FUEL COMPOSITION AND ITS USE

Info

Publication number: 20110308140
Type: Application
Filed: Jun 20, 2011
Publication Date: Dec 22, 2011
Applicant: SHELL OIL COMPANY (Houston, TX)
Inventors: Roger Francis CRACKNELL (Chester), Yajnanarayana Halmuthur JOIS (Katy, TX)
Application Number: 13/164,202

Abstract

A method for increasing flamespeed of an internal combustion engine by burning a certain gasoline composition is provided. The gasoline composition contains (a) a major amount of a mixture of hydrocarbons in the gasoline boiling range and (b) a minor amount of at least one hydrocarbon having 5 to 12 carbon atoms and containing at least one cyclopropyl group and at least one acetylenic group.

Description

Description

The present application claims the benefit of pending U.S. Provisional Patent Application Ser. No. 61/356,922, filed Jun. 21, 2010 the entire disclosure of which is hereby incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to a gasoline composition and its use, particularly, in combustion engines.

BACKGROUND OF THE INVENTION

Spark initiated internal combustion gasoline engines require fuel of a minimum octane level which depends upon the design of the engine. Petroleum refineries are constantly faced with the challenge of continually improving their products to meet increasingly severe governmental efficiency and emission requirements, and consumers' desires for enhanced performance. For example, in producing a fuel suitable for use in an internal combustion engine, petroleum producers blend a plurality of hydrocarbon containing streams to produce a product that will meet governmental combustion emission regulations and the engine manufacturers performance fuel criteria, such as research octane number (RON). Similarly, engine manufacturers conventionally design spark ignition type internal combustion engines around the properties of the fuel. For example, engine manufacturers endeavor to inhibit to the maximum extent possible the phenomenon of auto-ignition which typically results in knocking and, potentially engine damage, when a fuel with insufficient knock-resistance is combusted in the engine.

Under typical driving situations, engines operate under a wide range of conditions depending on many factors including ambient conditions (air temperature, humidity, etc.), vehicle load, speed, rate of acceleration, and the like. Fuel blenders have to design products which perform well under such diverse conditions. This naturally requires compromise, as often times fuel properties or engine parameters that are desirable under certain speed/load conditions prove detrimental to overall performance at other speed/load conditions. It is desirable to provide high burn velocity fuel, particularly for use under lean conditions to shorten the burn duration and thereby improve the thermodynamic efficiency. A faster burn velocity also serves to maximize conversion of the fuel, thereby increasing the overall fuel economy and reducing emissions. Thus, the flame speed (related to burning velocity) of combustible fuel plays an important role in fuels chemistry and in the performance of engines (power) and emissions from spark-ignition engines.

SUMMARY OF THE INVENTION

In accordance with certain of its aspects, in one embodiment of the present invention provides a gasoline composition comprising (a) a major amount of a mixture of hydrocarbons in the gasoline boiling range and (b) a minor amount of at least one hydrocarbon having 5 to 12 carbon atoms and containing at least one cyclopropyl group and at least one acetylenic group.

In another embodiment, the present invention provides a method of improving the flame speed of a gasoline which comprises adding to a major portion of a gasoline mixture, minor amount of the additive described above.

Yet in another embodiment, the present invention provides a method for operating a spark ignition engine which comprises burning in said engine such fuel composition described above.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 represents the Schlieren images of single combustion event 30 ms after ignition of Base Fuel-1 plus 20% Cyclopropylacetylene.

FIG. 2 represents the Schlieren images of single combustion event 30 ms after ignition of Base Fuel-1 only.

FIG. 3 represents improvement in Hyundai Acceleration Performance of the Faster Flame Speed fuel blends versus Base Fuel-2 (reference fuel); all additive concentrations in ppmw.

DETAILED DESCRIPTION OF THE INVENTION

We have found that the blended fuel composition described above significantly enhance the flame speed of gasoline fuels without compromise in RON. In an ideal case, flame speed is the measured rate of expansion of the flame front, generally measured in meters/second (m/s). In a spark engine, flame speed depends on gas pressure, temperature, and density change as a result of changes in volume due to piston motion (see Internal Combustion Engine Fundamentals, John B. Heywood. McGraw-Hill Book Co., 1988). Thus, “rate of expansion of the flame front” can also be measured by the increase in the pressure. Early pressure rise after spark (at 0 seconds) is also a measure of high burning velocity.

