FIELD OF THE INVENTION

The present invention relates to consumer goods products comprising functionalized lignin oligomer.

BACKGROUND OF THE INVENTION

Silicone is incorporated into consumer goods products to provide benefits such as softening and sheen benefits. However, the surface substantivity silicone can be poor, which can lead to poor silicone performance. The inventors have found that functionalizing lignin with silicone in the manner described by the present invention improves the performance of the silicone in the consumer goods product. In addition, the lignin provides anti-oxidant properties, this can be especially preferred for consumer goods products of skin applications. SUMMARY OF THE INVENTION

The present invention relates to a consumer goods product comprising a consumer goods product ingredient and a functionalised lignin oligomer, wherein the functionalised lignin oligomer: (a) has an average number of lignin monomers of from 3 to 8; (b) comprises a siloxane functional group; (c) comprises a functionalisation content between 85 and 0.5 % lignin (m/m).

DETAILED DESCRIPTION OF THE INVENTION

Consumer goods product: The consumer goods product comprises a consumer goods product ingredient and a functionalised lignin oligomer.

The consumer goods product may comprise an emollient and/or humectant.

The consumer goods product may comprise an emulsifier, this may be especially preferred when the lignin oligomer is in the form of an emulsion.

The product may be a skin treatment composition.

The product may be a hair treatment composition.

The product may be an oral care composition.

The product may be an antiseptic cream.

The product may be a shoe polish.

The product may be a detergent composition.

The consumer goods product may comprise chitin and/or chitin derivative. The consumer goods product is typically selected from: feminine pad; diaper; razor blade strip; hard surface cleaning sheet and/or wipe; and teeth treatment strip.

The consumer goods product is typically selected from: skin cream; skin lotion; shaving preparation gel or foam; handwash laundry detergent; handwash dishwashing detergent; soap bar; liquid handwash soap; body wash; toothpaste; shampoo; and conditioner.

Consumer goods product ingredient: Suitable consumer goods product ingredients include emmolient, humectants, emulsifiers, and any combination thereof. Functionalised lignin oligomer: The functionalised lignin oligomer: (a) has an average number of lignin monomers of from 3 to 8; (b) comprises a siloxane functional group; (c) comprises a functionalisation content between 85 and 0.5 % lignin (m/m).

The functionalised lignin oligomer may be crosslinked, and comprise at least one bonding motif of the following types between the lignin backbone and the functional group: lignin_backbone-('L') _m -'Si'-(L') _p -lignin_backbone wherein 'lignin_backbone' is a part of the lignin structural backbone;

wherein 'L' is a linking motif independently selected from the group: -0-, -C(0)0-, -C(0)NR'-, NR'-, and -NR'C(0)NR'-, wherein R' is H or C C ₆ alkyl,

wherein m is 0 or 1 ;

wherein 'S' is a spacing unit selected from the group: linear or branched, saturated or unsaturated, substituted or unsubstituted C2-C18 alkyl chain or a linear or branched, saturated or unsaturated, substituted or unsubstituted secondary hydroxy C2-C18 alkyl chain,

wherein p is 0 or 1 ; and

wherein 'Si' is a polysiloxane.

The functionalised lignin oligomer may be non-crosslinked and comprise a functional group having the structure comprising the functional group: lignin_backbone-0-L-'Si' wherein 'lignin_backbone' is the lignin structural backbone;

wherein L is a linker; and

wherein 'Si' is a polysiloxane,

wherein L has the chemical structure:

(a) wherein R and R are independently selected from H and linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Ci ₈ alkyl;

1 2

wherein X is independently selected from R , R , hydroxyl, amine, ether and ester;

wherein L' is a linking structural motif selected from linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Q ₈ alkyl;

wherein 'Si' is a polysiloxane; or

(b)

h ^c ' ^"L H

wherein-C- motif is a connecting motif selected from: -C(=0)-,— OC(=0)-, -C(=0)NR'-, wherein R' is selected from H, or C _\ -Ce alkyl;

wherein L' is a linking structural motif selected from linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Q ₈ alkyl;

wherein 'Si' is a polysiloxane.

The functionalised lignin oligomer may be crosslinked and comprise a functional group having the structure comprising the functional group: lignin_backbone-0-L-'Si"-L-0-lignin_backbone wherein 'lignin_backbone' is the lignin structural backbone;

wherein 'Si" is a polysiloxane; wherein L is a structural motif selected from: (a)

wherein R and R are independently selected H and linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Ci ₈ alkyl;

wherein X is independently selected from H, linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Ci ₈ alkyl, substituted or unsubstituted aromatic or

heteroaromatic groups, hydroxyl, amino, ether and ester;

wherein L' is a linking structural motif independently selected from linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Ci ₈ alkyl;

wherein 'Si" is a polysiloxane; or

(b)

j— C'-L ^, - ^, Si"-L'— C— j wherein the C- motif is a connecting motif selected from: -C(=0)-, -C(=0)0-, -C(=0)NR' -, wherein R' us selected from H, or C _\ -Ce alkyl;

wherein L' is a linking motif independently selected from linear or branched, saturated or unsaturated, substituted or unsubstituted Ci to Ci ₈ alkyl;

wherein 'Si" is a polysiloxane.

The functionalised lignin oligomer may be non-cross linked and comprise a functional group being linked via one of the following structural features:

(R ₁ )(R ₁ ')C=C(R ₂ )-N(R ₃ )(R3') wherein Ri, Ri ' and R2 are independently selected from hydrogen or lignin backbone, wherein at least one of Rj, Rj' and R2 is lignin backbone, wherein R ₃ and R ₃ ' are both independently selected from saturated or unsaturated, linear or branched, substituted or unsubstituted Q-C ₃ 2 alkyl , wherein at least one of R ₃ or R ₃ ' is bound to the 'Si' polysiloxane; or wherein both Rj and R2 are independently selected from hydrogen or lignin backbone, wherein at least one of Rj or R2 is lignin backbone,

wherein R ₃ is independently selected from saturated or unsaturated, linear or branched, substituted or unsubstituted Q-C ₃ 2 alkyl, wherein R ₃ is bound to the 'Si' polysiloxane.

