Name: separation of uranium and thorium for 230th-u dating of submarine hydrothermal sulfides
Uploaded: 2019-05-20T12:30:00
Description: Watch this Scientific Journal Video about Separation of Uranium and Thorium for 230Th-U Dating of Submarine Hydrothermal Sulfides at JoVE.com

This study was financially supported by Experimental Technology Innovation Foundation of Institute of Geology and Geophysics, Chinese Academy of Sciences (No. 11890940), and China Ocean Mineral Resources R &#38; D Association Project (No. DY135-S2-2-07).

1. Preparing the sample, reagents, and containers
<ol>
	<li>Clean the fume hood, hotplate and the balance room bench for the chemical experiment with sprayed alcohol or ultrapure water.</li>
	<li>Prepare sub-boiled acids (2 M HCl, 8 M HCl, 7 M HNO3, and 14 M HNO3), clean beakers and any apparatus before sample processed. 
	NOTE: Sulfide samples presented in this study were collected from newly discovered hydrothermal zones in the South Atlantic. Approximately 60 mg of powdered sample was used...

<ol>
	<li>Lalou, C., Brichet, E., Hekinian, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Age+dating+of+sulfide+deposits+from+axial+and+off-axial+structures+on+the+East+Pacific+Rise+near+12&#176;500N.">Age dating of sulfide deposits from axial and off-axial structures on the East Pacific Rise near 12&#176;500N.</a> Earth and Planetary Science Letters. 75 (1), 59-71 (1985).</li><li>Lalou, C., Brichet, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=On+the+isotopic+chronology+of+submarine+hydrothermal+deposits.">On the isotopic chronology of submarine hydrothermal deposits.</a> Chemical Geology. 65 (3-4), 197-207 (1987).</li><li>Lalou, C., Reyss, J. L., Brichet, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Actinide-series+disequilibrium+as+a+tool+to+establish+the+chronology+of+deep-sea+hydrothermal+activity.">Actinide-series disequilibrium as a tool to establish the chronology of deep-sea hydrothermal activity.</a> Geochimica et Cosmochimica Acta. 57 (6), 1221-1231 (1993).</li><li>Lalou, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=New+age+data+for+Mid-Atlantic+Ridge+hydrothermal+sites:+TAG+and+Snakepit+chronology+revisited.">New age data for Mid-Atlantic Ridge hydrothermal sites: TAG and Snakepit chronology revisited.</a> Journal of Geophysical Research. 98, 9705-9713 (1993).</li><li>Lalou, C., Reyss, J. L., Brichet, E., Rona, P. A., Thompson, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hydrothermal+activity+on+a+105-year+scale+at+a+slow-spreading+ridge,+TAG+hydrothermal+field,+Mid-Atlantic+Ridge+26&#176;+N.">Hydrothermal activity on a 105-year scale at a slow-spreading ridge, TAG hydrothermal field, Mid-Atlantic Ridge 26&#176; N.</a> Journal of Geophysical Research. 100 (B9), 17855-17862 (1995).</li><li>Kadko, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Radio+isotopic+studies+of+submarine+hydrothermal+vents.">Radio isotopic studies of submarine hydrothermal vents.</a> Reviews of Geophysics. 34 (3), 349-366 (1996).</li><li>Lalou, C., Mu &#776;nch, U., Halbach, P., Reyss, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Radiochronological+investigation+of+hydrothermal+deposits+from+the+MESO+zone,+Central+Indian+Ridge.">Radiochronological investigation of hydrothermal deposits from the MESO zone, Central Indian Ridge.</a> Marine Geology. 149 (149), 243-254 (1998).</li><li>Yejian, W., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hydrothermal+Activity+Events+at+Kairei+Field,+Central+Indian+Ridge+25&#176;S.">Hydrothermal Activity Events at Kairei Field, Central Indian Ridge 25&#176;S.</a> Resource Geology. 62 (2), 208-214 (2012).</li><li>Yejian, W., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mineralogy+and+geochemistry+of+hydrothermal+precipitates+from+Kairei+hydrothermal+field,+Central+Indian+Ridge.">Mineralogy and geochemistry of hydrothermal precipitates from Kairei hydrothermal field, Central Indian Ridge.</a> Marine Geology. 354 (3), 69-80 (2014).</li><li>Jun-ichiro, I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dating+of+Hydrothermal+Mineralization+in+Active+Hydrothermal+Fields+in+the+Southern+Mariana+Trough.">Dating of Hydrothermal Mineralization in Active Hydrothermal Fields in the Southern Mariana Trough.</a> Subseafloor Biosphere Linked to Hydrothermal Systems. , 289-300 (2015).