Arsenic removal by MF membrane with chemical sludge adsorption and NF membrane equipped with vibratory shear enhanced process

2003 ◽  
Vol 3 (5-6) ◽  
pp. 303-310 ◽  
Author(s):  
S.-H. Yi ◽  
S. Ahmed ◽  
Y. Watanabe ◽  
K. Watari
Keyword(s):  
Arsenic Removal ◽  
Membrane Surface ◽  
Membrane Process ◽  
Low Concentrations ◽  
Strong Shear ◽  
Low Levels ◽  
Removal Processes ◽  
Removal Of Arsenic ◽  
Concentration Polarization Layer ◽  
Chemical Sludge

Conventional arsenic removal processes have difficulty removing low concentrations of arsenic ion from water. Therefore, it is very hard to comply with stringent low levels of arsenic, such as below 10 μg/L. So, we have developed two arsenic removal processes which are able to comply with more stringent arsenic regulations. They are the MF membrane process combined with chemical sludge adsorption and NF membrane process equipped with the vibratory shear enhanced process (VSEP). In this paper, we examine the performance of these new processes for the removal of arsenic ion of a low concentration from water. We found that chemical sludge produced in the conventional rapid sand filtration plants can effectively remove As (V) ions of H2AsO4- and HAsO42- through anion exchange reaction. The removal efficiency of MF membrane process combined with chemical sludge adsorption increased to about 36%, compared to MF membrane alone. The strong shear force on the NF membrane surface produced by vibration on the VSEP causes the concentration polarization layer to thin through increased back transport velocity of particles. So, it can remove even dissolved constituents effectively. Therefore, As (V) ions such as H2AsO4- and HAsO42- can be removed. The concentration of As (V) ions decreased from 50 μg/L to below 10 μg/L and condensation factor in recirculating water increased up to 7 times by using NF membrane equipped with VSEP.

scholarly journals Hybrid Sorbents for Removal of Arsenic

2022 ◽  
Vol 320 (1) ◽  
pp. 32-41
Author(s):  
L. A. Zemskova ◽  
◽  
D. H. Shlyk ◽  
N. N. Barinov ◽  
◽  
...  
Keyword(s):  
Composite Materials ◽  
Transition Metal Oxides ◽  
Large Scale ◽  
Arsenic Removal ◽  
Tap Water ◽  
Carbon Composite ◽  
Low Concentrations ◽  
Carbon Composite Materials ◽  
The Stability ◽  
Removal Of Arsenic

The paper analyzes data on the removal of arsenic by sorption methods using materials that have prospects for large-scale application in water treatment. These materials include transition metal oxides in the micro- and nano-dimensional form, including those in the composition of composite materials with inorganic matrices, or hybrid sorbents in the composition with polymer resins or natural biopolymers. Examples of the use of composite (hybrid) sorbents for the removal of arsenic from solutions with low concentrations (at the level of MPC) are given. The objective of this article was to sum the up-to-date information about the most important features of chitosan-containing and chitosan-carbon materials we developed in view their use in arsenic removal processes at low concentrations to concentrations that meet WHO requirements. The paper presents data on the sorption properties of Mo-containing activated carbon fibers and chitosan-carbon composite materials towards arsenic (V) when it is extracted from bidistilled and tap water under static and dynamic conditions. The factors of the different behavior of the sorbents depending on the form of a biopolymer deposited on the fiber and the stability of the sorbents during the sorption of arsenic are discussed.

Arsenic Removal by Precipitation with Calcium Phosphate Hydroxyapatite

2012 ◽  
Vol 506 ◽  
pp. 413-416 ◽  
Author(s):  
W. Dungkaew ◽  
K.J. Haller ◽  
A.E. Flood ◽  
J.F. Scamehorn
Keyword(s):  
Calcium Phosphate ◽  
Water Sample ◽  
Removal Efficiency ◽  
Arsenic Removal ◽  
Arsenic Speciation ◽  
Arsenic Concentration ◽  
Contaminated Water ◽  
Low Levels ◽  
Removal Of Arsenic ◽  
Key Parameter