The lignin oligomer may comprise at least two different linking motifs.

Preferably, the lignin oligomer has a weight average molecular weight ( _w ) in the range of from 800 Da to 5,000 Da.

Preferably, the lignin oligomer has a number average molecular weight (M _n ) in the range of from 800 Da to 1,200 Da.

Preferably, the lignin oligomer is essentially free of sulphur.

Preferably, the lignin oligomer has an ester content in the range of from 0.0 mmol/g to 0.1 mmol/g.

Preferably, the lignin oligomer is derived from corn, sugar cane, wheat and any combination thereof.

Silicone: The silicone may be polydimethylsiloxane.

Suitable silicones are selected from the group consisting of silicone polyethers, silicone resins, silicone urethanes, and mixtures thereof provided that these structures contain not more than one reactive motif as decorating feature in a terminal or lateral position with respect to the backbone.

A preferred silicone according to the above definition is a polydialkylsilicone, alternatively a polydimethyl silicone (polydimethyl siloxane or "PDMS"), or a derivative thereof.

Preferably, the silicone meeting the above definitions has a viscosity at a temperature of 25°C and a shear rate of 1000s ^"1 in the range of from lOPa s to lOOPa s. Without wishing to be bound by theory, increasing the viscosity of the silicone improves the deposition of the perfume onto the treated surface. However, without wishing to be bound by theory, if the viscosity is too high, it is difficult to process and form the benefit delivery composition.

Other suitable silicones comprising one reative functional group are selected from an alkyloxylated silicone, preferably ethoxylated silicone, propoxylated silicone,

ethoxylated/propoxylated silicone, and any combination thereof as long as these functional groups are compatible with the presence of the for the linking necessary single amino-group present in the same molecule.

Suitable siliconeare selected from random or blocky organosilicone polymers having the following formula:

R ₁ R ₂ R3SiO-[(R4Si(X-Z)0] _k [R4R4SiO] _m -Si(X-Z)R ₄ R4 wherein:

k is an integer from 0 to about 200, in one aspect k is an integer from 0 to about 50;

when k = 0, at least one of Rj _, R2 or R3 is -X— Z;

m is an integer from 4 to about 5,000; in one aspect m is an integer from about 10 to about 4,000; in another aspect m is an integer from about 50 to about 2,000;

Rj is selected from the group of moieties of R10R11N-C -C32 alkyl, RK)RII -(CH2-CH2-0)P with p being an integer ranging from 1-X and Rjo and Rn being independently selected from H or linear or branced C1-C32 alkyl groups with at least one of them being H, n-RjoRnNKn-l)- hydroxy-Cn alkyl with n being an integer from 2 to 32 and Rjo and Rn being independently selected from H or linear or branced C1-C32 alkyl groups with at least one of them being H; alkyl residues mentioned in this list can be substituted, or partly or completely exchanged by C2- C32 alkoxy or C2-C32 substituted alkoxy.

R2 and R3 are each independently selected from the group consisting of H, OH, C1-C ₃ 2 alkyl, Ci- C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, C6-C ₃ 2 substituted alkylaryl, C1-C ₃ 2 alkoxy, C1-C ₃ 2 substituted alkoxy and X-Z;

each R4 is independently selected from the group consisting of H, OH, C1-C ₃ 2 alkyl, C1-C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, C ₆ - C ₃ 2 substituted alkylaryl, C1-C ₃ 2 alkoxy and C1-C ₃ 2 substituted alkoxy;

each X in said alkyl siloxane polymer comprises a substituted or unsubsitituted divalent alkylene radical comprising 2-12 carbon atoms, in one aspect each divalent alkylene radical is independently selected from the group consisting of -(CH2) _S - wherein s is an integer from about 2 to about 8, from about 2 to about 4; in one aspect, each X in said alkyl siloxane polymer comprises a substituted divalent alkylene radical selected from the group consisting of: -CH ₂ -

CH ₃

I

CH(OH)-CH ₂ -; -CH ₂ -CH ₂ -CH(OH)-; and— CH ₂ -CH-CH ₂ — _;

Q

I

each Z is selected independently from the group consisting of ^N Q,

with the proviso that when Z is a quat, Q cannot be an amide, imine, or urea moiety and if Q is an amide, imine, or urea moiety, then any additional Q bonded to the same nitrogen as said amide, imine, or urea moiety must be H or a C _\ -Ce alkyl, in one aspect, said additional Q is H; for Z A ^n~ is a suitable charge balancing anion. In one aspect A ^n~ is selected from the group consisting of CI ^" , Br ^" ,I ^" , methylsulfate, toluene sulfonate, carboxylate and phosphate ; and at least one Q in said organosilicone is independently selected from

-CH ₂ -CH(OH)-CH ₂ -R ₅ ; _;

each additional Q in said organosilicone is independently selected from the group comprising of H, Q-C3 ₂ alkyl, Q-C ₃₂ substituted alkyl, Cs-C ₃₂ or C6-C ₃₂ aryl, Cs-C ₃₂ or C6-C ₃₂ substituted aryl, C ₆ -C ₃₂ alkylaryl, C ₆ -C ₃₂ substituted alkylaryl, -CH ₂ -CH(OH)-CH ₂ -R ₅ ;

