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Sample records for monolayer adsorption capacity

  1. Adsorption of Ions at Uncharged Insoluble Monolayers

    Science.gov (United States)

    Peshkova, T. V.; Minkov, I. L.; Tsekov, R.; Slavchov, R. I.

    2016-08-01

    A method is proposed for the experimental determination of the adsorption of inorganic electrolytes at a surface covered with insoluble surfactant monolayer. This task is complicated by the fact that the change of the salt concentration alters both chemical potentials of the electrolyte and the surfactant. Our method resolves the question by combining data for the surface pressure versus area of the monolayer at several salt concentrations with data for the equilibrium spreading pressure of crystals of the surfactant (used to fix a standard state). We applied the method to alcohols spread at the surface of concentrated halide solutions. The measured salt adsorption is positive and has nonmonotonic dependence on the area per surfactant molecule. For the liquid expanded film, depending on the concentration, there is one couple of ions adsorbed per each 3–30 surfactant molecules. We analyzed which ion, the positive or the negative, stands closer to the surface, by measuring the effect of NaCl on the Volta potential of the monolayer. The potentiometric data suggest that Na+ is specifically adsorbed, while Cl– remains in the diffuse layer, i.e., the surface is positively charged. The observed reverse Hofmeister series of the adsorptions of NaF, NaCl, and NaBr suggests the same conclusion holds for all these salts. The force that causes the adsorption of Na+ seems to be the interaction of the ion with the dipole moment of the monolayer.

  2. Oxygen adsorption on palladium monolayer as a surface catalyst

    Science.gov (United States)

    Shah, Janki; Kansara, Shivam; Gupta, Sanjeev K.; Sonvane, Yogesh

    2017-09-01

    In the recent work, we study on the structural and electronic properties of the graphene like Pd monolayer with the adsorption of oxygen adatoms by using first-principles calculations. The electronic band structure and projected density of states investigate that Pd-surface with oxygen molecule adsorption gives metallic behaviour. We found that the behaviour changed at M-point in the electronic band structure as adding oxygen atoms. The oxygen adsorption was dissociative until the Pd surface immersed with oxygen atoms. The electron charge density increases as the number of oxygen atoms on Pd-surface increases. The noticeable observation is that by adding 7th oxygen atom, they started to ripple from fixed Pd-surface without making a bond due to oxygen coverage increases. The results show that Pd monolayer has different applications as a oxygen catalyst and it can be utilized as the pellet, surface, and film materials to safeguard sustenance from oxidation.

  3. Mono-layer BC2 a high capacity anode material for Li-ion batteries

    Science.gov (United States)

    Hardikar, Rahul; Samanta, Atanu; Han, Sang Soo; Lee, Kwang-Ryeol; Singh, Abhishek

    2015-04-01

    Mono-layer of graphene with high surface area compared to the bulk graphite phase, shows less Li uptake. The Li activity or kinetics can be modified via defects and/or substitutional doping. Boron and Nitrogen are the best known dopants for carbonaceous anode materials. In particular, boron doped graphene shows higher capacity and better Li adsorption compared to Nitrogen doped graphene. Here, using first principles density functional theory calculations, we study the spectrum of boron carbide (BCx) mono-layer phases in order to estimate the maximum gravimetric capacity that can be achieved by substitutional doping in graphene. Our results show that uniformly boron doped BC2 phase shows a high capacity of? 1400 mAh/g, much higher than previously reported capacity of BC3. Supported by Korea Institute of Science and Technology.

  4. Adsorption of anionic polyelectrolytes to dioctadecyldimethylammonium bromide monolayers

    Science.gov (United States)

    Engelking, J.; Menzel, H.

    Monolayers of dioctadecyldimethylammonium bromide (DODA) at the air/water interface were used as model for charged surfaces to study the adsorption of anionic polyelectrolytes. After spreading on a pure water surface the monolayers were compressed and subsequently transferred onto a polyelectrolyte solution employing the Fromherz technique. The polyelectrolyte adsorption was monitored by recording the changes in surface pressure at constant area. For poly(styrene sulfonate) and carboxymethylcellulose the plot of the surface pressure as function of time gave curves which indicate a direct correlation between the adsorbed amount and surface pressure as well as a solely diffusion controlled process. In the case of rigid rod-like poly(p-phenylene sulfonate)s the situation is more complicated. Plotting the surface pressure as function of time results in a curve with sigmoidal shape, characterized by an induction period. The induction period can be explained by a domain formation, which can be treated like a crystallization process. Employing the Avrami expression developed for polymer crystallization, the change in the surface pressure upon adsorption of rigid rod-like poly(p-phenylene sulfonate)s can be described.

  5. Bovine and human insulin adsorption at lipid monolayers: a comparison

    Directory of Open Access Journals (Sweden)

    Sergio eMauri

    2015-07-01

    Full Text Available Insulin is a widely used peptide in protein research and it is utilised as a model peptide to understand the mechanics of fibril formation, which is believed to be the cause of diseases such as Alzheimer and Creutzfeld-Jakob syndrome. Insulin has been used as a model system due to its biomedical relevance, small size and relatively simple tertiary structure. The adsorption of insu lin on a variety of surfaces has become the focus of numerous studies lately. These works have helped in elucidating the consequence of surface/protein hydrophilic/hydrophobic interaction in terms of protein refolding and aggregation. Unfortunately, such model surfaces differ significantly from physiological surfaces. Here we spectroscopically investigate the adsorption of insulin at lipid monolayers, to further our understanding of the interaction of insulin with biological surfaces.In particular we study the effect of minor mutations of insulin’s primary amino acid sequence on its interaction with 1,2-Dipalmitoyl-sn-glycero-3-phosphoglycerol (DPPG model lipid layers. We probe the structure of bovine and human insulin at the lipid/water interface using sum frequency generation spectroscopy (SFG. The SFG experiments are complemented with XPS analysis of Langmuir-Schaefer deposited lipid/insulin films. We find that bovine and human insulin, even though very similar in sequence, show a substantially different behavior when interacting with lipid films.

  6. Anion Adsorption on an Au Colloid Monolayer Based Cysteamine-Modified Gold Electrode

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Anion adsorption behavior on Au colloid surface was investigated in virture of depositing monolayers of Au colloid on the self-assembled monolayers of cysteamine on a gold electrode. Po tential-dependent anion adsorption-desorption waves via the nonfaradaic current were obtained by means of cyclic voltammetry at Au colloid-modified gold electrodes in the potential range of -200-600 mV. The adsorption sequence in the order of adsorption peak potentials(Epa) is OH->citrate3->H2PO4->Cl->SO42->ClO4->NO3-. Among them, citrate3-exhibited an en tirely irreversible adsorption. A rise in temperature can increase the rates of adsorption-desorp tion and improve the reversibility of the adsorption-desorption of CI-, SO24-, CIO4-, NO3- and H2PO4-. The adsorption peak potentials shifted more negatively for ca. 63 mV as the anion con centrations were increased by a decade factor. The change of pH from 7 to 1 slightly affected the adsorption peak potentials of Cl- and NO3-. Au colloids with a smaller size (16 nm) gave rise to a better reversibility of the adsorption-desorption process and lower adsorption currents. The ex perimental results of citrate ions adsorption on Au colloid surface show that Au colloids with a smaller size prepared by sodium citrate method exhibited a higher stability in the solution in com parison to those with larger sizes because of its higher ratio of charge/mass. In other words, the smaller gold nanoparticles are covered with citrate ions monolayer that can also be formed at larg er gold nanoparticles by means of electrochemical scan.

  7. Study of polystyrene-poly(ethylene oxide) diblock copolymer monolayers as barriers to protein adsorption

    Science.gov (United States)

    Jogikalmath, Gangadhar

    Protein adsorption resistant surfaces find use in many biomedical applications, such as catheters, dialysis devices and biosensors that involve blood contacting surfaces. To ensure long-term functioning of a device in an environment containing protein, there is a need to produce homogeneous surfaces that are resistant to protein adsorption. A polymer brush covered surface, produced by either physical adsorption or chemical grafting of hydrophilic polymers to surfaces, is one of the approaches used in creating such surfaces. High grafting densities needed to make an effective barrier are usually not realized in chemical grafting/adsorption from solution, due to self-exclusion of surface grafted molecules. In this dissertation polymer brush surfaces formed by chemically grafted PEO molecules and transferred monolayers of PS-b-PEO diblock copolymers are investigated using atomic force microscopy (AFM), surface plasmon resonance (SPR) and surface pressure measurement techniques. An AFM adhesion mapping technique was used to evaluate the surface heterogeneity of chemically modified PEO and transferred diblock copolymer monolayer surfaces. The behavior of PS-b-PEO molecules at the air-water interface was studied using Langmuir trough. The stability of transferred diblock copolymer monolayers was investigated using AFM. Using SPR, protein adsorption to the diblock copolymer layers was investigated as a function of protein size (using HSA and ferritin) as a function of grafting density of PEO in the monolayer. It was seen that a lower density of the PS-b-PEO monolayer was sufficient to prevent ferritin adsorption (larger protein) while a higher density brush layer was required to achieve complete prevention of HSA adsorption to the surface. The effect of mobility of the polymer brush layer on protein adsorption prevention was analyzed using SPR and surface pressure measurements. It was seen that the copolymer monolayer (at the air-buffer interface) rearranged itself to

  8. Structural Properties and Phase Transition of Na Adsorption on Monolayer MoS2.

    Science.gov (United States)

    He, Hai; Lu, Pengfei; Wu, Liyuan; Zhang, Chunfang; Song, Yuxin; Guan, Pengfei; Wang, Shumin

    2016-12-01

    First-principles calculations are performed to investigate the structural stability of Na adsorption on 1H and 1T phases of monolayer MoS2. Our results demonstrate that it is likely to make the stability of distorted 1T phase of MoS2 over the 1H phase through adsorption of Na atoms. The type of distortion depends on the concentration of adsorbed Na atoms and changes from zigzag-like to diamond-like with the increasing of adsorbed Na atom concentrations. Our calculations show that the phase transition from 1H-MoS2 to 1T-MoS2 can be obtained by Na adsorption. We also calculate the electrochemical properties of Na adsorption on MoS2 monolayer. These results indicate that MoS2 is one of potential negative electrodes for Na-ion batteries.

  9. Adsorption of tannic acid on polyelectrolyte monolayers determined in situ by streaming potential measurements.

    Science.gov (United States)

    Oćwieja, M; Adamczyk, Z; Morga, M

    2015-01-15

    Physicochemical characteristics of tannic acid (tannin) suspensions comprising its stability for a wide range of ionic strength and pH were thoroughly investigated using UV-vis spectrophotometry, dynamic light scattering and microelectrophoretic measurements. These studies allowed to determine the hydrodynamic diameter of the tannic acid that was 1.63 nm for the pH range 3.5-5.5. For pH above 6.0 the hydrodynamic diameter significantly decreased as a result of the tannin hydrolysis. The electrophoretic mobility measurements confirmed that tannic acid is negatively charged for these values of pH and ionic strength 10(-4)-10(-2) M. Therefore, in order to promote adsorption of tannin molecules on negatively charged mica, the poly(allylamine hydrochloride) (PAH) supporting monolayers were first adsorbed under diffusion transport conditions. The coverage of polyelectrolyte monolayers was regulated by changing bulk concentration of PAH and the adsorption time. The electrokinetic characteristics of bare and PAH-covered mica were determined using the streaming potential measurements. The zeta potential of these PAH monolayers was highly positive, equal to 46 mV for ionic strength of 10(-2) M. The kinetics of tannin adsorption on these PAH supporting monolayers was evaluated by the in situ the streaming potential measurements. The zeta potential of PAH monolayers abruptly decreases with the adsorption of tannin molecules that was quantitatively interpreted in terms of the three-dimensional electrokinetic model. The acid-base characteristics of tannin monolayers were acquired via the streaming potential measurements for a broad range of pH. The obtained results indicate that it is possible to control adsorption of tannin on positively charged surfaces in order to designed new multilayer structures of desirable electrokinetic properties and stability.

  10. Self-assembly of Carboxyl Functionalized Polystyrene Nanospheres into Close-packed Monolayers via Chemical Adsorption

    Institute of Scientific and Technical Information of China (English)

    LI,Zhi-Wei(李志伟); ZHOU,Jing-Fang(周静芳); ZHANG,Zhi-Jun(张治军); DANG,Hong-Xin(党鸿辛)

    2004-01-01

    The polyacrylic acid functionalized polystyrene nanospheres were synthesized and self-assembled into irregular,densely packed monolayers in non-aqueous media. The polymer nanoparticles were chemically adhered to substrates. The morphologies of the resulting films were investigated. The impact of the volume fraction of alcohol in the mixed solvents on the particle adsorption and fabrication of nanosphere assembled films was examined.

  11. Formaldehyde molecule adsorption on the doped monolayer MoS2: A first-principles study

    Science.gov (United States)

    Ma, Dongwei; Ju, Weiwei; Li, Tingxian; Yang, Gui; He, Chaozheng; Ma, Benyuan; Tang, Yanan; Lu, Zhansheng; Yang, Zongxian

    2016-05-01

    Based on first-principles calculations, formaldehyde (H2CO) adsorption on the pristine monolayer MoS2 and that doped with Cl, P, or Si was theoretically studied to explore the potential of the MoS2 sheets as H2CO gas sensors. It is found that under Mo-rich conditions it is viable for Cl to be filled into the S vacancies acting as n-type dopant and for P and Si acting as p-type dopants. The results on the H2CO adsorption on the pristine and the Cl-doped monolayer MoS2 indicate that both are insensitive to H2CO. In contrast, H2CO exhibits strong adsorption on the P or Si-doped monolayer MoS2. And there are large electron transfer from the P or Si-doped monolayer MoS2 to the H2CO and obvious change in the electronic densities of states of both systems induced by the H2CO adsorption. These suggest that P and Si can be appropriate dopants filled into MoS2 sheets for detecting H2CO molecule.

  12. Lead adsorption capacities of different components in natural surface coatings

    Institute of Scientific and Technical Information of China (English)

    DONG De-ming; HUA Xiu-yi; LI Yu; JI Liang; ZHANG Jing-jing

    2004-01-01

    Pb adsorption capacities of Fe oxide, Mn oxide and organic materials in natural surface coatings( biofilms and associated minerals) collected in three lakes, two ponds and a river in Jilin Province, China and Cayuga Lake in US were studied. A novel extraction technique was employed to remove one or more component(s) from the surface coatings. Pb adsorption to surface coatings before and after extraction was performed to determine the adsorptive properties of the extracted component(s). The statistical analysis of observed Pb adsorption was carried out using nonlinear least squares fitting(NLSF) to estimate the Pb adsorption capacity of each component of surface coatings. For each body of water, the estimated Pb adsorption capacity of Mn oxide(mol Pb/mol Mn) was significantly higher than that of Fe oxide( mol Pb/ mol Fe). The value of estimated adsorption capacities of organic materials with the unit mol Pb per kg COD was similar to or less than that of Fe oxides with the unit mol Pb per mol Fe. Comparison of components of surface coatings in different waters showed that the estimated Pb adsorption capacities of components in surface coatings developed in different natural waters were different,especially for Mn oxides.

  13. Band-gap manipulations of monolayer graphene by phenyl radical adsorptions: a density functional theory study.

    Science.gov (United States)

    Huang, Lin; Sk, Mahasin Alam; Chen, Peng; Lim, Kok Hwa

    2014-08-25

    Phenyl radical (Ph˙) adsorption on monolayer graphene sheets is used to investigate the band-gap manipulation of graphene through density functional theory. Adsorption of a single Ph˙ on graphene breaks the aromatic π-bond and generates an unpaired electron, which is delocalized to the ortho or para position. Adsorption of a second radical at the ortho or para position saturates the radical by electron pairing and results in semiconducting graphene. Adsorption of a second radical at the ortho position (ortho-ortho pairing) is found to be more favorable than adsorption at the para position (ortho-para pairing), and the ortho-ortho pairing has stronger effects on band-gap opening compared with ortho-para pairing. Adsorption of even numbers of Ph˙ on graphene by ortho-ortho and ortho-para pairings, in general, increases the band gap. Our study shows promise of band-gap manipulation in monolayer graphene by Ph˙ adsorption, leading to potential wider applications of graphene. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. CoFe2O4@MIL-100(Fe) hybrid magnetic nanoparticles exhibit fast and selective adsorption of arsenic with high adsorption capacity

    Science.gov (United States)

    Yang, Ji-Chun; Yin, Xue-Bo

    2017-01-01

    In this study, we report the synthesis and application of mesoporous CoFe2O4@MIL-100(Fe) hybrid magnetic nanoparticles (MNPs) for the simultaneous removal of inorganic arsenic (iAs). The hybrid adsorbent had a core-shell and mesoporous structure with an average diameter of 260 nm. The nanoscale size and mesoporous character impart a fast adsorption rate and high adsorption capacity for iAs. In total, 0.1 mg L−1 As(V) and As(III) could be adsorbed within 2 min, and the maximum adsorption capacities were 114.8 mg g−1 for As(V) and 143.6 mg g−1 for As(III), higher than most previously reported adsorbents. The anti-interference capacity for iAs adsorption was improved by the electrostatic repulsion and size exclusion effects of the MIL-100(Fe) shell, which also decreased the zero-charge point of the hybrid absorbent for a broad pH adsorption range. The adsorption mechanisms of iAs on the MNPs are proposed. An Fe-O-As structure was formed on CoFe2O4@MIL-100(Fe) through hydroxyl substitution with the deprotonated iAs species. Monolayer adsorption of As(V) was observed, while hydrogen bonding led to the multi-layer adsorption of neutral As(III) for its high adsorption capacity. The high efficiency and the excellent pH- and interference-tolerance capacities of CoFe2O4@MIL-100(Fe) allowed effective iAs removal from natural water samples, as validated with batch magnetic separation mode and a portable filtration strategy. PMID:28102334

  15. CoFe2O4@MIL-100(Fe) hybrid magnetic nanoparticles exhibit fast and selective adsorption of arsenic with high adsorption capacity

    Science.gov (United States)

    Yang, Ji-Chun; Yin, Xue-Bo

    2017-01-01

    In this study, we report the synthesis and application of mesoporous CoFe2O4@MIL-100(Fe) hybrid magnetic nanoparticles (MNPs) for the simultaneous removal of inorganic arsenic (iAs). The hybrid adsorbent had a core-shell and mesoporous structure with an average diameter of 260 nm. The nanoscale size and mesoporous character impart a fast adsorption rate and high adsorption capacity for iAs. In total, 0.1 mg L‑1 As(V) and As(III) could be adsorbed within 2 min, and the maximum adsorption capacities were 114.8 mg g‑1 for As(V) and 143.6 mg g‑1 for As(III), higher than most previously reported adsorbents. The anti-interference capacity for iAs adsorption was improved by the electrostatic repulsion and size exclusion effects of the MIL-100(Fe) shell, which also decreased the zero-charge point of the hybrid absorbent for a broad pH adsorption range. The adsorption mechanisms of iAs on the MNPs are proposed. An Fe-O-As structure was formed on CoFe2O4@MIL-100(Fe) through hydroxyl substitution with the deprotonated iAs species. Monolayer adsorption of As(V) was observed, while hydrogen bonding led to the multi-layer adsorption of neutral As(III) for its high adsorption capacity. The high efficiency and the excellent pH- and interference-tolerance capacities of CoFe2O4@MIL-100(Fe) allowed effective iAs removal from natural water samples, as validated with batch magnetic separation mode and a portable filtration strategy.

  16. High capacity adsorption media and method of producing

    Science.gov (United States)

    Tranter, Troy J.; Mann, Nicholas R.; Todd, Terry A.; Herbst, Ronald S.

    2010-10-05

    A method of producing an adsorption medium to remove at least one constituent from a feed stream. The method comprises dissolving and/or suspending at least one metal compound in a solvent to form a metal solution, dissolving polyacrylonitrile into the metal solution to form a PAN-metal solution, and depositing the PAN-metal solution into a quenching bath to produce the adsorption medium. The at least one constituent, such as arsenic, selenium, or antimony, is removed from the feed stream by passing the feed stream through the adsorption medium. An adsorption medium having an increased metal loading and increased capacity for arresting the at least one constituent to be removed is also disclosed. The adsorption medium includes a polyacrylonitrile matrix and at least one metal hydroxide incorporated into the polyacrylonitrile matrix.

  17. Carboxylic acid functionalized sesame straw: A sustainable cost-effective bioadsorbent with superior dye adsorption capacity.

    Science.gov (United States)

    Feng, Yanfang; Liu, Yang; Xue, Lihong; Sun, Haijun; Guo, Zhi; Zhang, Yingying; Yang, Linzhang

    2017-08-01

    This study prepared a carboxylic functionalized bioadsorbent that met the "4-E" criteria: Efficient, Economical, Environmentally friendly, and Easily-produced. Sesame straw (Sesamum indicum L.) was functionalized through treatment with citric acid (SSCA) and tartaric acid (SSTA). The products were examined for adsorption capacity and mechanisms. Langmuir model gave the best fit for the isotherm data, and the maximum monolayer adsorption capacity of SSCA was 650mgg(-1) for methylene blue (MB). The excellent dye adsorption capacity of SSCA can be attributed to the introduction of ester groups during citric-acid modification and the tube-like structures (i.e., sesame straw cell wall remnants). At last, the cost of carboxylic acid functionalized bioadsorbents was evaluated, which showed that SSCA would be the most cost-effective bioadsorbent. Additionally, this study presents a thermo-decomposition methodology for contaminant-loaded bioadsorbent. Results showed that SSCA is probably one of the few bioadsorbents that can be produced and applied in industrial scale. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. KINETIC, ISOTHERM AND EQUILIBRIUM STUDY OF ADSORPTION CAPACITY OF HYDROGEN SULFIDE-WASTEWATER SYSTEM USING MODIFIED EGGSHELLS

    Directory of Open Access Journals (Sweden)

    O A Habeeb

    2017-05-01

    Full Text Available The studies of adsorption equilibrium isotherm and kinetics of hydrogen sulfide-water systems on calcite-based adsorbents prepared from eggshell are undertaken. The effects of operating variables such as contact time and initial concentration on the adsorption capacity of hydrogen sulfide are investigated. The modified eggshells are characterized by using different analytical approaches such as Scanning Electron Microscopy (SEM and Fourier Transform Infrared (FTIR. The batch mode adsorption process is performed at optimum removal conditions: dosage of 1 g/L, pH level of pH 6, agitation speed of 150 rpm and contact time of 14h for adsorbing hydrogen sulfide with an initial concentration of 100-500 mg/L. In the current study, the Langmuir, Freundlich, Temkin, and Dubinin models are used to predict the adsorption isotherms. Our equilibrium data for hydrogen sulfide adsorption agrees well with those of the Langmuir equation. The maximum monolayer adsorption capacity is 150.07 mg/g. Moreover, the kinetics of H2S adsorption by using the modified calcite of eggshell follows a pseudo-second-order model. From the current work, we have found that the calcite eggshell is a suitable adsorbent for H2S embeded inside the waste water. Most importantly, chicken eggshell is a waste and vastly available; hence, it could serve as a practical mean for H2S adsorption.

  19. Tobacco mosaic virus adsorption on self-assembled and Langmuir–Blodgett monolayers studied by TIRF and SFM

    OpenAIRE

    Britt, David W.; Buijs, Jos; Hlady, V.

    1998-01-01

    The adsorption of tobacco mosaic virus (TMV) on self-assembled and Langmuir–Blodgett monolayers was investigated using total internal reflection fluorescence (TIRF) spectroscopy and scanning force microscopy (SFM). Substrates were chosen to probe electrostatic, hydrophobic and surface fluidity effects on TMV adsorption. Positively charged and hydrophobic surfaces demonstrated similar initial rates of TMV adsorption; however, their respective surface TMV coverages differed greatly. Likewise, p...

  20. Adsorption behavior of Fe atoms on a naphthalocyanine monolayer on Ag(111) surface

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Linghao; Wu, Rongting; Bao, Deliang; Ren, Junhai; Zhang, Yanfang; Zhang, Haigang; Huang, Li; Wang, Yeliang; Du, Shixuan; Huan, Qing; Gao, Hong-Jun

    2015-05-29

    Adsorption behavior of Fe atoms on a metal-free naphthalocyanine (H2Nc) monolayer on Ag(111) surface at room temperature has been investigated using scanning tunneling microscopy combined with density functional theory (DFT) based calculations. We found that the Fe atoms adsorbed at the centers of H2Nc molecules and formed Fe-H2Nc complexes at low coverage. DFT calculations show that the configuration of Fe at the center of a molecule is the most stable site, in good agreement with the experimental observations. After an Fe-H2Nc complex monolayer was formed, the extra Fe atoms self-assembled to Fe clusters of uniform size and adsorbed dispersively at the interstitial positions of Fe-H2Nc complex monolayer. Furthermore, the H2Nc monolayer grown on Ag(111) could be a good template to grow dispersed magnetic metal atoms and clusters at room temperature for further investigation of their magnetism-related properties.

  1. Electronic and optical properties of BxNyCz monolayers with adsorption of hydrogen atoms

    Science.gov (United States)

    Leite, L.; Azevedo, S.; de Lima Bernardo, B.

    2017-03-01

    We apply first-principles calculations, using density functional theory, to analyze the electronic and optical properties of monolayers of graphene with a nanodomain of 2D hexagonal boron nitrite (h-BN). It also investigated the effects of the adsorption of hydrogen atoms in different atoms at the edge of the h-BN nanodomain. We calculate the electronic band structure, the complex dielectric function and the optical conductivity. For such systems, the calculations demonstrate that the compounds exhibit a prominent excitement in the visible and near-infrared regions. In this form, the present study provides physical basis for potential applications of the considered materials in optoelectronic devices at the nanoscale.

  2. Adsorption of gas molecules on Cu impurities embedded monolayer MoS{sub 2}: A first- principles study

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, B.; Li, C.Y. [Hubei Nuclear Solid Physics Key Laboratory, Department of Physics, Wuhan University, Wuhan 430072 (China); Liu, L.L. [Key Lab for Special Functional Materials of Ministry of Eduaction, Henan Province, Henan University, Kaifeng 475004 (China); Zhou, B.; Zhang, Q.K. [Hubei Nuclear Solid Physics Key Laboratory, Department of Physics, Wuhan University, Wuhan 430072 (China); Chen, Z.Q., E-mail: chenzq@whu.edu.cn [Hubei Nuclear Solid Physics Key Laboratory, Department of Physics, Wuhan University, Wuhan 430072 (China); Tang, Z., E-mail: ztang@ee.ecnu.edu.cn [Key Laboratory of Polar Materials and Devices, Ministry of Education of China, East China Normal University, Shanghai 200241 (China)

    2016-09-30

    Highlights: • Embedded Cu atom is strongly constrained on the sulfur vacancy of monolayer MoS{sub 2}. • Transition-metal Cu atom can break the chemical inactivation of MoS{sub 2} surface. • MoS{sub 2}-Cu system is a promising for future application in gas molecules sensing. - Abstract: Adsorption of small gas molecules (O{sub 2}, NO, NO{sub 2} and NH{sub 3}) on transition-metal Cu atom embedded monolayer MoS{sub 2} was investigated by first-principles calculations based on the density-functional theory (DFT). The embedded Cu atom is strongly constrained on the sulfur vacancy of monolayer MoS{sub 2} with a high diffusion barrier. The stable adsorption geometry, charge transfer and electronic structures of these gas molecules on monolayer MoS{sub 2} embedded with transition-metal Cu atom are discussed in detail. It is found that the monolayer MoS{sub 2} with embedded Cu atom can effectively capture these gas molecules with high adsorption energy. The NH{sub 3} molecule acts as electron donor after adsorption, which is different from the other gas molecules (O{sub 2}, NO, and NO{sub 2}). The results suggest that MoS{sub 2}-Cu system may be promising for future applications in gas molecules sensing and catalysis, which is similar to those of the transition-metal embedded graphene.

  3. On the adsorption of hexaammineruthenium (III) at anionic self-assembled monolayers

    Energy Technology Data Exchange (ETDEWEB)

    Steichen, M.; Doneux, Th.; Buess-Herman, C. [Universite Libre de Bruxelles, Faculte des Sciences, Service de Chimie Analytique et Chimie des Interfaces, CP 255, Boulevard du Triomphe 2, B-1050 Bruxelles (Belgium)

    2008-09-01

    The binding of the electroactive hexaammineruthenium (III) complex ions to anionic self-assembled monolayers (SAMs) has been investigated by means of chronocoulometry and ac voltammetry. From chronocoulometric data recorded in 10{sup -2} M LiClO{sub 4} containing different [Ru(NH{sub 3}){sub 6}]{sup 3+} concentrations, we have established the adsorption isotherm of [Ru(NH{sub 3}){sub 6}]{sup 3+} on a compact monolayer of 2-mercaptobenzimidazole-5-sulfonate (MBIS) self-assembled on Au(1 1 1). The data were satisfactorily fitted to the linearized Langmuir adsorption isotherm and a binding constant of 4.0 ({+-}0.4) x 10{sup 6} M{sup -1} has been determined. The electrostatic binding of [Ru(NH{sub 3}){sub 6}]{sup 3+} to a dilute PNA-DNA monolayer formed after hybridization on a PNA-modified gold electrode by self-assembly from a mixed solution of mercaptobutan-1-ol and PNA oligonucleotides has been studied by ac voltammetry. The admittance of the PNA-modified electrode after hybridization with complementary DNA was measured in 0.01 M Tris-HCl buffer containing different [Ru(NH{sub 3}){sub 6}]{sup 3+} concentrations. Based on these data, a binding constant of [Ru(NH{sub 3}){sub 6}]{sup 3+} to the surface-confined PNA-DNA duplex was derived from the Langmuir isotherm and amounts to 2.9 ({+-}0.3) x 10{sup 5} M{sup -1}. As the interactions between [Ru(NH{sub 3}){sub 6}]{sup 3+} and the immobilized PNA-DNA hybrids on the gold surface are essentially electrostatic, the adsorption of the highly charged cationic redox complex at low concentrations to the negatively charged PNA-DNA modified surface is in large competition with other monovalent cations present in the electrolyte at higher concentrations. The influence of competing sodium cations was thus studied by adding different NaCl concentrations in the 0.01 M Tris-HCl electrolyte. (author)

  4. Effect of calcium on adsorption capacity of powdered activated carbon.

    Science.gov (United States)

    Li, Gang; Shang, Junteng; Wang, Ying; Li, Yansheng; Gao, Hong

    2013-12-01

    We investigated the effect of calcium ion on the adsorption of humic acid (HA) (as a target pollutant) by powered activated carbon. The HA adsorption isotherms at different pH and kinetics of two different solutions including HA alone and HA doped Ca(2+), were performed. It was showed that the adsorption capacity of powdered activated carbon (PAC) for HA was markedly enhanced when Ca(2+) was doped into HA. Also, HA and Ca(2+) taken as nitrate were tested on the uptake of each other respectively and it was showed that the adsorbed amounts of both of them were significantly promoted when HA and calcium co-existed. Furthermore, the adsorbed amount of HA slightly decreased with the increasing of Ca(2+) concentration, whereas the amount of calcium increased with the increasing of HA concentration, but all above the amounts without addition. Finally, the change of pH before and after adsorption process is studied. In the two different solutions including HA alone and HA doped Ca(2+), pH had a small rise, but the extent of pH of later solution was bigger.

  5. Adsorption of gas molecules on Cu impurities embedded monolayer MoS2: A first- principles study

    Science.gov (United States)

    Zhao, B.; Li, C. Y.; Liu, L. L.; Zhou, B.; Zhang, Q. K.; Chen, Z. Q.; Tang, Z.

    2016-09-01

    Adsorption of small gas molecules (O2, NO, NO2 and NH3) on transition-metal Cu atom embedded monolayer MoS2 was investigated by first-principles calculations based on the density-functional theory (DFT). The embedded Cu atom is strongly constrained on the sulfur vacancy of monolayer MoS2 with a high diffusion barrier. The stable adsorption geometry, charge transfer and electronic structures of these gas molecules on monolayer MoS2 embedded with transition-metal Cu atom are discussed in detail. It is found that the monolayer MoS2 with embedded Cu atom can effectively capture these gas molecules with high adsorption energy. The NH3 molecule acts as electron donor after adsorption, which is different from the other gas molecules (O2, NO, and NO2). The results suggest that MoS2-Cu system may be promising for future applications in gas molecules sensing and catalysis, which is similar to those of the transition-metal embedded graphene.

  6. Anomalous Lithium Adsorption Propensity of Monolayer Carbonaceous Materials: A Density Functional Study

    Indian Academy of Sciences (India)

    SWATI PANIGRAHI; DEIVASIGAMANI UMADEVI; G NARAHARI SASTRY

    2016-10-01

    Interaction between lithium and carbonaceous materials has gained a lot of importance in lithium battery industry as an important source of energy and storage. The size, dimension, curvature and chirality of the carbonaceous materials are found to be very important factors in controlling the sequential binding oflithium. The propensity of lithium binding to the monolayer carbonaceous materials has been studied using Density functional theory (DFT). Structural and energetical parameters of the complexes have been analyzed through interaction energy, sequential energy, Mulliken population analysis and spin density distribution. Spindensity of odd Li doped systems reveals the preferences for addition of further lithium atoms on the surface. Upon analyzing the interaction energy in armchair carbon nanotubes (A-CNTs) and zigzag carbon nanotubes (Z-CNTs), it has been observed that external and internal surfaces of CNTs have contrasting binding preferences for sequential addition of Li atoms. Internal surface is found to be more feasible site for lithium adsorption than the external surface. This current study provides fundamental understanding of the mechanism of lithium adsorption in lithium battery.

  7. Stabilization of Insulin by Adsorption on a Hydrophobic Silane Self-Assembled Monolayer.

    Science.gov (United States)

    Mauri, Sergio; Volk, Martin; Byard, Stephen; Berchtold, Harald; Arnolds, Heike

    2015-08-18

    The interaction between many proteins and hydrophobic functionalized surfaces is known to induce β-sheet and amyloid fibril formation. In particular, insulin has served as a model peptide to understand such fibrillation, but the early stages of insulin misfolding and the influence of the surface have not been followed in detail under the acidic conditions relevant to the synthesis and purification of insulin. Here we compare the adsorption of human insulin on a hydrophobic (-CH3-terminated) silane self-assembled monolayer to a hydrophilic (-NH3(+)-terminated) layer. We monitor the secondary structure of insulin with Fourier transform infrared attenuated total reflection and side-chain orientation with sum frequency spectroscopy. Adsorbed insulin retains a close-to-native secondary structure on both hydrophobic and hydrophilic surfaces for extended periods at room temperature and converts to a β-sheet-rich structure only at elevated temperature. We propose that the known acid stabilization of human insulin and the protection of the aggregation-prone hydrophobic domains on the insulin monomer by adsorption on the hydrophobic surface work together to inhibit fibril formation at room temperature.

  8. Adsorption of biopolymers human serum albumin and human gamma globulin to well-defined surfaces of self-assembled monolayers

    Science.gov (United States)

    Cregger, Tricia Ann

    The tenacity with which the blood proteins Human Serum Albumin (HSA) and Human Gamma Globulin (HGG) adsorb to a surface modified with a monomolecular coating varies with the packing of the alkyl chains in the coating. The adsorption of proteins onto well-defined surfaces of self-assembled monolayers (SAMs) was studied with X-ray reflectometry (XR), neutron reflectometry (NR), optical reflectometry, and total internal reflection fluorescence (TIRF). NR and XR was used to study adsorption in the absence of flow, while optical reflectometry and TIRF were used to probe the adsorption under flow conditions. In particular, competitive adsorption measurements of binary solutions of HSA, HGG and Fibrinogen (FIB) were performed with TIRE The properties of the surface were varied by altering the alkyl chains' packing density and the chain end functionality of the SAMs. The depth profiles of protein concentration near the adsorbing surface measured by NR were dependent upon the chain packing density in the case of HSA. The concentration depth profile of HGG was unaltered by varying chain packing density. Measurements performed under flow using optical reflectometry showed a different behavior: the surface excess of adsorbed HSA was relatively independent of the surface packing, while the surface excess of HGG depended on the packing density of the SAM. The tenacity with which the proteins adsorbed to different functionalized surfaces was determined by attempting to remove the protein using a strong surfactant, sodium dodecyl sulfate (SDS). Ex situ XR measurements suggested that both HSA and HGG adsorb more tenaciously to a less densely-packed monolayer, almost independent of surface functionality. Two exceptions were a less densely-packed vinyl-terminated monolayer and a less densely-packed bromine-terminated monolayer, from which HSA could not be removed at all.

  9. Markedly different adsorption behaviors of gas molecules on defective monolayer MoS2: a first-principles study.

    Science.gov (United States)

    Li, Hongxing; Huang, Min; Cao, Gengyu

    2016-06-01

    Sulfur vacancy (SV) is one of the most typical defects in two-dimensional monolayer MoS2, leading to reactive sites. We presented a systematic study of the adsorption behaviors of gas molecules, CO2, N2, H2O, CO, NH3, NO, O2, H2 and NO2, on monolayer MoS2 with single SV by first-principles calculations. It was found that CO2, N2 and H2O molecules physisorbed at the proximity of single SV. Our adsorption energy calculations and charge transfer analysis showed that the interactions between CO2, N2 and H2O molecules and defective MoS2 are stronger than the cases of CO2, N2 and H2O molecules adsorbed on pristine MoS2, respectively. The defective MoS2 based gas sensors may be more sensitive to CO2, N2 and H2O molecules than pristine MoS2 based ones. CO, NO, O2 and NH3 molecules were found to chemisorb at the S vacancy site and thus modify the electronic properties of defective monolayer MoS2. Magnetism was induced upon adsorption of NO molecules and the defective states induced by S vacancy can be completely removed upon adsorption of O2 molecules, which may provide some helpful information for designing new MoS2 based nanoelectronic devices in future. The H2 and NO2 molecules were found to dissociate at S vacancy. The dissociation of NO2 molecules resulted in O atoms located at the S vacancy site and NO molecules physisorbed on O-doped MoS2. The calculated results showed that NO2 molecules can help heal the S vacancy of the MoS2 monolayer.

  10. Oxygen Storage Capacity and Adsorptive Property of Praseodymium Oxides

    Institute of Scientific and Technical Information of China (English)

    万颖; 马建新; 方明; 刘毅廷

    2003-01-01

    Oxygen storage and adsorptive properties of praseodymium oxides were investigated by pulse experiments and temperature-programmed desportion/reduction (TPD/TPR) experiments. Pr2O3 possesses the similar oxygen storage properties to CeO 2, and its dynamic oxygen storage capacity is 14.9 μmolg-1. The studies on TPD of O2, H2O and CO and TPR show that Pr2O3 provides more active sur face oxygen species and at a lower temperature than CeO2. It is suggested that Pr2O3 can be a well candidate as an oxygen storage component in automobile three-way catalyst.

  11. Polanyi Evaluation of Adsorptive Capacities of Commercial Activated Carbons

    Science.gov (United States)

    Monje, Oscar; Surma, Jan M.

    2017-01-01

    Commercial activated carbons from Calgon (207C and OVC) and Cabot Norit (RB2 and GCA 48) were evaluated for use in spacecraft trace contaminant control filters. The Polanyi potential plots of the activated carbons were compared using to those of Barnebey-Cheney Type BD, an untreated activated carbon with similar properties as the acid-treated Barnebey-Sutcliffe Type 3032 utilized in the TCCS. Their adsorptive capacities under dry conditions were measured in a closed loop system and the sorbents were ranked for their ability to remove common VOCs found in spacecraft cabin air. This comparison suggests that these sorbents can be ranked as GCA 48 207C, OVC RB2 for the compounds evaluated.

  12. Adsorption of multi-heavy metals Zn and Cu onto surficial sediments: modeling and adsorption capacity analysis.

    Science.gov (United States)

    Li, Shanshan; Zhang, Chen; Wang, Meng; Li, Yu

    2014-01-01

    Improved multiple regression adsorption models (IMRAMs) was developed to estimate the adsorption capacity of the components [Fe oxides (Fe), Mn oxides (Mn), organic materials (OMs), residuals] in surficial sediments for multi-heavy metal Zn and Cu. IMRAM is an improved version over MRAM, which introduces a computer program in the model developing process. As MRAM, Zn(Cu) IMRAM, and Cu(Zn) IMRAM again confirmed that there is significant interaction effects that control the adsorption of compounded Zn and Cu, which was neglected by additional adsorption model. The verification experiment shows that the relative deviation of the IMRAMs is less than 13%. It is revealed by the IMRAMs that Mn, which has the greatest adsorption capability for compounded Zn and Cu (54.889 and 161.180 mg/l, respectively), follows by interference adsorption capacity of Fe/Mn (-1.072 and -24.591 mg/l respectively). Zn and Cu influence each other through different mechanisms. When Zn is the adsorbate, compounded Cu mainly affects the adsorption capacities of Fe/Mn and Fe/Mn/OMs; while when Cu is the adsorbate, compounded Zn mainly exerts its effect on Mn, Fe/Mn, and Mn/OMs. It also shows that the compounded Zn or Cu weakened the interference adsorption of Fe/Mn, and meanwhile, strengthened the interference adsorption of Mn/OMs.

  13. Molecular dynamics simulations of peptide adsorption on self-assembled monolayers

    Energy Technology Data Exchange (ETDEWEB)

    Xie Yun; Liu Meifeng [School of Chemistry and Chemical Engineering, Guangdong Provincial Key Lab for Green Chemical Product Technology, South China University of Technology, Guangzhou, Guangdong Province, 510640 (China); Zhou Jian, E-mail: jianzhou@scut.edu.cn [School of Chemistry and Chemical Engineering, Guangdong Provincial Key Lab for Green Chemical Product Technology, South China University of Technology, Guangzhou, Guangdong Province, 510640 (China)

    2012-08-01

    All-atom molecular dynamics simulations are performed to investigate the neuromedin-B peptide adsorption on the self-assembled monolayers (SAMs) of SH(CH{sub 2}){sub 10}N{sup +}(CH{sub 3}){sub 2}CH{sub 2}CH(OH)CH{sub 2}SO{sub 3}{sup -} (SBT), SH(CH{sub 2}){sub 10}OH and SH(CH{sub 2}){sub 10}CH{sub 3}. The force-distance profiles show that the surface resistance to peptide adsorption is mainly generated by the water molecules tightly bound to surfaces via hydrogen bonds (hydration water molecules); but surfaces themselves may also set an energy barrier for the approaching peptide. For the SBT-SAM, the surface first exerts a relatively high repulsive force and then a rather week attractive force on the approaching peptide; meanwhile the hydration water molecules exert a strong repulsive force on the peptide. Therefore, SBT-SAM has an excellent performance on resisting protein adsorption. For the OH-SAM and CH{sub 3}-SAM, surfaces show low or little energy barrier but strong affinity to the peptide; and the hydration water molecules apply merely a repulsive force within a much narrower range and with lower intensity compared with the case for the SBT-SAM. The analysis of structural and dynamical properties of the peptide, surface and water indicates that possible factors contributing to surface resistance include the hydrogen-bond formation capability of surfaces, mobility of water molecules near surfaces, surface packing density and chain flexibility of SAMs. There are a large number of hydrogen bonds formed between the hydration water molecules and the functional groups of the SBT-SAM, which greatly lowers the mobility of water molecules near the surface. This tightly-bound water layer effectively reduces the direct contact between the surface and the peptide. Furthermore, the SBT-SAM also has a high flexibility and a low surface packing density, which allows water molecules to penetrate into the surface to form tightly-bound networks and therefore reduces the

  14. Molecular dynamics simulations of peptide adsorption on self-assembled monolayers

    Science.gov (United States)

    Xie, Yun; Liu, Meifeng; Zhou, Jian

    2012-08-01

    All-atom molecular dynamics simulations are performed to investigate the neuromedin-B peptide adsorption on the self-assembled monolayers (SAMs) of SH(CH2)10N+(CH3)2CH2CH(OH)CH2SO3- (SBT), SH(CH2)10OH and SH(CH2)10CH3. The force-distance profiles show that the surface resistance to peptide adsorption is mainly generated by the water molecules tightly bound to surfaces via hydrogen bonds (hydration water molecules); but surfaces themselves may also set an energy barrier for the approaching peptide. For the SBT-SAM, the surface first exerts a relatively high repulsive force and then a rather week attractive force on the approaching peptide; meanwhile the hydration water molecules exert a strong repulsive force on the peptide. Therefore, SBT-SAM has an excellent performance on resisting protein adsorption. For the OH-SAM and CH3-SAM, surfaces show low or little energy barrier but strong affinity to the peptide; and the hydration water molecules apply merely a repulsive force within a much narrower range and with lower intensity compared with the case for the SBT-SAM. The analysis of structural and dynamical properties of the peptide, surface and water indicates that possible factors contributing to surface resistance include the hydrogen-bond formation capability of surfaces, mobility of water molecules near surfaces, surface packing density and chain flexibility of SAMs. There are a large number of hydrogen bonds formed between the hydration water molecules and the functional groups of the SBT-SAM, which greatly lowers the mobility of water molecules near the surface. This tightly-bound water layer effectively reduces the direct contact between the surface and the peptide. Furthermore, the SBT-SAM also has a high flexibility and a low surface packing density, which allows water molecules to penetrate into the surface to form tightly-bound networks and therefore reduces the affinity between the peptide and the surface. The results show that the protein

  15. The adsorption of CO and NO on the MoS{sub 2} monolayer doped with Au, Pt, Pd, or Ni: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Dongwei, E-mail: dwmachina@126.com [School of Physics, Anyang Normal University, Anyang 455000 (China); Ju, Weiwei [College of Physics and Engineering, Henan University of Science and Technology, Luoyang 471023 (China); Li, Tingxian; Zhang, Xiwei [School of Physics, Anyang Normal University, Anyang 455000 (China); He, Chaozheng, E-mail: hecz2013@nynu.edu.cn [Physics and Electronic Engineering College, Nanyang Normal University, Nanyang 473061 (China); Ma, Benyuan [Physics and Electronic Engineering College, Nanyang Normal University, Nanyang 473061 (China); Lu, Zhansheng; Yang, Zongxian [College of Physics and Electronic Engineering, Henan Normal University, Xinxiang 453007 (China)

    2016-10-15

    Graphical abstract: The MoS{sub 2} monolayers doped with Au, Pt, Pd, or Ni show enhanced adsorption and sensitivity toward CO or NO molecule. - Highlights: • CO and NO adsorption on the doped MoS{sub 2} monolayers is theoretically studied. • CO and NO are chemisorbed on the doped MoS{sub 2} monolayers. • Charge transfer can be observed between the adsorbed molecule and the substrates. • Molecular adsorption can induce the change in electronic structures of the doped MoS{sub 2} monolayers. - Abstract: By performing the first-principles calculation, the adsorption of CO and NO molecules on the Au, Pt, Pd, or Ni doped MoS{sub 2} monolayer has been studied. The interaction between CO or NO with the doped MoS{sub 2} monolayer is strong and belongs to the chemisorption, as evidenced by the large adsorption energy and the short distance between the adsorbed molecules and the dopants. The charge transfer and the electronic property induced by the molecule adsorption are discussed. It is found that for both CO and NO adsorption, for all the cases charge transfer between the substrates and the adsorbed molecules has been observed. For NO, the adsorption obviously induces new impurity states in the band gap or the redistribution of the original impurity states. These can lead to the change of the transport properties of the doped MoS{sub 2} monolayer, by which the adsorbed CO or NO can be detected. The present work shows that introducing appropriate dopants may be a feasible method to improve the performance of MoS{sub 2}-based gas sensors.

  16. Calcium adsorption and displacement: characterization of lipid monolayers and their interaction with membrane-active peptides/proteins

    Directory of Open Access Journals (Sweden)

    Gutsmann Thomas

    2006-05-01

    Full Text Available Abstract Background The first target of antimicrobial peptides (AMPs is the bacterial membrane. In the case of Gram-negative bacteria this is the outer membrane (OM, the lipid composition of which is extremely asymmetric: Whereas the inner leaflet is composed of a phospholipid mixture, the outer leaflet is made up solely from lipopolysaccharides (LPSs. LPS, therefore, represents the first target of AMPs. The binding and intercalation of polycationic AMPs is driven by the number and position of negatively charged groups of the LPS. Also, proteins other than cationic AMPs can interact with LPS, e.g. leading eventually to a neutralization of the endotoxic effects of LPS. We compared different biophysical techniques to gain insight into the properties of the electrical surface potentials of lipid monolayers and aggregates composed of LPSs and various phospholipids and their interaction with peptides and proteins. Results The net negative charge calculated from the chemical structure of the phospholipid and LPS molecules is linearly correlated with the adsorption of calcium to two-dimensional lipid monolayers composed of the respective lipids. However, the ζ-potentials determined by the electrophoretic mobility of LPS aggregates can only be interpreted by assuming a dependence of the plane of shear on the number of saccharides and charged groups. Various peptides and proteins were able to displace calcium adsorbed to monolayers. Conclusion To characterize the electrical properties of negatively charged phospholipids and LPSs and their electrostatic interaction with various polycationic peptides/proteins, the adsorption of calcium to and displacement from lipid monolayers is a suitable parameter. Using the calcium displacement method, the binding of peptides to monolayers can be determined even if they do not intercalate. The interpretation of ζ-potential data is difficulty for LPS aggregates, because of the complex three-dimensional structure of

  17. Gas-phase formaldehyde adsorption isotherm studies on activated carbon: correlations of adsorption capacity to surface functional group density.

    Science.gov (United States)

    Carter, Ellison M; Katz, Lynn E; Speitel, Gerald E; Ramirez, David

    2011-08-01

    Formaldehyde (HCHO) adsorption isotherms were developed for the first time on three activated carbons representing one activated carbon fiber (ACF) cloth, one all-purpose granular activated carbon (GAC), and one GAC commercially promoted for gas-phase HCHO removal. The three activated carbons were evaluated for HCHO removal in the low-ppm(v) range and for water vapor adsorption from relative pressures of 0.1-0.9 at 26 °C where, according to the IUPAC isotherm classification system, the adsorption isotherms observed exhibited Type V behavior. A Type V adsorption isotherm model recently proposed by Qi and LeVan (Q-L) was selected to model the observed adsorption behavior because it reduces to a finite, nonzero limit at low partial pressures and it describes the entire range of adsorption considered in this study. The Q-L model was applied to a polar organic adsorbate to fit HCHO adsorption isotherms for the three activated carbons. The physical and chemical characteristics of the activated carbon surfaces were characterized using nitrogen adsorption isotherms, X-ray photoelectron spectroscopy (XPS), and Boehm titrations. At low concentrations, HCHO adsorption capacity was most strongly related to the density of basic surface functional groups (SFGs), while water vapor adsorption was most strongly influenced by the density of acidic SFGs.

  18. Analytical insight into the lattice thermal conductivity and heat capacity of monolayer MoS2

    Science.gov (United States)

    Saha, Dipankar; Mahapatra, Santanu

    2016-09-01

    We report, a detailed theoretical study on the lattice thermal conductivity of a suspended monolayer MoS2, far beyond its ballistic limit. The analytical approach adopted in this work mainly relies on the use of Boltzmann transport equation (BTE) within the relaxation time approximation (RTA), along with the first-principles calculations. Considering the relative contributions from the various in-plane and out-of-plane acoustic modes, we derive the closed-form expressions of the mode specific heat capacities, which we later use to obtain the phonon thermal conductivities of the monolayer MoS2. Besides finding the intrinsic thermal conductivity, we also analyse the effect of the phonon-boundary scattering, for different dimensions and edge roughness conditions. The viability of the semi-analytic solution of lattice thermal conductivity reported in this work ranges from a low temperature (T∼30 K) to a significantly high temperature (T∼550 K), and the room temperature (RT) thermal conductivity value has been obtained as 34.06 Wm-1K-1 which is in good agreement with the experimental result.

  19. Enhanced chromium adsorption capacity via plasma modification of natural zeolites

    Science.gov (United States)

    Cagomoc, Charisse Marie D.; Vasquez, Magdaleno R., Jr.

    2017-01-01

    Natural zeolites such as mordenite are excellent adsorbents for heavy metals. To enhance the adsorption capacity of zeolite, sodium-exchanged samples were irradiated with 13.56 MHz capacitively coupled radio frequency (RF) argon gas discharge. Hexavalent chromium [Cr(VI)] was used as the test heavy metal. Pristine and plasma-treated zeolite samples were soaked in 50 mg/L Cr solution and the amount of adsorbed Cr(VI) on the zeolites was calculated at predetermined time intervals. Compared with untreated zeolite samples, initial Cr(VI) uptake was 70% higher for plasma-treated zeolite granules (50 W 30 min) after 1 h of soaking. After 24 h, all plasma-treated zeolites showed increased Cr(VI) uptake. For a 2- to 4-month period, Cr(VI) uptake increased about 130% compared with untreated zeolite granules. X-ray diffraction analyses between untreated and treated zeolite samples revealed no major difference in terms of its crystal structure. However, for plasma-treated samples, an increase in the number of surface defects was observed from scanning electron microscopy images. This increase in the number of surface defects induced by plasma exposure played a crucial role in increasing the number of active sorption sites on the zeolite surface.

  20. High-capacity adsorption of aniline using surface modification of lignocellulose-biomass jute fibers.

    Science.gov (United States)

    Gao, Da-Wen; Hu, Qi; Pan, Hongyu; Jiang, Jiping; Wang, Peng

    2015-10-01

    Pyromellitic dianhydride (PMDA) modified jute fiber (MJF) were prepared with microwave treatment to generate a biosorbent for aniline removal. The characterization of the biosorbent was investigated by SEM, BET and FT-IR analysis to discuss the adsorption mechanism. The studies of various factors influencing the adsorption behavior indicated that the optimum dosage for aniline adsorption was 3g/L, the maximum adsorption capacity was observed at pH 7.0 and the adsorption process is spontaneous and endothermic. The aniline adsorption follows the pseudo second order kinetic model and Langmuir isotherm model. Moreover, the biosorbent could be regenerated through the desorption of aniline by using 0.5M HCl solution, and the adsorption capacity after regeneration is even higher than that of virgin MJF. All these results prove MJF is a promising adsorbent for aniline removal in wastewater. Copyright © 2015 Elsevier Ltd. All rights reserved.

  1. Alkali metal cation doping of metal-organic framework for enhancing carbon dioxide adsorption capacity

    Institute of Scientific and Technical Information of China (English)

    Yan Cao; Yunxia Zhao; Fujiao Song; Qin Zhong

    2014-01-01

    Metal-organic frameworks (MOFs) have attracted much attention as adsorbents for the separation of CO2 from flue gas or natural gas. Here, a typical metal-organic framework HKUST-1(also named Cu-BTC or MOF-199) was chemically reduced by doping it with alkali metals (Li, Na and K) and they were further used to investigate their CO2 adsorption capacities. The structural information, surface chemistry and thermal behavior of the prepared adsorbent samples were characterized by X-ray powder diffraction (XRD), thermo-gravimetric analysis (TGA) and nitrogen adsorption-desorption isotherm analysis. The results showed that the CO2 storage capacity of HKUST-1 doped with moderate quantities of Li+, Na+ and K+, individually, was greater than that of unmodified HKUST-1. The highest CO2 adsorption uptake of 8.64 mmol/g was obtained with 1K-HKUST-1, and it was ca. 11%increase in adsorption capacity at 298 K and 18 bar as compared with HKUST-1. Moreover, adsorption tests showed that HKUST-1 and 1K-HKUST-1 displayed much higher adsorption capacities of CO2 than those of N2. Finally, the adsorption/desorption cycle experiment revealed that the adsorption performance of 1K-HKUST-1 was fairly stable, without obvious deterioration in the adsorption capacity of CO2 after 10 cycles.

  2. Chemical Modification on Reactive Dye Adsorption Capacity of Castor Seeds

    Directory of Open Access Journals (Sweden)

    V. Dharmalingam

    2011-01-01

    Full Text Available Abstract: The roles played by four major functional groups (amine, carboxyl, azo, hydroxyl groups in the biomass of castor seeds in adsorption of seven dyes were investigated. These functional groups in castor seeds were chemically modified individually to determine their contribution to the adsorption of ionic dyes. The dyes used were remazol red B, procino yellow, fast green FCF, brilliant cresyl blue, methylene blue, neutral red, red-141. It was found that hydroxyl group inhibited the adsorption of anionic dyes but it was major functional group in the adsorption of cationic dyes, hydroxyl group was important functional group in the adsorption of all seven dyes and the effect of methylation of amino group was not significant on the adsorption of seven dyes.

  3. Studies on The Adsorption Capacity for Bilirubin of The Adsorbent Chitosan-β-Cyclodextrin

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The adsorbent crosslinked chitosan-β-cyclodextrin (β-CD) was prepared by the reaction of glutaraldehyde with chitosan and β-cyclodextrin. This type of adsorbent has high adsorption capacity for unconjugated bilirubin. The adsorption capacity was related to the β-CD content of the adsorbent; phosphate buffer concentration; temperature; pH value; ionic strength and the adsorbent beads. The results indicated that the chitosan-β-CD was a good adsorbent for unconjugated bilirubin with high capacity.

  4. Adsorption Capacity of Kaolinite for Copper (II) under Magnetic Field

    Institute of Scientific and Technical Information of China (English)

    DONG Wei

    2004-01-01

    The adsorption of Cu2+ on kaolinite under magnetic field was studied at 25℃.The magnetic effects were investigated by designing the variation of exposure time,magnetic flux density and the method of magnetic exposure.The results from these study show that the magnetic treatment significantly enhance the fraction of adsorption of Cu2+,the adsorption of Cu2+ by kaolinite increases with the increase of pH value from 2 to 6.Both the magnetic exposure time and the magnetic flux density promote the fraction of adsorption Cu2+ on kaolinite.

  5. Experimental Investigation on Adsorption Capacity of a Variety of Activated Carbon/Refrigerant Pairs

    Directory of Open Access Journals (Sweden)

    Ahmed N. Shmroukh

    2015-04-01

    Full Text Available This study aims to develop a device with minimum heat and mass transfer limitations between adsorbent and adsorbate, and subsequently to obtain practically applicable adsorption capacity data. Also, 5 kW adsorption chillers (evaporators, condensers and adsorbers are designed based on the experimental output data of the whole tested pairs. A finned-tube heat exchanger was employed and installed at the center adsorber, and each employed adsorbent was immobilized on its surfaces by using an adhesive agent. A variety of pairs: are activated carbon powder (ACP/R-134a, ACP/R-407c, ACP/R-507A, activated carbon granules (ACG/R-507A, ACG /R-407c and ACG /R-134a, were examined at different adsorption temperatures of 25, 30, 35 and 50°C. It was found that, at the adsorption temperature of 25°C the maximum adsorption capacity was 0.8352 kg kg-1 for ACP/R-134a, while at the adsorption temperature of 50°C the maximum adsorption capacity was 0.3207 kg kg-1 for ACP/R- 134a. Therefore, the ACP/R-134a pair is highly recommended to be employed as adsorption refrigeration working pair because of its higher maximum adsorption capacity higher than the other examined pairs.

  6. Adsorptive

    Directory of Open Access Journals (Sweden)

    Vinod Kumar Gupta

    2017-05-01

    Full Text Available This work explores the feasibility of natural fibers derived from Ficus carica plant as an alternative precursor for the preparation of activated carbon via microwave assisted H3PO4 activation. The properties of activated carbon were investigated by scanning electron microscope (SEM and Fourier transform spectroscopy (FTIR. The operational parameters, chemical impregnation ratio, microwave power and irradiation time on the carbon yield and adsorption capability were investigated. Adsorption performance of Cu(II and Ni(II onto activated carbon was investigated as a function of pH, contact time, initial metal ion concentration and temperature. The adsorption capacity of Cu(II and Ni(II onto the adsorbent was found to be 23.08 and 18.78 mg/g, respectively. Adsorption of metal ions followed second order kinetics with best fit for Fraundlich adsorption isotherm. The values of thermodynamic parameters such as enthalpy change (ΔH°, entropy change (ΔS° and free energy change (ΔG° were evaluated for the adsorption of both the metal ions. Adsorption of metal ions onto activated carbon was spontaneous and endothermic in nature. The results suggested that activated carbon developed from natural fibers successfully improved the metal ions adsorption capacity. On the basis of our findings, the adsorbent could be used as a detoxifying agent for better management of industrial effluents.

  7. Thermodynamics of the adsorption of organic molecules on graphitized carbon black modified with a monolayer of 5-hydroxy-6-methyluracil

    Science.gov (United States)

    Gus'kov, V. Yu.; Ivanov, S. P.; Shaikhitdinova, Yu. F.; Kudasheva, F. Kh.

    2016-10-01

    Thermodynamic characteristics of the adsorption of alkanes, alcohols, arenes, and esters on graphitized carbon black with a deposited monolayer (0.17%) of 5-hydroxy-6-methyluracil are studied by means of inverse gas chromatography at infinite dilution. It is established that size effects (violation of the additivity of molar changes in internal energy and the entropy of adsorption for pairs of molecules of one homologous series that differ by one methyl group) are observed when organic molecules are adsorbed on the surface of the resulting adsorbent. The size effects are similar to those observed when 1% 5-hydroxy-6-methyluracil is deposited on graphitized carbon black. It is concluded that the observed violation of additivity is associated with cavities in the supramolecular structure.

  8. Oxygen and hydroxyl adsorption on MS{sub 2} (M = Mo, W, Hf) monolayers: a first-principles molecular dynamics study

    Energy Technology Data Exchange (ETDEWEB)

    Iordanidou, K.; Houssa, M.; Afanas' ev, V.V.; Stesmans, A. [Department of Physics and Astronomy, University of Leuven (Belgium); Pourtois, G. [IMEC, Leuven (Belgium)

    2016-11-15

    In this paper, we study the oxygen and hydroxyl adsorption on both pristine and S deficient MS{sub 2} (M = Mo, W, Hf) monolayers, using first-principles molecular dynamics calculations. Our simulations reveal that single-layer HfS{sub 2} suffers severely from oxidation, which results in the formation of strong Hf-O bonds, likely degrading the transport properties of the material. Oxygen adsorption on S deficient monolayers acts as a passivation mechanism, both ''structurally'' by saturating the dangling bonds of neighboring metal atoms and ''electronically'' by removing the S vacancy induced gap states. Hydroxyl adsorption on pristine monolayers generates spin-polarized gap states, and for HfS{sub 2} in particular, causes the Fermi level pinning close to the conduction band edge. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. Adsorption of alkali, alkaline-earth, simple and 3d transition metal, and nonmetal atoms on monolayer MoS2

    Directory of Open Access Journals (Sweden)

    X. D. Li

    2015-05-01

    Full Text Available Single adsorption of different atoms on pristine two-dimensional monolayer MoS2 have been systematically investigated by using density functional calculations with van der Waals correction. The adatoms cover alkali metals, alkaline earth metals, main group metal, 3d-transition metals, coinage metal and nonmetal atoms. Depending on the adatom type, metallic, semimetallic or semiconducting behavior can be found in direct bandgap monolayer MoS2. Additionally, local or long-range magnetic moments of two-dimensional MoS2 sheet can also attained through the adsorption. The detailed atomic-scale knowledge of single adsorption on MoS2 monolayer is important not only for the sake of a theoretical understanding, but also device level deposition technological application.

  10. Study of Static Adsorption Capacity of ACF for Xenon at 201 K

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The static adsorption performances of a series of active carbon fiber (ACF)for xenon at 201 K were measured with a model ASAP2010M specific surface area and aperture distribution instrument by changing the working gas of instrument from N2 to Xenon. Compared with grain active carbon(GAC): (1) the adsorption performance of Viscose-based ACF(VACF) adsorbents is better than that of GAC; (2) owing to the difference of aperture distribution, the adsorption performance of ACF with different radicales is different under the same experiment conditions though the specific surface area is similar; (3) there is no definite relationship between adsorption performance and specific surface area; (4) the VACF-A2 is the superior xenon adsorbent at the experimental temperature.Keyworls Active carbon fiber, CTBT, Xenon, Static adsorption, Adsorptive capacity, Adsorptive velocity

  11. Modeling high adsorption capacity and kinetics of organic macromolecules on super-powdered activated carbon.

    Science.gov (United States)

    Matsui, Yoshihiko; Ando, Naoya; Yoshida, Tomoaki; Kurotobi, Ryuji; Matsushita, Taku; Ohno, Koichi

    2011-02-01

    The capacity to adsorb natural organic matter (NOM) and polystyrene sulfonates (PSSs) on small particle-size activated carbon (super-powdered activated carbon, SPAC) is higher than that on larger particle-size activated carbon (powdered-activated carbon, PAC). Increased adsorption capacity is likely attributable to the larger external surface area because the NOM and PSS molecules do not completely penetrate the adsorbent particle; they preferentially adsorb near the outer surface of the particle. In this study, we propose a new isotherm equation, the Shell Adsorption Model (SAM), to explain the higher adsorption capacity on smaller adsorbent particles and to describe quantitatively adsorption isotherms of activated carbons of different particle sizes: PAC and SPAC. The SAM was verified with the experimental data of PSS adsorption kinetics as well as equilibrium. SAM successfully characterized PSS adsorption isotherm data for SPACs and PAC simultaneously with the same model parameters. When SAM was incorporated into an adsorption kinetic model, kinetic decay curves for PSSs adsorbing onto activated carbons of different particle sizes could be simultaneously described with a single kinetics parameter value. On the other hand, when SAM was not incorporated into such an adsorption kinetic model and instead isotherms were described by the Freundlich model, the kinetic decay curves were not well described. The success of the SAM further supports the adsorption mechanism of PSSs preferentially adsorbing near the outer surface of activated carbon particles.

  12. Evaluation of adsorption capacity of acetaminophen on activated ...

    African Journals Online (AJOL)

    vitro adsorption studies and scanning electron microscopy ... Faculty of Science, University of Nottingham Malaysia Campus, Jalan Broga, .... Materials. The adsorbate used all through was acetaminophen, pure standard (Sigma Aldrich®.

  13. Synthesis and Catalytic Activity of Pt Monolayer on Pd Tetrahedral Nanocrystals with CO-adsorption-induced Removal of Surfactants

    Energy Technology Data Exchange (ETDEWEB)

    Gong K.; Vukmirovic M.B.; Ma C.; Zhu Y.; Adzic R.R.

    2011-11-01

    We synthesized the Pt monolayer shell-Pd tetrahedral core electrocatalysts that are notable for their high activity and stable performance. A small number of low-coordination sites and defects, and high content of the (1 1 1)-oriented facets on Pd tetrahedron makes them a suitable support for a Pt monolayer to obtain an active O{sub 2} reduction reaction (ORR) electrocatalyst. The surfactants, used to control size and shape of Pd tetrahedral nanoparticles, are difficult to remove and cause adverse effects on the ORR. We describe a simple and noninvasive method to synthesize high-purity tetrahedral Pd nanocrystals (TH Pd) by combining a hydrothermal route and CO adsorption-induced removal of surfactants. Poly(vinylpyrrolidone) (PVP), used as a protecting and reducing agent in hydrothermal reactions, is strongly bonded to the surface of the resulting nanocrystals. We demonstrate that PVP was displaced efficiently by adsorbed CO. A clean surface was achieved upon CO stripping at a high potential (1.0 V vs RHE). It played a decisive role in improving the activity of the Pt monolayer/TH Pd electrocatalyst for the ORR. Furthermore, the results demonstrate a versatile method for removal of surfactants from various nanoparticles that severely limited their applications.

  14. Modification of cyanobacterial bloom-derived biomass using potassium permanganate enhanced the removal of microcystins and adsorption capacity toward cadmium (II)

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Jihai [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China); Hunan Provincial Key Laboratory of Farmland Pollution Control and Agricultural Resources Use, Hunan Agricultural University, Changsha 410128 (China); Gu, Ji-Dong [Hunan Provincial Key Laboratory of Farmland Pollution Control and Agricultural Resources Use, Hunan Agricultural University, Changsha 410128 (China); Laboratory of Environmental Microbiology and Toxicology, School of Biological Sciences, The University of Hong Kong, Hong Kong Special Administrative Region (Hong Kong); Peng, Liang; Luo, Si; Luo, Huili [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China); Yan, Zhiyong, E-mail: zhyyan111@163.com [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China); Wu, Genyi, E-mail: wugenyi99@163.com [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China)

    2014-05-01

    Highlights: • Potassium permanganate removed microcystins in the cyanobacterial bloom-derived biomass (CBDB). • Potassium permanganate oxidation caused the transformation of hydroxyl to carboxyl on the CBDB. • Manganese dioxide was formed on the surface of CBDB. • Potassium permanganate oxidation process increased the adsorption capacity of CBDB toward Cd(II). - Abstract: Cyanobacterial biomass shows high adsorption capacity toward heavy metal ions. However, the cyanotoxins in the cyanobacterial biomass inhibit its application in heavy metals removal. In order to safely and effectively remove Cd(II) from water using cyanobacterial bloom-derived biomass (CBDB), KMnO{sub 4} was used to modify CBDB. The results indicated that the microcystins in the CBDB were successfully removed by KMnO{sub 4}. Potassium permanganate oxidation caused the transformation of hydroxyl to carboxyl on the CBDB, and formed manganese dioxide on the surface of CBDB. The oxidized CBDB showed higher adsorption capacity toward Cd(II) than that of unoxidized treatment. The optimal KMnO{sub 4} concentration for increasing the adsorption capacity of CBDB toward Cd(II) was 0.2 g/L. The adsorption isotherm of Cd(II) by oxidized- or unoxidized-CBDB was well fitted by Langmuir model, indicating that the adsorption of Cd(II) by CBDB was monolayer adsorption. The desorption ratio of Cd(II) from oxidized CBDB was higher than that from unoxidized CBDB in the desorption process using NH{sub 4}NO{sub 3} and EDTA as desorbent. The results presented in this study suggest that KMnO{sub 4} modified CBDB may be used as a safe and high efficient adsorbent in Cd(II) removal from water.

  15. Adsorption and dissociation of H2S on monometallic and monolayer bimetallic Ni/Pd(111) surfaces: A first-principles study

    Science.gov (United States)

    Li, Yi; Huang, Pan; Tao, Dandan; Wu, Juan; Qiu, Mei; Huang, Xin; Ding, Kaining; Chen, Wenkai; Su, Wenyue; Zhang, Yongfan

    2016-11-01

    Periodic density functional theory calculations have been performed to investigate the adsorption structures and dissociative reaction pathways for H2S molecule on Ni(111), Pd(111) and Ni/Pd(111) monolayer bimetallic surfaces with surface monolayer and subsurface monolayer structures. Our results indicate that, for the molecular adsorption mode, the introducing Pd atoms on Ni(111) can enhance the binding strength between H2S and the surface, while an opposite effect is achieved when the Ni monolayer is formed on Pd(111) surface. The decompositions of H2S molecule on all Ni/Pd(111) surfaces are exothermic, especially for the surfaces that the top layer is composed of Ni atoms. According to the predicted minimum energy paths that connect the molecular and dissociative states, two elementary steps are found for all Ni/Pd(111) metal surfaces, and the breaking of the first Hsbnd S bond is the rate-determining step for the H2S dissociation. Our results reveal that in most cases, the decomposition of H2S molecule on the monometallic and Ni/Pd(111) monolayer bimetallic surfaces is easy to happen. However, on the monolayer Ni-Pd(111) surface, there is a competition between the trapping-desorption channel and activated dissociation channel, which implies that depositing one monolayer Ni on a Pd(111) surface may help reducing sulfur poisoning by hindering the dissociation of H2S molecule.

  16. Efficient removal and highly selective adsorption of Hg2+ by polydopamine nanospheres with total recycle capacity

    Science.gov (United States)

    Zhang, Xiulan; Jia, Xin; Zhang, Guoxiang; Hu, Jiamei; Sheng, Wenbo; Ma, Zhiyuan; Lu, Jianjiang; Liu, Zhiyong

    2014-09-01

    This study reported a new method for efficient removal of Hg2+ from contaminated water using highly selective adsorptive polydopamine (PDA) nanospheres, which were uniform and had a small diameter (150-200 nm). The adsorption isotherms, kinetics, thermodynamics were investigated. Also, the effects of ionic strength, co-existing ions on removing ability of PDA nanospheres for Hg2+ were studied. Adsorption of Hg2+ was very fast and efficient as adsorption equilibrium was completed within 4 h and the maximum adsorption capacities were 1861.72 mg/g, 2037.22 mg/g, and 2076.81 mg/g at 298 K, 313 K, and 328 K respectively, increasing with increasing of temperature. The PDA nanospheres exhibited highly selective adsorption of Hg2+ and had a total desorption capacity of 100% in hydrochloric acid solution, pH 1. The results showed that the structure of PDA nanospheres remained almost unchanged after recycling five times. Furthermore, X-ray photoelectron spectroscopy (XPS) was employed to determine the elements of PDA nanospheres before and after Hg2+ adsorption. Considering their efficient and highly Hg2+ selective adsorption, total recycle capacity, and high stability, PDA nanospheres will be feasible in a number of practical applications.

  17. Adsorption Capacity and Mechanism of Expanded Graphite for Polyethylene Glycol and Oils

    Directory of Open Access Journals (Sweden)

    Xiu-Yan Pang

    2010-01-01

    Full Text Available Expanded graphite (EG shows higher adsorption capacity for oils such as salad oil and SD300 oil than polyethylene glycol (PEG with different MW (4000, 10000, 20000. To illustrate their different adsorption mechanism, adsorption capacities of EG for these pollutants are firstly detected. And then stepwise adsorption for oils is carried out with EG which has been saturated first by PEG with different MW. Then difference between stepwise adsorbance of oil is checked with deviation analysis. Scanning electronic microscopy (SEM analysis is used to show structure difference of EG adsorbed different adsorbates. It is testified adsorption isotherms of PEG are all type I, PEG molecules lay flat on EG surface and equilibrium adsorbance decrease with the increase of PEG MW. Adsorbance for SD 300 oil and salad oil can reach 131.3 g/g and 127.8 g/g respectively. Deviation analysis for stepwise adsorbance of oil shows no statistical significance. EG saturated firstly by PEG, still has an average adsorption capacity of 98 g/g for SD300 oil and 85 g/g for salad oil and it does not change with the initial PEG concentration. SEM photos illustrate the adsorption of oil on EG is mainly filling. In the adsorption of PEG water solution, there is severe breakage of the V-type pore and shrinkage of the particle.

  18. Monolayer MoS2-Graphene Hybrid Aerogels with Controllable Porosity for Lithium-Ion Batteries with High Reversible Capacity.

    Science.gov (United States)

    Jiang, Lianfu; Lin, Binghui; Li, Xiaoming; Song, Xiufeng; Xia, Hui; Li, Liang; Zeng, Haibo

    2016-02-03

    Monolayer MoS2 nanosheets (NSs) are promising anode materials for lithium-ion batteries because all redox reactions take place at the surface without lithium-ion diffusion limit. However, the expanded band gap of monolayer MoS2 NSs (∼1.8 eV) compared to their bulk counterparts (∼1.2 eV) and restacking tendency due to the van der Waals forces result in poor electron transfer and loss of the structure advantage. Here, a facile approach is developed to fabricate the MoS2-graphene aerogels comprising controlled three-dimensional (3D) porous architectures constructed by interconnected monolayer MoS2-graphene hybrid NSs. The robust 3D architectures combining with the monolayer feature of the hybrid NSs not only prevent the MoS2 and graphene NSs from restacking, but also enable fast electrode kinetics due to the surface reaction mechanism and highly conductive graphene matrix. As a consequence, the 3D porous monolayer MoS2-graphene composite aerogels exhibit a large reversible capacity up to 1200 mAh g(-1) as well as outstanding cycling stability and rate performance, making them promising as advanced anode materials for lithium-ion batteries.

  19. Structural properties and adsorption capacity of holocellulose aerogels synthesized from an alkali hydroxide-urea solution

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, Gu-Joong; Kim, Dae-Young; Hwang, Jae-Hyun; Kang, Joo-Hyon [Dongguk University, Seoul (Korea, Republic of)

    2014-05-15

    A tulip tree was used to synthesize a holocellulose aerogel from an aqueous alkali hydroxide-urea solution with the substitution of an organic solvent followed by freeze-drying. For comparison, the synthesized holocellulose aerogels were divided into two groups according to the source of the hydrogel, an upper suspended layer and a bottom concentrated layer of the centrifuged solution of cellulose and NaOH/urea solvents. We investigated the effects of the temperature of the pre-cooled NaOH/urea solution (i.e., dissolution temperature) on the pore structure and the adsorption capacity of the holocellulose aerogel. A nano-fibrillar network structure of the holocellulose aerogel was observed, with little morphological difference in pore structure for different dissolution temperatures. Both micropores and mesopores were observed in the holocellulose aerogel. The specific surface area of the holocellulose aerogel was generally greater at lower dissolution temperatures. In a series of adsorption tests using methylene blue, the holocellulose aerogel showed the greatest adsorption capacity at the lowest dissolution temperature tested ( -2 .deg. C). However, the dissolution temperature generally had little effect on the adsorption capacity. The holocellulose aerogel produced from the upper suspended layer of the centrifuged hydrogel solution showed a greater porosity and adsorption capacity than the one produced from the bottom concentrated layer. Overall, the aerogel made by utilizing a delignified tulip tree display a high surface area and a high adsorption property, indicating its possible application in eco-friendly adsorption materials.

