Methods for preparing catalyst precursor materials

Patent metadata

Field	Value
Publication number	US-12479864-B2
Application number	US-202017600359-A
Country	US
Kind code	B2
Filing date	Mar 27, 2020
Priority date	Mar 31, 2019
Publication date	Nov 25, 2025
Grant date	Nov 25, 2025

Abstract

Methods for preparing a catalyst precursor material from dihalo-substituted metalloids are provided. The methods In include mixing a first solution of a halogenated alkane, at least one solvent, and a first component selected from a dihalo-substituted-group-14 metalloid or an organolithium reagent in a first reaction zone. Continuously adding the first solution to a second reaction zone, and continuously adding a second solution to the second reaction zone. The second solution including at least one solvent and a second component of either the dihalo-substituted-group-14 metalloid or the organolithium reagent, the second component is different from the first component. Mixing the first solution and the second solution in the second reaction zone.

First claim

The invention claimed is:

1 . A method, comprising:
reacting a halogenated alkane and a first component selected from one of a dihalo-substituted-group-14 metalloid or an organolithium reagent in a first reaction zone in the presence of at least one solvent to form a first solution; continuously adding the first solution to a second reaction zone; continuously adding a second solution to the second reaction zone, thereby reacting the organolithium reagent, the halogenated alkane, and the dihalo-substituted-group-14 metalloid, wherein the second solution comprises at least one solvent and a second component selected from one of the dihalo-substituted-group-14 metalloid or the organolithium reagent, wherein the second component is different from the first component; and mixing the first solution and the second solution in the second reaction zone, thereby further reacting the organolithium reagent, the halogenated alkane, and the dihalo-substituted-group-14 metalloid, wherein the dihalo-substituted-group-14 metalloid comprises dichlorodiisopropylsilane, di-tert-butyldichlorosilane, dichlorodiphenylsilane, dichlorodiisopropylgermane, di-tert-butyldichlorogermane, dichlorodiphenylgermane, or combinations thereof.

2 . The method of claim 1 , wherein the first component is the dihalo-substituted-group-14 metalloid and the second component is the organolithium reagent.

3 . The method of claim 1 , wherein the first component is the organolithium reagent and the second component is the dihalo-substituted-group-14 metalloid.

4 . The method of claim 1 , wherein the organolithium reagent comprises n-butyllithium, s-butyllithium, t-butyllithium, methyllithium, or combinations thereof.

5 . The method of claim 1 , wherein the halogenated alkane comprises a di-halogenated methane.

6 . The method of claim 1 , wherein the first reaction zone, the second reaction zone, or both have a temperature from 0° C. to −90° C.

7 . A method, comprising:
reacting an organolithium reagent and a halogenated alkane in a first reaction zone in the presence of at least one solvent to form a first solution; continuously adding the first solution and a second solution to a second reaction zone, thereby reacting the organolithium reagent, the halogenated alkane, and a dihalo-substituted-group-14 metalloid, wherein the second solution comprises the dihalo-substituted-group-14 metalloid and at least one solvent; and mixing the first solution and the second solution in the second reaction zone, thereby further reacting the organolithium reagent, the halogenated alkane, and the dihalo-substituted-group-14 metalloid, wherein the dihalo-substituted-group-14 metalloid comprises dichlorodiisopropylsilane, di-tert-butyldichlorosilane, dichlorodiphenylsilane, dichlorodiisopropylgermane, di-tert-butyldichlorogermane, dichlorodiphenylgermane, or combinations thereof.

8 . The method of claim 7 , further comprising separately cooling the organolithium reagent and the halogenated alkane to a temperature from 0° C. to −90° C. before continuously adding the first solution organolithium reagent and the halogenated alkane to the first reaction zone.

9 . The method of claim 7 , wherein the organolithium reagent comprises n-butyllithium, s-butyllithium, t-butyllithium, methyllithium, or combinations thereof.

10 . The method of claim 7 , wherein the halogenated alkane comprises a di-halogenated methane.

11 . The method of claim 7 , wherein the at least one solvent comprises an ethereal solvent, an alkyl solvent, an aromatic solvent, or combinations thereof.