R ₅ ⁰

-i-CH— CH— o — R ₅ ?i O H =( P-R ₅

M. k ■— C-O— R ₅ .— c N— R ₅ - ¾ . R ₅ · ₅

wherein each R5 is independently selected from the group consisting of H, Ci-C3 ₂ alkyl, Ci-C3 ₂ substituted alkyl, Cs-C3 ₂ or C6-C3 ₂ aryl, Cs-C3 ₂ or C6-C3 ₂ substituted aryl, C6-C3 ₂ alkylaryl, C - C32 substituted alkylaryl, -(CHR ₆ -CHR ₆ -0-) _w -L and a siloxyl residue;

each R6 is independently selected from H, Ci-Cis alkyl

each L is independently selected from -C(0)-R7 or

R ₇ ;

w is an integer from 0 to about 500, in one aspect w is an integer from about 1 to about 200; in one aspect w is an integer from about 1 to about 50;

each R ₇ is selected independently from the group consisting of H; Ci-C3 ₂ alkyl; Ci-C3 ₂ substituted alkyl, Cs-C3 ₂ or C6-C3 ₂ aryl, Cs-C3 ₂ or C6-C3 ₂ substituted aryl, C6-C3 ₂ alkylaryl; C - C32 substituted alkylaryl and a siloxyl residue;

OT CH ₂ OT

I

— CH ₂ — CH-CH ₂ -R _5; C IH-CH -R _{5 AND}

wherein each v in said organosilicone is an integer from 1 to about 10, in one aspect, v is an integer from 1 to about 5 and the sum of all v indices in each Q in the said organosilicone is an integer from 1 to about 30 or from 1 to about 20 or even from 1 to about 10. In another embodiment, the silicone may be chosen from a random or blocky

organosilicone polymer having the following formula:

R ₁ R ₂ R ₃ SiO-[(R4Si(X-Z)0] _k [R4R4SiO] _m -Si(X-Z)R ₄ R4 wherein

j is an integer from 0 to about 98; in one aspect j is an integer from 0 to about 48; in one aspect, j is 0; k is an integer from 0 to about 200; when k = 0, at least one of Rj _, I¾ or I¾= -X-Z, in one aspect, k is an integer from 0 to about 50

m is an integer from 4 to about 5,000; in one aspect m is an integer from about 10 to about 4,000; in another aspect m is an integer from about 50 to about 2,000;

Ri is selected from the group of moieties of R10R11N-C -C32 alkyl, RK)RII -(CH2-CH2-0)P with p being an integer ranging from 1-X and Rjo and Rn being independently selected from H or linear or branced C1-C32 alkyl groups with at least one of them being H, n-RjoRnNKn-l)- hydroxy-Cn alkyl with n being an integer from 2 to 32 and Rjo and Rn being independently selected from H or linear or branced C1-C32 alkyl groups with at least one of them being H; alkyl residues mentioned in this list can be substituted, or partly or completely exchanged by C2- C32 alkoxy or C2-C32 substituted alkoxy.

R2 and R3 are each independently selected from the group consisting of H, OH, C1-C ₃ 2 alkyl, Ci- C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, C6-C ₃ 2 substituted alkylaryl, C1-C ₃ 2 alkoxy, C1-C ₃ 2 substituted alkoxy and X-Z;

each R ₄ is independently selected from the group consisting of H, OH, C1-C ₃ 2 alkyl, C1-C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, C ₆ - C ₃ 2 substituted alkylaryl, C1-C ₃ 2 alkoxy and C1-C ₃ 2 substituted alkoxy;

each X comprises of a substituted or unsubstituted divalent alkylene radical comprising 2-12 carbon atoms; in one aspect each X is independently selected from the group consisting of - (CH ₂ ) _s -0- ; -CH ₂ -CH(OH)-CH ₂ -0-; ^— CH ₂ - CH-CH ₂ -0— >" _a nd _O H wherein each s independently is an integer from about 2 to about 8, in one aspect s is an integer from about 2 to about 4;

At least one Z in the said organosiloxane is selected from the group consisting of R5 ; 5;

wherein A ^" is a suitable charge balancing anion. In one aspect A ^" is selected from the group consisting of CI ^" , Br ^" ,

Γ, methylsulfate, toluene sulfonate, carboxylate and phosphate and

each additional Z in said organosilicone is independently selected from the group comprising of H, C ₁ -C ₃ 2 alkyl, Q-C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl,

C6-C ₃ 2 alkylaryl, C6-C ₃ 2 substituted alkylaryl, R5,

d N— R ₅

each R5 is independently selected from the group consisting of H; C ₁ -C ₃ 2 alkyl; C ₁ -C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl or C6-C ₃ 2 alkylaryl, or C6-C32 substituted alkylaryl,

-(CHR ₆ -CHR ₆ -0-) _w -CHR ₆ -CHR ₆ -L and siloxyl residue wherein each L is independently

†v

selected from -0-C(0)-R ₇ or -0-R ₇ ; ^N — ^R v; and

w is an integer from 0 to about 500, in one aspect w is an integer from 0 to about 200, one aspect w is an integer from 0 to about 50;

each R6 is independently selected from H or Ci-Qs alkyl; each R ₇ is independently selected from the group consisting of H; Q-C ₃ 2 alkyl; C ₁ -C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, and C6-C ₃ 2 substituted aryl, and a siloxyl residue;

each T is independently selected from H;

OT CH ₂ OT

I I

— CH ₂ — CH- CH ₂ -R ₅ ; CH CH ₂ — R ₅

wherein each v in said organosilicone is an integer from 1 to about 10, in one aspect, v is an integer from 1 to about 5 and the sum of all v indices in each Z in the said organosilicone is an integer from 1 to about 30 or from 1 to about 20 or even from 1 to about 10.

