A01N61/00

Methods to convert lignin to phenolic and carboxylate compounds
09775347 · 2017-10-03 · ·

A method of converting lignin to phenolic compounds and dicarboxylates in high yield is described. The method involves the use of peroxy acids to react with lignin at a moderated treatment conditions. The peroxy acids can be used along or in combination of other catalysts that have the capability to lower the molecular weight of lignin. A phenolic compounds yield is achieved (>60%) and these phenolic compounds represents high value precursors for various applications include but not limited to antioxidants, health improvement agents, anticorrosive agents, liquid fuel components and performance enhancing agents, resin and adhesives. Dicarboxylic acids can be used for polymer applications or hydrodeoxygenation to hydrocarbon fuel.

Methods to convert lignin to phenolic and carboxylate compounds
09775347 · 2017-10-03 · ·

A method of converting lignin to phenolic compounds and dicarboxylates in high yield is described. The method involves the use of peroxy acids to react with lignin at a moderated treatment conditions. The peroxy acids can be used along or in combination of other catalysts that have the capability to lower the molecular weight of lignin. A phenolic compounds yield is achieved (>60%) and these phenolic compounds represents high value precursors for various applications include but not limited to antioxidants, health improvement agents, anticorrosive agents, liquid fuel components and performance enhancing agents, resin and adhesives. Dicarboxylic acids can be used for polymer applications or hydrodeoxygenation to hydrocarbon fuel.

METHODS OF MAKING ANTIMICROBIAL COMPOSITIONS AND/OR VIRUCIDAL DISINFECTANT COMPOSITIONS FROM VEGETABLE OIL, AND RELATED ANTIMICROBIAL COMPOSITIONS AND/OR VIRUCIDAL DISINFECTANT COMPOSITIONS AND USES

The present disclosure relates to methods and systems for making one or more antimicrobial compositions and/or one or more virucidal disinfectant compositions. Said methods and systems include exposing a vegetable oil composition to ozone gas to cause ozonolysis of on one or more unsaturated fatty acids present in the vegetable oil composition, thereby forming an ozonated vegetable oil composition and exposing the ozonated vegetable oil composition to a temperature greater than 60° C. while in contact with water to decompose one or more ozonide compounds and form a heat-treated, ozonated vegetable oil composition. The present disclosure also relates to one or more uses of said one or more antimicrobial compositions and/or one or more virucidal disinfectant compositions.

Enhanced formulations, compositions and methods for pest control
11241008 · 2022-02-08 · ·

Formulations of pesticides are disclosed, specifically pesticidal blends of essential oils and other ingredients, that have been found to enhance the activity of the active pesticidal ingredients. The formulations may be, for example, emulsions or dust formulations. For example, a composition for controlling a target pest is disclosed that comprises at least one active agent and a formulation agent, wherein: the active agent is capable of interacting with a receptor in the target pest; the active agent has a first activity against the target pest when applied without the formulation agent and the composition has a second activity against the target pest; and the second activity is greater than the first activity.

Enhanced formulations, compositions and methods for pest control
11241008 · 2022-02-08 · ·

Formulations of pesticides are disclosed, specifically pesticidal blends of essential oils and other ingredients, that have been found to enhance the activity of the active pesticidal ingredients. The formulations may be, for example, emulsions or dust formulations. For example, a composition for controlling a target pest is disclosed that comprises at least one active agent and a formulation agent, wherein: the active agent is capable of interacting with a receptor in the target pest; the active agent has a first activity against the target pest when applied without the formulation agent and the composition has a second activity against the target pest; and the second activity is greater than the first activity.

Pesticidal compositions comprising a solid insecticide and an essential oil

A liquid composition for controlling a target pest by aerosol application to a space in need thereof is disclosed. The composition comprises a solid insecticide dissolved in a solvent comprising an essential oil or oils, wherein the solid insecticide is selected from the group consisting of pyrethroid, neonicotinoid and halogenated pyrrole insecticides, and wherein the solid insecticide is present at a concentration sufficient to control the target pest. Methods for controlling a target pest by aerosol application to a space in need thereof are also disclosed, such methods comprising the step of aerosolizing the liquid composition, thereby contacting the space with an insecticidally effective amount of the liquid composition.

Pesticidal compositions comprising a solid insecticide and an essential oil

A liquid composition for controlling a target pest by aerosol application to a space in need thereof is disclosed. The composition comprises a solid insecticide dissolved in a solvent comprising an essential oil or oils, wherein the solid insecticide is selected from the group consisting of pyrethroid, neonicotinoid and halogenated pyrrole insecticides, and wherein the solid insecticide is present at a concentration sufficient to control the target pest. Methods for controlling a target pest by aerosol application to a space in need thereof are also disclosed, such methods comprising the step of aerosolizing the liquid composition, thereby contacting the space with an insecticidally effective amount of the liquid composition.

HERBAL COMPOSITIONS AND METHOD FOR PREPARING THEREOF

The present invention relates to herbal compositions and method for preparing thereof. The herbal composition is derived from pulverizing at least two herbal materials selected from a group of herbal materials consisting of Panax ginseng, Glycyrrhiza uralensis, Agrimonia pilosa, Gynostemma pentaphyllum, asparagus, and mushroom. The pulverized herbal materials are combined to obtain a mixed herbal powder which is then extracted with a solvent to obtain a concentrated herbal extract, wherein the concentrated herbal extract is dried to obtain a dry powder of the herbal compositions.

Synergistic benzoxaborole-containing anti-fungicidal composition

An anti-fungal composition for the control of one or more target fungi (or a similar heterotrophic, hyphae-producing organism) that infect plant materials and are (is) separately controllable by a benzoxaborole and an anti-fungal compound of a preselected FRAC Target Site Code is disclosed, as is a method of its use. A composition contains a diluent medium having dissolved or dispersed therein a synergistic effective amount of each of a first and a second anti-fungal compound. The first anti-fungal compound is a benzoxaborole of Formula I. The second anti-fungal compound is other than a benzoxaborole and is known to control said one or more target species of fungus when utilized as the sole anti-fungal compound at a concentration greater than the synergistic effective amount and has a preselected FRAC Target Site Code of B, C, D, E, G, H, or M.

Synergistic benzoxaborole-containing anti-fungicidal composition

An anti-fungal composition for the control of one or more target fungi (or a similar heterotrophic, hyphae-producing organism) that infect plant materials and are (is) separately controllable by a benzoxaborole and an anti-fungal compound of a preselected FRAC Target Site Code is disclosed, as is a method of its use. A composition contains a diluent medium having dissolved or dispersed therein a synergistic effective amount of each of a first and a second anti-fungal compound. The first anti-fungal compound is a benzoxaborole of Formula I. The second anti-fungal compound is other than a benzoxaborole and is known to control said one or more target species of fungus when utilized as the sole anti-fungal compound at a concentration greater than the synergistic effective amount and has a preselected FRAC Target Site Code of B, C, D, E, G, H, or M.