SURFACE MODIFICATIONS OF ACTIVATED CARBON AND ITS IMPACT ON APPLICATION

2019 ◽  
Vol 26 (01) ◽  
pp. 1830006 ◽  
Author(s):  
MATHEUS PEGO ◽  
JANAÍNA CARVALHO ◽  
DAVID GUEDES
Keyword(s):  
Surface Modification ◽  
Activated Carbon ◽  
Surface Chemistry ◽  
Surface Structure ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Surface Modifications ◽  
Hazardous Substances ◽  
Carbon Surface ◽  
Corona Treatment

The main and new surface modification methods of activated carbon (AC) and their influence on application (adsorption capacity) were reviewed. Adsorption capacity is an important issue, contributing to hazardous substances environment management. According to literature, it is true that surface chemistry strongly affects adsorption capacity. Surface chemistry can be modified by several methods that lead to different activated carbon properties. Furthermore, adsorbate properties, and their relationships with surface structure, can impact adsorption properties. Surface modifications can be conducted by adding some atoms to the surface structure, making the surface more acidic or basic. Introduction of oxygen and ammonia atoms (chemical modification) are the main processes to make the surface more acidic and basic, respectively, although may bring chemical wastes to environment. Surface modification is done by chemical and physical modifications that lead activated carbons to present different properties. The main and new methods of chemical and physical modifications are compared and presented in this paper. Some new physical methods, like corona treatment, plasma discharge and microwave radiation, can be applied to cause surface modifications. Corona treatment can be a practical and new way to cause surface modification on an activated carbon surface.

scholarly journals Effect of Different Treatment on the Adsorption of p-Cresol by Activated Carbon

2017 ◽  
Vol 5 (1) ◽  
pp. 55 ◽  
Author(s):  
Sirous Nouri
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Molecular Form ◽  
Carbon Surface ◽  
Ionic Form ◽  
Freundlich Model ◽  
London Dispersion ◽  
Carbon Change ◽  
London Dispersion Forces

<p>Adsorption of p-Cresol by three activated carbons (one untreated and two treated) was carried out at 301 K and at controlled pH conditions. By treating the activated carbon the PZC and adsorption capacity (Q<sub>max</sub>) of carbon change. The adsorption capacity of each carbon, by using the homogenous Langmuir-Freundlich model, was found to comparing the effect of different treatment. At pH lower than pK<sub>a</sub> of p-cresol (molecular form), it was observed that the electron density of aromatic ring and also those of the carbon surface, are the main forces involved in the adsorption process, by affecting the extent of London dispersion forces. Treating by H<sub>2</sub> increase the PZC and treating by H<sub>2</sub>SO<sub>4</sub> decrease this factor. At higher pH (in ionic form), it was found that the electrostatic forces played a significant role on the extent of adsorption. In this condition the adsorption of the solute dependent on the concentration of anionic form of the solute. The effect of pH must be considered from its combined effects on the carbon surface and on the solute molecules. It was found that the uptake of the molecular form of the aromatic solute was dependent on the PZC of the carbon.</p>

scholarly journals Synergy Effect of Nitrogen and Molybdenum on Activated Carbon Matrix for Selective Adsorptive Desulfurization: Insights into Surface Chemistry Modification

2021 ◽  
Author(s):  
Musa O Azeez ◽  
Abdulkadir Tanimu ◽  
Khalid Alhooshani ◽  
Saheed A. Ganiyu
Keyword(s):  
Activated Carbon ◽  
Surface Chemistry ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Photoelectron Spectroscopy ◽  
Pore Volume ◽  
Carbon Surface ◽  
Synergy Effect ◽  
Adsorptive Desulfurization ◽  
X Ray

