Patent Application
20170253530
The invention generally relates to calcium silicate-based cements. More particularly, the invention relates to novel, carbonatable calcium silicate-based, white cements and methods of production and use thereof. The white cement disclosed herein may be used in a variety of cement and concrete applications in the infrastructure, construction, pavement and landscaping industries.
White Portland cements are cements produced to have a white or near white color for applications where light color or white concretes are employed for high aesthetic value. In order to obtain a white product, the level of iron and other species that contribute to color must be carefully controlled. The need for control of these species through raw material selection and processing constraints add considerable cost to the manufacture of a white Portland cement. Additionally, decreasing the level of iron and other colorant species creates a raw mix that is challenging to burn in the kiln, resulting in reduced throughput and increased fuel consumption.
A novel approach is needed to create a more economical white cement, which offers more flexibility in raw material selection and processing.
The present invention provides a new class of carbonatable calcium silicate clinkers and the ground cement product therefrom with a high brightness for use in products with high aesthetic considerations. Carbonatable calcium silicate-based cements are a novel class of non-hydraulic cements that gain strength primarily through a reaction with CO2(g) and can serve as a replacement for conventional hydraulic cements, such as Portland cement. The production and utilization of carbonatable calcium silicate-based cements results in significant reduction of associated energy consumption and enjoys a much favorable carbon footprint through sequestration of CO2 in concrete products.
In one aspect, the invention generally relates to a white carbonatable calcium silicate cement composition. The cement composition includes: one or more discrete calcium silicate phases selected from CS (wollastonite or pseudowollastonite), C3S2 (rankinite), C2S (belite, larnite, bredigite), and an amorphous calcium silicate phase, wherein the one or more discrete calcium silicate phases form about 30% or more by mass of the total phases, and wherein elemental Ca and elemental Si are present in the composition at a molar ratio from about 0.8 to about 1.2; and metal oxides of Al, Fe and Mg are present at about 30% or less by mass, wherein the total color-imparting oxides of one or more of metals selected from Fe, Ti, Mn and Cr are present at about 2.5% or less by mass of the total cement composition, wherein the cement composition is characterized by a reflectance value (L*) of greater than about 85%. The cement composition is suitable for carbonation with CO2 at a temperature of about 30° C. to about 90° C. to form a composite material comprising a binder matrix with a mass gain of about 10% or more.
In another aspect, the invention generally relates to a composite material formed by carbonation of a white carbonatable calcium silicate cement disclosed herein.
In yet another aspect, the invention generally relates to a method for producing a white carbonatable calcium silicate cement. The method includes: providing a raw material set primarily comprising of CaO and SiO2; grinding the raw material set to obtain a precursor mixture, wherein the molar ratio of CaO to SiO2 is from about 0.8 to about 1.2; firing the precursor mixture to a temperature of in the range from about 800° C. to about 1,400° C. to obtain a white carbonatable calcium silicate clinker; and grinding the white carbonatable calcium silicate clinker to a fineness of about 200 to about 800 m2/kg to produce the white carbonatable calcium silicate cement having a reflectance value (L*) of greater than about 85%.
Preferably, the precursor mixture includes less than about 21.2% (e.g., less than about 20%, less than about 17.5%, less than about 15%, less than about 12.5%) by mass the oxides of Al, Fe and Mg, and (ii) less than about 1.5% (e.g., less than about 1.3%, less than about 1.0%, less than about 0.8%, less than about 0.5%) by mass metal oxides of one or more metals selected from Fe, Ti, Mn and Cr.
The objects and features of the invention can be better understood with reference to the drawings described below, and the claims. The drawings are not necessarily to scale, emphasis instead generally being placed upon illustrating the principles of the invention. In the drawings, like numerals are used to indicate like parts throughout the various views.
CaSiO3 (calcium silicate)+CO2.
2Ca2SiO4.CaCO3+CO2.
MgCO3.
MgCO3 as a function of the proportion of CO2 in an inert gas.
The invention provides a new class of carbonatable calcium silicate-based, white clinkers and ground cements, as well as methods of their production and use thereof. The disclosed white clinkers and cements exhibit a high brightness and are suitable for use in products that require high aesthetic considerations.
Carbonatable calcium silicate cements are a novel class of non-hydraulic cements that gain strength primarily through a reaction with CO2 and can serve as a replacement for conventional hydraulic cements. These materials can be produced and utilized with significantly reduced energy requirement and CO2 emissions. The disclosed carbonatable calcium silicate compositions are made from widely available, low cost raw materials by a process suitable for large-scale production with flexible equipment and production requirements. Use of these special cements to make concrete products is accompanied by a permanent sequestration of CO2. A wide variety of applications can benefit from the invention, from construction, pavements and landscaping, to infrastructure and transportation through improved energy consumption and more desirable carbon footprint.
