scholarly journals Preparation of Chitosan—Graphene Oxide Composite Aerogel by Hydrothermal Method and Its Adsorption Property of Methyl Orange

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2169
Author(s):  
Wei Zhu ◽  
Xueliang Jiang ◽  
Fangjun Liu ◽  
Feng You ◽  
Chu Yao

Graphene based aerogel has become one of the most likely functional adsorption materials that is applicable to purify various contaminated water sources, such as dye wastewater, because of its high porosity, structural stability, large specific surface area, and high adsorption capacity. In this study, chitosan and graphene oxide were first selected as the matrix to prepare the composite hydrogel through the hydrothermal method, which was further frozen and dried to obtain the target aerogel. The microscopic structures and adsorption capacity of the composite aerogel were then characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and N2 (nitrogen) physical adsorption and desorption tests. The results show that the specific surface area of the composite aerogel was reached at 297.431 m2/g, which is higher than that of graphene oxide aerogel and chitosan aerogel. The aperture was reduced to about 3 nm. The adsorption rate of the composite aerogel for the methyl orange solution was as high as 97.2% at pH = 1, and the adsorption capacity was 48.6 mg/g. The adsorption process of the composite aerogel satisfies the Langmuir equation and can be described by the second-order adsorption kinetics. In addition, it is worth noting that this composite aerogel can provide a striking adsorption characteristic on methyl orange due to the combining effects from massive amino groups on chitosan and the structural conjugation of graphene oxide.

2020 ◽  
Vol 850 ◽  
pp. 16-21
Author(s):  
Hoc Thang Nguyen ◽  
Phong Thanh Dang

Diatomite or diatomaceous earth (DE) is one of materials which can be used as an adsorbent to treat heavy metal ions from waste water, even there are many factories used it to clean the water for drinking. However, natural DE (raw DE) has very low adsorption capacity because of low specific surface area. In this work, natural DE from Lam Dong province, Viet Nam was demagnetized to remove iron and activated by HCl solution for 90 minutes with concentration of 10% at room condition. Adsorbent capacity was evaluated using As solution and the results show that the activated diatomite has adsorption capacity three times higher than that of raw DE, and the specific surface area of activated diatomite was increased 47.5% with the main chemical composition of 90.8% SiO2 and high porosity


2018 ◽  
Vol 55 (1B) ◽  
pp. 109 ◽  
Author(s):  
Nguyen Huu Hieu

In this work, graphene oxide–manganese ferrite (GO–MnFe2O4) magnetic nanohybrids were synthesized by co–precipitation technique. The adsorption properties of GO–MnFe2O4 for efficient removal of Cd(II) from contaminated water were investigated. The nanohybrids were characterized by using X–ray diffraction, Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller specific surface area (BET), transmission electron microscopy, and vibrating sample magnetometry (VSM). VSM result showed the high saturation magnetization values Ms = 27.1 emu/g, the BET specific surface area was 84.236 m2/g. Adsorption experiments were carried out to evaluate the adsorption capacity of the GO–MnFe2O4 magnetic nanohybrids and compared with MnFe2O4 nanoparticles and GO nanosheets. The equilibrium time for adsorption of Cd(II) onto the nanohybrids was 240 minutes. Experimental adsorption data were well–fitted to the Langmuir isotherm and the pseudo–second–order kinetic equation. The experimental results showed that adsorption of Cd(II) using GO–MnFe2O4 magnetic nanohybrids was better than MnFe2O4 and GO with a maximum adsorption capacity of 121.951 mg/g at pH 8.  Reusability, ease of magnetic separation, high removal capacity, and fast kinetics lead the GO–MnFe2O4 nanohybrids to be promising adsorbents for removal heavy metals from contaminated water.


2019 ◽  
Vol 2019 ◽  
pp. 1-12
Author(s):  
Xin Wen ◽  
Siqin Zhao ◽  
S. Asuha

A series of nitrogen-doped mesoporous TiO2 nanomaterials and nitrogen-doped mesoporous TiO2/reduced graphene oxide (RGO) composites were successfully prepared by hydrothermal method using triammonium citrate as the nitrogen source. The effects of nitrogen and graphene oxide (GO) dopping on the photocatalytic properties of the TiO2 were investigated to optimize preparation conditions. The results showed that all prepared samples were mainly composed of the anatase phase and possessed a mesoporous structure. The use of the triammonium citrate not only significantly increased the specific surface area of the synthesized samples but also caused the partial reduction of GO to RGO, leading to further increase of the specific surface area and the improvement of quantum efficiency of the photogenerated electrons. All synthesized samples showed superior photocatalytic performance for methyl orange solution. Among them, the NMT/RGO-1.8-10 was found to be the best; the degradation rate of methyl orange solution on the sample reached 100% in 30 minutes under visible light irradiation.


