Kaolin products and their use

Information

  • Patent Grant
  • 7413601
  • Patent Number
    7,413,601
  • Date Filed
    Friday, August 17, 2001
    22 years ago
  • Date Issued
    Tuesday, August 19, 2008
    15 years ago
Abstract
The present invention relates to a particulate kaolin suitable for use as a filler material in compositions for making uncoated paper, the kaolin having a mean particle size ranging from 0.7 μm to 3 μm and a shape factor of at least 60. The invention also relates to compositions comprising a particulate kaolin, and methods for making uncoated paper sheets.
Description

The present invention relates to kaolin products and blends or compositions containing them. In particular, it relates to particulate kaolin products and blends containing them for use as fillers in making uncoated, e.g. supercalendered (SC) papers and their production.


Mineral fillers are used in the production of most papers for printing or writing applications. The incorporation of such fillers together with cellulose fibres in a paper making composition reduces the overall cost of the raw materials and can improve optical and printing properties of the paper. However, adding fillers causes reduction in the strength of the paper, so there is a practical limit to the amount of fillers normally used in the paper making composition.


Highly filled uncoated papers can compete with some coated paper grades.


Suitable smoothness, gloss, density per unit area and printing ink porosity can be achieved by multiple calendering of the filled paper sheets. The well known process of calendering involves passing the sheets of paper between rollers to compress the sheets.


Highly filled uncoated, calendered papers having properties approaching those of coated papers are generally known as supercalendered (SC) papers. Such papers can be used for various applications, particularly involving printing upon the paper by rotogravure or offset processes.


Kaolin materials have been widely used in the prior art as fillers for making papers, especially SC papers. One purpose of the present invention is to provide hydrous kaolin materials suitable for use as improved fillers in the production of uncoated writing and printing grade papers, especially SC papers.


According to the present invention in a first aspect there is provided a particulate kaolin suitable for use as a filler material in compositions for making uncoated paper, the kaolin having a mean particle size of between 0.7 μm and 3 μm and a shape factor of at least 60.


In this specification, mean particle size and all other particle size properties are as determined for a fully dispensed dilute aqueous suspension of the particulate material in question by sedimentation using a SEDIGRAPH™ 5100 machine, (supplied by the Micromeritics Corporation) in a well-known manner.


The mean particle size of the kaolin product may be from 0.9 μm to 2.5 μm, especially from 0.9 μm to 1.2 μm, or from 1.2 μm to 1.7 μm.


The powder brightness of the particulate kaolin according to the first aspect may be at least 80 ISO units, preferably at least 83 ISO units measured in a well-known manner according industry (TAPPI) standard procedures.


The shape factor of the particles of the particulate kaolin according to the invention is at least 60, preferably at least 65, in some cases at least 70 or more. The expression ‘shape factor’ as used herein means the average value (on a weight average basis) of the ratio of mean particle diameter to particle thickness for a population of particles of varying size and shape (i.e. in this case the particulate kaolin) as measured using the electrical conductivity method and apparatus described in GB-A-2240398, U.S. Pat. No. 5,128,606 and EP-A-528078 and using the equations derived in those patent specifications. ‘Mean particle diameter’ is here defined as the diameter of a circle, which has the same area as the largest face of the particle. In the electrical conductivity measurement method described in the said specifications, the electrical conductivity of a fully dispersed aqueous suspension of the particles under test is caused to flow through an elongated tube. Measurements of the electrical conductivity are taken between (a) a pair of electrodes separated longitudinally along the axis of the tube and (b) a pair of electrodes separated transversely across the tube. The shape factor of the particles under test is calculated from the two conductivity measurements.


The particulate kaolin according to the first aspect of the invention is a hydrous kaolin which may be obtained from a primary or secondary (sedimentary) source and may be processed using known procedures to have the specified properties. The processing procedures may for example involve comminution, e.g. grinding or milling, and particle size classification, e.g. using screens, centrifuges, cyclones, air classifiers and the like.


