P-chloroaniline Research Articles

Unveiling electron transfer and radical transformation pathways in coupled electrocatalysis and persulfate oxidation reactions for complex pollutant removal

The degradation of multiple organic pollutants in wastewater via advanced oxidation processes might involve different radicals, of which the types and concentrations vary upon interacting with different pollutants. In this study, electrochemical activation of peroxymonosulfate (E/PMS) using advanced activated carbon cloth (ACC) as electrode was applied for simultaneous degradation of mixed pollutants, e.g., metronidazole (MNZ) and p-chloroaniline (PCA). 92.5 % of MNZ and 91.4 % of PCA can be degraded at the cathode and anode at a low current density and PMS concentration, respectively. The rate constants for the simultaneous removal of MNZ and PCA in the E/PMS/MNZ(PCA) system were 118 times and 6 times higher than those in the sole PMS system, and 2.5 times and 1.6 times higher than those in the E/Na2SO4/MNZ(PCA) system, respectively. Different electrochemical characteristics, EPR spectra and radical quenching tests verified that the degradation of MNZ and PCA in the optimal system proceeded primarily through non-radical-dominated oxidation, involving electron transfer and 1O2 effect. The system also exhibited low energy consumption (0.215 kWh/m−3·order−1), broad operational pH range, excellent removal efficiency for water matrix, and low by-products toxicity, indicating its strong potential for practical applications. The ACC, with its super stable, low cost, and electrochemical activity, make it as a promising materials applicable in the E/PMS system for degradation of multiple pollutants. The study further elucidated the mechanism of pollutant interaction with electrode materials in terms of radical and non-radical transformation, providing fundamental insight into the application of this system for treatment of complex wastewater.

Biodegradation characteristics of p-Chloroaniline and the mechanism of co-metabolism with aniline by Pseudomonas sp. CA-1

Co-metabolism is a promising method to optimize the biodegradation of p-Chloroaniline (PCA). In this study, Pseudomonas sp. CA-1 could reduce 76.57 % of PCA (pH = 8, 70 mg/L), and 20 mg/L aniline as the co-substrate improved the degradation efficiency by 12.50 %. Further, the response and co-metabolism mechanism of CA-1 to PCA were elucidated. The results revealed that PCA caused deformation and damage on the surface of CA-1, and the –OH belonging to polysaccharides and proteins offered adsorption sites for the contact between CA-1 and PCA. Subsequently, PCA entered the cell through transporters and was degraded by various oxidoreductases accompanied by deamination, hydroxylation, and ring-cleavage reactions. Thus, the key metabolite 4-chlorocatechol was identified and two PCA degradation pathways were proposed. Besides, aniline further enhanced the antioxidant capacity of CA-1, stimulated the expression of catechol 2,3-dioxygenase and promoted meta-cleavage efficiency of PCA. The findings provide new insights into the treatment of PCA-aniline co-pollution.

Quantitative Insight into PCA Formation following Different Chlorhexidine Activation Methods in Endodontic Treatment.

The aim of the study was a quantitative analysis of p-chloroaniline (PCA) formation during 2% CHX activation with US and MDI methods in a root canal-like environment with the HPLC-DAD method and, thus, a safety assessment of US and MDI agitation of CHX in endodontic treatment. Two percent CHX was activated with the US method using ISO 30 and 35 K-file, and the MDI method using ISO 30.06 and 35.06 GP cones for 15, 30, 60, and 90 s. PCA concentration was assessed with the HPLC-DAD method. PCA concentration was also assessed for 2% CHX after 0, 3, 18, and 21 days of storage in ambient conditions. PCA was detected in all samples in all methods of activation. The concentration of PCA was dependent on time of activation in US ISO 30 and ISO 35 group (p < 0.05). In the MDI ISO 30.06 and ISO 35.06 groups, a similar trend was observed but without statistical significance (p > 0.05). PCA was detected in shelf-stored 2% CHX and the concentration was related to the time of storage. PCA is released after CHX activation with US and MDI, but mean concentrations are not higher than those observed from self-degradation of shelf-stored 2% CHX.

Dual Role of Silicon-based Matrices in Electron Exchange Matrices for Waste Treatment.

