scholarly journals Efficient Catalytic Degradation of Phenol with Phthalocyanine-Immobilized Reduced Graphene–Bacterial Cellulose Nanocomposite

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2218
Author(s):  
Binbin Wu ◽  
Yikai Sun ◽  
Qiujin Fan ◽  
Jiahui Chen ◽  
Weizheng Fang ◽  
...  

In this report, phthalocyanine (Pc)/reduced graphene (rG)/bacterial cellulose (BC) ternary nanocomposite, Pc-rGBC, was developed through the immobilization of Pc onto a reduced graphene–bacterial cellulose (rGBC) nanohybrid after the reduction of biosynthesized graphene oxide-bacterial cellulose (GOBC) with N2H4. Field emission scanning electron microscopy (FESEM) and Fourier transform infrared spectroscopy (FT-IR) were employed to monitor all of the functionalization processes. The Pc-rGBC nanocomposite was applied for the treatment of phenol wastewater. Thanks to the synergistic effect of BC and rG, Pc-rGBC had good adsorption capacity to phenol molecules, and the equilibrium adsorption data fitted well with the Freundlich model. When H2O2 was presented as an oxidant, phenol could rapidly be catalytically decomposed by the Pc-rGBC nanocomposite; the phenol degradation ratio was more than 90% within 90 min of catalytic oxidation, and the recycling experiment showed that the Pc-rGBC nanocomposite had excellent recycling performance in the consecutive treatment of phenol wastewater. The HPLC result showed that several organic acids, such as oxalic acid, maleic acid, fumaric acid, glutaric acid, and adipic acid, were formed during the reaction. The chemical oxygen demand (COD) result indicated that the formed organic acids could be further mineralized to CO2 and H2O, and the mineralization ratio was more than 80% when the catalytic reaction time was prolonged to 4 h. This work is of vital importance, in terms of both academic research and industrial practice, to the design of Pc-based functional materials and their application in environmental purification.

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1422
Author(s):  
Viktor V. Revin ◽  
Alexander V. Dolganov ◽  
Elena V. Liyaskina ◽  
Natalia B. Nazarova ◽  
Anastasia V. Balandina ◽  
...  

Currently, there is an increased demand for biodegradable materials in society due to growing environmental problems. Special attention is paid to bacterial cellulose, which, due to its unique properties, has great prospects for obtaining functional materials for a wide range of applications, including adsorbents. In this regard, the aim of this study was to obtain a biocomposite material with adsorption properties in relation to fluoride ions based on bacterial cellulose using a highly productive strain of Komagataeibacter sucrofermentans H-110 on molasses medium. Films of bacterial cellulose were obtained. Their structure and properties were investigated by FTIR spectroscopy, NMR, atomic force microscopy, scanning electron microscopy, and X-ray structural analysis. The results show that the fiber thickness of the bacterial cellulose formed by the K. sucrofermentans H-110 strain on molasses medium was 60–90 nm. The degree of crystallinity of bacterial cellulose formed on the medium was higher than on standard Hestrin and Schramm medium and amounted to 83.02%. A new biocomposite material was obtained based on bacterial cellulose chemically immobilized on its surface using atomic-layer deposition of nanosized aluminum oxide films. The composite material has high sorption ability to remove fluoride ions from an aqueous medium. The maximum adsorption capacity of the composite is 80.1 mg/g (F/composite). The obtained composite material has the highest adsorption capacity of fluoride from water in comparison with other sorbents. The results prove the potential of bacterial cellulose-based biocomposites as highly effective sorbents for fluoride.


Author(s):  
Falk Liebner ◽  
Nikita Aigner ◽  
Christian Schimper ◽  
Antje Potthast ◽  
Thomas Rosenau

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 508 ◽  
Author(s):  
Bo Wang ◽  
Fu-hua Lin ◽  
Xiang-yang Li ◽  
Xu-ran Ji ◽  
Si-xiao Liu ◽  
...  