</li><li>Takamasa, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=U-Th+radioactive+disequilibrium+and+ESR+dating+of+a+barite-containing+sulfide+crust+from+South+Mariana+Trough.">U-Th radioactive disequilibrium and ESR dating of a barite-containing sulfide crust from South Mariana Trough.</a> Quaternary Geochronology. 15 (1), 38-46 (2013).</li><li>Weifang, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=230Th/238U+dating+of+hydrothermal+sulfides+from+Duanqiao+hydrothermal+field,+Southwest+Indian+Ridge.">230Th/238U dating of hydrothermal sulfides from Duanqiao hydrothermal field, Southwest Indian Ridge.</a> Marine Geophysical Research. 38 (1-2), 71-83 (2017).</li><li>Lisheng, W., Zhibang, M., Hai, C., Wuhui, D., Jule, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Determination+of+230Th+age+of+Uranium-series+standard+samples+by+multiple+collector+inductively+coupled+plasma+mass+spectromerty.">Determination of 230Th age of Uranium-series standard samples by multiple collector inductively coupled plasma mass spectromerty.</a> Journal of China Mass Spectrometry Society. 37 (3), 262-272 (2016).</li><li>Wang, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=U+concentration+and+234U/238U+of+seawater+from+the+Okinawa+Trough+and+Indian+Ocean+using+MC-ICPMS+with+SEM+protocols.">U concentration and 234U/238U of seawater from the Okinawa Trough and Indian Ocean using MC-ICPMS with SEM protocols.</a> Marine Chemistry. 196, 71-80 (2017).</li><li>Hai, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Improvements+in+230Th+dating,+230Th+and+234U+half-life+values,+and+U-Th+isotopic+measurements+by+multi-collector+inductively+coupled+plasma+mass+spectrometry.">Improvements in 230Th dating, 230Th and 234U half-life values, and U-Th isotopic measurements by multi-collector inductively coupled plasma mass spectrometry.</a> Earth and Planetary Science Letters. , 82-91 (2013).</li><li>Edwards, R. L., Chen, J. H., Ku, T. -. L., Wasserburg, G. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Precise+timing+of+the+last+interglacial+period+from+mass+spectrometric+analysis+of+230Th+in+corals.">Precise timing of the last interglacial period from mass spectrometric analysis of 230Th in corals.</a> Science. 236 (4808), 1537-1553 (1987).</li><li>Edwards, R. L., Taylor, F. W., Wasserburg, G. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dating+earthquakes+with+high+precision+thorium-230+ages+of+very+young+corals+[J].">Dating earthquakes with high precision thorium-230 ages of very young corals [J].</a> Earth and Planetary Science Letters. 90 (4), 371-381 (1988).</li><li>Hai, C., Jess, A., Edwards, R. L., Boyle, E. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=U-Th+dating+of+deep-sea+corals.">U-Th dating of deep-sea corals.</a> Geochimica et Cosmochimica Acta. 64 (14), 2401-2416 (2000).</li><li>Ishibashi, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dating+of+Hydrothermal+Mineralization+in+Active+Hydrothermal+Fields+in+the+Southern+Mariana+Trough.">Dating of Hydrothermal Mineralization in Active Hydrothermal Fields in the Southern Mariana Trough.</a> Subseafloor Biosphere Linked to Hydrothermal Systems. , 289-300 (2015).</li><li>Jaffey, A. H., Flynn, K. F., Glendenin, L. E., Bentley, W. C., Essling, A. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Precision+measurement+of+half-lives+and+specific+activities+of+235U+and+238U.">Precision measurement of half-lives and specific activities of 235U and 238U.</a> Physical Review C. 4, 1889-1906 (1971).</li><li>Richter, S., Goldberg, S. A., Mason, P. B., Traina, A. J., Schwieters, J. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Linearity+tests+for+secondary+electron+multipliers+used+in+isotope+ratio+mass+spectrometry.">Linearity tests for secondary electron multipliers used in isotope ratio mass spectrometry.</a> International Journal of Mass Spectrometry. 206 (1-2), 105-127 (2001).</li></ol>

Some critical steps must be followed to ensure success of this protocol. Ensure that all operations are carried out in clean chemistry room under fume hood with clean air circulation. Purify all regents in this process in advance and clean the apparatus before use. Dissolve the samples completely in the process of making the 7 M HNO3 solution which is then loaded onto the 7 M HNO3-conditioned resins. If there is any insoluble substance in the sample, it will be redissolved after drying. Additional i...