The removal of arsenic from synthetic arsenic contaminated water sample by precipitating arsenic (in the form of arsenate oxyanion) with calcium phosphate hydroxyapatite, HAp, was studied under conditions that induce arsenate incorporated calcium phosphate hydroxyapatite, Ca (P/As)HAp, to form. Arsenate is able to substitute for a fraction of the phosphate in HAp host material as it forms. Consequently, arsenic is successfully removed from the contaminated water achieving up to 99% arsenic removal from 25 ppm initial arsenic concentration. The Ca:(P+As) and P:As mole ratios were found to play an important role in arsenic removal efficiency. Higher Ca:(P+As) and P:As mole ratios give higher arsenic removal efficiency. Surprisingly, the pH of the initial anion solution, a key parameter in arsenic speciation, was found to not have a significant effect on arsenic removal by this process. The advantage of this process is that the precipitation can occur rapidly at relatively low levels of arsenic contamination, implying an easy and inexpensive process for arsenic removal can be developed based on this approach.

scholarly journals Co-Occurrence of Regulated and Emerging Mycotoxins in Corn Silage: Relationships with Fermentation Quality and Bacterial Communities

Toxins ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 232
Author(s):  
Antonio Gallo ◽  
Francesca Ghilardelli ◽  
Alberto Stanislao Atzori ◽  
Severino Zara ◽  
Barbara Novak ◽  
...  
Keyword(s):  
Bacterial Community ◽  
Bacterial Communities ◽  
Dry Matter ◽  
Kojic Acid ◽  
Corn Silage ◽  
Fungal Metabolites ◽  
Fusarium Mycotoxins ◽  
Low Concentrations ◽  
Fermentation Quality ◽  
Low Levels

Sixty-four corn silages were characterized for chemicals, bacterial community, and concentrations of several fungal metabolites. Silages were grouped in five clusters, based on detected mycotoxins, and they were characterized for being contaminated by (1) low levels of Aspergillus- and Penicillium-mycotoxins; (2) low levels of fumonisins and other Fusarium-mycotoxins; (3) high levels of Aspergillus-mycotoxins; (4) high levels of non-regulated Fusarium-mycotoxins; (5) high levels of fumonisins and their metabolites. Altersetin was detected in clusters 1, 3, and 5. Rugulusovin or brevianamide F were detected in several samples, with the highest concentration in cluster 3. Emodin was detected in more than 50.0% of samples of clusters 1, 3 and 5, respectively. Kojic acid occurred mainly in clusters 1 and 2 at very low concentrations. Regarding Fusarium mycotoxins, high occurrences were observed for FB3, FB4, FA1, whereas the average concentrations of FB6 and FA2 were lower than 12.4 µg/kg dry matter. Emerging Fusarium-produced mycotoxins, such as siccanol, moniliformin, equisetin, epiequisetin and bikaverin were detected in the majority of analyzed corn silages. Pestalotin, oxaline, phenopirrozin and questiomycin A were detected at high incidences. Concluding, this work highlighted that corn silages could be contaminated by a high number of regulated and emerging mycotoxins.

Arsenic Removal from Wastewater Using Adsorptive Mediums

2011 ◽  
Vol 189-193 ◽  
pp. 404-409
Author(s):  
Fu Quan Peng ◽  
Zhen Cheng Xu ◽  
Jian Hong Huang ◽  
Qing Wei Guo ◽  
Feng Nie
Keyword(s):  
Arsenic Removal ◽  
Removal Rate ◽  
National Standards ◽  
Ferrous Oxide ◽  
Anion Resin ◽  
Quartz Sands ◽  
Long Time ◽  
Removal Of Arsenic ◽  
Adsorptive Properties

Different adsorptive mediums and adsorbents’ compounds were chosen to remove arsenic from Yangzonghai Lake wastewater. Results showed that Ca(OH)2, attapulgite, bentonite, LDHs these adsorptive mediums had adsorptive capacities of less than 2.5 mg/g of As removal and it took long time for sediment before monitoring; adsorbents compounds’ results showed Fe2O3 and quartz sands had best removal rate and quartz sands had little removal of arsenic. Both strong anion resin and hydrated ferrous oxide-loaded on polystyrene diethanolamine resin(designated as PDR-HFO) can decrease As concentration to less than 0.01 mg/L reaching national standards for arsenic; anions such as SO42- can not be removed when strong anion resin was regenerated causing its loss of exchange ions; PDR-HFO exhibited excellent adsorptive properties and recyclability.

