WO2012101127A1 - Sulphur cement products - Google Patents

Sulphur cement products Download PDF

Info

Publication number
WO2012101127A1
WO2012101127A1 PCT/EP2012/051058 EP2012051058W WO2012101127A1 WO 2012101127 A1 WO2012101127 A1 WO 2012101127A1 EP 2012051058 W EP2012051058 W EP 2012051058W WO 2012101127 A1 WO2012101127 A1 WO 2012101127A1
Authority
WO
WIPO (PCT)
Prior art keywords
sulphur
organosilane
sand
surface area
functional group
Prior art date
Application number
PCT/EP2012/051058
Other languages
French (fr)
Inventor
Willem Posthumus
Catherine Frances Smura
Guy Lode Magda Maria Verbist
Original Assignee
Shell Internationale Research Maatschappij B.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shell Internationale Research Maatschappij B.V. filed Critical Shell Internationale Research Maatschappij B.V.
Priority to KR1020137022066A priority Critical patent/KR101910792B1/en
Priority to CA2824915A priority patent/CA2824915C/en
Priority to JP2013550858A priority patent/JP2014503464A/en
Priority to US13/981,110 priority patent/US9174872B2/en
Priority to AU2012210627A priority patent/AU2012210627B2/en
Priority to BR112013018612-7A priority patent/BR112013018612B1/en
Priority to CN2012800062647A priority patent/CN103402945A/en
Priority to EA201300858A priority patent/EA022337B1/en
Priority to EP12701730.9A priority patent/EP2668146A1/en
Priority to MX2013008250A priority patent/MX348177B/en
Publication of WO2012101127A1 publication Critical patent/WO2012101127A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B40/00Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/40Compounds containing silicon, titanium or zirconium or other organo-metallic compounds; Organo-clays; Organo-inorganic complexes
    • C04B24/42Organo-silicon compounds
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B14/00Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02Granular materials, e.g. microballoons
    • C04B14/04Silica-rich materials; Silicates
    • C04B14/06Quartz; Sand
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/36Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing sulfur, sulfides or selenium
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B40/00Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
    • C04B40/0028Aspects relating to the mixing step of the mortar preparation
    • C04B40/0039Premixtures of ingredients