Submarine hydrothermal sulfides have been a steady source of metals like iron, copper, zinc and lead. They are also seen as economically viable resources of silver and gold. The location and size of the deposits are a record of the history of hydrothermal venting on the seafloor. Dating of a hydrothermal sulfide can provide important information regarding the formation and alteration mechanism of the sulfide ore deposit, seafloor hydrothermal activity history, and growth rate of large sulfide deposits1,2,3. 238U-234U-230Th disequilibrium dating is an effective isotopic method of age estimation for hydrothermal sulfides4,5,6,7,8,9,10,11,12, where the purification and separation of U and Th isotopes is necessary. This text describes a protocol for U and Th isotopes separation and 230Th-U dating of sulfides sample by MC-ICPMS.
Geological materials which contain U and Th remain undisturbed for several million years, and a state of secular equilibrium between all the nuclides in the radioactive series is established. However, a combination of chemical solubility and nuclear recoil factors often create disequilibrium, in which the members of the decay series are separated from each other through processes such as deposition, transport and weathering. For example, when a sulfide deposit is formed, the state of 238U, 234U and 230Th is of disequilibrium, and the long-lived 238U can decay gradually towards short-lived 234U and 230Th subsequently. Assuming (i) the system remains closed with respect to U and Th isotopes, and (ii) initial amount of 230Th and 232Th incorporated into sulfide samples is zero, it is possible to determine the time of deposition by measuring the present-day activity ratios of 230Th/238U and 234U/238U. However, the initial amount of Th is not zero in the sample, and we assume the initial 230Th/232Th atomic ratio is 4.4 &#177; 2.2 x 10-6. The applicable dating range of this method is approximately ~10-6 x 105 years13,14. However, the large difference between the abundance of uranium and thorium makes measurement challenging. Hence, it is very important to establish a chemical procedure for U-Th dating by MC-ICPMS.
In the past 30 years, most studies focused more measurements of carbonate materials14,15,16,17 and less on sulfide deposits11,12,18,19. Alpha-particle counting methods have traditionally been used for the study of 230Th/238U disequilibrium of submarine hydrothermal sulfides1. However, analytical uncertainty of 5-17% is a limiting factor that affects the precision of age determination of sulfides1,8,9. These techniques generally suffer from the use of relatively large columns and reagent volumes and the need for multiple column passes for purification and separation U-Th from a sample. Recent developments in MC-ICPMS have greatly improved the precision of U-Th isotopic measurements (&#60;5&#8240; for ages)14 and have significantly reduced the sample size (&#60;0.2 g) required for analysis. In these works, many chemical separation procedures have been developed, and have achieved excellent chemical yields with low chemical background12,13.
Here we present a chemical-based protocol to obtain samples that are sufficiently clean for MC-ICPMS analysis. It is suitable for the dating of hydrothermal sulfide samples of age &#60;6 x 105 years14. With this technique, the separated U and Th isotopic fractions can meet measuring requirements by MC-ICPMS. The age of the hydrothermal sulfide sample can be calculated from the extent of disequilibria between 230Th and 234U and between 234U and 238U by using the described activity decay equation.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>AG 1-X8 anion-exchange resin</td>
			<td>BIO-RAD</td>
			<td>140-1441</td>
			<td>Separating rare elements</td>
		</tr>
		<tr>
			<td>Ammonia solution</td>
			<td>Kanto Chemical CO., INC.</td>
			<td>1336-21-6</td>
			<td>Reagent</td>
		</tr>
		<tr>
			<td>Glass vials</td>
			<td>BOTEX</td>
			<td>None</td>
			<td>Sample collection</td>
		</tr>
		<tr>
			<td>Hydrochloric acid</td>
			<td>Sinopharem chemical reagent Co. Ltd</td>
			<td>7647-01-0</td>
			<td>Reagent</td>
		</tr>
		<tr>
			<td>Hydrofluoric acid</td>
			<td>EMD Millipore CO.</td>
			<td>7664-39-5</td>
			<td>Reagent</td>
		</tr>
		<tr>
			<td>Neptune Plus</td>
			<td>Thermo Fisher Scientific CO.</td>
			<td>None</td>
			<td>Apparatus</td>
		</tr>
		<tr>
			<td>Nitric acid</td>
			<td>Sinopharem chemical reagent Co. Ltd</td>
			<td>7697-37-2</td>
			<td>Reagent</td>
		</tr>
		<tr>
			<td>Perchloric acid</td>
			<td>Kanto Chemical CO., INC.</td>
			<td>32059-1B</td>
			<td>Reagent</td>
		</tr>
		<tr>
			<td>Ultrapure water</td>
			<td>Merck Millipore</td>
			<td>None</td>
			<td>Producted by Mill-Q Advantage systerm</td>
		</tr>
		<tr>
			<td>Wipe paper</td>
			<td>Kimberley-Clark</td>
			<td>0123-12</td>
			<td>Wipe and clean</td>
		</tr>
		<tr>
			<td>2 ml vial</td>
			<td>Nelgene</td>
			<td>5000-0020</td>
			<td>Sample collection</td>
		</tr>
		<tr>
			<td>229Th-233U-236U spike</td>
			<td>None</td>
			<td>None</td>
			<td>Reagent</td>
		</tr>
		<tr>
			<td>7 ml PFA beaker</td>
			<td>Savillex</td>
			<td>200-007-20</td>
			<td>Sample treatment</td>
		</tr>
		<tr>
			<td>10 ml centrifuge</td>
			<td>Nelgene</td>
			<td>3110-1000</td>
			<td>Sample treatment</td>
		</tr>
		<tr>
			<td>30 ml PFA beaker</td>
			<td>Savillex</td>
			<td>200-007-20</td>
			<td>Sample treatment</td>
		</tr>
	</tbody>
</table>

