Composition based on 1,3,3,3-tetrafluoropropene

Information

  • Patent Grant
  • 11591504
  • Patent Number
    11,591,504
  • Date Filed
    Monday, July 13, 2020
    4 years ago
  • Date Issued
    Tuesday, February 28, 2023
    a year ago
Abstract
A composition including a lubricant based on polyol esters (POEs) or PVE and a refrigerant F including from 1 to 99% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 1 to 99% by weight of 1,1,1,2-tetrafluoroethane. Also, the use of the composition including a lubricant and refrigerant in refrigeration, air conditioning and heat pumps.
Description
TECHNICAL FIELD

The present invention relates to a composition containing trans-1,3,3,3-tetrafluoropropene and 1,1,1,2-tetrafluoroethane and at least one lubricant, capable of being used in refrigeration, air-conditioning and heat pumps.


BACKGROUND

The problems presented by substances which deplete the atmospheric ozone layer were dealt with at Montreal, where the protocol was signed imposing a reduction in the production and use of chlorofluorocarbons (CFCs). This protocol has been the subject of amendments which have required the abandoning of CFCs and have extended the regulations to other products, including hydrochlorofluorocarbons (HCFCs).


The refrigeration and air-conditioning industry has invested a great deal in the replacement of these refrigerants and it is because of this that hydrofluorocarbons (HFCs) have been marketed.


In the motor vehicle industry, the air-conditioning systems of vehicles sold in many countries have been changed from a chlorofluorocarbon (CFC-12) refrigerant to a hydrofluorocarbon (1,1,1,2-tetrafluoroethane: HFC-134a) refrigerant, which is less harmful to the ozone layer. However, from the viewpoint of the objectives set by the Kyoto protocol, HFC-134a (GWP=1430) is considered to have a high heating power. The contribution of a refrigerant to the greenhouse effect is quantified by a criterion, the GWP (Global Warming Potential), which summarizes the heating power by taking a reference value of 1 for carbon dioxide.


Hydrofluoroolefins (HFOs) have a low heating power and thus meet the objectives set by the Kyoto protocol. Document JP 4-110388 discloses hydrofluoropropenes as heat-transfer agents.


In the industrial sector, the refrigerating machines most commonly used are based on cooling by evaporation of a liquid refrigerant. After vaporization, the refrigerant is compressed and then cooled in order to return to the liquid state and thus continue the cycle.


The refrigeration compressors used are of the reciprocating, scroll, centrifugal or screw type. In general, internal lubrication of the compressors is essential in order to reduce wear and heating of the moving members, complete their leaktightness and protect them against corrosion.


In addition to good heat-transfer agent properties, in order for a refrigerant to be commercially accepted, it must in particular exhibit thermal stability and compatibility with the lubricants. Specifically, it is highly desirable for the refrigerant to be compatible with the lubricant used in the compressor, present in the majority of refrigeration systems. This combination of refrigerant and lubricant is important for the implementation and the efficiency of the refrigeration system; in particular, the lubricant should be sufficiently soluble or miscible in the refrigerant over the entire operating temperature range.


Thus, polyalkylene glycols (PAGs) have been developed as lubricants of HFC-134a in motor vehicle air conditioning.


Tests for miscibility of 1,1,3,3,3-pentafluoropropene and 1,3,3,3-tetrafluoropropene with lubricants have been described in Example 2 of document WO 2004/037913. Compatibility tests have also been described in Example 3, with polyalkylene glycol. However, these tests do not specify the nature of the 1,3,3,3-tetrafluoropropene isomer.


Moreover, document WO 2005/108522 discloses an azeotropic composition of trans-1,3,3,3-tetrafluoropropene and 1,1,1,2-tetrafluoroethane.


Just recently, 2,3,3,3-tetrafluoropropene was chosen as a refrigerant for replacing HFC-134a in motor vehicle air conditioning.


SUMMARY

The applicant has now developed a refrigerant and lubricant pairing which can be used in refrigeration, air conditioning and heat pumps.


Embodiments of the present application include:


1) Composition comprising at least one lubricant based on polyol esters (POEs) or PVE and a refrigerant F comprising from 1 to 99% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 1 to 99% by weight of 1,1,1,2-tetrafluoroethane.


