scholarly journals Electrochemical removal of amphoteric ions

2021 ◽  
Vol 118 (40) ◽  
pp. e2108240118
Author(s):  
Amit N. Shocron ◽  
Eric N. Guyes ◽  
Huub H. M. Rijnaarts ◽  
P. M. Biesheuvel ◽  
Matthew E. Suss ◽  
...  
Keyword(s):  
Ionic Species ◽  
Factors Affecting ◽  
Salt Ions ◽  
Weak Bases ◽  
Effective Removal ◽  
Water Ph ◽  
Ph Dependent ◽  
High Concentrations ◽  
Local Water ◽  
Complex Phenomena

Several harmful or valuable ionic species present in seawater, brackish water, and wastewater are amphoteric, weak acids or weak bases, and, thus, their properties depend on local water pH. Effective removal of these species can be challenging for conventional membrane technologies, necessitating chemical dosing of the feedwater to adjust pH. A prominent example is boron, which is considered toxic in high concentrations and often requires additional membrane passes to remove during seawater desalination. Capacitive deionization (CDI) is an emerging membraneless technique for water treatment and desalination, based on electrosorption of salt ions into charging microporous electrodes. CDI cells show strong internally generated pH variations during operation, and, thus, CDI can potentially remove pH-dependent species without chemical dosing. However, development of this technique is inhibited by the complexities inherent to the coupling of pH dynamics and ion properties in a charging CDI cell. Here, we present a theoretical framework predicting the electrosorption of pH-dependent species in flow-through electrode CDI cells. We demonstrate that such a model enables insight into factors affecting species electrosorption and conclude that important design rules for such systems are highly counterintuitive. For example, we show both theoretically and experimentally that for boron removal, the anode should be placed upstream and the cathode downstream, an electrode order that runs counter to the accepted wisdom in the CDI field. Overall, we show that to achieve target separations relying on coupled, complex phenomena, such as in the removal of amphoteric species, a theoretical CDI model is essential.

scholarly journals Survival characteristics of Salmonella enterica serovar Enteritidis in chicken egg albumen

2006 ◽  
Vol 134 (5) ◽  
pp. 967-976 ◽  
Author(s):  
H. KANG ◽  
C. LOUI ◽  
R. I. CLAVIJO ◽  
L. W. RILEY ◽  
S. LU
Keyword(s):  
Salmonella Enterica ◽  
Iron Acquisition ◽  
Foodborne Pathogen ◽  
Human Infection ◽  
Salmonella Enterica Serovar Enteritidis ◽  
Factors Affecting ◽  
Chicken Egg ◽  
Egg Albumen ◽  
High Concentrations ◽  
Incubation Temperatures

Salmonella enterica serovar Enteritidis (SE) is a major foodborne pathogen primarily causing human infection through contaminated chicken eggs. To understand how SE survives in chicken egg albumen, we systematically and quantitatively analysed the survival properties of SE in egg albumen and identified factors affecting its survival. Survival assays of SE in egg indicate that egg albumen restricted the growth of SE. A major factor that controlled SE's growth in egg albumen was iron restriction, since egg albumen supplemented with iron allowed SE to grow, and iron acquisition mutants of SE showed decreased survival in egg albumen. In addition, low pH of albumen, high concentrations of bacteria and low incubation temperatures of bacteria with albumen facilitates the survival of SE. Our results suggest that egg albumen uses multiple mechanisms to control SE including iron limitation, surface interaction and possible enzymatic activities.

scholarly journals Phosphate-Catalyzed Hydrogen Peroxide Formation from Agar, Gellan, and κ-Carrageenan and Recovery of Microbial Cultivability via Catalase and Pyruvate

2017 ◽  
Vol 83 (21) ◽  
Author(s):  
Kosei Kawasaki ◽  
Yoichi Kamagata
Keyword(s):  
Hydrogen Peroxide ◽  
Phosphate Buffer ◽  
Laboratory Culture ◽  
Colony Count ◽  
Natural Environments ◽  
Ammonium Ions ◽  
Factors Affecting ◽  
Culture Techniques ◽  
Ph Dependent ◽  
Growth Inhibiting

