CA2151112A1 - High temperature polymerization process and products therefrom - Google Patents

Abstract

High temperature polymerization process and products obtained therefrom are provided. The polymerization is conducted at above 225C to produce polymershaving a degree of polymerization below 50. The products are useful as detergentadditives and for subsequent polymerization.

Description

i.; 2Islll2 ~~ HIGH TEMPERATURE POLYMERIZATION
PROCESS AND PRODUCTS THEREFROM

This invention relates to a high temperature polymerization process and products therefrom. In particular, this invention relates to a high temperature polymerization process to produce oligomers. More particularly, this invention relates to a high temperature polymerization process to produce terminally unsaturated oligomers. Oligomers, as used herein and in the appended claims, refers to polymers having degree of polymerization of below 50.

Low molecular weight polymers are known to be useful detergent additives, anti-redeposition agents, hard surface cleaners, scale inhibitors, pigment dispersants, mineral dispersants, clay dispersants, water treatment additives and the - like. However, production of very low molecular weight polymers of carboxylic monomers, especially acrylic acid, has proven to be a difficult task.

In certain applications, such as detergent additives, it is becoming increasingly important that the carboxylic acid polymers are biodegradable. It is known that biodegradability increases as molecular weight decreases. Therefore, processes which produce very low molecular weight polymers may provide routes to biodegradable polymer products.

The art has long sought an inexpensive, efficient and environmentally sound way to produce low molecular weight polymers.

One method of achieving low molecular weight polymers is through the use of efficient chain transfer agents, but this approach has several drawbacks. This approach incorporates the structure of the chain transfer agent into the polymerchain. This can be undesirable since that structure will have an increasing effect on the properties of the polymer as molecular weight decreases. Furthermore, the chain transfer agents commonly employed are mercaptans. These materials are expensive and have objectionable odors associated with their presence. Other common chain transfer agents are hypophospllites, bisulfites and alcohols. Thesealso add to the cost of the process, impart functionality to the polymer, can introduce salts into the product, and may necessitate a product separation step.
Another way of lowering the molecular weight of the polymers produced is by increasing the amount of initiator. This approach adds considerably to the cost of production and may result in polymer chain degradation, crosslinking, and high levels of unreacted initiator remaining in the product. In addition, high levels of initiator may also result in high levels of salt by-products in the polymer mixture which is known to be detrimental to performance in many applications. The same is true for chain stopping agents such as sodium metabisulfite. Among the preferred free-radical initiators for aqueous polymerization is hydrogen peroxide. It is relatively inexpensive, has low toxicity, and does not produce detrimental salt by-products. However, hydrogen peroxide does not generally decompose efficiently atconventional polymerization temperatures and large amounts must normally be used to generate enough radicals to carry out a polymerization.

High levels of metal ions together with high levels of initiator have also been tried as a means for controlling molecular weight. Such an approach is unsuitable for some products, such as water treatment polymers, which cannot tolerate metal ion contaminants in the polymer product. In addition, depending on the metal ions used, the product may be discolored due to the presence of the metal ions.

In the European Polymer Journal, 1972, Vol. 8, pp. 321-328, Feit describes a multistep synthesis technique for preparing terminally unsaturated oligomers. The process described therein requires a base-catalyzed addition of an acetic acid ester derivative to an activated olefin, followed by hydrolysis of one ester group, followed by a Mannich reaction to introduce a terminal double bond. This three step process is repeated to prepare a terminally unsaturated oligomer with one additional mer.
This process suffers the drawback of being fairly complex, expensive and time-consuming.

The present invention seeks to overcome the problems associated with the previously known methods for preparing terminally unsaturated oligomers.

In a first aspect of the present invention, there is provided a terminally unsaturated oligomer of the formula:

CH2=C~N~M~H
(I) COO

wherein N is a residue of the formula wherein Xl and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;

i 2151112 wherein M is the residue of a monoethylenically unsaturated monomer;
wherein m is O to 47;
wherein n is 2 to 50;
and wherein the sum of n and m is less than or equal to 50.

It is understood that the N and M residues in the terminally unsaturated oligomer may be randomly arranged. In other words, adjacent the terminally unsaturated moiety may be either an N or an M residue; the residue adjacent the residue adjacent the terminally unsaturated moiety may be either an N or an M
residue, and so on. It is also understood that In a second aspect of the present invention, there is provided an oligomer mixture, comprising:

(a) from 5 to 95 percent by weight of the oligomer mixture of terminally unsaturated oligomers of the formula:

CH2= C--E CH2 CH~ H
COOX, COOX2 wherein X1 and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
- wherein n is 1;

(b) from 5 to 95 percent by weight of the oligomer mixture of terminally unsaturated oligomers of the formula:

CH2= IC--E CH2--ICH~ M~ H
COOXl COOX2 wherein Xl and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
wherein M is the residue of a monoethylenically unsaturated monomer;
wherein m is O or 1;
wherein n is 1 or 2;
and wherein the sum of n and m is 2; and , i.. , 21S1112 (c) from O to 90 percent by weight of the oligomer mixture of terminally unsaturated oligomers of the formula:

CH2= IC~ CH2--ICH:~ M~ H

wherein X1 and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
wherein M is the residue of a monoethylenically unsaturated monomer;
wherein m is O to 5;
wherein n is 3 to 10;
wherein the sum of n and m is less than or equal to 10;
and wherein the sum of (a), (b) and (c) is equal to 100 percent.

In a third aspect of the present invention, there is provided a continuous process for preparing terminally unsaturated oligomers comprising:

(a) forming a reaction mixture comprising ;

(i) from 0.5 to 99.95 percent by weight of the reaction mixture of at least one monomer selected from the group consisting of acrylic acid and salts thereof, and acrylic acid and salts thereof in combination with at least one monoethylenically unsaturated monomer;

(ii) from 0.05 to 25 percent by weight based on the weight of the at least one monomer of at least one free-radical initiator; and (iii) optionally, from O to 99.5 percent by weight of the reaction mixture of atleast one solvent;

(b) continuously passing the reaction mixture through a heated zone wherein the reaction mixture is maintained at a temperature of at least 225C for from 0.1 seconds to 300 seconds to form terminally unsaturated oligomers.

In a fourth aspect of the present invention, there is provided a polymer product comprising, as polymerized units, the terminally unsaturated oligomers of the present invention.

'i............................................................. 2lslll2 In a fifth aspect of the present invention, there is provided a detergent composition comprising the terminally unsaturated oligomers of the present invention.

In a sixth aspect of the present invention, there is provided a detergent composition comprising a polymer product comprising, as polymerized units, the terminally unsaturated oligomers of the present invention.

