METHOD FOR DETECTING SILICA

Abstract

The present invention relates to utilization of lanthanide time resolved fluorescence for determining silica concentration. In the method sample comprising silica is admixed with a reagent comprising a lanthanide (III) ion and optionally a chelating agent, silica in the sample is allowed to interact with the reagent comprising the lanthanide (III) ion, followed by exciting the sample and detecting a signal deriving from the lanthanide (III) ion, and determining the concentration of the silica in the sample by using the detected signal.

Claims

1. A method for determining concentration of silica in a sample comprising silica, the method comprising: optionally diluting and/or purifying the sample; admixing the sample with a reagent comprising a lanthanide(III) ion; allowing the silica in the sample to interact with the reagent comprising the lanthanide(III) ion; exciting the sample at a excitation wavelength and detecting a sample signal deriving from the lanthanide(III) ion at a signal wavelength by using time-resolved fluorescence measurement; and determining the concentration of the silica in the sample by using the detected sample signal.

2. The method according to claim 1, wherein additionally a lanthanide chelating agent or agents is/are admixed with the sample.

3. The method according to claim 1, wherein concentration of the silica in a measurement mixture is in a range of 0.1-100 ppm, preferably 0.5-50 ppm, and more preferably 1-30 ppm.

4. The method according to claim 1, wherein concentration of the lanthanide(III) ion in a measurement mixture is in a range of 0.1-100 μM, preferably 0.1-50 μM, and more preferably 1-20 μM

5. The method according to claim 2, wherein concentration of the lanthanide chelating agent in a measurement mixture is in a range of 0.01-500 ppm, preferably 0.5-50 ppm, and more preferably 0.5-20 ppm.

6. The method according to claim 2, wherein the chelating agent comprises at least one or more functional groups capable of chelating lanthanide(III) ions, preferably one or more groups selected from esters, ethers, thiols, hydroxyls, carboxylates, sulfonates, amides, phosphates, phosphonates, amines or any combination thereof.

7. The method according to claim 2, wherein the chelating agent contain additionally aromatic group or groups.

8. The method according to claim 1, wherein the silica comprises silicic acid or oligomeric silicate soluble in water.

9. The method according to claim 1, wherein the lanthanide(III) ion is selected from europium, terbium, samarium or dysprosium ions, preferably europium or terbium ions.

10. The method according to claim 1, wherein the reagent comprises lanthanide(III) salt, preferably halogenide or oxyanion, more preferably hydrated halogenides or nitrates, most preferably chloride.

11. The method according to claim 1, wherein the sample is purified by using a purification method selected from the group consisting of centrifugation, size exclusion chromatography, cleaning with solid-phase extraction (SPE) cartridges, dialysis techniques, extraction methods for removing hydrocarbons, filtration, microfiltration, ultrafiltration, nanofiltration, membrane centrifugation and any combinations thereof.

12. The method according to claim 1, wherein a pH value of the sample is adjusted to a level in a range between pH 3 and pH 8, preferably in a range from pH 5 to pH 8.

13. Use of the method according to claim 1 for determining concentration of silica in a sample.

14. The use according to claim 12, wherein the sample originates from geothermal processes, cooling towers, desalination plants and water treatment process.

15. A device comprising means for performing the method according to claim 1 for determining concentration of silica in a sample.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0014] FIG. 1 illustrates time-resolved fluorescence signal of Europium as a function of sodium silicate concentration with and without polyacrylic acid chelating agent.

DETAILED DESCRIPTION

[0015] The present invention relates to a method for determining concentration of silica in a sample. More particularly the present invention relates to a method for determining concentration of silica in a sample comprising silica, the method comprising [0016] optionally diluting and/or purifying the sample, [0017] admixing the sample with a reagent comprising a lanthanide(III) ion, [0018] allowing the silica in the sample to interact with the reagent comprising the Ianthanide(III) ion, [0019] exciting the sample at a excitation wavelength and detecting a sample signal deriving from the lanthanide(III) ion at a signal wavelength by using time-resolved fluorescence measurement, and [0020] determining the concentration of the silica in the sample by using the detected sample signal.

[0021] In a preferred embodiment additionally a lanthanide chelating agent or chelating agents is/are admixed with the sample prior exciting the sample.

[0022] In one embodiment the reagent comprising lanthanide(III) ion and the chelating agent or agents are admixed together prior admixing with the sample.

[0023] In other embodiment the sample and the chelating agent or agents are admixed together prior admixing with the reagent comprising lanthanide(III) ion.

[0024] In other embodiment the reagent comprising lanthanide(III) ion and the sample are admixed together prior admixing with the chelating agent or agents.

[0025] The chelating agent comprises at least one or more functional groups capable of chelating lanthanide(III) ions. Preferably the one or more one functional groups are selected from esters, ethers, thiols, hydroxyls carboxylates, sulfonates, amides, phosphates, phosphonates, amines or any combination thereof.

[0026] In an embodiment, chelating agent contains additionally aromatic group or groups. The aromatic group(s) amplifies the signal of the lanthanide(III) ion.

[0027] The lanthanide(III) ion is selected from europium, terbium, samarium or dysprosium ions, preferably europium or terbium ions.

