Method for producing sulfur-containing compositions

By mixing and granulating sulfur and carbon sources to form spherical particles, then heating at controlled temperatures, the method efficiently produces sulfur-containing compositions with high sulfur content, addressing the inefficiencies of high-temperature methods.

JP7879703B2Active Publication Date: 2026-06-24MITSUBISHI UBE CEMENT CORP

Patent Information

Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
MITSUBISHI UBE CEMENT CORP
Filing Date
2022-03-02
Publication Date
2026-06-24

AI Technical Summary

Technical Problem

Existing methods for producing sulfur-containing compositions require high-temperature heating and large amounts of oxides, leading to low active ingredient content and inefficient production of heavy metal elution inhibitors.

Method used

A method involving mixing a sulfur source with a carbon source, granulating the mixture to form spherical particles, and heating at lower temperatures using a rotary kiln with controlled oxygen concentration to produce a sulfur-containing composition with high sulfur content.

Benefits of technology

The method achieves a high content of sulfur-containing compounds by ensuring uniform reaction and reducing side reactions, thereby lowering production costs and increasing the yield of sulfur-containing compounds like calcium sulfide.

✦ Generated by Eureka AI based on patent content.

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Abstract

To provide a method for producing a sulfur-containing composition with a high content of a sulfur-containing compound.SOLUTION: A method for producing a sulfur-containing composition includes a mixing step for mixing a sulfur source with a carbon source with over 70 mass% of particles passing through a sieve with a nominal opening of 1.18 mm; a granulating step for subjecting the starting mixture to rolling granulation, giving a granulated material; and a heating step for heating the granulated material.SELECTED DRAWING: None
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Description

Technical Field

[0001] The present invention relates to a method for producing a sulfur-containing composition.

Background Art

[0002] A method of producing a sulfur-containing composition by heating a sulfur source containing sulfur and a carbon source containing carbon is known. For example, Patent Document 1 discloses a method of obtaining calcium sulfide by mixing gypsum and a pulverized carbon source and heating them in a reducing atmosphere. Further, Patent Document 2 discloses a method for producing a heavy metal elution inhibitor containing a sulfide by adding an oxide to a raw material containing a reducing agent and a metal sulfate, granulating, and heating and melting. Further, Patent Document 2 describes a method for producing a heavy metal elution inhibitor containing a metal sulfide by melting a raw material containing a reducing agent such as carbon and a metal sulfate at 1200 to 1600°C in an oxidizing atmosphere.

Prior Art Documents

Patent Documents

[0003]

Patent Document 1

[0006] The present invention has been made in accordance with the circumstances described above, and aims to provide a method for producing a sulfur-containing composition with a high content of sulfur-containing compounds. [Means for solving the problem]

[0007] The present invention provides a method for producing a sulfur-containing composition, comprising a mixing step of mixing a sulfur source with a carbon source in which the proportion of particles passing through a sieve with a nominal mesh opening of 1.18 mm is 70% by mass or more to obtain a mixed raw material; a granulation step of tumbling the mixed raw material to obtain a granulated raw material; and a heating step of heating the granulated raw material.

[0008] The method for producing the sulfur-containing composition of the present invention may include a mixing step of mixing a sulfur source with a carbon source in which the proportion of particles passing through a sieve with a nominal mesh opening of 1.18 mm is 70% by mass or more to obtain a mixed raw material; a granulation step of granulating the mixed raw material to obtain a granulated raw material containing substantially spherical raw material particles; and a heating step of heating the granulated raw material.

[0009] The above granulation process may be carried out by the rolling granulation method.

[0010] The particle size of the above-mentioned granulation raw material may be 3 mm or larger.

[0011] The above heating process may be carried out using a rotary kiln, with the heating temperature inside the rotary kiln being 1200°C or less and the oxygen concentration being 20% ​​by volume or less.

[0012] The above sulfur-containing composition may contain metal sulfides.

[0013] The sulfur source may contain gypsum, and the sulfur-containing composition may contain calcium sulfide.