2) Composition according to embodiment 1, characterized in that the refrigerant F comprises from 5 to 95% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 5 to 95% by weight of 1,1,1,2-tetrafluoroethane.


3) Composition according to embodiment 1 or 2, characterized in that the refrigerant F comprises from 30 to 91% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 9 to 70% by weight of 1,1,1,2-tetrafluoroethane.


4) Composition according to any one of embodiments 1 to 3, characterized in that the POEs are obtained from polyols having a neopentyl backbone, such as neopentyl glycol, trimethylolpropane, pentaerythritol and dipentaerythritol.


5) Composition according to any one of embodiments 1 to 4, characterized in that the POEs are obtained from a linear or branched carboxylic acid containing from 2 to 15 carbon atoms.


6) Composition according to any one of embodiments 1 to 5, characterized in that the POE(s) represent(s) between 10 and 50% by weight of the composition.


7) Use of the composition according to any one of embodiments 1 to 6, in refrigeration, air conditioning and heat pumps.







DETAILED DESCRIPTION

A subject of the present application is therefore a composition comprising at least one lubricant based on polyol esters (POEs) or on polyvinyl ether (PVE) and a refrigerant F comprising from 1 to 99% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 1 to 99% by weight of 1,1,1,2-tetrafluoroethane.


Preferably, the composition according to the present invention comprises at least one lubricant based on polyol esters (POEs) or on polyvinyl ether (PVE) and a refrigerant F comprising from 5 to 95% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 5 to 95% by weight of 1,1,1,2-tetrafluoroethane.


The composition which is particularly preferred comprises at least one lubricant based on polyol esters (POEs) or on polyvinyl ether (PVE) and a refrigerant F comprising from 30 to 91% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) and from 9 to 70% by weight of 1,1,1,2-tetrafluoroethane.


The refrigerant F may also comprise other hydrofluorocarbons.


The fluid F has the advantage of being more effective than trans-HFO-1234ze and, in addition, the stability of the refrigerant in the presence of POE or PVE is greater compared with that of trans-HFO-1234ze in the presence of PAG.


Polyol esters are obtained by reaction of a polyol (an alcohol containing at least 2 hydroxyl groups —OH) with a monofunctional or plurifunctional carboxylic acid or with a mixture of monofunctional carboxylic acids. The water formed during this reaction is eliminated in order to prevent the reverse reaction (i.e. hydrolysis).


According to the present invention, the preferred polyols are those which have a neopentyl backbone, such as neopentyl glycol, trimethylolpropane, pentaerythritol and dipentaerythritol; pentaerythritol is the preferred polyol.


The carboxylic acids may contain from 2 to 15 carbon atoms, it being possible for the carbon backbone to be linear or branched. Mention may in particular be made of n-pentanoic acid, n-hexanoic acid, n-heptanoic acid, n-octanoic acid, 2-ethylhexanoic acid, 2,2-dimethylpentanoic acid, 3,5,5-trimethylhexanoic acid, adipic acid and succinic acid, and mixtures thereof.


Some alcohol functions are not esterified, however their proportion remains low. Thus, the POEs can comprise between 0 and 5 relative mol % of CH2—OH units relative to the —CH2—O—(C═O)— units.


The preferred POE lubricants are those which have a viscosity of from 1 to 1000 centiStokes (cSt) at 40° C., preferably from 10 to 200 cSt, and advantageously from 30 to 80 cSt.


The polyvinyl ether (PVE) oils are preferably copolymers of the following 2 units:




embedded image


The properties of the oil (viscosity, solubility of the refrigerant and miscibility with the refrigerant in particular) can be adjusted by varying the m/n ratio and the sum m+n. The preferred PVE oils are those which have 50 to 95% by weight of units 1.


According to one preferred embodiment of the invention, the lubricant represents between 10 and 50%, inclusive, by weight of the composition.


The refrigerant F may also comprise additives such as odorous compounds.


A subject of the present invention is also the use of the abovementioned composition in refrigeration, in particular domestic or commercial refrigeration, cold rooms, the food industry, the processing industry, refrigerated transport (trucks, boats); air conditioning, in particular domestic, commercial or industrial air conditioning, where the appliances used are chillers or direct expansion appliances; and heat pumps, in particular medium- and high-temperature heat pumps.


By virtue of their low glide temperature, the compositions according to the present invention can be used both in equipment with dry-expansion evaporators and in equipment with evaporators operating in a flooded system.


