Two models of a liquid-hydrogen (?-illegible) Cherenkov counter (illegible) been constructed (illegible). The first served as a prototype (?-illegible) and was (illegible) to demonstrate the feasibility (?-illegible) of the (illegible) concept (?-illegible) (illegible) liquid hydrogen does not give scintillation (?-illegible) (illegible) that of Cherenkov light. The second, final version (?-illegible), (illegible) in an experiment (?-illegible) in which particles brought to rest (?-illegible) (illegible) (illegible) electrons. In this second counter, the efficiency (?-illegible) (illegible) relativistic (?-illegible) particles (?-illegible) by their Cherenkov radiation in liquid hydrogen (?-illegible) was measured by stopping (illegible) mesons in the hydrogen and detecting their decay electrons outside (?-illegible) of the flask (?-illegible) after a suitable time delay. An average detection (?-illegible) efficiency (?-illegible) of 75% (?-illegible) was (illegible) taken over the volume of the hydrogen (?-illegible).

Document issued by the Office of the Attorney General of Texas in Austin, Texas, providing an interpretation of Texas law. It provides the opinion of the Texas Attorney General, Waggoner Carr, regarding a legal question submitted for clarification: Various questions relative to the “Rule Making Procedure” rule adopted by the Texas State Board of Examiners in Optometry.

Document issued by the Office of the Attorney General of Texas in Austin, Texas, providing an interpretation of Texas law. It provides the opinion of the Texas Attorney General, Waggoner Carr, regarding a legal question submitted for clarification: Whether certain advertising on specialized motor vehicles violate Article 1690 in Vernon’s Penal Code?

Technical report. From "3. Methods of Preparation" : "Pivadehyde cyanohydrin can be prepared by the reaction of pivadehyde with anhydrous HCN2 or by the sodium bisulfite process. Trimethyllactamide can be prepared by hydrolysis of pivaldehyde cyanohydrin with cold concentrated sulfuric acid. The procedure described here differs in the scale of preparation an in the use of cold fusing hydrochloric acid for hydrolizing the cyanohydrin."