Abstract: A two-component solventless laminating adhesive composition including: (A) at least one isocyanate component comprising at least one isocyanate; and (B) at least one polyol component comprising: (Bi) at least one amine-initiated polyol; (Bii) at least one aliphatic polyester polyol; and (Biii) at least one polyether polyol; a process for preparing the above solventless adhesive laminating composition; and a laminate structure made using the above solventless adhesive laminating composition.

Abstract: A two-component solventless adhesive composition including: (A) at least one isocyanate component formulated for application to a first substrate comprising either at least one aromatic-based isocyanate, or a blend of: (Ai) at least one aromatic-based isocyanate; and (Aii) at least one aliphatic-based isocyanate; and (B) at least one isocyanate-reactive component formulated for application to a second substrate comprising a blend of: (Bi) at least one amine-initiated polyol comprising two or more primary hydroxyl groups and a backbone incorporating tertiary amines; (Bii) at least one hydroxyl terminated polyurethane polyol; (Biii) at least one phosphate ester polyol; (Biv) at least one polyester polyol; (Bv) at least one polyether polyol and (Bvi) optionally, at least one silane adhesion promoter; and a process for preparing the above two-component solventless adhesive composition; and a laminate structure made using the above two-component solventless adhesive composition.

Abstract: Water-based acrylic adhesive compositions comprising (A) an acrylic emulsion comprising an acrylic copolymer particle dispersed in an aqueous medium, (B) a crosslinking agent comprising a hydrophilic aliphatic isocyanate, and (C) a silane compound incorporated into the crosslinking agent (B) are disclosed. In some embodiments, the silane compound (C) incorporated into the crosslinking agent (B) is selected from the group consisting of (3-Glycidyloxypropyl)trimethoxysilane, 3-(Triethoxysilyl)propyl isocyanate, and combinations thereof. Methods for preparing water-based acrylic adhesive compositions also disclosed. Methods for preparing a laminate structure suitable for use in a flexible food packaging article are still further disclosed. Flexible food packaging articles including the disclosed water-based acrylic adhesive compositions are also disclosed.

Abstract: Methods for forming a laminate structure comprising a two-component solventless polyurethane adhesive compositions are disclosed. The adhesive composition is formulated such that each component is applied independently to corresponding substrates prior to the substrates being brought together to form the laminate structure. The adhesive compositions are highly-reactive and can comprise amine-initiated polyols or catalysts providing for fast curing. The amine-initiated polyols comprise a functionality of from 2 to 12, a hydroxyl number of from 5 to 1,830, and a viscosity at 40° C. of from 500 to 20,000 mPa-s. The catalyst can be bismuth catalysts, zinc catalysts, zirconium catalysts, tin catalysts, and aluminum catalysts. Still further, a laminate formed according to the methods is disclosed.

Abstract: Methods for forming a laminate structure comprising a two-component solventless polyurethane adhesive compositions are disclosed. The adhesive composition is formulated such that each component is applied independently to corresponding substrates prior to the substrates being brought together to form the laminate structure. The adhesive compositions are highly-reactive and can comprise amine-initiated polyols or catalysts providing for fast curing. The amine-initiated polyols comprise a functionality of from 2 to 12, a hydroxyl number of from 5 to 1,830, and a viscosity at 40 C of from 500 to 20,000 mPa-s. The catalyst can be bismuth catalysts, zinc catalysts, zirconium catalysts, tin catalysts, and aluminum catalysts. Still further, a laminate formed according to the methods is disclosed.

Abstract: Two-component solventless polyurethane adhesive compositions are disclosed comprising an isocyanate component comprising an isocyanate blend, and a polyol component comprising an amine-initiated polyol comprising two or more primary hydroxyl groups and a backbone incorporating tertiary amines, wherein the amine-initiated polyol comprises a functionality of from 2 to 12, hydroxyl number of from 5 to 1,830, and a viscosity at 40° C. of from 500 to 20,000 mPa-s, and a silicone-based additive (e.g., an anti-foaming agent and/or a wetting agent). The adhesive compositions are formulated such that the isocyanate and polyol components can be applied to separate substrates prior to mixing. Laminate structures comprising the disclosed adhesive compositions and further comprising a polymeric barrier substrate are also disclosed.