  20. Enhancement of the anionic dye adsorption capacity of clinoptilolite by Fe{sup 3+}-grafting

    Energy Technology Data Exchange (ETDEWEB)

    Akgül, Murat, E-mail: makgul@hacettepe.edu.tr

    2014-02-01

    Graphical abstract: - Highlights: • Iron-grafted clinoptilolite was found to have higher adsorption capacity than that of raw clinoptilolite. • Iron-grafted clinoptilolite can be used as an efficient adsorbent for the removal of congo red at near-neutral pH. • pH dependency of adsorption process is different for raw and modified clinoptilolites. - Abstract: In this paper, a batch system was applied to study the adsorption behavior of congo red (CR) on raw and modified clinoptilolites. Raw clinoptilolite (Raw-CL) was treated with Fe(NO{sub 3}){sub 3} in ethanol to obtain its iron-grafted form (Fe-CL). Adsorbents were characterized by X-ray diffraction (XRD), Fourier transform-infrared (FT-IR), energy dispersive X-ray spectroscopy (EDX), thermogravimetric/differential thermal analysis (TG/DTA), zeta-potential measurement and N{sub 2} gas adsorption–desorption techniques. Effects of the experimental parameters (initial pH, dye concentration, temperature and adsorption time) were investigated to find optimum conditions that result in highest adsorption capacity for CR removal. The obtained results suggest that the solution pH appears to be a key factor of the CR adsorption process. The maximum dye adsorption was achieved with Fe-CL adsorbent at pH ∼6.3 and the corresponding adsorption capacity was found to be 36.7 mg/g, which is higher than that of its raw counterpart (16.9 mg/g). A significant decrease in CR removal was given by Fe-CL between pH 7 and 11 opposite to Raw-CL which has nearly constant q{sub e} in the same pH range. The Fe{sup 3+}-grafting increased the zeta potential of raw clinoptilolite, leading to a higher adsorption capacity compared to that of unfunctionalized adsorbent. Also, temperature change was found to have a significant effect on the adsorption process.

  1. Alkali metal adsorption on Ge(0 0 1)-c(2 × 4) surface: 0.25 monolayer of Na, K, Rb and Cs

    Energy Technology Data Exchange (ETDEWEB)

    Stankiewicz, B., E-mail: bst@ifd.uni.wroc.pl [Institute of Experimental Physics, University of Wrocław, Pl. Maxa Borna 9, 50-204 Wrocław (Poland); Mikołajczyk, P. [Nokia Solutions and Networks, Gen. J. Bema Str. 2, 50-265 Wrocław (Poland)

    2014-05-01

    Highlights: • We examine alkali metals adsorption on the Ge(0 0 1)-c(2 × 4) surface. • We calculated atomic and electronic structures using local-orbital and plane-waves methods. • We simulated expected scanning tunneling microscopy images. - Abstract: Alkali metals on Ge(0 0 1) surface reveal different adsorption energy depending on the initial substrate reconstruction and the adsorption site. The theoretical analysis of adsorption of 0.25 monolayer of alkali metals (Na, K, Rb and Cs) on Ge(0 0 1)-c(2 × 4) surface is presented. Stable adsorption sites are found and adsorption energy, atomic and electronic structures are given. The simulated STM images are also presented for the discussed adsorbed surface structures.

  2. Reduction of adsorption capacity of coconut shell activated carbon for organic vapors due to moisture contents.

    Science.gov (United States)

    Abiko, Hironobu; Furuse, Mitsuya; Takano, Tsuguo

    2010-01-01

    In occupational hygiene, activated carbon produced from coconut shell is a common adsorbent material for harmful substances including organic vapors due to its outstanding adsorption capacity and cost advantage. However, moisture adsorption of the carbon generally decreases the adsorption capacity for organic vapors. In a previous report, we prepared several coconut shell activated carbons which had been preconditioned by equilibration with moisture at different relative humidities and measured the breakthrough times for 6 kinds of organic vapor, in order to clarify the effect of preliminary moisture content in activated carbon on the adsorption capacity in detail. We found that the relative percent weight increase due to moisture adsorption of the carbon specimen had a quantitative effect, reducing the breakthrough time. In this report, we carried out further measurements of the effect of moisture content on the adsorption of 13 kinds of organic vapor, and investigated the relationship between moisture adsorption and the reduction of the breakthrough time of activated carbon specimens. We also applied the data to the Wood's breakthrough time estimation model which is an extension of the Wheeler-Jonas equation.

  3. Better adsorption capacity of SnO2 nanoparticles with different graphene addition

    Science.gov (United States)

    Paramarta, V.; Taufik, A.; Saleh, R.

    2016-11-01

    The adsorption capacity of SnO2 nanoparticle has been studied by graphene and nanographene platelets (NGP) additions using co-precipitation method. The crystalline phase, composition, and morphology of the samples are analyzed using X-Ray Diffraction (XRD), Energy Dispersive X-Ray (EDX), Fourier Transform Infrared Spectroscopy (FT-IR), and Transmission Electron Microscope (TEM). Tetragonal structure of SnO2 is shown for the nanoparticle and its composites. The presence of graphene and NGP is also confirmed. The adsorption capacity of the nanoparticle and its composites are analyzed by observing the degradation of methylene blue (MB) as the organic dye model using UV-Vis Spectroscopy. The result shows that SnO2 composite with graphene achieves higher adsorption capacity of about 20% than the composite with NGP. The fitting of equilibrium adsorption capacity result indicates that the adsorption mechanism of SnO2 composite with graphene tends to follow the Langmuir adsorption-isotherm model.

  4. Non-contact analysis of the adsorptive ink capacity of nano silica pigments on a printing coating base

    National Research Council Canada - National Science Library

    Jiang, Bo; Huang, Yu Dong

    2014-01-01

    .... First, the recording coating materials were prepared based on nano silica pigments. 80 samples of the recording coating materials were selected to develop the calibration of adsorptive ink capacity against ink adsorption (g/m2...

  5. Non-Contact Analysis of the Adsorptive Ink Capacity of Nano Silica Pigments on a Printing Coating Base: e109918

    National Research Council Canada - National Science Library

    Bo Jiang; Yu Dong Huang

    2014-01-01

    .... First, the recording coating materials were prepared based on nano silica pigments. 80 samples of the recording coating materials were selected to develop the calibration of adsorptive ink capacity against ink adsorption (g/m2...

  6. Surface-water interface induces conformational changes critical for protein adsorption: Implications for monolayer formation of EAS hydrophobin

    Directory of Open Access Journals (Sweden)

    Kamron eLey

    2015-11-01

    Full Text Available The class I hydrophobin EAS is part of a family of small, amphiphilic fungal proteins best known for their ability to self-assemble into stable monolayers that modify the hydrophobicity of a surface to facilitate further microbial growth. These proteins have attracted increasing attention for industrial and biomedical applications, with the aim of designing surfaces that have the potential to maintain their clean state by resisting non-specific protein binding. To gain a better understanding of this process, we have employed all-atom molecular dynamics to study initial stages of the spontaneous adsorption of monomeric EAS hydrophobin on fully hydroxylated silica, a commonly used industrial and biomedical substrate. Particular interest has been paid to the Cys3-Cys4 loop, which has been shown to exhibit disruptive behavior in solution, and the Cys7-Cys8 loop, which is believed to be involved in the aggregation of EAS hydrophobin at interfaces. Specific and water mediated interactions with the surface were also analyzed. We have identified two possible binding motifs, one which allows unfolding of the Cys7-Cys8 loop due to the surfactant-like behavior of the Cys3-Cys4 loop, and another which has limited unfolding due to the Cys3-Cys4 loop remaining disordered in solution. We have also identified intermittent interactions with water which mediate the protein adsorption to the surface, as well as longer lasting interactions which control the diffusion of water around the adsorption site. These results have shown that EAS behaves in a similar way at the air-water and surface-water interfaces, and have also highlighted the need for hydrophilic ligand functionalization of the silica surface in order to prevent the adsorption of EAS hydrophobin.

  7. Enantiopure chiral poly(glycerol methacrylate) self-assembled monolayers knock down protein adsorption and cell adhesion.

    Science.gov (United States)

    Li, Zheng; Köwitsch, Alexander; Zhou, Guoying; Groth, Thomas; Fuhrmann, Bodo; Niepel, Marcus; Amado, Elkin; Kressler, Jörg

    2013-10-01

    Chirality plays a fundamental role not only in biological systems, but also in synthetic materials intended for bio-applications. Self-assembled monolayers (SAMs) are prepared on gold surfaces through a "grafting to" method from racemic or enantiopure chiral poly(glycerol methacrylate)s (PGMA(rac), PGMA(R), and PGMA(S)), having a thiol endgroup. Such SAMs constitute a chemically and structurally well-defined model substrate for studying protein adsorption and cell adhesion as a function of the polymer chirality. Surface plasmon resonance measurements reveal that PGMA SAMs greatly reduce the adsorption of bovine serum albumin (BSA) compared to bare gold surfaces. Interestingly, enantiopure SAMs based on PGMA(R) or PGMA(S) show a significantly larger reduction in BSA adsorption than PGMA(rac)-covered surfaces. Studies with the monocytic cell line THP-1 show a similar relationship between enantiopurity of PGMA SAMs and the extent of cell adhesion. Ellipsometry and Raman spectroscopy measurements indicate that SAMs formed by PGMA(rac) have a higher grafting density compared to SAMs of PGMA(R) and PGMA(S). This seems to be due to the ability of PGMA(rac) to form more intermolecular hydrogen bonds among polymer chains compared to the enantiopure PGMAs. Circular dichroism spectroscopy provide evidence that enantiopure polymers adopt a chiral ordered conformation, most likely helical, in aqueous solutions. It is concluded that a higher water content of SAMs formed by enantiopure PGMA(S) and PGMA(R) SAMs arises from the macromolecular chiral conformation adopted by their enantiopure PGMA chains, and it is the decisive reason for the reduced BSA adsorption and cell adhesion as compared to PGMA(rac) SAMs.

  8. Oxygen adsorption and dissociation during the oxidation of monolayer Ti2C

    KAUST Repository

    Gan, Liyong

    2013-08-20

    Exfoliated two-dimensional early transition metal carbides and carbonitrides are usually not terminated by metal atoms but saturated by O, OH, and/or F, thus making it difficult to understand the surface structure evolution and the induced electronic modifications. To fill this gap, density functional theory and molecular dynamics simulations are performed to capture the initial stage of the oxidation process of Ti2C, a prototypical example from the recently fabricated class of two-dimensional carbides and carbonitrides. It is shown that the unsaturated Ti 3d orbitals of the pristine Ti2C surface interact strongly with the approaching O2 molecules, resulting in barrierless O2 dissociation. The diffusion of the dissociated O atoms is also found to be very facile. Molecular dynamics simulations suggest that both dissociation and diffusion are enhanced as the O2 coverage increases to 0.25 monolayer. For a coverage of less than 0.11 monolayer, the adsorbates lead to a minor modification of the electronic properties of Ti2C, while the modification is remarkable at 0.25 monolayer. The formed Ti2CO2 after O saturation is an indirect narrow gap semiconductor (0.33 eV) with high intrinsic carrier concentration at room temperature and high thermodynamic stability at intermediate temperature (e.g., 550 °C).

  9. The adsorption of CO and NO on the MoS2 monolayer doped with Au, Pt, Pd, or Ni: A first-principles study

    Science.gov (United States)

    Ma, Dongwei; Ju, Weiwei; Li, Tingxian; Zhang, Xiwei; He, Chaozheng; Ma, Benyuan; Lu, Zhansheng; Yang, Zongxian

    2016-10-01

    By performing the first-principles calculation, the adsorption of CO and NO molecules on the Au, Pt, Pd, or Ni doped MoS2 monolayer has been studied. The interaction between CO or NO with the doped MoS2 monolayer is strong and belongs to the chemisorption, as evidenced by the large adsorption energy and the short distance between the adsorbed molecules and the dopants. The charge transfer and the electronic property induced by the molecule adsorption are discussed. It is found that for both CO and NO adsorption, for all the cases charge transfer between the substrates and the adsorbed molecules has been observed. For NO, the adsorption obviously induces new impurity states in the band gap or the redistribution of the original impurity states. These can lead to the change of the transport properties of the doped MoS2 monolayer, by which the adsorbed CO or NO can be detected. The present work shows that introducing appropriate dopants may be a feasible method to improve the performance of MoS2-based gas sensors.

  10. Enhancement of the anionic dye adsorption capacity of clinoptilolite by Fe(3+)-grafting.

    Science.gov (United States)

    Akgül, Murat

    2014-02-28

    In this paper, a batch system was applied to study the adsorption behavior of congo red (CR) on raw and modified clinoptilolites. Raw clinoptilolite (Raw-CL) was treated with Fe(NO3)3 in ethanol to obtain its iron-grafted form (Fe-CL). Adsorbents were characterized by X-ray diffraction (XRD), Fourier transform-infrared (FT-IR), energy dispersive X-ray spectroscopy (EDX), thermogravimetric/differential thermal analysis (TG/DTA), zeta-potential measurement and N2 gas adsorption-desorption techniques. Effects of the experimental parameters (initial pH, dye concentration, temperature and adsorption time) were investigated to find optimum conditions that result in highest adsorption capacity for CR removal. The obtained results suggest that the solution pH appears to be a key factor of the CR adsorption process. The maximum dye adsorption was achieved with Fe-CL adsorbent at pH ∼6.3 and the corresponding adsorption capacity was found to be 36.7mg/g, which is higher than that of its raw counterpart (16.9mg/g). A significant decrease in CR removal was given by Fe-CL between pH 7 and 11 opposite to Raw-CL which has nearly constant qe in the same pH range. The Fe(3+)-grafting increased the zeta potential of raw clinoptilolite, leading to a higher adsorption capacity compared to that of unfunctionalized adsorbent. Also, temperature change was found to have a significant effect on the adsorption process.

  11. Optimization of layered double hydroxide stability and adsorption capacity for anionic surfactants

    OpenAIRE

    2007-01-01

    Low cost adsorption technology offers high potential to clean up laundry rinsing water. From an earlier selection of adsorbents, layered double hydroxide (LDH) proved to be an interesting material for the removal of anionic surfactant, linear alkyl benzene sulfonate (LAS) which is the main contaminant in rinsing water. The main research question was to identify the effect of process parameters of the LDH synthesis on the stability of the LDH structure and the adsorption capacity of LAS. LDH w...

  12. Correlation and prediction of adsorption capacity and affinity of aromatic compounds on carbon nanotubes.

    Science.gov (United States)

    Wu, Wenhao; Yang, Kun; Chen, Wei; Wang, Wendi; Zhang, Jie; Lin, Daohui; Xing, Baoshan

    2016-01-01

    Adsorption of 22 nonpolar and polar aromatic compounds on 10 carbon nanotubes (CNTs) with various diameters, lengths and surface oxygen-containing group contents was investigated to develop predictive correlations for adsorption, using the isotherm fitting of Polanyi theory-based Dubinin-Ashtakhov (DA) model. Adsorption capacity of aromatic compounds on CNTs is negatively correlated with melting points of aromatic compounds, and surface oxygen-containing group contents and surface area ratios of mesopores to total pores of CNTs, but positively correlated with total surface area of CNTs. Adsorption affinity is positively correlated with solvatochromic parameters of aromatic compounds, independent of tube lengths and surface oxygen-containing group contents of CNTs, but negatively correlated with surface area ratios of mesopores to total pores of CNTs. The correlations of adsorption capacity and adsorption affinity with properties of both aromatic compounds and CNTs clearly have physical significance, can be used successfully with DA model to predict adsorption of aromatic compounds on CNTs from the well-known physiochemical properties of aromatic compounds (i.e., solvatochromic parameters, melting points) and CNTs (i.e., surface area and total acidic group contents), and thus can facilitate the environmental application of CNTs as sorbents and environmental risk assessment of both aromatic contaminants and CNTs.

  13. Carbon nanotube membranes with ultrahigh specific adsorption capacity for water desalination and purification.

    Science.gov (United States)

    Yang, Hui Ying; Han, Zhao Jun; Yu, Siu Fung; Pey, Kin Leong; Ostrikov, Kostya; Karnik, Rohit

    2013-01-01

    Development of technologies for water desalination and purification is critical to meet the global challenges of insufficient water supply and inadequate sanitation, especially for point-of-use applications. Conventional desalination methods are energy and operationally intensive, whereas adsorption-based techniques are simple and easy to use for point-of-use water purification, yet their capacity to remove salts is limited. Here we report that plasma-modified ultralong carbon nanotubes exhibit ultrahigh specific adsorption capacity for salt (exceeding 400% by weight) that is two orders of magnitude higher than that found in the current state-of-the-art activated carbon-based water treatment systems. We exploit this adsorption capacity in ultralong carbon nanotube-based membranes that can remove salt, as well as organic and metal contaminants. These ultralong carbon nanotube-based membranes may lead to next-generation rechargeable, point-of-use potable water purification appliances with superior desalination, disinfection and filtration properties.

  14. Adsorption geometry and electronic properties of flat-lying monolayers of tetracene on the Ag(111) surface

    Science.gov (United States)

    Zaitsev, N. L.; Nechaev, I. A.; Höfer, U.; Chulkov, E. V.

    2016-10-01

    The geometrical and electronic properties of the monolayer (ML) of tetracene (Tc) molecules on Ag(111) are systematically investigated by means of DFT calculations with the use of a localized basis set. The bridge and hollow adsorption positions of the molecule in the commensurate γ -Tc/Ag(111) are revealed to be the most stable and equally favorable irrespective to the approximation chosen for the exchange-correlation functional. The binding energy is entirely determined by the long-range dispersive interaction. The former lowest unoccupied molecular orbital remains being unoccupied in the case of γ -Tc/Ag(111) as well as in the α phase with increased coverage. The unit cell of the α phase with point-on-line registry was adapted for calculations based on the available experimental data and computed structures of the γ phase. The calculated position of the Tc/Ag(111) interface state is found to be noticeably dependent on the lattice constant of the substrate, however its energy shift with respect to the Shockley surface state of the unperturbed clean side of the slab is sensitive only to the adsorption distance and in good agreement with the experimentally measured energy shift.

  15. High-Capacity and Photoregenerable Composite Material for Efficient Adsorption and Degradation of Phenanthrene in Water.

    Science.gov (United States)

    Liu, Wen; Cai, Zhengqing; Zhao, Xiao; Wang, Ting; Li, Fan; Zhao, Dongye

    2016-10-18

    We report a novel composite material, referred to as activated charcoal supported titanate nanotubes (TNTs@AC), for highly efficient adsorption and photodegradation of a representative polycyclic aromatic hydrocarbon (PAH), phenanthrene. TNTs@AC was prepared through a one-step hydrothermal method, and is composed of an activated charcoal core and a shell of carbon-coated titanate nanotubes. TNTs@AC offered a maximum Langmuir adsorption capacity of 12.1 mg/g for phenanthrene (a model PAH), which is ∼11 times higher than the parent activated charcoal. Phenanthrene was rapidly concentrated onto TNTs@AC, and subsequently completely photodegraded under UV light within 2 h. The photoregenerated TNTs@AC can then be reused for another adsorption-photodegradation cycle without significant capacity or activity loss. TNTs@AC performed well over a wide range of pH, ionic strength, and dissolved organic matter. Mechanistically, the enhanced adsorption capacity is attributed to the formation of carbon-coated ink-bottle pores of the titanate nanotubes, which are conducive to capillary condensation; in addition, the modified microcarbon facilitates transfer of excited electrons, thereby inhibiting recombination of the electron-hole pairs, resulting in high photocatalytic activity. The combined high adsorption capacity, photocatalytic activity, and regenerability/reusability merit TNTs@AC a very attractive material for concentrating and degrading a host of micropollutants in the environment.

  16. The effect of vanadium-carbon monolayer on the adsorption of tungsten and carbon atoms on tungsten-carbide (0001 surface

    Directory of Open Access Journals (Sweden)

    Moitra A.

    2011-01-01

    Full Text Available We report a first-principles calculations to study the effect of a vanadium-carbon (VC monolayer on the adsorption process of tungsten (W and carbon (C atoms onto tungsten-carbide (WC (0001 surface. The essential configuration for the study is a supercell of hexagonal WC with a (0001 surface. When adding the VC monolayer, we employed the lowest energy configuration by examining various configurations. The total energy of the system is computed as a function of the W or C adatoms’ height from the surface. The adsorption of a W and C adatom on a clean WC (0001 surface is compared with that of a W and C adatom on a WC (0001 surface with VC monolayer. The calculations show that the adsorption energy increased for both W and C adatoms in presence of the VC monolayer. Our results provide a fundamental understanding that can explain the experimentally observed phenomena of inhibited grain growth during sintering of WC or WC-Co powders in presence of VC.

  17. Adsorption of selected pharmaceuticals and an endocrine disrupting compound by granular activated carbon. 1. Adsorption capacity and kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Z.; Peldszus, S.; Huck, P.M. [University of Waterloo, Waterloo, ON (Canada). NSERC Chair in Water Treatment

    2009-03-01

    The adsorption of two representative PhACs (naproxen and carbamazepine) and one EDC (nonylphenol) were evaluated on two granular activated carbons (GAC) namely coal-based Calgon Filtrasorb 400 and coconut shell-based PICA CTIF TE. The primary objective was to investigate preloading effects by natural organic matter (NOM) on adsorption capacity and kinetics under conditions and concentrations (i.e., ng/L) relevant for drinking water treatment. Isotherms demonstrated that all compounds were significantly negatively impacted by NOM fouling. Adsorption capacity reduction was most severe for the acidic naproxen, followed by the neutral carbamazepine and then the more hydrophobic nonylphenol. The GAC with the wider pore size distribution had considerably greater NOM loading, resulting in lower adsorption capacity. Different patterns for the change in Freundlich KF and 1/n with time revealed different competitive mechanisms for the different compounds. Mass transport coefficients determined by short fixed-bed (SFB) tests with virgin and preloaded GAC demonstrated that film diffusion primarily controls mass transfer on virgin and preloaded carbon. Naproxen suffered the greatest deteriorative effect on kinetic parameters due to preloading, followed by carbamazepine, and then nonylphenol. A type of surface NOM/biofilm, which appeared to add an additional mass transfer resistance layer and thus reduce film diffusion, was observed. In addition, electrostatic interactions between NOM/biofilm and the investigated compounds are proposed to contribute to the reduction of film diffusion. A companion paper building on this work describes treatability studies in pilot-scale GAC adsorbers and the effectiveness of a selected fixed-bed model. 32 refs., 3 figs., 2 tabs.

  18. Adsorption Characteristics of DNA Nucleobases, Aromatic Amino Acids and Heterocyclic Molecules on Silicene and Germanene Monolayers

    KAUST Repository

    Hussain, Tanveer

    2017-09-14

    Binding of DNA/RNA nucleobases, aromatic amino acids and heterocyclic molecules on two-dimensional silicene and germanene sheets have been investigated for the application of sensing of biomolecules using first principle density functional theory calculations. Binding energy range for nucleobases, amino acids and heterocyclic molecules with both the sheets have been found to be (0.43-1.16eV), (0.70-1.58eV) and (0.22-0.96eV) respectively, which along with the binding distances show that these molecules bind to both sheets by physisorption and chemisorption process. The exchange of electric charges between the monolayers and the incident molecules has been examined by means of Bader charge analysis. It has been observed that the introduction of DNA/RNA nucleobases, aromatic amino acids and heterocyclic molecules alters the electronic properties of both silicene and germanene nano sheets as studied by plotting the total (TDOS) and partial (PDOS) density of states. The DOS plots reveal the variation in the band gaps of both silicene and germanene caused by the introduction of studied molecules. Based on the obtained results we suggest that both silicene and germanene monolayers in their pristine form could be useful for sensing of biomolecules.

  19. First-principles investigations of metal (V, Nb, Ta)-doped monolayer MoS2: Structural stability, electronic properties and adsorption of gas molecules

    Science.gov (United States)

    Zhu, Jia; Zhang, Hui; Tong, Yawen; Zhao, Ling; Zhang, Yongfan; Qiu, Yuzhi; Lin, Xianning

    2017-10-01

    Two-dimensional (2D) layered materials are at the forefront of research because of their unique structures and promising catalytic abilities. Here, the structural stability, electronic properties and gas adsorption of metal (V, Nb, Ta)-doped monolayer MoS2 have been investigated by density functional theory calculations. Our results show that the metal (V, Nb, Ta)-doped monolayer MoS2 is a stable catalyst under room temperature, due to the strong interaction between the doped metals (V, Nb, Ta) and S vacancy of monolayer MoS2. Compared with the gas adsorption (CO, NO2, H2O, NH3) on pristine monolayer MoS2, doped metal (V, Nb, Ta) can significantly improve the adsorption properties, chemical activity and the sensitivity of that of adsorbed gas molecules. This effect occurs due to the strong overlap between the metal nd orbitals and gas molecule orbitals, result in activation of the adsorbed gas molecules. Analysis of Bader charge shows that, more charge transfer (-0.66 e to -0.72 e) occur from metal (V, Nb, Ta)-doped monolayer MoS2 to the oxidizing gas molecules (NO2) acting as acceptors. While for the adsorption of CO molecules, the relative less electrons (about -0.24 e - -0.35 e) transfer occuring from substrate to the adsorbed gases. Whereas the direction of charge transfers is reversed for the adsorption of the reducing gas (H2O and NH3) behaving as donors, in which small electrons (0.04 e -0.09 e) transfer from adsorbed gas to metal (V, Nb, Ta)-doped monolayer MoS2. Our results suggested that metal (V, Nb, Ta)-doped monolayer MoS2 might be a good candidate for low-cost, highly active, and stable catalysts and gas sensors, providing an avenue to facilitate the design of high active MoS2-based two dimensional catalysts and gas sensors.

  20. Adsorption and dissociation of H{sub 2}S on monometallic and monolayer bimetallic Ni/Pd(111) surfaces: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yi, E-mail: liy99@fzu.edu.cn [College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350116 (China); Fujian Provincial Key Laboratory of Theoretical and Computational Chemistry, Xiamen, Fujian, 361005 (China); Huang, Pan; Tao, Dandan; Wu, Juan; Qiu, Mei; Huang, Xin; Ding, Kaining; Chen, Wenkai [College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350116 (China); Su, Wenyue [State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou, Fujian, 350002 (China); Zhang, Yongfan, E-mail: zhangyf@fzu.edu.cn [College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350116 (China); State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou, Fujian, 350002 (China)

    2016-11-30

    Highlights: • For the molecular adsorption, the introducing Ni monolayer on Pd(111) can reduce the binding strength between H{sub 2}S and the surface. • The decompositions of H{sub 2}S molecule on all Ni/Pd(111) surfaces are exothermic, especially for the surfaces that the top layer is composed of Ni atoms. • Monolayer Ni-Pd(111) surface may exhibit a good sulfur resistance performance because there is a competition between the desorption and decomposition of H{sub 2}S molecule. - Abstract: Periodic density functional theory calculations have been performed to investigate the adsorption structures and dissociative reaction pathways for H{sub 2}S molecule on Ni(111), Pd(111) and Ni/Pd(111) monolayer bimetallic surfaces with surface monolayer and subsurface monolayer structures. Our results indicate that, for the molecular adsorption mode, the introducing Pd atoms on Ni(111) can enhance the binding strength between H{sub 2}S and the surface, while an opposite effect is achieved when the Ni monolayer is formed on Pd(111) surface. The decompositions of H{sub 2}S molecule on all Ni/Pd(111) surfaces are exothermic, especially for the surfaces that the top layer is composed of Ni atoms. According to the predicted minimum energy paths that connect the molecular and dissociative states, two elementary steps are found for all Ni/Pd(111) metal surfaces, and the breaking of the first H−S bond is the rate-determining step for the H{sub 2}S dissociation. Our results reveal that in most cases, the decomposition of H{sub 2}S molecule on the monometallic and Ni/Pd(111) monolayer bimetallic surfaces is easy to happen. However, on the monolayer Ni-Pd(111) surface, there is a competition between the trapping-desorption channel and activated dissociation channel, which implies that depositing one monolayer Ni on a Pd(111) surface may help reducing sulfur poisoning by hindering the dissociation of H{sub 2}S molecule.

  1. Polyhydroxyl-aluminum pillaring improved adsorption capacities of Pb2+ and Cd2+ onto diatomite

    Institute of Scientific and Technical Information of China (English)

    朱健; 王平; 雷明婧; 张伟丽

    2014-01-01

    In order to greatly improve adsorption capacity, the diatomite was pillared by polyhydroxyl-aluminum.A series of adsorption tests were conducted to obtain the optimum condition for pillared diatomite synthesis. The scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), surface area and porosity analyzer and micro-electrophoresis were used to determine pore structure and surface property.The pillared diatomite attaining the optimal adsorption densities (qe) of Pb2+ and Cd2+ was synthesized with the following conditions: Addition of pillaring solution containing Al3+-oligomers with a concentration range of 0.1-0.2 mol/L to a suspension containing Na+-diatomite to obtain the required Al/diatomite ratio of 10 mmol/g; synthesis temperature of 80 °C for 120 min; aging at a temperature of 105 °C for 16 h. The adsorption capacities of Pb2+ and Cd2+ on pillared diatomite increase by 23.79% and 27.36% compared with natural diatomite, respectively. The surface property of pillared diatomite is more favorable for ion adsorption than natural diatomite. The result suggests that diatomite can be modified by pillaring with polyhydroxyl-aluminum to improve its adsorption properties greatly.

  2. Characterization and bisphenol A adsorption capacity of β-cyclodextrin-carboxymethylcellulose-based hydrogels.

    Science.gov (United States)

    Kono, Hiroyuki; Onishi, Kenta; Nakamura, Taichi

    2013-10-15

    Novel hydrogel beads having molecular adsorption abilities were prepared from carboxymethylcellulose sodium salt (CMC) and β-cyclodextrin (β-CD) by suspension crosslinking, using ethylene glycol diglycidyl ether (EGDE) in basic medium as a crosslinking agent. FTIR and solid-state NMR spectroscopic analysis revealed that the amount of incorporated β-CD and crosslinking densities within the hydrogel bead structures are strongly dependent on the molar feed ratio of β-CD to CMC during preparation. The hydrogel beads showed water-swelling capacities of 70-200 mL/g-polymer, with decreases in capacity associated with increased amounts of β-CD incorporated in the gel structure. The hydrogel beads also showed a high adsorption capacity toward bisphenol A (BPA) in water. Batch BPA-adsorption experiments were analyzed employing Langmuir isotherm models; hydrogel bead adsorption isotherms for BPA could be fitted to the Langmuir model. The maximum BPA-adsorption among the prepared series of hydrogel beads amounted to 167 μmol g(-1).

  3. High-capacity hydrogen and nitric oxide adsorption and storage in a metal-organic framework.

    Science.gov (United States)

    Xiao, Bo; Wheatley, Paul S; Zhao, Xuebo; Fletcher, Ashleigh J; Fox, Sarah; Rossi, Adriano G; Megson, Ian L; Bordiga, S; Regli, L; Thomas, K Mark; Morris, Russell E

    2007-02-07

    Gas adsorption experiments have been carried out on a copper benzene tricarboxylate metal-organic framework material, HKUST-1. Hydrogen adsorption at 1 and 10 bar (both 77 K) gives an adsorption capacity of 11.16 mmol H2 per g of HKUST-1 (22.7 mg g(-)1, 2.27 wt %) at 1 bar and 18 mmol per g (36.28 mg g(-)1, 3.6 wt %) at 10 bar. Adsorption of D2 at 1 bar (77 K) is between 1.09 (at 1 bar) and 1.20(at recovered on exposure of the resulting complex to water is enough to be biologically active, completely inhibiting platelet aggregation in platelet rich plasma.

  4. [Surface characteristics of alkali modified activated carbon and the adsorption capacity of methane].

    Science.gov (United States)

    Zhang, Meng-Zhu; Li, Lin; Liu, Jun-Xin; Sun, Yong-Jun; Li, Guo-Bin

    2013-01-01

    Coconut shell based activated carbon was modified by alkali with different concentrations. The surface structures of tested carbons were observed and analyzed by SEM and BET methods. Boehm's titration and SEM/EDS methods were applied to assay the functional groups and elements on the carbon surface. The adsorption of methane on tested carbons was investigated and adsorption behavior was described by the adsorption isotherms. Results showed that surface area and pore volume of modified carbon increased and surface oxygen groups decreased as the concentration of the alkali used increased, with no obvious change in pore size. When concentration of alkali was higher than 3.3 mol x L(-1), the specific surface area and pore volume of modified carbon was larger than that of original carbon. Methane adsorption capacity of alkali modified carbon increased 24%. Enlargement of surface area and pore volume, reduction of surface oxygen groups will benefit to enhance the methane adsorption ability on activated carbon. Adsorption behavior of methane followed the Langmuir isotherm and the adsorption coefficient was 163.7 m3 x mg(-1).

  5. Effect of purity on adsorption capacities of a Mars-like clay mineral at different pressures

    Science.gov (United States)

    Jenkins, Traci; Mcdoniel, Bridgett; Bustin, Roberta; Allton, Judith H.

    1992-01-01

    There has been considerable interest in adsorption of carbon dioxide on Marslike clay minerals. Some estimates of the carbon dioxide reservoir capacity of the martian regolith were calculated from the amount of carbon dioxide adsorbed on the ironrich smectite nontronite under martian conditions. The adsorption capacity of pure nontronite could place upper limits on the regolith carbon dioxide reservoir, both at present martian atmospheric pressure and at the postulated higher pressures required to permit liquid water on the surface. Adsorption of carbon dioxide on a Clay Mineral Society standard containing nontronite was studied over a wide range of pressures in the absence of water. Similar experiments were conducted on the pure nontronite extracted from the natural sample. Heating curves were obtained to help characterize and determine the purity of the clay sample.

  6. The influence of adsorption capacity on enhanced gas absorption in activated carbon slurries

    NARCIS (Netherlands)

    Holstvoogd, R.D.; Swaaij, van W.P.M.

    1990-01-01

    The enhanced absorption of gases in aqueous activated carbbon slurries of fine particles is studied with a non-steady-state absorption model, taking into account the finite adsorption capacity of the carbon particles. It has been found that, for the different gas/activated carbon slurry systems stud

  7. Detection of the adsorption of water monolayers through the ion oscillation frequency in the magnesium oxide lattice by means of low energy electron diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Guevara-Bertsch, M.; Avendaño, E. [Escuela de Física, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Centro de Investigación en Ciencia e Ingeniería de Materiales, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Ramírez-Hidalgo, G. [Centro de Investigación en Ciencia e Ingeniería de Materiales, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Sección de Física Teórica, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Chavarría-Sibaja, A.; Araya-Pochet, J. A. [Centro de Investigación en Ciencia e Ingeniería de Materiales, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Herrera-Sancho, O. A., E-mail: oscar-andrey.herrera@uibk.ac.at [Escuela de Física, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Centro de Investigación en Ciencia e Ingeniería de Materiales, Universidad de Costa Rica, 2060 San Pedro, San José (Costa Rica); Institut für Quantenoptik und Quanteninformation, Österreichische Akademie der Wissenschaften, Technikerstr. 21a, 6020 Innsbruck (Austria)

    2016-03-15

    We investigate the variation of the oscillation frequency of the Mg{sup 2+} and O{sup 2−} ions in the magnesium oxide lattice due to the interactions of the surface with water monolayers by means of Low Energy Electron Diffraction. Our key result is a new technique to determine the adsorbate vibrations produced by the water monolayers on the surface lattice as a consequence of their change in the surface Debye temperature and its chemical shift. The latter was systematically investigated for different annealing times and for a constant external thermal perturbation in the range of 110–300 K in order to accomplish adsorption or desorption of water monolayers in the surface lattice.

  8. Detection of the adsorption of water monolayers through the ion oscillation frequency in the magnesium oxide lattice by means of low energy electron diffraction

    Directory of Open Access Journals (Sweden)

    M. Guevara-Bertsch

    2016-03-01

    Full Text Available We investigate the variation of the oscillation frequency of the Mg2+ and O2− ions in the magnesium oxide lattice due to the interactions of the surface with water monolayers by means of Low Energy Electron Diffraction. Our key result is a new technique to determine the adsorbate vibrations produced by the water monolayers on the surface lattice as a consequence of their change in the surface Debye temperature and its chemical shift. The latter was systematically investigated for different annealing times and for a constant external thermal perturbation in the range of 110–300 K in order to accomplish adsorption or desorption of water monolayers in the surface lattice.

  9. Influence of the molecular-scale structures of 1-dodecanethiol and 4-methylbenzenethiol self-assembled monolayers on gold nanoparticles adsorption pattern.

    Science.gov (United States)

    Mamun, Abdulla Hel Al; Yoon, Sangwoon; Hahn, Jae Ryang

    2014-07-01

    In an effort to understand the effects of the molecular structures of self-assembled monolayers on the patterns formed by immobilized Au nanoparticles (AuNPs), we characterized and compared the morphologies and properties of AuNPs adsorbed onto self-assembled monolayers formed by 1-dodecanethiol (DDT-SAM) or 4-methylbenzenethiol (MBT-SAM) assembled on Au(111) surfaces. The AuNP adsorption pattern on the MBT-SAM surface was well-dispersed and characterized by a low degree of corrugation. By contrast, an aggregated and highly corrugated AuNP pattern was observed on the surface of the DDT-SAM. This difference was attributed to the retention or removal of citrate anions present on the AuNPs during adsorption onto the SAM surface. Direct interactions between the AuNPs and the highly corrugated hydrophobic surfaces of the DDT-SAMs could strip the citrate layers from the AuNP surfaces, leading to aggregated adsorption. The water molecules appeared to mediate the adsorption of the AuNPs by reducing the hydrophobicity of the MBT-SAM surface and promoting a more dispersed adsorption configuration.

  10. Influence of the inherent properties of drinking water treatment residuals on their phosphorus adsorption capacities.

    Science.gov (United States)

    Bai, Leilei; Wang, Changhui; He, Liansheng; Pei, Yuansheng

    2014-12-01

    Batch experiments were conducted to investigate the phosphorus (P) adsorption and desorption on five drinking water treatment residuals (WTRs) collected from different regions in China. The physical and chemical characteristics of the five WTRs were determined. Combined with rotated principal component analysis, multiple regression analysis was used to analyze the relationship between the inherent properties of the WTRs and their P adsorption capacities. The results showed that the maximum P adsorption capacities of the five WTRs calculated using the Langmuir isotherm ranged from 4.17 to 8.20mg/g at a pH of 7 and further increased with a decrease in pH. The statistical analysis revealed that a factor related to Al and 200 mmol/L oxalate-extractable Al (Alox) accounted for 36.5% of the variations in the P adsorption. A similar portion (28.5%) was attributed to an integrated factor related to the pH, Fe, 200 mmol/L oxalate-extractable Fe (Feox), surface area and organic matter (OM) of the WTRs. However, factors related to other properties (Ca, P and 5 mmol/L oxalate-extractable Fe and Al) were rejected. In addition, the quantity of P desorption was limited and had a significant negative correlation with the (Feox+Alox) of the WTRs (p<0.05). Overall, WTRs with high contents of Alox, Feox and OM as well as large surface areas were proposed to be the best choice for P adsorption in practical applications.

  11. The Adsorption Capacity, Pore Structure, and Thermal Behavior of the Modified Clay Containing SSA

    Directory of Open Access Journals (Sweden)

    Haijun Lu

    2016-01-01

    Full Text Available Sewage sludge ash (SSA was created by burning municipal sludge. The potential of clay containing 1 or 3 or 5% SSA was assessed for use as a landfill liner-soil material. Batch adsorption, low temperature N2 adsorption, and TG-DTA tests were performed to evaluate the adsorption capacity, micropore structure, thermostability, and components of soils under Cr(VI and Pb(II chemical solutions. With the increasing amount of SSA in modified clay, the adsorption capacity of Cr(VI and Pb(II to the modified clay increases gradually. After absorption, the pore size of modified clay ranges from 2 nm to 8 nm. With the increasing amount of absorption, the pore volume decreases and the specific surface area increases. With the increasing of adsorption concentration of Cr(VI and Pb(II, the mass loss percentage of modified clay increases to 23.4% and 12.6%, respectively. The modified clay containing SSA may be used as a good barrier material to attenuate contamination of Cr(VI and Pb(II in landfills.

  12. Enhanced formaldehyde-vapor adsorption capacity of polymeric amine-incorporated aminosilicas.

    Science.gov (United States)

    Nomura, Akihiro; Jones, Christopher W

    2014-05-19

    Airborne formaldehyde, which is a highly problematic volatile organic compound (VOC) pollutant, is adsorbed by polymeric amine-incorporated silicas (aminosilicas), and the factors that affect the adsorption performance are systematically investigated. Three different types of polymeric amines 1) poly(ethyleneimine) branched (PEIBR); 2) poly(ethyleneimine) linear (PEILI); and 3) poly(allylamine) (PAA) are impregnated into two types of porous silicas [SBA-15 and mesocellular foam (MCF) silicas] with systematic changes of the amine loadings. The adsorption results demonstrate that the adsorption capacity increases along with the amine loading until the polymeric amines completely fill the silica pores. This results in the MCF silica, which has a larger pore volume and hence can accommodate more polymeric amine before completely filling the pore, giving materials that adsorb more formaldehyde, with the largest adsorption capacity, q, of up to 5.7 mmolHCHO  g(-1) among the samples studied herein. Of the three different types of polymers, PAA, comprised of 100 % primary amines, showed the highest amine efficiency μ (mmolHCHO/mmolN) for capturing formaldehyde. The chemical structures of the adsorbed formaldehyde are analyzed by (13)C cross-polarization magic-angle spinning (CP-MAS) NMR, and it is demonstrated that the adsorbed formaldehyde is chemically attached to the aminosilica surface, forming hemiaminal and imine species. Because the chemical adsorption of formaldehyde forms covalent bonds, it is not desorbed from the aminosilicas below 130 °C based on temperature-programed-desorption (TPD) analysis. The high formaldehyde-adsorption capacity and stability of the trapped formaldehyde on the amine surface in this study reveal the potential utility of aminosilicas as formaldehyde abatement materials.

  13. Adsorption capacity of chosen sandy ground with respect to contaminants relocating with groundwater

    Directory of Open Access Journals (Sweden)

    Aniszewski Andrzej

    2017-03-01

    Full Text Available One of the most important problems concerning contaminant transport in the ground is the problem related to the definition of parameters characterizing the adsorption capacity of ground for the chosen contaminants relocating with groundwater. In this paper, for chloride and sulfate indicators relocating in sandy ground, the numerical values of retardation factors (Ra (treated as average values and pore groundwater velocities with adsorption (ux/Ra (in micro-pore ground spaces are taken into consideration. Based on 2D transport equation the maximal dimensionless concentration values (C*max c in the chosen ground cross-sections were calculated. All the presented numerical calculations are related to the unpublished measurement series which was marked in this paper as: October 1982. For this measurement series the calculated concentration values are compared to the measured concentration ones (C*max m given recently to the author of this paper. In final part of this paper the parameters characterizing adsorption capacity (Ra, ux/Ra are also compared to the same parameters calculated for the two earlier measurement series. Such comparison also allowed for the estimation of a gradual in time depletion of adsorption capacity for the chosen sandy ground.

  14. Influence of Main Components in Exhaust Gas on Mercury Adsorption Capacity of Brominated Activated Carbon

    Directory of Open Access Journals (Sweden)

    Tran Hong Con

    2016-01-01

    Full Text Available Brominated activated carbon (AC-Br, which was produced from coconut shell activated carbon (AC and brominated by wet way with elemental bromine, was determined as a material with super high adsorption capacity of mercury vapor. But in real exhaust gases, there are many components such as SO2, NOx, CO, CO2, HCl, H2O can influence on adsorption ability of the AC-Br. In this paper, these influences were studied and compared them between initial AC and AC-Br. Each component has different effect on AC and AC-Br and followed by its particular mechanism.

  15. Influence of diatomite microstructure on its adsorption capacity for Pb(II

    Directory of Open Access Journals (Sweden)

    Nenadović S.

    2009-01-01

    Full Text Available The effect of microstructural changes caused by mechanical modification on adsorption properties of diatomite samples were investigated. The microstructure has been characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM and atomic force microscopy (AFM while the degree of metal adsorption was evaluated by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP AES. The results show that metal sorption capacity of diatomite is considerably improved after mechanical modification and it can be attributed to amorphysation of the material. Immobilization efficiency increased from 22% for untreated to 81% for the treated sample after 5h at BPR 4.This qualifies natural diatomite as a material for wastewater remediation.

  16. Powder-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    Science.gov (United States)

    Janke, Christopher J.; Dai, Sheng; Oyola, Yatsandra

    2016-05-03

    A powder-based adsorbent and a related method of manufacture are provided. The powder-based adsorbent includes polymer powder with grafted side chains and an increased surface area per unit weight to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. A method for forming the powder-based adsorbent includes irradiating polymer powder, grafting with polymerizable reactive monomers, reacting with hydroxylamine, and conditioning with an alkaline solution. Powder-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  17. Novel biosorbent with high adsorption capacity prepared by chemical modification of white pine (Pinus durangensis) sawdust. Adsorption of Pb(II) from aqueous solutions.

    Science.gov (United States)

    Salazar-Rabago, J J; Leyva-Ramos, R

    2016-03-15

    The natural sawdust (NS) from white pine (Pinus durangensis) was chemically modified by a hydrothermal procedure using citric, malonic and tartaric acids. The adsorption capacity of modified sawdust (MS) towards Pb(II) was considerably enhanced due to the introduction of carboxylic groups on the surface of MS during the modification, and the adsorption capacity was almost linearly dependent on the concentration of carboxylic sites. The NS surface was acidic, and the MS surface became more acidic after the modification. At T = 25 °C and pH = 5, the maximum adsorption capacity of the optimal MS towards Pb(II) was 304 mg/g, which is exceptionally high compared to NS and other MS reported previously. The adsorption capacity of MS was considerably reduced from 304 to 154 mg/g by decreasing the solution pH from 5 to 3 due to electrostatic interactions. The adsorption of Pb(II) on MS was reversible at pH = 2, but not at pH = 5. The contribution percentage of ion exchange to the overall adsorption capacity ranged from 70 to 99% and 10-66% at the initial pH of 3 and 5, respectively. Hence, the adsorption of Pb(II) on MS was mainly due to ion exchange at pH = 3 and to both ion exchange and electrostatic attraction at pH = 5.

  18. Biochar Preparation, Characterization, and Adsorptive Capacity and Its Effect on Bioavailability of Contaminants: An Overview

    Directory of Open Access Journals (Sweden)

    Obemah D. Nartey

    2014-01-01

    Full Text Available This paper provides an updated review on the subjects, the available alternative to produce biochar from biomass, quantification and characterization of biochar, the adsorptive capacity for the adsorption of contaminants, and the effect of biochar addition to agricultural soils on contaminant bioavailability. The property of biochar produced is much dependent upon the composition and type of biomass and the conditions at which biomass is carbonized. The physical and chemical characterizations are necessary to identify the basic structure and property of biochar and to predict its potential in various environmental application. Biochar is a promising alternative to remedy the soils contaminated with heavy metals and organic compounds through adsorption and immobilization due to its large surface area, charged surface, and functional groups. Overall, the bioavailability of heavy metals and organic compounds decreases when biochar is amended into soils.

  19. The effect of food and ice cream on the adsorption capacity of paracetamol to high surface activated charcoal

    DEFF Research Database (Denmark)

    Høgberg, Lotte Christine Groth; Angelo, Helle Riis; Christophersen, Anne Bolette

    2003-01-01

    The effect of added food mixture (as if food was present in the stomach of an intoxicated patient) or 4 different types of ice cream (added as a flavouring and lubricating agent) on the adsorption of paracetamol (acetaminophen) to 2 formulations of activated charcoal was determined in vitro......, and paracetamol were mixed with either food mixture or ice cream followed by one hr incubation. The maximum adsorption capacity of paracetamol to activated charcoal was calculated using Langmuirs adsorption isotherm. Paracetamol concentration was analyzed using high pressure liquid chromatography. In the presence...... of food, the paracetamol adsorption capacity of the 2 activated charcoals was reduced by max. 19% (Pcream was mixed with the charcoal...

  20. Examination of zinc adsorption capacity of soils treated with different pyrolysis products

    Directory of Open Access Journals (Sweden)

    Rétháti Gabriella

    2014-11-01

    Full Text Available Organic matter input into soils is essential regarding agricultural, environmental and soil science aspects as well. However, the application of the pyrolysed forms of biochars and materials with different organic matter content gained more attention in order to decrease the emission of the green house gases (CO2, N2O from the soil. During pyrolysis, the materials containing high organic matter (biomass-originated organic matter are heated in oxygen-free (or limited amount of oxygen environment. As a result, the solid phase, which remains after eliminating the gases and liquid phase, is more stable compared to the original product, it cannot be mineralized easily in the soil and its utilization is more beneficial in terms of climatic aspects. Furthermore, it can improve soil structure and it can retain soil moisture and cations in the topsoil for long periods of time, which is very important for plants. In our experiment, the effects of biochar and bone char were examined on soils by zinc adsorption experiments. Based on our experiments, we concluded that the pyrolysis products can have significant Zn adsorption capacity compared to the soil. Bone ash can adsorb more Zn than the charcoal product. The Zn adsorption capacity of soils treated by pyrolysis products can be described by Langmuir adsorption isotherms. However, based on the amount of pyrolysis products, one or two term Langmuir isotherm fits well on the experiment data, which depends on the time the pyrolysis product has spent in the soil.

  1. Effect of surface modification of activated carbon on its adsorption capacity for NH3

    Institute of Scientific and Technical Information of China (English)

    SHAN Xiao-mei; ZHU Shu-quan; ZHANG Wen-hui

    2008-01-01

    To investigate the effects of carbon surface characteristics on NH3 adsorption, coal-based and coconut shell activated carbons were modified by treatment with oxidants. The surface properties of the carbons were characterized by low temperature nitrogen sorption, by Boehm's titrations and by XPS techniques. NH3 adsorption isotherms of the original and the modified carbons were determined. The results show that the carbons were oxidized by HNO3 and (NH4)2S2O8, and that there was an increase in oxygen containing functional groups on the surface. However, the pore-size distribution of the coal-based carbons was changed after KMnO4 treatment. It was found that the NH3 adsorption capacity of the modified carbons was enhanced and that the most pronounced enhancement results from (NH4)2S2O8 oxidation. Under our experimental conditions, the capacity is positively corrected to the number of surface functional groups containing oxygen, and to the number of micro-pores. Furthermore, an empirical model of the relationship between NH3 adsorption and multiple factors on the carbon surface was fit using a complex regression method.

  2. Activated carbons prepared from wood particleboard wastes: characterisation and phenol adsorption capacities.

    Science.gov (United States)

    Girods, P; Dufour, A; Fierro, V; Rogaume, Y; Rogaume, C; Zoulalian, A; Celzard, A

    2009-07-15

    The problems of valorisation of particleboard wastes on one hand, and contamination of aqueous effluents by phenolic compounds on the other hand, are simultaneously considered in this work. Preparation of activated carbons from a two steps thermo-chemical process, formerly designed for generating combustible gases, is suggested. The resultant carbonaceous residue is activated with steam at 800 degrees C. Depending on the preparation conditions, surface areas within the range 800-1300 m(2)/g are obtained, close to that of a commercial activated carbon (CAC) specially designed for water treatment and used as a reference material. The present work shows that particleboard waste-derived activated carbons (WAC) are efficient adsorbents for the removal of phenol from aqueous solutions, with maximum measured capacities close to 500 mg/g. However, most of times, the adsorption capacities are slightly lower than that of the commercial material in the same conditions, i.e., at equilibrium phenol concentrations below 300 ppm. Given the extremely low cost of activated carbons prepared from particleboard waste, it should not be a problem to use it in somewhat higher amounts than what is required with a more expensive commercial material. Phenol adsorption isotherms at 298 K were correctly fitted by various equations modelling type I and type II isotherms for CAC and WAC, respectively. Phenol adsorption isotherms of type II were justified by a 3-stages adsorption mechanism.

  3. Study of CO2 adsorption capacity of mesoporous carbon and activated carbon modified by triethylenetetramine (TETA)

    Science.gov (United States)

    Sulistianti, I.; Krisnandi, Y. K.; Moenandar, I.

    2017-04-01

    Mesoporous carbon was synthesized by soft template method using phloroglucinol and formaldehyde as a carbon source; and Pluronic F-127 as a mesoporous template. The synthesized mesoporous carbon and commercial activated carbon were modified with triethylenetetramine (TETA) to increase CO2 adsorption capacity. Based on FTIR characterization, the synthesized mesoporous carbon and the activated carbon without modification process has similarity pattern. After the modification, both of them showed absorption peaks in the area around 1580 to 1650 cm-1 which is known as N-H bending vibration and absorption peaks in the area around 3150 to 3380 cm-1 which is known as N-H stretching vibration. The XRD results showed two peaks at 2θ = 24.21° and 2θ = 43.85°, according to JCPDS index No. 75-1621 those peak are the typical peaks for hexagonal graphite carbon. In BET analysis, the synthesized mesoporous carbon and activated carbon modified TETA have surface area, pore volume and pore diameter lower than without modification process. In carbon dioxide adsorption testing, the synthesized mesoporous carbon showed better performance than the commercial activated carbon for CO2 adsorption both without modification and by modification. The synthesized mesoporous carbon obtained CO2 adsorption of 9.916 mmol/g and the activated carbon of 3.84 mmol/g for on 3.5 hours of adsorption. It is three times better than activated carbon for adsorption of carbon dioxide. The modified mesoporous carbon has the best performance for adsorption of gas CO2 if compared by unmodified.

  4. Dispersion of chitosan on perlite for enhancement of copper(II) adsorption capacity.

    Science.gov (United States)

    Hasan, Shameem; Ghosh, Tushar K; Viswanath, Dabir S; Boddu, Veera M

    2008-04-01

    Chitosan coated perlite beads were prepared by drop-wise addition of slurry, made of chitosan dissolved in oxalic acid and perlite, to an alkaline bath (0.7 M NaOH). The beads that contained 32% chitosan enhanced the accessibility of OH and amine groups present in chitosan for adsorption of copper ions. The experiments using Cu(II) ions were carried out in the concentration range of 50-4100 mg/L (0.78-64.1 mmol/L). Adsorption capacity for Cu(II) was pH dependent and a maximum uptake of 104 mg/g of beads (325 mg/g of chitosan) was obtained at pH 4.5 when its equilibrium concentration in the solution was 812.5 mg/L at 298 K. The XPS and TEM data suggested that copper was mainly adsorbed as Cu(II) and was attached to amine groups. The adsorption data could be fitted to one-site Langmuir adsorption model. Anions in the solution had minimal effect on Cu(II) adsorption by chitosan coated perlite beads. EDTA was used effectively for the regeneration of the bed. The diffusion coefficient of Cu(II) onto chitosan coated beads was calculated from the breakthrough curve and was found to be 2.02 x 10(-8) cm(2)/s.

  5. Synthesis, fine structural characterization, and CO2 adsorption capacity of metal organic frameworks-74.

    Science.gov (United States)

    Adhikari, Abhijit Krishna; Lin, Kuen-Song

    2014-04-01

    Two metal organic frameworks of MOF-74 group (zinc and copper-based) were successfully synthesized, characterized, and evaluated for CO2 adsorption. The both samples such as MOF-74(Zn) and MOF-74(Cu) were characterized with FE-SEM for morphology and particle size, XRD patterns for phase structure, FTIR for organic functional groups, nitrogen adsorption for pore textural properties, and X-ray absorption spectroscopy for fine structural parameters and oxidation states of central metal atoms. CO2 adsorption isotherms of MOF-74 samples were measured in a volumetric adsorption unit at 273 K and pressure up to 1.1 bar. The MOF-74(Zn) and MOF-74(Cu) adsorbents have the pore widths of 8.58 and 8.04 angstroms with the BET specific surface areas of 1,474 and 1,345 m2 g(-1), respectively. CO2 adsorption capacities of MOF-74(Zn) and MOF-74(Cu) were 4.10 and 3.38 mmol x g(-1), respectively measured at 273 K and 1.1 bar. The oxidation state of central atoms in MOF-74(Zn) was Zn(II) confirmed by XANES spectra while MOF-74(Cu) was composed of Cu(I) and Cu(II) central atoms. The bond distances of Zn--O and Cu--O were 1.98 and 1.94 angstroms, respectively.

  6. Enhancing the interaction strength and capacities of hydrogen storage via surface adsorption

    Science.gov (United States)

    Brown, Craig

    2008-03-01

    Storing Hydrogen molecules in porous media based on a physisorption mechanism is one possible approach to reach the US Department of Energy targets for on-board hydrogen storage. Although the storage capacities of metal-organic frameworks (MOFs) have progressed significantly over recent years, some technological obstacles pose challenges for their future improvement. These include the generally low H2 adsorption enthalpy limiting room temperature applications and the lack of understanding of surface packing density hindering the efficient improvement of H2 adsorption uptake. To improve the H2 affinity in MOFs, our previous work has shown that the coordinatively unsaturated metal centers (CUMCs) can greatly enhance the H2 binding strength. Our current study of MOF-74 will be presented, showing that its open Zn^2+ ions bind H2 strongly and are identified as being responsible for the large initial H2 adsorption enthalpy of 8.4 kJ/mol. In all, there are four H2 adsorption sites in MOF-74 identified by neutron powder diffraction. These four hydrogen adsorption sites are closely packed in MOF-74 and form a one dimensional nanoscale tube structure. We also demonstrate an interesting correlation that MOFs with CUMCs generally show larger surface packing densities than that of other MOFs without CUMCs. The implications of this will be addressed.

  7. Adsorption capacity of methylene blue, an organic pollutant, by montmorillonite clay

    KAUST Repository

    Feddal, I.

    2013-11-19

    The isotherms and kinetics of the adsorption of a cationic dye in aqueous solution, methylene blue, on a local Algerian montmorillonite clay mineral (raw, sodium and thermally activated at 300 and 500°C) were determined experimentally. Various parameters influencing the adsorption were optimized, mainly solid-liquid contact time, mass of adsorbent, initial concentration of dye, pH of the solution and temperature. Results showed that the adsorption kinetics were fast: 30 min for the raw clay mineral, and 20 min for sodium clay mineral (SC) and thermally activated at 300°C, whereas with the clay mineral calcined at 500°C, the equilibrium was reached after 150 min only. The maximum adsorption capacity was reached at pH 6.6. Results deducted from the adsorption isotherms also showed that the retention follows the Langmuir model. In addition, it was found that the kinetics were in the order of 2 (K = 2.457 × 106 g/mg.h) for sodium clay and were limited by an intra-particle diffusion. SC was found to be a better adsorbent to remove methylene blue from industrial wastewater. © 2013 Balaban Desalination Publications. All rights reserved.

  8. [Mechanism study of fluoride adsorption by hydrous metal oxides].

    Science.gov (United States)

    Guo, Hui-Chao; Li, Wen-Jun; Chang, Zhi-Dong; Wang, Huan-Ying; Zhou, Yue

    2011-08-01

    Hydrous oxides of cerium, aluminum, nickel and copper were prepared by alkaline precipitation method. Langmuir adsorption isotherm was studied and specific surface area was measured by BET method through N2 adsorption-desorption process. IR characterization of hydrous metal oxides before and after fluoride adsorption was also studied. Results show that different hydrous metal oxides have different specific surface areas and their pore size distributions also are not all the same. Adsorption capacity is not directly dependent on the specific surface area. Isotherm study indicates that the adsorption follows Langmuir model and shows the feature of monolayer adsorption. IR study before and after fluoride adsorption shows that different hydrous metal oxides have similar adsorption sites in the same IR region as well as adsorption sites in the different IR region. The comprehensive interaction of these adsorption sites with fluoride ions results in the different adsorption capacity of different hydrous metal oxides.

  9. Adsorption

    Directory of Open Access Journals (Sweden)

    Sushmita Banerjee

    2017-05-01

    Full Text Available Application of saw dust for the removal of an anionic dye, tartrazine, from aqueous solutions has been investigated. The experiments were carried out in batch mode. Effect of the parameters such as pH, initial dye concentration and temperature on the removal of the dye was studied. Equilibrium was achieved in 70 min. Maximum adsorption of dye was achieved at pH 3. Removal percent was found to be dependent on the initial concentration of dye solution, and maximum removal was found to be 97% at 1 mg/L of tartrazine. The removal increases from 71% to 97% when the initial concentration of dye solution decreases from 15 mg/L to 1 mg/L. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The (Langmuir adsorption capacity of the adsorbent is found to be 4.71 mg/g at 318 K. Kinetic modeling of the process of removal was carried out and the process of removal was found to follow a pseudo second order model and the value of rate constant for adsorption process was calculated as 2.7 × 10−3 g mg−1 min−1 at 318 K. The thermodynamic parameters such as change in free energy (ΔG°, enthalpy (ΔH° and entropy (ΔS° were determined and the negative values of ΔG° indicated that the process of removal was spontaneous at all values of temperatures. Further, the values of ΔH° indicated the endothermic nature of the process of removal.

  10. In vitro study of the effect of dog food on the adsorptive capacity of activated charcoal.

    Science.gov (United States)

    Wilson, Helen E; Humm, Karen R

    2013-01-01

    To evaluate the effect of dog food on the adsorptive capacity of activated charcoal. In vitro laboratory study. University veterinary teaching hospital. None. None. A fixed quantity of acetaminophen (50 mg) was added to a fixed quantity of activated charcoal (1 g), mixed with varying amounts of dog food (2-14 g). The admixture was agitated for 5 minutes, incubated at 38.5°C for 1 hour and then centrifuged for 30 minutes. The concentration of residual, nonadsorbed acetaminophen in the supernatant was quantitatively assayed by reverse phase high-pressure liquid chromatography with ultraviolet detection. Data were tested by linear regression analysis and statistical significance was set at P dog food (R(2) = 0.54; P = 0.0018). However, all measurements of residual acetaminophen were less than 100 mg/L, representing a reduction in acetaminophen concentration of more than 98.6%. The addition of dog food to activated charcoal reduces its total adsorptive capacity for acetaminophen. However, this reduction in adsorptive capacity is unlikely to be clinically significant in the presence of both the formulation of dog food and the ratio of dog food to charcoal used in this study. © Veterinary Emergency and Critical Care Society 2013.

  11. Oil Spill Adsorption Capacity of Activated Carbon Tablets from Corncobs in Simulated Oil-Water Mixture

    Directory of Open Access Journals (Sweden)

    Rhonalyn V. Maulion

    2015-12-01

    Full Text Available Oil spill in bodies of water is one of severe environmental problems that is facing all over the country and in the world. Since oil is an integral part of the economy, increasing trend for its demand and transport of has led to a great treat in the surface water. One of the promising techniques in the removal of the oil spills in water bodies is adsorption using activated carbon form waste material such as corn cobs. The purpose of this study is to determine the adsorption capacity of activated carbon tablets derived from corncobs in the removal of oil. The properties of activated carbon produced have a pH of 7.0, bulk density of 0.26 g//cm3 , average pore size of 45nm, particle size of 18% at 60 mesh and 39% at 80 mesh, iodine number of 1370 mg/g and surface area of 1205 g/m2. The amount of bentonite clay as binder (15%,20%,30%, number of ACT (1,2,3 and time of contact(30,60,90 mins has been varied to determine the optimum condition where the activated carbon will have the best adsorption capacity in the removal of oil. Results showed that at 15% binder, 60 mins contact time and 3 tablets of activated carbon is the optimum condition which give a percentage adsorption of 22.82% of oil. Experimental data also showed that a Langmuir isotherm was the best fit isotherm for adsorption of ACT.

  12. Influence of the inherent properties of drinking water treatment residuals on their phosphorus adsorption capacities

    Institute of Scientific and Technical Information of China (English)

    Leilei Bai; Changhui Wang; Liansheng He; Yuansheng Pei

    2014-01-01

    Batch experiments were conducted to investigate the phosphorus (P) adsorption and desorption on five drinking water treatment residuals (WTRs) collected from different regions in China.The physical and chemical characteristics of the five WTRs were determined.Combined with rotated principal component analysis,multiple regression analysis was used to analyze the relationship between the inherent properties of the WTRs and their P adsorption capacities.The results showed that the maximum P adsorption capacities of the five WTRs calculated using the Langmuir isotherm ranged from 4.17 to 8.20 mg/g at a pH of 7 and further increased with a decrease in pH.The statistical analysis revealed that a factor related to Al and 200 mmol/L oxalate-extractable Al (Alox) accounted for 36.5% of the variations in the P adsorption.A similar portion (28.5%) was attributed to an integrated factor related to the pH,Fe,200 mmol/L oxalate-extractable Fe (Feox),surface area and organic matter (OM) of the WTRs.However,factors related to other properties (Ca,P and 5 mmol/L oxalate-extractable Fe and Al) were rejected.In addition,the quantity of P desorption was limited and had a significant negative correlation with the (Feox + Alox) of the WTRs (p < 0.05).Overall,WTRs with high contents of Alox,Feox and OM as well as large surface areas were proposed to be the best choice for P adsorption in practical applications.

  13. Construction of horizontal stratum landform-like composite foams and their methyl orange adsorption capacity

    Science.gov (United States)

    Chen, Jiajia; Shi, Xiaowen; Zhan, Yingfei; Qiu, Xiaodan; Du, Yumin; Deng, Hongbing

    2017-03-01

    Chitosan (CS)/rectorite (REC)/carbon nanotubes (CNTs) composite foams with good mechanical properties were successfully fabricated by unidirectional freeze-casting technique. The morphology of the foam showed the well-ordered porous three-dimensional layers and horizontal stratum landform-like structure. The holes on the layers looked like the wings of butterfly. Additionally, the X-ray photoelectron spectroscopy and energy-dispersive X-ray spectroscopy results indicated the successful addition of CNTs and REC. The intercalated REC with CS chains was confirmed by small-angle X-ray diffraction. The surface structure of the foams was also analyzed by Raman spectroscopy. The adsorption experiments showed that when the mass ratio of CS to REC was 10:1 and CNTs content was 20%, the composite foam performed best in adsorbing low concentration methyl orange, and the largest adsorption capacity was 41.65 mg/g.

  14. Assessing changes in the physico-chemical properties and fluoride adsorption capacity of activated alumina under varied conditions

    Science.gov (United States)

    Craig, Laura; Stillings, Lisa; Decker, David L.

    2017-01-01

    Adsorption using activated alumina is a simple method for removing fluoride from drinking water, but to be cost effective the adsorption capacity must be high and effective long-term. The intent of this study was to assess changes in its adsorption capacity under varied conditions. This was determined by evaluating the physico-chemical properties, surface charge, and fluoride (F−) adsorption capacity and rate of activated alumina under conditions such as hydration period, particle size, and slow vs. fast titrations. X-ray diffraction and scanning electron microscopy analyses show that the mineralogy of activated alumina transformed to boehmite, then bayerite with hydration period and a corresponding reduction in adsorption capacity was expected; while surface area analyses show no notable changes with hydration period or particle size. The pH dependent surface charge was three times higher using slow potentiometric titrations as compared to fast titrations (due largely to diffusion into pore space), with the surface acidity generally unaffected by hydration period. Results from batch adsorption experiments similarly show no change in fluoride adsorption capacity with hydration period. There was also no notable difference in fluoride adsorption capacity between the particle size ranges of 0.5–1.0 mm and 0.125–0.250 mm, or with hydration period. However, adsorption rate increased dramatically with the finer particle sizes: at an initial F− concentration of 0.53 mmol L−1 (10 mg L−1), 90% was adsorbed in the 0.125–0.250 mm range after 1 h, while the 0.5–1.0 mm range required 24 h to achieve 90% adsorption. Also, the pseudo-second-order adsorption rate constants for the finer vs. larger particle sizes were 3.7 and 0.5 g per mmol F− per min respectively (24 h); and the initial intraparticle diffusion rate of the former was 2.6 times faster than the latter. The results show that adsorption capacity of activated alumina remains consistent and

  15. Adsorption of Pb(II) on mesoporous activated carbons fabricated from water hyacinth using H{sub 3}PO{sub 4} activation: Adsorption capacity, kinetic and isotherm studies

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Yang, E-mail: zzsfxyhy@163.com [Department of Chemistry and Environmental Science, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China); Li, Shunxing; Chen, Jianhua; Zhang, Xueliang; Chen, Yiping [Department of Chemistry and Environmental Science, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China)

    2014-02-28

    Activated carbons with high mesoporosity and abundant oxygen-containing functional groups were prepared from water hyacinth using H{sub 3}PO{sub 4} activation (WHAC) to eliminate Pb(II) in water. Characterizations of the WHAC were performed using Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The BET analysis showed that WHAC possesses a high mesoporosity (93.9%) with a BET surface area of 423.6 m{sup 2}/g. The presence of oxygen-containing functional groups including hydroxyl, carbonyl, carboxyl and phosphate groups renders the WHAC a favorable adsorbent for Pb(II) with the maximum monolayer capacity (q{sub m}) 118.8 mg/g. The adsorption behavior follows pseudo-first order kinetic and Langmuir isotherm. The desorption study demonstrated that the WHAC could be readily regenerated using 0.1 M HCl (pH = 1.0). The desorbed WHAC could be reused at least six times without significant adsorption capacity reduction. The adsorption process was spontaneous and endothermic with ΔG (−0.27, −1.13, −3.02, −3.62, −5.54, and −9.31 kJ/mol) and ΔH (38.72 kJ/mol). Under the optimized conditions, a small amount of the adsorbent (1.0 g/L) could remove as much as 90.1% of Pb(II) (50 mg/L) in 20 min at pH 6.0 and temperature of 298 K. Therefore, the WHAC has a great potential to be an economical and efficient adsorbent in the treatment of lead-contaminated water.

  16. A Valuable Biochar from Poplar Catkins with High Adsorption Capacity for Both Organic Pollutants and Inorganic Heavy Metal Ions.

    Science.gov (United States)

    Liu, Xia; Sun, Ju; Duan, Shengxia; Wang, Yanan; Hayat, Tasawar; Alsaedi, Ahmed; Wang, Chengming; Li, Jiaxing

    2017-08-30

    In this paper, biochar derived from poplar catkins was used as an economical and renewable adsorbent for adsorption organic and inorganic pollutants such as, dyes, organic compounds, and heavy metal ions from wastewater. Mesoporous activated carbonized poplar catkins (ACPCs) were produced from char as a by-product by carbonized poplar catkins (CPCs). With their high surface area, ACPCs exhibited the maximum adsorption capacities of 71.85 and 110.17 mg/g for the removal of inorganic U(VI) and Co(II). Compared other biochars adsorbents, ACPCs can also adsorb organic pollutants with the maximum adsorption capacities of 534, 154, 350, 148 and 384 mg/g for methylene blue (MB), methyl orange (MO), Congo red (CR), chloramphenicol (CAP) and naphthalene. The adsorption of organic pollutants was fitted with pseudo-first order, pseudo-second order, and intra-particle diffusion kinetic models figure out the kinetic parameters and adsorption mechanisms. Langmuir adsorption isotherm was found to be suitable for Co(II) and U(VI) adsorption and thermodynamic studies indicated adsorption processes to be endothermic and spontaneous. The adsorption process includes both outer-sphere surface complexes and hydrogen-bonding interactions. The results showed that biochar derived from poplar catkins was a potential material to remove pollutants in wastewater.

  17. A review on modification methods to cellulose-based adsorbents to improve adsorption capacity.

    Science.gov (United States)

    Hokkanen, Sanna; Bhatnagar, Amit; Sillanpää, Mika

    2016-03-15

    In recent decades, increased domestic, agricultural and industrial activities worldwide have led to the release of various pollutants, such as toxic heavy metals, inorganic anions, organics, micropollutants and nutrients into the aquatic environment. The removal of these wide varieties of pollutants for better quality of water for various activities is an emerging issue and a robust and eco-friendly treatment technology is needed for the purpose. It is well known that cellulosic materials can be obtained from various natural sources and can be employed as cheap adsorbents. Their adsorption capacities for heavy metal ions and other aquatic pollutants can be significantly affected upon chemical treatment. In general, chemically modified cellulose exhibits higher adsorption capacities for various aquatic pollutants than their unmodified forms. Numerous chemicals have been used for cellulose modifications which include mineral and organic acids, bases, oxidizing agent, organic compounds, etc. This paper reviews the current state of research on the use of cellulose, a naturally occurring material, its modified forms and their efficacy as adsorbents for the removal of various pollutants from waste streams. In this review, an extensive list of various cellulose-based adsorbents from literature has been compiled and their adsorption capacities under various conditions for the removal of various pollutants, as available in the literature, are presented along with highlighting and discussing the key advancement on the preparation of cellulose-based adsorbents. It is evident from the literature survey presented herein that modified cellulose-based adsorbents exhibit good potential for the removal of various aquatic pollutants. However, still there is a need to find out the practical utility of these adsorbents on a commercial scale, leading to the improvement of pollution control.

  18. Trimodal nanoporous silica as a support for amine-based CO2 adsorbents: Improvement in adsorption capacity and kinetics

    Science.gov (United States)

    Chen, Chao; Bhattacharjee, Samiran

    2017-02-01

    A trimodal nanoporous silica (TS) having unique trimodal pore structure viz., internal mesopores, textural mesopores and interconnected macropores, has been functionalized with amine using two different methods covalent grafting and wet impregnation. Both were studied as nanocomposite sorbents for CO2 capture. The effects of the amine loading, immobilization processes and the type of support were investigated. Commercially available silica gel (SG) with a purely mesoporous structure was studied as the support for the amine in order to compare differences in pore structure and amine loading with differences in CO2 adsorption capacity and kinetics. Amine-grafted TS exhibited much faster CO2 adsorption kinetics at 35 °C than amine-grafted SG. At the same amine loading, amine-impregnated TS showed higher CO2 adsorption capacity and faster CO2 adsorption kinetics than amine-impregnated SG. The CO2 adsorption capacity of amine-impregnated TS increased as the amine loading increased until 70%, with the highest value of 172 mg/g, while the amine-impregnated SG reached the highest CO2 adsorption capacity of only 78 mg/g at 40% amine loading. More importantly, amine-impregnated as-prepared TS exhibited even higher CO2 capture capacity than amine-impregnated TS when the amine loading was below 60%. Results suggest that amine-modified trimodal nanoporous silica sorbents meet the challenges of current CO2 capture technology.

  19. ADSORPTION CAPACITY OF ACTIVATED CARBON FIBER FABRIC IN CYANIDE LEACHING LIQUOR OF GOLD ORES

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Adsorption capacity of ACFF in cyanide leaching liquor of gold ores was studied withcyanide leaching liquor of gold ores, containing various kinds of ions. The adsorbed leaching liquorwas analyzed by atomic emission spectroscopy and colorimetric method. The contents of variouskinds of ions in ACFF were determined with X-ray photoctron spectroscopy. ACFF not onlyadsorbed gold but also adsorbed arsenic, nickel, zinc, calcium, sulphur, bismuth, copper, iron. silverand cyanide anion. Atomic percentage of C and those of O, N, Zr, Fe increase and decreaserespectively with the increase of the layer depth, while those of Ca, Au, Ag keep constant.

  20. Adsorption capacities of activated carbons for geosmin and 2-methylisoborneol vary with activated carbon particle size: Effects of adsorbent and adsorbate characteristics.

    Science.gov (United States)

    Matsui, Yoshihiko; Nakao, Soichi; Sakamoto, Asuka; Taniguchi, Takuma; Pan, Long; Matsushita, Taku; Shirasaki, Nobutaka

    2015-11-15

    The adsorption capacities of nine activated carbons for geosmin and 2-methylisoborneol (MIB) were evaluated. For some carbons, adsorption capacity substantially increased when carbon particle diameter was decreased from a few tens of micrometers to a few micrometers, whereas for other carbons, the increase of adsorption capacity was small for MIB and moderate for geosmin. An increase of adsorption capacity was observed for other hydrophobic adsorbates besides geosmin and MIB, but not for hydrophilic adsorbates. The parameter values of a shell adsorption model describing the increase of adsorption capacity were negatively correlated with the oxygen content of the carbon among other characteristics. Low oxygen content indicated low hydrophilicity. The increase of adsorption capacity was related to the hydrophobic properties of both adsorbates and activated carbons. For adsorptive removal of hydrophobic micropollutants such as geosmin, it is therefore recommended that less-hydrophilic activated carbons, such as coconut-shell-based carbons, be microground to a particle diameter of a few micrometers to enhance their equilibrium adsorption capacity. In contrast, adsorption by hydrophilic carbons or adsorption of hydrophilic adsorbates occur in the inner pores, and therefore adsorption capacity is unchanged by particle size reduction.

