scholarly journals Evaluation of Dissolved Organic Matter Removal Characteristics in GAC Adsorption Process in Drinking Water Treatment Process using LC-OCD-OND

2020 ◽  
Vol 42 (5) ◽  
pp. 239-250
Author(s):  
Heejong Son ◽  
Hoon-Sik Yoom ◽  
Chang-Dong Seo ◽  
Sang-Goo Kim ◽  
Yong-Soon Kim
Keyword(s):  
Water Treatment ◽  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Pore Volume ◽  
Adsorption Process ◽  
Pore Width ◽  
Column Test ◽  
Operation Period ◽  
Gac Adsorption

Objectives:In this study, we used liquid chromatograph-organic carbon detector-organic nitrogen detector (LC-OCD-OND) to evaluate adsorption and breakthrough characteristics of NOM fractions (biopolymers (BP), humic substances (HS), building blocks (BB) and low molecular weight organic substances (LMW-O)) according to the various characteristics of the different materials of granular activated carbons (GACs).Methods:Breakthrough characteristics, adsorption capacity and partition coefficients were evaluated by NOM fractions (BP, HS, BB, and LMW-O) using a lab-scale GAC adsorption column filled with coal-, coconut- and wood-based GAC. The GAC column test was operated with 10 minutes empty bed contact time (EBCT). The pore characteristics of each GAC were evaluated using an automated gas sorption analyzer (Autosorb iQ3, Quantachrome, USA) and the concentrations of NOM fractions in the influent and effluent were analyzed using chromatography LC-OCD-OND (Model 8, DOC-Labor, Germany).Results and Discussion:NOM adsorption capacity was evaluated for different materials of laboratory scale GAC adsorption column test. To study the adsorption behavior of individual NOM fractions according to the operation time, NOM was fractionated into BP, HS, BB and LMW-O by LC-OCD-OND, and the individual NOM fractions were quantified. Higher MW like BP was not adsorbed to GAC, in contrast, HS, BB, and LMW-O were well removed during the initial operation period, the concentrations in the effluent gradually increased as increase the operation period until reaching to the pseudo steady-state. Poor removal of BP in GAC adsorption may be a result of blocking the pores with large MW BP and hinder the access to the pores. However, in the case of HS, BB, and LMW-O, as the molecular size decreased, these organic matters easily access to the pores inside of GAC. It was confirmed through the partition coefficient that the adsorption capacity of these NOM fractions increased in proportion to the MW. In addition, in order to achieve a high NOM removal efficiency in the GAC adsorption process, not only the specific surface area, pore volume, and pore width of the GAC must be large, but also the pH<sub>zpc</sub> must be higher than the neutral pH level.Conclusions:In order to achieve a high NOM removal efficiency in the GAC adsorption process, not only the specific surface area, pore volume, and pore width of the GAC must be large, but also the pH<sub>zpc</sub> must be higher than the neutral pH level. In addition, in the NOM fractions, BP were not adsorbed to GAC, while the adsorption capacity of the remaining NOM fractions increased as the MW of the NOM fractions decreased. LMW-O was the most adsorbed, followed by BB, HS and BP. BP and HS play an important role in the membrane fouling that are introduced a lot into domestic and foreign water treatment plants. This study showed that the BP was not removed by the adsorption mechanism of the GAC process. In addition, HS was adsorbed and removed at the beginning of the operation, but the adsorption capacity of HS decreased rapidly as the operation period increased compared to other NOM fractions. Therefore, the GAC adsorption process is not expected to be an effective pre-treatment technology for reducing membrane foulants. Previous studies showed that the yields of DBPs (µmol･DBP/µmol･C) in the high MW humic and low MW non-humic fractions are similar. Therefore, it is suggested that the GAC adsorption process is more effective for DBP precursor control in water containing a larger percentage of LMW NOM.

Fuels Desulphurisation by Adsorbtion on Fe / Bentonite

2017 ◽  
Vol 68 (3) ◽  
pp. 483-486
Author(s):  
Constantin Sorin Ion ◽  
Mihaela Bombos ◽  
Gabriel Vasilievici ◽  
Dorin Bombos
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Pore Diameter ◽  
Adsorption Process ◽  
Continuous System ◽  
Gas Oil ◽  
Average Pore ◽  
Atmospheric Distillation

Desulfurisation of atmospheric distillation gasoline and gas oil was performed by adsorption process on Fe/ bentonite. The adsorbent was characterized by determining the adsorption isotherms, specific surface area, pore volume and average pore diameter. Adsorption experiments of atmospheric distillation gasoline and gas oil were performed in continuous system at 280�320oC, 5 atm and volume hourly space velocities of 1�2 h-1. The efficiency of adsorption on Fe / bentonite was better at desulphurisation of gasoline versus gas oil.