ABSTRACTPreviously, we reported that when agar is autoclaved with phosphate buffer, hydrogen peroxide (H2O2) is formed in the resulting medium (PT medium), and the colony count on the medium inoculated with environmental samples becomes much lower than that on a medium in which agar and phosphate are autoclaved separately (PS medium) (T. Tanaka et al., Appl Environ Microbiol 80:7659–7666, 2014,https://doi.org/10.1128/AEM.02741-14). However, the physicochemical mechanisms underlying this observation remain largely unknown. Here, we determined the factors affecting H2O2formation in agar. The H2O2formation was pH dependent: H2O2was formed at high concentrations in an alkaline or neutral phosphate buffer but not in an acidic buffer. Ammonium ions enhanced H2O2formation, implying the involvement of the Maillard reaction catalyzed by phosphate. We found that other gelling agents (e.g., gellan and κ-carrageenan) also produced H2O2after being autoclaved with phosphate. We then examined the cultivability of microorganisms from a fresh-water sample to test whether catalase and pyruvate, known as H2O2scavengers, are effective in yielding high colony counts. The colony count on PT medium was only 5.7% of that on PS medium. Catalase treatment effectively restored the colony count of PT medium (to 106% of that on PS medium). In contrast, pyruvate was not as effective as catalase: the colony count on sodium pyruvate-supplemented PT medium was 58% of that on PS medium. Given that both catalase and pyruvate can remove H2O2from PT medium, these observations indicate that although H2O2is the main cause of reduced colony count on PT medium, other unknown growth-inhibiting substances that cannot be removed by pyruvate (but can be by catalase) may also be involved.IMPORTANCEThe majority of bacteria in natural environments are recalcitrant to laboratory culture techniques. Previously, we demonstrated that one reason for this is the formation of high H2O2levels in media prepared by autoclaving agar and phosphate buffer together (PT medium). In this study, we investigated the factors affecting H2O2formation from agar. H2O2formation is pH dependent, and ammonium ions promote this phosphate-catalyzed H2O2formation. Amendment of catalase or pyruvate, a well-known H2O2-scavenging agent, effectively eliminated H2O2. Yet results suggest that growth-inhibiting factor(s) that cannot be eliminated by pyruvate (but can be by catalase) are present in PT medium.

RAMAN SPECTRA OF THE H2SO4–SO3 AND D2SO4–SO3 SYSTEMS: EVIDENCE FOR THE OCCURRENCE OF POLYSULPHURIC ACIDS

1962 ◽  
Vol 40 (4) ◽  
pp. 658-674 ◽  
Author(s):  
R. J. Gillespie ◽  
E. A. Robinson
Keyword(s):  
Sulphuric Acid ◽  
Raman Spectra ◽  
Ionic Species ◽  
The Self ◽  
Experimental Results ◽  
Similar Work ◽  
Stretching Vibrations ◽  
Sulphur Trioxide ◽  
High Concentrations

The Raman spectra of oleums, i.e. mixtures of sulphur trioxide and sulphuric acid, have been re-examined. Similar measurements on the sulphur trioxide – deuterosulphuric acid (D2SO4) system are also reported. The experimental results and conclusions of previous similar work on oleums are discussed. By comparison of the spectra of oleums with those of the polysulphuryl halides it is shown that the polysulphuric acids H2S2O7 and H2S3O10 are present in this system. The increase in the frequency of the SO2 stretching vibrations with increasing concentration of sulphur trioxide gives evidence for the existence of higher polysulphuric acids such as H2S4O13 at high concentrations of sulphur trioxide. In relatively concentrated oleum, sulphur trioxide monomer and trimer are also present. It is shown that the self-dissociation of liquid H2S2O7 gives mainly molecular H2S2O10 and H2SO4 and not ionic species. The conclusions reached from the interpretation of the Raman spectra of the D2SO4–SO3 system are similar to those arrived at for sulphuric acid oleums. The spectra of solutions of NaHSO4 in oleums were also examined, and are discussed.