Abstract This study reports the synthesis of mesoporous metal-modified nitrogen doped activated carbon (AC-N-Mo) from date seeds by ZnCl2 activation and its applicability for selective adsorptive desulfurization of dibenzothiophene (DBT). The AC-N-Mo exhibits higher adsorption capacity for DBT at 100 mg-S/L with the maximum value of 99.7% corresponding to 19.94 mg-S/g at room temperature than the unmodified carbon with 17.96 mg-S/g despite its highest surface area and pore volume of 1027 m2g− 1 and 0.55 cm3g− 1 respectively. The adsorption capacity breakthrough follows the order AC-N-Mo > AC-Mo > AC > AC-N. AC-N-Mo also displayed excellent selectivity in the presence of aromatics (toluene, naphthalene and 1-methylisoquinoline). The enhancement in the DBT uptake capacities of AC-N-Mo is attributed to synergy effect of nitrogen heteroatom that aid well dispersion of molybdenum nanoparticles on carbon surface thereby improving its surface chemistry and promising textural characteristics. The kinetic studies showed that the DBT adsorption proceeds via pseudo-second order kinetics while the isotherm revealed that both Freundlich and Langmuir fit the data but Freundlich fit the data more accurately for the best performing adsorbent. The physico-chemical properties (surface area, pore volume, carbon content, particle size etc.) of as-prepared adsorbents namely; AC, AC-N, AC-N-Mo and AC-Mo were characterized by N2- physisorption, X-ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Spectroscopy/Energy Dispersive Spectroscopy (SEM/EDS), Raman Spectroscopy (RS), Fourier Transform Infrared Spectroscopy (FTIR) and Ammonia-Temperature-Programmed Desorption (NH3-TPD).

scholarly journals Modification of the surface chemistry of activated carbon and its influence on methylene blue adsorption

2018 ◽  
Vol 5 (1) ◽  
pp. 374
Author(s):  
David Wibowo ◽  
Lanny Setyadhi ◽  
Suryadi Ismadji
Keyword(s):  
Methylene Blue ◽  
Activated Carbon ◽  
Surface Chemistry ◽  
Activated Carbons ◽  
Surface Acidity ◽  
Carbon Surface ◽  
Point Of Zero Charge ◽  
Titration Method ◽  
Zero Charge ◽  
Boehm Titration

The adsorption behavior of activated carbons is determined not only by their porous structures but also by the chemical nature of its surface. The surface chemistry of activated carbons can be selectively modified in order to improve their adsorption capacity. In this study, a NORIT granular activated carbon was treated by oxidant (HNO3) and non-oxidant acid (HCI) at different concentrations and temperatures. The surface chemistries of the materials were characterized by Boehm titration method and by the determination of the point of zero charge (pHPZC).The adsorption properties of the selected samples were studied by adsorption of methylene blue, which is one of the important dyes and found in many textile effluents. In addition, the pore structures of the modified carbons were also studied by argon adsorption at 87.29 K. As results, it was observed that both HN03 and HCI treatments could increase the surface acidity of activated carbons. Activated carbons modified by HCI gave the best performance on the adsorption of methylene blue.Keywords: Activated Carbon, Surface Chemistry, Chemical Treatment, Boehm Titration Method, Adsorption AbstrakKemampuan adsorpsi karbon akti.ftidak hanya ditentukan oleh struktur pori tetapijuga dipengaruhi oleh sifat kimia dari permukaannya. Sifat kimia permukaan karbon aktif dapat secara selektif dimodifikasi dengan tujuan untuk lebih meningkatkan kapasitas adsorpsinya. Pada penelitian ini, karbon aktif NORIT granular ditreatment dengan menggunakan asam oksidator (HNO) dan non-oksidator (HCI) pada berbagai konsentrasi dan suhu. Sifat kimia permukaan karbon aktif dikarakterisasi dengan menggunakan metode titrasi Boehm serta dengan penentuan point of zero charge (pHPZC). Kemampuan adsorpsinya diuji dengan mengadsorp larutan methylene blue, dimana methylene blue merupakan salah satu komponen dalam limbah tekstil. Sedangkan struktur pori karbon aktif dianalisa dengan adsorpsi Ar pada suhu 87,29 K. Penelitian ini menunjukkan bahwa baik treatment dengan HNO3 maupun HCI dapat mengakibatkan terjadinya peningkatan sifat asam pada permukaan karbon aktif. Karbon aktif yang diberi perlalatan dengan HCI memberikan kemampuan adsorpsi yang paling baik dalam adsorpsi larutan methylen biru.Kata Kunci: Karbon Aktif, Sifat Kimia Permukaan, Perlakuan dengan Larutan Kimia, Metode Titrasi Boehm, Adsorpsi

