Abstract: Anionic and cationic polymers are prepared by vinyl polymerizing a 2-alkenyloxazoline or 2-alkenyloxazine and reacting the resulting polymer which contains pendant oxazoline or oxazine moieties with a monobasic salt of sulfurous acid or a tertiary amine salt. Optionally, the 2-alkenyloxazoline or 2-alkenyloxazine can be polymerized with another ethylenically unsaturated monomer and/or a small amount of polyvinyl crosslinking monomer; and the resulting polymer is reacted with the desired salt to yield an anionic or cationic polymer.

Abstract: A process for modifying polymeric amine salts containing a halide ion by admixing with an epoxide to form a volatile halo-hydrin. By adjusting the amount of epoxide employed, the polymeric amine salt can be selectively modified by neutralization wherein partial or total conversion of the halide ion to a halo-hydrin is formed and by hydroxylation wherein the free amine sites formed from the conversion of the halide ion to a halo-hydrin are further reacted with excess epoxide to form a hydroxyl containing graft. The halo-hydrin is volatile and, therefore can be removed by distillation from the modified polymeric amine.

Abstract: The title salts are prepared in high purity by contacting in an aqueous reaction medium (a) 2-isopropenyl-2-oxazoline present in its free form in low concentration and (b) an acid selected from the group consisting of hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, nitric acid, organic carboxylic acids, alkyl or aryl sulfonic acids and mixtures thereof. The low concentration of 2-isopropenyl-2-oxazoline (IPO) in its free form can be achieved by adding the IPO slowly to the reaction mixture so that it does not accumulate or by maintaining a pH of less than about 2.5 in the reaction mixture so that nearly all of the IPO will be protonated.

Abstract: Anionic and cationic polymers are prepared by vinyl polymerizing a 2-alkenyloxazoline or 2-alkenyloxazine and reacting the resulting polymer which contains pendant oxazoline or oxazine moieties with a monobasic salt of sulfurous acid or a tertiary amine salt. Optionally, the 2-alkenyloxazoline or 2-alkenyloxazine can be polymerized with another ethylenically unsaturated monomer and/or a small amount of polyvinyl crosslinking monomer; and the resulting polymer is reacted with the desired salt to yield an anionic or cationic polymer.

Abstract: Lower trialkanolamines such as triethanolamine and triisopropanolamine are converted to the corresponding mono- and dialkanolamine by reacting with ammonia at about 150.degree. C.-275.degree. C. under superatmospheric pressure in the presence of a hydrogenation catalyst. The process is particularly useful for the recovery of alkanolamine values from still bottoms of alkanolamine production processes.

Abstract: The process of the invention for preparing a N-(2-substituted aminoethyl)amide of the formula: ##STR1## comprises contacting one or more compounds of the formula: ##STR2## with an amine of the formula: ##STR3## wherein A is nitrogen or a quaternary nitrogen of the formula: ##STR4## wherein B is ##STR5## when A is nitrogen and B is ##STR6## when A is IV; whereinX.sup..crclbar. is a counterion;b is zero or one; andR.sub.1 -R.sub.9 are as defined in the specification.In a preferred embodiment, the process is catalyzed by a Lewis acid or a protonic acid with a non-nucleophilic counterion.