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Main ideas:
Groups of runs. Groups are different but not identified as random choices, we have fixed blocking.
Problem of fixed blocking: Can’t use it to predict individual runs from future blocks
Experiments that consider fixed blocking need way more runs that experiments with random blocks. So
x runs in smallest random block, need 2x runs in smallest fixed size block.
Create design where blocks are nearly orthogonal with factor effects, If can’t block orthogonally show
how much variance increases.
Q what is the case? Iimprove shelf life of photosensitive vitamin supplement by adding fatty molecule to
it. Day to day variation exists in expt where apparatus that measures decay due to light is recalibrated
each day. Each day is a block. 8 days of experiment so 8 blocks.
Q.What is the problem? Can’t estimate 2-factor interactions independent of block effects. They are
completely confounded with block effects.
If you increase runs to 64, block effects double as well but still can’t estimate them
Q.What are the good points of this model? 1) The VIF for main effects and unconfounded 2-factor
interactions=1.So they can be estimated with maximum precision or minimum variance. Block effects
also have VIF=1.
Q.What could be potential solution? Use random blocks. Since each factor has 2 levels,
Right table:two VIFs from D-optimal design for random blocks. VIF of all factors is 1. Total VIF is VIF due
to blocking. Five of blocking factors has VIF of 1 and so can be estimated with maximal precision. None
of VIF is larger than 2.57. So can estimate all 2-factr interactions at the price of slightly imprecise
estimates.