The particulate kaolin according to the first aspect of the invention may be subjected to further refinement or beneficiation treatments to remove impurities and to improve properties, e.g. optical properties such as brightness. Such treatments may be known per se and may be selected for example from magnetic impurity separation, froth flotation, selective flocculation, impurity leaching and bleaching.


The particulate kaolin according to first aspect of the present invention may consist of at least 95% by weight kaolinite, preferably at least 98% by weight kaolinite.


The particulate kaolin according to the first aspect may be blended with other particulate filler materials for use in paper making compositions. Such other filler materials may be known per se and may be selected for example from other hydrous kaolin, calcined kaolin, talc, calcium sulphate, titanium dioxide and alkaline earth metal carbonate, especially calcium carbonate.


According to the present invention in a second aspect there is provided a blend or composition of fillers for use in compositions for making uncoated paper, especially so called wood containing or groundwood paper, comprises (a) particulate kaolin according to the first aspect and (b) a particulate calcium carbonate.


The blend according to the second aspect may comprise from 5% to 95%, especially from 20% to 80%, by weight of the kaolin according to the first aspect and from 95% to 5%, especially from 80% to 20%, by weight of the particulate calcium carbonate product.


For blends according to the second aspect where the kaolin according to the first aspect has a mean particle size of 1.2 μm or more the weight ratio of kaolin:calcium carbonate in the blend may be 50:50 or more, e.g. from 60:40 to 80:20 where the kaolin has a mean particle size greater than 1.2 μm and not greater than 1.7 μm.


For blends according to the second aspect where the kaolin according to the first aspect has a mean particle size of 1.2 μm or less the weight ratio of kaolin:calcium carbonate in the blend may be 50:50 or less, e.g. from 40:60 to 20:80 where the kaolin has a mean particle size less than 1.2 μm and not less than 0.9 μm.


The blend according to the second aspect of the invention benefits from the enhancement of properties such as brightness provided by the calcium carbonate as well as retaining desirable properties such as gloss and print quality provided by the kaolin.


We have found, unexpectedly, that the kaolin according to the first aspect shows a superior combination of properties when used as a filler in paper making compositions, especially when used in the form of a blend with calcium carbonate, compared with prior art kaolin fillers used in a comparable manner. Use of such fillers allows paper especially wood containing paper to be made having an improved combination of porosity, strength, sheet gloss, sheet brightness, print density and print gloss especially when printed upon by a gravure printing process or an offset printing process, especially a heatset offset process. Such an improved combination of properties is obtained especially when the paper sheet made using the said filler is heavily compressed by calendering, e.g. is supercalendered. The combination of properties may have a particularly good brightness when the composition is calcium carbonate rich and particularly good gloss and print quality properties when the composition is kaolin rich.


The papermaking composition in which the kaolin according to the first aspect or the blend according to the second aspect is used may be obtained from a groundwood pulp composition of cellulose fibres, i.e. from a pulp containing from 70% to 100% by weight of a so-called mechanical pulp, which is one that has been mechanically refined, e.g. obtained from logs and ground, refined and bleached or obtained from wood chips and refined (optionally under pressure and/or at elevated temperature and/or with the use of chemicals) and bleached. The composition may contain a minor percentage, e.g. up to 30% by weight, of a so called chemical pulp, i.e. one which has been chemically treated to remove lignin.


We have found that particularly beneficial results are obtained in use of the filler blend according to the second aspect of the invention when the filler blend comprises calcium carbonate having (i) a mean particle size of from 0.4 μm to 1.5 μm, especially from 0.7 μm to 1.3 μm; and (ii) a steepness factor of at least 40, preferably at least 50, especially at least 60.


The expression ‘steepness factor’, (sometimes referred to as ‘narrowness’) as used herein refers to the steepness of the particle size distribution curve as measured by the SEDIGRAPH 5100 machine in the manner described earlier and is given by the expression 100×(d30÷d70), where d30 is the value of the particle size less than which there are 30% by weight of the particles and d70 is the value of the particle size less than which there are 70% by weight of the particles.


The said calcium carbonate may comprise a so called ground carbonate, i.e. a product obtained from natural sources, e.g. marble, chalk or limestone, and processed to have appropriate properties by known treatments involving at least one grinding step.


