Actuator device, actuation method and manufacturing method
11274253 · 2022-03-15
Assignee
Inventors
- Johan Lub (Valkenswaard, NL)
- NICOLAAS PETRUS WILLARD (VALKENSWAARD, NL)
- Cornelis Petrus Hendriks (Eindhoven, NL)
- Karel Johannes Adrianus VAN DEN AKER (LIEMPDE, NL)
Cpc classification
F03G7/005
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C09K2019/3425
CHEMISTRY; METALLURGY
F03G7/06
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F03G7/009
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C09K19/2007
CHEMISTRY; METALLURGY
C09K2019/0448
CHEMISTRY; METALLURGY
F03G7/016
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F03G7/0613
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
B32B2307/40
PERFORMING OPERATIONS; TRANSPORTING
C09K19/24
CHEMISTRY; METALLURGY
C09K2219/00
CHEMISTRY; METALLURGY
C09K2019/0425
CHEMISTRY; METALLURGY
B29C70/00
PERFORMING OPERATIONS; TRANSPORTING
C09K2019/0437
CHEMISTRY; METALLURGY
International classification
F03G7/00
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C09K19/20
CHEMISTRY; METALLURGY
C09K19/04
CHEMISTRY; METALLURGY
C09K19/24
CHEMISTRY; METALLURGY
F03G7/06
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
H02N11/00
ELECTRICITY
C09K19/54
CHEMISTRY; METALLURGY
B29C70/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
An actuator device comprises a stack formed from a plurality of photoresponsive layers, which deform in response to light, which are partitioned by respective deformable non-photoresponsive layers. The deformable non-photoresponsive layers guide light between and to the photoresponsive layers, and can follow the deformation of the photoresponsive layers.
Claims
1. An actuator device comprising: a plurality of photoresponsive layers, wherein the plurality of photoresponsive layers deform in response to incident light; a deformable non-photoresponsive layer positioned at least partly between each adjacent pair of the plurality of photoresponsive layers, wherein the plurality of photoresponsive layers and the deformable non-photoresponsive layers are arranged in a stack, and wherein each deformable non-photoresponsive layer guides light between and to the plurality of photoresponsive layers; and a mechanical coupling disposed on at least one side of the stack in a stacking direction, wherein the mechanical coupling integrates one or more light sources, and wherein the one or more light sources are arranged to provide the incident light.
2. The actuator device as claimed in claim 1, wherein each of the plurality of photoresponsive layers comprises at least one liquid crystalline component and at least one photoresponsive group.
3. The actuator device as claimed in claim 2, wherein the at least one photoresponsive group is at least one of cinnamic acid-derived, cinnamylidene-derived, spiropyran-derived, and azobenzene-derived groups.
4. The actuator device as claimed in claim 1, wherein the thickness of each photoresponsive layer is 1 to 50 microns.
5. The actuator device as claimed in claim 1, wherein the mechanical coupling fixes the relative positions of the plurality of photoresponsive layers and the deformable non-photoresponsive layers in the stacking direction, and wherein the mechanical coupling allows contraction and expansion of the stack.
6. The actuator device as claimed in claim 5, wherein the mechanical coupling comprises a polymer, and wherein the polymer is an acrylate polymer.
7. The actuator device as claimed in claim 1, wherein the mechanical coupling fixes the relative positions of the plurality of photoresponsive layers and the deformable non-photoresponsive layers in the stacking direction, and wherein the mechanical coupling allows bowing of the stack.
8. The actuator device as claimed in claim 7, wherein the mechanical coupling comprises a polymer.
9. The actuator device as claimed in claim 8, wherein the polymer is an acrylate polymer.
10. The actuator device as claimed in claim 1, wherein each photoresponsive layer of the plurality of photoresponsive layers comprises a liquid crystalline component, and wherein the liquid crystalline component is curable.
11. The actuator device as claimed in claim 1, wherein the deformable non-photoresponsive layer comprises a polymer or rubber.
12. The actuator device as claimed in claim 1, wherein one or more other light sources are provided at the top and bottom of the stack of the plurality of photoresponsive layers and the deformable non-photoresponsive layers.
