Ni Metal Research Articles

Ni- and Co-Based MOF-Derived NixCo3-xO4 Materials: As an Efficient Anode for Direct Methanol Fuel Cell Application.

Finding inexpensive and efficient anode materials is crucial for the oxidation of methanol in the direct methanol fuel cell (DMFC), which is the key electrode reaction. Herein, we report metal-organic framework (MOF)-derived Co3O4, NiO, and NixCo3-xO4 (where x = 1.5, 1, and 0.6) materials deposited on nickel foam as efficient anode material for methanol oxidation. Among them, NiCo2O4 exhibited the highest methanol oxidation activity, owing to its lowest charge-transfer resistance (0.097 Ω) and high electrochemically active surface area (1950 cm2), resulting in the lowest onset potential of 0.35 V vs Hg/HgO. The optimized Ni-to-Co ratio and synergistic effect between Ni and Co metals enable NiCo2O4 to achieve the highest mass activity of 151 mA mg-1 and geometric current density of 288 mA cm-2, demonstrating excellent durability over 14 h at 0.6 V. In addition, to optimize methanol concentration, all the electrocatalysts were tested in a range of methanol concentrations, showing 0.5 M methanol as the optimal concentration. This study focuses on optimizing the metal ratio and methanol concentration to achieve the highest catalytic activity. Additionally, this lays the foundation for developing diverse MOF-derived electrocatalysts and advancing DMFCs.

Highly Efficient and Selective Hydrodeoxygenation of Guaiacol Using Ni-Supported Honeycomb-Structured Biochar and Phosphomolybdic Acid.

The sustainable development of energy has always been a concern. Upgrading biomass catalysis into hydrocarbon liquid fuels is one of the effective methods. In order to upgrade biomass derivative guaiacol by Hydrodeoxygenation (HDO) catalysis, this article report a three-dimensional honeycomb structure biochar loaded with Ni nanoparticles and phosphomolybdic acid demonstrating excellent catalytic performance in a short period of time. This is due to the porous structure of biochar, which allows Ni metal nanoparticles to be highly uniformly dispersed on the support, which enhances the catalytic hydrogenation of guaiacol in terms of both rate and efficiency. Furthermore, it was observed that the added phosphomolybdic acid dissolved within the temperature range of 78-90 °C, functioning as a homogeneous catalyst in the process. This proves advantageous, as the phosphomolybdic acid becomes accessible at any location within the porous Ni/C catalyst. The detailed characterization data revealed that the carbon support prepared in this study has a high specific surface area of up to 1375.61 m2/g. Additionally, the phosphomolybdic acid exhibited rich acidity, with Brønsted and Lewis acid contents of 2.55 μmol/g and 21.45 μmol/g, respectively. Reaction data demonstrated that at 240 °C for 180 min, 100 % conversion and 97.9 % cyclohexane selectivity were achieved. This study introduces a bifunctional catalyst with an unique catalyst's structure, facilitating a heterogeneous-homogeneous catalytic reaction and delivering an efficient catalytic effect.

Synthesis and properties of graphene-like porous carbon from modified cellulose

The work is devoted to the synthesis of graphene-like magnetic nanocomposites by direct pyrolysis of hemp microcrystalline cellulose modified with citric acid containing nickel or cobalt salts. Their chemical structure and morphology were characterized by X-ray diffraction (XRD), electron microscopy (SEM), Raman spectroscopy, low-temperature N2 adsorption-desorption, and Fourier transform infrared spectroscopy (FT-IR). Thermogravimetry has established a possible mechanism of pyrolysis of a modified cellulose matrix containing Ni and Co metals. X-ray diffraction analysis and Raman spectroscopy have shown that an increase in the number of carboxyl groups accelerates the process of graphitization of the cellulose matrix with transition metals (Ni and Co), as well as increases the degree of structural order and the level of graphitization. The conducted studies have shown that nanoparticles of metals of the zero-valence state are enclosed in graphene-like shells having a mainly mesoporous structure.