The acrylic acid used in the process of the present invention can be glacial acrylic acid or a solution of acrylic acid. Furthermore, the acrylic acid can be in the form of a salt such as an alkali metal salt, ammonium salt, alkaline earth metal salt or a combination thereof. Preferably, the acrylic acid is glacial acrylic acid or an aqueous solution of acrylic acid. The acrylic acid is present in the reaction mixture at a level of from 0.5 to 99.95 percent by weight, preferably from 1 to 95 percent by weight, most preferably from 5 to 90 percent by weight.

In addition to the acrylic acid, other monoethylenically unsaturated monomers may be used. Other suitable monoethylenically unsaturated monomers include other C3-C6 monoethylenically unsaturated monocarboxylic acids, and the alkali metal and ammonium salts thereof, such as, for example, methacrylic acid,crotonic acid, vinylacetic acid, and acryloxypropionic acid and salts thereof. Other suitable monoethylenically unsaturated monomers include C4-Cg monoethylenically unsaturated dicarboxylic acids and the alkali metal and ammonium salts thereof, and the anhydrides of the cis-dicarboxylic acids; such as, for example, maleic acid, maleic anhydride, itaconic acid, mesaconic acid, fumaric acid, citraconic acid, tetrahydrophthalic anhydrides, cyclohexene dicarboxylic acids and salts thereof. Other suitable monoethylenically unsaturated monomers includeacrylamide, t-butylacrylamide, N,N-dimethylacrylamide, and acrylonitrile. Other monoethylenically unsaturated monomers include alkyl esters of acrylic or methacrylic acids such as methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate and isobutyl methacrylate;
hydroxyalkyl esters of acrylic or methacrylic acids such as hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, and hydroxypropyl methacrylate; acrylamide, methacrylamide, N-tertiarybutylacrylamide, N-methylacrylamide, dimethylaminopropylmethacrylamide; methacrylonitrile, allyl alcohol, allylsulfonic acid, allylphosphonic acid, vinylphosphonic acid, dimethylaminoethyl acrylate, dimethylaminoethyl methacrylate, phosphoethyl methacrylate, N-vinylpyrrolidone, N-vinylformamide, N-vinylimidazole, vinyl acetate, styrene, styrenesulfonic acid and its salts, vinylsulfonic acid and its salts, and 2-acrylamido-2-methylpropanesulfonic acid and its salts. When used, the other , i..., 2151112 monoethylenically unsaturated monomers may be present in the reaction mixture at a level of from 0.05 to 99, preferably from 1 to 95, most preferably from 5 to 90.

The monoethylenically unsaturated monomers which are acids may be in their acid forms or in the form of the alkali metal, alkaline earth metal or ammonium salts of the acid, or a combination thereof. Suitable bases useful for neutralizing the monomer acids include sodium hydroxide, ammonium hydroxide, and potassium hydroxide. The acid monomers may be neutralized to a level of from 0 to 100 percent. Most preferably, the carboxylic acid monomers are used in the unneutralized form, however, partial neutralization of the carboxylic acid monomers may alleviate corrosion on parts of the reaction equipment. The monomers may be neutralized prior to or during the oligomerization reaction. Theterminally unsaturated oligomer products are often particularly useful in their partially or completely neutralized form. Partially neutralized terminally unsaturated oligomers, will have the formulae shown above, and in the claims below wherein X2 will be different among the mers of the terminally unsaturated oligomers.

Suitable initiators for the processes of the present invention are any conventional free-radical initiators including, but are not limited to, hydrogenperoxide, certain alkyl hydroperoxides, dialkyl peroxides, peresters, percarbonates, persulfates, peracids, oxygen, ketone peroxides, azo initiators and combinationsthereof. Specific examples of some suitable initiators include hydrogen peroxide, oxygen, t-butyl hydroperoxide, di-tertiary butyl peroxide, tertiary-amyl hydroperoxide, methylethyl ketone peroxide and combinations thereof. The initiators are normally used in amounts of from 0.05 percent to 25 percent based on the weight of total polymerizable monomer. A preferred range is from 0.5 to 20 percent by weight of the total polymerizable monomer.

The monomers are preferably polymerized as dilute solutions. The reaction mixture may contain one or more solvents at a level of from 0 to 99.5 percent byweight of the reaction mixture, preferably from 30 to 97 percent by weight of the reaction mixture, and most preferably from 50 to 95 percent by weight of the reaction mixture. As the relative amount of one or more solvents in the reactionmixture decreases, particularly below 60 percent, the molecular weight and the polydispersity (D) of the resulting oligomer mixture increases. Suitable solvents for the process of ~he present invention are capable of dissolving the one or more monomers and the oligomers formed therefrom. Suitable solvents for the present invention include, for example, water, acetone, methanol, isopropanol, propionicacid, acetic acid, methylethyl ketone, dimethylformamide, dimethylsulfoxide and i--, 2lslll2 ~~ combinations thereof. Water is the preferred solvent.

In the process of the present invention, the reaction mixture is continuously passed through a heated zone wherein the reaction mixture is maintained at a temperature of at least 225C under elevated pressure. Once the reaction mixture is formed, it is preferable to have the passing reaction mixture reach the polymerization temperature as rapidly as possible. Preferably, the reaction mixture reaches the polymerization temperature within 5 minutes, more preferably within 2 minutes, most preferably within 1 minute. Prior to reaching the reaction temperature, the reaction mixture may be at any suitable temperature, preferably at a temperature of from room temperature to 450C, most preferably from a temperature of from room temperature to 60C to 400C. The oligomerization is conducted at a temperature of at least 225C, and is preferably conducted at a temperature in the range of from 250C to 500C, and most preferably at a temperature in the range of from 275C to 450C. At temperatures below 225C, the molecular weight of the oligomer increases and the relative amount of by-products, particularly non-terminally unsaturated compounds, increases. The oligomerization at these elevated temperatures is rapid. Thus, the reaction mixture can be maintained at the polymerization temperature for as little as 0.1 seconds, preferably from 0.5 seconds to 5 minutes, most preferably from 1 second to 2 minutes. At extended periods of time at which the reaction mixture is exposed tothe polymerization temperature, the yield of terminally unsaturated oligomer decreases. However, extended periods at the polymerization temperature have been found to have little effect on both the conversion of monomer and the molecular weight of the products formed.

The elevated temperatures of the polymerization require that the polymerization reactor be equipped to operate at elevated pressure sufficient tomaintain the contents of the reactor as a fluid at the reaction temperature. In general, it is preferred to conduct the polymerization at from 1,000 to 5,000 pounds per square inch (psi), and more preferably at from 3,200 to 4,200 psi.

