Abstract: The present disclosure discloses a synthesis method of polyether for a low-modulus sealant, belonging to the technical field of organic compound synthesis. In the synthesis method of the present disclosure, a reaction is performed by using a mixture of monohydric alcohol polyoxypropylene ether and polyhydric alcohol polyoxypropylene ether as a starter, using epoxypropane as a chain extender and adding a metal complex catalyst, so as to obtain the polyether for the low-modulus sealant after the reaction is ended. The polyether prepared in the present disclosure can not only well enhance the rigid strength of the sealant but also reduce the elasticity modulus of the sealant, overcoming the problem that the existing polyether silane modified sealant is high in modulus. The synthesis method of the present disclosure is simple in synthesis process, easy to produce and control, short in production period and low in energy consumption.

Abstract: Disclosed a capacitive stylus pen, comprising a holding structure comprising a pen holder, and a pen tip assembly comprising a pen tip shaft and a strain sensor, the strain sensor comprising a resilient element and a strain gauge on the resilient element, and the resilient element being connected to the pen tip shaft and the holding structure, wherein the resilient element is L-shaped, the pen tip assembly further comprises an energy absorption structure arranged on the pen tip shaft, and the energy absorption structure is connected to the holding structure. The L-shaped resilient element in cooperation with the energy absorption structure forms a double-support elastic buffering structure and reduces deformation rate of the strain gauge with same load when the capacitive stylus pen itself rotates to different angles; and the energy absorption structure is added to share part of the stress on the resilient element to reduce the resilient element's deformation.

Abstract: The present invention relates to a synthesis method and synthesis reactor of high-selectivity 2-methylallyl chloride by taking isobutylene and chlorine gas as raw materials and performing a gas-phase chlorination reaction in a microchannel reactor with a cooling surface. The isobutylene and the chlorine gas are reacted in a T-shaped microchannel reactor, and the mixing speed is extremely fast. Meanwhile, the huge heat exchange area per unit volume can ensure that the reaction proceeds stably at a substantially constant temperature and has good controllability. Therefore, side reactions caused by excessive local temperature can be effectively suppressed, the reaction selectivity is high, and no coking phenomenon occurs.

Abstract: The present invention relates to a method for preparing 2-methylallyl chloride from 1,2-dichloroisobutane. The method is characterized in that 1,2-dichloroisobutane and a sodium hydroxide aqueous solution are used as raw materials; reactive rectification is performed in a combined rectifying tower to eliminate hydrogen chloride so as to obtain 2-methylallyl chloride. A plate tower is provided at the lower part of the combined rectifying tower; a packing tower is provided at the upper part of the combined rectifying tower; an inner reflux condenser is provided at the top of the combined rectifying tower. The sodium hydroxide aqueous solution is added from a first plate of the plate tower; and 1,2-dichloroisobutane is added from the middle part of the plate tower. The method has the advantages that the raw material 1 and 1,2-dichloroisobutane is fully converted; the selectivity of the 2-methylallyl chloride is high.

Abstract: The present invention relates to a method for preparing 2-methylallyl chloride from 1,2-dichloro-tert-butane. The method is characterized in that 1,2-dichloro-tert-butane and a sodium hydroxide aqueous solution are used as raw materials; reactive rectification is performed in a combined rectifying tower to eliminate hydrogen chloride so as to obtain 2-methylallyl chloride. A plate type tower is provided at the lower part of the combined rectifying tower; a packing tower is provided at the upper part of the combined rectifying tower; an inner reflux condenser is provided at the top of the combined rectifying tower. The sodium hydroxide aqueous solution is added from a first plate of the plate type tower; and 1,2-dichloro-tert-butane is added from the middle part of the plate type tower. The method has the advantages that the raw material 1 and 1,2-dichloro-tert-butane is fully converted; the selectivity of the 2-methylallyl chloride is high.

Abstract: The present invention relates to a synthesis method and synthesis reactor of high-selectivity 2-methylallyl chloride by taking isobutylene and chlorine gas as raw materials and performing a gas-phase chlorination reaction in a microchannel reactor with a cooling surface. The isobutylene and the chlorine gas are reacted in a T-shaped microchannel reactor, and the mixing speed is extremely fast. Meanwhile, the huge heat exchange area per unit volume can ensure that the reaction proceeds stably at a substantially constant temperature and has good controllability. Therefore, side reactions caused by excessive local temperature can be effectively suppressed, the reaction selectivity is high, and no coking phenomenon occurs.

Abstract: Provided in an embodiment of the present invention are a software key updating method and device. A trusted client device receives key information and verification information corresponding to the software and transmitted by a server, the key information containing a to-be-updated first software public key signature and a new second software public key signature, and the verification information containing software verification information; if a valid first software public key signature corresponding to the software and stored in the trusted client device is consistent with the received first software public key signature, then checking whether the software verification information is valid; and if the software verification information is valid, then updating the valid first software public key signature corresponding to the software and stored in the trusted client device as a second software public key signature.