Patent Application
20080083072
The method of the invention is used for drycleaning fabrics. Suitable fabrics include any textile articles that benefit from the drycleaning process. They include products made from a wide variety of natural and synthetic fibers, including, e.g., cotton, wool, silk, rayon, polyester, nylon, acetates, polyolefins, acrylics, spandex, and the like, and blends of these. Suitable fabric uses include garments and accessories, bedding, furniture coverings, rugs, wall coverings, draperies, napkins, tablecloths, and so on. The method can also be used to dryclean a fiber (e.g., wool fiber) before it is used to make a fabric.
The method uses a composition containing one or more dipropylene glycol C3-C4 alkyl ethers. Suitable glycol ethers include dipropylene glycol n-propyl ether (DPnP), dipropylene glycol isopropyl ether, dipropylene glycol n-butyl ether (DPnB), dipropylene glycol isobutyl ether, dipropylene glycol sec-butyl ether, dipropylene glycol tert-butyl ether (DPtB), and mixtures of these.
Dipropylene glycol C3-C4 alkyl ethers are normally produced as a mixture of isomers, which may have a primary or secondary hydroxyl group, and may have head-to-head or head-to-tail configuration of the oxypropylene groups. The major isomer depends on reaction conditions. Minor amounts of other compounds generated as by-products in the manufacture of the dipropylene glycol C3-C4 alkyl ethers may also be present. All of the dipropylene glycol propyl ether isomers have the molecular formula C9H20O3, while the butyl ethers all have the formula C10H22O3.
DPnP and DPnB are commercially available as Dowanol® DPnP and Dowanol® DPnB from Dow Chemical Company. DPnP, DPnB, and DPtB are commerically available as ARCOSOLV® DPnP, ARCOSOLV® DPnB, and ARCOSOLV® DPtB, from Lyondell Chemical Company.
Compositions useful in practicing the invention comprise from 30 to 90 wt. % of a dipropylene glycol C3-C4 alkyl ether. More preferably, the compositions contain from 45 to 80 wt. %, and most preferably from 60 to 70 wt. %, of the dipropylene glycol C3-C4 alkyl ether.
The drycleaning composition also includes one or more C10-C15 hydrocarbons. Usually, a blend of C10-C15 hydrocarbons, preferably a mixture of saturated aliphatic hydrocarbons, is used. Suitable hydrocarbon mixtures are formulated to provide a desired flash point or boiling point range. Particularly preferred are hydrocarbon mixtures that are predominantly C10-C13 hydrocarbons. Examples include ExxonMobil's DF-2000® and Actrel 3360L® solvents, Caled's Hydroclene® solvent, Shell's Shellsol D-600 solvent, and Chevron Phillips's EcoSolv® solvent. Other suitable though less preferred blends use mixtures with predominantly C13-C15 hydrocarbons. Examples include ExxonMobil's Isopar M®, and Exxsol D95® solvents.
To maximize safety in drycleaning operations, the hydrocarbons preferably have a flash point greater than 140° F. (i.e., greater than 60° C.). Each of the solvent mixtures listed above satisfies that criterion. The lower-boiling hydrocarbon mixtures typically have boiling ranges from 180° C to 210° C., while the higher-boiling hydrocarbon mixtures usually boil from 220° C. to 270° C.
Suitable drycleaning compositions have from 5 to 65 wt. % of the hydrocarbons, more preferably from 20 to 50 wt. %, and most preferably from 30 to 50 wt. %.
The compositions also contain from 1 to 10 wt. % of water, which helps to dissolve many soils, particularly those with substantial water solubility such as blood or tea. Too much water in the drycleaning formulation should be avoided, however, because it will cause many fabrics (e.g., cotton or wool) to shrink. Shrinkage values greater than about 2% are generally undesirable. Preferably, the amount of water present is 2 to 5 wt. %, more preferably 2.5 to 4 wt. %.
The relative amounts of the dipropylene glycol C3-C4 alkyl ether, hydrocarbons, and water are balanced to maximize the cleaning properties of the composition and to minimize the amount of residual solvent remaining in the drycleaned article. While either of glycol ethers or hydrocarbon mixtures have been taught elsewhere for drycleaning, any benefit arising from their combined use in the presence of a small proportion of water was unknown. In general, compositions useful herein provide acceptable cleaning performance when compared with commercially available drycleaning compositions. As an added bonus, however, the compositions offer better-than-expected evaporability.
While the hydrocarbon blends evaporate more quickly than dipropylene glycol C3-C4 alkyl ethers, we surprisingly found that mixtures of the glycol ethers and hydrocarbons evaporate faster than predicted from the evaporation times of the individual components, especially at elevated temperature (see Tables 1 to 6, below). To determine the improvement in evaporability, we first measured evaporation times for each of dipropylene glycol C3-C4 alkyl ether/water (95:5) and DF-2000 (hydrocarbon mixture) at room temperature and 77° C. By using a weighted average, we were able to predict an evaporation time for any mixture of glycol ether and hydrocarbons. For instance, a mixture of 90 wt. % of DPnP/water (95:5) and 10 wt. % of DF-2000 has a predicted evaporation time at 77° C. of 2,596 seconds (see sample calculations) compared with an observed value of 2,100 seconds. The observed value is therefore 19% faster than expected. Similar calculations were performed to predict evaporability for hydrocarbon mixtures with DPnB or DPtB.