The gasoline composition of the present invention contains component (b) of at least one hydrocarbon having 5 to 12 carbon atoms and containing at least one cyclopropyl group and at least one acetylenic group. The term “acetylenic group” refers to unsaturated hydrocarbons that have carbon atoms in chains linked by one or more triple bonds. The component (b) can be a compound having the formula:

wherein n is an integer from 0 to 7; R₁to R₆are independently hydrogen, alkyl group having 1 to 7 carbon atoms, alkenyl group having 1 to 7 carbon atoms, alkynyl group having 1 to 7 carbon atoms, cyclic group having 1 to 7 carbon atome, with the proviso that the total number of carbon atoms in the compound are from 5 to 12. Preferably n is an integer from 0 to 5, more preferably 0 to 3. Preferably R₁to R₆are independently hydrogen, alkyl group having 1 to 5, more preferably 1 to 3 carbon atoms, with the proviso that the total number of carbon atoms in the compound are from 5 to 12.

Some of these cyclopropyl group-containing acetylenic compounds are available from GSF Chemicals Corporation and Sigma-Aldrich Company Ltd. Various synthetic routes can be used in the preparation of the cyclopropyl group-containing acetylenic compounds useful in the invention. For example, cyclopropylacetylene can be prepared by chlorination of acetylcyclopropane with PCl₅in the presence of an org. base in a chlorinated hydrocarbon with dehydrochlorination of the mixt. of alpha,-alpha dichlorocyclopropane and alpha-chlorovinylcyclopropane (with base at reflux in a solvent) and simultaneous distillation. (see Dolgii, I. E.; Shvedova, I. B.; Shavrin, K. N.; Nefedov, O. M. (Zelinskii, N. D., Institute of Organic Chemistry, USSR). U.S.S.R. (1977)) Dicyclopropylacetylenic derivatives can be prepared using Favorskii reaction and common organic synthesis procedure (Nefedov, O. M.; Dolgii, I. E.; Shvedova, I. B.; Baidzhigitova, E. A. Inst. Org. Khim. Im. Zelinskogo, Moscow, USSR. Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya (1978), (6), 1339-44.) Cyclopropyl Cyanide can be prepared by the reaction of sodium amide with chlorobutyronitrile (Organic Syntheses, Volume 3, page 223. John Wiley & Sons, Inc. Submitted by M. J. Schlatter and checked by R. L. Shriner and Chris Best). Other methods can be used to prepare the cyclopropyl group-containing acetylenic compounds useful in the invention as are known to one who is skilled in the art of organic synthesis. The preferred cyclopropyl group-containing acetylenic compounds maybe, for example, cyclopropyl acetylene; 1-cyclopropyl-1-propyne; 1-cyclopropyl-2-propyne; 1-methyl-1-ethynyl-cyclopropane; 2-methyl-1-ethynyl-cyclopropane; 1,1-(3-methylene-1-propyne-1,3-diyl)bis-; 1,1-bicyclopropyl, 2,2-diethynyl-; 1-cyclopropylpenta-1,3-diyne; cyclopropane, 1,1-(1,3-butadiyne-1,4-diyl)bis-; cyclopropane, 1,1-(3-methyl-1-propyne-1,3-diyl)bis-; and 1,4-dicyclopropylbuta-1,3-diyne.

The fuel composition of the present invention comprises a major amount of a mixture of hydrocarbons in the gasoline boiling range and a minor amount of component (b). As used herein for component (b), the term “minor amount” means less than 50% by weight of the total fuel composition, preferably less than about 30% by weight of the total fuel composition. However, the term “minor amount” will contain at least some amount, preferably at least 0.001% by weight of the total fuel composition.

An effective amount of one or more compounds of component (b), more particularly Formula I, are introduced into the combustion zone of the engine in a variety of ways to improve flame speed. As mentioned, a preferred method is to add a minor amount of one or more compounds of component (b) to the fuel. For example, one or more compounds of component (b) may be added directly to the fuel or blended with one or more carriers to form an additive concentrate which may then be added at a later date to the fuel.

