CA2103499A1 - Finish for textile fibers containing silahydrocarbon lubricants and nonionic emulsifiers having a plurality of hydrocarbon chains - Google Patents

Abstract

ABSTRACT OF THE DISCLOSURE

A fiber finish composition, which may be applied as an aqueous emulsion, is provided having:
(a) from 50 to 95 parts by weight of a silahydrocarbon lubricant;
(b) from 5 to 50 parts by weight of an emulsifier selected from:
(i) ethoxylated C12-C36 branched alcohols;
(ii) alkoxylated polyhydric alcohols having at least 3 hydroxyl sites which are esterified with C12-C36 fatty acids;
(iii) alkoxylated glycerol esters of C12-C36 fatty acids having at least one hydroxyl functionality;
(c) up to 10 parts by weight of an ionic emulsifier; and (d) up to 5 parts by weight of an antisling additive.

Description

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'~. Case Number 10l~
~i FINIa~ FOR TEXTI~E FIBBR~ CONTAININ~
~ILAHY9ROCARBON LUBRICANT~ AND NONIONIC ~MUL8I~I~RB
~AVIN~ A PLURALITY OF HYDROCARBON C~AIN~
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. BACXGROUND OF T~E INVENTION
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This invention relates generally to a lubricating composition for finishing synthetic textile fibers, and in particular to a composition containing a silahydrocarbon oil and an improved emulsifier having a polyoxyalkylene chain and a hydrophobic component having a plurality of C4-C32 aliphatic groups .
Synthetic polymers are made into fibers in the form of .~ continuous filaments, usually by a process of melt spinning. The i filaments are cooled and converted into filament yarn, staple or tow. Typically, a lubricant composition or finish is applied to the fibers to aid in processing operations by reducing friction, dissipating static charges and modifying the pliability and yarn bundle forming characteristics of the fibers. The finish should be relatively non-absorbent, since this can adversely af~ect the strenqth and elasticity of the fibers. Also, as the finish is absorbed, the fibers tends to swell, lubrication is lost and ~1 friction increases. Another requirement of the finish is that it c should be removable from the fiber by conventional procedures.
Mineral oil was one of the first compositions used as a fiber finish for synthetic fibers. However, due to the high rl degree of absorption of mineral oil into some fibers, especially .~, '', 1 ~:', ,,', :.: :: - : :;.::. . ,:,;;,.
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elastomeric polyurethanes, mineral oils have been replaced by polysiloxane oils.
The polysiloxane oils provide better lubrication and are generally absorbed less by the fibers. In particular, polysiloxane oils have been useful in conjunction with polymers that are especially sensitive to the deleterious effects of absorption of lubricants, such as elastomeric polyurethane (spandex) fibers. Although polysiloxane oils have been used on elastomeric polyurethanes for well over twenty years, there are several drawbacks associated with the processing of fibers treated with these oils. The polysiloxane oils do not offer the cohesion needed to keep yarn bundles or packages together, and package degradation is noticed with time. The lack of boundary friction associated with the polysiloxane oils also leads to irregularities in yarn package formation, such as saddling and bulging, and limits yarn package size.
Safety and environmental concerns also militate against the use of polysiloxane oils as fiber finishes. Beam drippings of the polysiloxane on the floors of processing plants creates an environment ripe for slipping accidents. This danger is exacerbated by the difficulty of removing polysiloxane oils from the floor. Environmentally, the polysiloxane oils have come under attack in that the oils do not readily biodegrade.
Furthermore, since the polysiloxane oils tend to propagate a flame, oil which remains on the yarn after fabric formation can .

