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Smelting method of ferro molybdenum


The main raw material for smelting ferro molybdenum is molybdenite (MoS2). Molybdenum concentrate is usually oxidized by multi-hearth furnace before smelting to obtain roasted molybdenum ore with sulfur less than 0.07%. Iron molybdenum smelting generally adopts the outside furnace process. The furnace is a cylinder placed on a sand base, lined with clay bricks, with 75% silicon ferrosilicon and a small number of aluminum particles as reducing agents. After the charge is added to the furnace barrel, it is smelted by the upper ignition method. An initiator (saltpeter, aluminum chips or magnesium chips) is used on the surface of the material, which is a violent reaction after ignition, and then sedated, slagging, and demolition of the furnace tube. The ferro molybdenum ingot is first cooled in the sand pit, then sent to the cooling room for flushing and cooling, and finally broken and finished. The metal recovery rate is 92 ~ 99%. Molybdenum oxide compacted block has been widely used to replace ferro molybdenum in steelmaking industry in recent years.
Ferric molybdenum is usually smelted by the metal thermal process. Ferric molybdenum is a legally inspected commodity. The main producing areas are Jilin, Hebei, Jiangsu, Henan, Liaoning, etc., mainly exported to the United States, the Netherlands, Germany and so on.

Relevant information

Physical and chemical properties of molybdenum

Physical property Molybdenum is located in the mendeleev periodic table of the fifth cycle, the first VIB, as a transition metal element, molybdenum atomic number 42, atomic weight of 95.95, in the atomic electron configuration: 1 s22s22p63s23p64s23d104p64d55s1. Due to the semi-full valence orbital state, molybdenum is in a typical transition state between lithophile elements (8 electron ion configuration) and cuprophilic elements (18 electron ion configuration). Goldschmidt called it siderophile in the geochemical classification of elements. Molybdenum has seven stable natural isotopes. Chemical property Molybdenum is extremely difficult to throw away seven or eight electrons. This determines the chemical properties of molybdenum are relatively stable. At room temperature or at not too high a temperature, molybdenum is stable in air or water. Molybdenum is heated in the air, and the color begins to turn from white (color) to dark gray; When the temperature rises to 520℃, molybdenum begins to be slowly oxidized to form Mo2O3. When the temperature rises above 600℃, molybdenum is rapidly oxidized to MoO3. Molybdenum is heated in water vapor to 700~800 ° C and begins to form MoO2, which is further heated and molybdenum dioxide is continued to be oxidized to molybdenum trioxide. Molybdenum can spontaneously ignite in pure oxygen to form molybdenum trioxide. Molybdenum oxides have been reported a lot, but many are reaction intermediates, rather than thermodynamically stable phase states. There are only nine that are very reliable.

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Standard for the inspection of ferric molybdenum

(1) Quality inspection and acceptance. The quality inspection and acceptance of products shall comply with the requirements of GB/ T3650-95 "General Provisions for Ferroalloy acceptance, packaging, storage and transportation, marking and Quality Certificate". (2) Batch. When the products are delivered in a batch of one furnace or the supply and demand parties agree on a batch of furnaces, the difference between the highest or lowest molybdenum content in each batch of products and the average molybdenum content of the sample shall not exceed 3%. (3) Sampling. Samples for chemical analysis should be taken in accordance with GB/ T4010-94 "Sample Taking and Preparation for Chemical Analysis of Ferroalloys". (4) Sample preparation. The preparation of samples for chemical analysis is carried out according to GB/ T4010-94 "Sampling and Preparation of Samples for Chemical Analysis of Ferroalloys". (5) Chemical analysis methods. The corresponding elements are tested according to the following criteria: GB5059? Molybdenum content was determined by 1-85-8-hydroxyquinoline gravimetric method. Gb5059.2-85 malachite green spectrophotometric determination of antimony; Gb5059.3-85 atomic absorption spectrophotometry for the determination of copper content; Gb5059.4-88 polarographic determination of tin content; Gb5059.5-86 gravimetric measurement of silicon content; Gb5059.6-86 molybdenum blu-ray method for the determination of phosphorus content; Gb5059.7-88 infrared absorption method to determine carbon content; Gb5059.8-88 Coulomb method for carbon content determination; Gb5059.9-88 infrared absorption method for the determination of sulfur; Gb5059.10-88 Combustion potassium iodate titration method for determination of sulfur content.

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