The invention pertains to the field of technical textiles and in particular the field of textiles used as carrier, in particular as carrier for compounds that are active or can be activated. The invention therefore provides a pile fabric in glass, quartz or metal and a catalytic fabric.
The invention also concerns a method for manufacturing this fabric.
EP-1008565 describes the use of glass fibres coated with titanium oxide as photocatalyst. The glass fibres are coated using a sol-gel process. This document describes the decomposing of organic substances, in particular sterilisation or deodorising by means of these coated glass fibres.
In this document, the increase in the effective surface area of titanium dioxide is obtained by multiplying the coating steps with photocatalyst or by using a surfactant during this coating step.
EP-823280 concerns filtration using devices integrating a photocatalyst. This photocatalyst is carried on a carrier which may be in glass and may comprise projecting portions. Additives can be added to the photocatalyst or can be used as sub-layer to improve photocatalysis.
WO-2008/087339 describes a fabric web comprising optical fibres and binding yarns the surface of which can be coated with photocatalytic particles. The optical fibres comprise alterations allowing the sideways emission of light to activate photocatalytic particles. The fabric web described in this document is of warp and weft woven type. No indication is given to improve the efficacy or yield of the fabric web.
There is therefore a need to provide textiles in glass, metal and combinations thereof which can be used as carrier, in particular in the field of catalysis, and which give improved performance.
The invention therefore proposes a pile fabric in glass, quartz or metal, or combinations thereof, which brings a solution to all or part of the problems of prior art carriers or fabrics in glass or metal.
Advantageously, and the quantities of materials being equal, the fabric of the invention has an improved effective surface area. The pile yarns of the fabric of the invention allow an increased contact surface with the surrounding medium.
The invention therefore provides a pile fabric comprising:
Preferably, the fabric of the invention comprises a weft, a ground warp and a pile warp. Also preferably, the fabric of the invention comprises a weft, two ground warps and a pile warp.
Preferably, the fabric of the invention is a cut-pile or warp velvet or cut-pile warp velvet. Advantageously the pile height of the fabric of the invention is between 1 and 10 mm or between 2 and 8 mm.
The pile density of the fabric of the invention is between 50 and 200 pile yarn per cm2, preferably between 80 and 160 pile yarn per cm2, in particular between 60 and 120 pile yarn per cm2.
For the fabric of the invention, the yarns used can be in glass, metal or combinations thereof. The yarns used to manufacture the fabric of the invention are preferably in glass and in particular in silica, purified silica or quartz, more particularly yarns made from quartz crystals. Yarns in lead crystal or lead glass or even soda-lime glass are also suitable for producing the fabric of the invention.
As examples of glass yarns used to produce a fabric of the invention, mention can be made of yarns produced from highly pure silica fibres that are continuous, non-porous, homogeneous and amorphous. The purity of the silica may be higher than 90%, 95% or even higher than 99.99%.
The yarns used may also be in metal, preferably in steel, particularly in stainless steel.
The fabric of the invention may also be produced from mixtures of different yarns, in particular mixtures of different glass yarns or mixtures of glass yarns and metal yarns, in particular mixtures of quartz yarns and stainless steel yarns.
Preferably the yarns used for the fabric of the invention are non-elastic, have good resistance to UV radiation and to heat treatments, or to treatments with chemical agents.
These yarns can advantageously be selected from among cable yarns.
In general, the size of the yarns used may range from 10 to 500 tex or from 15 to 200 tex or from 20 to 100 tex or from 25 to 80 tex or from 40 to 75 tex.
The invention also concerns the manufacture of a pile fabric according to the invention. The invention therefore provides a method for manufacturing a fabric, comprising:
Preferably, the method of the invention therefore allows a fabric to be produced comprising a weft, a ground warp and a pile warp.
Also preferably the method of the invention therefore allows a fabric to be produced comprising a weft, two ground warps and a pile warp.
For the manufacturing method of the invention, the tension of the ground warp is preferably between 5 and 30 g/yarn (grams per yarn).
Also preferably the tension of the pile warp is between 5 and 30 g/yarn.
