CN102206171A - Carbon dissolving and decoloring method - Google Patents
Carbon dissolving and decoloring method Download PDFInfo
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- CN102206171A CN102206171A CN2011101227644A CN201110122764A CN102206171A CN 102206171 A CN102206171 A CN 102206171A CN 2011101227644 A CN2011101227644 A CN 2011101227644A CN 201110122764 A CN201110122764 A CN 201110122764A CN 102206171 A CN102206171 A CN 102206171A
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Abstract
The invention relates to a carbon dissolving and decoloring method. The method comprises the following steps of: pre-mixing activated carbon with water in a carbon dissolving tank equipped with an air induction device at the tank port, stirring by substituting a stirring device with compressed air, and decoloring the substances to be decolored with the sufficiently mixed carbon-water compound. According to the invention, the air induction device installed at the tank port of the carbon dissolving tank effectively avoids the flying phenomenon of activated carbon, reduces environmental pollution and harm to workers and reduces the loss of activated carbon; the compressed air is used to substitute the stirring device, which reduces mechanical wear, reduces maintenance cost, simultaneously reduces electric power consumption and saves energy; and the pre-mixing of activated carbon and water increases the contact area of activated carbon and the substances to be decolored, greatly increases the decoloring reaction speed, shortens reaction time and greatly improves the quality and yield of the decolored substances.
Description
Technical field
The present invention relates to a kind of molten carbon decoloring method.
Technical background
At present in the pharmaceutical engineering the general gac that adopts to the medicine processing of decolouring.Its process is generally: after medicine dissolution is in bleacher, directly add gac in bleacher.Because gac is a kind of very light pulverous atrament, in the process of adding, can cause very big dust pollution, and cause the loss of material, environment and production are all caused very big influence.
Summary of the invention
The purpose of this invention is to provide a kind of molten carbon decoloring method that can reduce environmental pollution and loss of material and effectively improve wait to decolour material mass and output.
The present invention solves the problems of the technologies described above the technical scheme of taking:
A kind of molten carbon decoloring method, it is characterized in that described method comprises the steps: to add entry in the jar mouth is fitted with the molten charcoal jar of blower unit, open blower unit, in described molten charcoal jar, drop into gac from the jar mouth then, in described molten charcoal jar, feed pressurized gas again and stir the mixture that obtains gac and water, at last the mixture of described gac and water is injected the bleacher that the material of waiting to decolour is housed and decolour; The weight ratio of gac and water is 1:5-10 in the described molten charcoal jar; The material of waiting in the described bleacher to decolour mixes with its weight 3-3.5 water doubly and obtains mixed solution, and the mixture of described gac and water and the weight ratio of described mixed solution are 1:5-7.
Material described to be decoloured is Paracetamol, 4-novalgin or quinizine.
A kind of molten charcoal jar of implementing above-mentioned molten carbon decoloring method is characterized in that it comprises tank body, is fitted in the jar mouthful blower unit of locating of tank body and feeds a jar intravital pressurized gas pipeline.
Two sections pressurized gas outlet sections of described pressurized gas pipeline are symmetric circular arc.
Beneficial effect of the present invention: the jar of the molten charcoal jar mouthful blower unit that increases has effectively been avoided the phenomenon of dispersing of gac among the present invention, has reduced to the pollution of environment with to workman's harm, and has reduced the loss of material of gac; The inventive method adopts pressurized air to replace whipping appts, has reduced mechanical wear, has reduced maintenance cost, has reduced power consumption simultaneously, has saved the energy; Two sections pressurized gas outlet sections are symmetric circular arc, and jar interior water is rotated to same direction, make gac and water thorough mixing; Because gac and water are pre-mixed, strengthened gac and the contact area of the material material of waiting to decolour, accelerated the speed of response of decolouring greatly, shortened the time of reaction, make the quality of the material of waiting to decolour and output that by a relatively large margin raising all be arranged.
Description of drawings
Fig. 1 is the structural representation of molten charcoal jar among the present invention.
In the accompanying drawings: 1 tank body, 2 blower units, 3 pressurized gas pipelines, 4 jars of mouths, 5a 5b reducing valve, 6 tensimeters, 7 water inlet pipes, 8 charcoal water mixture extrude pipeline, 9 liquidometers, 10 pressurized gas outlet sections.