scholarly journals The influence of active carbon contaminants on the ozonation mechanism interpretation

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lilla Fijołek ◽  
Joanna Świetlik ◽  
Marcin Frankowski
Keyword(s):  
Activated Carbon ◽  
Active Carbon ◽  
Alkali Metals ◽  
Activated Carbons ◽  
Carbon Surface ◽  
Bulk Solution ◽  
Ozone Decomposition ◽  
Reaction Products ◽  
Treatment Technology ◽  
Carbon Impurities

AbstractIn water treatment technology, activated carbons are used primarily as sorbents to remove organic impurities, mainly natural organic matter, but also as catalysts in the ozonation process. Commercially available activated carbons are usually contaminated with mineral substances, classified into two main groups: alkali metals (Ca, Na, K, Li, Mg) and multivalent metals (Al, Fe, Ti, Si). The presence of impurities on the carbon surface significantly affects the pHpzc values determined for raw and ozonated carbon as well as their acidity and alkalinity. The scale of the observed changes strongly depends on the pH of the ozonated system, which is related to the diffusion of impurities from the carbon to the solution. In an acidic environment (pH 2.5 in this work), the ozone molecule is relatively stable, yet active carbon causes its decomposition. This is the first report that indirectly indicates that contaminants on the surface of activated carbon (multivalent elements) contribute to the breakdown of ozone towards radicals, while the process of ozone decomposition by purified carbons does not follow the radical path in bulk solution. Carbon impurities also change the distribution of the reaction products formed by organic pollutants ozonation, which additionally confirms the radical process. The study showed that the use of unpurified activated carbon in the ozonation of succinic acid (SA) leads to the formation of a relatively large amount of oxalic acid (OA), which is a product of radical SA degradation. On the other hand, in solutions with purified carbon, the amount of OA generated is negligible.

scholarly journals Pinecone-Derived Activated Carbons as an Effective Medium for Hydrogen Storage

Energies ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2237
Author(s):  
Sara Stelitano ◽  
Giuseppe Conte ◽  
Alfonso Policicchio ◽  
Alfredo Aloise ◽  
Giovanni Desiderio ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Hydrogen Storage ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Hydrogen Adsorption ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Textural Properties ◽  
Biomass Waste ◽  
Wavelength Dispersive Spectrometry

Pinecones, a common biomass waste, has an interesting composition in terms of cellulose and lignine content that makes them excellent precursors in various activated carbon production processes. The synthesized, nanostructured, activated carbon materials show textural properties, a high specific surface area, and a large volume of micropores, which are all features that make them suitable for various applications ranging from the purification of water to energy storage. Amongst them, a very interesting application is hydrogen storage. For this purpose, activated carbon from pinecones were prepared using chemical activation with different KOH/precursor ratios, and their hydrogen adsorption capacity was evaluated at liquid nitrogen temperatures (77 K) at pressures of up to 80 bar using a Sievert’s type volumetric apparatus. Regarding the comprehensive characterization of the samples’ textural properties, the measurement of the surface area was carried out using the Brunauer–Emmett–Teller method, the chemical composition was investigated using wavelength-dispersive spectrometry, and the topography and long-range order was estimated using scanning electron microscopy and X-ray diffraction, respectively. The hydrogen adsorption properties of the activated carbon samples were measured and then fitted using the Langmuir/ Töth isotherm model to estimate the adsorption capacity at higher pressures. The results showed that chemical activation induced the formation of an optimal pore size distribution for hydrogen adsorption centered at about 0.5 nm and the proportion of micropore volume was higher than 50%, which resulted in an adsorption capacity of 5.5 wt% at 77 K and 80 bar; this was an increase of as much as 150% relative to the one predicted by the Chahine rule.