EXPERIMENTAL SECTION

The thermal stability trials are carried out according to standard ASHRAE 97-2007: “sealed glass tube method to test the chemical stability of materials for use within refrigerant systems”.


The test conditions are as follows:


weight of refrigerant: 2.2 g


weight of lubricant: 5 g


temperature: 200° C.


duration: 14 days


The lubricant is introduced into a 42.2 ml glass tube. The tube is then evacuated under vacuum and then the refrigerant F is added thereto. The tube is then welded in order to close it and placed in an oven at 200° C. for 14 days.


At the end of the test, various analyses are carried out:

    • the gas phase is recovered in order to be analysed by gas chromatography: the main impurities were identified by GC/MS (gas chromatography coupled with mass spectrometry). The impurities coming from the refrigerant F and those coming from the lubricant can thus be combined;
    • the lubricant is analysed: colour (by spectrocolorimetry, Labomat DR Lange LIC220 Model MLG131), water content (by Karl Fischer coulometry, Mettler DL37) and acid number (by quantitative determination with 0.01N methanolic potassium hydroxide). 3 commercial lubricants were tested: the PAG ND8 oil, the POE Ze-GLES RB68 oil and the PVE FVC 68D oil.
















PAG ND8
POE Ze-GLES RB68
PVE FVC 68D














Trans-HFO-

Trans-HFO-
Trans-HFO-


Refrigerant
HFC-134a
1234ze
HFC-134a
1234ze
1234ze





By-products in







the gas phase:



















from the
100
ppm
4000 ppm +
100
ppm
500 ppm +
3% + 1800 ppm












refrigerant

6000 ppm

1500 ppm
(HFO-1234yf)




(HFO-1234yf)

(HFO-1234yf)














from the
1.5%
2%
500
ppm
800 ppm
2%












lubricant







Analysis of the







lubricant:






















colour
400
Hazen
17
Gardner
300
Hazen
300
Hazen
6
Gardner


water content
1200
ppm
1100
ppm
160
ppm
500
ppm
500
ppm


acid number
1.5
mg KOH/g
10
mg KOH/g
0.3
mg KOH/g
0.6
mg KOH/g
1.1
mg KOH/g





It is noted that trans-HFO-1234ze in the presence of POE or PVE improves the stability of the lubricant. In addition, in the presence of POE, the stability of the refrigerant is also improved.






Applications


Thermodynamic performance of the systems using the mixtures in question


Calculation Tools


The RK-Soave equation is used for the calculation of the densities, enthalpies, entropies and the liquid-vapour equilibrium data of the mixtures. The use of this equation requires knowledge of the properties of the pure substances used in the mixtures in question and also the coefficients of interaction for each binary combination.


The data necessary for each pure substance are:


boiling point, critical pressure and temperature, curve of pressure as a function of temperature starting from the boiling point to the critical point, saturated liquid and saturated vapour densities as a function of temperature.


The data on HFCs are published in the ASHRAE Handbook 2005 chapter 20 and are also available under Refrop (software developed by NIST for calculating the properties of refrigerants).


The HFO temperature-pressure curve data are measured by the static method. The critical pressure and temperature are measured using a C80 calorimeter sold by Setaram. The densities, at saturation as a function of temperature, are measured by means of the vibrating tube densimeter technology developed by the laboratories of the dcole des Mines de Paris [French Engineering School].


Coefficient of Binary Interaction:


The RK-Soave equation uses coefficients of binary interaction to represent the behaviour of products in mixtures. The coefficients are calculated according to experimental liquid-vapour equilibrium data.


The technique used for the liquid-vapour equilibrium measurements is the static analytical cell method. The equilibrium cell comprises a sapphire tube and is equipped with two Rolsitm electromagnetic samplers. It is immersed in a cryothermostat bath (Huber HS40). Magnetic stirring driven by a magnetic field rotating at a variable speed is used to accelerate the reaching of the equilibria. The sample analysis is carried out by gas chromatography (HP5890 series II) using a katharometer (TCD).


HFC-134a/Trans-HFO-1234ze


The liquid-vapour equilibrium measurements on the HFC-134a/trans-HFO-1234ze binary combination are carried out for the following isotherm: 20° C.


