Cadmium Acetate Research Articles

Effect Of Annealing Temperature On The Optical And Structural Properties Of Zinc-Doped Cd2SnO4 Thin Films Prepared By Dip-Coating Method

As demand for solar PV modules steadily increases studies on cheaper alternative TCO materials, with low resistivity and high transmittances in the visible spectrum to replace ITO are been undertaken. Among TCO materials considered as alternative to Indium Tin Oxide (ITO) is Cd2SnO4, owing to its availability in large quantities at relatively lower costs. Studies on optical properties of N2 and F2 doped Cd2SnO4 films have revealed increased transmittance 99%, and reduced band gap 3.3 eV. On the other hand Fe doped films have been observed to exhibit higher refractive indices, extinction and absorption coefficients with lower transmittance and optical band gap. Although studies have been carried out on Zinc doped Cd2SnO4 films, the effect of annealing temperature on the properties of the films have not been reported. This study investigated the effect of annealing temperature on the optical and structural properties of Zinc-doped Cd2SnO4 films. Thin films of Zincdoped Cd2SnO4 were prepared by mixing 0.1 M Cadmium Acetate with 0.1 M Tin II Chloride in ratio 1:1 to prepare Cd2SnO4 which was doped with 0.1 M Zinc Nitrate then dip-coated on clean glass substrates. The coated substrates were dried at room temperature and annealed in air the films annealed at 350 o C, 400 o C and 450 o C for 90 minutes Optical transmittance and reflectance were measured in wavelength range 200-1200 nm and with the results: prominent XRD peak oriented in the (2 0 0) direction, transmittance of 78.7% at 700 nm wavelength, absorption coefficient of 3.891 - 5.591 x 104 cm-1 , extinction coefficient of 0.1852 - 0.2126, refractive indices of 1.983-2.121 at 588 nm wavelength and band gap values range 3.45-3.65 eV. Annealing was observed to reduce refractive index and does not affect transmittance therefore doesn’t enhance suitability of films as TCO materials for Photovoltaic applications.

Comparative studies on pinhole free CBD-CdZnS thin films on ITO and FTO substrate

The development of CdZnS thin films using the chemical bath deposition process in nonaqueous media is a technological challenge. In this work, 75 millilitres of ethylene glycol and ethanol (1:2 ratios) were used to develop a CdZnS thin film on ITO and FTO glass substrates using cadmium acetate, zinc sulphate, and thiourea. The ideal bath temperature was kept at 1300C and the anneal temperature of the film that had been deposited in the air was maintained at 3500C. The films have been examined using FTIR, WCA, FESEM, and XRD. XRD studies reveal that CdZnS films have a hexagonal crystal structure with a preference for orientation (002) during the deposition and annealing processes and the assessment of the various attributes have been done, such as dislocation density, micro strain, and grain size. FESEM study indicates that as deposited film on ITO glass have smooth surface and grains appear in the form of small needle shape of equal sizes where as FTO substrate reveals the grains of equal size throughout the entire surface in cluster form. It is also confirmed that both the CdZnS films formed on ITO and FTO substrates have hydrophilic quality. The presence of chemical bonds and functional groups was confirmed by FTIR analysis.

Designing Robust CdS Nanostructures for Superior Photostability and Enhanced Photocatalytic Degradation of Organic Pollutants

AbstractTill date it is a great challenge to synthesize CdS photocatalyst with a high stability. In this study, a stable CdS photocatalyst was successfully synthesized by a simple, cost‐effective hydrothermal route via cadmium acetate and thiourea as Cd and S precursors, respectively. The effect of different processing times (8 h and 24 h) and molar ratios on the photocatalytic activity and stability were mainly investigated. The samples were characterized in detail by XRD, FT‐IR, XPS, UV‐vis DRS, Photolummiscence spectroscopy and Surface photovoltage. The photocatalytic activity of the as‐obtained nanostructures was examined for methylene blue (MB) dye degradation under visible light irradiation (λ≥420 nm). After 70 min of irradiation, nearly 82 % of MB was degraded by CdS nanostructures, display an improved photocatalytic activity for MB degradation with an apparent rate constant (k) of 0.019 min−1. Additionally, CdS nanostructures sustained a good photostability after five consecutive cycles. The higher photocatalytic activity of CdS nanostructure is attributed to an efficient separation of photogenerated electron‐hole pairs stimulated by its optimal molar ratio, optimal temperature and surface morphology. Our synthesized stable nanostructures have potential for dye contaminated waste‐water treatment.