In the process of the present invention, the one or more monomers, the at least one initiator and, optionally, the one or more solvents are combined to form a reaction mixture. The order of combining the components of the reaction mixture is not critical to the process of the present invention. In one embodiment of the present invention, it may be desirable to use one or more solvents, heat the one or more solvents to an elevated temperature, and add the one or more monomers and the at least one initiator to the heated solvent to form the reaction mixture. It is preferred to add the at least one initiator last. The reaction mixture can be formed at i.., 2l5lll2 a temperature below, at or above the oligomerzation temperature. In one embodiment of the invention, it may be desirable to add an additional amount of one or more solvents to the oligomer product while the oligomer product is at anelevated temperature to maintain desirable fluidity and viscosity properties of the oligomer product.

The reaction mixture may optionally contain metal ions, such as copper, nickel or iron ions or combinations thereof.

The process of the present invention generally results in a relative conversion of the monomers into oligomer product of from 10 to greater than 95 percent relative to the initial amount of the one or more monomers present in the reaction mixture. If residual monomer levels in the oligomer mixture are unacceptably high for a particular application, their levels can be reduced by any of several techniques known to those skilled in the art. Preferably, any residual monomers which may be present in the oligomer mixture are distilled or "stripped" and recycled for later use.

The process of the present invention results in oligomers having low molecular weights and narrow polydispersities. ~urthermore, selected embodiments of the process result in products which do not require the removal of organic solvents and are not contaminated with high levels of salt. The process of the present invention can be used to produce oligomers having number average molecular weights below 5,000, preferably below 3,000, and most preferably from 200 to 1,000. The process of the present invention is useful for producing oligomers of the structural formula shown above wherein the sum of m and n is less than or equal to 50, preferably less than 20, most preferably less than 10.

In a preferred embodiment of the present invention, the oligomer product is predominantly a mixture of terminally unsaturated dimers, terminally unsaturatedtrimers and terminally unsaturated tetramers. Dimers are oligomeric products of formula (I) wherein the sum of n and m is 1; trimers are oligomeric products of formula (I) wherein the sum of n and m is 2; tetramers are oligomeric products of formula (I) wherein the sum of n and m is 3. The oligomer product preferably contains from 5 to 95 percent of terminally unsaturated dimer, more preferably from 15 to 80 percent of terminally unsaturated dimer based on the total weight of oligomer product in the oligomer mixture. The oligomer product preferably contains from 5 to 95 percent of terminally unsaturated trimer, more preferably from 15 to 80 percent of terminally unsaturated trimer based on the total weight of oligomer product in the oligomer mixture. The oligomer product preferably i... 21S1112 contains from O to 90 percent of terminally unsaturated tetramer, more preferably from 5 to 70 percent of terminally unsaturated tetramer based on the total weight of oligomer product in the oligomer mixture.

The oligomers prepared by the process of the present invention may be used, for example, as additives for detergents, including, for example, powdered laundry detergents, liquid laundry detergents, automatic machine dishwashing detergents,hand dishwashing detergents and deaners. The oligomers may also be used as water-treatment additives or scale inhibitors. The oligomers may also be used, for example, as dispersants for pigments, minerals, clays, cosmetics, and formulatedproducts such as soaps or agricultural chemical formulations. The oligomers may also be used as a soil humectant to prevent soil from drying and eroding.

When the terminally unsaturated oligomers of the present invention contain, for example, a carboxylic acid group, the oligomers can be reacted withpolyfunctional alcohols having two or more alcohol functionalities to form polyesters. Suitable polyfunctional alcohols include, for example, diols, triols and other polyols. Examples of suitable polyfunctional alcohols include, for example, sugars, glycerol, polysaccharides, poly(vinyl alcohols), ethylene glycol, propylene glycol, poly(ethylene glycol) and poly(propylene glycol). Preferably, the polyfunctional alcohol is ethylene glycol, sorbitol, sucrose, glucose or a mono-, oligo- or polysaccharide. The reaction of terminally unsaturated oligomers containing carboxylic acid groups with polyfunctional alcohols can be conducted in any suitable manner and is preferably conducted in the presence of an acid catalyst.

Similarly, when the terminally unsaturated oligomers of the present invention contain at least one carboxylic acid group, the at least one carboxylic acid group can undergo a condensation reaction with any suitable amine to form a compound which is an amide, polyamide or poly(ester amide). Also, any suitable amine can undergo a Michael-type addition to the terminally unsaturated moiety of the terminally unsaturated oligomer to form a compound which is a Michael adduct, which may also undergo a reaction to form a compound which is an amide, polyamide or poly(ester amide). Suitable amines, include for example, amino acids, alkylamines, diamines, triamines and alkanolamines. Particular examples of suitable amines include ammonia, methylamine, lysine, ethylenediamine, ethanolamine and Jeffamines sold by Exxon Corp.

, i.., 2lslll2 ~~ Polyesters, amides, polyamides, poly(ester amides) or Michael adduct containing, as reacted units, the terminally unsaturated oligomers, are useful, for example, as additives for detergents, including, for example, powdered laundry detergents, liquid laundry detergents, automatic machine dishwashing detergents,hand dishwashing detergents and cleaners, as water-treatment additives or scale inhibitors, as dispersants for pigments, minerals, clays, cosmetics, and formulated products such as soaps or agricultural chemical formulations.

Because the oligomers are terminally unsaturated, they can also be used, for example, as monomers in a subsequent polymerization, such as in a bulk polymerization, solution polymerization, emulsion polymerization, or suspension polymerization. The terminally unsaturated oligomers can be subsequently polymerized with themselves to form a homopolymer, or with one or more other ethylenically unsaturated monomers to form copolymers. The polymers resulting from the subsequent polymerization of the terminally unsaturated oligomers of the present invention may be useful, for example, in the same applications as the oligomers, or as adhesives, coatings, surfactants, adsorbents, ion-exchange resins and other polymeric applications.

The terminally unsaturated oligomers can also be grafted onto any suitable substrate. Compounds which are suitable substrates are those which contain hydrogen atoms which can be abstracted by a free-radical. Examples of suitable substrates include: polyhydric alcohols such as sugars, glycerol, polysaccharides, and poly(vinyl alcohol); poly(ethylene glycol); poly(propylene glycol); and certain esters such as polycaprolactone. Preferably, the graft substrate is poly(ethylene glycol) (PEG), sorbitol, sucrose, glucose, or other mono-, oligo- or polysaccharide.

