• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a novel stable colloidal polysaccharide suspension containing a (1-3) -gucan, an economical process for its preparation and possible applications of these polysaccharide suspensions.
    公开号:AT518612A1
    申请号:T56/2015
    申请日:2015-02-06
    公开日:2017-11-15
    发明作者:
    申请人:Chemiefaser Lenzing Ag；
    IPC主号:
    专利说明:

    Polysaccharide suspension, process for their preparation and their
    use
    The present invention relates to a novel stable colloidal polysaccharide suspension containing a (1-> 3) -glucan, an economical process for its preparation and possible applications of these polysaccharide suspensions. Such suspensions are often referred to as "gel" and in the present invention both terms are to be understood as synonymous.
    State of the art
    It is known that natural polysaccharides such as xanthan, alginate, guar gum, starch, etc. and also cellulose derivatives as well as e.g. Carboxymethvlcellulose. Hydroxymethylpropyl cellulose in water as colloids In solution and under certain conditions have a gelling ability. Due to their water solubility, the aforementioned substances do not form stable colloidal suspensions.
    Hdc wfilhudif am hüi unrUnrnmanrla pAlwearrharSH Set Hia ΓαΙΙμΙλοα Πια
    Preparation of Suspensions of Nanofibrillar Cellulose or Fibrous ^ Diadiuiurici i. uio esu ic; ucsnuiuacaiaoM uiuui auivvciacn. iai ucivai nil.
    V
    Related patents and publications are mentioned in WO2013 / 006876A1. The preparation of cellulose gels by the amine oxide process with cellulose II structure is described in WO2013 / 006876A1. In the meantime it has been found that 1% ΑΙΑ 2 A Ιλι * ΙαΙλΑ Λ Ο ^ AUI ΟΛ ΛαΙ | (.ΙαΑα aJi "* aU CiAAAK νοίΜίνοσ ^.) Is also produced from a spinning mass according to the amine oxide method with higher λ ^ΙΙιΐΐΑΧΛΜΑΐΐΑΧΛΜΑΑϋΑϋΛ σιιαιι ywi ι MQiopiciovvuiao iw wwvi ru wuiiuivoo / uwivii binoaia wmva
    High-pressure homogenizer a phase-stable cellulose suspension with a Μ II II
    Water retention of 500 to 5000% can be produced. P.elli ilncenele Hie narh Hem AmirtnviH.V / Experienced / ale IM i mncmittol Serves a Tertiary AmiertviH hewer *, int. M., Methwlmrrr, helir .. eviH ^ ought to know how to treat - 0 1 · - to refute niifciuiibuiiierier Ceiiuiyse udei anuetei Alien vun
    Nanocellulose has clear product advantages: they no longer have a pure fiber-like structure, but are largely isotropic. The particles are heavily swollen and form a 3-dimensional network. By precipitation u / jn vsrschisdsnsn form bodies from the spinning mass, weakening of these moldings by enzymatic treatment, coarse crushing and subsequent ivlahlung in a high-pressure homogenizer, these gels can be obtained.
    US 7,000,000 describes fibers made by spinning a solution of polysaccharides consisting essentially of hexose repeat units linked via a (1-> 3) glycosidic linkages. These polysaccharides can be prepared by contacting an aqueous solution of sucrose with GtfJ glucosyltransferase isolated from Streptococcus salivarius (Simpson et al., Microbiology, Vol 41, pp ^ Ί4.Ί4βη MOOGU In the Allelic Kan11 in Riaoameri, Iiiiiiiiiiii. IW · I 'f WW y I VWW ^ IU * V WWW II «MWI» We WWWWW kV »II» W1WWWI I · HIWWW · I II »IWI II IWI l ^ f that occasionally there may be defects within the polysaccharide chains, among others These polysaccharides are to be referred to as "a (1- * 3) glucan" for purposes of the present invention.
    A disclosure of the preparation of such glucans can be found in US 6,284,479 A1; The polysaccharide mixtures described therein are intended to contain a (1- »3) -, a (1-> 6) ·, (1 ~> 2) - and (1-> 4) -linked glucans in unspecified proportions. These products are intended to be used to replace all or part of starch or latex in coatings. More details on this can not be found in US Pat. No. 6,284,479 A1.
