Calcium nitrate based fertilizer

Chemistry: fertilizers – Processes and products – Inorganic material

Reexamination Certificate

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C071S028000, C071S031000, C071S059000, C071S062000, C071S064030, C071S063000, C023S3130FB, C023S3130FB

Reexamination Certificate

active

06171358

ABSTRACT:

The present invention relates to calcium nitrate based fertilizers containing sulphur and a process for making such fertilizers.
Calcium nitrate is widely used within horticulture and as a dry product on open fields. There are two major types of calcium nitrate, one made from acidulation of calcium carbonate by nitric acid and one obtained as a by-product from nitrophosphate fertilizer processes. The latter normally contains 75-81 weight % Ca(NO
3
)
2
, 5-9 weight % NH
4
NO
3
and 12-14 weight % water of crystallization. This type is usually called NH—CN (Norsk Hydro Calcium Nitrate). In the following the abbreviation CN will be used for both these types of fertilizer.
Over the last years there has been an ever increasing demand for sulphur in fertilizers in general, even for special applications of CN-fertilizers sulphur has been required. For some markets and crops there has also been a demand for CN-fertilizers containing Mg, Se, Co and some micronutrients in addition to sulphur.
In order to meet the demands for new fertilizers the simplest solution seemed to be blending various S-containing fertilizers like ammonium sulphate or potassium sulphate, but when other ingredients like Mg, Se etc. should be added, segregation problems would inherently arise. Another criteria will of course be the price of the various components and it would be advantageous to use cheap sulphur sources like gypsum, kieserite and langbeinite, but again segregation problems were experienced.
Preparation of homogeneous CN-based fertilizers by particulation of melts or solutions of CN and sulphur sources like ammonium- or potassium sulphate did however prove to be most difficult due to the low ability to tie up water of crystallization possessed by these two sulphur sources. Possible application of gypsum and/or kieserite for making homogeneous fertilizers was then investigated.
From Japanese patent application J54085957 it is known preparation of a fertilizer comprising mixing calcium nitrate, gypsum and superphosphate of lime and then granulating the mixture. Mixing is performed at 100-120° C. and the molten mixture is extruded, cut to a size of 2-3 mm and cooled and dried. The amount of superphosphate of lime is 50-70% of the calcium nitrate. Firstly, this fertilizer contains large amounts of phosphate and no magnesium. Secondly, the particulation process is most uneconomical.
Further it is known from J53027564 to coat CN-fertilizers with gypsum during the spraying of CN melt in cooling air containing gypsum powder. This fertilizer is stated to have a prolonged effect. Its sulphur content will however be far too low to meet the requirements which the present invention has to meet.
It is also known to add minor amounts of CN to granulated ammonium sulphate as a binder and to add minor amounts of ammonium sulphate and calcium nitrate to ammonium nitrate to improve its crushing strength, but none of these publications solve the problems related to making homogeneous CN-based fertilizers.
The main object of the present invention was to arrive at a homogeneous CN-based fertilizer containing sulphur and optionally magnesium, selenium, cobalt and micronutrients.
Another object was to arrive at a cost effective continuous process for making homogeneous sulphur containing CN-based fertilizers which could be particulated.
A further object was to arrive at a process for making homogeneous sulphur containing CN-based fertilizers containing magnesium and optionally selenium, cobalt and micronutrients.
Application of normal S-sources like ammonium sulphate and potassium sulphate were first investigated. It was then found that when these sources are mixed with CN melt the following reactions will take place:
1. (NH
4
)
2
SO
4
+Ca(NO
3
)
2
→CaSO
4
+NH
4
NO
3
2. K
2
SO
4
+Ca(NO
3
)
2
→KNO
3
+CaSO
4
The formation of gypsum consumes calcium nitrate and the melt loses its ability to solidify due to less power to tie up water of crystallization. Accordingly, the two S-sources were found to be too difficult to apply in CN-based fertilizers.
Gypsum (CaSO
4
1/2 H
2
O) was expected to not react with CN melt and should therefore constitute a cheap S-source. Even though gypsum is not water soluble, several agronomical examinations have shown that gypsum is readily available to plants. Different gypsum sources can be utilized, such as dead burned gypsum and gypsum with hydrate water up to dihydrate, the hemi hydrate form is however preferred.
Kieserite (MgSO
4
H
2
O) is both a Mg- and S-source which is considered to be water soluble. By mixing this salt into a CN melt the following reaction was found to take place:
3. MgSO
4
H
2
O+Ca(NO
3
)
2
→CaSO
4
+Mg(NO
3
)
2
+H
2
O
It was further found that if the Mg(NO
3
)
2
content became too high, solidification problems would occur. However, trials carried out revealed surprisingly that reaction no. 3 did not take place at a significant rate. During further laboratory tests at which kieserite was thoroughly mixed into CN melt for several minutes it was confirmed that said reaction did not result in solidification problems. The investigations also showed that reaction
3
indeed did take place at the surface of each kieserite crystal, but the gypsum formed a thin coating that protected the crystals from further attack by the CN melt. This formation of gypsum coating and the slow dissolving time of the kieserite mineral in general seemed to give possibilities for homogeneous distribution of fine kieserite crystals in the CN melt prior to solidification and thereby make it possible to utilize this for making a homogeneous CN-based fertilizer containing both sulphur and magnesium.
Based on the results from the above investigations, several tests were performed in a pilot plant. It was then confirmed that by using gypsum and slow reacting sulphate minerals like kieserite, langbeinite etc. together with a CN melt it would be possible to make homogeneous S-containing fertilizers which met the above stated objects of the invention.
Thus, according to the invention, solid gypsum and/or a slow reacting sulphate mineral could be mixed with melted calcium nitrate fertilizer at a temperature of 90-110° C. and kept at this temperature for 3-15 minutes and subsequently particulated at a temperature of 80-110° C.
The particulation by prilling should be performed at 95-110° C. and the granulation at 90-110° C.
Microamounts of Co and/or Se and/or micronutrients like Mn, Cu, B, and Zn could be added as solutions of their salts to the mixture prior to particulation.
One preferred method comprises mixing 4-23 weight % gypsum, based on the total composition, with a melted calcium nitrate fertilizer at 103-106° C. during stirring and keeping the mixture at this temperature for 5-10 minutes and then particulate the thus formed slurry.
Another preferred method comprises mixing 4-23 weight % kieserite during stirring with a melted calcium nitrate fertilizer for 6-12 minutes and subsequently particulate the thus formed slurry.
Fertilizers according to the invention comprise a homogeneous composition of a calcium nitrate fertilizer and gypsum and/or a slow reacting sulphate mineral comprising 0.1-5.0 weight % SO
4
—S, 14-19 weight % water soluble calcium and 16-21 weight % total calcium and 0-3.0 weight % water soluble magnesium. Preferably said new fertilizer contains 1.0-3.0 weight % SO
4
—S. The preferred content of magnesium is 0.1-4.0 weight %.
The scope and special features of the invention are as stated in the attached claims.
The invention is further explained by the following examples and the comments to these examples:


REFERENCES:
patent: 5698002 (1997-12-01), Hudson
patent: 1311065 (1973-03-01), None
patent: 1382870 (1975-02-01), None
patent: 53-27564 (1978-03-01), None
patent: 54-85957 (1979-07-01), None
WPI/Derwent's abstract, No. 79-60872B, week 7933, Abstract of JP 54085957 (Shimohiro I), Jul. 9, 1979.

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