Definitions

  • the present invention provides sulphur cement products including sulphur mortar and sulphur concrete.
  • the invention also provides a process for the preparation of sulphur cement products.
  • Elemental sulphur or modified sulphur can be used to bind aggregate and filler, thereby providing sulphur cement products such as sulphur mortar and sulphur concrete.
  • Sulphur concrete can be used in a variety of pre-cast concrete applications such as marine defences, paving slabs, road barriers and retaining walls.
  • Sand is very commonly used as a fine aggregate in sulphur mortar and sulphur concrete. It is desirable to use sand that is available locally for reasons of cost and convenience.
  • organosilanes having functional groups such as amino, epoxy and mercapto groups can be incorporated into sulphur mortar or concrete to reduce the water
  • the present inventors have found that sulphur mortar and sulphur concrete prepared from porous sand having a high surface area is also liable to disintegrate when exposed to water. This is not due to the presence of expandable clays (washing procedures do not affect the water stability of sulphur mortar and sulphur concrete prepared from the sand) .
  • the inventors have sought to improve the water stability of sulphur mortar and sulphur concrete prepared from this high-surface-area sand.
  • organosilanes having amino functional groups can improve the water stability of sulphur mortar and sulphur
  • Organosilanes having mercapto and sulphide functional groups do not have the same effect when used within the same concentration range.
  • the present invention provides a sulphur cement product comprising sulphur, filler, sand having a surface area of greater than 0.5m 2 /g, and an organosilane having at least one amino functional group.
  • the invention provides a process for the preparation of a sulphur cement product comprising the steps of:
  • sulphur cement product refers to a composite comprising sulphur, filler and aggregate.
  • Fillers and aggregate are particulate inorganic
  • Fillers have an average particle size in the range of from 0.1 ⁇ to 0.1 mm.
  • Fine aggregate has an average particle size in the range of from 0.1 to 5mm.
  • Sand is one type of fine aggregate.
  • Coarse aggregate has an average particle size in the range of from 5 to 40mm.
  • Sulphur mortar comprises sulphur, filler, sand and optionally additional fine aggregate, but does not comprise coarse aggregate.
  • Sulphur concrete comprises sulphur, filler, coarse aggregate, sand and optionally additional fine aggregate.
  • the sulphur cement product of the invention is a sulphur mortar.
  • the sulphur cement product of the invention is a sulphur concrete.
  • the amounts of sulphur, filler, sand and additional aggregate in the sulphur cement products of the invention can be chosen by the skilled person in view of the proposed application of the sulphur cement product. The skilled person will seek to ensure that sufficient sulphur is incorporated to bind the filler and aggregate, that sufficient filler and aggregate are incorporated to provide mechanical strength and that the balance of components provides a mixture with suitable workability for the proposed application.
  • Sulphur mortar preferably comprises from 5 to 40wt% sulphur, from 45 to 90wt% fine aggregate and from 1 to 10wt% filler; more preferably from 5 to 30wt% sulphur, from 55 to 75wt% fine aggregate and from 3 to 8wt% filler, where weight percentages are based upon the weight of the sulphur mortar.
  • Sulphur concrete preferably comprises from 5 to 40wt% sulphur, from 25 to 50wt% coarse aggregate, from 20 to 40wt% fine aggregate and from 1 to 10wt% filler; more preferably from 5 to 30wt% sulphur, from 30 to 40wt% coarse
  • the sand in the sulphur cement products of the invention has a surface area of greater than 0.5m 2 /g, preferably greater than lm /g, more preferably greater than 1.5m 2 /g and most preferably greater than 2m 2 /g.
  • the surface area of the sand is measured according to the BET technique using nitrogen, following the procedure as set forth in Example 1.
  • the surface area of quartz is usually about 0.25m 2 /g and the surface area of normsand (used in European standards as a typical sand used in concrete) is about 0.02m 2 g.
  • Sand may have a high surface area due to a surface layer of palygorskite . The presence of a
  • palygorskite surface layer in sand can be detected using energy dispersive x-ray spectroscopy.
  • the sulphur cement product may comprise additional fine aggregate such as sand,
  • the sand in the sulphur cement product will have a bulk surface area of greater than 0.5m 2 /g, preferably greater than lm 2 /g.
  • the (bulk) surface area will typically not be more than 10m 2 /g, preferably not be more than 5m 2 /g, more preferably not more than 3.5m 2 /g.
  • organosilane having at least one amino functional group.
  • An organosilane is a compound having at least one carbon-silicon bond or at least one carbon- oxygen-silicon group.
  • the organosilane may be
  • organosilanes include 3-aminopropyl triethoxy silane, bis (triethoxysilylpropyl) amine, ,3- bis (3-aminopropyl) -1,1,3, 3-tetramethyldisiloxane,
  • the amino groups may be primary, secondary or tertiary amino groups.
  • an organosilane having at least one amino functional group encompasses organosilanes having functional groups that are converted to amino functional groups under the processing
  • an organosilane having an imine group falls within the term "an organosilane having at least one amino functional group".
  • a suitable imine functionalised organosilane is N- ⁇ 3- ( triethoxysilyl ) -dihydroimidazole :
  • the amount of organosilane having at least one amino functional group in the sulphur cement product is preferably from 0.05 to 2wt% based upon the weight of the sand having a surface area of greater than 1.5m 2 /g, more preferably from 0.1 to lwt%.
  • the preferred amount of organosilane is a balance between incorporating
  • organosilane having at least one amino functional group it may be desirable to have at least one amino functional group.
  • organosilane compounds in the sulphur cement products of the invention (and also in the sulphur cement pre-composition and wax-based pre- composition of the invention) .
  • additional organosilane compounds in the sulphur cement products of the invention (and also in the sulphur cement pre-composition and wax-based pre- composition of the invention) .
  • organotitanate compounds may be any organotitanate compounds.
  • Suitable organosilane and organotitanate compounds are disclosed in WO 2008 148814, WO 2008
