WO2008043222A1 - Procédé de production directe d'acide phosphorique et de plusieurs sous-produits silicate ou aluminate à partir de matériaux de minerais bruts de phosphate - Google Patents

Procédé de production directe d'acide phosphorique et de plusieurs sous-produits silicate ou aluminate à partir de matériaux de minerais bruts de phosphate Download PDF

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Publication number
WO2008043222A1
WO2008043222A1 PCT/CN2007/001122 CN2007001122W WO2008043222A1 WO 2008043222 A1 WO2008043222 A1 WO 2008043222A1 CN 2007001122 W CN2007001122 W CN 2007001122W WO 2008043222 A1 WO2008043222 A1 WO 2008043222A1
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Prior art keywords
kiln
powder
phosphoric acid
phosphate rock
aluminate
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PCT/CN2007/001122
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English (en)
French (fr)
Inventor
Dingbin Zhang
Caizhou Tang
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Hubei Sanxin Phosphoric Acid Co. Ltd
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Application filed by Hubei Sanxin Phosphoric Acid Co. Ltd filed Critical Hubei Sanxin Phosphoric Acid Co. Ltd
Publication of WO2008043222A1 publication Critical patent/WO2008043222A1/zh

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/18Phosphoric acid
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/20Silicates

Definitions

  • the invention relates to the field of chemical industry, in particular to a method for preparing phosphoric acid and by-products a plurality of silicon and aluminates after the phosphate rock and other auxiliary materials are processed by milling, molding and sintering.
  • the industrial production methods of phosphoric acid mainly include the following: (1) Wet-process phosphoric acid: Decomposing phosphate rock with sulfuric acid to prepare phosphoric acid, this method requires a large amount of high-quality phosphate rock and sulfuric acid, and at the same time, a large amount of phosphogypsum waste residue is produced. (2) Thermal phosphoric acid: The production of yellow phosphorus by an electric furnace method, followed by combustion and absorption to obtain phosphoric acid, requires a large amount of electric energy and a medium-high grade phosphate ore lump ore.
  • the code into the tunnel kiln car is preheated in the tunnel kiln, and the temperature is raised to 1200 °C - 1600 °C, so that the coke in the block reacts with the phosphate rock to form phosphorus vapor P 4 and carbon monoxide.
  • the high temperature gas containing P 2 0 5 is pumped out through the heat exchanger and then into the hydration tower and absorbed by the circulating acid to obtain phosphoric acid. After the reaction, the bricks are cooled and heat exchanged and then the building is constructed. Brick product.
  • This patent has 1-3 times of immersion glaze process, the production process control is more complicated, and the immersion process also increases the production cost. Summary of the invention
  • the object of the invention is to directly use the P 2 0 5 ⁇ 6% phosphorus-containing ore and tailings in the phosphate rock or the selection process to prepare a high concentration phosphoric acid, the phosphorus thereof, on the basis of the patent application No. 200610018780.8.
  • the utilization rate reaches 95%, and a method for preparing phosphoric acid by direct reduction of phosphate rock of cement clinker or various silicate and aluminate press-formed products and by-product of various silicon and aluminate products is obtained.
  • the present invention provides a method for directly reducing phosphate rock to produce phosphoric acid and by-producting a plurality of silicon and aluminate articles, comprising the steps of:
  • the formed material is placed in a material container, and after being dried and preheated in a tunnel kiln or a roller kiln or a push-plate kiln, the temperature is raised to 1200-1600 ° C to react the materials in the container to generate Phosphorus vapour and carbon monoxide escape from the vessel and are further oxidized in the tunnel kiln? 2 0 5 and ( 0 2 ;
  • the reduction of phosphate rock and the oxidation of phosphorus are carried out by using a tunnel kiln or a roller kiln or a push-plate kiln as the main reaction equipment, and phosphoric acid is obtained by absorption through a hydration tower.
  • a tunnel kiln or a roller kiln or a push-plate kiln as the main reaction equipment
  • phosphoric acid is obtained by absorption through a hydration tower.
