LOAD BEARING TRACTION MEMBERS AND METHOD
20190161321 ยท 2019-05-30
Inventors
Cpc classification
C08G18/831
CHEMISTRY; METALLURGY
B29C41/003
PERFORMING OPERATIONS; TRANSPORTING
B29C41/08
PERFORMING OPERATIONS; TRANSPORTING
C09D5/00
CHEMISTRY; METALLURGY
B66B7/06
PERFORMING OPERATIONS; TRANSPORTING
B29K2063/00
PERFORMING OPERATIONS; TRANSPORTING
B29K2075/00
PERFORMING OPERATIONS; TRANSPORTING
C08G18/10
CHEMISTRY; METALLURGY
D07B1/22
TEXTILES; PAPER
B66B9/00
PERFORMING OPERATIONS; TRANSPORTING
D07B1/16
TEXTILES; PAPER
C08K5/29
CHEMISTRY; METALLURGY
B66B7/10
PERFORMING OPERATIONS; TRANSPORTING
C08G18/10
CHEMISTRY; METALLURGY
International classification
B66B7/06
PERFORMING OPERATIONS; TRANSPORTING
C09D5/00
CHEMISTRY; METALLURGY
Abstract
Disclosed is a method of making a load-bearing traction member. According to the method, a composition including a thermoplastic polyurethane and a compound with a plurality of epoxide groups or a compound with a plurality of groups having the formula
##STR00001##
wherein R.sub.1 and R.sub.2 are each groups in a polymer backbone or together form a group having the formula NR.sub.4, wherein R.sub.3 and R.sub.4 each independently represents an organic group, is heated to a fluid state and applied to at least one tension member, and solidified to form a polymer jacket around at least one tension member
Claims
1. A method of making a load-bearing traction member, comprising heating a composition comprising a thermoplastic polyurethane, and a compound comprising a plurality of epoxide groups or a compound comprising a plurality of groups having the formula ##STR00010## wherein R.sub.1 and R.sub.2 are each groups in a polymer backbone or together form a group having the formula NR.sub.4, wherein R.sub.3 and R.sub.4 each independently represents an organic group; and applying the fluid mixture to at least one member, and solidifying the fluid composition to form a polymer jacket around the at least one tension member.
2. The method of claim 1, wherein the composition comprises a compound comprising a plurality of groups having the formula ##STR00011##
3. The method of claim 2, wherein R.sub.1 and R.sub.2 are each polymer backbone groups.
4. The method of claim 2, wherein R.sub.1 and R.sub.2 together form a group having the formula NR.sub.4.
5. The method of claim 2, wherein the composition comprises 0.1-5.0 wt. % of the compound comprising a plurality of groups having the formula ##STR00012##
6. The method of claim 1, wherein the composition comprises a compound comprising a plurality of epoxide groups.
7. The method of claim 6, wherein the composition comprises 0.05-10.00 wt. % of the compound comprising a plurality of epoxide groups.
8. The method of claim 1, wherein the composition further comprises a catalyst.
9. The method of claim 1, wherein the composition is heated to a temperature of at least 150 C.
10. The method of claim 1, wherein the composition is heated to a temperature of less than 250 C.
11. A load bearing traction member, comprising one or more tension members; and a polymer jacket comprising the reaction product of a composition comprising a thermoplastic polyurethane and a compound comprising a plurality of groups having the formula ##STR00013## wherein R.sub.1 and R.sub.2 are each groups in a polymer backbone or together form a group having the formula NR.sub.4, wherein R.sub.3 and R.sub.4 each independently represents an organic group.
12. The load bearing traction member of claim 11, wherein the composition comprises a compound comprising a plurality of groups having the formula ##STR00014##
13. The load bearing traction member of claim 12, wherein R.sub.1 and R.sub.2 are each polymer backbone groups.
14. The load bearing traction member of claim 12, wherein R.sub.1 and R.sub.2 together form a group having the formula NR.sub.4.
15. The load bearing traction member of claim 12, wherein the composition comprises 0.1-5.0 wt. % of the compound comprising a plurality of groups having the formula ##STR00015##
16. The load bearing traction member of claim 11, wherein the composition comprises a compound comprising a plurality of epoxide groups.
17. The load bearing traction member of claim 16, wherein the composition comprises 0.05-10.00 wt. % of the compound comprising a plurality of epoxide groups.
