Patent Application
20240150276
The present invention relates to a process for the solidification of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI diethylamino hydroxybenzoyl hexyl benzoate, DHHB), wherein the process comprises a steps (a) of applying a shear rate of 800 s−1 or more to liquid hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate and (b) adding seed crystals of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate.
Hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI diethylamino hydroxybenzoyl hexyl benzoate), also referred to as DHHB, is an UV-A filter belonging to the group of benzophenone derivatives. It is sold under the tradename Uvinul A Plus by BASF. It has a melting point of about 54° C.
It is known in the art that solvent-free DHHB melt is hard to crystallize. An undercooled melt can stay in a metastable liquid state for weeks, until it finally crystallizes. An economical solidification process like flaking or pastillation on a cooling belt with such a very slowly crystallizing product is not known, so far. Currently, methods like crystallizing DHHB in tubs or drums and afterwards crushing it are applicable. However, these methods have a bad space time yield and lead to non-uniform particle shapes and sizes, which can lead to drawbacks, e.g., regarding its caking properties.
It was therefore an object of the present invention to provide an improved process for the solidification of DHHB. In particular, it was an object of the present invention to provide a process, which has economic advantages in comparison to the prior art methods. In this connection, it was particularly an object of the present invention to provide a process, which provides an improved space time yield. Moreover, it was an object to provide the solidified DHHB in uniform particle shapes and sizes, preferably exhibiting a good flowability and/or good storage stability.
It has surprisingly been found that at least one of the afore-mentioned objects can be achieved by the process of the present invention. In particular, it has surprisingly been found by the inventors of the present invention that applying a high shear rate to a DHHB melt or subcooled melt can provoke in combination with seeding a very accelerated crystallization of DHHB.
The present invention relates in a first aspect to a process for the solidification of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI diethylamino hydroxybenzoyl hexyl benzoate, DHHB), wherein the process comprises the step of (a) applying a shear rate of 800 s−1 or more to liquid hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate and (b) adding seed crystals of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate, while applying the shear rate of step (a).
In the following, preferred embodiments of the process of the first aspect are described in further detail. It is to be understood that each preferred embodiment is relevant on its own as well as in combination with other preferred embodiments.
In a preferred embodiment A1 of the first aspect, the liquid hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is provided as a melt, which preferably has a temperature from more than about 54 to about 70° C., preferably from more than about 54 to about 65° C., or
In a preferred embodiment A2 of the first aspect, the applied shear rate is 900 s−1 or more, preferably 1000 s−1 or more and/or wherein the shear rate is obtained by stirring the melt or subcooled at a stirring speed of 50 to 600 rpm, preferably of 90 to 500 rpm, preferably of 100 to 250 rpm.
In a preferred embodiment A3 of the first aspect, the temperature of the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate to be solidified in step (b) is from about 15 to about 54° C., preferably from about 25 to about 52° C.
In a preferred embodiment A4 of the first aspect, in step (b) from 0.0001 to 0.1 g, preferably from 0.0005 to 0.05 g, more preferably from 0.001 to 0.03 g, of seed crystals are added per 1 g of the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate to be solidified melt and/or the seed crystals have a particle size, determined according to sieve analysis, of less than 100000 μm, preferably from 1 to 10000 μm, more preferably from 5 to 5000 μm.
In a preferred embodiment A5 of the first aspect, step (a) is performed in an apparatus, preferably selected from the group consisting of an extruder, a scraped surface heat exchanger, a cooling disc crystallizer, or a stirred vessel, preferably with scraping agitator, which is cooled to a temperature of less than about 54° C., preferably about 40° C. or less.
In a preferred embodiment A6 of the first aspect, step (a) is performed in a scraped surface heat exchanger and the process further comprises the steps of
In a preferred embodiment A7 of the first aspect, in step (i-1), a temperature of more than about 54° C. is applied and/or
In a preferred embodiment A8 of the first aspect, step (b) provides the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of solidified strands.