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Case Number 1~13 significantly increase the flammability of fabric. Thus, the use of polysiloxane oils by the textile industry is coming under increased regulation.
A silahydrocarbon lubricant for textile fiber6 is disclosed by Plonsker, U.S. Patent No. 4,932,976. Plonsker suggests that the lubricant may be provided as an emulsion. However, suitable emulsifiers are not disclosed.
A polyalphaolefin based fiber finish and useful emulsifiers are disclosed in Ross et al., U.S. Patent No. 4,995,884. The patent discloses a finish composition comprising from 30 to 70 wt.% of a polyalphaolefin, 25 to 50 wt.% of an emulsifier and 5 to 20 wt.% of an antistatic agent. Specific examples of finish formulations having from 37.6 to 56.6 wt.% polyalphaolefin are provided in the patent. The finish composition is applied to the fiber as an agueous emulsion. Any suitable emulsifying agent may ~ be used and several commercially available emulsifiers are i~ recommended.
Seemuth, U. S. Patent No. 4,99g,120 discloses a finish for spandex fibers which is an aqueous emulsion of a .
polydimethylsiloxane lubricant and an ethoxylated, long-chained alkanol emulsifier. The solids portion of the emulsion contains ~ from 80% to 99.5% polydimethylsiloxane.
3 While it is often desirable to provide a finish as an emulRion from the viewpoint of ease of application and removal from the textile fiber, emulsifiers generally have a negative ,, ., . , :: . :,, ~, , ;'''~ ' ` . ' :

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Case Numbe~ 1~13 impact on performance of the lubricant. Additionally, the emulsifier may absorb into the textile fiber resulting in swelling and weakening of the fiber. Thus, selection of an emulsifier is critical to the performance of a finish composition.

~NARY OF T~E INVENTION

Therefore, one of the objects of the invention is to provide a fiber finish which will lubricate the fiber during processing operations, will not cause degradation or swelling of the fiber, will not adversely affect yarn package formation, and can be removed from the fiber by conventional washing and scouring operations.
Another object of the present invention is to provide a fiber finish adapted for use on synthetic fiber~, particularly elastomeric polyurethane fibers.
s Still another object of the invention is to provide a finish composition having a high percentage of silahydrocarbon oil which may be applied to the fiber as an aqueous emulsion, and wherein the emulsifier is not absorbed by the fiber or does not otherwise detract from finish performance.
Accordingly, a finish composition is provided with from 10 to 95 parts by weight of a silahydrocarbon oil and from 5 to 90 parts by weight of an emulsifier having a polyoxyalkylene chain and a hydrophobic component characterized by at least two C4-C32 ,,,, ., .

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C~se Number 1813 aliphatic chains or branches. Preferably, the hydrophobic component of the emulsifier has at least two C6-C24 aliphatic chains and an HLB value of from 6 to 13. In addition to the silahydrocarbon oil, other lubricants may be included in the composition, especially those having a plurality of hydrocarbon chain~ such as polyalphaolefins disclosed in Ross, et al., U.S.
Patent No. 4,995,884, incorporated by reference.
The finish composition imparts superior hydrodynamic and boundary frictional characteristics to fiber and yarn, has negligible adverse impact on the physical properties of the fiber, shows minimal absorption into synthetic fibers, especially spandex, and is relatively easy to remove from the fiber. The finish composition features a relatively high concentration of a branched hydrocarbon lubricant and an emulsifier with multiple hydrocarbon chains or branches. The finish may be applied to the fiber as an emulsion and is easily removed from the fiber by scouring.

D~CRIPTION OF T~ PR~F~RRED ~NBOD~MENT OF ~HB INVEN~ION

Without limiting the scope of the invention, the preferred features of the invention are set forth.
The fiber finish composition of the present invention contain a silahydrocarbon lubricant and an emulsifier. The composition may be applied to a textile fiber neat or as an oil in water emulsion. Emulsions may be prepared by any conventional , ". , , . : , .

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CRSe Number 1~13 technique, for example high speed mixing, using approximately 3 to 25 wt.% of the finish in the aqueous emulsion, preferably 10 to 20 wt.% of the finish in the aqueous emulsion.
Suitable silahydrocarbon lubricants include compounds having the formula:
Si R1 P2 R3 R4 and Rl R2 R3 Si - (CH2) n ~ Si R1 R2 R3 wherein R1, R2, R3 and R4 are independently selected from alkyl, aryl, aralkyl, alkaryl and cycloalkyl; and n is 2 to 8. The total number of carbon atoms in the compound should be at least 24 and further, the lubricant should be a liquid at ambient temperature.
~l Preferred silahydrocarbons are those in which Rl is methyl, ethyl or propyl, most preferably methyl, and R2, R3 and R4 are C8-C12 alkyl, most preferably straight chain alkyl. Examples of preferred lubricants include methyltri(decyl3silane, methyltri(octyl)6ilane and methyltri(dodecyl)silane.
Additional useful silahydrocarbon lubricants are disclosed in Plonsker, U.S. Patent No. 4,932,976, incorporated by i reference. Methods of synthesizing silahydrocarbons identified y~ as u~eful herein are well known to those skilled in the art.
The silahydrocarbon lubricant comprises from 10 to 95 parts by weight of the finish composition. It is desirable to maximize the concentration of lubricant in the finish composition, ~. .~

