Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258176Generated: October 25, 2026

Acetate → Calcium Acetate

https://huagongshe.com/reaction/258176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantFormateHCID 283—
ReactantFormaldehydeHCID 712—
ReactantPropionic AcidHCID 1032—
ReactantPropionate ionHCID 104745—
ReactantCalciumHCID 5460341—
SolventAcetic AcidHCID 176—
SolventFormic AcidHCID 284—
ProductCalcium AcetateHCID 6116—
ProductCalcium formateHCID 10997—
ProductCalcium propionateHCID 19999—

Reaction Steps

Calcium salts, such as calcium acetate, calcium formate or calcium proprionate, are obtained from aqueous liquors derived from the pyrolysis of lignocellulosic biomass containing cellulose, hemicelluloses or starch. The above biomass is subjected to rapid pyrolysis to obtain a crude product containing an aqueous phase and an organic phase. The product obtained, preferably as the aqueous phase, is then distilled to produce a distillate containing at least one acid selected from acetic acid, formic acid and propionic acid as well as their esters and formaldehyde. An alkaline source of calcium is added to this distillate to adjust the pH to an alkaline level sufficient to hydrolyze the esters, cause at least partial oxidation of the formaldehyde and prevent volatilization of acetate, formate or propionate ions as acetic acid, formic acid or propionic acid respectively. This pH adjusted alkaline liquid is then subjected to a further distillation to remove water and volatile organic components and produce at least one of calcium acetate, calcium formate and calcium propionate as solid residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264623
Source datasetuspto-grants-1993_11
ORD IDord-16b1ba1558904565bf5ed4916f00085d
Source noteuspto-grants-1993_11