Hydrodeoxygenation of guaiacol over modified coconut carbon supported Ni nanoparticles catalysts under alkaline condition

The efficient utilization of lignin from the papermaking black liquor has attracted interest due to its carbon-neutral value and industrial application. This work illustrates a simple support-phosphate-pretreatment strategy to develop superdispersed Ni species in activated carbon (AC) to enhance the hydrodeoxygenation (HDO) reactions of the lignin model compound guaiacol into biohydrocarbons under alkaline conditions. For the first time, sodium polyphosphate was applied as a pretreatment agent for coconut carbon in the synthesis of carbon-supported Ni catalysts. Superdispersed Ni nanoparticles were achieved on Ni/NaPnOAC with a particle size of 2.5 nm, which was much smaller than that on unmodified Ni/C (13.1 nm). The characterization results and reactions revealed that the P−O that formed served as anchoring sites for the Ni species and strengthened the interaction between the Ni species and support (SMSI), which resulted in significantly improved dispersion of the Ni metal sites and, thus, a nearly 6-fold greater yield of hydrocarbons was obtained on Ni/NaPnOAC (58.1 %) than on Ni/C (10.1 %). In addition, compared with Ni2P/NaPnOAC and NiS/NaPnOAC, Ni/NaPnOAC exhibited higher HDO activity, especially higher direct deoxygenation (DDO) activity and higher benzene yield, reducing hydrogen consumption during the HDO reaction.

Ni(II)-selenosemicarbazones complexes as promising anticancer and anti-tubercular agents: Synthesis, characterization, molecular docking and binding studies with HSA and ct-DNA

Reaction of nickel(II) acetate with selenosemicarbazones (2-HOxsesc, 3-MeHOxsesc, 6-ClHOxsesc, 3-HIndsesc, 3-AcHIndsesc, 9-HAnsesc, 1-HNapsesc, 2-HNapsesc) in 1:2 (M:L) molar ratio yielded complexes of formula, [Ni(sesc)2] 1–8 (sesc = 2-Oxsesc 1, 3-MeOxsesc 2, 6-ClOxsesc 3, 3-Indsesc 4, 3-AcIndsesc 5, 9-Ansesc 6, 1-Napsesc 7, 2-Napsesc 8).Complexes are characterized using elemental analysis, FTIR, NMR (1H and 13C) spectroscopy and Mass spectrometry. The full optimized energy for 2-HOxsesc and its complex was found through Density Functional Theory calculation using B3LYP level and predicted geometry parameters are compared with literature. Selenosemicarbazones and their complexes were tested for their anti-tuberculosis activity against M. tuberculosis H37RV strain and anticancer activity against PA-1 and DU145cell lines. The anti-TB activity of 3-AcHIndsesc (MIC = 25 μg/mL) got exceptionally enhanced on complexation with Ni(II) (complex 5, MIC = 0.8 μg/mL). Anticancer activity of ligands have got enhanced on complexation with Ni(II) metal ion and best results were obtained in case of complex 5 (PA-1, IC50 =1.28; DU145, IC50 =3.83). The binding constant of 6.5 × 103M-1 and 3 × 104M−1 obtained from absorption spectroscopy (UV–Vis) indicates strong binding of complex 5 with HSA and ct-DNA. The molecular interaction of 3-AcHIndsesc and complex 5 with mycobacterium tuberculosis enoyl reductase and DNA (PDB ID: 1BNA) were checked with docking studies. The docking studies with mycobacterium tuberculosis enoyl reductase and DNA (PDB ID: 1BNA) gave minimum binding energy of -8.9 Kcal/mol and -7.5 Kcal/mol respectively for complex 5. The docking results are in well agreement with experimental data.

Assessment of Neurotoxic Mechanisms of Individual and Binary Mixtures of Cobalt, Nickel and Lead in Hippocampal Neuronal Cells.

Many studies have focused on the neurotoxic effects of single metals, while investigation on the exposure to metal mixtures, which mainly occur in real-life situations, is scarce. This study sought to assess the neurotoxic effect of Ni, Co, and Pb binary mixtures and their individual effects in hippocampal neuronal cells (HT-22). Cells were exposed to Ni, Co, and Pb separately for 48 h at 37°C and 5% CO2, and cell viability was assessed. Morphological assessment of the cells exposed to binary mixtures of Co, Ni, and Pb and single metals was assessed using a microscope. Furthermore, acetylcholinesterase (AChE) activity, oxidative stress biomarkers (glutathione [GSH] and malondialdehyde [MDA] levels, catalase [CAT], and glutathione-S transferase [GST] activities) and nitric oxide [NO] levels were evaluated after treatment with the binary mixtures and single metals. Binary mixtures of the metals reduced cell viability, exerting an additivity action. The combinations also exerted synergistic action, as revealed by the combination index. Furthermore, a significant reduction in AChE activity, GSH levels, CAT and GST activities, and high MDA and NO levels were observed in neuronal cells. The additive interactions and synergistic actions of the binary mixtures might contribute to the significant reduction of AChE activity, GSH levels, GST, and CAT activities, and an increase in MDA and NO levels. The findings from this study revealed significant evidence that binary mixtures of Co, Pb, and Ni may induce impaired neuronal function and, ultimately, neurodegeneration.