separation of uranium and thorium for 230th-u dating of submarine hydrothermal sulfides

The age of a submarine hydrothermal sulfide is a significant index for estimating the size of hydrothermal ore deposits. Uranium and thorium isotopes in the samples can be separated for 230Th-U dating. This article presents a method to purify and separate U and Th isotopes in submarine hydrothermal sulfide samples. Following this technique, the separated U and Th fractions can meet measuring requirements by multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS). The age of the hydrothermal sulfide sample can be calculated by measuring the present-day activity ratios of 230Th/238U and 234U/238U. A super clean room is necessary for this experiment. Cleaned regents and supplies are used to reduce the contamination during the sample processes. Balance, hotplate, and centrifuge are also used. The sulfide sample is powdered for analysis and less than 0.2 g sample is used. Briefly, the sample is weighed, dissolved, added to 229Th-233U-236U double spike solution, Fe co-precipitated, and separated on an anion-exchange resin extraction column. Approximately 50 ng U is consumed for 230Th-U dating of sulfides sample by MC-ICPMS.

Using this procure, a submarine hydrothermal sulfide sample can be completely dissolved. Following this protocol, the Th fraction was eluted from the hydrothermal sulfide sample using 8 M HCl. Meanwhile, the U fraction of the hydrothermal sulfide sample was eluted with 0.1 M HNO3. U and Th fractions were dissolved in the 2% HNO3 (+0.1% HF) solution (see Figure 2) and stored in 2 mL capacity vials. The mixture was then analyzed by MC-ICPMS.
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Watch this Scientific Journal Video about Separation of Uranium and Thorium for 230Th-U Dating of Submarine Hydrothermal Sulfides at JoVE.com

Separation of Uranium and Thorium for 230Th-U Dating of Submarine Hydrothermal Sulfides

The protocol describes a method to purify and separate the U and Th nuclide in submarine hydrothermal sulfide sample with Fe co-precipitation and extraction chromatography for 230Th-U disequilibrium dating.

Separation of Uranium and Thorium for 230Th-U Dating of Submarine Hydrothermal Sulfides

The age of a submarine hydrothermal sulfide is a significant index for estimating the size of hydrothermal ore deposits. Uranium and thorium isotopes in ...

