Investigation of the Range of a Plastic pH Sensor Based on a Dibasic Ionophore

1992 ◽  
Vol 45 (2) ◽  
pp. 435 ◽  
Author(s):  
TJ Cardwell ◽  
RW Cattrall ◽  
LW Deady ◽  
KA Murphy
Keyword(s):  
Positive Charge ◽  
Ph Sensor ◽  
Low Ph ◽  
Membrane Electrode ◽  
Neutral Carrier ◽  
Ph Values ◽  
Response Range ◽  
Ph Scale ◽  
Ph Range ◽  
Sensitive Membrane

A study is reported of the use of a neutral carrier reagent containing two nitrogen atoms with very different basicities in a pH-sensitive membrane electrode with a view to obtaining a broad response range. This electrode responds well in the pH region of 6-12 but suffers anion interference in the region of pH 2-6. A study is included of the effect of adding various amounts of potassium tetrakis(4-chloropheny1)borate as an anion suppressing reagent to the membrane in order to reduce the anion interference at low pH values. The conclusion is drawn that an extension to the working pH range is not possible with this approach unless controlled amounts of anion suppressing reagent can be provided to approximately balance the positive charge of the carrier in each region of the pH scale.

Surface charge on kaolinites in aqueous suspension

Soil Research ◽  
1976 ◽  
Vol 14 (2) ◽  
pp. 197 ◽  
Author(s):  
MDA Bolland ◽  
AM Posner ◽  
JP Quirk
Keyword(s):  
Surface Charge ◽  
Positive Charge ◽  
Aqueous Suspension ◽  
Isomorphous Substitution ◽  
Ph Values ◽  
Negative Surface ◽  
Negative Surface Charge ◽  
Decreasing Ph ◽  
Ph Range ◽  
Exchange Technique

The surface charge of several natural kaolinites was measured in the pH range 3-10 using an exchange technique. The positive charge was found to increase with decreasing pH and sometimes to increase with increasing ionic strength; it occurred on the kaolinites at pH values as high as 9 and 10 and was particularly evident at high ionic strengths. The positive surface charge on kaolinites is thought to be due to exposed alumina such as is found on oxide surfaces. Aluminium was found to dissolve from kaolinite at pH values beiow about 6.5. Aluminium dissolution increased with decreasing pH and time. When the proportion of dissolved aluminium ions balancing negative surface charge was taken into account, the negative and net negative surface charge on kaolinite was concluded to be largely due to pH independent charge resulting from isomorphous substitution, together with some pH dependent charge due to exposed SiOH sites. If Na+ was the index cation, dissolved aluminium ions from the clay replaced some of the Na+ balancing the negative surface charge. However, when Cs+ was the index cation, less Cs+ balancing the negative surface charge on the clay was replaced by dissolved aluminium. As the concentration of either Na+ or Cs+ was increased, less dissolved aluminium replaced the index cation as a counteraction to the negative surface charge.

scholarly journals Near-Infrared pH Sensor Based on a SPEEK–Polyaniline Polyelectrolyte Complex Membrane

Proceedings ◽  
2018 ◽  
Vol 3 (1) ◽  
pp. 11 ◽  
Author(s):  
Nedal Y. Abu-Thabit
Keyword(s):  
Polyelectrolyte Complex ◽  
Near Infrared ◽  
Response Times ◽  
Oxidative Polymerization ◽  
Ph Sensor ◽  
Ph Sensing ◽  
Ph Values ◽  
Sensing Applications ◽  
Ph Range ◽  
Speek Membrane

A polyelectrolyte complex (PEC) membrane based on sulfonated poly (ether ether ketone) and polyaniline (SPEEK-PANI) was developed for pH sensing applications. Aniline was polymerized in the presence of the SPEEK membrane by using in situ chemical oxidative polymerization to yield an ionically crosslinked SPEEK-PANI membrane. The fabricated membrane exhibited sensitivity in the physiological pH range of 2–8. The PEC membrane pH sensor showed good absorption properties in the near-infrared region (NIR). The membrane showed fast response during a de-doping process (≈90 s), while longer response times are essential for doping processes from the alkaline/neutral pH region to the acidic pH region, which is attributed to the presence of highly acidic sulfonic acid groups with a high buffering capacity in the PEC membrane. The SPEEK-PANI membrane exhibited slightly higher water uptake compared to the neat SPEEK membrane. The membrane exhibited good stability, as it was stored in 1M HCl solution for more than 2 years without physical or visual deterioration. A preconditioning step in 1M HCl ensured that the results were reproducible and allows the pH sensor to be used repeatedly. The PEC sensor membranes are suitable for applications that start at low pH values and move upwards to higher pH values in the 2–8 pH range.

