IP Library Granted Patent US 12,297,121
Granted Patent B2
US 12,297,121 · App. 16/652,609 · Granted May 13, 2025

Stannous oxide powder and method for producing same

Inventors: Koichi Takemoto (Ibaraki, JP); Toru Imori (Ibaraki, JP)
Assignee: JX Advanced Metals Corporation
C01G19/02B01J14/00B01J19/0006B01J19/0013B01J19/0086C01P2004/03C01P2004/61C01P2006/11C01P2006/12C01P2006/82C25D17/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,297,121
App. No.
16/652,609
Granted
May 13, 2025
Kind
B2
Abstract

Provided is a method for producing stannous oxide, comprising a step of subjecting stannous sulfate to neutralization in an aqueous solution using ammonium carbonate or ammonium bicarbonate, and thereby precipitating stannous oxide. This production method is a novel means for producing stannous oxide in which chlorine, sulfur, sodium, and potassium are sufficiently reduced, and which has excellent solubility.

Claims (23)

1. A stannous oxide consisting of a stannous oxide content of 99.99% by mass or more, a chlorine content of 1 ppm or less, and optionally sulfur, sodium, potassium, and antimony.

2. The stannous oxide according to claim 1 , wherein the chlorine content is 1 ppm or less and the sulfur content is less than 10 ppm.

3. A stannous oxide powder comprising the stannous oxide according to claim 2 .

4. The stannous oxide according to claim 1 , wherein the stannous oxide has a sodium content of less than 5 ppm and a potassium content of less than 5 ppm.

5. A stannous oxide powder comprising the stannous oxide according to claim 4 .

6. The stannous oxide according to claim 1 , wherein the stannous oxide has an antimony content of 5 ppm or less.

7. A stannous oxide powder comprising the stannous oxide according to claim 6 .

8. A stannous oxide powder comprising the stannous oxide according to claim 1 .

9. The stannous oxide according to claim 8 , wherein the powder has a water content in a range of from 1 to 10% by weight.

10. The stannous oxide according to claim 8 , wherein the powder has a specific surface area in a range of from 0.1 to 1.0 m 2 /g.

11. The stannous oxide according to claim 8 , wherein the powder has a TAP density in a range of from 1.0 to 4.0 g/cm 3 .

12. The stannous oxide according to claim 8 , wherein the powder has a 50% particle diameter (D50) in a range of from 20 to 60 μm.

13. A method for producing stannous oxide according to claim 1 , the method comprising a step of subjecting stannous sulfate to a neutralization reaction with ammonium carbonate or ammonium bicarbonate in an aqueous solution to deposit stannous oxide,

wherein the neutralization reaction is carried out in an aqueous solution having a pH in a range of from pH 6.0 to pH 8.0,

wherein the step of subjecting stannous sulfate to the neutralization reaction to deposit stannous oxide comprises:

subjecting stannous sulfate to the neutralization reaction at a temperature in a range of from 50 to 80° C.; and

then maintaining the aqueous solution subjected to the neutralization reaction at a temperature in a range of from 60 to 100° C. to deposit stannous oxide.

14. The method according to claim 1 , wherein the step of subjecting stannous sulfate to the neutralization reaction to deposit stannous oxide comprises:

subjecting stannous sulfate to the neutralization reaction at a temperature in a range of from 50 to 80° C. for 1 to 10 hours; and

then maintaining the aqueous solution subjected to the neutralization reaction at a temperature in a range of from 60 to 100° C. for 1 to 10 hours to deposit stannous oxide.

15. The method according to claim 13 , wherein the neutralization reaction is carried out by adding an aqueous stannous sulfate solution to an aqueous ammonium bicarbonate solution.

16. The method according to claim 15 , wherein a concentration of ammonium bicarbonate in the aqueous ammonium bicarbonate solution is in a range of from 50 to 150 g/L.

17. The method according to claim 15 , wherein a concentration of tin in the aqueous stannous sulfate solution is in a range of from 10 to 130 g/L.

