Abstract: The invention provides a PHA copolymer including at least a 3-hydroxy-?-carboxyalkanoic acid represented by a formula (19) or (32) and simultaneously at least a unit represented by a formula (2) or a formula (3) in a molecule, a precursor PHA copolymer having a corresponding vinyl group or a corresponding alkoxycarbonyl group, a biosynthesis method thereof by microorganisms, and a method of producing a desired PHA copolymer from the precursor PHA copolymer: (wherein k, m, n are integers; R18 represents H, Na, K, R27? represents (A); R1 represents a substituent on a cyclohexyl group and represents H, CN, NO2, a halogen atom, CH3, C2H5, C3H7, CF3, C2F5, or C3F7; R includes a residue including a phenyl structure or a thienyl structure; these being independent for each unit).

Abstract: A developer carrying member which prevents toner from being excessively charged in a development apparatus and maintains a high charge quantity of toner, and which is difficult to cause deposition of toner thereto, and a development apparatus equipped with the developer carrying member are provided. A resin layer containing, as a binder, a resin containing polyhydroxyalkanoate having in the molecule at least one hydroxyalkanoic acid unit including sulfonic acid or a derivative thereof or carboxylic acid or a derivative thereof is formed on a substrate or on the surface of the substrate of the developer carrying member.

Abstract: To provide a toner for developing electrostatic images which is not easily cause the phenomenon of toner-spent, constituent materials are so selected that a charge control resin has hardness which is the same as the hardness of a binder resin or the charge control resin is harder than the binder resin, as measured with a scanning probe microscope in a viscoelasticity evaluation mode in respect to the binder resin and the charge control resin which are present in the particle interiors or particle surfaces of the toner.

Abstract: A polyhydroxyalkanoate characterized by having in the molecule a unit represented by Chemical Formula (1): wherein n may assume any one integral value within the range of from 1 to 8. Also disclosed are a process for producing the polyhydroxyalkanoate by the use of a microorganism having the ability to produce the polyhydroxyalkanoate and accumulate it in the bacterial body; a charge control agent, a toner binder and a toner which contain this polyhydroxyalkanoate; and an image-forming method and an image-forming apparatus which make use of the toner.

Abstract: A novel polyhydroxyalkanoate having a monomer unit represented by the formula (1), the unit having a carboxyl group substituting a ring structure at the end of side chain, obtainable by oxydizing vinyl or methyl group substituting a ring structure at the end of the side chain. The polyhydroxyalkanoate has high thermal stability, charge stablity, a high charge amount, improved dispersibility and biodegradability together, and therefore, suitable for resin moldings, and binders and charge controlling agents for toners used in the electrophotographic process.

Abstract: A polyhydroxyalkanoate copolymer comprises one kind of unit of —[OCH((CH2)x—SOC6H5R)CH2CO]— (n=1-7) ??(1) (wherein R is any one of H, halogen, CN, NO2, COOR?, SO2R? (R? is any one of H, Na, K, CH3 and C2H5; R? is any one of OH, ONa, OK, halogen, OCH3 and OC2H5), CH3, C2H5, C3H7, (CH3)2—CH and (CH3)3—C) and —[OCH((CH2)x—SO2C6H5R)CH2CO]— (n=1-7) ??(2) (wherein R is any one of H, halogen, CN, NO2, COO R?, SO2R? (R? is any one of H, Na, K, CH3 and C2H5; R? is any one of OH, ONa, OK, halogen, OCH3 and OC2H5), CH3, C2H5, C3H7, (CH3)2—CH and (CH3)3—C) and at least one unit of chemical formulae (3) to (6): —[OCH((CH2)m—Rz)CH2CO]— (n=1-8) ??(3) (wherein Rz comprises a residue having either a phenyl structure or a thienyl structure), —[OCH((CH2)k—C6H11Ra)CH2CO]— (n=1-8) ??(4) (wherein Ra is any one of H, CN, NO2, halogen, CH3, C2H5, C3H7, CF3, C2F5 and C3F7) —[OCH((CH2)n—CH?CH2)CH2CO]— (n=1-8) ??(5), and —[OCH((CH2)n—COORb)CH2CO]— (n=1-8) ??(6) (wherein Rb is any one of H, Na and K).

