GB737468A - Preparation of urea-formaldehyde condensate fertiliser compositions - Google Patents

Preparation of urea-formaldehyde condensate fertiliser compositions

Info

Publication number
GB737468A
GB737468A GB20549/52A GB2054952A GB737468A GB 737468 A GB737468 A GB 737468A GB 20549/52 A GB20549/52 A GB 20549/52A GB 2054952 A GB2054952 A GB 2054952A GB 737468 A GB737468 A GB 737468A
Authority
GB
United Kingdom
Prior art keywords
urea
formaldehyde
per cent
products
employed
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB20549/52A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB737468A publication Critical patent/GB737468A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05CNITROGENOUS FERTILISERS
    • C05C9/00Fertilisers containing urea or urea compounds
    • C05C9/02Fertilisers containing urea or urea compounds containing urea-formaldehyde condensates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Fertilizers (AREA)

Abstract

Urea-formaldehyde condensates for use as fertilizers are prepared by mildly agitating at 20-65 DEG C. and pH 1-6 a mixture of 1 mol. formaldehyde, 1.5-4.5 mols. of urea and 20-80 mols. of water. The pH of the mixture is adjusted to at least 6 and the precipitated urea-formaldehyde condensate separated or the precipitated product is separated and its pH adjusted to at least 6. Formamide, acetamide or propionamide may be added as chain-stoppers. The amount of agitation is sufficient to prevent settling of precipitated solids and is such that the initial precipitate having a particle size of 2-6 microns agglomerates to an average particle size of 20-200 microns. Neutralization is preferably effected with a base, e.g. CaCO3 which will remove from the solution the anion of the acid, e.g. H2SO4 used to obtain the desired acidity for the condensation. The product, if desired after screening, is granulated by tumbling in 75-200 per cent of water and then dried. Starch or urea may be added as granulating agents. Reaction may be batchwise, continuous or semi-continuous. If desired separate streams of reactants may be led into a tubular reactor. Preferably the filtrate from the precipitated product is recycled with appropriate quantities of fresh reactants. The formaldehyde may be used as an aqueous solution or as paraformaldehyde, trioxane, hexamethylenetetramine, dimethylol urea or as methylol urea as disclosed in Specification 641,703. Formic acid in aqueous formaldehyde solutions may be sufficient to give the desired pH. The urea may be added as solid or in solution. The reaction may be performed in a vessel of wood, stainless steel, glass, enamel or stoneware. The vessel may be jacketed or an external heat exchanger may be provided. The products may be employed as such or admixed with fertilizer ingredients, e.g. nitrates, potassium salts or phosphates. Products formed with a relatively high mol. ratio of urea may be employed as feed supplements for cattle. The products have an insoluble nitrogen content of at least 60 per cent and an availability index of at least 45 per cent both according to tests defined in the Specification.ALSO:Urea-formaldehyde condensates for use as fertilizers are prepared by mildly agitating at 20-65 DEG C. and pH 1-6 a mixture of 1 mol. formaldehyde, 1.5-4.5 mols. of urea and 20-80 mols. of water. The pH of the mixture is adjusted to at least 6 and the precipitated urea-formaldehyde condensate separated or the precipitated product is separated and its pH adjusted to at least 6. Formamide, acetamide or propionamide may be added as chain-stoppers. The amount of agitation is sufficient to prevent settling of precipitated solids and is such that the initial precipitate having a particle size of 2-6 microns agglomerates to an average particle size of 20-200 microns. Neutralization is preferably effected with a base, e.g. CaCO3 which will remove from the solution the anion of the acid, e.g. H2SO4 used to obtain the desired acidity for the condensation. The product, if desired, after screening is granulated by tumbling in 75-200 per cent of water and then dried. Starch or urea may be added as granulating agents. Reaction may be batchwise, continuous, or semi-continuous. If desired separate streams of reactants may be led into a tubular reactor. Preferably the filtrate from the precipitated product is recycled with appropriate quantities of fresh reactants. The formaldehyde may be used as an aqueous solution or as paraformaldehyde, trioxane, hexamethylenetetramine, dimethylol urea or as methylol urea as disclosed in Specification 641,703. Formic acid in aqueous formaldehyde solution may be sufficient to give the desired pH. The urea may be added as solid or in solution. The reaction may be performed in a vessel of wood, stainless steel, glass, enamel or stoneware. The vessel may be jacketed or an external heat exchanger may be provided. The products may be employed as such or admixed with fertilizer ingredients, e.g. nitrates, potassium salts or phosphates. Products formed with a relatively high mol. ratio of urea may be employed as feed supplements for cattle. The products have an insoluble nitrogen content of at least 60 per cent and an availability index of at least 45 per cent both according to tests defined in the Specification.ALSO:A urea-formaldehyde condensate with an insoluble nitrogen content of at least 60 per cent and an availability index as defined in the Specification of at least 45 per cent (see Group IV (a)) is employed as a feed supplement for cattle or other ruminants. The products, which are preferably granulated by tumbling in water, may also be employed as fertilizers, if desired in admixture with any other known fertilizer compositions or ingredients, e.g. nitrates, potassium salts or phosphates.
GB20549/52A 1951-09-12 1952-08-15 Preparation of urea-formaldehyde condensate fertiliser compositions Expired GB737468A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US737468XA 1951-09-12 1951-09-12