  1. Molecular Dynamics Simulations of Adsorption of Polymer Chains on the Surface of BmNn Graphyne-Like Monolayers

    Science.gov (United States)

    Rouhi, Saeed; Atfi, Amin

    2017-03-01

    Molecular dynamics simulations are used here to study the interactions between BmNn graphyne-like monolayers and four different polymer chains. BN, B1N9, and B2N8 graphyne-like monolayers are selected from the family of BmNn graphyne-like monolayers. It is observed that increasing the number of B atoms in the structure of BmNn graphyne-like monolayers results in larger interaction energies of nanosheet/polymer systems. It is also shown that the polymer chains with the linear adsorbed configurations on the nanosheets have larger interaction energies with the nanosheets. Investigating the effect of number of polymer repeat units on the polymer/nanosheet interaction energy, it is observed that increasing the number of repeat units of polymers leads to enhancing the polymer/nanosheet interaction energy.

  2. Synthesis and Characterization of Al-Cr-Pillared Montmorillonite with High Thermal Stability and Adsorption Capacity

    Institute of Scientific and Technical Information of China (English)

    CAO Ming-li; LIU Shi-zhen; YU Yong-fu

    2004-01-01

    Al-Cr-pillared montmorillonite was synthesized by using bentonite and Al-Cr pillaring solutionsas starting materials. The basal spacing and specific surface areas of the materials were significantly increased rela-tive to those of untreated clays. When the Al/Cr molar ratio ( R ) was 0.10, the d (001) value and specific surfacearea of pillared montmorillonite were 1.9194 nm and 165.7 m2 g- 1 , respectively. Thermal stability of the mate-rials was determined using calcined tests and X- ray diffraction (XRD) analysis. The materials formed at differentR(0.05;0.10;0.15;0.25) exhibit a high thermal stability at 300℃ , especially at initial R = 0.10, the basalinterlayer spacing of materials is stabilized at 1.7313 nm after calcined at 500℃ for 2 h. Adsorption behavior ofthe materials was studied by adsorption experiments. The results show that the Al- Cr-pillared montmorillonites ex-hibit much stronger adsorption capacity on Cr6+ in aqueous solution than untreated clays do.

  3. Diamine-appended metal-organic frameworks: enhanced formaldehyde-vapor adsorption capacity, superior recyclability and water resistibility.

    Science.gov (United States)

    Wang, Zhong; Wang, WenZhong; Jiang, Dong; Zhang, Ling; Zheng, Yali

    2016-07-28

    Capturing formaldehyde (HCHO) from indoor air with porous adsorbents still faces challenges due to their low uptake capacity, difficult regeneration, and especially, the sorption capacity reduction that is caused by the competitive adsorption of H2O when exposed to a humid atmosphere. In this work, MIL-101 is modified with ethylenediamine (ED) on its open-metal sites to substantially improve the HCHO adsorption properties. The HCHO uptake capacity of modified MIL-101 can be up to 5.49 mmol g(-1) in this study, which is among the highest-levels of various adsorbents reported thus far. Moreover, this modification both improved the material's recyclability and water resistibility, allowing for cyclic and selective tests with stable adsorption capacities, revealing the potential utility of amine-modified MOFs for indoor air purification.

  4. An adsorbent with a high adsorption capacity obtained from the cellulose sludge of industrial residues.

    Science.gov (United States)

    Orlandi, Géssica; Cavasotto, Jéssica; Machado, Francisco R S; Colpani, Gustavo L; Magro, Jacir Dal; Dalcanton, Francieli; Mello, Josiane M M; Fiori, Márcio A

    2017-02-01

    One of the major problems in effluent treatment plants of the cellulose and paper industry is the large amount of residual sludge generated. Therefore, this industry is trying to develop new methods to treat such residues and to use them as new products, such as adsorbents. In this regard, the objective of this work was to develop an adsorbent using the raw activated sludge generated by the cellulose and paper industry. The activated cellulose sludge, after being dried, was chemically activated with 42.5% (v/v) phosphoric acid at 85 °C for 1 h and was charred at 500 °C, 600 °C and 700 °C for 2 h. The efficiency of the obtained adsorbent materials was evaluated using kinetic tests with methylene blue solutions. Using the adsorption kinetics, it was verified that the three adsorbents showed the capacity to adsorb dye, and the adsorbent obtained at a temperature of 600 °C showed the highest adsorption capacity of 107.1 mg g(-1). The kinetic model that best fit the experimental data was pseudo-second order. The Langmuir-Freudlich isotherm adequately described the experimental data. As a result, the cellulose sludge generated by the cellulose and paper industries could be used as an adsorbent.

  5. Amine-functionalized PVA-co-PE nanofibrous membrane as affinity membrane with high adsorption capacity for bilirubin.

    Science.gov (United States)

    Wang, Wenwen; Zhang, Hao; Zhang, Zhifeng; Luo, Mengying; Wang, Yuedan; Liu, Qiongzhen; Chen, Yuanli; Li, Mufang; Wang, Dong

    2017-02-01

    In this study, poly(vinyl alcohol-co-ethylene) (PVA-co-PE) nanofibrous membrane was activated by sodium hydroxide and cyanuric chloride, and then the activated membranes were functionalized by 1,3-propanediamine, hexamethylenediamine and diethylenetriamine to be affinity membranes for bilirubin removal, respectively. The chemical structures and morphologies of membranes were investigated by SEM, FTIR and XPS. And the adsorption ability of different amine-functionalized nanofibrous membranes for bilirubin was characterized. Furthermore, the effects of temperature, initial concentration of bilirubin, NaCl concentration and BSA concentration on the adsorption capacity for bilirubin of diethylenetriamine-functionalized nanofibrous membrane were studied. Results indicated that the adsorption capacity for bilirubin of diethylenetriamine-functionalized nanofibrous membrane could reach 85mg/g membrane when the initial bilirubin concentration was 200mg/L while the adsorption capacity could be increased to 110mg/g membrane if the initial bilirubin concentration was more than 400mg/L. The dynamic adsorption of diethylenetriamine-functionalized nanofibrous membrane showed that the ligands of amine groups on the membrane surface could be used as far as possible by recirculating the plasma with certain flow rates. Therefore, the diethylenetriamine-functionalized PVA-co-PE nanofibrous membrane possessed high adsorption capacity for bilirubin and it can be candidate as affinity membrane for bilirubin removal.

  6. Ultra-high adsorption capacity of zeolitic imidazole framework-67 (ZIF-67) for removal of malachite green from water.

    Science.gov (United States)

    Lin, Kun-Yi Andrew; Chang, Hsuan-Ang

    2015-11-01

    Zeolitic imidazole frameworks (ZIFs), a new class of adsorbents, are proposed to adsorb Malachite Green (MG) in water. Particularly, ZIF-67 was selected owing to its stability in water and straightforward synthesis. The as-synthesized ZIF-67 was characterized and used to adsorb MG from water. Factors affecting the adsorption capacity were investigated including mixing time, temperature, the presence of salts and pH. The kinetics, adsorption isotherm and thermodynamics of the MG adsorption to ZIF-67 were also studied. The adsorption capacity of ZIF-67 for MG could be as high as 2430mgg(-1) at 20°C, which could be improved at the higher temperatures. Such an ultra-high adsorption capacity of ZIF-67 was almost 10-times of those of conventional adsorbents, including activated carbons and biopolymers. A mechanism for the high adsorption capacity was proposed and possibly attributed to the π-π stacking interaction between MG and ZIF-67. ZIF-67 also could be conveniently regenerated by washing with ethanol and the regeneration efficiency could remain 95% up to 4 cycles of the regeneration. ZIF-67 was also able to remove MG from the aquaculture wastewater, in which MG can be typically found. These features enable ZIF-67 to be one of the most effective and promising adsorbent to remove MG from water.

  7. Efficient removal and highly selective adsorption of Hg{sup 2+} by polydopamine nanospheres with total recycle capacity

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Xiulan [School of Chemistry and Chemical Engineering, Key Laboratory for Green Processing of Chemical Engineering of Xinjiang bingtuan, Shihezi University, Shihezi 832003 (China); Jia, Xin, E-mail: jiaxin@shzu.edu.cn [School of Chemistry and Chemical Engineering, Key Laboratory for Green Processing of Chemical Engineering of Xinjiang bingtuan, Shihezi University, Shihezi 832003 (China); Zhang, Guoxiang [Gansu Dayu Water-saving Group Co., Ltd, Jiuquan 735000 (China); Hu, Jiamei; Sheng, Wenbo; Ma, Zhiyuan; Lu, Jianjiang; Liu, Zhiyong [School of Chemistry and Chemical Engineering, Key Laboratory for Green Processing of Chemical Engineering of Xinjiang bingtuan, Shihezi University, Shihezi 832003 (China)

    2014-09-30

    Highlights: • The PDA nanospheres with uniform diameter of 150–200 nm were used to remove Hg{sup 2+} efficiently and selectively. • The desorption capacity of PDA nanospheres was 100% in pH 1. • The structure and removal capacity of PDA nanospheres remained almost unchanged after recycling five times. - Abstract: This study reported a new method for efficient removal of Hg{sup 2+} from contaminated water using highly selective adsorptive polydopamine (PDA) nanospheres, which were uniform and had a small diameter (150–200 nm). The adsorption isotherms, kinetics, thermodynamics were investigated. Also, the effects of ionic strength, co-existing ions on removing ability of PDA nanospheres for Hg{sup 2+} were studied. Adsorption of Hg{sup 2+} was very fast and efficient as adsorption equilibrium was completed within 4 h and the maximum adsorption capacities were 1861.72 mg/g, 2037.22 mg/g, and 2076.81 mg/g at 298 K, 313 K, and 328 K respectively, increasing with increasing of temperature. The PDA nanospheres exhibited highly selective adsorption of Hg{sup 2+} and had a total desorption capacity of 100% in hydrochloric acid solution, pH 1. The results showed that the structure of PDA nanospheres remained almost unchanged after recycling five times. Furthermore, X-ray photoelectron spectroscopy (XPS) was employed to determine the elements of PDA nanospheres before and after Hg{sup 2+} adsorption. Considering their efficient and highly Hg{sup 2+} selective adsorption, total recycle capacity, and high stability, PDA nanospheres will be feasible in a number of practical applications.

  8. Study on the Adsorption Capacities for Airborne Particulates of Landscape Plants in Different Polluted Regions in Beijing (China

    Directory of Open Access Journals (Sweden)

    Wei-Kang Zhang

    2015-08-01

    Full Text Available Urban landscape plants are an important component of the urban ecosystem, playing a significant role in the adsorption of airborne particulates and air purification. In this study, six common landscape plants in Beijing were chosen as research subjects, and the adsorption capacities for each different plant leaf and the effects of the leaf structures for the adsorption capacities for particulates were determined. Preliminary results show that needle-leaved tree species adsorbed more airborne particulates than broad-leaved tree species for the same leaf area. Pinus tabuliformis exhibits the highest adsorption capacity, at 3.89 ± 0.026 μg·cm−2, almost two times as much as that of Populus tomentosa (2.00 ± 0.118 μg·cm−2. The adsorption capacities for PM10 of the same tree species leaves, in different polluted regions had significant differences, and the adsorption capacities for PM10 of the tree species leaf beside the Fifth Ring Road were higher than those of the tree species leaves in the Botanical Garden, although the adsorption capacities for PM2.5 of the same tree species in different polluted regions had no significant differences. By determining the soluble ion concentrations of the airborne particulates in two regions, it is suggested that the soluble ion concentrations of PM10 in the atmosphere in the Botanical Garden and beside the Fifth Ring Road have significant differences, while those of PM2.5 in the atmosphere had no significant differences. In different polluted regions there are significant adaptive changes to the leaf structures, and when compared with slightly polluted region, in the seriously polluted region the epidermis cells of the plant leaves shrinked, the surface textures of the leaves became rougher, and the stomas’ frequency and the pubescence length increased. Even though the plant leaves exposed to the seriously polluted region changed significantly, these plants can still grow normally and healthily.

  9. Hydrophobic interaction chromatography of proteins. IV. Protein adsorption capacity and transport in preparative mode.

    Science.gov (United States)

    To, Brian C S; Lenhoff, Abraham M

    2011-01-21

    The adsorption isotherms of four model proteins (lysozyme, α-lactalbumin, ovalbumin, and BSA) on eight commercial phenyl hydrophobic interaction chromatography media were measured. The isotherms were softer than those usually seen in ion-exchange chromatography of proteins, and the static capacities of the media were lower, ranging from 30 to 110 mg/mL, depending on the ammonium sulfate concentration and the protein and adsorbent types. The protein-accessible surface area appears to be the main factor determining the binding capacity, and little correlation was seen with the protein affinities of the adsorbents. Breakthrough experiments showed that the dynamic capacities of the adsorbents at 10% breakthrough were 20-80% of the static capacities, depending on adsorbent type. Protein diffusivities in the adsorbents were estimated from batch uptake experiments using the pore diffusion and homogeneous diffusion models. Protein transport was affected by the adsorbent pore structures. Apparent diffusivities were higher at lower salt concentrations and column loadings, suggesting that adsorbed proteins may retard intraparticle protein transport. The diffusivities estimated from the batch uptake experiments were used to predict column breakthrough behavior. Analytical solutions developed for ion-exchange systems were able to provide accurate predictions for lysozyme breakthrough but not for ovalbumin. Impurities in the ovalbumin solutions used for the breakthrough experiments may have affected the ovalbumin uptake and led to the discrepancies between the predictions and the experimental results.

  10. Reservoir capacity estimates in shale plays based on experimental adsorption data

    Science.gov (United States)

    Ngo, Tan

    from different measurement techniques using representative fluids (such as CH4 and CO2) at elevated pressures, and the adsorbed density can range anywhere between the liquid and the solid state of the adsorbate. Whether these discrepancies are associated with the inherent heterogeneity of mudrocks and/or with poor data quality requires more experiments under well-controlled conditions. Nevertheless, it has been found in this study that methane GIP estimates can vary between 10-45% and 10-30%, respectively, depending on whether the free or the total amount of gas is considered. Accordingly, CO2 storage estimates range between 30-90% and 15-50%, due to the larger adsorption capacity and gas density at similar pressure and temperature conditions. A manometric system has been designed and built that allows measuring the adsorption of supercritical fluids in microporous materials. Preliminary adsorption tests have been performed using a microporous 13X zeolite and CO 2 as an adsorbing gas at a temperature of 25oC and 35oC and at pressures up to 500 psi. Under these conditions, adsorption is quantified with a precision of +/- 3%. However, relative differences up to 15-20% have been observed with respect to data published in the literature on the same adsorbent and at similar experimental conditions. While it cannot be fully explained with uncertainty analysis, this discrepancy can be reduced by improving experiment practice, thus including the application of a higher adsorbent's regeneration temperature, of longer equilibrium times and of a careful flushing of the system between the various experimental steps. Based on the results on 13X zeolite, virtual tests have been conducted to predict the performance of the manometric system to measure adsorption on less adsorbing materials, such as mudrocks. The results show that uncertainties in the estimated adsorbed amount are much more significant in shale material and they increase with increasing pressure. In fact, relative

  11. Adsorption capacity of hydrophobic SiO2 aerogel/activated carbon composite materials for TNT

    Institute of Scientific and Technical Information of China (English)

    ZHOU; XiaoFang; CUI; Sheng; LIU; Yu; LIU; XueYong; SHEN; XiaoDong; WU; ZhanWu

    2013-01-01

    The adsorption properties of TNT from wastewater by hydrophobic silica aerogel/activated carbon composite materials were investigated. The effects of adsorption time, pH value, adsorption temperature, and the amount of the composite materials on the adsorption rate were studied. The adsorption principle and mechanism of the composite materials were discussed along with the Freundlich equation. The results showed that the best adsorption rate of the hydrophobic silica aerogel/activated car-bon composite materials could reach 96.5% with adsorption conditions of adsorption temperature 25°C, pH value 7, the amount of SiO2aerogel dosage 3.33 g/L, and adsorption time of 120 min. The adsorption of hydrophobic SiO2aero-gel/activated carbon composite materials for TNT solution is mainly surface adsorption, and also has some chemical adsorp-tion when the aerogel hydrophobicity is modified.

  12. Action of Plant Growth Regulators. IV. Adsorption of Unsubstituted and 2,6-Dichloro-aromatic Acids to Oat Monolayers

    Science.gov (United States)

    Brian, R. C.

    1967-01-01

    The adsorption of chloro-aromatic acids to monomolecular layers of oat squashes is reported in earlier papers but it was not possible by the technique used, to measure unambiguously the adsorption of unsubstituted and 2,6-dichloro-aromatic acids. This has now been achieved by a modification of the earlier method and involves assessments of competitive adsorption between the unknown acid and a standard acid, using measurements of surface potential. Benzoic and phenoxyacetic acids were not adsorbed but phenylacetic acid was weakly adsorbed. The second ring in naphthalene and naphthoxyacetic acids greatly increased adsorption. Substitution of the 2 and 6 positions in the phenyl and phenoxyacetic acids resulted in low adsorption but 2,6-disubstituted phenoxybutyric and benzoic acids were more highly adsorbed. The adsorption values from earlier work are combined and discussed in relation to the growth-regulating activity of the acids. It is conciuded that there is no direct relation embracing all acids between adsorption and activity, notable exceptions being those substituted by chlorine in the 3-position of the aromatic ring. However, for a number of acids it is suggested that activity is limited not only by their ability to interact at enzyme sites but also by the amount of acid immobilised by adsorption when moving to these sites. It is also concluded that the hydrophilic/lipophilic balance of a growth regulator sometimes used as a guide to its activity, is an unreliable indication of interfacial behaviour. PMID:16656642

  13. Enhancing adsorption capacity of toxic malachite green dye through chemically modified breadnut peel: equilibrium, thermodynamics, kinetics and regeneration studies.

    Science.gov (United States)

    Chieng, Hei Ing; Lim, Linda B L; Priyantha, Namal

    2015-01-01

    Breadnut skin, in both its unmodified (KS) and base-modified (BM-KS) forms, was investigated for its potential use as a low-cost adsorbent for the removal of toxic dye, malachite green (MG). Characterization of the adsorbents was carried out using scanning electron microscope, X-ray fluorescence and Fourier transform infra-red spectroscopy. Batch adsorption experiments, carried out under optimized conditions, for the adsorption of MG were fitted using five isotherm models (Langmuir, Freundlich, Dubinin-Radushkevich, Temkin and Sips) and six error functions to determine the best-fit model. The adsorption capacity was greatly enhanced when breadnut skin was chemically modified with NaOH, leading to an adsorption capacity of 353.0 mg g(-1), that was far superior to most reported adsorbents for the removal of MG. Thermodynamics studies indicated that the adsorption of MG was spontaneous on KS and BM-KS, and the reactions were endothermic and exothermic, respectively. Kinetics studies showed that both followed the pseudo-second order. Regeneration experiments on BM-KS indicated that its adsorption capacity was still maintained at>90% even after five cycles. It can be concluded that NaOH-modified breadfruit skin has great potential to be utilized in real-life application as a low-cost adsorbent for the removal of MG in wastewater treatment.

  14. The Adsorption Capacity and Geotechnical Properties of Modified Clay Containing SSA Used as Landfill Liner-Soil Materials

    Directory of Open Access Journals (Sweden)

    Haijun Lu

    2015-01-01

    Full Text Available The potential of clay containing 0~5% sewage sludge ash (SSA is assessed for use as a landfill liner-soil material. Low temperature N2 adsorption, batch adsorption, permeability, and unconfined compressive strength tests are performed to evaluate pore structure, adsorption capacity, hydraulic conductivity, and unconfined compressive strength of the clays. The pore size distribution of the modified clay containing SSA is mainly composed of micropores (<2 nm and mesopores (2~7 nm. With the increasing of SSA from 0% to 5%, the adsorption capacity of Zn(II and Cu(II to the clay increases 37% and 273%, respectively. The hydraulic conductivity of modified clay is from 3.62 × 10−8 to 2.17 × 10−8 cm/s. At SSA = 3%, the unconfined compressive strength of the clay reaches the maximum value of 601.1 kPa. After the clay containing SSA is contaminated by acid and alkali chemical solutions, the amount of mesopores and hydraulic conductivity increase. The adsorption capacity and unconfined compressive strength of contaminated clay decrease about 2∼44% and 25.7∼38.2%, respectively. The modified clay containing SSA can meet the adsorption and geotechnical requirement of landfill liners.

  15. Preparation of a porous clay heterostructure and study of its adsorption capacity of phenol and chlorinated phenols from aqueous solutions.

    Science.gov (United States)

    Arellano-Cárdenas, Sofía; Gallardo-Velázquez, Tzayhrí; Osorio-Revilla, Guillermo; López-Cortez, Ma del Socorro

    2008-01-01

    A porous clay heterostructure (PCH) from a Mexican clay was prepared and characterized, and its aqueous phenol and dichlorophenols (DCPs) adsorption capacities were studied using a batch equilibrium technique. The PCH displayed a surface area of 305.5 m2/g, 37.2 A average porous diameter, and a basal space of 23.2 A. The adsorption capacity shown by the PCH for both phenol and DCPs from water (14.5 mg/g for phenol; 48.7 mg/g for 3,4-DCP; and 45.5 mg/g for 2,5-DCP) suggests that the PCH has both hydrophobic and hydrophilic characteristics, as a result of the presence of silanol and siloxane groups formed during the pillaring and calcination of the PCH. The values of maximal adsorption capacity for dichlorophenols were higher than those reported for aluminum pillared clays and some inorgano-organo clays and comparable with some ionic exchange resins.

  16. Enhancement of the adsorption capacity of the light-weight expanded clay aggregate surface for the metronidazole antibiotic by coating with MgO nanoparticles: Studies on the kinetic, isotherm, and effects of environmental parameters.

    Science.gov (United States)

    Kalhori, Ebrahim Mohammadi; Al-Musawi, Tariq J; Ghahramani, Esmaeil; Kazemian, Hossein; Zarrabi, Mansur

    2017-02-09

    The synthesized MgO nanoparticles were used to coat the light-weight expanded clay aggregates (LECA) and as a metronidazole (MNZ) adsorbent. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Fourier-transformed infrared (FTIR) techniques were employed to study the surface morphology and characteristics of the adsorbents. MgO/LECA clearly revealed the advantages of the nanocomposite particles, showing high specific surface area (76.12 m(2)/g), significant adsorption sites and functional groups. Between pH 5 and 9, the MNZ sorption was not significantly affected. Kinetic studies revealed that the MNZ adsorption closely followed the Avrami model, with no dominant process controlling the sorption rate. The study of the effects of foreign ions revealed that the addition of carbonate raised the MNZ removal efficiency of LECA by 8% and the total removal of MNZ by MgO/LECA. Furthermore, nitrate and hardness only marginally influenced the MNZ removal efficiency and their effects can be ranked in the order of carbonate>nitrate>hardness. The isotherm adsorption of MNZ was best fitted with the Langmuir model enlighten the monolayer MNZ adsorption on the homogeneous LECA and MgO/LECA surfaces. The maximum adsorption capacity under optimum conditions was enhanced from 56.31 to 84.55 mg/g for LECA and MgO/LECA, respectively. These findings demonstrated that the MgO/LECA nanocomposite showed potential as an efficient adsorbent for MNZ removal.

  17. Shape of the hydrogen adsorption regions of MOF-5 and its impact on the hydrogen storage capacity

    Science.gov (United States)

    Cabria, I.; López, M. J.; Alonso, J. A.

    2008-11-01

    The adsorption of molecular hydrogen on a metal-organic framework (MOF) material, MOF-5, has been studied using the density-functional formalism. The calculated potential-energy surface shows that there are two main adsorption regions: both near the OZn4 oxide cores at the vertices of the cubic skeleton of MOF-5. The adsorption energies in those regions are between 100 and 130 meV/molecule. Those adsorption regions have the shape of long, wide, and deep connected trenches and passage of the molecule between regions needs to surpass small barriers of 30-50 meV. The shape of these regions, and not only the presence of metal atoms, explains the large storage capacity measured for MOF-5. The elongated shape explains why some authors have previously identified only one type of adsorption site, associated to the Zn oxide core, and others identified two or three sites. One should consider adsorption regions rather than adsorption sites. A third region of adsorption is near the benzenic rings of the MOF-5. We have also analyzed the possibility of dissociative chemisorption. The chemisorption energy with respect to two separated H atoms is 1.33 eV/H atom; but, since dissociating the free molecule costs 4.75 eV, the physisorbed H2 molecule is more stable than the dissociated chemisorbed state by about 2 eV. Dissociation of the adsorbed molecule costs less energy, but the dissociation barrier is still high.

  18. Determinants of natural zeolite clinoptilolite adsorption capacity for removing NO2

    Directory of Open Access Journals (Sweden)

    Nabiollah Mansouri

    2010-09-01

    Full Text Available Background: NO2 is a poisonous gas that potential to cause major threat to human being health and the environment, as a result, removing this gas from environment seems to be essential. Methods: The study aimed to remove this gas from environment using Iranian natural zeolite, clinoptilolite. After crushing and preparing two sizes of 1 and 2 mm zeolite they were activated in 380 to 420 ºC for 20 minutes. NO2 was produced by reaction of copper (Cu and nitric acid (HNO3 and diluted with enough air to achieve desired concentration. A laboratory reactor set with different concentration of NO2 (20, 30, and, 45 ppm, flows through the zeolite absorbent bed was prepared. Different parameters affected No2 absorption, such as concentration, height, and diameter of zeolite bed, zeolite granulation, and activation temperature were examined.Results: In different condition, the adsorption range of the zeolite for NO2 was varied from 0.35% W for 2mm granulation and the 20 ppm concentration to 1.5% W using 1mm granulation and 45 ppm concentration of NO2. Activation temperature of 420 ºC for 20 min was the best condition removing NO2. Efficiency of 1mm granulation was higher than 2mm. Conclusion: Reducing parameters such as height and diameter of zeolite bed decreased but increasing concentration of gas flow increased adsorption capacity of zeolite. Using Iranian zeolite in gas masks still not recommended.

  19. Fiber-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    Energy Technology Data Exchange (ETDEWEB)

    Janke, Christopher J.; Dai, Sheng; Oyola, Yatsandra

    2016-09-06

    A fiber-based adsorbent and a related method of manufacture are provided. The fiber-based adsorbent includes polymer fibers with grafted side chains and an increased surface area per unit weight over known fibers to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. The polymer fibers include a circular morphology in some embodiments, having a mean diameter of less than 15 microns, optionally less than about 1 micron. In other embodiments, the polymer fibers include a non-circular morphology, optionally defining multiple gear-shaped, winged-shaped or lobe-shaped projections along the length of the polymer fibers. A method for forming the fiber-based adsorbents includes irradiating high surface area polymer fibers, grafting with polymerizable reactive monomers, reacting the grafted fibers with hydroxylamine, and conditioning with an alkaline solution. High surface area fiber-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  20. Preparation, characterization and phenol adsorption capacity of activated carbons from African beech wood sawdust

    Directory of Open Access Journals (Sweden)

    N.T. Abdel-Ghani

    2016-05-01

    Full Text Available In the present study, different activated carbons were prepared from carbonized African beech wood sawdust by potassium hydroxide activation. The activated carbons were characterized by brunauer–emmett–teller, scanning electron microscope, fourier transform infrared spectroscopy, and thermogravimetric analyzer. The phenol adsorption capacity of the prepared carbons was evaluated. The different factors affecting phenol’s removal were studied including: contact time, solution pH and initial phenol concentration. The optimum phenol removal was obtained after a contact time of 300 min. and at an initial phenol solution pH 7. The maximum removal percentages were determined at 5mg/l initial phenol concentration as 79, 93, 94 and 98% for AC0, AC1, AC2 and AC3; respectively. The adsorption of phenol on African beech sawdust activated carbons was found to follow the Lagergren first order kinetics and the intraparticle diffusion mechanism gave a good fit to the experimental data. The isothermal models applied fitted the experimental data in the order: Langmuir> Dubinin–Radushkevich> Freundlich and Temkin.

  1. Synthesis of polycationic bentonite-ionene complexes and their benzene adsorption capacity

    Directory of Open Access Journals (Sweden)

    Valquíria Campos

    2015-04-01

    Full Text Available The purpose of this work was to structurally modify clays in order to incorporate water-insoluble molecules, such as petroleum hydrocarbons. The potential for ion exchange of quaternary ammonium salts was studied, which revealed their ability to interact with anions on the cationic surface, for environmental applications of the material. Ionenes, also known as polycations, have many potential uses in environmental applications. In this work, cationic aliphatic ammonium polyionenes, specifically 3,6-ionene and 3,6-dodecylionene, were prepared for incorporation into clay to form bentonite-ionene complexes. The intercalation of bentonite with ionene polymers resulted in an increase in the basal spacing of 3,6-dodecylionene from 1.5-3.5 nm. The higher d001 spacing of 3,6-dodecylionene samples than that of 3,6-ionene samples may be attributed to their longer tail length. The behavior of the TG/DTG curves and the activation energy values suggest that 3,6-dodecylionene (E = 174.85 kJ mol–1 is thermally more stable than 3,6 ionene (E = 115.52 kJ mol–1 complexes. The adsorption of benzene by 3,6-ionene and 3,6-dodecylionene was also investigated. The increase in benzene concentrations resulted in increased benzene adsorption by the sorbents tested in this work. The sorption capacity of benzene on ionene-modified bentonite was in the order of 3,6-dodecylionene > 3,6-ionene.

  2. Fiber-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    Science.gov (United States)

    Janke, Christopher J; Dai, Sheng; Oyola, Yatsandra

    2014-05-13

    A fiber-based adsorbent and a related method of manufacture are provided. The fiber-based adsorbent includes polymer fibers with grafted side chains and an increased surface area per unit weight over known fibers to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. The polymer fibers include a circular morphology in some embodiments, having a mean diameter of less than 15 microns, optionally less than about 1 micron. In other embodiments, the polymer fibers include a non-circular morphology, optionally defining multiple gear-shaped, winged-shaped or lobe-shaped projections along the length of the polymer fibers. A method for forming the fiber-based adsorbents includes irradiating high surface area polymer fibers, grafting with polymerizable reactive monomers, reacting the grafted fibers with hydroxylamine, and conditioning with an alkaline solution. High surface area fiber-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  3. Protein adsorption to poly(ethylenimine)-modified Sepharose FF: I. a critical ionic capacity for drastically enhanced capacity and uptake kinetics.

    Science.gov (United States)

    Yu, Lin-Ling; Tao, Shi-Peng; Dong, Xiao-Yan; Sun, Yan

    2013-08-30

    To explore the details of protein uptake to polymer-grafted ion exchangers, Sepharose FF was modified with poly(ethylenimine) (PEI) to prepare anion exchanger of 10 different ionic capacities (ICs, 100-1220mmol/L). Adsorption equilibria and kinetics of bovine serum albumin (BSA) were then studied. It is found that ionic capacity, i.e., the coupling density of PEI, had significant effect on both adsorption capacity (qm) and effective protein diffusivity (De). With increasing ionic capacity, the qm value increased rapidly at IC740mmol/L, the qm value decreased significantly while the De value increased moderately with increasing the IC. The results indicate that PEI chains played an important role in protein adsorption and transport. In brief, there was a critical IC (cIC) or PEI chain density, above which protein adsorption and transport behaviors changed drastically. The cIC was identified to be about 600mmol/L. Estimation of PEI grafting-layer thickness suggests that PEI chains formed an extended three-dimensional grafting-layer at IC>cIC, which provided high flexibility as well as accessibility of the chains for protein binding. Therefore, at IC>cIC, the adjacent PEI chains became close and flexible enough, leading to facilitated transport of adsorbed protein molecules by the interactions of neighboring chains mediated by the bound molecules. It is regarded as "chain delivery" effect. At the same time, improved accessibility of binding sites led the significant increase of binding capacity. The decrease of qm value at IC>740mmol/L is considered due to the decrease of effective porosity. The research has thus provided new insight into protein adsorption and transport in polymer-grafted ion-exchange media.

  4. Water Vapor Adsorption Capacity of Thermally Fluorinated Carbon Molecular Sieves for CO2 Capture

    Directory of Open Access Journals (Sweden)

    Jin-Young Jung

    2013-01-01

    Full Text Available The surfaces of carbon molecular sieves (CMSs were thermally fluorinated to adsorb water vapor. The fluorination of the CMSs was performed at various temperatures (100, 200, 300, and 400°C to investigate the effects of the fluorine gas (F2 content on the surface properties. Fluorine-related functional groups formed were effectively generated on the surface of the CMSs via thermal fluorination process, and the total pore volume and specific surface area of the pores in the CMSs increased during the thermal fluorination process, especially those with diameters ≤ 8 Å. The water vapor adsorption capacity of the thermally fluorinated CMSs increased compared with the as-received CMSs, which is attributable to the increased specific surface area and to the semicovalent bonds of the C–F groups.

  5. ADSORPTION CAPACITY OF ACTIVATED CARBON FIBER FABRIC IN CYANIDE LEACHING LIQUOR OF GOLD ORES

    Institute of Scientific and Technical Information of China (English)

    LIUXiaozhen

    2002-01-01

    Adsorption capacity of ACFF in cyanide leaching liquor of gold ores was studied with cyanide leaching liquor of gold ores,containing various kinds of ions.The adsorbed leaching liquor was analyzed by atomic emission spectroscopy and colorimetric method.The contents of various kinds. of ions in ACFF were determined with X-ray photoctron spectroscopy.ACFF not only adsorbed gold but also adsorbed arsenic,nickel,zinc,calcium,sulphur,bismuth,copper,iron,silver and cyanide,anion.Atomic percentage of C and those of O,N,Zn,Fe increase and decrease respectively with the increase of the layer depth,while those of Ca,Au,Ag keep constant.

  6. Copper Accumulation, Availability and Adsorption Capacity in Sandy Soils of Vineyards with Different Cultivation Duration

    Science.gov (United States)

    Mallmann, F. J. K.; Miotto, A.; Bender, M. A.; Gubiani, E.; Rheinheimer, D. D. S.; Kaminski, J.; Ceretta, C. A.; Šimůnek, J.

    2015-12-01

    Bordeaux mixture is a copper-based (Cu) fungicide and bactericide applied in vineyards to control plant diseases. Since it is applied several times per year, it accumulates in large quantities on plants and in soil. This study evaluates the Cu accumulation in, and desorption kinetics and adsorption capability of a sandy Ultisol in a natural field and in 3 vineyards for 5 (V1), 11 (V2), and 31 (V3) years in South of Brazil. Soil samples were collected in 8 depths (0-60 cm) of all four soil profiles, which all displayed similar soil properties. The following soil properties were measured: pH, organic matter (OM), soil bulk density, Cu total concentration, and Cu desorption and adsorption curves. A two first-order reactions model and the Langmuir isotherm were fitted to the desorption and adsorption curves, respectively. An increase in the total mass of Cu in the vineyards followed a linear regression curve, with an average annual increase of 7.15 kg ha-1. Cu accumulated down to a depth of 5, 20, and 30 cm in V1, V2 and V3, respectively, with the highest Cu content reaching 138.4 mg kg-1 in the 0-5 cm soil layer of V3. Cu desorption parameters showed a high correlation with its total concentration. Approximately 57 and 19% of total Cu were immediately and slowly available, respectively, indicating a high potential for plant absorption and/or downward movement. Cu concentrations extracted by EDTA from soil layers not affected by anthropogenic Cu inputs were very low. The maximum Cu adsorption capacity of the 0-5 and 5-10 cm soil layers increased with the vineyard age, reaching concentrations higher than 900 mg kg-1. This increase was highly related to OM and pH, which both increased with cultivation duration. Despite of low clay content of these soils, there is low risk of groundwater Cu contamination for actual conditions. However, high Cu concentrations in the surface layer of the long-term vineyards could cause toxicity problems for this and for companion crops.

  7. Adsorption characteristics of adsorbent resins and antioxidant capacity for enrichment of phenolics from two-phase olive waste.

    Science.gov (United States)

    Wang, Zhihong; Wang, Chengzhang; Yuan, Jiaojiao; Zhang, Changwei

    2017-01-01

    In this study, the adsorption properties of nine resins including polyamide resin (30-60), polyamide resin (60-100) AB-8, S-8, D-101, NKA-9, NKA-II, XDA-1 and XDA-4 for enrichment phenolics of the olive waste were investigated. XDA-1 and NKA-II were chosen for further study due to their outstanding adsorption and desorption capacity. XDA-1 and NKA-II had similar adsorption and desorption behaviors for phenolics of olive waste. The adsorption mechanism could be better explained by pseudo second-order kinetics model and Freundlich isotherm model, and the adsorption processes were spontaneously and exothermic. The experiment of gradient elution were carried out through treated XDA-1 resins column, the result indicated the total phenolics were mainly obtained from the 40% and 60% ethanol fraction. The order of antioxidant capacity by DPPH  , ABTS(+) radical and FRAP assay was similar with the content of phenolics from fraction elution. The compositions of phenolics from different elution fractions were determined by reversed phase-HPLC-DAD method. Gallic acid, hydroxytyrosol, tyrosol and ferulic acid were the major constituent in the fraction elute, and the content of hydroxytyrosol reached to the 41.69mg/g. The above results revealed the synergistic effects of the different phenolics contribute to the antioxidant capacity.

  8. Synthesis, characterisation and adsorption properties of a porous copper(II) 3D coordination polymer exhibiting strong binding enthalpy and adsorption capacity for carbon dioxide.

    Science.gov (United States)

    Eckold, Pierre; Gee, William J; Hill, Matthew R; Batten, Stuart R

    2012-11-21

    The synthesis and characterisation of microporous coordination polymers containing copper(II) or cobalt(II) and 2-(pyridin-4-yl)malonaldehyde (Hpma) is described and the gas adsorption properties evaluated. Single-crystal X-ray structure determinations identified the structures as [M(pma)(2)]·2X (M = Cu, 1; Co, 2; X = MeOH, MeCN), which contain 3D networks with rutile topology and continuous 1D rectangular channels with diameters ranging from 3 to 4 Å. The materials exhibit low BET surface areas of 143 m(2) g(-1), but possess large capacities for carbon dioxide capture of 14.1 wt%. The small pore channels are shown to account for this, delivering a particularly strong binding enthalpy to adsorbed CO(2) of 38 kJ mol(-1), and a very large adsorption capacity relative to the low surface area.

  9. Expanded porous MOF-505 analogue exhibiting large hydrogen storage capacity and selective carbon dioxide adsorption.

    Science.gov (United States)

    Zheng, Baishu; Yun, Ruirui; Bai, Junfeng; Lu, Zhiyong; Du, Liting; Li, Yizhi

    2013-03-18

    An expanded 4,4-paddlewheel-connected porous MOF-505-type metal-organic framework (MOF), [Cu2(PDEB)(H2O)2]·xS (NJU-Bai12; NJU-Bai represents the Nanjing University Bai group and S represents noncoordinated solvent molecules) has been designed from a nanosized rectangular diisophthalate linker containing alkyne groups 5,5'-(1,4-phenylenedi-2,1-ethynediyl)bis(1,3-benzenecarboxylic acid). This MOF material possesses permanent microporosity with the highest Brunauer-Emmett-Teller surface area of 3038 m(2)·g(-1) and the largest unsaturated total hydrogen storage capacity of 62.7 mg·g(-1) at 77 K and 20 bar among reported MOF-505 analogues. Additionally, NJU-Bai12 also exhibits excellent carbon dioxide (CO2) uptake capacity (23.83 and 19.85 mmol·g(-1) at 20 bar for 273 and 298 K, respectively) and selective gas adsorption properties with CO2/CH4 selectivity of 5.0 and CO2/N2 selectivity of 24.6 at room temperature.

  10. Adsorption Capacity of The As-Synthetic Graphene Oxide for The Removal of Alizarin Red S Dye from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Prawit Nuengmatcha

    2016-06-01

    Full Text Available This research was aimed to study the adsorption of Alizarin Red S (ARS dye using graphene oxide (GO as an adsorbent compared with bare graphite powder (BGP. For optimum conditions, the effects of the initial concentration of ARS, solution pH, adsorbent dosage, and contact time were investigated in detail. The optimum conditions for this work were consisted of 350 mg/L initial concentration of ARS with 0.02 mg adsorbent at pH 2.0. The adsorption equilibrium was completely reached within 30 min. The maximum adsorption capacity of GO was 88.50 mg/g which was higher than that of BGP (34.13 mg/g. The adsorption kinetics well fitted using a pseudo second-order kinetic model. The intraparticle diffusion model described that the intraparticle diffusion was not the only rate-limiting step. In thermodynamics diversion, changes in free energy (DG˚, enthalpy (DH˚ and entropy (DS˚ were also evaluated. The overall adsorption process was exothermic and spontaneous in nature. The adsorption isotherms for GO and BGP fit well with the Langmuir and Freundlich models, respectively. It is, therefore, evident that the as-prepared GO can be used as a high potential adsorbent for the anionic dye and it can be reused for fourth time of adsorption.

  11. EFFECT OF MOLECULAR OXYGEN ON ADSORPTIVE CAPACITY AND EXTRACTION EFFICIENCY OF GRANULATED ACTIVATED CARBON FOR THREE ORTHO-SUBSTITUTED PHENOLS

    Science.gov (United States)

    Adsorptive capacity of activated carbon for several organic compounds was found to be strongly influenced by the presence of molecular oxygen. This influence is manifested by the polymerization of adsorbate on the surface of activated carbon. As a result, GAC exhibits much high...

  12. Dose-dependent adsorptive capacity of activated charcoal for gastrointestinal decontamination of a simulated paracetamol overdose in human volunteers

    DEFF Research Database (Denmark)

    Gude, Anne-Bolette Jill; Hoegberg, Lotte Christine Groth; Riis Angelo, Helle

    2010-01-01

    The amount of activated charcoal needed to treat drug overdoses has arbitrarily been set at a charcoal-drug ratio of 10:1. Recent in vitro studies have shown a larger adsorptive capacity for activated charcoal when used in a model of paracetamol overdose. In the present study, we investigated...

  13. Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity.

    Directory of Open Access Journals (Sweden)

    Zhujian Huang

    Full Text Available To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH2 was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt was functionalized with 3-aminopropyl triethoxysilane (APTES to obtain the APTES-Mt products (APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt, APTES4.0CEC-Mt with enhanced adsorption capacity for Co2+. The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co2+ onto Ca-Mt, APTES1.0CEC-Mt and APTES2.0CEC-Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co2+ onto APTES3.0CEC-Mt and APTES4.0CEC-Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt and APTES4.0CEC-Mt were 25.1, 33.8, 61.6, and 61.9 mg·g-1, respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co2+-rich wastewater.

  14. Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity.

    Science.gov (United States)

    Huang, Zhujian; Wu, Pingxiao; Gong, Beini; Dai, Yaping; Chiang, Pen-Chi; Lai, Xiaolin; Yu, Guangwei

    2016-01-01

    To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH2) was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt) was functionalized with 3-aminopropyl triethoxysilane (APTES) to obtain the APTES-Mt products (APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt, APTES4.0CEC-Mt) with enhanced adsorption capacity for Co2+. The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co2+ onto Ca-Mt, APTES1.0CEC-Mt and APTES2.0CEC-Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co2+ onto APTES3.0CEC-Mt and APTES4.0CEC-Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt and APTES4.0CEC-Mt were 25.1, 33.8, 61.6, and 61.9 mg·g-1, respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co2+-rich wastewater.

  15. The adsorptive capacity of vapor-phase mercury chloride onto powdered activated carbon derived from waste tires.

    Science.gov (United States)

    Lin, Hsun-Yu; Yuan, Chung-Shin; Wu, Chun-Hsin; Hung, Chung-Hsuang

    2006-11-01

    Injection of powdered activated carbon (PAC) upstream of particulate removal devices (such as electrostatic precipitator and baghouses) has been used effectively to remove hazardous air pollutants, particularly mercury-containing pollutants, emitted from combustors and incinerators. Compared with commercial PACs (CPACs), an alternative PAC derived from waste tires (WPAC) was prepared for this study. The equilibrium adsorptive capacity of mercury chloride (HgCl2) vapor onto the WPAC was further evaluated with a self-designed bench-scale adsorption column system. The adsorption temperatures investigated in the adsorption column were controlled at 25 and 150 degrees C. The superficial velocity and residence time of the flow were 0.01 m/sec and 4 sec, respectively. The adsorption column tests were run under nitrogen gas flow. Experimental results showed that WPAC with higher Brunauer-Emmett-Teller (BET) surface area could adsorb more HgCl2 at room temperature. The equilibrium adsorptive capacity of HgCl2 for WPAC measured in this study was 1.49 x 10(-1) mg HgCl2/g PAC at 25 degrees C with an initial HgCI2 concentration of 25 microg/m3. With the increase of adsorption temperature PAC. Furthermore, WPAC with higher sulfur contents could adsorb even more HgCl2 because of the reactions between sulfur and Hg2+ at 150 degrees C. It was demonstrated that the mechanisms for adsorbing HgCl2 onto WPAC were physical adsorption and chemisorption at 25 and 150 degrees C, respectively. Experimental results also indicated that the apparent overall driving force model appeared to have the good correlation with correlation coefficients (r) > 0.998 for HgCl2 adsorption at 25 and 150 degrees C. Moreover, the equilibrium adsorptive capacity of HgCl2 for virgin WPAC was similar to that for CPAC at 25 degrees C, whereas it was slightly higher for sulfurized WPAC than for CPAC at 150 degrees C.

  16. Adsorption

    Directory of Open Access Journals (Sweden)

    Denis J.L. Guerra

    2016-09-01

    Full Text Available Nontronite is an important phyllosilicate with a high concentration of ferric iron in the octahedral layer. A new occurrence of Brazilian nontronite sample was used for the organofunctionalization process with 3-aminopropyltriethoxysilane. Due to the increment of basic centers attached to the pendant chains, the metal adsorption capability of the final chelating material, was found to be higher than its precursor. The ability of these materials to remove Pb2+, Mn2+, and Zn2+ from aqueous solutions was followed by a series of adsorption isotherms at room temperature and pH 6.0, in batch adsorption experiments in order to explain the adsorption mechanism. In order to evaluate the phyllosilicate samples as adsorbents in a dynamic system, a glass column was fulfilled with nontronite samples (1.5 g and it was fed with 2.1 mmol dm−3 divalent cations at pH 6.0. The energetic effects caused by metal cations adsorption were determined through calorimetric titrations. The effects of three divalent metals adsorption in the zero point of charge of each material were investigated.

  17. Hierarchical flower-like nickel(II) oxide microspheres with high adsorption capacity of Congo red in water.

    Science.gov (United States)

    Zheng, Yingqiu; Zhu, Bicheng; Chen, Hua; You, Wei; Jiang, Chuanjia; Yu, Jiaguo

    2017-10-15

    Monodispersed hierarchical flower-like nickel(II) oxide (NiO) microspheres were fabricated by a facile solvothermal reaction with the assistance of ethanolamine and a subsequent calcination process. The as-synthesized samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, nitrogen adsorption-desorption isotherms, zeta potential measurement and Fourier transform infrared spectroscopy. Flower-like nickel(II) hydroxide microspheres with uniform diameters of approximate 6.3μm were obtained after the solvothermal reaction. After heat treatment at 350°C, the crystal phase transformed to NiO, but the hierarchical porous structure was maintained. The as-prepared microspheres exhibited outstanding performance for the adsorption of Congo red (CR), an anionic organic dye, from aqueous solution at circumneutral pH. The pseudo-second-order model can make a good description of the adsorption kinetics, while Langmuir model could well express the adsorption isotherms, with calculated maximum CR adsorption capacity of 534.8 and 384.6mgg(-1), respectively, for NiO and Ni(OH)2. The adsorption mechanism of CR onto the as-synthesized samples can be mainly attributed to electrostatic interaction between the positively charged sample surface and the anionic CR molecules. The as-prepared NiO microspheres are a promising adsorbent for CR removal in water treatment. Copyright © 2017 Elsevier Inc. All rights reserved.

  18. Edge-functionalized nanoporous carbons for high adsorption capacity and selectivity of CO2 over N2

    Science.gov (United States)

    Zhou, Sainan; Guo, Chen; Wu, Zhonghua; Wang, Maohuai; Wang, Zhaojie; Wei, Shuxian; Li, Shaoren; Lu, Xiaoqing

    2017-07-01

    Single-component adsorption and competitive behavior of binary CO2/N2 mixture in the edge-functionalized nanoporous carbons (NPCs) were investigated by grand canonical Monte Carlo simulation. Results demonstrated that edge-functionalization effectively improved the pore topology and morphological characteristics of NPCs. Evaluation of adsorption capacity and analyses of the isosteric heat and radial distribution functions confirmed that edge-functionalization can evidently enhance the single-component adsorption of CO2/N2. Temperature had a negative effect on the single-component adsorption of CO2/N2 whereas pressure had a positive effect before adsorption reaches a stable equilibrium state. Edge-functionalization can significantly increase the selectivity of CO2 over N2 in NPCs, which demonstrate the following sequence according to selectivity: NH2sbnd NPC > COOHsbnd NPC > OHsbnd NPC > Hsbnd NPC > NPC. The increased CO2 molar fraction in the binary CO2/N2 mixture decreased the selectivity and saturation pressure to reach a stable equilibrium state. Overall, this work highlighted the effects of edge-functionalization on the adsorption and separation of CO2/N2 in NPCs, and provided an effective strategy for designing and screening adsorbent materials for carbon capture and separation.

  19. Preparation of Urea Nitrogen Adsorbent of Complex Type and Adsorption Capacity of Urea Nitrogen onto the Adsorbent

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The urea nitroge n adsorbent of complex type, which consists of chitosan coated dialdehyde cellulose (CDAC) and immobilized urease in gelatin membrane (IE), was prepared. The cellulose, the dialdehyde cellulose (DAC) and the CDAC were characterized by scanning electronic microscope. The results indicate that the cellulose C2-C3 bond was broken under the oxidation of periodate and it was oxidated to DAC. The DAC was coated with chitosan and the CDAC was obtained. The adsorption of urea nitrogen onto the adsorbent in Na2HPO4-NaH2PO4 buffer solution was studied in batch system. The effects of the experiment parameters, including degree of oxidation of CDAC, initial urea nitrogen concentration, pH and temperature, on the adsorption capacity of urea nitrogen onto the adsorbent at CDAC/IE weight ratio 10:1 were investigated. The results indicate that these parameters affected significantly the adsorption capacity. The adsorption capacity of urea nitrogen onto the adsorbent was 36.7 mg/g at the degree of oxidation of CDAC 88%, initial urea nitrogen concentration 600 mg/L, pH 7.4 and temperature 37 ℃.

  20. Adsorption capacity of poly(ether imide) microparticles to uremic toxins.

    Science.gov (United States)

    Tetali, Sarada D; Jankowski, Vera; Luetzow, Karola; Kratz, Karl; Lendlein, Andreas; Jankowski, Joachim

    2016-01-01

    Uremia is a phenomenon caused by retention of uremic toxins in the plasma due to functional impairment of kidneys in the elimination of urinary waste products. Uremia is presently treated by dialysis techniques like hemofiltration, dialysis or hemodiafiltration. However, these techniques in use are more favorable towards removing hydrophilic than hydrophobic uremic toxins. Hydrophobic uremic toxins, such as hydroxy hipuric acid (OH-HPA), phenylacetic acid (PAA), indoxyl sulfate (IDS) and p-cresylsulfate (pCRS), contribute substantially to the progression of chronic kidney disease (CKD) and cardiovascular disease. Therefore, objective of the present study is to test adsorption capacity of highly porous microparticles prepared from poly(ether imide) (PEI) as an alternative technique for the removal of uremic toxins. Two types of nanoporous, spherically shaped microparticles were prepared from PEI by a spraying/coagulation process.PEI particles were packed into a preparative HPLC column to which a mixture of the four types of uremic toxins was injected and eluted with ethanol. Eluted toxins were quantified by analytical HPLC. PEI particles were able to adsorb all four toxins, with the highest affinity for PAA and pCR. IDS and OH-HPA showed a partially non-reversible binding. In summary, PEI particles are interesting candidates to be explored for future application in CKD.

  1. Preparation of Aminated Macroporous Polyvinyl Alcohol Resins and Evaluation for Bilirubin Adsorption

    Institute of Scientific and Technical Information of China (English)

    WANG Wei-chao; ZHANG Sheng-nan; HU Yue-han; XIE Hui; OU Lai-liang; YU Yao-ting; KONG De-ling; GU Han-qing

    2008-01-01

    In the present study we prepared macroporous polyvinyl alcohol beads. A series of bilirubin adsorbents were generated by immobilization of eight amine agents to the beads as ligands. The adsorption of bilirubin was evaluated by in vitro static and dynamic adsorption tests. The results show that these adsorbents have excellent adsorption efficiency and capacity. Among the eight ligands, trimethylamine (TMA), triethylamine (TEA) and 1,6- hexanediamine(HAD) showed the highest adsorption capacity. The adsorption equilibrium can be achieved in half an hour, and the adsorption percentage of bilirubin was up to 80%. Static electricity and hydrophobic interaction played the main role in bilirubin adsorption, and the adsorption was found to match the monolayer model. The excellent adsorption of these adsorbents indicates their potential in clinical treatment.

  2. Effect of O2 pressure on the hydrothermal growth of CuO hierarchical microstructures: characterization and hydrogen adsorption capacity

    Science.gov (United States)

    Roble, M.; Diaz-Droguett, D.

    2017-08-01

    In the present study, the effect of injected O2 pressure to a hydrothermal reactor on the growth, morphology, structure and hydrogen adsorption properties of CuO hierarchical microstructures was investigated. The synthesis consisted of a simple one-step hydrothermal reaction using copper chloride and aqueous ammonia. Hydrothermal reactions were carried at 200 °C at reaction times of 1 and 12 h injecting at the beginning of the synthesis O2 pressures of 0, 30 or 60 bar. The samples were characterized by SEM and EDS for morphological and chemical information, XRD for determination of crystalline phases, lattice parameters and crystallinity grade using Rietveld refinement. Specific surface area was determined using BET method from nitrogen adsorption/desorption isotherm measurements. Hydrogen adsorption capacities at 20 °C were studied for key samples using the quartz crystal microbalance technique under gas exposure pressures between 3 and 100 Torr. It was found that the samples were of monoclinic CuO phase consisting mainly of sphere-like hierarchical microstructures of different average sizes assembled by sheets. The effect of the reactor pressure was mainly seen on average size of the CuO microstructures due to changes in the growth rate, specifically during the first stages of the hydrothermal reaction. Reactor pressure induced changes on the crystallinity of the samples were determined but no correlation was stated. Hydrogen adsorption capacities of studied samples measured at 100 Torr ranged from 0.27 to 0.6 wt%, indicating a good performance as compared with other reported values. Oxygen deficiency in CuO can influence on the hydrogen adsorption capacity.

  3. [Blood plasma protein adsorption capacity of perfluorocarbon emulsion stabilized by proxanol 268 (in vitro and in vivo studies)].

    Science.gov (United States)

    Sklifas, A N; Zhalimov, V K; Temnov, A A; Kukushkin, N I

    2012-01-01

    The adsorption abilities of the perfluorocarbon emulsion stabilized by Proxanol 268 were investigated in vitro and in vivo. In vitro, the saturation point for the blood plasma proteins was nearly reached after five minutes of incubation of the emulsion with human/rabbit blood plasma and was stable for all incubation periods studied. The decrease in volume ratio (emulsion/plasma) was accompanied by the increase in the adsorptive capacity of the emulsion with maximal values at 1/10 (3.2 and 1.5 mg of proteins per 1 ml of the emulsion, for human and rabbit blood plasma, respectively) that was unchanged at lower ratios. In vivo, in rabbits, intravenously injected with the emulsion, the proteins with molecular masses of 12, 25, 32, 44, 55, 70, and 200 kDa were adsorbed by the emulsion (as in vitro) if it was used 6 hours or less before testing. More delayed testing (6 h) revealed elimination of proteins with molecular masses of 25 and 44 kDa and an additional pool of adsorpted new ones of 27, 50, and 150 kDa. Specific adsorptive capacity of the emulsion enhanced gradually after emulsion injection and reached its maximum (3.5-5 mg of proteins per 1 ml of the emulsion) after 24 hours.

  4. Effects of textural and surface characteristics of microporous activated carbons on the methane adsorption capacity at high pressures

    Energy Technology Data Exchange (ETDEWEB)

    Bastos-Neto, M. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Canabrava, D.V. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Torres, A.E.B. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Rodriguez-Castellon, E. [Departamento de Quimica Inorganica, Cristalografia y Mineralogia (Unidad Asociada al ICP-CSIC), Facultad de Ciencias, Universidad de Malaga, 29071 Malaga (Spain); Jimenez-Lopez, A. [Departamento de Quimica Inorganica, Cristalografia y Mineralogia (Unidad Asociada al ICP-CSIC), Facultad de Ciencias, Universidad de Malaga, 29071 Malaga (Spain); Azevedo, D.C.S. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil)]. E-mail: diana@gpsa.ufc.br; Cavalcante, C.L. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil)

    2007-04-30

    The objective of this study is to relate textural and surface characteristics of selected microporous activated carbons to their methane storage capacity. In this work, a magnetic suspension balance (Rubotherm, Germany) was used to measure methane adsorption isotherms of several activated carbon samples. Textural characteristics were assessed by nitrogen adsorption on a regular surface area analyzer (Autosorb-MP, by Quantachrome, USA). N{sub 2} adsorption was analysed by conventional models (BET, DR, HK) and by Monte Carlo molecular simulations. Elemental and surface analyses were performed by X-ray photoelectronic spectroscopy (XPS) for the selected samples. A comparative analysis was then carried out with the purpose of defining some correlation among the variables under study. For the system under study, pore size distribution and micropore volume seem to be a determining factor as long as the solid surface is perfectly hydrophobic. It was concluded that the textural parameters per se do not unequivocally determine natural gas storage capacities. Surface chemistry and methane adsorption equilibria must be taken into account in the decision-making process of choosing an adsorbent for gas storage.

  5. Thermodynamic and kinetic study of the intrinsic adsorption capacity of graphene oxide for malachite green removal from aqueous solution

    Directory of Open Access Journals (Sweden)

    Prawit Nuengmatcha

    2014-12-01

    Full Text Available Graphene oxide (GO was produced from bare graphite (BGP material and was used as anintrinsic adsorbent for the removal of malachite green (MG from aqueous solution. In an optimization study, the effects of the initial concentration of MG, solution pH, adsorbent dosage, contact time and ionic strength were investigated in detail. The water-soluble dye was analyzed at a maximum wavelength of 618 nm. The optimum conditions for MG removal from aqueous solution included a 300 mg/L initial concentration with 0.02 mg adsorbent at pH 5.1, and complete adsorption equilibrium was reached within 40 min. The maximum adsorption capacity of GO for MG was 384.62 mg/g, dramatically higher (over 10 times than that of BGP (28.73 mg/g.The adsorption process followed pseudo-second-order kinetics. Thermodynamic data demonstrated that dye adsorption onto the GO surface was mainly an exothermic spontaneous reaction. The remarkably different adsorption isotherms for GO and BGP fit well with the Langmuir and Freundlich models, respectively. It is therefore evident that the prepared GO can be used as a highly effective adsorbent for this toxic dye.

  6. Supercritical CO2 Assisted Synthesis of EDTA-Fe3O4 Nanocomposite with High Adsorption Capacity for Hexavalent Chromium

    Directory of Open Access Journals (Sweden)

    Gunjan Bisht

    2016-01-01

    Full Text Available Efficiency of EDTA functionalized nanoparticles in adsorption of chromium (VI from water was investigated in this study. Magnetic iron oxide nanoparticles (IONPs were synthesized by a simple chemical coprecipitation route and EDTA coating onto IONPs was attained via supercritical carbon dioxide (Sc CO2, a technology with green sustainable properties. The obtained nanoparticles were then characterized by UV-Visible spectroscopy, Fourier transform infrared spectroscopy (FTIR, X-ray powder diffraction (XRD, transmission electron microscopy (TEM, scanning electron microscopy (SEM, and vibrating magnetometric analysis (VSM. The synthesized nanoparticle and its modified variant were evaluated as adsorbent for chromium (VI removal from water through batch adsorption technique and the effect of analytic concentration; contact time and adsorbent concentration were studied at pH 2. The results showed higher removal efficiency for modified magnetic iron oxide nanoparticles (MIONPs (i.e., 99.9% than their nonmodified variant IONPs, that is, 34.06% for the same concentration after 18 hours of incubation. Also maximum adsorption capacity (qe = 452.26 mg/g of MIONPs attained can be related to their preparation in Sc CO2 as qe calculated from IONPs, that is, 170.33 mg/g, is lower than that of MIONPs. The adsorption data fit well with Freundlich isotherm equation while kinetic adsorption studies of chromium (VI were modeled by pseudo-second-order model.

  7. Summary of Adsorption Capacity and Adsorption Kinetics of Uranium and Other Elements on Amidoxime-based Adsorbents from Time Series Marine Testing at the Pacific Northwest National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Gill, Gary A. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Kuo, Li-Jung [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Strivens, Jonathan E. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Wood, Jordana R. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Schlafer, Nicholas J. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Janke, Christopher J. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Das, Sadananda [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Mayes, Richard [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Saito, Tomonori [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Brown, Suree S. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Tsouris, Constantinos [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Tsouris, Costas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Wai, Chien M. [Univ. of Idaho, Moscow, ID (United States); LCW Supercritical Technologies, Seattle, WA (United States); Pan, Horng-Bin [Univ. of Idaho, Moscow, ID (United States)

    2016-09-29

    The Pacific Northwest National Laboratory (PNNL) has been conducting marine testing of uranium adsorbent materials for the Fuel Resources Program, Department of Energy, Office of Nuclear Energy (DOE-NE) beginning in FY 2012. The marine testing program is being conducted at PNNL’s Marine Sciences Laboratory (MSL), located at Sequim Bay, along the coast of Washington. One of the main efforts of the marine testing program is the determination of adsorption capacity and adsorption kinetics for uranium and selected other elements (e.g. vanadium, iron, copper, nickel, and zinc) for adsorbent materials provided primarily by Oak Ridge National Laboratory (ORNL), but also includes other Fuel Resources Program participants. This report summarizes the major marine testing results that have been obtained to date using time series sampling for 42 to 56 days using either flow-through column or recirculating flume exposures. The major results are highlighted in this report, and the full data sets are appended as a series of Excel spreadsheet files. Over the four year period (2012-2016) that marine testing of amidoxime-based polymeric adsorbents was conducted at PNNL’s Marine Science Laboratory, there has been a steady progression of improvement in the 56-day adsorbent capacity from 3.30 g U/kg adsorbent for the ORNL 38H adsorbent to the current best performing adsorbent prepared by a collaboration between the University of Tennessee and ORNL to produce the adsorbent SB12-8, which has an adsorption capacity of 6.56 g U/kg adsorbent. This nearly doubling of the adsorption capacity in four years is a significant advancement in amidoxime-based adsorbent technology and a significant achievement for the Uranium from Seawater program. The achievements are evident when compared to the several decades of work conducted by the Japanese scientists beginning in the 1980’s (Kim et al., 2013). The best adsorbent capacity reported by the Japanese scientists was 3.2 g U/kg adsorbent for a

  8. Multilayer adsorption on fractal surfaces.

    Science.gov (United States)

    Vajda, Péter; Felinger, Attila

    2014-01-10

    Multilayer adsorption is often observed in liquid chromatography. The most frequently employed model for multilayer adsorption is the BET isotherm equation. In this study we introduce an interpretation of multilayer adsorption measured on liquid chromatographic stationary phases based on the fractal theory. The fractal BET isotherm model was successfully used to determine the apparent fractal dimension of the adsorbent surface. The nonlinear fitting of the fractal BET equation gives us the estimation of the adsorption equilibrium constants and the monolayer saturation capacity of the adsorbent as well. In our experiments, aniline and proline were used as test molecules on reversed phase and normal phase columns, respectively. Our results suggest an apparent fractal dimension 2.88-2.99 in the case of reversed phase adsorbents, in the contrast with a bare silica column with a fractal dimension of 2.54.

  9. Molecular basis for the high CO2 adsorption capacity of chabazite zeolites.

    Science.gov (United States)

    Pham, Trong D; Hudson, Matthew R; Brown, Craig M; Lobo, Raul F

    2014-11-01

    CO2 adsorption in Li-, Na-, K-CHA (Si/Al=6,=12), and silica chabazite zeolites was investigated by powder diffraction. Two CO2 adsorption sites were found in all chabazites with CO2 locating in the 8-membered ring (8MR) pore opening being the dominant site. Electric quadrupole-electric field gradient and dispersion interactions drive CO2 adsorption at the middle of the 8 MRs, while CO2 polarization due to interaction with cation sites controls the secondary CO2 site. In Si-CHA, adsorption is dominated by dispersion interactions with CO2 observed on the pore walls and in 8 MRs. CO2 adsorption complexes on dual cation sites were observed on K-CHA, important for K-CHA-6 samples due to a higher probability of two K(+) cations bridging CO2. Trends in isosteric heats of CO2 adsorption based on cation type and concentration can be correlated with adsorption sites and CO2 quantity. A decrease in the hardness of metal cations results in a decrease in the direct interaction of these cations with CO2.

  10. Quantitative evaluation of the effect of moisture contents of coconut shell activated carbon used for respirators on adsorption capacity for organic vapors.

    Science.gov (United States)

    Abiko, Hironobu; Furuse, Mitsuya; Takano, Tsuguo

    2010-01-01

    Activated carbon is an elemental material used for hygienic applications, particularly as an adsorbent for harmful gases and vapors. In Japanese industrial and occupational hygiene, activated carbon produced from coconut shell is a traditional and popular adsorbent material due to its excellent adsorption ability and cost advantage. In this research, in order to clarify the effect of the preliminary content of moisture on the adsorption capacity in detail, we prepared several coconut shell activated carbons which were preconditioned by equilibration with moisture at different relative humidities. We measured their adsorption capacities as breakthrough times for 6 kinds of organic vapor, and attempted to determine the relationships between the relative weight increase of water adsorption and the decrease of adsorption capacities of the activated carbon specimens for the organic vapors. The procedure of the quantitative evaluation of the effect of moisture and the results are useful for practical applications of activated carbon, particularly those used as adsorbents in workplaces.

  11. High gas storage capacities and stepwise adsorption in a UiO type metal-organic framework incorporating Lewis basic bipyridyl sites.

    Science.gov (United States)

    Li, Liangjun; Tang, Sifu; Wang, Chao; Lv, Xiaoxia; Jiang, Min; Wu, Huaizhi; Zhao, Xuebo

    2014-03-04

    A UiO type MOF with Lewis basic bipyridyl sites was synthesized and structurally characterized. After being activated by Soxhlet-extraction, this MOF exhibits high storage capacities for H2, CH4 and CO2, and shows unusual stepwise adsorption for liquid CO2 and solvents, indicating a sequential filling mechanism on different adsorption sites.

  12. Experimental evidence for the influence of charge on the adsorption capacity of carbon dioxide on charged fullerenes

    CERN Document Server

    Ralser, Stefan; Probst, Michael; Postler, Johannes; Renzler, Michael; Bohme, Diethard K; Scheier, Paul

    2016-01-01

    We show, with both experiment and theory, that adsorption of $CO_2$ is sensitive to charge on a capturing model carbonaceous surface. In the experiment we dope superfluid helium droplets with $C_{60}$ and $CO_2$ and expose them to ionising free electrons. Both positively and negatively charged $C_{60}(CO_2)_n^{+/-}$ cluster ion distributions are observed with a high-resolution mass spectrometer and these show remarkable and reproducible anomalies in intensities that are strongly dependent on the charge. The highest adsorption capacity is seen with $C_{60}^+$. Complementary density functional theory calculations and molecular dynamics simulations provided insight into the nature of the interaction of charged $C_{60}$ with $CO_2$ as well as trends in the packing of $C_{60}^+$ and $C_{60}^-$. The quadrupole moment of $CO_2$ itself was seen to be decisive in determining the charge dependence of the observed adsorption features. Our findings are expected to apply to adsorption of $CO_2$ by charged surfaces in gene...

  13. Simultaneous activation/sulfurization method for production of sulfurized activated carbons: characterization and Hg(II) adsorption capacity.

    Science.gov (United States)

    Shamsijazeyi, Hadi; Kaghazchi, Tahereh

    2014-01-01

    As an inexpensive method for modification of activated carbons (ACs), sulfurization has attracted significant attention. However, the resulting sulfurized activated carbons (SACs) often are less porous than the original ACs. In this work, we propose a new method for concurrent sulfurization/activation that can lead to preparation of SACs with more porosity than the corresponding non-sulfurized ACs. By using scanning electron microscopy, nitrogen adsorption/desorption, and iodine number experiments, the porous structure of the SACs has been compared with that of non-sulfurized ACs. The specific surface areas of SACs are higher than the corresponding ACs, regardless of the type of activation agents used. For instance, the specific surface area of SAC and AC activated with phosphoric acid is 1,637 and 1,338 m(2)/g, respectively. Additionally, sulfur contents and surface charges (pHpzc) of the SACs and non-sulfurized ACs are compared. In fact, the SACs have higher sulfur contents and more acidic surfaces. Furthermore, the Hg(II) adsorption capacity of SACs has been compared with the corresponding non-sulfurized ACs. The Hg(II) adsorption isotherms on a selected SAC is measured at different pH values and temperatures. Hg(II) adsorptions as high as 293 mg/g are observed by using SACs prepared by the method proposed in this study.

  14. Industrial surfaces behaviour related to the adsorption and desorption of hydrogen at cryogenic temperature [in LHC vacuum system

    CERN Document Server

    Moulard, G; Saitô, Y

    2001-01-01

    The determination of the hydrogen adsorption capacity on different industrial surfaces has been carried out by measuring isothermal adsorption. First results show that the adsorption capacity is mainly determined by surface porosity. Therefore, the samples may be classified into two categories: smooth and porous surfaces. Thermal desorption spectra reveal two adsorption energy levels for hydrogen physisorbed on porous materials, but only a single one on smooth samples. The value of the lowest energy level seems to be independent of the substrate nature. The physisorption process studied at low coverage, well below a monolayer, shows that these two levels are not well defined but an energy distribution exists for each of them. The influences of the isotherm temperature and an annealing at 7 K of an adsorbed monolayer on hydrogen adsorption capacity have been studied. (16 refs).

  15. An in vitro Study on the Adsorption, Absorption and Uptake Capacity of Zn by the Bioremediator Trichoderma atroviride

    Directory of Open Access Journals (Sweden)

    Mazyar Yazdani

    2010-01-01

    Full Text Available The concentrations of Zn in the sediment of a polluted river at the Serdang Industrial Area were determined. These polluted sediment samples revealed high level of Zn (219. 27 µg/g. Isolation of fungi from this polluted sediment was also carried out using Rose Bengal Agar (RBA. The isolated fungi were exposed to different concentrations of Zn (0-6000 mg/L on Potato Dextrose Agar (PDA to find the most tolerant isolate. Trichoderma atroviride was found to have the highest tolerance and it was studied for growth rate, Zn uptake capacity, its tolerance to Zn and also localization of Zn by using Potato Dextrose Broth (PDB as the liquid culture medium. In the present study the results found out that the uptake capacity of T. atroviride ranged from 18.1-26.7 mg/g in liquid media at Zn concentrations from 500 to 1000 mg/L. The isolate showed 47.6-64% adsorption and 30.4¬45.1% absorption for Zn. Based on the present study, 5.7-7.4% of Zn removal was observed due to biomass washing. The high adsorption, relatively low absorption and high uptake capacity of Zn suggest that T. atroviride is a potential bioremediator of Zn. However, further studies are needed to confirm its practical use as a bioremediating agent for Zn under field conditions.

  16. 2,4-D adsorption to biochars: effect of preparation conditions on equilibrium adsorption capacity and comparison with commercial activated carbon literature data.

    Science.gov (United States)

    Kearns, J P; Wellborn, L S; Summers, R S; Knappe, D R U

    2014-10-01

    Batch isotherm experiments were conducted with chars to study adsorption of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Chars generated from corncobs, bamboo and wood chips in a laboratory pyrolyzer at 400-700 °C were compared with traditional kiln charcoals collected from villages in S/SE Asia and with activated carbons (ACs). 2,4-D uptake by laboratory chars obtained from bamboo and wood chips after 14 h of pyrolysis at 700 °C, from wood chips after 96 h of pyrolysis at 600 °C, and one of the field-collected chars (basudha) was comparable to ACs. H:C and O:C ratios declined with pyrolysis temperature and duration while surface area increased to >500 m(2)/g. Increasing pyrolysis intensity by increasing temperature and/or duration of heating was found to positively influence adsorption capacity yield (mg(2,4-D/g(feedstock))) over the range of conditions studied. Economic analysis showed that high temperature chars can be a cost-effective alternative to ACs for water treatment applications.

  17. EFFECT OF SURFACE CHEMISTRY OF ACTIVATED CARBON ON ITS EQUILIBRIUM ADSORPTION CAPACITY FOR CO2%活性炭表面化学性质对二氧化碳吸附平衡的影响

    Institute of Scientific and Technical Information of China (English)

    张睿; 周贝; 段晓佳; 胡子君; 李俊宁; 金鸣林

    2011-01-01

    把氢氧化钾活化的石油焦基活性炭进行浓硫酸氧化,并对氧化物进行热处理,得到不同氧含量的活性炭,并用氮气物理吸附和XPS对活性炭的孔及其表面化学官能团进行了表征.研究了二氧化碳在不同氧含量活性炭上的吸附平衡容量随温度的变化以及氧含量对于二氧化碳吸附容量的影响.结果表明:在25℃~175℃和0.001 MPa~1.5 MPa的范围内,二氧化碳在活性炭上的吸附可以用Langmuir方程很好地描述,饱和覆盖度和黏附系数均随温度的升高而下降,吸附热随活性炭的氧化和热处理变化很小.随活性炭O/C比的增加,饱和覆盖度下降,而黏附系数增加.适合二氧化碳吸附的活性炭应具有适中的O/C比,O/C比太大和太小均不利于二氧化碳的吸附.%Activated carbon from petroleum coke by KOH activation was oxidized by concentrated sulfuric acid at 170 ℃ for 3 h, followed by heat treatment under protection of nitrogen at 450 and 750 'C for 3 h. The as-activated carbon, oxidized activated carbon and heat-treated carbon with different oxygen contents were characterized by nitrogen adsorption and X-ray photo-electron spectroscopy, and their adsorptive capacities for CO2 at 25 °C to 175 'C and 10 mbar to 15 000 mbar were investigated. It was found that their BET surface areas and pore size distributions were similar while their surface oxygen contents were different depending on the oxidation and heat treatment conditions. The adsorptive capacities for CO2 in the experimental conditions can be well fitted by Langmuir equation. The monolayer capacity and sticking coefficient decreased with adsorption temperature and the heat of adsorption changed little with the oxidation or heat treatment. The monolayer capacity decreased and sticking coefficient increased with O/C atom ratios. Suitable activated carbon should have a moderate O/C ratio for a better adsorption forCO2.

  18. PREDICTING THE ADSORPTION CAPACITY OF ACTIVATED CARBON FOR ORGANIC CONTAMINANTS FROM ADSORBENT AND ADSORBATE PROPERTIES

    Science.gov (United States)

    A quantitative structure-property relationship (QSPR) was developed and combined with the Polanyi-Dubinin-Manes model to predict adsorption isotherms of emerging contaminants on activated carbons with a wide range of physico-chemical properties. Affinity coefficients (βl

  19. Optimization of layered double hydroxide stability and adsorption capacity for anionic surfactants

    NARCIS (Netherlands)

    Schouten, Natasja; Ham, Louis G.J. van der; Euverink, Gert-Jan W.; Haan, André B. de

    2007-01-01

    Low cost adsorption technology offers high potential to clean up laundry rinsing water. From an earlier selection of adsorbents, layered double hydroxide (LDH) proved to be an interesting material for the removal of anionic surfactant, linear alkyl benzene sulfonate (LAS) which is the main contamina

  20. Optimization of layered double hydroxide stability and adsorption capacity for anionic surfactants

    NARCIS (Netherlands)

    Schouten, Natasja; Ham, van der Louis G.J.; Euverink, Gert-Jan W.; Haan, de André B.

