CA2218157C - Composite polymer devices for controlled release of semiochemicals - Google Patents

Abstract

Composite polymer dispensers capable of controlled release of semiochemicals have been developed. The dispensers make use of a solid elastomer matrix reservoir which is at least partially surrounded by a permeable release rate controlling polymer membrane. The matrix materials are polyurethanes compatible with many types of semiochemicals and additives. The release rates of semiochemicals from the dispensers can be varied over a wide range by manipulation of the reservoir conditions and by selection of the type of permeable polymer membrane surrounding the device. The dispensers can have a variety of forms and can be produced by a simple process. The semiochemical devices produced by this method are useful for managing insect and other pests through attraction to traps, for population monitoring or for mass trapping. The devices may also be used to dispense anti-aggregation pheromones or repellents in addition to use for mating confusion or disruption.

Description

COMPOSITE POLYMER MATRICES FOR CONTROLLED
RELEASE OF SEMIOCIiEMICALS
FIELD OF THE INVENTION
This invention pertains to novel and versatile devices for use as semiochemical controlled release dis-pensers. More particularly, hydroxy-terminated polybuta-diene resins, or other polyols, can be combined with semiochemicals, additives, and an isocyanate component to produce a solid phase reservoir surrounded at least par-tially by a permeable, release rate controlling polymer membrane.
BACKGROUND OF THE INVENTION
Semiochemicals are an extremely diverse group of chemicals encompassing many functional groups and having at least several hundred members. "Law and Regnier (1971) proposed the tE~rm 'semiochemicals' (Gk. semeon, a mark or signal) for chemicals that mediate interactions between living organisms" taken from (Norlund et al. 1981). This definition is well known and has been in common usage by persons skilled in the art for many years.
Semiochemicals transmit signals to members of the same species as well as different species. These chemicals have been identified in many organisms including bacteria, yeast, plants, insects and animals. The U.S. Environmental Protection Agency which regulates certain pest control uses of semiochemicals has used a slightly narrower definition:
"Chemicals emitted by plants or animals that modify the behaviour of receptor organisms of like or different kinds are semiochemicals." (1982 Pesticide Assessment Guidelines, Subdivision M, Biorational Pesticides [NTIS publication PB-83153965 page 2]). Often semiochemicals are not emitted as a pure chemical, but rather as a blend of several com-pounds. The most studied semiochemicals are the phero-mones, which transmit chemical signals within the same species (The Merck Index 11th ed. 1989) and have been identified in at least 1,600 species (Mayer and Mclaughlin 1990, Arn et al. 1992). Kairomones, allomones and synomones are other types of semiochemicals that are intra species signals (Norlund et al. 1981). Allomones are compounds that serve to benefit the emitting species, while kairomones benefit the perceiving species. Synomones are chemical signals which serve to benefit both the emitting and perceiving species . It is worth note that the terms pheromone, allomone and kairomone are not mutually exclus-ive. For example, a semiochemical may be a pheromone in one species while the same chemical acts as a kairomone for predators of that species.
The use of semiochemicals as a tools in inte-grated pest management (IPM) is increasing. Uses for semiochemicals have been found in forestry, agriculture and urban industrial locations (Mitchell 1981, Ridgeway et al.
1990). Other compounds of use in integrated pest manage-ment also include synthetic chemicals not found naturally (unnatural chemicals) that mimic the biological actions of semiochemicals, for example the "male lures" of terphritid fruit flies (Cunningham et al. 1990) . The chemical mixture known as "trimedlure" (t-butyl esters of 4- and 5-chloro-2-methylcyclohexan-1-carboxylic acid) is a secific illus-tration. The Mediterranean fruit fly, Ceratitis capitata, does not produce these chemicals, nor are they found in nature. However, females of this species respond to this mixture as if it were a male produce sex pheromone. Thus trimedlure is an unnatural synthetic behaviour-modifying chemical that mimics the the function of a semiochemical (sex pheromone). These synthetically prepared, unnatural chemicals that cause behavoiral responses that copy or mimic the actions of semiochemicals are herein defined as an unnatural synthetic behaviour-modifying chemicals and are functionally equivalent to their corresponding semio-chemicals. A skilled practitioner will be aware that chemicals such as pesticides, fungicides, bactericides, insecticides, nematocides, acaricides, molluscicides and growth regulators are not semiochemicals, nor are they semiochemical mimics.
In contrast to pesticides, semiochemicals do not work through toxic action and in general are of low toxic-ity to non-target species (Ridgeway et al. 1992). Pesti-cides tend to be broad spectrum in the organisms affected while semiochemicals are much more specific, affecting at most a few species. Semiochemicals can often replace or substantially reduce the amount of pesticide needed for pest control applications. Semiochemical use in pest management may include strategies such as population monitoring, quarantine trapping, mass trapping, barrier trapping, and mating disruption. The use of anti-aggrega-tion pheromones, alarm pheromones, anti-feedants, oviposition deterrents, pollination enhancement and other types of--behaviour modifications are known.
The widespread use of semiochemicals in pest control applications has been limited partly by diffi-culties encountered in controlled delivery of the chemicals to the environment. Semiochemical-based pest management relies to a large extent on precise slow release device technology for its successful implementation. For example, the use of insect pheromones to lure pests to traps used for population monitoring requires a very specific delivery rate. Too low a delivery rate may be below the threshold of perception, while too high a delivery rate may confuse or repel the insect and prevent the insect from entering the trap. In other applications such as mating disruption, too low a release rate or premature exhaustion of slow release devices can severely reduce the efficacy of the treatment, while too high a release rate or too long a lifespan of devices loaded with an expensive semiochemical may make the cost of treatments prohibitive. Zeoli et al.

(1982) have summarized controlled release technologies used for delivering semiochemicals and have categorized the dis-pensers types into four groups: monolithic systems, lami-nated structures, reservoir systems without rate control-s ling membranes and reservoir systems with rate controlling membranes.
1. Monolithic systems These one material systems consist of inert polymeric matrices impregnated with the semiochemical as the active ingredient (AI). Such homogenous devices are simple and they lend themselves to a number of applica-tions. However, the release characteristics depend largely on the shape of the device, and the capacity of the polymer to hold the semiochemical, both of which may limit the longevity of the device. Release of AI from monolithic devices tends to be logarithmic over time with much of the active agent being lost in the early part of the device lifespan. The most constant release from this type of device usually occurrs when the reservoir is almost exhausted. Examples of this technology are polyvinyl-chloride (PVC) impregnated with semiochemical (Fitzgerald et al. 1973) or silicone rubber impregnated with fragrances as in U.S. Patent No. 4,725,575 (Union Camp Co.), or sili-cone-urethane. copolymers used as matrices for dispensing fragrances or pheromones as in U.S. Patent Nos. 4,908,208 and 5,008,115 (Dow Corning Co.), urethane matrices for dispensing pesticides as in U.S. Patent No. 4,594,380 (AT&T
Bell Laboratories) or acrylate polymers impregnated with pheromones (Smith et al. 1991 and Kim et al. 1988).
2. Laminated structures These devices have relatively good release characteristics, approaching zero order (constant) release.
However, the manufacture of these devices requires multiple processing to produce the laminate. An example of this technology are laminated dispensers described in U.S.
Patent No. 4,639,393 (Herculite Protective Fabrics), and German Patent No. 3,524,180 (Montedison S.p.A.).
3. Reservoir systems without rate controlling membranes These can be exemplified by capillary release devices as described in U.S. Patent No. 4,017,030 (Albany International Co.). These devices have been used despite undesirable high initial losses of semiochemical (Weatherston et al. 1985) and difficulty in handling.
4. Reservoir systems with a rate controlling membrane Dispensers of this type generally provide near constant release characteristics which are governed by a permeable membrane. The membrane composition and surface area can be varied to effect changes in the release rates.
Examples are described in U.S. Patent Nos. 4,323,556 (Montedison S.p.A.), 4,445,641 (Bend Research Inc.), 4,979,673 (I. J. Wilk), 4923119 (Shin-Etsu Chemical Co.), 4,793,555 (Dow Corning Corp.) and German Patent No.
2,945,655 (Celamerck G.m.b.H.).
Polyurethane chemistry is well known in the plastics industry, however the use of these polymers in semiochemical slow release devices has been limited to silicone-urethane copolymers. The terminology used herein to describe the reactants and the reactive process to produce a polyurethane semiochemical reservoir conforms to the customary meanings as given in "Polyurethane Handbook"
ed. G. Oertel, Hanser Publishers or "The ICI Polyurethanes Book", 2nd Edition, ed. G. Woods, published by ICI
Polyurethanes and John Wiley & Sons. The term polyol refers to a molecule with at least two hydroxyl groups.
Polymeric polyols usually contain other chemical functionalities and the most common types of polyols used in urethane manufacture are polyether polyols (hydroxy-terminated polyethers) and polyester polyols (hydroxy-terminated polyesters). Generally polymeric polyols are not pure compounds, but rather mixtures which are usually characterized by the average properties of the mixture.
The isocyanates described herein are molecules which contain at least two isocyanate groups. The term MDI
refers to diphenylmethane diisocyanate (predominately 4,4' isomer) which is commonly used in industry as mixtures of pure MDI and polymeric MDI. At the molecular level, polyurethane polymers may consist of soft block domains which consist of long chains with few crosslinks, an elastic structure and a low glass transition temperature, or hard block domains which consist of highly crosslinked chains, a rigid structure and a high glass transition temperature. Some polyurethanes may contain both hard and soft segments.
The terminology thermoplastic and thermoset plastic have meanings commonly accepted in the industry, thermoset plastics cannot be melted without decomposition and loss of original physical properties while thermoplastics may be readily melted and cast into molds without loss of original physical attributes.
SUMMARY OF THE INVENTION
The invention is directed to composite semio-chemical release devices composed of a homogeneous polyurethane matrix containing a dissolved or dispersed active agent and an active agent permeable polymer membrane which at least partially surrounds the matrix. The polymer matrix is prepared from a reactive mixture comprising a polyol and an isocyanate cross linking agent reacted in the presence of unreactive semiochemicals and additives.