Para chloro aniline (PCA) is a common toxic pollutant found in pharmaceutical wastewater. Our study suggests a novel PCA treatment method based on a heterogeneous advanced oxidation process (AOP) that proceeds in an electron exchange matrix (EEM) prepared by the incorporation of redox-active specie in silica matrices using the sol-gel synthesis route. The results, which are supported by DFT calculations, show that the silicon skeleton of the EEM has two important roles, both as a porous matrix that hosts the redox species and as an oxidant species involved in the AOP. The calculations indicate that the formation of a radical on the nitrogen is favored. The suggested mechanism could shed light on the AOP, which proceeds in a heterogenous system, and on its application inside the understudied EEMs that, until now, have been a virtual black box. A better understanding of the mechanism could lead to improved control over the heterogeneous processes that can play a critical role in industries with the need to treat small amounts of toxic compounds at low concentrations, such as in the pharmaceutical industry.

Physicochemical characterization of titanium dioxide inks for digital textile printing based on newly developed polyurethane prepolymers

Purpose This paper aims to study the physical and chemical characteristics of inkjet titanium dioxide inks for cotton fabric digital printing. Design/methodology/approach Different dispersing agents through the reaction of glycerol monooleate and toluene diisocyanate were prepared and then performed by using three different polyols (succinic anhydride-modified polyethylene glycol PEG 600, EO/PO Polyether Monoamine and p-chloro aniline Polyether Monoamine), to obtain three different dispersing agents for water-based titanium dioxide inkjet inks. The prepared dispersants were characterized using FTIR to monitor the reaction progress. Then the prepared dispersants were formulated in titanium dioxide inkjet inks formulation and characterized by particle size, dynamic surface tension, transmission electron microscopy, viscosity and zeta potential against commercial dispersants. Also, the study was extended to evaluate the printed polyester by using the prepared inks according to washing and crock fastness. Findings The obtained results showed that p-chloro aniline Polyether Monoamine (J) and succinic anhydride modified polyethylene glycol PEG 600 (H) dispersants provided optimum performance as compared to commercial standards especially, particle size distribution data while EO/PO Polyether Monoamine based on dispersant was against and then failed with the wettability and dispersion stability tests. Practical implications These ink formulations could be used for printing on cotton fabric by DTG technique of printing and can be used for other types of fabrics. Originality/value The newly prepared ink formulation for digital textile printing based on synthesized polyurethane prepolymers has the potential to be promising in this type of printing inks, to prevent clogging of nozzles on the printhead and to improve the print quality on the textile fiber.

Efficient Remediation of p-chloroaniline Contaminated Soil by Activated Persulfate Using Ball Milling Nanosized Zero Valent Iron/Biochar Composite: Performance and Mechanisms.

In this study, efficient remediation of p-chloroaniline (PCA)-contaminated soil by activated persulfate (PS) using nanosized zero-valent iron/biochar (B-nZVI/BC) through the ball milling method was conducted. Under the conditions of 4.8 g kg-1 B-nZVI/BC and 42.0 mmol L-1 PS with pH 7.49, the concentration of PCA in soil was dramatically decreased from 3.64 mg kg-1 to 1.33 mg kg-1, which was much lower than the remediation target value of 1.96 mg kg-1. Further increasing B-nZVI/BC dosage and PS concentration to 14.4 g kg-1 and 126.0 mmol L-1, the concentration of PCA was as low as 0.15 mg kg-1, corresponding to a degradation efficiency of 95.9%. Electron paramagnetic resonance (EPR) signals indicated SO4•-, •OH, and O2•- radicals were generated and accounted for PCA degradation with the effect of low-valence iron and through the electron transfer process of the sp2 hybridized carbon structure of biochar. 1-chlorobutane and glycine were formed and subsequently decomposed into butanol, butyric acid, ethylene glycol, and glycolic acid, and the degradation pathway of PCA in the B-nZVI/BC-PS system was proposed accordingly. The findings provide a significant implication for cost-effective and environmentally friendly remediation of PCA-contaminated soil using a facile ball milling preparation of B-nZVI/BC and PS.

Alginate magnetic graphene oxide biocomposite synthesis for removal of aromatic amines from aqueous samples.