13. The actuator device as claimed in claim 1, wherein a photoresponsive layer of the plurality of photoresponsive layers comprises an acrylate functionalized liquid crystalline component.
14. The actuator device as claimed in claim 1, wherein the one or more light sources are provided at said at least one side of the stack of the plurality of photoresponsive layers and the deformable non-photoresponsive layers.
15. A method of manufacturing an actuator device, the method comprising: providing a plurality of photoresponsive layers, wherein the plurality of photoresponsive layers deform in response to incident light; disposing a respective deformable non-photoresponsive layer at least partly between each adjacent pair of the plurality of photoresponsive layers, wherein the plurality of photoresponsive layers and the deformable non-photoresponsive layers are arranged in a stack, wherein each deformable non-photoresponsive layer guides light between and to the plurality of photoresponsive layers, wherein a mechanical coupling is disposed on at least one side of the stack in a stacking direction, wherein the mechanical coupling integrates one or more light sources, and wherein the one or more light sources are arranged to provide the incident light.
16. The method as claimed in claim 15, further comprising: stacking the plurality of photoresponsive layers between interlamellar spacers; filling the interlamellar spaces with at least one curable material; and curing the at least one curable material.
17. The method as claimed in claim 15, further comprising: coating the plurality of photoresponsive layers with at least one curable material; stacking the coated plurality of photoresponsive layers; and curing the at least one curable material.
18. The method as claimed in claim 15, further comprising: stacking the plurality of photoresponsive layers between interlamellar spacers, wherein the stack has one or more sides; filling the interlamellar spaces, and coating at least one of the one or more sides of the stack, with at least one curable material; and curing the at least one curable material.
19. The method as claimed in claim 15, further comprising: coating the plurality of photoresponsive layers with at least one curable material, wherein the stack has one or more sides; stacking the coated plurality of photoresponsive layers, and coating at least one of the one or more sides of the stack with the at least one curable material; and curing the at least one curable material.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) Examples of the claimed device will now be described in detail with reference to the accompanying schematic drawings, in which:
(2)
(3)
(4)
(5)
DETAILED DESCRIPTION OF THE EMBODIMENTS
(6) The claims define an actuator device comprising an actuation structure that can provide actuation based on the presence of a photoresponsive portion which, when it receives actuation light, can deform and a light guiding layer, i.e. a light guide for guiding and providing the actuation light to the photoresponsive layer. The actuation structure is constructed such that the photoresponsive portion is illuminated more efficiently than a photoresponsive portion of the same volume and incorporated in an actuation structure. Hence, an improved actuation output (stroke and/or strain) can be obtained with a particular volume of photoresponsive portion.
(7) Whilst the layers closer to the light source will deform more than those further away due to attenuation of the light as it passes through progressively more layers, deformable non-photoresponsive layers (light guiding layers) are provided which partition adjacent photoresponsive layers. They guide unabsorbed light between the layers and also enable light to be coupled in from the sides. They follow the deformation of the layers. Thus the greater and lesser deformations of the photoresponsive layers depending on their proximity to the light source are combined into an overall mechanically useful stack deformation. To avoid loss of the force generated by the deformation of the photoresponsive layers, the deformable non-photoresponsive layers are sufficiently deformable such that the movement of the photoresponsive layers is easily followed by the deformation of the non-photoresponsive layers.
(8) The light guiding layers may be elastically or plastically deformable. In both cases the amount of energy needed to deform any light guiding portion should be relatively low compared to the work to be performed by the photoresponsive portions.
(9) The device as claimed herein will be described with reference to the below examples.
(10) In a first example, the actuator structure 100 of
(11)
(12) The examples of
(13) Although not shown, in a similar fashion the reverse situation may also be implemented in which 301, 301′ 301″ and 301′″ form patterned photoresponsive layers while the body 302 is a light guiding layer.
(14) Another device 400 according to the invention includes a stack of layers as shown in
(15) The light guiding layers can be made of many materials as will be elucidated below.