White clinkers are manufactured and ground to cement powder to provide a high brightness (L, or reflectance, from the Hunter L*a*b color scale >85%). These white cements are used to create white or pigmented concretes with high aesthetic standards. The color of the clinker, and consequently the cement, is controlled through the raw material chemistry and through processing.
Ordinary Portland clinkers and cement (OPC) typically contain a ferrite (Ca2(Al,Fe)O5) phase that can vary but is typically 10% by mass. This phase is responsible for the characteristic gray color of OPC. The ferrite phase can host a wide range of substitution ions at various oxidation states. Ions associated with the color of the ferrite phase in OPC include primarily transition metals with multiple valences, for example, Fe, Ti, Mn, Cr, and Zn. Mg has also been shown to have a substantial darkening effect when substituting into the ferrite in conjunction with the presence of various transition metals. The high levels of substitutions and resultant electronic effects in the impure ferrite phase create high absorbance of visible light and thus a dark color in OPC.
Compared to OPC, carbonatable calcium silicate-based cements disclosed herein have a much higher tolerance for species that serve as colorants in OPC. Due to the bulk chemistry of carbonatable calcium silicate cements disclosed herein, ferrite is present only in trace levels if present at all. The species commonly responsible for darkening OPC, for example, Fe, Ti, Mn, and Cr, are instead incorporated into either the melilite (Ca,Na)2(Al,Fe,Mg,Si)2SiO7) or amorphous phases. The differences in bonding and relative position of the colorant ions between the OPC ferrite and the carbonatable calcium silicate melilite and amorphous phases contributes to a reduced impact of each individual species on the color of the phase and thus the cement.
The ferrite phase present in OPC has a high index of refraction of approximately 1.9-2.0 (averaged from biaxial refractive index values) depending on composition. The high index of refraction contributes to the scattering of light from ferrite phase and, through the phenomenon of diffuse reflectance, contributes its color to the bulk of the cement.
In contrast, the melilite phase present in carbonatable calcium silicate cements disclosed herein has a low refractive index of approximately 1.5-1.8. This lower refractive index corresponds to a low reflectivity and scattering, resulting in minimal contribution to the color of the final cement from diffused reflection.
The bulk composition of a white OPC clinker typically contains <0.5% Fe2O3 and minimum TiO2, Mn2O3 and Cr2O3. The most common elements influencing the color of the cement—Fe2O3, TiO2 and Mn2O3 strongly influence brightness, while Cr2O3 can darken and add a green tint. Proper control of these species can allow OPC to achieve an L-value exceeding 85%. Typical white cements contain <0.3% Fe2O3 and <0.03% Mn2O3. To achieve such low levels of colorants in OPC, especially for iron, the raw materials must be carefully selected. This requirement results in a substantial increase in the cost of raw materials of OPC clinker because only low iron precursor sources of CaO, SiO2 and Al2O3 can be used.
In addition to the raw mix composition, several changes to the clinker production process are typically needed to ensure to produce white OPC. In some situations the raw material grinding, fuel choice, firing regime and clinker cooling must be modified to achieve a white product. Each of these additional process controls introduces added cost to the production of the white cement clinker.
In many cases the raw mill must be modified to use ceramic or other high hardness grinding media and surfaces to avoid contamination of the raw materials by the steel media typically used in the raw material and cement grinding process. This contamination can introduce Fe2O3, MnO and Cr2O3 into the kiln to the detriment of the color of the OPC product. Similarly, the ash produced by the combustion of coal in the kiln can be incorporated into the OPC clinker. This ash adds Fe2O3, TiO2, MnO, Cr2O3 and other trace colorants to the OPC clinker to the detriment of the product color. A similar negative impact can be attributed to many alternative fuels with a non-volatile combustion residue such as automotive tires or shredded plastic waste. Due to fuel ash, in some circumstances it may be necessary to use a more expensive, low ash coal, remove alternative fuel heat sources, or switch from coal combustion to oil or natural gas combustion entirely to achieve a white OPC product.
The low iron content of the raw mix from which the white OPC clinker derives its characteristic color also limits the liquid phase formation at normal processing temperatures. In order to achieve the proportion of liquid phase necessary for clinkering and the formation of C3 S (alite, Ca3SiO5) in white OPC clinker, the processing temperature must be higher, typically approaching 1,500° C. Achieving this high temperature has negative impacts on kiln operation, including increased fuel consumption and decreased clinker production rates. In some cases, fluxing agents such as fluorspar (CaF2) or calcium chloride (CaCl2) are added to enhance the burnability of the white OPC raw mix without increasing the iron content.