  • coke or coal or gangue or wood powder or petroleum coke and other carbonaceous raw materials are used as reducing agents, lime powder or silica powder is added, and kaolin is added or added in small amount to participate in reduction reaction to form calcium silicate.
  • the heat released by the oxidation reaction is used to maintain the reaction temperature, which can reduce fuel consumption, save energy, and reduce costs.
  • the uniform mixing after the step 1) is preferably carried out by mixing the phosphate rock and the carbonaceous reducing agent, the lime powder or the silica powder, and adding a small amount of the additive, and then adding the water to the spherical disk (D5-50mm material). Balls, either direct powder or extruded into various shapes.
  • the additive in the step 1) is preferably a 0.5-8% aluminum effect raw material, and can produce cement clinker and various silicate and aluminate press-formed products.
  • the aluminum effective raw material is preferably kaolin or alumina.
  • the additive described in step 1) is preferably 1-2% water glass, polyvinyl alcohol or methyl cellulose, and can be made into a pre-designed shaped building material.
  • the kiln in step 2) is a tunnel kiln or a roller kiln or a pusher kiln.
  • the material container described in step 2) is preferably a refractory product.
  • the method for preparing phosphoric acid by direct reduction of phosphate rock and byproduct of producing various silicon and aluminate products is basically the same as the application No. 200610018780.8, but the patent application uses a refractory container to physically perform molding materials. Protection, the glazing process is omitted, and the reduction rate of phosphorus is further improved.
  • the kiln After being filled, it is loaded into a 1.5xl.5M kiln car, and after drying, it is preheated into a 36.98xl.9xl.5M tunnel kiln.
  • the temperature is raised to 1200 °C, and the total running time of the material container in the kiln is 16 hours.
  • the running process is automatically controlled by PLC programming.
  • the high-temperature gas is extracted into ⁇ 1.4 ⁇ 8.2 ⁇ .
  • the hydration tower absorbs phosphoric acid by circulating acid. After testing, the obtained phosphoric acid concentration is 85%.
  • the kiln is Portland cement clinker or other silicon. Aluminate products. Its quality is in line with the quality standards of Portland cement clinker or the standard of sintered silicon and aluminum products. The product contains P 2 O 5 ⁇ 0.5%. Material containers can be reused.
  • Example 1 The mixture in Example 1 was added with 2% kaolin mud, uniformly added with about 6% water and mixed well, and then pressed into a 230x112x65mm brick or 240x60x8mm brick with a 160-ton friction press. After drying, it was filled into a 410x410x260mm square phosphate refractory material container. In the 38x 1.5M roller kiln, the preheating is carried out, the temperature is raised to 1450 ° C, and the total running time of the material container in the kiln is 8 hours. The running process is automatically controlled by PLC programming. The high-temperature gas is pumped into the ⁇ 1.4 ⁇ 8.2 ⁇ hydration tower to absorb phosphoric acid by circulating acid.
  • the phosphoric acid concentration is 85%, and the bricks of the material container are cooled by heat exchange to obtain 230x112x65mm refractory brick or 240x60x8mm decorative brick product.
  • P 2 O 5 ⁇ 0.7% in the product the product meets the quality requirements of insulation brick or decorative brick.
  • Example 1 Use the mixture in Example 1 and add 1-2% water glass or polyvinyl alcohol to the total weight of the material. Or methyl cellulose, evenly added with 6-8 % water and mix well, and then pressed with a friction press to make external wall bricks or other pre-designed special-shaped building materials in accordance with national standards. After drying, it is filled with 410x410x280mm square zirconium corundum. In the refractory material container, the 28 x 0. 5M push plate kiln is preheated and heated to 1550 ° C. The total operation time of the material container in the kiln is 10 hours. The operation process is automatically controlled by PLC programming, and the high temperature gas is extracted.
  • the hydration tower absorbs phosphoric acid with circulating acid, and the concentration of phosphoric acid is 85%. After the material and container products are cooled and exchanged, the exterior wall brick or the special-shaped building materials are designed. The product P 2 O 5 ⁇ 0.7% .