Alternatively, the calcium carbonate may be synthesised, e.g. by chemical precipitation, e.g. by the reaction in an aqueous medium of carbon dioxide and lime (calcium hydroxide). Carbonate products made in this way may be mixed materials optionally containing other fine solids, e.g. fibres or particulate solids, present in the aqueous medium when the precipitation reaction is carried out. Such other solids become bonded to the calcium carbonate crystals during the precipitation of the calcium carbonate crystals. Examples of composite filler materials produced in this way are described in our EP 892,019.


The calcium carbonate product used to form the blend according to the second aspect of the invention may include a chemical additive employed to provide resistance to acidic conditions which are present in some papermaking systems. Such an additive is described for example in U.S. Pat. No. 5,593,489.


The kaolin according to the first aspect and the blend according to the second aspect of the invention may be employed in a paper making composition and paper sheets, especially paper sheets to be calendered and printed upon by a gravure or offset printing process, may be made using such a composition all in a known manner.


Embodiments of the present invention will now be described by way of example with reference to the following Examples.







EXAMPLE 1
Comparative

A paper pulp composition was prepared using an 80:20 (by weight) blend of mechanical and chemical pulps. The composition was formed into a dilute aqueous suspension (containing less than 1% by weight solids) by addition of water. The filler consisted of a 70:30 (by weight) kaolin-rich blend of kaolin and precipitated calcium carbonate (pcc). The kaolin, Kaolin 1, had the following properties:

  • (i) percentage by weight of particles smaller than 2 μm: 50%;
  • (ii) mean particle size: 1.6 μm;
  • (iii) shape factor 45.


The pcc, PCC1, had the following properties:

  • (i) percentage by weight of particles smaller than 2 μm: 95%;
  • (ii) mean particle size: 0.9 μm;
  • (iii) additive: 5% by weight (active based on the dry weight of calcium carbonate) of a neutrally buffering chemical comprising a solution of an aluminium compound and phosphoric acid.


Retention aid chemical commercially available under the trade name Percol 292 was added in an amount of 0.02% by weight (active based on the dry weight of solids present) to the filler containing pulp suspension.


Handsheets of grammage 57 g.m−2 were made from the suspension using a standard semi-automatic handsheet former according to TAPPI standard procedures. The handsheets were conditioned for 24 hours in a room at a temperature of 23° C. and a relative humidity of 50%. The conditioned handsheets were calendered using a laboratory soft nip calender. The calendering conditions were as follows:

  • (i) roll temperature: 100° C.;
  • (ii) nip pressure: 300 kN.m−2;
  • (iii) speed: 30m.min−1;
  • (iv) number of nips: 4 per side.


The properties specified in Tables 1 to 3 later of the handsheets produced were measured according to industry standard (TAPPI) procedures well known to those skilled in the art. The results which were obtained for these measurements are also shown in Tables 1 to 3 later.


EXAMPLE 2
Invention Embodiment

The procedure used in Example 1 was repeated to prepare and measure the properties of handsheets except that the kaolin used in the filler composition was a different kaolin, Kaolin 2, having the following properties:

  • (i) percentage by weight of particles smaller than 2 um: 50%;
  • (ii) mean particle size: 1.6 μm;
  • (iii) shape factor: 70.


The resulting calendered handsheets had the properties which are shown in Tables 1 to 3 later.


EXAMPLE 3
Comparative

The procedure used in Example 1 to prepare and measure the properties of handsheets was repeated except that the percentage by weight of Kaolin 1 used in the filler composition was 30%, the percentage by weight of PCC 1 being 70%.


The resulting calendered handsheets had the properties which are also shown in Tables 1 to 3 later.


EXAMPLE 4
Invention Embodiment

The procedure used in Example 1 to prepare and measure the properties of handsheets was repeated except that (i) the percentages by weight of kaolin and pcc (PCC 1) were respectively 30% and 70% by weight and (ii) the kaolin used in the filler composition was a further different kaolin, Kaolin 3, having the following properties:

  • (ii) percentage by weight of particles smaller than 2 um: 75%;
  • (ii) mean particle size: 1.0 μm;
  • (iii) shape factor: 70.