_ 7 _ The term composite polymer device has been used herein to indicate that the devices are constructed from at least a binary combination of separate polymers, namely a homogeneous polyurethane core containing a semiochemical active ingredient and a semiochemical permeable, separate polymer membrane at least partially surrounding the polyurethane core.
The polyol may be selected from the group con-sisting of hydroxy-terminated polybutadiene resins, poly-ether polyols, polyester polyols and mixtures thereof. The isocyanate component may be selected from the group con-sisting of monomeric or polymeric diphenylmethane diiso-cyanates, toluene diisocyanates, isophorone diisocyanate and hexamethylene diisocyanate or mixtures thereof. Semio-chemicals compatible with the reactive process may be selected from the functional groups including: alkanes, alkenes, aromatic hydrocarbons, ethers, esters, epoxides, aldehydes, ketones, lactones, nitriles, imines, tertiary amines, thioethers, sulfoxides, sulfones, disulfide com-pounds, thioesters, organohalides, and mixtures thereof.
Semiochemicals not compatible or reactive with the matrix include the functional groups: alcohols, carboxylic acids, thiols, primary and secondary amines, and phenols.
The reaction mixture may include anti-oxidants, ultraviolet light absorbers, pigments, dyes, fillers, blowing agents, plasticizers, other resin modifying agents and mixtures thereof.
The reaction mixture is polymerized in a device at least partially surrounded by a polymer layer selected from the group consisting of: polyvinyl chloride (PVC), PVC/vinyl copolymers, low and high density polyethylene, polyethylene/vinyl copolymers, polyethylvinyl acetate and copolymers, polyethylene terpthalate and copolymers, polypropylene, polyamide, polyimide, polyurethane, _ g _ polyvinylidene fluoride, fluorinated ethylene proplyene polymers, polytetrafluoroethylene, silicone rubber, butyl rubber, neoprene rubber, isoprene rubber, cellulose acetate and laminated (co-extruded) membrane types (eg. PVC/fluori-nated ethylene propylene polymers, polyethylene/ethylvinyl acetate, polyethylene/polyethylene terpthalate and the like). Different semiochemicals will have different permeabilities with respect to the membrane used and this provides versatility in attaining various desired release rate characteristics.
In a further embodiment, the reactive urethane mixture can be cast in a semiochemical permeable polymeric tube. The tubing containing the urethane mixture and the semiochemical can be used as long cylinders or cut into short cylinders which serve as semiochemical dispensers.
In a broad aspect, the invention is directed to a composite polymer semiochemical controlled release rate dispenser comprising: (a) a polyurethane reservoir formed from a reaction mixture of a polyol, a polymeric isocyanate and an unreactive semiochemical compatible with the polyol and isocyanate reaction mixture; and (b) a semiochemical permeable polymeric membrane that covers at least part of the reservoir, and which regulates the release of the semiochemical from the dispenser.
The invention in another aspect pertains to a composite polymer semiochemical controlled release dis-penser comprising: (a) a polyurethane reservoir formed from a reaction mixture of (i) a polyol selected from the group consisting of hydroxy-terminated polybutadiene resins, hydroxy-terminated polyether resins and hydroxy-terminated polyester resins, (ii) an isocyanate component selected from the group consisting of monomeric or polymeric diphenylmethane diisocyanate, toluene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate and - g -polymeric hexamethylene diisocyanate, (iii) an unreactive semiochemical(s) having functional groups selected selected from the group consisting of alkanes, alkenes, alkynes, aromatic hydrocarbons, ethers, esters, epoxides, aldehydes, ketones, lactones, nitriles, imines, tertiary amines, thioethers, sulfoxides, sulfones, disulfide compounds, thioesters, organohalides, and mixtures thereof; and (b) a semiochemical permeable polymeric membrane covering at least a portion of the said polyurethane reservoir and controlling release of the semiochemical from the reser-voir, the membrane being selected from the group consisting of polyvinylchloride, polyvinylchloride/vinyl copolymers, low and high density polyethylene, polyethylene/vinyl copolymers, polyethylvinyl acetate and copolymers, polyethylene terpthalate and copolymers, polypropylene, polyamide, polyimide, polyurethane, polyvinylidene fluoride, fluorinated ethylene propylene polymers, polytetrafluoroethylene, silicone rubber, butyl rubber, neoprene rubber, isoprene rubber, cellulose acetate and laminated (co-extruded) membrane types including polyvinylchloride/fluorinated ethylene propylene polymers, polyethylene/ethylvinyl acetate, polyethylene/polyethylene terpthalate.
The semiochemical active ingredient can be selected from the group: E or Z-13-octadecenyl acetate, E
or Z-11-hexadecenal, E or Z-9-hexadecenal, hexadecanal, E
or Z-11 hexadecenyl acetate,E or Z-9-hexadecenyl acetate, E or Z-11-tetradecenal, E or Z-9-tetradecenal, tetradecanal, E or Z-11-tetradecenyl acetate, E or Z-9-tetradecenyl acetate, E or Z-7-tetradecenyl acetate, E or Z-5-tetradecenyl acetate, E or Z-4-tridecenyl acetate, E or Z-9-dodecenyl acetate, E or Z-8 dodecenyl acetate, E or Z-5-dodecenyl acetate, dodecenyl acetate, 11-dodecenyl acetate, dodecyl acetate, E or Z-7-decenyl acetate, E or Z-5-decenyl acetate, E or Z-3-decenyl acetate, Z or E,Z or E
3,13-octadecadienyl acetate, Z or E, Z or E 2,13-octadecdienyl acetate, Z,Z or E-7,11-hexadecadienyl acet-ate, Z,E 9,12-tetradecadienyl acetate, E,E-8,10-dodecadienyl acetate, Z,E 6,8-heneicosadien-11-one, E,E

