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Glass Composition And Glass Substrate For Display Devices

Abstract: The present invention discloses a substrate glass and a glass composition, wherein said glass composition comprises: SiO2 from about 63.3 to about 71.3 mole %; AI2O3 from about 8.1 to about 12.1 mole %; B2O3 from about 6.7 to about 12.7 mole %; CaO from about 8 to 8.6 mole %; MgO from about 3 to 3.5 mole % and CS2O from about 0.001 to about 0.9 mole %; wherein inclusion of the alkali metal CS2O decreases the melting point of the substrate glass composition and at the same time as the cesium has a high radii as compared with other alkali metals, has very low mobility and thereby does not diffuse out and interfere with the TFT operation.

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Notices, Deadlines & Correspondence

Patent Information

Application #
Filing Date
11 May 2011
Publication Number
25/2012
Publication Type
INA
Invention Field
CHEMICAL
Status
Email
Parent Application
Patent Number
Legal Status
Grant Date
2018-02-12
Renewal Date

Applicants

STERLITE TECHNOLOGIES LTD.
E1/E2/E3, MIDC, WALUJ, AURANGABAD - 431136, MAHARASHTRA, INDIA

Inventors

1. JEETENDRA SEHGAL
STERLITE TECHNOLOGIES LTD., E1,E2,E3 MIDC. WALUJ, AURANGABAD - 431136, MAHARASHTRA, INDIA.

Specification

FORM 2
THE PATENTS ACT, 1970 (39 of 1970)
THE PATENTS RULES, 2003
COMPLETE SPECIFICATION
(See Section 10 and Rule 13)
1. Title of the Invention:-
GLASS COMPOSITION AND GLASS SUBSTRATE FOR DISPLAY DEVICES.
2. Applicant(s):-
(a)Name: STERLITE TECHNOLOGIES LTD.
(b) Nationality: An Indian Company
(c) Address: E1/E2/E3, MIDC, Waluj, Aurangabad - 431136
Maharashtra, INDIA
3. Preamble to the Description:-
Complete Specification:
The following specification describes the invention in details

FIELD OF THE INVENTION
[0001] Embodiments in general relate to a glass composition and a glass substrate for use in display and in particular to a glass composition and a glass substrate for use in liquid crystal display [LCD], an electroluminescence display [ELD], a field emission display [FED], plasma display [PD], organic light emitting diode [OLED] display etc.
BACKGROUND OF THE INVENTION
[0002] Over the years active matrix liquid crystal displays (AMLCDs) have become ubiquitous features of our life, wherein they are used in cellular phones, mobiles, desktops, laptops computer screens and in large screen televisions.
[0003] One aspect of all the electronic devices that has turned out to be noteworthy over the years is energy utilization by the device and is obviously desired to be as low as possible. It is quite clear that CRT are replaced by flat panel display and in particular by AMLCD and organic light-emitting diode (OLED)-based devices.
[0004] A typical AMLCD comprises, inter alia, two sheets of glass, the first one is vapor-deposited with silicon that forms the basis for the thin-film transistor (TFT) array and whereas the second for the color filter (CF) materials that enables RGB displays. A gap between the two sheets of glass holds a very thin layer of liquid crystal, wherein the gap between the two sheets has to be

maintained within tight specifications. The glass (also referred to as "glass substrate") used for depositing the silicon for the thin-film transistor array has a unique material composition, which is specifically designed for the application.
[0005] One method of producing these substrate glasses is the down draw-fusion process [also known as the down-draw process] and is capable of producing a precision fire-polished surface that requires no additional modification such as grinding or polishing prior to use. The US patent numbers 3,338,696 and 3,682,609 disclose fusion downdraw processes which include allowing flow of molten glass over the edges or weirs of a forming wedge, referred to as isopipe. The molten glass flows over converging forming surfaces of the isopipe and the separate flows reunite at the apex or root where the two converging forming surfaces meet to form a glass sheet. Thus, in the fusion process the glass which has been in contact with the forming surfaces is located in the inner portion of the glass sheet and the exterior surfaces of the glass sheet are contact free. Pulling rolls positioned downstream of isopipe root capture edge portions of the glass sheet so formed to control the rate at which the glass sheet leaves the isopipe and thus aids in controlling the thickness of the finished sheet. As the glass sheet descends from the root of the isopipe past the pulling rolls, it cools to form a solid elastic glass sheet, which may be processed further.

