阅读说明：本技术 二氧化硅肥料及其用途 (Silica fertilizer and use thereof ) 是由 D·吉廷斯 C·伏吉亚齐 K·斯托瓦尔 J·米苏拉卡 于 2020-04-24 设计创作，主要内容包括：包含二氧化硅含量等于或大于40重量％的矿物质的水性悬浮液作为植物肥料的用途,其中,所述水性悬浮液包含等于或小于10％(w/v)的矿物质。一种给植物施肥的方法,所述方法包括：制备所述水性悬浮液,并将其施用于种子、植物或生长基质,例如种子或植物周围的土壤。一种二氧化硅含量等于或大于40重量％的矿物质的浓缩浆料,其中,所述浓缩浆料的固体含量等于或大于20重量％或者等于或大于30重量％,并且粘度为60cP至2000cP或者60cP至700cP。制备所述浓缩浆料的方法,所述方法包括将二氧化硅含量等于或大于40重量％的矿物质与水混合。制备所述水性悬浮液的方法,所述方法包括稀释所述浓缩浆料。(Use of an aqueous suspension comprising a mineral having a silica content equal to or greater than 40 wt%, wherein the aqueous suspension comprises equal to or less than 10% (w/v) mineral, as a plant fertiliser. A method of fertilizing a plant, the method comprising: the aqueous suspension is prepared and applied to the seed, plant or growing substrate, such as the soil surrounding the seed or plant. A concentrated slurry of minerals having a silica content equal to or greater than 40 wt%, wherein the concentrated slurry has a solids content equal to or greater than 20 wt% or equal to or greater than 30 wt% and a viscosity of 60cP to 2000cP or 60cP to 700 cP. A process for preparing the concentrated slurry, the process comprising mixing a mineral matter having a silica content of equal to or greater than 40 wt% with water. A method of preparing the aqueous suspension, the method comprising diluting the concentrated slurry.)

1. Use of an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40 wt% as a plant fertiliser, wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral.

2. A method of fertilizing a plant, the method comprising:

preparing an aqueous suspension comprising minerals having a silica content of equal to or greater than about 40% by weight from a powder or concentrated slurry of minerals having a silica content of equal to or greater than about 40% by weight; and is

Applying the aqueous suspension to a seed, plant or growing substrate, such as soil surrounding a seed or plant,

wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral matter.

3. The use of claim 1 or the method of claim 2, wherein the mineral is diatomaceous earth, wollastonite, or a combination thereof.

4. The use or method of any preceding claim, wherein the aqueous suspension comprises from about 0.5 wt% to about 5 wt% (w/v) mineral.

5. Use or method according to any one of the preceding claims, wherein the total solids content of the aqueous suspension is equal to or less than about 15 wt% and/or equal to or greater than about 0.5 wt%.

6. Use or method according to any one of the preceding claims, wherein the aqueous suspension is prepared by diluting the concentrated slurry according to any one of claims 7 to 13.

7. A concentrated slurry of minerals having a silica content equal to or greater than about 40 wt%, wherein the concentrated slurry has a solids content equal to or greater than about 20 wt% or equal to or greater than about 30 wt% and a viscosity of about 60cP to about 2000cP or about 60cP to about 700 cP.

8. The concentrated slurry of claim 7, wherein the concentrated slurry further comprises one or more dispersants, one or more thickeners, one or more wetting agents, or a combination thereof.

9. The concentrated slurry of claim 7 or 8, wherein the concentrated slurry comprises about 0.5 wt% to about 2 wt% total dispersant.

10. The concentrated slurry of any of claims 7-9, wherein the mineral having a silica content equal to or greater than about 40 wt% is wollastonite.

11. The concentrated slurry of claim 10, wherein the wollastonite has:

d₅₀(Settlement diagram) equal to or less than about 10 μm, such as equal to or less than about 9 μm, such as equal to or less than about 8 μm; and/or

d₅₀(Settlement diagram) equal to or greater than about 4 μm, such as equal to or greater than about 5 μm, such as equal to or greater than about 6 μm; and/or

d₉₀(Settlement diagram) equal to or less than about 25 μm, for example equal to or less than about 20 μm, for example equal to or less than about 10 μm; and/or

d₉₀(Settlement diagram) equal to or greater than about 5 μm, such as equal to or greater than about 10 μm, such as equal to or greater than about 15 μm; and/or

d₁₀(Settlement diagram) equal to or less than about 3 μm, such as equal to or less than about 2 μm, such as equal to or less than about 1 μm; and/or

d₁₀(Settlement diagram) equal to or greater than about 0.1. mu.m, such as equal to or greater than about 0.5. mu.m, such as equal to or greater than about 1 μm.

12. The concentrated slurry of any of claims 7-9, wherein the mineral matter having a silica content equal to or greater than about 40 wt% is diatomaceous earth.

13. The concentrated slurry of claim 12, wherein the diatomaceous earth has:

d₅₀(Settlement diagram) equal to or less than about 5 μm, such as equal to or less than about 4 μm, such as equal to or less than about 3 μm; and/or

d₅₀(Settlement diagram) equal to or greater than about 0.5 μm, for example equal to or greater than about 1 μm; and/or

d₉₀(Settlement diagram) equal to or less than about 15 μm, such as equal to or less than about 10 μm, such as equal to or less than about 8 μm; and/or

d₉₀(Settlement diagram) equal to or greater than about 4 μm, such as equal to or greater than about 5 μm, such as equal to or greater than about 6 μm; and/or

d₁₀(Settlement diagram) equal to or less than about 2 μm, such as equal to or less than about 1 μm, such as equal to or less than about 0.5 μm; and/or

d₁₀(Settlement diagram) equal to or greater than about 0.05 μm, such as equal to or greater than about 0.1 μm, such as equal to or greater than about 0.2 μm.

14. A method of making the concentrated slurry of any one of claims 7-13, comprising mixing a mineral matter having a silica content of equal to or greater than about 40 wt% with water and optionally one or more dispersants, one or more thickeners, one or more wetting agents, or a combination thereof.

15. A method of making an aqueous suspension comprising equal to or less than about 10% (w/v) of a mineral matter having a silica content equal to or greater than about 40% by weight, the method comprising diluting the concentrated slurry of any one of claims 7-13.

Technical Field

The present invention generally relates to the use of an aqueous suspension comprising a mineral having a silica content equal to or greater than about 40 wt.% as a fertilizer. The invention also relates to a method for fertilizing a plant, wherein the method comprises preparing an aqueous suspension comprising minerals having a silica content equal to or greater than about 40% by weight and applying it to the seed, the plant, or a growth substrate (e.g., soil) surrounding the seed or the plant. The invention also relates to mineral products for use in the aqueous suspensions described herein and concentrated slurries comprising said minerals from which aqueous suspensions for use as fertilisers can be prepared.

Background

Silicon can help promote the growth and development of plants. Thus, the silicon-containing material may be included in various plant fertilizers to provide a source of silicon. For example, the dissolved silicate may be used in liquid form. However, this is relatively expensive and requires specially adapted equipment to handle the liquid manure. Alternatively, the silica-containing material may be used in solid (particulate) form. However, these materials must have a relatively large particle size to be effective for application to plants (e.g., not blown away by wind). Solid materials (term SC) are directly incorporated into the growing substrate (e.g. soil) to avoid drift, which is labor intensive. The large particle size of these materials also reduces the rate at which silicon dissolves in water and is therefore available to plants. Alternatively, particulate matter containing tiny solids or droplets small enough to be inhaled can cause serious health problems. Some particles with a diameter of less than 10 microns can penetrate deep into the lungs and even into the blood. Particles less than about 2.5 microns in diameter pose the greatest risk to health. There is therefore a need to provide alternative and/or improved products and methods for providing a source of silicon to plants.

Disclosure of Invention

According to a first aspect of the present invention there is provided the use of an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40% by weight as a plant fertiliser, wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral. In certain embodiments, the aqueous suspension is made from a powder or concentrated slurry of minerals having a silica content equal to or greater than about 40% by weight.

According to a second aspect of the present invention, there is provided a method of fertilizing a plant, the method comprising:

preparing an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40% by weight from a powder or concentrated slurry of the mineral having a silica content of equal to or greater than about 40% by weight, and

applying the aqueous suspension to a seed, a plant or a growing substrate (e.g., soil) surrounding the seed or plant,

wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral matter.

According to a third aspect of the present invention, there is provided a fertilizer composition, wherein the fertilizer composition is an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40 wt%, and wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral.

According to a fourth aspect of the present invention, there is provided a concentrated slurry comprising minerals having a silica content of equal to or greater than about 40 wt%, wherein the concentrated slurry has a solids content of equal to or greater than about 30 wt% and a viscosity of about 60cP to about 700 cP.

According to a fifth aspect of the present invention, there is provided a concentrated slurry comprising minerals having a silica content of equal to or greater than about 40 wt%, wherein the concentrated slurry has a solids content of equal to or greater than about 20 wt% and a viscosity of about 60cP to about 2000 cP.