Abstract: A developer carrying member is disclosed which can prevent a toner from being excessively charged in a developing assembly while keeping the charge quantity of the toner at a somewhat higher level, and seldomly causes toner melt adhesion to the developer carrying member.

Abstract: A polyhydroxyalkanoate containing in a molecule at least one unit represented by the chemical formula (1). The polyhydroxyalkanoate is a biodegradable plastic with enhanced melt-processability and exhibits excellent charging stability, high chargeability, and enhanced dispersibility when used as a charge control agent of a toner in an electrophotographic process. (R denotes -A1(—SO2R1)x. R1 is selected from OH, a halogen atom, ONa, OK, and OR1a. R1a and A1 are selected from a substituted or unsubstituted aliphatic hydrocarbon structure, a substituted or unsubstituted aromatic ring structure, and a substituted or unsubstituted heterocyclic structure. Further, m and x are integers selected from 1 to 8, and when two or more units exist, each of R, R1 R1a, A1, m, and x is defined as above independently for each of the units.

Abstract: To provide a resin-coated carrier for an electrophotographic developer capable of providing an image with excellent image quality; and a two-component developer and a replenishing developer each of which contains the resin-coated carrier as a constituent.

Abstract: There is provided a resin-coated carrier with a coating layer attached to the surface of a core material in a stable manner, the electrophotographic carrier which can provide an image with excellent quality.

Abstract: The present invention provides a negataively chargeable charge controlling agent to control a charged state of a powder or granular material such as toner for electrophotography, where the agent comprises a polyhydroxyalkanoate having at least one kind of 3-hydroxy-?-carboxyalkanoic acid unit represented by the chemical formula (1): wherein n is an integer selected from 1 to 8; R1 is an H, Na or K atom, or and when more than one unit exists, n and R1 is the same or different between the units. The charge controlling agent is excellent in electrophtographic properties and propitious to environment because of the biodegradability of the polyhydroxyalkanoate. wherein n is an integer selected from the range shown in the same chemical formula; R1 is an H atom, Na atom, K atom, or and when more than one unit exists, n and R1 may differ from unit to unit.

Abstract: A polyhydroxyalkanoate is disclosed which has in the molecule a unit represented by Chemical Formula (1). wherein R is arbitrarily selected from a hydrogen atom, a halogen atom, CN, NO2, COOR?, SO2R?, CH3, C2H5, C3H7, C(CH3)2H and C(CH3)3; where R? is H, Na, K, CH3 or C2H5, and R? is OH, ONa, OK, a halogen atom, OCH3 or OC2H5; and x is an integer arbitrarily selected from 1 to 8; with the proviso that a polyhydroxyalkanoate is excluded which has a hydrogen atom as R and x in all the units is 2 or 4. Also disclosed is a process for producing the polyhydroxyalkanoate by the use of a microorganism having the ability to produce the polyhydroxyalkanoate and accumulate it in the bacterial body.

Abstract: Provided is a polyhydroxyalkanoate containing in a molecule thereof one or more units each selected from the following formulae (1) (2), (3) and (4): wherein R1 and R6 are each OH, halogen, ONa, OK, OCH3 or OC2H5; A1 and J6 are each a substituted or unsubstituted aliphatic hydrocarbon; m and n are each 0 to 7; r is 1 to 500; and R1? to R5? are each hydrogen or halogen.

Abstract: A polyhydroxyalkanoate comprises a unit of formula (1): —(O—CH((CH2)mSASO2R)CH2C(?O))— wherein R is selected from the group consisting of OH, a halogen atom, ONa, OK, OCH3 and OC2H5; A represents a substituted or unsubstituted aliphatic hydrocarbon structure; m is an integer number selected from 1 to 8; and in the case where a plurality of units exist in the same molecule, R, A and m in one unit can be different from them in another unit respectively.