This article presents a method to purify and separate uranium and thorium isotopes in submarine hydrothermal sulfide samples. With this technique, uranium and thorium isotopic can be measured by MC-ICPMS, as suitable for dating samples with age less than 600, 000 years and provide important information of sulfide ore deposits, seafloor hydrothermal activity history and growth rates of large sulfide deposits. With this technique, less than 0.2 gram powdered sulfide sample is used and only 50 nanogram uranium is consumed for uranium series dating by MC-ICPMS.Some critical steps must be followed to ensure success of this protocol. Purify all chemical reagents and clean the apparatus. Be sure all operations are carried out under the fume hood and clean air circulation.Avoid the cross-contamination from the adjacent samples during the sample processing and reaching the condition of uranium and the thorium in accordance with your technique. The major imitation of this technique is related to the uranium 238 and the thorium 232. Concentration of the sample, it is best to choose samples where the uranium is more than and the thorium is less than 10 ppb.First, use sprayed alcohol, or ultra pure water, to clean the fume hood, hot plate and the balance room bench for the chemical experiment. In the fume hood, prepare the sub-boiled hydrochloric acid and nitric acid and sulfide samples in vials. Label 30 milliliter PFA bottles twice, to prevent erasure and weigh the blank bottles on a balance accurate to plus or minus 0.0001 grams.Pour the samples into the PFA bottles, cover with a lid and weigh the bottles. Add approximately one liter of ultra-pure water into the bottle, rotate the bottle to rinse the inner wall and shake the bottle carefully to have water cover all the samples. Place the sample containing bottles in the fume hood, open the lid and use a pipette to add three milliliters of 14 molar nitric acid, or aqua regia, into each bottle containing the samples.Place the PFA bottles on the hot plate and set the hot plate temperature to 170 degrees Celsius to dissolve the samples completely. Leave the solution to cool for at least 30 minutes. Then add 100 to 300 milliliters of thorium-229, uranium-233 and uranium-236 spike solution of known activity into each sample solution.Place the bottles on the hot plate at 170 degrees Celsius for five hours to dry. Dissolve each sample in two drops of 14 molar nitric acid and dry them on the hot plate at 170 degrees Celsius again. Prepare clean, 15 milliliter centrifuge tubes, label and place them in a tube stand, add approximately 0.1 milliliters of two molar hydrochloric acid into each bottle containing the dried samples and shake gently to completely dissolve the samples.Transfer each sample into a centrifuge tube. Add several drops of ammonia solution into each tube until the acid is neutralized, showing a reddish-brown uranium and thorium isotope precipitate, biferric oxyhydroxide. Seal the centrifuge tubes, level them and centrifuge at 2340 times g for seven minutes.Discard the supernatant. Add ultra-pure water to the tubes and shake to resuspend. Centrifuge again to wash and repeat the wash two more times.Next, dissolve the precipitate with 1.5 milliliters of seven molar nitric acid. Transfer the solution into the corresponding bottle, add one drop of perchloric acid to remove organic matters and dry each sample on the hot plate at 170 degrees Celsius for about 30 minutes. To prepare an anion exchange column, insert frit into each PTFE column slowly at the bottom, with the help of a PTFE pipe.Put the columns on the holder, pipette cleaned anion exchange resins into the columns. Fill the whole column with ultra-pure water and add one drop of 14 molar nitric acid. Then add two column volumes of seven molar nitric acid twice to remove the trace elements.Dissolve each sample in 0.5 milliliters of 7 molar nitric acid. Load it onto the column carefully, let it drip across the column, into the waste beaker. Next, add two column volumes and one column volume of seven molar nitric acid successively into each column.Iron and other metal elements in the samples are removed, while uranium and thorium are retained by the resin. After that, add two column volumes and one column volume of eight molar hydrochloric acid successively into each column, to elute thorium fraction. Collect the thorium fraction, using a seven milliliter PFA bottle for each column.Add one drop of perchloric acid into the bottle and dry the fraction on a hot plate at 170 degrees Celsius for about 30 minutes. Next, elute uranium fraction from the resin with two column volumes of 0.1 molar nitric acid twice. Collect the eluate in new PFA bottles then add one drop of perchloric acid and dry it on the hot plate at 170 degrees Celsius for about 30 minutes.Now prepare and label two milliliter capacity vials. Dissolve each sample in one drop of 14 molar nitric acid and dry it on the hot plate at 170 degrees Celsius for less than five minutes, until half a drop is left. Transfer them, along with 0.2 milliliters of 2%nitric acid and 0.1%hydrofluoric acid, into the corresponding vials for instrument measurement.Using this procedure, submarine hydrothermal sulfide samples can be completely dissolved for uranium and thorium analysis. In this example, uranium content ranged from 178 to 5, 118.2 nanograms per gram and thorium content ranged from 603 to 7, 212 picograms per gram. Five samples had ages ranging from 567 to 21, 936 years before the year 2000 AD.Sample consumption was about 60 milligrams, except S32 wherein only 17 milligrams of sample was consumed.In these steps, the concentration was acid reagents but we determined actually, to ensure success. Following this procedure, uranium and thorium isotopes reduce out and they still find it also determined the It can provide real chemical information for sulfide deposits. Our reagents are harmful to human body.Please strictly comply with the relevant specifications to ensure personal safety.

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