[0006] In order to achieve a good quality substrate glass using the fusion technique, various material properties of the glass in the molten stage must be controlled within specified limits during the downdraw process. [0007] One such material property is the viscosity of the glass. It is desired to maintain the viscosity of the glass at the location where it leaves the isopipe at a value greater than about 105 poise, which if not maintained the glass sheet flatness and thickness across its width becomes difficult to control, which may result in a glass sheet not suitable for display applications.
[0008] Further, when the glass in molten stage is exposed to low temperatures for significant time period, crystal phase development is initiated. The maximum temperature where these crystal phases disappear is termed as Iiquidus temperature. It is desired that the liquidus temperature of the glass to be less than 1200 °C and preferably less than 1150 °C.
[0009] Another significant factor is liquidus viscosity of the glass substrate. It is desired to have lower liquidus temperatures and hence higher liquidus viscosities for the downdraw process. The lower liquidus temperature and higher liquidus viscosity results in the glass being resistant to crystallization during the forming process. Since the forming is done at glass viscosities of greater than 105 poise, it is desired that the glass exhibits a liquidus viscosity of greater than about 105 poise.

[00010] Additionally, the glass substrate when formed should qualify certain requirements.
[00011] Numerous processes in the fabrication of liquid crystal displays include steps that are performed at high temperatures. For example, active matrix of the LCD employs an active device such as a diode or thin film transistor at each pixel thereby enabling high contrast and high response speed. It is known that display devices at present make use of amorphous silicon (a-Si), the processing of which may be done at temperatures of about 450° C or less. It is preferred to have polycrystalline-silicon (poly-Si) processing as poly-Si has much higher drive current and electron mobility thereby increasing the response time of the pixels and that it is possible, to build the display drive circuitry directly on the glass substrate by use of poly-Si processing. However, the efficient poly-Si processing methods requires temperatures of at least 600° C or more, such processes enable formation of poly-Si films. Thus, the glass substrate on which the poly-Si is to be deposited must have strain points exceeding 600° C. Therefore it is desired to have strain point glass, which makes the glass substrate resistant to heat resulting in low thermal deformation and thermal compaction when subjected to high temperatures during various thermal processing steps during panel fabrication.

[00012] Further, the substrate glass is desired to exhibit high durability to chemical treatments during the TFT manufacturing and long term exposure to environmental conditions in service.
[00013] It is also desired that the substrate glass should not interact chemically and/or electronically with the TFT's during the course of operation. It is known that alkalis such as lithium and sodium are mobilized at elevated temperatures and may interfere with the TFT performance, if the alkali metals are added to glass composition. Thus, inclusion of alkali metal oxides hinders the electrical properties of the display panel. The known prior art claims that the glass composition should be alkali free due to above mentioned reasons.
[00014] However, if no alkali metals are added to the glass composition, the melting of the glass composition becomes difficult as the melting viscosity becomes very high. Typically, the melting temperature of the glass without alkali metals is known to be greater than 1600 °C.
[00015] Another problem that occurs if no alkali metals are added is during the step of refining. Refining is step of removal of bubbles or gas inclusion in the molten glass, which may, if not removed make the glass substrate made useless for the display application. It is observed that the refining temperature has to be greater than 1650 °C in glasses without alkali metals.