In contrast, the lower optical response to colorant species in the carbonatable calcium silicate-based cement clinker disclosed herein allows a significantly larger range of less pure and less expensive materials to be used to economically produce white cement clinker. The tolerance for colorant species also entails that few restrictions in the selection of grinding media or fuel sources to avoid contamination by colorant species.
The oxidation state of the iron component of OPC also plays a role in determining the final color of the cement clinker. Fe3+ has a stronger color effect than Fe2+. In order to encourage the reduction of Fe3+ to Fe2+ in the kiln and prevent its reoxidation during cooling, some specific burning and cooling strategies can be used. A bleaching process achieved by burning with a reducing or very low oxygen condition can be employed either on the main burner or using a secondary burner on the clinker leaving the kiln. In some instances, the secondary burner serves to create a reducing atmosphere. The clinker is then cooled rapidly without access to high concentrations of oxygen, in some cases by water cooling, from 1,400° C.-600° C. to prevent the oxidation of Fe2+. This process is important to produce white OPC cements in areas where creating a cement chemistry with <0.3% Fe2O3 content is difficult since it effectively decreases the amount of color-influencing Fe2O3. Running kiln burners without sufficient oxygen can reduce the effectiveness of combustion, increasing fuel consumption, increasing ash or residue, and result in the reduction of nitrogen and thus undesirable NOx emissions. Changes to the cooler, especially a water quenching process, can reduce the ability to effectively recycle and reintroduce heat to the kiln and preheater which reduces the thermal efficiency of the entire process.
The low impact of colorant species on the overall brightness of carbonatable calcium silicate-based cement clinker also reduces the need for special control of the clinker cooling. Process controls used to prevent the oxidation of Fe2+ produced at high kiln temperatures include rapid cooling under a reducing atmosphere or water quenching of the clinker. While these steps are needed for producing white OPC, they can be eliminated in white carbonatable calcium silicate cement production.
The term “calcium silicate” material, as used herein, generally refers to naturally-occurring minerals or synthetic materials that are comprised of one or more of a group of calcium silicate phases including CS (wollastonite or pseudowollastonite, and sometimes formulated CaSiO3 or CaO.SiO2), C3 S2 (rankinite, and sometimes formulated as Ca3Si2O7 or 3CaO.2SiO2), C2S (belite, β-Ca2SiO4 or larnite, Ca7Mg(SiO4)4 or bredigite, α-Ca2SiO4 or γ-Ca2SiO4, and sometimes formulated as Ca2SiO4 or 2CaO.SiO2), a calcium-silicate based amorphous phase, each of which material may include one or more other metal ions and oxides (e.g., aluminum, magnesium, iron or manganese oxides), or blends thereof, or may include an amount of magnesium silicate in naturally-occurring or synthetic form(s) ranging from trace amount (1%) to about 50% or more by weight.
In the production of carbonatable calcium silicate cement clinker, a combination of raw materials comprising of various limestones, clays, shales, sand or other sources of CaO and SiO2 are blended and ground in such a proportion to achieve a CaO/SiO2 molar ratio of approximately 1.0. To produce a white carbonatable calcium silicate clinker, the levels of Fe, Ti, Mn, Cr and Zn are controlled by selection of raw materials to limit the sum of the oxides of these elements to less then 1.5% by mass. Decreasing the limit of Fe, Ti, Mn, Cr and Zn oxides in the raw mix below this level may increase the whiteness of the resulting clinker, allowing for finer control of the clinker color through the selection of raw materials.
The reduction in transition metal oxides, especially Fe2O3, in the creating of white carbonatable calcium silicate clinker raw mix limits the liquid phase available for clinkering reactions in rotary kiln processing. To achieve a white carbonatable calcium silicate clinker the burning zone temperature is selected to about between about 1,300° C. and about 1,400° C., rather than the burning zone temperature of below 1,300° C. (1,200° C.-1,300° C.) when a non-white clinker is desired.
In one aspect, the invention generally relates to a white carbonatable calcium silicate cement composition. The cement composition includes: one or more discrete calcium silicate phases selected from CS (wollastonite or pseudowollastonite), C3S2 (rankinite), C2S (belite, larnite, bredigite), and an amorphous calcium silicate phase, wherein the one or more discrete calcium silicate phases form about 30% or more by mass of the total phases, and wherein elemental Ca and elemental Si are present in the composition at a molar ratio from about 0.8 to about 1.2; and metal oxides of Al, Fe and Mg are present at about 30% or less by mass, wherein the total color-imparting oxides of one or more of metals selected from Fe, Ti, Mn and Cr are present at about 2.5% or less by mass of the total cement composition, wherein the cement composition is characterized by a reflectance value (L*) of greater than about 85%. The cement composition is suitable for carbonation with CO2 at a temperature of about 30° C. to about 90° C. to form a composite material comprising a binder matrix with a mass gain of about 10% or more.