- ~lu~ 3 Case Number 1813 provided that a sufficient level of an emulsifier is present to facilitate removal of the lubricant from the textile fiber when so desired, and when the finish is applied as an emulsion, a sufficient level of emulsifier to maintain a stable emulsion.
Thus, ranges of silahydrocarbon in the finish composition of from 50 to 95 parts by weight are preferred, with ranges of 70 to 90 parts by weight being most preferred.
An emulsifier is present in the finish composition in ranges of from 5 to 90 parts by weight, preferably from 5 to 50 parts by weight, and more preferably from 10 to 25 parts by weight. It ; has been found that these relatively low levels of emulsifiers i may be used in the finish composition without sacrificing the performance of the finish by selecting relatively high molecular weight, nonionic emulsifiers having a plurality of hydrocarbon , chains or branches. Without being bound to a particular theory, it is hypothesized that the multiple hydrocarbon chains or branches of the hydrophobic component of the emulsifier (1) ' provide a site for enhanced interaction with the branched hydrocarbon functionality of the silahydrocarbons to form a ctable emulsion in an aqueous solution and to facilitate removal of the lubricant from the textile fiber during scouring; and (2) minimize absorption of the emulsifier into the textile fiber.
The following emulsifiers have been found to meet the performance criteria of the present fiber finish composition:

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Case Numbcr 1813 (A) branched alcohols having at least two aliphatic chains of C~-C32 and from 12 to 36 total carbon atoms, which have been alkoxylated with from 3 to 20 moles of alkylene oxides selected from ethylene oxide, propylene oxide and glycidol, preferred features include from 3 to 12 moles of alkylene oxides and at least 50 % of the moles of alkylene oxide being ethylene oxide.
More preferably, at least 75 mole % of the alkylene oxides are ethylene oxide. Especially useful are branched alcohols having C6-C24 alkyl chains and a total of 12 to 28 carbon atoms, notably C12-C28 Guerbet alcohols such as 2-octyldodecanol and isoeicosyl alcohol;
(B) C3-Cgo polyhydric alcohols, including long chain alcohols and oligomers of the same, having at least three hydroxyl sites, which have been alkoxylated with from 5 to 200 moles of alkylene oxides selected from ethylene oxide, propylene oxide, butylene oxide and glycidol, followed by esterification in an acidic medium with 1 to 6 moles of a C12-C36 fatty acid;
preferably the fatty acids are branched and have a total of 12 to 28 carbon atoms, for example iso-stearic acid. Decreased absorption of the emulsifier may be achieved by first reacting a secondary hydroxyl forming alkylene oxide such as propylene oxide or butylene oxide with any primary hydroxyl groups of the polyhydric alcohol, followed by alkoxylation as described above.
Preferred features include C3-C6 polyhydric alcohols, alkoxylation with 5 to 40 moles of alkylene oxides, and at least ,'.' '' ' ~,'i ' - ' - , ",.,.,:~- ' ' ~: ' ' ' . .,. ' , ,, .

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Case Number 1813 50 % of the moles of alkylene oxide being ethylene oxide, more preferably at least 75 mole % are ethylene oxide; and : (C) glyceryl esters of C12-C36 fatty acids wherein the fatty acids have at least one hydroxyl functionality, and the hydroxyl functionalities have been alkoxylated with a total of ; from S0 to 250 moles of alkylene oxides selected from ethylene oxide, propylene oxide and glycidol, preferred features include alkoxylation with 150 to 250 moles of alkylene oxides and at least 50% of the moles of alkylene oxide being ethylene oxide.
More preferably at least 75 mole % of the alkylene oxides are ethylene oxide. Glyceryl esters of C12-C24 fatty acids are preferred, for example, castor oil may be alkoxylated as ! ' described above to provide an emulsifier.