7,9-heneicosadien-11-one, Z-6-henicosen-11-one, 7,8-epoxy-2-methyloctadecane, 2-methyl-7-octadecene, 7,8-epoxyoctadecane, Z,Z,Z-1,3,6,9-nonadecatetraene, 5,11-dimethylheptadecane, 2,5-dimethylheptadecane, 6-ethyl-2,3-dihydro-2-methyl-4H-pyran-4-one, methyl jasmonate, alpha-pinene, beta-pinene, terpinolene, limonene, 3-carene, p-cymene, heptane, ethyl crotonate, myrcene, verbenene, camphene, camphor, cineol, alpha-cubebene, allyl anisole, undecanal, nonanal, heptanal, E-2-hexenal, E-3-hexenal, hexanal, verbenone, 3-methyl-2-cyclohexenone, 3-methyl-3-cyclohexenone, frontalin, exo and endo-brevicomin, lineatin, multistriatin, chalcogran, 7-methyl-1,6-dioxaspiro [4 . 5] decane, 4, 8-dimethyl-4 (E) , 8 (E) -decadienolide,ll-methyl-3(Z)-undecenolide,Z-3-dodecen-11-olide, Z,Z-3,6-dodecen-11-olide, Z-5-tetradecen-13-olide, Z,Z-5,8-tetradecen-13-olide, Z-14-methyl-8-hexadecenal, 4,8-dimethyldecanal, gamma-caprolactone, hexyl acetate, E-2-hexenyl acetate, butyl-2-methylbutanoate, propyl-hexanoate, hexylpropanoate, butylhexanoate, hexylbutanoate, butyl butyrate, E-crotylbutyrate, Z-9-tricosene, methyl eugenol, alpha-ionone, 4-(p-hydroxyphenyl)-2-butanone acetate, E-beta-farnasene, nepetalactone, 3-methyl-6-isopropenyl-9-decenyl acetate, Z-3-methyl-6-isopropenyl-3,9-decadienyl acetate, E or Z-3,7-dimethyl-2,7-octadecadienyl propionate, 3-methylene-7-methyl-7-octenyl propionate, 2,6-dimethyl-1,5-heptadien-3-of acetate, 2-2,2-dimethyl-3-isopropenylcyclobutanemethanol acetate, E-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, Z-5-(1-decenyl)dihydro-2(3H)-furanone, 2-phenethylpropionate, 3,11-dimethyl-2-nonacosanone, 8-methylene-5-(1-methylethyl)spiro[11-oxabicyclo[8.1.0]undecene-2,2-oxiran]-3-one, 2-propylthietane, 3-propyl-1,2-dithiolane, 3,3-dimethyl-1,2-dithiolane, 2,2-dimethylthietane, E or Z-2,4,5-trimethylthiazoline, 2-sec-butyl-2-thiazoline, isopentenyl methyl sulfide.
The active ingredient in composite polymer release devices can be an unnatural synthetic behavior-modifying chemical (semiochemical mimic) as defined above.
This group comprises chemicals not found in nature but that cause behaviors that mimic those of a semiochemical.
The semiochemical concentration in the reservoir of a composite polymer controlled release device can be between 0.001% and 80o by weight. The reservoir forming mixture can include substances selected from the group consisting of antioxidants, ultraviolet light absorbers, pigments, dyes, fillers, blowing agents and plasticizers.
The invention in a further aspect is directed to a composite semiochemical controlled release rate dispenser comprising: (a) a cylindrical polyurethane core formed from a polyol, a diisocyanate and an unreactive semiochemical;
and (b) a semiochemical permeable rate controlling mem-brane comprised of a dissimiliar polymeric tubing covering at least a portion of the core.
DRAWINGS
In the drawings, which represent specific embodi-ments of the invention, but which should not be regarded as restricting the spirit or scope of the invention in any way:
Figure 1 illustrate graphs which demonstrates cumulative verbenone release from urethane monolithic devices compared with identical urethane cores surrounded by a permeable PVC membrane.

Figure 2 illustrates a graph of average retained Z-11-hexadecenal residue per device aged in a Florida cotton field as a function over time. Figure 3 includes similarly shaped PVC monolithic devices for comparison.
Figure 3 illustrates a plot of mean release rate (mg/hour/device) of verbenone from composite polymer release devices according to the invention, as a function of time.
DETAILED DESCRIPTION OF THE INVENTION
The invention consists of versatile composite polymer devices used for dispensing semiochemicals at a controlled rate. Hydroxy-terminated polybutadiene resins and/or other polyols an be combined with additives, semio-chemical(s), and an isocyanate component to produce con-trolled-release reservoirs. By varying the semiochemical load, the cross-linking density of the matrix, the presence of various resin additives, as well as the type of per-meable membrane, a variety of release characteristics can be obtained. Semiochemical dispensers can be produced under very mild conditions using a simple process that is readily adapted to automated production of a variety of device forms. The main limitation of this method is that the reaction chemistry which forms the device matrix is not compatible with aqueous semiochemical mixtures and semio-chemicals that have active hydrogen donating groups .
This technology is an improvement in several aspects of semiochemical dispensers described in prior art.
The current technology may be conducted at room temperature and this represents an energy saving over processes using thermal curing (Fitzgerald et al. 1973 and Czechoslovakian Patent No. 8490), melting polymers during semiochemical loading (U.S. Patent Nos. 4,908,208 and 5,008,115) or radiation curing methods (Kim et al. 1988 and Smith et al.

1991). Moreover, since expensive volatile semiochemicals may be lost during thermal processing, the current technol-ogy offers further advantages over this type of prior art.
The invention allows the formation of a semio-chemical reservoir in a single step at room temperature.
This contrasts strongly with U.S. Patent Nos. 4,908,208 and 5,008,115 which disclose silicone urethane copolymers which first must be synthesized using inert atmosphere and high temperatures, solvents removed, the copolymer melted and mixed with the with active agent and hot viscous mixture cast into devices. Other prior art membrane bound con-trolled release devices such as those disclosed in U.S.
Patent No. 4,445,641 also require multiple processing steps. Clearly, the devices specified in the current invention are prepared by a much simpler process.
Other differences between U.S. Patent Nos.
4,908,208 and 5,008,115 and the current technology are also evident. The subject invention discloses a thermoset polyurethane semiochemical reservoir composed predominately of soft block segments. Prior art silicone urethane copolymers are thermoplastic which require both hard and soft block segments in order to function properly as a controlled release matrix. The urethane component of the copolymers disclosed by Lee and Gornowicz consists of hard block segments derived from short chain polyols and diisocyanates while the soft block component of the are derived from polydiorganosilane and or polyalkylene oxide.
Similar silicone urethane copolymers are disclosed as membrane material in U.S. Patent No. 4,793,555 for the release of aqueous mixtures and this is obviously outside the scope of the subject invention.
Data is presented in U.S. Patent Nos. 4,908,208 and 5,008,115 that would indicate the practical utility of devices prepared with some of these copolymer active ingredient combinations would be very limited. For example, the release rate data presented in Table II (col.