In a preferred embodiment A9 of the first aspect, step (b) provides the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of a melt suspension, which is solidified by the further steps of
In a preferred embodiment A10 of the first aspect, step (b) provides the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of a melt suspension, which is solidified by a further step of
In a preferred embodiment A11 of the first aspect, a cooling belt is applied and the cooling belt comprises at least one cooling zone, preferably wherein the at least one cooling zone is in the temperature range from about 0 to about 40° C., more preferably from about 10 to about 38° C., and in particular from about 20 to about 35° C.
In a preferred embodiment A12 of the first aspect, the cooling belt comprises at least two cooling zones, preferably wherein the temperature of the first cooling zone is higher than the temperature of the second cooling zone, more preferably wherein the first cooling zone is in the temperature range from about 15 to about 40° C. and the second cooling zone is in the temperature range from about 5 to about 30° C.
In a preferred embodiment A13 of the first aspect, the process is performed as a continuous process, wherein the liquid hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is continuously fed into the scraped surface heat exchanger and the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is continuously collected from the scraped surface heat exchanger in the form of solidified strands or in the form of a melt suspension.
In a second aspect, the present invention relates to solidified hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of
Before describing in detail exemplary embodiments of the present invention, definitions important for understanding the present invention are given.
As used in this specification and in the appended claims, the singular forms of “a” and “an” also include the respective plurals unless the context clearly dictates otherwise. In the context of the present invention, the term “approximately” denote an interval of accuracy that a person skilled in the art will understand to still ensure the technical effect of the feature in question. The term typically indicates a deviation from the indicated numerical value of ±15%, preferably ±10%, more preferably ±5%, and in particular ±3%. It is to be understood that the term “comprising” is not limiting. For the purposes of the present invention the term “consisting of” is considered to be a preferred embodiment of the term “comprising of”. If hereinafter a group is defined to comprise at least a certain number of embodiments, this is meant to also encompass a group which preferably consists of these embodiments only. It is to be understood that this invention is not limited to the particular methodology, protocols, reagents etc. described herein as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention that will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art.
As used herein the term “pourable or flowable particles” refers to any solid form being able to be poured or granulated and which is safe and easy to handle by the processor (e.g. having reduced electrostatic properties when compared to powder).
As used herein the term “pastilles” is a subtype of the pourable or flowable particles, which preferably are hemispherical structures. Pastilles are preferably obtained via the still liquid melt or melt suspension, which can be portioned into small drops and be placed onto the flat surface such that said pastilles are formed. After the melt or melt suspension has crystallized out, the pastilles can be removed and bottled.
As used herein the term “flakes” refers to a specific solid form, which can be obtained by pouring the still liquid melt or melt suspension onto a flat surface, preferably wherein the obtained layer has a thickness of 0.1 to 10 mm, more preferably of 0.2 to 8 mm or of 0.2 to 5 mm or of 0.2 to 2 mm. After the melt or melt suspension has crystallized out, the solid layer is removed from the plane as is customary and bottled, the thin layer usually being comminuted to a desired flake size by breakage.
The production process of pourable or flowable particles, pastilles, and flakes can take place discontinuously (batch process) or continuously, where, in a continuous method, a continuously circulating steel belt, for example, can be used as mold for the purposes of the present invention.
Preferred embodiments regarding the process according to the present invention are described hereinafter. It is to be understood that the preferred embodiments of the invention are preferred alone or in combination with each other.
As indicated above, the present invention relates in one embodiment to a process for the solidification of hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate (INCI diethylamino hydroxybenzoyl hexyl benzoate, DHHB), wherein the process comprises the step of
In a preferred embodiment, the liquid hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is provided as a melt or a subcooled melt.
Hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate has a melting point of about 54° C. The melting point may vary depending on potential impurities. Therefore, it is to be understood that when referring to the temperature values of the process according to the present invention it is referred to said temperature value ±2° C., preferably ±1° C. For example, if it is referred to the temperature value of the melting point of DHHB of about 54° C., it is referred to a temperature range of 54° C.±2° C., preferably ±1° C.