[00016] Further, as the substrate glass is to be used in portable devices such as laptops, clocks, mobiles, which are light-weight devices. This implies that the substrate glass which forms an important part should also have low weight, which in-turn implies that the substrate glass itself should be light weight. It is desired that the thickness of the glass is less than about 1.1 mm, preferably less than about 0.7 mm and most preferably less than about 0.5 mm.
[00017] Additionally, it is desired that the substrate glass should exhibit a low coefficient of thermal expansion (CTE). This is necessary in order to match the CTE of silicon metal. As the TFT material is CTE of poly-silicon whose CTE is in the range from about 30 x 10"7/°C to about 32 x 10"7/°C, the CTE of the glass must match that of poly-silicon, thereby the CTE of the glass substrate must be in the range of from about 28 x 10"7/°C to about 40 x 10"7/°C.
[00018] The above described attributes or properties are impacted by the substrate glass composition. Therefore, there is a need to have a substrate glass composition which meets almost all the above described attributes.
OBJECTS OF THE PRESENT INVENTION
Some of the objects of the present disclosure are described herein below:
[00019] An object is to provide a substrate glass and a glass composition.

[00020] Another object is to provide a substrate glass and a glass composition for display devices.
[00021] Still another object is to provide a substrate glass and a glass composition compatible with the down draw process.
[00022] Yet another object is to provide a substrate glass and a glass composition having higher viscosity at the root of the isopipe.
[00023] Another object is to provide a glass composition with low melting and refining temperatures.
[00024] Another object is to provide a glass composition wherein the electrical properties of the TFT are not hindered or compromised in addition to having low melting and refining temperatures.
[00025] Another object is to provide a substrate glass and a glass composition having high-strain point.
[00026] Another object is to provide a substrate glass and a glass composition having lower liquidus temperature.

[00027] Another object is to provide a substrate glass and a glass composition, wherein the liquidus viscosity of the glass is higher.
[00028] Another object is to provide a substrate glass and a glass composition which does not chemically interact with the TFTs.
[00029] Another object is to provide a substrate glass which is light-weight.
[00030] Another object is to provide a substrate glass with low coefficient of thermal expansion in the range from about 28 x 10"7/°C to about 40 x 10"7/°C.
[00031] Another object is have a substrate glass composition for use in liquid crystal display [LCD], an electroluminescence display [ELD], a field emission display [FED], plasma display [PD], organic light emitting diode [OLED] etc.
[00032] Other objects and advantages of the present invention will be more apparent from the following description when read in conjunction with the accompanying figures, which are not intended to limit the scope of the present invention.
SUMMARY OF THE INVENTION
[00033] These and other objects of the present disclosure are to a great extent dealt within the disclosure.

[00034] In accordance with the embodiments of the present invention a glass composition is disclosed, said glass composition comprising Si02 from about 63.3 to about 71.3 mole %, A1203 from about 8.1 to about 12.1 mole %, B203 from about 6.7 to about 12.7 mole %, CaO from about 8 to 8.6 mole %, MgO from about 3 to 3.5 mole% and Cs20 from about 0.001 to about 0.9 mole %, wherein said CS2O decreases the melting point of the glass composition and cesium does not diffuse out and interfere with the TFT operation, owning to high ionic radii and large atomic mass, hence electrical resistivity is not affected or reduced.
[00035] In accordance with the present invention the glass composition further comprises of at least one refining agent selected from the group consisting of AS2O3 in the range from about 0 to 0.8 mole %, Sb203 in the range from 0 to 0.1 mole % and N2O5 in the range from 0 to 0,2 mole % or a combination thereof.
[00036] In accordance with the present invention the glass has a density of less than about 2.5 g/cm3, a coefficient of thermal expansion less than 40 x 10" 7/°C, a logarithm of liquidus viscosity of greater than 5, a strain point of greater than about 630 °C, annealing temperature of greater than 650 °C and a liquidus temperature of less than 1270 °C.

