scholarly journals Highly Efficient Debromination of 4,4ʹ-dibrominated Diphenyl Ether by Organic-palygorskite Supported Pd/Fe Nanoparticles

2021 ◽  
Author(s):  
Jiang Shao ◽  
Yi Zhang ◽  
Zongtang Liu ◽  
Zhenghao Fei ◽  
Yufeng Sun ◽  
...  
Keyword(s):  
Hydrogen Transfer ◽  
Bimetallic Nanoparticles ◽  
Diphenyl Ether ◽  
Order Kinetic ◽  
Transfer Mode ◽  
Removal Capacity ◽  
Fe Nanoparticles ◽  
Initial Ph ◽  
Stepwise Reduction ◽  
Supported Pd

Abstract Organic-palygorskite (OP) supported Pd/Fe nanoparticles composite (OP-Pd/Fe) was prepared by stepwise reduction method. The removal capacity of 4,4ʹ-dibrominated diphenyl ether (BDE15) by OP-Pd/Fe was compared with other various materials. For better understanding the possible mechanism, the synthesized and reacted OP-Pd/Fe materials were characterized by TEM, SEM, XRD, and XPS, respectively. The effects of major influencing parameters on the degradation of BDE15 were also studied. Benefit from the synergistic effect of the carrier and bimetallic nanoparticles, BDE15 could be completely debrominated into diphenyl ether (DE) under suitable conditions. A two-stage adsorption/debromination removal mechanism was proposed. The degradation of BDE15 with OP-Pd/Fe was mainly stepwise debromination reaction, and hydrogen transfer mode was assumed as the dominated debromination mechanism. The removal process fitted well to the pseudo first-order kinetic equation. The observed rate constants increased with increasing Pd loading and OP-Pd/Fe dosage, while decreased with increasing initial BDE15 concentration, the tetrahydrofuran/water ratio, and the initial pH of the solution. The work provides a new approach for the treatment of PBDEs pollution.

Chitosan-based Magnetic Composites - Efficient Adsorbents for Removal of Pb(II) and Cu(II) from Aqueous Mono and Bicomponent Solutions

2018 ◽  
Vol 69 (9) ◽  
pp. 2323-2330 ◽  
Author(s):  
Daniela C. Culita ◽  
Claudia Maria Simonescu ◽  
Rodica Elena Patescu ◽  
Nicolae Stanica
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Chemical Properties ◽  
Order Kinetic ◽  
Mass Ratio ◽  
Magnetic Adsorbent ◽  
Magnetic Composites ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Physical And Chemical

A series of three chitosan-based magnetic composites was prepared through a simple coprecipitation method. It was investigated the influence of mass ratio between chitosan and magnetite on the physical and chemical properties of the composites in order to establish the optimum conditions for obtaining a composite with good adsorption capacity for Pb(II) and Cu(II) from mono and bicomponent aqueous solutions. It was found that the microspheres prepared using mass ratio chitosan / magnetite 1.25/1, having a saturation magnetization of 15 emu g--1, are the best to be used as adsorbent for the metal ions. The influence of different parameters such as initial pH values, contact time, initial concentration of metal ions, on the adsorption of Pb(II) and Cu(II) onto the chitosan-based magnetic adsorbent was investigated in details. The adsorption process fits the pseudo-second-order kinetic model in both mono and bicomponent systems, and the maximum adsorption capacities calculated on the basis of the Langmuir model were 79.4 mg g--1 for Pb(II) and 48.5 mg g--1 for Cu(II) in monocomponent systems, while in bicomponent systems were 88.3 and 49.5 mg g--1, respectively. The results revealed that the as prepared chitosan-based magnetic adsorbent can be an effective and promising adsorbent for Pb(II) and Cu(II) from mono and bicomponent aqueous solutions.

scholarly journals Factors influencing the adsorption and photocatalysis of direct red 80 in the presence of a TiO2: Equilibrium and kinetics modeling

2021 ◽  
pp. 174751982198996
Author(s):  
Moussa Abbas
Keyword(s):  
Elimination Rate ◽  
Threshold Value ◽  
Heterogeneous Photocatalysis ◽  
Order Kinetic ◽  
Batch Mode ◽  
Adsorption Capacities ◽  
Initial Ph ◽  
Equilibrium And Kinetics ◽  
Order Kinetic Model ◽  
Charge Point