The amount of component (b) used will depend on the particular variation of Formula I used, the engine, the fuel, and the presence or absence of carriers and additional detergents. Generally, each compound of component (b) is added in an amount up to about 20% by weight, especially from about 0.005% by weight, more preferably from about 0.05% by weight, even more preferably from about 0.5% by weight, most preferably from about 1% by weight, based on the total weight of the fuel composition.

Suitable liquid hydrocarbon fuels of the gasoline boiling range are mixtures of hydrocarbons having a boiling range of from about 25° C. to about 232° C. and comprise mixtures of saturated hydrocarbons, olefinic hydrocarbons and aromatic hydrocarbons. Preferred are gasoline mixtures having a saturated hydrocarbon content ranging from about 40% to about 80% by volume, an olefinic hydrocarbon content from 0% to about 30% by volume and an aromatic hydrocarbon content from about 10% to about 60% by volume. The base fuel is derived from straight run gasoline, polymer gasoline, natural gasoline, dimer and trimerized olefins, synthetically produced aromatic hydrocarbon mixtures, or from catalytically cracked or thermally cracked petroleum stocks, and mixtures of these. The hydrocarbon composition and octane level of the base fuel are not critical. The octane level, (R+M)/2, will generally be above about 85. Any conventional motor fuel base can be employed in the practice of the present invention. For example, hydrocarbons in the gasoline can be replaced by up to a substantial amount of conventional alcohols or ethers, conventionally known for use in fuels. The base fuels are desirably substantially free of water since water could impede a smooth combustion.

The word major amount is used herein because the amount of hydrocarbons in the gasoline boiling range is often 50 weight or volume percent or more.

Normally, the hydrocarbon fuel mixtures to which the invention is applied are substantially lead-free, but may contain minor amounts of blending agents such as methanol, ethanol, ethyl tertiary butyl ether, methyl tertiary butyl ether, tert-amyl methyl ether and the like, at from about 0.1% by volume to about 15% by volume of the base fuel, although larger amounts may be utilized. The fuels can also contain conventional additives including antioxidants such as phenolics, e.g., 2,6-di-tertbutylphenol or phenylenediamines, e.g., N,N′-di-sec-butyl-p-phenylenediamine, dyes, metal deactivators, dehazers such as polyester-type ethoxylated alkylphenol-formaldehyde resins. Corrosion inhibitors, such as a polyhydric alcohol ester of a succinic acid derivative having on at least one of its alpha-carbon atoms an unsubstituted or substituted aliphatic hydrocarbon group having from 20 to 50 carbon atoms, for example, pentaerythritol diester of polyisobutylene-substituted succinic acid, the polyisobutylene group having an average molecular weight of about 950, in an amount from about 1 ppm (parts per million) by weight to about 1000 ppm by weight, may also be present.

The fuel compositions of the present invention may also contain one or more detergents. When detergents are utilized, the fuel composition will comprise a mixture of a major amount of hydrocarbons in the gasoline boiling range as described hereinbefore, a minor amount of one or more compounds of component (b) as described hereinbefore and a minor amount of one or more detergents. As noted above, a carrier as described hereinbefore may also be included. As used herein for detergents, the term “minor amount” means less than about 10% by weight of the total fuel composition, preferably less than about 1% by weight of the total fuel composition and more preferably less than about 0.1% by weight of the total fuel composition. The one or more detergents are added directly to the hydrocarbons, blended with one or more carriers, blended with one or more compounds of component (b), or blended with one or more compounds of component (b) and one or more carriers before being added to the hydrocarbon. The compounds of component (b) can be added at the refinery, at a terminal, at a depot, at a retail site, or by the consumer.

The treat rate of the fuel additive detergent packages that contains one or more detergents in the final fuel composition is generally in the range of from about 0.007 weight percent to about 0.76 weight percent based on the final fuel composition. The fuel additive detergent package may contain one or more detergents, dehazer, corrosion inhibitor and solvent. In addition a carrier fluidizer may sometimes be added to help in preventing intake valve sticking at low temperature.

While the invention is susceptible to various modifications and alternative forms, specific embodiments thereof are shown by way of examples herein described in detail. It should be understood, that the detailed description thereto are not intended to limit the invention to the particular form disclosed, but on the contrary, the intention is to cover all modifications, equivalents and alternatives falling within the spirit and scope of the present invention as defined by the appended claims. The present invention will be illustrated by the following illustrative embodiment, which is provided for illustration only and is not to be construed as limiting the claimed invention in any way.