High-Entropy Engineering in Hollow Layered Hydroxide Arrays to Boost 5-Hydroxymethylfurfural Electrooxidation by Suppressing Oxygen Evolution.

The electricity-driven 5-hydroxymethylfurfural (HMF) oxidation reaction has exhibited increasing potential to produce high-value-added 2,5-furandicarboxylic acid (FDCA). Unfortunately, the competitive oxygen evolution reaction (OER) can decrease the yield and Faradaic efficiency (FE) of FDCA under high potentials. Here, we report a general MOF-templated strategy to construct a new class of hollow high-entropy layered hydroxide array (HE-LHA) electrocatalysts including quinary, senary, and septenary phases composed of CoNiMnCuZn with Cd and Mg on carbon cloth (CC) for boosting the HMF oxidation reaction (HMFOR) by suppressing the OER. Impressively, the septenary CC@CoNiMnCuZnCdMg-LHA exhibits a low potential of 1.42 VRHE for the HMFOR but a high potential of 1.68 VRHE for the OER to achieve 100 mA cm-2, ranking it among one of the best electrocatalysts for the HMFOR. Finite element simulations show its hollow array morphology can induce a strong local electric field over all of the shell, thus favoring the electrocatalytic process. In situ electrochemical impedance spectroscopy and theoretical calculations further reveal that the Co, Ni, Cu, Zn, Mn, Cd, and Mg metals in high-entropy LHAs can accelerate the HMFOR but suppress the OER by optimizing the adsorption energy of the HMF* and OH*. This work sheds light on the rational design and construction of high-entropy nanoarchitectures for advanced electrocatalysis.

Finding high-performance MOFs for effective SF6/N2 separation through high-throughput computational screening and machine learning

Abstract Given the rapidly expanding pool of synthesized and hypothetical metal–organic frameworks (MOFs), testing every single material for SF6/N2 separation by iterative experimental methods or computationally demanding molecular simulations is not practical. In this study, we integrated high-throughput computational screening and machine learning (ML) approaches to evaluate SF6/N2 mixture adsorption and separation performances of over 25 000 different types of synthesized and hypothetical MOFs (hypoMOFs), representing the largest set of structures studied for SF6/N2 separation to date. SF6/N2 mixture adsorption data that we produced for synthesized MOFs using molecular simulations were utilized to develop ML models to accurately and quickly predict SF6 and N2 uptakes, SF6/N2 selectivities, SF6 working capacities, adsorbent performance scores, and regenerabilities of both synthesized and hypoMOFs. Results showed the MOF space that we studied exhibits very high SF6/N2 selectivities in the range of 1.8–4204 at 1 bar in addition to high SF6 working capacities between 0.04–5.68 mol kg−1 at an adsorption pressure of 1 bar and desorption pressure of 0.1 bar at room temperature. The top-performing MOF adsorbents for SF6/N2 mixture separation were identified to have Zn, Cu, Ni metals; terphenyl, pyridine, naphthalene linkers; and medium pore sizes. Our comprehensive computational approach offers a highly efficient alternative to brute-force computer simulations by enabling the rapid assessment of the MOF adsorbents for SF6/N2 separation and provides molecular insights into the key structural features of the most promising adsorbents.

Influences of Ti3AlC2 content on tribological behavior of cold-sprayed Ni-Ti3AlC2 composite coatings