The resulting calendered handsheets had the properties which are shown in Tables 1 to 3 later.


Results


The results obtained for the measurements on the handsheets made in Examples 1 to 4 are given in Table 1 to 3 as follows.













TABLE 1







Sheet light





Percent by
scattering
Sheet
Bendtsen


Example
weight
coefficient
gloss
porosity


No.
CaCO3
(F8) m2kg−2
Tappi 75° %
ml · min−1



















1 (comp)
30
69
40
21


2 (inv)
30
67
42
19


3 (comp)
70
81.5
36
31


4 (inv)
70
79
43
25






















TABLE 2








Weight
Rotogravure

Roto



Example
Percent
Print
Rotogravure
Missing



No.
CaCO3
density
Print gloss
Dots %









1 (comp)
30
1.38
33
4.3



2 (inv)
30
1.39
34
3.5



3 (comp)
70
1.22
30
3.5



4 (inv)
70
1.24
32
3.5






















TABLE 3







Offset
Offset
Offset
Offset



Weight
Print
Print
Print
Print


Example
Percent
density
density
Gloss
gloss


No.
CaCO3
Dry
litho
Dry
litho







1 (comp)
30
1.24
1.14
41
23


2 (inv)
30
1.24
1.13
44
23


3 (comp)
70
1.25
1.17
41
18


4 (inv)
70
1.25
1.14
44
20









The results in Tables 1 to 3 illustrate the improved combination of properties obtained by using kaolins embodying the invention (Kaolins 2 and 3) in blends with particulate calcium carbonate.