Adsorption of Soluble Metal Ions from Red Mud by Modified Activated Carbon

2008 ◽  
Vol 368-372 ◽  
pp. 1541-1544 ◽  
Author(s):  
Hua Lei Zhou ◽  
Dong Yan Li ◽  
Guo Zhuo Gong ◽  
Ya Jun Tian ◽  
Yun Fa Chen
Keyword(s):  
Activated Carbon ◽  
Metal Ions ◽  
Adsorption Capacity ◽  
Red Mud ◽  
Activated Carbons ◽  
Valuable Metal ◽  
Surface Areas ◽  
Alumina Industry ◽  
Modified Activated Carbons ◽  
Almost All

Activated carbon was employed as the adsorption carrier for the metal ions in HCl solution of red mud, a solid waste produced in alumina industry. To improve the adsorption capacity to valuable metal ions, the activated carbon was modified by chemicals including HNO3, H2O2, H2SO4, H3PO4, NH3, Na2CO3, and tri-butyl phosphate (TBP). It was found that the modifications contributed the high adsorption capacity to almost all metal ions we focused on. In the case of TBP, remarkably higher adsorption capacity and selectivity of Sc3+ was observed. The correlation between the surface areas, IR spectra of those chemically modified activated carbons and adsorption was schemed.

Modification of Activated Carbon and its Application on Adsorption of UDMH Gas

2013 ◽  
Vol 634-638 ◽  
pp. 1026-1030 ◽  
Author(s):  
Huan Chun Wang ◽  
Xiao Li Gou ◽  
Xiao Meng Lv
Keyword(s):  
Activated Carbon ◽  
High Temperature ◽  
Transition Metal ◽  
Surface Structure ◽  
Functional Groups ◽  
Room Temperature ◽  
Activated Carbons ◽  
Metal Solution ◽  
Modified Activated Carbons

Two kinds of modified activated carbons were prepared by dipping with Zn(NO3)2 solution and by reducing in the atmosphere of N2 at high temperature respectively, which were characterized by FTIR,DSC,SEM and EDS. The surface structure was strongly changed in the process, along with the changes of chemical functional groups. The results of adsorption experiments revealed that the adsorbent capacities of UDMH gas at room temperature were enhanced obviously by modification compared with the raw activated carbon, especially dipped by transition metal solution. The mechanism probably involved was also discussed.

scholarly journals Various Impregnation Methods Used for the Surface Modification of the Adsorbent: A Review

2018 ◽  
Vol 7 (4.7) ◽  
pp. 330 ◽  
Author(s):  
C. R. Girish ◽  
. .
Keyword(s):  
Surface Modification ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Surface Properties ◽  
Chemical Treatment ◽  
Water Contamination ◽  
Recent Time ◽  
Operating Conditions ◽  
Physical Chemical

The water contamination is an important crisis which is to be addressed in the recent time. The pollutants present in wastewater are treated by adsorption using activated carbon, which is considered as one of the effective method. The adsorbent has to be modified to improve the adsorption capacity and the surface properties. Various methods such as physical, chemical treatment, impregnation and functionalization techniques are available. Impregnation is one of the effective method carried out for surface modification and to increase the adsorption capacity. Therefore, current study investigates the different impregnation methods used for the surface modification of the adsorbent. It also reviews the various precursors used for adsorbent preparation, the impregnating agent, the operating conditions and the adsorption capacity of the adsorbent.  

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