8 and 9) for active agents in various copolymers is pres-ented as a single value, implying a constant release (zero order kinetics). This is misleading as release kinetics of monolithic devices are known to be logarithmic. Close inspection of release rate data given in Table II (col. 8 and 9) show that 20% trimedlure in copolymer I, 70%
trimedlure in copolymer II and 20% glossyplure have release rates higher than the neat chemical. This data appears to be erroneous since it is impossible for inert polymers to increase the vapour pressure of a substance. More import-antly, in controlled release applications, the objective is to reduce the release rate from that of the neat chemical to provide sustained release over long periods of time.
Obviously these copolymer matricies, at the stated loadings, are not controlling the release of volatile active agents. Similiarly, syneresis is observed with 900 trimedlure in copolymer II (example 5) and 33% benzyl alcohol in copolymer II. This syneresis is an indication of insolubility of volatile agents with the copolymer at this loading level and is a serious dissadvantage in the storage and use of such devices. Clearly, some of these copolymer mixtures appear to be poor release rate regula-tors for trimedlure, glossyplure and benzyl alcohol. The shortcomings of this technology has limited the use of the devices in semiochemical applications.
The invention is an improvement over prior art monolithic silicone polyurethane copolymer or urethane matrices (U.S. Patent Nos. 4,908,208, 5,008,115 and 4,594,380). These patents disclose matrix compositions but do not mention nor demonstrate the use of release rate controlling membranes in conjunction with the matrix. In addition, none of these prior art patents indicate that the release rate of any given active agent may be manipulated by changes to the matrix and or the rate controlling membrane. The new composite devices of the invention comprise polyurethane reservoir systems bounded by a dissimiliar polymer which acts as a rate controlling membrane. In addition to regulating the release rate, the membrane of the composite devices has further advantages over monolithic devices since it also serves to screen out ultraviolet light and limit exposure to oxygen, both of which may contribute to semiochemical degradation in the matrix.
An example given by Chapin et al. in U.S. Patent No. 4,594,380 demonstrates the effect of an open container on the release of vapona. This example specifies a mono-lithic wafer supported in container of unknown composition and geometry with a 950 mm2 opening. There is no permeable membrane to regulate the release characteristics. Further-more, Chapin et al. at lines 21-27 of column 1, state:
"One class of methods comprises dispersion of the active agent throughout (or dissolution in) a substantially inert matrix from which the active agent is gradually released into the environment. The discussion herein will be limited to controlled-release methods of this type, and to devices using this method. Such devices are frequently referred to as 'monolithic' devices." U.S. Patent No.
4,594,380 therefore pertains to a homogenous, single compo-nent (monolithic) device. Clearly, Chapin et al. did not anticipate composite polymer devices using a semi-permeable enveloping membrane of a seperate polymer to regulate the release characteristics.
The teachings of U.S. Patent No. 4,594,380 are predominately directed to the delivery of toxic agents. It not obvious from these teachings that for many semiochemical uses a very precise delivery of active agent is necessary. U.S. Patent No. 4,594,380 does not teach that the reactive nature of the urethane curing process may be useful for removal of inhibitors from a semiochemical blend. In addition, no biological or field data demon-strating efficacy was presented by Chapin et al.
The invention has addressed several of the problems inherent in monolithic semiochemical release devices and other prior art devices. The new technology demonstrates that both the reservoir matrix and the device membrane may be membrane may be manipulated. This compli-mentary combination allows the composite polymer devices better controlled release of semiochemicals than can usually be attained using monolithic devices. Comparisons of the new devices and prior art monolithic dispensers are shown in Examples 1, 3 and 4.
Although the invention as described is not suited to the release of aqueous semiochemical mixtures and semiochemicals with active hydrogen donating groups, this reactivity can be used to purify relatively crude semio-chemicals in situ. Impurities of this nature can be trapped by chemical reaction with the isocyanate component during curing of the matrix. This method avoids the need for additional purification of semiochemicals containing low concentrations of impurities with hydroxyl, carboxyl, sulfhydryl and amino functional groups. Example 2 demon strates this principal.
The physical form of the subject invention can be highly variable. For example, fillers or blowing agents may be included in the formulation to produce a reservoir where a high surface area is desired. Additives may be used to absorb or reflect radiation (pigments, ultraviolet screening agents and carbon black), inhibit oxidation (antioxidants), to increase or decrease the viscosity of the mix and or the release rate of the semiochemical (plasticizers). Devices may be prepared by casting the reactive mixture in polymeric tubing or molds containing the polymer membrane. Layered or laminated devices may also be produced by casting the polyurethane reservoir on various barrier materials or membranes. For example a three layer laminate device might consist of an aluminum foil barrier, polyurethane layer containing the AI and a polyethylene membrane.
Hydroxy-terminated polybutadiene (poly BDTM) resins with a range of hydroxyl numbers and molecular weights are available and are preferred components in polymerizing the matrix. Those available from Atochem North America include the following poly BDTM resins: R45M
(average molecular weight 2800 and hydroxyl value 0.73 meq/g), R45HT (average molecular weight 2800 and hydroxyl value 0.83 meq/g), R20LM (average molecular weight 1200 and hydroxyl value 1.7 meq/g), and 605 (an epoxidized hydroxyl-terminated polybutadiene with an oxirane content of 6.5% by weight and hydroxyl value of 2.7 meq/g) . Poly BDTM resins alone or blended with polyether or polyester polyols are compatible with many classes of semiochemicals. Variation of the mixtures may be used to change the solubility parameter, hydrogen bonding and the extent of cross linking within the matrix by methods known in prior art.
U.S. Patent No. 4,594,380 has indicated the use of hydroxy or carboxy-terminated copolymers of butadiene and acrylonitrile or styrene as agents to modify a poly BDTM
based urethane release matrix. These materials are of high viscosity and are not easily incorporated into the matrix without considerable heating and the use of specialized mechanical mixing equipment. Of far more utility are low viscosity hydroxy-terminated polyethers which may be used to modify the release matrix. Examples of low viscosity polyether polyols compatible with poly BDTM resins include polymers of polyproplene glycol such as PluracolTM 220 (hydroxyl number 27), PluracolTM 2010 (molecular weight 2000, hydroxyl number 56) both available from BASF Corpor-ation, and AlkapolTM G-240 (molecular weight 700, hydroxyl number 240) available from Rhone-Poulanc Speciality Chemi-cals, Mississauga, Ontario). Similar materials are avail-able from several other manufacturers. The polyol compo-nent can also include materials to enhance the biodegradability of the matrix for example polycaprolactone diol or carbohydrate-based materials (cellulose esters and ethers ) .
Semiochemical controlled release device reser-voirs prepared with a high proportions of hydroxyterminated butadienes will be highly elastic and will consist of predominately of soft block domains. The isocyanate component is generally an MDI with LupranateTM MM-103 (isocyanate content 29.50 by weight available from BASF
Corporation) and IsonateTM 143L (70-80o MDI and 20-30%
polymerized MDI, available from Dow Chemical U.S.A.) as examples of suitable commercially available materials.
Other isocyanates including toluene diisocyanate, isophorone, diisocyanate and hexamethylene diisocyanate as well as other MDI blends can also be used in the process.
The process generally requires no catalysis, however, catalysts known from prior art may be used with some of the slower reacting isocyanate/polyol combinations. Since isocyanates react readily with water, precautions must be taken to insure that the semiochemical, polyol and other matrix additives used are substantially free of water.
The general method for preparation of the polyurethane reservoir is based on the "one shot" batch protocol outlined for the reaction of poly BDTM resins with MDI (Ryan 1971). Typical preparation of a semiochemical reservoir involves warming the polyol component and addi-tives to 35-75° C with stirring at a vacuum of 15-100 mm to remove traces of volatile contaminants. The vessel is returned to ambient temperature and pressure and the semiochemical (0-80o w/w) is added to the mix. The mixture is stirred under vacuum until homogeneous. The isocyanate component added (isocyanate index 1.05) and stirring under vacuum continued. The mixture is transferred to molds and left to polymerize. The time for polymerization can vary from a few minutes to several days and is accelerated by catalytic means or by curing at higher temperatures.
The polymeric matrix used for the reservoir is compatible with a large number of semiochemicals. The skilled practitioner will be aware that hundreds of semio-chemicals are known and complete listing of compounds compatible with the matrix is clearly impractical. Some examples demonstrating the range of active ingredients suited to incorporation into the composite polymer devices include: lepidopteran pheromones (E or Z-13-octadecenyl acetate, E or Z-11-hexadecenal, E or Z-9-hexadecenal, hexadecanal, E or Z-11 hexadecenyl acetate,E or Z-9-hexadecenyl acetate, E or Z-11-tetradecenal, E or Z-9-tetradecenal, tetradecanal, E or Z-11-tetradecenyl acetate, E or Z-9-tetradecenyl acetate, E or Z-7-tetradecenyl acetate, E or Z-5-tetradecenyl acetate, E or Z-4-tridecenyl acetate, E or Z-9-dodecenyl acetate, E or Z-8 dodecenyl acetate, E or Z-5-dodecenyl acetate, dodecenyl acetate, 11-dodecenyl acetate, dodecyl acetate, E or Z-7-decenyl acetate, E or Z-5-decenyl acetate, E or Z-3-decenyl acet-ate, Z or E,Z or E 3,13-octadecadienyl acetate, Z or E, Z
or E-2,13 octadecadienyl acetate, Z,Z or E-7,11-hexadecadienyl acetate, Z,E 9,12-tetradecadienyl acetate, E,E-8,10-dodecadienyl acetate, Z,E-6,8-heneicosadien-11-one, E,E 7,9-heneicosadien-11-one, Z-6-henicosen-11-one, 7,8-epoxy-2-methyloctadecane, 2-methyl-7-octadecene, 7,8-epoxyoctadecane, Z,Z,Z-1,3,6,9-nonadecatetraene, 5,11-dimethylheptadecane, 2,5-dimethylheptadecane, 6-ethyl-2,3-dihydro-2-methyl-4H-pyran-4-one, methyl jasmonate), bark beetle kairomones (alpha-pinene, beta-pinene, terpinolene, limonene, 3-carene, p-cymene, myrcene, verbenene, camphene, camphor, cineol, alpha-cubebene, allyl anisole, undecanal, nonanal, heptanal, E-2-hexenal, E-3-hexenal, hexanal, heptane, ethyl crotonate), bark beetle pheromones (verbenone, 3-methyl-2-cyclohexenone, 3-methyl-3-cyclohexenone, frontalin, exo and endo-brevicomin, lineatin, multistriatin, chalcogran, 7-methyl-1,6-dioxaspiro[4.5]decane), grain beetle pheromones (4,8-dimethyl-4(E),8(E)-decadienolide, 11-methyl-3(Z)-undecenolide, Z-3-dodecen-11-olide, Z,Z-3,6-dodecen-11-olide, Z-5-tetradecen-13-olide, Z,Z-5,8-tetradecen-13-olide), dermestid and tenebrionid beetle pheromones (Z-14-methyl-8-hexadecenal, 4,8-dimethyldecanal, gamma-caprolactone), apple maggot kairomones (hexyl acetate, E-2-hexenyl acetate, butyl-2-methylbutanoate, propylhexanoate, hexylpropanoate, butylhexanoate, hexylbutanoate), dipteran pheromones and synthetic attractants (Z-9-tricosene, tert-butyl-4 (or 5)-chloro-2-methyl-cyclohexanecarboxylate, methyl eugenol, alpha-ionone, 4-(p-hydroxyphenyl)-2-butanone acetate), aphid pheromones (E-beta-farnasene, nepetalactone), hemipteran pheromones (butylbutryate and E-crotylbutryate), homopteran pheromones (3-methyl-6-isopropenyl-9-decenyl acetate, Z-3-methyl-6-isopropenyl-3,9-decadienyl acetate, E or Z-3,7-dimethyl-2,7-octadecadienyl propionate, 3-methylene-7-methyl-7-octenyl propionate, 2,6-dimethyl-1,5-heptadien-3-of acetate, 2-2,2-dimethyl-3-isopropenylcyclobutanemethanol acetate, E-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate), Japanese beetle pheromone and attractants( Z-5-(1-decenyl)dihydro-2(3H)-furanone, 2-phenethylpropionate), cockroach pheromones (3,11-dimethyl-2-nonacosanone,8-methylene-5-(1-methylethyl)spiro[11-oxabicyclo[8.1.0]undecene-2,2-oxiran]-3-one), mammal predator kairomones (2-propylthietane, 3-propyl-1,2-dithiolane, 3,3-dimethyl-1,2-dithiolane, 2,2-dimethylthietane, E or Z-2,4,5-trimethylthiazoline, 2-sec-butyl-2-thiazoline, isopentenyl methyl sulfide). It should be noted that some semiochemicals such as 2,4,5-trimethylthiazoline (with an imine functionality) or tertiary amines, although not reactive (compatible) with the matrix, will act as catalytic agents in the polyurethane forming reaction. These materials are not well suited to the batch method on a large scale, but are easily incorporated in a reaction injection moulding (RIM) process to produce devices.
The presence of a permeable polymer membrane on the dispensers is significant feature of this technology.
There are a great number of polymer membrane types commer-cially available. With this large selection, membrane materials can range from almost impermeable to highly permeable for most semiochemicals. It is recognized that the optimal release rate characteristics will be attained when the membrane material is not a polyurethane composed predominately of hydroxy-terminated polybutadiene. The membrane material may be selected from polyvinyl chloride, PVC/vinyl copolymers, low and high density polyethylene, polyethylene/vinyl copolymers,polyethylvinyl acetate and copolymers, polyethylene terpthalate and copolymers, polypropylene, polyamide, polyimide, polyurethane, polyvinylidene fluoride, fluorinated ethylene proplyene polymers, polytetrafluoroethylene, silicone rubber, butyl rubber, neoprene rubber, isoprene rubber, cellulose acetate and laminated (co-extruded) membrane types (eg. polyvinyl-chloride/fluorinated ethylene propylene polymers, polyethylene/ethylvinyl acetate, polyethylene/polyethylene terpthalate and the like).
The composite polymer devices exhibit a charac-teristic release of semiochemical over time as demonstrated in Examples 1,3, and 5. After manufacture devices are usually stored in vapour tight containers until the dis-pensers are needed. During this time the semiochemical approaches equilibrium concentrations in the matrix, the surrounding membrane and the atmosphere within the storage container (based on the solubility of the semiochemical in these various media). When these dispensers are removed from storage they will exhibit a moderate to sharp decline in release rate as the semiochemical evaporates from the surface of the device. This drop in release rate takes place over several hours or weeks and depends upon environ-s mental conditions, the volatility of the semiochemical and the type of matrix and membrane combination. Once diffu-sion of the semiochemical from the matrix to the surface of the membrane has taken place the dispensers will release at more constant levels for prolonged periods. This period of relatively higher release has not hampered the use of these devices in dispensing anti-aggregation pheromones for tree protection or predator kairomones for mammal repellent applications or sex pheromones for mating disruption applications. When dispensers are produced for monitoring traps, they may be removed from storage and "pre-aged"
prior to field deployment or the traps simply set out an appropriate time earlier than the anticipated flight of the pest.
A single manufacturing method may be used to produce several different types of release devices using the current invention, exemplified by the casting of the urethane matrix in PVC tubing. Short pieces of tubing (0.2-10.0 cm) can be cut and distributed for ground-based semiochemical dispensers in repellent or mating disruption applications. Similarly, short pieces of the tubing serve as single point source semiochemical emitters used as lures in insect traps. Where point source emitters are not desired, long lengths of semiochemical loaded tubing may be used. For example several meters of loaded tubing may be attached to a tree to provide semiochemical release over a large area. Long lengths of semiochemical-loaded tubing have advantages over devices with small reservoirs in that semiochemical release is possible for extended periods of time. The new technology is capable of producing devices that control the release of AI from minute quantities (ng/day) to a release hundreds of milligrams or even grams of AI per day.