Embodiment
Embodiment 1
Adopt the molten carbon decoloring method of the present invention that Paracetamol is decoloured:
(1) molten charcoal: in the molten charcoal jar of the 800L that is fitted with blower unit 2, add 500L water by water inlet pipe 7, open blower unit 2, in described molten charcoal jar, drop into the 75kg gac from jar mouth 4, opening with the gac packing bag when dropping into gac places in jar mouth 4, blower unit 2 can make gac all enter in the molten charcoal jar, avoids the phenomenon of dispersing.Open the reducing valve 5a on the pressurized gas pipeline 3 when opening blower unit 2, in tank body 1, feed pressurized air, because two sections pressurized gas outlet sections 10 of pressurized gas pipeline 3 are below liquid level and be symmetric circular arc, pressurized air feeds the water from two sections pressurized gas outlet sections 10, water in the tank body 1 is rotated to same direction, thereby will send into gac and water thorough mixing in the tank body 1 from jar mouth 4, obtain the mixture of gac and water.
(2) decolouring: in the bleacher of 4500L, the 800kg Paracetamol is dissolved in the 2400kg water.Owing to constantly feed gas in the molten charcoal jar jar internal pressure is increased, tensimeter 6 can show the pressure in the tank body 1, when treating that pressure reaches 0.2Mpa, open the reducing valve 5b on the charcoal water mixture extrusion pipeline 8, the mixture of above-mentioned gac and water is pressed in the above-mentioned bleacher, Paracetamol is decoloured.Liquidometer 9 on the tank body 1 can show the liquid level in the tank body 1.Used water can be the water of process heat exchange in the pharmaceutical factory in the molten carbon decoloring method of the present invention, both can accelerate to mix and dissolved speed, can avoid the wasting of resources again.
Embodiment 2
Adopt the molten carbon decoloring method of the present invention that quinizine is decoloured:
(1) molten charcoal: in the molten charcoal jar of the 800L that is fitted with blower unit 2, add 375L water by water inlet pipe 7, open blower unit 2, in described molten charcoal jar, drop into the 75kg gac from jar mouth 4, opening with the gac packing bag when dropping into gac places in jar mouth 4, blower unit 2 can make gac all enter in the molten charcoal jar, avoids the phenomenon of dispersing.Open the reducing valve 5a on the pressurized gas pipeline 3 when opening blower unit 2, in tank body 1, feed pressurized air, because two sections pressurized gas outlet sections 10 of pressurized gas pipeline 3 are below liquid level and be symmetric circular arc, water in the tank body 1 is rotated to same direction, thereby will send into gac and water thorough mixing in the tank body 1 from jar mouth 4, obtain the mixture of gac and water.
(2) decolouring: in the bleacher of 4500L, the 685kg quinizine is dissolved in the 2400kg water.Owing to constantly feed gas in the molten charcoal jar jar internal pressure is increased, tensimeter 6 can show the pressure in the tank body 1, when treating that pressure reaches 0.2Mpa, open the reducing valve 5b on the charcoal water mixture extrusion pipeline 8, the mixture of above-mentioned gac and water is pressed in the above-mentioned bleacher, quinizine is decoloured.Liquidometer 9 on the tank body 1 can show the liquid level in the tank body 1.Used water can be the water of process heat exchange in the pharmaceutical factory in the molten carbon decoloring method of the present invention, both can accelerate to mix and dissolved speed, can avoid the wasting of resources again.
Adopt the molten carbon decoloring method of the present invention that the 4-novalgin is decoloured:
(1) molten charcoal: in the molten charcoal jar of the 800L that is fitted with blower unit 2, add 500L water by water inlet pipe 7, open blower unit 2, in described molten charcoal jar, drop into the 50kg gac from jar mouth 4, opening with the gac packing bag when dropping into gac places in jar mouth 4, blower unit 2 can make gac all enter in the molten charcoal jar, avoids the phenomenon of dispersing.Open the reducing valve 5a on the pressurized gas pipeline 3 when opening blower unit 2, in tank body 1, feed pressurized air, because two sections pressurized gas outlet sections 10 of pressurized gas pipeline 3 are below liquid level and be symmetric circular arc, water in the tank body 1 is rotated to same direction, thereby will send into gac and water thorough mixing in the tank body 1 from jar mouth 4, obtain the mixture of gac and water.
(2) decolouring: in the bleacher of 4500L, 750kg 4-novalgin is dissolved in the 2400kg water.Owing to constantly feed gas in the molten charcoal jar jar internal pressure is increased, tensimeter 6 can show the pressure in the tank body 1, when treating that pressure reaches 0.2Mpa, open the reducing valve 5b on the charcoal water mixture extrusion pipeline 8, the mixture of above-mentioned gac and water is pressed in the above-mentioned bleacher, the 4-novalgin is decoloured.Liquidometer 9 on the tank body 1 can show the liquid level in the tank body 1.Used water can be the water of process heat exchange in the pharmaceutical factory in the molten carbon decoloring method of the present invention, both can accelerate to mix and dissolved speed, can avoid the wasting of resources again.