Study of the Porous Structure and High Adsorption Capacity of Biomass-Based Activated Carbon Prepared from Aspen Wood by Ferric Nitrate III Activation

2021 ◽  
Vol 15 (2) ◽  
pp. 131-144
Author(s):  
Chunjiang Jin ◽  
Huimin Chen ◽  
Luyuan Wang ◽  
Xingxing Cheng ◽  
Donghai An ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Mass Ratio ◽  
Aspen Wood ◽  
Surface Functional Groups ◽  
Wood Sawdust

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.

Investigation of the methane adsorption characteristics of marine organic-rich shale: A case study of the lower Cambrian Niutitang Shale in the Fenggang block, northern Guizhou Province, South China

2018 ◽  
Vol 6 (4) ◽  
pp. T819-T833 ◽  
Author(s):  
Yang Gu ◽  
Wenlong Ding ◽  
Min Yin ◽  
Ruyue Wang ◽  
Baocheng Jiao ◽  
...  
Keyword(s):  
Specific Surface ◽  
Pore Size ◽  
Adsorption Capacity ◽  
Surface Area ◽  
South China ◽  
Pore Volume ◽  
Lower Cambrian ◽  
Methane Adsorption ◽  
Guizhou Province ◽  
Average Value

The marine shale in South China has great gas exploration potential, and exploration in the Sichuan Basin has been successful, but the degree of exploration remains low in the Guizhou Province. We used organic geochemical analyses (total organic carbon content and kerogen type), scanning electron microscopy (SEM), field emission SEM, nuclear magnetic resonance (NMR), X-ray diffraction analysis, and low-temperature [Formula: see text] and [Formula: see text] adsorption experimental methods to study the micropore types and pore structures and their effects on the methane adsorption capacity of organic-rich shales found in the Fenggang block in northern Guizhou Province. The results indicate that the microscopic surface porosity of the lower Cambrian Niutitang Formation ranges from 2.88% to 5.34%, with an average value of 3.86%. Based on nitrogen adsorption methods, the range of the average pore size distribution is 4.6–9.491 nm, with an average value of 6.68 nm. All of the samples exhibit significant unimodal distributions. The main pore size is less than 10 nm, and these pores account for most of the mesopore volume, which is generally consistent with the NMR results. The methane adsorption capacity of the shale samples gradually increases in the range of 0–8 MPa at 30°C and reaches a maximum at approximately 10 MPa. Positive correlations were found between the gas content and specific surface area, total pore volume, and micropore volume. These strong correlations indicate that the Niutitang Shale has a high specific surface area, a high pore volume, and narrow-diameter pores, demonstrating that it has a high gas adsorption capacity. The results of this study provide valuable information regarding the adsorption characteristics of marine shales and the factors that affect those characteristics.

scholarly journals Adsorption of Ammonium Nitrogen from Aqueous Solution on Chemically Activated Biochar Prepared from Sorghum Distillers Grain

2019 ◽  
Vol 9 (23) ◽  
pp. 5249 ◽  
Author(s):  
Derlin Hsu ◽  
Changyi Lu ◽  
Tairan Pang ◽  
Yuanpeng Wang ◽  
Guanhua Wang
Keyword(s):  
Aqueous Solution ◽  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Adsorption Process ◽  
Ammonium Nitrogen ◽  
Activated Biochar ◽  
Distillers Grain ◽  
Kinetics And Isotherms

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.

scholarly journals Polyamide-6 surface cracked forms nanofibers: A novel way for increasing the surface roughness, and porosity

2021 ◽  
Author(s):  
Sedigheh Aghayari
Keyword(s):  
Surface Roughness ◽  
Water Treatment ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Polyamide 6 ◽  
Bet Method ◽  
Before And After ◽  
The Web

Abstract Here away used to reduce the porosity of the nanofibers, which is removing PVA nanofibers from PVA/PA6 nanofibers by water treatment. Measuring the porosity of the electrospun web before and after treatment by the BET method proved this. The specific surface area of the web was 60 % reduced after water treatment. Surface roughness and pore volume have reduced after water treatment. Also, I introduced BET as the method for measuring the diameters of mesopores (or lower than 100nm). I used BET to prove that the cracks can make mesopores on the nanofibers.