Octane Test Methods

The Research Octane Number (RON) (ASTM D2699) and Motor Octane Number (MON) (ASTM D2700) will be the techniques used in determining the R+M/2 octane of the fuel. The RON and MON of a spark-ignition engine fuel is determined using a standard test engine and operating conditions to compare its knock characteristic with those of primary reference fuel blends of known octane number. Compression ratio and fuel-air ratio are adjusted to produce standard knock intensity for the sample fuel, as measured by a specific electronic detonation meter instrument system. A standard knock intensity guide table relates engine compression ratio to octane number level for this specific method. The specific procedure for the RON can be found in ASTM D-2699 and the MON can be found in ASTM D-2700.

Table I contains the engine conditions necessary in determine the RON and MON of a fuel.

TABLE I RON and MON Test Conditions Test Engine Conditions Research Octane Number Motor Octane Number Test Method ASTM D-2699-92 ASTM D-2700-92 Engine Cooperative Fuels Cooperative Fuels Research (CFR) Research (CFR) Engine Engine Engine RPM 600 RPM 900 RPM Intake Air Varies with Barometric 38° C. Temperature Pressure (eq 88 kPA = 19.4° C., 101.6 kPa = 52.2° C.) Intake Air 3.56-7.12 g H₂O/kg 3.56-7.12 g Humidity dry air H₂O/kg dry air Intake mixture not specified 149° C. temperature Coolant 100° C. 100° C. Temperature Oil 57° C. 57° C. Temperature Ignition 13 degrees BTDC Varies with Advance-fixed compression ratio (eq 14-26 degrees BTDC) Carburetor Set according to 14.3 mm Venture engine altitude (eq 0-500 m = 14.3, 500-1000 m = 15.1 mm)

Flame Speed Test Method

Flame Speed of the fuels were tested with Leeds Combustion Bomb Method as described in SAE Technical Paper Series 2000-01-0192, Aspects of Laminar and Turbulent Burning Velocity relevant to SI Engines, by L. Gillespie, M. Lawes, C. G. W. Sheppard and R. Woolley, SAE 2000 World Congress, Detroit, Mich., Mar. 6-9, 2000. Fuels were tested under laminar conditions with initial conditions of 5 bar absolute pressure and 360K. All the burning velocities were measured at an equivalence ratio φ=1 (i.e., stoichiometric). The tests were conducted using the Leeds Mk2 fan stirred combustion vessel (bomb) a stainless sphere of 30 liter volume and with extensive optical access. The fuels were injected into the bomb and allowed to vaporize fully, than a stoichiometric amount of air was added. The gases were mixed with stirring fans inside the vessel and the contents were heated to the desired temperature. The fans were turned off prior to ignition. Mixtures were ignited using a spark plug. Pressure transducers were flush mounted inside the bob and recorded the pressure rise as a function of time.

Base Fuel

The base fuel physical properties used in the tests can be found in Table II.

TABLE II Base Fuel Physical Properties Base Base Parameter Method Units Fuel-1 Fuel-2 RON ASTM D2699 95.4 95.3 MON ASTM D2700 86.6 86.4 Density @ 15° C. IP 365 g cm⁻³ 0.7300 0.7293 Oxidation Stability IP 40 mins >1440 (induction) Unwashed gum IP 131 mg/100 ml 6 8 Distillation IP 123 IBP ° C. 34.9 35.7 10% rec ° C. 51.8 54.9 20% rec ° C. 59.9 62.5 30% rec ° C. 68.1 70.6 40% rec ° C. 77.8 80.6 50% rec ° C. 89.7 92.7 60% rec ° C. 103.1 105.7 70% rec ° C. 115.6 118.4 80% rec ° C. 126.7 129.6 90% rec ° C. 139.6 141.3 95% rec ° C. 146.9 147.9 FBP ° C. 167.1 171.4 Residue % vol 1.0 1.0 Recovery % vol 95.5 97.8 Loss % vol 3.5 1.2 E70 % vol 32.0 29.1 E100 % vol 57.9 55.7 E120 % vol 74.0 71.4 E150 % vol 96.3 95.7 RVP IP 394/ kPa 59.8 56.0 ASTM 519 GC LTP/26 C 6.60 6.61 H 12.51 12.56 O 0.00 0.00 Paraffins % vol 7.41 7.29 Isoparaffins % vol 53.84 53.90 Olefins (including % vol 3.06 3.76 dienes) Dienes % vol 0.01 0.01 Napthenes % vol 6.28 6.14 Aromatics % vol 29.07 28.79 Oxygenates % vol 0.00 0.00 Unknowns % vol 0.35 0.13 Total % vol 100.01 100.01 Benzene % vol 0.48 0.52 (+Me Cyc5 ene) Sulphur - WD XRF ISO 20884 mg/kg 10 Sulphur - Antek ISO 20846 mg/kg 5