THE EQUIPMENT AND GENERAL PROCEDURE

A 10 foot long section of titanium tubing having an inner diameter of 1/16th inch and a wall thickness of O.OS0 inch was connected at one end to a high pressure pump (Hewlett Packard Model HP 1050 TI) and at another end to a back-pressure control device. Between the two ends, the section of tubing was coiled about a torus-shaped metal mandrel. The mandrel was situated above a primary coil of a transformer so that the coils of titanium tubing and the mandrel functioned as secondary coils of the transformer. The coils of titanium tubing were further equipped with one end of a temperature probe. The other end of the temperature probe was connected to a temperature controlling device. The temperature controlling device regulated the current supplied to the primary coil of the transformer which had the effect of regulating the heat of inductance imparted to ,~, ,.. , 2lslll2 the coiled steel tubing.

A reaction mixture was prepared by mixing solvent, monomer, and initiator.
Helium was bubbled through the mixture while stirring.

Deionized water was pumped through the tubing via the high pressure pump at a rate of from 0.05 to 10 milliliters per minute ("ml/min"). The pressure was maintained at a level of from 3300 to 5000 pounds per square inch ("psi").
Current was supplied to the primary coil of the transformer to increase the temperature within the tubing to the desired polymerization temperature. After about 15 minutes, the water being pumped through the tubing was replaced by the reaction mixture which was continuously pumped through the tubing at the same rate, temperature and pressure. After allowing a suitable amount of time for thewater to be cleared from the tubing, product was collected as the effluent from the back-pressure control device. When the reaction mixture was nearly gone, deionized water was pumped through the tubing at the same rate, pressure and temperature as the reaction mixture.

The molecular weights referred to are measured by gel permeation chromatography using a polyacrylic acid standard unless specifically stated otherwise. Terminal unsaturation was detected and measured by both IH NMR
spectroscopy and 13C NMR spectroscopy. Conversion was measured as a function of product solids, and was also determined by residual monomer analysis using high pressure liquid chromotagraphy.

Examples 1-6 Examples 1-6 are oligomerizations conducted according to the general procedure outlined above. The reaction mixture was a 5 percent by weight aqueoussolution of glacial acrylic acid and 1 percent by weight based on the weight of glacial acrylic acid of 90 percent by weight tert-butylhydroperoxide. The flow rate was adjusted to provide a residence time of 16 seconds. The polymerization temperature ("Temp."), percent "Conversion" of monomer to oligomer, Mw and Mn appear in Table I below. Analysis of the oligomer product, where formed, indicated that the oligomers were terminally unsaturated oligomers.

l 2 i.. , 2151112 TABLE I

Example Temp. (C)Conversion (%) Mw Mn The data in Table I show that terminally unsaturated oligomers were formed in polymerizations conducted at a temperature above 200C. The data also show that the Mw and Mn decrease as temperature increase.

Examples 7-14 Examples 7-14 are polymerizations conducted according to the general procedure outlined above using the same conditions as Examples 1-6 except that the initiator was hydrogen peroxide. The polymerization temperature ("Temp."), percent "Conversion" of monomer to oligomer, Mw and Mn appear in Table II
below. Analysis of the oligomer product indicated that the oligomers were terminally unsaturated oligomers.

TABLE II

Example Temp. (C)Conversion (%) Mw Mn 7 200 8 >4400 >3600 13~ 350 - 508 339 The residence time for Example 13 was 45 seconds The data in Table II show that terminally unsaturated oligomers were formed in polymerizations conducted at a temperature at, and above, 200C. The data also show that the Mw and Mn decrease as temperature increase and that conversion increases as temperature increases. The data also show that hydrogen peroxide is a suitable initiator.

. . .l. 2lslll2 ~ Examples 15-24 Examples 15-24 are polymerizations conducted according to the general procedure outlined above using the same conditions as Examples 1-6 except that the residence time was 24 seconds. The initiator type ("Initiator"), polymerization temperature ("Temp."), percent "Conversion" of monomer to oligomer, Mw and Mn appear in Table III below. Analysis of the oligomer product indicated that the oligomers were terminally unsaturated oligomers.

TABLE III

Example Initiator Temp. (C) Conversion (%) Mw Mn t-BHP 350 54 510 358 17 t-BHP 375 50 436 327 19 t-BHP 390 48 435 317 21 t-BHP 410 44 400 307 23 t-BHP 425 42 392 301 The data in Table III show that the Mw and Mn decrease as temperature increases, and that the polymerizations can be conducted at a temperature of at least 425C.

Examples 25-41 Examples 25-41 are polymerizations conducted according to the general procedure outlined above using the same conditions as Examples 1-6 except the residence time was 8 seconds. the concentration, in percent by weight, of the aqueous acrylic acid solution was the percent shown in Table IV below as "AA
Level"; the initiator was at a level shown in Table IV below ("Init. Level" reported as the percent by weight based on the weight of acrylic acid); the temperature for each of the polymerizations shown in Table IV below was 375C. Analysis of the oligomer product indicated that the oligomers were terminally unsaturated oligomers.

l 4 - ~ TABLE IV

Example AA Level Init. Level Conversion (%) Mw Mn 33 30 5 ~ 94 1795 476 Examples 37-40 Examples 37-40 are polymerizations conducted according to the general procedure outlined above using the same conditions as Examples 1-6 except no initiator was used and the residence time was 46 seconds. The polymerization temperature ("Temp.") and observations appear in Table V, below.

TABLE V

Example Temp (C) Observations 37 250no oligomer formation observed 38 325no oligomer formation observed 39 375no oligomer formation observed 425no oligomer formation observed The data in Table V show that no oligomer was formed in the absence of initiator.

Examples 41-46 Examples 41-46 are polymerizations conducted according to the general procedure outlined above using the same conditions as Examples 1-6 except the concentration, in percent by weight, of the aqueous acrylic acid solution was 2.5 percent; the reaction mixture contained an equal amount of methacrylic acid (based on the weight of acrylic acid); the tubing was made of stainless steel. The polymerization temperature ("Temp."), the percent of acrylic acid monomer converted to oligomer product (reported as "AA Conversion (%)"), the percent of methacrylic acid monomer converted to oligomer product (reported as "MAA
Conversion (%)"), Mw and Mn appear in Table VI below. Analysis of the oligomer l 5 21~1112 products indicated that the oligomers were terminally unsaturated oligomers.

TABLE VI

Temp. AA Conversion MAA Conversion Example (C) (%) (%) Mw Mn The data in Table VI show that the process of the invention produced terminally unsaturated oligomers from a mixture of monomers.