A suitable silicone is a blocky cationic organopolysiloxane having the formula:

M _w D _x T _y Q _z wherein:

M = [SiR ₁ R ₂ R30 _1/2 ], [SiR ₁ R ₂ G ₁ 0 _1/2 ], [SiR ₁ G ₁ G ₂ 0 _1/2 ], [SiG ₁ G ₂ G ₃ 0 ₁ /2], or combinations thereof; D = [SiR ₁ R ₂ 0 ₂ /2], [SiR ₁ G ₁ 0 _2/2 ], [SiG ₁ G ₂ 0 ₂ /2] or combinations thereof;

T = [S1R ₁ O _3/ 2], [S1G ₁ O _3/ 2] or combinations thereof;

Q = [Si0 _4/2 ]; w = is an integer from 1 to (2+y+2z);

x = is an integer from 5 to 15,000;

y = is an integer from 0 to 98;

z = is an integer from 0 to 98;

Rj is selected from the group of moieties of RK)RII -CI-C32 alkyl, with p being an integer ranging from 1-X and Rjo and Rn being independently selected from H or linear or branced C1-C32 alkyl groups with at least one of them being H, n-RjoRnNKn-l)- hydroxy-Cn alkyl with n being an integer from 2 to 32 and Rjo and Rn being independently selected from H or linear or branced C1-C32 alkyl groups with at least one of them being H; alkyl residues mentioned in this list can be substituted, or partly or completely exchanged by C2- C32 alkoxy or C2-C32 substituted alkoxy. R2 and R3 are each independently selected from the group consisting of H, OH, C ₁ -C ₃ 2 alkyl, Ci C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, C6-C ₃ 2 substituted alkylaryl, C ₁ -C ₃ 2 alkoxy, C ₁ -C ₃ 2 substituted alkoxy and X-Z;

only one of the moieties M and D contains only one group Rj

at least one of M, D, or T incorporates at least one moiety Gi, G2 or G _3; and Gi, G2, and G ₃ are each independently selected from the formula:

wherein:

X comprises a divalent radical selected from the group consisting of C ₁ -C ₃ 2 alkylene, C ₁ -C ₃ 2 substituted alkylene, C5-C ₃ 2 or C6-C ₃ 2 arylene, C5-C ₃ 2 or C6-C ₃ 2 substituted arylene, C6-C ₃ 2 arylalkylene, C6-C ₃ 2 substituted arylalkylene, C ₁ -C ₃ 2 alkoxy, C ₁ -C ₃ 2 substituted alkoxy, tertiary C ₁ -C ₃ 2 alkyleneamino, tertiary C ₁ -C ₃ 2 substituted alkyleneamino, ring-opened epoxide, and ring- opened glycidyl, with the proviso that if X does not comprise a repeating alkylene oxide moiety then X can further comprise a heteroatom selected from the group consisting of P, N and O; each R4 comprises identical or different monovalent radicals selected from the group consisting of H, C ₁ -C ₃ 2 alkyl, C ₁ -C ₃ 2 substituted alkyl, C5-C ₃ 2 or C6-C ₃ 2 aryl, C5-C ₃ 2 or C6-C ₃ 2 substituted aryl, C6-C ₃ 2 alkylaryl, and C6-C ₃ 2 substituted alkylaryl;

E comprises a divalent radical selected from the group consisting of C ₁ -C ₃ 2 alkylene, C ₁ -C ₃ 2 substituted alkylene, C5-C ₃ 2 or C6-C ₃ 2 arylene, C5-C ₃ 2 or C6-C ₃ 2 substituted arylene, C6-C ₃ 2 arylalkylene, C6-C32 substituted arylalkylene, C ₁ -C32 alkoxy, C ₁ -C32 substituted alkoxy, tertiary C ₁ -C ₃ 2 alkyleneamino, tertiary C ₁ -C ₃ 2 substituted alkyleneamino, ring-opened epoxide, and ring- opened glycidyl,, with the proviso that if E does not comprise a repeating alkylene oxide moiety then E can further comprise a heteroatom selected from the group consisting of P, N, and O; E' comprises a divalent radical selected from the group consisting of C ₁ -C ₃ 2 alkylene, C ₁ -C ₃ 2 substituted alkylene, C5-C ₃ 2 or C6-C ₃ 2 arylene, C5-C ₃ 2 or C6-C ₃ 2 substituted arylene, C6-C ₃ 2 arylalkylene, C6-C ₃ 2 substituted arylalkylene, C ₁ -C ₃ 2 alkoxy, C ₁ -C ₃ 2 substituted alkoxy, tertiary C ₁ -C ₃ 2 alkyleneamino, tertiary C ₁ -C ₃ 2 substituted alkyleneamino, ring-opened epoxide, and ring- opened glycidyl,, with the proviso that if E' does not comprise a repeating alkylene oxide moiety then E' can further comprise a heteroatom selected from the group consisting of P, N, and O; p is an integer independently selected from 1 to 50;

n is an integer independently selected from 1 or 2; when at least one of Gi, G2, or G3 is positively charged, A ^" ' is a suitable charge balancing anion or anions such that the total charge, k, of the charge-balancing anion or anions is equal to and opposite from the net charge on the moiety Gi, G2 or G3; wherein t is an integer independently selected from 1 , 2, or 3 ; and k < (p*2/t) + 1 ; such that the total number of cationic charges balances the total number of anionic charges in the organopolysiloxane molecule;

and wherein at least one E does not comprise an ethylene moiety.