(16)
(17)
(18) The light providing portion may be attached to the photoresponsive portions through the surfaces through which the light is provided to the photoresponsive portions. Alternatively, they may not be attached. This provides moveability. For example in the configurations of
(19) In the examples above, preferably the light source, or a plurality of light sources is located in the mechanical couplings so that light form these sources can be provided to the light guiding layers which act as light guides to distribute the light and provide it to the photoresponsive portion and sub-portions of the stack. The light guiding portions may have light scattering properties if operating as light guide. Hence, scattered light entering the light guiding layers form a source are guided and scattered to exit the light guiding layer towards or into the photoresponsive portions. Light guiding layers or portions/sub-portions are thus preferably made from light scattering materials such as opaque materials. One example is siloxane or silicone rubber. Other compliant layers can be used.
(20)
(21) In one set of examples, the structure may be designed to avoid bowing and provide a linear, in-plane, actuation by constraining the layers so that they cannot deform out of plane. Thus, the examples above show light-induced deformation in one direction but this should not be construed as limiting the stack to only such deformations in one in-plane dimension. If the layers are not attached to each other in the stacking direction, sliding can happen and optimized force output realized as described herein before. No compliant material needs to be used in such cases as the light providing layers do not need to comply with the actuation induced shape or size change induced by the photoresponsive portion.
(22) Alternatively,
(23) To induce the bowing behavior, the photoresponsive layers are coated with a light absorbing (black) layer 910 on one side. This means the photoresponsive layers 901 (which in this example could be thicker than 30 micrometers) can only be irradiated from one face (e.g. from above in the configuration shown in
(24) In
(25) Alternatively, the bowing shown in
(26) The mechanical couplings 103 may also be used to couple light laterally into the photoresponsive layers, to improve the uniformity of illumination, and thereby reduce internal stresses, increase the conversion efficiency and, if desired, reduce the tendency for the structure to bow rather than expand or contract linearly.
(27) One way to provide lateral light coupling is to provide light from the top and/or bottom, and to use the mechanical couplings as reflectors for redirecting the light from the stacking direction to the lateral direction. A prism shaped structure as shown in e.g
(28) Alternatively, there may be light sources mounted at the edges of the stack (as shown in
(29) The light may be provided by a local light source which is part of the actuator device, for example as shown in
(30) The light guiding portions (e.g. the layers) in an actuator structures may have the same or different dimensions (e.g. thickness). Preferably the dimensions (e.g. 104 and 105, or 205 and 204 or 304 and 306), which may be thicknesses in case of layers, are in the range 1 micron to 50 microns. Photoresponsive layers or films of such dimensions can shrink (and expand) effectively.
(31) For example, the dimension of a photoresponsive portion may be between 1 and 10 microns. In case of unsubstituted azobenzene based photoresponsive materials (e.g. Formula 4) or photoresponsive materials with comparable extinction at the actuation wavelength, this dimension may be 5 microns as this provides a favorable balance between providing effective shrinking (and expanding) behavior whilst allowing unabsorbed light to pass to other photoresponsive layers of the stack.
(32) Alternatively, a photoresponsive portion with a thickness of 30 to 50 microns may be employed if bowing is preferred over linear expansion and contraction. Also, if extinction is reduced at the actuation wavelength, then thicker portions of photoresponsive portions can be used. This will increase mechanical output of a device and improve to facilitate manufacturability.
(33) The thickness of a light guiding portion or sub-portion may be, for example, between 5 and 20 microns. A dimension in this range results in a deformable light guiding layers which is sufficiently thin to follow easily the deformations of the photoresponsive layers whilst being sufficiently thick to guide light between and to the photoresponsive layers.
(34) The number of photoresponsive layers in the stack may be between 2 and 50, for example between 2 and 30 or for example between 2 and 20. Thus the height of the stack may be between 3 microns and about 1 mm.
(35) For example, for a stack comprising 10 photoresponsive layers with a 10 micron thickness with a deformable non-photoresponsive layer thickness of 20 microns, the height of the stack is 0.3 mm.
(36) The length and breadth of the stack is dependent upon the intended application and as such these dimensions may range from the order of millimeters to centimeters.
(37) It will be clear from the Figs. that the shape of the mechanical couplings is not especially limited and can be, for instance, prismatic or cuboidal. The mechanical couplings may comprise a connection which extends in the stacking direction to connect all of the layers in the stack, so that the deformations of the individual actuators are combined in a total deformation of the stack. In this way, the mechanical coupling fixes the relative positions in the stacking direction, but allows contraction and expansion, or bowing of the stack.