Publications (1)

Publication Number Publication Date
GB737468A true GB737468A (en) 1955-09-28

Family

ID=22115569

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20549/52A Expired GB737468A (en) 1951-09-12 1952-08-15 Preparation of urea-formaldehyde condensate fertiliser compositions

Country Status (1)

Country Link
GB (1) GB737468A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1139134B (en) * 1957-08-23 1962-11-08 Erling Bjarne Johnson Process for the production of fertilizers containing micronutrients (trace elements)
US4145207A (en) * 1977-01-19 1979-03-20 Moore William P Preparation of improved foliar fertilizer
US4173582A (en) * 1975-04-22 1979-11-06 Fertilizers & Chemicals Ltd. Method for the manufacture of improved ureaform fertilizer
US4297130A (en) 1977-08-30 1981-10-27 Moore Jr William P Method for increasing the number of pods in legumes by foliar feeding
EP0095913A2 (en) * 1982-05-27 1983-12-07 Montedison S.p.A. A process for preparing fertilizers
US4564667A (en) * 1984-02-23 1986-01-14 Bip Chemicals Limited Urea-formaldehyde resin manufacture
EP0678084A1 (en) * 1993-01-08 1995-10-25 The Vigoro Corporation Metal ammonium phosphate-alkylene urea buffered fertilizer

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1139134B (en) * 1957-08-23 1962-11-08 Erling Bjarne Johnson Process for the production of fertilizers containing micronutrients (trace elements)
US4173582A (en) * 1975-04-22 1979-11-06 Fertilizers & Chemicals Ltd. Method for the manufacture of improved ureaform fertilizer
US4145207A (en) * 1977-01-19 1979-03-20 Moore William P Preparation of improved foliar fertilizer
US4297130A (en) 1977-08-30 1981-10-27 Moore Jr William P Method for increasing the number of pods in legumes by foliar feeding
EP0095913A2 (en) * 1982-05-27 1983-12-07 Montedison S.p.A. A process for preparing fertilizers
EP0095913A3 (en) * 1982-05-27 1984-04-11 Montedison S.P.A. A process for preparing fertilizers
US4564667A (en) * 1984-02-23 1986-01-14 Bip Chemicals Limited Urea-formaldehyde resin manufacture
EP0678084A1 (en) * 1993-01-08 1995-10-25 The Vigoro Corporation Metal ammonium phosphate-alkylene urea buffered fertilizer
EP0678084A4 (en) * 1993-01-08 1998-03-25 Vigoro Corp Metal ammonium phosphate-alkylene urea buffered fertilizer.

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