Method for dewatering a polymer and the polymer made therefrom
US-2018112043-A1 · Apr 26, 2018 · US
US12296522B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12296522-B2 |
| Application number | US-201816628368-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 2, 2018 |
| Priority date | Jul 4, 2017 |
| Publication date | May 13, 2025 |
| Grant date | May 13, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention concerns a method for preparing an adhesive composition using an extruder having at least two rotating screws, successively comprising:feeding a plasticizer into the extruder;degassing the plasticizer in the extruder;feeding a silylated prepolymer and mixing the latter with the plasticizer in the extruder; anddischarging the mixture from the extruder.
Opening claim text (preview).
The invention claimed is: 1. A method comprising preparing an adhesive composition, using an extruder having at least two rotating screws, by successively: feeding at least one plasticizer into the extruder; degassing the at least one plasticizer in the extruder, wherein the at least one plasticizer, after being degassed, contains an amount of water by weight lower than that present in the at least one plasticizer before degassing; feeding at least one silylated prepolymer and mixing the latter with the at least one plasticizer in the extruder; and discharging the mixture from the extruder, wherein the temperature of the extruder when degassing the at least one plasticizer is 5° C. to 100° C. above the ring-and-ball softening temperature of the at least one plasticizer measured according to standard ISO 4625. 2. The method according to claim 1 , wherein the extruder is a co-rotating, intermeshing twin-screw extruder. 3. The method according to claim 1 , wherein the extruder has screws having an outer diameter and an inner diameter with a geometry defined by the ratio of the outer diameter of the screws to the inner diameter of the screws, De/Di, being 1.3 to 1.8. 4. The method according to claim 1 , wherein the screws have a diameter D and the length of the extruder is defined by a multiple of the diameter D of the screws, being 28D to 100D. 5. The method according to claim 1 , wherein the at least one silylated prepolymer has a main chain that is a main polyether chain, main polyether-polyurethane chain, main polyester chain, main polyester-polyurethane chain, main polyether-polyester-polyurethane chain, main polyolefin chain, main polyolefin-polyurethane chain, main polyether-polyolefin-polyurethane chain, main polyacrylate chain or main polyether-polyacrylate chain, and comprises two hydrolysable alkoxysilane terminal groups. 6. The method according to claim 1 , wherein the at least one silylated prepolymer is a prepolymer of formula (I): wherein: R 1 is a divalent hydrocarbon radical having 5 to 15 carbon atoms and can be aromatic or aliphatic, linear, branched or cyclic; R 2 is a linear or branched, divalent alkylene radical having 1 to 4 carbon atoms; R 3 is a linear, divalent alkylene radical having 1 to 3 carbon atoms; R 4 and R 5 , the same or different, are each a linear or branched alkyl radical having 1 to 20 carbon atoms, with the possibility when there are several R 4 or R 5 radicals that they can be the same or different; n is an integer such that the number average molecular weight of the block polyether of formula—[OR 2 ] n — is between 300 Da and 30 kDa; m 1 is a zero or nonzero integer; n and m1 are such that the number average molecular weight of the polymer of formula (1) is between 600 Da and 60 kDa; p is an integer equal to 0, 1 or 2. 7. The method according to claim 1 , wherein the at least one silylated prepolymer is a polyether of formula (VI): wherein: R 1 is a divalent hydrocarbon radical having 5 to 15 carbon atoms and can be aromatic, aliphatic, linear, branched or cyclic; R 2 is a linear or branched, divalent alkylene radical having 1 to 4 carbon atoms; R 3 is a linear divalent alkylene radical having 1 to 3 carbon atoms; R 4 and R 5 , the same or different, are each a linear or branched alkyl radical having 1 to 4 carbon atoms, with the possibility when there are several R 4 or R 5 radicals that they can be the same or different; R 6 is a hydrogen atom, phenyl radical, 2-succinate radical or a linear, branched or cyclic alkyl radical having 1 to 6 carbon atoms; n is an integer such that the number average molecular weight of the block polyether of formula—[OR 2 ] n — is between 300 Da and 30 kDa; m 2 is a nonzero integer; n and m 2 are such that the number average molecular weight of the polymer of formula (VI) is between 600 Da and 60 kDa; p is an integer equal to 0, 1 or 2. 8. The method according to claim 1 , wherein the at least one plasticizer is or comprises a tackifying resin. 9. The method according to claim 8 , wherein the tackifying resin has a number average molecular weight of between 200 Da and 10 kDa and is: (i) resins obtained by polymerization of terpene hydrocarbons and phenols, in the presence of Friedel-Crafts catalysts; (ii) resins obtained with a method comprising polymerization of alpha-methyl styrene; (iii) rosins of natural or modified origin, and the derivatives thereof hydrogenated, dimerized, polymerized or esterified by monoalcohols or polyols; (iv) resins obtained by hydrogenation, polymerization or copolymerization of mixtures of unsaturated aliphatic hydrocarbons having about 5, 9 or 10 carbon atoms derived from petroleum fractions; (v) terpene resins; (vi) copolymers containing natural terpenes; or (vii) acrylic resins having viscosity at 100° C. lower than 100 Pa·s. 10. The method according to claim 1 , wherein the amount by weight of silylated prepolymer is 20 to 85% and the amount by weight of plasticizer is 15% to 80%, relative to the weight of the adhesive composition. 11. The method according to claim 1 , wherein the adhesive composition is free of crosslinking catalyst. 12. The method according to claim 1 , wherein the adhesive composition comprises a crosslinking catalyst, the method comprising the adding of the catalyst and mixing thereof with the at least one plasticizer and the at least one silylated prepolymer. 13. The method according to claim 12 , wherein the amount by weight of crosslinking catalyst is 0.01% to 8%, relative to the weight of the adhesive composition. 14. The method according to claim 1 , wherein the residence time of the at least one plasticizer in the extruder is 0.1 to 3 minutes. 15. The method according to claim 1 , wherein the at least one plasticizer, after being degassed, contains an amount of water by weight less than or equal to 500 ppm and/or the at least one plasticizer, before degassing, contains an amount of water by weight higher than or equal to 500 ppm. 16. The method according to claim 1 also comprising one or more additions to the extruder of one or more antioxidants, moisture scavengers, thermoplastic polymers, plasticizers, paraffinic or naphthenic oils, waxes of a polyethylene homopolymer, waxes of a polyethylene and vinyl acetate copolymer, pigments, coloring agents or fillers. 17. The method according to claim 1 , also comprising one or more additional degassing operations. 18. The method according to claim 1 , wherein the temperature of the extruder, from the feed point of the at least one plasticizer as far as the discharge point, increases from ambient temperature up to a maximum temperature Tmax when degassing the at least one plasticizer, Tmax being between 150° C. and 220° C. and then decreases down to a final temperature Tf when discharging of between ambient temperature and Tmax. 19. The method according to claim 18 , wherein the temperature of the extruder when mixing the at least one silylated prepolymer with the at least one plasticizer, Tm, is between Tf and Tmax. 20. A method comprising preparing an adhesive composition, using an extruder having at least two rotating screws, by
Polyurethanes · CPC title
Use of unspecified macromolecular compounds as filler (use of unspecified rubbers {B29K2421/00}) · CPC title
Use of {PU, i.e.} polyureas or polyurethanes {or derivatives thereof}, as moulding material · CPC title
for feeding, e.g. end guides for the incoming material {(B29B7/7615 takes precedence; feeding predetermined amounts for mixing in general B01F35/714)} · CPC title
Screws · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.