Calcium silicate compositions may contain amorphous (non-crystalline) calcium silicate phases in addition to the crystalline phases described above. The amorphous phase may additionally incorporate Al, Fe and Mg ions and other impurity ions present in the raw materials.
Each of these crystalline and amorphous calcium silicate phases is suitable for carbonation with CO2.
In certain embodiments, the cement composition includes one or more residual CaO (lime) and SiO2 (silica) phases. The calcium silicate composition may also include small quantities of C3S (alite, Ca3SiO5). The C2S phase present within the calcium silicate composition may exist in any α-Ca2SiO4, β-Ca2SiO4 or γ-Ca2SiO4 polymorph or combination thereof.
In certain embodiments, the cement composition includes one or more melilite type phases having the general formula (Ca,Na,K)2[(Mg, Fe2+,Fe3+,Al,Si)3O7].
In certain preferred embodiments, the molar ratio of elemental Ca to elemental Si of the cement composition is from about 0.80 to about 1.20. In certain preferred embodiments, the molar ratio of Ca to Si of the cement composition is from about 0.85 to about 1.15. In certain preferred embodiments, the molar ratio of Ca to Si of the cement composition is from about 0.90 to about 1.10. In certain preferred embodiments, the molar ratio of Ca to Si of the cement composition is from about 0.95 to about 1.05. In certain preferred embodiments, the molar ratio of Ca to Si of the cement composition is from about 0.98 to about 1.02. In certain preferred embodiments, the molar ratio of Ca to Si of the composition is from about 0.99 to about 1.01.
In certain embodiments, the cement composition includes one or more calcium silicate phases existing in an amorphous state and one or more calcium silicate phases existing in a crystalline state.
In certain embodiments, the cement composition includes calcium silicate phases existing only in an amorphous state.
In certain embodiments, the cement composition includes calcium silicate phases existing in both the crystalline state and the amorphous state.
In certain embodiments, the cement composition is a powder having a reflectance value (L*) of greater than about 85%. In certain embodiments, the cement composition is a powder having a reflectance value (L*) of greater than 90%. In certain embodiments, the cement composition is a powder having a reflectance value (L*) of greater than 95%.
In certain embodiments of the cement composition, the metal oxides of one or more metal selected from Fe, Ti, Mn and Cr are incorporated into a melilite type phase. In certain embodiments of the cement composition, the metal oxides of one or more metal selected from Fe, Ti, Mn and Cr are incorporated into an amorphous phase. In certain embodiments of the cement composition, the metal oxides of one or more metal selected from Fe, Ti, Mn and Cr are incorporated into a melilite phase and an amorphous phase.
In certain embodiments of the cement composition, the one or more melilite phases are characterized by a refractive index between about 1.5 and about 1.8 (e.g., about 1.5, 1.6, 1.7, 1.8).
The discrete calcium silicate phases in the cement composition that are suitable for carbonation will be referred to as reactive phases. The reactive phases may be present in the composition in any suitable amount. In certain embodiments, the reactive phases are present at about 50% or more by mass. In certain embodiments, the reactive phases are present at about 60% or more by mass. In certain embodiments, the reactive phases are present at about 70% or more by mass. In certain embodiments, the reactive phases are present at about 80% or more by mass. In certain embodiments, the reactive phases are present at about 90% or more by mass. In certain embodiments, the reactive phases are present at about 95% or more by mass.
The various reactive phases may account for any suitable portions of the overall reactive phases. In certain embodiments, the reactive phases of CS are present at about 10 to about 60 wt % (e.g., about 15 wt % to about 60 wt %, about 20 wt % to about 60 wt %, about 25 wt % to about 60 wt %, about 30 wt % to about 60 wt %, about 35 wt % to about 60 wt %, about 40 wt % to about 60 wt %, about 10 wt % to about 50 wt %, about 10 wt % to about 40 wt %, about 10 wt % to about 30 wt %, about 10 wt % to about 25 wt %, about 10 wt % to about 20 wt %); C3 S2 in about 5 to 50 wt % (e.g., about 10 wt % to 50 wt %, about 15 wt % to 50 wt %, about 20 wt % to 50 wt %, about 30 wt % to 50 wt %, about 40 wt % to 50 wt %, about 5 wt % to 40 wt %, about 5 wt % to 30 wt %, about 5 wt % to 25 wt %, about 5 wt % to 20 wt %, about 5 wt % to 15 wt %); and C2S in about 5 wt % to 60 wt % (e.g., about 10 wt % to about 60 wt %, about 20 wt % to about 60 wt %, about 25 wt % to about 60 wt %, about 30 wt % to about 60 wt %, about 35 wt % to about 60 wt %, about 40 wt % to about 60 wt %, about 5 wt % to about 50 wt %, about 5 wt % to about 40 wt %, about 5 wt % to about 30 wt %, about 5 wt % to about 25 wt %, about 5 wt % to about 20 wt %, about 5 wt % to about 20 wt %), and C in about 0 wt % to 3 wt % (e.g., 0 wt %, 1 wt % or less, 2 wt % or less, 3 wt % or less, about 1 wt % to 2 wt %, about 1 wt % to 3 wt %, about 2 wt % to 3 wt %).