    2007-01-01

    Low cost adsorption technology offers high potential to clean up laundry rinsing water. From an earlier selection of adsorbents (Schouten et al. 2007), layered double hydroxide (LDH) proved to be an interesting material for the removal of anionic surfactant, linear alkyl benzene sulfonate (LAS) whic

  1. Properties of poly(1-naphthylamine)/Fe3O4 composites and arsenic adsorption capacity in wastewater

    Science.gov (United States)

    Tran, Minh Thi; Nguyen, Thi Huyen Trang; Vu, Quoc Trung; Nguyen, Minh Vuong

    2016-03-01

    The research results of poly(1-naphthylamine)/Fe3O4 (PNA/Fe3O4) nanocomposites synthesized by a chemical method for As(III) wastewater treatment are presented in this paper. XRD patterns and TEM images showed that the Fe3O4 grain size varied from 13 to 20 nm. The results of Raman spectral analysis showed that PNA participated in part of the PNA/Fe3O4 composite samples. The grain size of PNA/Fe3O4 composite samples is about 25-30 nm measured by SEM. The results of vibrating sample magnetometer measurements at room temperature showed that the saturation magnetic moment of PNA/Fe3O4 samples decreased from 63.13 to 43.43 emu/g, while the PNA concentration increased from 5% to 15%. The nitrogen adsorption-desorption isotherm of samples at 77 K at a relative pressure P/ P 0 of about 1 was studied in order to investigate the surface and porous structure of nanoparticles by the BET method. Although the saturation magnetic moments of samples decreased with the polymer concentration increase, the arsenic adsorption capacity of the PNA/Fe3O4 sample with the PNA concentration of 5% is better than that of Fe3O4 in a solution with pH = 7. In the solution with pH > 14, the arsenic adsorption of magnetic nanoparticles is insignificant.

  2. Hyperbranched-polyol-tethered poly (amic acid) electrospun nanofiber membrane with ultrahigh adsorption capacity for boron removal

    Science.gov (United States)

    Wang, Zhe; Wu, Zhongyu; Zhang, Yufeng; Meng, Jianqiang

    2017-04-01

    The development of efficient adsorbents with high sorption capacity remains as a challenge for the removal of micropollutants occurred globally in water resources. In this work, poly (amic acid) (PAA) electrospun nanofiber membranes grafted with hyperbranched polyols were synthesized and used for boron removal. The PAA nanofiber was reacted with hyperbranched polyethylenimine (HPEI) and further with glycidol to introduce the vicinal hydroxyl groups. The chemical composition and surface characteristics of the obtained PAA-g-PG membranes were evaluated by FESEM, FTIR, XPS and water contact angles (WCA) measurements. The boron adsorption thermodynamics and kinetics were investigated systematically. The results showed that the PAA nanofiber spun from concentration of 15% had uniform morphology and narrow diameter distribution. The PAA-g-PG nanofiber membrane had a maximum boron uptake of 5.68 mmol/g and could adsorb 0.82 mmol/g boron from a 5 mg/L solution in 15 min. Both the high surface area of nanofibers and the hyperbranched structure should contribute to the high boron uptake and high adsorption rate. The nanofiber membrane obeyed the Langmuir adsorption model and the pseudo-first-order kinetic model. The regeneration efficiency of the nanofiber membrane remained 93.9% after 10 cycled uses, indicating good regenerability of the membrane.

  3. Synthesis, characterisation and methyl orange adsorption capacity of ferric oxide-biochar nano-composites derived from pulp and paper sludge

    Science.gov (United States)

    Chaukura, Nhamo; Murimba, Edna C.; Gwenzi, Willis

    2016-02-01

    A Fe2O3-biochar nano-composite (Fe2O3-BC) was prepared from FeCl3-impregnated pulp and paper sludge (PPS) by pyrolysis at 750 °C. The characteristics and methyl orange (MO) adsorption capacity of Fe2O3-BC were compared to that of unactivated biochar (BC). X-ray diffraction (XRD) and scanning electron microscopy (SEM) confirmed the composite material was nano-sized. Fourier transform infrared (FTIR) spectroscopy revealed the presence of hydroxyl and aromatic groups on BC and on Fe2O3-BC, but Brunauer-Emmett-Teller (BET) surface area and Barrett-Joyner-Halenda (BJH) porosity were lower for Fe2O3-BC than BC. Despite the lower BET surface area and porosity of Fe2O3-BC, its MO adsorption capacity was 52.79 % higher than that of BC. The equilibrium adsorption data were best represented by the Freundlich model with a maximum adsorption capacity of 20.53 mg g-1 at pH 8 and 30 min contact time. MO adsorption obeyed pseudo-second-order kinetics for both BC and Fe2O3-BC with R 2 values of 0.996 and 0.999, respectively. Higher MO adsorption capacity for Fe2O3-BC was attributed to the hybrid nature of the nano-composites; adsorption occurred on both biochar matrix and Fe2O3 nanocrystals. Gibbs free energy calculations confirmed the adsorption is energetically favourable and spontaneous with a high preference for adsorption on both adsorbents. The nano-composite can be used for the efficient removal of MO (>97 %) from contaminated wastewater.

  4. Synthesis, characterisation and methyl orange adsorption capacity of ferric oxide-biochar nano-composites derived from pulp and paper sludge

    Science.gov (United States)

    Chaukura, Nhamo; Murimba, Edna C.; Gwenzi, Willis

    2017-09-01

    A Fe2O3-biochar nano-composite (Fe2O3-BC) was prepared from FeCl3-impregnated pulp and paper sludge (PPS) by pyrolysis at 750 °C. The characteristics and methyl orange (MO) adsorption capacity of Fe2O3-BC were compared to that of unactivated biochar (BC). X-ray diffraction (XRD) and scanning electron microscopy (SEM) confirmed the composite material was nano-sized. Fourier transform infrared (FTIR) spectroscopy revealed the presence of hydroxyl and aromatic groups on BC and on Fe2O3-BC, but Brunauer-Emmett-Teller (BET) surface area and Barrett-Joyner-Halenda (BJH) porosity were lower for Fe2O3-BC than BC. Despite the lower BET surface area and porosity of Fe2O3-BC, its MO adsorption capacity was 52.79 % higher than that of BC. The equilibrium adsorption data were best represented by the Freundlich model with a maximum adsorption capacity of 20.53 mg g-1 at pH 8 and 30 min contact time. MO adsorption obeyed pseudo-second-order kinetics for both BC and Fe2O3-BC with R 2 values of 0.996 and 0.999, respectively. Higher MO adsorption capacity for Fe2O3-BC was attributed to the hybrid nature of the nano-composites; adsorption occurred on both biochar matrix and Fe2O3 nanocrystals. Gibbs free energy calculations confirmed the adsorption is energetically favourable and spontaneous with a high preference for adsorption on both adsorbents. The nano-composite can be used for the efficient removal of MO (>97 %) from contaminated wastewater.

  5. Evaluation of phosphorus adsorption capacity of sesame straw biochar on aqueous solution: influence of activation methods and pyrolysis temperatures.

    Science.gov (United States)

    Park, J H; Ok, Y S; Kim, S H; Cho, J S; Heo, J S; Delaune, R D; Seo, D C

    2015-12-01

    The phosphorus (P) adsorption characteristic of sesame straw biochar prepared with different activation agents and pyrolysis temperatures was evaluated. Between 0.109 and 0.300 mg L(-1) in the form of inorganic phosphate was released from raw sesame straw biochar in the first 1 h. The release of phosphate was significantly enhanced from 62.6 to 168.2 mg g(-1) as the pyrolysis temperature increased. Therefore, sesame straw biochar cannot be used as an adsorbent for P removal without change in the physicochemical characteristics. To increase the P adsorption of biochar in aqueous solution, various activation agents and pyrolysis temperatures were applied. The amount of P adsorbed from aqueous solution by biochar activated using different activation agents appeared in the order ZnCl2 (9.675 mg g(-1)) > MgO (8.669 mg g(-1)) ⋙ 0.1N-HCl > 0.1N-H2SO4 > K2SO4 ≥ KOH ≥ 0.1N-H3PO4, showing ZnCl2 to be the optimum activation agent. Higher P was adsorbed by the biochar activated using ZnCl2 under different pyrolysis temperatures in the order 600 °C > 500 °C > 400 °C > 300 °C. Finally, the amount of adsorbed P by activated biochar at different ratios of biochar to ZnCl2 appeared in the order 1:3 ≒ 1:1 > 3:1. As a result, the optimum ratio of biochar to ZnCl2 and pyrolysis temperature were found to be 1:1 and 600 °C for P adsorption, respectively. The maximum P adsorption capacity by activated biochar using ZnCl2 (15,460 mg kg(-1)) was higher than that of typical biochar, as determined by the Langmuir adsorption isotherm. Therefore, the ZnCl2 activation of sesame straw biochar was suitable for the preparation of activated biochar for P adsorption.

  6. Effects of sulfur impregnation temperature on the properties and mercury adsorption capacities of activated carbon fibers (ACFs)

    Science.gov (United States)

    Hsi, H.-C.; Rood, M.J.; Rostam-Abadi, M.; Chen, S.; Chang, R.

    2001-01-01

    Laboratory studies were conducted to determine the role of sulfur functional groups and micropore surface area of carbon-based adsorbents on the adsorption of Hg0 from simulated coal combustion flue gases. In this study, raw activated carbon fibers that are microporous (ACF-20) were impregnated with elemental sulfur between 250 and 650 ??C. The resulting samples were saturated with respect to sulfur content. Total sulfur content of the sulfur impregnated ACF samples decreased with increasing impregnation temperatures from 250 and 500 ??C and then remained constant to 650 ??C. Results from sulfur K-edge X-ray absorption near-edge structure (S-XANES) spectroscopy showed that sulfur impregnated on the ACF samples was in both elemental and organic forms. As sulfur impregnation temperature increased, however, the relative amounts of elemental sulfur decreased with a concomitant increase in the amount of organic sulfur. Thermal analyses and mass spectrometry revealed that sulfur functional groups formed at higher impregnation temperatures were more thermally stable. In general, sulfur impregnation decreased surface area and increased equilibrium Hg0 adsorption capacity when compared to the raw ACF sample. The ACF sample treated with sulfur at 400 ??C had a surface area of only 94 m2/g compared to the raw ACF sample's surface area of 1971 m2/g, but at least 86% of this sample's surface area existed as micropores and it had the largest equilibrium Hg0adsorption capacities (2211-11343 ??g/g). Such a result indicates that 400 ??C is potentially an optimal sulfur impregnation temperature for this ACF. Sulfur impregnated on the ACF that was treated at 400 ??C was in both elemental and organic forms. Thermal analyses and CS2extraction tests suggested that elemental sulfur was the main form of sulfur affecting the Hg0 adsorption capacity. These findings indicate that both the presence of elemental sulfur on the adsorbent and a microporous structure are important properties for

  7. Effects of sulfur impregnation temperature on the properties and mercury adsorption capacities of activated carbon fibers (ACFs).

    Science.gov (United States)

    Hsi, H C; Rood, M J; Rostam-Abadi, M; Chen, S; Chang, R

    2001-07-01

    Laboratory studies were conducted to determine the role of sulfur functional groups and micropore surface area of carbon-based adsorbents on the adsorption of Hg0 from simulated coal combustion flue gases. In this study, raw activated carbon fibers that are microporous (ACF-20) were impregnated with elemental sulfur between 250 and 650 degrees C. The resulting samples were saturated with respect to sulfur content. Total sulfur content of the sulfur impregnated ACF samples decreased with increasing impregnation temperatures from 250 and 500 degrees C and then remained constant to 650 degrees C. Results from sulfur K-edge X-ray absorption near-edge structure (S-XANES) spectroscopy showed that sulfur impregnated on the ACF samples was in both elemental and organic forms. As sulfur impregnation temperature increased, however, the relative amounts of elemental sulfur decreased with a concomitant increase in the amount of organic sulfur. Thermal analyses and mass spectrometry revealed that sulfur functional groups formed at higher impregnation temperatures were more thermally stable. In general, sulfur impregnation decreased surface area and increased equilibrium Hg0 adsorption capacity when compared to the raw ACF sample. The ACF sample treated with sulfur at 400 degrees C had a surface area of only 94 m2/g compared to the raw ACF sample's surface area of 1971 m2/g, but at least 86% of this sample's surface area existed as micropores and it had the largest equilibrium Hg0 adsorption capacities (2211-11,343 micrograms/g). Such a result indicates that 400 degrees C is potentially an optimal sulfur impregnation temperature for this ACF. Sulfur impregnated on the ACF that was treated at 400 degrees C was in both elemental and organic forms. Thermal analyses and CS2 extraction tests suggested that elemental sulfur was the main form of sulfur affecting the Hg0 adsorption capacity. These findings indicate that both the presence of elemental sulfur on the adsorbent and a

  8. A Novel Cobalt(Ⅲ) Complex with Macrocyclic Triamine Ligand for High Capacity Hydrogen Adsorption

    Institute of Scientific and Technical Information of China (English)

    ZHU Hai-Yan; GUO Hui; LI Sai

    2012-01-01

    The coordination complex of Co(Ⅲ) based on a macrocyclic triamine ligand 1,4-diacetate-1,4,7-triazacyclodecane (L) has been synthesized and characterized. The metal cation is bonded with three nitrogen atoms and two oxygen atoms of L and one chloride ion to form a distorted octahedral geometry. This complex coordinated with macrocyclic ligand possesses large pore volume that will be contributed to observe high H2 adsorption. With respect to the first-principles electronic structure calculations, the feasibility to store hydrogen in the complex is explored. Indeed, the complex has shown a very high total H2 adsorption of 7.2 wt% (wt% = (weight of adsorbed H2)/(weight of host material)), with a binding energy of 0.03 eV/H2

  9. The influence of metal- and N-species addition in mesoporous carbons on the hydrogen adsorption capacity

    Energy Technology Data Exchange (ETDEWEB)

    Cai, J. [Université Lyon 1, CNRS UMR5256, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Av. Einstein, 69626 Villeurbanne (France); Bennici, S., E-mail: simona.bennici@ircelyon.univ-lyon1.fr [Université Lyon 1, CNRS UMR5256, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Av. Einstein, 69626 Villeurbanne (France); Shen, J. [Laboratory of Mesoscopic Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China); Auroux, A. [Université Lyon 1, CNRS UMR5256, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Av. Einstein, 69626 Villeurbanne (France)

    2015-07-01

    Mesoporous carbon (MC) and two types of N-containing mesoporous carbons (N-MC and C{sub 3}N{sub 4}-MC) were prepared from cost-effective materials and used for hydrogen storage both at 77 K and room temperature (RT). The mesoporous structure was confirmed by N{sub 2} adsorption isotherm at 77 K, and the characterization of the bulk and surface properties performed by ICP analysis, TEM, XRD, and XPS. The maximum hydrogen uptakes were found on N-MC (1.1 wt% of hydrogen) at 100 bar and RT and on MC (3.07 wt% of hydrogen) at 40 bar and 77 K. Pt, Pd, and Ru noble-metal were also added to the three carbon based supports in order to verify the existence of any spillover effect due to the metals presence and evaluate the influence on hydrogen storage capacity. - Highlights: • Biomass derived mesoporous carbons were modified by N and noble metal addition. • N atoms enhance the H{sub 2} adsorption capacity of mesoporous carbon at room temperature. • Ru/N-MC reaches the maximum theoretical limit of H{sub 2} storage for carbon materials.

  10. Preparation and evaluation adsorption capacity of cellulose xanthate of sugarcane bagasse for removal heavy metal ion from aqueous solutions

    Science.gov (United States)

    Iryani, D. A.; Risthy, N. M.; Resagian, D. A.; Yuwono, S. D.; Hasanudin, U.

    2017-05-01

    The discharge of heavy metals from industrial effluents into aquatic system in surrounding area of Lampung bay become a serious problem today. The data shows that the concentrations of heavy metals in this area are above allowable limits for the discharge of toxic heavy metals in the aquatic systems. The most common of heavy metal pollutant is divalent metal ions. Cellulose xanthate is one of the selective adsorbent to solve this problem, since xanthate contains two negative sulfur atoms that is capable to catch divalent metal ions. Preparation of cellulose xanthate was conducted by reacting carbon disulfide (CS2) and cellulose from sugarcane bagasse. The morphological characteristics of cellulose xanthate were visualized via Scanning Electron Microscope (SEM) and the presence of sulfur groups on sugarcane bagasse xanthate were identified by FTIR spectroscopic study. The degree of substitution (DS), degree of polymerization (DP), and adsorption capacities of cellulose xanthate for Cu2+ and Pb2+ metal were studied. The results of study reveals that the maximum adsorption capacities of Cu2+ and Pb2+ metal on cellulose xanthate are 54.226 mg Cu2+/g, and 51.776 mg Pb2+/g, respectively. This study reveals that cellulose xanthate could be a solution to reduce environmental pollution caused by industrial wastewater.

  11. Phosphate Adsorption Capacity and Organic Matter Effect on Dynamics of P Availability in Upland Ultisol and Lowland Inceptisol

    Directory of Open Access Journals (Sweden)

    Marsi

    2011-05-01

    Full Text Available Ultisols and Inceptisols were used to investigate the adsorption-desorption capacity of P and the effect of organic matter on the dynamics of P availability in tropical acid soils. The experiment consisted of two sub-experiments. Sub-experiment I was to study the adsorption-desorption capacity of Ultisols, Fresh-water lowland Inceptisols, and tidal-swamp Inceptisols. Therefore, surface soils (0 to 30 cm of each tested soil were treated with 0, 10, 20, 30, 40, 60, 80, 100, 120, 140, 170, and 200 mg P kg-1 of soil. Sub-experiment II was to study the effects of organic matter application (0, 5, 10, and 15 Mg ha-1 on the dynamics of available P following 60d incubation under room temperature. P fertilizer application significantly affected water soluble-P (WSP (pUpland Ultisol>fresh-water Lowland Inceptisol. OM application increased the BKP in all tested soils as compared to the control. Differences in pattern of soil available P dynamics over time were detected between upland soil and two lowland soils used in the current experiment.

  12. Enhancing phosphate adsorption capacity of SDS-based magnetite by surface modification of citric acid

    Science.gov (United States)

    Yu, Zhigang; Zhang, Chang; Zheng, Zuhong; Hu, Liang; Li, Xuemei; Yang, Zhongzhu; Ma, Chi; Zeng, Guangming

    2017-05-01

    In this study, citric acid (CA) was employed as a low-molecule organic acid to influence the adsorption performance of phosphorus by as-obtained magnetite. The factors including initial phosphate concentrations, dosage of citric acid, pH value, ion strength, contact time and temperature were examined in detail. Results indicated that the dissolution of anion sodium dodecyl sulfate (SDS) covering on surface of magnetite, a slight decrease of Fe level and a superior structure of magnetite after CA modification occurred. The pH-dependence of phosphate adsorption was impeded and the surface potential of magnetite positively increased at pH > 5.0 when CA was added. Non-linear regression Langmuir-Freundlich model was fitted well in thermodynamics, and the opposite adsorption process as a function of temperatures with or without CA addition was due to the decrease of active energy and active mobility of phosphate ion. Finally, the declining adsorption efficiency with increasing cycles was observed while phosphate removal was approximately finished and had small change with 0.05 and 0.1 M of CA addition. Those improvements of removal efficiency of phosphorus by modified iron oxide were because of the removal of anionic SDS that increased the surface positive charge, and especially the dissolution of element Fe into solution to form precipitate with phosphorus ions. The enhanced stability of magnetite by CA also promoted the high removal efficiency of phosphorus. These implications of CA on phosphate removal can be extended to the field where phosphate pollution is notorious but urgent.

  13. Adsorption Capacity of a Volcanic Rock—Used in ConstructedWetlands—For Carbamazepine Removal, and Its Modification with Biofilm Growth

    Directory of Open Access Journals (Sweden)

    Allan Tejeda

    2017-09-01

    Full Text Available In this study, the aim was to evaluate the adsorption capacity of a volcanic rock commonly used in Mexico as filter medium in constructed wetlands (locally named tezontle for carbamazepine (CBZ adsorption, as well as to analyze the change in its capacity with biofilm growth. Adsorption essays were carried out under batch conditions by evaluating two particle sizes of tezontle, two values of the solution pH, and two temperatures; from these essays, optimal conditions for carbamazepine adsorption were obtained. The optimal conditions (pH 8, 25 °C and 0.85–2.0 mm particle-size were used to evaluate the adsorption capacity of tezontle with biofilm, which was promoted through tezontle exposition to wastewater in glass columns, for six months. The maximum adsorption capacity of clean tezontle was 3.48 µg/g; while for the tezontle with biofilm, the minimum value was 1.75 µg/g (after the second week and the maximum, was 3.3 µg/g (after six months with a clear tendency of increasing over time. The adsorption kinetic was fitted to a pseudo-second model for both tezontle without biofilm and with biofilm, thus indicating a chemisorption process. On clean tezontle, both acid active sites (AAS and basic active sites (BAS were found in 0.087 and 0.147 meq/g, respectively. The increase in the adsorption capacity of tezontle with biofilm, along the time was correlated with a higher concentration of BAS, presumably from a greater development of biofilm. The presence of biofilm onto tezontle surface was confirmed through FTIR and FE-SEM. These results confirm the essential role of filter media for pharmaceutical removal in constructed wetlands (CWs.

  14. Zeolite Y adsorbents with high vapor uptake capacity and robust cycling stability for potential applications in advanced adsorption heat pumps

    Energy Technology Data Exchange (ETDEWEB)

    Li, XS; Narayanan, S; Michaelis, VK; Ong, TC; Keeler, EG; Kim, H; Mckay, IS; Griffin, RG; Wang, EN

    2015-01-01

    Modular and compact adsorption heat pumps (AHPs) promise an energy-efficient alternative to conventional vapor compression based heating, ventilation and air conditioning systems. A key element in the advancement of AHPs is the development of adsorbents with high uptake capacity, fast intracrystalline diffusivity and durable hydrothermal stability. Herein, the ion exchange of NaY zeolites with ingoing Mg2+ ions is systematically studied to maximize the ion exchange degree (IED) for improved sorption performance. It is found that beyond an ion exchange threshold of 64.1%, deeper ion exchange does not benefit water uptake capacity or characteristic adsorption energy, but does enhance the vapor diffusivity. In addition to using water as an adsorbate, the uptake properties of Mg, Na-Y zeolites were investigated using 20 wt.% MeOH aqueous solution as a novel anti-freeze adsorbate, revealing that the MeOH additive has an insignificant influence on the overall sorption performance. We also demonstrated that the lab-scale synthetic scalability is robust, and that the tailored zeolites scarcely suffer from hydrothermal stability even after successive 108-fold adsorption/desorption cycles. The samples were analyzed using N-2 sorption, Al-27/Si-29 MAS NMR spectroscopy, ICP-AES, dynamic vapor sorption, SEM, Fick's 2nd law and D-R equation regressions. Among these, close examination of sorption isotherms for H2O and N-2 adsorbates allows us to decouple and extract some insightful information underlying the complex water uptake phenomena. This work shows the promising performance of our modified zeolites that can be integrated into various AHP designs for buildings, electronics, and transportation applications. (C) 2014 Elsevier Inc. All rights reserved.

  15. Zeolite Y Adsorbents with High Vapor Uptake Capacity and Robust Cycling Stability for Potential Applications in Advanced Adsorption Heat Pumps.

    Science.gov (United States)

    Li, Xiansen; Narayanan, Shankar; Michaelis, Vladimir K; Ong, Ta-Chung; Keeler, Eric G; Kim, Hyunho; McKay, Ian S; Griffin, Robert G; Wang, Evelyn N

    2015-01-01

    Modular and compact adsorption heat pumps (AHPs) promise an energy-efficient alternative to conventional vapor compression based heating, ventilation and air conditioning systems. A key element in the advancement of AHPs is the development of adsorbents with high uptake capacity, fast intracrystalline diffusivity and durable hydrothermal stability. Herein, the ion exchange of NaY zeolites with ingoing Mg(2+) ions is systematically studied to maximize the ion exchange degree (IED) for improved sorption performance. It is found that beyond an ion exchange threshold of 64.1%, deeper ion exchange does not benefit water uptake capacity or characteristic adsorption energy, but does enhance the vapor diffusivity. In addition to using water as an adsorbate, the uptake properties of Mg,Na-Y zeolites were investigated using 20 wt.% MeOH aqueous solution as a novel anti-freeze adsorbate, revealing that the MeOH additive has an insignificant influence on the overall sorption performance. We also demonstrated that the labscale synthetic scalability is robust, and that the tailored zeolites scarcely suffer from hydrothermal stability even after successive 108-fold adsorption/desorption cycles. The samples were analyzed using N2 sorption, (27)Al/(29)Si MAS NMR spectroscopy, ICP-AES, dynamic vapor sorption, SEM, Fick's 2(nd) law and D-R equation regressions. Among these, close examination of sorption isotherms for H2O and N2 adsorbates allows us to decouple and extract some insightful information underlying the complex water uptake phenomena. This work shows the promising performance of our modified zeolites that can be integrated into various AHP designs for buildings, electronics, and transportation applications.

  16. Determination of coalbed methane potential and gas adsorption capacity in Western Kentucky coals

    Science.gov (United States)

    Mardon, S.M.; Takacs, K.G.; Hower, J.C.; Eble, C.F.; Mastalerz, Maria

    2006-01-01

    The Illinois Basin has not been developed for Coalbed Methane (CBM) production. It is imperative to determine both gas content and other parameters for the Kentucky portion of the Illinois Basin if exploration is to progress and production is to occur in this area. This research is part of a larger project being conducted by the Kentucky Geological Survey to evaluate the CBM production of Pennsylvanian-age western Kentucky coals in Ohio, Webster, and Union counties using methane adsorption isotherms, direct gas desorption measurements, and chemical analyses of coal and gas. This research will investigate relationships between CBM potential and petrographic, surface area, pore size, and gas adsorption isotherm analyses of the coals. Maceral and reflectance analyses are being conducted at the Center for Applied Energy Research. At the Indiana Geological Survey, the surface area and pore size of the coals will be analyzed using a Micrometrics ASAP 2020, and the CO2 isotherm analyses will be conducted using a volumetric adsorption apparatus in a water temperature bath. The aforementioned analyses will be used to determine site specific correlations for the Kentucky part of the Illinois Basin. The data collected will be compared with previous work in the Illinois Basin and will be correlated with data and structural features in the basin. Gas composition and carbon and hydrogen isotopic data suggest mostly thermogenic origin of coalbed gas in coals from Webster and Union Counties, Kentucky, in contrast to the dominantly biogenic character of coalbed gas in Ohio County, Kentucky.

  17. Strategies for increasing hydrogen storage capacity and adsorption energy in MOFs

    Science.gov (United States)

    Yaghi, Omar

    2007-03-01

    Storage of hydrogen in its molecular form is difficult and expensive because it requires employing either extremely high pressures as a gas or very low temperatures as a liquid. Worldwide effort is focused on storage of hydrogen with sufficient efficiency to allow its use in stationary and mobile fueling applications. DOE has set performance targets for on-board automobile storage systems to have densities of 60 mg H2/g (gravimetric) and 45 g H2/L (volumetric) for year 2010. These are system goals. Metal-organic frameworks (MOFs) have recently been identified as promising adsorbents (physisorption) for H2 storage, although little data are available for their adsorption behavior at saturation: a critical parameter for gauging the practicality of any material. This presentation will report adsorption data collected for seven MOF materials at 77 K which leads to saturation at pressures between 25 and 80 bar with uptakes from 2% to 7.5%. Strategies for increasing the adsorption energy of hydrogen in MOFs will also be presented.

  18. Adsorption of hexavalent chromium by graphite–chitosan binary composite

    Indian Academy of Sciences (India)

    RAJENDRA S DONGRE

    2016-06-01

    Graphite chitosan binary (GCB) composite was prepared for hexavalent chromium adsorption from studied water. GCB was characterized by TGA, FTIR, SEM and X-ray diffraction techniques.Wide porous sorptive surface of 3.89 m$^2$ g$^{−1}$ and absorptive functionalities of GCB was due to 20% (w/w) graphite support on chitosan evidenced from FTIR and SEM that impart maximum adsorption at pH 4, agitation with 200 rpm for 180 min. Adsorption studies revealed intraparticle diffusion models and best-fitted kinetics was pseudo 2nd order one. A wellfitted Langmuir isotherm model suggested monolayer adsorption with an adsorption capacity ($q_m$) of 105.6 mg g$^{−1}$ and $R^2 = 0.945$. Sorption mechanisms based on metal ionic interactions, intrusion/diffusion and chemisorptions onto composite. This graphite chitosan binary composite improve sorbent capacity for Cr(VI).

  19. Dose-dependent adsorptive capacity of activated charcoal for gastrointestinal decontamination of a simulated paracetamol overdose in human volunteers.

    Science.gov (United States)

    Gude, Anne-Bolette Jill; Hoegberg, Lotte Christine Groth; Angelo, Helle Riis; Christensen, Hanne Rolighed

    2010-05-01

    The amount of activated charcoal needed to treat drug overdoses has arbitrarily been set at a charcoal-drug ratio of 10:1. Recent in vitro studies have shown a larger adsorptive capacity for activated charcoal when used in a model of paracetamol overdose. In the present study, we investigated whether this reserve capacity exists in vivo. This is clinically relevant in cases of large overdoses or if the full standard dose of 50 g activated charcoal cannot be administered. We performed a randomized, cross-over study (n = 16). One hour after a standard breakfast, 50 mg/kg paracetamol was administered, followed 1 hr later by an activated charcoal-Water slurry containing 50 (control), 25 or 5 g activated charcoal. The areas under the serum concentration-time curve (AUC) for paracetamol were used to estimate the efficacy of each activated charcoal dose. The AUC of the 25-g dose was found to be of similar size compared to the control, although statistics were weak. The AUC of the 5-g dose was 59% larger than the AUC of the 50-g dose (p = 0.0003). The terminal elimination half-life (t(1/2)) of paracetamol was 1.6 (CI 1.4-2.0) and 1.9 (CI 1.5-2.4) hr for 50 and 25 g, respectively (NS), and 2.5 (CI 1.8-3.0) hr for the 5-g dose (p = 0.003). The decrease in t(1/2) of paracetamol for the two larger activated charcoal doses indicates a possible effect of activated charcoal on paracetamol clearance and warrants further investigation. The large adsorptive reserve capacity of activated charcoal in vitro could not be reproduced for the smallest dose of activated charcoal. An activated charcoal-drug ratio of 10:1 is therefore still recommendable.

  20. Planned Monolayer Assemblies by Adsorption

    Science.gov (United States)

    1988-09-01

    tsWaerabas (above 1000 C), 3 si.- lane ucollayses cin ZnSe or Go are usually resistant und5er exposure to, similar treament only at thue amb~ient tauueatue...1h ’ -11-- -nam all species uniderwent a large. irreversible rindlomntion at sard 110 OC. Although heating affected slight disorientation of the... heated copper blocks. Tem- Com e euremens can coplament the FTIR reuls perature was monitored with a thermocouple. For long-chalned ampmlphillc

  1. One-step synthesis of a novel N-doped microporous biochar derived from crop straws with high dye adsorption capacity.

    Science.gov (United States)

    Lian, Fei; Cui, Guannan; Liu, Zhongqi; Duo, Lian; Zhang, Guilong; Xing, Baoshan

    2016-07-01

    N-doping is one of the most promising strategies to improve the adsorption capacity and selectivity of carbon adsorbents. Herein, synthesis, characterization and dye adsorption of a novel N-doped microporous biochar derived from direct annealing of crop straws under NH3 is presented. The resultant products exhibit high microporosity (71.5%), atomic percentage of nitrogen (8.81%), and adsorption capacity to dyes, which is about 15-20 times higher than that of original biochar. Specifically, for the sample NBC800-3 pyrolyzed at 800°C in NH3 for 3 h, its adsorption for acid orange 7 (AO7, anionic) and methyl blue (MB, cationic) is up to 292 mg g(-1) and 436 mg g(-1), respectively, which is among the highest ever reported for carbonaceous adsorbents. The influences of N-doping and porous structure on dye adsorption of the synthesized carbons are also discussed, where electrostatic attraction, π-π electron donor-accepter interaction, and Lewis acid-base interaction mainly contribute to AO7 adsorption, and surface area (especially pore-filling) dominates MB adsorption. The N-doped biochar can be effectively regenerated and reused through direct combustion and desorption approaches.

  2. High surface-area amidoxime-based polymer fibers co-grafted with various acid monomers yielding increased adsorption capacity for the extraction of uranium from seawater.

    Science.gov (United States)

    Oyola, Yatsandra; Dai, Sheng

    2016-06-07

    Uranium is dissolved in the ocean at a uniform concentration of 3.34 ppb, which translates to approximately 4-5 billion tons of uranium. The development of adsorbents that can extract uranium from seawater has been a long term goal, but the extremely dilute uranium concentration along with the competition of other metal salts (which are at higher concentrations) has hindered the development of an economical adsorption process. Several acid monomers were co-grafted with acrylonitrile (AN) to help increase the hydrophilicity of the adsorbent to improve access to the metal adsorption sites. Grafting various acid monomers on PE fibers was found to significantly affect the uranium adsorption in simulated seawater in the following order: acrylic acid (AA) uranium adsorption capacity significantly increased when Mohr's salt was added with acrylic acid, most likely due to the reduction of co-polymerization of the monomers. When testing under more realistic conditions, the acid-grafted PE fiber adsorbents were exposed to natural seawater (more dilute uranium), the uranium adsorption capacity increased in the following order: MAA uranium adsorption capacity with each acid monomer was related to higher grafting of AN and therefore a higher conversion to amidoxime (AO).

  3. Effect of cetyl trimethyl ammonium bromide concentration on structure, morphology and carbon dioxide adsorption capacity of calcium hydroxide based sorbents

    Energy Technology Data Exchange (ETDEWEB)

    Hlaing, Nwe Ni, E-mail: nwenihlaing76@gmail.com [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Department of International Development Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo (Japan); Department of Physics, University of Yangon, 11041 Kamayut, Yangon (Myanmar); Vignesh, K., E-mail: vignesh134@gmail.com [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Anano Sphere Sdn Bhd, Lorong Industri 11, Kawasan Industri Bukit Panchor, 14300 Nibong Tebal, Penang (Malaysia); Sreekantan, Srimala, E-mail: srimala@usm.my [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Pung, Swee-Yong [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Hinode, Hirofumi; Kurniawan, Winarto [Department of International Development Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo (Japan); Othman, Radzali [Faculty of Manufacturing Engineering, Universiti Teknikal Malaysia Melaka, Hang Tuah Jaya, 76100 Durian Tunggal, Malacca (Malaysia); Thant, Aye Aye [Department of Physics, University of Yangon, 11041 Kamayut, Yangon (Myanmar); Mohamed, Abdul Rahman [Low Carbon Economy (LCE) Research Group, School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Salim, Chris [Department of Environmental Engineering, Surya University, Tangerang 15810, Banten (Indonesia)

    2016-02-15

    Graphical abstract: Carbonation conversions of (a) CC, (b) CH-2, (c) CH-4, (d) CH-6, (e) CH-8 precursor adsorbents for 10 cycles. - Highlights: • Ca(OH){sub 2} precursor was synthesized using precipitation method. • The effect of CTAB concentration on the synthesis of Ca(OH){sub 2} was studied. • The sorbent synthesized using 0.8 M of CTAB showed good CO{sub 2} adsorption capacity. • The cyclic stability of Ca(OH){sub 2} was increased with increase of CTAB concentration. - Abstract: Calcium hydroxide (Ca(OH){sub 2}) has been proposed as an important material for industrial, architectural, and environmental applications. In this study, calcium acetate was used as a precursor and cetyl trimethyl ammonium bromide (CTAB) was used as a surfactant to synthesize Ca(OH){sub 2} based adsorbents for carbon dioxide (CO{sub 2}) capture. The effect of CTAB concentration (0.2–0.8 M) on the structure, morphology and CO{sub 2} adsorption performance of Ca(OH){sub 2} was studied in detail. The synthesized samples were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), BET surfaced area and thermogravimetry-differential thermal analysis (TG–DTA) techniques. The phase purity, crystallite size, Brunauer–Emmett–Teller (BET) surface area and CO{sub 2} adsorption performance of Ca(OH){sub 2} precursor adsorbents were significantly increased when the concentration of CTAB was increased. XRD results showed that pure Ca(OH){sub 2} phase was obtained at the CTAB concentration of 0.8 M. TGA results exhibited that 0.8 M of CTAB-assisted Ca(OH){sub 2} precursor adsorbent possessed a residual carbonation conversion of ∼56% after 10 cycles.

  4. Adsorptive removal of Cr3+ from aqueous solutions using chitosan microfibers immobilized with plant polyphenols as biosorbents with high capacity and selectivity

    Science.gov (United States)

    Zhang, Ting; Wang, Yujia; Kuang, Yiwen; Yang, Ruilin; Ma, Jun; Zhao, Shilin; Liao, Yang; Mao, Hui

    2017-05-01

    A novel biosorbent was facilely prepared by immobilizing bayberry tannin (BT, a typical natural polyphenols) onto chitosan microfiber (CM). The as-prepared CM-BT adsorbent featured to a well-defined microfibrous morphology and highly distributed adsorption sites, which was highly efficient and selective for the adsorptive removal of Cr3+ from aqueous solutions. Based on batch experiments, the adsorption of Cr3+ on CM-BT was pH-dependent, and the optimized adsorption pH was determined to be 5.5. The adsorption capacity of CM-BT to Cr3+ was high up to 20.90 mg/g. The co-existing cations, such as Mg2+, Ca2+, Fe3+ and Cu2+, exhibited no significant influences on the adsorption of Cr3+ on CM-BT. The adsorption kinetics were well fitted by the pseudo-second-order rate model (R2 > 0.99) while the adsorption isotherms were well described by the Langmuir model (R2 > 0.98). Importantly, CM-BT was effective for the continues treatment of low concentration Cr3+ (2.0 mg/L) contaminated wastewater. Before reached the breakthrough point (5% of the initial Cr3+ concentration, 0.1 mg/L), the treated volume was as high as 894 bed volume, manifesting the great potential of CM-BT in practical treatment of Cr3+ contaminated wastewater.

  5. [Adsorption of phenanthrene from aqueous solution on cetylpyridinium bromide (CPB) -modified zeolite].

    Science.gov (United States)

    Li, Jia; Lin, Jian-Wei; Zhan, Yan-Hui; Chen, Zu-Mei; Wang, Peng-Jun

    2014-02-01

    Surfactant-modified zeolites (SMZs) with different coverage types were prepared by loading of different amounts of cetylpyridinium bromide (CPB) onto natural zeolites and were used as adsorbents to remove phenanthrene from aqueous solution. The adsorption of phenanthrene from aqueous solution on monolayer and bilayer SMZs as a function of adsorbent dosage, initial phenanthrene concentration, contact time, and temperature was investigated using batch experiments. Results showed monolayer and bilayer SMZs were effective for the removal of phenanthrene from aqueous solution. The phenanthrene removal efficiency of SMZs increased with increasing adsorbent dosage, but the amount of phenanthrene adsorbed on SMZs decreased with increasing adsorbent dosage. The adsorption kinetics of phenanthrene on SMZs well followed a pseudo-second-order kinetic model. The equilibrium adsorption data of phenanthrene on SMZs at a low concentration of phenanthrene in solution could be described by the Linear equation and Freundlich equation. The main mechanism for phenanthrene adsorption onto monolayer SMZ is hydrophobic interaction, and the main mechanism for phenanthrene adsorption onto bilayer SMZ is organic partitioning. The calculated thermodynamic parameters such as Gibbs free energy change (deltaG(theta)), enthalpy changes (deltaH(theta)), and entropy change (deltaS(theta)) showed that the adsorption process of phenanthrene on SMZs is spontaneous and exothermic in nature. When the CPB loading amount of bilayer SMZ was twice as much as that of monolayer SMZ, the phenanthrene adsorption capacity for bilayer SMZ was slightly higher than that for monolayer SMZ. In a conclusion, both monolayer and bilayer SMZs are promising adsorbents for the removal of phenanthrene from water and wastewater, and monolayer SMZ is a more cost-effective adsorbent for phenanthrene removal than bilayer SMZ.

  6. Facile synthesis of hydroxy-modified MOF-5 for improving the adsorption capacity of hydrogen by lithium doping.

    Science.gov (United States)

    Kubo, Masaru; Hagi, Hayato; Shimojima, Atsushi; Okubo, Tatsuya

    2013-11-01

    A facile synthesis of partially hydroxy-modified MOF-5 and its improved H2-adsorption capacity by lithium doping are reported. The reaction of Zn(NO3)2·6H2O with a mixture of terephthalic acid (H2BDC) and 2-hydroxyterephthalic acid (H2BDC-OH) in DMF gave hydroxy-modified MOF-5 (MOF-5-OH-x), in which the molar fraction (x) of BDC-OH(2-) was up to 0.54 of the whole ligand. The MOF-5-OH-x frameworks had high BET surface areas (about 3300 m(2) g(-1)), which were comparable to that of MOF-5. We suggest that the MOF-5-OH-x frameworks are formed by the secondary growth of BDC(2-)-rich MOF-5 seed crystals, which are nucleated during the early stage of the reaction. Subsequent Li doping into MOF-5-OH-x results in increased H2 uptake at 77 K and 0.1 MPa from 1.23 to 1.39 wt.% and an increased isosteric heat of H2 adsorption from 5.1-4.2 kJ mol(-1) to 5.5-4.4 kJ mol(-1).

  7. MOF-derived ZnO and ZnO@C composites with high photocatalytic activity and adsorption capacity.

    Science.gov (United States)

    Yang, Seung Jae; Im, Ji Hyuk; Kim, Taehoon; Lee, Kunsil; Park, Chong Rae

    2011-02-15

    Nanostructured ZnO materials have unique and highly attractive properties and have inspired interest in their research and development. This paper presents a facile method for the preparation of novel ZnO-based nanostructured architectures using a metal organic framework (MOF) as a precursor. In this approach, ZnO nanoparticles and ZnO@C hybrid composites were produced under several heating and atmospheric (air or nitrogen) conditions. The resultant ZnO nanoparticles formed hierarchical aggregates with a three-dimensional cubic morphology, whereas ZnO@C hybrid composites consisted of faceted ZnO crystals embedded within a highly porous carbonaceous species, as determined by several characterization methods. The newly synthesized nanomaterials showed relatively high photocatalytic decomposition activity and significantly enhanced adsorption capacities for organic pollutants. Copyright © 2010 Elsevier B.V. All rights reserved.

  8. On the drug adsorption capacity of SBA-15 obtained from various detemplation protocols

    NARCIS (Netherlands)

    Zhang, Zheng; Santangelo, D.; ten Brink, Gert; Kooi, Bart; Moulijn, J.A.; Melian Cabrera, Ignacio

    2014-01-01

    The effect of the mild detemplation method, based on Fenton chemistry (with and without previous solvent extraction), and calcination was evaluated by the drug uptake capacity of SBA-15 materials. A number of characterization techniques were applied for evaluation and comparison of the materials pro

  9. Determinants of HDL Cholesterol Efflux Capacity after Virgin Olive Oil Ingestion: Interrelationships With Fluidity of HDL Monolayer.

    Science.gov (United States)

    Fernández-Castillejo, Sara; Rubió, Laura; Hernáez, Álvaro; Catalán, Úrsula; Pedret, Anna; Valls, Rosa-M; Mosele, Juana I; Covas, Maria-Isabel; Remaley, Alan T; Castañer, Olga; Motilva, Maria-José; Solá, Rosa

    2017-09-08

    Cholesterol efflux capacity of HDL (CEC) is inversely associated with cardiovascular risk. HDL composition, fluidity, oxidation, and size are related with CEC. We aimed to assess which HDL parameters were CEC determinants after virgin olive oil (VOO) ingestion. Post-hoc analyses from the VOHF study, a crossover intervention with three types of VOO. We assessed the relationship of 3-week changes in HDL-related variables after intervention periods with independence of the type of VOO. After univariate analyses, mixed linear models were fitted with variables related with CEC and fluidity. Fluidity and Apolipoprotein (Apo)A-I content in HDL was directly associated, and HDL oxidative status inversely, with CEC. A reduction in free cholesterol, an increase in triglycerides in HDL, and a decrease in small HDL particle number or an increase in HDL mean size, were associated to HDL fluidity. HDL fluidity, ApoA-I concentration, and oxidative status are major determinants for CEC after VOO. The impact on CEC of changes in free cholesterol and triglycerides in HDL, and those of small HDL or HDL mean size, could be mechanistically linked through HDL fluidity. Our work points out novel therapeutic targets to improve HDL functionality in humans through nutritional or pharmacological interventions. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.

  10. Spin heat capacity of monolayer and AB-stacked bilayer MoS2 in the presence of exchange magnetic field

    Science.gov (United States)

    Hoi, Bui Dinh; Yarmohammadi, Mohsen; Mirabbaszadeh, Kavoos

    2017-04-01

    Dirac theory and Green's function technique are carried out to compute the spin dependent band structures and corresponding electronic heat capacity (EHC) of monolayer (ML) and AB-stacked bilayer (BL) molybdenum disulfide (MoS2) two-dimensional (2D) crystals. We report the influence of induced exchange magnetic field (EMF) by magnetic insulator substrates on these quantities for both structures. The spin-up (down) subband gaps are shifted with EMF from conduction (valence) band to valence (conduction) band at both Dirac points in the ML because of the spin-orbit coupling (SOC) which leads to a critical EMF in the K point and EHC returns to its initial states for both spins. In the BL case, EMF results split states and the decrease (increase) behavior of spin-up (down) subband gaps has been observed at both K and K‧ valleys which is due to the combined effect of SOC and interlayer coupling. For low and high EMFs, EHC of BL MoS2 does not change for spin-up subbands while increases for spin-down subbands.

  11. Effect of carbonation temperature on CO{sub 2} adsorption capacity of CaO derived from micro/nanostructured aragonite CaCO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Hlaing, Nwe Ni, E-mail: nwenihlaing76@gmail.com [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Department of International Development Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo (Japan); Department of Physics, University of Yangon, 11041 Kamayut, Yangon (Myanmar); Sreekantan, Srimala, E-mail: srimala@usm.my [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Hinode, Hirofumi, E-mail: hinode@ide.titech.ac.jp; Kurniawan, Winarto, E-mail: Kurniawan.w.ab@m.titech.ac.jp [Department of International Development Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo (Japan); Thant, Aye Aye, E-mail: a2thant@gmail.com [Department of Physics, University of Yangon, 11041 Kamayut, Yangon (Myanmar); Othman, Radzali, E-mail: radzali@utem.edu.my [Faculty of Manufacturing Engineering, Universiti Teknikal Malaysia Melaka, Hang Tuah Jaya, 76100 Durian Tunggal, Malacca (Malaysia); Mohamed, Abdul Rahman, E-mail: chrahman@eng.usm.my [Low Carbon Economy (LCE) Research Group, School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Salime, Chris, E-mail: chris.salim@surya.ac.id [Environmental Engineering, Surya University, Tangerang, 15810 Banten (Indonesia)

    2016-07-06

    Recent years, CaO-based synthetic materials have been attracted attention as potential adsorbents for CO{sub 2} capture mainly due to their high CO{sub 2} adsorption capacity. In this study, micro/nanostructured aragonite CaCO{sub 3} was synthesized by a simple hydrothermal method with using polyacrylamide (PAM). The structural, morphological and thermal properties of the synthesized sample were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and thermogravimetry analysis (TG-DTA). The XRD and FESEM results showed that the obtained sample was aragonite CaCO{sub 3} with aggregated nanorods and microspheres composed of nanorods. A TG-DTA apparatus with Thermoplus 2 software was used to investigate the effect of carbonation temperature on the CO{sub 2} adsorption capacity of CaO derived from aragonite CaCO{sub 3} sample. At 300 °C, the sample reached the CO{sub 2} adsorption capacity of 0.098 g-CO{sub 2}/g-adsorbent, whereas the sample achieved the highest capacity of 0.682 g-CO{sub 2}/g-adsorbent at 700 °C. The results showed that the carbonation temperature significantly influenced on the CO{sub 2} adsorption capacity of the CaO derived from aragonite CaCO{sub 3}.

  12. Dendritic silica nanomaterials (KCC-1) with fibrous pore structure possess high DNA adsorption capacity and effectively deliver genes in vitro.

    Science.gov (United States)

    Huang, Xiaoxi; Tao, Zhimin; Praskavich, John C; Goswami, Anandarup; Al-Sharab, Jafar F; Minko, Tamara; Polshettiwar, Vivek; Asefa, Tewodros

    2014-09-16

    The pore size and pore structure of nanoporous materials can affect the materials' physical properties, as well as potential applications in different areas, including catalysis, drug delivery, and biomolecular therapeutics. KCC-1, one of the newest members of silica nanomaterials, possesses fibrous, large pore, dendritic pore networks with wide pore entrances, large pore size distribution, spacious pore volume and large surface area--structural features that are conducive for adsorption and release of large guest molecules and biomacromolecules (e.g., proteins and DNAs). Here, we report the results of our comparative studies of adsorption of salmon DNA in a series of KCC-1-based nanomaterials that are functionalized with different organoamine groups on different parts of their surfaces (channel walls, external surfaces or both). For comparison the results of our studies of adsorption of salmon DNA in similarly functionalized, MCM-41 mesoporous silica nanomaterials with cylindrical pores, some of the most studied silica nanomaterials for drug/gene delivery, are also included. Our results indicate that, despite their relatively lower specific surface area, the KCC-1-based nanomaterials show high adsorption capacity for DNA than the corresponding MCM-41-based nanomaterials, most likely because of KCC-1's large pores, wide pore mouths, fibrous pore network, and thereby more accessible and amenable structure for DNA molecules to diffuse through. Conversely, the MCM-41-based nanomaterials adsorb much less DNA, presumably because their outer surfaces/cylindrical channel pore entrances can get blocked by the DNA molecules, making the inner parts of the materials inaccessible. Moreover, experiments involving fluorescent dye-tagged DNAs suggest that the amine-grafted KCC-1 materials are better suited for delivering the DNAs adsorbed on their surfaces into cellular environments than their MCM-41 counterparts. Finally, cellular toxicity tests show that the KCC-1-based

  13. Estimating prion adsorption capacity of soil by BioAssay of Subtracted Infectivity from Complex Solutions (BASICS.

    Directory of Open Access Journals (Sweden)

    A Christy Wyckoff

    Full Text Available Prions, the infectious agent of scrapie, chronic wasting disease and other transmissible spongiform encephalopathies, are misfolded proteins that are highly stable and resistant to degradation. Prions are known to associate with clay and other soil components, enhancing their persistence and surprisingly, transmissibility. Currently, few detection and quantification methods exist for prions in soil, hindering an understanding of prion persistence and infectivity in the environment. Variability in apparent infectious titers of prions when bound to soil has complicated attempts to quantify the binding capacity of soil for prion infectivity. Here, we quantify the prion adsorption capacity of whole, sandy loam soil (SLS typically found in CWD endemic areas in Colorado; and purified montmorillonite clay (Mte, previously shown to bind prions, by BioAssay of Subtracted Infectivity in Complex Solutions (BASICS. We incubated prion positive 10% brain homogenate from terminally sick mice infected with the Rocky Mountain Lab strain of mouse-adapted prions (RML with 10% SLS or Mte. After 24 hours samples were centrifuged five minutes at 200 × g and soil-free supernatant was intracerebrally inoculated into prion susceptible indicator mice. We used the number of days post inoculation to clinical disease to calculate the infectious titer remaining in the supernatant, which we subtracted from the starting titer to determine the infectious prion binding capacity of SLS and Mte. BASICS indicated SLS bound and removed ≥ 95% of infectivity. Mte bound and removed lethal doses (99.98% of prions from inocula, effectively preventing disease in the mice. Our data reveal significant prion-binding capacity of soil and the utility of BASICS to estimate prion loads and investigate persistence and decomposition in the environment. Additionally, since Mte successfully rescued the mice from prion disease, Mte might be used for remediation and decontamination protocols.

  14. High adsorption capacity of two Zn-based metal-organic frameworks by ultrasound assisted synthesis.

    Science.gov (United States)

    Masoomi, Mohammad Yaser; Bagheri, Minoo; Morsali, Ali

    2016-11-01

    Micro- and nano-rods and plates of two 3D, porous Zn(II)-based metal-organic frameworks [Zn(oba)(4-bpdh)0.5]n·(DMF)1.5 (TMU-5) and [Zn(oba)(4-bpmb)0.5]n (DMF)1.5 (TMU-6) were prepared by sonochemical process and characterized by scanning electron microscopy, X-ray powder diffraction and IR spectroscopy. These MOFs were synthesized using a non-linear dicarboxylate (H2oba=4,4-oxybisbenzoic acid) and two linear N-donor (4-bpdh=2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene and 4-bpmb=N(1),N(4)-bis((pyridin-4-yl)methylene)benzene-1,4-diamine) ligands by ultrasonic irradiation. Sonication time and concentration of initial reagents influencing size and morphology of nano-structured MOFs, were also studied. Calcination of TMU-5 and TMU-6 at 550°C under air atmosphere yields ZnO nanoparticles. TMU-5 and TMU-6 exhibited maximum percent adsorption of 96.2% and 92.8% of 100ppm rhodamine B dye, respectively, which obeys first order reaction kinetics.

  15. Ti-decorated graphitic-C3N4 monolayer: A promising material for hydrogen storage

    Science.gov (United States)

    Zhang, Weibin; Zhang, Zhijun; Zhang, Fuchun; Yang, Woochul

    2016-11-01

    Ti-decorated graphitic carbon nitride (g-C3N4) monolayer as a promising material system for high-capacity hydrogen storage is proposed through density functional theory calculations. The stability and hydrogen adsorption of Ti-decorated g-C3N4 is analyzed by computing the adsorption energy, the charge population, and electronic density of states. The most stable decoration site of Ti atom is the triangular N hole in g-C3N4 with an adsorption energy of -7.58 eV. The large diffusion energy barrier of the adsorbed Ti atom of ∼6.00 eV prohibits the cluster formation of Ti atoms. The electric field induced by electron redistribution of Ti-adsorbed porous g-C3N4 significantly enhanced hydrogen adsorption up to five H2 molecules at each Ti atom with an average adsorption energy of -0.30 eV/H2. The corresponding hydrogen capacity reaches up to 9.70 wt% at 0 K. In addition, the hydrogen capacity is predicted to be 6.30 wt% at 233 K and all adsorbed H2 are released at 393 K according to molecular dynamics simulation. Thus, the Ti-decorated g-C3N4 monolayer is suggested to be a promising material for hydrogen storage suggested by the DOE for commercial applications.

  16. An insight into the removal of Cu (II) and Pb (II) by aminopropyl-modified mesoporous carbon CMK-3: Adsorption capacity and mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Hamad, Hussein, E-mail: hussein.hamad@ul.edu.lb [Platform for Research and Analysis in Environmental Sciences (PRASE), Lebanese University, Beirut (Lebanon); Ezzeddine, Zeinab; Lakis, Fatima; Rammal, Hassan [Platform for Research and Analysis in Environmental Sciences (PRASE), Lebanese University, Beirut (Lebanon); Srour, Mortada [Lebanese University, Faculty of Sciences (I), Hadath, Beirut (Lebanon); Hijazi, Akram [Platform for Research and Analysis in Environmental Sciences (PRASE), Lebanese University, Beirut (Lebanon)

    2016-08-01

    In this study, the adsorption of heavy metal ions onto ordered mesoporous carbon CMK-3 was investigated. CMK-3 has been synthesized using SBA-15 as the hard template and then directly amino-functionalized by the treatment with 3-aminopropyltrimethoxysilane (APTMS) without the need of oxidation before. The thus obtained modified mesoporous carbon has been characterized by nitrogen sorption, X-ray diffraction and infrared spectroscopy. Its adsorption efficiency for the removal of Cu{sup 2+} and Pb{sup 2+} from aqueous solutions was tested. The effects of contact time, pH and initial metal ions concentration were investigated as well. The adsorption capacities were very high (3.5 mmol g{sup −1} and 8.6 mmol g{sup −1} for Pb{sup 2+} and Cu{sup 2+} respectively). These values depend largely on the speciation of metal ions as a function of pH. The selectivity was also dependent on the nature of metal ions rather than the adsorbent used. The mechanism of adsorption is complex where several types of interaction between metal ions and the adsorbent surface are involved. - Highlights: • Mesoporous carbon CMK-3 was successfully synthesized and functionalized. • No oxidation treatment was done prior to aminopropyl functionalization. • The adsorbent adsorption capacity is high (3.5 mmol g{sup −1} for Cu{sup 2+} and 8.6 mmol g{sup −1} for Pb{sup 2+}). • The maximum Cu{sup 2+} adsorption capacity is related to its speciation as a function of pH. • The mechanism of adsorption is complex including different types of interaction.

  17. Determination of Adsorption Capacity and Kinetics of Amidoxime-Based Uranium Adsorbent Braided Material in Unfiltered Seawater Using a Flume Exposure System

    Energy Technology Data Exchange (ETDEWEB)

    Gill, Gary A. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Kuo, Li-Jung [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Strivens, Jonathan E. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Park, Jiyeon [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Bonheyo, George T. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Jeters, Robert T. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Schlafer, Nicholas J. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.; Wood, Jordana R. [Pacific Northwest National Lab. (PNNL), Sequim, WA (United States). Marine Sciences Lab.

    2015-08-31

    PNNL has developed a recirculating flume system for exposing braided adsorbent material to natural seawater under realistic temperature and flow-rate exposure conditions. The flumes are constructed of transparent acrylic material; they allow external light to pass into the flumes and permit photosynthetic growth of naturally present marine organisms (biofouling). Because the system consists of two flumes, replicate experiments can be conducted in which one of the flumes can be manipulated relative to the other. For example, one flume can be darkened to eliminate light exposure by placing a black tarp over the flume such that dark/light experiments can be conducted. Alternatively, two different braided adsorbents can be exposed simultaneously with no potential cross contamination issues. This report describes the first use of the PNNL flume system to study the impact of biofouling on adsorbent capacity. Experiments were conducted with the ORNL AI8 braided adsorbent material in light-exposed and darkened flumes for a 42-day exposure experiment. The major objective of this effort is to develop a system for the exposure of braided adsorbent material to unfiltered seawater, and to demonstrate the system by evaluating the performance of adsorption material when it is exposed to natural marine biofouling as it would be when the technology is used in the marine environment. Exposures of amidoxime-based polymeric braid adsorbents prepared by Oak Ridge Natural Laboratory (ORNL) were exposed to ambient seawater at 20°C in a flume system. Adsorption kinetics and adsorption capacity were assessed using time series determinations of uranium adsorption and one-site ligand saturation modeling. Biofouling in sunlight surface seawater has the potential to significantly add substantial biogenic mass to adsorption material when it is exposed for periods greater than 21 days. The observed biomass increase in the light flume was approximately 80% of the adsorbent mass after 42 days

  18. Determination of binding capacity and adsorption enthalpy between Human Glutamate Receptor (GluR1) peptide fragments and kynurenic acid by surface plasmon resonance experiments.

    Science.gov (United States)

    Csapó, E; Majláth, Z; Juhász, Á; Roósz, B; Hetényi, A; Tóth, G K; Tajti, J; Vécsei, L; Dékány, I

    2014-11-01

    The interaction between kynurenic acid (KYNA) and two peptide fragments (ca. 30 residues) of Human Glutamate Receptor 201-300 (GluR1) using surface plasmon resonance (SPR) spectroscopy was investigated. Because of the medical interest in the neuroscience, GluR1 is one of the important subunits of the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPAR). AMPARs are ionotoropic glutamate receptors, which are mediating fast synaptic transmission and are crucial for plasticity in the brain. On the other hand, KYNA has been suggested to have neuroprotective activity and it has been considered for apply in therapy in certain neurobiological disorders. In this article the adsorption of the GluR1201-230 and GluR1231-259 peptides were studied on gold biosensor chip. The peptides were chemically bonded onto the gold surface via thiol group of L-cysteine resulted in the formation of peptide monolayer on the SPR chip surface. Because the GluR1231-259 peptide does not contain L-cysteine the Val256 was replaced by Cys256. The cross sectional area and the surface orientation of the studied peptides were determined by SPR and theoretical calculations (LOMETS) as well. The binding capability of KYNA on the peptide monolayer was studied in the concentration range of 0.1-5.0 mM using 150 mM NaCl ionic strength at pH 7.4 (±0.02) in phosphate buffer solutions. In order to determine the binding enthalpy the experiments were carried out between +10°C and +40°C. The heat of adsorption was calculated by using adsorption isotherms at different surface loading of KYNA on the SPR chip.

  19. ADSORPTION OF DINITROPHENOLS ONTO POLYMERIC ADSORBENTS AND ITS MECHANISM

    Institute of Scientific and Technical Information of China (English)

    SHIZuoqing; XUMancai; 等

    2000-01-01

    The adsorption of 2,4-dinitrophenol and 2,6-dinitrophenol on non-polar and polar adsorbents was studied.The results showed that the equilibrium adsorption did not comply with the Langmuir equation and was not mono-layer adsorption .It is of interest to notice that the effect of pH on the adsorption of 2,4-or 2,6-dinitrophenol onto ADS-7 and ADS-21 was very small,The result is explained by hydrogen bonding interaction between 2,4-or 2,6-dinitrophenol and the adsorbent ADS-21.The large adsorption capacity of dinitrophenol onto ADS-21,which was about 500mg/g at an equilibrium concentration of 400mg/L,and the small dinitrophenol leakage in the effluent from ADS-21 column presented a good prospect for treatment of wastewater containing dinitrophenol with adsorbent ADS-21.

  20. Investigation of SO{sub 2} adsorption capacity of the activated carbon with O{sub 2}-NH{sub 3} treatment

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Yoon Hee; Seo, Kyung Won [Ajou University, Suwon (Korea, Republic of); Park, Dal Keun [KIST, Seoul (Korea, Republic of)

    1995-05-01

    Activated carbons, modified by oxygen and ammonia treatment, were tested for their catalytic activity in the SO{sub 2} adsorption. The modified activated carbons showed higher SO{sub 2} adsorption capacity compared with the untreated activated carbons. In this study the surface of activated carbon was modified to introduce the surface oxygen and nitrogen functional groups from NH{sub 3} and/or O{sub 2} treatment. In this experiment the conditions of modification varied with the NH{sub 3} concentrations(0{approx}25 vol%) and temperature (473{approx}1273 K) of the furnace, which directly affect surface functionalities, elemental composition, surface area and pore structure. The adsorption capacities were measured in an electric torsion balance(Cahn 2000). The activated carbons were characterized by temperature programmed desorption(TPD), Fourier transform infrared spectroscopy(FTIR), and acid-base titration. The maximum capacity of SO{sub 2} adsorption of the carbon sample(SO{sub 2} mg/m{sup 2} surface area) was obtained in the temperature range of 973{approx}1173 K. The activated carbons, treated with NH{sub 3}(up to 25% with O{sub 2} 3% of fixed amount), adsorbed SO{sub 2} about 48% more than the untreated activated carbons. (author). 9 refs., 11 figs., 1 tab.

  1. Surfactant-free synthesis of octahedral ZnO/ZnFe2O4 heterostructure with ultrahigh and selective adsorption capacity of malachite green

    OpenAIRE

    Jue Liu; Min Zeng; Ronghai Yu

    2016-01-01

    A new octahedral ZnO/ZnFe2O4 heterostructure has been fabricated through a facile surfactant-free solvothermal method followed by thermal treatment. It exhibits a record-high adsorption capacity (up to 4983.0 mg·g−1) of malachite green (MG), which is a potentially harmful dye in prevalence and should be removed from wastewater and other aqueous solutions before discharging into the environment. The octahedral ZnO/ZnFe2O4 heterostructure also demonstrates strong selective adsorption towards MG...

  2. In Situ Immobilization on the Silica Gel Surface and Adsorption Capacity of Poly[ N-(4-carboxyphenyl)methacrylamide] on Toxic Metal Ions

    Science.gov (United States)

    Yanovska, Elina; Savchenko, Irina; Sternik, Dariusz; Kychkiruk, Olga; Ol'khovik, Lidiya; Buriachenko, Iana

    2017-04-01

    In situ immobilization of poly[ N-(4-carboxyphenyl)methacrylamide] has been performed on silica gel surface. Infrared (IR) and mass spectroscopies as well as thermogravimetry (TG) analysis have been used to elucidate the structure of immobilized polymer. An adsorption capacity of the synthesized composite towards Cu(II), Pb(II), Mn(II), Fe(III), Co(II), and Ni(II) ions has been estimated. Adsorption activity to microquantities of Pb(II), Cu(II), and Ni(II) in a neutral aqueous medium has been observed.

  3. Effect of HNO{sub 3} treatment on the SO{sub 2} adsorption capacity of activated carbon prepared from Chinese low-rank coal

    Energy Technology Data Exchange (ETDEWEB)

    Hang Wenhui; Wang ling; Li Shurong [China Coal Research Institute, Beijing (China)

    1999-11-01

    SO{sub 2} removal from flue gas by activated carbon and HNO{sub 3} treated activated carbon from Chinese low-rank coal was studied. SO{sub 2} adsorption on activated carbon is mainly chemisorption. There was shown to be a correlation between adsorption capacity and the number of active sites on the carbon surface. HNO{sub 3} treatment transforms C-H bonds in activated carbon into active sites, for removal of SO{sub 2}. 2 figs., 2 tabs.

  4. 2, 4 dichlorophenol (2, 4-DCP) sorption from aqueous solution using granular activated carbon and polymeric adsorbents and studies on effect of temperature on activated carbon adsorption.

    Science.gov (United States)

    Ghatbandhe, A S; Yenkie, M K N

    2008-04-01

    Adsorption equilibrium, kinetics and thermodynamics of 2,4-dichlorophenol (2,4-DCP), one of the most commonly used chlorophenol, onto bituminous coal based Filtrasorb-400 grade granular activated carbon, were studied in aqueous solution in a batch system with respect to temperature. Uptake capacity of activated carbon found to increase with temperature. Langmuir isotherm models were applied to experimental equilibrium data of 2, 4-DCP adsorption and competitive studies with respect to XAD resin were carried out. Equilibrium data fitted very well to the Langmuir equilibrium model. Adsorbent monolayer capacity 'Q0, Langmuir constant 'b' and adsorption rate constant 'k(a)' were evaluated at different temperatures for activated carbon adsorption. This data was then used to calculate the energy of activation of adsorption and also the thermodynamic parameters, namely the free energy of adsorption, deltaG0, enthalpy of adsorption, deltaH0 and the entropy of adsorption deltaS0. The obtained results showed that the monolayer capacity increases with the increase in temperatures. The obtained values of thermodynamic parameters showed that adsorption of 2,4 DCP is an endothermic process. Synthetic resin was not found efficient to adsorb 2,4 DCP compared to activated carbon. The order of adsorption efficiencies of three resins used in the study found as XAD7HP > XAD4 > XAD1180.

  5. Detection of Volatile Organic Compounds by Self-assembled Monolayer Coated Sensor Array with Concentration-independent Fingerprints

    Science.gov (United States)

    Chang, Ye; Tang, Ning; Qu, Hemi; Liu, Jing; Zhang, Daihua; Zhang, Hao; Pang, Wei; Duan, Xuexin

    2016-04-01

    In this paper, we have modeled and analyzed affinities and kinetics of volatile organic compounds (VOCs) adsorption (and desorption) on various surface chemical groups using multiple self-assembled monolayers (SAMs) functionalized film bulk acoustic resonator (FBAR) array. The high-frequency and micro-scale resonator provides improved sensitivity in the detections of VOCs at trace levels. With the study of affinities and kinetics, three concentration-independent intrinsic parameters (monolayer adsorption capacity, adsorption energy constant and desorption rate) of gas-surface interactions are obtained to contribute to a multi-parameter fingerprint library of VOC analytes. Effects of functional group’s properties on gas-surface interactions are also discussed. The proposed sensor array with concentration-independent fingerprint library shows potential as a portable electronic nose (e-nose) system for VOCs discrimination and gas-sensitive materials selections.

  6. Fourier transform infra-red (FTIR) spectroscopy investigation, dose effect, kinetics and adsorption capacity of phosphate from aqueous solution onto laterite and sandstone.

    Science.gov (United States)

    Coulibaly, Lassina Sandotin; Akpo, Sylvain Kouakou; Yvon, Jacques; Coulibaly, Lacina

    2016-12-01

    Environmental pollution by phosphate in developing countries is growing with extensive and diffuse pollution. Solving these problem with intensive technologies is very expensive. Using natural sorbent such as laterite and sandstone could be a solution. The main objective of the study is to evaluate the P-removal efficiency of these materials under various solution properties. Laterite and sandstone used mainly contain very high levels of finely grained iron and aluminum oxy-hydroxides and diverse dioctahedral clays. Phosphate adsorption tests were carried out using crushed laterite and sandstone. Optimal doses and pH effects on phosphate adsorption were studied with a potassium hydrogeno-phosphate solution of 5 mg/L at 30 °C. The main results were that the optimal dosage is 15 and 20 mg/L respectively for laterite and sandstone. The phosphate adsorptions efficiency of laterite and sandstone are pH-dependent, they increase when the pH grows up to the Point of Zero Charge (PZC) and slowly decrease beyond. The adsorption capacities of the materials also increase proportionally with the initial phosphate concentration. The pseudo-second-order successfully described the kinetics of the phosphate adsorption on the two adsorbents. With this model, the adsorption capacity values are obtained, which give an idea of the maximum phosphate uptake that the laterite and sandstone could achieve. The changes on the FTIR spectra of raw materials and phosphate adsorbed material confirm the mechanism of chemisorptions. Considering the above, laterite and sandstone could be used as efficient and cheap adsorbent for the removal of phosphate in aqueous solution. Copyright © 2016 Elsevier Ltd. All rights reserved.

  7. A one-step thermal decomposition method to prepare anatase TiO2 nanosheets with improved adsorption capacities and enhanced photocatalytic activities

    Science.gov (United States)

    Li, Wenting; Shang, Chunli; Li, Xue

    2015-12-01

    Anatase TiO2 nanosheets (NSs) with high surface area have been prepared via a one-step thermal decomposition of titanium tetraisopropoxide (TTIP) in oleylamine (OM), and their adsorption capacities and photocatalytic activities are investigated by using methylene blue (MB) and methyl orange (MO) as model pollutants. During the synthesis procedure, only one type of surfactant, oleylamine (OM), is used as capping agents and no other solvents are added. Structure and properties of the TiO2 NSs were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption analysis, UV-vis spectrum, X-ray photoelectron spectroscopy (XPS) and Photoluminescence (PL) methods. The results indicate that the TiO2 NSs possess high surface area up to 378 m2 g-1. The concentration of capping agents is found to be a key factor controlling the morphology and crystalline structure of the product. Adsorption and photodegradation experiments reveal that the prepared TiO2 NSs possess high adsorption capacities of model pollutants MB and high photocatalytic activity, showing that TiO2 NSs can be used as efficient pollutant adsorbents and photocatalytic degradation catalysts of MB in wastewater treatment.

  8. Influence of alumina phases on the molybdenum adsorption capacity and chemical stability for {sup 99}Mo/{sup 99m}Tc generators columns

    Energy Technology Data Exchange (ETDEWEB)

    Guedes-Silva, Cecilia C.; Ferreira, Thiago dos Santos; Paula, Carolina M. de; Otubo, Larissa, E-mail: cecilia.guedes@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Carvalho, Flavio M.S. [Universidade de Sao Paulo (IGC/USP), SP (Brazil). Instituto de Geociencias

    2016-07-15

    Technetium-{sup 99m} is the clinically most used radionuclide worldwide. Although many techniques can be applied to separate {sup 99}Mo and {sup 99m}Tc, the most commonly used method is the column chromatography with alumina as stationary phase. However, the alumina nowadays used has limited adsorption capacity of molybdate ions which implies the need to develop or improve materials to produce high specific activity generators. In this paper, alumina was obtained by a solid state method and heat treatments at different conditions. The powders had a microstructure with porous particles of γ, δ, θ and α-Al{sub 2}O{sub 3} phases as well as specific surface area between 36 and 312 m{sup 2} g{sup -1}. Most interesting results were reached by powders calcined at 900 deg C for 5 hours which had high chemical stability and a molybdenum adsorption capacity of 92.45 mg Mo per g alumina. (author)

  9. Influence of organobentonite structure on toluene adsorption from water solution

    Directory of Open Access Journals (Sweden)

    Nuria Vidal

    2012-12-01

    Full Text Available Due to increase water pollution by organic compound derived from hydrocarbons such as toluene, several alternative technologies for remediation of polluted water have been originated. In this work natural bentonites were modified with cetyltrimethylammonium (CTMA+ for obtaining organophilic bentonites. The obtained CTMA-bentonites would be suitable for use as adsorbents of toluene present in water. The influence of structural characteristics of CTMA-bentonites on their adsorption capacity was studied. It was shown that adsorption of toluene depended on homogeneous interlayer space associated with arrangements of CTMA+ paraffin-monolayer and bilayer models, accompanied by a high degree ordering of the carbon chain of organic cation in both arrangements. However, packing density would not have an evident influence on the retention capacity of these materials. The solids obtained were characterized by chemical analysis, X-ray diffractions and infrared spectroscopy. Toluene adsorption was measured by UV-visible spectrophotometer. Adsorption capacity was studied by determining adsorption isotherms and adsorption coefficient calculation. The adsorption isotherms were straight-line indicating a partition phenomenon of toluene between the aqueous and organic phase present in organophilic bentonites.

  10. Influence of the pore structure and surface chemical properties of activated carbon on the adsorption of mercury from aqueous solutions.

    Science.gov (United States)

    Lu, Xincheng; Jiang, Jianchun; Sun, Kang; Wang, Jinbiao; Zhang, Yanping

    2014-01-15

    Reactivation and chemical modification were used to obtain modified activated carbons with different pore structure and surface chemical properties. The samples were characterized by nitrogen absorption-desorption, Fourier transform infrared spectroscopy and the Bothem method. Using mercury chloride as the target pollutant, the Hg(2+) adsorption ability of samples was investigated. The results show that the Hg(2+) adsorption capacity of samples increased significantly with increases in micropores and acidic functional groups and that the adsorption process was exothermic. Different models and thermodynamic parameters were evaluated to establish the mechanisms. It was concluded that the adsorption occurred through a monolayer mechanism by a two-speed process involving both rapid adsorption and slow adsorption. The adsorption rate was determined by chemical reaction.

  11. Improving Adsorption Capacity of Modified Activated Carbon by Wastewater Contained Manganese%含锰废水改性活性炭吸附性能研究

    Institute of Scientific and Technical Information of China (English)

    刘广兵; 谭文轶

    2012-01-01

    在实验室条件下,采用含锰废水浸泡改性活性炭,测定了改性活性炭基本吸附性能.实验测得原始活性炭的碘吸附质量比为95.07 mg/g,活性炭的SO2吸附质量比为95.51 mg/g.而经过含锰废水浸泡不同天数后的改性活性炭的碘吸附质量比分别为:(1 d)118.43mg/ g,(2 d)118.36mg/g,(3 d)160.69 mg/g和(4 d)133.17mg/g;它们对SO2的吸附质量比分别为(1 d)149.53 mg/ g,(2 d)122.14 mg/g,(3 d)117.12mg/g和(4 d)1 10.09 mg/g.这些实验结果表明,采用含锰废水改性活性炭的表面化学性质后可以提高活性炭的碘值和吸附能力,同时含锰废水得到再利用.%In this paper,activated carbon was modified by being immersed in wastewater contained manganese under laboratory conditions,and the basic adsorption capability of the modified activated carbon had been determined. The value of iodine adsorption of the original activated carbon was 95.07 mg/g and SO2 adsorption capacity was 95.51 mg/g,respectively. After immersed in wastewater contained manganese in different days,the value of iodine adsorption of the modified activated carbon were 118.43 mg/g (one day),118.36 mg/g (two days),160.69 mg/g (three days) and 133.17 mg/g (four days),respectively. The SO2 adsorption capacity were 149.53 mg/g (one day),122.14 mg/g (two days),117.12 mg/g (three days) and 110.09 mg/g (four days),respectively. The results show that after modified the surface chemical properties of activated carbon immersed in wastewater contained manganese,the value of iodine adsorption and adsorption capacity of activated carbon have been improved,and the wastewater contained manganese was reused at the same time.

