The present invention relates to a steam saving device.
Conventional steam explosion systems typically comprise a reactor vessel, having inlets and outlets, a piping system and a separation device for separating steam and other gasses from the pre-treated biomass. The reactor vessel comprises inlets for loading biomass and steam. The biomass/steam mixture is pressurized in the reactor vessel for a predefined time period. The steam-infused biomass material is then rapidly depressurized and conveyed via a piping system to the separation device. The so obtained biomass is than subjected to further processing steps.
A steam explosion system with the above elements is for example known from EP 2389480 and EP 2389445.
The present invention solves the problem of reducing the steam consumption in hydrothermal pre-treatment of biomass.
This problem is solved by the provision of a steam saving device or nozzle in accordance with claim 1.
The nozzle comprises a tubular body with a first open end and a second open end. The nozzle is adapted to be inserted into and coupled to an outlet opening of a steam explosion reactor, wherein the second open end is coupled to a conduit for conveying the pretreated biomass to at least one second device, preferably comprising a separator and the first open end is lining up with the inner wall of the reactor vessel or protruding into the reactor vessel. The inner surface of the tubular body of the nozzle comprises an engraved helical structure.
It was surprisingly found by the inventors, that the engraved helical structure of the nozzle reduces the steam consumption of the hydrothermal pre-treatment system considerably.
The dimensions of the nozzle depend on the process parameters and the biomass material to be treated. The dimensions of the nozzle therefore generally have to be adapted to the specific process conditions.
In a preferred embodiment the pitch of the engraved helical structure is in the range of from 1 to 300 mm, preferably from 10 to 150 mm, more preferably from 20 to 100 mm and most preferably from 30 to 60 mm. Particularly preferred are 30, 40, 50 and 60 mm.
The length of the nozzle is in the range of from 1 to 3500 mm, preferably from 10 to 1000 mm, and more preferably from 30 to 600 mm, further preferred from 60 to 500 mm. Most preferred are lengths of 50, 60, 80, 100, 200, 300, 400 and 500 mm. The length and the pitch of the engraved helical structure may suitable be chosen such that about 1 to 5 full convolutions and preferably 2 full convolutions are obtained.
The cross-sectional area of the inner surface of the nozzle is in the range of from 10 to 9000 mm2, preferably from 20 to 8000 mm2, more preferably from 50 to 700 mm2, also preferred of from 60 to 5000 mm2. Further preferred ranges are from 10 to 150 mm2, from 30 to 100 mm2 and from 50 to 80 mm2 as well as ranges of from 1000 mm2 to 8000 mm2, from 1500 to 7000 mm2 and from 2000 to 6000 mm2. The smaller the cross-sectional area of the inner surface of the nozzle, the smaller is the overall steam consumption.
The nozzle may have any suitable shape. However, preferably the cross-sectional shape of the inner surface of the nozzle is circular or ellipsoid, such that turbulences of the biomass material flow are reduced.
The depth of the engraved helical structure is in the range of from 0.1 to 15 mm, preferably of from 0.5 to 10 mm, and more preferably of from 1 to 5 mm, whereas of from 1.5 to 3 mm is also preferred.
The width of the engraved helical structure is in the range of from 0.1 to 3 mm, preferably of from 0.5 to 2 mm, and more preferably of from 1.0 to 1.5 mm.
The nozzle may generally be made from any material known to a person skilled in the art as suitable for the inventive purpose. The nozzles are preferably made from material of high abrasion resistance such as ceramic material, such as aluminium oxide, and more preferably from high purity aluminium oxide material, and most preferably from aluminium oxide having a purity of above 92% and more preferably having a purity of 99.7%, particularly preferred a purity of from 99.50 to 99.99%. An abrasion resistance of Vickers hardness of at least 1800 MPa is preferred. Particularly preferred is an abrasion resistance of at least 2000 MPa Vickers hardness wherein at least 2500 MPa are most preferred.
In a further aspect the present invention is also directed to a system for steam explosion treatment of biomass material, comprising a pressurized reactor vessel, with at least one outlet. A tubular nozzle as as defined within the application with an engraved helical structure at its inner wall surface is inserted into and coupled to the at least one outlet of the reactor vessel. Within a preferred embodiment, the system further comprises a conduit coupled to the nozzle for conveying the pretreated biomass to at least one second device, and at least one second device, preferably comprising a separator.
Any suitable separator may be used within the system of the present invention to separate the solids and steam. Within a preferred embodiment the system comprises a cyclone separator. It is also possible to use multiple cyclone separators for the separation of biomass and steam. Within a particularly preferred embodiment the system comprises means to separate pressurized steam from the solids. Pressurized steam may then be recycled into the reactor vessel and/or be utilized for other applications leading to an even further decrease of steam consumption. “Means to separate pressurized steam” according to the present applications may be realized as a combination of two devices wherein the first device functions as a mechanical separator for separating the pressurized steam from the pretreated material and a subsequent cyclone separator for further steam separation and to expand to atmospheric pressure. Within an alternative embodiment the separator may be a pressure cyclone separator.