Among the different photocatalysts, TiO2 ( Eg = 3.1 eV, zero charge point (pHpzc = 6.3), and surface = 55 m2/g) is currently the most efficient and the most studied semiconductor due to its strong photocatalytic activity, non-toxicity, and chemical stability. The elimination of DR-80 on TiO2 is studied by adsorption in batch mode and by application of heterogeneous photocatalysis onto TiO2 under UV irradiation. The effects of contact time (0–60 min), initial pH (3–11), dose of the adsorbent (0.5–3 g L−1), and DR-80 concentration (40–60 mg L−1) on the adsorption of DR-80 by TiO2 are studied for optimization of these parameters. The kinetic parameters, rate constants, and equilibrium adsorption capacities are calculated and discussed for each applied theoretical model. The adsorption of DR-80 is well described by the pseudo-first-order kinetic model. The fitting of the adsorption isotherms shows that the models of Langmuir and Temkin offering a better fit and an adsorption 64.102 mg/g at 25 °C of DR-80 are eliminated. The results showed that the photocatalytic efficiency strongly depends on the pH while the initial rate of photodegradation is proportional to the catalyst dose, and becomes almost constant above a threshold value. It was found that the photodegradation is favored at low DR-80 concentrations in accordance with the Langmuir–Hinshelwood model with the constants Kad = 6.5274 L/mg and KL–H = 0.17818 mg L−1 min. However, the adsorption is improved for high DR-80 concentrations. It is found that the degradation depends on both the temperature and the pH with a high elimination rate at high temperature. The photocatalyst TiO2 has a better activity for the degradation of DR-80, compared to some commercial catalysts that have been described in the literature.

scholarly journals The sorption of inorganic arsenic on modified sepiolite: Effect of hydrated iron(III)-oxide

2014 ◽  
Vol 79 (7) ◽  
pp. 815-828 ◽  
Author(s):  
Nikola Ilic ◽  
Slavica Lazarevic ◽  
Vladana Rajakovic-Ognjanovic ◽  
Ljubinka Rajakovic ◽  
Djordje Janackovic ◽  
...  
Keyword(s):  
Sorption Capacity ◽  
Arsenic Removal ◽  
Ph Value ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Deionized Water ◽  
Order Kinetic ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of inorganic arsenic species, As(III) and As(V), from water by sepiolite modified with hydrated iron(III) oxide was investigated at 25 ?C through batch studies. The influence of the initial pH value, the initial As concentrations, the contact time and types of water on the sorption capacity was investigated. Two types of water were used, deionized and groundwater. The maximal sorption capacity for As(III) from deionized water was observed at initial and final pH value 7.0, while the bonding of As(V) was observed to be almost pH independent for pH value in the range from 2.0 to 7.0, and the significant decrease in the sorption capacity was observed at pH values above 7.0. The sorption capacity at initial pH 7.0 was about 10 mg g?1 for As(III) and 4.2 mg g?1 for As(V) in deionized water. The capacity in groundwater was decreased by 40 % for As(III) and by 20 % for As(V). The Langmuir model and pseudo-second order kinetic model revealed good agreement with the experimental results. The results show that Fe(III)-modified sepiolite exhibits significant affinity for arsenic removal and it has a potential for the application in water purification processes.

Phosphorus removal from aqueous solution using a novel granular material developed from building waste

2017 ◽  
Vol 75 (6) ◽  
pp. 1500-1511 ◽  
Author(s):  
Shengjiong Yang ◽  
Pengkang Jin ◽  
Xiaochang C. Wang ◽  
Qionghua Zhang ◽  
Xiaotian Chen
Keyword(s):  
Granular Material ◽  
Chemical Precipitation ◽  
Phosphate Removal ◽  
Precipitation Process ◽  
Order Kinetic ◽  
Solution Ph ◽  
Experimental Conditions ◽  
Removal Capacity ◽  
Order Kinetic Model ◽  
Pseudo Second Order

In this study, a granular material (GM) developed from building waste was used for phosphate removal from phosphorus-containing wastewater. Batch experiments were executed to investigate the phosphate removal capacity of this material. The mechanism of removal proved to be a chemical precipitation process. The characteristics of the material and resulting precipitates, the kinetics of the precipitation and Ca2+ liberation processes, and the effects of dosage and pH were investigated. The phosphate precipitation and Ca2+ liberation processes were both well described by a pseudo-second-order kinetic model. A maximum precipitation capacity of 0.51 ± 0.06 mg g−1 and a liberation capacity of 6.79 ± 0.77 mg g−1 were measured under the experimental conditions. The processes reached equilibrium in 60 min. The initial solution pH strongly affected phosphate removal under extreme conditions (pH <4 and pH >10). The precipitates comprised hydroxyapatite and brushite. This novel GM can be considered a promising material for phosphate removal from wastewater.

scholarly journals Insights into Starch Coated Nanozero Valent Iron-Graphene Composite for Cr(VI) Removal from Aqueous Medium

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Prasanna Kumarathilaka ◽  
Vimukthi Jayaweera ◽  
Hasintha Wijesekara ◽  
I. R. M. Kottegoda ◽  
S. R. D. Rosa ◽  
...  
Keyword(s):  
Point Of Zero Charge ◽  
Inert Material ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Graphene Composite ◽  
Removal Capacity ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
First Time