In certain embodiments, the reactive phases include a calcium-silicate based amorphous phase, for example, at about 40% or more (e.g., about 45% or more, about 50% or more, about 55% or more, about 60% or more, about 65% or more, about 70% or more, about 75% or more, about 80% or more, about 85% or more, about 90% or more, about 95% or more, from about 40% to about 95%, from about 50% to about 95%, from about 60% to about 95%, from about 70% to about 95%, from about 40% to about 80%, from about 40% to about 60%) by mass of the total phases. It is noted that the amorphous phase may additionally incorporate impurity ions present in the raw materials.
The calcium silicate cement compositions of the invention are suitable for carbonation with CO2. In particular, the cement composition of calcium silicate is suitable for carbonation with CO2 at a temperature of about 30° C. to about 90° C. to form CaCO3 with mass gain of about 20% or more. The mass gain reflects the net sequestration of CO2 in the carbonated products. In certain preferred embodiments, the composition is suitable for carbonation with CO2 at a temperature of about 30° C. to about 90° C. (e.g., about 40° C. to about 90° C., about 50° C. to about 90° C., about 60° C. to about 90° C., about 30° C. to about 80° C., about 30° C. to about 70° C., about 30° C. to about 60° C., about 40° C. to about 80° C., about 40° C. to about 70° C., about 40° C. to about 60° C.) to form CaCO3 with mass gain of 10% or more (e.g., 15% or more, 20% or more, 25% or more, 30% or more).
In another aspect, the invention generally relates to a composite material formed by carbonation of a white carbonatable calcium silicate cement disclosed herein.
In yet another aspect, the invention generally relates to a method for producing a white carbonatable calcium silicate cement. The method includes: providing a raw material set comprising CaO and SiO2; grinding the raw material set to obtain a precursor mixture, wherein the molar ratio of CaO to SiO2 is from about 0.8 to about 1.2; firing the precursor mixture to a temperature of in the range from about 800° C. to about 1,400° C. to obtain a white carbonatable calcium silicate clinker; and grinding the white carbonatable calcium silicate clinker to a fineness of about 200 to about 800 m2/kg to produce the white carbonatable calcium silicate cement having a reflectance level (L*) of greater than about 85%.
Preferably, the precursor mixture includes less than about 21.2% (e.g., less than about 20%, less than about 17.5%, less than about 15%, less than about 12.5%) by mass the oxides of Al, Fe and Mg, and (ii) less than about 1.5% (e.g., less than about 1.3%, less than about 1.0%, less than about 0.8%, less than about 0.5%) by mass metal oxides of one or more metals selected from Fe, Ti, Mn and Cr.
In certain embodiments, the precursor mixture is prepared from a raw material set selected from one or more of limestone, sand, silts, sandstones, silica-rich clays, diatomaceous earths, marl, fly ash, and silica fume.
In certain embodiments, the raw material set is selected to achieve a precursor mixture with less than about 1.5% (e.g., less than about 1.3%, less than about 1.0%, less than about 0.8%, less than about 0.5%) by mass of transition metal oxides.
In certain embodiments, the raw material set is selected to obtain a precursor composition with less than 1.5% (e.g., less than about 1.3%, less than about 1.0%, less than about 0.8%, less than about 0.5%) by mass of metal oxides of one or more metal selected from Fe, Ti, Mn and Cr.
In certain embodiments, firing the precursor mixture is performed at a temperature between about 1,300° C. to about 1,400° C. (e.g., between about 1,300° C. to about 1,330° C., between about 1,300° C. to about 1,350° C., between about 1,330° C. to about 1,350° C., between about 1,350° C. to about 1,400° C., between about 1,350° C. to about 1,380° C., between about 1,380° C. to about 1,400° C.).
In certain embodiments, after firing the white carbonatable calcium silicate clinker is subjected to cooling by forced air in the range of 1,400° C. to 500° C. under an uncontrolled atmosphere. In certain embodiments, after firing the white carbonatable calcium silicate clinker is subjected to cooling by forced air in the range of 1,400° C. to 500° C. under a reducing atmosphere. In certain embodiments, after firing the white carbonatable calcium silicate clinker is subjected to a cooling in the range of 1,400° C. to 500° C. by quenching in water.
In certain embodiments, grinding the mixture of CaO and SiO2 to obtain a precursor mixture is performed in a grinder with a steel grinding surface.
