http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11161811-B2
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c860c0fe21a8ff1ca8f3234bf1f60628 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2208-32 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K8-035 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K8-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K8-74 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K8-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K8-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-14 |
filingDate | 2018-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2021-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73ac608df03403f04fe3f225ea1457ae http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d88c213e8ff64ea257e1ed99751f6586 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13b580b5168cbd1f50f19e0547345dfa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dca63650ce333a63bee0fbc980056b32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c63301ca31a1e524a1b52eca633ded08 |
publicationDate | 2021-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-11161811-B2 |
titleOfInvention | Process for preparing Mannich base quaternary ammonium salt high-temperature resistant corrosion inhibitor and applications thereof |
abstract | The present invention discloses a process for preparing a Mannich base quaternary ammonium salt high-temperature resistant corrosion inhibitor and applications thereof. The preparation process comprises the following steps: (1) dissolve an amine substance indole, benzhydrylpiperidine, diphenylethylamine, dibenzylamine or diisopropanolamine into an organic solvent, slowly add an aldehyde substance 3-(2-thienyl)benzaldehyde or cinnamaldehyde, then place in a constant-temperature water bath, stir to react at 60-80° C. for 1 to 3 hours, then add a ketone substance benzalacetone, diphenylstyryl acetone or 1,1-diphenylacetone, adjust the reaction system pH to 3 to 4 using a hydrochloric acid solution, and then react for 7 to 10 hours; after cooled to room temperature, perform distillation under a reduced pressure to remove the solvent, to obtain a Mannich base; (2) dissolve the Mannich base in an organic solvent, add quaternizing reagent chloromethylnaphthalene, benzyl chloride or triphenylchloromethane, then react at 70-90° C. for 14-16 h, after cooled to room temperature, perform distillation under a reduced pressure. The process is simple and feasible, and its raw material is non-toxic, safe and environmental-friendly, and the prepared corrosion inhibitor has obvious resistance to the acid corrosion of carbon steels in oil-gas wells. |
priorityDate | 2018-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 129.