scholarly journals Summertime PM<sub>2.5</sub> ionic species in four major cities of China: nitrate formation in an ammonia-deficient atmosphere

2009 ◽  
Vol 9 (5) ◽  
pp. 1711-1722 ◽  
Author(s):  
R. K. Pathak ◽  
W. S. Wu ◽  
T. Wang
Keyword(s):  
Gas Phase ◽  
Ionic Species ◽  
Mean Value ◽  
Average Concentration ◽  
Phase Reaction ◽  
Gas Phase Reaction ◽  
Particulate Pollution ◽  
Aerosol Acidity ◽  
Low Levels ◽  
High Concentrations

Abstract. Strong atmospheric photochemistry in summer can produce a significant amount of secondary aerosols, which may have a large impact on regional air quality and visibility. In the study reported herein, we analyzed sulfate, nitrate, and ammonium in PM2.5 samples collected using a 24-h filter system at suburban and rural sites near four major cities in China (Beijing, Shanghai, Guangzhou, and Lanzhou). Overall, the PM2.5 mass concentrations were high (with a mean value of 55–68 gμgm−3), which reflects the long-known particulate pollution in China's large urban centers. We observed very high concentrations of sulfate and nitrate at the Beijing and Shanghai sites, and, in particular, abnormally high levels of nitrate (24-h average concentration up to 42 gμgm−3 and contributing up to 25% of the PM2.5 mass) in the ammonium-poor samples. The Beijing and Shanghai aerosols were characterized by high levels of aerosol acidity (~220–390 nmol m−3) and low levels of in-situ pH (−0.77 to −0.52). In these samples, the formation of the observed high concentrations of particulate nitrate cannot be explained by homogeneous gas-phase reaction between ammonia and nitric acid. Examination of the relation of nitrate to relative humidity and aerosol loading suggests that the nitrate was most probably formed via the heterogeneous hydrolysis of N2O5 on the surface of the moist and acidic aerosols in Beijing and Shanghai. In comparison, the samples collected in Lanzhou and Guangzhou were ammonium-rich with low levels of aerosol acidity (~65–70 nmol m−3), and the formation of ammonium nitrate via the homogeneous gas-phase reaction was favored, which is similar to many previous studies. An empirical fit has been derived to relate fine nitrate to aerosol acidity, aerosol water content, aerosol surface area, and the precursor of nitrate for the data from Beijing and Shanghai.

scholarly journals Characteristics, seasonality and sources of carbonaceous and ionic components in the tropical Indian aerosols

2011 ◽  
Vol 11 (2) ◽  
pp. 3937-3976 ◽  
Author(s):  
C. M. Pavuluri ◽  
K. Kawamura ◽  
S. G. Aggarwal ◽  
T. Swaminathan
Keyword(s):  
Organic Carbon ◽  
Atmospheric Aerosols ◽  
Atmospheric Transport ◽  
Indian Subcontinent ◽  
Ionic Species ◽  
Water Soluble ◽  
Carbonaceous Aerosols ◽  
Mass Fractions ◽  
High Concentrations ◽  
Ionic Components

Abstract. To better characterize South and Southeast Asian aerosols, PM10 samples collected from tropical Chennai, India (13.04° N; 80.17° E) were analyzed for carbonaceous and water-soluble ionic components. Concentration ranges of elemental carbon (EC) and organic carbon (OC) were 2.4–14 μg m−3 and 3.2–15.6 μg m−3 in winter samples whereas they were 1.1–2.5 μg m−3 and 4.1–17.6 μg m−3 in summer samples, respectively. Concentration of secondary organic carbon (SOC) retrieved from EC-tracer method was 4.6 ± 2.8 μg m−3 in winter and 4.3 ± 2.8 μg m−3 in summer. SO42- (8.8 ± 2.5 μg m−3 and 4.1 ± 2.7 μg m−3 in winter and summer, respectively) was found as the most abundant ionic species (57% on average, n = 49), followed by NH4+ (15%) > NO3− > Cl− > K+> Na+ > Ca2+ > MSA− > Mg2+. The mass fractions of EC, organic matter (OM) and ionic species varied seasonally, following the air mass trajectories and corresponding source strength. Based on mass concentration ratios of selected components and relations of EC and OC to marker species, we found that biofuel/biomass burning is the major source of atmospheric aerosols in South and Southeast Asia. The high concentrations of SOC and WSOC/OC ratios (ave. 0.45; n = 49) as well as good correlations between SOC and WSOC suggest that the secondary production of organic aerosols during long-range atmospheric transport is also significant in this region. This study provides the baseline data of carbonaceous aerosols for southern part of the Indian subcontinent.

