IP Library Granted Patent US 12,202,974
Granted Patent B2
US 12,202,974 · App. 17/053,969 · Granted Jan 21, 2025

Method for manufacturing a silicone elastomer article using a 3D printer

Inventors: Christophe Marquette (Villeurbanne, FR); Edwin-Joffrey Courtial (Villeurbanne, FR); Jean-Marc Frances (Meyzieu, FR)
Assignees: ELKEM SILICONES FRANCE; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; UNIVERSITÉ CLAUDE BERNARD LYON; INSTITUT NATIONAL DES SCIENCES APPLIQUÉES LYON 1
C08L83/04B29C64/106B29C64/357B33Y70/00B29K2083/00B33Y10/00C08L71/02C08L2312/00
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Quick Facts
Patent No.
US 12,202,974
App. No.
17/053,969
Granted
Jan 21, 2025
Kind
B2
Abstract

The present invention relates to a process for manufacturing a silicone elastomer article comprising the following step: 1) providing a composition C, comprising water and at least 20% by weight of at least one poloxamer, into a container; 2) placing the container comprising the composition C at the required temperature T1 to form a gel; 3) printing a crosslinkable silicone composition X into the gel obtained in 2) with a 3D printer at the required temperature T1; 4) optionally allowing the printed composition X to partially or totally crosslink, optionally by heating, to obtain a silicone elastomer article, into the container; 5) optionally placing the container obtained in step 4) at a temperature T3 lower than the sol-gel transition temperature of composition C; 6) recovering the silicone elastomer article; and 7) optionally washing the obtained silicone elastomer article for example with water at a temperature T3 lower than the sol-gel transition temperature of composition C.

Claims (34)

1. A method for manufacturing a silicone elastomer article comprising:

1) providing a composition C, comprising water and at least 20% by weight of at least one poloxamer, into a container;

2) placing the container comprising the composition C at a required temperature T1 to form a gel;

3) printing a crosslinkable silicone composition X into the gel obtained in 2) with a 3D printer at the required temperature T1;

4) allowing the printed composition X to partially or totally crosslink, by heating at a temperature between 30° C. and 90° C. to obtain a silicone elastomer article, in the container;

5) placing the container obtained in 4) at a temperature T3 lower than the sol-gel transition temperature of composition C;

6) after 5), recovering the silicone elastomer article; and

7) optionally washing the obtained silicone elastomer article for example with water at the temperature T3 lower than the sol-gel transition temperature of composition C;

wherein after 5), composition C is recovered in a reusable form and is recycled in 1).

2. The method according to claim 1 wherein the poloxamer is a copolymer composed of poly(propylene oxide) and poly(ethylene oxide) blocks.

3. The method according to claim 1 wherein the poloxamer is a triblock copolymer composed of a central poly(propylene oxide) block and two terminal poly(ethylene oxide) blocks.

4. The method according to claim 1 , wherein the poloxamer comprises from 25 to 90% by weight of poly(ethylene oxide) units based on the total weight of the poloxamer.

5. The method according to claim 1 , wherein the poloxamer is a triblock copolymer composed of a central poly(propylene oxide) block and two terminal poly(ethylene oxide) block for which the two poly(ethylene oxide) block comprise each 100+/−10 repeat units and the poly(propylene oxide) block comprises 55+/−10 repeat units.

6. The method according to claim 1 wherein composition C comprises from 20 to 40% by weight of at least one poloxamer.

7. The method according to claim 1 , wherein the composition C further comprises one or more compounds chosen from the group consisting of:

a base;

an acid; and

a functionalized silane.

8. The method according to claim 7 , wherein the base is NaOH, and wherein the acid is acetic acid.

9. The method according to claim 7 , wherein the functionalized silane is functionalized with a moiety selected from the group consisting of amino, epoxy, hydroxy, and polyether groups.

10. The method according to claim 1 wherein:

T1 is comprised between 25 and 50° C., and/or

T3 is lower than 15° C.

11. The method according to claim 10 wherein:

T1 is comprised between 25 and 35° C., and/or

T3 is comprised between 0 and 10° C.

12. The method according to claim 10 wherein:

T1 is comprised between 25 and 40° C., and/or

T3 is comprised between 0 and 15° C.

13. The method according to claim 1 , wherein 5) and 6) are reversed.

14. The method according to claim 1 , wherein composition C comprises from 21.5 to 22.5% by weight of poloxamer based on the total weight of composition C.

15. The method according to claim 1 , wherein the crosslinkable composition X has a viscosity comprised between 1000 mPa·s and 1000000 mPa·s.

16. The method for manufacturing a silicone elastomer article according to claim 1 , wherein the silicone elastomer article is manufactured using a 3D printer.

17. The method according to claim 1 , wherein the crosslinking is made by heating at a temperature between 40 and 70° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 16, 2021
From: MARQUETTE, CHRISTOPHE; COURTIAL, EDWIN-JOFFREY; FRANCES, JEAN-MARC
To: ELKEM SILICONES FRANCE SAS; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; UNIVERSITÉ CLAUDE BERNARD LYON; INSTITUT NATIONAL DES SCIENCES APPLIQUÉES LYON 1
Reel/Frame 055267/0849 →
Priority Claims (1)
EP 18305570 · May 9, 2018 · regional
Continuity (1)
Related Publication 20210238418A1 · Aug 5, 2021
References Cited (21)
US 6569955B1 · Brewer et al. · 2003 [cited by applicant]
US 6942830B2 · Muelhaupt et al. · 2005 [cited by applicant]
US 10150258B2 · Feinberg et al. · 2018 [cited by applicant]
US 10400071B2 · Achenbach et al. · 2019 [cited by applicant]
US 11135777B2 · Luo et al. · 2021 [cited by applicant]
US 20030090034A1 · Muelhaupt et al. · 2003 [cited by applicant]
US 20120116568A1 · Murphy · 2012 [cited by examiner]
US 20160068678A1 · Luo et al. · 2016 [cited by applicant]
US 20160074558A1 · Murphy et al. · 2016 [cited by applicant]
US 20160167312A1 · Feinberg · 2016 [cited by examiner]
US 20180057682A1 · Angelini et al. · 2018 [cited by applicant]
US 20180066115A1 · Achenbach et al. · 2018 [cited by applicant]
US 20190291350A1 · Feinberg et al. · 2019 [cited by applicant]
US 20200131364A1 · Luo et al. · 2020 [cited by applicant]
US 20200330644A1 · MacQueen · 2020 [cited by examiner]
CN 103249567 · 2013 [cited by applicant]
CN 107412853 · 2017 [cited by applicant]
Wikipedia contributors. (Feb. 7, 2023). Phosphate-buffered saline. In Wikipedia, The Free Encyclopedia. Retrieved 18:04, May 26, 2023, from https://en.wikipedia.org/w/index.php?title=Phosphate-buffered_saline&oldid=1137… [cited by examiner]
International Search Report for PCT/EP2019/061736 dated Jul. 29, 2019. [cited by applicant]
European Search Report for related application EP 18 30 5570 dated Nov. 5, 2018. [cited by applicant]
Bhattacharjee, et al., “Writing in the granular gel medium”, Sep. 25, 2015, pp. 1-6, Science Advances, vol. 1 No. 8. [cited by applicant]