Examples 47-52 Examples 47-52 are polymerizations conducted according to the general procedure outlined above using the same conditions as Examples 1-6 except the concentration, in percent by weight, of the aqueous acrylic acid solution was 2.5 percent; the reaction mixture contained an equal amount of maleic acid (based onthe weight of acrylic acid); the tubing was made of stainless steel. The polymerization temperature ("Temp."), the percent of acrylic acid monomer converted to oligomer product (reported as "AA Conversion (%)"), the percent of maleic acid monomer converted to oligomer product (reported as "MAL
Conversion (%)"), Mw and Mn appear in Table VII below. Analysis of the oligomer products indicated that the oligomers were terminally unsaturated oligomers.

TABLE VII

Temp. AA Conversion MAL Conversion Example (C) (%) (%) Mw Mn l 6 l. . 2151112 ~, The data in Table VII show that the process of the invention produced terminally unsaturated oligomers from a mixture of monomers.

Examples 53-60 Examples 53-60 were carried out as follows: A 6 foot long section of stainless steel tubing having an inner diameter of 1/16th inch and a wall thickness of 0.050 inch was connected at one end to a high pressure pump (Hewlett Packard Model HP
1050 TI) and at another end to a back-pressure control device. Between the two ends, the section of tubing was immersed in a temperature-controlled sand bath maintained at 375C. A reaction mixture was prepared by mixing solvent, monomer, and initiator. Solvent was pumped through the tubing via the high pressure pump at a rate of about 10 ml/min. The pressure was maintained at a level of about 3500 psi. After about 15 minutes, the solvent being pumped through the tubing was replaced by the reaction mixture which was continuously pumped through the tubing at the same rate, temperature and pressure. After allowing a suitable amount of time for the solvent to be cleared from the tubing, product was collected as the effluent from the back-pressure control device.

The reaction mixtures contained various amounts of glacial acrylic acid (reported in Table VIII as "AA%" in percent by weight of acrylic acid based on the reaction mixture) and 1 percent by weight based on the weight of glacial acrylic acid of 90 percent by weight tert-butylhydroperoxide. The reaction mixture also contained various amounts and types of solvents (reported in Table VIII as "Water %" and "Other %" in percent by weight of the reaction mixture). The flow rate provided a residence time of 14 seconds. Mw and Mn appear in Table VIII below.
Analysis of the oligomer product, where formed, indicated that the oligomers were terminally unsaturated oligomers.

TABLE VIII

Example AA % Solvent Mw Mn Water % Other %

54 10 60isopropyl alcohol, 30 532 377 0isopropyl alcohol, 80 605 343 57 30 20isopropyl alcohol, 50 606 418 58 30 0isopropyl alcohol, 70 588 355 59 30 0 acetone, 70 1087 536 0 methanol, 70 576 346 ,. ... 2lslll2 Example 61 The oligomer product obtained from the process similar to the process of Example 27 was chilled in a refrigerator. A crystalline precipitate formed and was collected. Analysis by lH NMR spectroscopy confirmed the identity of the crystalline product as the terminally unsaturated dimer of acrylic acid (2-methylene glutaric acid). A reaction mixture was formed by dissolving 0.432 grams of the terminally unsaturated dimer of acrylic acid and 0.045 grams of ammonium persulfate in 5 milliliters of D2O. The reaction mixture was heated to 80C while stirring. Samples of the heated reaction mixture were analyzed by 1H NMR
spectroscopy to determine the conversion of the terminally unsaturated dimer into higher molecular weight polymer product after 1 hour, 2.5 hours, and 4 hours. The percent of terminally unsaturated dimer converted to higher molecular weight polymer product (reported as "Dimer Conversion (%)"), Mw and Mn of the higher molecular weight polymer product appear in Table IX below.

TABLE IX

Dimer TimeConversion (%) Mw Mn i 0 hour 0 144 144 1 hour 73 n.m.~ n.m.
2.5 hours 93 4659 1480 4 hours >98 4862 1960 "n.m." is not measured The data in Table IX show that the terminally unsaturated oligomers can be polymerized to form higher molecular weight polymers.

l 8 i 2151112 .
~-- Example 62 The same procedure was followed as in Example 62 except that the terminally unsaturated dimer was converted to the sodium salt with dilute aqueous sodium hydroxide before the polymerization. The data appear in Table X below.

TABLE X

Dimer Time Conversion (%) Mw Mn 0 hour 0 144 144 1 hour 47 n.m.~ n.m.
2.5 hours 70 836 480 4 hours 82 954 612 "n.m." is not measured The data in Table X show that the terminally unsaturated oligomers can be polymerized to form higher molecular weight polymers.

Example 63 To a one liter, 4-neck flask equipped with a mechanical stirrer, reflux condenser, thermometer, and inlets for the gradual addition of monomer and initiator solution was added 48.5 grams of deionized water. The contents of the flask were heated to 82C while stirring. An initiator solution of 3.1 grams of ammonium persulfate and 20.0 grams of deionized water was prepared. A
monomer solution of 30 grams of terminally unsaturated oligomers prepared in a manner similar to Example 27 having Mw of 535 and Mn Of 360 dissolved in 30 grams of deionized water was prepared. A neutralizer solution of 99.0 grams of 14.7% by weight aqueous sodium hydroxide was prepared. A solution of 0.5 grams of ammonium persulfate dissolved in 2 grams of water was added to the flask immediately prior to the addition of the monomer, initiator and neutralizer solutions which were added linearly and separately. The neutralizer solution wasadded over 30 minutes, and the initlator solution and the monomer solution were added over 1.5 hours. Once the addition was complete, the system was kept at 82C
for 30 minutes. The system was then cooled to ambient temperature.

The solids content of the resulting polymer solution was 20.3%, the Mw was 1980 and the Mn was 1780. The residual terminally unsaturated oligomer was <1%
based on the original amount of terminally unsaturated oligomer.

l 9 .j 2151112 Example 64 To a one liter, 4-neck flask equipped with a mechanical stirrer, reflux condenser, thermometer, and inlets for the gradual addition of monomer and initiator solution was added 15.0 grams of deionized water and 15 grams of 1-propanol. The contents of the flask were heated to 82C while stirring. An initiator solution of 3.1 grams of ammonium persulfate, 10.0 grams of deionized water and 10.0 grams of l-propanol was prepared. A monomer solution of 18.55 grams of terminally unsaturated oligomers prepared in a manner similar to Example 27 having Mw of 535 and Mn Of 360, 15.2 grams of 2-acrylamidomethylpropanesulfonic acid, and 4.5 grams of t-butylacrylamide dissolved in 18.6 grams of l-propanol was prepared. A neutralizer solution of 20.8 grams of 50.0% by weight aqueous sodiumhydroxide was prepared. A solution of 0.5 grams of ammonium persulfate dissolved in 1 gram of water and 1 gram of l-propanol was added to the flask immediately prior to the addition of the monomer, initiator and neutralizer solutions which were added linearly and separately. The neutralizer solution wasadded over 30 minutes, and the initiator solution and the monomer solution were added over 1.5 hours. Once the addition was complete, the system was kept at 82C
for 30 minutes. The system was then cooled to ambient temperature.