In the present work, alginate magnetic graphene oxide biocomposite was synthesized for the removal and extraction of aromatic amines (aniline, p-chloroaniline (PCA), and p-nitroaniline (PNA)) from water samples. The biocomposite was investigated for its physiochemical characteristics such as surface morphology, functional groups, phase determination, and elemental composition. The results revealed that the functional groups of graphene oxide and alginate retained in biocomposite with magnetic properties. The biocomposite was applied to water samples for the removal and extraction of aniline, p-chloroaniline, and p-nitroaniline through adsorption process. The adsorption process was studied under various experimental conditions like time, pH, concentration, dose, and temperature, and all the parameters were optimized. The maximum adsorption capacities at room temperature have an optimum pH = 4 for aniline = 18.39mgg-1, for PCA = 17.13mgg-1, and for PNA = 15.24mgg-1. Kinetic and isotherm models showed that the experimental data is best fitted to pseudo-second-order kinetic model and the Langmuir isotherm model. Thermodynamic study suggested that the adsorption process is exothermic and spontaneous. Ethanol was found to be the best eluent for the extraction of all the three analytes suggested by the extraction study. The maximum percent recoveries from spiked water samples were calculated for aniline = 98.82%, PCA = 96.65%, and PNA = 93.55% which showed that alginate magnetic graphene oxide biocomposite could be a useful and ecofriendly adsorbent for the removal of organic pollutants in water treatment processes.

Low loading Pt on TiO2 for the ultra‐selective hydrogenation of chloronitrobenzenes to chloroanilines

AbstractLow loading Pton TiO2 were prepared by an impregnation‐reduction process for chemoselective hydrogenation of chloronitrobenzenes (CNBs) to chloroanilines (CANs). The structure and physicochemical properties were characterized by N2 adsorption‐desorption, X‐ray diffraction, high resolution transmission electron microscopy, X‐ray photoelectron spectroscopy and temperature programmedreduction. The low loading Pt(≤0.08 wt %) on TiO2 exhibited outstanding chemoselectivity for the catalytic hydrogenation of CNBs to CANs, without any disturbance on carbon‐chlorine bond. The characterization data suggested that the Pt particles were highly dispersed on TiO2 and strongelectronicinteractionsoccur between the dispersedPt andTiO2support, which led toelectron deficiency of nearly all Pt and production of suboxide TiOx species (x&lt;2) in the 0.08 wt % Pt/TiO2. The electron‐deficient Pt and suboxide TiOx species favor N=O bondactivation, leading to its unique chemoselectivity.

2-[(4-Chloro-phen-yl)imino]-1,2-di-phenyl-ethanone.

The title Schiff base, C20H14ClNO, obtained from the reaction of 4-chloro aniline with benzil, has an approximate T shape. The dihedral angle between the phenyl rings of the benzil unit is 74.14 (15)°. The extended structure features C-H⋯O hydrogen bonds.

Synthesis, Characterization and Study the Biological Activity for Some New Heterocyclic Derivative from 4,5-dichloro Imidazole

Creating a multi-step method for synthesizing heterocyclic compounds is the goal of this research. The first step involves reacting 4,5-dichloro-2- phenylenediamine with 3- amino- 4-“hydroxybenzoic acid to produce an imidazole derivative (1), which then reacts with salicyldehyde to produce the azo compound (2). Two, a Schiff base derivative is produced via a reaction with p-chloro aniline (23). Final steps involve reactions (3) with chloroacetyl chloride, alanine, sodium azide, thioglycol acid, anthranilic acid, and maleic anhydride, yielding beta-lactam derivatives (4), imidazolidine (5), tetrazol(6), thiazolidine (7), hydroquinazoline”(8), and oxazepine (9), respectively. The spectroscopic techniques of fourier transform infrared (FTIR) and proton nuclear magnetic resonance (1HNMR) have been used to identify all of the compounds that have been prepared; next, the compounds’ biological effects on two types of cancer have been investigated.

Schiff bases from chlorine substituted anilines and salicylaldehyde: Synthesis, characterization, fluorescence, thermal features, biological studies and electronic structure investigations