  • a particularly preferred additional organosilane agent is bis ( 3-triethyoxysilylpropyl ) tetrasulphide .
  • the sulphur cement products of the invention are suitably prepared by a process wherein all the components are admixed at a temperature at which the sulphur is molten, i.e. typically above 120°C, preferably in the range of from 120 to 150°C, more preferably in the range of from 125 to 140°C.
  • the admixture is preferably poured into a mould.
  • the sulphur cement product is then
  • the sulphur cement product can be demoulded.
  • a selection of the components may be supplied to the mixing step in the form of a pre-composition or masterbatch.
  • sulphur and the organosilane having at least one amino functional group may be supplied as a sulphur pre- composition. Therefore, in a preferred embodiment of step (a) of the process of the invention a sulphur cement pre-composition comprising sulphur and an organosilane having at least one amino functional group is mixed with filler and sand having a surface area of greater than 0.5m 2 /g.
  • the sulphur cement pre-composition preferably comprises less than lwt% filler and less than lwt% aggregate; and most preferably comprises no filler and no aggregate.
  • the sulphur cement pre-composition preferably comprises from 0.01 to 20wt% of the organosilane having at least one amino functional group, more preferably from 0.01 to 10wt%, most preferably from 0.01 to lwt%, wherein weight percentages are based upon the weight of the sulphur cement pre-composition.
  • the sulphur cement pre- composition preferably comprises at least 80wt% sulphur.
  • the sulphur cement pre-composition may comprise higher quantities of organosilane having at least one amino functional group, e.g. from 5 to 20wt%, and may also comprise higher quantities of filler, e.g. from 5 to 20wt%, wherein weight percentages are based upon the weight of the sulphur cement pre-composition .
  • the sulphur cement pre-composition is a "concentrated" pre-composition and such a
  • concentration can be used in small quantities to provide significant amounts of organosilane having at least one amino functional group.
  • the organosilane having at least one amino functional group may be supplied as a wax-based pre-composition.
  • the wax functions primarily as a carrier material. Therefore, in another preferred embodiment of step (a) of the process of the invention, a wax-based pre-composition comprising wax and an
  • the wax-based pre- composition preferably comprises less than lwt%
  • the wax-based pre-composition additionally comprises a filler or mineral adsorbate, e.g. calcium silicate, carbon black or calcium carbonate.
  • the wax- based pre-composition preferably comprise up to 70wt% wax, up to 20wt% mineral adsorbate and greater than 10wt% organosilane having at least one amino functional group, where weight percentages are based upon the weight of the wax-based pre-composition.
  • the wax- based pre-composition may also comprise polymer and/or sulphur .
  • Sulphur cement products produced according to the invention can be used in a variety of applications.
  • Sulphur concrete may be used in pre-cast concrete
  • sulphur mortar was prepared using 25% (by mass of the total composite) sulphur, 28% quartz filler and 47% of high surface area sand (which was sieved to remove particles with diameter greater than 2.36 mm) .
  • the surface area of the sand was measured as 2.25m 2 /g for a washed sample and 2.34m 2 /g for an unwashed sample.
  • the BET surface area was determined as follows:
  • BET surface area was measured using TriStar II 3020 apparatus (Micromeritics Instrument Corporation) .
  • a sample of 5.5866 g of (high surface area) sand from Kuwait (washed, pre-sieved to below 2.36 mm particles size) was transferred to a 20 ml vial and dried in an oven at 125-
  • the sample was transferred to the sample holder of the set-up and measurements were done using nitrogen adsorption at temperature of 77K.
  • the relative pressure (p/po) was varied from 0.02 to 0.3 and in that interval 8 measurements points were collected for the adsorbed amount of nitrogen, obtaining in this way an isotherm plot.
  • the data were processed according to the BET adsorption model using the set-up software. From the linear fit of the BET surface area plot, the BET specific surface area was calculated.
  • organosilane was 0.2% by mass of the total composite. After further mixing (15 minutes), the final mix was placed into a pre-heated silicone mould of dimensions 4x4x16cm 3 and tapped to ensure a smooth surface and to eliminate trapped air. Once cooled, the mortar prisms were removed from the moulds and broken into two pieces that were left for at least 3 days before being submerged under water. Water uptake was monitored by following the mass increase of the samples at regular intervals of time. The organosilane additives used are shown in
  • the water uptake is shown in Figure 1.
  • the x axis represents time in days; the y axis represents % increase in mass, based upon the original mass of the dry sulphur mortar.
  • the water uptake is significantly reduced when compared to the Comparative Examples
  • organosilane was then added.
  • the organosilane was diluted in ethanol at 10wt%.
  • the amount of organosilane used was between 0.1 and 0.3wt%, based upon the mass of the total composite. However, in each case the mass was calculated in order to provide the same molar
  • Examples 3 to 11 of the invention show lower water absorption and better strength retention than comparative example 4 (wherein an organosilane having a mercapto functional group is included in the sulphur mortar) .
  • Example 9 shows that an imine compound acts as an organosilane having an amine functional group under the processing conditions .
  • Mortar samples were prepared from 47% Amsterdam sand (sieved to remove particles with diameter > 2.36 mm, and having a surface area greater than 2m 2 /g) , 27% quartz filler and 25% sulphur. All ingredients were placed in heated mantle at a temperature of 140°C and mixed manually. Once the sulphur was molten and the mix was fully homogeneous (approximately 30 minutes), the organosilane was added using a syringe. After further mixing (15 minutes), the final mix was placed into a pre heated silicone mould of dimensions 4x4x16cm 3 and tapped to ensure a smooth surface and to eliminate trapped air. Once cooled, the mortar prisms were removed from the moulds and left for at least 3 days before being
  • Examples 12 and 13 show lower water uptake and better flexural strength than comparative example 5 (wherein an organosilane having a chloro functional group is included in the sulphur mortar) .