In a preferred embodiment, the melt has a temperature from more than about 54 to about 70° C., preferably from more than about 54 to about 65° C.
In a preferred embodiment, the subcooled melt has a temperature from about 15 to about 54° C., preferably from about 20 to about 52° C.
In a preferred embodiment, the applied shear rate is 900 s−1 or more, preferably 1000 s−1 or more, more preferably 1500 s−1 or more, still more preferably 2000 s−1 or more, and in particular 5000 s−1 or more. Preferred shear rates are in the range of from 800 to 100000 s−1, preferably from 900 to 50000 s−1, more preferably from 1000 to 30000 s−1. In yet another preferred embodiment, the applied shear rate is in the range of from 800 to 50000 s−1, preferably from 900 to 30000 s−1, and in particular from 900 to 20000 s−1.
Such high shear rates further reduce the time period until nucleation starts, thereby increasing the efficiency of the solidification process.
As used herein, the term “shear rate” refers to the rate at which progressive shearing deformation is applied to the liquid DHHB. In general, the shear rate may be determined for a fluid flowing between two parallel plates, one moving at a constant speed and the other one stationary based on the following equation:
γ=v/h
In a preferred embodiment, the melt or subcooled melt is stirred at a stirring speed of more than 50 rpm, more preferably more than 80 rpm, and in particular more than 100 rpm. It is also preferred that the melt or subcooled melt is stirred at a stirring speed of 50 to 600 rpm, preferably of 80 to 500 rpm, more preferably of 100 to 250 rpm.
Preferably, the high shear rate is obtained by stirring the melt or subcooled at a stirring speed of 50 to 600 rpm, preferably of 80 to 500 rpm, preferably of 100 to 250 rpm.
In a preferred embodiment, the seed crystals are added at a temperature from about 30 to about 60° C., more preferably from about 35 to about 55° C., and still more preferably from about 40 to less than about 54° C.
In a preferred embodiment, after addition of the seed crystals the temperature of the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate to be solidified is kept in the range from about 15 to less than about 54° C., preferably from about 25 to about 52° C.
In a preferred embodiment, in step (b) from 0.0001 to 0.1 g, preferably from 0.0005 to 0.05 g, more preferably from 0.001 to 0.03 g, of seed crystals are added per 1 g of the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate to be solidified.
In a preferred embodiment, the seed crystals have a particle size, determined according to sieve analysis, of less than 100000 μm, preferably from 1 to 10000 μm, more preferably from 5 to 5000 μm.
In this connection, the determination of the particle size is preferably performed using two sieves, wherein the first sieve has a broader width than the second. Preferably, an amplitude of 1.5 mm is applied and the two sieves are positioned in a Retsch sieve apparatus, wherein the sieve having a mesh having the broader width is located at the upper position. After applying the sample on the upper located sieve, sieving is conducted. The residues are weighed out after intervals within 1 to 20 minutes in order to validate whether the residues of the three obtained fractions change. In general, the distribution of the three fractions does not change any more after 5 to 10 minutes.
Preferably, the determination of the particle size is performed using two sieves, wherein the first sieve has a mesh width of 5 mm and the second sieve has a mesh width of 0.1 mm. Preferably, an amplitude of 1.5 mm is applied and the two sieves are positioned in a Retsch sieve apparatus, wherein the sieve having a mesh width of 5 mm is located at the upper position. After applying the sample on the upper located sieve, sieving is conducted. The residues are weighed out after intervals within 1 to 20 minutes in order to validate whether the residues of the three obtained fractions change. In general, the distribution of the three fractions does not change any more after 5 to 10 minutes. The first fraction comprises particles having a particle size of less than 0.1 mm, the second fraction comprises particles having a particle size of 0.1 to 5 mm, and the third fraction comprises particles having a particle size of more than 5 mm.
In a preferred embodiment, the step (a) is performed in an apparatus, preferably selected from the group consisting of an extruder, a scraped surface heat exchanger, a cooling disc crystallizer, or a stirred vessel, preferably with scraping agitator, which is cooled to a temperature of less than about 54° C., preferably about 40° C. or less.
