CN219922921U - Phosphoric acid preparation facilities - Google Patents

Phosphoric acid preparation facilities Download PDF

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Publication number
CN219922921U
CN219922921U CN202321638884.4U CN202321638884U CN219922921U CN 219922921 U CN219922921 U CN 219922921U CN 202321638884 U CN202321638884 U CN 202321638884U CN 219922921 U CN219922921 U CN 219922921U
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China
Prior art keywords
tank
tail gas
outlet
dilute acid
acid pump
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CN202321638884.4U
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Chinese (zh)
Inventor
王�忠
黄政炜
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Guizhou Fuquan East Sichuan Chemical Co ltd
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Guizhou Fuquan East Sichuan Chemical Co ltd
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Abstract

The utility model discloses a phosphoric acid preparation device which comprises a phosphorus dissolving device, a venturi tube, a dilute acid pump, a dilute acid tank, a pressurizing device, a hydration tower, a circulating acid pump, a membrane remover, a condensing device, a filtering device, a finished product tank, a tail gas treatment tank and a tail gas combustion treatment device. The utility model realizes the maximization of the value, the production efficiency and the quality controllability of chemical products, is well integrated with the existing production system, is beneficial to the improvement of the production system, and finally realizes the simple flow, economy, high efficiency, self-circulation, less emission and accurate batching.

Description

Phosphoric acid preparation facilities
Technical Field
The utility model relates to the technical field of phosphorus chemical industry, in particular to a phosphoric acid preparation device.
Background
Phosphoric acid is colorless transparent or slightly colored thick liquid at normal temperature, has a specific gravity of 1.69, is easily dissolved in water and alcohol, is corrosive, and becomes pyrophosphoric acid after dehydration under heating at 212 ℃, and then becomes metaphosphoric acid. The solidification point of phosphoric acid is 21.1 ℃. Orthophosphoric acid is the simplest oxyacid, and the phosphate radical is a PO4 tetrahedron formed by combining phosphorus with oxygen. Orthophosphoric acid has two kinds of crystals, namely, anhydrous phosphoric acid, is colorless crystalline solid (melting point 42.35 ℃) and has no oxidizing power below 350 ℃, and semi-aqueous industrial phosphoric acid (melting point 29.3 ℃). Pure phosphoric acid is slow to crystallize, when impurities exist in phosphoric acid, the impurities act as crystal nuclei to crystallize rapidly, and when the content exceeds 100%, the freezing point of the system drops sharply. Phosphoric acid is a medium strength tribasic acid with a fairly strong hydrogen-bonded structure and therefore a very high viscosity.
Because of the high pollution and low profit of the phosphorus chemical industry, most crude phosphorus manufacturers in China now adopt high-energy consumption and low profit operation modes of mass production and batch sales, the economic benefit is poor, the environmental hazard is also large, and a plurality of products are not utilized efficiently, so that the waste of resources is caused.
Therefore, a phosphoric acid preparation device with simple flow, economy, high efficiency, self circulation, low emission and accurate batching is urgently needed in the market.
Disclosure of Invention
The utility model aims to provide a phosphoric acid preparation device with simple flow, economy, high efficiency, self circulation, less emission and accurate batching.
In order to achieve the above purpose, the present utility model adopts the following technical scheme: the phosphoric acid preparation device comprises a phosphorus dissolving device, a venturi tube, a dilute acid pump, a dilute acid tank, a pressurizing device, a hydration tower, a circulating acid pump, a membrane remover, a condensing device, a filtering device, a finished product tank, a tail gas treatment tank and a tail gas combustion treatment device;
the phosphorus dissolving device is matched with the raw material yellow phosphorus and is used for heating the yellow phosphorus into a liquid state;
after liquefaction, the outlet of the phosphorus dissolving device is connected with the outlet of the pressurizing device, and liquefied yellow phosphorus and air are mixed and pressurized and then sent into a hydration tower for containing acid liquor;
the discharging end of the hydration tower is respectively connected with a circulating acid pump and a venturi, wherein dilute acid is introduced into the venturi, and concentrated acid is introduced into the circulating acid pump;
the venturi tube is used for introducing the dilute acid into the dilute acid tank, and then the dilute acid is separated by the dilute acid pump, wherein the relatively diluted acid liquid flows back into the venturi tube, the relatively high-concentration acid liquid flows into the circulating acid pump after being treated by the membrane remover, and the vaporization part is introduced into the tail gas treatment tank in the process;
the concentrated dilute acid is mixed and prepared into the required concentration by a circulating acid pump, the vaporized part is introduced into a tail gas treatment tank in the process, the concentrated acid part flows back to a hydration tower, the qualified part is condensed by a condensing device and then filtered to remove impurity solids by a filtering device, and the liquid part is put into a finished product tank;
the vaporized gas after heat exchange by the condensing device is introduced into the tail gas treatment tank and is treated and then introduced into the tail gas combustion treatment device for treatment.
Compared with the prior art, the utility model has the following advantages:
(1) According to the utility model, through the system full-disc planning design, the energy of the production system is recovered to the greatest extent, and waste gas, waste water, dust and solid waste generated in all production links are not directly discharged into the external environment, but are recycled in the system until the waste becomes non-valuable waste, and the non-valuable waste is uniformly treated and then discharged to the external circulation system.
(2) The utility model comprehensively applies minerals, chemical industry and thermodynamics, not only achieves the maximum application of solid materials, but also achieves the maximum value, production efficiency and quality controllability of chemical products, and also achieves the cyclic utilization of heat energy to reduce the energy consumption of the whole reaction system, thus the material efficiency ratio and the energy efficiency ratio of the utility model are obviously superior to the prior art.
(3) In the design link of the utility model, the adjustment of the equipment corresponding to the existing mature production line and production process is not great, mainly the improvement on the process method and the increase of part of equipment (such as a catalytic cracking and gas collecting device), and the utility model is well integrated with the existing production system, thereby being beneficial to the improvement of the production system.
Drawings
FIG. 1 is a schematic diagram of the structure of the present utility model;
in the figure: the device comprises a phosphorus dissolving device 1, a venturi tube 2, a dilute acid pump 3, a dilute acid tank 4, a pressurizing device 5, a hydration tower 6, a circulating acid pump 7, a membrane remover 8, a condensing device 9, a filtering device 10, a finished product tank 11, a tail gas treatment tank 12 and a tail gas combustion treatment device 13.
Description of the embodiments
Examples
The phosphoric acid preparation device shown in figure 1 comprises a phosphorus dissolving device 1, a venturi tube 2, a dilute acid pump 3, a dilute acid tank 4, a pressurizing device 5, a hydration tower 6, a circulating acid pump 7, a membrane remover 8, a condensing device 9, a filtering device 10, a finished product tank 11, a tail gas treatment tank 12 and a tail gas combustion treatment device 13;
the phosphorus dissolving device 1 is matched with the yellow phosphorus serving as a raw material and is used for heating the yellow phosphorus into a liquid state;
after liquefaction, the outlet of the phosphorus dissolving device 1 is connected with the outlet of the pressurizing device 5, and liquefied yellow phosphorus and air are mixed and pressurized and then sent into the hydration tower 6 for containing acid liquor;
the discharge end of the hydration tower 6 is respectively connected with a circulating acid pump 7 and a venturi tube 2, wherein dilute acid is introduced into the venturi tube 2, and concentrated acid is introduced into the circulating acid pump 7;
the venturi tube 2 is used for introducing the entering dilute acid into the dilute acid tank 4, and then the dilute acid is separated by the dilute acid pump 3, wherein the relatively diluted acid liquid flows back into the venturi tube 2, the relatively high-concentration acid liquid flows into the circulating acid pump 7 after being treated by the membrane remover 8, and the vaporization part is introduced into the tail gas treatment tank 12 in the process;
the concentrated dilute acid is mixed and prepared into the required concentration by a circulating acid pump, the vaporized part is introduced into a tail gas treatment tank 12 in the process, the concentrated acid part flows back to a hydration tower 6, the qualified part is condensed by a condensing device 9 and then filtered to remove impurity solids by a filtering device 10, and the liquid part is put into a finished product tank 11;
the vaporized gas after heat exchange by the condensing device 9 is introduced into the tail gas treatment tank 12 and is treated and then introduced into the tail gas combustion treatment device 13 for treatment.
The equipment according to the embodiment not only realizes the maximization of the value, the production efficiency and the quality controllability of chemical products, but also is well integrated with the existing production system, is beneficial to the improvement of the production system, and finally realizes the advantages of simple flow, economy, high efficiency, self-circulation, less emission and accurate batching.
The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present utility model. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the utility model. Thus, the present utility model is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.

