Analytical method for precipitated particles during co-precipitation reaction

Patent metadata

Field	Value
Publication number	US-10782272-B2
Application number	US-201816035725-A
Country	US
Kind code	B2
Filing date	Jul 16, 2018
Priority date	Jul 15, 2017
Publication date	Sep 22, 2020
Grant date	Sep 22, 2020

Abstract

An analytical method for precipitated particles using a co-precipitation reaction in includes feeding streams and a tracking metal into a reaction vessel; collecting a precipitated product containing the tracking metal from the reaction vessel in increments of time to obtain product samples; filtering each collected product sample to separate precipitated particles from filtrate; and performing elemental analysis for the tracking metal in the precipitated particles of each collected product sample and measuring a concentration of the tracking metal in the precipitated particles, to obtain a residence time distribution of the precipitated particles in the reaction vessel according to the concentration of the tracking metal in the precipitated particles. Therefore the preferred residence time of the precipitated particles in the reaction vessel can be ascertained, so that it is clear when the precipitated particles should be collected from the reaction vessel.

First claim

What is claimed is:

1. An analytical method for precipitated particles using a co-precipitation reaction, comprising:
feeding two streams and a tracking metal into a reaction vessel; wherein the tracking metal is injected to the reaction vessel for a given time duration;
collecting a precipitated product containing the tracking metal from the reaction vessel in increments of time to obtain product samples;
filtering each collected product sample to separate precipitated particles from filtrate; and
performing elemental analysis for the tracking metal in the precipitated particles of each collected product sample and measuring a concentration of the tracking metal in the precipitated particles, to obtain a residence time distribution of the precipitated particles in the reaction vessel according to the concentration of the tracking metal in the precipitated particles.

2. The method of claim 1 , further comprising performing elemental analysis for the tracking metal in the filtrate of each collected product sample and measuring a concentration of the tracking metal in the filtrate, to obtain a residence time distribution of a fluid in the reaction vessel according to the concentration of the tracking metal in the filtrate.

3. The method of claim 2 , wherein the concentration of the tracking metal in the filtrate decays to a stable value faster than in the precipitated particles.

4. The method of claim 1 , wherein the method comprises feeding a stream (A) containing precipitation cation(s) and a stream (B) containing precipitation anion(s) into the reaction vessel, so that the stream (A) and the stream (B) are contacted to form the precipitated product.

5. The method of claim 4 , wherein the stream (A) is selected from first row transition metals and has a concentration from 0.001-6 (mol cation/L).

6. The method of claim 4 , wherein the stream (B) is selected from LiOH, NaOH, KOH, Na 2 CO 3 , NaHCO 3 , NH 3 *H 2 O, or any combination thereof and has a concentration from 0.001-14 (mol anion/L).

7. The method of claim 4 , wherein the tracking metal is dissolved in the stream (A) or in the stream (B) when adding to the reaction vessel.

8. The method of claim 4 , wherein the tracking metal is provided in a separate stream (C) when adding to the reaction vessel.

9. The method of claim 1 , wherein the tracking metal is tracking ion of Sn or Ba.

10. The method of claim 9 , wherein a feed concentration of the tracking ion is in a range between 0.001-1 (mol tracking ion/L).

11. The method of claim 10 , wherein the feed concentration of the tracking ion is in a range between 0.1-1 (mol tracking ion/L).

12. The method of claim 9 , wherein the tracking ion is selected from Ba(NO 3 ) 2 , BaO, Ba(OH) 2 *xH 2 O, BaS, BaCO 3 , BaSO 4 , BaCl 2 , BaBr 2 , BaF 2 , Ba(ClO 4 ) 2 , SnSO 4 , SnCl 2 , Sn(NO 3 ) 2 , SnBr 2 , SnF 2 , SnCO 3 , Sn(OH) 2 , or any combinations thereof.

13. The method of claim 1 , wherein at the start of a second 3 hr residence time from starting feeding, the tracking metal is added to the reaction vessel for 30 minutes, and at the end of the 30 minutes addition of the tracking metal to the reaction vessel, the precipitated product containing the tracking metal is collected and binned from the reaction vessel at intervals of 30 minutes.

Assignees

• Microvast Power Systems Co Ltd

Inventors

• Yonemoto Bryan
• Zhang Xiao
• Liu Mattis Wenjuan
• Zhang Zhifeng

Classifications

• C01G53/82 Primary

  Compounds containing nickel, with or without oxygen or hydrogen, and containing two or more other elements · CPC title

• G01N31/02

  using precipitation {(measuring deposition or liberation of materials from an electrolyte G01N27/42)} · CPC title

• C01P2002/89

  by mass-spectroscopy · CPC title

• B01J2208/00557

  controlling the residence time inside the reactor vessel · CPC title

• B01J8/006

  by filtration · CPC title