(38) Alternatively, or additionally, the light guiding portions/sub-portions and photoresponsive portions/sub-portions may be mechanically connected to each other via their interface either directly or through additional layers. This may for example be done using glue.
(39) Without wanting to be bound by theory, in the example where the portions are layers such that there is a stack of a light guiding (light guide) layer and a photoresponsive layer and both are elastically deformable, the elastic modulus of the light guiding layer (E1) is preferably equal to or lower than the elastic modulus of the photoresponsive layer (E2). The modulus of the light guiding layer (E1) can be related to the modulus of the photoresponsive layer (E2) according to Equation 1:
E1=<k*E2*(d.sub.1/(d.sub.1+d.sub.2)) Equation 1
Where d.sub.1 and d.sub.2 respectively correspond to the thickness of the photoresponsive layer and light guiding layer and where k is a constant factor. Preferably, k is equal to or smaller than a value chosen from the group consisting of: 1, 0.5, 0.25, 0.1, or 0.05. A preferred value of k is 0.1. For example, for a photoresponsive layer with an elastic modulus in the order of 1000 MPa, a suitable value for the elastic modulus of the light guiding layer is then in the order of 100 MPa. An elastic modulus of 100 MPa corresponds to a hardness of 60 ShoreA in the case of a silicone elastomer material.
(40) Assuming that the elastic modulus of the deformable light guiding layer is very low (so that we may neglect it in calculations) the maximum force (F) that can be exerted by the combined layers of the stack may be approximated by (Equation 2):
F=ΦnA{d.sub.1/(d.sub.1+d.sub.2)} Equation 2
Where Φ is the stress of the photoresponsive layer, n is the number of photoresponsive layers, A is the cross-sectional area of the total multilayer stack and d.sub.1 and d.sub.2 correspond to the thickness of the photoresponsive layer and light guiding layers respectively.
(41) A photoresponsive group of a photoresponsive portion responds to light by exhibiting an effect which may be on a molecular level such as a light-induced isomerization or chemical reaction such as e.g. a chemical dimerization. An isomerization means that the elemental composition of the photoresponsive group is unchanged but the spatial arrangement of the atoms of the molecule changes on undergoing this process. This isomerization or reaction may change the shape of the molecule(s) which can alter the arrangement/ordering of species immediately surrounding and/or attached to the involved molecule(s) In this way the molecular response of the photoresponsive group(s) to actuation light triggers a macroscopic structural change/deformation of the photoresponsive portion.
(42) The effect of light on an azobenzene-derived group may be the well-known isomerization of the molecule between cis and trans isomers; these isomers differing in respect to the arrangement of aryl rings either side of the N═N double bond. The more stable trans isomer of an azobenzene-derived group is converted to the cis isomer upon irradiation with UV or near-UV (blue) light (Equation 3 below) and
(43) ##STR00001##
(44) It is the so called n−π* transition with associated wavelength range that is responsible for the E-Z isomerisations.
(45) The photoresponsive portion/sub-portion may for example comprise at least one liquid crystalline component. Such materials are useful for turning light into mechanical action since the effect of the physical change of the photoresponsive group (such as photoisomerization) may influence the order/alignment of the liquid crystalline component(s) resulting in significant macroscopic deformation of the photoresponsive portion. US2008264058 describes such materials and how they are actuated and these materials can be used in the invention. Polymeric liquid crystalline components, also known as liquid crystalline elastomers, derived from liquid crystalline components which are curable, are useful for photoactuation since the mesogenic ordering of the liquid crystalline components can be combined with the elastic characteristics of a polymer network making for large and reversible anisotropic deformations.
(46) Curable liquid crystalline components are well-known per se and may comprise a mesogenic group connected to a curable group via a spacer. Mesogenic groups are well known per se. The mesogenic group may be, for example, a phenyl benzoate-derived group. Curable groups are similarly well-known; for example suitable curable groups may be acrylate groups. One or more curable groups, such as acrylate groups may be used in the curable liquid crystalline component. Spacer groups are also well-known; suitable examples may be alkyl or polymethylene ((CH.sub.2).sub.n) groups.