In certain embodiments, grinding the white carbonatable calcium silicate clinker achieves a fineness of about 200 m2/kg to about 800 m2/kg to produce the white carbonatable calcium silicate cement. In certain embodiments, grinding the white carbonatable calcium silicate clinker achieves a fineness of about 200 m2/kg to about 400 m2/kg to produce the white carbonatable calcium silicate cement. In certain embodiments, grinding the white carbonatable calcium silicate clinker achieves a fineness of about 400 m2/kg to about 800 m2/kg to produce the white carbonatable calcium silicate cement. In certain embodiments, grinding the white carbonatable calcium silicate clinker achieves a fineness of about 400 m2/kg to about 600 m2/kg to produce the white carbonatable calcium silicate cement.
It is noted that preferably the carbonatable calcium silicate cement compositions of the invention do not hydrate. However, minor amounts of hydratable calcium silicate phases (e.g., C2S, C3S and CaO) may be present. C2S exhibits slow kinetics of hydration when exposed to water and is quickly converted to CaCO3 during CO2 curing processes. C3 S and CaO hydrate quickly upon exposure to water and thus should be limited to less than about 5% by mass.
The calcium silicate phases included in the calcium silicate composition do not hydrate when exposed to water. Due to this composites produced using a calcium silicate composition as the binding agent do not generate significant strength when combined with water. The strength generation is controlled by exposure of calcium silicate composition containing composites to specific curing regimes in the presence of CO2.
It should be understood that, calcium silicate compositions, phases and methods disclosed herein can be adopted to use magnesium silicate phases in place of or in addition to calcium silicate phases. As used herein, the term “magnesium silicate” refers to naturally-occurring minerals or synthetic materials that are comprised of one or more of a groups of magnesium-silicon-containing compounds including, for example, Mg2SiO4 (also known as “fosterite”) and Mg3Si4O10(OH)2 (also known as “talc”) and CaMgSiO4 (also known as “monticellite”), each of which material may include one or more other metal ions and oxides (e.g., calcium, aluminum, iron or manganese oxides), or blends thereof, or may include an amount of calcium silicate in naturally-occurring or synthetic form(s) ranging from trace amount (1%) to about 50% or more by weight.
A major utility of the carbonatable composition of the invention is that it can be carbonated to form composite materials that are useful in a variety of application. The carbonation, for example, may be carried out reacting it with CO2 via a controlled Hydrothermal Liquid Phase Sintering (HLPS) process to create bonding elements that hold together the various components of the composite material. For example in preferred embodiments, CO2 is used as a reactive species resulting in sequestration of CO2 and the creation of bonding elements in the produced composite materials with in a carbon footprint unmatched by any existing production technology. The HLPS process is thermodynamically driven by the free energy of the chemical reaction(s) and reduction of surface energy (area) caused by crystal growth. The kinetics of the HLPS process proceed at a reasonable rate at low temperature because a solution (aqueous or nonaqueous) is used to transport reactive species instead of using a high melting point fluid or high temperature solid-state medium.
Discussions of various features of HLPS and related topics can be found in U.S. Pat. No. 8,114,367, U.S. Pub. No. US 2009/0143211 (application. Ser. No. 12/271,566), U.S. Pub. No. US 2011/0104469 (application. Ser. No. 12/984,299), U.S. Pub. No. 2009/0142578 (application. Ser. No. 12/271,513), U.S. Pub. No. 2013/0122267 (application. Ser. No. 13/411,218), U.S. Pub. No. 2012/0312194 (application. Ser. No. 13/491,098), WO 2009/102360 (PCT/US2008/083606), WO 2011/053598 (PCT/US2010/054146), WO 2011/090967 (PCT/US2011/021623), U.S. Provisional Patent Application No. 61/708,423 filed Oct. 1, 2012, and U.S. Pub. No. 2014/0127450 (application. Ser. No. 14/045,758), U.S. Pub. No. 2015/0266778 (application. Ser. No. 14/045,519), U.S. Pub. No. 2014/0127458 (application. Ser. No. 14/045,766), U.S. Pub. No. 2014/0342124 (application. Ser. No. 14/045,540), U.S. Pub. No. 2014/0272216 (application. Ser. No. 14/207,413), U.S. Pub. No. 2014/0263683 (application. Ser. No. 14/207,421), U.S. patent application Ser. Nos. 14/207,920, 14/209,238, filed Mar. 13, 2014, U.S. Pub. No. 2014/0363665 (application. Ser. No. 14/295,601), U.S. Pub. No. 2014/0361471 (application. Ser. No. 14/295,402), U.S. Pub. No. 2016/0355439 (application. Ser. No. 14/506,079), U.S. Pub. No. 2015/0225295 (application. Ser. No. 14/602,313), U.S. Pub. No. 2015/0056437 (application. Ser. No. 14/463,901), U.S. Pub. No. 2016/0168720 (application. Ser. No. 14/584,249), U.S. Pub. No. 2015/0336852 (application. Ser. No. 14/818,629), U.S. Pub. No. 2016/0031757 (application. Ser. No. 14/817,193), U.S. Pub. No. 2016/0272544 (application. Ser. No. 15/074,659), U.S. Pub. No. 2016/0096773 (application. Ser. No. 14/874,350), U.S. Pub. No. 2016/0340261 (application. Ser. No. 14/715,497), U.S. Pub. No. 2016/0272545 (application. Ser. No. 15/074,692), application. Ser. No. 15/290,328, filed Oct. 11, 2016, each of which is expressly incorporated herein by reference in its entirety for all purposes.
