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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436709Generated: October 27, 2026

Ammonia → Silver behenate

https://huagongshe.com/reaction/436709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantNitric AcidHCID 944—
ReactantSilver NitrateHCID 24470—
ReactantAmmonium iodideHCID 25487—
ReactantAmmonium BromideHCID 25514—
ReactantSilver behenateHCID 164971—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductSilver behenateHCID 164971—
ProductSilver bromoiodideHCID 57465667—

Reaction Steps

3.4 g of silver behenate was dissolved in 100 ml of toluene at 60° C. 100 ml of a diluted aqueous solution of nitric acid having a pH of 2.0 (25° C.) was mixed with this solution while stirring the solution with a stirrer. The mixture was stirred at 60° C. and 100 ml of an aqueous solution of silver ammonium complex salt which was prepared by adding an ammonia solution to about 80 ml of an aqueous solution containing 1.7 g of silver nitrate and adding water to make the total volume 100 ml and then 50 ml of an aqueous solution containing 0.047 g of ammonium bromide and 0.001 g of ammonium iodide were added thereto at the same time while stirring the solution. Thus silver behenate and silver iodobromide were formed at the same time. When the reaction product was allowed to stand for 20 minutes at room temperature, it separated into an aqueous phase and a toluene phase. After removal of the aqueous phase, the toluene phase was washed with 400 ml of fresh water by decantation. This washing treatment was repeated three times. Then 400 ml of water was added thereto and silver behenate - silver iodobromide was separated by centrifugal separation. Thus 4 g of a mixture wherein spindle shaped silver behenate crystals having a length of about 1 micron and a diameter of about 0.05 microns contacted with silver iodobromide was produced. 2.5 g of this silver behenate-silver iodobromide mixture was added to 20 ml of an isopropyl alcohol solution containing 2 g of polyvinyl butyral and the mixture was ball milled for 1 hour to produce a polymer dispersion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028129
Source datasetuspto-grants-1977_06
ORD IDord-978325f3951146d99f1e2b5f0dd1f210
Source noteuspto-grants-1977_06