Siloxane functionalisation of lignin:

Functionalisation via activated hydroxyl groups: Lignin (500 mg) is dissolved in water containing sodium hydroxide (amount corresponding to lequivalnt (eq.) to total acidic groups in the lignin, i.e., phenolic hydroxyl and carboxylic acid groups. After 1 h of stirring, the suitably terminated siloxane functional, e.g., an epoxide-terminated siloxane functional, is added (depending on the desired technical loading, e.g in the range of from 0.25 to 10.0 eq. to lignin phenolic hydroxyl groups) and the reaction mixture is stirred at 50 °C overnight. In order to assure appropriate mixing of lignin and terminated siloxane functional in the reaction mixture, additives such as emulsifiers, e.g., non-ionic surfactants, can be used.

After cooling to room temperature and acidifying to pH 2 using 10% (v/v) aqueous hydrogen chloride solution, the resulting suspension is centrifuged (15 min at 500 rpm) to recover the precipitated lignin. The functionalised lignin is then washed 3 times with 50 mL acidified water (pH 2) followed by renewed isolation via centrifugation (15 min at 500 rpm) each time. The final pellet was subsequently freeze-dried. The freeze-dried material is used for analysis and application without any additional manipulation.

Functionalisation via keto-groups: Lignin, or chemically oxidised lignin, or lignin oxidised biotechnologically using oxidative enzymes, such as, but not exclusively, laccases (EC 1.10.3), polyphenol oxidases (EC 1.14.18) and lipoxygenases (EC 1.13.11) as well as homogenic or heterogenic mixtures thereof, (500 mg) are dissolved or suspended in water or an enzyme- compatible buffer solution in the present of 5% (m/v) of an non-ionic surfactant, the suitably decorated siloxane functional, e.g., an amine-decorated-siloxane-functional, is added and the mixture is stirred for a maximum of 24 hours. In case the reaction is run in the absence of enzymes, the reaction temperature is at 30 °C. In case the reaction is run in the presence of one or more enzymes, the temperature is chosen according to a performance study on the enzymatic species revealing the optimum temperature for maximum enzyme activity.

After the desired reaction time, at room temperature, the reaction n mixture is acidified to pH 2 using 10% (v/v) aqueous hydrogen chloride solution. The resulting suspension is centrifuged (15 min at 500 rpm) to recover the precipitated lignin. The functionalised lignin is then washed 3 times with 50 mL acidified water (pH 2) followed by renewed isolation via centrifugation (15 min at 500 rpm) each time. The final pellet was subsequently freeze-dried. The freeze-dried material is used for analysis and application without any additional manipulation.

How to measure functionalisation content:

Evaluation of bonding type: For evaluating the presence of covalent bonding between the silicon and the lignin starting materials, gel permeation chromatography studies are performed.

For the starting materials as well as for the silicon-lignin hybrids, M _n and M _w are determined, e.g. as described elsewhere. Covalent bonding is indicated by significant augmentations of the signals obtained by the diode array detector at a wavelength of λ = 280 nm at elution times at which no signal augmentation was observed for the starting lignin, indicating UV-active species exhibiting molecular weights significantly larger than those observed for the starting lignin under identical analysis conditions.

Quantification of silicon content:

Functionalisation via activated hydroxyl groups: For evaluating the extend of silicon- lignin hybrid formation, an elemental analysis in the form of a CHNS-analysis was performed as described above using a Carlo-Erba NA 1500 analyzer. Ratios between lignin oligomers and silicon polymers were estimated according to the change in the carbon/hydrogen ratio found in the sample based on the mathematical change caused by the addition of five siloxane monomer units (-Si(CH ₃ ) ₂ 0-)to the average C ₉ -formula (C H _a O _b (OCH ₃ ) _c )) of the theoretical average monomer of the starting lignin, wherein a is a number between 7.5 and 9.5, b is a number between 2.5 and 6.0, and c is a number between 0.0 and 2.0. Ratios are given in % lignin (m/m).

Functionalisation via keto-groups: For evaluating the extend of silicon-lignin hybrid formation, an elemental analysis in the form of a CHNS-analysis was performed as described above using a Carlo-Erba NA 1500 analyzer. Ratios between lignin oligomers and silicon polymers were estimated according to the amount of nitrogen found in the sample with respect to the nitrogen content of the polymeric unit of the employed amine group-containing siloxane- functional. Ratios are given in % lignin (m/m).

Method of measuring sulphur content: The chemical composition of a lignin sample in terms of its carbon (C), hydrogen (H), nitrogen (N) and sulphur (S) content can be determined by elemental analysis in form of a CHNS analysis of at least three different representative samples of a given batch of the respective lignin. Typical sample sizes are 2.0 mg of a lignin sample that was oven-dried at 105°C until a steady weight was obtained. The samples are placed in aluminum dishes and analyzed using a Carlo-Erba NA 1500 analyzer, using helium as carrier gas. Carbon (C), hydrogen (H), nitrogen (N) and sulphur (S) were detected in form of carbon dioxide, water, nitrogen, and sulphur dioxide, which are chromatographically separated to exit the instrument in the order of nitrogen, carbon dioxide, water, and sulphur dioxide.

Quantification is achieved against calibrations using typical standard substances used for the calibration of elemental analysers, such as (bis(5-tert-butyl-2-benzo-oxazol-2-yl) thiophene, based on the peak areas of the chromatograms obtained for each lignin sample.

