CN104724752A - Normal-temperature synthesis method of tin tetrachloride - Google Patents
Normal-temperature synthesis method of tin tetrachloride Download PDFInfo
- Publication number
- CN104724752A CN104724752A CN201510089511.XA CN201510089511A CN104724752A CN 104724752 A CN104724752 A CN 104724752A CN 201510089511 A CN201510089511 A CN 201510089511A CN 104724752 A CN104724752 A CN 104724752A
- Authority
- CN
- China
- Prior art keywords
- tin tetrachloride
- tin
- normal
- synthesis method
- chlorine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Catalysts (AREA)
Abstract
The invention discloses a normal-temperature synthesis method of tin tetrachloride. The normal-temperature synthesis method comprises the following steps: immersing tin into tin tetrachloride liquid, adding metallic carbon nanotubes, further introducing chlorine gas, controlling the temperature in a kettle at 20-30 DEG C, controlling the pressure at 1-3Pa and controlling the flow rate of chlorine gas at 1-3m<3>/h. Tin tetrachloride is prepared by adopting gas-liquid-solid heterogeneous reaction, the metallic carbon nanotubes are taken as an auxiliary catalyst, the yield is greatly improved in comparison with gas-solid heterogeneous reaction, the improving capability can be improved by 5 times or more, and continuous and stable production can be realized.
Description
Technical field
The present invention relates to a kind of manufacture method of mineral compound, more particularly, the present invention relates to a kind of normal temperature synthesis method of tin tetrachloride.
Background technology
At present, usually use gas, Gu inhomogeneous reaction method manufactures tin tetrachloride.Because tin, chlorine reaction are thermopositive reaction, temperature of reaction exceedes the melting temperature (231.5 DEG C) of tin very soon within very short time, so the fusing usually due to tin in reaction process causes chlorine channel blockage, thus causes stopping production.In addition, because the flowing of chlorine in tin slab is flow channels, so chlorine is little in tin surfaces contact area, the residence time is short, causes chlorine utilization low, affects tin tetrachloride yield.Meanwhile, have greater environmental impacts because chlorine content in tail gas is too high.
Summary of the invention
The object of the invention is to overcome chlorine passage in above-mentioned prior art often block, the shortcomings such as tin tetrachloride yield is low, provide one not adopt gas, solid inhomogeneous reaction method, and the novel method satisfactory for result that tin tetrachloride yield is quite high
The technical scheme of employing of the present invention comprises: tin is immersed tin tetrachloride liquid, and add metallic carbon nanotubes, then pass into chlorine, and controls temperature in the kettle at 20-30 DEG C, and pressure-controlling is at 1-3Pa, and chlorine flowrate controls at 1-3m
3/ h.
The present invention produces tin tetrachloride owing to adopting gas, liquid, solid inhomogeneous reaction, and using metallic carbon nanotubes as cocatalyst, yield comparatively gas, solid non-phase reaction improves a lot, and raising ability can improve more than 5 times, can continuous and stable production.
Embodiment
Embodiment 1, in φ 200 × 6 normal-pressure reaction kettle, drops into 70kg tin in tin tetrachloride liquid, makes it to flood, and add Determination of trace gold attribute carbon nanotube.The medial temperature of still 30 DEG C, still internal pressure 1.6Pa.Chlorine flowrate 1.6m3/h, reacts 22 hours, obtains tin tetrachloride 152.8kg, tin tetrachloride yield 99.56%, chlorine utilization 98.9%.
Embodiment 2
In φ 200 × 6 normal-pressure reaction kettle, drop into 70kg tin in tin tetrachloride liquid, make it to flood, and add Determination of trace gold attribute carbon nanotube.The medial temperature of still 25 DEG C, still internal pressure 0.916Pa, chlorine flowrate 1.2m3/h, react 23 hours, obtains tin tetrachloride 148kg, tin tetrachloride yield 96.43%, chlorine utilization 92%.
Embodiment 3
In φ 200 × 6 normal-pressure reaction kettle, drop into 70kg tin in tin tetrachloride liquid, and add Determination of trace gold attribute carbon nanotube, the medial temperature of still 30 DEG C, still internal pressure 1.32Pa, chlorine flowrate 1.2m3/h, react 24 hours, obtain tin tetrachloride 150.5kg, tin tetrachloride yield 98.06%, chlorine utilization 97%.