In exemplary embodiments of carbonation of the composition of the invention, ground calcium silicate composition is used. The ground calcium silicate composition may have a mean particle size from about 1 μm to about 100 μm (e.g., about 1 μm to about 80 μm, about 1 μm to about 60 μm, about 1 μm to about 50 μm, about 1 μm to about 40 μm, about 1 μm to about 30 μm, about 1 μm to about 20 μm, about 1 μm to about 10 μm, about 5 μm to about 90 μm, about 5 μm to about 80 μm, about 5 μm to about 70 μm, about 5 μm to about 60 μm, about 5 μm to about 50 μm, about 5 μm to about 40 μm, about 10 μm to about 80 μm, about 10 μm to about 70 μm, about 10 μm to about 60 μm, about 10 μm to about 50 μm, about 10 μm to about 40 μm, about 10 μm to about 30 μm, about 10 μm to about 20 μm, about 1 μm, 10 μm, 15 μm, 20 μm, 25 μm, 30 μm, 40 μm, 50 μm, 60 μm, 70 μm, 80 μm, 90 μm, 100 μm), a bulk density from about 0.5 g/mL to about 3.5 g/mL (loose, e.g., 0.5 g/mL, 1.0 g/mL, 1.5 g/mL, 2.0 g/mL, 2.5 g/mL, 2.8 g/mL, 3.0 g/mL, 3.5 g/mL) and about 1.0 g/mL to about 1.2 g/mL (tapped), a Blaine surface area from about 150 m2/kg to about 700 m2/kg (e.g., 150 m2/kg, 200 m2/kg, 250 m2/kg, 300 m2/kg, 350 m2/kg, 400 m2/kg, 450 m2/kg, 500 m2/kg, 550 m2/kg, 600 m2/kg, 650 m2/kg, 700 m2/kg).
Any suitable aggregates may be used to form composite materials from the carbonatable composition of the invention, for example, calcium oxide-containing or silica-containing materials. Exemplary aggregates include inert materials such as trap rock, construction sand, pea-gravel. In certain preferred embodiments, lightweight aggregates such as perlite or vermiculite may also be used as aggregates. Materials such as industrial waste materials (e.g., fly ash, slag, silica fume) may also be used as fine fillers.
The plurality of aggregates may have any suitable mean particle size and size distribution. In certain embodiments, the plurality of aggregates has a mean particle size in the range from about 0.25 mm to about 25 mm (e.g., about 5 mm to about 20 mm, about 5 mm to about 18 mm, about 5 mm to about 15 mm, about 5 mm to about 12 mm, about 7 mm to about 20 mm, about 10 mm to about 20 mm, about ⅛″, about ¼″, about ⅜″, about ½″, about ¾″).
Chemical admixtures may also be included in the composite material; for example, plasticizers, retarders, accelerators, dispersants and other rheology-modifying agents. Certain commercially available chemical admixtures such as Glenium™ 7500 by BASF® Chemicals and Acumer™ by Dow Chemical Company may also be included. In certain embodiments, one or more pigments may be evenly dispersed or substantially unevenly dispersed in the bonding matrices, depending on the desired composite material. The pigment may be any suitable pigment including, for example, oxides of various metals (e.g., black iron oxide, cobalt oxide and chromium oxide). The pigment may be of any color or colors, for example, selected from black, white, blue, gray, pink, green, red, yellow and brown. The pigment may be present in any suitable amount depending on the desired composite material, for example in an amount ranging from about 0.0% to about 10% by weight.
A variety of composite products can be produced from the carbonatable calcium silicate compositions of the invention by a process that does not require autoclave(s) and is suitable for continuous, large-scale production. The production methods are much improved over conventional pervious concretes in terms of both economics and environmental impact.