Assignments (3)
CHANGE OF NAME Recorded Jul 30, 2024
From: JX METALS CORPORATION
To: JX ADVANCED METALS CORPORATION
Reel/Frame 068192/0507 →
CHANGE OF NAME Recorded Sep 21, 2023
From: JX NIPPON MINING & METALS CORPORATION
To: JX METALS CORPORATION
Reel/Frame 065016/0620 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2020
From: TAKEMOTO, KOICHI; IMORI, TORU
To: JX NIPPON MINING & METALS CORPORATION
Reel/Frame 052497/0994 →
Priority Claims (1)
JP 2017-220474 · Nov 15, 2017 · national
Continuity (1)
Related Publication 20200231461A1 · Jul 23, 2020
References Cited (68)
US 5246623A · Giersberg · 1993 [cited by examiner]
US 9067800B2 · Katase et al. · 2015 [cited by applicant]
US 11772981B2 · Takemoto · 2023 [cited by examiner]
US 11981581B2 · Takemoto · 2024 [cited by examiner]
US 20080032132A1 · Woodfield · 2008 [cited by examiner]
US 20120195822A1 · Werner · 2012 [cited by examiner]
US 20130084414A1 · Grandbois · 2013 [cited by examiner]
US 20130289133A1 · Doshita et al. · 2013 [cited by applicant]
US 20140079618A1 · Katase et al. · 2014 [cited by applicant]
US 20140127109A1 · Katase et al. · 2014 [cited by applicant]
US 20170009078A1 · Katase · 2017 [cited by examiner]
US 20180327274A1 · Hirano · 2018 [cited by examiner]
US 20200231461A1 · Takemoto et al. · 2020 [cited by applicant]
US 20210047198A1 · Takemoto · 2021 [cited by examiner]
US 20210331934A1 · Takemoto · 2021 [cited by examiner]
CN 101367543A · 2009 [cited by applicant]
CN 103043711A · 2013 [cited by applicant]
CN 105813980A · 2016 [cited by applicant]
CN 106587139A · 2017 [cited by applicant]
CN 105813980B · 2017 [cited by applicant]
CN 107001065A · 2017 [cited by applicant]
CN 110997570A · 2020 [cited by applicant]
CN 111836781A · 2020 [cited by applicant]
EP 3070055A1 · 2016 [cited by applicant]
EP 3260420A1 · 2017 [cited by applicant]
EP 3712114A1 · 2020 [cited by applicant]
EP 3763677A1 · 2021 [cited by applicant]
JP 60221319A · 1985 [cited by applicant]
JP S6252130A · 1987 [cited by applicant]
JP 11310415A · 1999 [cited by applicant]
JP H11310415A · 1999 [cited by applicant]
JP 2007302496A · 2007 [cited by applicant]
JP 2009132570A · 2009 [cited by applicant]
JP 2009132571A · 2009 [cited by applicant]
JP 201251762A · 2012 [cited by applicant]
JP 4975367B2 · 2012 [cited by examiner]
JP 2012236724A · 2012 [cited by applicant]
JP 201379186A · 2013 [cited by applicant]
JP 2016153361A · 2016 [cited by applicant]
JP 2016172885A · 2016 [cited by applicant]
JP 6095929B2 · 2017 [cited by applicant]
TW 1511928B · 2012 [cited by applicant]
TW 201704154A · 2017 [cited by applicant]
WO 2012096172A1 · 2012 [cited by applicant]
WO 2015133426A1 · 2015 [cited by applicant]
WO 2019171692A1 · 2019 [cited by applicant]
Machine Translation JP 4975367 (Year: 2012). [cited by examiner]
Translation CN-105668616 A (Year: 2016). [cited by examiner]
Decision of Refusal from Korean Patent Office for corresponding KR Patent Application No. 10-2020-7002015 dated Nov. 16, 2021, 8 pages (including English translation). [cited by applicant]
Korean Office Action with Translation for KR 10-2020-7002015 related to PCT/JP2018/034052 dated May 11, 2021, 10 pages. [cited by applicant]
Extended European Search Report for corresponding EP 18877744.5 dated Dec. 11, 2020, 7 pages. [cited by applicant]
Extended European Search Report for related EP 19768694.2 corresponding to PCT/JP2019/015848, dated Mar. 18, 2022, 7 pages. [cited by applicant]
Chinese Office Action for the corresponding Chinese Patent Application No. 201880049513.8 dated Nov. 22, 2021 with translation, 16 pages. [cited by applicant]
Chinese Office Action for related Chinese Patent Application No. 201980001813.3 dated Dec. 6, 2021. [cited by applicant]
International Search Report for related PCT/JP2018/045006 dated Aug. 1, 2019, 4 pages. [cited by applicant]
Extended European Search Report for related EP Application No. 18909201.8 dated May 31, 2021, 6 pages. [cited by applicant]
Chinese Office Action for Chinese Patent Application No. 201880090566.4 for related U.S. Appl. No. 16/978,439, dated Apr. 18, 2022, 14 pages (with translation). [cited by applicant]
Chinese Office Action related to the corresponding Chinese Patent Application No. 201880049513.8 dated Jun. 21, 2022, with translation, 11 pages. [cited by applicant]
Chinese Office Action for corresponding Chinese patent application No. 201980001813.3 dated Jul. 15, 2022, with translation, 15 pages. [cited by applicant]
U.S. Office Action for related U.S. Appl. No. 16/494,021 dated Jan. 4, 2023, 30 pages. [cited by applicant]
Chinese Office Action for corresponding Chinese Patent Application No. 201880090566.4, dated Dec. 2, 2022, 8 pages (including translation). [cited by applicant]
Chinese Office Action for corresponding Chinese Patent Application No. 201880049513.8, dated Dec. 13, 2022, 11 pages (including translation). [cited by applicant]
JP Office Action with English Translation for corresponding JP Patent Application No. 2020-504792 dated Oct. 5, 2022, 4 pages. [cited by applicant]
Chinese Office Action for related Chinese Patent Application No. 201980001813.3 dated Aug. 11, 2023 with Translation, 7 pages. [cited by applicant]
U.S. Office Action issued in corresponding case U.S. Appl. No. 16/978,439 dated Sep. 6, 2023, 65 pages. [cited by applicant]
Chinese Office Action for corresponding Chinese Patent Application No. 201880049513.8 dated May 26, 2023 with Translation, 10 pages. [cited by applicant]
Chinese Office Action for the corresponding Chinese Patent Application No. 201980001813.3 dated Mar. 31, 2023 with Translation, 11 pages. [cited by applicant]
Chinese Office Action for corresponding Chinese Patent Application No. 201880090566.4 with translation, dated Apr. 1, 2023, 8 pages. [cited by applicant]