  12. Mercury adsorption properties of sulfur-impregnated adsorbents

    Science.gov (United States)

    Hsi, N.-C.; Rood, M.J.; Rostam-Abadi, M.; Chen, S.; Chang, R.

    2002-01-01

    Carbonaceous and noncarbonaceous adsorbents were impregnated with elemental sulfur to evaluate the chemical and physical properties of the adsorbents and their equilibrium mercury adsorption capacities. Simulated coal combustion flue gas conditions were used to determine the equilibrium adsorption capacities for Hg0 and HgCl2 gases to better understand how to remove mercury from gas streams generated by coal-fired utility power plants. Sulfur was deposited onto the adsorbents by monolayer surface deposition or volume pore filling. Sulfur impregnation increased the total sulfur content and decreased the total and micropore surface areas and pore volumes for all of the adsorbents tested. Adsorbents with sufficient amounts of active adsorption sites and sufficient microporous structure had mercury adsorption capacities up to 4,509 ??g Hg/g adsorbent. Elemental sulfur, organic sulfur, and sulfate were formed on the adsorbents during sulfur impregnation. Correlations were established with R2>0.92 between the equilibrium Hg0/HgCl2 adsorption capacities and the mass concentrations of elemental and organic sulfur. This result indicates that elemental and organic sulfur are important active adsorption sites for Hg0 and HgCl2.

  13. Modeling Stimuli-Responsive Nanoparticle Monolayer

    Science.gov (United States)

    Yong, Xin

    2015-03-01

    Using dissipative particle dynamics (DPD), we model a monolayer formed at the water-oil interface, which comprises stimuli-responsive nanoparticles. The solid core of the nanoparticle encompasses beads arranged in an fcc lattice structure and its surface is uniformly grafted with stimuli-responsive polymer chains. The surface-active nanoparticles adsorb to the interface from the suspension to minimize total energy of the system and create a monolayer covering the interface. We investigate the monolayer formation by characterizing the detailed adsorption kinetics. We explore the microstructure of the monolayer at different surface coverage, including the particle crowding and ordering, and elucidate the response of monolayer to external stimuli. The collective behavior of the particles within the monolayer is demonstrated quantitatively by vector-vector autocorrelation functions. This study provides a fundamental understanding of the interfacial behavior of stimuli-responsive nanoparticles.

  14. Etching of Crystalline ZnO Surfaces upon Phosphonic Acid Adsorption: Guidelines for the Realization of Well-Engineered Functional Self-Assembled Monolayers.

    Science.gov (United States)

    Ostapenko, Alexandra; Klöffel, Tobias; Eußner, Jens; Harms, Klaus; Dehnen, Stefanie; Meyer, Bernd; Witte, Gregor

    2016-06-01

    Functionalization of metal oxides by means of covalently bound self-assembled monolayers (SAMs) offers a tailoring of surface electronic properties such as their work function and, in combination with its large charge carrier mobility, renders ZnO a promising conductive oxide for use as transparent electrode material in optoelectronic devices. In this study, we show that the formation of phosphonic acid-anchored SAMs on ZnO competes with an unwanted chemical side reaction, leading to the formation of surface precipitates and severe surface damage at prolonged immersion times of several days. Combining atomic force microscopy (AFM), X-ray diffraction (XRD), and thermal desorption spectroscopy (TDS), the stability and structure of the aggregates formed upon immersion of ZnO single crystal surfaces of different orientations [(0001̅), (0001), and (101̅0)] in phenylphosphonic acid (PPA) solution were studied. By intentionally increasing the immersion time to more than 1 week, large crystalline precipitates are formed, which are identified as zinc phosphonate. Moreover, the energetics and the reaction pathway of this transformation have been evaluated using density functional theory (DFT), showing that zinc phosphonate is thermodynamically more favorable than phosphonic acid SAMs on ZnO. Precipitation is also found for phosphonic acids with fluorinated aromatic backbones, while less precipitation occurs upon formation of SAMs with phenylphosphinic anchoring units. By contrast, no precipitates are formed when PPA monolayer films are prepared by sublimation under vacuum conditions, yielding smooth surfaces without noticeable etching.

  15. Carbon nanotubes for energy storage using their hydrogen adsorption capacity: state of the art and perspectives; Nanotubos de carbono para estocagem de energia por adsorcao de hidrogenio: estado da arte e perspectivas

    Energy Technology Data Exchange (ETDEWEB)

    Maestro, Luis Fernando; Luengo, Carlos Alberto [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Inst. de Fisica. Grupo de Combustiveis Alternativos], e-mail: lmaestro@ifi.unicamp.br

    2004-07-01

    It is presented an updated scope of the research in carbon nanotubes synthesis, their purification and a discussion of recent results in energy storage using their hydrogen adsorption capacity. The GCA activities in this area are also discussed. (author)

  16. Surface adsorption of poisonous Pb(II) ions from water using chitosan functionalised magnetic nanoparticles.

    Science.gov (United States)

    Christopher, Femina Carolin; Anbalagan, Saravanan; Kumar, Ponnusamy Senthil; Pannerselvam, Sundar Rajan; Vaidyanathan, Vinoth Kumar

    2017-06-01

    In this study, chitosan functionalised magnetic nano-particles (CMNP) was synthesised and utilised as an effective adsorbent for the removal of Pb(II) ions from aqueous solution. The experimental studies reveal that adsorbent material has finer adsorption capacity for the removal of heavy metal ions. Parameters affecting the adsorption of Pb(II) ions on CMNP, such as initial Pb(II) ion concentration, contact time, solution pH, adsorbent dosage and temperature were studied. The adsorption equilibrium study showed that present adsorption system followed a Freundlich isotherm model. The experimental kinetic studies on the adsorption of Pb(II) ions exhibited that present adsorption process best obeyed with pseudo-first order kinetics. The maximum monolayer adsorption capacity of CMNP for the removal of Pb(II) ions was found to be 498.6 mg g(-1). The characterisation of present adsorbent material was done by FTIR, energy disperse X-ray analysis and vibrating sample magnetometer studies. Thermodynamic parameters such as Gibbs free energy (ΔG°), enthalpy (ΔH°) and entropy (ΔS°) have declared that the adsorption process was feasible, exothermic and spontaneous in nature. Sticking probability reported that adsorption of Pb(II) ions on CMNP was favourable at lower temperature and sticking capacity of Pb(II) ions was very high.

  17. Characteristic Evaluation of Graphene Oxide for Bisphenol A Adsorption in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Thatchaphong Phatthanakittiphong

    2016-07-01

    Full Text Available This paper investigates the characteristics of graphene oxide (GO for Bisphenol A (BPA adsorption in water. Batch experiments on the influence of significant parameters were performed. While an improvement of the adsorption capacity of BPA was obtained by the increment of contact time and the initial BPA concentration, the increment of pH above 8, GO dosage, and temperature showed the reverse results. The thermodynamic study suggested that BPA adsorption on GO was an exothermic and spontaneous process. The kinetics was explained by the pseudo-second-order model which covers all steps of adsorption. The fit of the results with the Langmuir isotherm indicated the monolayer adsorption. At 298 K, the adsorption reached equilibrium within 30 min with the maximum adsorption capacity of 49.26 mg/g. The low BPA adsorption capacity of GO can be interpreted by the occurrence of oxygen-containing functional groups (OCFGs that are able to form hydrogen bonds with the surrounding OCFGs and water molecules. This effect inhibited the role of π–π interactions that are mainly responsible for the adsorption of BPA.

  18. Evaluation of Adsorption Capacity of Low Cost Adsorbent for the Removal of Congo Red Dye from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Dattatraya Jirekar

    2016-10-01

    Full Text Available Vigna unguiculata seed husk powder has been investigated as low cost adsorbent for the removal of hazardous chemicals like Congo Red (CR dye from aqueous solution. Various parameters such as effect of contact time, initial CR dye concentration, adsorbent dose, effect of pH, zero-point pH were studied. Batch adsorption technique was employed to optimize the process parameter. The result indicated that, the percentage adsorption of Congo Red increased with increase in contact time, dose of adsorbent and initial concentration of Congo Red and decreased with addition of salt. The adsorption of Congo Red was 78% at the optimum pH of 6. Adsorption equilibrium was found to be reached in 24 h for 5 to 25 g/50 mL Congo red concentrations. The Langmuir and Freundlich isotherm models were found to provide an excellent fitting of the adsorption data.  The adsorption of CR follows Second order rate kinetics. Thermodynamic parameter (δGo showed that it was an exothermic process. This adsorbent was found to be effective and economically attractive. DOI: http://dx.doi.org/10.17807/orbital.v8i5.834

  19. Fabrication of CMC-g-PAM superporous polymer monoliths via eco-friendly Pickering-MIPEs for superior adsorption of methyl violet and methylene blue

    Science.gov (United States)

    Wang, Feng; Zhu, Yongfeng; Wang, Wenbo; Zong, Li; Lu, Taotao; Wang, Aiqin

    2017-06-01

    A series of superporous carboxymethylcellulose-graft-poly(acrylamide) (CMC-g-PAM) polymer monoliths presenting interconnected pore structure and excellent adsorption properties were prepared by one-step free-radical grafting polymerization reaction of CMC and acrylamide (AM) in the oil-in-water (O/W) Pickering-medium internal phase emulsions (Pickering-MIPEs) composed of non-toxic edible oil as a dispersion phase and natural Pal nanorods as stabilizers. The effects of Pal dosage, AM dosage, and co-surfactant Tween-20 (T-20) on the pore structures of the monoliths were studied. It was revealed that the well-defined pores were formed when the dosages of Pal and T-20 are 9-14% and 3%, respectively. The porous monolith can rapidly adsorb 1585 mg/g of methyl violet (MV) and 1625 mg/g of methylene blue (MB). After the monolith was regenerated by adsorption-desorption process for 5 times, the adsorption capacities still reached 92.1% (for MV) and 93.5% (for MB) of the initial maximum adsorption capacities. The adsorption process was fitted with Langmuir adsorption isotherm model and pseudo-second-order adsorption kinetic model very well, which indicate that mono-layer chemical adsorption mainly contribute to the high-capacity adsorption for dyes. The superporous polymer monolith prepared from eco-friendly Pickering-MIPEs shows good adsorption capacity and fast adsorption rate, which is potential adsorbent for the decontimination of dye-containing wastewater.

  20. Synthesis of PGMA Microspheres with Amino Groups for High-capacity Adsorption of Cr(VI) by Cerium Initiated Graft Polymerizatio

    Institute of Scientific and Technical Information of China (English)

    李鹏飞; 杨良嵘; 何秀琼; 王娟; 孔鹏; 邢慧芳; 刘会洲

    2012-01-01

    Abstract A novel polyglycidylmethacrylate (PGMA) microspheres with high adsorption capacity of Cr(VI) was prepared by cerium(IV) initiated graft polymerization of tentacle-type polymer chains with amino group on polymer microspheres with hydroxyl groups. The micron-sized PGMA microspheres were prepared by a dispersion polym erization method and subsequently modified by ring-opening reaction to introduce functional hydroxyl groups. The polymer microspheres were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The results indicated that the polymer microspheres had an average diameter of 5 m with uniform size distribution. The free amino group content was determined to be 5.13 mmol·g^-1 for g;PGMA-NH2 microspheres by potentiometric and conductometric titration methods. The Cr(VI) adsorption results indicated that the graft polymerization of tentacle-type polymer chains on the polymer microspheres could produce adsorbents with high adsorption capacity (500 mg-g-l). The polymer microspheres with grafted tentacle polymer chains have potenial application in large-scale removal of Cr(VI) in aqueous solution.

  1. Surfactant-free synthesis of octahedral ZnO/ZnFe2O4 heterostructure with ultrahigh and selective adsorption capacity of malachite green

    Science.gov (United States)

    Liu, Jue; Zeng, Min; Yu, Ronghai

    2016-05-01

    A new octahedral ZnO/ZnFe2O4 heterostructure has been fabricated through a facile surfactant-free solvothermal method followed by thermal treatment. It exhibits a record-high adsorption capacity (up to 4983.0 mg·g-1) of malachite green (MG), which is a potentially harmful dye in prevalence and should be removed from wastewater and other aqueous solutions before discharging into the environment. The octahedral ZnO/ZnFe2O4 heterostructure also demonstrates strong selective adsorption towards MG from two kinds of mixed solutions: MG/methyl orange (MO) and MG/rhodamine B (RhB) mixtures, indicating its promise in water treatment.

  2. Ultrasond-assisted synthesis of Fe3O4/SiO2 core/shell with enhanced adsorption capacity for diazinon removal

    Science.gov (United States)

    Farmany, Abbas; Mortazavi, Seyede Shima; Mahdavi, Hossein

    2016-10-01

    Fe3O4/SiO2 core/shell nanocrystals were synthesized by ultrasond-assisted procedure. The core/shell nanocrystals were characterized using XRD, FT-IR spectroscopy, SEM and BET. The BET analysis confirmed that iron oxide nanocrystal with the surface area of 208.0 m2/g can be used as an excellent adsorbent for organic and inorganic pollutants. The core/shell nanocrystal was used as an adsorbent for removal of insecticide O,O-diethyl-O[2-isopropyl-6-methylpyridimidinyl] phosphorothioate (diazinon). In continue the influence of different parameters such as pH, adsorbent dosage and shaking time on the adsorption capacity were studied. The experimental data were fitted well with the pseudo-second-order kinetic model (R2=0.9706). The adsorption isotherm was described well by Langmuir isotherm.

  3. Fracture Characteristics of Monolayer CVD-Graphene

    OpenAIRE

    Hwangbo, Yun; Lee, Choong-Kwang; Kim, Sang-Min; Kim, Jae-Hyun; Kim, Kwang-Seop; Jang, Bongkyun; Lee, Hak-Joo; Lee, Seoung-Ki; Kim, Seong-Su; Ahn, Jong-Hyun; Lee, Seung-Mo

    2014-01-01

    We have observed and analyzed the fracture characteristics of the monolayer CVD-graphene using pressure bulge testing setup. The monolayer CVD-graphene has appeared to undergo environmentally assisted subcritical crack growth in room condition, i.e. stress corrosion cracking arising from the adsorption of water vapor on the graphene and the subsequent chemical reactions. The crack propagation in graphene has appeared to be able to be reasonably tamed by adjusting applied humidity and stress. ...

  4. Porous and Magnetic Molecularly Imprinted Polymers via Pickering High Internal Phase Emulsions Polymerization for Selective Adsorption of λ-Cyhalothrin

    Science.gov (United States)

    Wu, Yunlong; Ma, Yue; Pan, Jianming; Gu, Runxing; Luo, Jialu

    2017-01-01

    A novel macroporous magnetic molecularly imprinted polymer (MMIPs) of was prepared by W/O Pickering (high internal phase emulsions) HIPEs polymerization, and then it was adopted as adsorbent for selective adsorption of λ-cyhalothrin (LC). In static conditions, adsorption capacity of LC increased rapidly in the first 60 min and reached to equilibrium in ~2.0 h. Excellent conformity of the second-order model confirmed the chemical nature of the interaction between the LC and imprinted sites. The fitting adsorption isotherm was a Langmuir type, and the maximum monolayer adsorption capacity at 298 K was 404.4 μmol g−1. Thermodynamic parameters suggested the specific adsorption at 298 K was an exothermic, spontaneous, and entropy decreased process. Competitive recognition studies of the MMIPs were performed with diethyl phthalate (DEP) and the structurally similar compound fenvalerate (FL), and the MMIPs, which displayed high selectivity for LC.

  5. Adsorption of arsenazo (III due by phosphorus-containing polymer sorbent

    Directory of Open Access Journals (Sweden)

    Alosmanov Rasim M.

    2016-01-01

    Full Text Available Phosphorus-containing polymer sorbent was employed for removal hazardous Arsenazo (III dye from water. The adsorption characteristics were determined by the study at different parameters such as effect of solution pH, effect of initial dye concentration, sorbent dose, phase contact time, and temperature. The equilibrium data were analyzed on the basis of various adsorption isotherm models, namely Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich. The highest monolayer adsorption capacity has been obtained (24.75 mg g-1 at 55°C. Different thermodynamic parameters such as free energy, enthalpy, and entropy have been calculated and it was concluded that when temperature rises, adsorption increases, indicating the endothermic nature of the process. Kinetic parameters were derived by pseudo-first-order, pseudo-second-order and intraparticle kinetic models. Scanning Electron Microscopy and Fourier Transform Infrared spectroscopy were used to characterize the sorbent and also to validate the adsorption mechanism.

  6. 煅烧水滑石对硝态氮的吸附性能研究%Adsorption capacity of nitrate by calcination layered double hydroxide

    Institute of Scientific and Technical Information of China (English)

    蒋钦凤; 喻杏元; 艾玉明; 邱喜; 何欣; 陈金毅

    2016-01-01

    通过共沉淀法和煅烧法制备不同煅烧温度的水滑石,并对其进行XRD、FT-IR及BET表征.结果表明,煅烧水滑石后使水滑石的特征峰消失,层状结构塌陷,并生成了镁铝复合氧化物,比表面积增加,平均孔径减少.将水滑石进行硝态氮的吸附性能研究,结果表明,煅烧450℃水滑石除硝态氮效果优于其他煅烧温度下的水滑石,对10 mg/L的硝态氮吸附240 min后平衡浓度低于1 mg/L.最后,研究水滑石对硝态氮的吸附动力学与吸附等温线,结果表明准二级动力学模型和Langmuir吸附等温线能较好地描述硝态氮在水滑石上的吸附行为,吸附过程分为快速吸附阶段和慢速吸附阶段,水滑石对硝态氮的吸附过程主要为化学吸附,偏向于单分子层的吸附过程,但也不能排除多分子层吸附的存在.%Layered double hydroxide( LDH) were synthesized by co-precipitation method and its calcination products ( LDH450 ) was prepared by heating LDH at 450 ℃.The materials were characterized by X-ray diffraction ( XRD ) , Fourier transform infrared spectroscopy ( FT-IR ) and Brunauer-Emmett-Teller ( BET ) . Results indicate that the characteristic peaks (003) and (006) of LDH450 disappeared,a mixed oxide Mg(Al) O was formed, and the BET SSA of LDH450 increased, and the average pore size reduced.The adsorption capacity of hydrotalcite was studied.Results indicate that nitrate adsorption by LDH450 was superior to the others.When initial concentrations of nitrate was 10 mg/L,the adsorption reaction reached a balance in 240 min, and the equilibrium concentration was less than 1 mg/L.Finally,the adsorption kinetics and adsorption isotherm showed that the Pseudo-second-order kinetic model and Langmuir isotherm model could be used to describe nitrate adsorption satisfactorily.Adsorption process divided into two stages,included fast stage and slow stage,and mainly chemical adsorption,the adsorption

  7. Preparation of hybrid organic-inorganic mesoporous silicas applied to mercury removal from aqueous media: Influence of the synthesis route on adsorption capacity and efficiency.

    Science.gov (United States)

    Pérez-Quintanilla, Damián; Sánchez, Alfredo; Sierra, Isabel

    2016-06-15

    New hybrid organic-inorganic mesoporous silicas were prepared by employing three different synthesis routes and mercury adsorption studies were done in aqueous media using the batch technique. The organic ligands employed for the functionalization were derivatives of 2-mercaptopyrimidine or 2-mercaptothiazoline, and the synthesis pathways used were post-synthesis, post-synthesis with surface ion-imprinting and co-condensation with ion-imprinting. The incorporation of functional groups and the presence of ordered mesopores in the organosilicas was confirmed by XRD, TEM and SEM, nitrogen adsorption-desorption isotherms, (13)C MAS-NMR, (29)Si MAS-NMR, elemental and thermogravimetric analysis. The highest adsorption capacity and selectivity observed was for the material functionalized with 2-mercaptothiazoline ligand by means the co-condensation with ion-imprinting route (1.03 mmol g(-1) at pH 6). The prepared material could be potential sorbent for the extraction of this heavy metal from environmental and drinking waters. Copyright © 2016 Elsevier Inc. All rights reserved.

  8. Adsorption of ammonium dinitramide (ADN) from aqueous solutions. 1. Adsorption on powdered activated charcoal.

    Science.gov (United States)

    Santhosh, G; Venkatachalam, S; Ninan, K N; Sadhana, R; Alwan, S; Abarna, V; Joseph, M A

    2003-03-17

    Investigations on the adsorption of ammonium dinitramide (NH(4)N(NO(2))(2)) (ADN) from aqueous solutions on powdered activated charcoal (PAC) were carried out in order to find out an effective and easier method of separating ADN from aqueous solutions. The effectiveness of PAC in the selective adsorption of ADN from aqueous solutions of ADN (ADN-F) and ADN in presence of sulfate (SO(4)(2-)) and nitrate (NO(3)(-)) ions (ADN-PS) was examined and compared using batch and column methods. The adsorption process follows both Langmuir and Freundlich adsorption isotherms and the isotherm parameters for the models were determined. The observed data favor the formation of monolayer adsorption. The adsorption capacities were found to be 63.3, 119, 105.3 and 82 mg of ADN per g of PAC for ADN-F (batch), ADN-PS (batch), ADN-F (column) and ADN-PS (column), respectively. Break-through curves for ADN-F and ADN-PS were obtained for the optimization of separation of ADN from aqueous solutions. Elution curves were generated for the desorption of ADN from PAC using hot water as eluent.

  9. A Study on Astrazon Black AFDL Dye Adsorption onto Vietnamese Diatomite

    Directory of Open Access Journals (Sweden)

    Bui Hai Dang Son

    2016-01-01

    Full Text Available In the present paper, the adsorption of Astrazon Black AFDL dye onto Vietnamese diatomite has been demonstrated. The diatomite was characterized by XRD, SEM, TEM, EDS, and nitrogen adsorption/desorption isotherms. The results show that diatomite mainly constituted centric type frustules characterized by pores as discs or as cylindrical shapes. The adsorption kinetics and isotherms of dye onto Vietnam diatomite were investigated. The experimental data were fitted well to both Freundlich and Langmuir in the initial concentration range of 400–1400 mg L−1. The average value of maximum adsorption capacity, qm, calculated from Freundlich equation is statistically similar to the average value of maximum monolayer adsorption capacity calculated from Langmuir equation. The thermodynamic parameters evaluated from the temperature dependent on adsorption isotherms in the range of 303–343 K show that the adsorption process was spontaneous and endothermic. The Webber and pseudo-first/second-order kinetic models were used to analyze the mechanism of adsorption. The piecewise linear regression and Akaike’s Information Criterion were used to analyze experimental data. The results show that the dye adsorption onto diatomite was film diffusion controlled and the goodness of fit of experimental data for kinetics modes was dependent on the initial concentration.

  10. The water-based synthesis of chemically stable Zr-based MOFs using pyridine-containing ligands and their exceptionally high adsorption capacity for iodine.

    Science.gov (United States)

    Wang, Zhe; Huang, Ying; Yang, Jian; Li, Yongsheng; Zhuang, Qixin; Gu, Jinlou

    2017-06-13

    The primary pollutant, radioactive iodine (I2), has become a worldwide concern due to its serious ill effects of radiotoxicity on human health. Therefore, it is of great significance to develop novel adsorbents for effectively eliminating I2 from nuclear waste. Herein, we reported a Zr-based MOF adsorbent constructed by utilizing pyridine-containing pyridine-dicarboxylic acid (PYDC) as organic ligands (UiO-66-PYDC) as well as active sites for the efficient removal of I2. UiO-66-PYDC MOFs were synthesized by a hydrothermal strategy and featured good chemical and thermal stabilities, endowing them with the ability to work in harsh environments. The abundant and inherent pyridine moieties in the developed adsorbent worked as active adsorption sites to capture I2. The correlation between the most significant parameters such as the contact time, adsorbate concentration, and reusability was optimized, and the interaction mechanism between I2 and UiO-66-PYDC was investigated in detail. As for the current adsorbent, a pseudo-second order rate equation was used to explain the removal kinetics, and the Langmuir model exhibited a better fit to the adsorption isotherm than the Freundlich model. Thanks to the strong affinity of PYDC ligands to I2 and high porosity, the adsorption capacities of UiO-66-PYDC for I2 could reach as high as 1250 mg g(-1), which was much higher than those of many other reported MOFs. Additionally, the UiO-66-PYDC MOFs exhibited excellent renewable adsorption properties, prefiguring their great promise as green adsorbents for I2 removal in nuclear waste management.

  11. Changing the adsorption capacity of coal-based honeycomb monoliths for pollutant removal from liquid streams by controlling their porosity

    Energy Technology Data Exchange (ETDEWEB)

    Gatica, Jose M.; Harti, Sanae [Departamento C.M., I.M. y Quimica Inorganica, Universidad de Cadiz, Puerto Real 11510 (Spain); Vidal, Hilario, E-mail: hilario.vidal@uca.es [Departamento C.M., I.M. y Quimica Inorganica, Universidad de Cadiz, Puerto Real 11510 (Spain)

    2010-09-15

    Coal-based honeycomb monoliths extruded using methods developed for ceramic materials have been used to retain methylene blue and p-nitrophenol from aqueous solutions. The influence of the filters' thermal treatment on their textural properties and performance as adsorbents was examined. Characterization by N{sub 2} physisorption, mercury porosimetry and scanning electron microscopy along with adsorption tests under dynamic conditions suggest that, depending on the pollutant and its initial concentration, it can be more convenient to previously submit the monoliths to a simple carbonization or to an additional activation, with or without preoxidation, as a consequence of their different resulting pore structures. Infrared spectroscopy indicates that their different adsorption behaviour seems not to be related to differences in their surface chemical groups. In addition, axial crushing tests show that the monoliths have an acceptable mechanical resistance for the application investigated.

  12. Granular activated carbon adsorption of organic micro-pollutants in drinking water and treated wastewater--Aligning breakthrough curves and capacities.

    Science.gov (United States)

    Zietzschmann, Frederik; Stützer, Christian; Jekel, Martin

    2016-04-01

    Small-scale granular activated carbon (GAC) tests for the adsorption of organic micro-pollutants (OMP) were conducted with drinking water and wastewater treatment plant (WWTP) effluent. In both waters, three influent OMP concentration levels were tested. As long as the influent OMP concentrations are below certain thresholds, the relative breakthrough behavior is not impacted in the respective water. Accordingly, the GAC capacity for OMP is directly proportional to the influent OMP concentration in the corresponding water. The differences between the OMP breakthrough curves in drinking water and WWTP effluent can be attributed to the concentrations of the low molecular weight acid and neutral (LMW) organics of the waters. Presenting the relative OMP concentrations (c/c0) over the specific throughput of the LMW organics (mg LMW organics/g GAC), the OMP breakthrough curves in drinking water and WWTP effluent superimpose each other. This superimposition can be further increased if the UV absorbance at 254 nm (UV254) of the LMW organics is considered. In contrast, using the specific throughput of the dissolved organic carbon (DOC) did not suffice to obtain superimposed breakthrough curves. Thus, the LMW organics are the major water constituent impacting OMP adsorption onto GAC. The results demonstrate that knowing the influent OMP and LMW organics concentrations (and UV254) of different waters, the OMP breakthroughs and GAC capacities corresponding to any water can be applied to all other waters.

  13. Enhancement in CO2 Adsorption Capacity and Selectivity in the Chalcogenide Aerogel CuSb2S4 by Post-synthetic Modification with LiCl

    KAUST Repository

    Ahmed, Ejaz

    2015-09-11

    The new chalcogel CuSb2S4 was obtained by reacting Cu(OAc)2·H2O with KSbS2 in a water/formamide mixture at room temperature. In order to modify the gas adsorption capacity the synthesized CuSb2S4 aerogel was loaded with different amounts of LiCl. CO2 adsorption measurements on the CuSb2S4 aerogel before and after treatment with LiCl showed more than three times increased uptake of the LiCl-modified chalcogel. The selectivities of the gas pairs CO2/H2 and CO2/CH4 in the LiCl-treated chalcogel are 235 and 105 respectively and amongst the highest reported for chalcogenide-based aerogels. In comparison with other porous materials like zeolites, activated carbon and most of the Metal Organic Frameworks (MOFs) or Porous Organic Frameworks (POFs), our synthesized aerogels show good air and moisture stability. Although, the CO2 storage capacity of our aerogels is relatively low, however the selectivity of CO2 over H2 or CH4 in LiCl-loaded aerogels are higher than in zeolites, activated carbon as well as some MOFs like Cu-BTC and MOF-5 etc.

  14. Effect of immobilized amine density on cadmium(II) adsorption capacities for ethanediamine-modified magnetic poly-(glycidyl methacrylate) microspheres

    Science.gov (United States)

    Dong, Tingting; Yang, Liangrong; Pan, Feng; Xing, Huifang; Wang, Li; Yu, Jiemiao; Qu, Hongnan; Rong, Meng; Liu, Huizhou

    2017-04-01

    A series of ethanediamine (EDA) - modified magnetic poly-(glycidyl methacrylate) (m-PGMA-EDA)microspheres with different amine density were synthesized and their cadmium saturation adsorption capacities were examined. The results showed that the cadmium saturation adsorption capacity increased with the immobilized amine density. However, they did not show strong positive linear correlation in the whole range of amine density examined. The molar ratio of amine groups to the adsorbed cadmium decreased with the increase of amine density and eventually reached a minimum value about 4. It suggested that low immobilized amine density led to low coordination efficiency of the amine. It is hypothesized that the immobilized amine groups needed to be physically close enough to form stable amine-metal complex. When the amine density reached to a critical value 1.25 m mol m-2, stable amine-cadmium complex (4:1 N/Cd) was proposed to form. To illustrate the coordination mechanism (structure and number) of amine and Cd, FT-IR spectra of m-PGMA-EDA and m-PGMA-EDA-Cd , and X-ray photoelectron spectroscopy (XPS) of PGMA-EDA and PGMA-EDA-Cd were examined and analyzed.

  15. Ultrasond-assisted synthesis of Fe{sub 3}O{sub 4}/SiO{sub 2} core/shell with enhanced adsorption capacity for diazinon removal

    Energy Technology Data Exchange (ETDEWEB)

    Farmany, Abbas, E-mail: a.farmany@usa.com [Department of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of); Mortazavi, Seyede Shima, E-mail: s.s.mortazavi@iauh.ac.ir [Department of Chemistry, Hamedan Branch, Islamic Azad University, Hamedan (Iran, Islamic Republic of); Mahdavi, Hossein [Department of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of)

    2016-10-15

    Fe{sub 3}O{sub 4}/SiO{sub 2} core/shell nanocrystals were synthesized by ultrasond-assisted procedure. The core/shell nanocrystals were characterized using XRD, FT-IR spectroscopy, SEM and BET. The BET analysis confirmed that iron oxide nanocrystal with the surface area of 208.0 m{sup 2}/g can be used as an excellent adsorbent for organic and inorganic pollutants. The core/shell nanocrystal was used as an adsorbent for removal of insecticide O,O-diethyl-O[2-isopropyl-6-methylpyridimidinyl] phosphorothioate (diazinon). In continue the influence of different parameters such as pH, adsorbent dosage and shaking time on the adsorption capacity were studied. The experimental data were fitted well with the pseudo-second-order kinetic model (R{sup 2}=0.9706). The adsorption isotherm was described well by Langmuir isotherm. - Highlights: • Amino functionalized Fe{sub 3}O{sub 4}/SiO{sub 2} core/shell nanocrystals were synthesized ultrasonically. • High surface area of 208.0 m{sup 2}/g of nanocrystal makes it as excellent adsorbent for organic/inorganic pollutants. • High adsorbent capacity obtained for diazinon removal.

  16. Fabrication and testing of engineered forms of self-assembled monolayers on mesoporous silica (SAMMS) material

    Energy Technology Data Exchange (ETDEWEB)

    Mattigod, S.V.; Liu, J.; Fryxell, G.E.; Baskaran, S.; Gong, M.; Nie, Z. [Pacific Northwest National Lab., Richland, WA (United States); Feng, X. [Ferro Corp., Cincinnati, OH (United States); Klasson, K.T. [Oak Ridge National Lab., TN (United States)

    1998-09-01

    A number of engineered forms such as flexible extrudates, beads, and rods were fabricated using thiol-SAMMS (Self-Assembled Monolayers on Mesoporous Silica) and tested for their mercury adsorption capacities. The flexible extrudate form had a mercury adsorption capacity of 340 mg/g but was found to be structurally unstable. A structurally sound bead form of thiol-SAMMS was fabricated with 5, 10, 25, and 40% by weight clay binder (attapulgite) and successfully functionalized. A structurally stable but non-optimized rod form of thiol-SAMMS was also fabricated. Bench-scale processes were developed to silanize and functionalize mesoporous silica beads made with attapulgite clay binder. Contact angle measurements were conducted to assess the degree of surface coverage by functional groups on mesoporous silica materials.

  17. Dye-adsorption capacity of bituminous fly ash and its pozzolanic property after used as dye-adsorbent

    Directory of Open Access Journals (Sweden)

    Penpolcharoen, M.

    2004-02-01

    Full Text Available Bituminous fly ash, which is an industrial waste, was used as an adsorbent to remove dyestuff from the textile-dye wastewater. The batch kinetic and isotherm experiments of the synthetic wastewater were firstly conducted to determine the adsorption behavior and optimal conditions for adsorption. The optimal conditions were then applied to the actual textile-dye wastewater. Under the original conditions of fly ash and wastewater, the results indicated that the color could be removed up to 86.65% by 12 g of the fly ash /L of the wastewater within 30 min. Its adsorption was described by the Freundlich isotherm. The dye-adsorbed fly ash was further studied on its pozzolanic property in terms of compressive strength by using it as a partial substitute to Portland cement type I to produce mortar. The result revealed that the highest compressive strength was of the sample containing 10% by weight of the dye-adsorbed fly ash in replacement of cement. It possessed 215 kg/cm2 at 28 days, which is 92.67% of the sample containing 10% by weight of the original fly ash in replacement of cement, or 83.33 of the cement mortar. For the environmental concern, leachabilities of lead (Pb, chromium (Cr, copper (Cu and zinc (Zn from all mortars were also carried out. No leaching of the heavy metals from any samples could be detected. Hence, the dye-adsorbed fly ash can be used as an environmental friendly construction material.

  18. Cr(VI) Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms.

    Science.gov (United States)

    Cui, You-Wei; Li, Jie; Du, Zhao-Fu; Peng, Yong-Zhen

    Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI)) creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI)-containing wastewater; the adsorbent was prepared using red mud (RM) generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM), followed the pseudo-second-order model, with a rapid adsorption rate. Cr(VI) adsorption was positively associated with the absorbent dose, pH, temperature, and initial Cr(VI) concentration; coexisting anions had little impact. The maximum Cr(VI) adsorption capacity was 17.35 mg/g. Cr(VI) adsorption on La-RM was a mono-layer adsorption pattern, following the Langmuir isotherm model. Thermodynamic parameters showed the adsorption was spontaneous and endothermic. The adsorption of Cr(VI) on La-RM occurred as a result of LaOCl formation on the RM surface, which in turn further reacted with Cr(VI) in the wastewater. This study highlighted a method for converting industrial waste into a valuable material for wastewater treatment. The novel absorbent could be used as a potential adsorbent for treating Cr(VI)-contaminating wastewater, due to its cost-effectiveness and high adsorption capability.

  19. Adsorption removal of tannic acid from aqueous solution by polyaniline: Analysis of operating parameters and mechanism.

    Science.gov (United States)

    Sun, Chencheng; Xiong, Bowen; Pan, Yang; Cui, Hao

    2017-02-01

    Polyaniline (PANI) prepared by chemical oxidation was studied for adsorption removal of tannic acid (TA) from aqueous solution. Batch adsorption studies were carried out under different adsorbent dosages, pH, ionic strength, initial TA concentration and coexisting anions. Solution pH had an important impact on TA adsorption onto PANI with optimal removal in the pH range of 8-11. TA adsorption on PANI at three ionic strength levels (0.02, 0.2 and 2molL(-1) NaCl) could be well described by Langmuir model (monolayer adsorption process) and the maximum adsorption capacity was 230, 223 and 1023mgg(-1), respectively. Kinetic data showed that TA adsorption on PANI fitted well with pseudo-second-order model (controlled by chemical process). Among the coexisting anions tested, PO4(3-) significantly inhibited TA adsorption due to the enhancement of repulsive interaction. Continuous flow adsorption studies indicated good flexibility and adaptability of the PANI adsorbent under different flow rates and influent TA concentrations. The mechanism controlling TA adsorption onto PANI under different operating conditions was analyzed with the combination of electrostatic interactions, hydrogen bonding, π-π interactions and Van der Waals interactions. Copyright © 2016 Elsevier Inc. All rights reserved.

  20. Cr(VI) Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms

    Science.gov (United States)

    Cui, You-Wei; Li, Jie; Du, Zhao-Fu; Peng, Yong-Zhen

    2016-01-01

    Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI)) creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI)-containing wastewater; the adsorbent was prepared using red mud (RM) generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM), followed the pseudo-second-order model, with a rapid adsorption rate. Cr(VI) adsorption was positively associated with the absorbent dose, pH, temperature, and initial Cr(VI) concentration; coexisting anions had little impact. The maximum Cr(VI) adsorption capacity was 17.35 mg/g. Cr(VI) adsorption on La-RM was a mono-layer adsorption pattern, following the Langmuir isotherm model. Thermodynamic parameters showed the adsorption was spontaneous and endothermic. The adsorption of Cr(VI) on La-RM occurred as a result of LaOCl formation on the RM surface, which in turn further reacted with Cr(VI) in the wastewater. This study highlighted a method for converting industrial waste into a valuable material for wastewater treatment. The novel absorbent could be used as a potential adsorbent for treating Cr(VI)-contaminating wastewater, due to its cost-effectiveness and high adsorption capability. PMID:27658113

  1. AUSTRALIAN PINE CONES-BASED ACTIVATED CARBON FOR ADSORPTION OF COPPER IN AQUEOUS SOLUTION

    Directory of Open Access Journals (Sweden)

    MUSLIM A.

    2017-02-01

    Full Text Available The Australian Pine cones (APCs was utilised as adsorbent material by physical and chemical activation for the adsorption Cu(II in aqueous solution. FTIR and SEM analysis were conducted to obtain the active site and to characterise the surface morphology of the APCs activated carbon (APCs AC prepared through pyrolysis at 1073.15 K and alkaline activation of NaOH. The independent variables effect such as contact time, Cu(II initial concentration and the activator ratio in the ranges of 0-150 min, 84.88-370.21 mg/l and 0.2-0.6 (NaOH:APCs AC, respectively on the Cu(II adsorption capacity were investigated in the APCs activated carbon-solution (APCs ACS system with 1 g the APCs AC in 100 mL Cu(II aqueous solution with magnetic stirring at 75 rpm, room temperature of 298.15 K (± 2 K, 1 atm and pH 5 (±0.25. As the results, Cu(II adsorption capacity dramatically increased with increasing contact time and Cu(II initial concentration. The optimal Cu(II adsorption capacity of 26.71 mg/g was obtained in the APCs ACS system with 120-min contact time, 340.81 m/l initial Cu(II and 0.6 activator ratio. The kinetics study showed the Cu(II adsorption kinetics followed the pseudo-second-order kinetics with 27.03 mg/g of adsorption capacity, 0.09 g/mg.min of rate constant and 0.985-R2. In addition, the Cu(II adsorption isotherm followed the Langmuir model with 12.82 mg/g of the mono-layer adsorption capacity, 42.93 l/g of the over-all adsorption capacity and 0.954-R2.

  2. Adsorption of cadmium(II) on waste biomaterial.

    Science.gov (United States)

    Baláž, M; Bujňáková, Z; Baláž, P; Zorkovská, A; Danková, Z; Briančin, J

    2015-09-15

    Significant increase of the adsorption ability of the eggshell biomaterial toward cadmium was observed upon milling, as is evidenced by the value of maximum monolayer adsorption capacity of 329mgg(-1), which is markedly higher than in the case of most "green" sorbents. The main driving force of the adsorption was proven to be the presence of aragonite phase as a consequence of phase transformation from calcite occurring during milling. Cadmium is adsorbed in a non-reversible way, as documented by different techniques (desorption tests, XRD and EDX measurements). The optimum pH for cadmium adsorption was 7. The adsorption process was accompanied by the increase of the value of specific surface area. The course of adsorption has been described by Langmuir, Freundlich and Dubinin-Radushkevich isotherms. The adsorption kinetics was evaluated using three models, among which the best correlation coefficients and the best normalized standard deviation values were achieved for the pseudo-second order model and the intraparticle diffusion model, respectively.

  3. The Effect of Oxidation on the Surface Chemistry of Sulfur-Containing Carbons and their Arsine Adsorption Capacity

    Science.gov (United States)

    2010-01-01

    hydrogen sulfide . Carbon 2004;42(3):469–76. Fig. 6 – Water adsorption isotherms of the samples studied. 1786 C A R B O N 4 8 ( 2 0 1 0 ) 1 7 7 9 –1 7 8...that oxygen- and sulfur-containing groups participate in arsine oxida- tion to arsenic tri- and pentoxide and/or in the formation of arsenic sulfides ...technological difficulties, arsine is also a powerful toxin susceptible to oxidation with a strong exothermic effect. Of all the methods to separate

  4. Molecular diffusion in monolayer and submonolayer nitrogen

    DEFF Research Database (Denmark)

    Hansen, Flemming Yssing; Bruch, Ludwig Walter

    2001-01-01

    The orientational and translational motions in a monolayer fluid of physisorbed molecular nitrogen are treated using molecular dynamics simulations. Dynamical response functions and several approximations to the coefficient of translational diffusion are determined for adsorption on the basal pla...... where the ballistic approximation to the translational molecular self-correlation function is accurate....

  5. New V(IV)-based metal-organic framework having framework flexibility and high CO2 adsorption capacity.

    Science.gov (United States)

    Liu, Ying-Ya; Couck, Sarah; Vandichel, Matthias; Grzywa, Maciej; Leus, Karen; Biswas, Shyam; Volkmer, Dirk; Gascon, Jorge; Kapteijn, Freek; Denayer, Joeri F M; Waroquier, Michel; Van Speybroeck, Veronique; Van Der Voort, Pascal

    2013-01-07

    A vanadium based metal-organic framework (MOF), VO(BPDC) (BPDC(2-) = biphenyl-4,4'-dicarboxylate), adopting an expanded MIL-47 structure type, has been synthesized via solvothermal and microwave methods. Its structural and gas/vapor sorption properties have been studied. This compound displays a distinct breathing effect toward certain adsorptives at workable temperatures. The sorption isotherms of CO(2) and CH(4) indicate a different sorption behavior at specific temperatures. In situ synchrotron X-ray powder diffraction measurements and molecular simulations have been utilized to characterize the structural transition. The experimental measurements clearly suggest the existence of both narrow pore and large pore forms. A free energy profile along the pore angle was computationally determined for the empty host framework. Apart from a regular large pore and a regular narrow pore form, an overstretched narrow pore form has also been found. Additionally, a variety of spectroscopic techniques combined with N(2) adsorption/desorption isotherms measured at 77 K demonstrate that the existence of the mixed oxidation states V(III)/V(IV) in the titled MOF structure compared to pure V(IV) increases the difficulty in triggering the flexibility of the framework.

  6. The surface characteristics of hyperbranched polyamide modified corncob and its adsorption property for Cr(VI)

    Science.gov (United States)

    Lin, Hai; Han, Shaoke; Dong, Yingbo; He, Yinhai

    2017-08-01

    A low-cost anion adsorbent for Cr(VI) effectively removing was synthesized by hyperbranched polyamide modified corncob (HPMC). Samples were characterized by Brunauer-Emmett-Teller (BET) surface area analysis, field-emission scanning electron microscopy (FE-SEM) with energy-dispersive X-ray spectroscopy, Fourier transform infrared (FTIR) and zeta potential analysis. Kinetics, isotherms and thermodynamics studies of HPMC for Cr(VI) adsorption were investigated in batch static experiments, in the temperature range of 25-45 °C, pH = 2.0. Results showed that the adsorption was rapid and stable, with the uptake capacity higher than 80% after 30 min. Adsorption behavior and rate-controlling mechanisms were analyzed using three kinetic models (pseudo-first order, pseudo-second order, intra-particle kinetic model). Kinetic studies showed that the adsorption of HPMC to Cr(VI) relied the pseudo-second-order model, and controlled both by the intra-particle diffusion and film diffusion. Equilibrium data was tested by Langmuir and Freundlich adsorption isotherm models. Langmuir model was more suitable to indicate a homogeneous distribution of active sites on HPMC and monolayer adsorption. The maximum adsorption capacity from the Langmuir model, qmax, was 131.6 mg/g at pH 2.0 and 45 °C for HPMC. Thermodynamic parameters revealed spontaneous and endothermic nature of the Cr(VI) adsorption onto HPMC.

  7. Study on the adsorption capacity for mercury (Ⅱ) with chromium/cobaIt-doped graphene oxide materiaIs%负载铬钴石墨烯基材料对汞(Ⅱ)的吸附性能研究

    Institute of Scientific and Technical Information of China (English)

    王卓; 邓娟; 朱君妍; 周超; 周晓吉; 郭永福; 白仁碧

    2016-01-01

    The chromium and cobalt doped reduced graphene oxide (RGO/Cr,RGO/Co) composite materials have been synthesized by making use of the reducibility of RGO and the oxidability of transition metallic salts ,and app-lied to the adsorption for Hg2+. The results show that the specific surface area of RGO/Cr is higher than that of RGO/Co and RGO. The hydrophilicity of RGO is effectively improved after having been doped with chromium or cobalt. The theoretical monolayer adsorption capacities of RGO,RGO/Cr and RGO/Co fitting Langmuir model are 128.98,181.86, and 146.86 mg/g,respectively,and the adsorption processes of these three materials complies with the pseudo-first-order and pseudo-second-order kinetic model.%利用石墨烯的还原性与过渡金属盐类的氧化性,制备得到分别负载有铬和钴的还原氧化石墨烯(RGO)复合材料RGO/Cr和RGO/Co,并将其应用于对Hg2+的吸附。结果表明:RGO/Cr比RGO/Co及RGO具有更大比表面积,负载铬和钴后RGO的亲水性能显著增加。 Langmuir拟合RGO、RGO/Cr、RGO/Co对Hg2+的理论单层最大吸附容量分别为128.98、181.86、146.86 mg/g,同时吸附过程均符合伪一级和伪二级动力学模型。

  8. Preparation of biodegradable sponge and research on its adsorption capacity%可降解海绵的制备及其吸附性能的研究

    Institute of Scientific and Technical Information of China (English)

    陈晶晶; 张从阳

    2012-01-01

      研究了用魔芋葡甘露聚糖制备可降解海绵的方法,并用制备出的海绵对硝基苯胺进行了吸附实验.结果表明选择魔芋葡甘露聚糖来制备可降解海绵是可行的,并且制备出的可降解海绵对硝基苯胺有较强的吸附的能力,对浓度为10.0 mg/L硝基苯胺的去除率150 min内可达80%.%  The preparation method of biodegradable sponge by konjac glucomannan and its adsorption capacity were studied.The experimental results show that the preparation of biodegradable sponge konjac mannan is feasible , and the biodegradable sponge has strong adsorption of p -nitroaniline, and the removal rate reaches 80%in 150 min.

  9. MOFs for CO2 capture and separation from flue gas mixtures: the effect of multifunctional sites on their adsorption capacity and selectivity.

    Science.gov (United States)

    Zhang, Zhijuan; Zhao, Yonggang; Gong, Qihan; Li, Zhong; Li, Jing

    2013-01-25

    Microporous metal-organic frameworks (MOFs) have attracted tremendous attention because of their versatile structures and tunable porosity that allow almost unlimited ways to improve their properties and optimize their functionality, making them very promising for a variety of important applications, especially in the adsorption and separation of small gases and hydrocarbons. Numerous studies have demonstrated that MOFs with multifunctional groups, such as open metal sites (OMSs) and Lewis basic sites (LBSs), interact strongly with carbon dioxide and are particularly effective in its capture and separation from binary mixtures of CO(2) and N(2). In this feature article, we briefly review the current state of MOF development in this area, with an emphasis on the effect of multifunctional groups on the selectivity and capacity of MOFs for the CO(2) capture from flue gas mixtures.

  10. Efficient adsorption of 4-Chloroguiacol from aqueous solution using optimal activated carbon: Equilibrium isotherms and kinetics modeling

    Directory of Open Access Journals (Sweden)

    Afidah Abdul Rahim

    2016-10-01

    Full Text Available The optimal activated carbon produced from Prosopis africana seed hulls (PASH-AC was obtained using the impregnation ratio of 3.19, activation temperature of 780 °C and activation time of 63 min with surface area of 1095.56 m2/g and monolayer adsorption capacity of 498.67 mg/g. The adsorption data were also modeled using five various forms of the linearized Langmuir equations as well as Freundlich and Temkin adsorption isotherms. In comparing the legitimacy of each isotherm model, chi square (χ2 was incorporated with the correlation coefficient (R2 to justify the basis for selecting the best adsorption model. Langmuir-2 > Freundlich > Temkin isotherms was the best order that described the equilibrium adsorption data. The results revealed pseudo-second-order to be the most ideal model in describing the kinetics data.

  11. Isotherm and thermodynamic studies of Zn (II) adsorption on lignite and coconut shell-based activated carbon fiber.

    Science.gov (United States)

    Shrestha, Sohan; Son, Guntae; Lee, Seung Hwan; Lee, Tae Gwan

    2013-08-01

    The Zn (II) adsorption capacity of lignite and coconut shell-based activated carbon fiber (ACF) was evaluated as a function of initial Zn (II) concentration, temperature and contact time in batch adsorption process in this study. Adsorption uptake increased with initial Zn (II) concentration and temperature. Optimal contact time for the adsorption of Zn (II) ions onto lignite and coconut shell-based ACF was found to be 50 min. Removal percentage decreased from 88.0% to 78.54% with the increment in initial Zn (II) concentration from 5 to 50 mg L(-1). Equilibrium data fit well with Langmuir-I isotherm indicating homogeneous monolayer coverage of Zn (II) ions on the adsorbent surface. Maximum monolayer adsorption capacity of Zn (II) ions on ACF was found to be 9.43 mg g(-1). Surface morphology and functionality of ACF prior to and after adsorption were characterized by electron microscopy and infrared spectroscopy. Various thermodynamic parameters such as standard Gibbs free energy (ΔG°), standard enthalpy (ΔH°), and standard entropy (ΔS°) were evaluated.

  12. Adsorption characteristics of Cu(II) and Pb(II) onto expanded perlite from aqueous solution.

    Science.gov (United States)

    Sari, Ahmet; Tuzen, Mustafa; Citak, Demirhan; Soylak, Mustafa

    2007-09-01

    The adsorption characteristics of Cu(II) and Pb(II) onto expanded perlite (EP) from aqueous solution were investigated with respect to the changes in pH of solution, adsorbent dosage, contact time and temperature of solution. For the adsorption of both metal ions, the Langmuir isotherm model fitted to equilibrium data better than the Freundlich isotherm model. Using the Langmuir model equation, the monolayer adsorption capacity of EP was found to be 8.62 and 13.39 mg/g for Cu(II) and Pb(II) ions, respectively. Dubinin-Radushkevich (D-R) isotherm model was also applied to the equilibrium data and the mean free energies of adsorption were found as 10.82 kJ/mol for Cu(II) and 9.12 kJ/mol for Pb(II) indicating that the adsorption of both metal ions onto EP was taken place by chemical ion-exchange. Thermodynamic functions, the change of free energy (DeltaG degrees ), enthalpy (DeltaH degrees ) and entropy (DeltaS degrees ) of adsorption were also calculated for each metal ions. These parameters showed that the adsorption of Cu(II) and Pb(II) ions onto EP was feasible, spontaneous and exothermic at 20-50 degrees C. Experimental data were also evaluated in terms of kinetic characteristics of adsorption and it was found that adsorption process for both metal ions followed well pseudo-second-order kinetics.

  13. Basic dye adsorption onto an agro-based waste material--sesame hull (Sesamum indicum L.).

    Science.gov (United States)

    Feng, Yanfang; Yang, Fan; Wang, Yongqian; Ma, Li; Wu, Yonghong; Kerr, Philip G; Yang, Linzhang

    2011-11-01

    The aim of this project was to establish an economical and environmentally benign biotechnology for removing methylene blue (MB) from wastewater. The adsorption process of MB onto abandoned sesame hull (Sesamum indicum L.) (SH) was investigated in a batch system. The results showed that a wide range of pH (3.54-10.50) was favorable for the adsorption of MB onto SH. The Langmuir model displayed the best fit for the isothermal data. The exothermic adsorption process fits a pseudo-second-order kinetic model. The maximum monolayer adsorption capacity (359.88 mg g(-1)) was higher than most previously investigated low-cost bioadsorbents (e.g., peanut hull, wheat straw, etc.). This study indicated that sesame hull is a promising, unconventional, affordable and environmentally friendly bio-measure that is easily deployed for removing high levels of MB from wastewater. Copyright © 2011 Elsevier Ltd. All rights reserved.

  14. Tuning ethylene gas adsorption via metal node modulation: Cu-MOF-74 for a high ethylene deliverable capacity.

    Science.gov (United States)

    Liao, Yijun; Zhang, Lin; Weston, Mitchell H; Morris, William; Hupp, Joseph T; Farha, Omar K

    2017-08-17

    M-MOF-74s were examined for potential applications in ethylene abatement and/or storage/delivery. Due to labile binding resulting from a Jahn-Teller distortion, Cu-MOF-74 exhibits a gradual initial uptake that, in turn, translates into the highest deliverable capacity among the MOFs examined (3.6 mmol g(-1)). In contrast, Co-MOF-74 is the most promising candidate for ethylene abatement due to the sharp uptake at low pressure.

  15. Methylene Blue Adsorption on a Low Cost Adsorbent-Carbonized Peanut Shell.

    Science.gov (United States)

    Gülen, Jale; Zorbay, Fatih

    2017-09-01

      Carbonized peanut shell (CPS), a low cost adsorbent was investigated for adsorption of methylene blue from its aqueous solution. Some experimental parameters like the effect of initial dye concentration, initial solution pH, phases contact time and temperature were investigated. Langmuir, Freundlich and Harkins-Jura isotherm models were applied to the experimental data and Langmuir model fitted best. Monolayer adsorption capacity was 5.34 mg/g according to the Langmuir model. Adsorption capacity/uptake of CPS was found comparable to the some other adsorbent materials. The kinetic and intra particle diffusion models were applied to the experimental data. The experimental reaction was progressed via pseudo second order kinetic model. The thermodynamic parameters were also evaluated.

  16. Adsorption of methyl orange onto protonated cross-linked chitosan

    Directory of Open Access Journals (Sweden)

    Ruihua Huang

    2017-01-01

    Full Text Available The adsorption of methyl orange (MO from aqueous solutions on protonated cross-linked chitosan was studied in a batch system. The results showed that the adsorption of MO onto protonated cross-linked chitosan was affected significantly by initial MO concentration, adsorbent dosage, adsorption temperature, and contact time. The pH value of solution had a minor impact on the adsorption of MO in a pH range of 1.0–9.1. The equilibrium isotherms at different temperatures (293, 303, and 313 K and pH values (4.5, 6.7, and 9.1 were investigated. Langmuir model was able to describe these Equilibrium data fitted perfectly. The maximum monolayer adsorption capacities obtained from the Langmuir model were 89.29, 130.9, and 180.2 mg/g at 293, 303, and 313 K, respectively. Adsorption kinetics at different concentrations (100, 200 and 300 mg/L and pH values (4.5, 6.7 and 9.1 were also studied. The kinetics was correlated well with the pseudo second-order model.

  17. Synthesis of fungus-like MoS2 nanosheets with ultrafast adsorption capacities toward organic dyes

    Science.gov (United States)

    Song, HaoJie; You, Shengsheng; Jia, XiaoHua

    2015-11-01

    Fungus-like molybdenum disulfide (MoS2) nanosheets with a thickness of a few nanometers have been successfully synthesized via one-pot hydrothermal method. The as-prepared MoS2 nanosheets with a high surface area of 106.989 m2 g-1 exhibited excellent wastewater treatment performance with high removal capacities toward organic dyes. In addition, the fungus-like MoS2 nanosheets can absorb Congo red completely within 2 min. Successful access to high quality fungus-like MoS2 nanosheets will make it possible for their potential application in catalysis and other fields.

  18. The electronic properties, electronic heat capacity and magnetic susceptibility of monolayer boron nitride graphene-like structure in the presence of electron-phonon coupling

    Science.gov (United States)

    Yarmohammadi, Mohsen

    2017-03-01

    In this work, we have studied the influences of electron-phonon (e-ph) coupling and chemical potential on the boron nitride graphene-like sheet. In particular, by starting the Green's function technique and Holstein model, the electronic density of states (DOS), electronic heat capacity (EHC) and magnetic susceptibility (MS) of this system have been investigated in the context of self-consistent second order perturbation theory which has been implemented to find the electronic self-energy. Our findings show that the band gap size decreases (increases) with e-ph coupling (chemical potential) parameters. The Schottky anomaly (crossover) decreases in EHC (MS) as soon as e-ph coupling increases. Also, the corresponding temperature with Schottky anomaly is considerably affected by e-ph coupling.

  19. p-Chlorophenol adsorption on activated carbons with basic surface properties

    Science.gov (United States)

    Lorenc-Grabowska, Ewa; Gryglewicz, Grażyna; Machnikowski, Jacek

    2010-05-01

    The adsorption of p-chlorophenol (PCP) from aqueous solution on activated carbons (ACs) with basic surface properties has been studied. The ACs were prepared by two methods. The first method was based on the modification of a commercial CWZ AC by high temperature treatment in an atmosphere of ammonia, nitrogen and hydrogen. The second approach comprised the carbonization followed by activation of N-enriched polymers and coal tar pitch using CO 2 and steam as activation agent. The resultant ACs were characterized in terms of porous structure, elemental composition and surface chemistry (pH PZC, acid/base titration, XPS). The adsorption of PCP was carried out from an aqueous solution in static conditions. Equilibrium adsorption isotherm was of L2 type for polymer-based ACs, whereas L3-type isotherm was observed for CWZ ACs series. The Langmuir monolayer adsorption capacity was related to the porous structure and the amount of basic sites. A good correlation was found between the adsorption capacity and the volume of micropores with a width < 1.4 nm for polymer-based ACs. Higher nitrogen content, including that in basic form, did not correspond to the enhanced adsorption of PCP from aqueous solution. The competitive effect of water molecule adsorption on the PCP uptake is discussed.

  20. Nickel oxide grafted andic soil for efficient cesium removal from aqueous solution: adsorption behavior and mechanisms.

    Science.gov (United States)

    Ding, Dahu; Lei, Zhongfang; Yang, Yingnan; Feng, Chuanping; Zhang, Zhenya

    2013-10-23

    An andic soil, akadama clay, was modified with nickel oxide and tested for its potential application in the removal of cesium from aqueous solution. Scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), and powder X-ray diffraction (XRD) results revealed the nickel oxide was successfully grafted into akadama clay. N2 adsorption-desorption isotherms indicated the surface area decreased remarkably after modification while the portion of mesopores increased greatly. Thermogravimetric-differential thermal analysis (TG-DTA) showed the modified akadama clay had better thermostability than the pristine akadama clay. Decreases in cation exchange capacity (CEC) and ζ-potential were also detected after the modification. Adsorption kinetic and isotherm studies indicated the adsorption of Cs+ on the modified akadama clay was a monolayer adsorption process. Adsorption capacity was greatly enhanced for the modified akadama clay probably due to the increase in negative surface charge caused by the modification. The adsorption of Cs+ on the modified akadama clay was dominated by an electrostatic adsorption process. Results of this work are of great significance for the application of akadama clay as a promising adsorbent material for cesium removal from aqueous solutions.

  1. Adsorption of acids and bases from aqueous solutions onto silicon dioxide particles.

    Science.gov (United States)

    Zengin, Huseyin; Erkan, Belgin

    2009-12-30

    The adsorption of acids and bases onto the surface of silicon dioxide (SiO(2)) particles was systematically studied as a function of several variables, including activation conditions, contact time, specific surface area, particle size, concentration and temperature. The physical properties of SiO(2) particles were investigated, where characterizations were carried out by FT-IR spectroscopy, and morphology was examined by scanning electron microscopy (SEM). The SEM of samples showed good dispersion and uniform SiO(2) particles with an average diameter of about 1-1.5 microm. The adsorption results revealed that SiO(2) surfaces possessed effective interactions with acids and bases, and greatest adsorption capacity was achieved with NaOH, where the best fit isotherm model was the Freundlich adsorption model. The adsorption properties of raw SiO(2) particles were further improved by ultrasonication. Langmuir monolayer adsorption capacity of NaOH adsorbate at 25 degrees C on sonicated SiO(2) (182.6 mg/g) was found to be greater than that of the unsonicated SiO(2) (154.3mg/g). The spontaneity of the adsorption process was established by decreases in DeltaG(ads)(0), which varied from -10.5 to -13.6 kJ mol(-1), in the temperature range 283-338K.

  2. Removal of Basic Red 46 dye from aqueous solution by adsorption onto Moroccan clay.

    Science.gov (United States)

    Karim, A Bennani; Mounir, B; Hachkar, M; Bakasse, M; Yaacoubi, A

    2009-08-30

    In this study, Moroccan crude clay of Safi, which was characterized by X-ray diffraction, is used as adsorbent for the investigation of the adsorption kinetics, isotherms and thermodynamic parameters of the Basic Red 46 (BR46) in aqueous solutions at various dye concentrations, adsorbent masses and pH values. The results showed that the adsorption capacity of the dye increased by initial dye concentration and pH values. Two kinetic models (the pseudo-first-order and the pseudo-second-order) were used to calculate the adsorption rate constants. The adsorption kinetics of the basic dye followed pseudo-second-order model. The experimental data isotherms were analyzed using the Langmuir, Freundlich and Dubinin-Radushkevish equations. The monolayer adsorption capacity for BR46 dye is 54 mg/g of crude clay. Nearly 20 min of contact time was found to be sufficient for the dye adsorption to reach equilibrium. Thermodynamical parameters were also evaluated for the dye-adsorbent system and revealed that the adsorption process is exothermic in nature.

  3. A comprehensive adsorption study and modeling of antibiotics as a pharmaceutical waste by graphene oxide nanosheets.

    Science.gov (United States)

    Rostamian, Rahele; Behnejad, Hassan

    2017-08-22

    The adsorption behavior of tetracycline (TCN), doxycycline (DCN) as the most common antibiotics in veterinary and ciprofloxacin (CPN) onto graphene oxide nanosheets (GOS) in aqueous solution was evaluated. The four factors influencing the adsorption of antibiotics (initial concentration, pH, temperature and contact time) were studied. The results showed that initial pH ∼ 6 to 7 and contact time ∼ 100 - 200min are optimum for each drug. The monolayer adsorption capacity was reduced with the increasing temperature from 25°C to 45°C. Non-linear regressions were carried out in order to define the best fit model for every system. To do this, eight error functions were applied to predict the optimum model. Among various models, Hill and Toth isotherm models represented the equilibrium adsorption data of antibiotics while the kinetic data were well fitted by pseudo second-order (PSO) kinetic model (DCN and TCN) and Elovich (CPN) models. The maximum adsorption capacity (qmax) is found to be in the following order: CPN > DCN > TCN, obtained from sips equation at the same temperature. The GOS shows highest adsorption capacity towards CPN up to 173.4mgg(-1). The study showed that GOS can be removed more efficiently from water solution. Copyright © 2017 Elsevier Inc. All rights reserved.

  4. Synthesis of fungus-like MoS{sub 2} nanosheets with ultrafast adsorption capacities toward organic dyes

    Energy Technology Data Exchange (ETDEWEB)

    Song, HaoJie; You, Shengsheng [Jiangsu University, School of Materials Science and Engineering, Zhenjiang, Jiangsu (China); Jia, XiaoHua [Jiangsu University, School of Environment and Safety Engineering, Zhenjiang, Jiangsu (China)

    2015-11-15

    Fungus-like molybdenum disulfide (MoS{sub 2}) nanosheets with a thickness of a few nanometers have been successfully synthesized via one-pot hydrothermal method. The as-prepared MoS{sub 2} nanosheets with a high surface area of 106.989 m{sup 2} g{sup -1} exhibited excellent wastewater treatment performance with high removal capacities toward organic dyes. In addition, the fungus-like MoS{sub 2} nanosheets can absorb Congo red completely within 2 min. Successful access to high quality fungus-like MoS{sub 2} nanosheets will make it possible for their potential application in catalysis and other fields. (orig.)

  5. Functional monolayers for direct electrical biosensing

    Science.gov (United States)

    Clare, Tami Lasseter

    Frequency-dependent electrochemical impedance spectroscopy has been used to characterize changes in electrical response that accompany specific binding of a protein to its substrate, using the biotin-avidin system as a model. This thesis work shows that avidin, at concentrations in the nanomolar range, can be detected electrically in a completely label-free manner under conditions of zero average current flow and without the use of any auxiliary redox agents. Electrical circuit modeling of the interface was used to relate the frequency-dependent electrical response to the physical picture of the interface before and after avidin binding. The interaction of proteins with semiconductors such as silicon and diamond is of great interest for applications such as electronic biosensing. Investigations into the use of covalently bound oligo(ethylene glycol), EG, monolayers on diamond and silicon to minimize nonspecific protein adsorption were conducted. Protein adsorption was monitored by fluorescence scanning as a function the length of the ethylene glycol chain (EG3 through EG6) and the terminal functional group (methyl- versus hydroxyl-terminated EG3 monolayer). More quantitative measurements were made by eluting adsorbed avidin from the surface and measuring the intensity of fluorescence in the solution. This thesis work shows that high quality EG monolayers are formed on silicon and diamond and that these EG3 monolayers are as effective as EG3 self-assembled monolayers on gold at resisting nonspecific avidin adsorption. These results show promise for use of silicon and diamond materials in many potential applications such as biosensing and medical implants. Substrate roughness is shown to play a role in nonspecific protein adsorption, where carbon-based surfaces having features less than approximately 5 nm, are highly resistant to protein adsorption. Functionalization of the surfaces with hexaethylene glycol confers additional resistance to protein adsorption. These

  6. Equilibrium modeling and kinetic studies on the adsorption of basic dye by a low-cost adsorbent: coconut (Cocos nucifera) bunch waste.

    Science.gov (United States)

    Hameed, B H; Mahmoud, D K; Ahmad, A L

    2008-10-01

    In this paper, the ability of coconut bunch waste (CBW), an agricultural waste available in large quantity in Malaysia, to remove basic dye (methylene blue) from aqueous solution by adsorption was studied. Batch mode experiments were conducted at 30 degrees C to study the effects of pH and initial concentration of methylene blue (MB). Equilibrium adsorption isotherms and kinetics were investigated. The experimental data were analyzed by the Langmuir, Freundlich and Temkin models of adsorption. The adsorption isotherm data were fitted well to Langmuir isotherm and the monolayer adsorption capacity was found to be 70.92 mg/g at 30 degrees C. The kinetic data obtained at different concentrations have been analyzed using a pseudo-first-order, pseudo-second-order equation and intraparticle diffusion equation. The experimental data fitted very well the pseudo-second-order kinetic model.

  7. Preparation and Adsorptive Capacity of AM-g-CCMC%AM-g-CCMC树脂的制备及其吸附性能

    Institute of Scientific and Technical Information of China (English)

    石亮; 张晓梅; 陈超越; 罗再刚

    2016-01-01

    以交联羧甲基纤维素(CCMC)、丙烯酰胺(AM)为原料,过硫酸钾为引发剂,N,N'–亚甲基双丙烯酰胺为交联剂,通过微波辐射法制备了吸水性树脂丙烯酰胺接枝交联羧甲基纤维素(AM–g–CCMC)。研究了溶液pH值、盐溶液浓度对AM–g–CCMC树脂吸水倍率的影响;同时考察了染料pH值、吸附时间、染料浓度、吸附剂浓度对树脂吸附量[对碱性品红(BF)和亚甲基蓝(MB)]的影响。结果表明,AM–g–CCMC对去离子水和浓度为0.154 mol/L的NaCl,CaCl2,FeCl3溶液的最大吸水倍率分别为1735,165,82,43 g/g;在20℃,浓度0.25 g/L条件下,AM–g–CCMC对BF和MB的最大吸附量分别为370 mg/g和323.4 mg/g。同时对该树脂的循环利用性能进行了初步研究。结果表明,吸附MB的AM–g–CCMC的再生效果略好于吸附BF的树脂。%Water absorbent resin acrylamide grafted and crosslinked carboxymethyl cellulose (AM-g-CCMC) was prepared by aqueous solution polymerization through microwave radiation method using crosslinked carboxymethyl cellulose (CCMC) and acrylamide (AM) as raw materials,potassium sulfate as initiator,N,N'–methylene bisacrylamide as crosslinking agent. The effects of pH,saltsolution concentration on the water absorption and the effects of adsorption time,dye concentration,and the ratio of solid-to-liquid on the adsorption capacity of the resin for fuchsin (BF) and methylene blue (MB) were studied. The results show that the maximum absorption rates of the resins are 1 735,165,82,43 g/g in distilled water,NaCl,CaCl2 and FeCl3 solution with the same concentration of 0.154 mol/L,respectively. At concentration of 0.25 g/L,the saturated adsorption capacities of resin to BF and MB are 370 mg/g and 323.4 mg/g,respectively at 20℃. At the same time,the recycling performance of the water absorbent resin was studied. The results show that the regeneration effect of AM-g-CCMC absorbed by MB is slightly better

  8. Morphology and adsorption of chromium ion on uranium 1,2,4,5-benzenetetracarboxylic acid metal organic framework (MOF

    Directory of Open Access Journals (Sweden)

    Vala Remy M.K.

    2016-01-01

    Full Text Available In this paper, we report the synthesis of metal organic framework of uranium 1,2,4,5-benzene tetracarboxylic acid (U-H4btec MOF by solvothermal method. The obtained MOF was characterized by Fourier transform infrared spectroscopy (FTIR, Scanning electron microscopy (SEM, Transmission electron microscopy (TEM, X-ray diffraction spectroscopy (XRD, Energy dispersive spectroscopy (EDS, thermogravimetric and differential thermogravimetric analysis (TGA/DTA. The morphology of the uranium 1,2,4,5-benzene tetracarboxylic acid MOF observed by SEM, revealed the presence of flaky porous structure. Adsorption of Cr3+ from aqueous solution onto the uranium 1,2,4,5-benzene tetracarboxylic acid MOF was systematically studied. Langmuir and Freundlich adsorption isotherms were applied to determine the adsorption capacity of the MOF to form a monolayer. Kinetic determination of the adsorption of Cr3+ suggested both chemisorption and physisorption probably due to the presence of carbonyl groups within the MOF and its porous structure.

  9. Fabrication of CMC-g-PAM Superporous Polymer Monoliths via Eco-Friendly Pickering-MIPEs for Superior Adsorption of Methyl Violet and Methylene Blue

    Directory of Open Access Journals (Sweden)

    Feng Wang

    2017-06-01

    Full Text Available A series of superporous carboxymethylcellulose-graft-poly(acrylamide/palygorskite (CMC-g-PAM/Pal polymer monoliths presenting interconnected pore structure and excellent adsorption properties were prepared by one-step free-radical grafting polymerization reaction of CMC and acrylamide (AM in the oil-in-water (O/W Pickering-medium internal phase emulsions (Pickering-MIPEs composed of non-toxic edible oil as a dispersion phase and natural Pal nanorods as stabilizers. The effects of Pal dosage, AM dosage, and co-surfactant Tween-20 (T-20 on the pore structures of the monoliths were studied. It was revealed that the well-defined pores were formed when the dosages of Pal and T-20 are 9–14 and 3%, respectively. The porous monolith can rapidly adsorb 1,585 mg/g of methyl violet (MV and 1,625 mg/g of methylene blue (MB. After the monolith was regenerated by adsorption-desorption process for five times, the adsorption capacities still reached 92.1% (for MV and 93.5% (for MB of the initial maximum adsorption capacities. The adsorption process was fitted with Langmuir adsorption isotherm model and pseudo-second-order adsorption kinetic model very well, which indicate that mono-layer chemical adsorption mainly contribute to the high-capacity adsorption for dyes. The superporous polymer monolith prepared from eco-friendly Pickering-MIPEs shows good adsorption capacity and fast adsorption rate, which is potential adsorbent for the decontamination of dye-containing wastewater.

  10. Fabrication of CMC-g-PAM Superporous Polymer Monoliths via Eco-Friendly Pickering-MIPEs for Superior Adsorption of Methyl Violet and Methylene Blue

    Science.gov (United States)

    Wang, Feng; Zhu, Yongfeng; Wang, Wenbo; Zong, Li; Lu, Taotao; Wang, Aiqin

    2017-01-01

    A series of superporous carboxymethylcellulose-graft-poly(acrylamide)/palygorskite (CMC-g-PAM/Pal) polymer monoliths presenting interconnected pore structure and excellent adsorption properties were prepared by one-step free-radical grafting polymerization reaction of CMC and acrylamide (AM) in the oil-in-water (O/W) Pickering-medium internal phase emulsions (Pickering-MIPEs) composed of non-toxic edible oil as a dispersion phase and natural Pal nanorods as stabilizers. The effects of Pal dosage, AM dosage, and co-surfactant Tween-20 (T-20) on the pore structures of the monoliths were studied. It was revealed that the well-defined pores were formed when the dosages of Pal and T-20 are 9–14 and 3%, respectively. The porous monolith can rapidly adsorb 1,585 mg/g of methyl violet (MV) and 1,625 mg/g of methylene blue (MB). After the monolith was regenerated by adsorption-desorption process for five times, the adsorption capacities still reached 92.1% (for MV) and 93.5% (for MB) of the initial maximum adsorption capacities. The adsorption process was fitted with Langmuir adsorption isotherm model and pseudo-second-order adsorption kinetic model very well, which indicate that mono-layer chemical adsorption mainly contribute to the high-capacity adsorption for dyes. The superporous polymer monolith prepared from eco-friendly Pickering-MIPEs shows good adsorption capacity and fast adsorption rate, which is potential adsorbent for the decontamination of dye-containing wastewater. PMID:28642862

  11. Adsorption equilibrium of citric acid from supercritical carbon dioxide/ethanol on cyano column

    Institute of Scientific and Technical Information of China (English)

    Huisheng L; Guoqing Wang; Minhua Zhang; Zhongfeng Geng; Miao Yang; Yanpeng Sun

    2015-01-01

    Supercritical adsorption equilibrium has a significant role in defining supercritical adsorption behavior. In this paper, the adsorption equilibrium of citric acid from supercritical CO2/ethanol on a cyano column was systemat-ical y investigated with the elution by characteristic point method. Equilibrium loading was obtained at 313.15 K and 321.15 K with supercritical CO2/ethanol densities varying from 0.7068 g·cm−3 to 0.8019 g·cm−3. The exper-imental results showed that the adsorption capacity of citric acid decreased with increasing temperature and in-creasing density of the supercritical CO2/ethanol mobile phase. The adsorption equilibrium data were fitted wel by the Quadratic Hill isotherm model and the isotherms showed anti-Langmuir behavior. The monolayer satura-tion adsorption capacity of citric acid is in the range of 44.54 mg·cm−3 to 64.66 mg·cm−3 with an average value of 56.86 mg·cm−3.