Compression System


Consider a compression system equipped with an evaporator, a condenser, a liquid-vapour exchanger (internal exchanger), a screw compressor and a pressure regulator.


The system operates with 15° C. of overheat and an internal exchanger between the outlets of the condenser and of the evaporator.


The isentropic efficiency of the compressors depends on the compression ratio. This efficiency is calculated according to the following equation:










η
isen

=

a
-


b


(

τ
-
c

)


2

-

d

τ
-
e







(
1
)







For a screw compressor, the constants a, b, c, d and e of the isentropic efficiency equation (1) are calculated according to the standard data published in the “Handbook of air conditioning and refrigeration, page 11.52”.


The coefficient of performance (COP) is defined as being the useful power supplied by the system over the power provided or consumed by the system.


The Lorenz coefficient of performance (COPLorenz) is a reference coefficient of performance. It depends on temperatures and is used to compare the COPs of the various refrigerants.


The Lorenz coefficient of performance is defined as follows:


(the temperatures T are in K)

Taveragecondenser=Tinletcondenser−Toutletcondenser  (2)
Taverageevaporator=Toutletevaporator−Tinletevaporator  (3)


The Lorenz COP in the case of conditioned air and refrigeration:









COPlorenz
=


T
average
evaporator



T
average
condensor

-

T
average
evaporator







(
4
)







The Lorenz COP in the case of heating:









COPlorenz
=


T
average
condensor



T
average
condensor

-

T
average
evaporator







(
5
)







For each composition, the coefficient of performance of the Lorenz cycle is calculated as a function of the corresponding temperatures.


The % COP/COPLorenz is the ratio of the COP of the system relative to the COP of the corresponding Lorenz cycle.


Results in Cooling Mode


In cooling mode, the compression system operates between an evaporation temperature of −5° C. and a condensation temperature of 50° C.


The values of the constituents (HFC-134a, trans-HFO-1234ze) for each composition are given as percentage by weight.























Temp
Temp

T









evap
comp
T
pressure

























inlet
outlet
condensation
regulator
Evap P
Cond P
Ratio

Comp
%
% COP/


Cooling mode
(° C.)
(° C.)
(° C.)
inlet
(bar)
(bar)
(w/w)
Glide
efficiency
CAP
COPLorenz





HFO-1234ze
−5
73
50
42
1.8
10.0
5.6
0.00
74.8
100
54



















HFO-1234ze
HFC-134a













 5
95
−5
81
50
42
2.4
13.1
5.4
0.03
75.9
136
56


10
90
−5
81
50
42
2.4
13.0
5.4
0.07
75.8
135
55


20
80
−5
80
50
42
2.3
12.8
5.5
0.16
75.6
131
55


30
70
−5
79
50
42
2.3
12.6
5.5
0.26
75.3
128
55


40
60
−5
79
50
42
2.2
12.3
5.6
0.34
75.1
124
54


50
50
−5
78
50
42
2.1
12.0
5.6
0.40
74.9
120
54


60
40
−5
78
50
42
2.1
11.7
5.7
0.44
74.7
116
54


70
30
−5
77
50
42
2.0
11.3
5.7
0.43
74.6
112
54


80
20
−5
76
50
42
1.9
10.9
5.7
0.37
74.5
108
54


90
10
−5
75
50
42
1.8
10.5
5.7
0.24
74.6
104
54


95
 5
−5
74
50
42
1.8
10.3
5.7
0.14
74.6
102
54









Results in Heating Mode


In heating mode, the compression system operates between an evaporation temperature of −5° C. and a condensation temperature of 50° C.


The values of the constituents (HFC-134a, trans-HFO-1234ze) for each composition are given as percentage by weight.























Temp
Temp

T









evap
comp
T
pressure

























inlet
outlet
condensation
regulator
Evap P
Cond P
Ratio

Comp
%
% COP/


Heating mode
(° C.)
(° C.)
(° C.)
inlet
(bar)
(bar)
(w/w)
Glide
efficiency
CAP
COPLorenz