[00037] Further, in accordance with the present invention the glass has a resistivity comparable or greater than commercially available LCD substrate glass.
[00038] In accordance with one embodiment of the present invention the glass is down-drawable or slot drawn or press-formable in a mold or drawable through roller press or drawable through float process.
DETAILED DESCRIPTION OF THE INVENTION
[00039] The embodiments herein and the various features and advantageous details thereof are explained with reference to the non-limiting embodiments in the following description. Descriptions of well-known components and processing techniques are omitted so as to not unnecessarily obscure the embodiments herein. The examples used herein are intended merely to facilitate an understanding of ways in which the embodiments herein may be practiced and to further enable those of skill in the art to practice the embodiments herein. Accordingly, the examples should not be construed as limiting the scope of the embodiments herein
[00040] The present invention is concerned with enhanced glasses for use as. substrates in displays. In particular, the glasses meet the various property requirements of such substrates.

[00041] In accordance with the present invention, the glass substrate composition comprises of the major components of the glass, for use in glass substrates, namely, Silica (S1O2), Alumina (A1203), Boron Oxide (B2O3), and alkaline earth oxides (AEO) such as MgO and CaO.
[00042] In accordance with the present invention silica (Si02) behaves as the basic glass former, wherein the former (silica in this case) forms the basic skeleton or network. Formers alone may form glass however the melting point in some cases (particularly when the former is silica) will be so high so as to make it impractical to commercially melt the glasses. In other cases wherein B2O3 or P2O5 is utilized as former the chemical durability will be so poor that it is impractical to use it in any application in its hundred percent forms.
[00043] In accordance with the present invention modifiers such as alkali oxides (AO) and Alkaline earth oxides (AEO) are utilized to modify the network structure formed by the glass formers so as to reduce the melting temperature and thereby improve other glass forming processes e.g., refining. In accordance with the present invention a trace amount of CS2O is utilized as the modifier for reasons discussed herein below.
[00044] In accordance with one embodiment of the present invention alkaline earth oxides such as CaO and MgO is added as modifiers.

[00045] Further, in accordance with the present invention intermediates such as alumina is added to the glass composition.
[00046] In accordance with one embodiment the present invention, the substrate glass composition, comprises SiO2 from about 63.3 to about 71.3 mole %; A1203 from about 8.1 to about 12.1 mole %; B203 from about 6.7 to about 12.7 mole %; CaO from about 8 to 8.6 mole %; MgO from about 3 to 3.5 mole % and CS2O from about 0.001 to about 0.9 mole %; wherein inclusion of the alkali metal Cs20 decreases the melting point of the substrate glass composition and at the same time as the cesium has a high radii as compared with other alkali metals, has very low mobility and thereby does not diffuse out and interfere with the TFT operation.
[00047] In accordance with one embodiment the substrate glass composition may contain AS2O3 in the range from about 0 to about 0.3 mole %, wherein AS2O3 is acts as a fining agent and aids in removal of bubbles or gaseous inclusions from the molten glass.
[00048] In accordance with one embodiment the substrate glass composition may contain Sb2O3 in the range from about 0 to about 0.1 mole %, wherein Sb203 also acts as a fining agent and aids in removal of bubbles or gaseous inclusions from the molten glass.

[00049] In accordance with one embodiment the substrate glass composition may contain N2O5 in the range from about 0 to 0.2 mole %, wherein addition of N2O5 enhances the refining agents refining capacity of AS2O3 and Sb203.
[00050] In accordance with the present invention the non-green components such as BaO and SrO are eliminated completely so as to produce an environmentally friendly "green" product, and in particular lessening or getting rid of barium is preferred since barium is one of the listed metals in the Resources Conservation and Recovery Act (RCRA) and is therefore classified by the US EPA as hazardous.
[00051] In accordance with this embodiment of the present invention, the substrate glass composition, comprises SiCh from about 63.3 to about 71.3 mole %; AI2O3 from about 8.1 to about 12.1 mole %; B2O3 from about 6.7 to about 12.7 mole %; CaO from about 8 to 8.6 mole %; MgO from about 3 to 3.5 mole % and CS2O from about 0.001 to about 0.9 mole %; wherein inclusion of the trace amount of alkali metal CS2O decreases the melting point of the substrate glass composition and at the same time as the cesium has a high radii and large atomic mass as compared with other alkali metals, has very low mobility and thereby does not diffuse out and interfere with the TFT operation.