[0014] The gypsum mentioned above is waste gypsum board containing paper, and the process may include a crushing step for crushing the waste gypsum board. [Effects of the Invention]

[0015] According to the present invention, it is possible to provide a method for producing a sulfur-containing composition with a high content of sulfur-containing compounds. [Modes for carrying out the invention]

[0016] A method for producing a sulfur-containing composition according to one embodiment of the present invention comprises a mixing step of mixing a sulfur source and a carbon source having a particle content of 70% by mass or more that passes through a sieve with a nominal mesh size of 1.18 mm to obtain a mixed raw material, a granulation step of tumbling granulation of the mixed raw material to obtain a granulated raw material, and a heating step of heating the granulated raw material. Alternatively, the method for producing a sulfur-containing composition according to this embodiment may also comprise a mixing step of mixing a sulfur source and a carbon source having a particle content of 70% by mass or more that passes through a sieve with a nominal mesh size of 1.18 mm to obtain a mixed raw material, a granulation step of granulating the mixed raw material to obtain a substantially spherical granulated raw material, and a heating step of heating the granulated raw material.

[0017] According to the manufacturing method of this embodiment, a sulfur-containing composition with a high content of sulfur-containing compounds can be obtained. The reason for this effect is that rolling granulation is performed on the mixed raw materials in the granulation process. Conventionally, when granulation is performed before heating the mixed raw materials, a method of compressing the raw materials, such as briquette granulation, has been employed. As a result, the granulated raw materials (particles) are compressed in a specific direction and have a flattened or columnar shape. Even when such raw materials are heated in a rotary kiln or the like, the granulated raw material particles do not roll properly, and heating proceeds only in a specific direction, resulting in uneven heating and inadequate reaction within the particles. As a result, a large amount of unreacted material remains. Furthermore, if the heating temperature is increased to promote the reaction, the combustion reaction of sulfur contained in the raw materials and the generated sulfur-containing compounds progresses, generating oxides. As a result, the content of sulfur-containing compounds in the obtained sulfur-containing composition actually decreases. On the other hand, in the manufacturing method according to this embodiment, since the mixed raw materials are roll-granulated, it is easy to obtain granulated raw materials (raw material particles) that are roughly spherical. The roughly spherical raw material particles can easily change orientation by rolling during heating, allowing the reaction to proceed uniformly within the particles and reducing unreacted material. Furthermore, because the reaction proceeds uniformly, the heating temperature can be lowered, reducing costs and suppressing side reactions that would otherwise occur as sulfur-containing compounds react and produce oxides. Additionally, the heating time can be shortened.

[0018] (Mixing process) In the mixing process, the raw materials, the sulfur source and the carbon source, are first mixed. The mixing method is not particularly limited and may be done using a mixer or the like. The mixing may be carried out either wet or dry.

[0019] As a sulfur source, any raw material containing sulfur is acceptable. The sulfur source may contain a compound with a positive oxidation state of sulfur, and may be a compound containing sulfur oxoacids (such as sulfur oxoates). Examples of such compounds include sulfates, sulfites, and bisulfates (hydrogen sulfates). These salts may also be hydrates. The sulfur source may contain one or more sulfur-containing compounds.

[0020] Further, the sulfur source may contain a metal element. The metal element is not particularly limited and may be an alkali metal, an alkaline earth metal, or the like. Examples of the alkali metal include lithium, sodium, potassium, rubidium, cesium, and the like. Examples of the alkaline earth metal include magnesium, calcium, barium, strontium, and the like, and may be magnesium or calcium. The metal element contained in the sulfur source may be one or more kinds.

[0021] Specifically, the sulfur source may contain gypsum. The sulfur source containing gypsum is not particularly limited, and examples include gypsum waste materials such as anhydrite, hemihydrate gypsum, dihydrate gypsum, waste gypsum board, gypsum mold for casting molding, and gypsum mold for industrial model. The waste gypsum board may contain paper. When using a waste gypsum board as the sulfur source, it may have a pulverizing step of pulverizing the waste gypsum board before the mixing step. The pulverizing step can be carried out using an ordinary pulverizer. The particle size of the sulfur source may be 20 mm or less, may be 10 mm or less, or may be 1 mm or less. The particle diameter of the sulfur source can be measured by a metal sieve conforming to JIS Z 8801-1:2019.

[0022] Examples of the carbon source include carbon, coal, coke, charcoal, wood, etc. In addition, coal ash containing unburned carbon discharged from a coal-fired power plant, gasification slag discharged from a coal gasification furnace, pulp sludge, waste plastic, waste wood, harvested wood, and other biomass wastes discharged from a paper mill can be mentioned. The carbon contained in the carbon source can reduce the sulfur when heated, provided that the sulfur source contains a compound containing sulfur having a positive oxidation number.