    The US 7,000,000 first discloses possibilities for the enzymatic production of a (1-> 3) »glucan from monosaccharides. In this way, relatively short-chain polysaccharides can be prepared without any dependence on monomer units, since the polymer chains are built up from the monomer units. In contrast to the production of short-chain cellulose molecules, the shorter the polymer chains, the cheaper the production of a (1-> 3) -glucan, since then only a short residence time is necessary in the reactors.
    A further possibility for the enzymatic production of a (1- * 3) -glucan from monosaccharides is disclosed in WO2013 / 036966A1 and WO2013 / 036918A2. By this method, a particularly pure a (1- »3) -glucan can be prepared, essentially without the formation of other polysaccharides.
    Glucan gels are known in the literature, but none are found containing a (1-> 3) * glucan. In the literature, one finds either a (1-> 4) -glucans, which were prepared by glucan phosphorylases (JP2006211989) and were processed by dissolution in alkaline and reprecipitation into a gel (US2003185863, WO201207301ΘΑ1). Or ß (1- * 3) -gucucans, which are water-soluble and are processed by addition of starch and plasticizers to a gel (US2003185863). Direct preparation of such gels without prior dissolution and precipitation or other chemical pretreatments is not known.
    task
    The object was compared to this prior art is a 4Ι · Ι I I · * I A I ·, «I Λ ..,).,. .14. . * ». ... .4..11 .. piiddcii ^ aiduiic, rvunuiuaic ruiyaauuuaiiu-ouayoiisiun £ ui venuguiiy lm οισιισιι whose production no chemical or enzymatic pretreatment of prttwoojjwonno srfcrdsri lind sins HSHS Snsmissffizisnz siifvvsisi Qsr i uiyoawwiιαιiuaivuiisiuii ounic pioiavvcu noiAuatoiiCH ociii uiiu uoi
    Surprisingly, this object could be achieved by the use of uiütechnölöyisch hergesteiitern and never dried a {1- »3) -Gluean be solved in comparison with existing description of the invention. From the polymer residue described in US Pat. No. 7,000,000 and in particular WO2013 / 036968A1 and WO2013 / 03891S.A2, it is possible to prepare, by mere mechanical treatment, a polysaccharide suspension which has no fibrillar structure and forms a 3-dimensional network, as long as it has never been dried ,
    The a (1- * 3) -glucan can be prepared by contacting an aqueous solution of sucrose with GtfJ glucosyltransferase isolated from Streptococcus salivarius (Simpson et al., Microbiology, vol 41, pp 1451-1460 (1995)).
    Thus, the solution to the above problem is to provide a phase-stable, colloidal polysaccharide suspension which is available in the form of a colloidal polysaccharide suspension of the type described in US Pat. No. 5,420,786 > WW | WMWW WMW I WLVVW VWWKHVVVVWV that consists of a (1-> 3) glucan, that the a (1- »3) glucan was never dried during its preparation, that the suspension of a presscake having a polysaccharide content between 4 and 60% by weight, preferably between 15 and 45% by weight, and that the polysaccharide concentration of the suspension is between 0.01 and 50% by weight, preferably between 1, 0 and 20 wt .-%, is.
    The a (1- »3) -glucan content of the polysaccharide may be between 1 and 100% by weight, more preferably between 80 and 100% by weight. The remaining polysaccharides may in particular be cellulose gels, particularly preferably those prepared by the amine oxide process with cellulose II structure. Such gels can be prepared, for example, according to WO2013 / 006876A1. You can also according to your Arrnnoxid method, as already described above, from a spinning mesa with higher cellulose content (for example, 13 wt.% Cellulose) by using a high pressure homogenizer with a f'all, UcAl / Aniantretinn> ηι / ί »ηαη f Λ ι · η # Ι λ f Παιι / 0 /. Hornaetollt uianlan
    WtlWIWWWMWI UBWI IWIMtlWI I aalf IWWI rvi W p 1 M (IW I | W WW Ψ9 * t W I IWI gwwiwilt IfWT WWMI VVöitömii'i can öS äiOii uöi uqi'i fösiiiCnön rüiySäCCnäriu üin uöm
    One skilled in the art gel-forming polysaccharides such as
    A ".αΙΙι ilncorloriv / at» KAieniAlcwiMaicA ParKnvv / mAthx / lollipop iIaca αγΙαγ etArlAr act. Such mixtures can be used advantageously, for example, in the paper industry.
    The remaining polysaccharides may also be other glucans, in particular a (1- * 6) -, (1-> 2) - and (1-> 4) -linked glucans.