scholarly journals Clostridium chromiireducens sp. nov., isolated from Cr(VI)-contaminated soil

2011 ◽  
Vol 61 (11) ◽  
pp. 2626-2631 ◽  
Author(s):  
K. S. Inglett ◽  
H. S. Bae ◽  
H. C. Aldrich ◽  
K. Hatfield ◽  
A. V. Ogram
Keyword(s):  
Contaminated Soil ◽  
Clostridium Beijerinckii ◽  
Rrna Gene ◽  
Acid Fermentation ◽  
Mixed Acid ◽  
Morphological Studies ◽  
Group I ◽  
Low Concentrations ◽  
Low Levels ◽  
Sequence Similarities

A Cr(VI)-resistant, Gram-positive, spore-forming, obligate anaerobe, designated GCAF-1T, was isolated from chromium-contaminated soil by its ability to reduce Cr(VI) in low concentrations. Mixed acid fermentation during growth on glucose resulted in accumulation of acetate, butyrate, formate and lactate. Morphological studies indicated the presence of peritrichous flagella, pili and an S-layer. The major cellular fatty acids (>5 %) were C16 : 0, C14 : 0, summed feature 3 (comprising iso-C15 : 0 2-OH and/or C16 : 1ω7c), C18 : 1ω7c, C16 : 1ω9c, summed feature 4 (comprising iso-C17 : 1 I and/or anteiso-C17 : 1 B) and C18 : 1ω9c. The DNA G+C content of strain GCAF-1T was 30.7 mol%. Phylogenetic interference indicated that strain GCAF-1T clustered with group I of the genus Clostridium. Of strains within this cluster, strain GCAF-1T shared the highest 16S rRNA gene sequence similarities (98.1–98.9 %) with Clostridium beijerinckii DSM 791T, C. saccharobutylicum NCP 262T, C. saccharoperbutylacetonicum N1-4T, C. puniceum DSM 2619T and C. roseum DSM 51T. However, strain GCAF-1T could be clearly distinguished from its closest phylogenetic neighbours by low levels of DNA–DNA relatedness (<50 %) and some phenotypic features. Based on the evidence presented here, strain GCAF-1T ( = DSM 23318T  = KCTC 5935T) represents a novel species of the genus Clostridium, for which the name Clostridium chromiireducens sp. nov. is proposed.

Arsenic removal from groundwater by Anjili tree sawdust impregnated with ferric hydroxide and activated alumina

2015 ◽  
Vol 16 (1) ◽  
pp. 115-127 ◽  
Author(s):  
P. Dhanasekaran ◽  
P. M. Satya Sai ◽  
C. Anand Babu ◽  
R. Krishna Prabhu ◽  
K. K. Rajan
Keyword(s):  
Arsenic Removal ◽  
Heart Diseases ◽  
Ferric Hydroxide ◽  
Sorption Kinetics ◽  
Activated Alumina ◽  
Maximum Sorption Capacity ◽  
Maximum Sorption ◽  
Freundlich Adsorption Isotherm ◽  
Pseudo Second Order ◽  
Removal Of Arsenic

Arsenic is a toxic element found naturally in groundwater. Due to its carcinogenicity, risk for heart diseases and diabetes, arsenic needs to be removed from groundwater for potable application. ‘Anjili’ tree sawdust was chemically modified with ferric hydroxide and activated alumina (SFAA) and used as an adsorbent for the removal of arsenic from groundwater. The adsorbent was characterized using scanning electron microscopy (SEM), Fourier transform infrared (FTIR) to study the pore structure and surface functional groups. Effect of contact time, initial concentration, pH, particle size and temperature was studied. Arsenic adsorbed by SFAA followed Freundlich adsorption isotherm. Maximum sorption of arsenic by SFAA adsorbent occurred at pH 6.5. Arsenic sorption kinetics followed a pseudo-second-order model. The maximum sorption capacity at 303 K was found to be 54.32 mg/g for As(III) and 77.60 mg/g for As(V). Interference of other ions on the adsorption was in the order of PO43− &gt; SO42− &gt; HCO3− &gt; NO3−.