The solids content of the resulting polymer solution was 29.2%, the Mw was 2249 and the Mn was 893. The residual terminally unsaturated oligomer was c1%
based on the original amount of terminally unsaturated oligomer.

Example 65 To a one liter, 4-neck flask equipped with a mechanical stirrer, reflux condenser, thermometer, and inlets for the gradual addition of monomer and initiator solution was added 20.0 grams of deionized water. The contents of the flask were heated to 82C while stirring. An initiator solution of 3.1 grams of ammonium persulfate and 3.9 grams of deionized water was prepared. A
monomer solution of 19.5 grams of terminally unsaturated oligomers prepared in amanner similar to Example 27 having Mw of 535 and Mn Of 360, 10.5 grams of hydroxyethylmethacrylate and 20 grams of deionized water was prepared. A
neutralizer solution of 2.2 grams of 30.0% by weight aqueous ammonium hydroxide dissolved in 4.8 grams of deionized water was prepared. A solution of 0.5 grams of ammonium petsulfate dissolved in 2 grams of water was added to the flask immediately prior to the addition of the monomer, initiator and neutralizer solutions which were added linearly and separately. The neutralizer solution wasadded over 30 minutes, and the initiator solution and the monomer solution were added over 1.5 hours. Once the addition was complete, the system was kept at 82C
for 30 minutes. The system was then cooled to ambient temperature. The contents ,, , 1., 2l5lll2 of the flask were neutralized 13.4 grams of 30% by weight aqueous ammonium hydroxide.

The sollds content of the resulting polymer solution was 33.8%, the Mw was 5520 and the Mn was 3590. The residual terminally unsaturated oligomer was <1%
based on the original amount of terminally unsaturated oligomer. The residual hydroxyethylmethacrylate was 355 ppm based on the original amount of hydroxyethylmethacrylate.

Example 66 To a one liter, 4-neck flask equipped with a mechanical stirrer, reflux condenser, thermometer, and inlets for the gradual addition of monomer and initiator solution was added 35.0 grams of deionized water. The contents of the flask were heated to 80C while stirring. An initiator solution of 3.1 grams of ammonium persulfate and 20.0 grams of deionized water was prepared. A
monomer solution of 18 grams of terminally unsaturated oligomers prepared in a manner similar to Example 27 having Mw of 535 and Mn Of 360, and 26.6 grams of 2-acrylamidomethylpropanesulfonic acid dissolved in 18 grams of deionized water was prepared. A neutralizer solution of 20 grams of 50.0% by weight aqueous sodium hydroxide was prepared. A solution of 0.5 grams of ammonium persulfate dissolved in 2 grams of water was added to the flask immediately prior to the addition of the monomer, initiator and neutralizer solutions which were added linearly and separately. The neutralizer solution was added over 30 minutes, andthe initiator solution and the monomer solution were added over 1.5 hours. Once the addition was complete, the system was kept at 80C for 30 minutes. The system was then cooled to ambient temperature.

The solids content of the resulting polymer solution was 30.2%, the Mw was 4460 and the Mn was 3810. The residual terminally unsaturated oligomer was <1%
based on the original amount of terminally unsaturated oligomer.

Example 67 To a 250 milliliter, 4-neck flask equipped with a mechanical stirrer, Dean-Stark condenser, thermometer, and an inlet and an outlet for nitrogen was added 31.7 grams of ~rminally unsaturated oligomer of acrylic acid (Mw of 490, Mn of 219) and 9.2 grams of ethylene glycol. The flask was immersed in an oil bath maintained at 150C while stirring the contents of the flask for 6.5 hours, then allowed to cool to room temperature. To the stirred contents of the flask was added 200 milliliters of deionized water and a sufficient amount of a 50 percent by weight aqueous solution of sodium hydroxide to form a homogeneous solution. The resulting polyester had .,, .'i... ' 2lslll2 a Mw of 22300 and Mn of 2030.

Example 68 A polyester was prepared in a similar manner as Example 67 except the terminally unsaturated oligomer of acrylic acid had Mw of 228 and Mn of 167; andthe flask was immersed in an oil bath maintained at 170C while stirring the contents of the flask for 2.0 hours. The resulting polyester had a Mw of 2530 and Mn of 1560.

Example 69 A polyester was prepared in a similar manner as Example 68 except the ethylene glycol was replaced with an equimolar amount of poly(ethylene glycol) having Mw of 400. The resulting polyester had a Mw of 2070 and Mn of 391.

Example 70 A polyester was prepared in a similar manner as Example 69 except the poly(ethylene glycol) had Mw of 1000. The resulting polyester had a Mw of 2150 and Mn of 403.
i Example 71 To a 500 milliliter three-neck flask equipped with a mechanical stirrer and reflux condenser was added 100.1 grams of terminally unsaturated oligomer of acrylic acid (Mw of 184, Mn of 139) and 92.5 grams of lysine. The contents of the flask were heated to 150C for 1 hour with continuous stirring, then allowed to cool to room temperature. A 10 gram sample was transferred from the flask to a beaker, and the beaker was placed in an oven maintained at 170C for 2 hours with manual stirring every 30 minutes. After 2 hours, the beaker was removed from the oven and allowed to cool to room temperature. To the beaker was added, while stirring, 50 milliliters of deionized water and a sufficient amount of a 50 percent by weight aqueous solution of sodium hydroxide to form a homogeneous solution. The resulting polyamide had a Mw of 1780 and Mn of 466.

Example 72 A polyamide was prepared in a similar manner as Example 71 except the beaker was placed in an oven maintained at 170C for 2.5 hours. The resulting polyamide had a Mw of 6790 and Mn of 886.

.. ', .,1., 2lslll2 Example 73 A polyamide was prepared in a similar manner as Example 71 except the beaker was placed in an oven maintained at 170C for 3 hours. The resulting polyamide had a Mw of 12,400 and Mn of 962.