Advantageously the weaving speed of the method of the invention is between entre 70 rounds/min and 300 rounds/min, preferably between 80 rounds/min and 200 rounds/min.
With respect to warping, the warping speed is generally between 10 and 80 m/min, preferably between 20 and 40 m/min, for example 30 m/min.
The pile fabric of the invention can be produced using a fabric manufacturing device comprising:
Advantageously, the means for preparing the weft is a shuttle or needles.
The cutting means are advantageously selected from among metal rods having a width of between 0.1 mm and 2 mm or a height between 0.5 mm and 15 mm, or from among a circular knife or razors allowing a pile height to be cut of between 0.5 mm and 15 mm.
Preferably, a device D1 can be used to manufacture a fabric of the invention which comprises:
It is also possible to use a device D2 to manufacture a fabric of the invention, which comprises:
The fabric of the invention can be used in numerous technical fields. In particular, it can be used as carrier.
The mechanical characteristics and the thermal properties of the pile fabric according to the invention can advantageously be given use as insulating materials or fabric, in particular in the building and aeronautics sectors.
Advantageously, the invention concerns a fabric of the invention as carrier, in particular as carrier of at least one active compound such as a catalyst or a photocatalyst.
The invention therefore provides a catalytic pile fabric comprising:
Preferably, the catalyst carried by the pile fabric of the invention is a photocatalyst e.g. a catalyst comprising titanium, tungsten, zinc or mixtures thereof.
As preferred catalysts, titanium dioxide (TiO2) or zinc oxide (ZnO) or the mixtures thereof are particularly advantageous, in particular titanium dioxide.
In general, the catalytic fabric of the invention is defined in accordance with all the characteristics of the pile fabric of the invention both with regard to its general characteristics and its particular advantageous or preferred characteristics combined with at least one catalyst.
The invention therefore provides a catalytic fabric comprising a catalyst such as a photocatalyst in particular in titanium, tungsten, zinc catalyst or mixtures thereof, in particular TiO2 and ZnO, preferably TiO2, carried on a pile fabric of the invention combining the following characteristics in whole or in part:
Advantageously, the invention provides a catalytic pile fabric comprising:
The catalytic fabric of the invention is prepared using a method comprising the depositing of the catalyst on the pile fabric of the invention.
This deposit can performed for example using different methods known to persons skilled in the art. In particular it can be performed by spraying the catalyst onto the fabric or by dipping the fabric in a catalyst sol-gel solution or by high-powered pulsed magnetron, via Metal Organic Chemical Vapour Deposition (MOCVD), via Metal Organic Vapour Phase Epitaxy (MOVPE)), via Atomic Layer Deposition (ALD) or Chemical Vapour Phase (CVD).
The invention also concerns the use of the catalytic fabric of the invention in different technical fields requiring at least one carried catalyst. The pile fabric of the invention has a particularly high surface area and allows a catalytic fabric to be obtained having improved efficacy compared with catalyst carriers in the prior art.
Therefore, the catalytic fabric of the invention can be given advantageous use in the field of the purification of liquid or gaseous fluids, or for the deodorising of gaseous fluids.
The catalytic fabric of the invention can also be used in the field of chemical catalysis.
The invention therefore provides a method for purifying a liquid or gaseous fluid, comprising the use of a catalytic fabric of the invention.
The purification method of the invention can be applied in particular to air treatment in homes, medical air treatment, to high level air treatments. The method can therefore advantageously be used for the treatment of air in hospital wards, in clean rooms, refrigerated storage areas, breeding enclosures, rooms in the home, living spaces, offices, etc. and for the treatment of industrial discharges.
The purification method of the invention can also be given advantageous use for the deodorising of air in particular in the aforementioned applications, for example in the treatment of food odours, industrial discharges, solvent odours, etc.
The purification method of the invention can be also be used to depollute aqueous effluent.
A description will now be given of the present invention with the help of non-limiting examples.
Using silica yarns (Quartzel C9 33×2 S150 QS13 by Saint-Gobain, France) of 33 tex with two ends (tex 67 for the yarn used) and with 150-turn twist, a double-layer quartz fabric of the invention was prepared.