    The polysaccharide suspension of the invention is particularly advantageous because it was prepared without chemical or enzymatic pretreatment, without high pressures and without high shear rates during comminution and without solution or precipitation steps.
    In a preferred embodiment, in the preparation of the polysaccharide suspension from the press cake, a dispersing unit is used which produces a low shear rate compared to high-pressure homogenizers, for example an Ultraturrax® mixer or a colloid mill.
    The above-mentioned residual polysaccharides may preferably be added to the a (1- »3) -glucan during this suspension preparation.
    According to the invention, the polysaccharide suspension in addition to the polysaccharide and 1 to 200 wt .-%, based on the amount of polysaccharide, to incorporated additives selected from the group comprising pigments, titanium oxides, especially stoichiometric titanium dioxide, barium sulfate, ion exchangers, polyethylene, polypropylene, polyester , Latex, activated carbon, polymeric superabsorbents and flame retardants.
    In a preferred embodiment of the process according to the invention, at least 90% of the a (1-r »3) -glucan consists of hexose units and at least 50% of the hexose units are linked by a (1-» 3) -glycosidic bonds. It is used in its never-dried form.
    The suspension according to the invention is based on a water-containing, in particular initially moist, a (1-> 3) -glucan which has never been dried after its preparation. a (1-> 3) -glucan does not dissolve in water as a colloid in solution. A solution or subsequent precipitation step, as described in glucan gels known in the literature, is not necessary.
    Typically, for the preparation of cellulose gels, a pretreatment to weaken the surface structure (enzyme treatment, chemical treatment) with a subsequent treatment by means of
    High pressure homogenizers applied. To prepare the polysaccharide suspensions according to the invention, the abovementioned production steps are not necessary; a grinding by means
    Dispersing aggregate (e.g., Ultraturrax® or colloid mill) is sufficient. This reduces the total energy required in comparison to a cellulose gel many times. By avoiding a solution step during the preparation of the suspensions according to the invention, the entry of solution residues into the final suspension is prevented, making it particularly suitable for applications in sensitive areas (food, pharmacy and cosmetics) ,
    The polysaccharide as the starting material for the suspension is preferably npmM IIR 7 ΟΠΟ ΟΠΗ and inshesnnrprA according to WO 013 / fl3fiflfiAA1 and
    W '· V
    A Ai n rA PPAi Λ A Λ I. ...... a.IU R.JK .. .t, ... ... ... ... U Π ... {- I S-iii-l /. , , .LA "---- · - ---. ,. , J - ... ,,., -.... ......., used, i. it was never dried before suspension production. It consists at least partially of a (1- »3) -glucan. In the last process step of its preparation, it is pressed to a solids content of between 4 and 60% by weight (based on the total press cake), preferably 15 to 45% by weight. The desired polysaccharide concentration, between 0.01 and 50% by weight (based on the total suspension), preferably between 1.0 and 20% by weight, is adjusted by addition of water and then comminuted by suitable comminution units (eg Ultraturrax ®, colloid mill,.,.), The polysaccharide suspension is prepared. Pretreatments to weaken the moldings and subsequent high shear treatments (for example, in the high pressure homogenizer) are not essential to the formation of these polysaccharide gels. This represents a great advantage over cellulose gels. The solids content of the polysaccharide suspensions according to the invention should be between 0.01 and 50% by weight, preferably between 0.1 and 20%, the polysaccharide never being allowed to be dried during production.
    In summary, the process according to the invention for the preparation of a polysaccharide suspension is characterized in that a) as initial material a press cake from an initial moisture
    Polysaccharide material is used, which consists at least partially of a (1- »3) -glucan, b) the press cake has a solids content between 4 and 0% by weight (based on the total press cake), preferably 15 to 45% by weight c) the desired polysaccharide concentration (usually by adding water) is adjusted to between 0.01 and 50% by weight (based on the total suspension), preferably between 1.0 and 20% by weight, and d ) followed by comminution with a dispersing unit.
    By additional treatment with a high-pressure homogenizer (HDH) as a grinding unit, the homogeneity of the suspension can be slightly improved if necessary.
    On the other hand, if the polysaccharide prepared according to US Pat. No. 7,000,000 and in particular according to WO2013 / 036968A1 and WO2013 / 03691ΘΑ2 has already been dried once prior to suspension formation, i. if it is no longer initially wet, only limited gels are formed on renewed suspension in water, which show only slight suspension stabilities and hardly noticeable increases in viscosity.
