When I teach medical physics (PHY 326 here at Oakland University), I go over this derivation in class, but the students still need practice. I have them analyze some related examples as homework. For instance, the oscillating magnetic field can be in the y direction, B1 = B1 cos(ωt) j, or can be shifted in time, B1 = B1 sin(ωt) i. Sometimes I even ask them to analyze what happens when the oscillating magnetic field is in the z direction, B1 = B1 cos(ωt) k, parallel to the static field. This orientation is useless for exciting spins, but is useful as practice.
Yet another way to excite spins is using a circularly polarized magnetic field, B1 = B1 cos(ωt) i – B1 sin(ωt) j. The analysis of this case is similar to the one in IPMB, with one twist: you don’t need to average over time! Below is a new homework problem illustrating this.
Problem 13 1/2. Assume you have a static magnetic field in the z direction and an oscillating, circularly polarized magnetic field in the x-y plane, B =Bo k + B1 cos(ωt) i – B1 sin(ωt) j.
a) Use Eq. 18.12 to derive the equations for the magnetization M in the laboratory frame of reference (ignore relaxation).
b) Use Eq. 18.18 to transform to the rotating coordinate system and derive equations for M'.
c) Interpret these results physically.I get the same equations as derived in IPMB (Eq. 18.25) except for a factor of one half; the angular frequency in the rotating frame is ω1 = γ B1. Not having to average over time makes the result easier to visualize. You don’t get a complex motion that—on average—rotates the magnetization. Instead, you get a plain old rotation. You can understand this behavior qualitatively without any math by realizing that in the rotating coordinate system the RF circularly polarized magnetic field is stationary, pointing in the x’ direction. The spins simply precess around the seemingly static B1'= B1 i', just like the spins precess around the static Bo = Bo k in the laboratory frame.
Now let’s assume that an RF excitation pulse rotates the magnetization so it aligns with the x' rotating axis. Once the pulse ends, what happens? Well, nothing happens unless we account for relaxation. Without relaxation the magnetization precesses around the static field, which means it just sits there stationary in the rotating frame. But we know that relaxation occurs. Consider the mechanism of dephasing, which underlies the T2* relaxation time constant. Slight heterogeneities in Bo mean that different spins precess at different Larmor frequencies, causing the spins to lose phase coherence, decreasing the net magnetization.
Next, consider the case of spin lock. Imagine an RF pulse rotates the magnetization so it is parallel to the x' rotating axis. Then, when the excitation pulse is over, immediately apply a circularly polarized RF pulse at the Larmor frequency, called B2, which is aligned along the x' rotating axis. In the rotating frame the magnetization is parallel to B2, so nothing happens. Why bother? Consider those slight heterogeneities in Bo that led to T2* relaxation. They will cause the spins to dephase, picking up a component in the y' direction. But a component along y' will start to precess around B2. Rather than dephasing, B2 causes the spins to wobble around in the rotating frame, precessing about x', with no net tendency to dephase. You just killed the mechanism leading to T2*! Wow!
Will the spins just precess about B2 forever? No, eventually other mechanisms will cause them to relax toward their equilibrium value. Their time constant will not be T1 or T2 or even T2*, but something else called T1ρ. Typcially, T1ρ is much longer than T2*. To measure T1ρ, apply a 90 degree excitation pulse, then apply a RF spin lock oscillation and record the free induction decay. Fit the decay to an exponential, and the time constant you obtain is T1ρ. (I am not a MRI expert: I am not sure how you can measure a free induction decay when a spin lock field is present. I would think the spin lock field would swamp the FID.)
T1ρ is sometimes measured to learn about the structure of cartilage. It is analogous to T1 relaxation in the laboratory frame, which explains its name. Because B2 is typically much weaker than Bo, T1ρ is sensitive to a different range of correlation times than T1 or T2 (see Fig. 18.12 in IPMB).
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