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Methodology - Mixability

Mixability™

Definition
Mixability™ is defined as the ability of a product to be distributed homogeneously in a premix or a feed.

The Mixability™ depends on:

  • The product to be incorporated.

  • The carrier.

  • The mixer.

Benefits
The results of the measurement of Mixability™ parameters make it possible to choose carriers which are best suited to the manufacture of a given premix and to specify the methods of incorporation of the vitamin products. They also make it possible to optimize the mixing parameters and to objectively interpret analytical results.

Poor Mixability™ leads to heterogeneous mixtures or to insufficient dispersions of the active material. It may be the cause of erroneous interpretation of the analytical results and of counter-productiveness in animal productions.


Parameters for assessing Mixability™
Assessment of practical Mixability™ of a vitamin product is determined by three factors:

  • Theoretical Mixability™ determined on the vitamin product to test.

  • Efficiency of the mixer.

  • Analytical performances.

Theoretical Mixability™ determined on the vitamin product to test
The theoretical Mixability™ of a vitamin product indicates whether the number of active particles in the product is (or is not) sufficient to yield an acceptable distribution in the intended mix. The objective entails obtaining a sufficient number of active particles per unit of volume, and to obtain an homogeneous distribution in the mixture.



Total variance = Theorical mixability variance + Mixer variance + Analytical variance + Residual variance

 

The theoretical Mixability™ is determined in three steps:

- step one: determine the particle size profile and of the specific density.

The particle size profile corresponds to the distribution of the product by standard particle size classes. It is measured by screening (ISO method 2591).

Relationship between the particle size profile
and the number of particles
Size of Particles
Particle number in 1.0 gram (specific gravity = 1.0) from D.E.Axe (1995)
U.S Sieve series
Diameter
microns (μm)
Tyler equivalent designation
N° 18
1000
16 mesh
1,530
N° 20
841
20 mesh
2,580
N° 25
707
24 mesh
4,350
N° 30
595
28 mesh
7,460
N° 35
500
32 mesh
 
N° 40
420
35 mesh
20,800
N° 45
354
42 mesh
 
N° 60
250
60 mesh
84,700
N° 80
177
80 mesh
281,000
N° 100
149
100 mesh
392,000
N° 120
125
115 mesh
 
N° 140
105
150 mesh
1,200,000
N° 170
88
170 mesh
 
N° 200
74
200 mesh
3,260,000
N° 230
63
250 mesh
 
N° 325
44
325 mesh
15,600,000
Bold letters: ISO recommendation

The specific density is defined as the weight of a volume of product excluding all of the interparticulate volume (air). It is measured by fluid displacement methods such as pycnometry. In practice, the specific density of a vitamin is given in tables (K. Behnke 1995 (1)).

- step two: calculate the number of active particles per gram of vitamin product (K. Behnke - 1995 (2)).

- step three: statistically calculate the theoretical Mixability™ according to the method of Bruggeman and Niesar (1965). The result of the theoritical Mixability™ calculation is expressed by the variation coefficient, wich is representative of the distribution of the product in the mixture.

This step requires the information from steps one and two and also involves the unit size of the sample and the level of incorporation of the product in premixes or feeds.

The concept of theorical mixability is used to:

  • Determine the minimum size of feed or premix samples to obtain a significant result of analysis (i.e. containing sufficient active particles).

  • Determine the valid tracer and the size of the sample in the case of testing the efficiency of the mixer.

  • Assess the validity of a tracer and the adequate sample sizeto use in a de-mixing test.

Adisseo has developed a computer program for calculating the theoretical Mixability™ of a vitamin product, as well as scales for interpretation of the Mixability™ of vitamins in premixes and feeds.

Comment:
In practice, the electrostaticity and the dustiness of the product, as well as the form of its particles, may modify the theoretical Mixability™ measurement results.


RPAN vitamin Mixability™ interpretation scale
(Variation coefficient %)

Compatibility of the carrier
A carrier is compatible if two criteria are met:

  • The particle size profile of the carrier encompasses that of the vitamin product to be mixed.

  • The density of the carrier (de) is of the same order as that of the vitamin (dv)'

In practice, it is accepted that it is possible to obtain a stable mixture when the ratio of the two components (dc / dv) is between 1 and 3.

Unstable mixture (magnesium oxide + ground corn):
de / dv > 3

Stable mixture (Microvit™ A Supra + ground corn):
de / dv < 3

Efficiency of the mixer
The efficiency of the mixer characterizes the ability of the mixer to disperse the vitamin products homogeneously in the premix or the feed. Measurement of the efficiency of the mixer takes into account the effect of shear (energy transmitted to the mixture) and the mixing duration.

The efficiency of the mixer is determined experimentally and should be supplied by the manufacturer of the mixer.

Analytical performances
The analytical performance depends on the product to analyze and the laboratories which carries out the analyses. The laboratory must be able to provide its analytical performance for each required product.

Conclusion
In order to obtain and verify good mixing of a vitamin product in a premix, it is necessary to satisfy the following three criteria:

  • Theoretical Mixability™.

  • Compatibility of the carrier.

  • Efficiency of the mixer.

The vitamin producer can directly control only the theoretical Mixability™ of the product. However, during the development of its product, the vitamin producer should have taken into account the standard conditions used in premix or feed plants (encompassed by the other two elements).

Under specific conditions, the premix manufacturer will have to choose the most suitable carriers and/or modify the mixing parameters.

Solubility

Solubility and water dispersibility of vitamin products
Certain animal production programs require the distribution of vitamins in drinking water. In this case, it is necessary to use vitamin products either in the form of soluble or water-dispersible powders or in liquid form (vitamin hydrosols).
The actual solubility of water-soluble B vitamins will vary according to their chemical form.

Solubility of B vitamins

Common name
of vitamin
Chemical form
Solubility
(mg/ml of water)
  B1
Thiamin hydrochloride
Thiamin mononitrate
1,000
27
  B2
Riboflavin
Sodium
riboflavin-5-phosphate
0.1
30
  B2 ou PP
Nicotinic acid
Nicotinamide
17
1,000
  B5
Calcium pantothenate
357
  B6
Not hygroscopic / Stable
222
  B9
Folic acid
0.02
  H
D - biotin
0.2
  B12
Cyanocobalamin
12
  C
Ascorbic acid
330
Source : V. Bulher, 2nd edition, 2001

The fat soluble (vitamins A, D3 and E) are not soluble in water. A suitable formulation allows very fine suspensions to be produced when these products are mixed in water. Water-dispersible complexes exist for vitamin K3 (MSB).

The most soluble chemical forms for the B vitamins or formulations specially adapted for the fat soluble vitamins will preferably be chosen for the preparation of water-soluble vitamin complexes.

Adisseo has developed a method for measuring the water dispersibility of fat soluble vitamins (RPAN - D 080).