    The degree of polymerization of the ot (1-> 3) glucan used in the process according to the invention, expressed as weight average DPW, can be between 200 and 2,000; Values between 400 and 1,000 are preferred. Due to the enzymatically controlled production of these glucans their molecular weight distribution is very narrow. Such narrow distributions do not occur with natural polysaccharides.
    Depending on the suspension concentration set, the suspensions according to the invention exhibit film-forming properties and are particularly suitable for producing polysaccharide layers, in particular films or coatings of other bodies, for example for coatings on different surfaces. These include, for example
    Paper and packaging applications. If the suspensions according to the invention form films or layers, they act as barriers for many substances because of their uniform and dense structure. Likewise, the polysaccharide suspension according to the invention is used as an additive to existing coating mixtures, e.g. suitable in the paper industry. These films or layers can be formed by knife coating, spraying or brushing and / or by evaporation of the aqueous phase and / or additional measures, such as heating or pressing. These films or layers may be firmly bonded to the pad (especially if this pad also contains polysaccharides), or may be present separately. For the purpose of film formation, wet strength agents or plasticizers may also be added to the polysaccharide suspension according to the invention. It is also possible to crosslink the films or layers. The coatings can be closed or even patchy. As incomplete coatings come, for example, perforations or the production of artistically designed patterns or ornaments in question.
    In addition to the production of films or coatings, the production of other moldings from the polysaccharide suspension according to the invention is possible, for example by extrusion or by the use of suitable molds. For this purpose, it is advantageous to use the polysaccharide suspension according to the invention as concentrated as possible or to add suitable additives thereto,
    Furthermore, the suspensions according to the invention are very suitable for all applications in which viscosity modifiers are required in order to produce a creamy consistency of the end products. The swollen polysaccharide particles can bind large amounts of water and therefore have a thickening effect even at lower concentrations than the polysaccharide suspensions prepared according to the prior art.
    The polysaccharide suspension according to the invention can be used as starting material for the preparation of dried polysaccharide powder, which is also the subject of the present invention. By simple drying of the suspensions according to the invention are formed by
    Formation of hydrogen bonds Agglomerates and compact layers, whereby the film-forming properties can be explained. Special drying methods (spray drying, freeze drying) produce separated particles and less agglomerates. Spray drying also offers the possibility to produce hybrid particles. The additives can be admixed during the production of the suspension according to the invention or metered in only during the drying process. Another drying option is supercritical drying. In this case, the aqueous phase is exchanged for a suitable apolar solvent. The strength of the hydrogen bonds is reduced upon removal of the solvent by means of supercritical CO 2 and the 3-dimensional network of the gel is retained; so-called aerogels are formed.
    So-called "spacers" may also be added to the suspension according to the invention before the drying step The spacers may be, for example, inorganic salts, polyethylene glycol, cellulose derivatives or other substances known in the field of gels as spacers. These spacers attach themselves between the polysaccharide molecules and thereby prevent the formation of strong hydrogen bonds. Although agglomerates are formed in this case, they can be redispersed. The formation of these agglomerates may be advantageous in metering applications.
    In the following, the spray-drying is discussed in more detail; The substrate to be dried, i. The polysaccharide gel according to the invention is atomized via a nozzle into fine droplets. The droplets are discharged with the stream of hot air in a separation cyclone, thereby evaporating water. The particle structure can be influenced by various parameters such as the solids concentration, the size of the spray nozzle or the temperature difference between supply air and exhaust air flow. The resulting polysaccharide particles have an average diameter of less than 1 pm up to 5 pm. The principle and scheme of spray drying are shown in Fig. Θ. That is; A: Supply of polysaccharide suspension B: Supply of spray air (= compressed air) TE: Temperature measurement of supply air TA: Temperature measurement of exhaust air 1: Intake air intake 2: Electric heater 3: Spray nozzle 4: Spray cylinder 5: Exhaust air 6: Separation cyclone 7: Exhaust air output filter Θ: Collecting vessel for the dried particles
    The suspensions according to the invention have shear-thinning properties and, because of the simple application methods (brushing, spraying, etc.), can also be used as binders for other materials and are nutty enough to be used for small, delicate bathtubs. In this case, the other material is preferably present in a proportion of from 2GC to 1000% by weight, based on the amount of polysaccharide. During drying, hydrogen bonds form and thus a corresponding "adhesive effect" is achieved.
