A METHOD FOR DETERMINING HYDROLYSIS DEGREE AND CHARGE DENSITY OF POLYELECTROLYTES AND PHOSPHONATES

Abstract

The present invention relates to a method for determining hydrolysis degree and charge density of polyelectrolyte or phosphonate in a sample. In the method the sample is mixed with a reagent comprising a lanthanide(lll) ion. The mixture is excited at an excitation wavelength and a signal deriving from the lanthanide(lll) ion is detected by using time-resolved fluorescence measurement, followed by determining the hydrolysis degree and the charge density of the polyelectrolyte or phosphonate by using the detected sample signal.

Claims

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

2. The method according to claim 1, wherein the polyelectrolyte contains one or more groups selected from ester, ether, carboxylic acid/carboxylate, amide, phosphonate, amine groups or any combination thereof.

3. The method according to claim 1, wherein the method is for determining of hydrolysis degree of polyelectrolytes or phosphonate.

4. The method according to claim 1, wherein the method is for determining of charge density of polyelectrolytes or phosphonate.

5. The method according to claim 1, wherein the reagent comprising a lanthanide(lll) ion is a lanthanide(lll) salt.

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

7. The method according to claim 5, wherein the lanthanide(lll) salt is selected from halogenides and oxyanions, preferably from hydrated halogenides or nitrates, more preferably chloride.

8. The method according to claim 1, wherein concentration of the lanthanide(lll) ion in the measurement mixture is in the range of 0.01-100 μM, preferably 0.1-20 μM, and more preferably 1-20 μM.

9. The method according to claim 1, wherein concentration of the polyelectrolyte or phosphonate in the measurement mixture is in the range of 0.01-100 ppm, preferably 0.1-50 ppm, and more preferably 0.5-20 ppm.

10. The method according to claim 1, wherein a signal modifier is added to the sample before the excitation of the sample, preferably the signal modifier comprises a metal ion selected from the group consisting of copper, nickel, chromium, iron, gold, silver, cobalt, and any of their mixtures.

11. The method according to claim 1, wherein the sample is 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.

12. The method according to claim 1, wherein a 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 7.5.

13. Use of the method according to claim 1 for determining hydrolysis degree of polyelectrolyte or phosphonate or charge density of polyelectrolyte or phosphonate in a sample.

14. The use according to claim 13, wherein the sample originates from water treatment, paper making processes, pharmaceutical industry, well drilling, mineral processing, enhanced oil recovery, an oilfield or an oil well or from an oil production process.

15. A device comprising means for performing the method according to claim 1 for determining hydrolysis degree or charge density of polyelectrolyte in a sample.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0023] FIG. 1 illustrates TRF response of polyacrylamides with different hydrolysis degree.

[0024] FIG. 2 illustrates TRF signal as a function of hydrolysis degree of polyacrylamide.

[0025] FIG. 3 illustrates TRF signals of polyacrylic acid and sodium polyacrylate for determining charge densities.

DETAILED DESCRIPTION

[0026] The present invention relates to a method for determining hydrolysis degree or charge density of polyelectrolyte or phosphonate in a sample. More particularly the present invention relates to a method for determining hydrolysis degree or charge density of polyelectrolyte or phosphonate in a sample comprising polyelectrolyte or phosphonate, the method comprising [0027] optionally diluting and/or purifying the sample, [0028] admixing the sample with a reagent comprising a lanthanide(III) ion, [0029] allowing the polyelectrolyte or phosphonate in the sample to interact with the reagent comprising the lanthanide(III) ion, [0030] exciting the sample at an excitation wavelength and detecting a sample signal deriving from the lanthanide(III) ion at a signal wavelength by using time-resolved fluorescence measurement, and [0031] determining the hydrolysis degree or the charge density of the polyelectrolyte or phosphonate in the sample by using the detected sample signal.