2012 ◽  
Vol 512-515 ◽  
pp. 1980-1985
Author(s):  
Ya Jun Luo ◽  
Xue Li ◽  
Xiao Li Hu ◽  
Deng Liang He ◽  
Peng Lin

SiO2aerogel is prepared under normal conditions by taking tetraethyl orthosilicate (TEOS) as the silica source, N-hexane as the displacer, trimethylchlorosilane hexane as the modifier and hydrolysis environment provided by hydrochloric acid and ammonia water. The effect of pH value, time, temperature, initial concentration on the adsorption of nitrobenzene by aerogel has been studied. The results show that the best range of the pH value for adsorption is 10.72. When adsorption time is 100 min, adsorption equilibrium can be reached. The best temperature for adsorption is 40 °C. The adsorption capacity becomes larger with the concentration increasing of the nitrobenzene solution. When the concentration reaches 500 mg/L, the adsorption reaches 32.402 mg/g. The adsorption equation matches Langmuir model. Scanning Electron Microscopes (SEM), infrared absorption spectrum and specific surface area measurements have shown that the adsorption property of SiO2aerogel for the nitrobenzene is related to cellular structure of the aerogel and large specific surface area.


2022 ◽  
Author(s):  
Kainan Li ◽  
Ke Zheng ◽  
Zhifang Zhang ◽  
Kuan Li ◽  
Ziyao Bian ◽  
...  

Abstract Construction of metal selenides with a large specific surface area and a hollow structure is one of the effective methods to improve the electrochemical performance of supercapacitors. However, the nano-material easily agglomerates due to the lack of support, resulting in the loss of electrochemical performance. Herein, we successfully design a three-dimensional graphene (3DG) encapsulation-protected hollow nanoboxes (CoSe2-SnSe2) composite aerogel (3DG/CoSe2-SnSe2) via a co-precipitation method coupled with self-assembly route, followed by a high temperature selenidation strategy. The obtained aerogel possesses porous 3DG conductive network, large specific surface area and plenty of reactive active sites. It could be used as a flexible and binder-free electrode after a facile mechanical compression process, which provided a high specific capacitance of 460 F g-1 at 0.5 A g-1, good rate capability of 212.7 F g-1 at 10 A g-1, and excellent cycle stability due to the fast electron/ion transfer and electrolyte diffusion. With the as-prepared 3DG/CoSe2-SnSe2 as positive electrodes and the AC (activated carbon) as negative electrodes, an asymmetric supercapacitor (3DG/CoSe2-SnSe2//AC) was fabricated, which delivered a high specific capacity of 38 F g-1 at 1A g-1 and an energy density of 11.89 W h kg-1 at 749.9 W kg-1, as well as a capacitance retention of 91.1% after 3000 cycles. This work provides a new method for preparing electrode material.


2021 ◽  
Vol 15 (2) ◽  
pp. 131-144
Author(s):  
Chunjiang Jin ◽  
Huimin Chen ◽  
Luyuan Wang ◽  
Xingxing Cheng ◽  
Donghai An ◽  
...  

In this study, aspen wood sawdust was used as the raw material, and Fe(NO3)3 and CO2 were used as activators. Activated carbon powder (ACP) was produced by the one-step physicochemical activation method in an open vacuum tube furnace. The effects of different mass ratios of Fe(NO3)3 and aspen wood sawdust on the pore structure of ACP were examined under single-variable experimental conditions. The mass ratio was 0–0.4. The detailed characteristics of ACP were examined by nitrogen adsorption, scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The adsorption capacity of ACP was established by simulating volatile organic compounds (VOCs) using ethyl acetate. The results showed that ACP has a good nanostructure with a large pore volume, specific surface area, and surface functional groups. The pore volume and specific surface area of Fe-AC-0.3 were 0.26 cm3/g and 455.36 m2/g, respectively. The activator played an important role in the formation of the pore structure and morphology of ACP. When the mass ratio was 0–0.3, the porosity increased linearly, but when it was higher than 0.3, the porosity decreased. For example, the pore volume and specific surface area of Fe-AC-0.4 reached 0.24 cm3/g and 430.87 m2/g, respectively. ACP presented good VOC adsorption performance. The Fe-AC-0.3 sample, which contained the most micropore structures, presented the best adsorption capacity for ethyl acetate at 712.58 mg/g. Under the action of the specific reaction products nitrogen dioxide (NO2) and oxygen, the surface of modified ACP samples showed different rich C/O/N surface functional groups, including C-H, C=C, C=O, C-O-C, and C-N.


