Miller Brewing Company

Millercoors LLC

Aki A Murakami

Henry Goldstein

David S Ryder

Patrick L Ting

Lance T Lusk

Jay R Refling

Michael A VanSanford

Alfonso L Navarro

John R Seabrooks

Velta D Young

William G Schulze

Disclosed are methods for the production of light stable hop products, useful for the brewing of beer or ale to be stored in clear or green glass containers, which beer or ale will not develop objectionable flavor as a result of exposure to light. Light stable hop products are prepared by double extraction of liquid/supercritical COextracted hop solids with ethanol to remove alpha/iso-alpha-acids. Such alpha/iso-alpha-acids may be further removed from the ethanol extraction filtrate obtained in the double extraction process by subjecting such filtrate to an ion exchange medium, or precipitation by a metal ion, heavy metal ion, or alkali metal ion, or hydrogenation to provide an alpha/iso-alpha-acids free filtrate which may be added to the light stable double extracted hop solid residues obtained in the initial double extraction process.

Preparation of light stable hop products

Disclosed are methods for the production of light stable hops, useful for the brewing of beer or ale to be stored in clear or green glass containers, which beer or ale will not develop objectionable flavor as a result of exposure to light. Light stable hops are prepared by double extraction of liquid/supercritical COextracted hop solids with ethanol to remove alpha/iso-alpha-acids. Such alpha/iso-alpha-acids may be further removed from the ethanol extraction liquor obtained in the double extraction process by subjecting such liquor to an ion exchange medium, or precipitation by a metal ion, heavy metal ion, or alkali metal ion, to provide an alpha/iso-alpha-acid is free extraction liquor which may be added to the light stable hops residue obtained in the initial double extraction process.

Preparation of light stable hops

The isolation of at least one water soluble glycoside comprising an aromatic moiety group conjugated to mono-, di-, and trisaccharides from hop plant parts other than hop cones is disclosed. A glycoside preparation made by extraction of hop plant leaves with an aqueous alcohol was discovered to confer a pleasant grape flavor to the beer to which the glycoside preparation was added. The glycoside composition of the glycoside preparation made from aqueous alcohol-extracted hop plant leaves was found to differ from a similar preparation made from hop cones.

Use of glycosides extracted from hop plant parts to flavor malt beverages

The isolation and characterization of a group of odorless and non-volatile glycosides from extracted hops (hop solids which have been previously extracted with non-polar solvents) is disclosed. These glycosides are water soluble and consist of a group of aromatic compounds conjugated to mono-, di-, and trisaccharides. These glycosides are responsible for the formation of kettle hop flavor and taste through both chemical and biological transformations. When these glycosides are transformed, they yield an essence and flavorant which imparts a kettle hop flavor and taste when the essence and flavorant is added to an unhopped beer. These kettle hop flavor essences and flavorants provide economy, consistency, flexibility, quality, and convenience to the brewing process because only one unhopped wort is required to brew a stock of unhopped beer. The unhopped beer can then be dosed with the desired amount of kettle hop flavor essence and flavorant.

Methods of making and using purified kettle hop flavorants

The invention is an apparatus and method for preparing volatiles collected from a sample for gas chromatographic analysis. Volatiles are collected from the sample in a volatile trap, such as a porous polymer trap. The volatile trap is then connected to a transfer line. The trap is heated to thermally desorb the volatiles, and an inert gas, such as helium, flows through the heated trap to transport volatiles through the transfer line into a capillary column located in a gas chromatograph oven. Inside of the oven, a portion of the capillary column is cooled with a cooling fluid such as liquid nitrogen to form a cold trap. When the cold trap is cooled, the desorbed volatiles are trapped in the cold trap. Then the cold trap is heated to allow the volatiles to be released and the volatiles are carried to the remainder of the capillary column for chromatographic analysis by an inert carrier gas.

Growing community of inventors

Mequon, WI, United States of America

Aki A Murakami