12 . The method of claim 7 , wherein the first solution is cooled to a temperature from 0° C. to −90° C. before the first solution is continuously added to the second reaction zone.

13 . The method of claim 7 , wherein at least one of the first reaction zone and the second reaction zone have a temperature from −40° C. to −70° C.

14 . A method of forming a catalyst precursor material, comprising:
reacting a halogenated alkane and a dihalo-substituted-group-14 metalloid in a first reaction zone in the presence of at least one solvent to form a first solution; adding the first solution and a second solution as continuous streams to a second reaction zone, thereby reacting the halogenated alkane, the dihalo-substituted-group-14 metalloid, and a organolithium reagent and forming a catalyst precursor material, wherein the second solution comprises at least one solvent and the organolithium reagent; mixing the first solution and the second solution in the second reaction zone contemporaneously with continued addition of the first solution and the second solution as continuous streams, thereby further reacting the halogenated alkane, the dihalo-substituted-group-14 metalloid, and the organolithium reagent and forming additional catalyst precursor material; and producing at least a portion of the catalyst precursor material from the second reaction zone contemporaneously with the continued addition of the first solution and second solution to the second reaction zone, wherein:
the first solution and the second solution are added as continuous streams to the second reaction zone for a period of greater than 20 hours, and
the first reaction zone and the second reaction zone have a temperature from 0° C. to −90° C.

15 . The method of claim 14 , wherein:
the dihalo-substituted-group-14 metalloid comprises dichlorodiisopropylsilane, di-tert-butyldichlorosilane, dichlorodiphenylsilane, dichlorodiisopropylgermane, di-tert-butyldichlorogermane, dichlorodiphenylgermane, or combinations thereof; the organolithium reagent comprises n-butyllithium, s-butyllithium, t-butyllithium, methyllithium, or combinations thereof; or combinations thereof.

16 . The method of claim 14 , wherein at least one of the first reaction zone and the second reaction zone have a temperature of from −40° C. to −70° C.

17 . A method of forming a catalyst precursor material, comprising:
reacting an organolithium reagent and a halogenated alkane in a first reaction zone in the presence of at least one solvent to form a first solution; adding the first solution and a second solution as continuous streams to a second reaction zone, thereby reacting the organolithium reagent, the halogenated alkane, and a dihalo-substituted-group-14 metalloid and forming a catalyst precursor material, wherein the second solution comprises the dihalo-substituted-group-14 metalloid and at least one solvent; mixing the first solution and the second solution in the second reaction zone contemporaneously with continued addition of the first solution and the second solution as continuous streams, thereby further reacting the organolithium reagent, the halogenated alkane, and the dihalo-substituted-group-14 metalloid and forming additional catalyst precursor material; and producing at least a portion of the catalyst precursor material from the second reaction zone contemporaneously with the continued addition of the first solution and second solution to the second reaction zone, wherein:
the first solution and the second solution are added as continuous streams to the second reaction zone for a period of greater than 6 hours, and
the first reaction zone and the second reaction zone have a temperature from 0° C. to −90° C.

18 . The method of claim 17 , wherein:
the dihalo-substituted-group-14 metalloid comprises dichlorodiisopropylsilane, di-tert-butyldichlorosilane, dichlorodiphenylsilane, dichlorodiisopropylgermane, di-tert-butyldichlorogermane, dichlorodiphenylgermane, or combinat

Assignees

• Dow Global Technologies Llc

Inventors

• Devaraj Jayachandran
• Zhang Chunming
• Feist Shawn D
• Pan Heqi
• Blaylock Donnie W
• Gillespie Ian B
• Heider Patrick L
• Davis Clark S
• Yvon-Bessette Andre

Classifications

• C08F10/02

  Ethene · CPC title

• C07F7/30

  Germanium compounds · CPC title

• C07F7/12

  Organo silicon halides · CPC title

• C07F7/081 Primary

  comprising at least one atom selected from the elements N, O, halogen, S, Se or Te · CPC title

• C07F1/02 Primary

  Lithium compounds · CPC title