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LignosulfonatesLignosulfonates, or sulfonated lignin, (CAS number 8062-15-5) are water-soluble anionic polyelectrolyte polymers: they are byproducts from the production of wood pulp using sulfite pulping.[1] Additional recommended knowledgeMost delignification in sulfite pulping involves acidic cleavage of ether bonds, which connect many of the constituents of lignin.[2] The electrophilic carbocations produced during ether cleavage react with bisulfite ions (HSO3-) to give sulfonates.
The primary site for ether cleavage is the α-carbon (carbon atom attached to the aromatic ring) of the propyl (linear three carbon) side chain. The following structures do not specify the structure since lignin and its derivatives are complex mixtures: the purpose is to give a general idea of the structure of lignosulfonates. The groups labeled "Q" can be a wide variety of groups found in the structure of lignin. Sulfonation occurs on the side chains, not on the aromatic rings, like in p-toluenesulfonic acid. Lignosulfonate have very broad ranges of molecular mass (they are very polydisperse). A range of from 1000–140,000 da has been reported for softwood lignosulfonates with lower values reported for hardwoods.[1] PreparationLignosulfonates are recovered from the spent pulping liquids (red or brown liquor) from sulfite pulping. The most widely used industrial process is the Howard process, in which 90–95% yields of calcium lignosulfonates (CAS number 904-76-3), are precipitated by adding of excess calcium hydroxide. Ultrafiltration and ion-exchange can also be used to separate lignosulfonates from the spent pulping liquid.[1] A list of CAS numbers for the various metal salts of lignosulfonate is available.[3] UsesLignosulfonates have a wide variety of applications.[4] The single largest use for lignosulfonates is as plasticizers in making concrete,[1] where they allow concrete to be made with less water (giving stronger concrete) while maintaining the ability of the concrete to flow. Lignosulfonates are also used during the production of cement, where they act as grinding aids in the cement mill and as a rawmix slurry deflocculant (that reduces the viscosity of the slurry). The ability of lignosulfonates to reduce the viscosity of mineral slurries is used to advantage in oil drilling mud, where it replaced tannic acids from quebracho (a tropical tree). Lignosulfonates are used to disperse pesticides, dyes,[5] carbon black,[6] and other insoluble solids and liquids into water. They are used in tanning leather. They are also used to suppress dust on unpaved roads.[7] Oxidation of lignosulfonates from softwood trees produced vanillin (artificial vanilla flavor), but this is not a current use.[8] Dimethyl sulfide and dimethyl sulfoxide (an important organic solvent) are produced from lignosulfonates. The first step involves heating lignosulfonates with sulfides or elemental sulfur to produce dimethyl sulfide. The methyl groups come from methyl ethers present in the lignin. Oxidation of dimethyl sulfide with nitrogen dioxide produces dimethyl sulfoxide (DMSO). [1] References
Categories: Organic polymers | Polyelectrolytes |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Lignosulfonates". A list of authors is available in Wikipedia. |