; The nonionic emulsifiers may be employed alone or in combination.
The above emulsifiers may be synthesized by base-catalyzed lkoxylation with, for example, a potassium hydroxide catalyst.
Comparable results may be achieved by other techniques known to !l those with skill in the art. Ethylene oxide and propylene oxide ;l are generally preferred alkylene oxides.
! Emulsifiers having an HLB value of between 6 and 13 are recom~ended, with those having an HLB between 7 and 12 being preferred. HLB values of between 8.5 and 10.5 are most preferred.

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~ Case Number 1813 In addition to the non-ionic emulsifiers described above, up to 10 parts by weight of the finish composition may be a cationic or anionic emulsifier, preferably from 3 to 7 parts by weight of an ionic emulsifier. By way of example, the ionic emulsifiers may be selected from phosphated C10-Cl5 monohydric alcohol alkoxylates, having from 4 to 10 moles of ethylene oxide residues and ethoxylated quaternary amine compounds such as Cordex AT-172, manufactured by Finetex, Inc., Spencer, North Carolina.
Minor amounts of additives may constitute up to 15 parts by weight of the finish composition. For example, viscosity modifiers, low sling additives such as polyisobutylene (up to 5 , parts by weight), antistatic agents (up to 5 parts by weight) and water may be added to the finish composition without deviating ~2 from the scope of the invention.
~he finish composition is applied to a textile fiber by any , number of known methods, such as from a kiss roll, pad, bath or spray nozzle, to provide a lubricated fiber comprising approximately 0.4 to 7 wt.% of the finish composition.
Typically, the finish composition comprises from .7 to 3 wt~% of the lubricated fiber.
The finish composition may be used neat, with the addition ~, of minor amounts of water or as an emulsion containing from 3 to 25 wt.% of the composition in water. For most applications, emulsions which are stable for 8 hours will be adequate. If it is de~irable to operate with the maximum level of silahydrocarbon ~' .,: . . ~ .

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~ 9 Casc Number 1813 lubricant, emulsions which are stable for less than 8 hours may be employed, provided the emulsion is used relatively quickly or is agitated.
The finish composition herein is useful on a wide range of a textile fibers, particularly synthetic textile fibers such as polyurethanes, especially elastomeric polyurethanes (spandex), polyesters, polyamides, especially Nylon 6 and Nylon 66, polyole~ins, especially polypropylene, polyethylene and block and random copolymers thereof, and acrylics. The finish composition is particularly useful whenever there is a tendency of the fiber to absorb the finish, as is the case with several of the synthetic fibers. In the past, spandex fibers have proven difficult to lubricate during finishing operations without the finish absorbing into the fiber or otherwise causing fiber degradation. As used throughout, the terms "spandex" or "elastomeric polyurethanes" are intended to refer to block copolymers made by reaction of diisocyantes with hydroxyl-terminated, low molecular weight polymers (macroglycols) and diamines or glycols (chain extenders) which creates relatively ~oft and hard segments in the copolymer. See Encyclopedia of Polymer Science and Engineering/ Volume 6, pp. 718-19, 733-55 ;,; (1986).
Preferably, the finish composition has the following properties:

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~ J'1~3 Case Numbor 1813 1. A neat viscosity of less than 200 centipoise Q ~5C.

2. A polyurethane absorp1:ion of less than 3 percent by weight of elastomeric polyurethane.

3. An emulsification effectiveness as measured by the presence of a stable emulsion at 25 C
lasting for at least 8 hours.
~, 4. Fiber to metal hydrodynamic friction on polyester and nylon of less than 1.06 and 0.99, respectively.
5. Fiber to fiber boundary friction on polyester and nylon of less than 0.27 and 0.37, respectively.
The invention may be further understood by reference to the following examples, but the invention is not intended to be unduly limited thereby. Unless otherwise indicated, all parts and percentages are by weight. The abbreviations EO and PO
~ represent ethylene oxide and propylene oxide residues "~ respectively.
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Examples l and 2 demonstrate preferred formulations of the finish compositlon for application to a textile fiber as an emulsion.

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Case Number 1813 ~ PLZ

In a typical experiment, 80 grams of methyltri(decyl)silane, provided by the Ethyl Corporation, was placed in a 250 ml beaker equipped with a magnetic stir bar. Twenty grams of 2-octyldodecanol 7E0 was then added to the beaker. The mixture was then agitated to provide a uniform mixture. To this mixture, 5.3 grams of C12-C15 5E0 phosphate, and 4.5 grams castor oil 200E0 was added respectively. The resulting mixture was allowed to stir for 5 minutes. Two and nine-tenths (2.9) grams of water was then added to provide a clear stable mixture.