scholarly journals Chemoenzymatic synthesis of the pH responsive surfactant octyl β-D-glucopyranoside uronic acid

2019 ◽  
Vol 104 (3) ◽  
pp. 1055-1062 ◽  
Author(s):  
Ngoc T. N. Ngo ◽  
Carl Grey ◽  
Patrick Adlercreutz
Keyword(s):  
Substrate Concentration ◽  
Uronic Acid ◽  
Catalyst System ◽  
Low Ph ◽  
Chemoenzymatic Synthesis ◽  
Ph Responsive ◽  
Ph Values ◽  
Wide Ph Range ◽  
Carboxyl Derivative ◽  
Ph Range

AbstractMethodology was developed to expand the range of benign alkyl glycoside surfactants to include also anionic types. This was demonstrated possible through conversion of the glycoside to its carboxyl derivative. Specifically, octyl β-D-glucopyranoside (OG) was oxidised to the corresponding uronic acid (octyl β-D-glucopyranoside uronic acid, OG-COOH) using the catalyst system T. versicolor laccase/2,2,6,6-tetramethylpiperidinyloxy (TEMPO) and oxygen from air as oxidant. The effects of oxygen supply methodology, concentrations of laccase, TEMPO and OG as well as reaction temperature were evaluated. At 10 mM substrate concentration, the substrate was almost quantitatively converted into product, and even at a substrate concentration of 60 mM, 85% conversion was reached within 24 h. The surfactant properties of OG-COOH were markedly dependent on pH. Foaming was only observed at low pH, while no foam was formed at pH values above 5.0. Thus, OG-COOH can be an attractive low-foaming surfactant, for example for cleaning applications and emulsification, in a wide pH range (pH 1.5–10.0).

An aminoquinoline based biocompatible fluorescent and colourimetric pH sensor designed for cancer cell discrimination

2018 ◽  
Vol 42 (24) ◽  
pp. 19818-19826 ◽  
Author(s):  
Jayanta Mandal ◽  
Pravat Ghorai ◽  
Paula Brandão ◽  
Kunal Pal ◽  
Parimal Karmakar ◽  
...  
Keyword(s):  
Cancer Cells ◽  
Cancer Cell ◽  
Low Cost ◽  
Ph Sensor ◽  
Low Ph ◽  
Cell Permeability ◽  
Ph Range ◽  
Cell Discrimination

A simple, low cost aminoquinoline based pH sensor,HLwas prepared and it works at a low pH range.HLexhibits cell permeability and used as an effective tool for differentiating between normal and cancer cells.

scholarly journals Aqueous Colloidal Stability of Graphene Oxide and Chemically Converted Graphene

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Swarnima Kashyap ◽  
Shashank Mishra ◽  
Shantanu K. Behera
Keyword(s):  
Graphene Oxide ◽  
Colloidal Stability ◽  
Low Ph ◽  
Particle Charge ◽  
Chemically Converted Graphene ◽  
Ph Scale ◽  
Ph Range ◽  
Average Size ◽  
Poor Stability ◽  
The Ideal

Graphene oxide (GO) was prepared by modified Hummer’s method, and chemically converted graphene (CCG) was prepared by further reduction of the aqueous GO colloid. The effect of pH on particle size, particle charge, and light absorption of the aqueous colloids of GO and CCG was studied with titration against HCl or NaOH, to find the ideal characteristics for a stable dispersion. The GO colloid was stable in the pH range of 4–11, whereas the CCG colloid gained stability at a relatively narrower pH range of 7–10. Poor stability of the colloids was observed for both GO and CCG colloids at both extremes of the pH scale. Both of the colloids exhibited average size of ~1 micron in the low pH range, whereas for higher pH the size ranged between 300 and 500 nm. The UV-Vis spectra showed absorption peak at 230 nm for GO colloids that shifted to 260 nm for the CCG colloid. Such shift can be ascribed to restoring of electronic conjugation of the C=C bonds in CCG.

Novel optical pH sensor for high and low pH values

2003 ◽  
Vol 90 (1-3) ◽  
pp. 143-150 ◽  
Author(s):  
Afsaneh Safavi ◽  
Mozhgan Bagheri
Keyword(s):  
Ph Sensor ◽  
Low Ph ◽  
Ph Values ◽  
Optical Ph Sensor

Changes in charge charactistics of soils after treatment with 0.5M calcium chloride at pH 1.5

Soil Research ◽  
1967 ◽  
Vol 5 (2) ◽  
pp. 247 ◽  
Author(s):  
CK Tweneboah ◽  
DJ Greenland ◽  
JM Oades
Keyword(s):  
Clay Minerals ◽  
Calcium Chloride ◽  
Negative Charge ◽  
Positive Charge ◽  
Low Ph ◽  
Rapid Rate ◽  
Constant Rate ◽  
Ph Range ◽  
Kinetics Of

