Patent Application
20170066653
The present disclosure relates to a process for making hollow particles using a template approach, onto which a shell material is deposited, and the template material removed to generate the hollow particle. More particularly, the disclosure relates to a process in which template material can be recycled.
Nano core/shell particles are submicroscopic colloidal systems composed of a solid or liquid core surrounded by a thin polymer or inorganic shell. This solid or liquid core is removed to form hollow nanospheres. Such core-shell systems may be prepared by deposition of the shell material onto a template particle, wherein the shell material can be either organic, inorganic, or hybrid. The selective removal of the core (template) material without disturbing the shell generates hollow particles.
In many cases where a template approach to hollow particles is used, the methods for removing the core are destructive. Typically, the template material is irreversibly changed, and cannot be used again. The most common ways of removing an organic template particle is calcination, whereupon the core material is burned. Alternatively, in the case of acid-labile metal carbonates (such as CaCO3, for example), the core material can be dissolved in acid, generating a water-soluble metal salt and CO2.
Therefore, a need exists to generate template-based methods for the preparation of hollow particle in which core materials can be recycled.
In the first aspect, the disclosure provides a process for making hollow inorganic particles through a template approach, and allows for recycling of the template material. The process for preparing the hollow particles comprises:
Typically the recyclable template particle, which may be a solid particle or a hollow particle, is removed by thermal depolymerization, typically by heating at temperatures of about 60° C. to about 500° C., or by acid or base.
In this disclosure “comprising” is to be interpreted as specifying the presence of the stated features, integers, steps, or components as referred to, but does not preclude the presence or addition of one or more features, integers, steps, or components, or groups thereof. Additionally, the term “comprising” is intended to include examples encompassed by the terms “consisting essentially of” and “consisting of.” Similarly, the term “consisting essentially of” is intended to include examples encompassed by the term “consisting of.”
In this disclosure, when an amount, concentration, or other value or parameter is given as either a range, typical range, or a list of upper typical values and lower typical values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or typical value and any lower range limit or typical value, regardless of whether ranges are separately disclosed. Where a range of numerical values is recited herein, unless otherwise stated, the range is intended to include the endpoints thereof, and all integers and fractions within the range. It is not intended that the scope of the disclosure be limited to the specific values recited when defining a range.
In this disclosure, terms in the singular and the singular forms “a,” “an,” and “the,” for example, include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to “hollow particle”, “the hollow particle”, or “a hollow particle” also includes a plurality of hollow particles.
This disclosure provides a process for preparing the hollow inorganic particles, through intermediacy of template particles, onto which the shell material is deposited, to generate core/shell particles. The core material is removed to generate hollow particles. This process details the method for generating hollow particles through non-destructive core removal, thereby allowing core material recycling.
The particles described herein are between about a 100 to about 900 nm in size, more typically between about 150 and about 800 nm, and still more typically between about 230 and about 700 nm. The disclosure provides the process for making hollow particles through a template approach in which template material is isolable and recyclable.
The process for preparing the hollow particles comprises:
Typically the recyclable template particle, that may be a solid particle or a hollow particle, is removed by thermal depolymerization, typically by heating at temperatures of about 60° C. to about 500° C., or by acid or base.
The recyclable template particle or core is prepared using typically an organic monomer which is polymerized to generate template particles. Some monomes for the template include styrene, methyl methacrylate, α-methylstyrene, lactic acid, or formaldehyde, more typically methyl methacrylate, lactic acid, or α-methylstyrene, and still more typically methyl methacrylate or α-methylstyrene. Similarly, a group of two monomers can be chosen for a copolymerization, such as a variety of diacids and dialcohols for polyester polymers (like polyethylene terephthalate, PET), diacids and diamides for various polyamides (like Nylon 6,6, or other Nylons), etc. The monomers are present in the amount of about 1 to about 60 wt %, more typically about 2 to about 50 wt %, still more typically about 5 to about 40 wt %, based on the total weight of the components used in the preparation of the recyclable template particle. Typically, the particle size of the template is tunable, and the particle size distribution of the template particles achieved is narrow, which is advantageous. For example, preparation of the recyclable template particle or core by emulsion polymerization is achieved by emulsification of the water-insoluble monomer or a monomer mixture in water, and polymerized using radical or photopolymerization conditions. Radical initiators such as potassium- or ammonium persulfate, and 2,2-azobis(2-methylpropionamidine) hydrochloride (AIBA) can be used, more typically AIBA. Surfactant can also typically be used. Some examples of suitable surfactants include sodium dodecylsulfate (SDS), cetyltrimethylammonium bromide (CTAB), poly-(vinylpyrrolidinone) PVP, etc. In some cases, it might be advantageous to use copolymers in order to introduce charge on the surface of the particle, like for example vinyltimethylammonium chloride benzene, 2-(methacryloxy)ethyltrimethylammonium chloride, etc. In cases where silica is deposited onto the template surface, it might be beneficial to use a copolymer with a silyl group, to promote the silica deposition on the particle surface like for instance 3-(trimethoxysilyl)propylmethacrylate, or other silyl-containing monomers. In some cases, it might be preferable to use comonomers that can crosslink two growing polymer chains, thereby strengthening the template particle-some of those materials include divinylbenzene or ethylene glycol dimethacrylate. In order to perform the polymerization, the reaction temperature is kept between about 0 and about 100° C., more typically about 15 to about 90° C., still more typically about 25° C. to about 70° C.