According to a sixth aspect of the present invention there is provided a method of preparing the concentrated slurry of the fourth or fifth aspect of the present invention, the method comprising mixing a mineral matter having a silica content of equal to or greater than about 40% by weight with water and optionally one or more dispersants, one or more thickeners, one or more wetting agents or a combination thereof.

According to a seventh aspect of the present invention there is provided a method of preparing an aqueous suspension comprising equal to or less than about 10% (w/v) of a mineral substance having a silica content equal to or greater than about 40% by weight, the method comprising diluting the concentrated slurry of the fourth or fifth aspect of the present invention.

Certain embodiments of any aspect of the present invention may provide one or more of the following advantages:

providing plant-usable silicon;

providing silicon in liquid form for plant use;

reducing the particle size of the mineral, for example, which may increase the rate at which silicon is obtained by the plant;

increased yield;

increase in protein content.

Further details, embodiments and preferences related to any particular one or more of the described aspects of the invention will be described herein and equally apply to all aspects of the invention. Unless otherwise indicated herein or otherwise clearly contradicted by context, any combination of the embodiments, examples, and preferences described herein is intended to be encompassed by the invention in all possible variations thereof.

Detailed Description

The present invention is based on the unexpected discovery that silica-containing minerals can be used as fertilizers in the form of aqueous suspensions. In particular, the silica-containing mineral powder can be used as a fertilizer by applying the silica-containing mineral powder in the form of an aqueous suspension. The present invention is also based on the unexpected discovery that silica-containing minerals can be used in the form of aqueous suspensions to increase the yield and/or protein content of plants.

The present invention is also based on the unexpected discovery that concentrated slurries of minerals having a silica content equal to or greater than about 40 weight percent can be prepared. Advantageously, the concentrated slurry has a viscosity such that it is pourable. This allows minerals having a silica content of equal to or greater than about 40% by weight to be shipped to customers (e.g., farmers) in a suitable and convenient form for preparing aqueous suspensions containing equal to or less than about 10% (w/v) minerals for use as fertilizers.

Accordingly, provided herein is the use of an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40 wt% as a plant fertiliser, wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral. In certain embodiments, the aqueous suspension is prepared from a powder or concentrated slurry of minerals having a silica content equal to or greater than about 40% by weight, for example, by mixing the powder or concentrated slurry with an aqueous solvent such as water.

Also provided herein is a method of fertilizing a plant, the method comprising:

preparing an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40% by weight from a powder or concentrated slurry of the mineral having a silica content of equal to or greater than about 40% by weight, and

applying the aqueous suspension to a seed, a plant or a growing substrate (e.g., soil) surrounding the seed or plant,

wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral matter.

The term "fertilizer" refers to any product that facilitates the growth and/or development of a plant. For example, the fertilizer may serve as a source of one or more nutrients essential or useful for plant growth and/or development, for example as a source of silicon, nitrogen, phosphorus and/or potassium.

The term "powder" refers to a solid particulate material. The aqueous suspensions described herein may be made from mineral powders having a silica content equal to or greater than about 40% by weight.

The term "concentrated slurry" refers to a suspension having a solids content of equal to or greater than about 20 wt% or equal to or greater than about 30 wt%. For example, the solids content of the concentrated slurry of wollastonite may be equal to or greater than about 50 weight percent, or equal to or greater than about 60 weight percent, or equal to or greater than about 70 weight percent. For example, the solids content of the concentrated slurry of diatomaceous earth may be equal to or greater than about 20 wt%, or equal to or greater than about 30 wt%, or equal to or greater than about 32 wt%, or equal to or greater than about 34 wt%.

The aqueous suspensions described herein can be made from concentrated slurries of minerals having a silica content equal to or greater than about 40% by weight. For example, the concentrated slurry may be an aqueous suspension. For example, the aqueous solvent may be water. The concentrated slurry can comprise, consist essentially of, or consist of water and minerals having a silica content equal to or greater than about 40 wt%. The concentrated slurry may, for example, comprise one or more other additives, such as one or more dispersants, one or more wetting agents, one or more thickeners, or any combination thereof. The concentrated slurry can comprise, consist essentially of, or consist of water and a mineral matter having a silica content equal to or greater than about 40 wt% and one or more dispersants, one or more thickeners, one or more wetting agents, or a combination thereof.

The concentrated slurry may, for example, be a stable concentrated slurry, for example, at least about 90% of the particles may remain suspended for up to 30 days after preparation of the concentrated slurry. This can be measured by a change in viscosity over 30 days. For example, the viscosity of the stable slurry changes by less than about 100cP or less than about 50cP over 30 days.

One or more other additives may each be present in the concentrated slurry in an amount from about 0.01% (w/v) to about 5% (w/v). For example, the one or more additional additives may each be present in the concentrated slurry in an amount of from about 0.05% (w/v) to about 4% (w/v), or from about 0.1% (w/v) to about 3% (w/v), or from about 0.5% (w/v) to about 2% (w/v), or from about 0.5% (w/v) to about 1.5% (w/v).

The total amount of other additives in the concentrated slurry may be, for example, equal to or less than about 10% (w/v). For example, the total amount of other additives in the concentrated slurry may be equal to or less than about 8% (w/v), or equal to or less than about 6% (w/v), or equal to or less than about 5% (w/v), or equal to or less than about 4% (w/v), or equal to or less than about 2% (w/v). For example, the total amount of other additives in the concentrated slurry may be from about 0.01% (w/v) to about 10% (w/v) or from about 0.1% (w/v) to about 5%.

For example, the solids content of the concentrated slurry can be equal to or greater than about 20 wt%. For example, the solids content of the concentrated slurry can be equal to or greater than about 21 wt%, or equal to or greater than about 22 wt%, or equal to or greater than about 23 wt%. For example, the solids content of the concentrated slurry can be equal to or greater than about 32 wt%. For example, the solids content of the concentrated slurry can be equal to or greater than about 34 wt%, or equal to or greater than about 35 wt%, or equal to or greater than about 38 wt%, or equal to or greater than about 40 wt%, or equal to or greater than about 45 wt%, or equal to or greater than about 50 wt%, or equal to or greater than about 55 wt%, or equal to or greater than about 60 wt%, or equal to or greater than about 65 wt%, or equal to or greater than about 70 wt%. For example, the solids content of the concentrated slurry can be equal to or less than about 90 wt%, or equal to or less than about 85 wt%, or equal to or less than about 80 wt%, or equal to or less than about 75 wt%.

When the concentrated slurry comprises wollastonite, the solids content of the concentrated slurry may be equal to or greater than about 50 weight percent, such as equal to or greater than about 55 weight percent, or equal to or greater than about 60 weight percent, or equal to or greater than about 65 weight percent, or equal to or greater than about 70 weight percent. When the concentrated slurry comprises wollastonite, the solids content of the concentrated slurry may be equal to or less than about 85 weight percent, such as equal to or less than about 80 weight percent, or equal to or less than about 75 weight percent, or equal to or less than about 73 weight percent. For example, when the concentrated slurry comprises wollastonite, the solids content of the concentrated slurry can be about 50 wt% to about 85 wt%, or about 60 wt% to about 80 wt%, or about 65 wt% to about 75 wt%, or about 65 wt% to about 73 wt%.

When the concentrated slurry comprises diatomaceous earth, the solids content of the concentrated slurry may be equal to or greater than about 20 wt.%, such as equal to or greater than about 21 wt.%, or equal to or greater than about 22 wt.%, or equal to or greater than about 23 wt.%. When the concentrated slurry comprises diatomaceous earth, the solids content of the concentrated slurry may be equal to or greater than about 30 wt.%, such as equal to or greater than about 32 wt.%, or equal to or greater than about 34 wt.%, or equal to or greater than about 35 wt.%. When the concentrated slurry comprises diatomaceous earth, the solids content of the concentrated slurry may be equal to or greater than about 40 wt.%, such as equal to or greater than about 41 wt.%, or equal to or greater than about 42 wt.%, or equal to or greater than about 43 wt.%. When the concentrated slurry comprises diatomaceous earth, the solids content of the concentrated slurry may be equal to or less than about 60 wt%, such as equal to or less than about 55 wt%, or equal to or less than about 50 wt%, or equal to or less than about 45 wt%, or equal to or less than about 40 wt%, or equal to or less than about 37 wt%. For example, when the concentrated slurry comprises diatomaceous earth, the solids content of the concentrated slurry may be from about 20 wt% to about 60 wt%, or from about 20 wt% to about 50 wt%. For example, when the concentrated slurry comprises diatomaceous earth, the solids content of the concentrated slurry may be from about 30 wt% to about 60 wt%, or from about 30 wt% to about 50 wt%, or from about 30 wt% to about 40 wt%, or from about 32 wt% to about 37 wt%.