~XAMPL~ 2 In a typical experiment, 80 grams of a methyltri(decyl)silane, provided by the Ethyl Corporation, was placed in a 250 ml beaker equipped with a magnetic stir bar. Ten grams of 2-octyldodecanol 7E0 and 10 grams of Sorbitol 2P0 28E0 penta-isostearate was then added to the beaker. The mixture was then agitated to provide a uniform mixture. To this mixture, 5.3 grams of C12-C15 5E0 phosphate, and 4.5 grams castor oil 200~0 was added respectively. The resulting mixture was allowed to stir for 5 minutes. Two and nine-tenths (2.9) grams of water was then added to provide a clear stable mixture.

Example 3 demonstrates a preferred formulation of the finish composition for application to a textile fiber neat.

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~,~NumbeT1813 BXAMPLE, 3 In a typical experiment, 90 grams of methyltri(decyl)silane, provided by the Ethyl Corporation, was placed in a 250 ml beaker equipped with a magnetic stir bar. Ten grams of Sorbitol 2PO
2~EO penta-isostearate was then added to the beaker. The mixture was then agitated to provide a uniform mixture. The resulting mixture was allowed to stir for 5 minutes.

Examples 4 demonstrates a preferred formulation of the finish composition for application to a textile fiber neat with a low sling additive, Tebeflex 200, a polyisobutylene mixture.

; EXAMPLE 4 In a typical experiment, 90 grams of methyltri(decyl)silane, provided by the Ethyl Corporation, was placed in a 250 ml beaker equipped with a magnetic stir bar. Ten grams of Sorbitol 2PO
28EO penta-isostearate and 2 grams of Tebeflex 200, purchased from Boehme Filatex, was then added to the beaker. The mixture was then agitated to provide a uniform mixture. The resulting mixture was allowed to stir for 5 minutes.

~VALUATION OF ~H~ PRODUCT
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The following tests were run on the spin finish to evaluate frictional characteristics versus polysiloxanes and also compatibility with polyurethane fiber.

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Case Number 1813 ~ Y~ro~ynami~ Friction was evaluated using a Rothschild frictometer. The finish was applied to 70/34 polyester and 70/34 Nylon 6 at 0.75 percent on weight of fiber (OWF) and allowed to condition for at least 24 hours at 72F and 63 percent relative humidity. After conditioning, the hydrodynamic fiber to metal friction was obtained on the Rothschild frictometer at fiber speeds of 100 meters/minute and pretensions of 20 grams.
Boundary frictions were performed likewise, except that the yarn speed was 0.0071 meters/minute and the pretension set at 50 grams.
The compositions or Examples 1-4 were applied to the fiber tested with an Atlab Finish Applicator, at a level of 0.75 OWF.
Polyurethane absorption was measured according to the following procedure:
An elastomeric polyurethane film (2-3 grams) was weighed on an analytical balance, placed in 100 mls. of a 20 wt. % emulsion of the finish composition in water and the mixture stirred for 6 minutes. The polyurethane film was then removed, rinsed with water, and allowed to dry. The resulting weight increase of the polyurethane film was then calculated and expressed as the percent absorption.
~i ~i~co~ity ~ea~ure~ents were performed using a Brookfield Viscometer operating at either 30 or ~0 rpm's and employing a number 1 spindle. All measurements were taken at 25C.

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Table 1 represents various polyurethane absorption data as measured by the described procedure, for the preceding examples.

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PRODUCT PERCENT
ABSORPTION
- ;l EXAMPLE 1 0.67 EXAMPLE 2 0.31 EXAMPLE 3 0.91 _ _ . _ _ Table 2 lists the viscosity as measured by the described procedures for the examples of this invention.

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FINISH SCOSll~l,cps EX~MPLE 1 6~.5 EXAMPLE 2 73~
EXAMPLE 3 19.0 E~AMPLE 4 23.0 .~ ~ . ~

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Case Numbcr 1813 Tables 3 and 4 lists the hydrodynamic and boundary frictions on nylon and polyester, respectively, as measured by the described procedure, for the examples of the invention. The silicone finish tested was a 20 centistoke, polydimethylsiloxane.