Abstract: Two-component solventless polyurethane adhesive compositions are disclosed comprising an isocyanate component comprising an isocyanate, and a polyol component comprising an amine-initiated polyol comprising two or more primary hydroxyl groups and a backbone incorporating tertiary amines, wherein the amine-initiated polyol comprises a functionality of from 2 to 12, a hydroxyl number of from 5 to 1,830, and a viscosity at 40° C. of from 500 to 20,000 mPa-s, and a silicone-based additive (e.g., an anti-foaming agent and/or a wetting agent). The adhesive compositions are formulated such that the isocyanate and polyol components can be applied to separate substrates prior to mixing. Laminate structures comprising the disclosed adhesive compositions and further comprising a metal or metallized substrate are also disclosed.

Abstract: Methods for forming a laminate structure comprising a two-component solventless polyurethane adhesive compositions are disclosed. The adhesive composition is formulated such that each component is applied independently to corresponding substrates prior to the substrates being brought together to form the laminate structure. The adhesive compositions are highly-reactive and can comprise amine-initiated polyols or catalysts providing for fast curing. The amine-initiated polyols comprise a functionality of from 2 to 12, a hydroxyl number of from 5 to 1,830, and a viscosity at 40 C of from 500 to 20,000 mPa-s. The catalyst can be bismuth catalysts, zinc catalysts, zirconium catalysts, tin catalysts, and aluminum catalysts. Still further, a laminate formed according to the methods is disclosed.

Abstract: Disclosed herein are nanoactuating rotaxanes comprising a threading component, the threading component comprising a oligoviologen, and at least two macrocylic components, wherein the oligoviologen is threaded through each of the macrocylic components. Also disclosed are methods for making and using the rotaxanes.

Abstract: Methods for recovering gold from gold-bearing materials are provided. The methods rely upon on the self-assembly of KAuBr4 and ?-cyclodextrin (?-CD) in aqueous solution to form a co-precipitate, a 1:2 complex, KAuBr4•(?-CD)2 (“?•Br”), either alone or in an extended {[K(OH2)6][AuBr4]?(?-CD)2}n chain superstructure (FIG. 1). The co-precipitation of ?•Br is selective for gold, even in the presence of other metals, including other square-planar noble metals. The method enables one to isolate gold from gold-bearing materials from diverse sources, as further described.

Abstract: Disclosed herein are nanoactuating rotaxanes comprising a threading component, the threading component comprising a oligoviologen, and at least two macrocylic components, wherein the oligoviologen is threaded through each of the macrocylic components. Also disclosed are methods for making and using the rotaxanes.

Abstract: A redox-active triangular prism is provided. The redox-active triangular prism includes a plurality of pure enantiomers selected from a group consisting of (?)-NDI-? and (+)-NDI-?. Methods for their preparation as solvent-templated supramolecular structures and a characterization of their redox-active behavior are provided.

Abstract: Methods for recovering gold from gold-bearing materials are provided. The methods rely upon on the self-assembly of KAuBr4 and ?-cyclodextrin (?-CD) in aqueous solution to form a co-precipitate, a 1:2 complex, KAuBr4•(?-CD)2 (“?•Br”), either alone or in an extended {[K(OH2)6][AuBr4]?(?-CD)2}n chain superstructure (FIG. 1). The co-precipitation of ?•Br is selective for gold, even in the presence of other metals, including other square-planar noble metals. The method enables one to isolate gold from gold-bearing materials from diverse sources, as further described.

Abstract: Methods for recovering gold from gold-bearing materials are provided. The methods rely upon on the self-assembly of KAuBr4 and ?-cyclodextrin (?-CD) in aqueous solution to form a co-precipitate, a 1:2 complex, KAuBr4•(?-CD)2 (“?•Br”), either alone or in an extended {[K(OH2)6][AuBr4]?(?-CD)2}n chain superstructure (FIG. 1). The co-precipitation of ?•Br is selective for gold, even in the presence of other metals, including other square-planar noble metals. The method enables one to isolate gold from gold-bearing materials from diverse sources, as further described.

Abstract: A redox-active triangular prism is provided. The redox-active triangular prism includes a plurality of pure enantiomers selected from a group consisting of (?)-NDI-? and (+)-NDI-?. Methods for their preparation as solvent-templated supramolecular structures and a characterization of their redox-active behavior are provided.

Abstract: Methods for recovering gold from gold-bearing materials are provided. The methods rely upon on the self-assembly of KAuBr4 and ?-cyclodextrin (?-CD) in aqueous solution to form a co-precipitate, a 1:2 complex, KAuBr4•(?-CD)2 (“?•Br”), either alone or in an extended {[K(OH2)6][AuBr4]?(?-CD)2}n chain superstructure (FIG. 1). The co-precipitation of ?•Br is selective for gold, even in the presence of other metals, including other square-planar noble metals. The method enables one to isolate gold from gold-bearing materials from diverse sources, as further described.