Claims (1)

1. A phosphoric acid production device, characterized in that: the preparation device comprises a phosphorus dissolving device (1), a venturi tube (2), a dilute acid pump (3), a dilute acid tank (4), a pressurizing device (5), a hydration tower (6), a circulating acid pump (7), a membrane remover (8), a condensing device (9), a filtering device (10), a finished product tank (11), a tail gas treatment tank (12) and a tail gas combustion treatment device (13);
the phosphorus dissolving device (1) is matched with the yellow phosphorus serving as a raw material;
the outlet of the phosphorus dissolving device (1) is connected with the outlet of the pressurizing device (5), and the outlet of the phosphorus dissolving device and the outlet of the pressurizing device are connected with the feeding end of the hydration tower (6) together;
the discharge end of the hydration tower (6) is respectively connected with a circulating acid pump (7) and a venturi tube (2);
the outlet end of the venturi tube (2) is connected with a dilute acid tank (4), and the dilute acid tank (4) is connected with a dilute acid pump (3);
a centrifugal separation device is arranged in the dilute acid pump (3), and is respectively connected with the flow venturi tube (2) and the membrane remover (8) after centrifugal separation;
the discharging end of the membrane remover (8) is connected with a circulating acid pump (7), and the gas outlet is connected with the gas inlet end of the tail gas treatment tank (12);
the gas outlet of the circulating acid pump is connected with the gas inlet end of the tail gas treatment tank (12), the reflux port is connected with the hydration tower (6), the discharge port is connected with the feed end of the filtering device (10) through the condensing device (9), and the discharge end of the filtering device (10) is connected with the finished product tank (11);
the gas outlet of the condensing device (9) is connected with the gas inlet end of the tail gas treatment tank (12), and the gas outlet end of the tail gas treatment tank (12) is connected with the tail gas combustion treatment device (13).
CN202321638884.4U 2023-06-27 2023-06-27 Phosphoric acid preparation facilities Active CN219922921U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202321638884.4U CN219922921U (en) 2023-06-27 2023-06-27 Phosphoric acid preparation facilities

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202321638884.4U CN219922921U (en) 2023-06-27 2023-06-27 Phosphoric acid preparation facilities

Publications (1)

Publication Number Publication Date
CN219922921U true CN219922921U (en) 2023-10-31

Family

ID=88489351

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202321638884.4U Active CN219922921U (en) 2023-06-27 2023-06-27 Phosphoric acid preparation facilities

Country Status (1)

Country Link
CN (1) CN219922921U (en)

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