scholarly journals Effect of Sample Preparation and Extended Mix Times with Different Salt Particle Sizes on the Uniformity of Mix of a Corn-Soybean Meal Swine Diet

Author(s):  
M. Saensukjaroenphon ◽  
C. K. Jones ◽  
C. H. Fahrenholz ◽  
C. R. Stark
2018 ◽  
Vol 61 (2) ◽  
pp. 743-746
Author(s):  
Marut Saensukjaroenphon ◽  
Cassandra K. Jones ◽  
Charles H. Fahrenholz ◽  
Charles R. Stark

Abstract. The uniformity of a feed mixture is determined from the coefficient of variation (CV) of ten samples in a single batch of feed. The feed industry standard is a CV of less than 10% using a single source tracer such as salt, trace minerals, or iron filings. The uniformity of mix can be affected by many factors, including mixer design, particle size of the ingredients, sample preparation, and mix time. Previous research has determined the minimum mix time to maximize the mixing efficiency, but some hypothesize that over-mixing may lead to ingredient segregation. However, there are limited data regarding the effects of extended mixing, appropriate particle size of the analytical marker, and the analytical sample preparation for maximum precision of the assay. The objectives of these experiments were to determine (1) the effects of extended mix time, (2) particle size of the marker, and (3) sample preparation of the CV in a corn-soy swine diet. Experiment 1 treatments were arranged in a 3 × 7 factorial with three salt particle sizes (fine-350 µm, medium-464 µm, and coarse-728 µm) and seven mix times (2, 3, 5, 15, 30, 45, and 60 min). Experiment 2 treatments were arranged in a 2 × 3 × 3 factorial with two sample preparations (unground and ground), three salt particle sizes (fine-350 µm, medium-464 µm, and coarse-728 µm), and three mix times (3, 30, and 60 min). There were three replicates per treatment and ten samples per replicate. Salt concentrations were determined using a Quantab chloride titrator. The results of experiment 1 indicated no interaction between mix time and salt particle size (p = 0.4366). The extended mix time did not result in segregation (p = 0.3073; 11.5%, 13.8%, 12.9%, 13.1%, 13.9%, 11.6% and 11.3% CV for 2, 3, 5, 15, 30, 45, and 60 min, respectively). Particle size of the salt significantly affected the mixture uniformity (p < 0.0001; 21.2%, 8.6%, and 7.9% CV for coarse, medium, and fine salt, respectively). The results of experiment 2 indicated no interaction of sample preparation, salt particle size, and mix time (p = 0.3823). However, there was an interaction between sample preparation and salt particle size (p = 0.0002). The difference in the % CV between unground and ground samples was significantly greater for the mixture with coarse salt (8.89%) than for mixtures with medium (2.59%) and fine (1.35%) salt. The ground treatment had a significantly lower % CV than the unground treatment (p < 0.0001; 8.7% and 13.0% for ground and unground samples, respectively). The fine and medium salt treatments had significantly lower % CV as compared to the coarse salt treatment (p < 0.0001; 7.4%, 7.7%, and 17.4% for fine, medium, and coarse, respectively). These results indicate that feed did not segregate after mixing for 1 h and that a greater number of particles per gram of the marker increased the precision of the analysis. This was likely due to an increased probability that the marker was present in greater proportionate quantities in the sample tested. However, when coarse salt is used in a manufacturing process, the samples should be ground prior to analysis. Keywords: Mix time14734540-4533900dgw:448Sgw Method S319.2:2.50Sgw Method S319.4:470.40% < 300 m:44 %dgw:448Sgw Method S319.2:2.50Sgw Method S319.4:470.40% < 300 m:44 %, Particle size, Salt, Uniformity.


2002 ◽  
Vol 56 (1-2) ◽  
pp. 63-72
Author(s):  
Branislav Zivkovic ◽  
Stanimir Kovcin ◽  
Mihal Fabjan

The paper will demonstrate the quality of some feed used in swine diet. The emphasis will be on feed whose incorporation into mixes could result in unfavorable effects on production, health and economic production of swine. Data will be presented on maize and its possible negative effects, having in mind toxins. Soybean meal, or genetically modified soybean meal, will also be observed. The next feed which will be discussed will be soybean whey obtained by different procedures and the potential dangers of its use in swine diet rations. Sunflower meal, feed of animal origin, with emphasis on fish flour and meat-bone flour will also be covered in the work. A feed which has been attracting particular attention lately is yeast imported from Italy. Its quality characteristics will be discussed, the so-called non-protein nitrogen. Analyses of mineral feed will include sources of phosphorus, phosphates (monocalciumphosphate, dicalcium phosphate) phytases and resolving the problem of phosphorus in swine rations. Finally, an inevitable segment are synthetic amino acids, especially lysine and its role in swine diet.


Author(s):  
M. Saensukjaroenphon ◽  
C. E. Evans ◽  
C. K. Jones ◽  
C. H. Fahrenholz ◽  
C. B Paulk ◽  
...  