As a type of lightweight and high-strength materials, aluminum alloys have been widely applied in such fields as aerospace and automobile manufacturing, which, however, easily wear out in harsh and complex environments due to their defects like poor wear resistance, low hardness, and easy deformation. For this reason, it is necessary to prepare a coating on the surface of aluminum alloys to enhance their wear resistance. In this work, Ni-Ti3AlC2 composite coatings were prepared on the aluminum alloy surface through cold spraying technology, and the influences of Ti3AlC2 content on the microstructure, mechanical properties, and tribological behavior of the Ni-Ti3AlC2 composite coatings were explored. It turned out that the mechanical properties and tribological behavior of the composite coatings were significantly improved with the increase of Ti3AlC2 content. Therein, the Ni-50%Ti3AlC2 composite coating exhibited a porosity of 0.384 %, a hardness of 310 HV0.2, and a bonding strength of 51.6 MPa, while its wear rate significantly declined to 1.87 × 10−5 mm3/N∙m. Because of the increase of Ti3AlC2 ceramic content, the compaction effect and shot peening effect of the ceramic hard phase were gradually enhanced, which further aggravated the deformation degree of Ni metal, thus improving the density, hardness, bonding strength, and wear resistance of composite coatings.

The active site of Mδ+ tailed by B (or N)-doped graphyne for nitrogen reduction reaction through DFT study

NN bond activation is one of the technical problems in the conversion of N2-to-NH3. In this work, we researched Cr, Mn, Co, Ni, Cu and Pt metal single atoms anchored on B/N-doped graphyne (M/X-GY) catalysts systematically by means of DFT. The results of Bader charge and charge density verified the charge transfers between single metal and the doped graphyne in M/X-GY catalysts. Cr (+1.001 e) and Mn (+0.800 e) exhibit higher positive valence, which is favorable for N2 adsorption. Based on the "donation and back-donation" mechanism, the energies gaps of 5σ-N2 and d-M for M=Cr, Mn and Co have the lower values of 3.01, 3.18, 3.18 eV, respectively, and the N2 adsorption energies on Cr/GY (−2.046 eV) and Mn/GY (−1.622 eV) have the more negative values. As a result, the catalyst of Cr metal atom anchored on GY is promising candidate. The substitution of B can effectively promote the activation of N2 and suppress the hydrogen evolution, while the substitution of N has the minimum ΔG*N-NH of 0.26 eV and ΔGNH3 of 0.08 eV. Compared with two different NRR pathways, the distal mechanism process is more preferential than the alternating pathway. The catalyst of Cr/N-GY has higher stability and can effectively activate N2 to generate *N2H, which can serves as promising catalysts throughout the NRR process.

Heteroleptic complexes of hydrazone Scaffold of picolinoyl N- oxide and 2,4 dihydroxy phenyl moieties; evaluation of antioxidant activity, DNA and protein binding properties and in vitro antiproliferation studies

The present study deals with design and synthesis of new mononuclear Cu(II), Co(II), Ni(II) and Zn(II) metal complexes of hydrazone of 2-(2-(2,4-dihydroxybenzylidene)hydrazinecarbonyl)pyridine-1-oxide (H2L), in a view to study their potential relevance for the biological applications. Structural aspects of the title compound (H2L) and metal complexes synthesized were evaluated by spectral and analytical methods viz. 1H NMR, 13C NMR, LC-MS, FT-IR, UV–Visible, SEM, EDX, Powder XRD, ESR, TGA and DTA. Ligational properties of H2L were explored by employing pH metric equilibrium studies for recognizing metal ion binding potential donor sites, and further HyperChem 7.5 software for computing properties of frontier molecular orbitals to ascertain orientation of highest occupied molecular orbitals from which presumably electrons are donated to metal ion in complex formation. The affinity of all title compounds to bind with CT-DNA and the type of interaction, therein have been studied by conducting UV–VIS absorption and fluorescence emission titrations. The protein-binding ability of all metal complexes with two serum proteins (BSA and HSA) were explored by absorption titrations, and further fluorescence titrations for BSA binding were also performed. Antioxidant activity of the title compounds was carried out by the method of free radical scavenging using spectrophotometric technique. Additionally, cytotoxicity of all metal complexes and ligand was measured by CTG cell proliferation assay after treating them with MDA-MB-231 and SKOV-3 cell lines. The cell cycle arrest and apoptosis assay in above cell lines after treatment with title compounds were also investigated by flow cytometry. In addition, molecular docking studies at target CDK2 protein inferred binding affinity of the title compounds through non covalent bonding interactions.

Synthesis, Spectral Characterization and Biological, DNA Binding, Molecular Docking and ADMET Studies of a New Benzyl (Z)-N’-((E)- 3-Ethoxy-2-Hydroxybenzylidene) Carbamohydrazonothioate and Its Co (II), Ni (II), Cu (II) and Zn (II) Metal Complexes Derived From S-Benzyl Thiosemicabazide-Salicylaldehyde.