HFO-1234ze
−5
73
50
42
1.8
10.0
5.6
0.00
74.8
100
62



















HFO-1234ze
HFC-134a













 5
95
−5
81
50
42
2.4
13.1
5.4
0.03
75.9
136
63


10
90
−5
81
50
42
2.4
13.0
5.4
0.07
75.8
135
63


20
80
−5
80
50
42
2.3
12.8
5.5
0.16
75.6
131
63


30
70
−5
79
50
42
2.3
12.6
5.5
0.26
75.3
128
63


40
60
−5
79
50
42
2.2
12.3
5.6
0.34
75.1
124
62


50
50
−5
78
50
42
2.1
12.0
5.6
0.40
74.9
120
62


60
40
−5
78
50
42
2.1
11.7
5.7
0.44
74.7
116
62


70
30
−5
77
50
42
2.0
11.3
5.7
0.43
74.6
112
62


80
20
−5
76
50
42
1.9
10.9
5.7
0.37
74.5
108
62


90
10
−5
75
50
42
1.8
10.5
5.7
0.24
74.6
104
62


95
 5
−5
74
50
42
1.8
10.3
5.7
0.14
74.6
102
62








Claims
  • 1. A composition comprising at least one lubricant comprising at least one polyol ester or at least one polyvinyl ether and a refrigerant comprising from 5 to 10% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze),from 5 to 50% by weight of 1,1,1,2-tetrafluoroethane, andat least one selected from the group of hydrofluorocarbons and hydrofluoroolefins, wherein the at least one selected from the group of hydrofluorocarbons and hydrofluoroolefins includes 2,3,3,3-tetrafluoropropene.
  • 2. The composition according to claim 1, wherein the refrigerant further comprises a hydrofluorocarbon.
  • 3. The composition according to claim 1, wherein the refrigerant comprises: from 5 to 10% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze),from 5 to 40% by weight of 1,1,1,2-tetrafluoroethane, andat least one selected from the group of hydrofluorocarbons and hydrofluoroolefins, wherein the at least one selected from the group of hydrofluorocarbons and hydrofluoroolefins includes 2,3,3,3-tetrafluoropropene.
  • 4. The composition according to claim 1, wherein the refrigerant comprises: from 5 to 10% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze),from 10 to 30% by weight of 1,1,1,2-tetrafluoroethane, andat least one selected from the group of hydrofluorocarbons and hydrofluoroolefins, wherein the at least one selected from the group of hydrofluorocarbons and hydrofluoroolefins includes 2,3,3,3-tetrafluoropropene.
  • 5. The composition according to claim 1, wherein the refrigerant comprises: from 5 to 10% by weight of trans-1,3,3,3-tetrafluoropropene (trans-HFO-1234ze),from 20 to 30% by weight of 1,1,1,2-tetrafluoroethane, andat least one selected from the group of hydrofluorocarbons and hydrofluoroolefins, wherein the at least one selected from the group of hydrofluorocarbons and hydrofluoroolefins includes 2,3,3,3-tetrafluoropropene.
  • 6. The composition according to claim 1, wherein the at least one lubricant comprises at least one polyol ester, wherein the at least one polyol ester is obtained from a polyol having a neopentyl backbone.
  • 7. The composition according to claim 6, wherein the polyol having a neopentyl backbone is selected from the group consisting of neopentyl glycol, trimethylolpropane, and dipentaerythritol.
  • 8. The composition according to claim 1, wherein the at least one lubricant comprises at least one polyol ester, wherein the at least one polyol ester is obtained from a linear or branched carboxylic acid containing from 2 to 15 carbon atoms.
  • 9. The composition according to claim 1, wherein the at least one lubricant comprises at least one polyol ester, wherein the at least one polyol ester is between 10 and 50% by weight of the composition.
  • 10. The composition according to claim 1, wherein the polyvinyl ether represents between 10 and 50% by weight of the composition.
  • 11. The composition according to claim 1, wherein the at least one lubricant comprises at least one polyvinyl ether, wherein the polyvinyl ether is a copolymer of the following two units:
  • 12. The composition according to claim 11, wherein the polyvinyl ether has from 50 to 95% by weight of Unit 1.
  • 13. The composition according to claim 1, wherein out of the total wt % of trans-HFO-1234ze and 1,1,1,2-tetrafluoroethane, trans-HFO-1234ze contributes an amount of 20-30% by weight and 1,1,1,2-tetrafluoroethane contributes an amount of 70-80% by weight.
Priority Claims (1)
Number Date Country Kind
10.57483 Sep 2010 FR national
CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. application Ser. No. 16/143,505, filed on Sep. 27, 2018, which is a continuation of U.S. application Ser. No. 13/232,106, filed on Sep. 14, 2011, now U.S. Pat. No. 10,119,056, which claims the benefit of French Application No. 10.57483, filed on Sep. 20, 2010. The entire contents of each of U.S. application Ser. No. 16/143,505, U.S. application Ser. No. 13/232,106 and French Application No. 10.57483 are hereby incorporated herein by reference in their entirety.