Method of measuring M _n and M _w : The number average molecular weight, M _n , as well as the weight average molecular weight, M _w , can be determined using gel permeation chromatography (GPC). Prior to analysis, representative lignin samples are acetobrominated as reported in archival literature (J. Asikkala, T. Tamminen, D. S. Argyropoulos, J. Agric. Food Chem. 2012, 60, 8968-8973.) to ensure complete solubilisation in tetrahydrofuran (THF). 5mg lignin is suspended in lmL glacial acetic acid/acetyl bromide (9: 1 v/v) for 2 h. The solvent is then removed under reduced pressure, and the residue is dissolved in HPLC-grade THF and filtered over a 0.45 μπι syringe filter prior to injection into a 20 μL· sample loop. Typical analysis set-ups resemble the following specific example: GPC-analyses are performed using a Shimadzu instrument consisting of a controller unit (CBM-20A), a pumping unit (LC 20AT), a degasser unit (DGU-20A3), a column oven (CTO-20AC), a diode array detector (SPD-M20A), and a refractive index detector (RID- 1 OA); the instrumental set-up is controlled using the Shimadzu LabSolution software package (Version 5.42 SP3). Three analytical GPC columns (each 7.5 x 30 mm) are connected in series for analyses: Agilent PLgel 5 μπι 10000 A, followed by Agilent PLgel 5 μπι 1000 A and Agilent PLgel 5 μπι 500 A. HPLC-grade THF (Chromasolv®, Sigma- Aldrich) is used as eluent (isocratic at 0.75 mL min ^"7 , at 40 °C). Standard calibration is performed with polystyrene standards (Sigma Aldrich, MW range 162 - 5 x 106 g mol ^"7 ), and lower calibration limits are verified / adjusted by the use of synthesized dimeric and trimeric lignin models. Final analyses of each sample is performed using the intensities of the UV signal at λ = 280 nm employing a tailor-made MS Excel-based table calculation, in which the number average molecular weight (M _n ) and the weight average molecular weight ( _w )) is calculated based on the measured absorption (in a.u.) at a given time (min) after corrections for baseline drift and THF-stemming artifacts.

M _n is calculated according to the formula in which M _n is the number average molecular weight

W; is obtained via w,- =— h,-——— with M being molecular weight

^{1 1 1} d(log M) ^{6 6}

hi being the signal intensity of a given logM measurement point

V being the volume of the curve over a given logM interval d(logM).

Mi is a given molecular weight.

The analysis is run in triplicate, and final values are obtained as the standard average.

M _w is calculated according to the formula

∑WiMi

w = in which M _w is the number average molecular weight

W; is obtained via w,- =— hi , ^dV , with M being the molecular weight

^{1 1 1} d(log M) ^{6 6}

hi being the signal intensity of a given logM measurement point

V being the volume of the curve over a given logM interval d(logM).

Mi is a given molecular weight.

The analysis is run in triplicate, and final values are obtained as the standard average.

Eventually necessary adjustment of M _n and M _w with respect to the desired applications is achieved by mechanical breaking of polymeric lignin using a ball mill, by chemically or enzymatically polymerising oligomeric lignin.

Method of measuring aromatic hydroxyl and aliphatic hydroxyl content: Typically, a procedure similar to the one originally published can be used (A. Granata, D. S. Argyropoulos, J. Agric. Food Chem. 1995, 43, 1538-1544). A solvent mixture of pyridine and (CDC13) (1.6: 1 v/v) is prepared under anhydrous conditions. The NMR solvent mixture is stored over molecular sieves (4 A) under an argon atmosphere. Cholesterol is used as internal standard at a concentration of 0.1 mol/L in the aforementioned NMR solvent mixture. 50 mg of Cr(III) acetyl acetonate are added as relaxation agent to this standard solution.

Ca. 30 mg of the lignin are accurately weighed in a volumetric flask and suspended in 400 μL· of the above prepared solvent solution. One hundred microliters of the internal standard solution are added, followed by 100 μΐ. of 2-chloro-4,4,5,5-tetramethyl-l,3,2-dioxaphospholane (Cl-TMDP). The flask is tightly closed, and the mixture is stirred for 120 min at ambient temperature. 3 IP NMR spectra are recorded using suitable equipment, similar or identical to the following example: On a Bruker 300 MHz NMR spectrometer, the probe temperature is set to 20 °C. To eliminate NOE effects, the inverse gated decoupling technique is used. Typical spectral parameters for quantitative studies are as follows: 90° pulse width and sweep width of 6600 Hz. The spectra are accumulated with a delay of 15 s between successive pulses. Line broadening of 4 Hz is applied, and a drift correction is performed prior to Fourier transform. Chemical shifts are expressed in parts per million from 85 % H3P04 as an external reference. All chemical shifts reported are relative to the reaction product of water with Cl-TMDP, which has been observed to give a sharp signal in pyridine/CDC13 at 132.2 ppm. To obtain a good resolution of the spectra, a total of 256 scans are acquired. The maximum standard deviation of the reported data is 0.02 mrnol/g, while the maximum standard error is 0.01 mrnol/g. (A. Granata, D. S. Argyropoulos, J. Agric. Food Chem. 1995, 43, 1538-1544). Quantification on the basis of the signal areas at the characteristic shift regions (in ppm, as reported in A. Granata, D. S. Argyropoulos, J. Agric. Food Chem. 1995, 43, 1538-1544) is done using a tailor-made table calculation in which the abundances, given in mmol/g, of the different delineable phosphitylated hydroxyl groups are determined on the basis of the integral obtained for the signal of the internal standard, that is present in the analysis sample at a concentration of 0.1 m, creating a signal at the interval ranging from 144.5 ppm to 145.3 ppm. The area underneath the peak related to the internal standard is set to a value of 1.0 during peak integration within the standard processing of the crude NMR data, allowing for determining abundances using simple rule-of -proportion mathematics under consideration of the accurate weight of the sample used for this analysis. The analysis is run in triplicate, and final values are obtained as the standard average. Method of measuring hydrolysable ester content: The total ester content of the lignin can be determined by subjecting the lignin to alkaline hydrolysis conditions: Ca. 500 mg of lignin are dissolved in an excess of 1 M sodium hydroxide solution and heated to temperatures of above 70 - 80 °C for 12 h. The lignin is subsequently precipitated by acidifying the reaction mixture, isolated and freeze-dried.