18. The load bearing traction member of claim 11, wherein the composition further comprises a catalyst.
19. An elevator system comprising the load bearing traction member of claim 11.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] The following descriptions should not be considered limiting in any way. With reference to the accompanying drawings, like elements are numbered alike:
[0018]
[0019]
[0020]
[0021]
[0022]
DETAILED DESCRIPTION
[0023] A detailed description of one or more embodiments of the disclosed apparatus and method are presented herein by way of exemplification and not limitation with reference to the Figures.
[0024] Shown in
[0025] The sheaves 18 each have a diameter 20, which may be the same or different than the diameters of the other sheaves 18 in the elevator system 10. At least one of the sheaves could be a drive sheave 26. The drive sheave 26 is driven by a machine 24. Movement of the drive sheave 26 by the machine 24 drives, moves and/or propels (through traction) the one or more belts 16 that are routed around the drive sheave 26. At least one of the sheaves 18 could be a diverter, deflector or idler sheave 18. Diverter, deflector or idler sheaves 18 are not driven by the machine 24, but help guide the one or more belts 16 around the various components of the elevator system 10.
[0026] In some embodiments, the elevator system 10 could use two or more belts 16 for suspending and/or driving the elevator car 12. In addition, the elevator system 10 could have various configurations such that either both sides of the one or more belts 16 engage the one or more sheaves 18 (such as shown in the exemplary elevator systems in
[0027]
[0028] Referring to
[0029] As mentioned above, the jacket 30 can be formed from a polymer composition that is applied in a fluid state to the cords 28 and solidified. The polymer composition comprises a thermoplastic polyurethane (TPU) as a base polymer material. TPU can be prepared from a polyaddition reaction of diisocyanates and long-chain and short-chain polyols. Various commercially-available TPU compositions can provide targeted properties including but not limited to hardness, elasticity, tensile strength, torsion modulus, tear strength, creep performance, dependence of any of the above or other properties on temperature (e.g., heat-resistance). Blends of different TPU's can be used to achieve targeted performance parameters. In some embodiments, the TPU can be characterized by a hardness of at least 75 Shore A, according to according to DIN ISO 7619-1 (3s).
[0030] The polymer composition further comprises a compound comprising a plurality of epoxide groups and/or a compound comprising a plurality of groups having the formula
##STR00006##
wherein R.sub.1 and R.sub.2 are each groups in a polymer backbone or together form a group having the formula NR.sub.4, wherein R.sub.3 and R.sub.4 each independently represents an organic group. Regarding compounds with a plurality of epoxide groups (i.e., polyepoxides), in some embodiments, the compound includes an n-functional polyepoxide (i.e., average number of epoxide groups per molecule) in which n can be a number from 2 to 8000, more specifically from 20 to 6000, and even more specifically from 200 to 4000. Examples of compounds comprising a plurality of epoxide groups include, but are not limited to epoxide derivatives of diols, triols, and other polyols such as bisphenol A diglycidyl ether, epoxide-terminated polyether pre-polymers or polymers (which can be produced by a ring opening reaction of the aforementioned epoxide groups). In some embodiments, the a polyepoxide can have the formula
##STR00007##
Other examples of polyepoxides include oligomers or polymers having a plurality of epoxide groups appended to an oligomer or polymer backbone such as acrylic oligomers or polymer including pendant epoxide groups, e.g., polyglycidyl methacrylate copolymers produced by an addition polymerization reaction of a monomer mixture comprising glycidyl methacrylate along with other (meth)acrylate monomers and optionally other addition polymerizable monomers.
[0031] Compounds having the formula
##STR00008##
include carbodiimides and polymeric carbodiimides. Examples of carbodiimides (i.e., compounds in which R.sub.1 and R.sub.2 together represent the group NR.sub.4, so that the compound has the formula R.sub.4NCNR.sub.3) include but are not limited to dicyclohexylcarbodiimide (DCC), N,N-isopropylcarbodiimide (DIC), or N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide.
[0032] Polymeric carbodiimides represent compounds in which R.sub.1 and R.sub.2 each represents a group on a polymer backbone adjacent to the imido carbon (C in the above formula) that is also on the backbone. Polymeric carbodiimides are characterized by repeat units having the formula
##STR00009##
and can be prepared by catalyzed living polymerization of the carbodiimides using titanium (IV) catalysts or other catalysts such as copper, nickel, or zirconium catalysts.