Schiff bases have been developed as potent biological agents due to their advanced physical, chemical and biomedical characteristics. Herein, 2 and 4 chloro anilines containing salicylaldehyde Schiff bases (2CAS and 4CAS) were successfully synthesised. Both simulated and experimental FTIR, UV–vis, 1H NMR, 13C NMR spectroscopic techniques were employed to characterise the synthesised compounds and the comparable spectra confirm the formation of products. The obtained fluorescence intensity values 219 (2CAS) and 1369, 2429 (4CAS) strongly suggest the fluorescence nature of the compounds. Using thermogravimetric analysis, thermal stability of the compounds were measured that were found to be 288 and 299 °C respectively. DFT optimised the geometry.Calculated energy gap for both the compounds were found to be 4.01 and 3.98 eV respectively.Molecular electrostatic potential analysis showed that carbon and oxygen atoms for both the compounds are susceptable to electrophillic attack. Mullicken charge analysis identified, for both compounds carbon atoms showed positive and negative charges, hydrogen atoms showed positive charges only,electronegative atoms such as chlorine,oxygen and nitrogen atoms showed negative charges only. NBO analysis explained detailed hyperconjugative interactions present in both the compounds. Wave function studies such as ELF found that delocalised electron density were found on the Cl, N and C atoms of both compounds and its delocalised orbitals positions were present in Cl, N, C and localised orbitals positions in hydrogen atoms of both compounds, which were identified by LOL. RDG maps demonstrates regions where van der waals interactions weak and the steric effects dominates in the prepared compounds. The antimicrobial study of the synthesised compounds showed higher activity than the commercial amoxicillin against gram positive staphylococcus aureus bacteria and moderate activity against candida albicans fungi. Furthermore, the compounds were subjected to molecular docking studies using PDB:4F2T protein of staphylococcus aureus with lowest binding attractions were determined to be- 4.94 (2CAS) and −5.02 (4CAS) kcal/ml respectively and the results were comparable to the experimental data.

Significant roles of surface functional groups and Fe/Co redox reactions on peroxymonosulfate activation by hydrochar-supported cobalt ferrite for simultaneous degradation of monochlorobenzene and p-chloroaniline

CoFe2O4/hydrochar composites (FeCo@HC) were synthesized via a facile one-step hydrothermal method and utilized to activate peroxymonosulfate (PMS) for simultaneous degradation of monochlorobenzene (MCB) and p-chloroaniline (PCA). Additionally, the effects of humic acid, Cl-, HCO3-, H2PO4-, HPO42- and water matrices were investigated and degradation pathways of MCB and PCA were proposed. The removal efficiencies of MCB and PCA were higher in FeCo@HC140–10/PMS system obtained under hydrothermal temperature of 140 °C than FeCo@HC180–10/PMS and FeCo@HC220–10/PMS systems obtained under higher temperatures. Radical species (i.e., SO4•-, •OH) and nonradical pathways (i.e., 1O2, Fe (IV)/Co (IV) and electron transfer through surface FeCo@HC140–10/PMS* complex) co-occurred in the FeCo@HC140–10/PMS system, while radical and nonradical pathways were dominant in degrading MCB and PCA respectively. The surface functional groups (i.e., C-OH and CO) and Fe/Co redox cycles played crucial roles in the PMS activation. MCB degradation was significantly inhibited in the mixed MCB/PCA solution over that in the single MCB solution, whereas PCA degradation was slightly promoted in the mixed MCB/PCA solution. These findings are significant for the provision of a low-cost and environmentally-benign synthesis of bimetal-hydrochar composites and more detailed understanding of the related mechanisms on PMS activation for simultaneous removal of the mixed contaminants in groundwater.

Nano porous PtRu alloy catalyst with enhanced synergic effect for selective hydrogenation of chloronitrobenzene

Selective hydrogenation of chloronitrobenzene (CNB) to chloroaniline (CAN) is a critical reaction for producing multiple valuable fine chemicals. Inhibiting the dechlorination is extremely vital for this reaction. In this work, we synthesize supported nano porous PtRu alloy catalyst for this catalytic reaction. The special structure of alloy catalyst, mutual-accessible Ru enriched surface and Pt enriched core, strengthens the synergic effect between Ru and Pt, thus improves the catalytic performance. As a result, 100% of o-chloronitrobenzene (o-CNB) conversion and 99.9% of o-chloroaniline (o-CAN) selectivity are achieved by the most optimal catalyst. Besides, the catalyst shows superior selectivity of o-CAN (98%) even under harsh reaction conditions such as high temperature of 150 °C and high pressure of 6 MPa. The excellent catalytic performance is also observed in selective hydrogenation of m-chloronitrobenzene (m-CNB) and p-chloronitrobenzene (p-CNB) as well.

