Abstract: Provided is a high-concentration carbonyl sulfide conversion-absorption type desulfurizer for use at medium-low temperature and preparation method thereof. The desulfurizer comprises 50%-75% magnetic iron oxide red (Fe21.333O32), 5%-10% alkali metal oxide (K2O), 5-35% anatase TiO2, and 5-10% shaping binder. The method of preparing the desulfurizer comprises: uniformly mixing a metatitanic acid prepared using ferrous sulfate recycled as a by-product from titanium dioxide production with K2CO3, calcining to activate at 500° C.-700° C., mixing with the magnetic iron oxide red and binder, roll molding at room temperature to form balls which are dried at 100° C.-150° C. to obtain the desulfurizer. The desulfurizer has a hydrolysis conversion of carbonyl sulfide higher than 99%, and has a higher sulfur capacity more than 25%.

Abstract: A method of preparing magnetic iron oxide Fe21.333O32, which includes the steps of preparing a solid green rust and calcining the solid green rust to obtain the magnetic iron oxide Fe21.333O32. Also provided is the application of magnetic iron oxide Fe21.333O32 as an active material in desulfurization at a medium temperature. Also provided is a desulfurizer which uses magnetic iron oxide Fe21.333O32 and the application thereof. The present preparation method has simple steps and a short production period.

Abstract: The present invention relates to a novel use of magnetic iron oxide red Fe21.333O32 as a catalyst in oxidizing methanthiol to prepare dimethyl disulfide. The magnetic iron oxide red Fe21.333O32 according to the present invention has extremely high catalytic selectivity in catalyzing and oxidizing methanthiol to prepare dimethyl disulfide. The magnetic iron oxide red Fe21.333O32 is prepared with a carbonate and a ferrite as raw materials, has advantages of low cost and simple preparation process, and is suitable for industrial production.

Abstract: Provided is a high-concentration carbonyl sulfide conversion-absorption type desulfurizer for use at medium-low temperature and preparation method thereof. The desulfurizer comprises 50%-75% magnetic iron oxide red (Fe21.333O32), 5%-10% alkali metal oxide (K2O), 5-35% anatase TiO2, and 5-10% shaping binder. The method of preparing the desulfurizer comprises: uniformly mixing a metatitanic acid prepared using ferrous sulfate recycled as a by-product from titanium dioxide production with K2CO3, calcining to activate at 500° C.-700° C., mixing with the magnetic iron oxide red and binder, roll molding at room temperature to form balls which are dried at 100° C.-150° C. to obtain the desulfurizer. The desulfurizer has a hydrolysis conversion of carbonyl sulfide higher than 99%, and has a higher sulfur capacity more than 25%.

Abstract: A method for preparing amorphous iron oxide hydroxide, comprising following steps: (1) preparing a ferrous salt solution with solid soluble ferrous salt; (2) preparing a hydroxide solution; (3) mixing said hydroxide solution and said ferrous salt solution in a co-current manner for reaction at an alkali ratio of 0.6˜0.8 and a reaction temperature not exceeding 30° C.; (4) after the reaction in step (3) is finished, yielding a first mixture, then charging said first mixture with a gas containing oxygen for oxidation, and controlling the first mixture at a pH value of 6˜8 until the oxidation is finished to yield a second mixture; and (5) filtering, washing with water and drying said second mixture obtained in step (4) to yield the amorphous iron oxide hydroxide.

Abstract: The present invention provides a process for preparing ball-type desulfurizer with high sulfur capacity, comprising the following steps: placing initial balls in a rolling equipment; wetting the surface of the initial balls with an aqueous solution of an organic binder; then alternately adding non-crystalline iron oxide hydroxide and the aqueous solution of the organic binder to gradually form small balls of non-crystalline iron oxide hydroxide with high sulfur capacity and different diameters; and adjusting the shape of the small balls and then roasting or naturally drying the small balls. In the desulfurizer prepared by this method, the initial balls constitutes 0.98 wt %-9.03 wt % of the desulfurizer, the non-crystalline iron oxide hydroxide constitutes 90.29 wt %-98.62 wt % of the desulfurizer, and the organic binder constitutes 0.58 wt %-0.89 wt % of the desulfurizer.

Abstract: A method for preparing amorphous iron oxide hydroxide, comprising following steps: (1) preparing a ferrous salt solution with solid soluble ferrous salt; (2) preparing a hydroxide solution; (3) mixing said hydroxide solution and said ferrous salt solution in a co-current manner for reaction at an alkali ratio of 0.6˜0.8 and a reaction temperature not exceeding 30° C.; (4) after the reaction in step (3) is finished, yielding a first mixture, then charging said first mixture with a gas containing oxygen for oxidation, and controlling the first mixture at a pH value of 6˜8 until the oxidation is finished to yield a second mixture; and (5) filtering, washing with water and drying said second mixture obtained in step (4) to yield the amorphous iron oxide hydroxide.