Isotactic polypropylene (iPP) is a commonly used thermoplastic polymer with many excellent properties. But high brittleness, especially at low temperatures, limits the use of iPP. The presence of transcrystallization of iPP makes it possible for fiber-reinforced iPP composites with higher strength. Bacterial cellulose (BC) is a kind of cellulose with great potential to be used as a new filler to reinforce iPP due to its high crystallinity, biodegradability and efficient mechanical properties. In this study, the iPP/BC hamburger composite was prepared by a simple hot press and maleic anhydride grafted polypropylene (MAPP) was used to improve the interface compatibility of iPP and BC. The polarizing microscope (POM) photograph shows that BC successfully induces the transcrystallization of iPP. The differential Scanning Calorimeter (DSC) date proves that the addition of BC could improve the thermal properties and crystallization rate of the composite. Especially, this change is more obvious of the iPP/MAPP/BC. The mechanical properties of the iPP/BC composites were greatly increased. This DSC date is higher than BC; we used BC particles to enhance the iPP in our previous research. The scanning Electron Microscope (SEM) analysis intuitively shows that the interface of the iPP/MAPP/BC is more smooth and flat than the iPP/BC. The fourier Transform infrared spectroscopy (FT-IR) analysis of the iPP/BC hamburger composites was shown that a new C=O group vibration appeared at 1743 cm−1, which indicated that the hydrogen bond structure of BC molecules was weakened and some hydroxyl groups were substituted after modification which can increase the lipophilicity of BC. These results indicated that the BC fiber can easily induce the transcrystallization of iPP, which has excellent mechanical properties. Moreover, the addition of MAPP contributes greatly to the interface compatibility of iPP and BC.


Crystals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 675 ◽  
Author(s):  
Jinbo Ouyang ◽  
Jian Chen ◽  
Limin Zhou ◽  
Fangze Han ◽  
Xin Huang

To improve the physicochemical properties of valnemulin (VLM), different solid forms formed by VLM and organic acids, including tartaric acid (TAR), fumaric acid (FUM), and oxalic acid (OXA), were successfully prepared and characterized by using differential scanning calorimetry (DSC), scanning electron microscope (SEM), X-ray powder diffraction (XRPD), and Fourier-transform infrared spectroscopy (FT-IR). The excess enthalpy Hex between VLM and other organic acids was calculated by COSMOthermX software and was used to evaluate the probability of forming multi-component solids between VLM and organic acids. By thermal analysis, it was confirmed that multi-component solid forms of VLM were thermodynamically more stable than VLM itself. Through dynamic vapor sorption (DVS) experiments, it was found that three multi-component solid forms of VLM had lower hygroscopicity than VLM itself. Furthermore, the intrinsic dissolution rate of VLM and its multi-component forms was determined in one kind of acidic aqueous medium by using UV-vis spectrometry. It was found that the three multi-component solid forms of VLM dissolved faster than VLM itself.


2020 ◽  
Vol 10 (20) ◽  
pp. 7329
Author(s):  
Srikanth Vuppala ◽  
Marco Stoller

In this study, a synthetic phenol solution of water and raw olive mill wastewater (OMW) were considered to achieve purification of the aqueous streams from pollutants. Only OMW was initially submitted to a coagulation/flocculation process, to reduce the turbidity, phenols, and chemical oxygen demand (COD). This first treatment appeared to be mandatory in order to remove solids from wastewater, allowing the successive use of laboratory-made core-shell nanocomposites. In detail, the optimal coagulant concentration, i.e., chitosan, was 500 mg/L, allowing a reduction of the turbidity and the COD value by 90% and 33%, respectively. After this, phenol wastewater was tested for photocatalysis and then OMW was treated by employing the laboratory-made nanocomposites in a photoreactor equipped with visible light sources and using optimal catalyst concentrations, which allowed for an additional 45% reduction of the COD of the OMW. In addition to this, the effect of the operating temperature was investigated on the photocatalytic process, and suitable kinetic models proposed.