Description

一种以磷矿为原料直接制备磷酸
并副产多种硅、 铝酸盐制品的方法 技术领域
本发明涉及化工领域, 具体的说, 把磷矿和其它辅料通过制粉、 成型、 烧结后, 吸收气相制备磷酸并副产多种硅、 铝酸盐的方法。
背景技术
磷酸的工业化生产方法主要有以下几种: (1 )湿法磷酸: 用硫酸 分解磷矿石制取磷酸, 该方法需要大量优质磷矿石和硫酸, 同时产生 大量磷石膏废渣。 (2 )热法磷酸: 用电炉法生产黄磷, 然后燃烧吸收 制取磷酸,该方法需要大量电能和中高品位磷矿块矿。( 3 )窑法磷酸: 这种工艺生产中未见成功应用, 但专利方法中有报道, 如: 中国长沙 矿冶院的专利号为 93111447.0 "—种直接还原磷矿石生产磷酸的方 法" 的发明专利, 该方法需要中品位磷矿石, 磷的利用率只有 80%左 右; 中国化工部化肥研究所的专利申请号为 89100292.8 "—种制取高 浓度磷酸的方法" 的专利, 也需要中品位磷矿石。 申请人之前申请的 "利用磷矿选矿后的含磷尾矿制取高浓度磷酸并副产建筑用砖的方 法,, 的专利, 申请号为 200610018780.8, 磷的还原率可以达到 90%。
本申请人于 2006年 4月 14日申请了名称为 "利用磷矿选矿后的 含磷尾矿制取磷酸并副产建筑用砖的方法"的发明专利, 其主要工艺 过程是将含磷尾矿和碳质还原剂、硅石粉混合后加入得到混合料, 再 加入粘和剂混合, 经陈腐均化, 真空挤出机挤出或压砖机压成坯体, 经烘干后再浸釉 1-3 次, 码入隧道窑车在隧道窑内经预热, 升温到 1200°C-1600°C , 使料块中的焦碳与磷矿反应生成磷蒸气 P4和一氧化 碳, 往窑内通入空气使 P4和 CO氧化成?205和(:02, 把含有 P205的 高温气体抽出来经换热器降温后入水合塔并用循环酸吸收得磷酸,反 应完毕后的砖块经冷却换热后即为建筑砖产品。 此专利有 1-3次浸釉 工序, 其生产过程控制较为复杂, 浸釉工序也增加了生产成本。 发明内容
本发明的目的是在申请号为 200610018780.8专利的基础上,直接 利用磷矿或釆选过程中的 P205≥6%含磷贫矿和尾矿为原料,制取高浓 度磷酸, 其磷的利用率达到 95%, 并得到水泥熟料或各种硅酸盐、 铝 酸盐压制成型制品的直接还原磷矿制备磷酸并副产多种硅、铝酸盐制 品的方法。
为了实现本发明的目的,本发明提供了一种直接还原磷矿制备磷 酸并副产多种硅、 铝酸盐制品的方法, 包括如下步骤:
1 )将磷矿粉和碳质还原剂、 石灰粉或硅石粉、 不加或者少量加 入添加剂混合均匀后成型;
2 )将成型后的物料盛放于物料容器中, 在隧道窑或者辊道窑或 者推板窑中经过烘干、 预热后, 升温到 1200~1600°C , 使容器中的物 料反应, 生成磷蒸汽和一氧化碳从容器中逸出, 在隧道窑中进一步氧 化成?205和( 02
3 )把含有 P205的高温气体抽出来经换热器降温后, 进入水合塔 并用循环酸吸收得到磷酸, 容器中的物料经冷却换热后即为多种硅、 铝酸盐制品。
本发明的工作原理如下:
以隧道窑或者辊道窑或者推板窑为主要反应设备来完成磷矿的 还原和磷的氧化反应, 通过水合塔吸收制得磷酸。磷矿的还原用焦碳 或煤或煤矸石或木粉或者石油焦等含碳原料作为还原剂,加入石灰粉 或硅石粉, 不加入或少量加入高岭土参与还原反应, 生成硅酸钙
( nCaOSi02 ) ,铝酸三钙 ( 3CaOAl203 )。 化学反应如下:
4Ca5(PO4)3F+30C+mSiO2+Al2O3'2SiO2 +nCaO→
( n+17 ) CaO- ( m+1 ) Si02+3CaO-Al203 +SiF4†+30CO†+3P4† 应:
P4 +502→2P205 +ΔΗ
2CO+02→20Ο2+ ΔΗ
氧化反应放出的热量用于维持反应温度, 可以减少燃料用量, 节 约能源, 降低成本。
所述磷矿中 P205含量优选≥6%, 按照质量比优选为: 磷矿粉: 硅石粉 =4 : 0.1-2; 或者磷矿粉: 石灰粉 =1 : 0.1-2;碳质还原剂优选为 焦碳、 煤或煤矸石, 以固定碳含量计: P2O5%:C%=l:0.3-1.5。