Abstract: A polyhydroxyalkanoate comprises a unit of formula (1): —(O—CH((CH2)mSASO2R)CH2C(═O))— wherein R is selected from the group consisting of OH, a halogen atom, ONa, OK, OCH3 and OC2H5; A represents a substituted or unsubstituted aliphatic hydrocarbon structure; m is an integer number selected from 1 to 8; and in the case where a plurality of units exist in the same molecule, R, A and m in one unit can be different from them in another unit respectively.

Abstract: Provided is a polyhydroxyalkanoate containing in a molecule thereof one or more units each selected from the group consisting of the following formulae (1), (2), (3) and (4): 1

Abstract: A method is provided for controlling the molecular weight of a polyhydroxyalkanoate containing at least one of a unit: —[OCH((CH2)mR1)CH2C(O)]— (m=1-8; R1 is a residue having a ring structure of any of phenyl and thienyl structure), and a unit: —[OCH((CH2)kC6H1)R2)CH2C(O)]— (k=0-8; R2 denotes a substituent on the cyclohexyl group including H, CN, NO2, halogen atom, CH3, C2H5, C3H7, CF3, C2F5 or C3F7), wherein a microorganism is cultivated in the presence of a hydroxyl group-containing compound, which is capable of producing the polyhydroxyalkanoate from R3(CH2)qCH2CH2COOH (q=1-8; R3 contains a residue having a ring structure of phenyl or thienyl) or R4C6H10(CH2)rCH2CH2COOH (r=0-8; R4 denotes a substituent on the cyclohexyl group including H, CN, NO2, halogen, CH3, C2H5, C3H7, CF3, C2F5, or C3F7).

Abstract: A polyhydroxyalkanoate (PHA) having a desired configuration is produced using a raw material containing &ohgr;-(4-vinylphenyl)-alkanoic acid and (&ohgr;-substituted alkanoic acid in which a group having a ring structure selected from phenyl, thienyl, and cyclohexyl structures substitutes therefor on the end thereof by producing a PHA copolymer containing the corresponding 3-hydroxy-&ohgr;-(4-vinylphenyl)-alkanoate unit and the corresponding 3-hydroxy-&ohgr;-substituted alkanoate unit by making use of a microorganism capable of producing the PHA or by oxidizing a predetermined portion of the corresponding PHA.

Abstract: A method is provided for controlling the molecular weight of a polyhydroxyalkanoate containing at least one of a unit: —[OCH((CH2)mR1)CH2C(O)]— (m=1-8; R1 is a residue having a ring structure of any of phenyl and thienyl structure), and a unit: —[OCH ((CH2)kC6H10R2) CH2C(O)]— (k=0-8; R2 denotes a substituent on the cyclohexyl group including H, CN, NO2, halogen atom, CH3, C2H5, C3H7, CF3, C2F5 or C3F7), wherein a microorganism is cultivated in the presence of a hydroxyl group-containing compound, which is capable of producing the polyhydroxyalkanoate from R3(CH2)qCH2CH2COOH (q=1-8; R3 contains a residue having a ring structure of phenyl or thienyl) or R4C6H10(CH2)rCH2CH2COOH (r=0-8; R4 denotes a substituent on the cyclohexyl group including H, CN, NO2, halogen, CH3, C2H5, C3H7, CF3, C2F5, or C3F7).

Abstract: A polyhydroxyalkanoate (PHA) having a desired configuration is produced using a raw material containing &ohgr;-(4-vinylphenyl)-alkanoic acid and &ohgr;-substituted alkanoic acid in which a group having a ring structure selected from phenyl, thienyl, and cyclohexyl structures substitutes therefor on the end thereof by producing a PHA copolymer containing the corresponding 3-hydroxy-&ohgr;-(4-vinylphenyl)-alkanoate unit and the corresponding 3-hydroxy-&ohgr;-substituted alkanoate unit by making use of a microorganism capable of producing the PHA or by oxidizing a predetermined portion of the corresponding PHA.