For example, the solid material in the concentrated slurry can include equal to or greater than about 90 wt% minerals having a silica content equal to or greater than about 40 wt%. For example, the solid material in the slurry may comprise equal to or greater than about 92 wt%, or equal to or greater than about 94 wt%, or equal to or greater than about 95 wt%, or equal to or greater than about 96 wt%, or equal to or greater than about 98 wt% of minerals having a silica content equal to or greater than about 40 wt%. For example, the solid material in the slurry may comprise from about 90 wt% to about 100 wt%, or from about 92 wt% to about 99 wt%, or from about 94 wt% to about 98 wt% of minerals having a silica content equal to or greater than about 40 wt%.

When the concentrated slurry further comprises one or more dispersants, the solids content of the concentrated slurry may be higher than the solids content of a concentrated slurry that does not comprise a dispersant. For example, when the concentrated slurry further comprises one or more dispersants, the solids content of the concentrated slurry can be equal to or greater than about 30 wt%, or equal to or greater than about 35 wt%, or equal to or greater than about 40 wt%, or equal to or greater than about 45 wt%, or equal to or greater than about 50 wt%, or equal to or greater than about 55 wt%, or equal to or greater than about 60 wt%, or equal to or greater than about 65 wt%, or equal to or greater than about 70 wt%. For example, the solids content of the concentrated slurry of one or more dispersants may be from about 30 wt% to about 90 wt%, or from about 40 wt% to about 90 wt%, or from about 50 wt% to about 90 wt%, or from about 60 wt% to about 90 wt%, or from about 70 wt% to about 90 wt%.

For example, the concentrated slurry may have a viscosity of about 60cP to about 2000cP, such as about 100cP to about 1500cP, or about 200cP to about 1000cP, or about 400cP to about 800 cP.

For example, the concentrated slurry can have a viscosity of about 60cP to about 700cP, such as about 100cP to about 500cP, or about 200cP to about 400 cP.

When the concentrated slurry comprises wollastonite, the viscosity of the concentrated slurry may be equal to or less than about 500cP, for example equal to or less than about 450cP, or equal to or less than about 400cP, or equal to or less than about 350 cP. For example, when the concentrated slurry comprises wollastonite, the viscosity of the concentrated slurry can be equal to or greater than about 200cP, such as equal to or greater than about 250cP, or equal to or greater than about 300 cP. For example, when the concentrated slip comprises wollastonite, the viscosity of the concentrated slip can be from about 200cP to about 500cP, alternatively from about 250cP to about 450cP, alternatively from about 300cP to about 400 cP.

When the concentrated slurry comprises diatomaceous earth, the viscosity of the concentrated slurry may be equal to or less than about 2000cP, such as equal to or less than about 1500cP, such as equal to or less than about 1000cP, such as equal to or less than about 800 cP. When the concentrated slurry comprises diatomaceous earth, the viscosity of the concentrated slurry may be equal to or less than about 700cP, for example equal to or less than about 650cP, or equal to or less than about 600cP, or equal to or less than about 550cP, or equal to or less than about 500cP, or equal to or less than about 450cP, or equal to or less than about 400 cP. For example, when the concentrated slurry comprises diatomaceous earth, the viscosity of the concentrated slurry may be equal to or greater than about 200cP, such as equal to or greater than about 250cP, or equal to or greater than about 300cP, such as equal to or greater than about 350 cP. For example, when the concentrated slurry comprises diatomaceous earth, the viscosity of the concentrated slurry may be from about 200cP to about 2000cP, alternatively from about 250cP to about 1500cP, alternatively from about 300cP to about 1000cP, alternatively from about 500cP to about 1000 cP. For example, when the concentrated slurry comprises diatomaceous earth, the viscosity of the concentrated slurry may be from about 200cP to about 700cP, alternatively from about 250cP to about 600cP, alternatively from about 300cP to about 500 cP.

For example, the concentrated slurry may be pourable and pumpable.

Viscosity measurements were made directly after mixing the slurries at room temperature. The viscosity can be measured using a Brookfield DV2T LV viscometer with spindle 3 running at 20rpm or 50rpm or 100rpm, or with spindle 5 running at 20 rpm. The most appropriate rotor will provide the most consistent reading and may be selected by the technician.

For example, the concentrated slurry may comprise diatomaceous earth, and have a solids content of about 20 wt% to about 60 wt% and a viscosity of about 100cP to about 2000 cP. For example, the concentrated slurry may comprise diatomaceous earth, and have a solids content of about 20 wt% to about 60 wt% and a viscosity of about 100cP to about 1000 cP. For example, the concentrated slurry may comprise diatomaceous earth, and have a solids content of about 30 wt% to about 50 wt% and a viscosity of about 500cP to about 800 cP.

For example, the concentrated slurry may comprise diatomaceous earth, and have a solids content of about 30 wt% to about 60 wt% and a viscosity of about 100cP to about 600 cP. For example, the concentrated slurry may comprise diatomaceous earth, and have a solids content of about 30 wt% to about 60 wt% and a viscosity of about 100cP to about 500 cP. For example, the concentrated slurry may comprise diatomaceous earth, and have a solids content of about 30 wt% to about 50 wt% and a viscosity of about 100cP to about 400 cP.

For example, the concentrated slurry may comprise diatomaceous earth and from about 0.01% (w/v) to about 5% (w/v) of one or more dispersants, and have a solids content of from about 20 wt% to about 60 wt% and a viscosity of from about 100cP to about 2000 cP. For example, the concentrated slurry may comprise diatomaceous earth and from about 0.01% (w/v) to about 2% (w/v) of one or more dispersants, and have a solids content of from about 20 wt% to about 50 wt% and a viscosity of from about 100cP to about 1000 cP. For example, the concentrated slurry may comprise diatomaceous earth and from about 0.01% (w/v) to about 2% (w/v) of one or more dispersants, and have a solids content of from about 20 wt% to about 50 wt% and a viscosity of from about 500cP to about 800 cP.

For example, the concentrated slurry may comprise diatomaceous earth and from about 0.01% (w/v) to about 5% (w/v) of one or more dispersants, and have a solids content of from about 30 wt% to about 60 wt% and a viscosity of from about 100cP to about 600 cP. For example, the concentrated slurry may comprise diatomaceous earth and from about 0.01% (w/v) to about 2% (w/v) of one or more dispersants, and have a solids content of from about 35% to about 60% by weight and a viscosity of from about 100cP to about 500 cP. For example, the concentrated slurry may comprise diatomaceous earth and from about 0.01% (w/v) to about 2% (w/v) of one or more dispersants, and have a solids content of from about 40 wt% to about 60 wt% and a viscosity of from about 100cP to about 400 cP.

For example, the concentrated slurry may comprise wollastonite and have a solids content of about 40 wt.% to about 80 wt.% and a viscosity of about 100cP to about 600 cP. For example, the concentrated slurry may comprise wollastonite and have a solids content of about 50 wt% to about 80 wt% and a viscosity of about 100cP to about 500 cP. For example, the concentrated slurry may comprise wollastonite and have a solids content of about 50 wt.% to about 80 wt.% and a viscosity of about 100cP to about 400 cP.

For example, the concentrated slurry may comprise wollastonite and from about 0.01% (w/v) to about 5% (w/v) of one or more dispersants, and have a solids content of from about 40 wt% to about 80 wt% and a viscosity of from about 100cP to about 600 cP. For example, the concentrated slurry may comprise wollastonite and from about 0.01% (w/v) to about 2% (w/v) of one or more dispersants, and have a solids content of from about 50 wt% to about 80 wt% and a viscosity of from about 100cP to about 500 cP. For example, the concentrated slurry may comprise wollastonite and from about 0.01% (w/v) to about 2% (w/v) of one or more dispersants, and have a solids content of from about 60 wt% to about 80 wt% and a viscosity of from about 100cP to about 400 cP.

Aqueous suspensions suitable for use as fertilizers as described herein (aqueous suspensions of minerals having a silica content equal to or greater than about 40% by weight equal to or less than about 10% (w/v)) can be made, for example, from powders or concentrated slurries of minerals having a silica content equal to or greater than about 40% by weight.

Aqueous suspensions suitable for use as fertilizers as described herein may be prepared, for example, by mixing a powder or concentrated slurry of minerals having a silica content equal to or greater than about 40% by weight with an aqueous solvent such as water. Any suitable mixing device may be used.

An aqueous suspension for use as a fertilizer comprises a mineral having a silica content equal to or greater than about 40% by weight. For example, the aqueous suspension used as a fertilizer may consist essentially of, or consist of, minerals having a silica content equal to or greater than about 40% by weight. For example, an aqueous suspension for use as a fertilizer may consist essentially of, or consist of, a mineral having a silica content equal to or greater than about 40% by weight and optionally one or more other additives as described herein. The term "consisting of … …" does not include any additional components not specifically recited. The term "consisting essentially of … …" limits the presence of other additives such that the total amount of additional components is equal to or less than about 10% (w/v), or equal to or less than about 5% (w/v), or equal to or less than about 2% (w/v), or equal to or less than about 1% (w/v).

