Mobile microfluidic determination of analytes

Patent metadata

Field	Value
Publication number	US-2017082551-A1
Application number	US-201515126225-A
Country	US
Kind code	A1
Filing date	Mar 26, 2015
Priority date	Mar 28, 2014
Publication date	Mar 23, 2017
Grant date	—

Abstract

A method includes providing a water sample for analysis at a well site, or at a location proximate the well site, where the water sample is collected from at least one water source and the water sample comprises at least one analyte. The water sample and a reagent are introduced into a microfluidic mixing cell to produce a mixture of the reagent and water sample, and the mixture has a detectable characteristic indicative of concentration of the at least one analyate in the water sample. The detectable characteristic is measured by spectrophotometry to determine concentration of the at least one analyte. Then a subterranean formation treatment fluid is prepared using water from the at least one water source based on the concentration of the at least one analyte. The introducing into the microfluidic mixing cell and the measuring by spectrophotometry are conducted over an elapsed time period of about 5 minutes or less.

First claim

1 . A method comprising:
providing a water sample for analysis, wherein the water sample is collected from at least one water source and wherein the water sample comprises at least one analyte; injecting the water sample and a reagent into a microfluidic mixing cell to produce a mixture of the reagent and water sample, the mixture comprising a detectable characteristic indicative of concentration of the at least one analyate in the water sample; measuring the detectable characteristic by spectrophotometry to determine concentration of the at least one analyte; preparing a subterranean formation treatment fluid comprising the at least one water source based on the concentration of the at least one analyte;
wherein the injecting and the measuring are conducted over an elapsed time period of about 5 minutes or less.

2 . The method of claim 1 further comprising injecting the water sample into a rotating valve and passing the water sample through a sample loading loop fluidly connected with the rotating valve, then injecting the water sample and a reagent into the microfluidic mixing cell, wherein the elapsed time period between the injecting the water sample into the rotating valve and the measuring is about 5 minutes or less.

3 . (canceled)

4 . The method of claim 1 further comprising:
injecting a carrier fluid and the reagent into the microfluidic mixing cell to produce a mixture of the reagent and the carrier fluid;
measuring the mixture of the reagent and the carrier fluid by spectrophotometry to a determine a baseline;

wherein the mixture of the reagent and the carrier fluid is substantially free of the water sample.

5 . The method of claim 4 wherein the injecting the carrier fluid and the reagent into the microfluidic mixing cell and the measuring the mixture of the reagent and the carrier fluid by spectrophotometry are conducted separate from the injecting the water sample and the reagent into the microfluidic mixing cell and the measuring the detectable characteristic.

6 . The method of claim 5 wherein the measured baseline and the measured detectable characteristic are compared to determine concentration of the at least one analyte, and wherein the method is conducted over elapsed time period of about 5 minutes or less.

7 . (canceled)

8 . The method of claim 1 wherein the injecting and the measuring are conducted over an elapsed time period of about 2 minutes or less.

9 . The method of claim 1 further comprising passing the mixture of the reagent and water sample through an optical cell concurrent with the measuring the detectable characteristic by spectrophotometry.

10 . The method of claim 1 further comprising:
injecting the water sample and an Nth reagent into a Nth microfluidic mixing cell to produce a mixture of the Nth reagent and water sample, the mixture comprising a Nth detectable characteristic indicative of concentration of a Nth analyte in the water sample;
measuring the Nth detectable characteristic by spectrophotometry to determine concentration of the Nth analyte;
preparing a subterranean formation treatment fluid comprising the at least one water source based on the concentration of the at least one analyte and the Nth analyte;

wherein the injecting and the measuring are conducted over an elapsed time period of about 5 minutes or less.

11 . The method of claim 1 wherein the at least one analyte is selected from the group consisting of boron, manganese, iron, nitrate, nitrate, sulfate, phosphate, calcium, magnesium, strontium, sulfide, zirconium, titanium, barium, alkalinity, pH, salinity and any combinations thereof.

12 . The method of claim 1 wherein the reagent is selected from the group consisting of carminic acid, ferrozine, o-phenanthroline, chromotropic acid, griess reagent, vanadomolybdate, o-cresolphthalein, calgamite, tannic acid, methylene blue, hydroxyanthraquinone, phenolphthalein, thymol blue, bromocresol, and any combinations thereof.

13 . A method comprising:
providing at least one water source, wherein the at least one water source comprises at least one analyte; delivering an aqueous stream from the at least one water source to a mixer and to a microfluidic mixing cell; injecting a water sample from the at least one water source and a reagent into a microfluidic mixing cell to produce a mixture of the reagent and water sample, the mixture comprising a detectable characteristic indicative of concentration of the at least one analyate in the water sample; measuring the detectable characteristic by spectrophotometry to determine concentration of the at least one analyte; mixing one or more additional components in the mixer with the aqueous stream, in an amount based on the concentration of the at least one analyte; pumping a treatment fluid comprising the at least one water source and the one or more additional components into a wellbore penetrating a subterranean formation; wherein the injecting and the measuring are conducted over a time period of about 5 minutes or less.

14 . The method of claim 13 further comprising injecting the water sample into a rotating valve and passing the water sample through a sample loading loop fluidly connected with the rotating valve, then injecting the water sample and a reagent into the microfluidic mixing cell, wherein the elapsed time period between the injecting the water sample into the rotating valve and the measuring is about 5 minutes or less.

15 . (canceled)

16 . The method of claim 15 further comprising:
injecting a carrier fluid and the reagent into the microfluidic mixing cell to produce a mixture of the reagent and the carrier fluid;
measuring the mixture of the reagent and the carrier fluid by spectrophotometry to a determine a baseline;
wherein the mixture of the reagent and the carrier fluid is substantially free of the water sample.

17 . The method of claim 16 wherein the injecting the carrier fluid and the reagent into the microfluidic mixing cell and the measuring the mixture of the reagent and the carrier fluid by spectrophotometry are conducted separate from the injecting the water sample and the reagent into the microfluidic mixing cell and the measuring the detectable characteristic.

18 . The method of claim 17 wherein the measured baseline and the measured detectable characteristic are compared to determine concentration of the at least one analyte.

19 . The method of claim 18 wherein the injecting and the measuring are conducted over an elapsed time period of about 1 minutes or less.

20 . The method of claim 13 wherein the injecting and the measuring are conducted over an elapsed time period of about 1 minutes or less.

21 . The method of claim 13 further comprising passing the mixture of the reagent and water sample through an optical cell concurrent with the measuring the detectable characteristic by spectrophotometry.

22 . The method of claim 13 further comprising:
injecting the water sample and an Nth reagent into a Nth microfluidic mixing cell to produce a mixture of the Nth reagent and water sample, the mixture comprising a Nth detectable characteristic indicative of concentration of the at least one analyate in the water sample;
measuring the Nth detectable characteristic by spectrophotometry to determine concentration of the Nth analyte;
mixing one or more additional components in the mixer with the aqueous stream, in an amount based on the concentrations of the at least one analyte and the

Assignees

• Schlumberger Technology Corp

Inventors

• Mackay Bruce Alexander
• Mostowfi Farshid
• Sieben Vincent
• Floquet Cedric

Classifications

• E21B43/2607

  Surface equipment specially adapted for fracturing operations · CPC title

• G01N2021/0346

  Capillary cells; Microcells · CPC title

• B01L3/5027

  by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip · CPC title

• G01N21/78 Primary

  producing a change of colour · CPC title

• B01F3/1207

  Operations & Transport · mapped topic