Properties of psammozems of the Kama terraces above the floodplain and assessment of their sustainability to pollution by Cu and Cd

Pine forests growing on psammozems, found on sandy Kama terraces above the floodplain within the territory of Perm, encompass roughly 2 thousand hectares. The study was conducted on psammozems under the influence of advancing pollution caused by heavy metals, highlighting the significance of soil’s buffering capacity in preserving the ecosystem’s stability. It is of great interest to investigate the morphogenetic properties of psammozems and evaluate the risks linked to the accumulation of Cu and Cd in these soils through the analysis of changes in soil enzyme activity (catalase, urease, and invertase) and the occurrence of phytotoxicity. The psammozems found in the Kama region originated from periglacial sandy alluvium, which was deposited during glacial melting in the Mesozoic era. The variety of humus psammozems includes typical, podzolized, illuvial-ferruginous, and pseudofibrous subtypes. These soils are highly acidic, have a very low absorption capacity, low base saturation, and reduced activity of soil enzymes. The contents of Cu, Cd, Zn, and Pb in psammozems are notably lower compared to the regional soil clarks; however, in the underdeveloped humus horizons, the concentrations of these metals are slightly higher than in soil-forming sands. The experiment was conducted to determine the ecotoxicological load, where mixed soil samples from a 0–20 cm layer of humus psammozems were treated with solutions containing copper acetate and cadmium acetate. The application of solutions was done individually, with Cu and Cd ranging from 2.5 to 250 mg/kg of soil. Upon introducing Cu and Cd into the soil at the rate of 2.5–10 mg/kg, a decrease in invertase activity, deterioration of the physiological and biochemical parameters of the test crop (Lepidium sativum L.), along with the inhibition of Cd catalase activity, were observed.

Iodination of Substituted Alkynes in the Presence of Cadmium(II) Acetate

AbstractA convenient and selective method for the preparation of substituted iodoalkynes, iodoalkenes based on the interaction of propargylic compounds with iodine in the presence of readily available cadmium (II) acetate in some solvents was developed. The highest yields of iodoalkynes and iodoalkenes were recorded using DMSO as the solvent. An excess of the alkylpropargyl substrate unambiguously led to iodolkynes. By varying the reaction conditions using a twofold excess of iodine in DMSO, methanol or ethanol it was possible to achieve a one‐pot preparation of triiodoalkenes. The interaction of iodine with propargyl substrates could be represented in two ways: formation and further nucleophilic transformation of the iodonium complex under the influence of the acetate ion and generation of π‐coordinated species and elimination of acetic acid.

Investigation of Optical Characteristics and Synthesis of Cobalt-Doped Cds (Cds: Co) Using Simple and Rapid Microwave Activated Method

Cobalt-doped cadmium sulphide semiconductor nanoparticles (CdS: Co NPs) were made using a microwave-assisted method with different cobalt concentrations. Chemicals like sodium sulphide, cobalt chloride, and cadmium acetate were used. The Debye-Scherer equation helped find the nanoparticles' size, revealing a 2 to 4 nm range. X-ray diffraction showed a zinc-blend structure. The optical bandgap energies were found to be undoped and doped are 2.44eV and 2.58eV, respectively. For pure CdS, the XRD spectra display three main peaks at 2θ = 26.68°, 44.16°, and 52.32°. Modest alterations have been noted in 2θ for Co doping levels of 3% in CdS NPs. The peaks point to the samples' cubic structure and correlate to the (1 1 1), (2 2 0), and (3 1 1) planes. The sizes of the nanoparticles, which are 2.29 nm, 3.64 nm, for pure and Co (3%) doped CdS, were determined using the FWHM and Debye Scherer equation. The substitution of Co2+ion for Cd2+ion may be the cause of the decrease in nanoparticle size observed in the Co-doped CdS sample as concentration rises. The difference in the ionic radii of Cd2+ (0.98 Å) and Co2+ (0.72 Å) shows that when the concentration of Co-doped CdS increases, the lattice constant falls. The peak at 3646 cm-1 in the higher energy area of the 400–4000 cm–1 FTIR spectra is attributed to the O–H stretching of absorbed water on the surface of CdS. Its bending vibration confirms the existence of water. Using HRTEM, the size of the produced nanoparticles was examined. Additionally, it confirms the sample's nanocrystalline structure. For 3% Co-doped CdS, the average size of randomly chosen nanoparticles is determined.