The biomass material to be treated by the system may be lignocellulosic material. Lignocellulosic material includes, but is not limited to plant material such as wheat straw, barley straw, rice straw, wood, wood chips, sawmill and paper mill discards, corn stover, sugarcane bagasse, and other agricultural residues, dedicated energy crops, municipal paper waste, and any other biomass material comprising cellulose, hemicellulose and lignin. The biomass material preferably has a dry matter (DM) content of from 30 to 70 wt.-%, further preferred of from 40 to 60 wt.-% and also preferred of from 45 to 55 wt.-%.
Features described in relation to one aspect may equally be applied to other aspects of the invention.
The invention will be further described, by way of example only, with reference to the accompanying drawings in which:
In
In a hydrothermal pre-treatment process, biomass and steam are conveyed to the reactor vessel 10 via inlets 12. The biomass material is pressurized with steam in the reactor vessel 10 at elevated temperatures for a predetermined amount of time. After the heat/pressure treatment the outlet valve 14 is opened and the hydrothermally pre-treated biomass is allowed to expand. The expansion process is also referred to as “steam explosion”. By rapidly releasing the pressure, the steam expands within the biomass material and bursts the cells of the biomass material or defibrillates the biomass material. In the depicted embodiment in
In a preferred embodiment of the invention, the steam saving device is a tubular nozzle 16 as depicted in
The nozzle 16 depicted in
In the following, experimental results for steam consumption in a hydrothermal pre-treatment process according to the state of the art (without nozzle) and with a nozzle according to the invention are shown.
In this example the biomass material was wheat straw bales, which were loosened up in a bale crusher equipped with rotating scrappers operated at 3000 rpm yielding particles with particle sizes from 10 to 40 cm. This particle size ensures smooth transport of the straw and operation of the subsequent milling step. The biomass material was pneumatically transported to a hammer mill operated at 3000 rpm with 30 mm sieves where the straw was cut to pieces with particle sizes from 1 to 5 cm.
The cut straw was transported to the thermal pre-treatment system with a pin drum feeder followed by a transportation screw and plug screw. In the reactor vessel the wheat straw was continuously pre-treated in a reactor at 160° C. for 5 min without addition of any chemicals. After this hydrothermal pre-treatment, the biomass material was transported to a cyclone to separate the organic materials form the gases.
The reactor vessel used in thermal pre-treatment had an outlet with a cross-sectional area of about 283 mm2. The steam was measured to amount to 4.6 kg steam per 1 kg dry matter as depicted in
A nozzle with engraved helical structure according to the present invention was inserted into the outlet of the reactor vessel. The nozzle was made from aluminium oxide ceramic (99.7%), having a length of 60 mm and was provided with an engraved helical structure at the inner wall surface. The helical structure had a pitch of 30 mm. The two grooves of the helical structure had a depth of 1.0 mm and a width of 1.5 mm.
The further process parameter were identical to the process parameters of the comparative example.
In Table 1 and
In contrast thereto, using the nozzle according to the present invention, for the same amount of dry matter feed, the steam consumption was reduced to 364.7 kg/h. This corresponds to a specific steam consumption of only 0.91 kg steam per 1 kg dry matter, which represents an effective reduction of steam consumption by factor 5.
As a final advantage, the resulting pressure in the conduit between the nozzle and the separator device was reduced when a nozzle according to the present invention was used. Reduced pressure beneficially affects the lifetime of the piping system.
Number | Date | Country | Kind |
---|---|---|---|
15199879 | Dec 2015 | EP | regional |
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/EP2016/079272 | 11/30/2016 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2017/102330 | 6/22/2017 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
2017043 | Galliot | Oct 1935 | A |
20020043221 | Hytonen | Apr 2002 | A1 |
20050183542 | Uesaka et al. | Aug 2005 | A1 |
20050258281 | Schwegler et al. | Nov 2005 | A1 |
20090010825 | Polti | Jan 2009 | A1 |
20120211512 | Pschorn et al. | Aug 2012 | A1 |
20140110069 | Rawls | Apr 2014 | A1 |
20150233053 | Stromberg | Aug 2015 | A1 |
20160059248 | Yamauchi | Mar 2016 | A1 |
20160158722 | Knapper | Jun 2016 | A1 |
Number | Date | Country |
---|---|---|
101348804 | Jan 2009 | CN |
103321073 | Sep 2013 | CN |
203291824 | Nov 2013 | CN |
204356320 | May 2015 | CN |
2389445 | Nov 2011 | EP |
2389480 | Nov 2011 | EP |
2007108021 | Sep 2007 | WO |
Entry |
---|
Stanford Advanced Materials, Alumina, 2014, Stanford Advanced Materials (Year: 2014). |
Number | Date | Country | |
---|---|---|---|
20200011011 A1 | Jan 2020 | US |