Aqueous suspensions suitable for use as fertilizers contain equal to or less than about 10% (w/v) mineral matter having a silica content equal to or greater than about 40% by weight. For example, an aqueous suspension for use as a fertilizer may contain equal to or less than about 9.5% (w/v), or equal to or less than about 8% (w/v), or equal to or less than about 7.5% (w/v), or equal to or less than about 7% (w/v), or equal to or less than about 6.5% (w/v), or equal to or less than about 6% (w/v), or equal to or less than about 5.5% (w/v), or equal to or less than about 5% (w/v) equal to or less than about 4.5% (w/v), or equal to or less than about 4% (w/v), or equal to or less than about 3.5% (w/v), or equal to or less than about 3% (w/v), or equal to or less than about 2.5% (w/v), of minerals having a silica content equal to or greater than about 40% by weight. For example, an aqueous suspension for use as a fertilizer may contain equal to or greater than about 0.01% (w/v) of minerals having a silica content equal to or greater than about 40% by weight. For example, an aqueous suspension for use as a fertilizer may contain equal to or greater than about 0.05% (w/v), or equal to or greater than about 0.1% (w/v), or equal to or greater than about 0.5% (w/v), or equal to or greater than about 1% (w/v), or equal to or greater than about 1.5% (w/v), or equal to or greater than about 2% (w/v) of a mineral having a silica content equal to or greater than about 40 wt%. For example, an aqueous suspension for use as a fertilizer may comprise from about 0.01% (w/v) to about 10% (w/v) of a mineral having a silica content equal to or greater than about 40% by weight, or from about 0.05% (w/v) to about 8% (w/v) of a mineral having a silica content equal to or greater than about 40% by weight, or from about 0.05% (w/v) to about 5% (w/v) of a mineral having a silica content equal to or greater than about 40% by weight, or from about 0.5% (w/v) to about 4% (w/v) of a mineral having a silica content equal to or greater than about 40% by weight.

The aqueous suspension comprises an aqueous solvent. For example, the aqueous solvent may be water.

The aqueous suspension for use as a fertilizer may optionally comprise one or more further additives. For example, the aqueous suspension for use as a fertilizer may further comprise one or more other fertilizers. For example, the aqueous suspension for use as a fertilizer may comprise one or more dispersants, one or more wetting agents, one or more thickeners, or any combination thereof.

Examples of dispersants suitable for use in the aqueous suspensions and concentrated slurries described herein may be made, for example, from monomers and/or comonomers selected from the group consisting of: acrylic acid, methacrylic acid, itaconic acid, crotonic acid, fumaric acid, maleic anhydride, isocrotonic acid, aconitic acid (cis or trans), mesaconic acid, sinapic acid, undecylenic acid, angelic acid, canellic acid, hydroxyacrylic acid, acrolein, acrylamide, acrylonitrile, dimethylaminoethyl methacrylate, vinylpyrrolidone, vinylcaprolactam, ethylene, propylene, isobutylene, diisobutylene, vinyl acetate, styrene, alpha-methylstyrene, methyl vinyl ketone, esters of acrylic acid and methacrylic acid, and mixtures thereof. The dispersing agent may for example be polyacrylic acid and/or polymethacrylic acid and/or salts thereof, e.g. sodium polyacrylate, sodium polyacrylate. Nonionic dispersants such as polyethylene glycol and its derivatives are also suitable for use in the aqueous suspensions and concentrated slurries described herein. Carboxymethyl cellulose and hydroxyethyl cellulose are also examples of dispersants suitable for use in the aqueous suspensions and concentrated slurries described herein.

Certain dispersants may also be used as thickeners in the aqueous suspensions and concentrated slurries described herein. For example, cellulose and cellulose derivatives such as carboxymethyl cellulose, hydroxyethyl cellulose and hydrophobically modified cellulose, and polymers of acrylic acid and methacrylic acid may also act as thickeners. For example, polymers of acrylic acid and methacrylic acid modified with hydrophobic copolymers may be used as thickeners.

Other mineral products, such as bentonite and/or attapulgite, may also be used as thickeners.

Other examples of thickeners include ethylene oxide and/or propylene oxide polymers or copolymers, polyethylene oxide (polyethylene glycol), ethylene oxide urethanes, hydrophobically modified hydroxylated urethanes, hydrophobically modified alkali-swellable emulsion thickeners, diisobutylene-maleic anhydride copolymers, tannic acid, itaconic acid, glycerol monostearate, and natural thickeners such as lignin, sulfonated lignin, starch, hydrophobically modified starch, guar gum, gelatin, and xanthan gum.

Examples of wetting agents for use in the aqueous suspensions and concentrated slurries described herein include organosilicones, such as nonionic organosilicones, e.g., methylated silicones.

The one or more other additives may each be present in the aqueous suspension in an amount of from about 0.01% (w/v) to about 5% (w/v). For example, the one or more additional additives may each be present in the aqueous suspension in an amount of from about 0.05% (w/v) to about 4% (w/v), alternatively from about 0.1% (w/v) to about 3% (w/v), alternatively from about 0.5% (w/v) to about 2% (w/v).

The total amount of other additives in the aqueous suspension may be, for example, equal to or less than about 10% (w/v). For example, the total amount of other additives in the aqueous suspension may be equal to or less than about 8% (w/v), or equal to or less than about 6% (w/v), or equal to or less than about 5% (w/v), or equal to or less than about 4% (w/v), or equal to or less than about 2% (w/v). For example, the total amount of other additives in the aqueous suspension may be from about 0.01% (w/v) to about 10% (w/v), or from about 0.1% (w/v) to about 5%.

For example, the total solids content of an aqueous suspension suitable for use as a fertilizer may be equal to or less than about 15% by weight. For example, the total solids content of an aqueous suspension suitable for use as a fertilizer may be equal to or less than about 14 wt%, or equal to or less than about 13 wt%, or equal to or less than about 12 wt%, or equal to or less than about 11 wt%, or equal to or less than about 10 wt%, or equal to or less than about 9 wt%, or equal to or less than about 8 wt%, or equal to or less than about 7 wt%, or equal to or less than about 6 wt%, or equal to or less than about 5 wt%, or equal to or less than about 4 wt%, or equal to or less than about 3 wt%. For example, an aqueous suspension suitable for use as a fertilizer may have a solids content of equal to or greater than about 0.5 wt%, or equal to or greater than about 1 wt%, or equal to or greater than about 1.5 wt%, or equal to or greater than about 2 wt%. For example, aqueous suspensions suitable for use as fertilizers have a total solids content of from about 0.5% to about 15% by weight, or from about 1% to about 10% by weight.

For example, the solid material in the aqueous suspension may comprise equal to or greater than about 90 wt% minerals having a silica content equal to or greater than about 40 wt%. For example, the solid material in the aqueous suspension may comprise equal to or greater than about 92 wt%, or equal to or greater than about 94 wt%, or equal to or greater than about 95 wt%, or equal to or greater than about 96 wt%, or equal to or greater than about 98 wt% of minerals having a silica content equal to or greater than about 40 wt%. For example, the solid material in the aqueous suspension may comprise from about 90 wt% to about 100 wt%, or from about 92 wt% to about 99 wt%, or from about 94 wt% to about 98 wt% of minerals having a silica content equal to or greater than about 40 wt%.

Aqueous suspensions suitable for use as fertilizers and concentrated slurries described herein contain minerals having a silica content equal to or greater than about 40% by weight. The following description of minerals having a silica content of equal to or greater than about 40% by weight, including particle size characteristics, is equally applicable to minerals used in aqueous suspensions and concentrated slurries suitable for use as fertilizers.

The term "mineral" as used herein refers to a naturally occurring inorganic solid material having a fixed structure and chemical composition. The term "silica" as used herein refers to silicon dioxide, SiO₂。

For example, minerals having a silica content of equal to or greater than about 40 wt% may have a silica content of equal to or greater than about 45 wt%, or equal to or greater than about 50 wt%, or equal to or greater than about 55 wt%, or equal to or greater than about 60 wt%, or equal to or greater than about 65 wt%, or equal to or greater than about 70 wt%, or equal to or greater than about 75 wt%, or equal to or greater than about 80 wt%, or equal to or greater than about 85 wt%, or equal to or greater than about 90 wt%. For example, minerals having a silica content of equal to or greater than about 40 wt% can have a silica content of equal to or less than about 100 wt%, or equal to or less than about 99 wt%, or equal to or less than about 95 wt%, or equal to or less than about 90 wt%, or equal to or less than about 80 wt%, or equal to or less than about 70 wt%, or equal to or less than about 60 wt%. For example, minerals having a silica content equal to or greater than about 40 wt% can have a silica content of about 40 wt% to about 99 wt%, or about 40 wt% to about 95 wt%, or about 40 wt% to about 60 wt%, or about 60 wt% to about 99 wt%.

The silica content of the mineral may be determined, for example, by quantitative X-ray diffraction, such as the Rietveld method.

Minerals having a silica content equal to or greater than about 40 wt% can be selected from, for example, diatomaceous earth, wollastonite, zeolites, kaolinites, bentonites, talc, chlorites, and combinations thereof. For example, minerals having a silica content equal to or greater than about 40 weight percent can be selected from diatomaceous earth, wollastonite, or a combination thereof.