In this connection it is to be understood that every apparatus, which can be cooled and which enables stirring may be used.
In a preferred embodiment the process is a continuous process.
Preferably, a continuously operated process comprises using a scraped surface heat exchanger and a storage vessel where the DHHB melt can be stored above its melt temperature. A scraped surface heat exchanger, which can be fed with DHHB melt from the storage vessel, is used to generate a melt suspension. In the scraped surface heat exchanger, liquid DHHB is cooled down by means of a cooled internal surface (also referred to as scraped surface) and stirred by the scraper. According to the present invention seed crystals are added. After the onset of crystallization, crystals are generated on a cold internal surface and scraped off by means of a scraper comprised in the scraped surface heat exchanger. During the startup phase, the generated melt suspension is fed back to the storage vessel until the desired solid content in the generated melt suspension is reached. As soon as crystallization starts significantly, an increase of the turbidity of the DHHB melt suspension can be observed (e.g. via the signal of the turbidity probe). Moreover, a color change from brownish to bright yellow can be observed when crystallization starts significantly.
As soon as the desired solid content is reached, the melt suspension can be continuously applied to a maturing belt, preferably a cooling belt (more preferably with multiple temperature zones).
In a preferred embodiment, step (a) is performed in a scraped surface heat exchanger and the process further comprises the steps of
Preferably, in step (i-1), a temperature of more than about 54° C. is applied. It is also preferred that in step (i-1), a temperature of from more than about 54 to about 70° C., more preferably from more than about 54 to about 65° C. is applied.
Preferably, step (i-2) is performed under heating of the feed to a temperature of more than about 54° C. It is also preferred that step (i-2) is performed under heating of the feed to a temperature of from more than about 54 to about 70° C., more preferably from more than about 54 to about 65° C.
Preferably, the temperature in the scraped surface heat exchanger is less than about 54° C., preferably less than about 52° C.
Preferably, the internal surface of the scraped surface heat exchanger has a temperature of less than about 50° C., more preferably less than about 40° C., still more preferably less than about 30° C., and in particular less than about 20° C. It is also preferred that the internal surface of the scraped surface heat exchanger has a temperature of from about 1 to about 50° C., more preferably from about 2 to about 40° C., still more preferably from about 3 to about 30° C., and in particular from about 5 to about 20° C.
In this connection it is to be understood that the scraped surface heat exchanger is cooled via its internal surface. Therefore, when referred to the temperature in the scraped surface heat exchanger, it is referred to the approximate temperature of the melt/melt suspension, which is cooled via the cooled internal surface. When referred to the temperature of the internal surface it is referred to the temperate of the internal surface of the scraped surface heat exchanger.
In a preferred embodiment, in step (i-1), a temperature of more than about 54° C. is applied, the step (i-2) is performed under heating of the feed to a temperature of more than about 54° C. and the temperature in the scraped surface heat exchanger is less than about 54° C.
In a preferred embodiment, step (a) is performed in a stirred vessel and the process further comprises the steps of
Preferably, in step (ii-1), a temperature of more than about 54° C. is applied. It is also preferred that in step (ii-1), a temperature of from more than about 54 to about 70° C., more preferably from more than about 54 to about 65° C. is applied.
Preferably, in step (ii-2), the subcooled melt has a temperature of less than about 54° C. It is also preferred that in step (ii-2), the subcooled melt has a temperature in the range from about 15 to about 54° C., preferably from about 20 to about 52° C.
In a preferred embodiment, in step (ii-1), a temperature of more than about 54° C. is applied and in step (ii-2), the subcooled melt has a temperature of less than about 54° C.
In a preferred embodiment, step (b) provides a melt suspension.
It is to be understood that according to the present invention the term “melt suspension” denotes a melt comprising solids. For examples a melt suspension of DHHB comprises DHHB in liquid, i.e. molten form, and in solid form.
The melt suspension provided by step (b) may be poured on any suitable container in order to allow the melt suspension to further cool and solidify.
In a preferred embodiment, step (b) provides the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of solidified strands.