This example show two similiar but separate experiments demonstrating the effect of a membrane on the release characteristics of the bark beetle anti-aggregation pheromone verbenone from a polyurethane matrix. In these experiments, the matrix was prepared via the basic method outlined that contain verbenone (active ingredient) and a polyurethane composed of poly BDTM R45HT and LupranateTM
MM103. The matrix mixture was divided and used to prepare both composite polymer devices and homogenous monolithic devices in both experiments.
In the first experiment (series A), a mixture containing 9.86% verbenone is allowed to polymerize in PVC
tubing (0.5 mm thick and 3.8 mm i.d.) for 16 hours at room temperature in a sealed polyethlene nylon laminate bag.
The tubing is cut into 10 cm lengths and in one group of devices, the outer PVC membrane is carefully removed to produce monolithic devices. Each device core contained a calculated load of approximately 100 mg of verbenone.
In the second experiment (series B), a mixture containing 8.96% verbenone is allowed to polymerize in: 1) PVC tubing ( 0 . 5 mm thick and 3 . 0 mm i . d. ) which was heat sealed every 10 cm along its length 2) glass tubing 50 cm long x 3.0 mm i.d. capped at both ends with a rubber septa.
The loaded tubes were left at room temperature in a sealed polyethylene/nylon laminate bag for one week. The loaded PVC tubing was cut every 10 cm at centre of the heat seal to provide composite polymer devices (a urethane core completely surrounded by a permeable PVC membrane). The glass tubes were carefully broken and the resulting urethane rod was cut into 10 cm lengths to provide mono-lithic (unsheathed) devices. Each device core contained a calculated load of approximately 78 mg of verbenone.
In both experiments, four replicates of the composite polymer devices and four monolithic devices were aged in a temperature controlled environment chamber at 30°
for the A series (first experiment) or at 35°C for the B
series (second experiment) with an air flow through the chamber at a rate of 15 cfm. Devices were weighed at regular intervals on a balance with a precision of 0.05 mg.
The average cumulative percentage weight loss per device was plotted against time for the first experiment is shown in Figure 1, A series and the second experiment is shown in Figure 1, B series.
In both experiments, the effect of the permeable polymer membrane was dramatic, the monolithic devices A and B rapidly lost verbenone such that 50-70 % was evaporated in the first 2-3 days. In contrast, the composite polymer devices A and B released verbenone relatively smoothly throughout the test period. After 30 days the monolithic devices had released approximately 85% of the loaded verbenone while the composite devices had released 14-22 of the loaded verbenone. In addition, as demonstrated by the smooth curves, the rate of verbenone release from the composite devices was much more constant than that of the monolithic devices. The composite polymer devices, both A
and B, in these experiment were clearly superior in the controlled release of verbenone to the environment over long periods of time.
The two experiments show the similarities between the monolithic devices A and B or the composite devices A
and B at both 30°C and 35°C. There is not much difference between the composite devices A or B. Likewise, the curves for the monolithic devices A and B substancially overlap.