Features of analytical control of glyphosate salts in preparative formulations

Goal. Development of a method of analytical control of glyphosate in preparative forms of herbicides.
 Methods. Determination of glyphosate was carried out by the chromatographic method of thin-layer chromatography (TLC) using Sorbfil plates with a thin layer of silica gel KSK adsorbent. The active substance was identified by the value of Rf, quantitative determination was based on the formalized dependence of the size of the area of the chromatographic zones on the amount of glyphosate.
 Results. Physicochemical properties of herbicides — electrolytes, to which glyphosate belongs, create special problems when developing methods for its determination in various matrices. In herbicides and desiccants, glyphosate (as a salt) usually takes the form of a deprotonated acid residue and a corresponding cation. Therefore, the determination of the active substance is carried out by the acid residue, which is important for the quantitative assessment of its content in the matrix both in the acid equivalent and in the form of the corresponding salt. The density of the preparative form serves, in particular, as a criterion for controlling the form of the glyphosate salt. The method is based on dissolution of the preparation form in 44% ethanol and quantitative determination by TLC method. The determination of the active substance is not hindered by other components of the preparations, derivatives of glycine and amines.The optimal conditions of analysis were chosen using the conceptual designs of the laboratory «Algorithm of chemical-analytical monitoring of pesticides» and «System of multi-quantitative determination of pesticides in matrices», according to which the main stages of the process are extraction/dissolution, purification of extracts, elution (chromatographic process), identification and quantitative analysis . Selective conditions for TLC determination — mobile phase with pH 9: distilled water + ethanol + aqueous ammonia (22 + 20 + 0.25 by volume), developing reagent: a specific complex of ninhydrin with cadmium acetate in an acidic medium. Quantitative determination is carried out taking into account the coefficients of conversion of the corresponding salt form to the acid equivalent.
 Conclusions. The use of the chromatographic method of thin-layer chromatography makes it possible to control the content of the active substance glyphosate in various salt formulations in preparative forms of herbicides and desiccants with high accuracy and reproducibility.

Investigation of structural, linear, and nonlinear optical properties of nanosized zinc oxide and cadmium oxide particles ingrained in graphitic carbon nitrides

The study aims to evaluate the third-order optical nonlinearity caused by laser irradiation in transition metal oxide incorporated into graphitic carbon nitrides. The work describes the synthesis of nano-sized hybrid g-C3N4/ZnO (14%) and g-C3N4/CdO (14%). Nano-sized transition metal oxides: ZnO and CdO, have been prepared by thermally decomposing the organic precursors; Zinc Acetate Dihydrate, Cadmium Acetate Dihydrate, and Urea at 873 K. Graphitic carbon nitrides are synthesized from urea, which also functions as a reducing agent. The synthesized sample’s structural and morphological characterization are investigated using x-ray diffraction (XRD), Fourier transforms infrared (FTIR), UV–vis. spectra, field emission scanning electron microscopy (FESEM), and energy dispersive x-ray spectroscopy (EDX). The grain size of the ZnO and CdO nanoparticles is observed to be ∼21 nm and ∼28 nm, respectively. The absorption in the samples is found to be 250–450 nm and transmit the light in the visible spectrum as observed in UV–vis. spectra. The bandgap values calculated from Tauc’s plot for the hybrid structure of g-C3N4/ZnO and g-C3N4/CdO are found to be 2.97 eV and 2.30 eV.The z-scan method is adopted to evaluate the nonlinear susceptibility (χ3), intensity-dependent absorption coefficient (β), and nonlinear index of refraction (n2) using a pulsed Nd:YAG laser (∼532 nm). The results of the composite of g-C3N4/ZnO and g-C3N4/CdO show good third-order susceptibility and hence are useful for use as an optical limiter.