[0032] The analyte, polyelectrolyte or phosphonate, in the sample bears one or more groups that can hydrolyze and/or that the sample bears one or more groups that are capable of dissociating in aqueous solution to form either anion or cation groups. The analyte can be zwitterionic, i.e. contain both cationic and anionic groups. The charging of the group can depend on the environment pH (acidic or basic groups, such as carboxylic acids and amino groups). Therefore, the groups capable for dissociation can be neutral in certain pH (e.g. carboxylic acid group in acidic and amino groups in basic environment). The polyelectrolyte can be basic or acidic.

[0033] In one embodiment the polyelectrolyte contains one or more groups selected from, carboxylic acid/carboxylate, amide, phosphonate, amine, or any combination thereof.

[0034] In a preferred method the polyelectrolyte contain aromatic groups. The aromatic group(s) amplify the signal of lanthanide(III) ion.

[0035] In one embodiment the polyelectrolyte has molecular weight of at least 1000 g/mol.

[0036] In another embodiment the phosphonate has molecular weight of at least 100 g/mol.

[0037] The lanthanide(III) ion is selected from europium, terbium, samarium or dysprosium ions, preferably europium or terbium ions.

[0038] In a preferred embodiment the lanthanide(III) ion is a 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 hydrated chloride.

[0039] In one embodiment the method of the present invention is utilized for determining charge density of polyelectrolytes or phosphonates. In another embodiment the method of the present invention is utilized for determining of hydrolysis degree of polyelectrolytes such as amide containing polyelectrolytes or phosphonates.

[0040] In one embodiment hydrolysis degree or charge density of polyelectrolyte is determined.

[0041] In other embodiment hydrolysis degree or charge density of phosphonate is determined.

[0042] The sample may be optionally diluted or purified prior mixing the sample with the reagent comprising a lanthanide(III) ion.

[0043] 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. It should be understood that the purification treatment step means preferably removal or dilution of molecules that may disturb the examination of charged molecules of interest, not isolation of the polyelectrolyte e.g. by chromatography.

[0044] The polyelectrolyte or phosphonate 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. If the polymer solution contains some interfering compounds, suitable pretreatment procedures may be applied prior to the dilution steps. Preferably the sample is an aqueous solution.

[0045] In one embodiment concentration of the lanthanide(III) ion in the measurement mixture comprising the sample and the lanthanide (III) ion is in range of 0.1-100 μM, preferably 0.1-20 μM, and more preferably 1-20 μM.

[0046] In other embodiment concentration of the polyelectrolyte or phosphonate in the measurement mixture comprising the sample and the lanthanide (III) ion is in range of 0.01-100 ppm, preferably 0.5-50 ppm, and more preferably 0.5-20 ppm.

[0047] In case the concentration of the polyelectrolyte in the sample is higher, the sample can be diluted

[0048] By term “measurement mixture” is meant the admixture in the measurement.

[0049] In one embodiment a signal modifier is added to the sample before the excitation of the sample. The signal modifier comprises a metal ion selected from a group comprising copper, nickel, chromium, iron, gold, silver, cobalt, and any of their mixtures.

[0050] In one embodiment a pH value of the sample is adjusted prior the mixing to a level in range between pH 3 and pH 8, preferably in range from pH 5 to pH 7.5.

[0051] In a preferred embodiment buffer is used in the measurement for standardization of the pH. Preferably, the buffer is non-chelating, zwitterionic Good's buffer, such as HEPES or tris-bis propane. The pH of the buffer solution is adjusted to a suitable range, preferably to pH 5-7.5. The pH should not be excessively alkaline in order to prevent possible precipitation of the lanthanide hydroxides.

[0052] Unknown hydrolysis degree of the polyelectrolyte or phosphonate in the sample is determined from the measurement by comparing the sample signal to calibration curve. The calibration standard samples have known hydrolysis degree and known concentration. The calibration curve is produced by measurement of known samples having known hydrolysis degrees. The known samples should have same polyelectrolyte or phosphonate concentration as the unknown samples. The hydrolysis degree of the samples (both calibration samples and unknown samples) may vary e.g. in the range of 1-100 mol-%, preferably in the range of 5-60 mol-%.

