Catalytic Degradation and Directional Upgrading of Zhunnan Lignite: Double Constraint of Active Hydrogen and Effective Acquisition of Derived Arenes over Nickel Ferrite

2021 ◽  
Author(s):  
Guang-Hui Liu ◽  
Zhi-Wen Zhang ◽  
Xia-Long Li ◽  
Yu-Hong Kang ◽  
Cui-Ying Lu ◽  
...  
Keyword(s):  
Nickel Ferrite ◽  
Catalytic Degradation ◽  
Active Hydrogen ◽  
Double Constraint

Microwave Catalytic Degradation of Antibiotic Molecules by 2D Sheets of Spinel Nickel Ferrite

2020 ◽  
Vol 59 (36) ◽  
pp. 15839-15847
Author(s):  
Sandhya Mishra ◽  
Prashant Kumar ◽  
Sujoy Kumar Samanta
Keyword(s):  
Nickel Ferrite ◽  
Catalytic Degradation

Photo-catalytic degradation of gaseous pollutants in paper mills of southern China

TAPPI Journal ◽  
2018 ◽  
Vol 17 (03) ◽  
pp. 167-178 ◽  
Author(s):  
Xin Tong ◽  
Jiao Li ◽  
Jun Ma ◽  
Xiaoquan Chen ◽  
Wenhao Shen
Keyword(s):  
Degradation Rate ◽  
Southern China ◽  
Catalytic Degradation ◽  
Pulp And Paper ◽  
Gaseous Pollutants ◽  
Pulp And Paper Mills ◽  
Paper Mills ◽  
Initial Concentration ◽  
First Order ◽  
First Order Kinetics

Studies were undertaken to evaluate gaseous pollutants in workplace air within pulp and paper mills and to consider the effectiveness of photo-catalytic treatment of this air. Ambient air at 30 sampling sites in five pulp and paper mills of southern China were sampled and analyzed. The results revealed that formaldehyde and various benzene-based molecules were the main gaseous pollutants at these five mills. A photo-catalytic reactor system with titanium dioxide (TiO2) was developed and evaluated for degradation of formaldehyde, benzene and their mixtures. The experimental results demonstrated that both formaldehyde and benzene in their pure forms could be completely photo-catalytic degraded, though the degradation of benzene was much more difficult than that for formaldehyde. Study of the photo-catalytic degradation kinetics revealed that the degradation rate of formaldehyde increased with initial concentration fitting a first-order kinetics reaction. In contrast, the degradation rate of benzene had no relationship with initial concentration and degradation did not conform to first-order kinetics. The photo-catalytic degradation of formaldehyde-benzene mixtures indicated that formaldehyde behaved differently than when treated in its pure form. The degradation time was two times longer and the kinetics did not reflect a first-order reaction. The degradation of benzene was similar in both pure form and when mixed with formaldehyde.

Impedance Spectroscopy of Copper Substituted Nickel Ferrite Nan particles

2017 ◽  
Vol 49 (003) ◽  
pp. 591--596
Author(s):  
K. A. KALHORO ◽  
M. KHALID ◽  
A. D. CHANDIO ◽  
M. A. KALHORO ◽  
N. CHANNA
Keyword(s):  
Impedance Spectroscopy ◽  
Nickel Ferrite

Tổng hợp vật liệu cấu trúc spinel nickel ferrite NIxFE3-xO4 bằng phương pháp sol-gel và khảo sát hoạt tính quang xúc tác

2018 ◽  
Vol 54(7) ◽  
pp. 20
Author(s):  
Nguyễn Trương Xuân Vinh ◽  
Đoàn Văn Hồng Thiện ◽  
Huỳnh Kỳ Phương Hạ
Keyword(s):  
Nickel Ferrite ◽  
Sol Gel

scholarly journals Synthesis, characterization and heavy metal removal efficiency of nickel ferrite nanoparticles (NFN’s)

