Abstract: A bubbler chamber assembly comprising one chamber or two or more chambers connected in series, all chambers being in substantially vertical orientation. A solid or liquid source of the compound is contained in the chamber or chambers. The ratio between the length of the chamber or combined length of chambers connected in series with respect to the direction of flow of the carrier gas through the chamber or chambers and the average diameter equivalent of the cross section of the chamber or chambers with respect to the direction of flow of the carrier gas through the chamber or chambers is not less than about 6:1.

Abstract: Polymethylaluminoxane compositions having increased solution stability in organic solvent and, in some cases, increased polymerization activity, which comprise moieties derived from an organic compound containing an electron-rich heteroatom (e.g., from Group V and/or Group VI of the Periodic Table) and a hydrocarbyl moiety. These compositions can be formed by reaction of trimethylaluminum, the organic compound, and water. They can also be formed by reaction of pre-formed polymethylaluminoxane the organic compound, which can be a hydrocarbyl group-containing compound containing an electron-rich heteroatom (e.g., oxygen, nitrogen, or sulfur), either with or without an active hydrogen atom connected to the heteroatom. The organic compound, in some embodiments, has also been found to be effective in increasing the catalytic activity of modified polymethylaluminoxane which, in addition to methyl, contain C.sub.2 and higher alkyl groups for enhanced solution stability.

Abstract: Polymethylaluminoxane compositions having increased solution stability in organic solvent and, in some cases, increased polymerization activity, which comprise moieties derived from an organic compound containing an electron-rich heteroatom (e.g., from Group V and/or Group VI of the Periodic Table) and a hydrocarbyl moiety. These compositions can be formed by reaction of trimethylaluminum, the organic compound, and water. They can also be formed by reaction of pre-formed polymethylaluminoxane the organic compound, which can be a hydrocarbyl group-containing compound containing an electron-rich heteroatom (e.g., oxygen, nitrogen, or sulfur), either with or without an active hydrogen atom connected to the heteroatom. The organic compound, in some embodiments, has also been found to be effective in increasing the catalytic activity of modified polymethylaluminoxane which, in addition to methyl, contain C.sub.2 and higher alkyl groups for enhanced solution stability.

Abstract: The efficient production of alkylaluminoxane by the reaction of water, e.g., in the form of atomized water, and trialkylaluminum, e.g., trimethylaluminum, in an organic solvent medium can be achieved using a preformed alkylaluminoxane as a reaction moderator in the reaction mixture.

Abstract: Aluminoxanes can be produced by contacting an organic solvent containing a trialkylaluminum compound with an atomized spray of water. If desired, a pore-formed aluminoxane can be present as a reaction moderator.

Abstract: Trimethylaluminum can be formed by reacting a methylaluminum chloride, such as dimethylaluminum chloride, with sodium in the presence of an effective amount of an alkali or alkaline earth metal fluoride (e.g., sodium fluoride) to enhance the reaction.

Abstract: Dimethylzinc is prepared by heating a dimethylaluminum halide, e.g., dimethylaluminum chloride, and a dialkylzinc, e.g., diethylzinc, with distillative removal of dimethylzinc from the reaction mixture which results therefrom.

Abstract: Post-precipitation of solids from a hydrocarbon solution of an organomagnesium compound is prevented by addition of an appropriate amount of an alkyllithium compound.

Abstract: A process for the preparation of 2,4,5-trichlorophenol and 2,4,5-trichlorophenoxyacetic acid free of 2,3,7,8-tetrachloro-dibenzo-p-dioxin contamination by the steps of nitrating 1,2,4-trichlorobenzene, reducing the resulting 1,2,4-trichloro-5-nitrobenzene, diazotizing the resulting 2,4,5-trichloroaniline, hydrolyzing the resulting 2,4,5-trichlorobenzenediazonium salt and recovering 2,4,5-trichlorophenol. The 2,4,5-trichlorophenol is reacted with monochloroacetic acid to give 2,4,5-trichlorophenoxyacetic acid. Both the 2,4,5-trichlorophenol and the 2,4,5-trichlorophenoxyacetic acid produced by the process are analytically free of 2,3,7,8-tetrachloro-dibenzo-p-dioxin in analytical tests sensitive to 1 part per billion.