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Civil Engineering (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Silicon Compounds (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Oil, Petroleum & Natural Gas (AREA)

Abstract

A sulphur cement product comprising sulphur, filler, sand having a surface area of greater than 0.5m2/g, and an organosilane having at least one amino functional group is disclosed. Further, a process for the preparation of such cement sulphur product is disclosed.

Description

SULPHUR CEMENT PRODUCTS
Field of the Invention
The present invention provides sulphur cement products including sulphur mortar and sulphur concrete. The invention also provides a process for the preparation of sulphur cement products.
Background of the Invention
Elemental sulphur or modified sulphur can be used to bind aggregate and filler, thereby providing sulphur cement products such as sulphur mortar and sulphur concrete. Sulphur concrete can be used in a variety of pre-cast concrete applications such as marine defences, paving slabs, road barriers and retaining walls.
Sand is very commonly used as a fine aggregate in sulphur mortar and sulphur concrete. It is desirable to use sand that is available locally for reasons of cost and convenience.
US 4,376,830 discusses the problem of using
aggregates that are contaminated with water-expandable clays. These clays can cause the sulphur mortar or concrete to disintegrate when exposed to water. It is possible to remove the clays by washing procedures, but this is uneconomical. The λ830 patent teaches that organosilanes having functional groups such as amino, epoxy and mercapto groups can be incorporated into sulphur mortar or concrete to reduce the water
expandability of the water-expandable clay.
The present inventors have found that sulphur mortar and sulphur concrete prepared from porous sand having a high surface area is also liable to disintegrate when exposed to water. This is not due to the presence of expandable clays (washing procedures do not affect the water stability of sulphur mortar and sulphur concrete prepared from the sand) . The inventors have sought to improve the water stability of sulphur mortar and sulphur concrete prepared from this high-surface-area sand.
Summary of the Invention
The present inventors have surprisingly found that organosilanes having amino functional groups can improve the water stability of sulphur mortar and sulphur
concrete prepared from sand having a high surface area.
Organosilanes having mercapto and sulphide functional groups do not have the same effect when used within the same concentration range.
Accordingly, the present invention provides a sulphur cement product comprising sulphur, filler, sand having a surface area of greater than 0.5m2/g, and an organosilane having at least one amino functional group.
In a further aspect, the invention provides a process for the preparation of a sulphur cement product comprising the steps of:
(a) admixing sulphur, filler, sand having a surface area of greater than 0.5m2/g, and an organosilane having at least one amino functional group; and
(b) solidifying the molten sulphur cement product.
Detailed Description of the Invention
The term "sulphur cement product" refers to a composite comprising sulphur, filler and aggregate.
Fillers and aggregate are particulate inorganic
materials. Fillers have an average particle size in the range of from 0.1 μπι to 0.1 mm. Fine aggregate has an average particle size in the range of from 0.1 to 5mm. Sand is one type of fine aggregate. Coarse aggregate has an average particle size in the range of from 5 to 40mm. Sulphur mortar comprises sulphur, filler, sand and optionally additional fine aggregate, but does not comprise coarse aggregate. Sulphur concrete comprises sulphur, filler, coarse aggregate, sand and optionally additional fine aggregate.
According to one preferred embodiment, the sulphur cement product of the invention is a sulphur mortar.
According to another preferred embodiment, the sulphur cement product of the invention is a sulphur concrete.
The amounts of sulphur, filler, sand and additional aggregate in the sulphur cement products of the invention can be chosen by the skilled person in view of the proposed application of the sulphur cement product. The skilled person will seek to ensure that sufficient sulphur is incorporated to bind the filler and aggregate, that sufficient filler and aggregate are incorporated to provide mechanical strength and that the balance of components provides a mixture with suitable workability for the proposed application. Sulphur mortar preferably comprises from 5 to 40wt% sulphur, from 45 to 90wt% fine aggregate and from 1 to 10wt% filler; more preferably from 5 to 30wt% sulphur, from 55 to 75wt% fine aggregate and from 3 to 8wt% filler, where weight percentages are based upon the weight of the sulphur mortar. Sulphur concrete preferably comprises from 5 to 40wt% sulphur, from 25 to 50wt% coarse aggregate, from 20 to 40wt% fine aggregate and from 1 to 10wt% filler; more preferably from 5 to 30wt% sulphur, from 30 to 40wt% coarse
aggregate, from 25 to 35wt% fine aggregate and from 3 to 8wt% filler, where weight percentages are based upon the weight of the sulphur concrete.
The sand in the sulphur cement products of the invention has a surface area of greater than 0.5m2/g, preferably greater than lm /g, more preferably greater than 1.5m2/g and most preferably greater than 2m2/g. The surface area of the sand is measured according to the BET technique using nitrogen, following the procedure as set forth in Example 1.
The surface area of quartz is usually about 0.25m2/g and the surface area of normsand (used in European standards as a typical sand used in concrete) is about 0.02m2 g. Sand may have a high surface area due to a surface layer of palygorskite . The presence of a
palygorskite surface layer in sand can be detected using energy dispersive x-ray spectroscopy.
In addition to the sand having a surface area of greater than 0.5m2/g, the sulphur cement product may comprise additional fine aggregate such as sand,