TAI~LE 3 O~ ~lC~ ~ff~ ON~
¦ I~YDRODYNMiIC BOUNDAI~Y

F/MF/M F/F F/F
CNEMICAL F/M F/F KINETICSTATICKINETIC STATIC
__ _ SILICONE 028 020 0.130.17 020 035 EX~MPLE 1 0.65 036 0.09 0.12 0.15 0.19 EXAMPLE 2 0.66 037 0.07 0.11 0.15 0.19 EX~MPLE 3 0.62 036 0.08 0.08 0.17 021 J EX~MPLE 4 0.68 03C 0.09 0.11 0.17 0.21 1, , ,- _ .

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J _ J, F/M F/M F/F F/F
_ RODUCT F/MF/FKINETICSTATIC KINETIC ¦ STATIC
_ SILICONE O.S7 028 0.08 0.11 0.14 ¦ 021 EXAMPLE 10.78 037 0.060.10 0.12 ¦0.18 EXAMPIE 201~1 OAl 0.080.10 0.09 10.14 ::, EXAMPLE 30.74 039 0.060.07 0.12 ¦0.14 ` EXAMI'LE 4 0$1 037 0.06 0.08 0.12 1 0.14 ~,., . --,i ' ..
There are, of course, many alternate embodiments and . modifications which are intended to be included within the scope ., of the following claims.

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Claims (20)

1. A fiber finish composition comprising on a neat basis:
(a) from 10 to 95 parts by weight of a silahydrocarbon selected from compounds having the formula:
Si R1 R2 R3 R4 and R1 R2 R3 Si - (CH2)n-Si-R1 R2 R3 wherein R1, R2, R3 and R4 are independently selected from alkyl, aryl, or aralkyl, alkaryl and cycloalkyl; and n is an integer from 2 to 8, provided that said silahydrocarbon has at least 24 carbon atoms and is liquid at ambient temperature;
(b) from 5 to 90 parts by weight of an emulsifier selected from:
(i) branched alcohols having at least two aliphatic chains of C4-C32 and from 12 to 36 total carbon atoms, which have been alkoxylated with from 3 to 30 moles of alkylene oxides selected from ethylene oxide, propylene oxide and glycidol; and (ii) C3-C90 polyhydric alcohols having at least three hydroxyl sites, which have been alkoxylated with from 5 to 200 moles of alkylene oxides selected from ethylene oxide, propylene oxide, butylene oxide and glycidol, provided that if any of said hydroxyl sites are primary alcohols, then said primary alcohols are reacted with a secondary hydroxyl forming alkylene oxide prior to alkoxylation, followed by esterification in an acidic medium with 1 to 6 moles of a C12-C36 fatty acid.

2. The composition of Claim 1 wherein said silahydrocarbon comprises primarily compounds of the formula Si R1 R2 R3 R4 wherein R1 is methyl and R2, R3 and R4 are independently selected from C8-C12 alkyl.

3. The composition of Claim 2 wherein at least 50 % of said alkylene oxides comprising said emulsifiers are ethylene oxide.

4. The composition of Claim 3 wherein said emulsifiers have an HLB of between 6 and 13.

5. The composition of Claim 4 having a viscosity of less than 200 centipoise @ 25°C, a polyurethane absorption of less than 3 percent by weight of elastomeric polyurethane, a fiber to metal hydrodynamic friction on polyester and nylon of less than 1.06 and 0.99, respectively and a fiber to fiber boundary friction on polyester and nylon of less than 0.27 and 0.37, respectively.

6. A fiber finish composition comprising on a neat basis:
(a) from 50 to 95 parts by weight of a silahydrocarbon having the formula:
Si R1 R2 R3 R4 wherein R1, R2, R3 and R4 are independently selected from alkyl, aryl, aralkyl, alkaryl and cycloalkyl;
provided that said silahydrocarbon has at least 24 carbon atoms and is liquid at ambient temperature;
(b) from 5 to 50 parts by weight of an emulsifier selected from:
(i) branched alcohols having at least two alkyl chains of C6-C24 and from 12 to 28 total carbon atoms, which have been alkoxylated with from 3 to 12 moles of alkylene oxides selected from ethylene oxide and propylene oxide; and (ii) C3-C6 polyhydric alcohols having at least three hydroxyl sites, which have been alkoxylated with from 5 to 40 moles of alkylene oxides selected from ethylene oxide and propylene oxide, followed by esterification in an acidic medium with 3 to 6 moles of a C12-C28 branched, fatty acid.