    Especially when used as binders, for example for nonwovens or similar open structures, the polysaccharide suspension according to the invention can be applied so that either the entire structure or only parts thereof are penetrated by the suspension or a superficial coating is produced. This again leads to a significant increase in the strength of the resulting composite material over the original structure. Upon contact with water, such structures solidified with a (1- »3) glucan-containing suspensions can be broken up again, which results in applications in the
    Area of "flushable wipes", i.e. wipes that can be shredded by the wastewater stream.
    By the uniform introduction of additives further functionalities can be introduced into the polysaccharide suspension according to the invention. A variety of organic (chitosan, ...) and inorganic (nanosilver, zinc oxide, ...) additives and color pigments can be introduced into the suspension.
    In the following the invention will be described by way of examples. However, the invention is expressly not limited to these examples, sinners as well as other embodiments based on the same inventive concept.
    Examples
    AlhftmftjnAs; % Appendices are always to be understood as fiaw% 711, unless stated otherwise.
    Example 1:
    A presscake of hydrous, irsitiaifeuchtem a (1-s-3) -G! Ucan (dry matter content (TS) = 17.6 wt .-%) is suspended in deionized water and by means of an Ultraturrax® ("UT"), type IKA T50 basic, 6,000 rpm, crushed for 4 minutes The suspension to be comminuted in this experiment contained 3.05% by weight of a (1- »3) -glucan (atro) .The suspension thus prepared was divided into two parts A partial quantity was additionally pumped through a high-pressure homogenizer (HDH), type GEA Niro Soavi NS 1001L-2K, operating pressure 1,000 bar, for 2 passes, and the two glucan suspensions were subsequently characterized by viscosity and WRV.
    The water retention capacity (WRV) of the glucan particles was determined as follows: A precisely defined amount of suspension was introduced into special centrifuge tubes (with drainage for the water). The mixture was then spun off for 15 minutes at 3,000 rpm and the moist glucan immediately weighed. The wet glucan was dried overnight at 105 ° C and then the dry weight determined. The calculation of the WRV took place according to the following formula:
    The calculated dry contents and WRV are summarized in Table 1. Table 1: Dry contents and WRV of the glucan suspensions
    The viscosities of the two suspensions show shear thinning behavior and do not differ in their course (FIG. 1). In Fig. 1, as well as the other figures, "shear rate", "viscosity" and "Viscosity" were used, viscosities were measured by means of a Malvern Kinexus rheometer with a cone-plate measuring system (CP4 / 40S0687 SS) in a shear rate range of 10-200 s "1 determined.
    For comparison, experiments were carried out with dried glucans. Linear glucans with different degrees of polymerization (DPW 1,000 and DP * 500) and a branched glucan were used. In all three cases, no uniform gels were formed and phase separation occurred. The suspensions were adjusted to a solids content of 2-3%, pre-crushed by treatment in Ultraturrax® (UT, IKA T50 basic, 6,000 rpm) for 4 min and then treated with the high-pressure homogenizer for 2 passes at a working pressure of 1,000 bar. In the following, dry content and WRV were determined (Table 2). The WRV is well below the values of the gels prepared from initially moist glucan. Likewise, these suspensions show no viscosity increase.
    Table 2: Dry contents and WRV of dried glucan gels
    The so treated suspensions were swelled overnight to make the surface more accessible. The next day, the samples were again treated for 4 passes at 1,000 bar with the HDH. It was found that the dried glucans used are unsuitable for suspension production: even after 6 passes on the HDM, phase separations still occurred and particles were optically recognizable (FIG. 2).
    Example 2:
    It was to be proved that even large amounts of polysaccharide can be processed into a homogeneous suspension without the use of high-pressure homogenizers by using a larger amount of 4% by weight glucan in a pilot plant test with a colloid mill (type IKA Colloid Mill MK2000 / 10). Gel was made.
    From 3.69 kg of never dried, initial wet a (1-> 3) -glucan (TS = 16.25%) and 11.3 kg of water was a glucan gel with a solids content of 3.9% by grinding in the colloid mill (IKA Colloid Mill MK2000 / 10). After 15 minutes grinding at a 0.1 mm gap at maximum power, the glucan gel was ready. It was then characterized as follows:
    Viscosity: The Glucan gel was measured on the Malvern Kinexus Rheometer using a cone-plate measuring system (CP4 / 40 S0687 SS) with a shear rate of 10-200 s'1. The suspension according to the invention showed shear-thinning behavior (FIG. 3).