typically from a different geological formation, that has a surface area of 0.5m2/g or less. However, it is conventional to use only one type of sand, for example sand from one geological formation, in a sulphur cement product. It will be appreciated that the surface area of the sand is being measured by taking representative samples from the sand and measure the average, bulk, surface area of the samples according to the BET
technique using nitrogen, following the procedure set forth in Example 1. According to a preferred embodiment, the sand in the sulphur cement product will have a bulk surface area of greater than 0.5m2/g, preferably greater than lm2/g. The (bulk) surface area will typically not be more than 10m2/g, preferably not be more than 5m2/g, more preferably not more than 3.5m2/g.
The sulphur cement product of the invention
comprises an organosilane having at least one amino functional group. An organosilane is a compound having at least one carbon-silicon bond or at least one carbon- oxygen-silicon group. The organosilane may be
functionalised with one amino group or with several amino groups. Suitable organosilanes include 3-aminopropyl triethoxy silane, bis (triethoxysilylpropyl) amine, ,3- bis (3-aminopropyl) -1,1,3, 3-tetramethyldisiloxane,
Dynasylan™ 1146 and Dynasylan™ 1151. Structures are shown below:
Figure imgf000006_0001
The amino groups may be primary, secondary or tertiary amino groups. Also, the term "an organosilane having at least one amino functional group" encompasses organosilanes having functional groups that are converted to amino functional groups under the processing
conditions for preparing sulphur cement products. For example, imine groups will hydrolyse under the processing conditions for preparing sulphur cement products, so an organosilane having an imine group falls within the term "an organosilane having at least one amino functional group". A suitable imine functionalised organosilane is N- { 3- ( triethoxysilyl ) -dihydroimidazole :
Figure imgf000007_0001
The amount of organosilane having at least one amino functional group in the sulphur cement product is preferably from 0.05 to 2wt% based upon the weight of the sand having a surface area of greater than 1.5m2/g, more preferably from 0.1 to lwt%. The preferred amount of organosilane is a balance between incorporating
sufficient organosilane to achieve effective water stability and minimising the cost due to organosilane addition .
In addition to the organosilane having at least one amino functional group, it may be desirable to
incorporate additional organosilane compounds in the sulphur cement products of the invention (and also in the sulphur cement pre-composition and wax-based pre- composition of the invention) . Alternatively or
additionally, organotitanate compounds may be
incorporated into the sulphur cement products (and the sulphur cement pre-composition and wax-based pre- composition) . Suitable organosilane and organotitanate compounds are disclosed in WO 2008 148814, WO 2008
152054, WO 2009 150193, WO 2010 012601 and WO 2010 086391. A particularly preferred additional organosilane agent is bis ( 3-triethyoxysilylpropyl ) tetrasulphide .
The sulphur cement products of the invention are suitably prepared by a process wherein all the components are admixed at a temperature at which the sulphur is molten, i.e. typically above 120°C, preferably in the range of from 120 to 150°C, more preferably in the range of from 125 to 140°C. The admixture is preferably poured into a mould. The sulphur cement product is then
solidified by cooling to a temperature at which the sulphur solidifies. After cooling, the sulphur cement product can be demoulded.
In the process of the invention, a selection of the components may be supplied to the mixing step in the form of a pre-composition or masterbatch. For example, sulphur and the organosilane having at least one amino functional group may be supplied as a sulphur pre- composition. Therefore, in a preferred embodiment of step (a) of the process of the invention a sulphur cement pre-composition comprising sulphur and an organosilane having at least one amino functional group is mixed with filler and sand having a surface area of greater than 0.5m2/g. The sulphur cement pre-composition preferably comprises less than lwt% filler and less than lwt% aggregate; and most preferably comprises no filler and no aggregate. The sulphur cement pre-composition preferably comprises from 0.01 to 20wt% of the organosilane having at least one amino functional group, more preferably from 0.01 to 10wt%, most preferably from 0.01 to lwt%, wherein weight percentages are based upon the weight of the sulphur cement pre-composition. The sulphur cement pre- composition preferably comprises at least 80wt% sulphur. In one embodiment, the sulphur cement pre-composition may comprise higher quantities of organosilane having at least one amino functional group, e.g. from 5 to 20wt%, and may also comprise higher quantities of filler, e.g. from 5 to 20wt%, wherein weight percentages are based upon the weight of the sulphur cement pre-composition .
In this embodiment, the sulphur cement pre-composition is a "concentrated" pre-composition and such a
"concentrated" pre-composition can be used in small quantities to provide significant amounts of organosilane having at least one amino functional group.
Alternatively, the organosilane having at least one amino functional group may be supplied as a wax-based pre-composition. The wax functions primarily as a carrier material. Therefore, in another preferred embodiment of step (a) of the process of the invention, a wax-based pre-composition comprising wax and an
organosilane having at least one amino functional group is mixed with sulphur, filler and sand having a surface area of greater than 0.5m2/g. The wax-based pre- composition preferably comprises less than lwt%
aggregate; and most preferably comprises no aggregate. Preferably the wax-based pre-composition additionally comprises a filler or mineral adsorbate, e.g. calcium silicate, carbon black or calcium carbonate. The wax- based pre-composition preferably comprise up to 70wt% wax, up to 20wt% mineral adsorbate and greater than 10wt% organosilane having at least one amino functional group, where weight percentages are based upon the weight of the wax-based pre-composition. In addition to wax, the wax- based pre-composition may also comprise polymer and/or sulphur .