The kinetics of the removal of iron, aluminium, and silicon from soils and clays in the pH range 0-3 have been studied using a number of oxides, clay minerals, and soils. At pH 1.5, aluminium is removed but little iron or silicon. An initial rapid rate of aluminium extraction is followed by a slower constant rate. The rapidly released aluminium is extracted in approximately 12 hr using 0.5M CaCl2 at pH 1.5.reatment of a range of soils and clays by this method reduced the positive charge developed at low pH very substantially but had little effect on the negative charge. It is suggested that the positive charges in the soils studied are mostly due to the 'active' aluminium oxides.

scholarly journals Influence of particle properties on iron flocculation

2017 ◽  
Vol 18 (5) ◽  
pp. 1617-1624
Author(s):  
D. J. de Ridder ◽  
D. van Halem
Keyword(s):  
Positive Charge ◽  
Water Phase ◽  
Significant Delay ◽  
Iron Species ◽  
Particle Properties ◽  
Charged Species ◽  
Ph Values ◽  
Ph Range ◽  
Positively Charged ◽  
Charge Interactions

Abstract In this study, the importance of charge interactions during flocculation of Fe3+ in the presence of particles and anions/cations at various pH values was investigated. SiO2, (s) and ZnO(s) were dosed as particles to promote charge interactions and/or serve as a nucleus to accelerate floc formation. In the pH range 6–9, SiO2, (s) is negatively charged, while ZnO(s) carries a positive charge. Ca2+ and HPO42− were selected to investigate charge interactions in the water phase. A significant delay in floc growth due to charge repulsion between negatively charged iron species was observed at pHini 9. For positively charged species at pHini 6, a delay in floc growth was observed as well, but to a lesser degree. These effects could be neutralized by either dosing (positively charged) ZnO(s) or Ca2+ at pHini 9, or (negatively charged) SiO2, (s) at pHini 6. The addition of phosphate did not hinder floc growth at pHini 6. While phosphate completely inhibited floc growth at pHini 7–9 in the presence of negatively charged SiO2, (s), the presence of positively charged ZnO(s) partly neutralized the detrimental influence of phosphate on floc growth. Similarly, dosing Ca2+ partly neutralized the effect of phosphate.

Conserved amphiphilic feature is essential for periplasmic chaperone HdeA to support acid resistance in enteric bacteria

2008 ◽  
Vol 412 (2) ◽  
pp. 389-397 ◽  
Author(s):  
Ye E. Wu ◽  
Weizhe Hong ◽  
Chong Liu ◽  
Lingqing Zhang ◽  
Zengyi Chang
Keyword(s):  
Pathogenic Bacteria ◽  
Acid Resistance ◽  
Enteric Bacteria ◽  
Structural Features ◽  
Low Ph ◽  
Hydrophobic Region ◽  
Ph Values ◽  
Ph Conditions ◽  
Stomach Ph ◽  
Ph Range

The extremely acidic environment of the mammalian stomach (pH 1–3) represents a stressful challenge for enteric pathogenic bacteria, including Escherichia coli, Shigella and Brucella. The hdeA (hns-dependent expression A) gene was found to be crucial for the survival of these enteric bacteria under extremely low pH conditions. We recently demonstrated that HdeA is able to exhibit chaperone-like activity exclusively within the stomach pH range by transforming from a well-folded conformation at higher pH values (above pH 3) into an unfolded conformation at extremely low pH values (below pH 3). This study was performed to characterize the action mechanisms and underlying specific structural features for HdeA to function in this unfolded conformation. In the present study, we demonstrate that the conserved ‘amphiphilic’ feature of HdeA, i.e. the exposure of the conserved hydrophobic region and highly charged terminal regions, is essential for exhibiting chaperone-like activity under extremely low pH conditions. Mutations that disrupt this amphiphilic feature markedly reduced the chaperone-like activity of HdeA. The results also strongly suggest that this acid-induced chaperone-like activity of HdeA is crucial for acid resistance of the enteric bacteria. Moreover, our new understanding of this amphiphilic structural feature of HdeA helps to better interpret how this unfolded (disordered) conformation could be functionally active.

Color tunable, ratiometric pH sensor for high and low pH values base on 9-(cycloheptatrienylidene)fluorene derivatives

2007 ◽  
Vol 122 (2) ◽  
pp. 389-394 ◽  
Author(s):  
Guorong Zheng ◽  
Zixing Wang ◽  
Lei Tang ◽  
Ping Lu ◽  
William P. Weber
Keyword(s):  
Ph Sensor ◽  
Low Ph ◽  
Ph Values ◽  
Color Tunable
Sign in / Sign up

Export Citation Format

Share Document