If we have to use nitrogen gas for packaging like food, pharmaceuticals, ampules filling etc.... then what minimum purity of nitrogen gas and pressure would be required as per USP or BP standards. Any documentary reference would be appreciated.
for food standards USDA and 3A may also have something to do about that also.
just remember when working with multiple government agencies.....their standards can conflict with each other........come to think, even in a single agency like USDA-3A its own standards can conflict with its own....and is left to the inspectors interpedation....so be good to the inspectors.
p911
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“ When people get what they want, they are often surprised when they get what they deserve " - James Wood
It will depend on the application. For example if the product is pro-ported to be sterile, for babies or for those with imparted immune systems etc then the requirements will be different when compared to say bag of chips (or whatever food item).
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"New and stirring things are belittled because if they are not belittled, the humiliating question arises, 'Why then are you not taking part in them?' " - H. G. Wells
You have to be careful to specify what process you are undertaking. Broadly speaking, it makes a difference whether it is a pharmaceutical process (http://www.us.lindegas.com/international/web/lg/us/likelgus30.nsf/docbyalias/nav_industry_pharm_usp) or a food process (http://www.linde-gas.ae/international/web/lg/com/likelgcom30.nsf/docbyalias/nav_biogon) or a general industrial process. As a matter of curiosity with regard to different standards for different purposes, medical oxygen is not as pure an oxygen as some industrial oxygen, but nevertheless industrial oxygen is not to be used for medical purposes.