By aqueous monomer dispersion we mean water or a mixture of water and surfactant, initiator, defoaming agent, or a suitable buffer in cases where pH needs to be kept in a particular range.
The recyclable template particle or core, that may be a solid particle or a hollow particle, is then coated with a shell material to generate a core/shell particle. To generate a silica treatment comprising a coating, layer or shell, at least one water-based silica precursor is used.
The water-based silica precursor in step (c) is sodium silicate, potassium silicate or pre-formed silicic acid; more typically sodium silicate or potassium silicate; still more typically sodium silicate.
The concentration of water-based silica precursor is about 0.005 wt % to about 20 wt %, more typically about 0.005 wt % to about 15 wt %, based on the total weight of the dispersion. Typically, the suspension of recyclable template particles in water is treated with water-based silica precursor, which results in silica deposition of the recyclable particles, generating core/shell particles.
The pH is maintained at about 2 to about 10, more typically about 5 to about 9, to form a silica layer on the recyclable template particle and the reaction times are held between about 1 to about 24 hours, more typically about 1.5 to about 18 hours, still more typically about 2 to about 12 hours. This results in the deposition of a silica treatment comprising a coating, layer or shell on the recyclable template particle or core. The reaction is kept at temperatures between about 25 to about 100° C., more typically between about 40 and about 90° C., still more typically between about 50 and about 80° C.
The core/shell particles are removed from the aqueous solution by centrifugation or filtration, more typically by centrifugation.
Depending on the nature of the recyclable template particle, the recyclable template particle that constitutes the core can be recycled either through thermal depolymerization, or acid- or base hydrolysis. Typically, core materials made out of poly-(α-methylstyrene), PMMA, various polyamides, as well as styrene are depolymerized at increased temperatures, with the temperatures of depolymerization varying with the polymer used. Some suitable temperature ranges include about 250 to about 450° C., more typically about 275 to about 400° C., still more typically from about 290 to about 325° C., to generate hollow particles as well as core monomer. For example, poly(methylmethacrylate)@silica core/shell particles can be heated above around about 300° C. to generate methyl methacrylate monomer and hollow silica particles. Further, poly(α-methylstyrene)@silica can be heated to about above 60° C. to generate hollow silica particles and α-methylstyrene monomer.
Alternatively, acid- or base-labile core materials can be hydrolyzed instead of thermally depolymerized to generate hollow particles with the possibility of monomer recycling. Polymers such as Delrin® (polyacetal), poly(lactic acid), as well as other polyesters can be depolymerized through acid hydrolysis. For example, treating polyacetal@silica with acid should generate hollow silica as well as aldehyde monomer that can be recycled in template particle synthesis. Similarly, polyesters or polyamides from core/shell particles can be recycled in the same fashion to generate diacid/dialcohol (diacid/diamine) monomer couples as well as hydroxylic or amino acids as monomers (like in the case of polylactic acid, for example).
These depolymerization methods allow for hollow particle formation, as well as, being non-destructive toward core monomers, allowing for template material recycling.
These inorganic hollow particle dispersions are useful as hiding or opacifying agents in coating and molding compositions. They are also useful as drug delivery systems in the pharmaceutical and medical industries; in food, personal care and cosmetics; and agriculture.
To a three-necked 250 mL round bottom flask with 100.0 mL water was added methyl methacrylate (9.5 g, 94.89 mmol), 2-(methacryloxy)ethyltrimethylammonium chloride (0.125 g of 80% aqueous solution, mmol), ethylene glycol dimethacrylate (0.4 g, mmol), and AIBA (0.1 g, mmol). Trimethoxysilyl propyl methacrylate (0.5 g 2.01 mmol) was then added. The mixture was degassed by purging N2 for 10 min, and then heated to 70° C. under nitrogen overnight, to generate a white slurry of PMMA particles.
To a 100 ml three-necked round bottom flask, equipped with an overhead stirrer and a reflux condenser was added 25 mL of PMMA suspension from Example 1, and the pH of the mixture was adjusted to 9 with addition of aqueous NaOH. To this mixture was added sodium silicate (4.72 g of 26.5 wt % aqueous solution, diluted to 10 mL with water), and HCl (10 mL of 1.40M solution), using two syringe pumps simultaneously, to maintain the pH in the 8-9 range. The rate of addition was 2 mL/h. After the addition, the temperature of the reaction was increased to 80° C., and the mixture was left stirring overnight. After that time, the mixture was cooled down, and the solids isolated by centrifugation, and washed with water and ethanol, to generate a while solid (2.73 g), whose TEM confirmed the core/shell structure.
500 mg of the sample from Example 2 was placed in a tube furnace and heated to 500 C at a 1° C./min rate, and kept at 500 C for ten hours. Upon cooling, 233 mg of white solid was obtained, whose TEM images confirmed the hollow structure.
Upon washing, of the material from Example 2, the core/shell particles are placed in a 50 mL round bottom flask, and the flask is placed inside a bulb-to-bulb distillation apparatus. The material is heated to 300° C. under nitrogen, and the distillate is collected in the cooled (−20° C.) receiving adapter, to capture the released MMA monomer. The hollow particle material remains in the distillation flask.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US15/17904 | 2/27/2015 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 61950875 | Mar 2014 | US |