Fe–Mn Oxide Composite Activated Peroxydisulfate Processes for Degradation of p-Chloroaniline: The Effectiveness and the Mechanism

The chemical co-precipitation method was used to prepare magnetically separable Fe–Mn oxide composites, and the degradation of p-chloroaniline (PCA) using MnFe2O4 activated peroxydisulfate (PDS). The MnFe2O4 catalyst exhibited highly catalytic activity in the experiments. XRD, FTIR, SEM and TEM were used to characterize the catalytic materials. MnFe2O4 calcined at 500 °C was more suitable as a catalytic material for PCA degradation. The elevated reaction temperature was beneficial to the degradation of PCA in neutral pH solution. The reaction mechanism of the MnFe2O4 catalyzed oxidative degradation of PCA by PDS was investigated by free radical quenching experiments and XPS analysis. The results showed that sulfate radicals (SO4•−), hydroxyl radicals (•OH) and singlet oxygen (1O2) may all be participated in the degradation of PCA. XPS spectra showed that the electron gain and loss of Mn2+ and Fe3+ was the main cause of free radical generation. The possible intermediates in the degradation of PCA were determined by HPLC-MS, and possible degradation pathways for the degradation of PCA by the MnFe2O4/PDS system were proposed.

Peroxydisulfate activation by 2D MOF-derived Ni/Fe3O4 nanoparticles decorated in 3D graphene oxide network

Metal organic framework (MOF)-derived materials normally have three-dimensional (3D) structure, while little attention has been paid to two-dimensional (2D) MOF-derived materials with high catalytic activity. Nevertheless, the underlying agglomeration and metal leaching issues of 2D MOF-derived catalysts hinder their real applications. In this work, we report a bimetallic nanocomposite (Ni-Fe-C-600-acid/GO) derived from 2D Ni-Fe-MOF and graphene oxide (GO) network. Employing Ni(0) and Fe3O4 as active site, the Ni-Fe-C-600-acid/GO shows high efficiency in peroxydisulfate (PDS) activation for the removal of p-chloroaniline (PCA), and the catalyst/PCA dosage ratio (0.8) is substantially lower than those of the previous studies (3.9–156.9). The prepared catalysts demonstrate high catalytic activity over a wide pH range of 3–9 and maintain high efficiency after five cycles with good tolerance to inorganic anions. The singlet oxygen is identified as the predominant active species and relatively weak contributions from sulfate free radicals and hydroxyl radicals are confirmed. This catalysis system presents new insights in 2D MOF-derived catalysts in advanced oxidation processes.

Impact of P-Chloroaniline on Oxidative Stress and Biomacromolecules Damage in the Clam Ruditapes philippinarums: A Simulate Toxicity Test of Spill Incident.

As a hazardous chemical, p-chloroaniline (PCA) shows intensive adsorption and accumulation after entering the aquatic ecosystem, which can be enriched in organisms and cause damage. With the objective of achieving an integrated and mechanistic view of the toxic effects of PCA in the marine sentinel organism Ruditapes philippinarum, Manila clams were exposed to different concentration of PCA (0.5, 2 and 5 mg/L) for 15 days. Focusing on the gills, first targeting the toxic and digestive gland, the metabolic detoxification organ, we detected dose- and time-related changes inantioxidase activities and biomacromolecular damages in treated clams. Glutathione S-transferase (GST) activity and glutathione (GSH) contents were significantly induced, and superoxide dismutase (SOD) activity increased at the beginning of exposure and then decreased. The malondialdehyde (MDA) and protein methylation (PC) contents which represent lipid peroxidation and carbonylation of proteins, increased first with exposure time and then decreased in the digestive gland. DNA strand break levels were consistently higher than those in the control group. The digestive gland showed more sensitivity to the stress of PCA than the gills. GST and MDA in the gill and GST, GSH, SOD, DNA strand break level in the digestive gland showed significant correlation with PCA exposure, which indicated that these parameters can be used as sensitive biomarkers to indicate toxic effects from chloraniline leakage.

Theoretical investigation on the mechanism and kinetics of the OH•‒initiated atmospheric degradation of p-chloroaniline via OH•‒addition and hydrogen abstraction pathways

Atmospheric oxidative degradation of p-chloroaniline (PCA) initiated by OH• has been studied theoretically at the M06-2X/aug-cc-pVTZ and CBS-QB3//M06-2X/aug-cc-pVTZ levels, coupled with kinetic calculations using the RRKM/ZCT method over the temperature range of 250–350 K. The calculations exhibit that the OH• addition and hydrogen atom abstraction pathways are thermodynamically favorable. RRKM results revealed that the atmospheric oxidation of PCA is dominated by OH addition to the C1 and C2 atoms and hydrogen atom abstraction from amino group. The individual and overall rate coefficients of PCA reaction triggered by OH• at 1 bar are negatively linear dependent on the temperature and their values are consistent with the experimental data. RRKM calculations also show that the transition state theory approximation for estimation of rate coefficients at ambient pressure breaks down and very high pressures are essential to be valid. The atmospheric life-time at the benchmark CBS-QB3 level is smaller than 2 days.

