Mr. Jason Perry , NC A&T State University, Department
of Physics
Lifetime of the Neutral Pion via the Primakoff Effect
Jason Perry
Greensboro, NC
Guilford County
Faculty Advisor(s): Samuel Danagoulian
Department of Physics, North Carolina A&T
State University
The Primakoff effect is a process of beam
particle scattering off the target nucleus at small angles. In this process
the scattering occurs in the electromagnetic field of the nucleus without
creating a large background of nuclear particles. In the reaction of pion
production via the Primakoff effect, the beam of photons is directed to the
atomic nucleus producing neutral pions at very small angle. Produced pions
later decay into two more photons. If we know the energy of the initial photons,
the energy and the emerging angles of the decay photons, then we can calculate
the lifetime of the pion. I was involved in the construction of several
detectors for this experiment.
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Ms. Nikia Isley-George: Department of Political Science,
NC A&T State University
Racial Profiling in Greensboro Police
Department: Examination of Minority Trust
Abstract
The purpose of this research project is
to examine the role of racial profiling in the relationship between
Law Enforcement and Minority Communities in Greensboro, N.C.
Racial Profiling refers to the Phenomenon of targeting people of color
in traffic enforcement as a pretext to further investigation or search.
Racial Profiling is a very controversial topic and has received a great deal
of attention in the national media. More importantly, members
of Congress, President Bush and Attorney General Ashcroft have suggested
this issue will be a top priority in the new administration.
Two Bills have been introduced in Congress to mandate collection of data
at the federal level. Several states and local law enforcement agencies
are collecting data on Traffic Stops.
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Ms. Deidra Felton, Department of Human Environment and Family
Sciences, NC A&T State University
Microbiological Quality and Shelf-Life of Fish
as Influenced by Bifidobacteria and Chemical Preservatives
Deidra Felton
Faculty Advisors: S.A. Ibrahim,
and C.W. Seo
Food Microbiology and Biotechnology
laboratory, 171 Carver Hall, North Carolina A&T State University, Greensboro,
NC 27411
Abstract
In this study tilapia samples
were immersed into the following solutions for 2 minutes: 1) 0.1 M sodium
acetate, 2) 0.1 M sodium phosphate, 3) 10% Tween-20, 4) 0.1 M EDTA, 5) bifidobacteria
fermented broth and 6) combinations of bifidobacteria and each of the four
food preservative solutions. Samples, which received no treatment,
served as controls. Fish samples were stored at 4( C for
the period of 14 days and analyzed for bacterial count. Samples treated
with bifidobacteria alone or in combination with EDTA or Tween 20 showed
significantly reduction in microbial population followed by EDTA alone.
Samples treated with sodium acetate delayed microbial growth in comparison
with control treatment. Significant increase in microbial population
was found in control samples during the storage period. Bifidobacteria
alone or in combination with other food preservatives could be used to increase
the shelf-life of fish and fish products. This method has the potential
for use as a low-cost means to extend the shelf-life of fish and possibly
other food products.
Mr. Somphavanh Phetsamphou, Department of Human Environment
and Family Sciences, NC A&T State University
Encapsulation of Lactobacillus reuteri with
Sodium Alginate for Continuous Production of Lactic Acid
S. Phetsomphou
Faculty Advisor: S.A.
Ibrahim,
Food Microbiology and Biotechnology
laboratory, 171 Carver Hall, North Carolina A&T State University, Greensboro,
NC 27411
Abstract
In this study, the production
of lactic acid was compared using two types of fermentation methods:
Batch and Batch bead fermentation. Five strains of L. reuteri, were used.
These strains were grown in lactobacillus MRS at 37(C for 24 hours. The cells
were then washed and suspended in 10-ml peptone water. Sodium alginate
beads were prepared by resuspending the 10-ml culture in 7% sodium alginate
solution. Beads were manufactured by dropping sodium alginate
culture into ice-cold (2( C) 0.4M calcium chloride using a separatory
funnel. Under comparable conditions the sodium alginate encapsulated
cells were allowed to ferment in 500-ml lactobacillus MRS and whey based medium
at 37(C for 24 hrs. Results showed that the pH reached 4.00 within
15 hrs with beads fermentation and reached 5.40 using conventional batch.
Our results suggest that using immobilized cells of L. reuteri could have
potential use to produce lactic acid for commercial applications in food
and pharmaceutical industries.
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