This study presents the synthesis, characterization, and biological evaluation of metal complexes derived from benzyl carbamohydrazonothioate. The ligand was synthesized through a condensation reaction and subsequently complexed with various metal ions, including Cu(II), Ni(II), Co(II), and Zn(II). The resulting metal complexes were characterized using a range of spectroscopic techniques, including FT-IR, UV-Vis, and NMR spectroscopy, confirming the successful coordination of the metal ions with the ligand. The structural elucidation was further supported by elemental analysis and molar conductance measurements. The biological activities of the synthesized complexes were evaluated for their antibacterial, antifungal, and antioxidant properties. The results indicated that the metal complexes exhibited enhanced biological activities compared to the free ligand, suggesting their potential as effective antimicrobial and antioxidant agents. This study highlights the significance of metal complexation in enhancing the biological efficacy of organic ligands.

Rhenium and related valuable metals in the oil shales of the Volga basin

The results of study of the content of rhenium and other valuable metals in the oil shales of the Volga basin are presented. The new data on precise determination of Re, Co, Ni, Cu, Zn, U and other metals by inductively coupled plasma mass spectrometry have been published. The content of the studied metals were compared with clarks in carbonaceous shales. The association of metals with rhenium (Mo, U, Co, Ni, Cu, Zn, Se, Ag, Sb) has been isolated in oil shales. The organic matter of oil shales acts as a rhenium concentrator, and apparently Mo, U. The preferred petrographic type of oil shales for the concentration of rhenium in them is the colloalginite-vitrinite-clay type. The rhenium-bearing and metalliferous content of the Volga shales is compared with the contents of rhenium and a number of other valuable metals in dictyonema shales of the Baltic sedimentary basin.

Modulation of electronic and magnetic characteristics of Ni and Cr-based transition metal halide monolayers using strain engineering

Modulation of electronic and magnetic characteristics of Ni and Cr-based transition metal halide monolayers using strain engineering

Exploration of a Novel Electric-Fuse Device with a Simple Structure of Ni Metal on a SiO2 Dielectric for Electrostatic Discharge Protection under a Human Body Model.

On-chip electrostatic discharge (ESD) protection poses a challenge in the chip fabrication process. In this study, a novel electric fuse (E-fuse) device featuring a simple structure of Ni metal on a SiO2 dielectric for ESD protection was proposed, and the physical mechanism of its operation was investigated in detail. Experimental evaluations, utilizing transmission line pulse (TLP) testing and fusing performance analyses, reveal that the E-fuse, constructed with a Ni metal layer measuring 5 μm in width, 100 μm in length, and 5 nm in thickness, achieved a significant ESD protection voltage of 251 V (VHBM) and demonstrates low-voltage fusing at a bias voltage of 7 V. Compared to traditional ESD protection devices, the E-fuse boasts a smaller size and removability. To assess fusing performance, devices of varying sizes were tested using a fusing lifetime model. This study supports both theoretical and empirical evidence, enabling the adoption of cost-effective, straightforward E-fuse devices for ESD protection.

Production of Bio-Oil from Sugarcane Bagasse through Hydrothermal Liquefaction Processes with Modified Zeolite Socony Mobil-5 Catalyst

In response to the increasing global demand for sustainable energy alternatives, this research explores the efficient conversion of sugarcane bagasse to bio-oil through hydrothermal liquefaction (HTL) processes with modified Zeolite Socony Mobil-5 catalysts (ZSM-5). The study systematically investigates the impact of feedstock quantity, reaction temperature, duration, and catalyst loading on bio-oil yield and quality. Optimisation experiments revealed that a feedstock amount of 10 grammes, an HTL temperature of 340 °C for 60 min and a ZSM-5 catalyst loading of 3 grammes resulted in the highest bio-oil yield. Furthermore, the introduction of Ni and Fe metals to ZSM-5 exhibited enhanced catalytic activity without compromising the structure of the zeolites. Comprehensive characterisation of modified catalysts using SEM-EDS, XRD, TGA, TEM, and FTIR provided insight into their structural and chemical properties. The successful incorporation of Ni and Fe into ZSM-5 was confirmed, highlighting promising applications in hydrothermal liquefaction. Gas chromatography–mass spectrometry (GC-MS) analysis of bio-oils demonstrated the effectiveness of the 2% Fe/ZSM-5 catalyst, highlighting a significant increase in hydrocarbon content. FTIR analysis of the produced bio-oils indicated a reduction in functional groups and intensified aromatic peaks, suggesting a shift in chemical composition favouring aromatic hydrocarbons. This study provides valuable information on HTL optimisation, catalyst modification, and bio-oil characterisation, advancing the understanding of sustainable biofuel production. The findings underscore the catalytic prowess of modified ZSM-5, particularly with iron incorporation, in promoting the formation of valuable hydrocarbons during hydrothermal liquefaction.