1985 ◽  
Vol 48 (3) ◽  
pp. 240-243 ◽  
Author(s):  
KURT E. RICHARDSON ◽  
WINSTON M. HAGLER ◽  
CAROL A. HANEY ◽  
P. B. HAMILTON

Several Fusarium isolates known to produce zearalenone or T-2 toxin were tested for their toxigenic potential on heatsterilized whole and cracked soybeans, on soybean meal, and on rice. Moisture concentration levels and particle sizes of substrate were varied to determine effects on the amount and type of toxin produced. Only one of the three Fusarium isolates known to produce zearalenone, Fusarium roseum ‘Graminearum’, produced detectable amounts of this mycotoxin on soybeans. Fusarium sporotrichioides NRRL 3299, the T-2 toxin-producing isolate tested, produced T-2 toxin as well as T-2 tetraol, HT-2 toxin and neosolaniol on soybeans. HT-2 toxin production was greatly enhanced on soybean meal in comparison to rice cultures. These findings plus previous field observations suggest that soybean products present a mycotoxic hazard which warrants attention.


2013 ◽  
Vol 316-317 ◽  
pp. 404-407
Author(s):  
Yu Zhen Wang ◽  
Shu Zhong Wang ◽  
Yang Guo ◽  
Dong Hai Xu ◽  
Guang Xin Yu ◽  
...  

Salt deposition from supercritical water has been identified as a key issue in the development of supercritical water technologies. In order to better understand salt deposition behavior, the salt particle – supercritical water flow in a 90° bend pipe with smooth walls was simulated using discrete element method (DEM) coupled with computational fluid dynamics (CFD). The transport behavior of pure supercritical water flow and salt particle-supercritical water flow with diiferent particle sizes were both simulated. The numerical results indicates that for the pure supercritical water flow, the primary flow accelerated near the inner wall and a secondary flow moving from the outer to the inner wall of the bend. The salt particle accumulation in the inner wall of horizontal pipe is the most notable feature in the salt - supercritical water flow.


2021 ◽  
Vol 328 ◽  
pp. 05007
Author(s):  
Nizar Amir ◽  
Makhfud Efendy ◽  
Rachmad Hidayat ◽  
Misri Gozan

The salt quality was studied by dewatering methods such as centrifugal hydro extraction, fixed bed dryer, and rotary drum dryer. The effect of different salt particle sizes was also analyzed. The centrifugal hydro extractor is found to be effective when reducing the high-water content of salt and suitable for reducing water content after the salt wash stage. Fixed bed dryers produce lower water content than rotary drum dryers. A water content lower than 1% can be achieved using fixed bed dryers. Finally, all dewatering methods such as centrifugal hydro extractors, fixed bed dryers, and rotary bed dryers are suitable for salt production methods. Reduced salt particle size from 30 to 60 mesh also improved the drying performance.


2008 ◽  
Vol 55-57 ◽  
pp. 805-808 ◽  
Author(s):  
Thadsanee Thongkanluang ◽  
Pichet Limsuwan ◽  
P. Rakkwamsuk

This research article reports a development on green pigments having high reflectance of NIR radiation from the sun. The aim of the development is to use the green pigments as a component of building paint to reduce heat penetrating into the building. Cr2O3, a green pigment oxide, was used as the host component and the mixtures of Al2O3, V2O5 and TiO2 were used as the guest components. Al2O3, V2O5 and TiO2 were mixed at different 36 compositions according to triaxial diagram. For each sample preparation, 80% wt Cr2O3 was mixed with 20%wt of guest component for each composition. Then the mixed sample were calcined at 1150 °C for 4 hours and were ground with an agate ball mill for 7 minutes at a speed of 250 rev/min. Finally, the pigments were sieved to obtain the particle sizes of 0.5 - 2.0 µm. The pigment powders were compressed in a mold to get samples in the form of thin disks, each one with a diameter of 2.7 cm and a thickness of 4 mm. The reflectance for all samples was measured using a spectrophotometer in the wavelength ranging from 300 – 2100 nm in accordance with ASTM E891. It was found that the maximum reflectance, in the wavelengths ranging from 780 – 2100 nm, of 82.83% was obtained from the sample with a composition of 80%Cr2O3, 14%Al2O3, 4%TiO2 and 2% V2O5.


Author(s):  
Kiran Bhadriraju ◽  
Jayesh Bellare

Freeze-fracture replication TEM and Cryo-TEM are developed techniques for studying surfactant dispersions. Application of freeze-fracture cryo-SEM with direct imaging to such systems has the advantages of observing a greater range of particle sizes, large depth of field implying larger tilts together with rotation, and freeze-etching/freeze drying the sample while imaging it. A procedure for cryo-SEM of liquid colloids, which uses a simple sample preparation setup, and its results for liposomal dispersions, are described here.Samples are plunge-frozen by a freezing device (Fig.l) made from a standard desoldering tool (Fig.2) used as a plunging unit. Fracture plates (Fig.3) are made from 0.1 mm thin copper sheet made adhesive to the liquid by 400 mesh TEM grids that are bent over the two edges of the plates and stuck on the non-sample side with a rubber adhesive. The sample is sandwiched between a pair of fracture plates (Fig.3) and plunged into liquid Freon-22 kept at its freezing point (-160°C) in an electrically heated cup (Fig.l) cooled by a liquid liquid nitrogen bath.


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