Diatomaceous earth (also referred to as "diatomaceous earth" and "DE") is generally a deposit rich in biogenic silica (i.e., silica produced or brought by organisms) in the form of the siliceous framework (frustules) of diatoms. Diatoms are a diverse group of microscopic, unicellular, golden brown algae, generally belonging to the class diatoms (Bacillariophyceae), with an ornate siliceous skeleton, diverse and complex in structure, comprising two valves, which are combined like a kit in live diatoms.

Diatomaceous earth is typically made by processing very finely divided diatomaceous earth (including diatomaceous earth minerals). Generally, natural diatomaceous earth is a sedimentary biogenetic silica deposit (including fossil skeletons or diatoms), a unicellular algae plant that accumulates in marine or freshwater environments. Diatomaceous earth is available from saline or fresh water sources and typically has a honeycomb silica structure, which provides it with useful properties such as absorption capacity, high surface area, chemical stability and low bulk density.

For example, DE may contain one or more natural impurities, such as clays and organics. Prior to its first use, DE may undergo one or more chemical and/or physical modification processes, which may, for example, remove one or more natural impurities. Physical modification processes include, for example, grinding, drying, and classification. Chemical modification processes include, for example, silylation and calcination. Alternatively, the DE may not be treated after mining or extraction prior to first use.

The diatomaceous earth may comprise from about 65% to about 98% by weight silica, such as from about 68% to about 93% by weight silica, or from about 70% to about 90% by weight silica, or from about 80% to about 90% by weight silica. The natural diatomaceous earth may, for example, comprise about 90% by weight silica mixed with other substances. For example, the crude diatomaceous earth may comprise about 90% by weight silica and one or more metal oxides, such as Al, Fe, Ca, and Mg oxides. For example, DE may comprise from about 1 wt% to about 5 wt%, e.g., from about 2 wt% to about 4 wt%, of alumina (Al)₂O₃). For example, the DE may comprise from about 0.1 wt% to about 4 wt%, such as from about 0.5 wt% to about 2 wt%, iron oxide.

Wollastonite is a calcium silicate mineral (CaSiO)₃) It may contain small amounts of iron, magnesium and/or manganese in place of calcium. It is typically formed when impure limestone or dolomitic rock is subjected to high temperatures and pressures, sometimes in the presence of a siliceous fluid.

For example, the wollastonite can comprise about 40 weight percent to about 60 weight percent silica, such as about 42 weight percent to about 53 weight percent silica, or about 45 weight percent to about 52 weight percent silica, or about 48 weight percent to about 52 weight percent silica.

Depending on the acid extraction process, for example, the Si availability of minerals having a silica content equal to or greater than about 40 wt% may be equal to or greater than about 3%. Depending on the acid extraction process, for example, the mineral having a silica content of equal to or greater than about 40 wt% may have a Si availability of equal to or greater than about 4%, or equal to or greater than about 5%, or equal to or greater than about 6%, or equal to or greater than about 7%, or equal to or greater than about 8%, or equal to or greater than about 9%, or equal to or greater than about 10%, or equal to or greater than about 11%, or equal to or greater than about 12%, or equal to or greater than about 13%, or equal to or greater than about 14%, or equal to or greater than about 15%, or equal to or greater than about 16%. Depending on the acid extraction process, for example, the mineral having a silica content of equal to or greater than about 40 wt% may have a Si availability of equal to or less than about 50%, or equal to or less than about 40%, or equal to or less than about 30%, or equal to or less than about 25%, or equal to or less than about 20%, or equal to or less than about 18%. Depending on the acid extraction process, for example, the mineral having a silica content equal to or greater than about 40 wt% may have a Si availability of about 3% to about 50%, alternatively about 5% to about 40%, alternatively about 6% to about 30%, alternatively about 8% to about 25%, alternatively about 10% to about 25%, alternatively about 12% to about 20%.

Acid extraction methods (NIAES, 1987) are disclosed in Masayoshi Koshino: second review of The Methods of Analysis of fetilizers (Details), page 144-146, Yoknendo, Tokyo (1988), The contents of which are incorporated herein by reference. The process uses a test portion of 1g of mineral having a silica content equal to or greater than about 40% by weight, which is stirred with 150ml of HCl at about 30 ℃ for 1 hour, then cooled to room temperature and filtered. Si availability was determined by using additional HCl, potassium fluoride solution that converted soluble silica to fluorosilicic acid (H)₂SiF₆) The reaction of fluorosilicic acid with added potassium chloride forms a large amount of potassium fluorosilicate (K)₂SiF₆) And (4) precipitating. The precipitate is treated with a base (K)₂SiF₆+4NaOH->2KF+4NaF+H₄SiO₄) And (4) titrating. This process is further described in the examples below.

Depending on the alkali extraction process, for example, the Si availability of minerals having a silica content equal to or greater than about 40 wt% may be equal to or greater than about 1%. Depending on the alkali extraction process, for example, the mineral having a silica content of equal to or greater than about 40 wt% may have an Si availability of equal to or greater than about 1.5%, or equal to or greater than about 2%, or equal to or greater than about 2.5%, or equal to or greater than about 3%, or equal to or greater than about 3.5%, or equal to or greater than about 4%, or equal to or greater than about 4.5%, or equal to or greater than about 5%, or equal to or greater than about 5.5%, or equal to or greater than about 6%. Depending on the alkali extraction process, for example, the Si availability of minerals having a silica content equal to or greater than about 40 wt% may be equal to or less than about 20%, or equal to or less than about 15%, or equal to or less than about 10%, or equal to or less than about 8%. Depending on the alkaline extraction process, for example, the Si availability of minerals having a silica content equal to or greater than about 40 wt% may be from about 1% to about 20%, alternatively from about 2% to about 15%, alternatively from about 2% to about 10%.

The alkali extraction method is described in Sebastian et al, Journal of AOAC International, Vol.96, No. 2, 2013, which is incorporated herein by reference. 0.2g of a test portion of minerals having a silica content equal to or greater than about 40% by weight was added to 100ml of Na₂CO₃Solution (0.094M) and 100ml of NH₄NO₃Solution (0.20M) and stirred for 1 hour. The sample was left undisturbed for 5 days, and then Si availability was determined colorimetrically at a wavelength of 660nm using ammonium molybdate complex on a U2001 Hitachi spectrophotometer. Tartaric acid was added to complex all the phosphorus in the solution. Standard silicon curves were 0, 0.5, 1.0 and 2.0 mg/l.

According to CaCl₂Extraction methods, for example, the Si availability of minerals having a silica content equal to or greater than about 40 wt% can be equal to or greater than about 0.001%. According to CaCl₂Extraction methods, for example, minerals having a silica content of equal to or greater than about 40 wt% can have a Si availability of equal to or greater than about 0.005%, or equal to or greater than about 0.01%, or equal to or greater than about 0.05%, or equal to or greater than about 0.1%. According to CaCl₂Extraction methods, for example, minerals having a silica content of equal to or greater than about 40 wt% may have a Si availability of equal to or less than about 5%, or equal to or less than about 2%, or equal to or less than about 1%, or equal to or less than about 0.5%. According to alkaline extraction methods, e.g. silicaThe mineral content equal to or greater than about 40 wt% may have an Si availability of about 0.001% to about 5%, alternatively about 0.005% to about 2%, alternatively about 0.01% to about 1%.

CaCl₂The extraction method uses 1g of a test portion of minerals having a silica content equal to or greater than about 40% by weight. The test portion was mixed with 100ml of 0.01M CaCl₂The solution was stirred for 2 hours (Korndorfer et al, 1999). The solution was then filtered and the Si content determined by ICP-OES atomic spectroscopy (Jones and Dreher, 1996).

For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₅₀And may be equal to or less than about 50 μm. E.g. d of said minerals₅₀May be equal to or less than about 45 μm, or equal to or less than about 40 μm, or equal to or less than about 35 μm, or equal to or less than about 30 μm, or equal to or less than about 25 μm, or equal to or less than about 20 μm, or equal to or less than about 15 μm, or equal to or less than about 10 μm, or equal to or less than about 5 μm, or equal to or less than about 3 μm. E.g. d of said minerals₅₀May be equal to or greater than about 0.1 μm, or equal to or greater than about 0.5 μm, or equal to or greater than about 1 μm, or equal to or greater than about 2 μm, or equal to or greater than about 3 μm, or equal to or greater than about 4 μm, or equal to or greater than about 5 μm. E.g. d of said minerals₅₀May be from about 0.1 μm to about 50 μm, alternatively from about 0.1 μm to about 10 μm, alternatively from about 0.1 μm to about 5 μm, alternatively from about 0.1 μm to about 3 μm, alternatively from about 0.5 μm to about 10 μm, alternatively from about 0.5 μm to about 5 μm, alternatively from about 0.5 μm to about 3 μm, alternatively from about 4 μm to about 10 μm.

When the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₅₀May be equal to or less than about 5 μm, or equal to or less than about 4.5 μm, or equal to or less than about 4 μm, or equal to or less than about 3.5 μm, or equal to or less than about 3 μm. When the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₅₀May be equal to or greater than about 0.1 μm, or equal to or greater than about 0.5 μm, or equal to or greater than about 1 μm.For example, when the mineral having a silica content equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₅₀May be from about 0.1 μm to about 5 μm, alternatively from about 0.5 μm to about 4 μm, alternatively from about 0.5 μm to about 3 μm.