步骤 1 )中的混合均匀后成型优选为将磷矿和碳质还原剂、 石灰 粉或硅石粉、 可以少量加入添加剂混合均匀后, 通过再加水, 在成球 盘中制成 (D5-50mm料球、 或者是直接粉料、 或者挤压成各种形状的 制品。
步骤 1 ) 中所述添加剂优选为物料总重量 0.5-8%铝质效正原料, 可以生产水泥熟料和各种硅酸盐、 铝酸盐压制成型制品。
所述铝质效正原料优选为高岭土或铝土。
步骤 1 ) 中所述添加剂优选为物料总重量 1-2%水玻璃、 聚乙烯 醇或甲基纤维素, 可以制成预先设计的异型建筑材料。
步骤 2 ) 中所述窑炉为隧道窑或者辊道窑或者推板窑。
步骤 2 ) 中所述物料容器优选为耐火材料制品。
本发明提供的直接还原磷矿制备磷酸并副产多种硅、铝酸盐制品 的方法, 工作原理与申请号为 200610018780.8 专利基本相同, 但本 专利申请釆用了耐火材料容器对成型物料进行物理保护,省略了上釉 工序, 还进一步提高了磷的还原率。
具体实施方式
为了更好地理解本发明的实质,下面用实施例的方式来具体地说 明和解释本发明。
实施例 1 用湖北神农架矿业公司磷矿粉、 石灰粉或硅石粉、 焦碳粉分别按 下述质量比: (1)磷矿粉: 石灰粉 =1: 0.1或者磷矿粉: 硅石粉 =1: 0.1, P205%: C%=1: 0.8; (2)磷矿粉: 石灰粉 =1: 0.5或者磷矿粉: 硅石粉 =1: 0.5, P205%: C%=1: 0.3; (3)磷矿粉: 石灰粉 =1: 1或 者磷矿粉: 硅石粉 =1: 1, P205%: C%=1: 1.5; (4)磷矿粉: 石灰粉 =1: 1.8或者磷矿粉: 硅石粉 =1: 1.8, P205%:C%=1: 1.0混合好, 混合料要求细度≥120目; 拌匀后在成球盘中均匀加入 8%左右水把料 做成 Φ30πιπι小球状, 再装入 610x610x450mm方形炭化硅物料容器 中, 装满后码入 1.5xl.5M窑车, 经烘干后进入 36.98xl.9xl.5M隧道 窑经过预热, 升温到 1200°C, 物料容器在窑内总运行时间 16小时, 其运行过程釆用 PLC编程自动控制。 其高温气体抽出入 Φ1.4Χ8.2Μ 水合塔用循环酸吸收得磷酸, 经检测, 得到的磷酸浓度为 85%; 物 料容器经冷却换热后出窑就是硅酸盐水泥熟料或者其它硅、铝酸盐制 品。 其质量符合硅酸盐水泥熟料质量标准或者烧结硅、 铝制品标准。 制品含 P2O5≤0.5%。 物料容器可重复使用。
实施例 2
用例 1中的混合料外加 2%高岭土泥浆,均匀外加 6%左右水分拌 匀后用 160吨摩擦压力机压制成 230x112x65mm砖块或 240x60x8mm 片砖, 经烘干后装入 410x410x260mm方形磷酸盐耐火物料容器中, 推入 38x 1.5M辊道窑经过预热,升温到 1450°C,物料容器在窑内总运 行时间 8小时, 其运行过程釆用 PLC编程自动控制。 其高温气体抽 出入 Φ1.4Χ8.2Μ水合塔用循环酸吸收得磷酸,经检测, 得到磷酸浓度 为 85%, 物料容器的砖块经冷却换热后得 230x112x65mm耐火保温 砖或 240x60x8mm装饰砖产品, 制品中 P2O5≤0.7%, 产品符合保温砖 或装饰砖质量要求。
实施例 3
用例 1 中的混合料, 再加入物料总重量 1-2%水玻璃或聚乙烯醇 或甲基纤维素, 均匀外加 6-8 %水分拌匀后,用摩擦压力机压制成符合 国家标准规定的外墙砖或其他预先设计的异型建筑材料,经烘干后装 入 410x410x280mm方形锆刚玉耐火物料容器中,推入 28 x 0. 5M推板 窑经过预热, 升温到 1550°C , 物料容器在窑内总运行时间 10小时, 其运行过程釆用 PLC编程自动控制, 其高温气体抽出入 Φ1.4χ8.2Μ 水合塔用循环酸吸收得磷酸, 磷酸浓度为 85 % , 物料容器产品经冷 却换热后得外墙砖或所设计的异型建筑材料, 制品中 P2O5≤0.7%。