[0023] The particle size of the carbon source can be measured, for example, using a metal sieve conforming to JIS Z 8801-1:2019 "Test sieves - Part 1: Metal mesh sieves". Specifically, the proportion of particles passing through a sieve with a nominal mesh size of 1.18 mm in the carbon source used in this embodiment is 70% by mass or more, may be 80% by mass or more, may be 90% by mass or more, or may be 95% by mass or more, relative to the total amount of carbon source. By setting the proportion of particles passing through a sieve with a nominal mesh size of 1.18 mm in the carbon source within the above range, improved reactivity can be obtained due to an increase in the surface area of ​​the carbon source, and the increased density of the granules makes it less likely for the sulfur source (raw material) and the sulfur-containing compound (product) to come into contact with O2 and be oxidized, thereby suppressing the formation of oxides.

[0024] In the carbon source used in this embodiment, the proportion of particles passing through a sieve with a nominal aperture of 600 μm may be 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more based on the total amount of the carbon source. In the carbon source used in this embodiment, the proportion of particles passing through a sieve with a nominal aperture of 300 μm may be 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more based on the total amount of the carbon source. In the carbon source used in this embodiment, the proportion of particles passing through a sieve with a nominal aperture of 150 μm may be 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more based on the total amount of the carbon source. In the carbon source used in this embodiment, the proportion of particles that cannot pass through a sieve with a nominal aperture of 300 μm may be 3% by mass or less, 2% by mass or less, 1% by mass or less, or 0.7% by mass or less based on the total amount of the carbon source. In the carbon source used in this embodiment, the proportion of particles that cannot pass through a sieve with a nominal aperture of 150 μm may be 15% by mass or less, 0.1 - 10% by mass, 0.5 - 8% by mass, or 1 - 7% by mass based on the total amount of the carbon source. In the carbon source used in this embodiment, the proportion of particles that pass through a sieve with a nominal aperture of 300 μm but cannot pass through a sieve with a nominal aperture of 150 μm may be 15% by mass or less, 0.1 - 10% by mass, 0.5 - 8% by mass, or 1 - 7% by mass based on the total amount of the carbon source.

[0025] The proportion of the carbon source with a particle size of less than 1 mm in the carbon source may be 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more based on the total amount of the carbon source used. The carbon source may have a proportion of those with a predetermined particle size of less than 1 mm being 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more. The predetermined particle size may be 0.6 mm or less, 0.3 mm or less, or 0.15 mm or less.

[0026] The carbon source content of less than 0.6 mm may be 70% or more by mass, 80% or more by mass, 90% or more by mass, or 95% or more by mass, relative to the total amount of carbon source. The carbon source content of less than 0.3 mm may be 70% or more by mass, 80% or more by mass, 90% or more by mass, or 95% or more by mass, relative to the total amount of carbon source. The carbon source content of less than 0.15 mm may be 70% or more by mass, 80% or more by mass, 90% or more by mass, or 95% or more by mass, relative to the total amount of carbon source.

[0027] The molar ratio of carbon in the carbon source to sulfur in the sulfur source in the mixed raw materials may be 1.0 or higher, 1.5 or higher, 2.0 or higher, or 2.2 or higher, from the viewpoint of increasing the content of sulfur-containing compounds in the resulting sulfur-containing composition. Furthermore, the molar ratio of carbon in the carbon source to sulfur in the sulfur source in the mixed raw materials may be 10 or lower, 5 or lower, 3 or lower, or 2.5 or lower, from the viewpoint of reducing unreacted carbon and suppressing the generation of oxides due to excessive reaction.

[0028] For example, if the sulfur source contains gypsum (CaSO4), the ratio of the carbon source to the sulfur source can be expressed as [C] / [CaSO4], which is the molar ratio of carbon (C) to CaSO4 contained in the carbon source.

[0029] The mixed raw materials may contain a granulation accelerator in addition to the sulfur source and carbon source. The granulation accelerator may be inorganic or organic. Examples of inorganic accelerators include bentonite. Examples of organic accelerators include molasses, starch, alginic acid, polyvinyl alcohol, and carboxymethylcellulose.

[0030] The mixed raw materials may contain ash derived from a carbon source (e.g., SiO2, Al2O3).