Claims
  • 1. A particulate kaolin, wherein the kaolin has a mean particle size ranging from 0.9 μm to 2.5 μm, and a shape factor of at least 60.
  • 2. The particulate kaolin according to claim 1, wherein the shape factor is at least 65.
  • 3. A composition comprising filler materials, wherein the composition comprising filler materials comprises the particulate kaolin according to claim 1, andat least one additional filler chosen form hydrous kaolin, calcined kaolin, talc, calcium sulfate and alkaline earth metal carbonates.
  • 4. The composition according to claim 3, wherein the composition comprises particulate kaolin in amount ranging from at least 50% by weight, relative to the total weight of the composition.
  • 5. The composition according to claim 4, wherein the composition comprises particulate kaolin in amount ranging from 60% to 80% by weight, relative to the total weight of the composition.
  • 6. The composition according to claim 3, wherein the at least one additional filler comprises calcium carbonate.
  • 7. The composition according to claim 6, wherein the calcium carbonate comprises a material obtained from a natural source and processed by grinding.
  • 8. The composition according to claim 6, wherein the calcium carbonate comprises a material prepared by chemical synthesis.
  • 9. The composition according to claim 8, wherein at least one additional solid is bonded to the calcium carbonate.
  • 10. The composition according to claim 6, wherein the calcium carbonate has a mean particle size ranging from 0.5 μm to 1.5 μm.
  • 11. The composition according to claim 10, wherein the calcium carbonate has a mean particle size ranging from 0.7 μm to 1.3 μm.
  • 12. The composition according to claim 6, wherein the calcium carbonate has a steepness factor of at least 40.
  • 13. The composition according to claim 12, wherein the calcium carbonate has a steepness factor of at least 50.
  • 14. The composition according to claim 6, wherein the calcium carbonate is in the form of a composition containing at least one chemical additive in an amount ranging from greater than 0 to 15% by weight on an active basis, wherein said at least one chemical additive is capable of stabilizing the carbonate in acidic conditions.
  • 15. The composition according to claim 6, wherein the particulate kaolin has a mean particle size of at least 1.2 μm, and wherein the weight ratio of kaolin:calcium carbonate in the composition is at least 50:50.
  • 16. The composition according to claim 15, wherein the particulate kaolin has a mean particle size ranging from 1.2 μm to 1.7 μm, and wherein the weight ratio of kaolin:calcium carbonate in the composition ranges from 60:40 to 80:20.
  • 17. The composition according to claim 6, wherein the particulate kaolin has a mean particle size ranging from 0.9 μm to 1.2 μm, and wherein the weight ratio of kaolin:calcium carbonate in the composition to 50:50 or less.
  • 18. The composition according to claim 17, wherein the particulate kaolin has a mean particle size ranging from 1.2 μm to 0.9 μm, and wherein the weight ratio of kaolin:calcium carbonate ranges from 40:60 to 20:80.
  • 19. A method of making uncoated paper sheets, comprising preparing an aqueous paper-making composition from a pulp and mineral filler particles, and forming the composition into paper sheets,wherein the mineral filler particles comprise a composition according to claim 3.