Example 74 A polyamide was prepared in a similar manner as example 71 except the beaker was placed in an oven maintained at 170C for 3.5 hours. The resulting polyamide ha~ a Mw of 36,600 and Mn of 1950.

Liquid Detergent Formulation and Performance Evaluation The efficacy of the oligomers in a liquid detergent formulation was evaluated by washing soiled cotton fabrics in a prototypical, ultra-heavy duty liquid laundry detergent composition utilizing Sears Kenmore(~ Ultra Fabric Care brand washing machines (model Heavy Duty 80 Series) set to typical U.S. laundering parameters.Washing conditions are detailed in Table XI below, and the liquid detergent -formulation used for the evaluations was that shown in Table XII.

Cotton cloth ("Cotton") was purchased from Test Fabrics, Inc. (Middlesex, NJ) and cut to a specified size (3 1/2" x 4 1/2"). The cloths were then soiled using a China bristle brush (#10) by applying either from 0.7 to 0.8 grams of a 25% clay slurry (in water). The soil was "painted" onto the cloth inside a 2" diameter circle and allowed to air dry overnight prior to laundering. The clays used to soil the cloths were of two types: a) a deep-orange clay (designated "Clay 1" in Table XIII, below), and b) a reddish-brown particulate clay (designated "Clay 2" in Table XIII, below). In addition, cotton cloths pre-soiled with clay (designated "Clay 3" in Table XIII, below), were purchased from Scientific Services (Oakland, NJ.). The clay used by Scientific Services was a brown clay.

Cotton cloths pre-soiled with a dust/sebum mixture, cotton/polyester blend cloths pre-soiled with a dust/sebum mixture ("PE/C"), and polyester cloth ("PE")pre-soiled with a dust/sebum mixture were also purchased from Scientific Services (Oakland, NJ).

Reflectance of each of the cloths was measured using a Pacific Scientific Colorimeter (Colorgard System 1000) and the data recorded using the X,Y,Z color scale. The reflectance (Y) of the soiled cloths was measured before laundering so that only cloths of the same reflectance were used in a test. Reflectance was then measured after laundering to evaluate the efficacy of the detergent. The Y values reported in Table XIII are the reflectance values obtained after laundering the cloths ,,1, , 1,," 2151112 as described above.

Each of the three clay soils were evaluated with four replicates. The data appearing in Table XIII are composite averages of the reflectance values obtained from all of the clay soils laundered with the builder/adjuvant listed.

TABLE XI
WASH CONDITIONS

APPARATUS - SEARS KENMORE BRAND WASHING MACHINE
TEMPERATURE- WARM (95F) WATER HARDNESS - MODERATE (200 ppm) AGITATION- HIGH
WASH CYCLE - MEDIUM (10 MIN.) WATER CAPACITY - 16.7 GALLONS/LOAD

TABLE XII
BASE LIQUID DETERGENT FORMULATION
Component parts by weight Surfactants Linear Dodecylbenzene Sulfonate 15.0 Alcohol Ethoxylate (Nonionic) 9.5 Sodium Alcohol Ethoxysulfate 5.0 Builder/Adjuvant Sodium Citrate or oligomer 12.5 Hydrotrope/Solubilizing Agent Monoethanolamine 2.5 Triethanolamine 2.0 Propylene Glycol 2.5 Sodium Xylene Sulfonate 5.0 * Misc. and Water up until total formulation is 100 parts.
* Misc. includes perfume, colorants, fatty acids, whiteners and opacifiers.

2 ~
TABLE XIII
Reflectance Values Reflectance (Y) Reflectance (Y) Dust/Sebum soils Builder/Adjuvant Clay 1 Clay 2 Clay 3 Cotton PE/C PE
none 63.5 50.8 61.5 59.7 62.1 51.6 oligomer~ 65.5 52.3 65.4 61.4 64.2 53.9 (MW=270) oligomer~ 66.0 51.4 65.9 60.5 63.7 54.2 (Mw=370) citrate 65.5 51.5 64.0 60.1 63.7 52.6 ~ terminally unsaturated oligomer of acrylic acid prepared in a similar manner as Example 6.

These results demonstrate that the terminally unsaturated oligomers produced by the present invention are effective as additives, and potential partial or complete replacements for citrate, in liquid laundry detergents.

Powder Detergent Formulation and Performance Evaluation The efficacy of the oligomers and polymers containing the oligomers as polymerized units were evaluated in a powder detergent formulation by washing soiled cotton and cotton/terry blended fabrics in a prototypical, powdered laundry detergent composition shown in Table XV, below. Cloths were stained in the manner described above. The clay used to soil the cloths was a reddish-brown particulate clay.

The detergent compositions were tested in a Terg-o-Tometer at the following conditions; 40C, 100 rpm, 100 ppm hardness (50% city tap water/50% de-ionized water), 12 minute wash with one 3 minute rinse, 1300 ppm detergent and 5 cloths per pot (3 of them soiled). The wash water was pre-heated, the fabric swatches were added and then dissolved detergent (2.6 grams of a 50% slurry in 100 milliliterswater) was added. Following the wash period the swatches were wrung, and following the rinse cycle the swatches were wrung again and then air dried.
Swatches washed in a detergent containing no polymer or oligomer were always run as a control.

. ,.'i. 2l5lll~
`~ Reflectance was measured using a Pacific Scientific Colorimeter (Colorgard System 1000) and the data recorded using the L,a,b color scale. Detergency values (E), a measure of soil removal, and whiteness index (W.I.), a measure of anti-redeposition, are calculated as:

E = ((Ls-L)2+(as-a)2+(bs-b)2)05 W.I. = (L/100)~(L-(5.715~b)) where Ls, as, and bs are the reflectivity reading for the soiled swatches and L,a,b are the reflectivity readings for the washed swatches. Each polymer was evaluated inthree separate washing experiments. The detergent composition and levels of the components in parts by weight ("pbw") are shown in Table XV. This composition was used for the above described performance evaluation and the results of the detergent performance evaluation are listed in Table XVI. The reflectance of thesoiled cloths was measured before laundering so that only cloths of the same reflectance were used in a test. Reflectance was then measured after laundering to evaluate the efficacy of the polymer in the detergent. The values reported in Table XVI are the average of the change in detergency and whiteness index of three cloths relative to the control cloths laundered in detergent not containing polymer.
Positive numbers indicate an increase in detergency or whiteness index.