2011 ◽  
Vol 694 ◽  
pp. 936-945
Author(s):  
Wu Bin ◽  
Duo Li Chai

In this study, we developed an efficient catalysis-oxidation method for the degradation of phenol in wastewater, in which the Fe3O4 nanocrystals and H2O2 were employed as catalyst and oxidation agents respectively. Firstly, Fe3O4 nanocrystal coated with PEG was prepared via an oxygenation-deposition hydrothermal method, TEM, FT-IR, BET and XRD characterization indicated that the prepared Fe3O4 nanocrystals had an average size of 26 nm and the specific surface of 35.25 m2/g. Using the prepared Fe3O4 nanocrystals as catalyst, the phenol in wastewater was efficiently degraded by H2O2. The degradability of the phenol was investigated by FT-IR, HPLC and UV–visible spectrophotometer, and the experimental results showed that the phenol was efficiently degraded by H2O2 and the Fe3O4 nanocrystals could be efficiently recycled. Finally, the possible catalytic reaction mechanisms and pathways of phenol degradation were discussed.


2015 ◽  
Vol 1119 ◽  
pp. 24-28
Author(s):  
Rey Alfred G. Rañola ◽  
Isabella Concina ◽  
Elisabetta Comini ◽  
Fortunato B. Sevilla ◽  
Giorgio Sberveglieri

A graphene/polyaniline (rGO/PANi) nanocomposite was synthesized by solution blending method and deposited on to a nylon-6 membrane via vacuum assisted self-assembly (VASA) method to fabricate a flexible material applied as a chemoresistive gas sensor for trimethylamine (TMA). The morphological and structural characterization of surfaced adsorbed polymer nanocomposite was carried out by FT-IR, SEM, UV-Vis and surface profilometry. While, electrical property was carried out by four-point probe measurement. Prepared rGO/PANi nanocomposite has a percolation threshold around 0.40% vol. fraction, with a conductivity of 8.28 S/m (rsd = 3.0%, n=3) and thickness around 38.58 μm (rsd = 7.63%, n=3. The composite sensor exhibited linear range from 45 to 230 mg/L (r2= 0.9962) and the calculated limit of detection was 25.30 mg/L. It exhibited a repeatable response to TMA gas.


2017 ◽  
Vol 41 (16) ◽  
pp. 7893-7907 ◽  
Author(s):  
Sudhakar Pichaikaran ◽  
Arumugam Pandurangan

Rh/Ni bimetallic supported bifunctional 3D porous aluminosilicate and Rh/Ni supported reduced graphene oxide (r-GO) catalysts were synthesised and their structural properties evaluated by XRD, BET-surface area, FT-IR, NH3-TPD, H2-TPR, ICP-OES, HRTEM-EDAX and XPS analysis.


2013 ◽  
Vol 7 (2) ◽  
pp. 202-209
Author(s):  
Chiu-Wen Chen ◽  
Yu-Ling Liao ◽  
Chih-Feng Chen ◽  
Cheng-Di Dong

2017 ◽  
Vol 1142 ◽  
pp. 225-229
Author(s):  
Yong Ling Pan ◽  
Chuan Guo Ma ◽  
Hua Mei Wan ◽  
De Shui Huang ◽  
Jin Xing Wang ◽  
...  

Graphene oxide (GO) was prepared by modified Hummer’s method, and reduced by solvothermal method using ethanol as the solvent and modified diethylene triamine (amine curing agent 593) as reducing agent and modifier. The effect of reduction time and temperature on the structure and conductive property of reduced graphene oxide (593-rGO) was investigated by SEM, FT-IR and XRD. The results show that the graphene modified by 593 is obviously improved in dispersibility and sedimentation stability in dichloromethane, as well as in conductivity. The optimal reduction processing is that the mass ratio of GO to 593 is 2:1, the reduction time and temperature is 6 h and 160°C, respectively.


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