[0028] In a preferred embodiment the reagent comprises lanthanide(III) salt. The lanthanide(III) salt is selected from halogenides and oxyanions, such as nitrates, sulfates or carbonates, preferably from hydrated halogenides or nitrates, more preferably chloride.

[0029] The silica in the sample can be any suitable silica. Preferably the silica comprises silicic acid or oligomeric silicate soluble in water.

[0030] In one embodiment concentration of the silica in the measurement mixture is in the range of 0.1-100 ppm, preferably 0.5-50 ppm, and more preferably 1-30 ppm.

[0031] In case the concentration of the silica in the sample is higher, the sample can be diluted.

[0032] In another embodiment concentration of the lanthanide(III) ion in the measurement mixture is in the range of 0.1-100 μM, preferably 0.1-50 μM, and more preferably 1 μM 20 μM.

[0033] In preferred embodiment concentration of the lanthanide chelating agent in the measurement mixture is in the range of 0.01-500 ppm, preferably 0.5-50 ppm, and more preferably 0.5-20 ppm.

[0034] By term “measurement mixture” is meant the admixture in the measurement.

[0035] The sample is optionally diluted to suitable aqueous solution e.g. deionized water or brine containing monovalent and/or divalent ions. Preferably, the dissolution brine does not contain any trivalent ions. Preferably the sample is an aqueous solution.

[0036] If the sample solution contains some interfering compounds such as trivalent metal cations or chelating agents that may affect TRF signal, suitable purification procedures may be applied prior to the dilution steps.

[0037] The sample is optionally purified by using a purification method selected from centrifugation, size exclusion chromatography, cleaning with solid-phase extraction (SPE) cartridges, dialysis techniques, extraction methods for removing hydrocarbons, filtration, microfiltration, ultrafiltration, nanofiltration, membrane centrifugation and any combinations thereof.

[0038] In one embodiment pH value of the sample is adjusted to a level in range between pH 3 and pH 8, preferably in range from pH 5 to pH 8

[0039] Unknown concentration of the silica in the sample is determined by comparing the sample signal to calibration curve. The calibration curve is obtained from TRF measurement of calibration standard samples with varying silica concentrations and the optional chelating agent in fixed concentration. Same dilution and/or purification steps and measurement parameters have to be used for both the sample and calibration samples.

[0040] The lanthanide(III) ion is excited at excitation wavelength and measured at emission wavelength and detected by using time-resolved fluorescence (TRF). Any TRF reader can be employed. Excitation and emission wavelengths are selected so that the S/N is the best. Also the delay time can be optimized.

[0041] The excitation and emission wavelengths and the delay time are chosen based on the requirements of the lanthanide ion.

[0042] In an exemplary embodiment excitation wavelength and emission wavelength and delay time for Europium is 395 nm and 615 nm and 400 μs respectively.

[0043] The present invention further relates to use of the method of the present invention for determining concentration of silica in a sample.

[0044] The sample can originate from originates from geothermal processes, cooling towers, desalination plants and water treatment process.

[0045] The present invention further relates a device comprising means for performing the method according to the present invention for determining concentration of silica in a sample.

[0046] The examples are not intended to limit the scope of the invention but to present embodiments of the present invention.

EXAMPLES

Example 1. Silica Detection in the Absence of Chelating Agent

[0047] All the reagents were diluted into brine, which composition is presented in Table 1. EuCl.sub.3.6 H.sub.2O was used as lanthanide source. The europium salt was diluted into brine so that the concentration of europium was 22.48 μM. Silica sample solution was prepared by diluting sodium silicate (Na.sub.2SiO.sub.3) into the brine. The Na.sub.2SiO.sub.3 concentration was varied between 0 and 30 ppm. 100 μl of both lanthanide and silica solutions were pipetted into microplate (MICROPLATE BIOCHEM 96WELL BLACK), and the TRF signal of the mixture was measured using Tecan Spark multiplate reader. The lag time, excitation and emission wavelengths used were 400 μs, 295 nm and 615 nm, respectively.

Example 2. Silica Detection in the Presence of Chelating Agent

[0048] All the reagents were diluted into brine, which composition is presented in Table 1. EuCl.sub.3.6 H.sub.2O was used as lanthanide source. The europium salt was diluted into brine so that the concentration of europium was 22.48 μM. 200 ppm chelating agent solution was prepared by diluting the chelating agent into brine. Polyacrylic acid type polymer can be used as chelating agent. Silica sample solution was prepared by diluting sodium silicate (Na.sub.2SiO.sub.3) into the brine. The Na.sub.2SiO.sub.3 concentration was varied between 0 and 120 ppm. 100 μl of lanthanide solution was first pipetted into microplate (MICROPLATE BIOCHEM 96WELL BLACK), after which 50 μl of silica solution and 50 μl of chelating agent were added to the plate. The TRF signal of the mixture was measured using Tecan Spark multiplate reader. The lag time, excitation and emission wavelengths used were 400 μs, 295 nm and 615 nm, respectively.

[0049] FIG. 1 presents the TRF signals of the measurements of Examples 1 and 2.

TABLE-US-00001 TABLE 1 Brine composition used in tests. Salts are weighed and diluted in 10 liters of MQ water. Salt Mass (g) NaCl 350.3 CaCl.sub.2*2H.sub.2O 22.4 MgCl2*6H.sub.2O 14.6 KCl 2.1 BaCl.sub.2*2H.sub.2O 1.3