Chemistry Project Grade 11 (I Am Jerish Alan)
Chemistry Project Grade 11 (I Am Jerish Alan)
Chemistry Project Grade 11 (I Am Jerish Alan)
FOOD ADULTERATION
Submitted by,
R. Jerish Alan
XII- A
ACKNOWLEDGEMENT
REGISTRATION NO:
2. Acknowledgement
3. Introduction
4. Theory
5. Activity
Aim
Apparatus required
Procedure
Result
Precautions
Conclusion
OBJECTIVE
The Objective of this project is to study some of the
common food adulterants present in different food
stuffs.
INTRODUCTION
Food is one of the basic necessities for sustenance
of life. Pure, fresh and healthy diet is most
essential for the health of the people. It is no
wonder to say that community health is national
wealth. Adulteration of food-stuffs was so
rampant, widespread and persistent that nothing
short of a somewhat drastic remedy in the form
of a comprehensive legislation became the need
of the hour. To check this kind of antisocial evil a
concerted and determined onslaught was
launched by the Government by introduction of
the Prevention of Food Adulteration Bill in the
Parliament to herald an era of much needed hope
and relief for the consumers at large.
About the middle of the 19th century chemical
and microscopal knowledge had reached the
stage that food substances could be
analyzed, and the subject of food adulteration
began to be studied from the standpoint of the
rights and welfare of the consumer. In 1860
the first food law framed in the interest of the
purchaser was passed.
That law, lacking sufficient means of enforcement,
remained largely ineffective until 1872, when
administrative officials were appointed
and penalties for violation provided.
In the United States the federal Food and Drug
Act of 1906 was the result of a long and stormy
campaign led by Dr. Harvey Washington Wiley.
This law defined food adulteration and the
misbranding of products; it provided regulations
covering the interstate movement of food and
penalties for violations. The 1906 act
was superseded in 1938 by the more rigorous
Food, Drug, and Cosmetic Act administered since
1940 by the Food and Drug Administration (now
within the Dept. of Health and Human
Services).The FDA is charged with enforcing
truthful and informative labeling of essential
commodities, maintaining staff laboratories, and
formulating definitions and standards promoting
fair dealing in the interests of the consumer. The
1938 act broadened the definitions of
adulteration, misbranding, and lack of informative
labeling; it provided for factory inspections; and it
increased the penalties for violations. It was
amended in 1958 and 1962 to define and regulate
food additives and food coloring. The federal law
controls traffic from one state to another and is
supplemented by local regulations that require
food handlers to be licensed, thereby
discouraging the spread of disease; it provides for
the inspection by health officers of meat and
other foods, of restaurants, and of dairies and
cold storage methods. Imported goods that
violate the provisions of the act may be denied
admittance to the United States and if not
removed within a given time may be destroyed.
STATEMENT OF OBJECTS AND
REASON:
ACT 37 OF 1954:
GOVERNMENT MEASURES:
EXPERIMENT I
EXPERIMENT II
insoluble impurities
do not dissolve.
presence of chalk
sample of sugar.
EXPERIMENT III
powder: To a sample of
turmeric powder: To a