[0031] (granulation process) In the granulation process, the mixed raw materials obtained in the mixing process are granulated. The granulation process may be carried out by rolling granulation. The rolling granulation method is not particularly limited, but may be carried out using a pan-type granulator, drum-type granulator, vibrating granulator, high-speed mixer, etc. The size and particle size distribution of the granulated raw materials can be changed and adjusted by appropriately adjusting the granulation conditions according to the granulation method. For example, with a pan-type granulator, water can be sprayed in a mist onto the powdered raw materials placed in the pan, causing the particles to roll along the rotation direction of the granulation container and collide and bond with each other, thereby granulating particles of the required size. For other granulation methods, the granulation size and particle size distribution can be adjusted by appropriately adjusting the amount of water and binder added, the rotation speed of the drum and stirring screw, the motor vibration frequency, etc. Furthermore, the aspect ratio (=short axis length / long axis length) of the raw material particles after granulation may be 0.7 to 1, 0.8 to 1, or 0.9 to 1.

[0032] The particle size of the raw material particles may be 1 mm or larger, 3 mm or larger, greater than 3 mm, 5 mm or larger, or 10 mm or larger, from the viewpoint of reducing the purification of oxides, which are by-reaction products. Furthermore, the particle size of the raw material particles may be 50 mm or smaller, 30 mm or smaller, or 20 mm or smaller, from the viewpoint of ensuring sufficient reaction within the particles. The particle size of the raw material particles can be measured using a metal sieve in accordance with JIS Z 8801-1:2019.

[0033] When measuring the particle size of raw material particles using a sieve, the particle size may be the particle size measured after granulation and drying of the raw material particles. For example, the percentage of raw material particles that passed through a sieve with a nominal mesh size of 3.35 mm may be 5 to 50% by mass, or 5 to 20% by mass. Also, of the raw material particles that did not pass through the sieve with a nominal mesh size of 3.35 mm, the percentage that passed through a sieve with a nominal mesh size of 9.5 mm may be 5 to 80% by mass, or 20 to 80% by mass. Also, the percentage of raw material particles that did not pass through a sieve with a nominal mesh size of 9.5 mm may be 50 to 95% by mass, or 80 to 95% by mass. The percentage of raw material particles that did not pass through a sieve with a nominal mesh size of 3.35 mm may be 50% or more by mass, 70% or more by mass, 80% or more by mass, 90% or more by mass, or 95% or more by mass. The proportion of raw material particles that could not pass through a sieve with a nominal mesh size of 9.5 mm may be 50% by mass or more, 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more.

[0034] The moisture content of the granulation raw material may be 1 to 30% by mass, 3 to 25% by mass, or 5 to 20% by mass relative to the total amount of the granulation raw material.

[0035] (Heating process) The heating method is not particularly limited, but may be carried out in a heating furnace. The heating furnace is not particularly limited as long as it can heat to a predetermined temperature, such as an internal combustion burner rotary kiln, an external heating rotary kiln, a double-cylinder rotary kiln type carbonization furnace, a batch type carbonization furnace, etc.

[0036] The heating temperature may be 1200°C or lower, or 1100°C or lower. The oxygen concentration inside the heating furnace may be 20% by volume or lower, or 17% by volume or lower, 15% by volume or lower, 13% by volume or lower, or 10% by volume or lower. The oxygen concentration inside the heating furnace may be 3 to 20% by volume, or 5 to 15% by volume.

[0037] The resulting sulfur-containing composition may be subjected to classification. Classification can be carried out, for example, using a sieve in accordance with JIS Z 8801-1:2019.

[0038] Examples of sulfur compounds included in the sulfur-containing composition obtained by the heating process include compounds containing sulfur with a lower oxidation state than the sulfur contained in the sulfur source of the raw material, such as metal sulfides and metal sulfites (i.e., compounds in which the sulfur has been reduced). Such sulfur-containing compounds containing sulfur with a lower oxidation state can be used as a reducing agent for hexavalent chromium. Examples of metal sulfides include calcium sulfide, calcium polysulfide, and magnesium sulfide. Examples of metal sulfites include calcium sulfite and magnesium sulfite.

[0039] In the heating process, for example, if gypsum (CaSO4) is used as the sulfur source, the reaction represented by the following reaction equation (1) proceeds. Simultaneously, the reaction represented by the following reaction equation (2) may also proceed, and SO2 may be generated. CaSO4 + 2C → CaS + 2CO2 (1) CaSO4 + CaS → 2CaO + 2SO2(2)

[0040] In the heating process, it is preferable that the number of moles of gypsum (CaSO4) supplied to the heating section and the number of moles of the carbon source (C) satisfy the following formula (3), more preferably the following formula (4), and even more preferably the following formula (5). This makes the reaction between gypsum and the carbon source proceed more easily. C / CaSO4≧3 (3) C / CaSO4>4 (4) C / CaSO4>5 (5)

[0041] The sulfur-containing composition may contain components other than sulfides. Such components include calcium oxide, unreacted gypsum, and impurities derived from raw materials such as gypsum. By adding the sulfur-containing composition containing sulfides to the grinding process, which is one of the cement manufacturing processes for producing cement compositions, and grinding it together with cement clinker and gypsum, a cement composition capable of reducing the amount of hexavalent chromium leached can be produced. The sulfur-containing composition may also be added in the grinding process as a dry powder or alkaline slurry.