2021 ◽  
Vol 14 (02) ◽  
pp. 2151011
Author(s):  
Jingwen Jia ◽  
Longfu Wei ◽  
Ziting Guo ◽  
Fang Li ◽  
Changlin Yu ◽  
...  

Metal–organic frameworks (MOFs) are the electrocatalytic materials with large specific surface area, high porosity, controllable structure and monodisperse active center, which is a promising candidate for the application of electrochemical energy conversion. However, the electrocatalytic performance of pure MOFs is seriously limited its poor conductivity and stability. In this work, high-performance electrocatalyst was fabricated through combining NiFe/MOF on nickel foam (NF) via in-situ growth strategy. Through rational control of the time and ratio in reaction precursors, we realized the effective manipulation of the growth behavior, and further investigated the electrocatalytic performance in water splitting. The catalyst presented excellent electrocatalytic performance for water splitting, with low overpotential of 260 mV in alkaline condition at a current density of 50 mA[Formula: see text], which is benefited from the large specific surface area and active sites. This study demonstrates that the rational design of NiFe MOF/NF plays a significant role in high-performance electrocatalyst.


2019 ◽  
Vol 9 (23) ◽  
pp. 5249 ◽  
Author(s):  
Derlin Hsu ◽  
Changyi Lu ◽  
Tairan Pang ◽  
Yuanpeng Wang ◽  
Guanhua Wang

Chemically activated biochars prepared from sorghum distillers grain using two base activators (NaOH and KOH) were investigated for their adsorption properties with respect to ammonium nitrogen from aqueous solution. Detailed characterizations, including scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetry (TG), and specific surface area analyses, were carried out to offer a broad evaluation of the prepared biochars. The results showed that the NaOH- and KOH-activated biochars exhibited significantly enhanced adsorption capacity, by 2.93 and 4.74 times, respectively, in comparison with the pristine biochar. Although the NaOH-activated biochar possessed larger specific surface area (132.8 and 117.7 m2/g for the NaOH- and KOH-activated biochars, respectively), the KOH-activated biochar had higher adsorption capacity owing to its much higher content of functional groups. The adsorption kinetics and isotherms of the KOH-activated biochar at different temperatures were further studied. The biochar had a maximum adsorption capacity of 14.34 mg/g at 45 °C, which was satisfactory compared with other biochars prepared using different feedstocks. The adsorption process followed pseudo-second-order kinetics, and chemical adsorption was the rate-controlling step. The equilibrium data were consistent with the Freundlich isotherm, and the thermodynamic parameters suggested that the adsorption process was endothermic and spontaneous. Consequently, this work demonstrates that chemically activated biochar from sorghum distillers grain is effective for ammonium nitrogen removal.


Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2362 ◽  
Author(s):  
Qinya Fan ◽  
Liqiang Cui ◽  
Guixiang Quan ◽  
Sanfei Wang ◽  
Jianxiong Sun ◽  
...  

Biochar has been studied for remediation of heavy metal-contaminated soils by many researchers. When in external conditions, biochar in soils ages, which can transform its structural properties and adsorption capacity. This study was conducted with two oxidation processes, HNO3/H2SO4 and NaOH/H2O2, to simulate the effects of biochar in acid and alkaline soil conditions. The results show that the oxygen-containing functional groups increased in aged biochar, which led to improve the ratio of oxygen and carbon (O/C). Nitro functional groups were found in the acid-oxidation treated biochar. Destroyed ditches and scars were observed on the surface of aged biochar and resulted in growth in their specific surface area and porosity. Specific surface area increased by 21.1%, 164.9%, and 63.0% for reed-derived biochar treated with water washing, acid oxidation, and basic oxidation, respectively. Greater peaks in the Fourier Transform Infrared Spectroscopy (FTIR) results were found in C–O and O–H on the surface of field-aged biochar. Meanwhile, mappings of energy-dispersive spectroscopy showed that biochar aged in soil was abundant in minerals such as silicon, iron, aluminum, and magnesium. In summary, biochar subjected to wet oxidation aging had an increased capacity to immobilize Cd compared to unaged biochar, and the adsorption capacity of oxidized biochar increased by 28.4% and 13.15% compared to unaged biochar due to improvements in porosity and an increase in functional groups.


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