Self-Healing Polyurethane Elastomers

Patent Title: POLYURETHANE

 Number/Link: W02016185172

Applicant/Assignee: Croda

Publication date: 24-11-2016

Gist”: PU from polyols which contain both a fatty dimer residue and an H-bonding group, show self-healing properties

Why it is interesting: Polyurethane elastomers with ‘intrinsic’ self-healing properties (i.e. without the need for external chemicals like encapsulated monomers) can be prepared by reacting isocyanates with polyols that have at least one urethane, amide or carbonate group and at least one fatty dimer residue. It is theorized that the fatty dimer allows the soft-phase of the polymer to flow and H-bonds to form, thus restoring most of the properties after damage.  In the examples polyols with internal urethane groups were prepared by reacting C36 dimer diol with HDI, which were then reacted with MDI and BDO. Samples of the resulting elastomers were cut in half, and manually stuck together again under mild heating (60°C), thus recovering most of their tensile and elongation properties.

A dimer diol

A dimer diol

Reactive Polyurethane Plasticizer

Patent Title: REACTIVE POLYURETHANE PLASTICIZERS AND ADHESIVES MADE THEREFROM

 Number/Link: W02016179131

Applicant/Assignee: Dow

Publication date: 10-11-2016

Gist”: An EO/PO monol is reacted with an excess of 4,4′-MDI

Why it is interesting: The invention is about reactive PU plasticizers which are said to be especially useful for polyurethane moisture curing adhesives used in automotive glass bonding. As opposed to conventional plasticizers they will supposedly not migrate and therefore not degrade adhesive properties over time or cause window fogging. The reactive plasticizers are prepared by reacting a slight excess of 4,4′-MDI with and EO/PO monol of MW between 500 and 2000 Da and an EO:PO ratio of about 1:1, such that the resulting in NCO content is between 0.1 and 1%.  Obviously at such low NCO values most of the MDI will have reacted twice with monol, and the resulting non-reactive plasticizer may (in my opinion) well migrate depending on the composition of both monol and adhesive.

4,4'-MDI

4,4′-MDI

 

Non-Isocyanate Polyurethanes from Sucrose-Fatty Acid Esters

Patent Title: BIOBASED CYCLIC CARBONATE FUNCTIONAL RESINS AND POLYURETHANE THERMOSETS THEREFROM

 Number/Link: US2016/0312060

Applicant/Assignee: NDSU

Publication date: 27-10-2016

Gist”: Epoxidized sucrose-fatty acid esters are reacted with CO2, then with polyamines

Why it is interesting:  Esters of unsaturated fatty acids and sucrose have been known since the 1960s and are useful in e.g. coatings.  Highly subsituted sucrose esters with an average of 7.7 fatty acid chains per molecule, a molecular weight of about 2400 and a relatively low viscosity of 300-400 mPa.s are commercially available. According to this invention, epoxidized sucrose-fatty acid esters can be further reacted with carbon dioxide resulting in a resin with a ‘pluraility’ of cyclocarbonate groups. Curing with polyamines results in highly crosslinked poly(hydroxyurethanes) useful for coatings, composites and adhesives.

Epoxidized sucrose-fatty acid ester

Epoxidized sucrose-fatty acid ester

 

 

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