Sulphur cement products produced according to the invention can be used in a variety of applications. Sulphur concrete may be used in pre-cast concrete
applications such as marine defences, paving slabs, road barriers and retaining walls.
Examples
The invention is further illustrated by means of the following non-limiting examples.
Five samples were prepared using the following method. Approximately 200g of sulphur mortar was prepared using 25% (by mass of the total composite) sulphur, 28% quartz filler and 47% of high surface area sand (which was sieved to remove particles with diameter greater than 2.36 mm) . The surface area of the sand was measured as 2.25m2/g for a washed sample and 2.34m2/g for an unwashed sample. The BET surface area was determined as follows:
BET surface area was measured using TriStar II 3020 apparatus (Micromeritics Instrument Corporation) . A sample of 5.5866 g of (high surface area) sand from Qatar (washed, pre-sieved to below 2.36 mm particles size) was transferred to a 20 ml vial and dried in an oven at 125-
150°C for 2 days. The sample was transferred to the sample holder of the set-up and measurements were done using nitrogen adsorption at temperature of 77K. The relative pressure (p/po) was varied from 0.02 to 0.3 and in that interval 8 measurements points were collected for the adsorbed amount of nitrogen, obtaining in this way an isotherm plot. The data were processed according to the BET adsorption model using the set-up software. From the linear fit of the BET surface area plot, the BET specific surface area was calculated.
All ingredients were placed in a heated mantle at a temperature of 140°C and mixed manually. Once the sulphur was molten and the mix was fully homogeneous (approximately 30 minutes), an organosilane additive (if used) was added using a syringe. The amount of
organosilane was 0.2% by mass of the total composite. After further mixing (15 minutes), the final mix was placed into a pre-heated silicone mould of dimensions 4x4x16cm3 and tapped to ensure a smooth surface and to eliminate trapped air. Once cooled, the mortar prisms were removed from the moulds and broken into two pieces that were left for at least 3 days before being submerged under water. Water uptake was monitored by following the mass increase of the samples at regular intervals of time. The organosilane additives used are shown in
Table 1.
Table 1
Figure imgf000011_0001
The water uptake is shown in Figure 1. The x axis represents time in days; the y axis represents % increase in mass, based upon the original mass of the dry sulphur mortar. In the Examples of the invention (wherein an organosilane having an amino functional group is included in the sulphur mortar) , the water uptake is significantly reduced when compared to the Comparative Examples
(wherein no organosilane is included, or wherein
polysulphide or mercapto organosilanes are included) .
Further samples consisting of 25wt% sulphur, 24wt% quartz and 51wt% washed Qatar sand (which was sieved to remove particles with diameter greater than 2 mm) were prepared using the following method. The surface area of this sand was greater than 2m2/g. All components were pre-heated and weighed into a mixing vessel; the
organosilane was then added. The organosilane was diluted in ethanol at 10wt%. The amount of organosilane used was between 0.1 and 0.3wt%, based upon the mass of the total composite. However, in each case the mass was calculated in order to provide the same molar
concentration of silicon. The contents of the vessel were heated to 140°C and mixed for approximately 1 hour to give a homogeneous consistency. The mix was then placed into pre-heated 4xlxlcm3 silicone moulds. Once cooled, the prism samples were removed from the moulds. Prisms were submerged under water and mass increase was followed as a function of time. The organosilane used in each sample is recorded in Table 2, which also shows the increase in weight due to water uptake over a period of 4 weeks and the strength retention of the samples. The strength of both dry and wet samples were measured, using a 3-point bending test. The strength retention was calculated from the wet strength divided by the initial, dry strength. Some of the strength results appear to be greater than 100%. Strength retention of greater than 100% is unlikely in practice but these results are due to errors inherent in the measurement methods.
Examples 3 to 11 of the invention (wherein an organosilane having an amino functional group is included in the sulphur mortar) show lower water absorption and better strength retention than comparative example 4 (wherein an organosilane having a mercapto functional group is included in the sulphur mortar) . Example 9 shows that an imine compound acts as an organosilane having an amine functional group under the processing conditions .
Table 2
Figure imgf000014_0001
Mortar samples were prepared from 47% Qatar sand (sieved to remove particles with diameter > 2.36 mm, and having a surface area greater than 2m2/g) , 27% quartz filler and 25% sulphur. All ingredients were placed in heated mantle at a temperature of 140°C and mixed manually. Once the sulphur was molten and the mix was fully homogeneous (approximately 30 minutes), the organosilane was added using a syringe. After further mixing (15 minutes), the final mix was placed into a pre heated silicone mould of dimensions 4x4x16cm3 and tapped to ensure a smooth surface and to eliminate trapped air. Once cooled, the mortar prisms were removed from the moulds and left for at least 3 days before being
submerged under water. Water uptake was monitored by following the mass increase of the samples at regular intervals of time. After 106 days, the prisms were removed from the water and the flexural strength was measured. The results are shown in Table 3.
Table 3
Figure imgf000015_0001
Examples 12 and 13 (wherein an organosilane having an amino functional group is included in the sulphur mortar) show lower water uptake and better flexural strength than comparative example 5 (wherein an organosilane having a chloro functional group is included in the sulphur mortar) .

