In standard weight box used for calibration of analytical
balance there are two numbers (Qty) of 20mg, 200mg,2.oGM
weights. Why?
Answers were Sorted based on User's Feedback
Answer / g. subrahmanyam
In standard weights box we receive single 1 mg, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and 500 mg, 1.0 gram, 5.0 grams, 10.0 grams and 100.0 grams weights. But we will receive two numbers of 2.0 mg, 20.0 mg, 200.0 mg, 2.0 grams, 20.0 grams and 200.0 grams weights in the box.
In order to weigh 4 mg, 9 mg, 14 mg, 25 mg, 34 mg, 44 mg, 54 mg, 64 mg, 74 mg, 84 mg, 94 mg, 104 mg, 19 mg, 29 mg, 39 mg, 49 mg, 59 mg, 69 mg, 79 mg, 89 mg and 99 mg we require two numbers of 2 mg in combination with other weights. Similarly the above same case apply with 20 mg, 2.0 grams, 20 grams and with 200 grams when we go the above level.
| Is This Answer Correct ? | 10 Yes | 2 No |
Answer / nilesh
in box u receive 1,2,5,10,20,50,100,200,500
now for 30 mg u able to use 10+20. but what about 40mg,90mg,140mg,190mg,400mg
| Is This Answer Correct ? | 8 Yes | 2 No |
What is the difference between the optics of UV and PDA Detectors ?
What is primary & Secondary Standard ? Give Example
what is the difference between LOSS ON DRYING IN ORDINARY OVEN TECHNIQUE AND VACUUM OVEN TECHNIQUE
i want to know about headspace and interview question on headspace
1 Answers Srikem Laboratories,
In which cases factor of KF Reaget got higher side
What are the different zones in stability according to ICH?
what is mean by least count balance?
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
0 Answers Reddy Labs, Vimta Labs,
What is the composition of K.F
What is the lab normality??
principle of UV , PDA , RI detector in HPLC
Can anybody tell me how to measure Redox potential in an aerobic matrix, for e.g., soil etc.?