[0042] The calcium sulfide content of a sulfur-containing composition can be determined by analyzing the diffraction pattern obtained by powder X-ray diffraction measurement using the Rietveld method. The calcium sulfide content of the sulfur-containing composition is preferably 5% by mass or more, more preferably 30% by mass or more, even more preferably 50% by mass or more, and particularly preferably 70% by mass or more. From the viewpoint of ease of manufacture, the calcium sulfide content of the sulfur-containing composition may be 95% by mass or less.

[0043] The particle size of the sulfur-containing composition may be 1 mm or larger, 3 mm or larger, greater than 3 mm, 5 mm or larger, or 10 mm or larger, from the viewpoint of reducing the formation of oxides as by-reaction products. Furthermore, the particle size of the sulfur-containing composition may be 50 mm or smaller, 30 mm or smaller, or 20 mm or smaller, from the viewpoint of ensuring sufficient reaction within the particles.

[0044] The particle size of the sulfur-containing composition can be measured using a metal sieve in accordance with JIS Z 8801-1:2019. For example, the percentage of the sulfur-containing composition that passed through a sieve with a nominal mesh size of 3.35 mm may be 5 to 50% by mass, or 5 to 20% by mass. Also, of the sulfur-containing composition that did not pass through the sieve with a nominal mesh size of 3.35 mm, the percentage that passed through a sieve with a nominal mesh size of 9.5 mm may be 5 to 80% by mass, or 20 to 80% by mass. Also, the percentage of the sulfur-containing composition that did not pass through the sieve with a nominal mesh size of 9.5 mm may be 50 to 95% by mass, or 80 to 95% by mass. The percentage of the sulfur-containing composition that did not pass through the sieve with a nominal mesh size of 3.35 mm may be 50% by mass or more, 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more. The proportion of the sulfur-containing composition that could not pass through a sieve with a nominal mesh size of 9.5 mm may be 50% by mass or more, 70% by mass or more, 80% by mass or more, 90% by mass or more, or 95% by mass or more. [Examples]

[0045] A carbon source with the particle size distribution shown in Table 1 was prepared. Coarse slag 1 is coal gasification coarse slag (manufactured by Ube Industries, Ltd.), and coarse slag 2 is coarse slag crushed using a ball mill. Waste gypsum board is crushed waste gypsum board (containing 94% dihydrate gypsum by mass, including paper), and pulverized coal is produced by crushing general coal using a vertical roller mill. The particle size distribution of each carbon source was measured using a metal sieve in accordance with JIS Z 8801-1:2019 "Test sieves - Part 1: Metal wire mesh sieves". In Table 1, for convenience, for each carbon source, particles that pass through a 150 μm sieve are expressed as "≤150 μm", particles that pass through a 300 μm sieve but not a 150 μm sieve are expressed as "150 μm <, ≤300 μm", particles that pass through a 600 μm sieve but not a 300 μm sieve are expressed as "300 μm <, ≤600 μm", particles that pass through a 1.18 mm sieve but not a 600 μm sieve are expressed as "600 μm <, ≤1.18 mm", and particles that do not pass through a 1.18 mm sieve are expressed as "1.18 mm <". The percentage (mass %) of each particle is listed in Table 1.

[0046] [Table 1]

[0047] (Examples 1 and 2) A powdered mixed raw material was obtained by mixing gypsum and a carbon source in a ratio of [C] / [CaSO4] = 2.4 (molar ratio) according to the mixing ratios shown in Table 2. The obtained mixed raw material was granulated by tumbling in a high-speed mixer (Earth Technica Co., Ltd., FS100) to obtain a roughly spherical granulated raw material. Tumbling granulation was performed by adding water to the mixed raw material placed in the granulation container. Note that the moisture content in Table 2 is the ratio of moisture to the total amount of water and raw materials. The obtained granulated raw material was granulated in a rotary kiln (total length approximately 3m, rotation speed 0.5min) -1 A sulfur-containing composition was obtained by heating under the conditions shown in Table 2. The obtained sulfur-containing composition contained unreacted gypsum (CaSO4) and the products calcium sulfide (CaS) and calcium oxide (CaO). The amount of CaS and CaO produced was converted to the amount of CaSO4 used as a raw material, and the content of these (gypsum equivalent %) relative to the total amount of unreacted CaSO4 and the converted CaS and CaO is shown in Table 2. In Table 2, the reaction rate is the ratio (%) of the total amount of converted CaS and CaO relative to the total amount in the obtained sulfur-containing composition.