  • 20. The method according to claim 19, wherein the paper sheets are calendared by a supercalendar process.
  • 21. The method according to claim 19, wherein the pulp comprises mechanical pulp in an amount ranging from at least 70% by weight.
  • 22. The method according to claim 19, wherein the paper sheets are suitable for printing upon by a process chosen from a gravure printing process and an offset printing process.
  • 23. A method of making uncoated paper sheets, comprising preparing an aqueous paper-making composition from a pulp and mineral filler particles, andforming the composition into paper sheets,wherein the mineral filler particles comprise a particulate kaolin according to claim 1.
  • 24. The method according to claim 23, wherein the paper sheets are calendared by a supercalendar process.
  • 25. The method according to claim 23, wherein the pulp comprises mechanical pulp in an amount ranging from at least 70% by weight.
  • 26. The method according to claim 23, wherein the paper sheets are suitable for printing upon by a process chosen from a gravure printing process and an offset printing process.
Priority Claims (1)
Number Date Country Kind
0020179.8 Aug 2000 GB national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/GB01/03707 8/17/2001 WO 00 5/1/2003
Publishing Document Publishing Date Country Kind
WO02/16509 2/28/2002 WO A
US Referenced Citations (151)
Number Name Date Kind
2158987 Maloney May 1939 A
2414391 Peaker Jan 1947 A
2531396 Carter et al. Nov 1950 A
2883356 Gluesenkamp Apr 1959 A
3034859 Gunn et al. May 1962 A
3171718 Gunn et al. Mar 1965 A
3291769 Woodford et al. Dec 1966 A
3463350 Unger Aug 1969 A
3526768 Rai et al. Sep 1970 A
3615806 Torock et al. Oct 1971 A
3635662 Lyons Jan 1972 A
3663260 Poppe et al. May 1972 A
3790402 Eastes Feb 1974 A
3798044 Whitley et al. Mar 1974 A
4082880 Zboril Apr 1978 A
4102974 Boni Jul 1978 A
4125411 Lyons Nov 1978 A
4176148 Magder et al. Nov 1979 A
4183991 Smiley et al. Jan 1980 A
4198333 van Bonin et al. Apr 1980 A
4221697 Osborn et al. Sep 1980 A
4225496 Columbus et al. Sep 1980 A
4227920 Chapman et al. Oct 1980 A
4233199 Abolins et al. Nov 1980 A
4234469 Ohta et al. Nov 1980 A
4241142 Kaliski et al. Dec 1980 A
4243574 Manwiller Jan 1981 A
4250077 van Bonin et al. Feb 1981 A
4251576 Osborn et al. Feb 1981 A
4298711 Moulson et al. Nov 1981 A
4311635 Pearson Jan 1982 A
4359497 Magder et al. Nov 1982 A
4381948 McConnell et al. May 1983 A
4409344 Moulson et al. Oct 1983 A
4414352 Cohen et al. Nov 1983 A
4427450 Kostansek Jan 1984 A
4467057 Dieck et al. Aug 1984 A
4528235 Sacks et al. Jul 1985 A
4543287 Briggs et al. Sep 1985 A
4546126 Breitenfellner et al. Oct 1985 A
4549930 Dessauer Oct 1985 A
4582866 Shain Apr 1986 A
4584333 Prigent et al. Apr 1986 A
4708975 Shain Nov 1987 A
4728478 Sacks et al. Mar 1988 A
4795776 Milner Jan 1989 A
4800103 Jeffs Jan 1989 A
4816074 Raythatha et al. Mar 1989 A
4820761 Saito et al. Apr 1989 A
4873116 Ancker Oct 1989 A
4888315 Bowman et al. Dec 1989 A
4889886 Wada et al. Dec 1989 A
4918127 Adur et al. Apr 1990 A
4943324 Bundy et al. Jul 1990 A
4966638 Mudgett Oct 1990 A
4981521 Bettacchi et al. Jan 1991 A
5085707 Bundy et al. Feb 1992 A
5104925 Honda et al. Apr 1992 A
5109051 Kroenke et al. Apr 1992 A
5112782 Brown et al. May 1992 A
5128606 Gate et al. Jul 1992 A
5153039 Porter et al. Oct 1992 A
5167707 Freeman et al. Dec 1992 A
5168083 Matthews et al. Dec 1992 A
