Abstract: A graphical user interface displayed by a processing device in operative communication with an ultrasound device may include a preset filter option that provides an easy way to switch between different presets which belong to a preset family. The user uses the preset filter feature to cycle through the different presets in the family while remaining on the same screen that is showing ultrasound images collected in real time. The imaging depth remains the same while the user is using the preset filter feature to select the preset within a family Other settings such as time-gain compensation may not remain the same when cycling between presets. The preset filter feature allows a user to continuously view and assess the ultrasound images being collected in real time while cycling through the presets in the family.

Abstract: A fishback assembly which is mounted on top of a separation device on an agricultural combine. The fishback assembly comprises a series of vertical fishback flanges that are coupled to one another by upstream and downstream mounting brackets. The mounting bracket is mounted to the separation device by mounting bolts passing through mounting holes formed ion the mounting brackets.

Abstract: The present invention provides a process for the preparation of 1,4:3,6-dianhydro-D-glucitol-5-nitrate, in which(a) 1,4:3,6-dianhydro-D-glucitol is acetylated with 0.5 to 1.5 mole equivalents of acetic anhydride in the presence of a catalyst, a mixture of 1,4:3,6-dianhydro-D-glucitol-2-acetate, 1,4:3,6-dianhydro-D-glucitol-5-acetate and 1,4:3,6-dianhydro-D-glucitol-2,5-diacetate being obtained;(b) the mixture is nitrated with nitric acid, a mixture of 1,4:3,6-dianhydro-D-glucitol-2-acetate-5-nitrate and 1,4:3,6-dianhydro-D-glucitol-5-acetate-2-nitrate being obtained; and(c) hydrolysis is carried out with an inorganic base to give 1,4:3,6-dianhydro-D-glucitol-5-nitrate;wherein, in step (a), the reaction is carried out in the presence of a basic catalyst and the 1,4:3,6-dianhydro-D-glucitol-2,5-diacetate is substantially removed before further working up.

Abstract: The present invention provides a process for the preparation of 5-(4'-chloro-5'-sulfamoyl-2'-thenylamino)-phenyltetrazole by condensing 5-(4'-chloro-5'-sulfamoyl-2'-aminophenyl)-tetrazole with thiophene-2-aldehyde in the presence of an acid catalyst and reducing the 5-[4'-chloro-5'-sulfamoyl-2'-(thenylidene-2-amino)-phenyl]tetrazole so obtained with a boranate, wherein the condensation is carried out in dimethyl sulfoxide as solvent, with azeotropic distilling off of the water formed and the reduction is carried out in the same medium, without isolation of the 5-[4'-chloro-5'-sulfamoyl-2'-(thenylidene-2-amino)-phenyl]-tetrazole.

Abstract: The present invention provides a process for the preparation of 4-hydroxycarbazole by the dehydration of 1,2,3,4-tetrahydro-4-oxocarbazole, wherein the reaction is carried out in aqueous alkaline solution, using Raney nickel as catalyst.

Abstract: The process for the chromatographic fractionation of whey comprising passing whey through a column of an ion exchange material, thereafter passing water through said column as eluant, and collecting the aqueous effluent from said column as a plurality of fractions. Advantageously the ion exchange material is a polystyrene resin containing sulfonic acid groups neutralized with calcium ions and cross-linked with about 2 to 4% by weight of divinyl-benzene, and the eluant is demineralized water.