Removal of color substances using photocatalytic oxidation for membrane filtration processes

2001 ◽  
Vol 43 (10) ◽  
pp. 319-325 ◽  
Author(s):  
J. H. Tay ◽  
D. Chen ◽  
D. D. Sun
Keyword(s):  
Hydrogen Peroxide ◽  
Membrane Filtration ◽  
Photocatalytic Oxidation ◽  
Removal Rate ◽  
Membrane Surface ◽  
Rejection Rate ◽  
Solution Treated ◽  
Low Concentrations ◽  
Photo Catalytic Oxidation ◽  
Positive Effect

This study aims to remove the color substances, which normally cause difficulties in membrane filtration processes due to fouling using heterogeneous UV/TiO2/H2O2 reactor. It is confirmed that the technique used in this study was effective to remove TOC at 38% and color400 at 89% within 150-min irradiation. The experiment results showed that low concentrations of hydrogen peroxide dosage (less than 0.016 M) to UV/TiO2 system accelerated the TOC and Color400 removal rate from 9% to 38% and 40% to 89% respectively, while over-dosage made this positive effect decline. The humic acid solution treated by photo catalytic oxidation in UV/TiO2/H2O2 reactor did not change the zeta potential on membrane surface and membrane rejection rate.

scholarly journals Tumor necrosis factor-dependent production of human immunodeficiency virus 1 in chronically infected HL-60 cells

Blood ◽  
1993 ◽  
Vol 82 (9) ◽  
pp. 2742-2748 ◽  
Author(s):  
K Kitano ◽  
CI Rivas ◽  
GC Baldwin ◽  
JC Vera ◽  
DW Golde
Keyword(s):  
Human Immunodeficiency Virus ◽  
Tumor Necrosis Factor ◽  
Tumor Necrosis ◽  
Virus Production ◽  
Viral Production ◽  
Low Concentrations ◽  
Immunodeficiency Virus ◽  
Lag Period ◽  
Low Levels ◽  
Necrosis Factor

Abstract Tumor necrosis factor (TNF) may play a central role in proviral activation and release from latency in cells infected with the human immunodeficiency virus (HIV). We studied viral production and its relation to TNF in a HL-60 cell line (J22-HL-60) infected with a monocytotropic strain of HIV-1JR-FL. Viral production was stimulated to similar levels by TNF, 12-O-tetradecanoyl-phorbol-13-acetate (TPA), and 1,25-dihydroxyvitamin D3 (1,25[OH]2D3). Production of the virus was not suppressed by 3′-azido-3′-deoxythymidine (AZT), indicating that viral production was not caused by superinfection. Low concentrations of TNF (0.1 ng/mL) induced viral production with a short lag period of 8 hours, and this proviral activation was specifically suppressed by anti- TNF antibodies. However, induction of virus production by 1,25(OH)2D3 showed an extended lag period of 2 to 3 days. The effect of 1,25(OH)2D3 on virus production was also blocked by anti-TNF antibodies, which suggests the direct participation of TNF in this process. TNF accumulated in the culture supernatant of cells stimulated with 1,25(OH)2D3 with a kinetics consistent with its involvement in the action of 1,25(OH)2D3 on viral production. The J22-HL-60 cell line produced low levels of virus when cultured in the absence of an external stimulus; however, this basal viral production was suppressed greater than 80% in the presence of anti-TNF antibodies. Corresponding low levels of TNF were detected in the culture supernatants. Viral production decreased slowly with increasing passage of the cells, and no virus was detected in the supernatants of cells maintained in culture for several months. Concomitantly, TNF was no longer detected in the supernatant of these cells, which suggests that endogenous autocrine production of TNF drives viral production in the unstimulated cells. However, viral production was stimulated in these cells by low concentrations (0.1 ng/mL) of added TNF. These results argue for a central role for TNF in HIV proviral activation in chronically infected myeloid cells.

Disposal of wastes resulting from arsenic removal processes

2003 ◽  
pp. 483-489 ◽  
Author(s):  
Michael J. MacPhee ◽  
John T. Novak ◽  
David A. Cornwell ◽  
Rodney N. Mutter
Keyword(s):  
Arsenic Removal ◽  
Removal Processes
Sign in / Sign up

Export Citation Format

Share Document