Patent classifications
C07C409/32
Formulation of di(4-tert-butylcyclohexyl) peroxydicarbonate
Powder formulation comprising 20-75 wt % of di(4-tert-butylcyclohexyl) peroxydicarbonate and 25-80 wt % of a phlegmatizer selected from the group consisting of ethylene glycol dibenzoate, phenyl benzoate, trimethylol propane tribenzoate, dimethylsulfon, ethylene glycol ditoluate, 1,3-propanediol ditoluate, ethylene glycol 4-tert-butylbenzoate, ethylene glycol monobenzoate monotoluate, 2,3-butanediol dibenzoate, 4-methylphenyl benzoate acid ester, and combinations thereof.
SOLID ORGANIC PEROXIDE COMPOSITION
Organic peroxide composition that is solid at room temperature, said composition comprising (i) at least about 40 wt %—based on the weight of the entire composition—of an organic peroxide that is solid at room temperature, said organic peroxide being selected from peroxydicarbonates and diacylperoxides, and (ii) about 0.001 to about 5 wt %—based on the weight of organic peroxide in the composition—of an HCl scavenger that is solid at room temperature.
SOLID ORGANIC PEROXIDE COMPOSITION
Organic peroxide composition that is solid at room temperature, said composition comprising (i) at least about 40 wt %—based on the weight of the entire composition—of an organic peroxide that is solid at room temperature, said organic peroxide being selected from peroxydicarbonates and diacylperoxides, and (ii) about 0.001 to about 5 wt %—based on the weight of organic peroxide in the composition—of an HCl scavenger that is solid at room temperature.
Online continuous flow process for the synthesis of organic peroxides using hydrogen peroxide as raw material
An online continuous flow production process for directly preparing organic peroxides by using hydrogen peroxide as a raw material. This production process uses hydrogen peroxide, catalyst, and an oxidation substrate as a raw material. Substrate will be turned to designated peroxides sequentially through oxidation and workup. This process is performed in a plug-and-produce integrated continuous flow reactor, and the raw materials are continuously fed to the reactor. So, specified peroxide can be continuously obtained at the outlet of the plug-and-produce integrated continuous flow reactor.
Online continuous flow process for the synthesis of organic peroxides using hydrogen peroxide as raw material
An online continuous flow production process for directly preparing organic peroxides by using hydrogen peroxide as a raw material. This production process uses hydrogen peroxide, catalyst, and an oxidation substrate as a raw material. Substrate will be turned to designated peroxides sequentially through oxidation and workup. This process is performed in a plug-and-produce integrated continuous flow reactor, and the raw materials are continuously fed to the reactor. So, specified peroxide can be continuously obtained at the outlet of the plug-and-produce integrated continuous flow reactor.
Online continuous flow process for the preparation of organic peroxides direct from alcohols or alkanes
A continuous flow production process for preparing organic peroxides directly from alcohols or alkanes takes very safe alcohols or alkanes as starting materials, and directly reacts to obtain designated peroxides. The production process is carried out in an integrated continuous flow reactor, and a safe starting source of alcohol or alkane is continuously added at the feed inlet of the integrated continuous flow reactor, and continuously provided with a designated peroxide at the discharge port of the integrated continuous flow reactor.
FORMULATION OF DI(4-TERT-BUTYLCYCLOHEXYL) PEROXYDICARBONATE
Powder formulation comprising 20-75 wt % of di(4-tert-butylcyclohexyl) peroxydicarbonate and 25-80 wt % of a phlegmatizer selected from the group consisting of ethylene glycol dibenzoate, phenyl benzoate, trimethylol propane tribenzoate, dimethylsulfon, ethylene glycol ditoluate, 1,3-propanediol ditoluate, ethylene glycol 4-tert-butylbenzoate, ethylene glycol monobenzoate monotoluate, 2,3-butanediol dibenzoate, 4-methylphenyl benzoate acid ester, and combinations thereof.
BCHPC having a reduced burning rate
The invention relates to the reduction of the burning rate of di-(4-tert-butylcyclohexyl)-peroxydicarbonate (BCHPC) by adding desensitizers as well as to the use of BCHPC preparations having a reduced burning rate as an initiator in chemical reactions.
BCHPC having a reduced burning rate
The invention relates to the reduction of the burning rate of di-(4-tert-butylcyclohexyl)-peroxydicarbonate (BCHPC) by adding desensitizers as well as to the use of BCHPC preparations having a reduced burning rate as an initiator in chemical reactions.
ONLINE CONTINUOUS FLOW PROCESS FOR THE PREPARATION OF ORGANIC PEROXIDES DIRECT FROM ALCOHOLS OR ALKANES
A continuous flow production process for preparing organic peroxides directly from alcohols or alkanes takes very safe alcohols or alkanes as starting materials, and directly reacts to obtain designated peroxides. The production process is carried out in an integrated continuous flow reactor, and a safe starting source of alcohol or alkane is continuously added at the feed inlet of the integrated continuous flow reactor, and continuously provided with a designated peroxide at the discharge port of the integrated continuous flow reactor.