The curves shown in Figure 1 also demonstrate the permeability of the PVC membrane to verbenone. In the second experiment the composite polymer devices were completely enclosed in the PVC membrane, while in the first experiments the composite polymer devices were open-ended cylinders. In both experiments the effect of the PVC
polymer membrane was very clear when compared to the monolithic devices. The release characteristics of both types of composite polymer devices A and B are similar, the effects of the open ends is minimal, even at different temperatures, in comparison to the absence of the membrane.
Furthermore, the effects of the open ends is minimized when the geometry of the device is a cylinder many times longer than it is in diameter, as was the case in these experi ments.

This experiment demonstrates the capability of the reservoir forming reaction to purify a crude semio-chemical mixture in situ during the curing process. The main component in the pheromone of Choristoneura fumiferana is E-11-tetradecenal together with a small percentage of the Z isomer (Silk et al. 1980). The insect response to this pheromone blend is inhibited by E-11-tetradecenol (Sanders 1972) which is often the synthetic precursor to the aldehyde and may be present as a contaminant in some batches of pheromone. A mixture of 34.2 mg of E-11-tetradecenal (92.5% E isomer, 5.3% Z isomer, free of detectable alcohols) and 4.7 mg of E-11-tetradecenol (990 pure) was prepared and a sample subjected to capillary gas chromatography (GC). Under the conditions used, the ratio of peak areas of E-11-tetradecenol to E-11-tetradecenal was 0.1322. Another sample of the aldehyde/alcohol mixture (approximately 2.0% w/w) was polymerized with 20% w/w of dioctyladipate and poly BDTM R45HT and LupranateTM MM 103 (isocyanate index 1.1). After polymerization the resulting plug was loosened from the vial walls and extracted with five volumes of hexanes overnight. A sample of the extract was diluted six fold and subjected again to GC analysis.
After this analysis the ratio of peak areas of E-11-tetradecenol to E-11-tetradecenal was now 0.0049. The results demonstrate that approximately 96% of the original E-11-tetradecenol had been removed during the curing process. This example also serves to demonstrate why semiochemicals with active hydrogen donating groups are not compatible with this type of polyurethane reservoir.

This example demonstrates that the composite polymer devices have sustained release capabilities for a labile lepidopteran pheromone. The new dispensers are compared with prior art monolithic devices. A polymeric core formulated from poly BDTM R45HT, IsonateTMTM 143 L, 14.50 dioctyladipate w/w and 1.37 % Z-11-hexadecenal w/w as the active ingredient AI was cast into PVC tubing 4.8 mm diameter with 0.5 mm wall thickness. Cylinders 42 mm long were cut from the tubing to form the devices used in this test. Devices were tethered to cotton plants and exposed to ambient conditions in Florida during August - October 1991. Sample devices were collected at weekly intervals, sealed in nylon polyethylene laminate bags and stored at 5°
C or lower until analysis. Samples consisting of three devices were repeatedly extracted with hexanes, the extracts were pooled, treated with Hexadecane as an inter-nal standard and analyzed by capillary column gas chroma-tography. The extracts were analyzed for AI and Z-11-Hexadecenoic acid, an expected oxidation product of the AI.
The results of the residue analysis are graphed as a function over time in Figure 2. Results from similarly shaped PVC monolithic devices are included for comparison in Figure 2. Clearly, the composite polymer devices have superior controlled release properties when compared to the monolithic devices. The results demonstrate that the composite polymer device affords some protection of the pheromone from oxidation. Except for an initial sharp drop in the residue weights in the first two weeks, the devices exhibit a smooth release of AI for over 60 days under relatively high temperature field conditions. Such a device is potentially useful for mating disruption of Heliocoverpa (Heliothis) species.

In this example, composite polymer lures were compared with two types of monolithic PVC lures in sticky traps. The biological assay was conducted at sites in Oregon, Washington, California and Idaho in 1991. The devices were 4 mm diameter with a wall thickness of 0.5 mm with a core composition containing poly BDTM R45HT, IsonateTM 143L, 50% w/w dioctyladipate and 0.001 % w/w of Z-6-Henicosen-11-one as AI. The PVC devices were 5 mm long and the urethane cored devices were 8 mm long, with all devices containing equivalent weights (approximately 500 ng each) of AI. The results of this test are shown in Table 1.

TABLE 1: Summary of Douglas-~r tussock moth lure evaluation.
Lure Type PVC 1 PVC 2 CON~OSITE

# of sites (4 blocks/site)27 27 27 Sum of avg # insects 414.92 596.00 685.83 trapped/block Avg # insects trapped/block15.37 22.07 25.40 Standard Deviation 23.63 23.71 24.66 1 Maximum # trapped/block 87.50 81.75 75.75 o The results demonstrate that composite polymer devices show good biological activity and no inhibitors of the biological response were present. These devices are useful as an early warning monitoring tool for detecting Douglas-Fir tussock moth populations.

In this example two different urethane semiochemical blends were cast into lengths of ethylvinyl acetate / ethylene copolymer tube stock 12 micron thick to produce pouches 5.2 x 10.0 cm. After loading with semio-chemical and polymer, the packages were heat sealed and allowed to polymerize. The composite polymer devices were made to contain 5.0 g each of verbenone as the semio-chemical. Sample A devices contained 80o verbenone w/w and 20o polyurethane prepared from poly BDTM R45-HT and LupranateTM MM-103. Sample B devices contained 20%
verbenone w/w and 80o polyurethane prepared from poly BDTM
R20LM and lupranate~ MM-103. The devices were aged in a temperature controlled chamber at 24° C with a flow of air through the chamber of 15 cfm. Release rate of semio-chemical from the controlled devices was determined by weight loss. The observed mean release of verbenone from these devices over time is shown in Figure 3. The results demonstrate that resin type and pheromone load can substan-tially alter the release rate characteristics of these devices. Devices such as these are useful for dispensing anti-aggregation pheromones of bark beetles.

Many different composite polymer devices have been used to deliver semiochemicals under conditions of actual field use. The type of membranes used has included polyvinyl chloride, PVC/vinyl copolymers, low and high density polyethylene, polypropylene, nylon, polyethylene/vinyl copolymers, polyethylvinyl acetate and copolymers, polypropylene, nylon (polyamide), and laminated (coextruded) polyethylene/nylon. The types of semio-chemicals has included: Z-11-hexadecenal, Z-9-hexadecenal, E-11-tetradecenal, Z-9-tetradecenal, E or Z-11-tetradecenyl acetate, E and Z-9-dodecenyl acetate, Z-7-decenylacetate, Z,E 9,12-tetradecadienyl acetate, Z,E 6,8-heneicosadien-11-one, E,E 7,9-heneicosadien-11-one, Z-6-henicosen-11-one,7,8-epoxy-2-methyloctadecane,2-methyl-7-octadecene, 7,8-epoxyoctadecane, alpha-pinene, terpinolene, limonene, 3-carene, p-cymene, heptane, allyl anisole, undecanal, nonanal, hexanal, verbenone, frontalin, exo-brevicomin, conophthorin (7-methyl-1,6-dioxaspiro[4.5]decane), Z-14-methyl-8-hexadecenal, hexyl acetate, E-2-hexenyl acetate, butyl-2-methylbutanoate, propylhexanoate, hexylpropanoate, butylhexanoate, hexylbutanoate), butylbutrate, E-crotylbutyrate, 2-9-tricosene, 2-propylthietane, 3-propyl-1,2-dithiolane, 2,2-dimethylthietane, E and Z-2,4,5-trimethylthiazoline, and isopentenyl methyl sulfide).