Claims

权 利 要 求 书
1、 一种以磷矿为原料直接制备磷酸并副产多种硅、 铝酸盐制品 的方法, 包括如下步骤:
1 )将磷矿粉和碳质还原剂、 石灰粉或者硅石粉、 不加入或者少 量加入添加剂混合均匀后成型;
2 )将成型后的物料盛放于物料容器中, 在隧道窑或者辊道窑或 者推板窑中经过烘干、 预热后, 升温到 1200〜160(TC , 使容器中的物 料发生还原反应, 生成的磷蒸汽和一氧化碳从容器中逸出, 在窑炉中 进一步氧化成 P205和 co2;
3 )把含有 P205的气体抽出来后, 进入水合塔并用循环酸吸收得 到磷酸, 容器中的物料经冷却换热后即为多种硅、 铝酸盐制品。
2、 根据杈利要求书 1所述的方法, 其特征在于, 步骤 2 ) 中所 用主要反应设备窑炉为工业隧道窑或者辊道窑或者推板窑。
3、 根据权利要求书 1所述的方法, 其特征在于, 步骤 2 ) 中所 述物料容器为耐火材料制品。
4、根据杈利要求书 1所述的方法,其特征在于,所述磷矿中 P205 含量≥6%, 按照质量比为: 磷矿粉: 石灰粉 =1 : 0.1-2 或者磷矿粉-. 硅石粉 =1: 0.1-2;碳质还原剂为焦碳、煤或煤矸石、木粉或者石油焦, 以固定碳含量计: P205%:C%=1 :0.3-1.5。
5、 根据杈利要求 1所述的方法, 其特征在于, 步骤 1 ) 中的混 合均匀后成型为将磷矿粉和碳质还原剂、 石灰粉或者硅石粉、不加或 者加入少量添加剂混合均匀后, 通过再加水, 在成球盘中制成 <D5-50mm料球、 或者是直接粉料、 或挤压成各种形状的制品。
6、 根据权利要求书 1所述的方法, 其特征在于, 步骤 1 ) 中所 述添加剂为物料总重量 0.5-8%铝质效正原料。
7、 根据权利要求书 4所述的方法, 其特征在于, 所述铝质效正 原料为高岭土或铝土。 、 根据权利要求书 1所述的方法, 其特征在于, 步骤 1 ) 中所述添加 剂为物料总重量 1-2%水玻璃、 聚乙烯醇或甲基纤维素。
PCT/CN2007/001122 2006-09-30 2007-04-06 Procédé de production directe d'acide phosphorique et de plusieurs sous-produits silicate ou aluminate à partir de matériaux de minerais bruts de phosphate WO2008043222A1 (fr)

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Cited By (7)

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US7910080B2 (en) 2004-06-04 2011-03-22 Jdcphosphate, Inc. Phosphorous pentoxide producing methods
US8734749B2 (en) 2011-11-29 2014-05-27 Jdcphosphate, Inc. Phosphorous pentoxide producing methods and phosphate ore feed agglomerates
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CN112250051A (zh) * 2020-10-16 2021-01-22 昆明理工大学 一种磷矿浆吸收磷石膏焙烧烟气联产磷酸和水泥熟料的方法
CN112624641A (zh) * 2020-12-25 2021-04-09 武汉理工大学 一种无废渣全资源化利用磷尾矿的方法
CN114380617A (zh) * 2022-01-07 2022-04-22 武汉科技大学 一种磷尾矿-煤矸石基轻质隔热材料及其制备方法
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Publication number Priority date Publication date Assignee Title
US7910080B2 (en) 2004-06-04 2011-03-22 Jdcphosphate, Inc. Phosphorous pentoxide producing methods
US8734749B2 (en) 2011-11-29 2014-05-27 Jdcphosphate, Inc. Phosphorous pentoxide producing methods and phosphate ore feed agglomerates
US9783419B2 (en) 2014-09-26 2017-10-10 Jdcphosphate, Inc. Phosphorous pentoxide producing methods and systems with increased agglomerate compression strength
US11858811B2 (en) 2019-06-30 2024-01-02 Novaphos Inc. Phosphorus production methods and systems and methods for producing a reduction product
CN112250051A (zh) * 2020-10-16 2021-01-22 昆明理工大学 一种磷矿浆吸收磷石膏焙烧烟气联产磷酸和水泥熟料的方法
CN112250051B (zh) * 2020-10-16 2023-08-22 昆明理工大学 一种磷矿浆吸收磷石膏焙烧烟气联产磷酸和水泥熟料的方法
CN112624641A (zh) * 2020-12-25 2021-04-09 武汉理工大学 一种无废渣全资源化利用磷尾矿的方法
CN112624641B (zh) * 2020-12-25 2022-09-20 武汉理工大学 一种无废渣全资源化利用磷尾矿的方法
CN114380617A (zh) * 2022-01-07 2022-04-22 武汉科技大学 一种磷尾矿-煤矸石基轻质隔热材料及其制备方法

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