TABLE XIV
WASH CONDITIONS

APPARATUS- Terg-o-tometer washing machine AGITATION- 100 revolutions per minute WATER HARDNESS - 100 parts per million ("ppm") WASH CYCLE - 12 minutes RINSE CYCLE- 3 minutes WATER LEVEL - 1 liter DETERGENT DOSAGE - 1,300 ppm BALLAST- 5 cloths per load (3 soiled/2 unsoiled) '' 2l5lll2 ~, TABLE XV
Experimental Powdered Detergent Composition Detergent Component pbw sodium carbonate 40.0 zeolite A 28.2 sodium silicate 4.9 LAS 7.4 lauryl sulfate 14.5 oligomer, polymer, polyester or polyamide 0 or 5.0 TABLE XVI

Product of Example #Detergency (E) Whiteness Index none 0 0 67~ 2.4 16.6 67 3.6 25.7 68* 1.1 11.8 68 2.6 14.4 69 1.8 18.2 1.2 11.3 71~ 1.1 11.8 71 2.8 17.9 72 3.4 27.8 73 2.2 15.5 74 2.7 22.0 ~ The oligomer starting material was tested.

Test of Terminally Unsaturated Oligomers as Inorganic Pigment Dispersants Examples 75 and 76 The slurries appearing in Table XVII, below, were made in the following way:
0.842 grams of dispersant and 0.689 grams of sodium carbonate were added to deionized water and diluted with additional deionized water to 210.0 grams. Thismixture was stirred with a spatula until it was completely mixed. Then, 490.0 grams of dried clay was added to the mixture and the mixture was stirred at high speed on a Waring blender for five minutes to provide a 70 percent by weight dispersed slurry of clay with a "Dispersant Level" of 0.172 percent by weight based on theweight of clay. The viscosity of the slurry was then measured at 23C using a Brookfield viscometer, model RVT, spindle #2 at 20 rpm (reported in Table XVII as "Initial Viscosity" in centipoises ("cps")). The slurry was then allowed to stand for 2 2l5lll2 weeks at 70C and the viscosity was measured in the same manner (reported in Table XVII as "Heat Aged Viscosity" in cps).

Examples 77 and 78 Slurries were prepared in a similar manner as Examples 75 and 76 except 0.876 grams of dispersant and 0.717 grams of sodium carbonate were used to provide a slurry of clay with a Dispersant Level of 0.178 percent by weight based on theweight of clay.

In Table XVII, below, Dispersant Type A is the sodium salt of a terminally unsaturated oligomer of acrylic acid having Mw of 1076, and Dispersant Type B isthe sodium salt of a homopolymer of acrylic acid having Mw of 1,000.

TABLE XVII

ExampleDispersant Dispersant Initial Viscosity HeatAged Type Level (cps) Viscosity (cps) A 0.172 410 1090 76 B 0.172 482 1440 77 A 0.178 484 790 78 B 0.178 920 1830 The data in Table XVII show that terminally unsaturated oligomers are effective as dispersants of inorganic pigments as shown by the lower viscosities of slurries containing them relative to slurries containing known polymeric dispersants, both immediately after the dispersed slurry is prepared and after the slurry has been heated and aged.

Claims (18)

1. A terminally unsaturated oligomer of the formula:

(I) wherein N is a residue of the formula wherein X1 and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
wherein M is the residue of a monoethylenically unsaturated monomer;
wherein m is 0 to 47;
wherein n is 2 to 50;
and wherein the sum of n and m is less than or equal to 50.

2. The terminally unsaturated oligomer of claim 1, wherein the sum of n and m less than or equal to 10.

3. The terminally unsaturated oligomer of claim 2, wherein m is zero.

4. An oligomer mixture, comprising:

(a) from 5 to 95 percent by weight of the oligomer mixture of terminally unsaturated oligomers of the formula:

wherein X1 and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
wherein n is 1;

(b) from 5 to 95 percent by weight of the oligomer mixture of terminally unsaturated oligomers of the formula:

wherein X1 and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
wherein M is the residue of a monoethylenically unsaturated monomer;
wherein m is 0 or 1;
wherein n is 1 or 2;
and wherein the sum of n and m is 2; and (c) from 0 to 90 percent by weight of the oligomer mixture of terminally unsaturated oligomers of the formula:

wherein X1 and X2 are independently selected from the group consisting of H, NH4, alkali metals and alkaline earth metals;
wherein M is the residue of a monoethylenically unsaturated monomer;
wherein m is 0 to 5;
wherein n is 3 to 10;
wherein the sum of n and m is less than or equal to 10;
and wherein the sum of (a), (b) and (c) is equal to 100 percent.

5. A continuous process for preparing terminally unsaturated oligomers comprising:

(a) forming a reaction mixture comprising (i) from 0.5 to 99.95 percent by weight of the reaction mixture of at least one monomer selected from the group consisting of acrylic acid and salts thereof, and acrylic acid and salts thereof in combination with at least one monoethylenically unsaturated monomer;

(ii) from 0.05 to 25 percent by weight based on the weight of the at least one monomer of at least one free-radical initiator; and (iii) optionally, from 0 to 99.5 percent by weight of the reaction mixture of atleast one solvent;

(b) continuously passing the reaction mixture through a heated zone wherein the reaction mixture is maintained at a temperature of at least 225°C for from 0.1 seconds to 300 seconds to form terminally unsaturated oligomers.

6. The process of claim 5, wherein the at least one solvent is selected from thegroup consisting of water, acetone, methanol, isopropanol, propionic acid, acetic acid, methylethyl ketone, dimethylformamide, dimethylsulfoxide and combinations thereof.

7. The process of claim 5, wherein the at least one solvent is water.

8. The process of claim 5, wherein the reaction mixture is heated to a temperature in the range of from 250°C to 500°C.

9. The process of claim 5, wherein the reaction mixture is heated to a temperature in the range of from 275°C to 450°C.

10. A polymer product comprising, as polymerized units, the terminally unsaturated oligimers of claim 1.

11. The polymer product of claim 10, wherein the polymer product is prepared by a process selected from the group consisting of bulk polymerization, solution polymerization, emulsion polymerization and suspension polymerization.

12. The polymer product of claim 10, wherein the terminally unsaturated oligomeris grafted onto a substrate.

13. The polymer product of claim 10, wherein the polymer product is a polyester.

14. A compound selected from the group consisting of amides, polyamides, poly(ester amides) and Michael adducts comprising, as reacted units, the terminally unsaturated oligomers of claim 1.

15. A detergent composition comprising the terminally unsaturated oligomer of claim 1.

16. A detergent composition comprising the polymer product of claim 10.

17. A dispersant composition comprising the terminally unsaturated oligomer of claim 1.

18. A dispersant composition comprising the terminally unsaturated oligomer of claim 10.