Abstract: Diethylaminoethyl (DEAE)-Cotton, prepared so that the tertiary amine nitrogens have unshared electrons and are thus in the Lewis-base form, is reacted with an alcoholic solution of an alpha-omega dihaloalkane to quaternize amino groups. The fabric produced by this process is crosslinked between tertiary amine nitrogen groups in cellulose and every alkylene group introduced is connected to two quaternary ammonium ions. The products of this process have strong base anion exchange properties and fabrics of high nitrogen content are imparted both wet and dry crease resistance.

Abstract: Strong base quaternary ammonium cellulose derivatives prepared under anhydrous conditions are further chemically modified in selected organic solvents by a sequential process that produces a partial cellulose ether in fibrous form that can be used in electro-chemical reactions covering a range of oxidation-reduction potentials. These new derivatives can be prepared such that they stabilize a given anion in the cellulose matrix until such time as its oxidation or reduction power is needed in desired chemical reactions. Although prepared in nonaqueous media, these red-ox cellulosic anion exchangers can be used to regulate oxidation-reduction reactions in aqueous media. Some of these new red-ox anion exchangers are dispersible in water and can be reprecipitated by organic solvents without losing their red-ox abilities during the process. Others are water insoluble.

Abstract: Partially carboxymethylated-cotton fabric prepared by a non-aqueous procedure is reacted with either ethylene carbonate or propylene carbonate in a heated, evacuated oven. The product of either reaction is a fabric with high conditioned and high wet wrinkle recovery.