Abstract: A method for preparing magnetic iron oxide Fe21333O32, comprising the following steps: (1) preparing a ferrous salt solution with solid soluble ferrous salt; (2) preparing a hydroxide solution; (3) mixing said hydroxide solution and said ferrous salt solution in a co-current manner for reaction at an alkali ratio of 0.6-0.8 and a reaction temperature not exceeding 30° C.; (4) after the reaction in step (3) is finished, yielding a first mixture, then charging said first mixture with a gas containing oxygen for oxidation, and controlling the first mixture at a pH value of 6-8 until the oxidation is finished to yield a second mixture; (5) filtering, washing with water and drying said second mixture obtained in step (4) to yield a precursor; and (6) calcining the precursor obtained in step (5) at 250-400° C.

Abstract: The present invention provides a process for preparing ball-type desulfurizer with high sulfur capacity, comprising the following steps: placing initial balls in a rolling equipment; wetting the surface of the initial balls with an aqueous solution of an organic binder; then alternately adding non-crystalline iron oxide hydroxide and the aqueous solution of the organic binder to gradually form small balls of non-crystalline iron oxide hydroxide with high sulfur capacity and different diameters; and adjusting the shape of the small balls and then roasting or naturally drying the small balls. In the desulfurizer prepared by this method, the initial balls constitutes 0.98 wt %-9.03 wt % of the desulfurizer, the non-crystalline iron oxide hydroxide constitutes 90.29 wt %-98.62 wt % of the desulfurizer, and the organic binder constitutes 0.58 wt %-0.89 wt % of the desulfurizer.

Abstract: Provided is a preparation method of magnetic iron oxide Fe21.333O32, comprising the following steps, preparing a solid green rust; and then calcining said solid green rust to obtain a magnetic iron oxide Fe21.333O32. Also provided is the application of the magnetic iron oxide Fe21.333O32 as active materials of desulfurization at medium temperature. Also provided is a desulfurizer comprising the magnetic iron oxide Fe21.333O32 and the application thereof. The preparation method has simple steps and short production period.

Abstract: The present invention relates to a trifunctional catalyst used in catalytic cracking device in petroleum refining industry and a method for preparing the same. The trifunctional catalyst of the invention comprises absorbent, cerium dioxide and vanadium pentoxide acting as oxidative catalyst and cerium oxyfluoride acting as structural promoter. The oxidative catalyst and structural promoter are dispersed over the absorbent. The absorbent is spinel-based composite oxides having a general formula of MgAl2-xFexO4.yMgO, where the x is 0.01-0.5 and y is 0.2-1.2. In the trifunctional catalyst, the raw material for forming the chemical compound containing rare-earth cerium is hamartite powder. The method for preparing the trifunctional catalyst of the invention is shown as follows: the components relating to the preparation of the finished product are dissolved or dispersed into liquid materials; then the trifunctional catalyst is obtained after the mixing, drying and calcining of such liquid materials.

Abstract: The present invention discloses a composition for a desulfurizer with a high sulfur capacity and a process for making the same. The composition comprises the active components of three kinds of iron oxides and is used in the desulfurizer to remove hydrogen sulfide from the gaseous and liquid state feed stocks. The process for preparing the composition comprises the following steps: (1) mixing a solid ferrous compound with a solid hydroxide at a molar ratio of iron to hydroxyl being in the range from 1:2 to 1:3; (2) kneading the mixture feeds obtained in step (1) and making them react completely; (3) drying the products obtained in step (2) in the air; (4) washing and filtering the feeds obtained in the step (3); (5) naturally drying or baking the solids obtained in step (4) to form a composition for a desulfurizer with a high sulfur capacity.

Abstract: The present invention relates to a novel process for refining the liquefied petroleum gas (LPG) in a commercial scale. The process comprises: sequentially performing fine desulfurization and mercaptan conversion of the LPG after alcohol amine treatment through desulfurizer and catalyst set in fixed bed reactor in the absence of alkali, wherein, during the fine desulfurization, the resultants of reaction between hydrogen sulfide in the LPG and Fe—Ca oxides or their hydrates adhered on the desulfurizer, and during the mercaptan conversion, the mercaptan in the LPG reacts with the residual trace amount of air in the LPG under the action of the catalyst to produce the disulfides; letting the formed disulfides along with the LPG flow out of the fixed bed reactor; rectifying the LPG after the mercaptan conversion to obtain the refined LPG products, with further rectification to obtain the valuable disulfide products.