium, and complex kinetics are observed as a function of sodium concentration. On the other hand, in 140mm Na⁺ the rate of calcium transport exhibits simple saturation kinetics as a function of calcium concentration. Ca⁺⁺/O₂ ratios determined for many different rates of transport give a ratio of about 0.5, a value much lower than similar ratios determined for other transport mechanisms. The calcium transport mechanism in the ectoderm responds to changes in transport rate very sluggishly, taking 30 to 50 min to give a maximum response. The differences between the calcium transport mechanism in this membrane and other known transport systems are discussed and it is suggested that these differences may represent the adaptations necessary for transcellular calcium transport.     

Erbium(III) ion-doped borate-based glasses for 1.53 μm broad band applications

Novel erbium(III) ion-doped borate-based glasses (Er³⁺:BCNF) by conventional melt-quenching technique were designed and synthesized. The glasses were characterized for their structural, vibrational and spectroscopic properties. The nephelauxetic ratio, bonding parameters, and Judd–Ofelt (JO) intensity parameters (Ω_λ λ = 2, 4 and 6) were determined by using absorption spectrum of 1 mol% Er₂O₃ doped glass. These JO parameters were utilized to derive radiative properties for various excited states of erbium(III) ions. Emission cross-section for ⁴I_13/2 → ⁴I_15/2 transition of erbium(III) ions was computed through McCumber theory. The decay curves for (²H_11/2, ⁴S_3/2) and ⁴I_13/2 levels were recorded and analysed. All the results of Er³⁺:BCNF glasses revealed that the studied glasses are efficient and thermally stable and could be suitable for display devices, optical amplification and green laser applications.