Page 145, Table II, fourth column heading should read: Erratum e = (At/t34)103 Our apologies to the following authors and to our readers Due to the fact that the printer advanced our deadline on the March 1976 issue, we were unable to wait for all authors' galley proofs to be returned before going to press. We offer our apologies to the following authors: Patrick Valentin and Georges Guiochon Toshihido Hanai and Kazumi Fujimura N. Moiseyev and I. Platzner C. David Pearson Corrections to their articles appear below. Typographical spelling errors, where the meaning is clear, have not been included. The following are corrections to the article, "Determination of Gas-Liquid and Gas-Solid Equilibrium Isotherms by Chromatography: II. Apparatus, Specifications, and Results, " by Patrick Valentin and Georges Guiochon, Journal of Chromatographic Science, 14(3) 132-139 (1976). Page 134, equation 14, should read: Page 135, first column, sentence beginning on line 29, should read: Refilling can be done periodically or constantly for high concentrations. Page 135, caption to Figure 2 should read: Figure 2. Diffusion cell: (a) Principle; (1) Mixing volume; (2) Diffusion tube; (3) Liquid in equilibrium with its vapor, (b) Device used for preparation of large concentration mixtures: (1) Mixing volume; (2) Diffusion volume; (3) Liquid; (4) Sintered metal disk; (5) Refilling. Page 139, equation 17 should read: = t f\ D + 4 A - k^B - XA Page 147, equation 22 should read: H(t) = 1/y 2[ 1 _ 1 Ni(t) Eq. 22 Page 147, column two, last sentence of first paragraph, "In addition . . . isotope effect" should be deleted. The following are corrections to the article, "The Determination of Trace Mercaptans and Sulfides in Natural Gas by a Gas Chromatography-Flame Photometric Detector Technique," by C. David Pearson, Journal of Chromatographic Science, 14(3) 154-158 (1976). Page 156, first column, third paragraph under the heading Calculation, the tenth line should read: E = slope of log plot = (log A1 /A2)/(log P1 /P2) where A1 and A2 are areas, and P1 and P2 are the pressures corresponding to those areas. Page 156, first column, last sentence should read: Stainless steel columns and connections are much more robust and cause fewer problems with leaks and absorption than Teflon, particularly at higher temperatures. Page 156, second column, last line of second paragraph (b) under heading Gas Chromatographic Column should read: elution time (see Figure 8). Page 157, caption to Figure 6 should read: Figure 6. Chromatogram of commercial odorant, Scentinel E. Conditions identical to Figure 5. Page 158, caption to Figure 7 should read: Figure 7. Chromatogram of commercial odorant, Scentinel F 50. Conditions identical to Figure 5. Eq.17 2 Pure Consistency*** 3p dp AA + k BA " k AB " k BB Page 139, reference 15 should read: 15. A. Raymond and G. Guiochon, J. Chromatog. Sci. 13 173 (1975). The following are corrections to the article, "Non-Aqueous Solvent Chromatography V: The Comparison of Organic and Inorganic Adsorbents," by Toshihiko Hanai and Kazumi Fujimura, Journal of Chromatographic Science, 14(3) 140-143 (1976). Toshihiko Hanai's present address is the Institute of Chemical Analysis, Applications, and Forensic Science, 341 Mugar, Northeastern University, Boston, Massachusetts 02115. Page 140, column two, sentence beginning on the fourth line under Table I should read: The plate numbers (N) were calculated from N 16(7"/ W) 2 where T is the retention time (min) of the sample and W is its peak width (min). The following are corrections to the article, "Isotope Effect in Gas-Solid Chromatography of SF6," by N. Moiseyev and I. Platzner, Journal of Chromatographic Science 14(3) 143-148 (1976). Page 144, column one, tenth line should read: Partial separation of 1 2 c - 1 3 c and 16o - 18o isotopic isomers of methane and carbon dioxide (13), 1 0B - 1 1 B (14), 12c - 13c (15) and 32s - 34$ (15) as their volatile fluorides, has also been reported. Hong Kong Buenos Aires Pick your city. Or lab. Anywhere. Any time. Your thin layer chromatography on EM plates will be consistent with other separations performed anywhere on EM plates. How? Why? Because the uniformity, homogeneity and chromatographic properties of EM precoated TLC plates have established new standards. Because of: a range of sorbents, guaranteed free from defects a choice of layer thicknesses. Plus the versatility of switching from EM's pre-coated glass, plastic or aluminum backings to other EM chromatographic media. For separating non-polar samples, use our new Reverse Phase Plates. Once a chromatographic combination has been chosen, results will be uniform, lab to lab, and applicable to other forms of the same sorbent. It's all part of the EM System Concept of Chromatography. Send for complete details. a sorbent layer with controlled pore volume, particle size, layer thickness and Inert binder "M EM Laboratories, Inc. E. Merck, Darmstadt, Germany 900 Executive Boulevard Elmsford, NY. 10523 (914) 992-488O laboratory reagents and indicator strips sorbents, plates and columns for chromatography biochemical specialties Instrumentation chemicals Circle number 25 JOURNAL OF CHROMATOGRAPHIC SCIENCE • VOL. 14 Denver APRIL 1976
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