[00052] In accordance with the present invention an advantage of the glass substrate made from the glass composition is that it exhibit higher viscosity, typically of the order of 10s poise or greater.
[00053] In accordance with the present invention the glass substrate made from the glass composition exhibit a high-strain point greater than about 630 °C.
[00054] In accordance with the present invention the glass substrate made from the glass composition has lower liquidus temperature of less than about 1270°C.
[00055] In accordance with the present invention the glass substrate made from the glass composition exhibits a high liquidus viscosity of about 105 or greater.
[00056] In accordance with the present invention the glass substrate made from the glass composition does not chemically interact with the TFTs due to presence to Cs20 and hence also have a reduced melting point.
[00057] In accordance with the present invention, the substrate glass has light-weight owing to the low density of less than about 2.5 g/cm3.

[00058] In accordance with the present invention, the substrate glass has lower coefficient of thermal expansion of less than about 40 x 10"7/°C
[00059] Thus, the present invention provides a substrate glass composition for display devices compatible with the down draw fusion process.
[00060] In accordance with the present invention the substrate glass composition may be used in liquid crystal display [LCD], an electroluminescence display [ELD], a field emission display [FED], plasma display [PD], organic light emitting diode [OLED] display etc,

[00061] Exemplary compositions of the glass of the present disclosure are listed in Table 1.
Table 1

EXAMPLES I II III IV Y VI vu Mil IX X
SiO; 67.91 6S.93 70.02 "1.3 66.91 65.91 64.91 63.3 63.3 63.3
A1203 10.21 9.21 8.1 S.l 11.21' 12.1 12.3 12.1 11.57 11.57
B:0, 10.04 10.04 10.04 S.76 10.04 10.15 31.15 12.7 12.7 12."
CaO S S £ S S S 8 8.07 S.6 S.l
VIgO 3 3 3 3 3 3 3 3 3 3.5
SrO 0 0 0 0 0 0 0 0 0 0
Cs:0 0.4 0.4 0.4 0.4 0.4 0.4 0.4 0.4 04 0.4
As:0; 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3
Sb;0; 0.1 0.1 0.1 0.1 " 0.1 0.1 0.1 0.3 0.1 0,1
N:Oj 0 0.19 0.19 0.39 0.19 0.39 0.19 0.19 0.19 0.19
PROPEJ ITIES
Density (gfcoi*) 2,41 2.41 2.41 2.41 2.41 2.41 2.42 2.42 2.43 2.43
CTE (K 10-7;C) 35.69 35.7" 35S6 35.61 35.60 H tf 35.75 36.14 37.04 36.59
Log (Liquidus Viscosity) 6.63 6.74 6.S7 7.00 65! 6.39 6.29 6.12 6.07 6.06
Strain Point ("Q 64S 646 643 6}} 651 652 644 631 62S 628
Liquidus Temperature 1229 2239 1250 1268 1220 1210 1196 2173 11-2 1 ISO
Ajinealing Temperature (;C) 691 6S7 6S2 691 696 699 692 6S1 677 676
Foaming at 1420 C CO No No No No No No No No No No

Table 1 continued ...