As will be apparent to those skilled in the art in the light of the foregoing disclosure, many alterations and modifications are possible in the practice of this invention without departing from the spirit or scope thereof. Accordingly, the scope of this invention is to be construed in accordance with the substance defined by the following claims.

- 3~ -REFERENCES
Arn H., et al., ed. 1992: "List of Sex Pheromones of Lepidoptera and Related Attractants", 2nd edition, Interna-tional Organization for Biological Control, West Palearctic Regional Section, Montfavet.
Budavari, S., ed. 1989: "The Merck Index", 11th edition, Merck & Co. Inc., Rahway.
Cunningham, R.T., et al. 1990: "The Male Lures of Tephritid Fruit Flies" in Behaviour Modifying Chemicals for Insect Pest Management Applications of Pheromones and Other Attractants, ed. R.L. Ridgeway et al., Marcel Dekker Inc., New York, p 255-267.
Fitzgerald, T.D., et al. 1973: Environmental Entomology, Vol. 2, #4, p.607-610.
Kim, J, et al. 1988: Appl. Radiat. Isot., Vol. 39, #11, p.
1145-52.
Mayer, M.S., and J.R. McLaughlin 1990: "CRC Handbook of Insect Pheromones and Sex Attractants", CRC Press Inc., Boca Raton.
Mitchell, E.R. ed. 1981: "Management of Insect Pests with Semiochemicals Concepts and Practice", Plenum Press, New York.
Norlund D.A. 1981: "Semiochemicals: A Review of the Termi-nology", in Semiochemicals Their Role in Pest Control, ed.
D.A. Norlund et al., John Wiley & Sons, p 13-23.
Oertel, G., ed. 1985: "Polyurethane Handbook" Hanser Publishers, Munich.

- 3~ -Ridgway R.L., et al. ed. 1990: "Behaviour Modifying Chemi-cals for Insect Pest Management Applications of Pheromones and Other Attractants", Marcel Dekker Inc., New York.
Ridgway R.L., et al., ed. 1992: "Insect Pheromones an Other Behaviour-Modifying Chemicals" BCPC monograph No. 51, British Crop Protection Council, Farnham.
Ryan, P.W., 1971: Journal of Elastoplastics, Vol 3, p 57-71.
Sanders, C.J. 1972: Canadian Forestry Service, Bi-Monthly Research Notes, 28, p 9-10.
Silk, P.J., et al. 1980: Environmental Entomology, Vol 9, p 640-644.
Smit, C.N. et al. 1991: Intern. Symp. Control Rel. Bioact.
Mater., Controlled Release Society, Inc. p 81-82.
Weatherston, I., et al. 1985: Journal of Chemical Ecology, Vol. 11, ##8, p 953-965, p 967-978 Woods, G., 1986: "The ICI Polyurethanes Book" 2nd Ed., ICI
Polyurethanes and John Wiley & Sons, Chichester.
Zeoli, L.T., et al. 1982: "Controlled Release Technol-ogies" in Insect Suppression with Controlled Release Pheromone Systems, Vol. 1, ed G. Zweig, CRC Press Inc., Boca Raton, Florida, p.131-144.

Claims (12)

1. A composite polymer semiochemical controlled release dispenser comprising:
(a) a polyurethane reservoir formed from a reaction mixture of a polyol, an isocyanate and as an active ingredient an unreactive semiochemical compatible with the polyol and isocyanate reaction mixture; and (b) a semiochemical permeable polymeric membrane covering at least part of the reservoir, and regulating the release of the semiochemical from the dispenser.

2. A composite polymer semiochemical controlled release dispenser comprising:
(a) a polyurethane reservoir formed from a reaction mixture of (i) a polyol selected from the group consisting of hydroxy-terminated polybutadiene resins, hydroxy-terminated polyether resins, and hydroxy-terminated polyester resins;
(ii) an isocyanate selected from the group consisting of monomeric or polymeric diphenylmethane diisocyanate, toluene diisocyanate, isophorone diisocyanate,hexamethylenr diisocyanate and polymeric hexamethylene diisocyanate; and (iii) a semiochemical unreactive with the polyol and isocyanate selected from the functional groups consisting of alkanes, alkenes, alkynes, aromatic hydrocarbons, ethers, esters, epoxides, aldehydes, ketones, lactones, nitriles, imines, tertiary amines, thioethers, sulfoxides, sulfones, disulfide compounds, thioesters, organohalides, and mixtures thereof; and (b) a surrounding permeable polymeric membrane covering at least a portion of the polyurethane reservoir and controlling the release of the semiochemical from the reservoir, said membrane being selected from the group consisting of consisting of polyvinylchloride, polyvinylchloride/vinyl copolymers,low and high density polyethylene, polyethylene/vinyl copolymers, polyethylvinyl acetate and copolymers, polyethylene terpthalate and copolymers, polypropylene, polyamide, polyimide, polyurethane, polyvinylidene fluoride, fluorinated ethylene propylene polymers, polytetrafluoroethylene, silicone rubber, butyl rubber, neoprene rubber, isoprene rubber, cellulose acetate and laminated (co-extruded) membrane types including polyvinylchloride/fluorinated ethylene propylene polymers, polyethylene/ethylvinyl acetate, and polyethylene/polyethylene terpthalate.

3. A composite polymer semiochemical controlled release dispenser according to claim 2 wherein the semiochemical active ingredient is selected from the group:
E or Z-13-octadecenyl acetate, E or Z-11-hexadecenal, E or Z-9-hexadecenal, hexadecanal, E or Z-11 hexadecenyl acetate, E or Z-9-hexadecenyl acetate, E or Z-11-tetradecenal, E or Z-9-tetradecenal, tetradecanal, E or Z-11-tetradecenyl acetate, E or Z-9-tetradecenyl acetate, E or Z-7-tetradecenyl acetate, E or Z-5-tetradecenyl acetate, E or Z-4-tridecenyl acetate, E or Z-9-dodecenyl acetate, E or Z-8 dodecenyl acetate, E or Z-5-dodecenyl acetate, dodecenyl acetate, 11-dodecenyl acetate, dodecyl acetate, E or Z-7-decenyl acetate, E or Z-5-decenyl acetate, E or Z-3-decenyl acetate, Z or E,Z or E 3,13-octadecadienyl acetate, Z or E, Z or E 2,13-octadecdienyl acetate, Z,Z or E-7,11-hexadecadienyl acetate, Z,E 9,12-tetradecadienyl acetate, E,E-8,10-dodecadienyl acetate, Z,E 6,8-heneicosadien-11-one, E,E 7,9-heneicosadien-11-one, Z-6-henicosen-11-one, 7,8-epoxy-2-methyloctadecane, 2-methyl-7-octadecene, 7,8-epoxyoctadecane, Z,Z,Z-1,3,6,9-nonadecatetraene, 5,11-dimethylheptadecane, 2,5-dimethylheptadecane, 6-ethyl-2,3-dihydro-2-methyl-4H-pyran-4-one, methyl jasmonate, alphapinene, beta-pinene, terpinolene, limonene, 3-carene, p-cymene, heptane, ethyl crotonate, myrcene, verbenene, camphene, camphor, cineol, alpha-cubebene, allyl anisole, undecanal, nonanal, heptanal, E-2-hexenal, E-3-hexenal, hexanal, verbenone, 3-methyl-2-cyclohexenone, 3-methyl-3-cyclohexenone, frontalin, exo and endo-brevicomin, lineatin, multistriatin, chalcogran, 7-methyl-1,6-dioxaspiro[4.5]decane, 4,8-dimethyl-4(E),8(E)-decadienolide,11-methyl-3(Z)-undecenolide,Z-3-dodecen-11-olide, Z,Z-3,6-dodecen-11-olide, Z-5-tetradecen-13-olide, Z,Z-5,8-tetradecen-13-olide, Z-14-methyl-8-hexadecenal,

4,8-dimethyldecanal, gamma-caprolactone, hexyl acetate, E-2-hexenyl acetate, butyl-2-methylbutanoate, propylhexanoate, hexylpropanoate, butylhexanoate, hexylbutanoate, butyl butyrate, E-crotylbutyrate, Z-9-tricosene, methyl eugenol, alpha-ionone, 4-(p-hydroxyphenyl)-2-butanone acetate, E-beta-farnasene, nepetalactone, 3-methyl-6-isopropenyl-9-decenyl acetate, Z-3-methyl-6-isopropenyl-3,9-decadienyl acetate, E or Z-3,7-dimethyl-2,7-octadecadienyl propionate, 3-methylene-7-methyl-7-octenyl propionate, 2,6-dimethyl-1,5-heptadien-3-olacetate,Z-2,2-dimethyl-3-isopropenylcyclobutanemethanol acetate,E-6-isopropyl-3,9-dimethyl-5,8-decadienylacetate, Z-5-(1-decenyl) dihydro-2 t3H)-furanone, 2-phenethylpropionate, 3,11-dimethyl-2-nonacosanone, 8-methylene-5-(1-methylethyl)spiro[11-oxabicyclo[8.1.0]undecene-2,2-oxiran]-3-one, 2-propylthietane, 3-propyl-1,2-dithiolane, 3,3-dimethyl-1,2-dithiolane, 2,2-dimethylthietane, E or Z-2,4,5-trimethylthiazoline, 2-sec-butyl-2-thiazoline, isopentenyl methyl sulfide.