In a preferred embodiment, step (b) provides the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of a melt suspension, which is solidified by the further steps of
In a preferred embodiment, step (b) provides the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of a melt suspension, which is solidified by a further step of
In a preferred embodiment, a cooling belt is applied and the cooling belt comprises at least one cooling zone. Preferably, the at least one cooling zone is in the temperature range from about 0 to about 40° C., more preferably from about 10 to about 38° C., and in particular from about 20 to about 35° C.
Preferably, the cooling belt comprises at least two cooling zones, more preferably wherein the temperature of the first cooling zone is higher than the temperature of the second cooling zone. Preferably, the temperature in the first cooling zone is about 5° C., more preferably about 10° C., higher than the temperature in the second cooling zone. Preferably, the first cooling zone is in the temperature range from about 15 to about 40° C., more preferably from about 22 to about 38° C., and the second cooling zone is in the temperature range from about 5 to about 30° C., more preferably from about 10 to about 20° C.
In a preferred embodiment, the process is performed as a continuous process, wherein the liquid hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is continuously fed into a scraped surface heat exchanger or an extruder and the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is continuously collected from the scraped surface heat exchanger or the extruder in the form of solidified strands or in the form of a melt suspension.
If the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate is still not completely solidified after the residence time of the cooling belt a ripening belt can be used subsequent to the cooling belt.
In a second aspect, the present invention relates to solidified hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]benzoate in the form of
In a preferred embodiment, the pourable or flowable particles have a particle size, determined according to sieve analysis, of 0.01 to 30 mm, more preferably of 0.1 to 30 mm, still more preferably of more than 5 to 30 mm, and in particular of 10 to 25 mm.
Any suitable method for determining the particle size of the pourable or flowable particles may be applied.
The particle size of the pourable or flowable particles may be determined via sieve analysis. Preferably, the determination of the particle size are performed using two sieves, wherein the first and the second sieves have a mesh width, which is suitable for the determination of e.g. 1 to 30 mm. Preferably, an amplitude of 1.5 mm is applied and the two sieves are positioned in a Retsch sieve apparatus, wherein the sieve having the broader mesh width is located at the upper position. After applying the sample on the upper located sieve, sieving is conducted for 1 to 20 minutes until no change of the distribution of the three fractions is detected.
The particle size of the pourable or flowable particles may also be determined according to caliper. In this connection it is to be understood that the Feretmax. of Feret's diameter is decisive for the particle size.
Sieving is preferably used for of the pourable or flowable particles having a particle size of less than 20 mm, more preferably less than 10, and in particular of 5 mm and less.
Image analysis or caliper are preferably used for the pourable or flowable particles having a particle size of more than 5 mm, more preferably more than 10 mm.
Preferably, the pourable or flowable particles have a bulk density of 0.35 g/mL or more, more preferably of 0.35 to 0.5 g/mL.
In a preferred embodiment, the pastilles have a particle size of 1 to 30 mm, more preferably of 2 to 30 mm, still more preferably of more than 5 to 30 mm, and in particular of 6 to 20 mm.
Any suitable method for determining the particle size of the pastilles may be applied.
The particle size of the pastilles may be determined according to image analysis. Therefore, 100 pastilles are randomly selected from the final product. The particle sizes are determined and the average particle diameter is derived therefrom.
The particle size of the pastilles may also be determined according to caliper. In this connection it is to be understood that the Feretmax. of Feret's diameter is decisive for the particle size. Using the caliper method is preferred for pastilles having a particle size of more than 5 mm.
Preferably, the pastilles have a bulk density of 0.35 g/mL or more, more preferably of 0.35 to 0.5 g/mL.
In a preferred embodiment, the flakes have a particle size of 1 to 100 mm, more preferably of 5 to 90 mm, even more preferably of more than 5 to 85 mm, still more preferably of 7 to 80 mm, and in particular of 10 to 80 mm.
Any suitable method for determining the particle size of the flakes may be applied.