  12. 改性沸石和膨润土对氟离子吸附性能研究%Study on the adsorption capacity of modified zeoIite and bentonite for fIuoride ions

    Institute of Scientific and Technical Information of China (English)

    赵文生; 孙彦红; 赵万明

    2016-01-01

    High-temperature roasting,sulphuric acid,and magnesium sulphate have been used for the modification of natural zeolite and bentonite. The effects of three kinds of modification methods on the adsorption capacity of zeo-lite and bentonite for fluoride ions have been investigated. The experimental results show that high-temperature roasting,sulphuric acid modification and magnesium sulphate modification can all increase the adsorption capacity of zeolite and bentonite for fluoride ions. The adsorption of modified zeolite for fluoride ions complies with Langmuir isothermal adsorption;the adsorption of sulphuric acid modified and magnesium sulphate modified bentonite for fluo-ride ions can be described with both Langmuir model and Freundlich model;while the adsorption of high-tempera-ture roasting modified bentonite for fluoride ions complies with Freundlich model.%选用高温焙烧、硫酸、硫酸镁改性天然沸石和膨润土,考察了3种改性方法对沸石和膨润土吸附氟离子性能的影响。实验结果表明,高温焙烧、硫酸改性和硫酸镁改性均提高了沸石和膨润土对氟离子的吸附能力。改性沸石对氟离子的吸附符合Langmuir等温吸附模型;硫酸改性、硫酸镁改性膨润土对氟离子的吸附可用Langmuir模型和Freundlich模型描述,高温焙烧改性膨润土对氟离子的吸附则符合Freundlich模型。

  13. Ti-decorated graphitic-C{sub 3}N{sub 4} monolayer: A promising material for hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Weibin [Department of Physics, Dongguk University, Seoul 04620 (Korea, Republic of); Zhang, Zhijun [Department of Physics, Dongguk University, Seoul 04620 (Korea, Republic of); School of Materials Science and Engineering, Shanghai University, Shanghai 200072 (China); Zhang, Fuchun [College of Physics and Electronic Information, Yan’an University, Yan’an 716000 (China); Yang, Woochul, E-mail: wyang@dongguk.edu [Department of Physics, Dongguk University, Seoul 04620 (Korea, Republic of)

    2016-11-15

    Highlights: • Ti atoms are stably decorated at the triangular N hole in g-C{sub 3}N{sub 4} with an adsorption energy of −7.58 eV. • Electron redistribution of Ti-adsorbed porous g-C{sub 3}N{sub 4} significantly enhanced hydrogen adsorption up to five H{sub 2} molecules at each Ti atom. • The hydrogen capacity of the Ti-decorated g-C{sub 3}N{sub 4} system reaches up to 9.70 wt%. • All H{sub 2} absorbed in the Ti/g-C{sub 3}N{sub 4} system can be released at 393 K according to the molecular dynamic analysis. • Ti/g-C{sub 3}N{sub 4} as a hydrogen storage system is suitable and reversible at the temperature range required for practical applications. - Abstract: Ti-decorated graphitic carbon nitride (g-C{sub 3}N{sub 4}) monolayer as a promising material system for high-capacity hydrogen storage is proposed through density functional theory calculations. The stability and hydrogen adsorption of Ti-decorated g-C{sub 3}N{sub 4} is analyzed by computing the adsorption energy, the charge population, and electronic density of states. The most stable decoration site of Ti atom is the triangular N hole in g-C{sub 3}N{sub 4} with an adsorption energy of −7.58 eV. The large diffusion energy barrier of the adsorbed Ti atom of ∼6.00 eV prohibits the cluster formation of Ti atoms. The electric field induced by electron redistribution of Ti-adsorbed porous g-C{sub 3}N{sub 4} significantly enhanced hydrogen adsorption up to five H{sub 2} molecules at each Ti atom with an average adsorption energy of −0.30 eV/H{sub 2}. The corresponding hydrogen capacity reaches up to 9.70 wt% at 0 K. In addition, the hydrogen capacity is predicted to be 6.30 wt% at 233 K and all adsorbed H{sub 2} are released at 393 K according to molecular dynamics simulation. Thus, the Ti-decorated g-C{sub 3}N{sub 4} monolayer is suggested to be a promising material for hydrogen storage suggested by the DOE for commercial applications.

  14. Adsorptive potential of cationic Basic Yellow 2 (BY2) dye onto natural untreated clay (NUC) from aqueous phase: Mass transfer analysis, kinetic and equilibrium profile

    Science.gov (United States)

    Öztürk, A.; Malkoc, E.

    2014-04-01

    In this work, natural untreated clay (NUC) was studied for the removal of Basic Yellow 2 (BY2) from aqueous solution in batch system. The effects of initial BY2 concentration, contact time, solution temperature and solution pH on BY2 adsorption were investigated. Nitrogen sorption measurements were employed to investigate the variation in surface and pore properties after dye adsorption. The adsorbent was characterized by means of FTIR, PSD, TEM, XRD and BET analysis. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Temkin and Scatchard isotherm models. The maximum monolayer adsorption capacity was found to be 833.33 mg/g at 25 °C (at room temperature). The pseudo-second-order kinetic model provided the best fit to the experimental datas compared with pseudo-first-order kinetic adsorption models. To explain mass transfer mechanism of BY2 adsorption, obtained experimental datas were applied Weber and Morris model, Body and Frusawa and Smith models. The results show that the adsorption process is controlled by film diffusion. The thermodynamic parameters such as, Gibbs free energy changes (ΔG°), standard enthalpy change (ΔH°) and standard entropy change (ΔS°) were determined. Adsorption of BY2 on NUC is exothermic and spontaneous in nature. The calculated activation energy of adsorption was found to be 5.24 kJ/mol for BY2. This value indicates that the adsorption process is a physisorption.

  15. Adsorption of Rh(III) complexes from chloride solutions obtained by leaching chlorinated spent automotive catalysts on ion-exchange resin Diaion WA21J

    Energy Technology Data Exchange (ETDEWEB)

    Shen Shaobo, E-mail: shaoboshen@metall.ustb.edu.cn [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China); Department of Physical Chemistry, School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Pan Tonglin; Liu Xinqiang; Yuan Lei [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China); Wang Jinchao [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China); Department of Physical Chemistry, School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhang Yongjian; Guo Zhanchen [Key Laboratory of Ecological and Recycling Metallurgy, Ministry of Education of China, Beijing 100083 (China)

    2010-07-15

    It was found that Rh, Pd and Pt contained in the spent ceramic automotive catalysts could be effectively extracted by dry chlorination with chlorine. In order to concentrate Rh(III) ions contained in the chloride solutions obtained, thermodynamic and kinetics studies for adsorption of Rh(III) complexes from the chloride solutions on an anionic exchange resin Diaion WA21J were carried out. Rh, Pd, Pt, Al, Fe, Si, Zn and Pb from the chloride solution could be adsorbed on the resin. The distribution coefficients (K{sub d}) of Rh(III) decreased with the increase in initial Rh(III) concentration or in adsorption temperature. The isothermal adsorption of Rh(III) was found to fit Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich models under the adsorption conditions. The maximum monolayer adsorption capacities Q{sub max} based on Langmuir adsorption isotherms were 6.39, 6.61 and 5.81 mg/g for temperatures 18, 28 and 40 deg. C, respectively. The apparent adsorption energy of Rh was about -7.6 kJ/mol and thus Rh(III) adsorption was a physical type. The experimental data obtained could be better simulated by pseudo-first-order kinetic model and the activation energy obtained was 6.54 J/mol. The adsorption rate of Rh(III) was controlled by intraparticle diffusion in most of time of adsorption process.

  16. Batch Study for Insecticide Carbofuran Adsorption onto Palm-Oil-Fronds-Activated Carbon

    Directory of Open Access Journals (Sweden)

    Jassem M. Salman

    2013-01-01

    Full Text Available The adsorption of insecticide, carbofuran from aqueous solution onto activated carbon derived from palm oil fronds (PFAC was investigated through batch study. The effects of both initial concentration and pH of the carbofuran over the range of 25 to 250 mg/L and 2 to 12, respectively, on the adsorption of the prepared PFAC were studied in batch experiments. Equilibrium data were fitted to the Langmuir, the Freundlich, and the Temkin isotherm models. The results obtained from application of these models show that the best fits were achieved with the Langmuir model, and a maximum monolayer adsorption capacity of 164 mg/g was obtained at 30°C. The regeneration efficiency of spent activated carbon was studied and it was found to be 90.0–96.4%. The results indicated that PFAC has good capability as adsorbent for the removal of carbofuran from aqueous solutions.

  17. Study on the adsorption of DNA on the layered double hydroxides (LDHs)

    Science.gov (United States)

    Li, Bin; Wu, Pingxiao; Ruan, Bo; Liu, Paiyu; Zhu, Nengwu

    2014-03-01

    Four kinds of layered double hydroxides (LDHs) were prepared by chemical coprecipitation method and used as DNA adsorbents. Multiple characterization tools such as power X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and Standard electronic modules (SEM) were employed to characterize the LDHs. By examining the effect of initial concentration, solution pH, adsorption experiments were carried out to investigate the adsorption capacities of LDHs for DNA. The results revealed that the LDHs with Mg/Al = 3 had higher ability on adsorbing the DNA and were not affected by pH values. The LDHs exhibited excellent adsorption properties and completely adsorbed DNA within 2 h. The adsorption equilibrium data were fitted to the Langmuir and Freundlich models, showing that the Langmuir model which represented monolayer adsorption had better correlation with the adsorption linear equation. In addition, Circular dichroism (CD) spectrum, UV-vis spectorscopy and agarose gel electrophoresis revealed the integrity of DNA structure, suggesting that there had no damage on the DNA structure during the adsorption process.

  18. Characterization and application of tourmaline and beryl from Brazilian pegmatite in adsorption process with divalent metals

    Institute of Scientific and Technical Information of China (English)

    Denis L.Guerra; Silze P.Oliveira; Ricardo A.R.Silva; Victor Leidens; Adriano C.Batista

    2012-01-01

    In this study,the original tourmaline and beryl mineral samples have been collected from a Brazilian pegmatite.The objective of this study was to examine the adsorption behavior of Brazilian ciclosilicate sampies,towards divalent metals (Pb2+,Mn2+,and Zn2+) in ethanol solution has been studies by a batch technique.The ciclosilicate samples were characterized by elemental analysis,Fourier transform infrared spectroscopy,helium picnometry,mercury porosity,and nitrogen adsorption-desorption.The Langmuir expression for adsorption isotherm was applied in order to determine the adsorption capacity to form a monolayer and the constant related to the adsorption intensity.In aqueous solution there was a significant adsorption increase with the temperature and pronounced synergistic effects were observed.The maximum number of moles adsorbed was determined to be 12.48 and 11.49 mmol/g for systems Pb2+/beryl and Pb2+/tourmaline,respectively.The energetic effects caused by metal cations adsorption were determined through calorimetric titrations.Thermodynamics indicated the existence of favorable conditions for such Pb2+-,Mn2+-,and Zn2+-OH interactions.

  19. Carbonaceous materials for adsorptive refrigerators

    Science.gov (United States)

    Buczek, B.; Wolak, E.

    2012-06-01

    Carbon monoliths prepared from hard coal precursors were obtained. The porous structure of the monoliths was evaluated on the basis of nitrogen adsorption — desorption equilibrium data. The investigated monoliths have a well-developed microporous structure with significant specific surface area (S BET ). Equilibrium studies of methanol vapour adsorption were used to characterize the methanol adsorptive capacity that was determined using a volumetric method. The heat of wetting by methanol was determined in order to estimate the energetic effects of the adsorption process. The results of the investigations show that all monoliths exhibit high adsorption capacity and high heat of wetting with methanol.

  20. Aspects of vapor adsorption on solids

    Science.gov (United States)

    Beaglehole, David

    1997-02-01

    The paper describes three unexpected phenomena which were observed during studies of the vapour adsorption onto solids. A quadratic variation of the adsorption of water onto borosilicate glass is found at low pressures. Water films condensed onto mica start to conduct electricity at a thickness of almost exactly one monolayer, with fluctuations in the conductivity in the region of onset. Diffusion through a background atmosphere slows the adsorption process and asymetrical fluctuations in thickness are observed.

  1. Adsorption and recovery of nonylphenol ethoxylate on a crosslinked beta-cyclodextrin-carboxymethylcellulose polymer.

    Science.gov (United States)

    Bonenfant, Danielle; Niquette, Patrick; Mimeault, Murielle; Hausler, Robert

    2010-01-01

    A study of adsorption/recovery of nonylphenol 9 mole ethoxylate (NP9EO) on a crosslinked beta-cyclodextrin-carboxymethylcellulose (beta-CD-CMC) polymer was carried out by ultraviolet-visible (UV-vis) and Fourier transform infrared (FTIR) spectroscopies. The adsorption was performed in mixtures containing 500 mg of the beta-CD-CMC polymer and aqueous NP9EO solutions at concentrations 12-82 mg/L, whereas the recovery of NP9EO was effectuated by shaking the beta-CD-CMC polymer loaded with methanol. The assays were made at 25 degrees C and atmospheric pressure under agitation. The results have shown that the adsorption is a rapid process and the beta-CD-CMC polymer exhibits a high NP9EO adsorption capacity of 83-92 w% (1.1-6.8 mg NP9EO/g beta-CD-CMC polymer) dependent of the initial NP9EO concentration in liquid phase. This adsorption may involve the formation of an inclusion complex beta-CD-NP9EO and a physical adsorption in the polymer network. The adsorption equilibrium measurements, which were analyzed using the Langmuir isotherm, have indicated a monolayer coverage and the homogeneous distribution of active sites at the surface of the beta-CD-CMC polymer. Moreover, the negative value obtained for the free energy change (-13.2 kJ/mol) has indicated that the adsorption process is spontaneous. In parallel, the beta-CD-CMC polymer exhibited a high NP9EO recovery efficiency of 97 w% that may occur through a decrease of binding strength between beta-CD-CMC polymer and NP9EO. Together, these results suggest that the beta-CD-CMC polymer could constitute a good adsorbent for removing nonylphenol ethoxylates from wastewater due to its high adsorption capacity and non-toxic character of beta-CD and CMC to environment.

  2. Efficient adsorption of both methyl orange and chromium from their aqueous mixtures using a quaternary ammonium salt modified chitosan magnetic composite adsorbent.

    Science.gov (United States)

    Li, Kun; Li, Pei; Cai, Jun; Xiao, Shoujun; Yang, Hu; Li, Aimin

    2016-07-01

    A quaternary ammonium salt modified chitosan magnetic composite adsorbent (CS-CTA-MCM) was prepared by combination of Fe3O4 nanoparticles. Various techniques were used to characterize the molecular structure, surface morphology, and magnetic feature of this composite adsorbent. CS-CTA-MCM was employed for the removal of Cr(VI) and methyl orange (MO), an anionic dye, from water in respective single and binary systems. Compared with chitosan magnetic adsorbent (CS-MCM) without modification, CS-CTA-MCM shows evidently improved adsorption capacities for both pollutants ascribed to the additional quaternary ammonium salt groups. Based on the adsorption equilibrium study, MO bears more affinity to CS-CTA-MCM than Cr(VI) causing a considerable extent of preferential adsorption of dye over metal ions in their aqueous mixture. However, at weak acidic solutions, Cr(VI) adsorption is evidently improved due to more efficient Cr(VI) forms, i.e. dichromate and monovalent chromate, binding to this chitosan-based adsorbent. Thus chromium could be efficient removal together with MO at suitable pH conditions. The adsorption isotherms and kinetics indicate that adsorptions of Cr(VI) and MO by CS-CTA-MCM both follow a homogeneous monolayer chemisorption process. This magnetic adsorbent after saturated adsorption could be rapidly separated from water and easily regenerated using dilute NaOH aqueous solutions then virtually reused with little adsorption capacity loss.

  3. Models of pure CO2 and pure CH4 adsorption on the late paleozoic coals from the Kailuan Coalfield, Hebei, China

    Science.gov (United States)

    Dai, S.; Zhang, B.; Peng, S.; Zhang, X.; Chou, C.

    2009-01-01

    Isothermal adsorption experiments of pure CO2 and CH4 on different coals in rank (the No. 11 Coal from the Linnancang Mine and the No. 9 Coal from the Majiagou Mine) from the Kailuan Coalfield of Hebei Province, China, have been studied. Four different models (Langmuir, BET, D-R, and D-A) were used to fit the experimental data of CO2 and CH4 adsorption and their fitting degree were investigated. The results showed that the adsorption capacity of the Majiagou coal(Ro, ran = 1. 21%) is higher than that of the Linnancang coal (Ro, ran = 0. 58%). The adsorption capacity of CO2 is higher than that of CH4 on the same coal under the same pressure. The adsorption isotherms of pure CO 2 and pure CH4 on the Majiagou coal can be classified as Type I and their fitting errors of curves are very weak; thus the experimental data can be presented using the Langmuir isotherm. However, the adsorption of Linnancang coal is more complicated, and can be presented using D-A model because of its minimum error. Monolayer adsorption occurs during the adsorption of pure CO2 and pure CH4 on the No. 11 Coal and that of pure CH4 on the No. 9 Coal.

  4. Kinetic Modeling and Isotherm Studies for Copper(II Adsorption onto Palm Oil Boiler Mill Fly Ash (POFA as a Natural Low-Cost Adsorbent

    Directory of Open Access Journals (Sweden)

    Abdul Shukor Abdul Aziz

    2013-11-01

    Full Text Available Adsorption characteristics of palm oil boiler mill fly ash (POFA for the removal of Cu(II from aqueous solution were investigated using batch adsorption studies. The effects of relevant parameters such as contact time, solution pH, adsorbent dosage, and initial concentration of copper were examined. Fundamental batch investigations indicated that 90% of the Cu(II was removed in the first 30 min, achieving equilibration after only 270 min of agitation. The Cu(II uptake mechanism is particularly pH- and concentration-dependant, favoring a pH value of 6.0. A decrease in adsorption capacity (qe with an increase in Cu(II removal efficiency (RE % was obtained as the adsorbent dosage increased. The adsorption behavior of Cu(II fit well to the Langmuir isotherm, with a monolayer adsorption capacity of 17 mg/g. The applicability of the Langmuir isotherm suggested the formation of monolayer coverage of Cu(II ions onto equivalent sites of the adsorbent. Kinetics experimental data followed the trend of pseudo second-order kinetics, which is consistent with chemisorption with intraparticle diffusion as one of the rate-determining steps. Therefore, this study indicates that POFA could be used successfully as a natural low-cost adsorbent for Cu(II removal from aqueous solutions.

  5. Liquid phase adsorptions of Rhodamine B dye onto raw and chitosan supported mesoporous adsorbents: isotherms and kinetics studies

    Science.gov (United States)

    Inyinbor, A. A.; Adekola, F. A.; Olatunji, G. A.

    2016-04-01

    Irvingia gabonensis endocarp waste was charred (DNc) and subsequently coated with chitosan (CCDNc). Physicochemical characteristics of the two adsorbents were established, while Fourier transform infrared (FTIR), Scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) surface area methods were further employed for characterization. Efficiencies of the prepared adsorbents in the uptake of Rhodamine B (RhB) from aqueous effluent were investigated and adsorption data were tested using four isotherms and four kinetics models. The BET surface areas of the prepared adsorbent were 0.0092 and 4.99 m2/g for DNc and CCDNc, respectively, and maximum adsorption was recorded at pH between 3 and 4, respectively. While monolayer adsorption dominates the uptake of RhB onto DNc, uptake of RhB onto CCDNc was onto heterogeneous surface. The maximum monolayer adsorption capacities (q max) obtained from the Langmuir equation are 52.90 and 217.39 mg/g for DNc and CCDNc, respectively. Pseudo second order and Elovich kinetic models well described the kinetics of the two adsorption processes. The mean sorption energy (E) calculated from the D-R model and desorption efficiencies suggests that while the uptake of RhB onto DNc was physical in nature, for RhB-CCDNc system chemisorption dominates.

  6. Liquid phase adsorptions of Rhodamine B dye onto raw and chitosan supported mesoporous adsorbents: isotherms and kinetics studies

    Science.gov (United States)

    Inyinbor, A. A.; Adekola, F. A.; Olatunji, G. A.

    2017-09-01

    Irvingia gabonensis endocarp waste was charred (DNc) and subsequently coated with chitosan (CCDNc). Physicochemical characteristics of the two adsorbents were established, while Fourier transform infrared (FTIR), Scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) surface area methods were further employed for characterization. Efficiencies of the prepared adsorbents in the uptake of Rhodamine B (RhB) from aqueous effluent were investigated and adsorption data were tested using four isotherms and four kinetics models. The BET surface areas of the prepared adsorbent were 0.0092 and 4.99 m2/g for DNc and CCDNc, respectively, and maximum adsorption was recorded at pH between 3 and 4, respectively. While monolayer adsorption dominates the uptake of RhB onto DNc, uptake of RhB onto CCDNc was onto heterogeneous surface. The maximum monolayer adsorption capacities ( q max) obtained from the Langmuir equation are 52.90 and 217.39 mg/g for DNc and CCDNc, respectively. Pseudo second order and Elovich kinetic models well described the kinetics of the two adsorption processes. The mean sorption energy ( E) calculated from the D-R model and desorption efficiencies suggests that while the uptake of RhB onto DNc was physical in nature, for RhB-CCDNc system chemisorption dominates.

  7. Solid-supported monolayers and bilayers of amphiphilic ß-Cyclodextrin

    NARCIS (Netherlands)

    Cristiano, Antonella; Lim, C.W.; Rozkiewicz, D.I.; Reinhoudt, David; Ravoo, B.J.

    2007-01-01

    This paper describes the adsorption and spreading of B-cyclodextrin (CD) vesicles on hydrophobic and hydrophilic substrates, which involves a transition from bilayer vesicles to planar molecular monolayers or bilayers. On substrates that are patterned with self-assembled monolayers by microcontact

  8. Electronic storage capacity of ceria: role of peroxide in Aux supported on CeO2(111) facet and CO adsorption.

    Science.gov (United States)

    Liu, Yinli; Li, Huiying; Yu, Jun; Mao, Dongsen; Lu, Guanzhong

    2015-11-07

    Density functional theory (DFT+U) was used to study the adsorption of Aux (x = 1-4) clusters on the defective CeO2(111) facet and CO adsorption on the corresponding Aux/CeO2-x catalyst, in this work Aux clusters are adsorbed onto the CeO2-x + superoxide/peroxide surface. When Au1 is supported on the CeO2(111) facet with an O vacancy, the strong electronegative Au(δ-) formed is not favorable for CO adsorption. When peroxide is adsorbed on the CeO2(111) facet with the O vacancy, Aux was oxidized, resulting in stable Aux adsorption on the defective ceria surface with peroxide, which promotes CO adsorption on the Aux/CeO2-x catalyst. With more Au atoms in supported Aux clusters, CO adsorption on this surface becomes stronger. During both the Au being supported on CeO2-x and CO being adsorbed on Aux/CeO2-x, CeO2 acts as an electron buffer that can store/release the electrons. These results provide a scientific understanding for the development of high-performance rare earth catalytic materials.

  9. Adsorption of iron(III), cobalt(II), and nickel(II) on activated carbon derived from Xanthoceras Sorbifolia Bunge hull: mechanisms, kinetics and influencing parameters.

    Science.gov (United States)

    Zhang, Xiaotao; Hao, Yinan; Wang, Ximing; Chen, Zhangjing

    2017-04-01

    Xanthoceras Sorbifolia Bunge hull activated carbon (XSA) was prepared and characterized by Brunauer-Emmett-Teller analysis, scanning electron microscopy and energy dispersive X-ray (EDX) spectroscopy. The ability of XSA as an adsorbent was investigated for the removal of the iron group ions Fe(III), Co(II), and Ni(II) from aqueous solution. Optimum adsorption parameters were determined based on the initial concentrations of the iron group ions, pH, adsorption temperature, and adsorption time in adsorption studies. The maximum monolayer adsorption capacities were 241.13 mg/g for Fe(III), 126.05 mg/g for Co(II), and 187.96 mg/g for Ni(II), respectively. Adsorption kinetics and isotherms showed that the adsorption process best fitted the nonlinear pseudo-second-order and Langmuir models, and the affinity of the ions for XSA decreased as follows: Fe(III) > Ni(II) > Co(II). Regeneration studies indicated that XSA could be used after several consecutive adsorption/desorption cycles using HNO3. Fourier transform infrared and EDX spectra revealed the chemical adsorption value of XSA as an adsorbent for removing iron group ions from aqueous solutions.

  10. Adsorption capacity for heavy metal ions in wastewater by ultrasonic-modified bentonite%超声波改性膨润土对废水中重金属离子的吸附性能研究

    Institute of Scientific and Technical Information of China (English)

    张雪萍; 马静; 苏国钧

    2014-01-01

    Bentonite has been modified by ultrasonic wave,for the preparation of a series of modified bentonites. The results show that:the adsorption for heavy metal ions Cu2+,Zn2+,Mn2+,Co2+by modified bentonite is better than that by raw bentonite. The longer the ultrasonic time is ,the better the adsorption capacity. The adsorption volume of ul-trasonic-modified bentonite in mixed ion system declines in different degrees ,when compared with single ion system. Modified bentonite is closely related to the adsorption sequence of the four kinds of metal ions and the hydration of heavy metal ions.%超声波对膨润土进行改性制得一系列改性土。研究结果表明:改性土对重金属离子Cu2+、Zn2+、Mn2+、Co2+的吸附好于原土,且超声时间越长吸附性能越好。与单一离子体系比较,超声改性土在混合离子体系中对各离子的吸附量均有不同程度的下降。超声改性土对四种金属离子的吸附顺序与重金属离子的水合能密切相关。

  11. Adsorption of Ni(II) onto Chemically Modified Spent Grated Coconut (Cocos Nucifera)

    Science.gov (United States)

    Hamzah, F. I.; Khalid, K.; Hanafiah, M. A. K. M.

    2017-06-01

    A new adsorbent of plant waste origin from coconut processing food factory was explored for removing Ni(II) from aqueous solutions. Several parameters such as pH, dosage, concentration and contact time were studied to obtain optimum conditions for treatment of Ni(II) contaminated wastewater. Spent grated coconut (Cocos nucifera) treated with sulfuric acid (SSGC) showed good adsorption capacity for Ni(II) ion. The amount adsorbed was affected by solution pH with the highest value achieved at pH 5. Other optimum conditions found were; dosage of 0.02 g, and 60 min of equilibrium time. Ni(II) adsorption obeyed the pseudo-second order kinetic model which suggested that chemisorption mechanism occurred in the adsorption process. The equilibrium data presented a better fitting to the Langmuir isotherm model, an indication that monolayer adsorption occurred onto a homogeneous surface. The maximum adsorption capacity, qmax was 97.09 mg g-1, thus SSGC can be classified as good and comparable with other plant waste adsorbents.

  12. Adsorption/desorption of Direct Yellow 28 on apatitic phosphate: Mechanism, kinetic and thermodynamic studies

    Directory of Open Access Journals (Sweden)

    H. El Boujaady

    2014-10-01

    Full Text Available In this study, the adsorption potential of apatitic tricalcium phosphate for the removal of Direct Yellow 28 (DY28 from aqueous solution has been investigated by using batch mode experiments. The effects of different parameters such as pH, adsorbent dosage, initial dye concentration, contact time, addition of ions and temperature have been studied to understand the adsorption behavior of the adsorbent under various conditions. The adsorbent has been characterized by pHzpc measurement, chemical analyses, FTIR, XRD and TEM. The Langmuir and Freundlich models are found to be the best to describe the equilibrium isotherm data, with a maximum monolayer adsorption capacity of 67.02 mg g−1. Thermodynamic parameters including the Gibbs free energy ΔG, enthalpy ΔH, and entropy ΔS have revealed that the adsorption of DY28 on the apatitic tricalcium phosphate is feasible, spontaneous and endothermic. Among the kinetic models tested for apatitic tricalcium phosphate, the pseudo-second-order model fits the kinetic data well. The introduction of orthophosphate ions in the medium causes a decrease of adsorption. The addition of Ca2+ ions favors the adsorption. The results of this study have demonstrated the effectiveness and feasibility of the apatitic tricalcium phosphate for the removal of DY28 from aqueous solution.

  13. Adsorption characteristics of trace levels of bromate in drinking water by modified bamboo-based activated carbons.

    Science.gov (United States)

    Chen, Ho-Wen; Chuang, Yen Hsun; Hsu, Cheng-Feng; Huang, Winn-Jung

    2017-09-19

    This study was undertaken to investigate the adsorption kinetics and isotherms of bromate (BrO3(-)) on bamboo charcoals that are activated with nitrogen and water vapor. Bamboo-based activated carbon (AC) was dipped in acid and oxidized in a mixture of potassium permanganate and sulfuric acid. Oxidation treatment considerably improved the physicochemical properties of AC, including purity, pore structure and surface nature, significantly enhancing BrO3(-) adsorption capacity. AC with many oxygenated groups and a high mesopore volume exhibited a particularly favorable tendency for BrO3(-) adsorption. Its adsorption of BrO3(-) is best fitted using Langmuir isotherm, and forms a monolayer. A kinetic investigation revealed that the adsorption of BrO3(-) by the ACs involved chemical sorption and was controlled by intra-particle diffusion. The competitive effects of natural organic matter (NOM) on AC were evaluated, and found to reduce the capacity of carbon to adsorb BrO3(-). Residual dissolved ozone reacted with AC, reducing its capacity to absorb BrO3(-). Proper dosing and staging of the ozonation processes can balance the ozone treatment efficiency, BrO3(-) formation, and the subsequent removal of BrO3(-).

  14. Characterization of sorption properties of selected soils from Lublin region by using water vapour adsorption method

    Science.gov (United States)

    Skic, Kamil; Boguta, Patrycja; Sokołowska, Zofia

    2016-04-01

    *The studies were carried out within the framework of a research project. The project was financed from funds of National Science Center on the base of decision number DEC-2013/11/D/NZ9/02545 Among many methods proposed to study sorption properties of soils an analysis of adsorption/ desorption isotherm is probably the easiest and most convenient one. It characterizes both quantity and quality of mineral and organic components and also their physical and physicochemical properties. The main aim of this study is comparison of sorption properties of selected Polish soils by using water vapour adsorption method. Samples were taken from the depth of 0-20 cm, from the Lublin region, eastern Poland. Soils were selected on the basis of their different physicochemical properties and were classified as: Haplic Fluvisol, Haplic Chernozem, Mollic Gleysol, Rendzic Phaeozem, Stagnic Luvisol, Haplic Cambisol (WG WRB 2006). Data taken from experimental adsorption isotherms were used to determine parameters of monolayer capacity, specific surface area and the total amount of vapour adsorbed at relative pressure of 0.974. Obtained adsorption and desorption isotherms reviled that adsorbate molecules interacted with the soil particles in different extent. Similar monolayer capacity was observed for Haplic Fluvisol, Haplic Chernozem and Stagnic Luvisol, while for Mollic Gleysol was more than 4 times higher. Mollic Gleysol was also characterized by highest values of specific surface area as well as quantity of adsorbed vapour at relative pressure of 0.974. Higher sorption was caused by presence of soil colloids which contains functional groups of a polar nature (mainly hydroxyls, phenolic and carboxyls). These groups similarly to silicates, oxides, hydratable cations as well as electric charge form adsorption centres for water vapour molecules.

  15. Adsorption and magnetic removal of neutral red dye from aqueous solution using Fe{sub 3}O{sub 4} hollow nanospheres

    Energy Technology Data Exchange (ETDEWEB)

    Iram, Mahmood, E-mail: iram@home.ipe.ac.cn [Key Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190 (China); Guo, Chen [Key Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190 (China); Guan Yueping [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Ishfaq, Ahmad [Institute of Applied Mathematics, Academy of Mathematics and System Science, Chinese Academy of Science, Beijing 100190 (China); Liu Huizhou [Key Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190 (China)

    2010-09-15

    Fe{sub 3}O{sub 4} hollow nanospheres were prepared via a simple one-pot template-free hydrothermal method and were fully characterized. These magnetic spheres have been investigated for application as an adsorbant for the removal of dye contaminants from water. Because of the high specific surface area, nano-scale particle size, and hollow porous material, Fe{sub 3}O{sub 4} hollow spheres showed favorable adsorption behavior for Neutral red. Factors affecting adsorption, such as, initial dye concentration, pH and contact time were evaluated. Langmuir and the Freundlich adsorption isotherms were selected to explicate the interaction of the dye and magnetic adsorbant. The characteristic parameters for each isotherm have been determined. The overall trend followed an increase of the sorption capacity with increasing dye concentration with a maximum of 90% dye removal. The monolayer adsorption capacity of magnetic hollow spheres (0.05 g) for NR in the concentration range studied, as calculated from the Langmuir isotherm model at 25 deg. C and pH 6, was found to be 105 mg g{sup -1}. Adsorption kinetic followed pseudo-second-order reaction kinetics. Thermodynamic study showed that the adsorption processes are spontaneous and endothermic. The combination of the superior adsorption and the magnetic properties of Fe{sub 3}O{sub 4} nanospheres can be useful as a powerful separation tool to deal with environmental pollution.

  16. Microwave-assisted preparation and adsorption performance of activated carbon from biodiesel industry solid reside: influence of operational parameters.

    Science.gov (United States)

    Foo, K Y; Hameed, B H

    2012-01-01

    Preparation of activated carbon has been attempted using KOH as activating agent by microwave heating from biodiesel industry solid residue, oil palm empty fruit bunch (EFBAC). The significance of chemical impregnation ratio (IR), microwave power and activation time on the properties of activated carbon were investigated. The optimum condition has been identified at the IR of 1.0, microwave power of 600 W and activation time of 7 min. EFBAC was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy and nitrogen adsorption isotherm. The surface chemistry was examined by zeta potential measurement, determination of surface acidity/basicity, while the adsorptive property was quantified using methylene blue as dye model compound. The optimum conditions resulted in activated carbon with a monolayer adsorption capacity of 395.30 mg/g and carbon yield of 73.78%, while the BET surface area and total pore volume were corresponding to 1372 m2/g and 0.76 cm3/g, respectively.

  17. Membrane Insertion by Trichosanthin Using the Monolayer Method

    Institute of Scientific and Technical Information of China (English)

    薛毅; 夏晓峰; 隋森芳

    2003-01-01

    A monolayer technique was used to investigate the interaction between the ribosome inactivating protein trichosanthin (TCS) and phospholipid membrane.The adsorption experiments show that the negatively charged 1,2-dipalmitoyl-sn-glycerol-3-phosphoglycerol (DPPG) causes obvious enrichment of TCS beneath the monolayer, indicating electrostatic attraction between TCS and the negatively charged phospholipid.When TCS was incorporated into the DPPG monolayer at low pH, it could not be completely squeezed out until the monolayer collapsed.The results suggest that the electrostatic attraction and the hydrophobic force are involved in the interaction between TCS and phospholipids at different stages.These findings may be correlated with the membrane translocation mechanism of TCS.

  18. Fracture Characteristics of Monolayer CVD-Graphene

    Science.gov (United States)

    Hwangbo, Yun; Lee, Choong-Kwang; Kim, Sang-Min; Kim, Jae-Hyun; Kim, Kwang-Seop; Jang, Bongkyun; Lee, Hak-Joo; Lee, Seoung-Ki; Kim, Seong-Su; Ahn, Jong-Hyun; Lee, Seung-Mo

    2014-03-01

    We have observed and analyzed the fracture characteristics of the monolayer CVD-graphene using pressure bulge testing setup. The monolayer CVD-graphene has appeared to undergo environmentally assisted subcritical crack growth in room condition, i.e. stress corrosion cracking arising from the adsorption of water vapor on the graphene and the subsequent chemical reactions. The crack propagation in graphene has appeared to be able to be reasonably tamed by adjusting applied humidity and stress. The fracture toughness, describing the ability of a material containing inherent flaws to resist catastrophic failure, of the CVD-graphene has turned out to be exceptionally high, as compared to other carbon based 3D materials. These results imply that the CVD-graphene could be an ideal candidate as a structural material notwithstanding environmental susceptibility. In addition, the measurements reported here suggest that specific non-continuum fracture behaviors occurring in 2D monoatomic structures can be macroscopically well visualized and characterized.

  19. Fe(II)Ti(IV)O3 mixed oxide monolayer at rutile TiO2(011): Structures and reactivities

    Science.gov (United States)

    Wen, Zhan-Hui; Halpegamage, Sandamali; Gong, Xue-Qing; Batzill, Matthias

    2016-11-01

    Mixed-metal oxide monolayer grown at an oxide support is of great potential in applications like heterogeneous catalysis. In this work, the experimentally obtained ordered mixed FeTiO3 oxide monolayer supported by rutile TiO2(011) surface has been carefully studied with density functional theory calculations. The genetic algorithm based optimization scheme has been employed to improve the searching capacity for possible structures, and a well ordered mixed Fe(II)Ti(IV)O3 monolayer oxide structure much more stable than the one proposed previously has been successfully located. The new surface structure consists of uniformly distributed Ti and Fe cations in the ratio of 2:1. The simulated Scanning Tunneling Microscopy image based on this model is well consistent with the experimental one. Our calculations have shown that the O vacancy formation energy is rather high at the surface. We have also studied the adsorption of O2 and CO at the exposed Fe sites on the surface as well as their reactions. The adsorption energies of O2 are generally higher than those of CO. The catalytic cycle of CO oxidation following an Eley-Rideal type mechanism has been located for CO to react with surface adsorbed O2 and O.

  20. Surface chemistry of lipid raft and amyloid Aβ (1-40) Langmuir monolayer.

    Science.gov (United States)

    Thakur, Garima; Pao, Christine; Micic, Miodrag; Johnson, Sheba; Leblanc, Roger M

    2011-10-15

    Lipid rafts being rich in cholesterol and sphingolipids are considered to provide ordered lipid environment in the neuronal membranes, where it is hypothesized that the cleavage of amyloid precursor protein (APP) to Aβ (1-40) and Aβ (1-42) takes place. It is highly likely that the interaction of lipid raft components like cholesterol, sphingomylein or GM1 leads to nucleation of Aβ and results in aggregation or accumulation of amyloid plaques. One has investigated surface pressure-area isotherms of the lipid raft and Aβ (1-40) Langmuir monolayer. The compression-decompression cycles and the stability of the lipid raft Langmuir monolayer are crucial parameters for the investigation of interaction of Aβ (1-40) with the lipid raft Langmuir monolayer. It was revealed that GM1 provides instability to the lipid raft Langmuir monolayer. Adsorption of Aβ (1-40) onto the lipid raft Langmuir monolayer containing neutral (POPC) or negatively charged phospholipid (DPPG) was examined. The adsorption isotherms revealed that the concentration of cholesterol was important for adsorption of Aβ (1-40) onto the lipid raft Langmuir monolayer containing POPC whereas for the lipid raft Langmuir monolayer containing DPPG:cholesterol or GM1 did not play any role. In situ UV-vis absorption spectroscopy supported the interpretation of results for the adsorption isotherms.

  1. Macromolecule simulation and CH4 adsorption mechanism of coal vitrinite

    Science.gov (United States)

    Yu, Song; Yan-ming, Zhu; Wu, Li

    2017-02-01

    The microscopic mechanism of interactions between CH4 and coal macromolecules is of significant practical and theoretical importance in CBM development and methane storage. Under periodic boundary conditions, the optimal energy configuration of coal vitrinite, which has a higher torsion degree and tighter arrangement, can be determined by the calculation of molecular mechanics (MM) and molecular dynamics (MD), and annealing kinetics simulation based on ultimate analysis, 13C NMR, FT IR and HRTEM. Macromolecular stabilization is primarily due to the van der Waals energy and covalent bond energy, mainly consisting of bond torsion energy and bond angle energy. Using the optimal configuration as the adsorbent, GCMC simulation of vitrinite adsorption of CH4 is conducted. A saturated state is reached after absorbing 17 CH4s per coal vitrinite molecule. CH4 is preferentially adsorbed on the edge, and inclined to gathering around the branched chains of the inner vitrinite sites. Finally, the adsorption parameters are calculated through first principle DFT. The adsorbability order is as follows: aromatic structure> heteroatom rings > oxygen functional groups. The adsorption energy order is as follows: Top < Bond < Center, Up < Down. The order of average RDF better reflects the adsorption ability and that of [-COOH] is lower than those of [sbnd Cdbnd O] and [Csbnd Osbnd C]. CH4 distributed in the distance of 0.99-16 Å to functional groups in the type of monolayer adsorption and the average distance order manifest as [sbnd Cdbnd O] (1.64 Å) < [Csbnd Osbnd C] (1.89 Å) < [sbnd COOH] (3.78 Å) < [-CH3] (4.11 Å) according to the average RDF curves. CH4 enriches around [sbnd Cdbnd O] and [Csbnd O-C] whereas is rather dispersed about [-COOH] and [CH3]. Simulation and experiment data are both in strong agreement with the Langmuir and D-A isothermal adsorption model and the D-A model fit better than Langmuir model. Preferential adsorption sites and orientations in vitrinite are

  2. The effect of low-NOx combustion on residual carbon in fly ash and its adsorption capacity for air entrainment admixtures in concrete

    DEFF Research Database (Denmark)

    Pedersen, Kim Hougaard; Jensen, Anker Degn; Dam-Johansen, Kim

    2010-01-01

    been combusted in an entrained flow reactor to test the impact of changes in operating conditions and fuel type on the AEA adsorption of ash and NOx formation. Increased oxidizing conditions, obtained by improved fuel-air mixing or higher excess air, decreased the AEA requirements of the produced ash...

  3. Monitoring the hydration of DNA self-assembled monolayers using an extensional nanomechanical resonator.

    Science.gov (United States)

    Cagliani, Alberto; Kosaka, Priscila; Tamayo, Javier; Davis, Zachary James

    2012-05-08

    We have fabricated an ultrasensitive nanomechanical resonator based on the extensional vibration mode to weigh the adsorbed water on self-assembled monolayers of DNA as a function of the relative humidity. The water adsorption isotherms provide the number of adsorbed water molecules per nucleotide for monolayers of single stranded (ss) DNA and after hybridization with the complementary DNA strand. Our results differ from previous data obtained with bulk samples, showing the genuine behavior of these self-assembled monolayers. The hybridization cannot be inferred from the water adsorption isotherms due to the low hybridization efficiency of these highly packed monolayers. Strikingly, we efficiently detect the hybridization by measuring the thermal desorption of water at constant relativity humidity. This finding adds a new nanomechanical tool for developing a label-free nucleic acid sensor based on the interaction between water and self-assembled monolayers of nucleic acids.

  4. 膨润土的有机改性及吸附性能%Modification of Bentonite and Analysis of Its Adsorptive Capacity

    Institute of Scientific and Technical Information of China (English)

    张秀英

    2011-01-01

    以十六烷基三甲基溴化铵( CTMAB)为改性剂制得有机膨润土,通过X射线衍射图谱分析了有机膨润土的结构,研究了该有机膨润土对亚甲基蓝的吸附效果,结果表明:在浓度为40 mg/L的200 mL亚甲基蓝弱酸性溶液中,加入2 g有机膨润土,常温下震荡吸附40 min,亚甲基蓝的去除率可达到98.69%,远好于钙基膨润土的吸附效果,因此,有机膨润土对亚甲基蓝具有较强的吸附能力.%Organic-bentonite was prepared by using cetyltrimethyl ammonium bromide (CTMAB) as modifier. Its mi-crostructure were characterized by XRD. The adsorption of organic-bentonite on methylene blue was studied. The results showed that the adsorptive percentage of methylene blue reached 98. 69% under the condition of adsorption: thickness of methylene blue is 40 mg/L,the dosage of wastewater and organic-bentonite respective is 200 mL and 2 g,at weakly acidic and reaction time is 40min in room temperature and weakly acidic . The performance of organic-bentonite for adsorption of the methylene blue is better than Ca-bentonite. The adsorption ability of organic-bentonite is strong.

  5. Effect of the β-propiolactone treatment on the adsorption and fusion of influenza A/Brisbane/59/2007 and A/New Caledonia/20/1999 virus H1N1 on a dimyristoylphosphatidylcholine/ganglioside GM3 mixed phospholipids monolayer at the air-water interface.

    Science.gov (United States)

    Desbat, Bernard; Lancelot, Eloïse; Krell, Tino; Nicolaï, Marie-Claire; Vogel, Fred; Chevalier, Michel; Ronzon, Frédéric

    2011-11-15

    The production protocol of many whole cell/virion vaccines involves an inactivation step with β-propiolactone (BPL). Despite the widespread use of BPL, its mechanism of action is poorly understood. Earlier work demonstrated that BPL alkylates nucleotide bases, but its interaction with proteins has not been studied in depth. In the present study we use ellipsometry to analyze the influence of BPL treatment of two H1N1 influenza strains, A/Brisbane/59/2007 and A/New Caledonia/20/1999, which are used for vaccine production on an industrial scale. Analyses were conducted using a mixed lipid monolayer containing ganglioside GM3, which functions as the viral receptor. Our results show that BPL treatment of both strains reduces viral affinity for the mixed monolayer and also diminishes the capacity of viral domains to self-assemble. In another series of experiments, the pH of the subphase was reduced from 7.4 to 5 to provoke the pH-induced conformational change of hemagglutinin, which occurs following endocytosis into the endosome. In the presence of the native virus the pH decrease caused a reduction in domain size, whereas lipid layer thickness and surface pressure were increased. These observations are consistent with a fusion of the viral membrane with the lipid monolayer. Importantly, this fusion was not observed with adsorbed inactivated virus, which indicates that BPL treatment inhibits the first step of virus-membrane fusion. Our data also indicate that BPL chemically modifies hemagglutinin, which mediates the interaction with GM3.

  6. 扬子地区古生界泥页岩吸附性及控制机理%Adsorption capacity and controlling mechanisms of Paleozoic shales in Yangtze region

    Institute of Scientific and Technical Information of China (English)

    徐良伟; 刘洛夫; 刘祖发; 孟召平

    2016-01-01

    As a gas⁃rich shale layer, the Paleozoic in Yangtze region is a main target for shale gas exploration and development in China. Adsorption state is one of the most important occurrence modes of shale gas;hence it is very necessary to study the adsorption capacity and controlling mechanisms of shales. We collected some shale samples from Paleozoic in Yangtze area, and then carried out TOC analysis, Rock⁃Eval, XRD and water content analyses, isother⁃mal adsorption experiments, and ultra⁃high pressure isothermal adsorption experiments. The adsorption properties of shales vary during different ages and in different areas due to the combined effects of TOC content and mineral compo⁃sition. The TOC content and methane adsorption of shales do not have a positive relationship as proposed by previous researchers, because that shale samples are limited and are in the high⁃mature and over⁃mature stages. The methane adsorption isotherms of kerogens in different ages show that older kerogens have a stronger methane adsorption capacity. Removing the effects of organic matter abundance and maturity, the kerogens of typeⅢadsorb more methane than those of typeⅡ. If organic matter abundance and type are the same, the methane adsorption amount of high matu⁃rity kerogen is more than that of low maturity kerogen. Soluble organic matter can dissolve and adsorb methane, and hence improve the methane adsorption capacity of shales. The relationship between clay mineral and methane adsorp⁃tion which is normalized by TOC is not obvious, this is mainly because the samples contain water.Maturity, porosity and permeability may affect the maximum methane adsorption of shales. Compared with low pres⁃sure, the methane adsorption characteristics under high pressure have a certain continuity. There are several influencing factors, which demand deep research to reveal the influence of each single factor on shale adsorption characteristics.%扬子地区古生界地层为富气

  7. Methane adsorption capacity of extracted coals under control of solvent polarity%溶剂极性控制下的煤抽余物吸附甲烷能力研究

    Institute of Scientific and Technical Information of China (English)

    陈润; 王治洋; 秦勇; 王琳琳; 韦重韬; 王优阳

    2015-01-01

    Based upon isothermal methane adsorption on raw and solvent extracted coals, relationship between solvent polarity and methane adsorption capacity change of the coal was analyzed, and the possible geochemical mechanism was discussed from polarity of the solvents. The results show that methane isothermal adsorption curves on the extracted coals follow the Langmuir equation. Extraction with CS2 and C6 H6 enhances methane adsorption capacities on extracted coals, and that with tetrahydrofuran ( THF) and acetone is opposite. There is a negative correlation between methane adsorption capacity change of the coal and the solvent polarity, which can be explained by similarity-intermiscibility theory. The polarities of CS2 and C6 H6 are weaker, which can extract more alkane and aromatic hydrocarbons with nonpolar molecule structure (-CH3 and -CH2-) to increase the adsorbed space of coal surface for methane adsorption. The polarities of THF and acetone are stronger, which can extract more non-hydrocarbon and asphaltene with polar molecule structure (-CHO, -OH and -COOH) to reduce the adsorbed space of coal surface for methane adsorption.%基于原煤和有机溶剂抽余物的等温吸附实验结果,对比分析溶剂极性与其煤抽余物吸附甲烷能力变化关系,探讨抽提溶剂极性差异对煤抽余物吸附甲烷能力控制的地球化学机理。结果表明,煤溶剂抽余物等温吸附甲烷曲线都遵循Langmuir方程,且二硫化碳( CS2)和苯( C6 H6)溶剂抽提作用增大了煤吸附甲烷量,四氢呋喃( THF)和丙酮溶剂抽提作用减小了煤吸附甲烷量。实验发现,煤抽余物吸附甲烷能力变化与抽提溶剂极性成负相关关系,该现象可用相似相容原理解释:CS2和C6 H6溶剂极性较弱,抽提出较多具有非极性结构(-CH3和-CH2-)的烷烃和芳烃,为甲烷在煤表面吸附增多了吸附位而增强了抽余物吸附甲烷能力,THF和丙酮溶剂极性较强,抽提出较

  8. Adsorption of Crystal violet on raw and acid-treated montmorillonite, K10, in aqueous suspension.

    Science.gov (United States)

    Sarma, Gautam Kumar; Sen Gupta, Susmita; Bhattacharyya, Krishna G

    2016-04-15

    Crystal violet is used as a dye in cotton and silk textiles, paints and printing ink. The dye is hazardous and exposure to it may cause permanent injury to the cornea and conjunctiva including permanent blindness, and in severe cases, may lead to respiratory and kidney failure. The present work describes removal of Crystal violet from aqueous solution by adsorption on raw and acid-treated montmorillonite, K10. The clay mineral was treated with 0.25 and 0.50 M sulfuric acid and the resulting materials were characterized by XRD, zeta potential, SEM, FTIR, cation exchange capacity, BET surface area and pore volume measurements. The influences of pH, interaction time, adsorbent amount, and temperature on adsorption were monitored and explained on the basis of physico-chemical characteristics of the materials. Basic pH generally favors adsorption but considerable removal was possible even under neutral conditions. Adsorption was very rapid and equilibrium could be attained in 180 min. The kinetics conformed to second order model. Langmuir monolayer adsorption capacity of raw montmorillonite K10 was 370.37 mg g(-1) whereas 0.25 M and 0.50 M acid treated montmorillonite K10 had capacities of 384.62 and 400.0 mg g(-1) respectively at 303 K. Adsorption was exothermic and decreased in the temperature range of 293-323 K. Thermodynamically, the process was spontaneous with Gibbs energy decreasing with rise in temperature. The results suggest that montmorillonite K10 and its acid treated forms would be suitable for removing Crystal violet from aqueous solution. Copyright © 2016 Elsevier Ltd. All rights reserved.

  9. A New Method For The Simulation Of Lipid Monolayer Dynamics

    CERN Document Server

    Griesbauer, J; Seeger, H M; Schneider, M F

    2010-01-01

    In this paper we present a predictive numerical model to describe dynamic properties of lipid monolayers. Its thermodynamic basis simply assumes a hexagonal lattice which can be occupied by lipids which may be ordered or disordered. Since the lattice sites are translational lose and interconnected by Newtonian springs, dynamic movements of the lipids are included. All necessary parameters directly follow from experiments. This approach allows the calculation of isotherms of lipid monolayers, which can be directly compared to experimentally determined ones, both quantitatively and qualitatively. Apart from that the monolayers heat capacity profile can be calculated, which otherwise cannot be easily extracted.

  10. Cross-linked chitosan/sepiolite composite for the adsorption of methylene blue and reactive orange 16.

    Science.gov (United States)

    Marrakchi, F; Khanday, W A; Asif, M; Hameed, B H

    2016-12-01

    Cross-linked chitosan/sepiolite composite was prepared from sepiolite clay and chitosan, and was cross-linked using epichlorohydrin. Among the various weight ratio percentage of chitosan and sepiolite clay composites, CS50SP50 was selected as the best adsorbent for both methylene blue (MB) and reactive orange 16 (RO 16). At an optimum adsorbent dosage of 0.2g/100mL, the effects of initial dye concentration (25-400mg/L) and pH (3-11) on MB and RO 16 adsorption onto CS50SP50 composite were studied. Monolayer adsorption capacities of CS50SP50 composite for MB and RO 16 were 40.986mg/g and 190.965mg/g, respectively at 30°C. Freundlich, Langmuir and Temkin isotherms applied on the adsorption data for both the dyes reveal that data fitted best for Freundlich model. For both the dyes pseudo-second-order kinetics were found to describe the adsorption process better than pseudo-first-order kinetics. The adsorption capacity of CS50SP50 composite for both the dyes was found better compared to previous studies thus making it potentially low-cost adsorbent for removal of both cationic and reactive dyes. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Magnetic hydrogel beads based on PVA/sodium alginate/laponite RD and studying their BSA adsorption.

    Science.gov (United States)

    Mahdavinia, Gholam Reza; Mousanezhad, Sedigheh; Hosseinzadeh, Hamed; Darvishi, Farshad; Sabzi, Mohammad

    2016-08-20

    In this study double physically crosslinked magnetic hydrogel beads were developed by a simple method including solution mixing of sodium alginate and poly(vinyl alcohol) (PVA) containing magnetic laponite RD (Rapid Dispersion). Sodium alginate and PVA were physically crosslinked by Ca(2+) and freezing-thawing cycles, respectively. Magnetic laponite RD nanoparticles were incorporated into the system to create magnetic response and strengthen the hydrogels. All hybrids double physically crosslinked hydrogel beads were stable under different pH values without any disintegration. Furthermore, adsorption of bovine serum albumin (BSA) on the hydrogel beads was investigated on the subject of pH, ion strength, initial BSA concentration, and temperature. Nanocomposite beads exhibited maximum adsorption capacity for BSA at pH=4.5. The experimental adsorption isotherm data were well followed Langmuir model and based on this model the maximum adsorption capacity was obtained 127.3mgg(-1) at 308K. Thermodynamic parameters revealed spontaneous and monolayer adsorption of BSA on magnetic nanocomposites beads.

  12. On the adsorptive capacity of carbon nano-tubes for low-concentrated erythromycin in water%碳纳米管对水中低浓度红霉素的吸附特性研究

    Institute of Scientific and Technical Information of China (English)

    汪涛; 刘振中; 詹健; 匡彬

    2016-01-01

    The article is to make efforts in studying the multiwalled carbon nanotubes (MWNTs) when they were used as the adsorbents to remove erythromycin (EM) from the water media.At the same time,the gravimetTic method can also adopted for calculating the adsorption isotherm and kinetic curves of EM on to the carbon nanotubes.The experiments we have done demonstrate that it takes only 200 min for MWNTs to reach its equilibrium,though the first 40 min should be taken as the rapid adsorption stage during which the removal efficiency of EM can be expected to increase by a rate of 80%.In addition,the adsorption kinetics and isotherm can also be well described by using a pseudo-second-order rate model and Freundlich isotherm,respectively.In so doing,the pseudo-second-order model proves that the adsorption process can be controlled by the particle diffusion condition both in and outside of the reaction when the Freundlich isotherm is found favorable for the adsorption.Besides,we have managed to find the thermodynamic parameters,such as the standard free energy changes (△G),the standard enthalpy change (△H) and the standard entropy change (△S),indicating that the adsorption of the EM onto the MWNTs is spontaneous and endothermic.Besides,the value of Ea also shows that the strong adsorption of EM on MWNTs is a typical chemical adsorption process.The adsorption capacity of the carbon nanotubes on the erythromycin should be put into the category of chemical bond of π-π.To make it clear,we have done the experiments on the influential factors including the decisive parameters,such as the sorbent type,dosage,temperature,time,pH,humic acids and inorganic salts.The results of our experiments prove that the carbon nanotubes treated through nitric acid can be better than the original ones for its adsorptive capacity for EM tends to increase by over 25%.The results of our experiments have thus verified the presence of the small amount of humic acids and higher pH value from 5 to

  13. Catalytic monolayer voltammetry and in situ scanning tunneling microscopy of copper nitrite reductase on cysteamine-modified Au(111) electrodes

    DEFF Research Database (Denmark)

    Zhang, Jingdong; Welinder, A.C.; Hansen, Allan Glargaard

    2003-01-01

    We have studied the adsorption and electrocatalysis of the redox metalloenzyme blue copper nitrite reductase from Achromobacter xylosoxidans (AxCuNiR) on single-crystal Au(111)-electrode surfaces modified by a self-assembled monolayer of cysteamine. A combination of cyclic voltammetry and in situ...... biotechnology at the monolayer and toward the single-molecule level....

  14. Ab Initio Prediction and Characterization of Mo2C Monolayer as Anodes for Lithium-Ion and Sodium-Ion Batteries.

    Science.gov (United States)

    Sun, Qilong; Dai, Ying; Ma, Yandong; Jing, Tao; Wei, Wei; Huang, Baibiao

    2016-03-17

    Identifying suitable electrodes materials with desirable electrochemical properties is urgently needed for the next generation of renewable energy technologies. Here we report an ideal candidate material, Mo2C monolayer, with not only required large capacity but also high stability and mobility by means of first-principles calculations. After ensuring its dynamical and thermal stabilities, various low energy Li and Na adsorption sites are identified, and the electric conductivity of the host material is also maintained. The calculated minor diffusion barriers imply a high mobility and cycling ability of Mo2C. In addition, the Li-adsorbed Mo2C monolayer possesses a high theoretical capacity of 526 mAh·g(-1) and a low average electrode potential of 0.14 eV. Besides, we find that the relatively low capability of Na-adsorbed Mo2C (132 mAh·g(-1)) arises from the proposed competition mechanism. These results highlight the promise of Mo2C monolayer as an appealing anode material for both lithium-ion and sodium-ion batteries.

  15. Hydrogen sorption in Pd monolayers in alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Martin, M.H. [Departement de chimie, Universite de Sherbrooke, 2500 blvd. de l' Universite, Sherbrooke, Quebec, J1K 2R1 (Canada); Lasia, A. [Departement de chimie, Universite de Sherbrooke, 2500 blvd. de l' Universite, Sherbrooke, Quebec, J1K 2R1 (Canada)], E-mail: a.lasia@usherbrooke.ca

    2009-09-01

    Hydrogen adsorption/absorption at palladium monolayers (ML) deposited on monocrystalline Au(1 1 1) electrode was studied in 0.1 M NaOH solution. H charge isotherms demonstrated that adsorption started at potentials more positive than at thicker nanometric Pd/Au(polycrystal) deposits. Due to 3-dimensional deposit growth, absorption could be seen at all deposits thicker than 1 ML. Besides, H sorption at Pd/Au(1 1 1) monolayers was more reversible than at nanometric Pd/Au(polycrystal) deposits. Strong geometric and electronic effects due to the Au substrate were observed up to 5 Pd ML. Influence of benzotriazole (BTA) on H sorption was also investigated. BTA blocked H adsorption above 250 mV vs. RHE. At less positive potentials adsorbed BTA layer seemed to undergo a reorientation allowing H adsorption. Stationary and dynamic electrochemical impedance spectroscopy was used to obtain double layer capacitance and charge transfer resistance. BTA also promoted kinetically H sorption into Pd/Au(1 1 1) monolayer and Pd/Au(polycrystal) nanometric deposits.

  16. Acid Blue 25 adsorption on base treated Shorea dasyphylla sawdust: Kinetic,isotherm, thermodynamic and spectroscopic analysis

    Institute of Scientific and Technical Information of China (English)

    Megat Ahmad Kamal Megat Hanafiah; Wan Saime Wan Ngah; Shahira Hilwani Zolkafly; Lee Ching Teong; Zafri Azran Abdul Majid

    2012-01-01

    The potential of base treated Shorea dasyphylla (BTSD) sawdust for Acid Blue 25 (AB 25) adsorption was investigated in a batch adsorption process.Various physiochemical parameters such as pH,stirring rate,dosage,concentration,contact time and temperature were studied.The adsorbent was characterized with Fourier transform infrared spectrophotometer,scanning electron microscope and Brunauer,Emmett and Teller analysis.The optimum conditions for AB 25 adsorption were pH 2,stirring rate 500 r/min,adsorbent dosage 0.10 g and contact time 60 min.The pseudo second-order model showed the best conformity to the kinetic,data.The equilibrium adsorption of AB 25 was described by Freundlich and Langmuir,with the latter found to agree well with the isotherm model.The maximum monolayer adsorption capacity of BTSD was 24.39 mg/g at 300 K,estimated from the Langmuir model.Thermodynamic parameters such as Gibbs free energy,enthalpy and entropy were determined.It was found that AB 25 adsorption was spontaneous and exothermic.

  17. Synthesis, characterization, and potential application of Mn2+-intercalated bentonite in fluoride removal: adsorption modeling and mechanism evaluation

    Science.gov (United States)

    Mudzielwana, Rabelani; Gitari, Wilson M.; Akinyemi, Segun A.; Msagati, Titus A. M.

    2017-09-01

    The study synthesizes a low-cost adsorbent made from Mn2+-modified bentonite clay for groundwater defluoridation. The clays were characterized using X-ray diffraction, X-ray fluorescence, scanning electron microscopy, and Fourier transform infrared techniques. The fluoride adsorption capacity of the modified clay was evaluated using batch experiments. The adsorption kinetics results showed that the optimum fluoride (F-) uptake was achieved within the 30 min' contact time. The data fitted well to pseudo-second-order of reaction kinetics indicating that adsorption of F- occurred via chemisorption. In addition, the adsorption isotherm data fitted well to Langmuir isotherm model indicating that adsorption occurred on a mono-layered surface. Maximum F- removal of 57% was achieved from groundwater with an initial F- concentration of 5.4 mg L-1 and natural pH of 8.6 using adsorbent dosage of 1 g/100 mL. Fluoride adsorption occurred through ligands and ion exchange mechanisms. The synthesized adsorbent was successfully regenerated for up to five times. The study shows that Mn2+-intercalated bentonite clay has potential for application in defluoridation of groundwater.

  18. Adsorption of U(VI) ions from aqueous solutions by activated carbon prepared from Antep pistachio (Pistacia vera L.) shells

    Energy Technology Data Exchange (ETDEWEB)

    Donat, Ramazan [Pamukkale Univ., Denizli (Turkey). Dept. of Chemistry; Erden, Kadriye Esen [Pamukkale Univ., Kinikli-Denizli (Turkey). Denizli Vocational School of Technical Sciences

    2017-08-01

    Antep pistachio (Pistacia vera L.) shells an abundant and low cost natural resource in Turkey was used to prepare activated carbon by physiochemical activation and carbon dioxide (CO{sub 2}) atmosphere as the activating agents at 700 C for 2 h. The adsorption equilibrium of U(VI) from aqueous solutions on such carbon has been studied using a batch system. The parameters that affect the U(VI) adsorption, such as particle size of adsorbent, contact time, of pH of the solution, and temperature, have been investigated and conditions have also been optimized. The equilibrium data for U(VI) ions' adsorption onto activated carbon well fitted to the Langmuir equation, with a maximum monolayer adsorption capacity of 8.68 mg/g, The Freundlich and Dubinin-Radushkevich (D-R) isotherms have been applied and the data correlated well with Freundlich model and that the adsorption is physical in nature (E{sub a}=15.46 kJ/mol). Thermodynamic parameters [ΔH{sub s}=11.33 kJ/mol, ΔS=0.084 kJ/molK, ΔG (293.15 K)=-13.29 kJ/mol] showed the endothermic heat of adsorption and the feasibility of the process.

  19. Comparison of the adsorption capacities of an activated-charcoal--yogurt mixture versus activated-charcoal--water slurry in vivo and in vitro

    DEFF Research Database (Denmark)

    Høgberg, Lotte Christine Groth; Christophersen, Anne-Bolette; Christensen, Hanne Rolighed

    2005-01-01

    BACKGROUND: An activated charcoal--yogurt mixture was evaluated in vivo to determine the effect on the gastrointestinal absorption of paracetamol, as compared to activated-charcoal--water slurry. The potential advantage of the activated-charcoal--yogurt mixture is a better palatability and general......, ability to swallow, and overall impression of the mixtures. The time spent to consume the activated charcoal was also registered. In vitro: Activated charcoal, simulated gastric (pH 1.2) or intestinal (pH 7.2) fluid, and paracetamol were mixed with yogurt followed by 1 h incubation. The maximum adsorption...

  20. Adsorption in air treatment; Adsorption en traitement de l'air

    Energy Technology Data Exchange (ETDEWEB)

    Le Cloirec, P. [Ecole des Mines de Nantes, Dept. Systemes Energetiques et Environnement, 44 - Nantes (France)

    2003-01-01

    The aim of this article is to present the concepts and technologies of adsorption in air treatment. The following points are more particularly developed: 1 - approach of mechanisms: gas-solid transfer, equilibrium equations, multi-composed adsorption, adsorption influencing parameters, adsorption-desorption capacities and energies, specific case of hydrogen sulfide, the case of ketones; 2 - adsorbents implemented; 3 - adsorption and dynamical adsorber: flow and pressure drop in a porous medium, breakthrough curves, adsorption capacities, modeling of breakthrough curves; 4 - implementation of adsorber: models, dimensioning and practical operating data, process safety; 5 - regeneration of activated charcoals: reactivation, in-situ thermal regeneration. (J.S.)

  1. Preparation of char from lotus seed biomass and the exploration of its dye removal capacity through batch and column adsorption studies.

    Science.gov (United States)

    Nethaji, S; Sivasamy, A; Kumar, R Vimal; Mandal, A B

    2013-06-01

    Char was obtained from lotus seed biomass by a simple single-step acid treatment process. It was used as an adsorbent for the removal of malachite green dye (MG) from simulated dye bath effluent. The adsorbent was characterized for its surface morphology, surface functionalities, and zero point charge. Batch studies were carried out by varying the parameters such as initial aqueous pH, adsorbent dosage, adsorbent particle size, and initial adsorbate concentration. Langmuir and Freundlich isotherms were used to test the isotherm data and the Freundlich isotherm best fitted the data. Thermodynamic studies were carried out and the thermodynamic parameters such as ∆G, ∆H, and ∆S were evaluated. Adsorption kinetics was carried out and the data were tested with pseudofirst-order model, pseudosecond-order model, and intraparticle diffusion model. Adsorption of MG was not solely by intraparticle diffusion but film diffusion also played a major role. Continuous column experiments were also conducted using microcolumn and the spent adsorbent was regenerated using ethanol and was repeatedly used for three cycles in the column to determine the reusability of the regenerated adsorbent. The column data were modeled with the modeling equations such as Adam-Bohart model, Bed Depth Service Time (BDST) model, and Yoon-Nelson model for all the three cycles.

  2. Preparation of Graphene Oxide Decorated Fe3O4@SiO2 Nanocomposites with Superior Adsorption Capacity and SERS Detection for Organic Dyes

    Directory of Open Access Journals (Sweden)

    Song Yang

    2015-01-01

    Full Text Available The fast detection and removal of organic dyes from contaminated water has become an urgent environmental issue due to their high toxicity, chemical stability, and low biodegradability. In this paper, we have developed graphene oxide decorated Fe3O4@SiO2 (Fe3O4@SiO2-GO as a novel adsorbent aiming at the rapid adsorption and trace analysis of organic dyes followed by surface enhanced Raman scattering (SERS. The structure and morphology of the nanocomposites were characterized by transmission electron microscopy (TEM, Fourier infrared spectrometry (FT-IR, X-ray diffraction (XRD, and vibrating sample magnetometer (VSM. The obtained nanocomposites were used to adsorb methylene blue (MB in aqueous solution based on π-π stacking interaction and electrostatic attraction between MB and GO, and the adsorption behaviors of MB were investigated. Moreover, the obtained nanocomposites with adsorbed dyes were separated from the solution and loaded with silver nanoparticles for SERS detection. These nanocomposites showed superior SERS sensitivity and the lowest detectable concentration was 1.0 × 10−7 M.

  3. Understanding Volumetric and Gravimetric Hydrogen Adsorption Trade-off in Metal-Organic Frameworks.

    Science.gov (United States)

    Gómez-Gualdrón, Diego A; Wang, Timothy C; García-Holley, Paula; Sawelewa, Ruth M; Argueta, Edwin; Snurr, Randall Q; Hupp, Joseph T; Yildirim, Taner; Farha, Omar K

    2017-04-07

    Metal-organic frameworks (MOFs) are porous crystalline materials that are promising for adsorption-based, on-board storage of hydrogen in fuel-cell vehicles. Volumetric and gravimetric hydrogen capacities are the key factors that determine the size and weight of the MOF-filled tank required to store a certain amount of hydrogen for reasonable driving range. Therefore, they must be optimized so the tank is neither too large nor too heavy. Because the goals of maximizing MOF volumetric and gravimetric hydrogen adsorption loadings individually are incompatible, an in-depth understanding of the trade-off between MOF volumetric and gravimetric loadings is necessary to achieve the best compromise between these properties. Here we study, both experimentally and computationally, the trade-off between volumetric and gravimetric cryo-adsorbed hydrogen deliverable capacity by taking an isoreticular series of highly stable zirconium MOFs, NU-1101, NU-1102, and NU-1103 as a case study. These MOFs were studied under recently proposed operating conditions: 77 K/100 bar →160 K/5 bar. We found the difference between highest and lowest measured deliverable capacity in the MOF series to be ca. 40% gravimetrically, but only ca. 10% volumetrically. From our molecular simulation results, we found hydrogen "monolayer" adsorption to be proportional to the surface area, whereas hydrogen "pore filling" adsorption is proportional to the pore volume. Thus, we found that the higher variability in gravimetric deliverable capacity in contrast to the volumetric capacity, occurs due to the proportional relation between gravimetric surface area and pore volume in the NU-110x series in contrast to the inverse relation between volumetric surface area and void fraction. Additionally, we find better correlations with geometric surface areas than with BET areas. NU-1101 presents the highest measured volumetric performance with 46.6 g/L (9.1 wt %), whereas NU-1103 presents the highest gravimetric one

  4. Carbons prepared from Spartina alterniflora and its anaerobically digested residue by H3PO4 activation: characterization and adsorption of cadmium from aqueous solutions.

    Science.gov (United States)

    Wang, Zhengfang; Nie, Er; Li, Jihua; Zhao, Yongjun; Luo, Xingzhang; Zheng, Zheng

    2011-04-15

    Two series of activated carbons were prepared from Spartina alterniflora and from its anaerobically digested residue by H(3)PO(4) activation at various process conditions, and used as adsorbents for the removal of cadmium (II) in aqueous solutions. The surface areas and pore volumes of carbons were derived from adsorption isotherms (N(2) at 77K). The surface chemistry of carbons was investigated by infrared spectroscopy. Comparison study indicated that physicochemical properties of the activated carbons were strongly dependent not only on activation conditions but also on biopolymer contents of precursors. Several isotherm models were investigated and the adsorption isotherm data were best represented by the Langmuir isotherm model, with a maximum monolayer adsorption capacity of 47.85 mg/g at 25 °C. The results showed that the activated carbon produced from S. alterniflora could be employed as a promising adsorbent for removing cadmium (II) from aqueous solutions.

  5. Preparation of High-capacity IDA Chelating Resin and Its Adsorption Properties%高容量亚胺基二乙酸型螯合树脂的制备及吸附性能

    Institute of Scientific and Technical Information of China (English)

    董佳斌; 吴建波; 杨静; 宋玮; 戴小军; 冶正得; 龚波林

    2013-01-01

    A new high-capacity iminodiacetic acid (IDA) chelating resin was synthesized via surface-initiated atom transfer radical polymerization ( SI-ATRP) method. Glycidyl methacrylate ( GMA) was grafted onto the surface of the chloromethyl polystyrene resin by SI-ATRP using the organic metal compound formed in the Cu-Br/2,2'-bipyridine(Bpy) system as catalyst at room temperature. The IDA chelating resin was synthesized by grafting IDA on the surface of polyglycidyl methacrylate ( PGM A) modified polystyrene resin. The chelating resin was characterized by means of elementary analysis, and evaluated in details to determine its adsorption properties and parameters of kinetics and the thermodynamics. The amount of IDA on the surface of polystyrene resin was calculated to be 8. 15 mg/m . Adsorption capacity of copper( II) increased with increasing initial metal ion concentration and temperature, and its highest adsorption capacity was 1339. 66 mg/g at pH = 2. 2. The experimental results showed that the equilibrium adsorption data fitted well to both Langmuir and Freundlich isotherms. The thermodynamic equilibrium functions were also determined. △G<0, △H=270. 60 kJ/mol, △S>0, so the adsorption was spontaneous, endothermic and entropy increasing. The kinetic experimental data were correlated with second-order kinetic model.%以甲基丙烯酸缩水甘油酯(GMA)为单体,氯甲基化的交联聚苯乙烯树脂(CMCPS)为大分子引发剂,CuBr/2,2’-联吡啶(Bpy)为催化剂,采用表面引发原子转移自由基聚合(SI-ATRP)技术,使甲基丙烯酸缩水甘油酯聚合在CMCPS树脂表面,制得了环氧化聚合物.将该聚合物与亚胺基二乙酸(IDA)反应,制备了高容量亚胺基二乙酸型螯合树脂(IDA-PGMA-CMCPS),用元素分析对其进行了表征.考察了螯合树脂对Cu2+的吸附性能及动力学和热力学参数.该螯合树脂表面IDA接枝密度达8.15 mg/m2.研究结果表明,树脂对Cu2+的吸附量随离子浓度和温度的

  6. Rapid and high-capacity ultrasonic assisted adsorption of ternary toxic anionic dyes onto MOF-5-activated carbon: Artificial neural networks, partial least squares, desirability function and isotherm and kinetic study.

    Science.gov (United States)

    Askari, Hanieh; Ghaedi, Mehrorang; Dashtian, Kheibar; Azghandi, Mohammad Hossein Ahmadi

    2017-07-01

    The present paper focused on the ultrasonic assisted simultaneous removal of fast green (FG), eosin Y (EY) and quinine yellow (QY) from aqueous media following using MOF-5 as a metal organic framework and activated carbon hybrid (AC-MOF-5). The structure and morphology of AC-MOF-5 was identified by SEM, FTIR and XRD analysis. The interactive and main effects of variables such as pH, initial dyes concentration (mgL(-1)), adsorbent dosage (mg) and sonication time (min) on removal percentage were studied by central composite design (CCD), subsequent desirability function (DF) permit to achieved real variable experimental condition. Optimized values were found 7.06, 5.68, 7.59 and 5.04mgL(-1), 0.02g and 2.55min for pH, FG, EY and QY concentration, adsorbent dosage and sonication time, respectively. Under this conditions removal percentage were obtained 98.1%, 98.1% and 91.91% for FG, EY and QY, respectively. Two models, namely partial least squares (PLS) and multi-layer artificial neural network (ANN) model were used for building up to construct an empirical model to predict the dyes under study removal behavior. The obtained results show that ANN and PLS model is a powerful tool for prediction of under-study dyes adsorption by AC-MOF-5. The evaluation and estimation of equilibrium data from traditional isotherm models display that the Langmuir model indicated the best fit to the equilibrium data with maximum adsorption capacity of 21.230, 20.242 and 18.621mgg(-1), for FG, EY and QY, respectively, while the adsorption rate efficiently follows the pseudo-second-order model. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Comparison of the adsorption capacities of an activated-charcoal--yogurt mixture versus activated-charcoal--water slurry in vivo and in vitro

    DEFF Research Database (Denmark)

    Høgberg, Lotte Christine Groth; Christophersen, Anne-Bolette; Christensen, Hanne Rolighed

    2005-01-01

    , ability to swallow, and overall impression of the mixtures. The time spent to consume the activated charcoal was also registered. In vitro: Activated charcoal, simulated gastric (pH 1.2) or intestinal (pH 7.2) fluid, and paracetamol were mixed with yogurt followed by 1 h incubation. The maximum adsorption...... paracetamol 50 mg/kg as a simulated overdose. Each study day volunteers were given a standard meal 1 h before paracetamol, then 50 g activated charcoal 1 h later in either of two preparations: standard water slurry or mixed with 400 mL yogurt. Paracetamol serum concentrations were measured using HPLC....... The areas under the concentration-time curve (AUC) of the two preparations were compared and used to estimate the efficacy of each preparation. The palatability of both preparations was evaluated using a visual-analogue scale where the volunteers were asked to evaluate the appearance, smell, flavor, texture...

  8. Adsorption behavior and mechanism of Cr(VI) using Sakura waste from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Wenfang [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Zhao, Yingxin, E-mail: yingxinzhao@tju.edu.cn [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Tianjin Engineering Center of Urban River Eco-Purification Technology, Tianjin 300072 (China); Zheng, Xinyi [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Ji, Min [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Tianjin Engineering Center of Urban River Eco-Purification Technology, Tianjin 300072 (China); Zhang, Zhenya [Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba 3058572 (Japan)

    2016-01-01

    Graphical abstract: The main chemical components of Sakura leaves are cellulose 16.6%, hemicellulose 10.4%, lignin 18.3%, ash 11.4%, and others 43.3%. The adsorption capacity of Cr(VI) onto Sakura leaves can achieve 435.25 mg g{sup −1}, much higher than other similar agroforestry wastes. - Highlights: • Sakura leaves were prepared to remove Cr(VI) from aqueous solution. • The maximum adsorption capacity of Cr(VI) reached 435.25 mg g{sup −1}. • Cr(VI) adsorption fitted pseudo-second-order kinetic model. • Isotherm models indicated Cr(VI) adsorption occurred on a monolayer surface. • The influence order of coexisting ions followed PO{sub 4}{sup 3−} > SO{sub 4}{sup 2−} > Cl{sup −}. - Abstract: A forestall waste, Sakura leave, has been studied for the adsorption of Cr(VI) from aqueous solution. The materials before and after adsorption were characterized by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). To investigate the adsorption performance of Sakura waste, batch experiments were conducted under different adsorbent dosage, contact time, initial concentration of Cr(VI), and co-existing ions. Results showed the data fitted pseudo-second-order better than pseudo-first-order kinetic model. Equilibrium data was analyzed with Langmuir, Freundlich and Redlich–Peterson isotherm models at temperature ranges from 25 °C to 45 °C. The maximum adsorption capacity from the Langmuir model was 435.25 mg g{sup −1} at pH 1.0. The presence of Cl{sup −}, SO{sub 4}{sup 2−} and PO{sub 4}{sup 3−} would lead to an obvious negative effect on Cr(VI) adsorption, and their influence order follows PO{sub 4}{sup 3−} > SO{sub 4}{sup 2−} > Cl{sup −}. The study developed a new way to reutilize wastes and showed a great potential for resource recycling.

