Disclosed are methods for preparing cannabigerol (CBG) or a CBG analog, embodiments of the method comprising providing a compound (I); combining the compound (I) with geraniol and a solvent to form a reaction mixture; and combining the reaction mixture with an acid catalyst to form a product mixture comprising the CBG or the CBG homolog. The method may further comprise separating the CBG or the CBG analog from the product mixture and may further comprise purifying the CBG or CBG analog. Methods for preparing cannabigerolic acid (CBGA) or a cannabigerolic acid analog are also disclosed. The present disclosure also provides highly purity CBG, CBGA, and analogs thereof.

Provided are methods for producing levulinic acid from hemp hurds. In some embodiments, the methods include dissolving hemp hurds in an ionic liquid medium to produce a cellulose-rich product; hydrolyzing cellulose present in the cellulose-rich product to produce a glucose-rich product; dehydrating glucose present in the glucose-rich product, and/or fructose resulting from isomerization of the glucose, to produce 5-hydroxymethyl furfural (HMF); and hydrolyzing the HMF to levulinic acid. Also provided are methods for method for producing levulinic acid from sugar sources generally, which can include providing a sugar source, wherein the sugar source is a hydrolysis product produced by hydrolyzing a cellulose-rich product generated from hemp hurds and/or a cellulase digestion product of softwood pre-treated with phosphoric acid (H3PO4) or another acid; dehydrating the glucose present in the sugar source, and/or fructose resulting from isomerization of glucose present in the sugar source, to produce 5-hydroxymethyl furfural (HMF); and hydrolyzing the HMF to produce levulinic acid.

Provided are methods for producing levulinic acid from hemp hurds. In some embodiments, the methods include dissolving hemp hurds in an ionic liquid medium to produce a cellulose-rich product; hydrolyzing cellulose present in the cellulose-rich product to produce a glucose-rich product; dehydrating glucose present in the glucose-rich product, and/or fructose resulting from isomerization of the glucose, to produce 5-hydroxymethyl furfural (HMF); and hydrolyzing the HMF to levulinic acid. Also provided are methods for method for producing levulinic acid from sugar sources generally, which can include providing a sugar source, wherein the sugar source is a hydrolysis product produced by hydrolyzing a cellulose-rich product generated from hemp hurds and/or a cellulase digestion product of softwood pre-treated with phosphoric acid (H3PO4) or another acid; dehydrating the glucose present in the sugar source, and/or fructose resulting from isomerization of glucose present in the sugar source, to produce 5-hydroxymethyl furfural (HMF); and hydrolyzing the HMF to produce levulinic acid.

Provided are methods for producing levulinic acid from hemp hurds. In some embodiments, the methods include dissolving hemp hurds in an ionic liquid medium to produce a cellulose-rich product; hydrolyzing cellulose present in the cellulose-rich product to produce a glucose-rich product; dehydrating glucose present in the glucose-rich product, and/or fructose resulting from isomerization of the glucose, to produce 5-hydroxymethyl furfural (HMF); and hydrolyzing the HMF to levulinic acid. Also provided are methods for method for producing levulinic acid from sugar sources generally, which can include providing a sugar source, wherein the sugar source is a hydrolysis product produced by hydrolyzing a cellulose-rich product generated from hemp hurds and/or a cellulase digestion product of softwood pre-treated with phosphoric acid (H3PO4) or another acid; dehydrating the glucose present in the sugar source, and/or fructose resulting from isomerization of glucose present in the sugar source, to produce 5-hydroxymethyl furfural (HMF); and hydrolyzing the HMF to produce levulinic acid.

The invention relates to carbon dioxide dioxaphosphetane compositions, including solid carbon dioxide dioxaphosphetane compositions. The invention includes compositions and methods for the capture, storage, and recycling of carbon, including methods of boric acid catalyzed reduction of carbonates in aqueous media and the use of phosphate solutions for capture and recycling of carbon.

The invention relates to carbon dioxide dioxaphosphetane compositions, including solid carbon dioxide dioxaphosphetane compositions. The invention includes compositions and methods for the capture, storage, and recycling of carbon, including methods of boric acid catalyzed reduction of carbonates in aqueous media and the use of phosphate solutions for capture and recycling of carbon.

Disclosed are methods for preparing cannabigerol (CBG) or a CBG analog, embodiments of the method comprising providing a compound (I); combining the compound (I) with geraniol and a solvent to form a reaction mixture; and combining the reaction mixture with an acid catalyst to form a product mixture comprising the CBG or the CBG homolog. The method may further comprise separating the CBG or the CBG analog from the product mixture and may further comprise purifying the CBG or CBG analog. Methods for preparing cannabigerolic acid (CBGA) or a cannabigerolic acid analog are also disclosed. The present disclosure also provides highly purity CBG, CBGA, and analogs thereof.

Disclosed are methods for preparing cannabigerol (CBG) or a CBG analog, embodiments of the method comprising providing a compound (I); combining the compound (I) with geraniol and a solvent to form a reaction mixture; and combining the reaction mixture with an acid catalyst to form a product mixture comprising the CBG or the CBG homolog. The method may further comprise separating the CBG or the CBG analog from the product mixture and may further comprise purifying the CBG or CBG analog. Methods for preparing cannabigerolic acid (CBGA) or a cannabigerolic acid analog are also disclosed. The present disclosure also provides highly purity CBG, CBGA, and analogs thereof.

The present disclosure relates to methods, systems and products for converting carbon dioxide to one or more small organic compounds. In certain embodiments, the present disclosure provides a method of converting CO.sub.2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO.sub.2 and/or the related form thereof to a beta particle activated high band-gap semiconductor and thereby converting the CO.sub.2 and/or the related form thereof to the one or more small organic compounds.

The present disclosure relates to methods, systems and products for converting carbon dioxide to one or more small organic compounds. In certain embodiments, the present disclosure provides a method of converting CO.sub.2 and/or a related form thereof to one or more small organic compounds, the method comprising exposing the CO.sub.2 and/or the related form thereof to a beta particle activated high band-gap semiconductor and thereby converting the CO.sub.2 and/or the related form thereof to the one or more small organic compounds.