[0033] In some embodiments, the polymer composition can optionally include additional reactive components, including but not limited to polyols (e.g., diol chain extenders or higher functionality alcohol crosslinkers) or polyamines (e.g., diamine chain extenders or higher functionality amine crosslinkers) or blocked or unblocked polyisocyanates. Diols include ethylene glycol, propylene glycol, butylene glycol, 1,4-butanediol, butenediol, butynediol, xylylene glycols, amylene glycols, 1,4-phenylene-bis-beta-hydroxy ethyl ether, 1,3-phenylene-bis-beta-hydroxy ethyl ether, bis-(hydroxy-methyl-cyclohexane), hexanediol, and thiodiglycol; diamines including ethylene diamine, propylene diamine, butylene diamine, hexamethylene diamine, cyclohexylene diamine, phenylene diamine, tolylene diamine, xylylene diamine, 3,3-dichlorobenzidine, and 3,3-dinitrobenzidine; alkanol amines including ethanol amine, aminopropyl alcohol, 2,2-dimethyl propanol amine, 3-aminocyclohexyl alcohol, and p-aminobenzyl alcohol; and combinations of any of the aforementioned chain extenders. Higher molecular weight reactive components such as polyester polyols or polyether polyols can also be included. Polyester polyols can be produced from a reaction of a dicarboxylic acid and a glycol having at least one primary hydroxyl group. Dicarboxylic acids include but are not limited to adipic acid, methyl adipic acid, succinic acid, suberic acid, sebacic acid, oxalic acid, glutaric acid, pimelic acid, azelaic acid, phthalic acid, terephthalic acid, or isophthalic acid, and combinations thereof. Glycols for use in producing the polyester polyols include but are not limited to ethylene glycol, butylene glycol, hexanediol, bis(hydroxymethylcyclohexane), 1,4-butanediol, diethylene glycol, 2,2-dimethyl propylene glycol, or 1,3-propylene glycol. Polyether polyols include but are not limited to polytetramethylene glycol, polyethylene glycol, or polypropylene glycol.
[0034] In some example embodiments, technical effects can be achieved such as good mechanical properties and good hydrolytic stability. Unlike 2K systems that require special handling and continuous metering for iscosyanate crosslinkers, compositions disclosed herein can be used to produce load bearing traction members using conventional extrusion or molding equipment using large stable master batch materials.
[0035] The relative amounts of the compound with a plurality of epoxide groups and/or the carbodiimide or polymeric carbodiimide can be varied by the skilled person to achieve targeted properties or results. In some embodiments, the compound with a plurality of epoxide groups can be present in the heated TPU composition at a level of up to 10 wt. % (i.e., present in amount greater than zero and less than or equal to 10 wt. % based on the total weight of the composition). In some embodiments, the compound with a plurality of epoxide groups can be present at a level 0.05 wt. % to 10 wt. %. In some embodiments, the carbodiimide or polymeric carbodiimide can be present in the heated TPU composition at a level of up to 5 wt. % (i.e., present in amount greater than zero and less than or equal to 5 wt. % based on the total weight of the composition). In some embodiments, the compound with a plurality of epoxide groups can be present at a level 0.1 wt. % to 5 wt. %. The remainder of the composition is primarily the TPU, although other materials can be present, including but not limited to blend polymers, flame retardants, friction additives, adhesion promoters, mold release agents, antioxidants or other stabilizers.
[0036] Referring to
[0037] The term about is intended to include the degree of error associated with measurement of the particular quantity based upon the equipment available at the time of filing the application. For example, about can include a range of 8% or 5%, or 2% of a given value.
[0038] The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the present disclosure. As used herein, the singular forms a, an and the are intended to include the plural forms as well, unless the context clearly indicates otherwise. Unless otherwise stated, the term or means and/or. It will be further understood that the terms comprises and/or comprising, when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, element components, and/or groups thereof.
[0039] While the present disclosure has been described with reference to an exemplary embodiment or embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the present disclosure. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the present disclosure without departing from the essential scope thereof. Therefore, it is intended that the present disclosure not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this present disclosure, but that the present disclosure will include all embodiments falling within the scope of the claims.