(47) Molecules comprising mesogenic group connected to a curable group via a spacer are well-known per se. Non-limiting examples of a curable liquid crystalline component which may be used in the photoresponsive layers of the stack are compounds according to Formulae 1 to 3:
(48) ##STR00002##
(49) Acrylate-functionalized curable liquid crystalline components such as compounds according to Formulae 1 to 3 display effective mesogenic properties due to a linear rod-like structure and the acrylate group(s) may be employed in polymerization/cross-linking reactions with other curable components such as other curable liquid crystalline components. Also polymerization/cross-linking reactions may occur between the curable liquid crystalline component, such as a compound according to Formulae 1 to 3 and/or the polymers therefrom, with curable polymeric or monomeric photoresponsive groups.
(50) The term photoresponsive group is intended to mean a chemical group or moiety which responds to light. The photoresponsive group responds to light by exhibiting a physical change. The at least one photoresponsive group may be incorporated as part of the at least one liquid crystalline component and/or may be employed separately from the liquid crystalline component. The terms ‘incorporated as part of’ and ‘employed separately from’ can be interpreted to mean that chemical bonds respectively join or do not join the photoresponsive group to the liquid crystalline component. The photoresponsive group may itself have mesogenic or liquid crystalline properties such that it can also be a liquid crystalline component. This physical change of the photoresponsive group when illuminated may influence the ordering/alignment of the at least one liquid crystalline component in order to effect a macroscopic change/deformation of the photoresponsive layer.
(51) A photoresponsive group which is curable permits the photoresponsive group to be polymerized or cross-linked, and it may be attached to another curable group. This can be achieved by the photoresponsive group being functionalized with at least one curable group such as an acrylate group. The photoresponsive group may be connected to the curable group using a spacer group such as an alkyl or polymethylene (—(CH.sub.2).sub.n) group. A suitable photoresponsive group may be azobenzene-derived hence a suitable curable photoresponsive group may be an acrylate-functionalized azobenzene-derived group.
(52) Curable photoresponsive groups comprising a photoresponsive group connected to a curable group via spacer group are well-known per se. A non-limiting example of such a curable photoresponsive group which may be used in the photoresponsive portions of the invention is a compound according to Formula 4:
(53) ##STR00003##
Where q is the number of methylene groups in the spacer group. For example, q may be equal to 3 or 6.
The diacrylate-functionalized azobenzene-derived curable photoresponsive group according to Formula 4 may itself display mesogenic properties due to its linear rod-like structure. In a non-limiting example, the acrylate groups of the curable photoresponsive group according to Formula 4 may be employed in polymerization/cross-linking reactions with other curable components such as other curable photoresponsive groups, for example other curable photoresponsive groups according to Formula 4 or the homopolymers therefrom.
(54) The photoresponsive layer may be prepared by preparing a mixture of the curable liquid crystalline component, such as one or more of the compounds according to Formulae 1 to 3, and the photoresponsive group, such as a molecule according to Formula 4, aligning the mesogenic groups of the liquid crystalline component, for example using parallel rubbed surfaces, and polymerizing or curing the mixture. The method of polymerization is not especially limited and may be carried out photochemically, thermally, catalytically etc.
(55) The resulting photoresponsive layer may comprise one or more of a photoresponsive group which is curable such as an acrylate-functionalized azobenzene-derived group, a homopolymer of a curable photoresponsive group, a copolymer of a curable photoresponsive group with a curable liquid crystalline component, a copolymer comprising a homopolymer of a curable photoresponsive group and a curable liquid crystalline component, and a copolymer comprising a homopolymer of a curable photoresponsive group with a homopolymer of a curable liquid crystalline component.
(56) The homopolymer or polymer of a photoresponsive group can be formed by polymerizing or cross-linking (also called curing) two or more of the curable photoresponsive groups. In an example, the curable photoresponsive group is incorporated as part of the liquid crystalline component hence a homopolymer of a curable photoresponsive group would advantageously provide photoresponsive properties, the molecular ordering/alignment properties of liquid crystals combined with the elastic properties of an elastomeric polymer network.
