The present invention relates to a method for preparing a humic acid-containing synergistic carrier for accelerating urea conversion. The preparation method includes steps of, for example, preparing an extractant for humic acid, preparing a humic acid extract and preparing a humic acid-containing synergistic carrier. Combination of the humic acid-containing synergistic carrier with urea can accelerate urea conversion, and the residual urea rate will be reduced by 22.7%-29.1% than a commercially available urea. The present invention provides a new idea for improving the utilization rate of nitrogen fertilizer in soil with low urease activity. Compared with a commercially available urea, the urea containing the humic acid-containing synergistic carrier of the present invention can increase the rice yield and the utilization rate of nitrogen fertilizer by 9.7% and 8.3%, respectively.

An anticaking agent having a coating and a mineral matrix of a coarse mineral and a fine mineral is described. A method of making the anticaking agent is disclosed, as well as a method of applying the anticaking agent to a hygroscopic fertilizer to reduce caking in high temperature and high humidity environments. The coarse mineral may be a diatomaceous earth.

An anticaking agent having a coating and a mineral matrix of a coarse mineral and a fine mineral is described. A method of making the anticaking agent is disclosed, as well as a method of applying the anticaking agent to a hygroscopic fertilizer to reduce caking in high temperature and high humidity environments. The coarse mineral may be a diatomaceous earth.

An improved solvent system for the formulation and application of N-alkyl thiophosphoric triamide urease inhibitors. These formulations provide safety and performance benefits relative to existing alternatives and enable storage, transport and subsequent coating or blending with urea based or organic based fertilizers. These formulations are comprised primarily of environmentally friendly aprotic and protic solvents (particularly dimethyl sulfoxide and alcohols/polyols) to stabilize the urease inhibitor.

An improved solvent system for the formulation and application of N-alkyl thiophosphoric triamide urease inhibitors. These formulations provide safety and performance benefits relative to existing alternatives and enable storage, transport and subsequent coating or blending with urea based or organic based fertilizers. These formulations are comprised primarily of environmentally friendly aprotic and protic solvents (particularly dimethyl sulfoxide and alcohols/polyols) to stabilize the urease inhibitor.

Disclosed are compositions and methods of making a liquid fertilizer additive of biodegradable polymeric and/or oligomeric nitrification inhibitors comprised of utilizing a non-aqueous polar, aprotic organo liquid (NAPAOL) as the reaction medium for the reaction of aldehyde(s) with cyano-containing nitrification inhibitors that have one or more aldehyde reactive groups selected from the group consisting of a) primary, b) secondary amines, c) amides, d) thiols, e) hydroxyls and f) phenols.

Disclosed are compositions and methods of making a liquid fertilizer additive of biodegradable polymeric and/or oligomeric nitrification inhibitors comprised of utilizing a non-aqueous polar, aprotic organo liquid (NAPAOL) as the reaction medium for the reaction of aldehyde(s) with cyano-containing nitrification inhibitors that have one or more aldehyde reactive groups selected from the group consisting of a) primary, b) secondary amines, c) amides, d) thiols, e) hydroxyls and f) phenols.

An improved solvent system for the formulation and application of N-alkyl thiophosphoric triamide urease inhibitors. These formulations provide safety and performance benefits relative to existing alternatives and enable storage, transport and subsequent coating or blending with urea based or organic based fertilizers. These formulations are comprised primarily of environmentally friendly aprotic and protic solvents (particularly dimethyl sulfoxide and alcohols/polyols) to stabilize the urease inhibitor.

An improved solvent system for the formulation and application of N-alkyl thiophosphoric triamide urease inhibitors. These formulations provide safety and performance benefits relative to existing alternatives and enable storage, transport and subsequent coating or blending with urea based or organic based fertilizers. These formulations are comprised primarily of environmentally friendly aprotic and protic solvents (particularly dimethyl sulfoxide and alcohols/polyols) to stabilize the urease inhibitor.

Methods of forming a fertilizer composition having slow-release nitrogen compounds with a molten process are disclosed. The methods include mixing of a crystalline polyethylene wax with urea and formaldehyde to form a molten methylene urea mixture. The contents of the molten methylene urea mixture react to form slow-release nitrogen compounds. Fertilizer compositions formed of or including the slow-release nitrogen compounds are also disclosed.