EXAMPLES XI XII XIII XIV xv XM xvn XVIII XIX C-I
SiO; 6"7 6S.S 6S.7 6S.7 6S.7 6S.7 6S.7 6S.S 67.7 69.43
A1:0; 12.1 32.1 1.2.1 12 U.9 11 S 11.7 32.3 12.1 10.46
B;Oi 7-76 6.7 6- 6.7 6.7 6.7 67 6.7 7.7 9.S1
CaO 8.6 S.6 S.6 S.6 S.6 S.6 $.6 £.6 8.6 9.4
MgO J 5 3 3 3 3 3 3.3 3.5 0.2
SrO 0 0 0 0 0 0 0 0 0 0.4S
CVO 0.4 0.4 0 5 0.6 0.7 O.S 0.9 0.1 0.001 0
As:Oj 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0
Sb:o3 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0
N:Oj 0.19 0.19 0.19 019 0.19 0.19 0.19 0.19 0.19
PROPEF .TIES
Density (g'cm") 2.43 2 42 2,43 2.43 2-43 2.43 2.43 2.43 2.43 2.39
CTE(x3D-7/;C) 36.06 37.00 37.00 38.00 3S.00 3S.00 39.00 35.52 35.69 35.64
Log (Liquidui Viscosity) 6.51 6,62 6.61 6.62 6.63 6.63 6.64 6.56 6,42 -.00
: Strain Point f"C) 669 67S 677 677 676 676 6" 67S 669 65S
Liquidus Temperature (:C) 1237 1252 1252 1251 1251 1250 1250 125" 1245 1203
Annealing Temperature (:C) 713 720 720 719 71S 71S "17 720 713 704
Foaming at 1420 C r-C) No No No No No No No No No Yes
[00062] In the Table I provided herein above, examples I to XIX are glass compositions in accordance with the embodiments of the present invention,

whereas C-I is a comparative example of glass composition in accordance with known prior art. It is observed that owing to presence of Cs20 in the composition, the resistivity of the glass made from the composition is comparable with that of the commercially available LCD substrate glass or even better.
[00063] The foregoing description of the specific embodiments will so fully reveal the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the embodiments as described herein.

We claim:
1. A glass composition comprising:
S1O2 from 63.3 to 71.3 mole %;
A1203 from 8.1 to 12.1 mole %;
B203 from 6.7 to 12.7 mole %;
CaO from 8 to 8.6 mole %;
MgO from 3 to 3.5 mole%; and
Cs20 from about 0.001 to about 0.9 mole %.
2. The glass as claimed in claim 1, wherein the glass further comprises of refining agents selected from a group consisting of Sb203 in the range from 0 to 0.8 mole % and AS2O3 in the range from 0 to 0.8 mole % in conjunction with N2O5.
3. The glass as claimed in claim 1, wherein said CS2O decreases the melting point of the glass composition and cesium does not diffuse out and interfere with the TFT operation, owning to high ionic radii and higher atomic mass.
4. The glass as claimed in claim 1, wherein said glass has a density of less than about 2.5 g/cm3.

5. The glass as claimed in claim 1, wherein said glass has a coefficient of thermal expansion less than 40 x 10"7/°C.
6. The glass as claimed in claim 1, wherein said glass has a logarithm of liquidus viscosity of greater than 5.
7. The glass as claimed in claim 1, wherein said glass has a strain point greater than 630 °C.
8. The glass as claimed in claim 1, wherein said glass has a liquidus temperature of less than 1270 °C.
9. The glass as claimed in claim 1, wherein said glass is down-drawable or slot drawn or press-formable in a mold or drawable through roller press or drawable through float process.
10. A glass sheet prepared from the glass as claimed in claim 1.
11. An electronic device, the electronic device comprising a glass substrate, the glass substrate comprising the glass composition as claimed in claim