Photocatalytic desulfurization of gas condensate using zinc diacetate and cadmium diacetate liquid catalysts

This inquiry studied the application of photocatalytic desulfurization as an effective method for removing sulfur-containing organic compounds from gas condensate extracted from oil wells. To this end, cadmium diacetate and zinc diacetate compounds were prepared as the liquid catalysts. Then their structures were confirmed and their properties were determined by common methods, including FTIR, NMR, and UV. Subsequently, their performances as catalysts were investigated by an optical technique for the desulfurization process. Accordingly, the study used a photoreactor equipped with a 250 W mercury ultraviolet lamp with a maximum wavelength of 365 nm, and investigated and optimized the effect of the ratios of the influencing parameters on the total sulfur removal efficiency. These included the ratios of fuel to photocatalyst, H2O2, and acetonitrile. Ratios of 1:2:3:2 and 1:3:2:1 (fuel: catalyst: oxidant: solvent) of zinc and cadmium diacetate led to 93.5 % and 87.1 % reduction of the total sulfur content, respectively, after 60 min since the exposure process. Also, under sunlight, the total sulfur removal was 67.0 % for the Zn diacetate and 42.0 % for Cd diacetate. Liquid diacetate photocatalysts were successfully recycled over five cycles with only a maximum of 10 % reduction in efficiency. The kinetics of the systems studied were evaluated under optimal conditions and it was found that both systems fit the pseudo-first order model with rate constants of 0.148 min−1 and 0.098 min−1, respectively. In the final step, some physicochemical properties of the desulfurized sample crucial in evaluation of fuel quality were determined under optimal conditions and compared with the properties of the original sample. The results indicated that the liquid photocatalysts used in the experiment increased the quality of the fuel by changing its important indicators by reducing its freezing point in addition to increasing its cetane number.

Synthesis of Cadmium Oxyorthosilicate by a Sol-Gel Method

Cadmium silicates are materials of interest due to their stability and possible application as phosphors. There are three stable forms: cadmium metasilicate, CdSiO3, cadmium orthosilicate, Cd2SiO4 and cadmium oxyorthosilicate, Cd3SiO5. Of these, oxyorthosilicate is particularly challenging to obtain, leading to fewer studies. We have successfully prepared Cd3SiO5 using a sol-gel approach, employing cadmium acetate and tetraethylorthosilicate as precursors in a stoichiometric proportion of 2:1. Additionally, cetyltrimethylammonium bromide served as a template for creating a mesoporous structure. Adjusting the pH to 3 and subjecting the material to calcination at 800 °C for 6 h, we achieved the formation of cadmium oxyorthosilicate compound, identified by X-ray diffraction. Electron diffractometry and energy dispersive X-ray spectrometry confirm the phase purity. Characterization via nitrogen adsorption analysis and transmission microscopy shows aggregates of nanoparticles with a surface area of 6 m2 g-1 and a narrow pore diameter distribution centered at 5 nm.

Study of structural, morphological and optical properties of Mn+2 doped CdS nanoparticles synthesized at various doping concentration

Manganese-doped cadmium sulphide semiconductor nanoparticles (CdS: Mn) NPs have been created utilizing a microwave-assisted solvothermal technique at different Mn concentrations (0, 1%, 3%, and 5%). The chemicals utilized for the preparation of Mndoped CdS nanoparticles were sodium sulphide (Na2S.xH2O), manganese chloride (MnCl2.4H2O), and cadmium acetate (CH3COO)2Cd., H2O). To determine the structural dimensions of the generated nanoparticles, the Debye-Scherer equation was used to calculate the average crystallite size at the full-width half maximum (FWHM) of the diffraction peaks. FTIR spectra analysis was used to look at the various functional and vibrational groups present in the Mn-doped CdS nanoparticle sample. The structure features of the produced nanoparticles have been examined using X-ray diffraction patterns. Energy dispersive X-rays were employed to ascertain the chemical composition of the synthesized nanoparticles. The optical properties and quantification of the energy band gap of the nanoparticles have been done using UV-V spectroscopy. According to XRD calculations, the cubic zinc-blend structure of the generated NPs had a crystal size of between 4 and 7 nm. By using EDX spectroscopy, the incorporation of Mn at the CdS lattice was confirmed.