    Microscopy: The glucan gel was filled between two slides, forming a thin layer. This layer was examined microscopically. An adhesive tape (Scotch tape, matt, approx. 0.3 mm) was glued to the lower slide at the edge to obtain a uniform layer thickness. The images were taken at the stereomicroscope ZEISS Discovery V12 with a 50x magnification with underlight (Figure 4). It can be seen agglomerates, which form from the smallest particles in the suspension. However, these agglomerates are not felt when rubbed between the fingers and disintegrate under the slightest shear again.
    Glass tube method: 10 g of glucan gel were weighed into glass tubes (length = approx. 9.7 cm, 0 2.5 cm) with cap, shaken, turned upside down and photographed after 10 sec. The glass tube was positioned against a black background and lit from above with a table lamp (distance to the ground about 22 cm).
    Photography was taken with a digital camera Canon EOS450D. Again, no particles are visible (Figure 5). It forms a uniform, dense film along the glass wall.
    The film forming properties of these suspensions were tested on different surfaces.
    The suspension according to the invention from Example 2 was knife-coated or sprayed onto polyester (PES) films or glass. Both coating methods resulted in continuous, even films that adhere well to the bases. Fig. 6 shows the transparency of such films on PES films: the right side of the image is covered with the coated PES film; the left side is not covered.
    Of the air-dried films, SEM photographs were taken (Hitachi S-4000 SEM scanning electron microscope); Here one can see the structure of the dense layer, which at the same time has a large inner surface (FIG. 7).
    In addition, SEM images were taken of the freeze-dried glucan gel (Figure 8). Here one recognizes the 3-dimensional sponge-like network which is formed in the glucan gel and gives the suspension according to the invention its unique properties.
    Example 3:
    Glucan gels with different solids concentrations were prepared analogously to Example 2. At higher solids content, the viscosities of the suspensions increase (Figure 9), while the water retention capacity (WRV) decreases. While suspensions with a solids content of 3 and 4% can still be processed with an HDH, suspensions with a solids content of 5% can only be comminuted with a device with lower shear, for example an Ultraturrax IKA T50 basic ("IKA"), since the HDM is such can no longer promote highly viscous suspensions. Table 3 shows that the viscosity increases with increasing solids content, but at the same time the WRV decreases.
    Table 3: Comparison of the viscosities and WRV of the different glucan gels after comminution.
    Example 4:
    In the following example, the 3% glucan gel from example 3 was dried in a laboratory spray dryer (Büchi Mini Spray Dryer 8-290, see FIG. 10). The particle size distribution was determined by means of laser diffraction (measuring device from Helos) in isopropanol. Parameters: 180 ° C supply air and 62 ° C extract air temperature; 1.4 mm nozzle size. The particle size distribution gave; Χίο = 0.79 pm; xso = 2.2 pm; xgo = 5.29 pm; xeeB 8.27 pm.
    Example 5:
    From 1.887 kg never dried, initial moist a (1-> 3) -G! Ucan (TS * 39.74%) and 5.613 kg of water was prepared by means of IKA mill (Colloid Mill IKA MK2000 / 10) a suspension with 10% glucan, After 20 minutes grinding at a 0.1 mm gap at maximum power, the glucan suspension is ready. It formed a stable suspension, which is comparable in viscosity with the 4% glucan suspension of Example 2 (Figure 12).
    Further, microscopic images (Fig. 13) were made of the gel of Example 5 under the conditions described in Example 2. Again, small particles are recognizable, but again they are not felt between the fingers.
    权利要求:
    Claims (13)
    [1]
    claims
    1. A phase-stable, colloidal polysaccharide suspension, characterized in that the polysaccharide consists at least partially of a (1- + 3) -glucan, that the a (1-> 3) -glucan was never dried during its preparation that the Suspension of a press cake with a polysaccharide content between 4 and 0% by weight, preferably between 15 and 45 wt .-% was prepared and that the polysaccharide concentration of the suspension between 0.01 and 50 wt .-%, preferably between 1.0 and 20 wt .-%, is.
    [2]
    2. Suspension according to claim 1, characterized in that the a (1-> 3) -glucan content of the polysaccharide is between 1 and 100 wt .-%, particularly preferably between 80 and 100 wt .-%.