Regulating Crystal Facets of MnO2 for Enhancing Peroxymonosulfate Activation to Degrade Pollutants: Performance and Mechanism

On the catalyst surface, crystal facets with different surface atom arrangements and diverse physicochemical properties lead to distinct catalytic activity. Acquiring a highly reactive facet through surface regulation is an efficient strategy to promote the oxidative decomposition of wastewater organic pollutants via peroxymonosulfate (PMS) activation. However, the mechanism through which crystal facets affect PMS activation is still unclear. In this study, three facet-engineered α-MnO2 with different exposed facets were prepared via a facile hydrothermal route. The prepared 310-MnO2 exhibited superior PMS activation performance to 100-MnO2 and 110-MnO2. Moreover, the 310-MnO2/PMS oxidative system was active over a wide pH range and highly resistant to interfering substances from wastewater. These advantages of the 310-MnO2/PMS system make it highly promising for practical wastewater treatment. Based on quenching experiments, electron paramagnetic resonance (EPR) analysis, solvent exchange, and electrochemical measurements, mediated electron transfer was found to be the dominant nonradical pathway for p-chloroaniline (PCA) degradation. A sulfhydryl group (-SH) masking experiment showed that the highly exposed Mn atoms on the 310-MnO2 surface were sites of PMS activation. In addition, density functional theory (DFT) calculations confirmed that the dominant {310} facet promoted adsorption/activation of PMS, which favored the formation of more metastable complexes on the α-MnO2 surface. The reaction mechanism obtained here clarifies the relationship between PMS activation and crystal facets. This study provides significant insights into the rational design of high-performance catalysts for efficient water remediation.

New insight into the kinetic study on the different loadings of the CuO/CNT catalyst and its optimization for p-chloroaniline photodegradation.

The effect of the copper (Cu) content on Cu oxide loaded onto a carbon nanotube (CuO/CNT) catalyst on the mechanistic, kinetic, and photonic efficiency of the photodegradation of p-chloroaniline (PCA) under visible (Vis) and ultraviolet (UV) light irradiation has been explored. For low-loading (1–5 wt%) CuO/CNTs, photodegradation performed better under UV (>84%) rather than the Vis system; this may be due to the presence of abundant defect sites on both CuO and CNTs, which allowed the multielectron reduction of oxygen at their impurity levels to generate more hydrogen peroxide and subsequent ·OH radicals. The active species under UV were in the following order: h+ ≫ e− > ·OH, while it was vice versa for the Vis system with a well-balanced 50 wt% CuO/CNT catalyst that exhibited a similar performance. The kinetic study showed the transition of the kinetic order from the zeroth to the first order on increasing the PCA concentration under the Vis system and vice versa for the UV system. The Thiele modulus (ϕ) further confirmed that the effect of internal mass transfer was negligible under UV light. In contrast, the transition from mass transfer to kinetic control limitation was observed under the Vis system. The optimum PCA degradation predicted from the response surface analysis was 97.36% at the reaction pH of 7.3, catalyst dosage of 0.45 g L−1, and initial PCA concentration of 11.02 mg L−1. The condition obtained was fairly close to the forecasted value with an error of 0.26%.

Thermal stability of new formazan complexes derived from thiophene-2-carboxaldehyde

Novel formazan ligand was prepared from the condensation of p-phenylenediamine and thiophene-2-carboxaldehyde, with diazonium salt of 4-chloro aniline and its derived metal transition complexes of Co (II), Cu (II) and Ni (II) have been synthesized by reaction of metal chlorides with formazan ligand in the molar ratio 1:1 (M: L). The formazan ligand and its metal complexes were identified by different spectroscopic and analytical techniques, these studies result propose that the metal complexes have tetrahedral geometry. Thermal decomposition of the complexes has been studied by thermogravimetry analysis. The results showed that all values of ∆G are positive which indicate that all steps are non-spontaneous, the decomposition processes were endothermic from the positive rate of ∆H and the complexes more ordered than the reactants from the negative rate of ∆S .Thermodynamic data (∆H, ∆S, ∆G) were calculated by using the Coats-Redfern.