Synthesis, crystal structure and Hirshfeld surface analysis of di-acetato-bis-[4-(2-amino-eth-yl)morpholine]cadmium tetra-hydrate.

The title coordination compound, [Cd(C2H3O2)2(C6H14N2O)2]·4H2O, was synthesized by mixing 2 moles of 4-(2-amino-eth-yl)morpholine and 1 mole of cadmium acetate in double-distilled water. The Cd atom is octa-hedrally coord-inated by two N,N'-bidentate ligands [4-(2-amino-eth-yl)morpholine] and two trans-located acetate mol-ecules. The Cd atom is located on a center of inversion, whereas the 4-(2-amino-eth-yl)morpholine and four water mol-ecules are adjacent to the acetate mol-ecules. The chair conformation of the morpholine mol-ecules is confirmed. In the crystal, adjacent metal complexes and uncoord-inated water mol-ecules are linked via N-H⋯O and O-H⋯O hydrogen-bonding inter-actions, generating R 2 2(6), R 6 6(16), R 6 6(20) and S 1 1(6) motifs and forming a three-dimensional network. A Hirshfeld surface analysis indicated the contributions of various contacts: H⋯H (71.8%), O⋯H/H⋯O (27.1%), and C⋯H/H⋯C (1.0%).

Iodination of propargylpyrazole in the presence of cadmium (II) acetate

This paper describes an efficient synthetic method of iodine addition to the triple bond and substitution of the CH-acid hydrogen atom of propargylpyrazole in the presence of cadmium (II) acetate at room temperature, the role of solvents and the ratio of reagents during iodination are optimized.

Iodination of Propargylpyrazole in the Presence of Cadmium(II) Acetate

Iodination of Propargylpyrazole in the Presence of Cadmium(II) Acetate

Cadmium acetate induced biochemical alterations in serum (blood) of Kuroiler chicks

Cadmium acetate induced biochemical alterations in serum (blood) of Kuroiler chicks

Synthesis, structure and Hirshfeld surface analysis of a coordination compound of cadmium acetate with 2-amino-benzoxazole.

A first coordination compound of 2-amino-benzoxazole (2AB), namely, bis-(2-amino-benzoxazole-κN 3)bis-(acetato-κ2 O,O')cadmium(II), [Cd(CH3COO)2(2AB)2], has been synthesized from ethanol solutions of Cd(CH3(COO)2 and 2AB. In the monoclinic crystals with the space group C21/c, the cadmium ions coordinate two neutral 2AB mol-ecules in a monodentate fashion through the oxazole N atom, while two acetate ligands are coordinated through the O atoms in a bidentate manner. The coordination polyhedron of the central ion is substanti-ally distorted octa-hedral. There are two relatively strong intra-molecular hydrogen bonds in the complex mol-ecule. Additionally, two inter-molecular hydrogen bonds associate complex mol-ecules into columns running in the [10] and [110] directions. The Hirshfeld surface analysis shows that 45.7% of the inter-molecular inter-actions are from H⋯H contacts, 24.7% are from O⋯H/H⋯O contacts and 18.8% are from C⋯H/H⋯C contacts, while other contributions are from N⋯H/H⋯N and O⋯O contacts.