4. A composite polymer semiochemical controlled release dispenser according to claim 2 wherein the reservoir forming mixture includes substances selected from the group consisting of anti-oxidants, ultraviolet light absorbers, pigments, dyes, fillers, blowing agents, and plasticizers.

5. A composite polymer semiochemical controlled release dispenser according to claim 2 wherein the semiochemical concentration in the said reservoir is between 0.001% and 80% by weight of the reservoir.

6. A composite polymer semiochemical controlled release dispenser comprising:
(a) a cylindrical polyurethane core formed from a polyol, a diisocyanate, and an unreactive semiochemical compatible with the polyol and diisocyanate; and (b) a semiochemical permeable rate controlling membrane comprised of a separate polymeric tubing covering at least a portion of the cylindrical polyurethane core.

7. A composite polymer controlled release dispenser according to claim 1 wherein the active ingredient is an unnatural synthetic behaviour-modifying chemical (semiochemical mimic).

8. A composite polymer controlled release dispenser according to claim 2 wherein the active ingredient is an unnatural synthetic behaviour-modifing chemical (semiochemical mimic).

9. A composite polymer controlled release dispenser according to claim 4 wherein the active ingredient is an unnatural synthetic behaviour-modifying chemical (semiochemical mimic).

10. A composite polymer controlled release dispenser according to claim 5 wherein the active ingredient is an unnatural synthetic behaviour-modifying chemical (semiochemical mimic).

11. A composite polymer controlled release dispenser according to claim 6 wherein the active ingredient is an unnatural synthetic behaviour-modifying chemical (semiochemical mimic).

12. A composite polymer semiochemical controlled release dispenser comprising:
(a) a polyurethane reservoir formed from a reaction mixture of (i) a polyol selected from the group consisting of hydroxy-terminated polybutadiene resins, hydroxy-terminated polyether resins, and hydroxy-terminated polyester resins;
(ii) an isocyanate selected from the group consisting of monomeric or polymeric diphenylmethane diisocyanate, toluene diisocyanate, isophorone diisocyanate,hexamethylene diisocyanate and polymeric hexamethylene diisocyanate; and (iii) a semiochemical unreactive with the polyol and isocyanate selected from the group consisting of E or Z-13-octadecenyl acetate, E or Z-11-hexadecenal, E or Z-9-hexadecenal, hexadecanal, E or Z-11 hexadecenyl acetate, E or Z-9-hexadecenyl acetate, E or Z-11-tetradecenal, E or Z-9-tetradecenal, tetradecanal, E or Z-11-tetradecenyl acetate, E or Z-9-tetradecenyl acetate, E or Z-7-tetradecenyl acetate, E or Z-5-tetradecenyl acetate, E or Z-4-tridecenyl acetate, E or Z-9-dodecenyl acetate, E or Z-8 dodecenyl acetate, E or Z-5-dodecenyl acetate, dodecenyl acetate, 11-dodecenyl acetate, dodecyl acetate, E or Z-7-decenyl acetate, E or Z-5-decenyl acetate, E or Z-3-decenyl acetate, Z or E, Z or E 3,13-octadecadienyl acetate, Z or E, Z
or E 2,13-octadecdienyl acetate, Z,Z or E-7,11-hexadecadienyl acetate, Z,E 9,12-tetradecadienyl acetate, E, E- 8,10-dodecadienyl acetate, Z, E
6,8-heneicosadien-11-one, E,E 7, 9-heneicosadien-11-one, Z-6-henicosen-11-one, 7, 8-epoxy-2-methyloctadecane, 2-methyl-7-octadecene, 7, 8-epoxyoctadecane, Z, Z, Z-1, 3, 6, 9-nonadecatetraene, 5 , 11-dimethylheptadecane, 2 , 5-dimethylheptadecane, 6-ethyl-2, 3-dihydro-2-methyl-4H-pyran-4-one, methyl jasmonate, alpha-pinene, beta-pinene, terpinolene, limonene, 3-carene, p-cymene, heptane, ethyl crotonate, myrcene, verbenene, camphene, camphor, cineol, alpha-cubebene, allyl anisole, undecanal, nonanal, heptanal, E-2-hexenal, E-3-hexenal, hexanal, verbenone, 3 -methyl - 2 - cyclohexenone, 3-methyl-3-cyclohexenone, frontalin, exo and endobrevicomin, lineatin, multistriatin, chalcogran, 7-methyl-1, 6-dioxaspiro [4.5] decane, 4, 8-dimethyl-4 (E), 8(E)-decadienolide, 11-methyl-3(Z)-undecenolide, Z-3-dodecen-11-olide, Z, Z-3, 6-dodecen-11-olide, Z-5-tetradecen-13-olide, Z, Z-5, 8-tetradecen-13-olide, Z-14-methyl-8-hexadecenal, 4, 8-dimethyldecanal, gammacaprolactone, hexyl acetate, E-2-hexenyl acetate, butyl-2-methylbutanoate, propylhexanoate, hexylpropanoate, butylhexanoate, hexylbutanoate, butyl butyrate, E-crotylbutyrate, Z-9-tricosene, methyl eugenol, alpha-ionone, 4-(p-hydroxyphenyl)-2-butanone acetate, E-beta-farnasene, nepetalactone, 3-methyl-6-isopropenyl-9-decenyl, acetate, Z-3-methyl-6-isopropenyl-3, 9-decadienyl acetate, E or Z-3,7-dimethyl-2,7-octadecadienyl propionate, 3-methylene-7-methyl-7-octenyl propionate, 2, 6-dimethyl-1, 5-heptadien-3-ol acetate, Z-2,2-dimethyl-3-isopropenylcyclobutanemethanol acetate, E-6-isopropyl-3, 9-dimethyl-5, 8-decadienyl acetate, Z-5- (1-decenyl) dihydro-2 (3H) -furanone, 2-phenethylpropionate, 3,11-dimethyl-2-nonacosanone, 8-methylene-5-(1-methylethyl)spiro[11-oxabicyclo[8.1.0]undecene-2,2-oxiran]-3-one, 2-propylthietane, 3-propyl-1,2-dithiolane, 3,3-dimethyl-1,2-dithiolane,2,2-dimethylthietane, E or Z-2,4,5-trimethylthiazoline, 2-sec-butyl-2-thiazoline, isopentenyl methyl sulfide; and (b) a surrounding permeable polymeric membrane covering at least a portion of the polyurethane reservoir and controlling the release of the semiochemical from the reservoir, said membrane being selected from the group consisting of consisting of polyvinylchloride, polyvinylchloride/vinyl copolymers, low and high density polyethylene, polyethylene/vinyl copolymers, polyethylvinyl acetate and copolymers, polyethylene terpthalate and copolymers, polypropylene, polyamide, polyimide, polyurethane, polyvinylidene fluoride, fluorinated ethylene propylene polymers, polytetrafluoroethylene, silicone rubber, butyl rubber, neoprene rubber, isoprene rubber, cellulose acetate and laminated (co-extruded) membrane types including polyvinylchloride/fluorinated ethylene propylene polymers, polyethylene/ethylvinyl acetate, and polyethylene/polyethylene terpthalate.