US Referenced Citations (43)
Number Name Date Kind
5202044 Hagihara et al. Apr 1993 A
5452586 Hamid Sep 1995 A
8951432 Boutier et al. Feb 2015 B2
9005468 Rached Apr 2015 B2
9315706 Boussand Apr 2016 B2
9512343 Rached et al. Dec 2016 B2
9574124 Rached Feb 2017 B2
9683154 Rached Jun 2017 B2
10029963 Bonnet et al. Jul 2018 B2
10119056 Rached et al. Nov 2018 B2
10266465 Bonnet et al. Apr 2019 B2
10308854 Rached Jun 2019 B2
10450489 Rached Oct 2019 B2
10759983 Rached Sep 2020 B2
10858564 Rached Dec 2020 B2
20050245421 Singh et al. Nov 2005 A1
20060243944 Minor et al. Nov 2006 A1
20080099190 Singh et al. May 2008 A1
20080111099 Singh et al. May 2008 A1
20100038582 Shimomura et al. Feb 2010 A1
20100038583 Shimomura et al. Feb 2010 A1
20100122545 Minor et al. May 2010 A1
20110023507 Yana Motta et al. Feb 2011 A1
20120068104 Rached et al. Mar 2012 A1
20120068105 Rached et al. Mar 2012 A1
20120272668 Van Horn et al. Nov 2012 A1
20130055733 Rached Mar 2013 A1
20130055739 Rached Mar 2013 A1
20130061613 Rached Mar 2013 A1
20130299733 Boussand Nov 2013 A1
20140110623 Boutier et al. Apr 2014 A1
20150013942 Minor Jan 2015 A1
20150184051 Rached Jul 2015 A1
20160031773 Bonnet et al. Feb 2016 A1
20160032165 Boussand Feb 2016 A1
20160215193 Low Jul 2016 A1
20170037291 Rached et al. Feb 2017 A1
20180079943 Rached Mar 2018 A1
20180312453 Bonnet et al. Nov 2018 A1
20190023956 Rached et al. Jan 2019 A1
20190233700 Rached Aug 2019 A1
20190375971 Rached Dec 2019 A1
20220389298 Minor Dec 2022 A1
Foreign Referenced Citations (32)
Number Date Country
2094856 Oct 1993 CA
0913457 May 1999 EP
0913457 Jul 1999 EP
1227108 Jul 2002 EP
2138558 Dec 2009 EP
H04110388 Apr 1992 JP
H06145104 May 1994 JP
H08104896 Apr 1996 JP
H08503975 Apr 1996 JP
H09302370 Nov 1997 JP
H11228984 Aug 1999 JP
2006291142 Oct 2006 JP
2007538115 Dec 2007 JP
2008544072 Dec 2008 JP
2016103039 Jun 2016 JP
9324585 Dec 1993 WO
WO 2004037913 May 2004 WO
2004037913 Jan 2005 WO
2005108522 Nov 2005 WO
2006094303 Sep 2006 WO
2007002625 Jan 2007 WO
2007002625 May 2007 WO
2006094303 Jun 2007 WO
2007126414 Nov 2007 WO
2007126414 Jan 2008 WO
2008105256 Sep 2008 WO
2008105366 Sep 2008 WO
2010083100 Jul 2010 WO
2010129920 Nov 2010 WO
WO 2010129920 Nov 2010 WO
2011101620 Aug 2011 WO
2011101622 Aug 2011 WO
Non-Patent Literature Citations (1)
Entry
Japanese Office Action and English-language (machine) translation issued in JP 2016-103039, dated Jun. 6, 2017, Japanese Intellectual Property Office, Tokyo, JP, 4 pages.
Related Publications (1)
Number Date Country
20200339855 A1 Oct 2020 US
Continuations (2)
Number Date Country
Parent 16143505 Sep 2018 US
Child 16927242 US
Parent 13232106 Sep 2011 US
Child 16143505 US