  9. Green synthesis of nickel nanoparticles using Ocimum sanctum and their application in dye and pollutant adsorption

    Institute of Scientific and Technical Information of China (English)

    Chitra Jeyaraj Pandian; Rameshthangam Palanivel; Solairaj Dhananasekaran

    2015-01-01

    Nickel nanoparticles as an eco-friendly adsorbent was biosynthesized using Ocimum sanctum leaf extract. The phys-iochemical properties of green synthesized nickel nanoparticles (NiGs) were characterized by UV–Vis spectroscopy (UV–Vis), Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electron Microscope (SEM) and Transmission Electron Microscope (TEM). NiGs were used as adsorbent for the removal of dyes such as crystal violet (CV), eosin Y (EY), orange I (OR) and anionic pol utant nitrate (NO3−), sulfate (SO42−) from aqueous solution. Adsorption capacity of NiGs was examined in batch modes at different pH, contact time, NiG dosage, initial dye and pol utant concentration. The adsorption process was pH dependent and the adsorption capacity increased with increase in contact time and with that of NiG dosage, whereas the adsorption capacity decreased at higher con-centrations of dyes and pol utants. Maximum percentage removal of dyes and pol utants were observed at 40, 20, 30, 10 and 10 mg·L−1 initial concentration of CV, EY, OR, NO3−and SO42−respectively. The maximum adsorption capacities in Langmuir isotherm were found to be 0.454, 0.615, 0.273, 0.795 and 0.645 mg·g−1 at pH 8, 3, 3, 7 and 7 for CV, EY, OR, NO3−and SO42−respectively. The higher coefficients of correlation in Langmuir isotherm sug-gested monolayer adsorption. The mean energies (E), 2.23, 3.53, 2.50, 5.00 and 3.16 kJ·mol−1 for CV, EY, OR, NO3−and SO42−respectively, calculated from the Dubinin–Radushkevich isotherm showed physical adsorption of adsor-bate onto NiGs. Adsorption kinetics data was better fitted to pseudo-second-order kinetics with R2 N 0.870 for al dyes and pol utants. NiGs were found to be an effective adsorbent for the removal of dyes and pol utants from aque-ous solution and can be applied to treat textile and tannery effluents.

  10. Adsorption behavior of lead on aquatic sediments contaminated with cerium dioxide nanoparticles.

    Science.gov (United States)

    Wang, Chao; Fan, Xiulei; Wang, Peifang; Hou, Jun; Ao, Yanhui; Miao, Lingzhan

    2016-12-01

    Aquatic sediments serve as an important sink for engineered nanomaterials (ENMs), such as metal oxide nanoparticles (MeO NPs) and carbon nanotubes (CNTs). Owing to their remarkable properties, ENMs demonstrate significant potential to disturb the adsorption behavior of other contaminants in aquatic sediments, thereby altering the bioavailability and toxicity of these contaminants. Thus far, most studies have investigated the effect of CNTs on the adsorption of other contaminants on sediments. Cerium dioxide nanoparticles (CeO2 NPs), as one of the important MeO NPs, are also inevitably discharged into aquatic sediments because of their widespread use. In this study, we investigated the adsorption behavior of Pb(2+) on sediments spiked with CeO2 NPs at a weight ratio of 5.0%. The results showed that the adsorption rates at three stages occurring during adsorption clearly increase for sediments contaminated with CeO2 NPs. Moreover, the results obtained from the adsorption isotherms indicated that the Langmuir isotherm model best fits the isotherm data for both sediments and those contaminated with CeO2 NPs. After spiking the sediments with CeO2 NPs, the theoretical maximum monolayer adsorption capacity (Qmax) for Pb(2+) increased from 4.433 to 4.995 mg/g and the Langmuir isotherm coefficient (KL) decreased from 8.813 to 7.730 L/g. The effects of CeO2 NPs on the surface charge and pore surface properties of sediments were also studied as these properties affect the adsorption of several chemicals in sediments. The results showed that pHzpc, SBET, Sext, and average pore size of sediments clearly decrease for sediments contaminated with CeO2 NPs. Hence, the strong adsorption capacity of CeO2 NPs and the changes of sediment surface charge and pore surface properties caused by CeO2 NPs are important factors affecting the adsorption behavior of Pb(2+). The potential risk of Pb(2+) in aquatic environment may increase with CeO2 NPs buried in sediments.

  11. Water adsorption on goethite: Application of multilayer adsorption models

    Science.gov (United States)

    Hatch, C. D.; Tumminello, R.; Meredith, R.

    2016-12-01

    Adsorbed water on the surface of atmospheric mineral dust has recently been shown to significantly affect the ability of mineral dust aerosol to act as cloud condensation nuclei. We have studied water adsorption as a function of relative humidity (RH) on goethite (α-FeO(OH)), a common component of atmospheric mineral dust. The goethite surface area and particle size was determined using BET analysis and with N2 as an adsorbate and scanning electron microscopy, respectively. Water adsorption on the sample was monitored using horizontal attenuated total reflectance Fourier transform infrared (HATR-FTIR) spectroscopy equipped with a flow cell. Water content was determined using Beer's law and the optical constants for bulk water. The results were analyzed using Type II adsorption isotherms to model multilayer adsorption, including BET (Brunauer, Emmet and Teller), FHH (Frenkel, Halsey and Hill) and Freundlich. BET fits to experimental data provide parameters of monolayer coverage, while the FHH and Freundlich isotherms provide insights into multilayer adsorption mechanisms. Results indicate that goethite contains 5% H2O by mass at 50% RH, which increases to 12% by mass at 90% RH. Adsorption parameters and experimental results will be presented.

  12. Pb2+ adsorption from aqueous solutions on activated carbons obtained from lignocellulosic residues

    Directory of Open Access Journals (Sweden)

    L. Giraldo

    2008-03-01

    Full Text Available Activated carbons obtained from cane sugar bagasse (ACB, African palm pit (ACP and sawdust (ACS were prepared through an impregnated with HNO3 and thermal treatment in an atmosphere in N2/steam water at 1173 K. Adsorption isotherms of N2 at 77 K and of CO2 at 273 K were determined for the activated carbons for which surface area and pore volume values were from 868 to 1100 m²g-1 and from 0.27 to 0.55cm³ g-1, respectively. These results were correlated, with the ones obtained for adsorption the adsorption isotherms of Pb2+ in aqueous solutions. Impregnation of the lignocellulosic materials with nitric acid produced acid-type activated carbons with total acid site contents between 4.13 and 6.93 mmol g-1 and pH at the point of zero charge values between 2.7 and 4.1, which were within range of the adsorption, at different pH values, since they determined, the surface charge of the activated carbons. Adsorption isotherms of Pb2+ at different pH values (2-8 at 298 K were determined. The ion adsorption capacity on ACB, ACP and ACS were 13.7, 15.2 and 17.5 mg.g-1, respectively. Experimental data were fitted to the Langmuir and Freundlich models and all cases the former fit better. The highest values for the quantity adsorbed on the monolayer, qm, were at pH 4, whereas the surface, charge of activated carbons was negative and the lead species mainly present was Pb2+. For higher pHs, the quantity of Pb2+ adsorbed decreased, and this had an important effect on adsorption, the surface characteristics of the solids and the hydroxilated lead species that were formed in the system.

  13. Copper adsorption in tropical oxisols

    Directory of Open Access Journals (Sweden)

    Silveira Maria Lucia Azevedo

    2003-01-01

    Full Text Available Cu adsorption, at concentrations between 0 to 800 mg L-1, was evaluated in surface and subsurface samples of three Brazilian soils: a heavy clayey-textured Rhodic Hapludalf (RH, a heavy clayey-textured Anionic ''Rhodic'' Acrudox (RA and a medium-textured Anionic ''Xanthic'' Acrudox (XA. After adsorption, two consecutive extractions were performed to the samples which received 100 mg L-1 copper. Surface samples adsorbed higher amounts of Cu than the subsurface, and exhibited lower Cu removed after the extractions, reinforcing the influence of the organic matter in the reactions. Cu adsorption was significant in the subsurface horizons of the Oxisols, despite the positive balance of charge, demonstrating the existence of mechanisms for specific adsorption, mainly related to the predominance of iron and aluminum oxides in the mineral fractions. In these samples, Cu was easily removed from the adsorption sites. RH demonstrated a higher capacity for the Cu adsorption in both horizons.

  14. Photoresponsive Wettability in Monolayer Films from Sinapinic Acid

    Directory of Open Access Journals (Sweden)

    Cleverson A. S. Moura

    2013-01-01

    Full Text Available Sinapinic acid is an interesting material because it is both antioxidant and antibacterial agent. In addition, when illuminated with ultraviolet light, it can exhibit the so-called photodimerization process. In this paper, we report on the investigation of monolayer films from 3,5-dimethoxy-4-hydroxycinnamic acid (sinapinic acid, SinA deposited onto poly(allylamine hydrochloride, PAH, films. SinA monolayers were prepared by using the layer-by-layer (LbL self-assembly technique. Adsorption kinetics curves were well fitted by a biexponential function suggesting that the adsorption process is determined by two mechanisms: nucleation and growth of aggregates. By using wetting contact angle analysis, we have found that SinA monolayers exhibit photoresponsive wettability under UV irradiation (365 nm; that is, wettability decreases with increasing UV irradiation time. The photoresponse of wettability was attributed to photodimerization process. This hypothesis was supported by the dependence of surface morphological structure and absorption on UV irradiation time. The mechanism found in the well-known transcinnamic acid crystals is used to explain the photodimerization process in SinA monolayers.

  15. Competitive adsorption of heavy metal ions on peat

    Institute of Scientific and Technical Information of China (English)

    LIU Zhi-rong; ZHOU Li-min; WEI Peng; ZENG Kai; WEN Chuan-xi; LAN Hui-hua

    2008-01-01

    The uptake capacities, and the adsorption kinetics, of copper, Cu(Ⅱ), nickel, Ni(Ⅱ), and cadmium, Cd(Ⅱ), on peat have been studied under static conditions. The results show that the adsorption rates are rapid: equilibrium is reached in twenty minutes. The adsorption of copper, nickel and cadmium is pH dependent over the pH range from 2 to 6. The adsorption kinetics can be excellently described by the Elovich kinetic equation. The adsorption isotherm fits a Langmuir model very well. The adsorption capacifies follow the order Cu2+>Ni2+>Cd2+ in single-component systems and the competitive adsorption capacities fall in the decreasing order Cu2+> Ni2+>Cd2+ in multi-component systems. The adsorption capacities of these three heavy metal ions on peat are consistent with their observed competitive adsorption capacities.

  16. Adsorption Characteristics of Remazol Black B on Anoxic Sludge

    Institute of Scientific and Technical Information of China (English)

    HUANG Man-hong; CHEN Liang; CHEN Dong-hui; CHEN Chao-peng

    2009-01-01

    The adsorption characteristics of Remazol Black B on anoxic sludge were investigated. The parameters, such as initial pH, sulphate concentration, and temperature,affecting the dye adsorption were studied. The adsorption data were analyzed with three adsorption isotherm models,namely Langmuir, Freudlich, and linear partition. The results showed that adsorption of Remazol Black B on the sterilized sludge reached equilibrium in 4 h. It also indicated that pH had significant effect on anoxic sludge adsorption behavior. The adsorption capacity of anoxic sludge decreased with the increase of pH value and the maximum adsorption capacity of dyes occurred at pH = 3. The adsorptive capacities increased with the decrease of temperature and increase of sulphate concentration. Results also indicated that the adsorption equilibrium of Remazol Black B on anoxic sludge could be well fitted by Freundlich model.

  17. Nanoscale zerovalent iron (nZVI) supported by natural and acid-activated sepiolites: the effect of the nZVI/support ratio on the composite properties and Cd(2+) adsorption.

    Science.gov (United States)

    Habish, Amal Juma; Lazarević, Slavica; Janković-Častvan, Ivona; Jokić, Bojan; Kovač, Janez; Rogan, Jelena; Janaćković, Đorđe; Petrović, Rada

    2017-01-01

    Natural (SEP) and partially acid-activated (AAS) sepiolites were used to prepare composites with nanoscale zerovalent iron (nZVI) at different (SEP or AAS)/nZVI ratios in order to achieve the best nZVI dispersibility and the highest adsorption capacity for Cd(2+). Despite the higher surface area and pore volume of AAS, better nZVI dispersibility was achieved by using SEP as the support. On the other hand, a lower oxidation degree was achieved during the synthesis using AAS. X-ray photoelectron spectroscopy (XPS) analysis of the composite with the best nZVI dispersibility, before and after Cd(2+) adsorption, confirmed that the surface of the nZVI was composed of oxidized iron species. Metallic iron was not present on the surface, but it was detected in the subsurface region after sputtering. The content of zerovalent iron decreased after Cd(2+) adsorption as a result of iron oxidation during Cd(2+) adsorption. The XPS depth profile showed that cadmium was present not only at the surface of the composite but also in the subsurface region. The adsorption isotherms for Cd(2+) confirmed that the presence of SEP and AAS decreased the agglomeration of the nZVI particles in comparison to the pure nZVI, which provided a higher adsorption capacity. The results showed that the prevention of both aggregation and oxidation during the synthesis was necessary for obtaining an SEP/AAS-nZVI composite with a high adsorption capacity, but oxidation during adsorption was beneficial for Cd(2+) removal. The formation of strong bonds between Cd(2+) and the adsorbents sites of different energy until monolayer formation was proposed according to modeling of the adsorption isotherms.

  18. Adsorption of arsenic from aqueous solution using magnetic graphene oxide

    Science.gov (United States)

    Sherlala, A. I. A.; Raman, A. A.; Bello, M. M.

    2017-06-01

    A binary of graphene oxide (GO) and iron oxide (IO) was prepared and used for the removal of arsenic from aqueous solution. The synthesized compound was characterized using XRD analysis. The prepared composite was used for the adsorption of arsenic from aqueous solution. Central Composite Design was used to design the adsorption experiments and to investigate the effects of operational parameters (initial concentration of arsenic, adsorbent dosage, pH and time) on the adsorption capacity and efficiency. The adsorbent shows a high adsorption capacity for the arsenic. The adsorption efficiency ranges between 33.2 % and 99.95 %. The most significant factors affecting the adsorption capacity were found to be the initial concentration of arsenic and the adsorbent dosage. The initial pH of the solution slightly affects the adsorption capacity, with the maximum adsorption capacity occurring around pH 6 - 7. Thus, the developed adsorbent has a potential for effective removal of arsenic from aqueous solution.

  19. Self-assembled biomimetic monolayers using phospholipid-containing disulfides.

    Science.gov (United States)

    Chung, Yi Chang; Chiu, Yi Hong; Wu, Yin Wei; Tao, Yu Tai

    2005-05-01

    Several phospholipid-based disulfide molecules were synthesized and attached onto the gold-coated silicon wafer using the self-assembling method. The syntheses of these surface-modifying agents were conducted by introducing bromoethylphosphorate (PBr), phosphorylcholine (PC) or phosphorylethanolamine (PE) groups on the terminals of a dialkyl disulfide. After disulfides adsorption onto gold substrate surfaces, the composition, the film thickness, and the conformational order of self-assembled monolayer surfaces were explored and discussed in detail based on reflection-absorption infrared spectroscopy, contact angle measurement, Auger electron spectroscopy, X-ray photoelectron spectroscopy, and so on. The monolayer having the PBr end group could also be converted to a PC surface by treating with trimethylamine. The model functional surfaces of Au-SC11-PC, -PE, -PBr, -OH or corresponding mixed layers were used to mimic biomembrane surfaces. The monolayer having PC groups was found to reduce fibrinogen adsorption as evaluated from protein adsorption experiments using quartz crystal microbalance. It also showed relatively low platelet adherence compare to the glass, PBr and PE surfaces. The cell viability test also revealed that the PC surface displayed lower cytotoxicity than other surfaces.

  20. Anti-fouling chemistry of chiral monolayers: enhancing biofilm resistance on racemic surface.

    Science.gov (United States)

    Bandyopadhyay, Debjyoti; Prashar, Deepali; Luk, Yan-Yeung

    2011-05-17

    This work reports the resistance to protein adsorption and bacterial biofilm formation by chiral monolayers of polyol-terminated alkanethiols surrounding micrometer-sized patterns of methyl-terminated alkanethiols on gold films. We discover that patterned surfaces surrounded by chiral polyol monolayers can distinguish different stages of biofilm formation. After inoculation on the surfaces, bacteria first reversibly attached on the chiral polyol monolayers. Over time, the bacteria detached from the polyol surfaces, and attached on the hydrophobic micropatterns to form biofilms. Interestingly, while both enantiomers of gulitol- and mannonamide-terminated monolayer resisted adsorption of proteins (bovine serum albumin, lysozyme, and fibrinogen) and confined biofilms formed on the micropatterns, the monolayers formed by the racemic mixture of either pair of enantiomers exhibited stronger antifouling chemistry against both protein adsorption and biofilm formation than monolayers formed by one enantiomer alone. These results reveal the different chemistries that separate the different stages of biofilm formation, and the stereochemical influence on resisting biofoulings at a molecular-level.

  1. Adsorption mechanism of cadmium on juniper bark and wood

    Science.gov (United States)

    Eun Woo Shin; K. G. Karthikeyan; Mandla A. Tshabalala

    2007-01-01

    In this study the capacity of sorbents prepared from juniper wood (JW) and bark (JB) to adsorb cadmium (Cd) from aqueous solutions at different pH values was compared. Adsorption behavior was characterized through adsorption kinetics, adsorption isotherms, and adsorption edge experiments. Results from kinetics and isotherm experiments showed that JB (76.3–91.6 lmol Cd...

  2. STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles.

    Science.gov (United States)

    Kudernac, Tibor; Shabelina, Natalia; Mamdouh, Wael; Höger, Sigurd; De Feyter, Steven

    2011-01-01

    Despite their importance in self-assembly processes, the influence of charged counterions on the geometry of self-assembled organic monolayers and their direct localisation within the monolayers has been given little attention. Recently, various examples of self-assembled monolayers composed of charged molecules on surfaces have been reported, but no effort has been made to prove the presence of counterions within the monolayer. Here we show that visualisation and exact localisation of counterions within self-assembled monolayers can be achieved with scanning tunnelling microscopy (STM). The presence of charges on the studied shape-persistent macrocycles is shown to have a profound effect on the self-assembly process at the liquid-solid interface. Furthermore, preferential adsorption was observed for the uncharged analogue of the macrocycle on a surface.

  3. The adsorption behavior and mechanism investigation of Pb(II) removal by flocculation using microbial flocculant GA1.

    Science.gov (United States)

    Feng, Jing; Yang, Zhaohui; Zeng, Guangming; Huang, Jing; Xu, Haiyin; Zhang, Yuanyuan; Wei, Shumei; Wang, Like

    2013-11-01

    In this work, microbial flocculant GA1 (MBFGA1) was used to remove Pb(II) ions from aqueous solution. A series of experimental parameters including initial pH, MBFGA1 dose, temperature and initial calcium ions concentration on Pb(II) uptake was evaluated. Meanwhile, the flocculation mechanism of MBFGA1 was investigated. The removal efficiency of Pb(II) reached up to 99.85% when MBFGA1 was added in two stages, separately. The results indicated that Pb(II) adsorption could be described by the Langmuir adsorption model, and being the monolayer capacity negatively affected with an increase in temperature. The adsorption process could be described by pseudo-second-order kinetic model. Fourier transform-infrared spectra and environmental scanning electron microscope analysis indicated that MBFGA1 had a large number of functional groups, which had strong capacity for removing Pb(II). The main mechanisms of Pb(II) removal by MBFGA1 could be charge neutralization and adsorption bridging.

  4. ADSORPTION OF Pb2+ IONS FROM AQUEOUS SOLUTIONS ONTO BAEL TREE LEAF POWDER: ISOTHERMS, KINETICS AND THERMODYNAMICS STUDY

    Directory of Open Access Journals (Sweden)

    P. SENTHIL KUMAR

    2009-12-01

    Full Text Available In this study, bael tree (BT leaf powder was used as an adsorbent for removal of Pb2+ ions from aqueous solutions through batch equilibrium technique. The influence of pH, equilibrium time, temperature, adsorbent dosage and initial concentration of metal ions on adsorbed amount of metals ions were investigated. Studies showed that the pH of aqueous solutions affected Pb2+ ions removal as a result of removal efficiency increased with increasing solution pH. The experimental isotherm data were analyzed using the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich equations. The monolayer adsorption capacity is 4.065 mg/g with the correlation coefficient of 0.993. The experiments showed that highest removal rate was 84.93% at solution pH 5, contact time 60 min and initial concentration of 50 mg/L. Thermodynamic parameters such as Gibbs free energy, enthalpy, and entropy have also been evaluated and it has been found that the sorption process was feasible, spontaneous and exothermic in nature. Three simplified kinetic models including a pseudo-first-order equation, pseudo-second-order equation and intraparticle diffusion equation were selected to follow the adsorption process. Kinetic parameters, rate constants, equilibrium sorption capacities and related correlation coefficients, for each kinetic model were calculated and discussed. It was shown that the adsorption of Pb2+ ions could be described by the pseudo-second order equation, suggesting that the adsorption process is presumable a chemisorption.

  5. High performance NiFe layered double hydroxide for methyl orange dye and Cr(VI) adsorption.

    Science.gov (United States)

    Lu, Yi; Jiang, Bin; Fang, Liang; Ling, Faling; Gao, Jiemei; Wu, Fang; Zhang, Xihua

    2016-06-01

    The NiFe layered double hydroxides (LDHs) with different mole ratio of Ni/Fe (4:1, 3:1, 7:3 and 1:1) were prepared by a simple coprecipitation method. The adsorption performance were evaluated by the removal of methyl orange (MO) dye and hexavalent chromium(VI) heavy metal ion. It is found that Ni4Fe1-LDH can remove more than 92% of MO in 10 min at the 10 mg/L MO initial concentration, and 97% of Cr(VI) in 1 h at 4 mg/L Cr2O7(2-) initial concentration. The saturated adsorption capacity of Ni4Fe1-LDH is found to be as large as 205.76 mg/g for MO and 26.78 mg/g for Cr(VI). The adsorption behavior of this new adsorbent is fitted well with Langmuir isotherm and the pseudo-second-order kinetic model, indicative of a monolayer and chemical adsorption that synergistically originates from exchangeable anions mechanism and layer charge density. Due to the excellent removal capacity of MO and Cr(VI), the NiFe-LDHs could be a promising adsorbent for wastewater treatment.

  6. Interactions of gas molecules with monolayer MoSe2: A first principle study

    Science.gov (United States)

    Sharma, Munish; Jamdagni, Pooja; Kumar, Ashok; Ahluwalia, P. K.

    2016-05-01

    We present a first principle study of interaction of toxic gas molecules (NO, NO2 and SO2) with monolayer MoSe2. The predicted order of sensitivity of gas molecule is NO2 > SO2 > NO. Adsorbed molecules strongly influence the electronic behaviour of monolayer MoSe2 by inducing impurity levels in the vicinity of Fermi energy. NO and SO2 is found to induce p-type doping effect while semiconductor to metallic transitions occur on NO2 adsorption. Our findings may guide the experimentalist for fabricating sensor devices based on MoSe2 monolayer.

  7. Adsorptional removal of methylene blue by guar gum-cerium (IV) tungstate hybrid cationic exchanger.

    Science.gov (United States)

    Gupta, V K; Pathania, Deepak; Singh, Pardeep; Kumar, Amit; Rathore, B S

    2014-01-30

    Guar gum-cerium (IV) tungstate nanocomposite (GG/CTNC) cationic exchanger was synthesized using simple sol gel method. The GG/CTNC was characterized using X-ray diffraction (XRD), Fourier transmission infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and energy dispersive X-ray spectrophotometer (EDX). The XRD studies confirmed amorphous and fibrous in nature of GG/CTNC. The high percentage of oxygen in the nanocomposite material confirmed the functionality tungstate (WO4(-)). The ion exchange capacity of GG/CTNC for Na(+) ion was observed to be 1.30 mequivg(-1). The hybrid exchanger was used as potential adsorbent for the removal of methylene blue (MB) from aqueous system. The correlation coefficients value indicated a good fit of monolayer Langmuir model to the adsorption of methylene blue onto GG/CTNC. The adsorption kinetic study revealed that the adsorption process followed the pseudo second order kinetic. The Gibbs free energy (ΔG) values confirmed the spontaneous nature of adsorption process.

  8. Studies on adsorption of mercury from aqueous solution on activated carbons prepared from walnut shell.

    Science.gov (United States)

    Zabihi, M; Haghighi Asl, A; Ahmadpour, A

    2010-02-15

    The adsorption ability of a powdered activated carbons (PAC) derived from walnut shell was investigated in an attempt to produce more economic and effective sorbents for the control of Hg(II) ion from industrial liquid streams. Carbonaceous sorbents derived from local walnut shell, were prepared by chemical activation methods using ZnCl(2) as activating reagents. Adsorption of Hg(II) from aqueous solutions was carried out under different experimental conditions by varying treatment time, metal ion concentration, pH and solution temperature. It was shown that Hg(II) uptake decreases with increasing pH of the solution. The proper choice of preparation conditions were resulted in microporous activated carbons with different BET surface areas of 780 (Carbon A, 1:0.5 ZnCl(2)) and 803 (Carbon B, 1:1 ZnCl(2))m(2)/g BET surface area. The monolayer adsorption capacity of these particular adsorbents were obtained as 151.5 and 100.9 mg/g for carbons A and B, respectively. It was determined that Hg(II) adsorption follows both Langmuir and Freundlich isotherms as well as pseudo-second-order kinetics.

  9. Single and binary adsorption of reactive dyes from aqueous solutions onto clinoptilolite.

    Science.gov (United States)

    Sismanoglu, Tuba; Kismir, Yasemin; Karakus, Selcan

    2010-12-15

    The adsorption of Reactive Blue 21 (RB21) and Reactive Red 195 (RR195) onto clinoptilolite type natural zeolite (ZEC) has been investigated at 298.15K. The uptake of single and binary reactive dyes from aqueous solutions has been determined by UV-vis spectroscopy. Two mono-component (RB21 and RR195) and binary component (RB21 with RR195, and RR195 with RB21), isotherms were determined. The mono-component Langmuir isotherm model was applied to experimental data and the isotherm constants were calculated for RB21 and RR195 dyes. The monolayer coverage capacities of clinoptilolite for RB21 and RR195 dyes in single solution system were found as 9.652 and 3.186 mg/g, respectively. Equilibrium adsorption for binary systems was analyzed by using the extended Langmuir models. The rate of kinetic processes of single and binary dye systems onto clinoptilolite was described by using two kinetics adsorption models. The pseudo-second-order model was the best choice among the kinetic models to describe the adsorption behaviour of single and binary dyes onto clinoptilolite.

  10. Comprehending the interaction between chitosan and ionic liquid for the adsorption of palladium.

    Science.gov (United States)

    Kumar, A Santhana Krishna; Sharma, Shivani; Reddy, R Sudheer; Barathi, M; Rajesh, N

    2015-01-01

    Biopolymers and ionic liquids are of prime importance in numerous applications. Recovery of industrially important noble metals such as palladium is of paramount significance considering their diverse applications. The main idea behind this work was to develop an effective strategy involving the impregnation of Aliquat-336 (ionic liquid) onto chitosan as a novel adsorbent for the adsorption of Pd(II). The analytical characterization was systematically done through FT-IR, XRD, SEM and EDX analysis. The interaction of the amino and hydroxyl functional groups in chitosan with the cationic nitrogen in the ionic liquid could be established through the above characterization. Several key parameters such as pH influence, amount of adsorbent, isotherms, kinetics and thermodynamic studies were also studied in detail for the adsorption of palladium. The effectiveness of adsorption was observed between pH 3.5-4.0 with 50 mL of 120 mg L(-1) Pd(II) solution giving a commendable monolayer adsorption capacity of 187.61 mg g(-1).

  11. Adsorption of Hg(II from Aqueous Solution Using Adulsa (Justicia adhatoda Leaves Powder: Kinetic and Equilibrium Studies

    Directory of Open Access Journals (Sweden)

    Mohd Aslam

    2013-01-01

    Full Text Available The ability of Adulsa leaves powder (ALP to adsorb Hg(II from aqueous solutions has been investigated through batch experiments. The ALP biomass was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The experimental parameters that were investigated in this study included pH, adsorbent dosage, and effect of contact time along with initial metal ion concentration. The adsorption process was relatively fast, and equilibrium was achieved after 40 min of contact time. The maximum removal of Hg(II, 97.5% was observed at pH 6. The adsorption data were correlated with Langmuir, Freundlich, and Temkin isotherms. Isotherms results were amply fitted by the Langmuir model determining a monolayer maximum adsorption capacity (qm of ALP biomass equal to 107.5 mg g−1 and suggesting a functional group-limited sorption process. The kinetic process of Hg(II adsorption onto ALP biomass was tested by applying pseudofirst-order, pseudosecond-order, Elovich, and intraparticle-diffusion models to correlate the experimental data and to determine the kinetic parameters. It was found that the pseudosecond order kinetic model for Hg(II adsorption fitted very well. The rate determining step is described by intraparticle diffusion model. These studies considered the possibility of using Adulsa plant leaves biomass as an inexpensive, efficient, and environmentally safe adsorbent for the treatment of Hg(II contaminated wastewaters.

  12. Kinetics and isothermal modeling of liquid phase adsorption of rhodamine B onto urea modified Raphia hookerie epicarp

    Science.gov (United States)

    Inyinbor, A. A.; Adekola, F. A.; Olatunji, G. A.

    2016-09-01

    Epicarp of Raphia hookerie, a bioresource material, was modified with urea (UMRH) to adsorb Rhodamine B (RhB) from aqueous solution. Adsorbent morphology and surface chemistry were established by Brunauer-Emmett-Teller (BET) surface area determination, Fourier transform infrared spectroscopic (FTIR) analysis, scanning electron microscopy (SEM), as well as the pH point of zero charge (pHpzc) determination. Prepared material was subsequently utilized for the uptake of Rhodamine B (RhB). Operational parameters, such as adsorbent dosage, concentration, time, and temperature, were investigated. Evidence of effective urea modification was confirmed by vivid absorption bands at 1670 and 1472 cm-1 corresponding to C=O and C-N stretching vibrations, respectively. Optimum adsorption was obtained at pH 3. Freundlich adsorption isotherm best fits the equilibrium adsorption data, while evidence of adsorbate-adsorbate interaction was revealed by Temkin isotherm model. The maximum monolayer adsorption capacity (q max) was 434.78 mg/g. Kinetics of the adsorption process was best described by the pseudo-second-order kinetics model. Desorption efficiency was less than or equal to 25 % for all the eluents, and it follows the order HCl > H2O > CH3COOH.

  13. Arsenic(V) adsorption-desorption in agricultural and mine soils: Effects of organic matter addition and phosphate competition.

    Science.gov (United States)

    Arco-Lázaro, Elena; Agudo, Inés; Clemente, Rafael; Bernal, M Pilar

    2016-09-01

    High total and bioavailable concentrations of As in soils represent a potential risk for groundwater contamination and entry in the food chain. The use of organic amendments in the remediation of As-contaminated soils has been found to produce distinct effects on the solubility of As in the soil. Therefore, knowledge about As adsorption-desorption processes that govern its solubility in soil is of relevance in order to predict the behaviour of this element during these processes. In this paper, the objective was to determine As adsorption and desorption in four different soils, with and without compost addition, and also in competition with phosphate, through the determination of sorption isotherms. Batch experiments were carried out using three soils affected differently by previous mining activity of the Sierra Minera of La Unión-Cartagena (SE Spain) and an agricultural soil from Segovia province (central Spain). Adsorption was higher in the mining soils (and highest in the acidic one) than in the agricultural soils, although the latter were not affected negatively by organic matter or phosphate competition for sorption sites. The results show that As adsorption in most soils, both with and without compost, fitted better a multimolecular layer model (Freundlich), whereas As adsorption in competition with P fitted a monolayer model (Langmuir). Moreover, the use of compost and phosphate reduced the adsorption of As in the mining soils, while in the agricultural soils compost increased their low adsorption capacity. Therefore, the use of compost can be a good option to favour As immobilisation in soils of low adsorption, but knowledge of the soil composition will be crucial to predict the effects of organic amendments on As solubility in soils and its associated environmental risk. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. One-pot solvothermal synthesis of dual-phase titanate/titania Nanoparticles and their adsorption and photocatalytic Performances

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Yu Hua; Gong, Dangguo; Tang, Yuxin; Ho, Jeffery Weng Chye; Tay, Yee Yan; Lau, Wei Siew; Wijaya, Olivia; Lim, Jiexiang; Chen, Zhong, E-mail: aszchen@ntu.edu.sg

    2014-06-01

    Dual phase titanate/titania nanoparticles undergo phase transformation gradually with the increase of solvothermal synthesis temperature from 100 °C to 200 °C, and eventually are fully transformed into anatase TiO{sub 2}. The crystal structure change results in the changes of optical absorption, sensitizer/dopant formation and surface area of the materials which finally affect the overall dye removal ability. Reactions under dark and light have been conducted to distinguish the contributions of surface adsorption from photocatalytic degradation. The sample synthesized at 160 °C (S160) shows the best performances for both adsorption under dark and photocatalytic degradation of methylene blue (MB) under visible light irradiation. The adsorption mechanism for S160 is determined as monolayer adsorption based on the adsorption isotherm test under dark condition, and an impressive adsorption capacity of 162.19 mg/g is achieved. For the photocatalytic application, this sample at 0.1 g/L loading is also able to degrade 20 ppm MB within 6 hours under the visible light (>420 nm) condition. - Graphical abstract: The effect of solvothermal synthesis temperature on the formation and dye removal performance of dual phase titanate/titania nanoparticles was unveiled and optimized. - Highlights: • Low temperature one-pot solvothermal synthesis of dual-phase photocatalysts. • Correlation of the synthesis temperature is made with the phase composition. • Adsorption isotherm, kinetics, photocatalytic degradation were studied. • Synthesis at 160 °C yields the best material for adsorption of MB in dark. • The same sample also shows the best visible light degradation of MB.

  15. Studies of the adsorptive decoloration of aqueous solutions by MDFSD

    Directory of Open Access Journals (Sweden)

    Khaled Hartani

    2016-09-01

    Breakthrough plots were obtained beside the three isotherms. The breakthrough times were found as CV > MB > BG. These results were compatible to the adsorptivity estimated from the isotherms. It was found through this study that adsorption of CV followed pseudo-first order kinetics, the adsorption rate constant increases with increasing temperature, adsorbent concentration, MDFSD dose and pH. The adsorption equilibrium was shifted toward higher adsorption capacity by increasing the substrate concentration, temperature and pH. The adsorption data fit Freundlich, Langmuir, but attained a better correlation with the Langmuir model. Langmuir and freundlich constants, activation enthalpy of adsorption and the adsorption thermodynamic parameters were obtained.

  16. Effects of CO2 adsorption on coal deformation during geological sequestration

    National Research Council Canada - National Science Library

    Kan Yang; Xiancai Lu; Yangzheng Lin; Alexander V. Neimark

    2011-01-01

      CO2 adsorption capacity in coals is determined CO2 adsorption-induced coal deformation is evaluated Geological sequestration of CO2 is deeply discussed Adsorption-induced deformation of coal during...

  17. Stability of defects in monolayer MoS2 and their interaction with O2 molecule: A first-principles study

    Science.gov (United States)

    Zhao, B.; Shang, C.; Qi, N.; Chen, Z. Y.; Chen, Z. Q.

    2017-08-01

    The stability of various defects in monolayer MoS2, as well as their interactions with free O2 molecules were investigated by density functional theory (DFT) calculations coupled with the nudged elastic band (NEB) method. The defects including S vacancy (monosulfur and disulfue vacancies), antisite defect (MoS) and external Mo atom can exist steadily in monolayer MoS2, and introduce defect levels in these defective systems, which breaks the surface chemical inertness and significantly enhances the adsorption capacity for free O2. The adsorption energy calculations and electronic properties analysis suggest that there is a strong interaction between O2 molecule and defective system. The adsorbed O2 on the defective surface can dissociate with a lower activation energy barrier, which produce two active oxygen atoms. Especially, two Mo atoms can occupy one Mo lattice site, and adsorbed O2 on the top of the Mo atom can then dissociate directly with the lowest activation energy barrier. Hence, our work may provide useful information to design MoS2-based gas sensor or catalysts.

  18. Evaluation of the capacity of heavy metal adsorption in exfoliated vermiculite; Avaliacao da capacidade de adsorcao de metal pesado em vermiculitas esfoliadas

    Energy Technology Data Exchange (ETDEWEB)

    Lima, J.F.; Silva, P.S.; Hanken, R.B.L. [Universidade Federal de Campina Grande (UAEMa/UFCG), PB (Brazil). Unidade Academica de Engenharia de Materiais; Raposo, C.M.O., E-mail: raposo@dmg.ufcg.edu.b [Universidade Federal de Campina Grande (UAMG/UFCG), Bodocongo, PB (Brazil). Unidade Academica de Mineracao e Geologia

    2009-07-01

    Many groups from modern society have seen with attention the issues of pollutants, generally present in nature, those same that have caused irreversible damages to the environment. The Vermiculite, a phyllosilicate, with t-o-t structure, have high interlamelar charge, has been studied as cationic exchanger, whose application when exfoliated, are increased. This work has the objective of evaluate the absorption capacity of chromium (III), in different concentrations, in high, slim and medium concentrations of exfoliated vermiculites. The results obtained from the characterization by spectroscopy in infrared and by diffraction of x-ray from prepared solids showed important variations in the quantity of adsorbed metal in order the size of the concentrated particles. (author)

  19. Mechanisms of fibrinogen adsorption at solid substrates.

    Science.gov (United States)

    Adamczyk, Zbigniew; Bratek-Skicki, Anna; Żeliszewska, Paulina; Wasilewska, Monika

    2014-01-01

    The aim of this work was to critically review recent results pertinent to fibrinogen adsorption at solid/electrolyte interfaces with the emphasis focused on a quantitative analysis of these processes in terms of the electrostatic interactions. Accordingly, in the first part, the primary chemical structure of fibrinogen is analyzed. Physicochemical data pertinent to the bulk properties derived from hydrodynamic, dynamic light scattering and micro-electrophoretic measurements aided by theoretical modeling are discussed. Possible conformations and the effective charge distribution over the fibrinogen molecule for various pH an ionic strength are defined, especially the semi-collapsed conformation prevailing at physiological conditions. Adsorption kinetics of fibrinogen at hydrophilic and hydrophobic (polymer modified) substrates determined by various techniques is described. Adsorption at polymeric carrier particles, pertinent to immunological assays, studied in terms of electrokinetic and concentration depletion methods, are also considered. The reversibility of adsorption, fibrinogen molecule orientations and maximum coverages are thoroughly discussed. The stability of fibrinogen monolayers formed at these carrier particles in respect to pH and ionic strength cyclic changes is also discussed. In the final section interactions and deposition of model colloid particles on fibrinogen monolayers are analyzed which allows one to derive valuable information about molecule orientations. Based on the physicochemical data, adsorption kinetics and colloid particle deposition measurements, probable adsorption mechanisms of fibrinogen on solid/electrolyte interfaces are defined.

  20. A novel zerovalent manganese for removal of copper ions: synthesis, characterization and adsorption studies

    Science.gov (United States)

    Dada, A. O.; Adekola, F. A.; Odebunmi, E. O.

    2015-11-01

    Synthesis of nanoscale zerovalent manganese (nZVMn) by chemical reduction was carried out in a single pot system under inert environment. nZVMn was characterized using a combination of analytical techniques: Ultraviolet-Visible Spectroscopy, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Transmission Electron Microscopy, Energy Dispersive X-ray, BET surface area and Point of Zero Charge. The adsorption physicochemical factors: pH, contact time, adsorbent dose, agitation speed, initial copper ion concentration and temperature were optimized. The kinetic data fitted better to Pseudo second-order, Elovich, fractional power and intraparticle diffusion models and their validity was tested by three statistical models: sum of square error, Chi-square (χ 2) and normalized standard deviation (Δq). Seven of the two-parameter isotherm models [Freundlich, Langmuir, Temkin, Dubinin-Kaganer-Raduskevich (DKR), Halsey, Harkin-Jura and Flory-Huggins] were used to analyse the equilibrium adsorption data. The Langmuir monolayer adsorption capacity (Q max = 181.818 mg/g) obtained is greater than other those of nano-adsorbents utilized in adsorption of copper ions. The equilibrium adsorption data were better described by Langmuir, Freundlich, Temkin, DKR and Halsey isotherm models considering their coefficient of regression (R 2 > 0.90). The values of the thermodynamic parameters: standard enthalpy change ∆H° (+50.27848 kJ mol-1), standard entropy change ∆S° (203.5724 J mol-1 K-1) and the Gibbs free energy change ∆G° revealed that the adsorption process was feasible, spontaneous, and endothermic in nature. The performance of this novel nanoscale zerovalent manganese (nZVMn) suggested that it has a great potential for effective removal of copper ions from aqueous solution.

  1. A novel zerovalent manganese for removal of copper ions: synthesis, characterization and adsorption studies

    Science.gov (United States)

    Dada, A. O.; Adekola, F. A.; Odebunmi, E. O.

    2017-06-01

    Synthesis of nanoscale zerovalent manganese (nZVMn) by chemical reduction was carried out in a single pot system under inert environment. nZVMn was characterized using a combination of analytical techniques: Ultraviolet-Visible Spectroscopy, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Transmission Electron Microscopy, Energy Dispersive X-ray, BET surface area and Point of Zero Charge. The adsorption physicochemical factors: pH, contact time, adsorbent dose, agitation speed, initial copper ion concentration and temperature were optimized. The kinetic data fitted better to Pseudo second-order, Elovich, fractional power and intraparticle diffusion models and their validity was tested by three statistical models: sum of square error, Chi-square ( χ 2) and normalized standard deviation (Δ q). Seven of the two-parameter isotherm models [Freundlich, Langmuir, Temkin, Dubinin-Kaganer-Raduskevich (DKR), Halsey, Harkin-Jura and Flory-Huggins] were used to analyse the equilibrium adsorption data. The Langmuir monolayer adsorption capacity ( Q max = 181.818 mg/g) obtained is greater than other those of nano-adsorbents utilized in adsorption of copper ions. The equilibrium adsorption data were better described by Langmuir, Freundlich, Temkin, DKR and Halsey isotherm models considering their coefficient of regression ( R 2 > 0.90). The values of the thermodynamic parameters: standard enthalpy change ∆ H° (+50.27848 kJ mol-1), standard entropy change ∆ S° (203.5724 J mol-1 K-1) and the Gibbs free energy change ∆ G° revealed that the adsorption process was feasible, spontaneous, and endothermic in nature. The performance of this novel nanoscale zerovalent manganese (nZVMn) suggested that it has a great potential for effective removal of copper ions from aqueous solution.

  2. Surface heterogeneity: a friend or foe of protein adsorption - insights from theoretical simulations.

    Science.gov (United States)

    Penna, Matthew; Ley, Kamron; Maclaughlin, Shane; Yarovsky, Irene

    2016-10-06

    A lack in the detailed understanding of mechanisms through which proteins adsorb or are repelled at various solid/liquid interfaces limits the capacity to rationally design and produce more sophisticated surfaces with controlled protein adsorption in both biomedical and industrial settings. To date there are three main approaches to achieve anti biofouling efficacy, namely chemically adjusting the surface hydrophobicity and introducing various degrees of surface roughness, or a combination of both. More recently, surface nanostructuring has been shown to have an effect on protein adsorption. However, the current resolution of experimental techniques makes it difficult to investigate these three phase systems at the molecular level. In this molecular dynamics study we explore in all-atom detail the adsorption process of one of the most surface active proteins, EAS hydrophobin, known for its versatile ability to self-assemble on both hydrophobic and hydrophilic surfaces forming stable monolayers that facilitate further biofilm growth. We model the adsorption of this protein on organic ligand protected silica surfaces with varying degrees of chemical heterogeneity and roughness, including fully homogenous hydrophobic and hydrophilic surfaces for comparison. We present a detailed characterisation of the functionalised surface structure and dynamics for each of these systems, and the effect the ligands have on interfacial water, the adsorption process and conformational rearrangements of the protein. Results suggest that the ligand arrangement that produces the highest hydrophilic chain mobility and the lack of significant hydrophobic patches shows the most promising anti-fouling efficacy toward hydrophobin. However, the presence on the protein surface of a flexible loop with amphipathic character (the Cys3-Cys4 loop) is seen to facilitate EAS adsorption on all surfaces by enabling the protein to match the surface pattern.

  3. Adsorption of Ar on individual carbon nanotubes, graphene, and graphite

    Science.gov (United States)

    Dzyubenko, Boris; Kahn, Joshua; Vilches, Oscar; Cobden, David

    2015-03-01

    We compare and contrast results of adsorption measurements of Ar on single-walled carbon nanotubes, graphene, and graphite. Adsorption isotherms on individual suspended nanotubes were obtained using both the mechanical resonance frequency shift (sensitive to mass adsorption) and the electrical conductance. Isotherms on graphene mounted on hexagonal boron nitride were obtained using only the conductance. New volumetric adsorption isotherms on bulk exfoliated graphite were also obtained, paying special attention to the very low coverage region (less than 2% of a monolayer). This allowed us to compare the degree of heterogeneity on the three substrate types, the binding energies, and the van der Waals 2D parameters. Research supported by NSF DMR 1206208.

  4. Hydrogen adsorption on bimetallic PdAu(111) surface alloys

    DEFF Research Database (Denmark)

    Takehiro, Naoki; Liu, Ping; Bergbreiter, Andreas

    2014-01-01

    The adsorption of hydrogen on structurally well defined PdAu-Pd(111) monolayer surface alloys was investigated in a combined experimental and theoretical study, aiming at a quantitative understanding of the adsorption and desorption properties of individual PdAu nanostructures. Combining...... the structural information obtained by high resolution scanning tunneling microscopy (STM), in particular on the abundance of specific adsorption ensembles at different Pd surface concentrations, with information on the adsorption properties derived from temperature programmed desorption (TPD) spectroscopy...... and high resolution electron energy loss spectroscopy (HREELS) provides conclusions on the minimum ensemble size for dissociative adsorption of hydrogen and on the adsorption energies on different sites active for adsorption. Density functional theory (DFT) based calculations give detailed insight...

  5. Human fibrinogen monolayers on latex particles: role of ionic strength.

    Science.gov (United States)

    Bratek-Skicki, Anna; Żeliszewska, Paulina; Adamczyk, Zbigniew; Cieśla, Michał

    2013-03-19

    The adsorption of human serum fibrinogen on polystyrene latex particles was studied using the microelectrophoretic and concentration depletion methods. Measurements were carried out for pH 3.5 and an ionic strength range of 10(-3) to 0.15 M NaCl. The electrophoretic mobility of latex was determined as a function of the amount of adsorbed fibrinogen (surface concentration). A monotonic increase in the electrophoretic mobility (zeta potential) of the latex was observed, indicating a significant adsorption of fibrinogen on latex for all ionic strengths. No changes in the latex mobility were observed for prolonged time periods, suggesting the irreversibility of fibrinogen adsorption. The maximum coverage of fibrinogen on latex particles was precisely determined using the depletion method. The residual protein concentration after making contact with latex particles was determined by electrokinetic measurements and AFM imaging where the surface coverage of fibrinogen on mica was quantitatively determined. The maximum fibrinogen coverage increased monotonically with ionic strength from 1.8 mg m(-2) for 10(-3) M NaCl to 3.6 mg m(-2) for 0.15 M NaCl. The increase in the maximum coverage was interpreted in terms of the reduced electrostatic repulsion among adsorbed fibrinogen molecules. The experimental data agree with theoretical simulations made by assuming a 3D unoriented adsorption of fibrinogen. The stability of fibrinogen monolayers on latex was also determined in ionic strength cycling experiments. It was revealed that cyclic variations in NaCl concentration between 10(-3) and 0.15 M induced no changes in the latex electrophoretic mobility, suggesting that there were no irreversible molecule orientation changes in the monolayers. On the basis of these experimental data, a robust procedure of preparing fibrinogen monolayers on latex particles of well-controlled coverage was proposed.

  6. Electronic and vibrational properties of graphene monolayers with iron adatoms: A density functional theory study

    Energy Technology Data Exchange (ETDEWEB)

    Dimakis, Nicholas, E-mail: dimakis@utpa.edu [Department of Physics and Geology, University of Texas-Pan American, Edinburg, TX (United States); Navarro, Nestor E. [Department of Chemistry, University of Texas-Pan American, Edinburg, TX (United States); Velazquez, Julian; Salgado, Andres [Department of Physics and Geology, University of Texas-Pan American, Edinburg, TX (United States)

    2015-04-15

    Highlights: • Periodic density functional calculations were performed on graphene monolayers with and without an iron adatom. • Densities of states, charge transfers, and overlap populations were used to elucidate the effects of weak iron adsorption on graphene compared to CO adsorption on Pt. • Infrared intensities and normal mode analysis verify weak iron adsorption on graphene by studying the shift in prominent vibrational modes and changes in lattice dynamics. - Abstract: Periodic density functional calculations on graphene monolayers with and without an iron adatom have been used to elucidate iron-graphene adsorption and its effects on graphene electronic and vibrational properties. Density-of-states calculations and charge density contour plots reveal charge transfer from the iron s orbitals to the d orbitals, in agreement with past reports. Adsorbed iron atoms covalently bind to the graphene substrate, verified by the strong hybridization of iron d-states with the graphene bands in the energy region just below the Fermi level. This adsorption is weak and compared to the well-analyzed CO adsorption on Pt: It is indicated by its small adsorption energy and the minimal change of the substrate geometry due to the presence of the iron adatoms. Graphene vibrational spectra are analyzed though a systematic variation of the graphene supercell size. The shifts of graphene most prominent infrared active vibrational modes due to iron adsorption are explored using normal mode eigenvectors.

  7. Novel sandwich structure adsorptive membranes for removal of 4-nitrotoluene from water

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Yuexin [College of Chemistry, Beijing Normal University, Beijing 100875 (China); School of Pharmacy, North China University of Science and Technology, Tangshan 063000 (China); Jia, Zhiqian, E-mail: zhqjia@bnu.edu.cn [College of Chemistry, Beijing Normal University, Beijing 100875 (China)

    2016-11-05

    Highlights: • Novel sandwich PES-SPES/PS-PDVB/PTFE adsorptive membranes were prepared. • The removal efficiency for 4-nitrotoluene is greater than 95% after five recycles. • The membrane showed higher adsorption capacity than that of mixed matrix membrane. - Abstract: Novel sandwich PES-SPES/PS-PDVB/PTFE adsorptive membranes were prepared by a filtration/immersion precipitation method and employed for the removal of 4-nitrotoluene from water. The static adsorption thermodynamics, kinetics, dynamic adsorption/desorption and membrane reusability were investigated. The results showed that the Freundlich model describes the adsorption isotherm satisfactorily. With increased PS-PDVB content, the maximum static adsorption capacity, partition coefficient, apparent adsorption rate constant, and dynamic adsorption capacity all significantly increased. The sandwich membranes showed much higher removal efficiency and adsorption capacity than those of mixed matrix membranes. With respect to dynamics adsorption/desorption, the sandwich membranes exhibited excellent reusability, with a removal efficiency greater than 95% even after five recycles.

  8. 改性橘子皮对水中金属离子的吸附%The Adsorptive Capacity of Zinc and Iron of Water by Modified Orange Peel

    Institute of Scientific and Technical Information of China (English)

    毛娜

    2014-01-01

    将橘子皮用氢氧化钾、乙醇和氯化钙进行皂化处理,得到改性橘子皮生物吸附剂( SCOP)。在保持pH、起始金属离子浓度和温度不变的情况下进行吸附试验,研究不同氢氧化钾浓度浸泡下的SCOP及不同固液比、接触时间的改性橘子皮对水中锌、铁离子的吸附量大小。通过火焰原子吸收分光光度计定性测得SCOP对锌离子有较好的吸附,对铁则吸附较少。%A novel absorbent was prepared by modifying orange peel with potassium hydroxide and calcium chloride. Keeping pH, initial concentration of metal ions and experimental temperature not change, the absorption behavior of Zn( II) and Fe ( II ) on modified orange peel under varying concentration of sodium hydroxide, contract time and absorption of different quantity were studied. SCOP had a better adsorption capacities for Zn ( II ) but with a fewer for Fe( II) by flame atomic absorption spectrometry.

  9. Synthesis of magnetic γ-Fe2O3-based nanomaterial for ultrasonic assisted dyes adsorption: Modeling and optimization.

    Science.gov (United States)

    Asfaram, Arash; Ghaedi, Mehrorang; Hajati, Shaaker; Goudarzi, Alireza

    2016-09-01

    γ-Fe2O3 nanoparticles were synthesized and loaded on activated carbon. The prepared nanomaterial was characterized by field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transforms infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). The γ-Fe2O3 nanoparticle-loaded activated carbon (γ-Fe2O3-NPs-AC) was used as novel adsorbent for the ultrasonic-assisted removal of methylene blue (MB) and malachite green (MG). Response surface methodology and artificial neural network were applied to model and optimize the adsorption of the MB and MG in their individual and binary solutions followed by the investigation on adsorption isotherm and kinetics. The individual effects of parameters such as pH, mass of adsorbent, ultrasonication time as well as MB and MG concentrations in addition to the effects of their possible interactions on the adsorption process were investigated. The numerical optimization revealed that the optimum adsorption (>99.5% for each dye) is obtained at 0.02g, 15mgL(-1), 4min and 7.0 corresponding to the adsorbent mass, each dye concentration, sonication time and pH, respectively. The Freundlich, Langmuir, Temkin and Dubinin-Radushkevich isotherms were studied. The Langmuir was found to be most applicable isotherm which predicted maximum monolayer adsorption capacities of 195.55 and 207.04mgg(-1) for the adsorption of MB and MG, respectively. The pseudo-second order model was found to be applicable for the adsorption kinetics. Blank experiments (without any adsorbent) were run to investigate the possible degradation of the dyes studied in presence of ultrasonication. No dyes degradation was observed.

  10. Phosphate adsorption on lanthanum loaded biochar.

    Science.gov (United States)

    Wang, Zhanghong; Shen, Dekui; Shen, Fei; Li, Tianyu

    2016-05-01

    To attain a low-cost and high-efficient phosphate adsorbent, lanthanum (La) loaded biochar (La-BC) prepared by a chemical precipitation method was developed. La-BC and its pristine biochar (CK-BC) were comparatively characterized using zeta potential, BET surface area, scanning electron microscopy/energy dispersive spectrometer (SEM-EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). The adsorption ability and the mechanisms during adsorption process for the La-BC samples were also investigated. La loaded on the surface of biochar can be termed as La-composites (such as LaOOH, LaONO3 and La(OH)3), leading to the decrease of negative charge and surface area of biochar. La-BC exhibited the high adsorption capacity to phosphate compared to CK-BC. Adsorption isotherm and adsorption kinetic studies showed that the Langmuir isotherm and second order model could well describe the adsorption process of La-BC, indicating that the adsorption was dominated by a homogeneous and chemical process. The calculated maximum adsorption capacity was as high as 46.37 mg g(-1) (computed in P). Thermodynamic analysis revealed that the adsorption was spontaneous and endothermic. SEM, XRD, XPS and FT-IR analysis suggested that the multi-adsorption mechanisms including precipitation, ligand exchange and complexation interactions can be evidenced during the phosphate adsorption process by La-composites in La-BC.

  11. Monolayer patterning using ketone dipoles.

    Science.gov (United States)

    Kim, Min Kyoung; Xue, Yi; Pašková, Tereza; Zimmt, Matthew B

    2013-08-14

    The self-assembly of multi-component monolayers with designed patterns requires molecular recognition among components. Dipolar interactions have been found to influence morphologies of self-assembled monolayers and can affect molecular recognition functions. Ketone groups have large dipole moments (2.6 D) and are easily incorporated into molecules. The potential of ketone groups for dipolar patterning has been evaluated through synthesis of two 1,5-disubstituted anthracenes bearing mono-ketone side chains, STM characterization of monolayers self-assembled from their single and two component solutions and molecular mechanics simulations to determine their self-assembly energetics. The results reveal that (i) anthracenes bearing self-repulsive mono-ketone side chains assemble in an atypical monolayer morphology that establishes dipolar attraction, instead of repulsion, between ketones in adjacent side chains; (ii) pairs of anthracene molecules whose self-repulsive ketone side chains are dipolar complementary spontaneously assemble compositionally patterned monolayers, in which the two components segregate into neighboring, single component columns, driven by side chain dipolar interactions; (iii) compositionally patterned monolayers also assemble from dipolar complementary anthracene pairs that employ different dipolar groups (ketones or CF2 groups) in their side chains; (iv) the ketone group, with its larger dipole moment and size, provides comparable driving force for patterned monolayer formation to that of the smaller dipole, and smaller size, CF2 group.

  12. Monitoring the hydration of DNA self-assembled monolayers using an extensional nanomechanical resonator

    DEFF Research Database (Denmark)

    Cagliani, Alberto; Kosaka, Priscila; Tamayo, Javier;

    2012-01-01

    We have fabricated an ultrasensitive nanomechanical resonator based on the extensional vibration mode to weigh the adsorbed water on self-assembled monolayers of DNA as a function of the relative humidity. The water adsorption isotherms provide the number of adsorbed water molecules per nucleotid...

  13. Self-assembled monolayers on gold of ferrocene-terminated thiols and hydroxyalkanethiols

    NARCIS (Netherlands)

    Auletta, T.; van Veggel, F.C.J.M.; Reinhoudt, David

    2002-01-01

    this paper, a study on the adsorption of mixed self-assembled monolayers (SAMs) for two different combinations of thiols (Fc(CH2)6SH/HO(CH2)2SH and Fc(CH2)16SH/HO(CH2)11SH (Fc = ferrocene)) is presented, to obtain surfaces with single isolated ferrocenylalkanethiols embedded in shorter

  14. Selective adsorption of tannins onto hide collagen fibres

    Institute of Scientific and Technical Information of China (English)

    LIAO; Xuepin(廖学品); LU; Zhongbing(陆忠兵); SHI; Bi(石碧)

    2003-01-01

    Hide collagen of animals is used to prepare adsorbent material and its adsorption properties to tannins are investigated. It is indicated that the collagen fibres has excellent adsorption selectivity and high adsorption capacity to tannins. The adsorption rate of tannins is more than 90% whilst less than 10% of functional components are retained by the adsorbent. The adsorption mechanism of tannins onto hide collagen fibres is hydrogen-bonding association. Freundlich model can be used to describe the adsorption isotherms, and the pseudo-second-order rate model can be used to describe adsorption kinetics.

  15. From monomer to monolayer: a global optimisation study of (ZnO)n nanoclusters on the Ag surface.

    Science.gov (United States)

    Demiroglu, Ilker; Woodley, Scott M; Sokol, Alexey A; Bromley, Stefan T

    2014-12-21

    We employ global optimisation to investigate how oxide nanoclusters of increasing size can best adapt their structure to lower the system energy when interacting with a realistic extended metal support. Specifically, we focus on the (ZnO)@Ag(111) system where experiment has shown that the infinite Ag(111)-supported ZnO monolayer limit corresponds to an epitaxially 7 : 8 matched graphene-like (Zn(3)O(3))-based hexagonal sheet. Using a two-stage search method based on classical interatomic potentials and then on more accurate density functional theory, we report global minina candidate structures for Ag-supported (ZnO)n cluster with sizes ranging from n = 1-24. Comparison with the respective global minina structure of free space (ZnO)n clusters reveals that the surface interaction plays a decisive role in determining the lowest energy Ag-supported (ZnO)n cluster structures. Whereas free space (ZnO)n clusters tend to adopt cage-like bubble structures as they grow larger, Ag-supported (ZnO)n clusters of increasing size become progressively more like planar cuts from the infinite graphene-like ZnO single monolayer. This energetic favourability for planar hexagonal Ag-supported clusters over their 3D counterparts can be partly rationalised by the ZnO-Ag(111) epitaxial matching and the increased number of close interactions with the Ag surface. Detailed analysis shows that this tendency can also be attributed to the capacity of 2D clusters to distort to improve their interaction with the Ag surface relative to more rigid 3D bubble cluster isomers. For the larger sized clusters we find that the adsorption energies and most stable structural types appear to be rather converged confirming that our study makes a bridge between the Ag-supported ZnO monomer and the infinite Ag-supported ZnO monolayer.

  16. Phonons on the clean metal surfaces and in adsorption structures

    Science.gov (United States)

    Rusina, Galina G.; Chulkov, Evgenii V.

    2013-06-01

    The state-of-the-art studies of the vibrational dynamics of clean metal surfaces and metal surface structures formed upon the sub-monolayer adsorption of the atoms of various elements are considered. A brief historical survey of the milestones of investigations of surface phonons is presented. The results of studies of the atomic structure and vibration characteristics of surfaces with low and high Miller indices and adsorption structures are analyzed. It is demonstrated that vicinal surfaces of FCC metals tend to exhibit specific vibrational modes located on the step and polarized along the step. Irrespective of the type and position of adsorption or the substrate structure, the phonon spectra of sub-monolayer adsorption structures always tend to display two modes for combined translational displacements of adatoms and for coupled vibrations of substrate atoms and adatoms polarized in the direction normal to the surface. The bibliography includes 202 references.

  17. Adsorption of octadecyltrichlorosilane on mesoporous SBA-15

    Energy Technology Data Exchange (ETDEWEB)

    Mirji, S.A. [Physical Chemistry Division, National Chemical Laboratory, Pune 411008 (India)]. E-mail: mirji@dalton.ncl.res.in; Halligudi, S.B. [Inorganic and Catalysis Division, National Chemical Laboratory, Pune 411008 (India); Sawant, Dhanashri P. [Inorganic and Catalysis Division, National Chemical Laboratory, Pune 411008 (India); Jacob, Nalini E. [Inorganic and Catalysis Division, National Chemical Laboratory, Pune 411008 (India); Patil, K.R. [Center for Material Characterization, National Chemical Laboratory, Pune 411008 (India); Gaikwad, A.B. [Center for Material Characterization, National Chemical Laboratory, Pune 411008 (India); Pradhan, S.D. [Center for Material Characterization, National Chemical Laboratory, Pune 411008 (India)

    2006-04-15

    Adsorption of octadecyltrichlorosilane (OTS) on mesoporous SBA-15 has been studied by using Brunauer-Emmett-Teller (BET) surface area analysis, scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and thermo-gravimetric analysis (TGA) techniques. BET surface area analysis shows decrease of surface area from 930 to 416 m{sup 2}/g after OTS adsorption. SEM pictures show close attachment of SBA-15 particles. EDAX measurements show increase of carbon weight percentage and decrease of oxygen and silicon weight percentage. XPS results closely support EDAX analysis. FTIR spectra shows presence of methyl (-CH{sub 3}) and methylene (-CH{sub 2}) bands and oriented OTS monolayer on SBA-15. Thermo-gravimetric analysis shows that the OTS adsorbed on SBA-15 are stable up to a temperature of 230 deg. C and that the OTS monolayers decompose between 230 and 400 deg. C.

  18. Electron-induced ammonia adsorption on iron

    CERN Document Server

    Narkiewicz, U; Trybuchowicz, A; Arabczyk, W

    2003-01-01

    The adsorption of ammonia on an iron surface at ambient temperature has been investigated using Auger electron spectroscopy (AES). The effect of the electron beam on the process of the ammonia adsorption has been studied. The polycrystalline iron samples precovered with different amounts of oxygen (0.15-1 ML) or sulphur (1 ML) were used. The initial sticking coefficient of ammonia to oxygen precovered iron surface was estimated as s sub 0 approx 5x10 sup - sup 4 (independently on the oxygen coverage) for the adsorption experiments without the effect of the electron beam. The strong inhibiting effect of sulphur precoverage on the ammonia adsorption has been found (s sub 0 approx 6.5x10 sup - sup 6). The electron beam has favourable effect on the adsorption of ammonia, and this effect increases with the oxygen coverage (one monolayer of adsorbed nitrogen atoms at the saturation state and s sub 0 approx 1 for the iron surface precovered with one monolayer of oxygen). The proposed explanation is the favourable ef...

  19. An investigation into the adsorption of thorium(IV) from aqueous solutions by a carboxylate-functionalised graft copolymer derived from titanium dioxide-densified cellulose.

    Science.gov (United States)

    Anirudhan, T S; Sreekumari, S S; Jalajamony, S

    2013-02-01

    The use of a carboxylate-functionalized graft copolymer (PGTDC-COOH) based on titanium dioxide-densified cellulose (TDC) for the removal and recovery of thorium(IV) [Th(IV)] from industrial wastewater is reported in this paper. Infrared spectroscopy and X-ray diffractometer were used to characterize the adsorbent material. Batch equilibrium experiments showed that the adsorbent exhibited 98.6 ± 3.1% adsorption from an initial concentration of 10 mg/L Th(IV) solution at pH 5.0. The sorption kinetics have been analysed by pseudo-first-order and pseudo-second-order kinetic models and the adsorption kinetics was described by pseudo-second-order model. The experimental data obeyed Langmuir isotherm and the maximum monolayer adsorption capacity for Th(IV) was also found to be 92.23 ± 2.4 mg/g at 30 °C. The desorption capacity of HCl concentrations of different strengths ranging from 0.001 to 0.1 M was also studied. Maximum desorption of 98.2 ± 2.8% for Th(IV) occurred with 0.1 M HCl. The adsorption efficiency towards Th(IV) ion removal was tested using artificial sea water. Almost complete removal was possible with 3.5 g of the adsorbent from 1 L of the sea water.

  20. Equilibrium adsorption isotherm studies of Cu (II) and Co (II) in high concentration aqueous solutions on Ag-TiO2-modified kaolinite ceramic adsorbents

    Science.gov (United States)

    Ajenifuja, E.; Ajao, J. A.; Ajayi, E. O. B.

    2017-09-01

    Photocatalytic ceramic adsorbents were prepared from locally sourced kaolinite clay minerals for the removal of copper and cobalt ions from high concentration aqueous solutions. The minerals were treated with mild acid before modification using silver nanoparticles sources and titanium-oxide nanoparticles. Batch adsorption experiment was carried out on the targeted ions and the results were analyzed by Langmuir and Freundlich equation at different concentrations (100-1000 mg/l). As-received raw materials do not exhibit any adsorption capacity. However, the adsorption isotherms for modified kaolinite clay ceramic adsorbents could be fitted well by the Langmuir model for Cu2+ and Co2+ with correlation coefficient ( R) of up to 0.99705. The highest and lowest monolayer coverage ( q max) were 93.023 and 30.497 mg/g for Cu2+ and Co2+, respectively. The separation factor ( R L ) was less than one (ceramic adsorbent is favorable. The highest adsorbent adsorption capacity ( K f ) and intensity ( n) constants obtained from Freundlich model are 14.401 (Cu2+ on KLN-T) and 6.057 (Co2+ on KLN-T).

  1. Comparative study on composition, structure, and adsorption behavior of activated carbons derived from different synthetic waste polymers.

    Science.gov (United States)

    Lian, Fei; Xing, Baoshan; Zhu, Lingyan

    2011-08-15

    The composition, structure, and adsorption behavior of activated carbons (ACs) derived from three different types of waste polymers, i.e., tire rubber (TR), polyvinyl chloride (PVC), and polyethyleneterephtalate (PET), by KOH activation were compared. The AC derived from PET exhibited the largest surface area (2831 m(2)/g) and pore volume (1.68 cm(3)/g) due to the homogenous aromatic composition of PET. The AC derived from PVC exhibited relatively lower surface area (2666 m(2)/g) but more narrowed pore size distribution (2-3 nm). The complex composition and high ash content of tire particles resulted in AC product with significantly lower surface area (398.5 m(2)/g) and heterogeneous pore width. Adsorption data of methylene blue (MB) were fitted well by Langmuir equation, indicating monolayer coverage on the ACs. The high oxygen content of PET-derived AC heavily affected its adsorption to MB and iodine. Due to the remarkable surface area and highly mesoporous structures, ACs based on both PET and PVC exhibited much higher adsorption capacities than that of TR and commercial coal-based AC (F400). This study demonstrates that the properties of ACs are highly dependent on their starting polymers and the potential of converting synthetic polymer waste into effective adsorbents for environmental remediation and cleanup.

  2. [Adsorption characteristics of ciprofloxacin in ustic cambosols].

    Science.gov (United States)

    Cui, Hao; Wang, Shu-ping

    2012-08-01

    In order to understand the adsorption characteristics of ciprofloxacin in ustic cambosols, static adsorption experiments were used to investigate dynamic and isothermal adsorption characteristics of ciprofloxacin in ustic cambosols, influence of pH on the adsorption process. Results showed that the absorption process of ciprofloxacin can be divided into two stages: fast adsorption and slow balance. The adsorption processes followed the pseudo-second-order kinetics, with adsorption rate of 1.138 x 10(-3) - 2.849 x 10(-2) kg x (min x mg)(-1). Adsorption isotherms of ciprofloxacin in ustic cambosols were well described by the Freundlich and Langmuir equation, Freundlich equation is more applicable than Langmuir equation, with the adsorption capacity (lgKf) of 2.725. Moreover, at the tested pH interval of 4-9, lgKd values of ciprofloxacin increased and then decreased with the increase of pH in ustic cambosols; the maximum adsorption of ciprofloxacin in ustic cambosols can be obtained when the pH value was 5 with lgKd value was 3.11; strong acid or alkali conditions were unfavorable to ciprofloxacin adsorption. It could be deduced that cationic adsorptions was one of the significant sorption mechanisms for ciprofloxacin in ustic cambosols.

  3. An investigation of Cu(II) adsorption by raw and acid-activated bentonite: A combined potentiometric, thermodynamic, XRD, IR, DTA study

    Energy Technology Data Exchange (ETDEWEB)

    Eren, E. [Department of Chemistry, Faculty of Arts and Sciences, Ondokuz Mayis University, 55139 Kurupelit-Samsun (Turkey)], E-mail: erdalern@omu.edu.tr; Afsin, B. [Department of Chemistry, Faculty of Arts and Sciences, Ondokuz Mayis University, 55139 Kurupelit-Samsun (Turkey)

    2008-03-01

    Adsorption of Cu(II) by raw bentonite (RB) and acid-activated bentonite (AAB) samples was investigated as a function of the initial Cu(II) concentration, solution pH, ionic strenght, temperature, the competitive and complexation effects of ligands (Cl{sup -}, SO{sub 4}{sup 2-}, PO{sub 4}{sup 3-}). Langmuir monolayer adsorption capacity of the RB (42.41 mg g{sup -1}) was found greater than that of the AAB (32.17 mg g{sup -1}). The effect of structural charges on the reactivity of the edge groups was evidenced by the particular proton adsorption behaviour of the bentonite samples. The spontaneity of the adsorption process is established by decrease in {delta}G which varied from -0.34 to -0.71 kJ mol{sup -1} (RB), -1.13 to -1.49 kJ mol{sup -1} (AAB) in temperature range 303-313 K. Infrared (IR) spectra of the bentonite samples showed that the positions and shapes of the fundamental vibrations of the OH and Si-O groups were influenced by the adsorbed Cu(II) cations. Differential thermal analysis (DTA) results showed that adsorbed Cu(II) cations have a great effect on the thermal behaviour of the bentonite samples. The X-ray diffraction (XRD) spectra indicated that the Cu(II) adsorption onto the bentonite samples led to changes in unit cell dimensions and symmetry of the parent bentonites.

  4. Monolayers and mixed-layers on copper towards corrosion protection

    Energy Technology Data Exchange (ETDEWEB)

    Sinapi, F. [Fonds pour la Formation a la Recherche dans l' Industrie et dans l' Agriculture, Rue d' Egmont 5, B-1000 Brussels (Belgium); Julien, S.; Auguste, D.; Hevesi, L.; Delhalle, J. [Laboratory of Chemistry and Electrochemistry of Surfaces, University of Namur, FUNDP, Rue de Bruxelles, 61, B-5000 Namur (Belgium); Mekhalif, Z. [Laboratory of Chemistry and Electrochemistry of Surfaces, University of Namur, FUNDP, Rue de Bruxelles, 61, B-5000 Namur (Belgium)], E-mail: zineb.mekhalif@fundp.ac.be

    2008-05-01

    In order to improve the protection abilities of (3-mercaptopropy)trimethoxysilane (MPTS) self-assembled monolayers on copper surfaces, mixed monolayers have been formed successfully by successive immersions in MPTS and in n-dodecanethiol (DT). A newly synthesised molecule, (11-mercaptoundecyl)trimethoxysilane (MUTS), has also been employed to form a thicker organic film on copper surfaces and, thereby, enhance the inhibitory action of the coating. The grafting has been confirmed by X-ray photoelectron spectroscopy (XPS), polarization modulation infrared reflection adsorption spectroscopy (PM-IRRAS) and water contact angle. The protective efficiency of each protective organic film has been evidenced by cyclic voltammetry (CV) and polarization curve measurements (CP). It was shown that the MUTS and unhydrolyzed MPTS/DT films exhibited significant corrosion protection properties.

  5. Adsorption isotherm of non-azeotropic solution onto porous adsorbents

    Science.gov (United States)

    Bono, A.; Ramlan, N. A.; Anisuzzaman, S. M.; Chu, C. M.; Farm, Y. Y.

    2016-06-01

    Adsorption isotherm is essential component in the understanding of the adsorption process. Several methods of the measurements, analysis and interpretation of adsorption from solution have been reported in the literature. Most of the measurements of adsorption isotherm from solution were involved the measurement of excess isotherm conducted at low region of sorbates concentration. Direct interpretation of excess adsorption isotherm as adsorption isotherm is always been practice. Therefore, in this work a study on the measurement of the adsorption isotherm from solution of non-azeotropic organic solvent mixture onto porous adsorbents for whole range of liquid concentration was conducted. The study included the measurement of excess adsorption isotherm using conventional technique. Theoretical analysis and interpretation of adsorption isotherm from the excess isotherm were conducted using Pseudo Ideal Adsorption, Gibbs Dividing Plane Model and Langmuir-Fruendlich binary isotherm model. For organic solvents, acetone and propanol were chosen as the adsorbates due to the non-azeotropic properties in the mixture. Activated carbon and silicalite were chosen as adsorbents due to the different in their porosity such as macro porous and micro porous structure. The result of the study has revealed that the adsorption isotherm of non-azeotropic mixture onto activated carbon and silicalite can be interpreted as monolayer type of adsorption.

  6. Adsorption isotherm studies of Cu (II) and Co (II) in high concentration aqueous solutions on photocatalytically modified diatomaceous ceramic adsorbents

    Science.gov (United States)

    Ajenifuja, E.; Ajao, J. A.; Ajayi, E. O. B.

    2017-01-01

    Photocatalytically modified ceramic adsorbents were synthesized for the removal of high concentration Cu (II) and Co (II) ions from their aqueous solutions. The raw material, diatomaceous aluminosilicate mineral was modified using silver and anatase titanium oxide nanoparticles. Batch adsorption experiment was carried out on the targeted metal ions and the results were analyzed by the Langmuir and Freundlich equation at different concentrations (100-1000 mg/l) and the characteristic parameters for each adsorption isotherm were determined. As-received raw materials do not exhibit any sorption capacity for high concentration Cu2+ and Co2+ adsorbates. However, the adsorption isotherms for modified diatomaceous ceramic adsorbents could be fitted well by the Langmuir model for both Cu2+ and Co2+ with correlation coefficient (R) of up to 0.99953. The highest and lowest monolayer coverage (q max) were 121.803 and 31.289 mg/g for Cu2+ and Co2+, respectively. The separation factor (R L) in the experiment was less than one (capacity (K f) and intensity (n) constants obtained from Freundlich model are 38.832 (Cu2+ on ZEO-T) and 5.801 (Co2+ on STOX-Z).