When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₅₀May be equal to or less than about 10 μm, or equal to or less than about 9.5 μm, or equal to or less than about 9 μm, or equal to or less than about 8.5 μm, or equal to or less than about 8 μm. When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₅₀May be equal to or greater than about 4 μm, or equal to or greater than about 4.5 μm, or equal to or greater than about 5 μm, or equal to or greater than about 5.5 μm, or equal to or greater than about 6 μm. For example, when the mineral having a silica content equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₅₀Can be from about 4 μm to about 10 μm, alternatively from about 5 μm to about 9 μm, alternatively from about 6 μm to about 8 μm.

For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₉₀And may be equal to or less than about 80 μm. For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₉₀May be equal to or less than about 75 μm, or equal to or less than about 70 μm, or equal to or less than about 65 μm, or equal to or less than about 60 μm, or equal to or less than about 55 μm, or equal to or less than about 50 μm, or equal to or less than about 45 μm, or equal to or less than about 40 μm, or equal to or less than about 35 μm. For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₉₀May be equal to or greater than about 5 μm, or equal to or greater than about 10 μm, or equal to or greater than about 15 μm, or equal to or greater than about 20 μm. For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₉₀May be from about 5 μm to about 80 μm, alternatively from about 5 μm to about 70 μm, alternatively from about 5 μm to about 60 μm, alternatively from about 5 μm to about 50 μm, alternatively from about 5 μm to about 20 μm, alternatively from about 5 μm to about 10 μm.

When the silica content is equal to or greater than aboutWhen 40% by weight of the mineral is diatomaceous earth, the mineral has a d₉₀And may be equal to or less than about 15 μm. For example, when the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₉₀May be equal to or less than about 14 μm, or equal to or less than about 13 μm, or equal to or less than about 12 μm, or equal to or less than about 11 μm, or equal to or less than about 10 μm, or equal to or less than about 9 μm, or equal to or less than about 8 μm. When the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₉₀May be equal to or greater than about 4 μm, or equal to or greater than about 4.5 μm, or equal to or greater than about 5 μm, or equal to or greater than about 5.5 μm, or equal to or greater than about 6 μm. For example, when the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₉₀Can be from about 4 μm to about 15 μm, or from about 5 μm to about 10 μm.

When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₉₀And may be equal to or less than about 25 μm. For example, when the mineral having a silica content equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₉₀And may be equal to or less than 20 μm, or equal to or less than about 15 μm, or equal to or less than about 10 μm, or equal to or less than about 8 μm. When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₉₀May be equal to or greater than about 5 μm, or equal to or greater than about 5.5 μm, or equal to or greater than about 6 μm, or equal to or greater than about 10 μm, or equal to or greater than about 15 μm. When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₉₀May be from about 5 μm to about 25 μm, alternatively from about 5 μm to about 20 μm, alternatively from about 6 μm to about 15 μm, alternatively from about 6 μm to about 10 μm.

For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₁₀And may be equal to or less than about 5 μm. For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₁₀May be equal to or less than about 4 μm, or equal to or less than about 3 μm, or equal to or less than about 2 μm, or equal to or less than about 1 μm, or equal to or less than about 0.5 μm, or equal to or less than about 0.2 μm. For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₁₀May be equal to or greater than about 0.01 μm, or equal to or greater than about 0.05 μm, or equal to or greater than about 0.1 μm. For example, d for minerals having a silica content of equal to or greater than about 40 weight percent₁₀Can be from about 0.01 μm to about 5 μm, alternatively from about 0.05 μm to about 2 μm, alternatively from about 0.1 μm to about 1 μm, alternatively from about 0.1 μm to about 0.5 μm.

When the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₁₀And may be equal to or less than about 2 μm. For example, when the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₁₀And may be equal to or less than about 1.5 μm, or equal to or less than about 1 μm. When the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₁₀May be equal to or greater than about 0.05 μm, or equal to or greater than about 0.1 μm, or equal to or greater than about 0.5 μm. For example, when the mineral having a silica content of equal to or greater than about 40% by weight is diatomaceous earth, the mineral has a d₁₀Can be about 0.05 μm to about 2 μm, or about 0.1 μm to about 1 μm.

When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₁₀And may be equal to or less than about 3 μm. For example, when the mineral having a silica content equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₁₀And may be equal to or less than 2.5 μm, or equal to or less than about 2 μm. When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₁₀May be equal to or greater than about 0.1 μm, or equal to or greater than about 0.5 μm, or equal to or greater than about 1 μm. When the mineral having a silica content of equal to or greater than about 40 weight percent is wollastonite, the mineral has a d₁₀Can be from about 0.1 μm to about 3μ m, alternatively from about 0.5 μm to about 2.5 μm, alternatively from about 0.1 μm to about 2 μm.

The particle size characteristics referred to herein are measured by precipitation of the particulate material in an aqueous medium under conditions of complete dispersion in a well-known manner using a Sedigraph 5100 machine (referred to herein as the "Micromeritics Sedigraph 5100 unit") supplied by Micromeritics Instruments Corporation, Norcross, Georgia, USA (www.micromeritics.com) and based on the application of stokes law. Such machines provide measurements and maps of the cumulative weight percent of particles of a certain size, known in the art as the "equivalent spherical diameter" (e.s.d), which is less than a given e.s.d value. Average particle diameter d₅₀The value of the particles e.s.d is determined in such a way that 50% by weight of the particles have a value smaller than d₅₀Equivalent spherical diameter of value. The particle size characteristics may be determined according to ISO 13317-3 or its equivalent.

The mineral having a silica content of equal to or greater than about 40 wt% for use in the aqueous suspensions and concentrated slurries described herein can be, for example, diatomaceous earth and has a d from about 0.5 μm to about 2.5 μm₅₀. For example, a mineral having a silica content equal to or greater than about 40 weight percent can be d₅₀Is about 0.5 μm to about 2.5 μm and d₉₀Diatomaceous earth equal to or less than about 10 μm. For example, a mineral having a silica content equal to or greater than about 40 weight percent can be d₅₀Is about 0.5 μm to about 2.5 μm and d₉₀Equal to or less than about 10 μm and d₁₀Diatomaceous earth equal to or less than about 1 μm. For example, a mineral having a silica content equal to or greater than about 40 weight percent can be d₅₀Is about 0.5 μm to about 2.5 μm and d₉₀Is about 4 μm to about 10 μm and d₁₀Diatomaceous earth ranging from about 0.1 μm to about 0.5 μm.

The mineral having a silica content of equal to or greater than about 40 weight percent for use in the aqueous suspensions and concentrated slurries described herein can be, for example, wollastonite and has a d of from about 5 μm to about 10 μm₅₀. For example, a mineral having a silica content equal to or greater than about 40 weight percent can be d₅₀Is from about 5 μm to about 10 μm and d₉₀Equal to or less than about 20Mu m wollastonite. For example, a mineral having a silica content equal to or greater than about 40 weight percent can be d₅₀Is from about 5 μm to about 10 μm and d₉₀Equal to or less than about 20 μm and d₁₀Wollastonite of about 5 μm or less. For example, a mineral having a silica content equal to or greater than about 40 weight percent can be d₅₀Is from about 5 μm to about 10 μm and d₉₀Is about 10 μm to about 15 μm and d₁₀Wollastonite of about 0.5 μm to about 5 μm.

The aqueous suspensions described herein are useful as plant fertilizers. For example, the aqueous suspensions described herein may be used in a method of fertilizing a plant, which may, for example, comprise applying the aqueous suspension to a seed, a plant, or a growing substrate (e.g., soil) surrounding the seed or plant. The term "growth substrate" refers to any material from which a seed or plant can obtain nutrients to aid in its growth and development, such as soil, compost, minerals, hydroponics, or combinations thereof. The term "seed or plant environment" refers to any area from which a seed or plant can acquire nutrients to aid in its growth and development. This may depend on the type and size of the seed or plant (e.g. the length of its roots). The aqueous suspension may be applied, for example, to a growth substrate (e.g., soil) within about 1m of the seed or plant, or within about 0.5m of the seed or plant, or within about 0.3m of the seed or plant, or within about 0.2m of the seed or plant.

For example, the aqueous suspension may be applied to the seed, the plant, or a growing substrate (e.g., soil) surrounding the seed or plant by any suitable means. The aqueous suspension may be applied to the seed, the plant or a growth substrate (e.g. soil) surrounding the seed or plant, for example by spraying, for example by foliar spraying (spraying directly onto the leaves of the plant). For example, the aqueous suspension may be applied to the seed, the plant, or a growth substrate (e.g., soil) surrounding the seed or plant by an irrigation system (i.e., by fertigation).