Claims

C L A I M S
1. A sulphur cement product comprising sulphur, filler, sand having a surface area of greater than 0.5m2/g, and an organosilane having at least one amino functional group .
2. A sulphur cement product according to claim 1, wherein the amount of organosilane having at least one amino functional group in the sulphur cement product is from 0.05 to 2wt%, based upon the weight of the sand having a surface area of greater than 0.5m2/g.
3. A process for the preparation of a sulphur cement product comprising the steps of:
(a) admixing sulphur, filler, sand having a surface area of greater than 0.5m2/g, and an organosilane having at least one amino functional group; and
(b) solidifying the molten sulphur cement product.
4. A process for the preparation of a sulphur cement product according to claim 3, wherein step (a) a sulphur cement pre-composition comprising sulphur and an
organosilane having at least one amino functional group is mixed with filler and sand having a surface area of greater than 0.5m2/g.
5. A process for the preparation of a sulphur cement product according to claim 4, wherein step (a) a wax- based pre-composition comprising wax and an organosilane having at least one amino functional group is mixed with sulphur, filler and sand having a surface area of greater than 0.5m2/g.
6. A process for the preparation of a sulphur cement product according to claim 5, wherein step (a) the wax- based pre-composition additionally comprises a mineral adsorbate .
PCT/EP2012/051058 2011-01-25 2012-01-24 Sulphur cement products WO2012101127A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
KR1020137022066A KR101910792B1 (en) 2011-01-25 2012-01-24 Sulphur cement products
CA2824915A CA2824915C (en) 2011-01-25 2012-01-24 Sulphur cement products
JP2013550858A JP2014503464A (en) 2011-01-25 2012-01-24 Sulfur cement product
US13/981,110 US9174872B2 (en) 2011-01-25 2012-01-24 Sulphur cement products
AU2012210627A AU2012210627B2 (en) 2011-01-25 2012-01-24 Sulphur cement products
BR112013018612-7A BR112013018612B1 (en) 2011-01-25 2012-01-24 SULFUR CEMENT PRODUCT, AND, PROCESS FOR THE PREPARATION OF A SULFUR CEMENT PRODUCT
CN2012800062647A CN103402945A (en) 2011-01-25 2012-01-24 Sulphur cement products
EA201300858A EA022337B1 (en) 2011-01-25 2012-01-24 Sulphur cement products
EP12701730.9A EP2668146A1 (en) 2011-01-25 2012-01-24 Sulphur cement products
MX2013008250A MX348177B (en) 2011-01-25 2012-01-24 Sulphur cement products.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11151973.2 2011-01-25
EP11151973 2011-01-25

Publications (1)

Publication Number Publication Date
WO2012101127A1 true WO2012101127A1 (en) 2012-08-02

Family

ID=44226004

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2012/051058 WO2012101127A1 (en) 2011-01-25 2012-01-24 Sulphur cement products

Country Status (11)

Country Link
US (1) US9174872B2 (en)
EP (1) EP2668146A1 (en)
JP (1) JP2014503464A (en)
KR (1) KR101910792B1 (en)
CN (1) CN103402945A (en)
AU (1) AU2012210627B2 (en)
BR (1) BR112013018612B1 (en)
CA (1) CA2824915C (en)
EA (1) EA022337B1 (en)
MX (1) MX348177B (en)
WO (1) WO2012101127A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014076280A1 (en) 2012-11-19 2014-05-22 Shell Internationale Research Maatschappij B.V. Sulphur cement product

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012101127A1 (en) * 2011-01-25 2012-08-02 Shell Internationale Research Maatschappij B.V. Sulphur cement products
US10030122B2 (en) * 2015-02-09 2018-07-24 Wacker Chemical Corporation Curable compositions
US9856173B2 (en) 2015-02-09 2018-01-02 Wacker Chemical Corporation One component ready-to-use tile grout

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2015568A (en) * 1978-03-02 1979-09-12 Chevron Res Plasticized sulfur composition
EP0048106A1 (en) * 1980-09-12 1982-03-24 Sulphur Development Institute of Canada (SUDIC) Moldable sulphur compositions, molded articles based on sulphur and mineral aggregate and a method of production thereof
US4376830A (en) 1981-08-10 1983-03-15 Chevron Research Company Sulfur cement-aggregate-organosilane compositions and methods for preparing
WO2008148814A2 (en) 2007-06-07 2008-12-11 Shell Internationale Research Maatschappij B.V. Modified sulphur and product comprising modified sulphur as binder
WO2008152054A1 (en) 2007-06-13 2008-12-18 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and process for preparing such sulphur cement pre-composition
WO2009150193A1 (en) 2008-06-11 2009-12-17 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and process for preparing such sulphur cement pre-composition
WO2010012601A1 (en) 2008-08-01 2010-02-04 Shell Internationale Research Maatschappij B.V. Processes for preparing sulphur composites and organosilane coupling agents
WO2010086391A1 (en) 2009-01-29 2010-08-05 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and sulphur cement product
WO2010133580A1 (en) * 2009-05-20 2010-11-25 Shell Internationale Research Maatschappij B.V. Process for preparing a sulphur cement product
WO2011000837A1 (en) * 2009-07-01 2011-01-06 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and sulphur cement product