  7. Sodium alginate/graphene oxide aerogel with enhanced strength-toughness and its heavy metal adsorption study.

    Science.gov (United States)

    Jiao, Chenlu; Xiong, Jiaqing; Tao, Jin; Xu, Sijun; Zhang, Desuo; Lin, Hong; Chen, Yuyue

    2016-02-01

    Ordered porous sodium alginate/graphene oxide (SAGO) aerogel was fabricated by in situ crosslinking and freeze-drying method. GO, as reinforcing filler, can be easily incorporated with SA matrix by self-assembly via hydrogen bonding interaction. Compared with pure SA aerogel, the as-prepared SAGO exhibited excellent mechanical strength and elasticity, and the compression strength of SAGO can reach up to 324 kPa and remain 249 kPa after five compression cycles when 4 wt% GO was added, which were considered significant improvements. SEM result presents that the addition of GO obviously improves the porous structures of aerogel, which is beneficial for the enhancement of strength-toughness and adsorbability. As a consequence, the adsorption process of SAGO is better described by pseudo-second-order kinetic model and Langmuir isotherm, with maximum monolayer adsorption capacities of 98.0 mg/g for Cu2+ and 267.4 mg/g for Pb2+, which are extremely high adsorption capacities for metal ions and show far more promise for application in sewage treatment.

  8. Phenomenological Modeling for Langmuir Monolayers

    Science.gov (United States)

    Baptiste, Dimitri; Kelly, David; Safford, Twymun; Prayaga, Chandra; Varney, Christopher N.; Wade, Aaron

    Experimentally, Langmuir monolayers have applications in molecular optical, electronic, and sensor devices. Traditionally, Langmuir monolayers are described by a rigid rod model where the rods interact via a Leonard-Jones potential. Here, we propose effective phenomenological models and utilize Monte Carlo simulations to analyze the phase behavior and compare with experimental isotherms. Research reported in this abstract was supported by UWF NIH MARC U-STAR 1T34GM110517-01.

  9. Surface area, porosity and water adsorption properties of fine volcanic ash particles

    Science.gov (United States)

    Delmelle, Pierre; Villiéras, Frédéric; Pelletier, Manuel

    2005-02-01

    Our understanding on how ash particles in volcanic plumes react with coexisting gases and aerosols is still rudimentary, despite the importance of these reactions in influencing the chemistry and dynamics of a plume. In this study, six samples of fine ash (500 Å. All the specimens had similar pore size distributions, with a small peak centered around 50 Å. These findings suggest that fine ash particles have relatively undifferentiated surface textures, irrespective of the chemical composition and eruption type. Adsorption isotherms for water vapour revealed that the capacity of the ash samples for water adsorption is systematically larger than predicted from the nitrogen adsorption as values. Enhanced reactivity of the ash surface towards water may result from (i) hydration of bulk ash constituents; (ii) hydration of surface compounds; and/or (iii) hydroxylation of the surface of the ash. The later mechanism may lead to irreversible retention of water. Based on these experiments, we predict that volcanic ash is covered by a complete monolayer of water under ambient atmospheric conditions. In addition, capillary condensation within ash pores should allow for deposition of condensed water on to ash particles before water reaches saturation in the plume. The total mass of water vapour retained by 1 g of fine ash at 0.95 relative water vapour pressure is calculated to be ~10-2 g. Some volcanic implications of this study are discussed.

  10. Kinetics, Equilibrium, and Thermodynamic Studies on Adsorption of Methylene Blue by Carbonized Plant Leaf Powder

    Directory of Open Access Journals (Sweden)

    V. Gunasekar

    2013-01-01

    Full Text Available Carbon synthesized from plant leaf powder was employed for the adsorption of methylene blue from aqueous effluent. Effects of pH (2, 4, 6, 8, and 9, dye concentration (50, 100, 150, and 200 mg/dm3, adsorbent dosage (0.5, 1.0, 1.5, and 2.0 g/dm3, and temperature (303, 313, and 323 K were studied. The process followed pseudo-second-order kinetics. Equilibrium data was examined with Langmuir and Freundlich isotherm models and Langmuir model was found to be the best fitting model with high R2 and low chi2 values. Langmuir monolayer adsorption capacity of the adsorbent was found to be 61.22 mg/g. From the thermodynamic analysis, ΔH, ΔG, and ΔS values for the adsorption of MB onto the plant leaf carbon were found out. From the values of free energy change, the process was found out to be feasible process. From the magnitude of ΔH, the process was found to be endothermic physisorption.

  11. Adsorption Batch Studies on the Removal of Pb(II Using Maize Tassel Based Activated Carbon

    Directory of Open Access Journals (Sweden)

    Mambo Moyo

    2013-01-01

    Full Text Available The demand for clean water is on the increase as rapid industrialization is still contributing to pollution. Nowadays, as water is the basic need for mankind, efforts have gathered momentum to decontaminate it in order to address the acute shortage of clean and pure water. Maize tassel was used as the precursor for making activated carbon for the adsorption of Pb(II ions. The product obtained was characterized and utilized for the removal of Pb(II from aqueous solutions over a wide range of initial metal ion concentration (10–50 mg/L, contact time (5–300 min, adsorbent dose (0.1–2.5 g, and pH (2–12. The optimum set of conditions for biosorption of Pb(II ion were found to be initial concentration 10 mg/L, dosage 1.2 g, and pH 5.4. The adsorption data conformed to both the Langmuir and the Freundlich isotherms but fitted best into the Langmuir model. The R2 for Langmuir equation was 0.9997 and that for Freundlich was 0.9515. The Langmuir monolayer adsorption capacity of the activated carbon was calculated to be 37.31 mg/g. The results indicate that activated carbon might be used to effectively adsorb Pb(II ions from wastewater treatment plants.

  12. Adsorption behavior of {sup 99}Mo using AG1-X8 anionic resin

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Jacinete L. dos; Yamaura, Mitiko; Damasceno, Marcos O.; Forbicini, Christina A.L.G.O., E-mail: jlsantos@ipen.br, E-mail: myamaura@ipen.br, E-mail: marcos956@bol.com.br, E-mail: cforbici@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    The significant growth in demand of {sup 99}Mo in developed and developing countries, like Brazil, requires large production capacity and availability of this radioisotope. With the global crisis on its supply to Brazil rethought the need to become independent in their production and the solution was to start the Brazilian Multipurpose Reactor (RMB) project, which aims to meet the national demand of {sup 99}Mo for the medical field. This work aims to study the {sup 99}Mo adsorption in AG1-X8 strong anion resin, which is one of the intermediate steps of separation and purification, retaining it in the form of molybdate ions. In process evaluated the resin properties with respect to pH and concentration of {sup 99}Mo in the solution. The adsorbed amount of {sup 99}Mo was determined indirectly by the amount in the supernatant after adsorption and the data fitted to the Langmuir and Freundlich isotherms. Among the models, the Langmuir showed a closer relationship with the experimentally obtained data. This suggests the occurrence of monolayer adsorption and heterogeneous conditions at the surface, where both phenomena can coexist in the experimental conditions tested. (author)

  13. Molecular simulation of C{sub 60} adsorption onto a TiO{sub 2} rutile (1 1 0) surface

    Energy Technology Data Exchange (ETDEWEB)

    Palace Carvalho, A.J., E-mail: ajpalace@uevora.pt [Centro de Quimica de Evora, Universidade de Evora, R. Romao Ramalho 59, 7000-671 Evora (Portugal); Departamento de Quimica, Universidade de Evora, R. Romao Ramalho 59, 7000-671 Evora (Portugal); Prates Ramalho, J.P. [Centro de Quimica de Evora, Universidade de Evora, R. Romao Ramalho 59, 7000-671 Evora (Portugal); Departamento de Quimica, Universidade de Evora, R. Romao Ramalho 59, 7000-671 Evora (Portugal)

    2010-06-15

    A Monte Carlo molecular simulation study is presented on the adsorption and growth of C{sub 60} films on the surface of the (1 1 0) face of rutile. Simulations are performed for a temperature of 600 K using atomistic models both for the fullerene molecules and the TiO{sub 2} surface. It is found in this work that C{sub 60} is adsorbed preferably in an ordered arrangement along the surface depressions over the exposed undercoordinated Ti cations. At low densities adsorption occurs preferably at alternate rows, with locations in consecutive rows being occupied appreciably only at higher C{sub 60} densities. At low densities, the fullerene molecules tend to aggregate into islands in the surface plane. Additional layers of C{sub 60} form only as the density increases, and do so before a monolayer is completed in all consecutive rows. Full monolayer capacity obtained at the highest densities is about 0.9 C{sub 60} molecules per nm{sup 2}, but this is only achieved by completing the packing of molecules in interstices at a slightly upper level. The fraction of the molecules that lie closest to the surface only amounts to 0.6 molecules per nm{sup 2}.

  14. Mapping interfacial chemistry induced variations in protein adsorption with scanning force microscopy.

    Science.gov (United States)

    Ta, T C; McDermott, M T

    2000-06-01

    In this work, we demonstrate the sensitivity of scanning force microscopy (SFM), operated in friction force mode, to adsorbed protein conformation or orientation. We employ patterned films of methyl- and carboxylate-terminated alkanethiolate monolayers on gold as substrates for protein adsorption to observe the effect of each functional group in the same image. Infrared spectroscopic and SFM studies of bovine fibrinogen (BFG) adsorption to single-component monolayers indicate that complete films of BFG that are stable to imaging are formed at each functional group. After adsorption of BFG to a patterned monolayer, we observe a contrast in friction images due to differences in adsorbed BFG conformation or orientation induced by each functional group. We also observe frictional contrast in films of other proteins adsorbed on patterned monolayers. These observations lead to the conclusion that SFM-measured friction is sensitive to adsorbed protein state.

  15. Polymethylmethacrylate open tubular ion exchange columns: nondestructive measurement of very small ion exchange capacities.

    Science.gov (United States)

    Zhang, Min; Yang, Bingcheng; Dasgupta, Purnendu K

    2013-08-20

    We describe an approach to prepare an open tubular ion exchange (OTIE) column by coating a monolayer of anion exchange nanoparticle to a 16-20 μm bore polymethylmethacrylate (PMMA) capillary. The latex nanoparticle was electrostatically attached to carboxylate groups on the inner wall of capillary, pretreated with strong base for hydrolyzing the ester. Several approaches to nondestructively measure ion exchange capacities (IEC) of the columns were examined: (a) adsorption-desorption of an intensely fluorescent ion, e.g. fluorescein, and off-line fluorometry, (b) loading a weakly retained ion (e.g., IO3(-)), frontal displacement by a strongly bound ion (e.g., Cl(-)), and online optical or conductometric boundary detection, and (c) similar to the above except displacement being accompanied by reaction (e.g., acid-base titration). To our knowledge, this is the first time on-column titration has been used to measure capacities. By using different pH displacer solutions, we demonstrate for the first time the possibility of pKa-differentiated ion exchange capacity measurements. The cation exchange capacity of bare PMMA capillaries was on the order of 1 pequiv/mm(2) with little dependence on time and temperature of hydrolysis conditions. After AS18 latex coating, the strong base anion exchange capacity was on the order of 10 pequiv/mm(2), very close to what would be estimated on the basis of monolayer coverage of the surface by individual latex particles. The latex used contained a significant, additional amount of weak base character, about the same as the strong base ion exchange capacity.

  16. Evaluation of natural organic matter adsorption on Fe-Al binary oxide: Comparison with single metal oxides.

    Science.gov (United States)

    Kim, Kyung-Jo; Jang, Am

    2017-10-01

    The adsorption characteristics of three types of standard natural organic matter (NOM) on iron-aluminum (Fe-Al) binary oxide (FAO) and heated aluminum oxide (HAO) under natural surface water condition were investigated using various adsorption isotherms and kinetic models. FAO was synthesized by Fe oxide and Al oxide, mixed using the sol-gel hydrothermal method, and aluminum sulfate was used to make HAO. The amount of adsorbed NOM was increased to 79.6 mg g(-1) for humic acid (HA), 101.1 mg g(-1) for sodium alginate (SA) in the FAO, but the maximum adsorption capacity of bovine serum albumin (BSA) (461.3 mg g(-1)) was identified on the HAO. The adsorption of HA, BSA, and SA dramatically increased (>70%) on FAO in 5 min and HA was significantly removed (90%) among the three NOM. Mutual interaction among the adsorbed NOM (BSA) occurred on the HAO surface during adsorption due to formation of monolayer by protein molecules at neutral pH. The pseudo second order clearly represented the adsorption kinetics for both adsorbents. The equilibrium isotherm data of FAO was better exhibited by the Langmuir isotherm model than by the Freundlich isotherm, but HAO was a slightly non-linear Langmuir type. Also, the free energy, enthalpy, and entropy of adsorption were determined from the thermodynamic experiments. Adsorption on FAO was spontaneous and an exothermic process. Fluorescence excitation-emission matrix (FEEM) spectra were used to elucidate the variation in organic components. The results obtained suggests that the significant changes in the surface property of the adsorbent (large surface area, increased crystalline intensity, and fine particle size) were effectively determined by the Fe-synthesized Al oxide mixed using the sol-gel hydrothermal method. The results also suggest that the changes enhanced the adsorption capacity, whereby three NOM were notably removed on FAO regardless of NOM characteristics (hydrophobic and hydrophilic). Copyright © 2017 Elsevier

  17. Adsorption of amylase enzyme on ultrafiltration membranes.

    Science.gov (United States)

    Beier, Søren Prip; Enevoldsen, Ann Dorrit; Kontogeorgis, Georgios M; Hansen, Ernst B; Jonsson, Gunnar

    2007-08-28

    A method to measure the static adsorption on membrane surfaces has been developed and described. The static adsorption of amylase-F has been measured on two different ultrafiltration membranes, both with a cutoff value of 10 kDa (a PES membrane and the ETNA10PP membrane, which is a surface-modified PVDF membrane). The adsorption follows the Langmuir adsorption theory. Thus, the static adsorption consists of monolayer coverage and is expressed both as a permeability drop and an adsorption resistance. From the adsorption isotherms, the maximum static permeability drops and the maximum static adsorption resistances are determined. The maximum static permeability drop for the hydrophobic PES membrane is 75%, and the maximum static adsorption resistance is 0.014 m2.h.bar/L. The maximum static permeability drop for the hydrophilic surface-modified PVDF membrane (ETNA10PP) is 23%, and the maximum static adsorption resistance is 0.0046 m2.h.bar/L. The difference in maximum static adsorption, by a factor of around 3, affects the performance during the filtration of a 5 g/L amylase-F solution at 2 bar. The two membranes behave very similarly during filtration with almost equal fluxes and retentions even though the initial water permeability of the PES membrane is around 3 times larger than the initial water permeability of the ETNA10PP membrane. This is mainly attributed to the larger maximum static adsorption of the PES membrane. The permeability drop during filtration exceeds the maximum static permeability drop, indicating that the buildup layer on the membranes during filtration exceeds monolayer coverage, which is also seen by the increase in fouling resistance during filtration. The accumulated layer on the membrane surface can be described as a continually increasing cake-layer thickness, which is independent of the membrane type. At higher concentrations of enzyme, concentration polarization effects cannot be neglected. Therefore, stagnant film theory and the osmotic

  18. Adsorption of Pb(II) ions present in aqueous solution on the oxy hydroxides: boehmite (γ-AIOOH), goethite (α-FeOOH) and manganite (γ-MnOOH); Adsorcion de iones Pb(II) presentes en solucion acuosa sobre los oxihidroxidos: boehmita (γ-AlOOH), goetita (α-FeOOH) y manganita (γ-MnOOH)

    Energy Technology Data Exchange (ETDEWEB)

    Arreola L, J. E.

    2013-07-01

    Boehmite, goethite and manganite were synthesized by different methods and characterized using X-ray diffraction (XRD), infrared spectroscopy (IR), thermogravimetric study , N{sub 2} physisorption measurements, scanning electron microscopy (Sem), semiquantitative elemental analysis (EDS), as well as additional studies were determined the surface active sites concentration and zero point of charge. Furthermore, we studied the Pb(II) ion adsorption capacity present in aqueous solution on these synthesized materials by batch-type experiments at room temperature, as a function of contact time between the phases liquid-solid system (adsorption kinetics), initial concentration of the adsorbate (adsorption isotherms), ph and temperature. The adsorption equilibrium time of adsorption processes in these studied systems was found at 60 minutes for boehmite and 30 minutes for goethite and manganite respectively after contacting the solid-liquid phase systems. The adsorption capacity of the lead ions on these adsorbent materials depended of lead concentration, ph and temperature of the systems. Were evaluated lead adsorption capacities in these materials to different contact times using an initial concentration of 20 mg/L of Pb(II) ions at ph = 4, the results of three systems were adjusted to second pseudo kinetic model order. With respect to the study of the adsorbate concentration effect, boehmite-Pb(II) and goethite-Pb(II) systems were adjusted to Langmuir isotherm model which proposes that the adsorption is carried out in a monolayer, moreover manganite-Pb(II) system was adjusted Temp kin isotherm model, which assumes that the adsorption heat of all the molecules in the layer decreases linearly with coverage due to adsorbent-adsorbate interactions and adsorption is characterized by a uniform distribution of the binding energies. Were studied the ph effect of Pb(II) ions solution on the adsorption capacity of such adsorbents, it was found that as the ph increases lead

  19. Adsorption of Atenolol on Kaolinite

    Directory of Open Access Journals (Sweden)

    Yingmo Hu

    2015-01-01

    Full Text Available In this study the adsorption of atenolol (AT, a β-blocker, on kaolinite, a clay mineral of low surface charge, was investigated under varying initial AT concentration, equilibrium time, solution pH, ionic strength, and temperature conditions. The results showed that the amounts of AT uptake by kaolinite were close to its cation exchange capacity value and the AT adsorption was almost instantaneous, suggesting a surface adsorption. The adsorption was exothermic and the free energy of adsorption was small negative, indicating physical adsorption. The increase in ionic strength of the solution drastically reduced AT uptake on kaolinite. A significant reduction in AT uptake was found at solution pH below 5 or above 10. The FTIR results showed band shifting and disappearance for NH bending vibration and benzene ring skeletal vibration at 3360 and 1515 cm−1 and band splitting at 1412 and 1240 cm−1 attributed to C–N valence vibration coupled with NH bending vibrations and alkyl aryl ether linkage, suggesting the participation of NH, –O–, and benzene ring for AT adsorption on kaolinite.

  20. Interactions of doxorubicin with self-assembled monolayer-modified electrodes: electrochemical, surface plasmon resonance (SPR), and gravimetric studies.

    Science.gov (United States)

    Nieciecka, Dorota; Krysinski, Pawel

    2011-02-01

    We present the results on the partitioning of doxorubicin (DOX), a potent anticancer drug, through the model membrane system, self-assembled monolayers (SAMs) on gold electrodes. The monolayers were formed from alkanethiols of comparable length with different ω-terminal groups facing the aqueous electrolyte: the hydrophobic -CH(3) groups for the case of dodecanethiol SAMs or hydrophilic -OH groups of mercaptoundecanol SAMs. The electrochemical experiments combined with the surface plasmon resonance (SPR) and gravimetric studies show that doxorubicin is likely adsorbed onto the surface of hydrophilic monolayer, while for the case of the hydrophobic one the drug mostly penetrates the monolayer moiety. The adsorption of the drug hinders further penetration of doxorubicin into the monolayer moiety.

  1. Decoupling of crystalline and conformational degrees of freedom in lipid monolayers

    DEFF Research Database (Denmark)

    Ipsen, John Hjorth; Mouritsen, Ole G.; Zuckermann, Martin J.

    1989-01-01

    by a liquid-conformationally ordered phase. This prediction is consistent with synchrotron x-ray experiments which show that the chain-ordering transition and the crystallization process need not take place at the same lateral pressure. A characterization is provided of the nonequilibrium effects and pattern-formation...... of the experimentally observed isotherms of lipid monolayer phase behavior. It is pointed out that cholesterol, which promotes lipid-chain conformational order, has a unique capacity of acting as a `crystal breaker' in the solid monolayer phases and therefore provides a molecular mechanism for decoupling crystalline...... and conformational order in lipid monolayers containing cholesterol. The phase diagram of mixed cholesterol–lipid monolayers is derived and discussed in relation to monolayer experiments. The Journal of Chemical Physics is copyrighted by The American Institute of Physics....

  2. Oligo(ethylene glycol)-terminated monolayers on silicon surfaces and their nanopatterning with a conductive atomic force microscope

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Functionalization of silicon substrate surfaces with a stable monolayer for resisting non-specific adsorption of proteins has attracted great interest,since it is directly relevant to the development of miniature,silicon-based biosensors and implantable microdevices,such as silicon-neuron interfaces.This brief review summarizes our contribution to the development of robust monolayers grown by surface hydrosilylation on atomically flat,hydrogen-terminated silicon surfaces.The review also outlines our strategy and progress on the fabrication of single molecule patterns on such monolayer platforms.

  3. Equilibrium Kinetics and Isotherm Studies of Cu (II Adsorption from Waste Water onto Alkali Activated Oil Palm Ash

    Directory of Open Access Journals (Sweden)

    Zaira Z. Chowdhury

    2011-01-01

    Full Text Available Problem statement: Heavy metal accumulation in waste water could affect aquatic life, human health and overall ecosystem adversely. Therefore, in recent years much emphasis has been given for the use of industrial waste material as low cost adsorbents for removal of metallic contaminants from waste water. Approach: Present study deals with the adsorption equilibrium and kinetics of Cu (II cation using sodium hydroxide activated Oil Palm Ash (OPA. Adsorption was investigated in a batch system with respect to various parameters such as initial metal ion concentration, contact time and pH of the solution. Surface characterization of the prepared adsorbent was done by using surface area analyzer, Scanning Electron Microscope (SEM and X-ray Fluorescence and compared with natural oil palm ash. The adsorption equilibrium data were best represented by Langmuir, Freundlich and Temkin model. Equilibrium kinetics studies were performed by Pseudo first order, Pseudo second order and Intra-particle diffusion. Results: Maximum monolayer adsorption capacity observed at 30°C was 18.86 mg g−1. Kinetic data correlated well with the pseudo second order model, suggesting that the adsorption process might be chemical sorption. The linear plots of intra particle diffusion revealed that the adsorption process was mainly governed by pore diffusion. Equilibrium uptake was increased with increase of initial concentration and contact time. Experimental data showed that about 96.03% of copper can be removed at pH 5.5. Conclusion: The research concluded that activation by alkali treatment of natural OPA would produce sufficient porosities and surface area and it has got good potential to remove Cu (II from waste water.

  4. 焦木素对苯酚吸附性能的研究%STUDY ABOUT ADSORPTION PROPERTIES OF PYROXYLIN FOR PHENOL

    Institute of Scientific and Technical Information of China (English)

    李丽敏; 彭学伟; 焦为成

    2001-01-01

    With pyroxy as an adsorbent,the adsorption of pyroxylin for phenol in sewage,the rate of adsorption,the capacity of adsorption and the effect of pH on the adsorption of phenol were studied.The resullts indicated that the pyroxylin had well properties of adsorption,the adsorption isotherms were conformed to Freundlich equation.

  5. Surface Analysis of 4-Aminothiophenol Adsorption at Polycrystalline Platinum Electrodes

    Science.gov (United States)

    Rosario-Castro, Belinda I.; Fachini, Estevao R.; Contes, Enid J.; Perez-Davis, Marla E.; Cabrera, Carlos R.

    2008-01-01

    Formation of self-assembled monolayer (SAM) of 4-aminothiophenol (4-ATP) on polycrystalline platinum electrodes has been studied by surface analysis and electrochemistry techniques. The 4-ATP monolayer was characterized by cyclic voltammetry (CV), Raman spectroscopy, reflection absorption infrared (RAIR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). Cyclic voltammetry (CV) experiments give an idea about the packing quality of the monolayer. RAIR and Raman spectra for 4-ATP modified platinum electrodes showed the characteristic adsorption bands for neat 4-ATP indicating the adsorption of 4-ATP molecules on platinum surface. The adsorption on platinum was also evidenced by the presence of sulfur and nitrogen peaks by XPS survey spectra of the modified platinum electrodes. High resolution XPS studies and RAIR spectrum for platinum electrodes modified with 4-ATP indicate that molecules are sulfur-bonded to the platinum surface. The formation of S-Pt bond suggests that ATP adsorption gives up an amino terminated SAM. Thickness of the monolayer was evaluated via angle-resolved XPS (AR-XPS) analyses. Derivatization of 4-ATP SAM was performed using 16-Br hexadecanoic acid.

  6. Fator capacidade de fósforo em solos de pernambuco mineralogicamente diferentes e influência do pH na capacidade máxima de adsorção Phosphate capacity factor in mineralogically different soils in Pernambuco and the influence of pH on the maximum capacity of adsorption

    Directory of Open Access Journals (Sweden)

    Fábio Broggi

    2011-02-01

    -plant relations. Moreover, the soil pH has affected adsorption, and in other cases, it has shown small and inconsistent change in the maximum adsorption capacity of P (CMAP. Thus, this study aimed to determine the different FCP soil mineralogy in Pernambuco; to correlate physical and chemical characteristics of soils with PBC and to evaluate the effect of pH on the CMAP. Subsurface soil samples from four different soils were characterized chemically and physically determined, and the PBC was determined. These samples were corrected with CaCO3 and MgCO3 in a 4:1 ratio and incubated for 30 days, except the Vertisol. The CMAP was determined before and after correction of the soil. The experiment consisted of a 4 x 2 factorial (four soils with and without correction, distributed in randomized blocks with three replicates. Soil characteristics that best reflected the PBC were the remaining P (P-rem and MPAC. Regardless of the constituents of clay mineralogy, soil with high aluminum levels had increased CMAP after correction. The energy of adsorption (EA in the limed soils was on average significantly lower, regardless of the soil.

  7. Adsorption of Helium Atoms on Two-Dimensional Substrates

    Science.gov (United States)

    Burganova, Regina; Lysogorskiy, Yury; Nedopekin, Oleg; Tayurskii, Dmitrii

    2016-01-01

    The study of the adsorption phenomenon of helium began many decades ago with the discovery of graphite as a homogeneous substrate for the investigation of physically adsorbed monolayer films. In particular, helium monoatomic layers on graphite were found to exhibit a very rich phase diagram. In the present work we have investigated the adsorption phenomenon of helium atoms on graphene and silicene substrates by means of density functional theory with Born-Oppenheimer approximation. Helium-substrate and helium-helium interactions were considered from first principles. Vibrational properties of adsorbed monolayers have been used to explore the stability of the system. This approach reproduces results describing the stability of a helium monolayer on graphene calculated by quantum Monte Carlo (QMC) simulations for low and high coverage cases. However, for the moderate coverage value there is a discrepancy with QMC results due to the lack of helium zero point motion.

  8. Adsorption of Helium Atoms on Two-Dimensional Substrates

    Science.gov (United States)

    Burganova, Regina; Lysogorskiy, Yury; Nedopekin, Oleg; Tayurskii, Dmitrii

    2016-12-01

    The study of the adsorption phenomenon of helium began many decades ago with the discovery of graphite as a homogeneous substrate for the investigation of physically adsorbed monolayer films. In particular, helium monoatomic layers on graphite were found to exhibit a very rich phase diagram. In the present work we have investigated the adsorption phenomenon of helium atoms on graphene and silicene substrates by means of density functional theory with Born-Oppenheimer approximation. Helium-substrate and helium-helium interactions were considered from first principles. Vibrational properties of adsorbed monolayers have been used to explore the stability of the system. This approach reproduces results describing the stability of a helium monolayer on graphene calculated by quantum Monte Carlo (QMC) simulations for low and high coverage cases. However, for the moderate coverage value there is a discrepancy with QMC results due to the lack of helium zero point motion.

  9. The Adsorption of NOx on Magnesium Aluminium Hydrotalcite

    Institute of Scientific and Technical Information of China (English)

    Zhe Ming NI; Wei Hua YU; Shao Fen ZHAO; Zhong Hua GE

    2004-01-01

    Magnesium aluminium hydrotalcite (Mg-Al-HT) with molar ratio of Mg-to-Al of 3 to 1 was prepared and characterized by X-ray diffraction (XRD) and infrared spectra (IR).The performances of Mg-Al-HT for the adsorption and desorption of NOx were studied.The results indicated that the adsorption capacity of the hydrotalcite for NOx was 1398.2 mg/g, and it was higher than the acticarbon's.The adsorption capacities depended on adsorption time and temperature.Mg-Al-HT could be regenerated by thermal decomposition, and the adsorption efficiency had not changed markedly after three cycles.

  10. 榴莲壳内皮果胶多糖和黄酮对重金属吸附作用的研究%Study on pectin polysaccharides and flavonoids extraction of durian inner shell on adsorption capacity of heavy metals

    Institute of Scientific and Technical Information of China (English)

    王晓波; 车海萍; 陈海珍; 刘冬英; 王梅

    2011-01-01

    目的:从榴莲壳内皮中提取果胶多糖和黄酮,并评价果胶多糖和黄酮对重金属的吸附作用。方法:以榴莲壳内皮为原料,采取水提乙醇沉淀法从榴莲壳内皮中提取高酯果胶及黄酮,采用碱化法将高酯果胶转化为低酯果胶,并用原子吸收光谱法测定高酯果胶、低酯果胶及黄酮对重金属的吸附率,从而评价其吸附能力。结果:在模拟胃液及肠液条件下,高酯果胶、低酯果胶和黄酮对铅的吸附能力:高酯果胶〉低酯果胶〉黄酮,对镉的吸附能力:低酯果胶〉高酯果胶〉黄酮;对钙、铁及锌离子均无吸附能力。结论:榴莲壳内皮中提取物果胶及黄酮对重金属元素有一定的选择性吸附作用,具有进一步研究和开发价值。%Objective:Study on pectin polysaccharides and flavonoids from durian inner shell and the adsorption capacity of the heavy metal. Methods:The durian inner shell as raw materials to ethanol precipitation,water extraction were directly extracted,high ester pectin and flavonoids,using alkaline method into the high-ester pectin with low ester pectin,to evaluate their adsorption capacity by atomic absorption spectrometry. Results:In simulated gastric and intestinal fluid conditions,the high ester pectin,low ester pectin and flavonoids adsorption capacity of Pb2+:high ester pectinlow ester pectinflavonoids,the adsorption capacity of Cd2+:low ester pectinhigh ester pectinflavonoids. There was no significant influence on Fe2+,Zn2+,Ca2+ absorption. Conclusion:The pectin and flavonoids extraction from durian inner shell had a certain heavy metal adsorption capacity,with research and development value.

  11. Adsorption of Methylene Blue from Aqueous Solution onto a Low-Cost Natural Jordanian Tripoli

    Directory of Open Access Journals (Sweden)

    Atef S. ALzaydien

    2009-01-01

    of the MB dye solution at specified concentrations was continuously stirred at 160 rpm with 0.5 g of Tripoli at 25◦C. Samples were withdrawn at appropriate time intervals and then centrifuged at 4000 rpm for 15 min and the absorbance of the supernatant was measured. The concentration of the residual dye was measured using UV/visible spectrometer at a λmax corresponding to the maximum absorption for the dye solution (λmax= 661 nm. Results: Four kinetic models are the pseudo-first-order, pseudo-second-order, Elovich and intraparticle diffusion equations, were selected to interpret the adsorption data. The kinetic parameters were calculated from the experimental data and it was shown that they could be fitted well to the pseudo-second-order kinetic and intra-particle diffusion models. The linear Langmuir and Freundlich models were applied to describe equilibrium isotherms The adsorption data obtained were well described by the Langmuir adsorption isotherm model. The maximum adsorption capacity was found to be 16.6 mg g−1 from the Langmuir isotherm model at 25 °C. The Langmuir isotherm constant, KL, was used to evaluate the changes of free energy . The negative value of free energy change indicated the spontaneous nature of sorption and confirmed affinity of natural Jordanian tripoli for the methylene blue basic dye .Conclusion: The present study shows that the natural Jordanian tripoli, an abundant low-cost clay, can be used as sorbent for the removal of methylene blue dye from aqueous solutions. The amount of dye sorbed was found to vary with initial pH, tripoli dose, methylene blue concentration and contact time. The value of The monolayer saturation capacity of tripoli was comparable to the adsorption capacities of some other adsorbent materials for MB dye .

  12. Adsorption of organic molecules at the mercury-solution interface: effect of anion specific adsorption on double layer properties. [Benzyl alcohol

    Energy Technology Data Exchange (ETDEWEB)

    Buckfelder, J.J. III

    1980-08-01

    Adsorption of iso-pentanol, pentanoic acid, and benzyl alcohol at the mercury-solution interface was studied in HC1O/sub 4/, H/sub 2/SO/sub 4/, NaNO/sub 3/, and NaF electrolytes. The Frumkin isotherm equation Ba = (theta/(1-theta))exp(2..cap alpha..theta) together with the implied charge vs. surface excess relation: q = (1-theta)q/sub w/ + thetaQ were used to analyze the experimental data. Linear charge vs surface excess plots were obtained for the aliphatic compounds over the entire potential region studied; for benzyl alcohol, plots were linear only at anodic potentials. The slopes of these lines agreed with those predicted by the above equation, with Q = C/sub org/(V-V/sub n/), for cathodic potentials. At potentials anodic to the electrocapillary maximum, deviations between experimental and theoretical slopes appeared. In the model proposed, the double layer consists of two parts. The layer closest to the surface is restricted to water molecules and specifically adsorbed ions. The second layer contains organic molecules exclusively; any charge necessary to balance the surface charge is considered to be in a monolayer adjacent to the organic layer. From the slope of the charge vs surface excess plots, it is possible to calculate the charge on the covered portion of the surface and then calculate the amount of specific adsorption. The relative amounts of specific adsorption are in agreement with known strengths of adsorption of the anions of the electrolyte. Capacity curves were also calculated and were in good agreement with experimental curves.

  13. Kinetic modelling and mechanism of dye adsorption on unburned carbon

    Energy Technology Data Exchange (ETDEWEB)

    Wang, S.B.; Li, H.T. [Curtin University of Technology, Perth, WA (Australia). Dept. of Chemical Engineering

    2007-07-01

    Textile dyeing processes are among the most environmentally unfriendly industrial processes by producing coloured wastewaters. The adsorption method using unburned carbon from coal combustion residue was studied for the decolourisation of typical acidic and basic dyes. It was discovered that the unburned carbon showed high adsorption capacity at 1.97 x 10{sup -4} and 5.27 x 10{sup -4} mol/g for Basic Violet 3 and Acid Black 1, respectively. The solution pH, particle size and temperature significantly influenced the adsorption capacity. Higher solution pH favoured the adsorption of basic dye while reduced the adsorption of acid dye. The adsorption of dye increased with increasing temperature but decreased with increasing particle size. Sorption kinetic data indicated that the adsorption kinetics followed the pseudo-second-order model. The adsorption mechanism consisted of two processes, external diffusion and intraparticle diffusion, and the external diffusion was the dominating process.

  14. Phase separated anionic domains in ternary mixed lipid monolayers at the air-water interface.

    Science.gov (United States)

    Maloney, K M; Grainger, D W

    1993-04-01

    A series of ternary mixed monolayers containing varying amounts of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and equimolar additions of 1-palmitoyl-2-hydroxy-sn-glycero-3-phosphocholine (LYSO-PC) and palmitic acid (PA) were studied at the air-water interface. These mixed monolayers were used to model phospholipid biomembrane interfaces resulting from phospholipase A2 (PLA2) hydrolysis. Recent work [D.W. Grainger A. Reichert, H. Ringsdorf and C. Salesse (1989) Biochim. Biophys. Acta. 1023, 365-379] has shown that PLA2 hydrolysis of pure phospholipid monolayers results in formation of large PLA2 domains at the air-water interface. These domains are proposed to result from PLA2 adsorption to phase separated regions in the hydrolyzed monolayer. To elucidate the phase behaviour in these monolayer systems, surface pressure-area isotherms were measured for the ternary mixtures on pure water and buffered subphases. Fluorescence microscopy at the air-water interface was used to image fluorescent probe-doped monolayer mixtures during isothermal compressions. A water-soluble cationic carbocyanine dye was used to probe the interfacial properties of the mixed monolayers. Isotherm data do not provide unambiguous evidence for either phase separation or ideal mixing of monolayer components. Fluorescence microscopy is more revealing, showing that lateral phase separation of microstructures containing palmitic acid occurred only when monolayer subphases contained Ca2+ ions at alkaline pH. At either low pH or on Ca(2+)-free subphases, phase separation was not observed.

  15. Effect of H-vacancy defect on the adsorption of CO and NO on graphane: A DFT study

    Science.gov (United States)

    Zhou, Qingxiao; Ju, Weiwei; Yong, Yongliang; Su, Xiangying; Li, Xiaohong; Fu, Zhibing; Wang, Chaoyang

    2017-10-01

    We investigated the adsorption of CO and NO molecules on hydrogenated graphene (graphane) monolayer using density functional theory (DFT) calculations. The geometry, adsorption stability, and electronic properties of CO and NO molecules absorbed on pure and H-vacancy defected graphane sheet were performed. The calculated results suggested that the small adsorption energy indicated the adsorption of CO and NO molecules on pure graphane were physisorption. However, the presence of H-vacancy improved the reactivity of graphane and the adsorption on H-vacnacy defected graphane changed to chemisorption. The adsorption also induced obvious change into the band gaps, which can be seen as signal to detect the CO and NO gas.

  16. Adsorption behavior of methylene blue by bone char

    Science.gov (United States)

    Jia, Puqi; Tan, Hongwei; Liu, Kuiren; Gao, Wei

    2017-07-01

    This work studies the adsorption behavior of methylene blue (MB) from water by bone char (BC). The effects of pH, initial dye concentration and dosage of adsorbent on the adsorption were investigated. It was found that the adsorption capacity of MB was affected by the mount of OH-, initial concentration gradient driving force of MB, the surface charge and adsorption site of BC.

  17. Adsorption of D113 Resin for Dysprosium(Ⅲ)

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The adsorption behavior and mechanism of D113 resin for Dy(Ⅲ) was investigated by using the method of resin adsorption. Experimental results show that the optimum medium pH of adsorption of D113 resin for Dy3+ is pH=6.00 in the HAc-NaAc medium. The static adsorption capacity of D113 resin for Dy3+chemical analysis and IR spectra.

  18. Adsorption of Amido Black 10B from aqueous solutions onto Zr (IV) surface-immobilized cross-linked chitosan/bentonite composite

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Lujie; Hu, Pan; Wang, Jing; Huang, Ruihua, E-mail: hrh20022002@163.com

    2016-04-30

    Graphical abstract: - Highlights: • Zr-CCB was prepared and characterized. • The adsorption of AB10B followed the Langmuir isotherm model. • The pseudo-second-order model described the kinetic behavior. - Abstract: Zr(IV) surface-immobilized cross-linked chitosan/bentonite composite was synthesized by immersing cross-linked chitosan/bentonite composite in zirconium oxychloride solution, and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, Scanning electron microscopy techniques. The adsorption of an anionic dye, Amido Black 10B, from aqueous solution by Zr(IV) loaded cross-linked chitosan/bentonite composite was investigated as a function of loading amount of Zr(IV), adsorbent dosage, pH value of initial dye solution, and ionic strength. The removal of Amido Black 10B increased with an increase in loading amount of Zr(IV) and adsorbent dosage, but decreased with an increase in pH or ionic strength. The adsorption of AB10B onto Zr(IV) loaded cross-linked chitosan/bentonite composite was favored at lower pH values and higher temperatures. The Langmuir isotherm model fitted well with the equilibrium adsorption isotherm data and the maximum monolayer adsorption capacity was 418.4 mg/g at natural pH value and 298 K. The pseudo-second-order kinetic model well described the adsorption process of Amido Black 10B onto Zr(IV) loaded cross-linked chitosan/bentonite composite. The possible mechanisms controlling Amido Black 10B adsorption included hydrogen bonding and electrostatic interactions.

  19. Adsorption of monoclonal antibodies to glass microparticles.

    Science.gov (United States)

    Hoehne, Matthew; Samuel, Fauna; Dong, Aichun; Wurth, Christine; Mahler, Hanns-Christian; Carpenter, John F; Randolph, Theodore W

    2011-01-01

    Microparticulate glass represents a potential contamination to protein formulations that may occur as a result of processing conditions or glass types. The effect of added microparticulate glass to formulations of three humanized antibodies was tested. Under the three formulation conditions tested, all three antibodies adsorbed irreversibly at near monolayer surface coverages to the glass microparticles. Analysis of the secondary structure of the adsorbed antibodies by infrared spectroscopy reveal only minor perturbations as a result of adsorption. Likewise, front-face fluorescence quenching measurements reflected minimal tertiary structural changes upon adsorption. In contrast to the minimal effects on protein structure, adsorption of protein to suspensions of glass microparticles induced significant colloidal destabilization and flocculation of the suspension.

  20. Adsorption of lipids on silicalite-1

    Science.gov (United States)

    Atyaksheva, L. F.; Ivanova, I. I.; Ivanova, M. V.; Tarasevich, B. N.; Fedosov, D. A.

    2017-05-01

    The adsorption of egg lecithin and cholesterol from chloroform solutions onto silicalite-1 (hydrophobic silica with MFI zeolite structure) is investigated. Adsorption isotherms of the L-type for lecithin and the S-type for cholesterol are obtained in the 0.05-4.5 mg/mL range of equilibrium lipid concentrations. The maximum adsorption for lecithin is 30 mg/g; for cholesterol it is 70 mg/g. Chloroform treatment results in the desorption of no more than 10% of the lecithin and up to 50% of the cholesterol from the silicalite-1 surface. The lecithin molecules in the monolayer on the silicalite-1 are oriented such that their hydrophobic tails are oriented toward the surface and are partially inside the pores of the adsorbent.

  1. Effect of piezoelectric material on hydrogen adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xuan [Department of Materials Science and Engineering, Michigan Technological University, 1400 Townsend Drive, Houghton, MI, 49931 (United States); Civil and Environmental Engineering School, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing, 100083 (China); Hwang, Jiann-Yang; Shi, Shangzhao; Sun, Xiang; Zhang, Zheng [Department of Materials Science and Engineering, Michigan Technological University, 1400 Townsend Drive, Houghton, MI, 49931 (United States)

    2010-09-15

    In hydrogen storage applications, the primary issue for physisorption of hydrogen onto solid-state materials is the weak interaction force between hydrogen molecules and the adsorbents. It is found that enhanced adsorption can be obtained under an external electric field, because it appears the electric field increases the hydrogen adsorption energy. Experiments were carried out to determine hydrogen adsorption on activated carbon using the piezoelectric material PMN-PT as the charge supplier under hydrogen pressure. Results indicate that more than 20% hydrogen adsorption enhancement was obtained. Parameters related to hydrogen adsorption enhancement include the amount of the charge and temperature. Higher voltage and lower temperature promote the increase of adsorption capacity but room temperature results are very encouraging. (author)

  2. ADSORPTION AND RELEASING PROPERTIES OF BEAD CELLULOSE

    Institute of Scientific and Technical Information of China (English)

    A. Morales; E. Bordallo; V. Leon; J. Rieumont

    2004-01-01

    The adsorption of some dyes on samples of bead cellulose obtained in the Unit of Research-Production "Cuba 9"was studied. Methylene blue, alizarin red and congo red fitted the adsorption isotherm of Langmuir. Adsorption kinetics at pH = 6 was linear with the square root of time indicating the diffusion is the controlling step. At pH = 12 a non-Fickian trend was observed and adsorption was higher for the first two dyes. Experiments carried out to release the methylene blue occluded in the cellulose beads gave a kinetic behavior of zero order. The study of cytochrome C adsorption was included to test a proteinic material. Crosslinking of bead cellulose was performed with epichlorohydrin decreasing its adsorption capacity in acidic or alkaline solution.

  3. Adsorption and Desorption of Methiopyrsulfuron in Soils

    Institute of Scientific and Technical Information of China (English)

    WU Chun-Xian; WANG Jin-Jun; ZHANG Su-Zhi; ZHANG Zhong-Ming

    2011-01-01

    Methiopyrsulfuron is a new low-rate sulfonylurea herbicide for weed control in wheat; however, there is a lack of published information on its behavior in soils. In this study, methiopyrsulfuron adsorption and desorption were measured in seven soils sampled from Heilongjiang, Shandong, Jiangxi, Sichuan, Anhui, and Chongqing provinces of China using a batch equilibrium method. The Freundlich equation was used to described its adsorption and desorption. Adsorption isotherms were nonlinear with the values of Kf-ads, the Freundlich empirical constant indicative of the adsorption capacity,ranging from 0.75 to 2.46, suggesting that little of this herbicide was adsorbed by any of the seven soils. Soil pH and organic matter content (OM) were the main factors influencing adsorption; adsorption was negatively correlated with pH and positively correlated with OM. Methiopyrsulfuron desorption was hysteretic on the soils with high OM content and low pH.

  4. Characterization of Formation Kinetics of Self-Assembled Thiol Monolayers on Gold by Electrochemical Impedance Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Self-assembled monolayers of octadecanethiol (ODT) on gold have been studied by electrochemical impedance spectroscopy (EIS). The fractional coverage has been examined as a function of immersion time of Au in ODT deposition solution. The fractional coverage exhibits two distinct adsorption steps: an initial rapid step followed by a slow one. The fractional coverage of ODT monolayer increases sharply from zero to more than 99% of its maximum within the first minute. However, it takes a day for the fractional coverage to approach its final value.

  5. Structure of self-assembled monolayer of NPAN on Au(111) electrode

    Institute of Scientific and Technical Information of China (English)

    YANG Guangzheng; ZENG Qingdao; WAN Lijun; BAI Chunli

    2003-01-01

    Adsorption of 4-(4-nitrophenylazo)-1-naphthol (NPAN), an azobenzene derivative, on Au(111) has been investigated in aqueous HClO4 solution by using the cyclic voltammetry and scanning tunneling microscopy (STM). The molecule is found to form a stable monolayer on the electrode with a (6×4) structure relative to the underlying Au(111) lattice. Cyclic voltammograms show that the redox reactions occurring on the electrode are retarded by the formation of the monolayer. A structural model is proposed for the two-dimensional adlayer.

  6. Combined paracetamol and amitriptyline adsorption to activated charcoal

    DEFF Research Database (Denmark)

    Hoegberg, Lotte Christine Groth; Groenlykke, Thor Buch; Abildtrup, Ulla;

    2010-01-01

    Objectives. High-gram drug doses seen in multiple-drug poisonings might be close to the adsorption capacity of activated charcoal (AC). The aim was to determine the maximum adsorption capacities (Q(m)) of amitriptyline and paracetamol, separately and in combination, to AC. Methods. ACs (Carbomix...

  7. Positional order in Langmuir monolayers

    DEFF Research Database (Denmark)

    Kaganer, V.M.; Brezesinski, G.; Möhwald, H.;

    1998-01-01

    We find that a structural solid-solid phase transition in a two-dimensional Langmuir film is accompanied by strong positional disorder. Specifically, we find by a grazing-incidence x-ray diffraction experiment that in monolayers of octadecanol both the hexagonal phase LS and the centered rectangu......We find that a structural solid-solid phase transition in a two-dimensional Langmuir film is accompanied by strong positional disorder. Specifically, we find by a grazing-incidence x-ray diffraction experiment that in monolayers of octadecanol both the hexagonal phase LS and the centered...

  8. Electromelting of Confined Monolayer Ice

    CERN Document Server

    Qiu, Hu

    2013-01-01

    In sharp contrast to the prevailing view that electric fields promote water freezing, here we show by molecular dynamics simulations that monolayer ice confined between two parallel plates can melt into liquid water under perpendicularly applied electric field. The melting temperature of the monolayer ice decreases with the increasing strength of the external field due to field-induced disruption of the water-wall interaction induced well-ordered network of hydrogen bond. This electromelting process should add an important new ingredient to the physics of water.

  9. Multicomponent Adsorption Model for Polar and Associating Mixtures

    DEFF Research Database (Denmark)

    Nesterov, Igor; Shapiro, Alexander; Kontogeorgis, Georgios M.

    2015-01-01

    of these problems could be due to the fact that the original MPTA assumes that a given adsorbent has the same adsorption capacity (for example, porous volume) for all the adsorbed substances and is adjusted simultaneously to many data. This is a simplified picture, as experimental data indicate that the adsorption....... Thus, we feel that there is no need to use more complex potentials provided that the difference in the individual adsorption capacities is accounted for....

  10. Effect of solution acidity on adsorption capacity and magnetic performances of magnetic activated carbon%溶液酸度对磁性活性炭吸附性能和磁性能的影响

    Institute of Scientific and Technical Information of China (English)

    王燕; 解强; 唐瀚滢; 姚鑫; 刘娟; 宫国卓

    2012-01-01

    Magnetic activated carbons (MACs) were prepared from Taixi anthracite in the pres- ence of Fe3O4. The MACs were soaked in hydrochloric acid solution with different concentra- tions. The iodine number and methylene blue value of MACs samples before and after acid so- lution soaking were determined, and X-ray diffraction and a vibrating sample magnetometer were exploited to characterize the Fe-containing components and magnetic performances of MACs, respectively. The results show that the adsorption capacity and magnetic property of MACs are strongly influenced by solution acidity. When the MACs was soaked by hydrochloric acid solution of 1 tool/L, the iodine number is increased by 7. 9% and the maximum iodine number is up to 732.49 mg/g, meanwhile its specific susceptibility reduces from 259 × 10^-7 to 7. 16× 10^-7m^3/kg. But it is still effective for magnetic sorting recycling. MACs thoroughly losses its magnetism when the concentration of the soaking acid solution is 2 mol/L.%以太西无烟煤为原料、Fe3O4为添加剂制备煤基磁性活性炭,用不同浓度的盐酸溶液浸泡,测定酸液浸泡前后活性炭的碘值和亚甲蓝值,采用X射线衍射仪和振动样品磁强计分别测定、表征活性炭中含铁化合物的组成和磁性能.结果表明,溶液酸度对磁性活性炭的吸附性能和磁性能均有影响,当溶液酸浓度达到1mol/L时,磁性活性炭浸泡后的碘值提高了7.9%、达732.49mg/g,比磁化系数从259×10-7 m3/kg降低到7.16×10-7 m3/kg,但仍能采用磁场分选回收;当溶液酸浓度达到2mol/L时,磁性活性炭完全失磁.

  11. Teor e capacidade máxima de adsorção de arsênio em Latossolos brasileiros Content and maximum capacity of arsenic adsorption in Brazilian Oxisols

    Directory of Open Access Journals (Sweden)

    Mari Lucia Campos

    2007-12-01

    Full Text Available A alta toxicidade do As aos animais e humanos e a possibilidade de existência de grande número de áreas contaminadas tornam imprescindível o conhecimento do teor semitotal em solos ditos não-contaminados e dos processos de adsorção do As em solos de carga variável. O objetivo deste trabalho foi determinar o teor e a capacidade máxima de adsorção de As (CMADS AS em Latossolos. O teor total foi determinado pelo método USEPA 3051A, e a CMADS As, com auxílio de isotermas de Langmuir com base nos valores de adsorção obtidos em dose de As (0, 90, 190, 380, 760 e 1.150 µmol L-1 (relação solo:solução final = 1:100, a pH 5,5 e força iônica de 15 mmol L-1. Os 17 Latossolos apresentaram teor médio total de As de 5,92 mg kg-1 e CMADS As média de 2.013 mg kg-1. O teor de argila e os óxidos de Fe e Al apresentaram influência positiva na CMADS As.In view of the toxicity of As for man and animals and the possibility of existence of a great number of contaminated areas it is imperative to know the total As content in soils considered uncontaminated and about As sorption processes in soils of variable charge. The objective of this work was to determine the total content and maximum capacity of As adsorption (CMADS As in Oxisols. The total content was determined by the USEPA 3051A method. The cmADS As was determined by the Langmuir Isotherms using six solution concentrations (0, 0.09, 0.19, 0.38, 0.76, 1.15 mmol L-1 (1:100 soil: solution ratio, pH values 5.5 and ionic strength 15 mmol L-1. In the 17 Oxisols the average total As content was 5.92 mg kg-1 and mean cmADS As was 2.013 mg kg-1. Clay, and Fe and Al oxides content influenced cmADSs positively.

  12. Adsorption of phenolic compound by aged-refuse

    Energy Technology Data Exchange (ETDEWEB)

    Chai Xiaoli [State Key Laboratory of Pollution Control and Resource Reuse, School of Enviromental Science and Engineering, Tongji University, Siping Road 1239, Shanghai 200092 (China)]. E-mail: xlchai@mail.tongji.edu.cn; Zhao Youcai [State Key Laboratory of Pollution Control and Resource Reuse, School of Enviromental Science and Engineering, Tongji University, Siping Road 1239, Shanghai 200092 (China)

    2006-09-01

    The adsorption of phenol, 2-chlorophenol, 4-chlorophenol and 2,4-dichlorophenol by aged-refuse has been studied. Adsorption isotherms have been determined for phenol, 2-chlorophenol, 4-chlorophenol and 2,4-dichlorophenol and the data fits well to the Freundlich equation. The chlorinated phenols are absorbed more strongly than the phenol and the adsorption capacity has an oblivious relationship with the numbers and the position of chlorine subsistent. The experiment data suggests that both the partition function and the chemical adsorption involve in the adsorption process. Pseudo-first-order and pseudo-second-order model were applied to investigate the kinetics of the adsorption and the results show that it fit the pseudo-second-order model. More than one step involves in the adsorption process and the overall rate of the adsorption process appears to be controlled by the chemical reaction. The thermodynamic analysis indicates that the adsorption is spontaneous and endothermic.

  13. Capacidade de adsorção de fósforo em solos de várzea do Estado do Rio Grande do Sul Phosphorus adsorption capacity in lowland soils of Rio Grande do Sul State

    Directory of Open Access Journals (Sweden)

    Sidnei Kuster Ranno

    2007-02-01

    highly reactive elements such as phosphorus. Low-crystallinity forms of iron oxides and hydroxides become predominant with time. They could be the most important components in phosphorus adsorption during dry periods, and could control phosphorus release after flooding. The objective of this study was to evaluate the maximum phosphorus adsorption capacity (MPAC of some lowland soils in Rio Grande do Sul State (RS, Brazil and relate it with soil chemical and physical properties. Soil samples from 16 different areas in RS with widely varied soil chemical and physical properties were collected from the surface layer (0-20 cm. They were air-dried, sieved (2 mm, and the MPAC measured using adsorption isotherms. Each soil was kept in contact with increasing levels of P (0, 50, 100, 200, 300, 600, 900, and 1.800 mg kg-1 of P soil for 16 hours. The equilibrium P in the solution was determined and the data fit to the Langmuir equation. The MPAC varied considerably among the RS lowland soils (from 71 to 933 mg kg-1 of P; the variation was significantly correlated with the clay, organic matter and iron oxide contents extracted by dithionite and ammonium oxalate. The different MPAC affected the phosphorous doses necessary to increase available phosphorous by the Mehlich-1extractant in lowland soils.

  14. Induction of homochirality in achiral enantiomorphous monolayers.

    Science.gov (United States)

    Parschau, Manfred; Romer, Sara; Ernst, Karl-Heinz

    2004-12-01

    We report the induction of homochirality in enantiomorphous layers of achiral succinic acid on a Cu(110) surface after doping with tartaric acid (TA) enantiomers. Succinic acid becomes chiral upon adsorption due to symmetry-breaking interactions with the Cu(110) surface. The doubly deprotonated bisuccinate forms mirror domains on the surface, which leads to a superposition of (11,-90) and (90,-11) patterns observed by low-energy electron diffraction (LEED). On average, however, the surface layer is racemic. An amount of 2 mol % of (R,R)- or (S,S)-tartaric acid in the monolayer, corresponding to an absolute coverage of 0.001 tartaric acid molecule per surface copper atom, is sufficient to make the LEED spots of one enantiomorphous lattice disappear. After thermally induced desorption of TA, the succinic acid lattice turns racemic again. In analogy to the "sergeants-and-soldiers" principle described for helical polymers, this effect is explained by a lateral cooperative interaction within the two-dimensional lattice.

  15. Protein Adsorption in Three Dimensions

    Science.gov (United States)

    Vogler, Erwin A.

    2011-01-01

    Recent experimental and theoretical work clarifying the physical chemistry of blood-protein adsorption from aqueous-buffer solution to various kinds of surfaces is reviewed and interpreted within the context of biomaterial applications, especially toward development of cardiovascular biomaterials. The importance of this subject in biomaterials surface science is emphasized by reducing the “protein-adsorption problem” to three core questions that require quantitative answer. An overview of the protein-adsorption literature identifies some of the sources of inconsistency among many investigators participating in more than five decades of focused research. A tutorial on the fundamental biophysical chemistry of protein adsorption sets the stage for a detailed discussion of the kinetics and thermodynamics of protein adsorption, including adsorption competition between two proteins for the same adsorbent immersed in a binary-protein mixture. Both kinetics and steady-state adsorption can be rationalized using a single interpretive paradigm asserting that protein molecules partition from solution into a three-dimensional (3D) interphase separating bulk solution from the physical-adsorbent surface. Adsorbed protein collects in one-or-more adsorbed layers, depending on protein size, solution concentration, and adsorbent surface energy (water wettability). The adsorption process begins with the hydration of an adsorbent surface brought into contact with an aqueous-protein solution. Surface hydration reactions instantaneously form a thin, pseudo-2D interface between the adsorbent and protein solution. Protein molecules rapidly diffuse into this newly-formed interface, creating a truly 3D interphase that inflates with arriving proteins and fills to capacity within milliseconds at mg/mL bulk-solution concentrations CB. This inflated interphase subsequently undergoes time-dependent (minutes-to-hours) decrease in volume VI by expulsion of either-or-both interphase water and

  16. Comparative evaluation of adsorption kinetics of diclofenac and isoproturon by activated carbon.

    Science.gov (United States)

    Torrellas, Silvia A; Rodriguez, Araceli R; Escudero, Gabriel O; Martín, José María G; Rodriguez, Juan G

    2015-01-01

    Adsorption mechanism of diclofenac and isoproturon onto activated carbon has been proposed using Langmuir and Freundlich isotherms. Adsorption capacity and optimum adsorption isotherms were predicted by nonlinear regression method. Different kinetic equations, pseudo-first-order, pseudo-second-order, intraparticle diffusion model and Bangham kinetic model, were applied to study the adsorption kinetics of emerging contaminants on activated carbon in two aqueous matrices.

  17. Effect of Doping on Hydrogen Evolution Reaction of Vanadium Disulfide Monolayer

    Science.gov (United States)

    Qu, Yuanju; Pan, Hui; Kwok, Chi Tat; Wang, Zisheng

    2015-12-01

    As cheap and abundant materials, transitional metal dichalcogenide monolayers have attracted increasing interests for their application as catalysts in hydrogen production. In this work, the hydrogen evolution reduction of doped vanadium disulfide monolayers is investigated based on first-principles calculations. We find that the doping elements and concentration affect strongly the catalytic ability of the monolayer. We show that Ti-doping can efficiently reduce the Gibbs free energy of hydrogen adsorption in a wide range of hydrogen coverage. The catalytic ability of the monolayer at high hydrogen coverage can be improved by low Ti-density doping, while that at low hydrogen coverage is enhanced by moderate Ti-density doping. We further show that it is much easier to substitute the Ti atom to the V atom in the vanadium disulfide (VS2) monolayer than other transitional metal atoms considered here due to its lowest and negative formation energy. It is expected that the Ti-doped VS2 monolayer may be applicable in water electrolysis with improved efficiency.

  18. Equilibrium and kinetics study on hexavalent chromium adsorption onto diethylene triamine grafted glycidyl methacrylate based copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Maksin, Danijela D., E-mail: dmaksin@vinca.rs [University of Belgrade, Vinca Institute of Nuclear Sciences, P.O. Box 522, Belgrade (Serbia); Nastasovic, Aleksandra B., E-mail: anastaso@chem.bg.ac.rs [University of Belgrade, Institute of Chemistry, Technology and Metallurgy, Njegoseva 12, Belgrade (Serbia); Milutinovic-Nikolic, Aleksandra D., E-mail: snikolic@nanosys.ihtm.bg.ac.rs [University of Belgrade, Institute of Chemistry, Technology and Metallurgy, Njegoseva 12, Belgrade (Serbia); Surucic, Ljiljana T., E-mail: ljilja_m@yahoo.com [University of Belgrade, Faculty of Forestry, Kneza Viseslava 1, Belgrade (Serbia); Sandic, Zvjezdana P., E-mail: zvjezdana.sandic@gmail.com [Faculty of Science, Mladena Stojanovica 2, Banja Luka, Bosnia and Herzegovina (Bosnia and Herzegowina); Hercigonja, Radmila V., E-mail: radah@ffh.bg.ac.rs [University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11001 Belgrade (Serbia); Onjia, Antonije E., E-mail: onjia@vinca.rs [University of Belgrade, Vinca Institute of Nuclear Sciences, P.O. Box 522, Belgrade (Serbia)

    2012-03-30

    Highlights: Black-Right-Pointing-Pointer Methacrylate based copolymers grafted with diethylene triamine as Cr(VI) sorbents. Black-Right-Pointing-Pointer Chemisorption and pore diffusion are characteristics of this sorption system. Black-Right-Pointing-Pointer Langmuir isotherm provided best fit and maximum adsorption capacity was 143 mg g{sup -1}. Black-Right-Pointing-Pointer Cr(VI) sorption onto amino-functionalized copolymer was endothermic and spontaneous. Black-Right-Pointing-Pointer A simple, efficient and cost-effective hexavalent chromium removal method. - Abstract: Two porous and one non-porous crosslinked poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) [abbreviated PGME] were prepared by suspension copolymerization and functionalized with diethylene triamine [abbreviated PGME-deta]. Samples were characterized by elemental analysis, mercury porosimetry, scanning electron microscopy with energy-dispersive X-ray spectroscopy, and transmission electron microscopy. Kinetics of Cr(VI) sorption by PGME-deta were investigated in batch static experiments, in the temperature range 25-70 Degree-Sign C. Sorption was rapid, with the uptake capacity higher than 80% after 30 min. Sorption behavior and rate-controlling mechanisms were analyzed using five kinetic models (pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion and Bangham model). Kinetic studies showed that Cr(VI) adsorption adhered to the pseudo-second-order model, with definite influence of pore diffusion. Equilibrium data was tested with Langmuir, Freundlich and Tempkin adsorption isotherm models. Langmuir model was the most suitable indicating homogeneous distribution of active sites on PGME-deta and monolayer sorption. The maximum adsorption capacity from the Langmuir model, Q{sub max}, at pH 1.8 and 25 Degree-Sign C was 143 mg g{sup -1} for PGME2-deta (sample with the highest amino group concentration) while at 70 Degree-Sign C Q{sub max} reached the high value of 198

  19. Micron-sized Magnetic Polymer Microspheres for Adsorption and Separation of Cr(VI) from Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    王强; 官月平; 刘翔; 杨明珠; 任秀峰

    2012-01-01

    The magnetic poly-(methacrylate-divinyl benzene) microspheres with micron size were synthesized by modified suspension polymerization method. Adsorption of Cr(VI) from aqueous solution by magnetic poly-(MA-DVB) microspheres with surface amination was investigated. The adsorption processes were carried out under diversified conditions of pH value, adsorption time and temperature to evaluate the perlbrmance of the magnetic microspheres. The optimum pH value for Cr(VI) adsorption was found as 3. The adsorption capacity increased with adsorption time and attained an optimum at 60 rain. The adsorption processes for magnetic microspheres was endothermic reaction, and the adsorption capacity increased with increasing temperature.

  20. Adsorption characteristics of siloxanes in landfill gas by the adsorption equilibrium test

    Energy Technology Data Exchange (ETDEWEB)

    Nam, Sangchul; Namkoong, Wan [Department of Environmental Engineering, Konkuk University, Hwayang-Dong, Gwangjin-Gu, Seoul 143-701 (Korea, Republic of); Kang, Jeong-Hee; Park, Jin-Kyu [Department of Environmental Engineering, Anyang University, Anyang 5-Dong, Manan-Gu, Anyang-Si, Gyeonggi-Do 430-714 (Korea, Republic of); Lee, Namhoon, E-mail: nhlee@anyang.ac.kr [Department of Environmental Engineering, Anyang University, Anyang 5-Dong, Manan-Gu, Anyang-Si, Gyeonggi-Do 430-714 (Korea, Republic of)

    2013-10-15

    Highlights: • Equilibrium test was attempted to evaluate adsorption characteristics of siloxane. • L2 had higher removal efficiency in carbon compared to noncarbon adsorbents. • Total adsorption capacity of siloxane was 300 mg/g by coal activated carbon. • Adsorption characteristics rely on size of siloxane molecule and adsorbent pore. • Conversion of siloxane was caused by adsorption of noncarbon adsorbents. - Abstract: Due to the increase in energy cost by constantly high oil prices and the obligation to reduce greenhouse effect gases, landfill gas is frequently used as an alternative energy source for producing heat and electricity. Most of landfill gas utility facilities, however, are experiencing problems controlling siloxanes from landfill gas as their catalytic oxidizers are becoming fouled by silicon dioxide dust. To evaluate adsorption characteristics of siloxanes, an adsorption equilibrium test was conducted and parameters in the Freundlich and Langmuir isotherms were analyzed. Coconut activated carbon (CA1), coal activated carbon (CA2), impregnated activated carbon (CA3), silicagel (NCA1), and activated alumina (NCA2) were used for the adsorption of the mixed siloxane which contained hexamethyldisiloxane (L2), octamethylcyclotetrasiloxane (D4), and decamethylcyclopentasiloxane (D5). L2 had higher removal efficiency in noncarbon adsorbents compared to carbon adsorbents. The application of Langmuir and Freundlich adsorption isotherm demonstrated that coconut based CA1 and CA3 provided higher adsorption capacity on L2. And CA2 and NCA1 provided higher adsorption capacity on D4 and D5. Based on the experimental results, L2, D4, and D5 were converted by adsorption and desorption in noncarbon adsorbents. Adsorption affinity of siloxane is considered to be affect by the pore size distribution of the adsorbents and by the molecular size of each siloxane.

  1. Functionalized SBA-15 materials for bilirubin adsorption

    Science.gov (United States)

    Tang, Tao; Zhao, Yanling; Xu, Yao; Wu, Dong; Xu, Jun; Deng, Feng

    2011-05-01

    To investigate the driving force for bilirubin adsorption on mesoporous materials, a comparative study was carried out between pure siliceous SBA-15 and three functionalized SBA-15 mesoporous materials: CH 3-SBA-15 (MS), NH 2-SBA-15 (AS), and CH 3/NH 2-SBA-15 (AMS) that were synthesized by one-pot method. The obtained materials exhibited large surface areas (553-810 m 2/g) and pore size (6.6-7.1 nm) demonstrated by XRD and N 2-ad/desorption analysis. The SEM images showed that the materials had similar fiberlike morphology. The functionalization extent was calculated according to 29Si MAS NMR spectra and it was close to the designed value (10%). The synthesized mesoporous materials were used as bilirubin adsorbents and showed higher bilirubin adsorption capacities than the commercial active carbon. The adsorption capacities of amine functionalized samples AMS and AS were larger than those of pure siliceous SBA-15 and MS, indicating that electrostatic interaction was the dominant driving force for bilirubin adsorption on mesoporous materials. Increasing the ionic strength of bilirubin solution by adding NaCl would decrease the bilirubin adsorption capacity of mesoporous material, which further demonstrated that the electrostatic interaction was the dominant driving force for bilirubin adsorption. In addition, the hydrophobic interaction provided by methyl groups could promote the bilirubin adsorption.

  2. A QCM study on the adsorption of colloidal laponite at the solid/liquid interface.

    Science.gov (United States)

    Xu, Dan; Hodges, Chris; Ding, Yulong; Biggs, Simon; Brooker, Anju; York, David

    2010-06-01

    The adsorption of colloidal laponite at the solid/liquid interface on various substrates and over a range of laponite concentrations (10-1000 ppm) has been investigated. Although a wide range of surfaces were studied, only on a positively charged poly(diallyldimethylammonium chloride) (PDADMAC) surface was any adsorption of the laponite observed. This shows that when fully wetted, laponite adsorption depends primarily on the surface charge rather than the degree of hydrophobicity of the surface. The adsorption of spherical Ludox silica nanoparticles on PDADMAC surfaces was also examined for comparison with the disklike laponite. The QCM data for both laponite and Ludox show strong adsorption on PDADMAC surfaces; however, larger frequency shifts were seen for Ludox than laponite at all concentrations tested. Within the concentration range examined in this work, the dissipation data from the QCM suggested a simple monolayer formation for Ludox but a monolayer to multilayer transition for laponite as the concentration increases.

  3. Mesoporous activated coconut shell-derived hydrochar prepared via hydrothermal carbonization-NaOH activation for methylene blue adsorption.

    Science.gov (United States)

    Islam, Md Azharul; Ahmed, M J; Khanday, W A; Asif, M; Hameed, B H

    2017-12-01

    Mesoporous activated carbon was prepared using a hydrochar derived from coconut shell waste through hydrothermal carbonization and NaOH chemical activation process (COSHTC). Three sets of activated carbons were obtained with different hydrochar:NaOH impregnation ratios (1:1, 1:2, and 1:3). Among these ratios, 1:3 (COSHTC3) exhibited the optimum adsorption for methylene blue (MB). COSHTC3 adsorbed MB with an initial concentration of 25-250 mg/L at pH 3-11 and 30 °C. The adsorption isotherm of MB on COSHTC3 demonstrated that Langmuir isotherm could be better applied at a maximum monolayer adsorption capacity of 200.01 mg/g at 30 °C. The data was well fitted to the pseudo-second-order (PSO) kinetic model. These results show that the COSHTC3 prepared from low-cost agricultural waste (coconut shell) with average pore diameter 28.6 Å and surface area 876.14 m(2)/g acts as a better adsorbent for removal of cationic dyes and could pave the way for more low-cost adsorbents for dye removal. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Aggregation of silica nanoparticles directed by adsorption of lysozyme.

    Science.gov (United States)

    Bharti, Bhuvnesh; Meissner, Jens; Findenegg, Gerhard H

    2011-08-16

    The interaction of the globular protein lysozyme with silica nanoparticles of diameter 20 nm was studied in a pH range between the isoelectric points (IEPs) of silica and the protein (pH 3-11). The adsorption affinity and capacity of lysozyme on the silica particles is increasing progressively with pH, and the adsorbed protein induces bridging aggregation of the silica particles. Structural properties of the aggregates were studied as a function of pH at a fixed protein-to-silica concentration ratio which corresponds to a surface concentration of protein well below a complete monolayer in the complete-binding regime at pH > 6. Sedimentation studies indicate the presence of compact aggregates at pH 4-6 and a loose flocculated network at pH 7-9, followed by a sharp decrease of aggregate size near the IEP of lysozyme. The structure of the bridged silica aggregates was studied by cryo-transmission electron microscopy (cryo-TEM) and small-angle X-ray scattering. The structure factor S(q) derived from the scattering profiles displays characteristic features of particles interacting by a short-range attractive potential and can be represented by the square-well Percus-Yevick potential model, with a potential depth not exceeding 3k(B)T.

  5. Direct imaging of hexaamine-ruthenium(III) in domain boundaries in monolayers of single-stranded DNA

    DEFF Research Database (Denmark)

    Grubb, Mikala; Wackerbarth, Hainer; Wengel, J.;

    2007-01-01

    We describe adsorption and identification of the binding sites of [Ru(NH3)(6)](3+) (RuHex) molecules in a closely packed monolayer of a 13-base ss-DNA on Au(111) electrodes by electrochemical in situ scanning tunneling microscopy (STM), cyclic voltammetry and interfacial capacitance data. In situ...

  6. Catalytic monolayer voltammetry and in situ scanning tunneling microscopy of copper nitrite reductase on cysteamine-modified Au(111) electrodes

    DEFF Research Database (Denmark)

    Zhang, Jingdong; Welinder, A.C.; Hansen, Allan Glargaard

    2003-01-01

    We have studied the adsorption and electrocatalysis of the redox metalloenzyme blue copper nitrite reductase from Achromobacter xylosoxidans (AxCuNiR) on single-crystal Au(111)-electrode surfaces modified by a self-assembled monolayer of cysteamine. A combination of cyclic voltammetry and in situ...

  7. Highly Polymer-Repellent yet Atomically Flat Surfaces Based on Organic Monolayers with a Single Fluorine Atom

    NARCIS (Netherlands)

    Wang, Zhanhua; Pujari, S.P.; Lagen, van B.; Smulders, M.M.J.; Zuilhof, H.

    2016-01-01

    Organic monolayers or polymer brushes, often in combination with surface structuring, are widely used to prevent nonspecific adsorption of polymeric or biological material on sensor and microfluidic surfaces. Here it is demonstrated for the first time how robust, covalently attached alkyne-derived m

  8. Carbon dioxide adsorption in graphene sheets

    Directory of Open Access Journals (Sweden)

    Ashish Kumar Mishra

    2011-09-01

    Full Text Available Control over the CO2 emission via automobiles and industrial exhaust in atmosphere, is one of the major concerns to render environmental friendly milieu. Adsorption can be considered to be one of the more promising methods, offering potential energy savings compared to absorbent systems. Different carbon nanostructures (activated carbon and carbon nanotubes have attracted attention as CO2 adsorbents due to their unique surface morphology. In the present work, we have demonstrated the CO2 adsorption capacity of graphene, prepared via hydrogen induced exfoliation of graphitic oxide at moderate temperatures. The CO2 adsorption study was performed using high pressure Sieverts apparatus and capacity was calculated by gas equation using van der Waals corrections. Physical adsorption of CO2 molecules in graphene was confirmed by FTIR study. Synthesis of graphene sheets via hydrogen exfoliation is possible at large scale and lower cost and higher adsorption capacity of as prepared graphene compared to other carbon nanostructures suggests its possible use as CO2 adsorbent for industrial application. Maximum adsorption capacity of 21.6 mmole/g was observed at 11 bar pressure and room temperature (25 ºC.

  9. Inhibition of copper corrosion by the formation of Schiff base self-assembled monolayers

    Science.gov (United States)

    Zhang, Jing; Liu, Zheng; Han, Guo-Cheng; Chen, Shi-Liang; Chen, Zhencheng

    2016-12-01

    Self-assembled monolayers (SAMs) of 4-((2-thiophenecarboxylic acid hydrazide) methylene) benzoic acid (HD2) (denoted as HD2-SAMs) were formed on copper surface. The SAMs were characterized by scanning electron microscopy and X-ray photoelectron spectroscopy. Polarization curve and weight loss methods indicated that the highest inhibition efficiency was 93.9% for CO2-saturated simulative oilfield water at a self-assembled time of 3 h. Potential-time curve, electrochemical impedance tests showed that HD2-SAMs on copper surface exhibited excellent inhibition effect at 30 °C. The adsorption behavior of HD2-SAMs on the copper surface followed the Langmuir adsorption isotherm, which was indicative of typically chemical adsorption. Quantum chemistry calculation showed that O and N atoms can interact with Cu atoms by coordination bonds which were the mainly active area of the adsorption of HD2 molecules.

  10. Preparation and characterization of alkylphosphonic acid self-assembled monolayers on titanium alloy by chemisorption and electrochemical deposition.

    Science.gov (United States)

    Metoki, Noah; Liu, Liang; Beilis, Edith; Eliaz, Noam; Mandler, Daniel

    2014-06-17

    Ti-6Al-4V alloy is the most commonly used alloy for dental and orthopedic implants. In order to improve osseointegration, different surface modification methods are usually employed, including self-assembled monolayers (SAMs). This study presents an investigation of both active (electroassisted) and passive (adsorption) approaches for the modification of Ti-6Al-4V using alkylphosphonic acid. The monolayers were characterized by cyclic voltammetry, double-layer capacitance, contact angle measurements, X-ray photoelectron spectroscopy, polarization modulation infrared reflection adsorption spectroscopy, electrochemical impedance spectroscopy, and corrosion potentiodynamic polarization measurements. It is shown that the electrochemically assisted monolayers, which are assembled faster, exhibit better control over surface properties, a superior degree of order, and a somewhat higher packing density. The electrosorbed SAMs also exhibit better blockage of electron transfer across the interface and thus have better corrosion resistance.

  11. Adsorptive removal of Cd(II) and Pb(II) ions from aqueous solutions by using Turkish illitic clay.

    Science.gov (United States)<