Examples 1-8

For examples 1-3, the additives were each added to Base Fuel 1 (Octane 91) at 20% in weight. These samples were then tested thrice for RON, MON, and flame speed. The average of three runs was tabulated in Table III. Similar blending method was used for examples 4-8 with Base Fuel 2 (Octane 91) at concentrations indicated in Table III.

TABLE III Flame- speed Pressure Additive in (in bomb(bar) weight %) at Example Base in 0.1 s after # blend Gasoline ignition RON MON (R + M)/2 1 Base None 17.35 95.4 86.6 91.0 Fuel 1 2 Base 20% of 32.33 97.0 81.8 89.4 Fuel 1 Cyclopropyl- acetylene 3 Base 20% of 26.59 93.2 81.8 87.5 Fuel 1 1-Pentyne 4 Base None 21.66 95.2 86.9 91.0 Fuel 2 5 Base 5% of 25.09 96.1 85.3 90.7 Fuel 2 Cyclopropyl- acetylene 6 Base 10% of 32.74 96.3 84.6 90.4 Fuel 2 Cyclopropyl- acetylene 7 Base 5% of 24.22 95.3 85.6 90.4 Fuel 2 1-Pentyne 8 Base 10% of 24.36 94.9 84.9 89.9 Fuel 2 1-Pentyne

Addition of molecules containing cyclopropyl and acetylenic group significantly enhanced the flame speed of the given fuel composition. The increase in cylinder pressure compared to the reference fuel after 0.1 seconds after ignition is used as the measure of the laminar flame speed. Results showed that Cyclopropylacetylene and 1-Pentyne at blend concentrations of 10% and 5% produced a statistically significant (at99%) improvement in chamber pressure compared to the reference fuel. We chose another molecule with three member ring, without acetylene moiety (carbon triple bond carbon), for example, Carene. Carene was tested at 20% in Base Fuel 2. This blend showed no statistically significant improvement in pressure difference compared to the Base Fuel 2 (reference fuel).

At a concentration of 20 wt. % Cyclopropylacetylene in the Base Fuel-1 shows the pressure increase in the combustion chamber 0.1 seconds after ignition of the homogeneous charge is statistically (>95%) significantly greater than the Base Fuel-1 (reference fuel). For example, Schlieren images of the combustion, 30 ms after the ignition event shown in the Figures clearly show a large difference in both the flame size and structure (Cyclopropylacetylene being more cellular). It is noted that at nearly 33 ms the flame for the fuel blend containing cyclopropylacetylene fills the viewing window; the Base Fuel-1 (reference fuel) takes nearly 38.5 ms to fill the viewing window, so it is not possible to show differences in flame size after this point. Hence the images are not shown at 100 ms (0.1 seconds) after ignition to help corroborate the pressure data. However, pressure at 0.1 seconds been tabulated in Table III.

Cyclopropylacetylene, 1-Pentyne were blended at 0.5% and 1.0% into Base Fuel-2. Each fuel blend was tested in a single day along with the reference fuel (base fuel without the additive) in an A-B-A-B . . . type test design on the chassis dynamometer. A Hyundai Coupe was used for the testing. As this vehicle has shown to be insensitive to changes in fuel octane the improvements in acceleration performance achieved between the test and reference fuel are attributed to changes in the laminar flame speed of the fuel. A standard chassis dynamometer power and acceleration test procedure on a Hyundai Coupe was used to obtain these results as shown in FIG. 3. The figure shows over 0.2% acceleration performance improvements with 1% cyclopropylacetylene as an additive as compared to the base fuel without the additive.