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8137456B2 (en) * 2005-12-09 2012-03-20 Shell Oil Company Process for the preparation of sulphur cement or a sulphur cement-aggregate composite
MX2009013182A (en) 2007-06-07 2010-01-15 Shell Int Research Sulphur cement pre-composition and process for preparing such sulphur cement pre-composition.
DE102008063965C5 (en) * 2008-12-19 2019-02-21 Evonik Degussa Gmbh Hydrophobic cementitious compositions
WO2012101127A1 (en) * 2011-01-25 2012-08-02 Shell Internationale Research Maatschappij B.V. Sulphur cement products

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2015568A (en) * 1978-03-02 1979-09-12 Chevron Res Plasticized sulfur composition
EP0048106A1 (en) * 1980-09-12 1982-03-24 Sulphur Development Institute of Canada (SUDIC) Moldable sulphur compositions, molded articles based on sulphur and mineral aggregate and a method of production thereof
US4376830A (en) 1981-08-10 1983-03-15 Chevron Research Company Sulfur cement-aggregate-organosilane compositions and methods for preparing
WO2008148814A2 (en) 2007-06-07 2008-12-11 Shell Internationale Research Maatschappij B.V. Modified sulphur and product comprising modified sulphur as binder
WO2008152054A1 (en) 2007-06-13 2008-12-18 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and process for preparing such sulphur cement pre-composition
WO2009150193A1 (en) 2008-06-11 2009-12-17 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and process for preparing such sulphur cement pre-composition
WO2010012601A1 (en) 2008-08-01 2010-02-04 Shell Internationale Research Maatschappij B.V. Processes for preparing sulphur composites and organosilane coupling agents
WO2010086391A1 (en) 2009-01-29 2010-08-05 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and sulphur cement product
WO2010133580A1 (en) * 2009-05-20 2010-11-25 Shell Internationale Research Maatschappij B.V. Process for preparing a sulphur cement product
WO2011000837A1 (en) * 2009-07-01 2011-01-06 Shell Internationale Research Maatschappij B.V. Sulphur cement pre-composition and sulphur cement product

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014076280A1 (en) 2012-11-19 2014-05-22 Shell Internationale Research Maatschappij B.V. Sulphur cement product

Also Published As

Publication number Publication date
US9174872B2 (en) 2015-11-03
EP2668146A1 (en) 2013-12-04
CA2824915A1 (en) 2012-08-02
JP2014503464A (en) 2014-02-13
EA022337B1 (en) 2015-12-30
MX2013008250A (en) 2013-09-13
BR112013018612B1 (en) 2020-03-03
CA2824915C (en) 2019-05-21
MX348177B (en) 2017-06-02
AU2012210627B2 (en) 2016-04-07
AU2012210627A1 (en) 2013-08-01
CN103402945A (en) 2013-11-20
KR101910792B1 (en) 2018-12-28
BR112013018612A2 (en) 2016-10-18
US20140007792A1 (en) 2014-01-09
KR20140020255A (en) 2014-02-18
EA201300858A1 (en) 2013-12-30

Similar Documents

Publication Publication Date Title
JP5152605B2 (en) Sulfur cement pre-composition and method for preparing such sulfur cement pre-composition
KR101346041B1 (en) Process for the preparation of sulphur cement or a sulphur cement-aggregate composite
CA2824915C (en) Sulphur cement products
WO2010012601A1 (en) Processes for preparing sulphur composites and organosilane coupling agents
EP2448879B1 (en) Sulphur cement pre-composition and sulphur cement product
EP2382168B1 (en) Sulphur cement pre-composition and sulphur cement product
WO2014009501A1 (en) Sulphur cement pre-composition and process for preparing such sulphur cement pre-composition
WO2012101128A1 (en) Sulphur cement pre-composition and sulphur cement product
EP2920130B1 (en) Sulphur cement product
EP2733130A1 (en) Sulphur cement product
EP3027577A1 (en) Sulphur cement products

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12701730

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2824915

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: MX/A/2013/008250

Country of ref document: MX

ENP Entry into the national phase

Ref document number: 2013550858

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2012210627

Country of ref document: AU

Date of ref document: 20120124

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 20137022066

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2012701730

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 201300858

Country of ref document: EA

WWE Wipo information: entry into national phase

Ref document number: 13981110

Country of ref document: US

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112013018612

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112013018612

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20130719