Claims (4)
1. molten carbon decoloring method, it is characterized in that described method comprises the steps: to add entry in the jar mouth is fitted with the molten charcoal jar of blower unit, open blower unit, in described molten charcoal jar, drop into gac from the jar mouth then, in described molten charcoal jar, feed pressurized gas again and stir the mixture that obtains gac and water, at last the mixture of described gac and water is injected the bleacher that the material of waiting to decolour is housed and decolour; The weight ratio of gac and water is 1:5-10 in the described molten charcoal jar; The material of waiting in the described bleacher to decolour mixes with its weight 3-3.5 water doubly and obtains mixed solution, and the mixture of described gac and water and the weight ratio of described mixed solution are 1:5-7.
2. a kind of molten carbon decoloring method according to claim 1 is characterized in that material described to be decoloured is Paracetamol, 4-novalgin or quinizine.
3. a molten charcoal jar of implementing the molten carbon decoloring method of claim 1 is characterized in that it comprises tank body (1), is fitted in jar blower unit (2) that mouthful (4) are located of tank body (1) and feeds the interior pressurized gas pipeline (3) of tank body (1).
4. a kind of molten charcoal jar according to claim 3 is characterized in that two sections pressurized gas outlet sections (10) of described pressurized gas pipeline (3) are symmetric circular arc.
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CN201110122764.4A CN102206171B (en) | 2011-05-13 | 2011-05-13 | A kind of molten carbon decoloring method |
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CN201110122764.4A CN102206171B (en) | 2011-05-13 | 2011-05-13 | A kind of molten carbon decoloring method |
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CN102206171B CN102206171B (en) | 2016-01-20 |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102941033A (en) * | 2012-11-26 | 2013-02-27 | 济南华明生化有限公司 | Solution mixing device for itaconic acid bleaching tank |
CN104447386A (en) * | 2014-12-13 | 2015-03-25 | 常熟华港制药有限公司 | Decoloring process of paracetamol |
CN107815707A (en) * | 2017-09-30 | 2018-03-20 | 安徽华星化工有限公司 | Reactive tank stirs practicality improved method after primary brine |
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CN101450801A (en) * | 2007-11-28 | 2009-06-10 | 北京有色金属研究总院 | Modified silicon carbide powder and preparation method thereof |
CN101891683A (en) * | 2010-07-22 | 2010-11-24 | 河北冀衡(集团)药业有限公司 | Aminopyrine production method |
CN202096923U (en) * | 2011-05-13 | 2012-01-04 | 河北冀衡(集团)药业有限公司 | Carbon dissolving tank |
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2011
- 2011-05-13 CN CN201110122764.4A patent/CN102206171B/en active Active
Patent Citations (3)
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CN101450801A (en) * | 2007-11-28 | 2009-06-10 | 北京有色金属研究总院 | Modified silicon carbide powder and preparation method thereof |
CN101891683A (en) * | 2010-07-22 | 2010-11-24 | 河北冀衡(集团)药业有限公司 | Aminopyrine production method |
CN202096923U (en) * | 2011-05-13 | 2012-01-04 | 河北冀衡(集团)药业有限公司 | Carbon dissolving tank |
Non-Patent Citations (2)
Title |
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《染整技术》 20040831 程刚 溶药系统中搅拌装置的改造 摘要、图1 1-4 第26卷, 第4期 * |
程刚: "溶药系统中搅拌装置的改造", 《染整技术》, vol. 26, no. 4, 31 August 2004 (2004-08-31), pages 1 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102941033A (en) * | 2012-11-26 | 2013-02-27 | 济南华明生化有限公司 | Solution mixing device for itaconic acid bleaching tank |
CN104447386A (en) * | 2014-12-13 | 2015-03-25 | 常熟华港制药有限公司 | Decoloring process of paracetamol |
CN107815707A (en) * | 2017-09-30 | 2018-03-20 | 安徽华星化工有限公司 | Reactive tank stirs practicality improved method after primary brine |
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CN102206171B (en) | 2016-01-20 |
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Address after: 053000 No.1, Weiwu street, high tech Zone, Hengshui City, Hebei Province Patentee after: Hebei Jiheng Pharmaceutical Co.,Ltd. Address before: 053000 No.368 Jianshe North Street, Hengshui City, Hebei Province Patentee before: HEBEI JIHENG (Group) PHARMACEUTICAL Co.,Ltd. |
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