The particle size of the flakes may be determined according to image analysis. Therefore, 100 flakes are randomly selected from the final product. The particle sizes are determined and the average particle diameter is derived therefrom.
The particle size of the flakes may also be determined according to caliper. In this connection it is to be understood that the Feretmax. of Feret's diameter is decisive for the particle size. Using the caliper method is preferred for flakes having a particle size of 5 mm and more.
Preferably, the flakes have a bulk density of 0.35 g/mL or more, more preferably of 0.35 to 0.5 g/mL.
The present invention is further illustrated by the following examples.
To evaluate the solidification behavior of thin layers (1-3 mm) of a DHHB melt, cooling plate experiments have been performed at a fixed cooling plate temperature of 20° C. In the experiment a thin layer of DHHB melt was placed on the surface of the thermostated cooling plate surface (material: stainless steel). To apply a low shear rate of approximately 50 s−1, a spatula was used to stir the liquid DHHB melt gently for several minutes. No crystallization was observed within 2 h.
The following example is in line with Example 6 of EP 2155660 B1: 5 kg of DHHB is poured in a 5 L aluminum vessel. The melt is stirred by an PTFE propeller stirrer (60 mm diameter), which is stirred by an electrical motor. The melt is stirred at 25° C. with a stirring speed of 250 rpm (approximately 1000 s−1). After 11 h of stirring, melt viscosity increases significantly so that stirring is not possible any more. First crystals are observed after 5 h of stirring. Complete solidification is achieved after 24 h.
The following example is in line with Example 10 of EP 2155660 B1: DHHB seed particles are added to 5 kg DHHB melt. The melt temperature at which seed particles (<100 μm) are added is about 40° C. Afterwards the DHHB melt is allowed to cool down to room temperature. First crystals are observed after 10 days. Complete solidification is achieved after 2 months. The melt is not stirred during the experiment.
A scraped surface heat exchanger covering a melt volume of approximately 90 L was used in the experiment. A melt of DHHB was fed from a storage tank into the scraped surface heat exchanger, where it was cooled down below its melt temperature (i.e. below about 54° C.). The stirring speed of the scraper was maintained at 120 rpm throughout the experiment. As soon as the DHHB melt temperature was below 54° C. DHHB seed particles were added to the melt. DHHB powder of approximately <200 μm was used as seed particles. After approximately 2-3 h crystallization was observed to start significantly. To monitor the crystallization process, samples of the DHHB melt were taken from the scraped surface heat exchanger (every 30 min). The start of crystallization could be observed visually by eye (increase of turbidity) and an increase of the scraper torque. Also, a color change of the product from brownish to yellow could be observed. After the desired (high) solid content in the DHHB melt suspension was reached, the melt suspension was poured onto a cooling belt. Depending on the tool used for applying the melt suspension on the cooling belt, DHHB pastilles or a DHHB layer was produced on the cooling belt. The cooling belt comprised of two different cooling zones. The first section of the cooling belt length was maintained at 30° C., whereas the second section was maintained at 15° C. This temperature profile was identified to lead to a high solidification progress until the DHHB pastilles or DHHB layer was scraped off at the end of the cooling belt. When an DHHB layer was applied on the cooling belt, DHHB flakes were produced (Inventive Example 1.1). Complete solidification of the DHHB pastilles (Inventive Example 1.2) and DHHB flakes (Inventive Example 1.1) was achieved after approximately 2-3 h of ripening at room temperature after they were scraped off from the cooling belt. Notably, ripening can also be carried out on an additional ripening belt at room temperature. Further experimental parameters are summarized in Table 1.
The obtained pastilles (Inventive Example 1.2) have an average height of 3.5 to 4.5 mm and an average diameter of 7 to 9.5 mm. Hence, their particle size as understood according to the present invention is from 7 to 9.5 mm (i.e. the Feretmax.).
The complete solidification of the DHHB melt suspension can be obtained surprisingly faster when seed crystals are applied in combination with high shear rates.
| Number | Date | Country | Kind |
|---|---|---|---|
| 21160497.0 | Mar 2021 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2022/055089 | 3/1/2022 | WO |