Genotypical response of barley to increased cadmium content in soil

The results of a comparative evaluation of spring barley (Hordeum vulgare L.) varieties obtained by different methods on control and provocative soil background for cadmium are presented. A total of 10 varieties were studied: Rodnik Prikamya, Novichok, Dina, Zazersky 85, Triumph, Tallon (hybridization and selection); Forward, Bionic, Vitrum (cell selection); In memory of Dudin (mutagenesis). The studies were carried out in 2021 under the climatic conditions of the Kirov region. Seeds of the plants of each variety were sown in vegetation containers filled with soddy-podzolic soil. Cadmium provocative background (6.4 ± 0.5 mg/kg) was created by adding cadmium acetate to the soil. The average yield of barley varieties in the control (soil background without cadmium) was 279 g/m2; against a provocative background – 216 g/m2. Under the conditions of cadmium stress, the yield of hybrids decreased compared to the control by 12.2 %, regenerants – by 29.6 %, mutant – by 42.4 %. Among the studied varieties, the Bionic variety, which has a regenerated origin, showed a consistently high yield both on the control (334 g/m2) and cadmium background (263 g/m2). Productive bushiness of hybrid barley varieties against the control background varied from 2.8 to 4.1; in regenerants – from 3.4 to 4.8; mutant varieties – 4.3 pieces. Under the conditions of cadmium stress, productive bushiness decreased by an average of 2.7 – in hybrids; for 3.4 – for regenerants, for 2.6 pieces – a mutant. Bionic, regardless of the soil background, compared with other varieties, had the highest productive bushiness. Significant differences in the content of polyphenols in the grain of the studied varieties on the control and provocation soil background for cadmium were not revealed. Under the conditions of cadmium stress, a decrease in the content of flavonoids in grain was noted, as well as the accumulation of cadmium (0.29–0.92 mg/kg). Varieties of hybrid origin showed the ability to accumulate cadmium in grain to a greater extent.

Cadmium acetate induced immunotoxico and histopathological modulations in thymus of Kuroiler chicks

Cadmium acetate induced immunotoxico and histopathological modulations in thymus of Kuroiler chicks

Study on the synthesis and properties of porous cadmium zeolitic imidazolate framework for environmental treatment

In this study, cadmium imidazolate frameworks were synthesized by a solvothermal method from cadmium acetate and 2-methylimidazole in an ethanol/methanol mixture. The Cd(Im)2 processed at 150 oC after 8 hours with the mixture of solvents has high crystallinity. The appearance of the absorption band at 407.73 cm-1 shows a link formation of Cd (II) and N within HIm’s molecule. Cadmium imidazolate only formats zeolite crystal, the network fibers were potent, and the pores were alike. The dimension of pores is approximately 200 nm. The XRD diagram shows that the Cd(Im)2 has high crystallinity. The Cd(Im)2 phase is obvious from reflections at 7o, 10o, 12o, 14o, 15,6o and 17o. The surface area of Cd(Im)2 was 662.894 m2/g or 858.389 m²/g with BET or Langmuir calculations, respectively. The maximum adsorption capacity of Cd-ZIF-8 for the RhB is 64.52 mg.g-1, and the adsorption data were fitted well with a pseudo-second-order model.

Effect of Doping with Zinc Oxide on The Structural, Surface, and Optical Properties of Titanium Dioxide Thin Films

Titanium oxide thin films that are both undoped and doped with zinc have been produced in rates of (0, 2 and 4) %. The titanium oxide films doped with zinc were made by combining cadmium acetate with zinc acetate in a solution of titanium acetate with (0.2 M). X-ray diffraction tests showed that the films of undoped TiO2 and (TiO2: Zn) are polycrystalline with (121) orientation. Additionally, the crystallization of films rises as zinc doping level rises. With zinc doping concentration, the grain size of the deposited films is around (15.55-17.91) nm, while the strain (%) parameter decreases from 22.29 to 19.35 with zinc. The grain size was in the range of (90.9), (67.8), and (37.7) nm for the (Ti O2, TiO2: 2% Zn, and TiO2:4% Zn) accordingly in Atomic Force Macroscopy pictures of the film surface morphology. Surface roughness and rms values for the deposited films for undoped TiO2 and TiO2:2% Zn, and TiO2:4%Zn were (6.72, 3.34, and 2.034) nm and (8.80, 8.03, and 4.24), respectively. The spectrum of absorbance and transmission was used to study the optical characteristics. The investigation revealed that the films have robust transmission throughout the visible spectrum and that this transmission decreases with increased doping with zinc content. In addition, the edge of the films' absorbance changes to high wavelengths, which supports a drop in energy gap values. Also computed and discovered to vary with increased doping with zinc concentration were the absorption coefficient, refractive index, and extinction coefficient.