Understanding the trends and controlling factors of Indian Ocean acidification

2021 ◽  
Author(s):  
Kunal Madkaiker ◽  
Vinu Valsala
Keyword(s):  
Indian Ocean ◽  
Spatial Variability ◽  
Dissolved Inorganic Carbon ◽  
Total Alkalinity ◽  
Global Ocean ◽  
Strong Negative Correlation ◽  
Chemical Balance ◽  
Factors Affecting ◽  
Water Ph ◽  
The Individual

&lt;p&gt;The Indian Ocean (IO) is witnessing acidification of its surface waters as a consequence of the continuous rising of atmospheric CO&lt;sub&gt;2&lt;/sub&gt; concentration thus disrupting the biological and chemical balance of the ecosystem in the region. The basin wide spatial variability of biogeochemical properties induces spatial variability of surface water pH. This study investigates the seasonality and trends of surface pH over the IO bioprovinces and regionally assesses the individual contribution of the factors affecting its variability. Simulations from global ocean models (OTTM and ROMS) coupled with suitable biogeochemical modules were validated with pH observations over the basin, and used to discern the regional response of pH seasonality (1990-2010) and trend (1961-2010) to changes in ocean temperature (SST), Dissolved Inorganic Carbon (DIC), Total Alkalinity (ALK) and Salinity (S). DIC and SST are the major contributors to the seasonal variability of pH in almost all bioprovinces consistent in both model simulations. The acidification in IO basin of 0.0675 units during 1961-2010 is attributed to 69.28% contribution of DIC followed by 13.82% contribution of SST. For most of the regions DIC remains a dominant contributor to changing trend in pH except for the Northern Bay of Bengal and Around India (NBoB-AI) region, wherein pH trend is dominated by ALK (55.6%) and SST (16.8%). The interdependence of SST and S over ALK is significant in modifying the carbonate chemistry and biogeochemical dynamics of NBoB-AI and a part of tropical, subtropical IO. The strong negative correlation between SST and pH infers the increasing risk of acidification in the bioprovinces with the rising SST.&lt;/p&gt;&lt;p&gt;This study is an attempt to identify the regional influencers of pH variability so that adequate mitigation action can be planned and the acidification can be decelerated in near future.&lt;/p&gt;

scholarly journals Assessment of the Rheological Behavior of Polymer–Oxidant Mixtures and the Influence of the Groundwater Environment on Their Properties

Water ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1698
Author(s):  
Qi Xu ◽  
Jiajun Chen ◽  
Xinran Song
Keyword(s):  
Xanthan Gum ◽  
Control Method ◽  
Shear Thinning ◽  
Mobility Control ◽  
Retention Rates ◽  
Viscosity Reduction ◽  
Leading Role ◽  
Salt Ions ◽  
Groundwater Environment ◽  
Water Ph

