5 research outputs found
Chelate titrations of Ca2+ and Mg2+ using microfluidic paper-based analytical devices
We developed microfluidic paper-based analytical devices (μPADs) for the chelate titrations of Ca2+ and Mg2+ in natural water. The μPAD consisted of ten reaction zones and ten detection zones connected through narrow channels to a sample zone located at the center. Buffer solutions with a pH of 10 or 13 were applied to all surfaces of the channels and zones. Different amounts of ethylenediaminetetraacetic acid (EDTA) were added to the reaction zones and a consistent amount of a metal indicator (Eriochrome Black T or Calcon) was added to the detection zones. The total concentrations of Ca2+ and Mg2+ (total hardness) in the water were measured using a μPAD containing a buffer solution with a pH of 10, whereas only Ca2+ was titrated using a μPAD prepared with a potassium hydroxide solution with a pH of 13. The μPADs permitted the determination of Ca2+ and Mg2+ in mineral water, river water, and seawater samples within only a few minutes using only the naked eye—no need of instruments
Chelate titrations of Ca2+ and Mg2+ using microfluidic paper-based analytical devices
We developed microfluidic paper-based analytical devices (μPADs) for the chelate titrations of Ca2+ and Mg2+ in natural water. The μPAD consisted of ten reaction zones and ten detection zones connected through narrow channels to a sample zone located at the center. Buffer solutions with a pH of 10 or 13 were applied to all surfaces of the channels and zones. Different amounts of ethylenediaminetetraacetic acid (EDTA) were added to the reaction zones and a consistent amount of a metal indicator (Eriochrome Black T or Calcon) was added to the detection zones. The total concentrations of Ca2+ and Mg2+ (total hardness) in the water were measured using a μPAD containing a buffer solution with a pH of 10, whereas only Ca2+ was titrated using a μPAD prepared with a potassium hydroxide solution with a pH of 13. The μPADs permitted the determination of Ca2+ and Mg2+ in mineral water, river water, and seawater samples within only a few minutes using only the naked eye—no need of instruments
Acid–Base Titrations Using Microfluidic Paper-Based Analytical Devices
Rapid
and simple acid–base titration was accomplished using
a novel microfluidic paper-based analytical device (μPAD). The
μPAD was fabricated by wax printing and consisted of ten reservoirs
for reaction and detection. The reaction reservoirs contained various
amounts of a primary standard substance, potassium hydrogen phthalate
(KHPth), whereas a constant amount of phenolphthalein was added to
all the detection reservoirs. A sample solution containing NaOH was
dropped onto the center of the μPAD and was allowed to spread
to the reaction reservoirs where the KHPth neutralized it. When the
amount of NaOH exceeded that of the KHPth in the reaction reservoirs,
unneutralized hydroxide ion penetrated the detection reservoirs, resulting
in a color reaction from the phenolphthalein. Therefore, the number
of the detection reservoirs with no color change determined the concentration
of the NaOH in the sample solution. The titration was completed within
1 min by visually determining the end point, which required neither
instrumentation nor software. The volumes of the KHPth and phenolphthalein
solutions added to the corresponding reservoirs were optimized to
obtain reproducible and accurate results for the concentration of
NaOH. The μPADs determined the concentration of NaOH at orders
of magnitude ranging from 0.01 to 1 M. An acid sample, HCl, was also
determined using Na<sub>2</sub>CO<sub>3</sub> as a primary standard
substance instead of KHPth. Furthermore, the μPAD was applicable
to the titrations of nitric acid, sulfuric acid, acetic acid, and
ammonia solutions. The μPADs were stable for more than 1 month
when stored in darkness at room temperature, although this was reduced
to only 5 days under daylight conditions. The analysis of acidic hot
spring water was also demonstrated in the field using the μPAD,
and the results agreed well with those obtained by classic acid–base
titration