(57) Alternatively, the copolymer of a curable photoresponsive group and a curable liquid crystalline component can be formed by copolymerizing or cross-linking (also called curing) one or more of the curable photoresponsive group(s) with one or more of the curable liquid crystalline component(s). The curable photoresponsive group is thereby connected to the liquid crystalline component which may advantageously enhance the effect of the light-induced response of the photoresponsive group on the molecular ordering/alignment properties of liquid crystals and hence on the macroscopic deformation of the photoresponsive layer. Furthermore, the copolymer also favorably includes the elastic properties of an elastomeric polymer network.
(58) Alternatively, the copolymer comprising a homopolymer of a curable photoresponsive group and a curable liquid crystalline component can be formed by copolymerizing or cross-linking (also called curing) at least one of the homopolymers of the curable photoresponsive group(s) with at least one of the curable liquid crystalline component(s). The homopolymer of the curable photoresponsive group is thereby connected to the liquid crystalline component which may advantageously enhance the effect of the light-induced response of the photoresponsive group on the molecular ordering/alignment properties of liquid crystals and hence on the macroscopic deformation of the photoresponsive layer. Furthermore, the copolymer also favorably includes the elastic properties of an elastomeric polymer network.
(59) Alternatively, the copolymer comprising a homopolymer of a curable photoresponsive group and a homopolymer of a curable liquid crystalline component can be formed by copolymerizing or cross-linking (also called curing) at least one of the homopolymers of the curable photoresponsive group(s) with at least one of the homopolymers of the curable liquid crystalline component(s). The homopolymer of the curable photoresponsive group is thereby connected to the homopolymer of the liquid crystalline component which may advantageously enhance the effect of the light-induced response of the photoresponsive group on the molecular ordering/alignment properties of liquid crystals and hence on the macroscopic deformation of the photoresponsive layer. Furthermore, the copolymer also favourably includes the elastic properties of an elastomeric polymer network.
(60) The stack may be used as a single actuator, or else there may be a line or array of the stacks, for example to provide control of a 2D or 3D contour. Such actuator devices may find application in flexible foils for fluidics, catheters, actuators for drug delivery, soft robotics in cushions or garments (such as active pressure stockings) which can give mechanical support to elderly or disabled persons or to help and guide physiotherapy or help to prevent pressure ulcers. Other possible applications are in products which use UV LEDs, for instance oral healthcare (curing of teeth whitening coatings) and photodynamic therapy (for treating psoriasis, acne). Such devices may also be used in photo-catalytic oxidation applications (water and air purification).
(61) The present invention further relates to the fabrication of the stack. In a non-limiting example, the photoresponsive layers or films are prepared in 10 micron cells in which parallel rubbed surfaces are filled with a mixture of the curable liquid crystalline component according to Formula 1 and the photoresponsive group according to Formula 2. After alignment and photopolymerization with the aid of a photo initiator, a 10 micron film is obtained which can be removed from the cell and cut into the photoresponsive layers for the stack.
(62) In one implementation, the 10 micron photoresponsive layers are stacked between 10 micron spacers. The gaps between the photoresponsive layers are then filled with a curable silicone material which can also be applied at the sides of the stack, which may assist in dividing light over several layers. Thus light is guided to the photoresponsive layers both in the stacking direction and perpendicularly to the stacking direction by light being guided via non-photoresponsive material disposed at the peripheries of the stack. The silicone material is then cured to form the silicone polymer/rubber of the deformable non-photoresponsive layers. The extremes of the stack are then connected via a mechanical coupling that is formed from acrylate monomers by thermal or photochemical polymerization.
(63) In an alternative implementation, the photoresponsive layers are coated with 10 micron of uncured silicone material by a technique such as doctor blading. The coated photoresponsive layers are then stacked followed by curing of the silicone material to form a silicone polymer/rubber. Mechanical couplings may be applied before or after curing of the silicone material.
(64) Other variations to the disclosed embodiments can be understood and effected by those skilled in the art in practicing the claimed invention, from a study of the drawings, the disclosure, and the appended claims. In the claims, the word “comprising” does not exclude other elements or steps, and the indefinite article “a” or “an” does not exclude a plurality. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs in the claims should not be construed as limiting the scope.