1. Process route

Allyl Chloride high-temperature chlorination method: Propylene and chlorine gas are obtained by directly replacing the hydrogen atom on the methyl group of propylene with chlorine under high temperature conditions without a catalyst. The reaction equation is: H₂C=CH-CH₃+Cl₂ → H₂C=CH-CH₂Cl+HCl

2. Process flow

3. Technical advantages

Shandong Catech Technology Co., Ltd. is one of the few enterprises in the world that has mastered this technology, with multiple patents. Currently, all the Allyl chloride units in operation in China are provided by Catech with technology. For many years, Catech Technology has continuously optimized its process technology, and now the process has the following advantages: simple process flow, mild reaction conditions, high selectivity and product yield, and minimal corrosion to equipment. In addition, in order to improve the production efficiency and product quality of Allyl chloride, and reduce production and operating costs, Catech Technology has developed a 25000 ton reactor and has been successfully applied and verified.

4. Downstream market direction

Allyl chloride is widely used downstream and can be roughly divided into the following product routes:

① Allyl chloride → epichlorohydrin → glycerol, epoxy resin, chlorohydrin rubber, nitroglycerin explosives;

② Allyl chloride → Allyl alcohol (propylene alcohol) → Allyl bromide;

③ Allyl chloride → allyl isothiocyanate (mustard oil)/diallyl phthalate (DPA) and other allyl ester products;

④ Allyl chloride → allyl phenyl ether/trimethylolpropane diallyl ether/ α- Allyl ether products such as allyl glycerol ether;

⑤ Allyl chloride → silane coupling agent;

⑥ Allyl chloride → 1-bromo-3-chloropropane;

⑦ Allyl chloride → allyl thiourea;

⑧ Allyl chloride → 1,2,3-trichloropropane (TCP);

⑨ Allyl chloride → allylamines.