Documents

Application Documents

# Name Date
1 1445-MUM-2011-FORM 4 [13-06-2024(online)].pdf 2024-06-13
1 Other Document [29-02-2016(online)].pdf 2016-02-29
2 Form 13 [29-02-2016(online)].pdf 2016-02-29
2 1445-MUM-2011-RELEVANT DOCUMENTS [30-09-2023(online)].pdf 2023-09-30
3 Examination Report Reply Recieved [04-03-2016(online)].pdf 2016-03-04
3 1445-MUM-2011-RELEVANT DOCUMENTS [01-10-2021(online)]-1.pdf 2021-10-01
4 Description(Complete) [04-03-2016(online)].pdf 2016-03-04
4 1445-MUM-2011-RELEVANT DOCUMENTS [01-10-2021(online)].pdf 2021-10-01
5 Correspondence [04-03-2016(online)].pdf 2016-03-04
5 1445-MUM-2011-RELEVANT DOCUMENTS [06-04-2020(online)].pdf 2020-04-06
6 Claims [04-03-2016(online)].pdf 2016-03-04
6 1445-MUM-2011-RELEVANT DOCUMENTS [30-03-2019(online)].pdf 2019-03-30
7 Petition Under Rule 137 [24-10-2016(online)].pdf 2016-10-24
7 1445-MUM-2011-ABSTRACT(11-5-2012).pdf 2018-08-10
8 Other Document [24-10-2016(online)].pdf 2016-10-24
8 1445-mum-2011-abstract.pdf 2018-08-10
9 HEARING ADJOURNMENT [24-10-2016(online)].pdf 2016-10-24
9 1445-MUM-2011-CLAIMS(11-5-2012).pdf 2018-08-10
10 1445-MUM-2011-CORRESPONDENCE(11-5-2012).pdf 2018-08-10
10 Petition Under Rule 137 [22-11-2016(online)].pdf 2016-11-22
11 1445-MUM-2011-CORRESPONDENCE(5-6-2012).pdf 2018-08-10
11 Other Patent Document [22-11-2016(online)].pdf 2016-11-22
12 1445-MUM-2011-CORRESPONDENCE(8-3-2013).pdf 2018-08-10
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13 1445-MUM-2011-CORRESPONDENCE(IPO)-(10-8-2011).pdf 2018-08-10
13 1445-MUM-2011-IntimationOfGrant12-02-2018.pdf 2018-02-12
14 1445-MUM-2011-DESCRIPTION(COMPLETE)-(11-5-2012).pdf 2018-08-10
14 1445-MUM-2011-RELEVANT DOCUMENTS [31-03-2018(online)].pdf 2018-03-31
15 1445-mum-2011-description(provisional).pdf 2018-08-10
15 1445-MUM-2011_EXAMREPORT.pdf 2018-08-10
16 1445-MUM-2011-FORM 1(11-5-2012).pdf 2018-08-10
16 1445-MUM-2011-OTHERS-090316.pdf 2018-08-10
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18 1445-MUM-2011-FORM 18(5-6-2012).pdf 2018-08-10
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19 1445-mum-2011-form 5.pdf 2018-08-10
19 1445-MUM-2011-FORM 2(11-5-2012).pdf 2018-08-10
20 1445-MUM-2011-FORM 2(TITLE PAGE)-(11-5-2012).pdf 2018-08-10
20 1445-MUM-2011-FORM 5(11-5-2012).pdf 2018-08-10
21 1445-mum-2011-form 2(title page).pdf 2018-08-10
21 1445-mum-2011-form 3.pdf 2018-08-10
22 1445-mum-2011-form 2.pdf 2018-08-10
22 1445-MUM-2011-FORM 3(8-3-2013).pdf 2018-08-10
23 1445-MUM-2011-FORM 3(11-5-2012).pdf 2018-08-10
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24 1445-MUM-2011-FORM 3(8-3-2013).pdf 2018-08-10
25 1445-mum-2011-form 3.pdf 2018-08-10
25 1445-mum-2011-form 2(title page).pdf 2018-08-10
26 1445-MUM-2011-FORM 5(11-5-2012).pdf 2018-08-10
26 1445-MUM-2011-FORM 2(TITLE PAGE)-(11-5-2012).pdf 2018-08-10
27 1445-MUM-2011-FORM 2(11-5-2012).pdf 2018-08-10