Claims (1)
1. a normal temperature synthesis method for tin tetrachloride, is characterized in that comprising: tin is immersed tin tetrachloride liquid, and add metallic carbon nanotubes, then pass into chlorine, and controls temperature in the kettle at 20-30 DEG C, and pressure-controlling is at 1-3Pa, and chlorine flowrate controls at 1-3m
3/ h.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510089511.XA CN104724752A (en) | 2015-02-27 | 2015-02-27 | Normal-temperature synthesis method of tin tetrachloride |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510089511.XA CN104724752A (en) | 2015-02-27 | 2015-02-27 | Normal-temperature synthesis method of tin tetrachloride |
Publications (1)
Publication Number | Publication Date |
---|---|
CN104724752A true CN104724752A (en) | 2015-06-24 |
Family
ID=53449256
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510089511.XA Pending CN104724752A (en) | 2015-02-27 | 2015-02-27 | Normal-temperature synthesis method of tin tetrachloride |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104724752A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105645466A (en) * | 2016-01-27 | 2016-06-08 | 柳州豪祥特科技有限公司 | Synthetic method of stannic chloride |
CN105668620A (en) * | 2016-01-27 | 2016-06-15 | 柳州豪祥特科技有限公司 | Process for preparing stannic chloride |
CN107089678A (en) * | 2017-05-26 | 2017-08-25 | 南通艾德旺化工有限公司 | A kind of preparation method and applications of butter of tin |
-
2015
- 2015-02-27 CN CN201510089511.XA patent/CN104724752A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105645466A (en) * | 2016-01-27 | 2016-06-08 | 柳州豪祥特科技有限公司 | Synthetic method of stannic chloride |
CN105668620A (en) * | 2016-01-27 | 2016-06-15 | 柳州豪祥特科技有限公司 | Process for preparing stannic chloride |
CN105668620B (en) * | 2016-01-27 | 2017-11-21 | 柳州豪祥特科技有限公司 | A kind of technique for preparing butter of tin |
CN105645466B (en) * | 2016-01-27 | 2017-11-21 | 柳州豪祥特科技有限公司 | A kind of synthetic method of butter of tin |
CN107089678A (en) * | 2017-05-26 | 2017-08-25 | 南通艾德旺化工有限公司 | A kind of preparation method and applications of butter of tin |
CN108704669A (en) * | 2017-05-26 | 2018-10-26 | 南通艾德旺化工有限公司 | A kind of preparation method and applications of butter of tin |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103088230B (en) | High-copper alloy strip for heat sink of automobile | |
CN104724752A (en) | Normal-temperature synthesis method of tin tetrachloride | |
CN104148599B (en) | A kind of clad material solid-liquid compound horizontal casting former and method | |
EP1405924A4 (en) | Method for producing granular metal | |
CN104610068B (en) | A kind of preparation method of 2,4,6-trifluoro benzylamine compound | |
WO2009051254A1 (en) | Copper alloy powder and method for producing the same | |
CN102180514A (en) | Production process of tin tetrachloride | |
CN104497026B (en) | A kind of production unit of ortho-chlorotolu'ene Grignard reagent and preparation technology | |
CN104745868A (en) | Thin-wall titanium alloy pipe processing technique | |
CN204604747U (en) | A kind of mould producing plastic products | |
CN103980133B (en) | A kind of method preparing 2-methyl-4,6-diaminoresorcinol dihydrochloride | |
CN106001467A (en) | Preparing method of ultralow tin-copper tin contact line | |
CN104745844A (en) | Low-cost vanadium-aluminum alloy preparation technology | |
CN202762404U (en) | Diamond synthetic block | |
CN103588911A (en) | Preparation method for hydrogenated butyronitrile rubber | |
CN104209144A (en) | Catalytic system, preparation method thereof, and preparation method of vinyl acetylene by the same | |
CN202983635U (en) | High-quality diamond synthesizing block | |
CN104551455A (en) | -70 degrees centigrade low-temperature steel welding bar | |
CN105622934A (en) | Electrode material polyaniline synthesis method | |
CN102659544A (en) | Method for preparing 2,3-difluorobenzaldehyde | |
CN102328909A (en) | Method for preparing hydrogen chloride from concentrated sulfuric acid | |
CN102836731A (en) | Catalyst used in preparation of paradichlorobenzene and method for preparing paradichlorobenzene by using such catalyst | |
CN103275815A (en) | Palmitoleic acid hydrogenation technology | |
CN106916976A (en) | A kind of Al-V-Mo-Fe alloy preparation technology | |
CN104278187A (en) | Golf club balancing weight and production technology thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20150624 |