A carbonatable calcium silicate clinker (Experimental Cement 1) was produced using a 4-stage preheater kiln. No special consideration was made for the raw mix grinding, which proceeded using a typical steel media closed circuit ball mill also used for the grinding of gray cement raw meal. The kiln was fired with a mixture of coal and shredded plastic waste. The burning temperature in the kiln was approximately 1,260° C. and was operating a normal (approximately 5% excess oxygen) burning atmosphere. The clinker was cooled using a reciprocating grate cooler with no special cooling procedure employed. The result of grinding this clinker is a carbonatable calcium silicate cement with a reflectance (L-value) of 77.7. The findings of this production are summarized in TABLE 1. An exemplary photo of Experimental Cement 1 is shown in
A carbonatable calcium silicate clinker (Experimental Cement 2) was produced using a 2-stage preheater kiln. No special consideration was made for the raw mix grinding, which proceeded using a typical steel vertical roller mill also used for the grinding of gray cement raw meal. The kiln was fired using natural gas. The burning temperature in the kiln was approximately 1,250° C. and was operating under a normal (approximately 5% excess oxygen) burning atmosphere. The clinker was cooled using a rotary cooler with no special cooling procedure employed. The result of grinding this clinker is a carbonatable calcium silicate cement with a reflectance (L-value) of 80.0. The findings of this production are summarized in TABLE 2. An exemplary photo of Experimental Cement 2 is shown in
A carbonatable calcium silicate clinker was produced using a 5-stage precalciner kiln. No special consideration was made for the raw mix grinding, which proceeded using a vertical roller mill also used for grinding of ordinary gray cement raw meal (steel grinding surfaces). The kiln was fired with a low-ash coal. The burning temperature in the kiln was approximately 1,350° C. and was operating under a normal (approximately 5% excess oxygen) burning atmosphere. No bleaching process was employed. The cement clinker was cooled using a reciprocating grate cooler with no special cooling procedure employed. The result of grinding this clinker is carbonatable calcium silicate cement with a reflectance (L-value) of 88.8%. The findings of this production are summarized in TABLE 3. An exemplary photo of Experimental Cement 3 is shown in
A carbonatable calcium silicate clinker was produced using a 4-stage preheater kiln. No special consideration was made for the raw mix grinding, which proceeded using a ball mill also used for grinding of ordinary gray cement raw meal (steel grinding surfaces). The kiln was fired with a coal and waste plastic fuel mixture similar to that used in gray cement production. The burning temperature in the kiln was about 1,300° C. and was operating under a normal (about 5% excess oxygen) burning atmosphere. No bleaching process was employed. The cement clinker was cooled using a reciprocating grate cooler with no special cooling procedure employed. The result of grinding this clinker is carbonatable calcium silicate cement with a reflectance (L-value) of 82.1%. The findings of this production are summarized in TABLE 4. An exemplary photo of Experimental Cement 3 is shown in
Applicant's disclosure is described herein in preferred embodiments with reference to the Figures, in which like numbers represent the same or similar elements. Reference throughout this specification to “one embodiment,” “an embodiment,” or similar language means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, appearances of the phrases “in one embodiment,” “in an embodiment,” and similar language throughout this specification may, but do not necessarily, all refer to the same embodiment.
The described features, structures, or characteristics of Applicant's disclosure may be combined in any suitable manner in one or more embodiments. In the description herein, numerous specific details are recited to provide a thorough understanding of embodiments of the invention. One skilled in the relevant art will recognize, however, that Applicant's composition and/or method may be practiced without one or more of the specific details, or with other methods, components, materials, and so forth. In other instances, well-known structures, materials, or operations are not shown or described in detail to avoid obscuring aspects of the disclosure.
In this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural reference, unless the context clearly dictates otherwise.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present disclosure, the preferred methods and materials are now described. Methods recited herein may be carried out in any order that is logically possible, in addition to a particular order disclosed.
References and citations to other documents, such as patents, patent applications, patent publications, journals, books, papers, web contents, have been made in this disclosure. All such documents are hereby incorporated herein by reference in their entirety for all purposes. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material explicitly set forth herein is only incorporated to the extent that no conflict arises between that incorporated material and the present disclosure material. In the event of a conflict, the conflict is to be resolved in favor of the present disclosure as the preferred disclosure.
The representative examples disclosed herein are intended to help illustrate the invention, and are not intended to, nor should they be construed to, limit the scope of the invention. Indeed, various modifications of the invention and many further embodiments thereof, in addition to those shown and described herein, will become apparent to those skilled in the art from the full contents of this document, including the examples which follow and the references to the scientific and patent literature cited herein. The following examples contain important additional information, exemplification and guidance that can be adapted to the practice of this invention in its various embodiments and equivalents thereof.
This application claims the benefit of priority from U.S. Provisional Application Ser. No. 62/304,107, filed on Mar. 4, 2016, the entire content of which is incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62304107 | Mar 2016 | US |