27 1445-mum-2011-form 5.pdf 2018-08-10
28 1445-MUM-2011-FORM 18(5-6-2012).pdf 2018-08-10
28 1445-MUM-2011-FORM 9(5-6-2012).pdf 2018-08-10
29 1445-mum-2011-form 1.pdf 2018-08-10
29 1445-MUM-2011-FORM PCT-ISA-237(8-3-2013).pdf 2018-08-10
30 1445-MUM-2011-FORM 1(11-5-2012).pdf 2018-08-10
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31 1445-mum-2011-description(provisional).pdf 2018-08-10
31 1445-MUM-2011_EXAMREPORT.pdf 2018-08-10
32 1445-MUM-2011-DESCRIPTION(COMPLETE)-(11-5-2012).pdf 2018-08-10
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33 1445-MUM-2011-CORRESPONDENCE(IPO)-(10-8-2011).pdf 2018-08-10
33 1445-MUM-2011-IntimationOfGrant12-02-2018.pdf 2018-02-12
34 1445-MUM-2011-CORRESPONDENCE(8-3-2013).pdf 2018-08-10
34 1445-MUM-2011-PatentCertificate12-02-2018.pdf 2018-02-12
35 1445-MUM-2011-CORRESPONDENCE(5-6-2012).pdf 2018-08-10
35 Other Patent Document [22-11-2016(online)].pdf 2016-11-22
36 1445-MUM-2011-CORRESPONDENCE(11-5-2012).pdf 2018-08-10
36 Petition Under Rule 137 [22-11-2016(online)].pdf 2016-11-22
37 HEARING ADJOURNMENT [24-10-2016(online)].pdf 2016-10-24
37 1445-MUM-2011-CLAIMS(11-5-2012).pdf 2018-08-10
38 Other Document [24-10-2016(online)].pdf 2016-10-24
38 1445-mum-2011-abstract.pdf 2018-08-10
39 Petition Under Rule 137 [24-10-2016(online)].pdf 2016-10-24
39 1445-MUM-2011-ABSTRACT(11-5-2012).pdf 2018-08-10
40 Claims [04-03-2016(online)].pdf 2016-03-04
40 1445-MUM-2011-RELEVANT DOCUMENTS [30-03-2019(online)].pdf 2019-03-30
41 Correspondence [04-03-2016(online)].pdf 2016-03-04
41 1445-MUM-2011-RELEVANT DOCUMENTS [06-04-2020(online)].pdf 2020-04-06
42 Description(Complete) [04-03-2016(online)].pdf 2016-03-04
42 1445-MUM-2011-RELEVANT DOCUMENTS [01-10-2021(online)].pdf 2021-10-01
43 1445-MUM-2011-RELEVANT DOCUMENTS [01-10-2021(online)]-1.pdf 2021-10-01
43 Examination Report Reply Recieved [04-03-2016(online)].pdf 2016-03-04
44 1445-MUM-2011-RELEVANT DOCUMENTS [30-09-2023(online)].pdf 2023-09-30
44 Form 13 [29-02-2016(online)].pdf 2016-02-29
45 1445-MUM-2011-FORM 4 [13-06-2024(online)].pdf 2024-06-13
45 Other Document [29-02-2016(online)].pdf 2016-02-29

ERegister / Renewals

3rd: 12 May 2018

From 11/05/2013 - To 11/05/2014

4th: 12 May 2018

From 11/05/2014 - To 11/05/2015

5th: 12 May 2018

From 11/05/2015 - To 11/05/2016

6th: 12 May 2018

From 11/05/2016 - To 11/05/2017

7th: 12 May 2018

From 11/05/2017 - To 11/05/2018

8th: 12 May 2018

From 11/05/2018 - To 11/05/2019

9th: 12 May 2018

From 11/05/2019 - To 11/05/2020

10th: 08 May 2020

From 11/05/2020 - To 11/05/2021

11th: 04 May 2021

From 11/05/2021 - To 11/05/2022

12th: 04 May 2022

From 11/05/2022 - To 11/05/2023

13th: 25 Apr 2023

From 11/05/2023 - To 11/05/2024

14th: 14 Jun 2024

From 11/05/2024 - To 11/05/2025

15th: 02 May 2025

From 11/05/2025 - To 11/05/2026