For example, each treatment of the aqueous suspension may be applied such that the mineral matter having a silica content equal to or greater than about 40 wt.% is applied in an amount of from about 1kg/ha to about 40kg/ha, such as from about 5kg/ha to about 30kg/ha, or from about 10kg/ha to about 25kg/ha, or from about 15kg/ha to about 20 kg/ha.

Treatment with one or more aqueous suspensions containing minerals having a silica content equal to or greater than about 40% by weight may be applied to the plants. For example, two or three treatments may be performed using the aqueous suspension. For example, up to six or up to five or up to four treatments may be performed using the aqueous suspension.

The aqueous suspension may be used as a fertilizer for any suitable plant. The plant may for example be selected from cereals (e.g. wheat, barley, oats, rye, corn, maize, rice, sorghum, millet), legumes (e.g. kidney beans, lima beans, black beans, broad beans, peas, chickpeas, lentils, dried beans), fruits, vegetables and nuts. For example, the plant may be wheat or lettuce.

For example, the aqueous suspension may be applied to the seed or plant at any suitable stage of its growth and development.

For example, when the plant is wheat, the aqueous suspension may be applied at and/or after the visible flag leaf stage (Zadock stage GS 47). For example, the aqueous suspension may be administered to wheat at and/or after Zadock stage GS59 and/or at and/or after Zadock stage GS 75. For example, the aqueous suspension may be applied to all Zadock stages GS47, GS59 and GS 75.

For example, the use of an aqueous suspension as a fertilizer can increase the yield of plants. For example, the yield of a plant can be increased by at least about 2%, or at least about 3%, or at least about 4%, or at least about 5%, or at least about 6% as compared to the yield without treatment with an aqueous suspension comprising a mineral having a silica content equal to or greater than about 40% by weight. For example, the yield may be increased by up to about 20%, or up to about 10%, or up to about 8% as compared to the yield without treatment with an aqueous suspension comprising a mineral having a silica content equal to or greater than about 40% by weight.

For example, the use of an aqueous suspension as a fertilizer may increase the protein content of a plant. For example, the protein content of the plant can be increased by at least about 1% (i.e., 1 percentage point), alternatively at least about 2%, alternatively at least about 3%, alternatively at least about 4%, alternatively at least about 5%, alternatively at least about 6%, as compared to the protein content of a plant not treated with an aqueous suspension comprising a mineral having a silica content equal to or greater than about 40% by weight. For example, the protein content of the plant may be increased by up to about 20%, or up to about 10%, or up to about 8% as compared to the protein content without treatment with an aqueous suspension comprising a mineral having a silica content equal to or greater than about 40% by weight.

The following numbered paragraphs define specific embodiments of the present invention:

1. use of an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40 wt% as a plant fertiliser, wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral.

2. A method of fertilizing a plant, the method comprising:

preparing an aqueous suspension comprising a mineral having a silica content of equal to or greater than about 40% by weight from a powder or concentrated slurry of the mineral having a silica content of equal to or greater than about 40% by weight, and

applying the aqueous suspension to a seed, plant, or growing substrate, such as soil surrounding a seed or plant, wherein the aqueous suspension comprises equal to or less than about 10% (w/v) mineral matter.

3. The use of paragraph 1 or the method of paragraph 2 wherein the mineral has a silica content of equal to or greater than about 45 wt%, or equal to or greater than about 65 wt%.

4. The use or method of any preceding paragraph, wherein the mineral is diatomaceous earth, wollastonite, or a combination thereof.

5. The use or method of any preceding paragraph, wherein d of the mineral is₅₀(Settlement diagram) equal to or greater than about 0.1 μm and/or equal to or less than about 50 μm.

6. The use or method of any preceding paragraph, wherein d of the mineral is₉₀(Settlement diagram) equal to or greater than about 5 μm and/or equal toOr less than about 80 μm.

7. The use or method of any preceding paragraph, wherein d of the mineral is₁₀(Settlement diagram) equal to or greater than about 0.01 μm and/or equal to or less than about 5 μm.

8. The use or method of any preceding paragraph, wherein the aqueous suspension comprises equal to or greater than about 0.01% (w/v) mineral.

9. The use or method of any preceding paragraph, wherein the aqueous suspension comprises about 0.5 wt% to about 5 wt% (w/v) mineral substance.

10. The use or method of any preceding paragraph, wherein the aqueous suspension has a total solids content of equal to or less than about 15 wt% and/or equal to or greater than about 0.5 wt%.

11. The use or method of any preceding paragraph, wherein the aqueous suspension is applied to the seed or plant by foliar spraying.

12. The use or method of any preceding paragraph, wherein the aqueous suspension is applied to the seed or plant or growth substrate, for example the soil surrounding the seed or plant, by an irrigation system.

13. The use or method of any preceding paragraph, wherein the yield of the plant is increased, and/or wherein the protein content of the plant is increased.

14. The use or method of any preceding paragraph, wherein the plant is wheat or lettuce.

15. The use or method of any preceding paragraph, wherein the aqueous suspension is prepared by diluting the concentrated slurry of any one of paragraphs 16 to 40.

16. A concentrated slurry of minerals having a silica content equal to or greater than about 40 wt%, wherein the concentrated slurry has a solids content equal to or greater than about 20 wt% or equal to or greater than about 30 wt% and a viscosity of about 60cP to about 2000cP or about 60cP to about 700 cP.

17. The concentrated slurry of paragraph 16, wherein the concentrated slurry further comprises one or more dispersants, one or more thickeners, one or more wetting agents, or a combination thereof.

18. The concentrated slurry of paragraphs 16 or 17, wherein the concentrated slurry comprises about 0.5 wt% to about 2 wt% total dispersant.

19. The concentrated slurry of any of paragraphs 16 to 18, wherein the mineral having a silica content of equal to or greater than about 40% by weight is wollastonite.

20. The concentrated slurry of paragraph 19 wherein the wollastonite has a d₅₀(Settlement diagram) equal to or less than about 10 μm, for example equal to or less than about 9 μm, for example equal to or less than about 8 μm.

21. The concentrated slurry of paragraph 19 or 20 wherein the wollastonite has a d₅₀(Settlement diagram) equal to or greater than about 4 μm, such as equal to or greater than about 5 μm, such as equal to or greater than about 6 μm.

22. The concentrated slurry of any of paragraphs 19 to 21, wherein the d of wollastonite₉₀(Settlement diagram) equal to or less than about 25 μm, for example equal to or less than about 20 μm, for example equal to or less than about 10 μm.

23. The concentrated slurry of any of paragraphs 19 to 22, wherein the d of wollastonite₉₀(Settlement diagram) equal to or greater than about 5 μm, such as equal to or greater than about 10 μm, such as equal to or greater than about 15 μm.

24. The concentrated slurry of any of paragraphs 19 to 23, wherein the d of wollastonite₁₀(Settlement diagram) equal to or less than about 3 μm, for example equal to or less than about 2 μm, for example equal to or less than about 1 μm.

25. The concentrated slurry of any of paragraphs 19 to 24, wherein the d of wollastonite₁₀(Settlement diagram) equal to or greater than about 0.1. mu.m, such as equal to or greater than about 0.5. mu.m, such as equal to or greater than about 1 μm.

26. The concentrated slurry of any of paragraphs 19 to 25, wherein the concentrated slurry has a solids content of equal to or greater than about 50 wt.%, such as equal to or greater than about 60 wt.%, such as equal to or greater than about 70 wt.%.

27. The concentrated slurry of any of paragraphs 19 to 26, wherein the concentrated slurry has a solids content of equal to or less than about 85 wt.%, or equal to or less than about 80 wt.%, or equal to or less than about 75 wt.%.

28. The concentrated slurry of any of paragraphs 19 to 27, wherein the concentrated slurry has a viscosity equal to or less than about 500cP, for example equal to or less than about 400 cP.

29. The concentrated slurry of any of paragraphs 19 to 28, wherein the viscosity of the concentrated slurry is equal to or greater than about 200cP, for example equal to or greater than about 300 cP.

30. The concentrated slurry of any of paragraphs 16 to 18, wherein the mineral matter having a silica content equal to or greater than about 40% by weight is diatomaceous earth.

31. The concentrated slurry of paragraph 30 wherein d of diatomaceous earth₅₀(Settlement diagram) equal to or less than about 5 μm, for example equal to or less than about 4 μm, for example equal to or less than about 3 μm.

32. The concentrated slurry of paragraphs 30 or 31 wherein the d of the diatomaceous earth₅₀(Settlement diagram) equal to or greater than about 0.5 μm, for example equal to or greater than about 1 μm.

33. The concentrated slurry of any of paragraphs 30 to 32, wherein d of the diatomaceous earth₉₀(Settlement diagram) equal to or less than about 15 μm, for example equal to or less than about 10 μm, for example equal to or less than about 8 μm.

34. The concentrated slurry of any of paragraphs 30 to 33, wherein d of the diatomaceous earth₉₀(Settlement diagram) equal to or greater than about 4 μm, such as equal to or greater than about 5 μm, such as equal to or greater than about 6 μm.