Ca. 30 mg of the lignin are accurately weighed in a volumetric flask and suspended in 400 μL· of the above prepared solvent solution. One hundred microliters of the internal standard solution are added, followed by 100 μΐ. of 2-chloro-4,4,5,5-tetramethyl-l,3,2-dioxaphospholane (Cl-TMDP). The flask is tightly closed, and the mixture is stirred for 120 min at ambient temperature. ³¹ P NMR spectra are recorded using suitable equipment under the conditions reported above for the determination of aliphatic and aromatic hydroxyl contents. Quantification of the acid content is done on the basis of the signal intensities at the characteristic shift regions (in ppm) using a tailor-made table calculation referring to the signal of the internal standard. Abundances are typically given in mmol/g. The ester content is obtained as the difference in the abundances of acid groups, aliphatic hydroxyl groups, and aromatic hydroxyl groups found in untreated vs. the lignin treated with sodium hydroxide as outlined above. The analysis is run in triplicate, and final values are obtained as the standard average.

Emollient: Suitable emollients are silicon based emollients. Silicone-based emollients are organo-silicone based polymers with repeating siloxane (Si 0) units. Silicone-based emollients of the present invention are hydrophobic and exist in a wide range of molecular weights. They include linear, cyclic and crosslinked varieties. Silicone oils are generally chemically inert and usually have a high flash point. Due to their low surface tension, silicone oils are easily spreadable and have high surface activity. Examples of silicon oil include: Cyclomethicones, Dimethicones, Phenyl-modified silicones, Alkyl-modified silicones, Silicones resins, Silica. Other emollients useful in the present invention can be unsaturated esters or fatty esters.

Examples of unsaturated esters or fatty esters of the present invention include: Caprylic Capric Triglycerides in combination with Bis-PEG/PPG-1 6/16 PEG/PPG-16/16 Dimethicone and C12- C15 Alkylbenzoate.

The basic reference of the evaluation of surface tension, polarity, viscosity and spreadability of emollient can be found under Dietz, T., Basic properties of cosmetic oils and their relevance to emulsion preparations. SOFW- Journal, July 1999, pages 1-7. Humectant: A humectant is a hygroscopic substance used to keep things moist. Typically, it is often a molecule with several hydrophilic groups, most often hydroxyl groups; however, amines and carboxyl groups, sometimes esterified, can be encountered as well (its affinity to form hydrogen bonds with molecules of water is the crucial trait). A humectant typically attracts and retains the moisture in the air nearby via absorption, drawing the water vapour into and/or beneath the organism/object's surface.

Suitable humectants include: Propylene glycol, hexylene glycol, and butylene glycol, Glyceryl triacetate, Neoagarobiose, Sugar alcohols (sugar polyols) such as glycerol, sorbitol, xylitol, maltitol, Polymeric polyols such as polydextrose, Quillaia, Urea, Aloe vera gel, MP diol, Alpha hydroxy acids such as lactic acid, Honey, Lithium chloride

Emulsifier:_An emulsifier generally helps disperse and suspend a discontinuous phase within a continuous phase in an oil-in-water emulsion. A wide variety of conventional emulsifiers are suitable for use herein. Suitable emulsifiers include: hydrophobically-modified cross-linked polyacrylate polymers and copolymers, polyacrylamide polymers and copolymers, and polyacryloyldimethyl taurates. More preferred examples of the emulsifiers include:

acrylates/C 10-30 alkyl acrylate cross-polymer having tradenames PemulenTM TR-1,

PemulenTM TR-2 (all available from Lubrizol); acrylates/steareth-20 methacrylate copolymer with tradename ACRYSOLTM 22 (from Rohm and Hass); polyacrylamide with tradename SEPIGEL 305 (from Seppic).

EXAMPLES

Example 1: The following samples were evaluated by the method described below.

Sample A is silicone functionalized lignin oligomer in accordance with the present invention. Sample B is unfunctionalised lignin mixed with silicone* (comparative example).

Av. # lignin Functionalisation Functionalisation monomers Content

Lignin oligomer of 3-8 Polydimethylsiloxane 49% (m/m)

Sample A (PDMS) linked via

ether bond

Lignin oligomer of 3-8 unfunctionalised 0% (m/m)

Sample B *Sample B comprises the lignin starting material and the silicone starting material used in the synthesis of the silicone functionalized lignin oligomer of Sample A as a chemically unreactive derivative (i.e. a derivative in which the functional group used to link it to the lignin has been consumed by activated methanol) (i.e. Sample B is the silicone and lignin substrate used to make Sample A).

Preparation of contact angle samples: Weigh out O. lg of silicone functionalised lignin oligomer and disperse in 1 litre of non-ionic based hard surface cleaning product water dispersion (Flash diluted in de-ionised water at the recommended dosage of 4.8ml/l) and stir it for 15 minutes at 200 rpm at room temperature. Using sodium carbonate, pH was adjusted to pH 10.5. Then, glass slides were dipped for 30 minutes and allowed to dry two hours at room temperature. Following this preparatory procedure contact angle of deionized water on the treated surface was measured using First Ten Angstroms 200 equipment.