The benefit of this increase in flame speed is best utilized in performance a applications such as racing fuel and premium fuel. Addition of such molecules in fuels typically results in less pollution, more power and better efficiency. Faster burning fuels allow engines to run on lean mixtures of gasoline and air, potentially reducing nitrogen oxide and hydrocarbon emissions. As seen in the above Table, the flame speed of the cyclopropyl acetylene in gasoline is greatly increased without lowering the RON value. Further, the fuel composition of the invention increases fuel sensitivity. There are industry reports that indicate fuel with higher sensitivity (lower MON) has better anti-knock quality. (see SAE Technical Paper Series 2001-01-3584, Fuel Anti-Knock quality-Part I. Engine Studies, by G. T. Kalghatgi and SAE Technical Paper Series 2001-01-3585, Fuel Anti-Knock Quality-Part II. Vehicle Studies—How Relevant is Motor Octane Number (MON) in Modern Engines, by G. T. Kalghatgi.) An increase in fuel sensitivity increases the “octane index” of the fuel which is a better measure of the anti-knock quality of the fuel, and leads to improved power and acceleration performance. As seen from the above Table III, while RON value of the cyclopropyl acetylene containing formulation is higher than the reference fuel without the cyclopropyl acetylene, MON value of the cyclopropyl acetylene containing formulation is lower than the reference fuel without the cyclopropyl acetylene.

Claims

1. A gasoline composition comprising (a) a major amount of a mixture of hydrocarbons in the gasoline boiling range and (b) a minor amount of at least one hydrocarbon having 5 to 12 carbon atoms and containing at least one cyclopropyl group and at least one acetylenic group.

2. The fuel composition of claim 1 wherein component (b) is present in an amount from about 0.005% by weight to 20% by weight base on the total weight of the fuel.

3. The fuel composition of claim 1 wherein component (b) has a formula: wherein n is an integer from 0 to 7; R1 to R6 are independently hydrogen, alkyl group having 1 to 7 carbon atoms, alkenyl group having 1 to 7 carbon atoms, alkynyl group having 1 to 7 carbon atoms, cyclic group having 1 to 7 carbon atoms, with the proviso that the total number of carbon atoms in the compound are from 5 to 12.

4. The fuel composition of claim 2 wherein component (b) is selected from the group consisting of cyclopropyl acetylene; 1-cyclopropyl-1-propyne; 1-cyclopropyl-2-propyne; 1-methyl-1-ethynyl-cyclopropane; 2-methyl-1-ethynyl-cyclopropane; 1,1-(3-methylene-1-propyne-1,3-diyl)bis-; 1,1-bicyclopropyl, 2,2-diethynyl-; 1-cyclopropylpenta-1,3-diyne; cyclopropane, 1,1-(1,3-butadiyne-1,4-diyl)bis-; cyclopropane, 1,1-(3-methyl-1-propyne-1,3-diyl)bis-; and 1,4-dicyclopropylbuta-1,3-diyne.

5. The fuel composition of claim 2 wherein component (b) is cyclopropyl acetylene.

6. The fuel composition of claim 4 wherein component (b) is present in an amount of 0.05 wt % to 20 wt %.

7. The fuel composition of claim 3 further comprising (c) a minor amount of a fuel detergent.

8. The fuel composition of claim 4 further comprising (c) a minor amount of a fuel detergent.

9. The fuel composition of claim 3 wherein n is an integer from 0 to 5.

10. The fuel composition of claim 9 wherein R1 to R6 are independently hydrogen, alkyl group having 1 to 5 carbon atoms, with the proviso that the total number of carbon atoms in the compound are from 5 to 12.

11. A method of improving the flamespeed of a gasoline which comprises adding to a major portion of a gasoline mixture minor amounts of at least one hydrocarbon having 5 to 12 carbon atoms and containing at least one cyclopropyl group and at least one acetylenic group.

12. A method for increasing flamespeed of an internal combustion engine which comprises burning in said engine a fuel composition of claim 1.

13. A method for increasing flamespeed of an internal combustion engine which comprises burning in said engine a fuel composition of claim 3.

14. A method for increasing sensitivity of a gasoline which comprises adding to a major portion of a gasoline mixture minor amounts of a at least one hydrocarbon having 5 to 12 carbon atoms and containing at least one cyclopropyl group and at least one acetylenic group.