Hydrogen spillover on Ni@Graphene enables robust and efficient catalytic hydrogenation of aqueous levulinic acid to γ-valerolactone

Hydrogenation of biomass-derived aqueous levulinic acid (LA) to produce γ-valerolactone (GVL) is a promising approach from biomass to sustainable platform chemicals. However, the practical application of this method is limited because aqueous LA is highly corrosive to metal-based hydrogenation catalyst in high-temperature hydrothermal environments. Herein, we encapsulated metallic Ni0 particles with a few layers of graphene using a hydrothermal carbon coating method to obtain Ni@FLG-600 catalyst, which exhibited efficient catalytic activity and excellent cycling stability for the hydrogenation of aqueous LA to GVL. The defect-rich graphene shell prevents the Ni0 from acid corrosion meanwhile selectively permits the passage of small H2 molecules. The resulted active H* on Ni0 spills over to the outer surface of graphene shell and reacts with LA. Remarkably, the amount of H* on graphene shell can be the descriptor of activity. This finding presents a new strategy for the fabrication of acid-resistant catalysts for aqueous biomass hydrogenation.

In-situ exsolved Ni nanoparticles for boosting CO2 reduction in solid oxide electrolysis cell

Due to their excellent high Faraday efficiency, perovskite solid oxide cells (SOECs) have attracted considerable attention. Nevertheless, they still face significant challenges in terms of stability and electrocatalytic activity during CO₂ electrolysis. In this study, Ni particles in La0.65Ba0.35Mn1-xNixO3-δ are successfully separated by a unique in-situ exsolved method of metal nanoparticles, which are uniformly anchored to the electrode surface as Ni nanometal particles. This effectively suppresses the generation of carbon deposits on the cathode surface. Under test conditions of 850 °C, 1.6 V and 50 sccm flow rate, the CO yield of the modified cathode material reached 5.9 mL min−1 cm−2, which is nearly four times higher than that before doping. The synergistic effect of in-situ exsolution of Ni metal nanoparticles with oxygen defects generated by the perovskite, creating more active locations for CO2 adsorption and electrolysis, is responsible for the significant improvement in electrochemical performance. This work provides new strategies and ideas for the development of efficient and durable SOEC cathode materials.

Growth behavior of anisotropic monometallic MOFs derivatives with the high absorbing and thermal properties

The growth behavior and morphological characteristics of metal-organic frameworks (MOFs) should be considered as important factors in understanding their structure. Therefore, MOFs with atypical shapes, heterogeneous structures or abnormal properties that grow anisotropic can serve as components and templates for further directed assembly or conversion into MOF derivatives with excellent performance in electromagnetic wave absorption. Cobalt (Co) and nickel (Ni) metals have good magnetic properties and are common materials for the preparation of monometallic MOF-derived. In this study, various MOF materials with anisotropic properties, such as rod-like, flower-like, and braided, were prepared by adjusting the molar ratio of Co and Ni solvent to the organic ligand. Due to the rich inter-facial polarization and strong magnetic coupling network of the magnetic composites, Ni-MOF-b (Ni-MOF with braided shape) was prepared for the first time when the molar ratio of nickel nitrate to linker was 1:1.2. The Ni-C-b was obtained after pyrolysis of Ni-MOF-b, the minimum reflection loss of Ni-C-b was –50.7 dB at 4.0 mm. In addition, the thermal conductivity of the film prepared with Ni-C-b as filler is 2.2 W/mK. The film with integrated good heat dissipation and wave absorbing properties provides a research idea for the design of multifunctional integrated film.

Biosorption of Ni (II), Pb (II) and Cu (II) Metal Ions on the Chitin Isolated from Spider Species of Drassodes lapidosus

Biosorption of Ni (II), Pb (II) and Cu (II) Metal Ions on the Chitin Isolated from Spider Species of Drassodes lapidosus