5169443 Willis et al. Dec 1992 A
5214091 Tanaka et al. May 1993 A
5234763 Rosen Aug 1993 A
5292365 Delfosse Mar 1994 A
5294654 Hellstern-Burnell et al. Mar 1994 A
5302404 Rissanen et al. Apr 1994 A
5332493 Ginn et al. Jul 1994 A
5364899 Watanabe et al. Nov 1994 A
5376237 Ishiguro et al. Dec 1994 A
5411587 Willis et al. May 1995 A
5416151 Tanaka May 1995 A
5439558 Bergmann et al. Aug 1995 A
5454865 Ginn et al. Oct 1995 A
5478388 Gane et al. Dec 1995 A
5516829 Davis et al. May 1996 A
5522924 Smith et al. Jun 1996 A
5573946 Haxell et al. Nov 1996 A
5578659 Anada et al. Nov 1996 A
5624488 Forbus et al. Apr 1997 A
5635279 Ma et al. Jun 1997 A
5645635 Behl et al. Jul 1997 A
5665183 Kresge et al. Sep 1997 A
5685900 Yuan et al. Nov 1997 A
5695608 Yagi et al. Dec 1997 A
5700560 Kotani et al. Dec 1997 A
5707912 Lowe et al. Jan 1998 A
5735946 Bloodworth et al. Apr 1998 A
5749958 Behl et al. May 1998 A
5810998 Arrington-Webb et al. Sep 1998 A
5846309 Freeman et al. Dec 1998 A
5879512 McGenity et al. Mar 1999 A
5883173 Elspass et al. Mar 1999 A
5897411 Stark et al. Apr 1999 A
5916420 Wurster et al. Jun 1999 A
5925454 Bekele Jul 1999 A
5948156 Coutelle et al. Sep 1999 A
5952093 Nichols et al. Sep 1999 A
6031036 Rosenquist et al. Feb 2000 A
6087016 Feeney et al. Jul 2000 A
6117541 Frisk Sep 2000 A
6149723 Pruett et al. Nov 2000 A
6186335 Arrington-Webb et al. Feb 2001 B1
6193831 Overcash et al. Feb 2001 B1
6232389 Feeney et al. May 2001 B1
6238793 Takahashi et al. May 2001 B1
6245395 Falat et al. Jun 2001 B1
6262161 Betso et al. Jul 2001 B1
RE37385 Okada et al. Sep 2001 E
6312511 Bilimoria et al. Nov 2001 B1
6358576 Adur et al. Mar 2002 B1
6402826 Yuan et al. Jun 2002 B1
6416817 Rangwalla et al. Jul 2002 B1
6447845 Nanavati et al. Sep 2002 B1
6447860 Mueller et al. Sep 2002 B1
6465064 Branch Oct 2002 B1
6531183 Cason et al. Mar 2003 B1
6531196 Aho et al. Mar 2003 B1
6537363 Golley et al. Mar 2003 B1
6545079 Nurmi et al. Apr 2003 B1
6554892 Manasso et al. Apr 2003 B1
6564199 Pruett et al. May 2003 B1
6610137 Golley et al. Aug 2003 B2
6616749 Husband et al. Sep 2003 B1
6623866 Migliorini et al. Sep 2003 B2
6632868 Qian et al. Oct 2003 B2
6758895 Wesley Jul 2004 B2
6759463 Lorah et al. Jul 2004 B2
6790896 Chaiko Sep 2004 B2
6794042 Merlin et al. Sep 2004 B1
6838507 Chou et al. Jan 2005 B2
6841211 Knoll et al. Jan 2005 B1
6884450 Wu et al. Apr 2005 B2
6887302 Rajagopalan et al. May 2005 B2
6887351 Lunden et al. May 2005 B1
6914095 Lorah et al. Jul 2005 B2
6942897 Joyce et al. Sep 2005 B2
7214264 Jones et al. May 2007 B2
7226005 Jones et al. Jun 2007 B2
7306668 Pring et al. Dec 2007 B2
20030187120 Chaiko et al. Oct 2003 A1
20040033379 Grunlan et al. Feb 2004 A1
20040161594 Joyce et al. Aug 2004 A1
20040241475 Morabito Dec 2004 A1
20050145138 Raju et al. Jul 2005 A1
20050171243 Hemmings et al. Aug 2005 A1
20050228096 Kirsten et al. Oct 2005 A1
20050228104 Feeney et al. Oct 2005 A1
Foreign Referenced Citations (174)
Number Date Country
2 089 613 Sep 1993 CA
2 467 284 Nov 2004 CA
2 241 577 Mar 1973 DE
24 49 656 Dec 1975 DE
26 58 814 Feb 1978 DE
28 18 954 Nov 1978 DE
27 39 620 Mar 1979 DE
30 12 235 Oct 1980 DE
30 47 269 Jul 1982 DE
36 32 606 Apr 1987 DE
35 36 371 May 1987 DE
35 40 524 May 1987 DE
37 50 864 Apr 1988 DE
38 84 605 Aug 1988 DE
43 01 730 Jul 1993 DE
42 13 746 Oct 1993 DE
100 10 941 Sep 2001 DE
0 001 066 Apr 1980 EP
0 026 075 Apr 1981 EP
0 054 424 Jun 1982 EP
0 132 094 Jan 1985 EP
0 132 228 Jan 1985 EP