scholarly journals The influence factors for gas adsorption with different ranks of coals

2017 ◽  
Vol 36 (3-4) ◽  
pp. 904-918 ◽  
Author(s):  
Deyong Guo ◽  
Xiaojie Guo
Keyword(s):  
Moisture Content ◽  
Specific Surface ◽  
Pore Structure ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Gas Adsorption ◽  
Total Pore Volume ◽  
Factors Influencing

In this paper, scanning electron microscopy, low-temperature N2 adsorption and CH4 isothermal adsorption experiments were performed on 11 coal samples with Ro,max between 0.98 and 3.07%. The pore structure characteristics of coals (specific surface area, total volume distribution) were studied to assess the gas adsorption capacity. The results indicate that there is significant heterogeneity on coal surface, containing numerous channel-like pores, bottle-shaped pores and wedge-shaped pores. Both Langmuir volume (VL) and Langmuir pressure (PL) show a stage change trend with the increase of coalification degree. For different coalification stages, there exist different factors influencing the VL and PL values. For low-rank coals (Ro,max < 1.1%), the increase of VL values and decrease of PL values are mainly due to the abundant primary pore and fracture within coal. For middle-rank coals (1.1% < Ro,max < 2.1%), the moisture content, vitrinite content and total pore volume are all the factors influencing VL, and the reduction of PL is mainly attributed to the decrease of moisture content and inertinite content. Meanwhile, this result is also closely related to the pore shape. For high-rank coals (Ro,max > 2.1%), VL values gradually increase and reach the maximum. When the coal has evolved into anthracite, liquid hydrocarbon within pore begins pyrolysis and gradually disappears, and a large number of macropores are converted into micropores, leading to the increase of specific surface area and total pore volume, corresponding to the increase of VL. In addition, the increase of vitrinite content within coal also contributes to the increase of VL. PL, reaches the minimum, indicating that the adsorption rate reaches the largest at the low pressure stage. The result is mainly controlled by the specific surface area and total pore volume of coal samples. This research results will provide a clearer insight into the relationship between adsorption parameters and coal rank, moisture content, maceral composition and pore structure, and it is of great significance for better assessing the gas adsorption capacity.

The Adsorption/Desorption Dynamics Properties of N-Alkanes in Light Naphtha on 5A Zeolites

2013 ◽  
Vol 807-809 ◽  
pp. 2643-2646
Author(s):  
Xiang Ji ◽  
Qing Sheng Zhang ◽  
Qun Cui ◽  
Hai Yan Wang
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Fixed Bed ◽  
Light Naphtha ◽  
Bet Specific Surface Area ◽  
Purge Gas ◽  
Adsorption Desorption

Self-made JH4 zeoite was characterized by BET, mercury and other methods. The dynamic adsorption capacity of nC5/nC6 in light naphtha on JH4 zeolite fixed bed was investigated. The effect of cyclic purge exhaust composition, which simulate different condensation conditions, on desorption performance of JH4 zeolite bed was studied. The results shows that, the microporous BET specific surface area and pore volume of JH4 zeolite is 710.05 m2/g and 0.32 cm3/g; macropore specific surface area and pore volume is 3.64 m2/g and 0.29 cm3/g, respectively. Under the adsorption conditions of 0.1 MPa, 165 °C, adsorption capacity of n-pentane and n-hexane in light naphtha on JH4 zeolite reaches, 7.24 g/100gadsand 3.11 g/100gadsrespectively.If the content of pentane and hexane achieves 3.68% and 0.21% in nitrogen purge gas, total desorption amount of JH4 zeolite is 2.07 g/100gads, falling 60.19% than that of pure N2purge.

scholarly journals Nanometer Pore Structure Characterization of Taiyuan Formation Shale in the Lin-Xing Area Based on Nitrogen Adsorption Experiments

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 298
Author(s):  
Chenlong Ding ◽  
Jinxian He ◽  
Hongchen Wu ◽  
Xiaoli Zhang
Keyword(s):  
Specific Surface ◽  
Pore Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
Shale Gas ◽  
Pore Volume ◽  
Ordos Basin ◽  
Total Pore Volume ◽  
Nitrogen Adsorption ◽  
Taiyuan Formation