On an adapted loom the following steps were carried out:
A double-layer quartz velvet of the invention was thus obtained.
Using identical yarn to the yarn used in Example 1, a single layer quartz velvet of the invention was prepared.
On an adapted loom, the following steps were carried out:
In this manner a single-layer velvet of the invention was obtained.
Several samples of a single-layer quartz velvet of the invention were prepared from Example 2.
These samples were shaped by cutting and sewing and then cleaned (degreasing) by wet dipping at about 80° C. in a 0.5% aqueous solution of ethoxylated fatty alcohol polyglycol (8 OE) (Zuzolat 1008/25 by Zschimmer et Schwarz).
The catalyst TiO2 was then deposited by spraying or dipping in a sol-gel of TiO2 and silica at 400 mL/m2.
The efficacy of the photocatalytic fabric of the invention was evaluated by degradation of formic acid compared with different prior art carried catalysts.
A sample of quartz velvet fabric (surface area: 9 cm2) was prepared in accordance with Example 3.
70 mL of an aqueous formic acid solution were prepared (50 mg/L).
The photocatalytic fabric was immersed in the solution under stirring for 30 min.
The solution containing the photocatalytic fabric was irradiated (UVC, 3.2 mW/cm2) for 180 min.
Degradation of the formic acid was monitored by cation exchange column HPLC eluting with dilute sulphuric acid and with UV absorption detection.
Under the same conditions, the efficacy of different carried photocatalysts of the prior art was compared with the efficacy of the photocatalytic fabric of the invention.
The results are grouped together in Table 1.
It was found that the initial degradation velocity of formic acid obtained with the photocatalytic fabric of the invention is higher than that of all the carried catalysts of the state of the art.
In addition the endurance of the photocatalytic fabric of the invention, measured with 4 successive tests, showed that this photocatalytic fabric is efficient without loss of photocatalytic activity.
Number | Date | Country | Kind |
---|---|---|---|
12 54299 | May 2012 | FR | national |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/EP2013/059539 | 5/7/2013 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2013/167625 | 11/14/2013 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
2381218 | Jacob | Aug 1945 | A |
2385577 | Jacob | Sep 1945 | A |
3764448 | Nisbet | Oct 1973 | A |
3953913 | Brown et al. | May 1976 | A |
4010004 | Brown | Mar 1977 | A |
4167482 | Muller | Sep 1979 | A |
4416782 | Kerres | Nov 1983 | A |
5985411 | Pfeffer | Nov 1999 | A |
5989677 | Stuhler | Nov 1999 | A |
6468428 | Nishii et al. | Oct 2002 | B1 |
6771866 | Iimura | Aug 2004 | B2 |
20030026585 | Iimura | Feb 2003 | A1 |
20070264467 | Wang | Nov 2007 | A1 |
20100029157 | Brochier et al. | Feb 2010 | A1 |
20100029471 | Wang | Feb 2010 | A1 |
20140234163 | Faurie | Aug 2014 | A1 |
Number | Date | Country |
---|---|---|
202507979 | Oct 2012 | CN |
202820825 | Mar 2013 | CN |
203493344 | Mar 2014 | CN |
203493344 | Mar 2014 | CN |
104761989 | Jul 2015 | CN |
106113751 | Nov 2016 | CN |
1008565 | Jun 2000 | EP |
2 258 893 | Dec 2010 | EP |
3013042 | May 2015 | FR |
964 508 | Jul 1964 | GB |
2000271415 | Oct 2000 | JP |
2004230065 | Aug 2004 | JP |
2008237793 | Oct 2008 | JP |
2011036405 | Feb 2011 | JP |
WO-2015071429 | May 2015 | WO |
Entry |
---|
International Search Report for PCT/EP2013/059539 dated Mar. 13, 2014. |
French Search Report for FR 1254299 dated Feb. 7, 2013. |
Number | Date | Country | |
---|---|---|---|
20150099090 A1 | Apr 2015 | US |