(1), is approximately 3 s and is further reduced by interactions with the glass container wall and the formation of van der Waals complexes. For the addition of co-adsorbing water vapor, a vessel filled with 10 ml of liquid water and 3.1 kPa of water vapor was connected to the shuttle system. After the shuttling system was evacuated following the SEOP procedure described in Section 2.1, the water vessel was opened and allowed the system to be filled with water vapor. The vessel was then closed again and delivery of hp 131Xe gas was

carried out on top of the approximate 3.1 kPa water vapor (see Fig. 1 for details). T1 values for hp 131Xe were calculated by nonlinear least-squares selleck compound fitting of the 131Xe signal intensity as a function of time and number of applied medium flip angle radio frequency pulses. Since each data point in T1 measurements was an Dasatinib cost average of four replicate measurements, the errors reported in this work were calculated as standard deviations. Quadrupolar splittings, 2νQ, and linewidths were obtained from 131Xe NMR spectra after deconvolution by multi-peak fitting routine using Lorentzian functions. Data analysis

and simulations of the polarization curves were performed using Igor Pro, Version 6.11 from Wavemetrics, OR, USA. As detailed in the introduction, spin-exchange optical pumping of 131Xe has been explored previously, but these studies focused exclusively on phenomena within the SEOP cells. Although the separation of hp Janus kinase (JAK) 3He, hp 129Xe (both spin I = 1/2) [5], [65] and [66], and more recently hp 83Kr

(I = 9/2) [64], [67], [68] and [69] from the SEOP alkali metal vapor is well developed, the separation of the hp 131Xe from the alkali metal vapor has never been reported. The major obstacle for producing alkali metal free hp 131Xe are the large nuclear electric quadrupole interactions found with this isotope. Quadrupolar interactions caused by binary gas-phase collisions [21] and [26], the formation of gas-phase van der Waals complexes, [24], [25], [26] and [27], and brief periods of adsorption on surfaces [68] lead to fast longitudinal relaxation that diminishes the level of hyperpolarization. In contrast to 129Xe, which has a T1 time on the order of hours at ambient pressure and temperature [70], a T1 time below 5 s was observed in this work for gas-phase hp 131Xe at a pressure of 120 kPa (using mixture III (93% Xe) at 9.4 T in a 12.6 mm inner diameter glass cell). This value is much shorter than the value of T1 ≈ 23 s that was expected from the pure gas-phase relaxation given by Eq. (1) [21] because of the relatively large surface to volume ratio in the NMR detection tubes and because of relaxation contributions arising from van der Waals complexes.