Shear-thinning polymers have been introduced to contaminant remediation in the subsurface as a mobility control method applied to mitigate the inefficient delivery of remedial agents caused by geological heterogeneity. Laboratory experiments have been conducted to assess the compatibility of polymers (xanthan and hydrolyzed polyacrylamide (HPAM)) and oxidants (KMnO4 and Na2S2O8) through quantitative evaluation of the viscosity maintenance, shear-thinning performance, and oxidant consumption. The mechanism that causes viscosity loss and the influence of the groundwater environment on the mixture viscosity were also explored. The xanthan–KMnO4 mixture exhibited the best performance in both viscosity retention and shear-thinning behavior with retention rates higher than 75% and 73.5%, respectively. Furthermore, the results indicated that xanthan gum has a high resistance to MnO4− and that K+ plays a leading role in its viscosity reduction, while HPAM is much more sensitive to MnO4−. The viscosity responses of the two polymers to Na2S2O8 and NaCl were almost consistent with that of KMnO4; salt ions displayed an instantaneous effect on the solution’s viscosity, while the oxide ions could cause the solution’s viscosity to decrease continuously with time. Since xanthan exhibited acceptable oxidant consumption as well, xanthan–KMnO4 is considered to be the optimal combination. In addition, the results implied that the effects of salt ions and the water pH on the mixture solution could be acceptable. In the 2D tank test, it was found that when xanthan gum was introduced, the sweeping efficiency of the oxidant in the low-permeability zone was increased from 28.2% to 100%. These findings demonstrated the feasibility of using a xanthan–KMnO4 mixture for actual site remediation.

Factors affecting the viscosity of caseinates in dispersions of high concentrations

1968 ◽  
Vol 35 (1) ◽  
pp. 31-47 ◽  
Author(s):  
J. F. Hayes ◽  
Pamela M. Southby ◽  
L. L. Muller
Keyword(s):  
Methyl Cellulose ◽  
Calcium Content ◽  
Gel Formation ◽  
High Concentration ◽  
Factors Affecting ◽  
Physical Effects ◽  
High Concentrations ◽  
Commercial Applications ◽  
Reversible Gel

SummaryThe physical effects of various cations in caseinate dispersions of high concentrations were investigated over a range of temperature and pH.With calcium and strontium the temperature-viscosity relationships of the caseinates were abnormal in that the viscosity decreased rapidly from 30 to about 40 °C and a gel formed at temperatures in the region of 50–60 °C. On cooling, the gel reliquefied. No gel formed with barium, aluminium or magnesium. On cooling, magnesium preparations separated into 2 phases.The supernatant phase from the magnesium caseinate and a corresponding phase prepared by centrifuging the calcium caseinate showed depletion of α-casein and enrichment of κ-casein and β-casein. The supernatant phase from the calcium caseinate showed the reversible gel formation on heating. The magnesium supernatant phase did not. κ-Casein and a mixture of κ- and β-caseins gave reversible gels at similar levels of calcium and pH.For reversible gel formation to occur, calcium caseinate was required to be in fairly high concentration, to have a calcium content of about 1·0% of the protein and to be within the pH limits 5·2–6·0. The temperature at which gelation occurred was affected by the concentration of calcium and protein and by pH.The behaviour of the material was compared with that of methyl cellulose with and without addition of urea.Some potential commercial applications of the findings on viscosity relationships are outlined.

scholarly journals Effect of polyamines on the stability of brain-cortex ribosomes

1969 ◽  
Vol 114 (4) ◽  
pp. 847-854 ◽  
Author(s):  
R. K. Datta ◽  
Suchandra Sen ◽  
J. J. Ghosh
Keyword(s):  
Melting Temperature ◽  
Brain Cortex ◽  
Temperature Dependent ◽  
Enzymic Digestion ◽  
Ph Dependent ◽  
High Concentrations ◽  
The Stability ◽  
Goat Brain

1. Ribosomes isolated from the cortex tissue of goat brain contain very small amounts of spermidine and spermine. Ribosomes isolated from spermidine-treated slices have a higher spermidine content. 2. The polyamines partially prevent the temperature-dependent breakdown of ribosomes into acid-soluble nucleotides. 3. The ‘melting’ temperature of ribosomes rises slightly when the ribosomes are heated slowly in the presence of polyamines. 4. The pH-dependent breakdown of ribosomes into protein, RNA and acid-soluble nucleotide is markedly decreased by polyamines present in media in which ribosomes are suspended. 5. The breakdown of ribosomes in the presence of high concentrations of salts and EDTA is partially checked by the concurrent presence of polyamines. 6. Spermidine and spermine make ribosomes less susceptible to enzymic digestion by crystalline trypsin and ribonuclease.

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