Contact Angle Data:

Sample A in accordance with the present invention showed superior surface modification properties than the comparison example (Sample B). Example 2, Illustrative examples:

Shampoo Compositions:

Ingredient Wt. % Wt. %

Product I Product II

Water Balance Balance

Cetyl Alcohol 4.18% 4.18% Stearyl Alcohol 7.52% 7.52%

Sodium laureth-3 sulfate (28% 10.00% 10.00% Active)

Lignin 0.01% 1.00%

Hair Conditioning:

Hand Dishwashing:

Water Balance Balance

Granular laundry detergent compositions designed for front-loading automatic washing machines:

Wt% Wt%

Product I Product II

Linear alkylbenzenesulfonate 8 8

CI 2- 14 Alkylsulfate 1 1

AE7 2.2 2.2

C _J O- ₁ 2 Dimethyl

hydroxyethylammonium

chloride 0.75 0.75

Crystalline layered silicate (δ- Na ₂ Si ₂ 0 ₅ ) 4.1 4.1

Zeolite A 5 5

Citric Acid 3 3

Sodium Carbonate 15 15

Silicate 2R (Si0 ₂ :Na ₂ 0 at ratio

2:1) 0.08 0.08

Soil release agent 0.75 0.75

Acrylic Acid/Maleic Acid

Copolymer 1.1 1.1

Carboxymethylcellulose 0.15 0.15

Protease - Purafect® (84 mg

active/g) 0.2 0.2

Amylase - Stainzyme Plus® (20

mg active/g) 0.2 0.2 Lipase - Lipex® (18.00 mg

active/g) 0.05 0.05

Amylase - Natalase® (8.65 mg

active/g) 0.1 0.1

TAED 3.6 3.6

Percarbonate 13 13

Na salt of Ethylenediamine- Ν,Ν'-disuccinic acid, (S,S)

isomer (EDDS) 0.2 0.2

Hydroxyethane di phosphonate

(HEDP) 0.2 0.2

MgS0 ₄ 0.42 0.42

Perfume 0.5 0.5

Suds suppressor agglomerate 0.05 0.05

Soap 0.45 0.45

Sulphonated zinc phthalocyanine

(active) 0.0007 0.0007

S-ACMC 0.01 0.01

Lignin 0.01 1.0

Sulfate/ Water & Miscellaneous Balance Balance

Beauty Lotion/Cream:

Wt% Wt% Product I Product II

Water Balance Balance

Glycerin 7 7

Disodium EDTA 0.05 0.05

Methylparaben 0.1 0.1

Sodium Dehydroacetate 0.5 0.5

Benzyl alcohol 0.25 0.25

GLW75CAP-MP (75% aq. 0.5 0.5

Ti02 dispersion) ¹ Palmitoyl-dipeptide 0.0001 0.0001

N-acetyl glucosamine 2 2

Salicylic Acid 1.5 1.5

Isohexadecane 3 3

PPG 15 Stearyl Ether 4 4

Isopropyl Isostearate 1.3 1.3

Sucrose polyester 0.7 0.7

Phytosterol 0.5 0.5

Cetyl alcohol 0.4 0.4

Stearyl alcohol 0.5 0.5

Behenyl alcohol 0.4 0.4

PEG- 100 stearate 0.1 0.1

Cetearyl glucoside 0.1 0.1

Poly aery lamide/C 13-14 2 2 isoparaffin/laureth-7

Dimethicone/dimethiconol 2 2

Polymethylsilsequioxane 0.25 0.25

Lignin 0.01 1.00

Personal Care product containing skin lightening:

Wt% wt%

Component

Product I Product II

Disodium EDTA 0.100 0.100

Phlorogine BG 2.000 0 deoxyArbutin 0 2.000

Niacinamide 5.000 5.000

Isohexadecane 3.000 3.000

Isopropyl isostearate 1.330 1.330

Sucrose polycottonseedate 0.670 0.670

Polymethylsilsesquioxane 0.250 0.250

Cetearyl glucoside + cetearyl

0.200 0.200 alcohol Behenyl alcohol 0.400 0.400

Ethylparaben 0.200 0.200

Propylparaben 0.100 0.100

Cetyl alcohol 0.320 0.320

Stearyl alcohol 0.480 0.480

Tocopheryl acetate 0.500 0.500

PEG- 100 stearate 0.100 0.100

Glycerin 7.000 7.000

Titanium dioxide 0.604 0.604

Poly aery lamide + CI 3- 14

2.000 2.000

isoparaffin + laureth-7

Panthenol 1.000 1.000

Benzyl alcohol 0.400 0.400

Dimethicone + dimethiconol 2.000 2.000

Lignin 0.010 1.000

Water (to lOOg) Balance Balance

Automatic Dishwashing Cleaning composition:

Powder (wt% based on Powder (wt% based on 19 g portion) 19 g portion)

STPP 34-38 34-38

Alcosperse ¹ 7-12 7-12

SLF-18 Polytergent 1-2 1-2

Esterified substituted benzene 0.1-6.0 0.1-6.0

sulfonate ³

Polymer ⁴ 0.2-6.0 0.2-6.0

Sodium perborate 2-6 2-6

monohydrate

Carbonate 20-30 20-30

2.0r silicate 5-9 5-9

Sodium disilicate 0-3 0-3

Enzyme system 0.1-5.0 0.1-5.0 Pentaamine cobalt(III)chloride 10-15 10-15

dichloride salt

TAED 0-3 0-3

Perfume, dyes, water and other Balance to 100% Balance to 100%

components

Liquid (wt% based on Liquid (wt% based on

1.9 g portion) 1.9 g portion)

Dipropylene Glycol 35-45 35-45

SLF-19 Polytergent 40-50 40-50

Neodol ® C11E09 1-3 1-3

Lignin 0.01 1.0

Dyes, water and other Balance Balance

components such as Alcosperse® 246 or 247, a sulfonated copolymer of acrylic acid from Alco Chemical Co.

linear alcohol ethoxylate from Olin Corporation

such as those described above

⁴ a sulfonated polymer such as those described above

⁵ one or more enzymes such as protease, mannaway, natalase, lipase and mixture thereof.

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as "40 mm" is intended to mean "about 40 mm."