Overall, we surprisingly found that the evaporability of mixtures containing dipropylene glycol C3-C4 alkyl ethers, C10-C15 hydrocarbons, and water is temperature dependent. Room temperature measurements indicated that evaporability was, at best, marginally better than predicted from the weighted average calculations (see Tables 2, 4, and 6). At elevated temperature, however, the mixtures evaporated faster than the calculations predict. In particular, the evaporability of DPnP at 77° C. was 12-22% faster than expected (Table 1). For DPnB and DPtB, evaporabilities at 77° C. were up to 31% or 19% faster than expected (see Tables 3 and 5, respectively).
Optionally, compositions used in the invention contain additional components commonly used in the drycleaning industry. For example, the compositions can include other organic solvents, such as other glycol ethers, glycol esters, glycol ether esters, alcohols (C8-C12 aliphatic alcohols) or the like, and mixtures of these. The compositions can also contain detergents, anti-static agents, surfactants, fabric softeners, brighteners, disinfectants, anti-redeposition agents, fragrances, and the like. For more on conventional additives, see U.S. Pat. No. 6,086,634, the teachings of which are incorporated herein by reference.
A variety of well-known drycleaning techniques can be employed. In a first step, garments and/or other drycleanable articles are agitated in the presence of a cleaning composition. In commercial processes, garments are typically rotated in a tumble-type washer that contains a drycleaning solvent, detergents, and other additives. The cleaning composition is drained from the tumbler, and the garments are spun to remove the cleaning composition from the garments. The garments are then contacted in a dryer with heated air to remove the remaining cleaning composition. The temperature of the heated air can be adjusted to optimize removal of the remaining cleaning composiiton. For practicing this invention, a temperature range of 50 to 90° C. is preferred for removing the remaining cleaning composition. In our experiments, we used 77° C., to simulate typical drycleaning conditions. The cleaning composition is preferably recovered and reused. If desired, it can be purified by adsorption, distillation, or a combination of these methods.
The following examples merely illustrate the invention. Those skilled in the art will recognize many variations that are within the spirit of the invention and scope of the claims.
A. Method for Measuring Evaporation Time at Room Temperature
A Falex evaporometer is calibrated and the evaporation times of the solvents are measured according to ASTM D 3539-87, with two exceptions. The evaporation times are recorded when 100% of the solvent evaporates (rather than 90%), and the data is collected electronically (rather than using a strip chart). Calibration of the evaporometer is performed with n-butyl acetate by adjusting the “air-flow” ports (N2 gas, 21 L/min), until the evaporation time of n-butyl acetate is 470±10 sec. After the instrument is calibrated, 0.7 mL of a solvent blend is added to the filter paper. The evaporation time at room temperature is measured when approximately 100% of the solvent has evaporated from the filter paper. Room temperature evaporability results for mixtures containing DPnP, DPnB, and DPtB are reported in Tables 2, 4, and 6, respectively.
B. Method for Measuring Evaporation Time at 77° C.
An 8.5″×11″ piece of neutral worsted flannel cloth (wool oil content <0.5%, Test Fabrics Inc. #523) is folded in half four times, stapled together (at the corner, to form a pad), and trimmed at the edges until the weight is 10±0.1 g. After 2 g±0.1 of solvent (see Tables 1, 3, and 5 at columns 1 and 2 for compositions) is added to the pad, it is placed into a forced draft oven, which is maintained at 77° C. Periodically, the cloth is removed from the oven and weighed until 100% of the solvent has evaporated. Evaporability results at 77° C. for mixtures containing DPnP, DPnB, and DPtB are reported in Tables 1, 3, and 5, respectively.
At 77° C.:
DPnP and Water/DF-2000 Composition (90/10)
Actual ET(100% DPnP/H2O)×(DPnP/H2O wt. %)=2,800×0.90=2,520 s
Actual ET(100% DF-2000)×(DF-2000 wt. %)=760×0.10=76 s
Total=2,520+76=2,596 s
At Room Temperature:
DPnP and Water/DF-2000 Composition (80/20)
Actual ET(100% DPnP/H2O)×(DPnP/H2O wt. %)=47,000×0.80=37,600 s
Actual ET(100% DF-2000)×(DF-2000 wt. %)=10,000×0.20=2,000 s
Total=37,600+2,000=39,600 s
At 77° C.:
(Predicted ET−Actual ET)/Predicted ET×100=(2,596−2,100 s)/2,596 s×100=19%
At Room Temperature:
(39,600−38,000 s)/39,600 s×100=4.0%