[0048] (Comparative Examples 1 and 2) Except for not performing granulation and changing the kiln operating conditions as shown in Table 2, the raw materials were mixed and heated in the same manner as in Example 1 to obtain a sulfur-containing composition.

[0049] (Comparative Example 3) A sulfur-containing composition was obtained by mixing and heating the raw materials in the same manner as in Example 1, except that the mixed raw materials were granulated using a briquette machine (Furukawa Sangyo Co., Ltd., KP-102H) to obtain flat, almond-shaped granulated raw materials, and the kiln operating conditions were changed as shown in Table 2. The granulation size of Comparative Example 3 is an actual measurement value using calipers. The typical particle size was 10 mm × 24 mm × 16 mm (aspect ratio = 0.417).

[0050] (Comparative Example 4) Except for using coarse slag 1 as the carbon source and changing the kiln operating conditions as shown in Table 2, the raw materials were mixed and heated in the same manner as in Example 1 to obtain a sulfur-containing composition.

[0051] (Comparative Example 5) Except for using coarse slag 2 as the carbon source, not performing granulation, and changing the kiln operating conditions as shown in Table 2, the raw materials were mixed and heated in the same manner as in Example 1 to obtain a sulfur-containing composition.

[0052] [Table 2]

[0053] In Comparative Examples 1 and 2, where only gypsum and a carbon source were mixed and fired, most of the gypsum was converted to CaO, and the proportion obtained as CaS was small. In Comparative Example 3, where raw materials granulated into almond shapes using a briquette machine were used, the reaction rate of the gypsum was insufficient, and the proportion of CaO was also high. In Comparative Example 4, where the carbon source was not crushed, although about half of the gypsum was converted to CaS, more than 10% was CaO. On the other hand, in Examples 1 and 2, almost all of the gypsum reacted, and the proportion of CaS was also high. In Comparative Example 5, which used coarse slag 2 but was not granulated, the reaction proceeded too far, and almost no CaS was present.

Claims

1. A mixing step to obtain a mixed raw material by mixing a sulfur source with a carbon source in which the proportion of particles passing through a sieve with a nominal mesh size of 1.18 mm is 70% by mass or more, A granulation step is performed to obtain granulation material by tumbling the mixed raw materials, A heating step for heating the granulation raw material, It has, A method for producing a sulfur-containing composition, comprising mixing the sulfur source and the carbon source in a mixing step such that the molar ratio of carbon contained in the carbon source to the sulfur contained in the sulfur source in the mixed raw materials is 2.0 or more.

2. A mixing step to obtain a mixed raw material by mixing a sulfur source with a carbon source in which the proportion of particles passing through a sieve with a nominal mesh size of 1.18 mm is 70% by mass or more, A granulation step is performed to obtain a granulated raw material containing roughly spherical raw material particles by granulating the aforementioned mixed raw materials, A heating step for heating the granulation raw material, It has, A method for producing a sulfur-containing composition, comprising mixing the sulfur source and the carbon source in a mixing step such that the molar ratio of carbon contained in the carbon source to the sulfur contained in the sulfur source in the mixed raw materials is 2.0 or more.

3. A method for producing a sulfur-containing composition according to claim 2, wherein the granulation step is carried out by a rolling granulation method.

4. A method for producing a sulfur-containing composition according to any one of claims 1 to 3, wherein the particle size of the granulated raw material is 3 mm or more.

5. A method for producing a sulfur-containing composition according to any one of claims 1 to 4, wherein the heating step is performed by a rotary kiln, the heating temperature in the rotary kiln is 1200°C or less, and the oxygen concentration is 20% by volume or less.

6. A method for producing the sulfur-containing composition according to any one of claims 1 to 5, wherein the sulfur-containing composition contains a metal sulfide.

7. A method for producing a sulfur-containing composition according to any one of claims 1 to 6, wherein the sulfur source contains gypsum and the sulfur-containing composition contains calcium sulfide.

8. A method for producing a sulfur-containing composition according to claim 7, wherein the gypsum is waste gypsum board containing paper, and the method includes a grinding step of grinding the waste gypsum board.