35. The concentrated slurry of any of paragraphs 30 to 34, wherein d of the diatomaceous earth₁₀(Settlement diagram) equal to or less than about 2 μm, for example equal to or less than about 1 μm, for example equal to or less than about 0.5 μm.

36. The concentrated slurry of any of paragraphs 30 to 35, wherein d of the diatomaceous earth₁₀(Settlement diagram) equal to or greater than about 0.05 μm, such as equal to or greater than about 0.1 μm, such as equal to or greater than about 0.2 μm.

37. The concentrated slurry of any of paragraphs 30 to 36, wherein the concentrated slurry has a solids content of equal to or greater than about 30 wt%, for example equal to or greater than about 35 wt%.

38. The concentrated slurry of any of paragraphs 30 to 37, wherein the solids content of the concentrated slurry is equal to or less than about 60 wt.%, or equal to or less than about 50 wt.%, or equal to or less than about 40 wt.%.

39. The concentrated slurry of any of paragraphs 30 to 38, wherein the concentrated slurry has a viscosity equal to or less than about 700cP, for example equal to or less than about 600cP, for example equal to or less than about 500 cP.

40. The concentrated slurry of any of paragraphs 30 to 39, wherein the concentrated slurry has a viscosity equal to or greater than about 200cP, for example equal to or greater than about 300 cP.

41. A method of making the concentrated slurry of any of paragraphs 16 to 40, comprising mixing a mineral matter having a silica content of equal to or greater than about 40% by weight with water and optionally one or more dispersants, one or more thickeners, one or more wetting agents, or a combination thereof.

42. A method of preparing an aqueous suspension comprising equal to or less than about 10% (w/v) of a mineral substance having a silica content equal to or greater than about 40% by weight, the method comprising diluting the concentrated slurry of any one of paragraphs 16 to 40.

Examples

Example 1

Materials and methods

The effect of treatment with Diatomaceous Earth (DE) or wollastonite (W) on lettuce growth was determined.

The DE tested had a d of 1.28 μm₅₀(Settlement diagram) and d of 11.7 μm₅₀(laser).

W tested had a d of 12 μm₅₀(laser).

D of DE and W₅₀(laser) is measured by laser diffraction, for example using an instrument available from Malvern Panalytical or Microtrac.

Application of the samples was carried out in a commercial plastic greenhouse lettuce culture in the Chrysoupoli (Kavala, North Greece) area. Each sample was applied at 2 doses (20kg/ha and 200kg/ha) 1 week after transplantation into 0.1 hectare of hydroponic culture. The samples were aqueous suspensions of DE or W with a mineral content of 2% (W/v) and were applied by fertigation.

Lettuce plants with 4 leaves were transplanted at a distance of 20cm within a row of lettuce plants and at a distance of 40cm between rows of lettuce plants. The experiment was repeated in 3 plots per treatment.

Visual assessment of nutritional deficiencies or phytotoxicity was achieved throughout the experiment.

Samples were taken 2 months after transplantation at the commercial harvest stage and the overall yield was assessed. The total yield was estimated as the average of 3 plots per treatment. Plant size was assessed based on a random sampling of 70 plants per treatment.

The overall yield is expressed in tons per 0.1 hectare. After the foreign matter was removed, the weight of the individual plants was weighed to two decimal places.

To determine the nutrient content of the leaves, the plant tissue was washed, dried, ashed, then the trace and macro elements were extracted and measured in inductively coupled plasma emission spectroscopy (ICP-OES). The total nitrogen content was measured in a Kjeldahl system (Kjeldahl system).

Statistical analysis was performed by ANOVA analysis using the SPSS statistical package (SPSS v21.0, Chicago, USA). Different letters indicate statistically significant differences according to the Duncan multiple difference test with a significance level p of 0.05.

Results

During visual inspection of the lettuce cultures under greenhouse conditions, no signs of nutrient deficiency or phytotoxicity were observed.

The yield difference is shown in Table 1.

TABLE 1

The data obtained from this experiment show that lettuce treated with 20kg/ha of DE increased by 5.3 tonnes per hectare. Despite the high crop density, the overall yield increased by 7.6% compared to the control.

The average size of each lettuce (n ═ 70) at harvest after fertilization with DE and W at concentrations of 0 (control), 20 and 200kg/ha is shown in table 2.

TABLE 2

The size of individual lettuce treated with 20kg/ha of DE increases significantly, which increases the commercial value of the crop.

According to nutrient analysis, the total nitrogen concentration increased after DE treatment at concentrations of 200kg/ha and 200 kg/ha. The phosphorus concentration increased in response to DE treatment at 20kg/ha and 200 kg/ha. Manganese concentrations increased in response to 20kg/ha of DE and W treatment. The zinc concentration increased in response to DE treatment at 200kg/ha and in response to W treatment at 20kg/ha and 200 kg/ha. The iron concentration increased after treatment with 20kg/ha and 200kg/ha of W. The copper concentration increased after DE and W treatment at 200 kg/ha.

Example 2

The effect of treatment with Diatomaceous Earth (DE) or wollastonite (W) on wheat growth was determined. The same DE and W as used in example 1 were used in this example.

The following treatments were tested:

treatment 1: spraying DE once on the leaf surface of a visible flag leaf stage (Zadock stage GS47)

And (3) treatment 2: spraying W once on the leaf surface of a visible flag leaf stage (Zadock stage GS47)

And (3) treatment: spraying three times on leaves (first spraying in visible flag leaf stage (Zadock stage GS47), second spraying two weeks later (Zadock stage GS59), third spraying two weeks later (Zadock stage GS75))

And (4) treatment: spraying three times on leaves (spraying for the first time in the visible flag leaf stage (Zadock stage GS47), spraying for the second time two weeks after the first spraying (Zadock stage GS59), spraying for the third time two weeks after the second spraying (Zadock stage GS75))

And (4) treatment 5: control treatment (without foliar fertiliser)

The experiments were performed in Sessajou, Greece. The experiment included four replicates of each treatment in a fully randomized block design. It consists of 20 plots, 5m x 9m in size.

The treatment groups were sprayed onto the tree crowns 30cm using a field sprayer equipped with a fan nozzle operating at 3 bar pressure. Sprayed (5% (w/v)) with a dose of 20kg/ha diluted with 400l/ha of water.

During harvest, seed and shoot samples were collected from each plot. The moisture content was estimated by overdrying the seed samples for 24 hours to 105 ℃. Seed samples were used to evaluate weight per liter, protein content, gluten content, and grain color. The nutrient composition was evaluated using seed and shoot samples. Grain and sprout samples are analyzed using a Near Infrared (NIR) analyzer (e.g., Foss model GRAINANALYSER Mill or percen 8800).

The average yield was estimated after normalizing the results for the fresh weight of seeds for all treatments based on a common moisture of 10%.

Results

The grain yield and quality parameters obtained for each treatment are shown in table 3.

TABLE 3

Seed protein in the treated wheat was up to 1% (1 percentage point) higher compared to the control.

In terms of average yield, treatment 1 was 4.9t/ha, treatment 2 was 5.02t/ha, treatment 3 was 4.85t/ha, treatment 4 was 4.94t/ha, and treatment 5 was 4.81 t/ha.

Example 3

The diatomaceous earth minerals used in examples 1 and 2 above were formulated into a concentrated slurry (DE 1). Additional diatomaceous earth minerals (DE 2) and wollastonite minerals (W) were also formulated as concentrated slurries.

A 7 wt% suspension of each mineral in a 0.2 wt% sodium hexametaphosphate solution was prepared. The particle size distribution of the minerals was determined from the sedimentation diagram. The results are shown in Table 4.

TABLE 4

	d50(μm)	d10(μm)	d90(μm)
				W	6.71	1-1.5	～20
DE 1	1.28	<0.3	～5-6
				DE 2	1.96	～0.4	～8-10

Each mineral was then gradually added to 200mL of tap water at room temperature or a 1% sodium polyacrylate solution at room temperature with stirring. The samples were mixed under high shear for 5 minutes prior to viscosity testing or observation. The fluidity of the viscosity of the slurry was visually evaluated. The highest percent solids obtained in each case was determined by the ability to visually observe the free flow and agitation of the suspension without significant resistance. The results are shown in Table 5.

TABLE 5

The viscosity of each mineral was then analyzed in 100mL of water and the solids content was gradually increased. The samples were mixed under high shear for 5 minutes prior to viscosity testing. Similarly, minerals are gradually added to the aqueous sodium polyacrylate solution. The viscosity was measured using a Brookfield DV2T viscometer, spindle 3 running at 100 rpm. The percent solids to achieve 500cP and 800cP is reported in Table 6 below.

TABLE 6

The viscosities of the various slurries of W and DE1 used in this example were also measured using a Brookfield DV2T LV viscometer with spindle 3 running at 20rpm (wollastonite) or spindle 5 running at 20rpm (DE). Viscosity measurements were made directly after mixing the slurries at room temperature. The results are shown in Table 7.

TABLE 7

The foregoing describes certain embodiments of the present invention broadly and without limitation. Variations and modifications which are obvious to a person skilled in the art are intended to be included within the scope of the invention as defined by the accompanying claims.