Embedding nanoparticles into an inert material like graphene is a viable option since hybrid materials are more capable than those based on pure nanoparticulates for the removal of toxic pollutants. This study reports for the first time on Cr(VI) removal capacity of novel starch stabilized nanozero valent iron-graphene composite (NZVI-Gn) under different pHs, contact time, and initial concentrations. Starch coated NZVI-Gn composite was developed through borohydrate reduction method. The structure and surface of the composite were characterized by scanning electron microscopy (SEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), and point of zero charge (pHpzc). The surface area and pHpzc of NZVI-Gn composite were reported as 525 m2 g−1 and 8.5, respectively. Highest Cr(VI) removal was achieved at pH 3, whereas 67.3% was removed within first few minutes and reached its equilibrium within 20 min obeying pseudo-second-order kinetic model, suggesting chemisorption as the rate limiting process. The partitioning of Cr(VI) at equilibrium is perfectly matched with Langmuir isotherm and maximum adsorption capacity of the NZVI-Gn composite is 143.28 mg g−1. Overall, these findings indicated that NZVI-Gn composite could be utilized as an efficient and magnetically separable adsorbent for removal of Cr(VI).

Preparation of cationic waste paper and its application in poisonous dye removal

2013 ◽  
Vol 67 (11) ◽  
pp. 2560-2567 ◽  
Author(s):  
Fan Yang ◽  
Xiaojie Song ◽  
Lifeng Yan
Keyword(s):  
Low Cost ◽  
Aqueous Suspension ◽  
Order Kinetic ◽  
Acid Orange 7 ◽  
Anionic Dyes ◽  
Experimental Conditions ◽  
Adsorption Models ◽  
Acid Orange ◽  
Initial Ph ◽  
Pseudo Second Order

Cationic paper was prepared by reaction of paper with 2,3-epoxypropyltrimethylammonium chloride in aqueous suspension, and tested as low-cost adsorbent for wastewater treatment. The experimental results revealed that anionic dyes (Acid Orange 7, Acid Red 18, and Acid Blue 92) were adsorbed on the cationic paper nicely. The maximum amount of dye Acid Orange 7 adsorbed on cationic paper was 337.2 mg/g in experimental conditions. The effects of initial dye concentration, temperature, and initial pH of dye solution on adsorption capacity of cationic paper were studied. The pseudo-first-order and pseudo-second-order kinetic models were applied to describe the kinetic data. The Freundlich and Langmuir adsorption models were used to describe adsorption equilibrium. The thermodynamic data indicated that the adsorption process of dye on cationic paper occurred spontaneously.

Self-hydrogen transfer hydrogenolysis of β-O-4 linkages in lignin catalyzed by MIL-100(Fe) supported Pd–Ni BMNPs

2017 ◽  
Vol 19 (19) ◽  
pp. 4538-4543 ◽  
Author(s):  
Jia-wei Zhang ◽  
Guo-ping Lu ◽  
Chun Cai
Keyword(s):  
Hydrogen Transfer ◽  
Catalytic Performance ◽  
Model Compounds ◽  
Lignin Model Compounds ◽  
Organosolv Lignin ◽  
Lignin Model ◽  
Intramolecular Transfer ◽  
Supported Pd

A MIL-100(Fe) supported Pd–Ni BMNP catalyst has been fabricated, and the catalyst exhibits superior catalytic performance toward intramolecular transfer hydrogenolysis of lignin model compounds and organosolv lignin.

Adsorption of Chromium (VI) from Aqueous Solution by Agricultural Waste Derived Activated Carbon

2013 ◽  
Vol 726-731 ◽  
pp. 2100-2106 ◽  
Author(s):  
Hua Zhang ◽  
Xue Hong Zhang ◽  
Yi Nian Zhu ◽  
Shou Rui Yuan
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Agricultural Waste ◽  
Order Kinetic ◽  
Chromium Vi ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Grapefruit Peel ◽  
Pseudo Second Order ◽  
C 30

Activated carbon prepared from grapefruit peel, an agricultural solid waste by-product, has been used for the adsorption of Cr(VI) from aqueous solution. The effects of adsorbent dosage, pH and temperature on adsorption of Cr(VI) were investigated. The maximum adsorption yield was obtained at the initial pH of 3. The dynamical data fit very well with the pseudo-second-order kinetic model and the calculated adsorption capacities (23.98, 24.33 and 24.81 mg/g) were in good agreement with experiment results at 20°C, 30°C and 40 °C for the 100 mg/L Cr(VI) solution. The Freundlich model (R2 values were 0.9198-0.9871) fitted adsorption data better than the Langmuir model. The calculated parameters confirmed the favorable adsorption of Cr(VI) on the activated carbon prepared from grapefruit peel.

Sign in / Sign up

Export Citation Format

Share Document