[0053] The unknown charge density of the polyelectrolyte or phosphonate in the sample is determined from the measurement by comparing the sample signal to the calibration curve. The calibration standard samples have known charge density and known concentration. The calibration curve is produced by measurement of known samples having known charge densities. The known samples should have same polyelectrolyte or phosphonate concentration as the unknown samples.

[0054] 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.

[0055] The excitation and emission wavelengths and the delay time are chosen based on the requirements of the lanthanide ion.

[0056] In an exemplary embodiment 250-400 nm can be used as excitation wavelength region and 575-625 nm can be used as emission wavelength region for Europium.

[0057] In another exemplary embodiment excitation wavelength and emission wavelength and delay time for Europium is 395 nm and 615 nm and 400 μs respectively.

[0058] The present invention further relates to use of the method of the present invention for determining hydrolysis degree of polyelectrolyte or phosphonate or charge density of polyelectrolyte or phosphonate in a sample.

[0059] The sample can originate from water treatment, paper making processes, pharmaceutical industry, well drilling, mineral processing, enhanced oil recovery, an oilfield or an oil well or from an oil production process.

[0060] The present invention further relates a device comprising means for performing the method according to the present invention for determining hydrolysis degree or charge density of polyelectrolyte or phosphonate in a sample.

[0061] The examples are not intended to limit the scope of the present invention, but to present embodiments of the present invention.

EXAMPLES

[0062] Polymers (polyacrylamide or polyacrylate) are dissolved into brine. The brines contain alkaline and earth alkaline metals as chlorides or bicarbonates. The TDS of the brines varies between 20 000 and 40 000 ppm. The diluted polymer samples are eluted through GE NAP-10 column to UV cuvette. HEPES buffer solution (adjusted to pH 7.4) and EuCl.sub.3 is added into the cuvette. The concentrations of polymer in the measurement vary between ˜3 and 17 ppm. The concentrations of HEPES and Eu are 5 mM and 10μM in the measurement mixture. The samples are measured with TRF reader. The lag time, excitation and emission wavelengths used were 401 μs, 396 nm and 615 nm, respectively.

[0063] Table 1 presents hydrolysis degree measurements of polyacrylamides. TRF signal of polyacrylamides with varying polymer concentration (3.3-16.7 ppm in the measurement mixture) and hydrolysis degree (20-60 mol-%), and 3 parallel measurements are measured for each sample and concentration. In the last column, the TRF signal of the sample is compared to that of 40 mol-% hydrolyzed polymer sample.

TABLE-US-00001 TABLE 1 Polyacrylamide concentration Recovery-% in the measurement Hydrolysis Photon (Signal/40% mixture (ppm) degree count AVERAGE polymer signal) 3.3 60 11675 11345 116.4 11447 10914 40 9417 9750 100 9765 10069 25 3337 3209 32.9 3161 3129 21.6 2007 1994 20.4 1926 2048 16.7 60 12835 11806 40.3 10018 12564 40 30179 29279 100 27280 30377 25 9141 9138 31.2 9452 8822 21.6 3447 3685 12.6 3552 4055 13.3 40 26730 26186 100 27798 24031 25 8682 8576 32.7 8044 9002 21.6 3222 3433 13.1 3544 3533

[0064] FIG. 1 presents TRF response of polyacrylamides with different hydrolysis degree. Sample concentrations in the measurement mixture are A) 3.3 ppm: B) 16.7 ppm.

[0065] FIG. 2 presents TRF signals (calibration curves) as a function of hydrolysis degree of polyacrylamide. Average results from the three parallel measurements are presented in the FIG. 2. It can be seen that TRF signal depends on the hydrolysis degree and polymer concentrations (the concentrations presented are concentrations in the measurement mixture).

[0066] FIG. 3 presents TRF signals of polyacrylic acid (pH 6.66) and sodium polyacrylate (pH 3.90) (calibration curves). The TRF signal decreases when the fraction of polyacrylate fraction increases. The signal change is utilized for charge measurement of polyacrylic acids/polyacrylates. It can be seen that the TRF signal depends on the concentration polyacrylic acid and sodium polyacrylate fractions. The concentrations presented in the FIG. 3 are concentrations in the measurement mixture.