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Waheed Ali Khoso ◽  
Noor Haleem ◽  
Muhammad Anwar Baig ◽  
Yousuf Jamal
Keyword(s):  
Heavy Metals ◽  
Nickel Ferrite ◽  
Contact Time ◽  
Metal Removal ◽  
Heavy Metal Removal ◽  
Ferrite Nanoparticles ◽  
Batch Adsorption ◽  
Aqueous Environment ◽  
Human Beings ◽  
Nickel Ferrite Nanoparticles

AbstractThe heavy metals, such as Cr(VI), Pb(II) and Cd(II), in aqueous solutions are toxic even at trace levels and have caused adverse health impacts on human beings. Hence the removal of these heavy metals from the aqueous environment is important to protect biodiversity, hydrosphere ecosystems, and human beings. In this study, magnetic Nickel-Ferrite Nanoparticles (NFNs) were synthesized by co-precipitation method and characterized using X-Ray Diffraction (XRD), Energy Dispersive Spectroscopy (EDS) and Field Emission Scanning Electronic Microscopy (FE-SEM) techniques in order to confirm the crystalline structure, composition and morphology of the NFN’s, these were then used as adsorbent for the removal of Cr(VI), Pb(II) and Cd(II) from wastewater. The adsorption parameters under study were pH, dose and contact time. The values for optimum removal through batch-adsorption were investigated at different parameters (pH 3–7, dose: 10, 20, 30, 40 and 50 mg and contact time: 30, 60, 90, and 120 min). Removal efficiencies of Cr(VI), Pb(II) and Cd(II) were obtained 89%, 79% and 87% respectively under optimal conditions. It was found that the kinetics followed the pseudo second order model for the removal of heavy metals using Nickel ferrite nanoparticles.

scholarly journals UV Stimulated Manganese Dioxide for the Persulfate Catalytic Degradation of Bisphenol A

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 502
Author(s):  
Guihua Dong ◽  
Bing Chen ◽  
Bo Liu ◽  
Stanislav R. Stoyanov ◽  
Yiqi Cao ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Reaction Mechanisms ◽  
Reduction Rate ◽  
Catalytic Degradation ◽  
Gas Chromatography Mass Spectrometry ◽  
Degradation Pathways ◽  
Industrial Chemicals ◽  
Oh Groups ◽  
Long Term Adverse Effects

One of the most commonly produced industrial chemicals worldwide, bisphenol A (BPA), is used as a precursor in plastics, resins, paints, and many other materials. It has been proved that BPA can cause long-term adverse effects on ecosystems and human health due to its toxicity as an endocrine disruptor. In this study, we developed an integrated MnO2/UV/persulfate (PS) process for use in BPA photocatalytic degradation from water and examined the reaction mechanisms, degradation pathways, and toxicity reduction. Comparative tests using MnO2, PS, UV, UV/MnO2, MnO2/PS, and UV/PS processes were conducted under the same conditions to investigate the mechanism of BPA catalytic degradation by the proposed MnO2/UV/PS process. The best performance was observed in the MnO2/UV/PS process in which BPA was completely removed in 30 min with a reduction rate of over 90% for total organic carbon after 2 h. This process also showed a stable removal efficiency with a large variation of pH levels (3.6 to 10.0). Kinetic analysis suggested that 1O2 and SO4•− played more critical roles than •OH for BPA degradation. Infrared spectra showed that UV irradiation could stimulate the generation of –OH groups on the MnO2 photocatalyst surface, facilitating the PS catalytic degradation of BPA in this process. The degradation pathways were further proposed in five steps, and thirteen intermediates were identified by gas chromatography-mass spectrometry. The acute toxicity was analyzed during the treatment, showing a slight increase (by 3.3%) in the first 30 min and then a decrease by four-fold over 2 h. These findings help elucidate the mechanism and pathways of BPA degradation and provide an effective PS catalytic strategy.

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