7. The composition of Claim 6 wherein said silahydrocarbon comprises primarily compounds of the formula Si R1 R2 R3 R4 wherein R1 is methyl and R2, R3 and R4 are independently selected from C8-C12 alkyl.

8. The composition of Claim 7 wherein at least 50 % of said alkylene oxides comprising said emulsifiers are ethylene oxide.

9. The composition of Claim 8 wherein said emulsifiers have an HLB of between 7 and 12.

10. The composition of Claim 9 having a viscosity of less than 200 centipoise @ 25°C, a urethane absorption of less than 3 percent by weight of elastomeric polyurethane, a fiber to metal hydrodynamic friction on polyester and nylon of less than 1.06 and 0.99, respectively and a fiber to fiber boundary friction on polyester and nylon of less than 0.27 and 0.37, respectively.

11. An aqueous emulsion comprising from 3 to 25 wt.% of a finish composition having:
(a) from 50 to 95 parts by weight of a silahydrocarbon having the formula:
Si R1 R2 R3 R4 wherein R1, R2, R3 and R4 are alkyl; provided that said silahydrocarbon has at least 24 carbon atoms and is liquid at ambient temperature;

(b) from 5 to 50 parts by weight of an emulsifier selected from:
(i) branched alcohols having at least two alkyl chains of C6-C24 and from 12 to 28 total carbon atoms, which have been alkoxylated with from 3 to 12 moles of alkylene oxides selected from ethylene oxide and propylene oxide: and (ii) C3-C6 polyhydric alcohols having at least three hydroxyl sites, which have been alkoxylated with from 5 to 40 moles of alkylene oxides selected from ethylene oxide and propylene oxide, followed by esterification in an acidic medium with 3 to 6 moles of a C12-C28 fatty acid.

12. The emulsion of Claim 11 wherein said silahydrocarbon comprises primarily compounds of the formula Si R1 R2 R3 R4 wherein R1 is methyl and R2, R3 and R4 are independently selected from C8-C12 alkyl.

13. The emulsion of Claim 12 wherein at least 50 % of said alkylene oxides comprising said emulsifiers are ethylene oxide.

14. The emulsion of Claim 13 wherein said finish composition comprises from 70 to 90 part by weight of said silahydrocarbon and from 10 to 25 parts of said emulsifier.

15. The emulsion of Claim 14 wherein said emulsifiers have an HLB of between 7 and 12.

16. The emulsion of Claim 14 having a viscosity of less than 200 centipoise @ 25°C, a urethane absorption of less than 3 percent by weight of elastomeric polyurethane, a fiber to metal hydrodynamic friction on polyester and nylon of less than 1.06 and 0.99, respectively and a fiber to fiber boundary friction on polyester and nylon of less than 0.27 and 0.37, respectively.

17. The composition of Claim 5 wherein said emulsifier is a branched alcohol having at least two aliphatic chains of C4-C32 and from 12 to 36 total carbon atoms, which has been alkoxylated with from 3 to 30 moles of alkylene oxides selected from ethylene oxide, propylene oxide, butylene oxide and glycidol.

18. The composition of Claim 10 wherein said emulsifier is a branched alcohol having at least two alkyl chains of C6-C24 and from 12 to 28 total carbon atoms, which has been alkoxylated with from 3 to 12 moles of alkylene oxides selected from ethylene oxide and propylene oxide.

19. The composition of Claim 12 wherein said emulsifier is a branched alcohol having at least two alkyl chains of C6-C24 and from 12 to 28 total carbon atoms, which has been alkoxylated with from 3 to 12 moles of alkylene oxides selected from ethylene oxide and propylene oxide.

20. The composition of Claim 11 wherein said emulsifier is a Guerbet alcohol having at least two alkyl chains of C6-C24 and from 12 to 28 carbon atoms, which has been alkoxylated with from 3 to 20 moles of alkylene oxides selected from ethylene oxide and propylene oxide.