Ordos Basin is an important continental shale gas exploration site in China. The micropore structure of the shale reservoir is of great importance for shale gas evaluation. The Taiyuan Formation of the lower Permian is the main exploration interval for this area. To examine the nanometer pore structures in the Taiyuan Formation shale reservoirs in the Lin-Xing area, Northern Shaanxi, the microscopic pore structure characteristics were analyzed via nitrogen adsorption experiments. The pore structure parameters, such as specific surface area, pore volume, and aperture distribution, of shale were calculated; the significance of the pore structure for shale gas storage was analyzed; and the main controlling factors of pore development were assessed. The results indicated the surface area and hole volume of the shale sample to be 0.141–2.188 m2/g and 0.001398–0.008718 cm3/g, respectively. According to the IUPAC (International Union of Pure and Applied Chemistry) classification, mesopores and macropores were dominant in the pore structure, with the presence of a certain number of micropores. The adsorption curves were similar to the standard IV (a)-type isotherm line, and the hysteresis loop type was mainly similar to H3 and H4 types, indicating that most pores are dominated by open type pores, such as parallel plate-shaped pores and wedge-shaped slit pores. The micropores and mesopores provide the vast majority of the specific surface area, functioning as the main area for the adsorption of gas in the shale. The mesopores and macropores provide the vast majority of the pore volume, functioning as the main storage areas for the gas in the shale. Total organic carbon had no notable linear correlation with the total pore volume and the specific surface area. Vitrinite reflectance (Ro) had no notable correlation with the specific surface area, but did have a low “U” curve correlation with the total pore volume. There was no relationship between the quartz content and specific surface area and total pore volume. In addition, there was no notable correlation between the clay mineral content and total specific surface area and total pore volume.

scholarly journals Titanium Carbide Nanocrystals Synthesized from a Metatitanic Acid-Sucrose Precursor via a Carbothermal Reduction

2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Hyunho Shin ◽  
Jun-Ho Eun
Keyword(s):  
Process Control ◽  
Titanium Carbide ◽  
Specific Surface ◽  
Surface Area ◽  
Pore Volume ◽  
Carbothermal Reduction ◽  
Crystal Size ◽  
Reduction Process ◽  
Specific Pore Volume ◽  
Metatitanic Acid

A TiC powder is synthesized from a micron-sized mesoporous metatitanic acid-sucrose precursor (precursor M) by a carbothermal reduction process. Control specimens are also prepared using a nanosized TiO2-sucrose precursor (precursor T) with a higher cost. When synthesized at 1500°C for 2 h in flowing Ar, the characteristics of the synthesized TiC from precursor M are similar to those of the counterpart from precursor T in terms of the crystal size (58.5 versus 57.4 nm), oxygen content (0.22 wt% versus 0.25 wt%), and representative sizes of mesopores: approximately 2.5 and 19.7–25.0 nm in both specimens. The most salient differences of the two specimens are found in the TiC from precursor M demonstrating (i) a higher crystallinity based on the distinctive doublet peaks in the high-two-theta XRD regime and (ii) a lower specific surface area (79.4 versus 94.8 m2/g) with a smaller specific pore volume (0.1 versus 0.2 cm3/g) than the counterpart from precursor T.

The relationship between geotechnical index properties and the pore-size distribution of compacted clayey silts

2015 ◽  
Vol 22 (6) ◽  
Author(s):  
Nazile Ural
Keyword(s):  
Specific Surface ◽  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Correlation Coefficients ◽  
Liquid Limit ◽  
Index Properties

AbstractIn this study, the relationships between geotechnical index properties and the pore-size distribution of compacted natural silt and artificial soil mixtures, namely, silt with two different clays and three different clay percentages (10%, 20%, and 40%), were examined and compared. Atterberg’s limit tests, standard compaction tests, mercury intrusion porosimetry, X-ray diffraction, scanning electron microscopy (SEM) analysis, and Brunauer-Emmett-Teller specific surface analysis were conducted. The results show that the liquid limit, the cumulative pore volume, and specific surface area of artificially mixed soils increase with an increase in the percentage of clay. The cumulative pore volume and specific surface area with geotechnical index properties were compared. High correlation coefficients were observed between the specific areas and both the liquid limit and the plasticity index, as well as between the cumulative pore volume and both the clay percentage and the

Sign in / Sign up

Export Citation Format

Share Document