    [3]
    3. polysaccharide suspension according to claim 1, wherein the a (1 - + 3) - glucan consists of at least 90% of hexose units and at least 50% of the hexose units are linked by a (1- + 3) -glycosidische bonds ,
    [4]
    4. polysaccharide suspension according to claim 1, which in addition to the polysaccharide 1 to 200 wt .-%, based on the amount of polysaccharide, to incorporated additives selected from the group comprising pigments, titanium oxides, in particular hypostoichiometric titanium dioxide, barium sulfate, ion exchanger, polyethylene, Polypropylene, polyester, latex, activated carbon, polymeric superabsorbents and flame retardants.
    [5]
    5. A process for the preparation of a polysaccharide suspension, characterized in that a. the starting material used is a press cake of an initially moist polysaccharide material which at least partially consists of a (1- + 3) -glucan, b. the press cake has a solids content of between 4 and 80% by weight (based on the total press cake), preferably 15 to 45% by weight, c. the desired polysaccharide concentration is adjusted to between 0.01 and 50% by weight (based on the total suspension), preferably between 1.0 and 20% by weight, d. followed by comminution with a dispersing unit.
    [6]
    6. The method according to claim 5, wherein after step d. an additional treatment with a dispersing aggregate, preferably with a high-pressure homogenizer, takes place.
    [7]
    7. The method according to claim 5, wherein the degree of polymerization of the employed a (1- * 3) glucan, expressed as weight average DPW, between 200 and 2,000, preferably between 400 and 1,000, is located. Θ. Use of the polysaccharide suspension according to claim 1 for the preparation of polysaccharide layers.
    [9]
    9. Use of the polysaccharide suspension according to claim 1 as a binder for other materials, wherein the adhesion effect is achieved by drying and formation of hydrogen bonds.
    [10]
    10. Use of the polysaccharide suspension according to claim 9, wherein the other material is a non-wovens material.
    [11]
    11. Use of the polysaccharide suspension according to claim 9, wherein the other material in a proportion of 200 to 1000 wt .-%, based on the amount of polysaccharide present.
    [12]
    12. Use of the polysaccharide suspension according to claim 1 for the preparation of dried polysaccharide powder.
    [13]
    13. Dry polysaccharide powder prepared by spray drying according to claim 12.
    [14]
    14. Use of the polysaccharide suspension according to claim 1 as a viscosity modifier.
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    同族专利:
    公开号 | 公开日
    WO2016123644A1|2016-08-11|
    US20190218373A1|2019-07-18|
    CN107207626B|2021-05-28|
    JP6727522B2|2020-07-22|
    JP2018507293A|2018-03-15|
    EP3253803A1|2017-12-13|
    KR20170115552A|2017-10-17|
    CN107207626A|2017-09-26|
    US11098179B2|2021-08-24|
    US20200079932A1|2020-03-12|
    AT518612B1|2019-03-15|
    US20180273731A1|2018-09-27|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    ATA56/2015A|AT518612B1|2015-02-06|2015-02-06|Polysaccharide suspension, process for its preparation and its use|ATA56/2015A| AT518612B1|2015-02-06|2015-02-06|Polysaccharide suspension, process for its preparation and its use|
    EP16709674.2A| EP3253803A1|2015-02-06|2016-02-03|Polysaccharide suspension, method for producing same and use thereof|
    JP2017541265A| JP6727522B2|2015-02-06|2016-02-03|Polysaccharide suspension, its preparation method and its use|
    KR1020177022947A| KR20170115552A|2015-02-06|2016-02-03|Polysaccharide suspensions, methods for producing them, and uses thereof|
    US15/932,303| US20180273731A1|2015-02-06|2016-02-03|Polysaccharide suspension, method for its preparation, and use thereof|
    PCT/AT2016/000007| WO2016123644A1|2015-02-06|2016-02-03|Polysaccharide suspension, method for producing same and use thereof|
    CN201680008823.6A| CN107207626B|2015-02-06|2016-02-03|Polysaccharide suspensions, method for the production thereof, and use thereof|
    US16/248,254| US20190218373A1|2015-02-06|2019-01-15|Polysaccharide suspension, method for its preparation, and use thereof|
    US16/681,226| US11098179B2|2015-02-06|2019-11-12|Polysaccharide suspension, method for its preparation, and use thereof|
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