0 160 777 Nov 1985 EP
0 163 427 Dec 1985 EP
0 217 626 Apr 1987 EP
0 222 138 May 1987 EP
0 222 298 May 1987 EP
0 239 986 Oct 1987 EP
0 245 553 Nov 1987 EP
0 262 649 Apr 1988 EP
0 274 888 Jul 1988 EP
0 341 981 Nov 1989 EP
0 352 714 Jan 1990 EP
0 456 363 Nov 1991 EP
0 204 324 Feb 1992 EP
0 475 434 Mar 1992 EP
0 524 635 Jan 1993 EP
0 528 078 Feb 1993 EP
0 543 793 May 1993 EP
0 586 904 Mar 1994 EP
0 588 239 Mar 1994 EP
0 589 461 Mar 1994 EP
0 596 442 May 1994 EP
0 494 594 Oct 1995 EP
0 691 375 Jan 1996 EP
0 764 739 Mar 1997 EP
0 804 505 Nov 1997 EP
0 824 130 Feb 1998 EP
0 991 530 Apr 2000 EP
0 991 815 Apr 2000 EP
1 088 852 Apr 2001 EP
1 245 730 Oct 2002 EP
1 484 176 Dec 2004 EP
1 512 552 Mar 2005 EP
1 299 089 Jul 1962 FR
2 150 953 Apr 1973 FR
2 273 040 Dec 1975 FR
2 359 874 Feb 1978 FR
2 389 645 Dec 1978 FR
2 452 511 Oct 1980 FR
2 558 168 Jul 1985 FR
2 774 689 Aug 1999 FR
2 822 086 Sep 2002 FR
819 050 Aug 1959 GB
1032536 Jun 1966 GB
1 100 496 Jan 1968 GB
1 101 950 Feb 1968 GB
1118723 Jul 1968 GB
1 136 350 Dec 1968 GB
1 241 177 Jul 1971 GB
1 310 933 Mar 1973 GB
1375057 Nov 1974 GB
1469028 Mar 1977 GB
1493393 Nov 1977 GB
1 496 088 Dec 1977 GB
1513657 Jun 1978 GB
1597213 Sep 1981 GB
2223758 Apr 1990 GB
2240398 Jul 1991 GB
2 306 392 May 1997 GB
2310215 Aug 1997 GB
51005383 Jan 1976 JP
53016063 Feb 1978 JP
54010394 Jan 1979 JP
54047751 Apr 1979 JP
55 129439 Oct 1980 JP
55131024 Oct 1980 JP
59074152 Apr 1984 JP
60023448 Feb 1985 JP
60038455 Feb 1985 JP
60084364 May 1985 JP
60161443 Aug 1985 JP
60235858 Nov 1985 JP
62116667 May 1987 JP
62232452 Oct 1987 JP
63132964 Jun 1988 JP
63175047 Jul 1988 JP
02-018362 Jan 1990 JP
02034653 Feb 1990 JP
02045551 Feb 1990 JP
04122752 Apr 1992 JP
4 270650 Sep 1992 JP
05262974 Oct 1993 JP
06016918 Jan 1994 JP
06065490 Mar 1994 JP
06502684 Mar 1994 JP
06145442 May 1994 JP
07502068 Mar 1995 JP
07 251486 Oct 1995 JP
08022945 Jan 1996 JP
09 111696 Apr 1997 JP
10114854 May 1998 JP
10 298358 Nov 1998 JP
11 129379 May 1999 JP
11 129381 May 1999 JP
2000 265391 Sep 2000 JP
2000 303386 Oct 2000 JP
2000345032 Dec 2000 JP
2001 020200 Jan 2001 JP
2001098149 Apr 2001 JP
2002 363885 Dec 2002 JP
2003 192861 Jul 2003 JP
2003 292678 Oct 2003 JP
2004 003118 Jan 2004 JP
2004 034390 Feb 2004 JP
77224 Aug 1983 PT
WO 8001167 Jun 1980 WO
WO 8002430 Nov 1980 WO
WO 8805804 Aug 1988 WO
WO 9011605 Oct 1990 WO
WO 9304119 Mar 1993 WO
WO 9407956 Apr 1994 WO
WO 9615321 May 1996 WO
WO 9622329 Jul 1996 WO
WO 9700910 Jan 1997 WO
WO 9732934 Sep 1997 WO
WO 9734956 Sep 1997 WO
WO 9837152 Aug 1998 WO
WO 9854409 Dec 1998 WO
WO 9854410 Dec 1998 WO
WO 9856598 Dec 1998 WO
WO 9856860 Dec 1998 WO
WO 9856861 Dec 1998 WO
WO 9858613 Dec 1998 WO
WO 9901504 Jan 1999 WO
WO 9961703 Feb 1999 WO
WO 9941309 Aug 1999 WO
WO 9951815 Oct 1999 WO
WO 9958613 Nov 1999 WO
WO 0005311 Feb 2000 WO
WO 0059840 Oct 2000 WO
WO 0059841 Oct 2000 WO
WO 0066657 Nov 2000 WO
WO 0076862 Dec 2000 WO
WO 0078540 Dec 2000 WO
WO 0112708 Feb 2001 WO
WO 0146307 Jun 2001 WO
WO 0153159 Jul 2001 WO
WO 0159215 Aug 2001 WO
WO 0166627 Sep 2001 WO
WO 0166635 Sep 2001 WO
WO 0166655 Sep 2001 WO
WO 0187580 Nov 2001 WO
WO 0187596 Nov 2001 WO
WO 0216509 Feb 2002 WO
WO 03039228 May 2003 WO
WO 2004046463 Jun 2004 WO
WO 2004074574 Sep 2004 WO
WO 2005013704 Feb 2005 WO
WO 2005014283 Feb 2005 WO
WO 2005044938 May 2005 WO
WO 2005047372 May 2005 WO
WO 2005061608 Jul 2005 WO
WO 2005108222 Nov 2005 WO
Related Publications (1)
Number Date Country
20050126730 A1 Jun 2005 US