FeCu bimetallic metal organic frameworks photo-Fenton synergy efficiently degrades organic pollutants: Structure, properties, and mechanism insight.

The high ion leaching, low photogenerated charge separation efficiency, and slow metal valence cycling of Fe-based metal organic frameworks (MOFs) have limited their application in the deep treatment of organic pollutants. Herein, FeCu bimetallic MOFs (FeCuBDC) were synthesized using a modified solvothermal method, and a coupled photo-Fenton degradation system was successfully constructed. Degradation performance tests showed that FeCuBDC could efficiently degrade 99.3% ± 0.1% of 50 mg/L phenol within 40 min. The reaction rate constants of the photo-Fenton system were 11.0 and 64.7 times higher than those of the single Fenton reaction and photocatalysis, respectively. FeCuBDC also exhibits good cycling stability, degradation generalization, and excellent photoelectric catalytic properties. Such a considerable enhancement in the overall performance pertains to the following. First, the introduction of Cu into Fe-MOFs not only improves the crystallinity and stability, but also reduces the band gap value, increases the absorption capacity of visible light, and promotes the generation of photogenerated carriers. Second, the FeCu in MOFs are all mixed valence. Initially, the high-valence FeCu captures photogenerated electrons and promotes photogenerated charge separation and transfer. Then, the low-valence FeCu adsorbs and decomposes H2O2, accelerating the valence cycling of the bimetallic sites. The core of the reaction mechanism is that FeCuBDC effectively promotes the photo-Fenton synergy.

Core-shell structure of sulphur vacancies-CdS@CuS: Enhanced photocatalytic hydrogen generation activity based on photoinduced interfacial charge transfer.

To regulate the charge flow of the photocatalyst in photocatalytic hydrogen reactions is highly desirable. In this study, a highly efficient sulphur vacancies-CdS@CuS core-shell heterostructure photocatalyst (denoted CdS-SV@CuS) was developed through the surface modification of CdS-sulphur vacancies (SV) nanoparticles by CuS based on photoinduced interfacial charge transfer (IFCT). This novel photocatalyst with modulated charge transfer was prepared by hydrothermal treatment and subsequent cation-exchange reactions. The SV confined in CdS and the IFCT facilitate the charge carrier's efficient spatial separation. The optimized CdS-SV@CuS(5%) catalyst exhibited a remarkably higher H2 production rate of 1654.53 µmol/g/h, approximately 6.7 and 4.0 times higher than those of pure CdS and CdS-SV, respectively. The high photocatalytic performance is attributed to the rapid charge separation, caused by the intimate interactions between CdS-SV and CuS in the core-shell heterostructure. This is the first time that a straightforward method is adopted to construct a metal sulphide core-shell structure for superior H2-production activity by IFCT.

Surface oxygen vacancies enriched FeOOH/Bi2MoO6 photocatalysis- fenton synergy degradation of organic pollutants.

To achieve rapid separation of photogenerated charges, increase photocatalytic degradation activity, a visible light-driven FeOOH/Bi2MoO6-OVs photocatalyst was designed and successfully fabricated via solvothermal synthesis and calcination. H2O2 was added under visible light irradiation to form a heterogeneous photocatalysis-Fenton synergy system. Using visible light irradiation, 10% FeOOH/Bi2MoO6-OVs had the best degradation activity. The removal efficiency of phenol was 100% within 3 h, which was 1.54 times and 1.33 times of the degradation efficiency of photocatalysis and Fenton alone, respectively. The catalyst has high removal activity for various pollutants and good cycle stability. Hydroxyl radicals and superoxide radicals have proven to be the main active substances and a reasonable catalytic mechanism was proposed. Surface oxygen vacancy can not only reduce the width of band gap, promote the separation and migration of photogenerated electron-hole pairs, but also make the OO bond of H2O2 elongate and weaken, making it easier to react with FeOOH and realize the synergistic effect of photocatalysis-Fenton. Simultaneously, the oxygen vacancies located near the valence band can capture holes, and the holes are rapidly transferred to the surface of the catalyst and participated in the degradation of pollutants.

Tuning the Supramolecular Structures of Metal-Free Porphyrin via Surfactant Assisted Self-Assembly to Enhance Photocatalytic Performance.

Metal-free porphyrin with good planarity is beneficial to π-π stack interactions, which promotes electron coupling and the separation and transfer of photogenerated carriers. It is necessary to develop metal-free porphyrin-based photocatalysts and exploit the photocatalytic mechanism. Herein, metal-free porphyrin (5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin, TCPP) was self-assembled through an acid-based neutralization reaction and mixing dual-solvents under surfactants to form different aggregates. Morphology structures, optical and optoelectronic properties of the TCPP aggregates were characterized in detail. TCPP self-assemblies showed higher photocatalytic activities for the degradation of phenol under visible light than untreated TCPP powders, and the aggregates of nanorods formed through the acid-based neutralization reaction in the presence of hexadecyl trimethyl ammonium bromide (CTAB) possessed 2.6 times more activity than the nanofiber aggregates formed through mixing dual-solvents. It was proved that self-assembly methods are crucial for controlling the aggregation of porphyrins to form different aggregations, which have a profound impact on the photocatalytic activity.

Enhancement of Photocatalytic Activity under Visible Light Irradiation via the AgI@TCNQ Core-Shell Structure.

In this paper, a AgI@TCNQ photocatalyst with a core-shell structure was reported. A two-dimensional TCNQ (7,7,8,8-Tetracyanoquinodimethane) nanosheet, with a π-π conjugate structure, was used as a shell layer to realize the flexible coating on the surface of AgI nanoparticles. These special core-shell structure composites solve the key problems of the small interface of the bulk composites and the lesser charge transfer paths, which could accelerate the migration of photogenerated carriers. Thus, the AgI@TCNQ photocatalysts showed the better photodegradation performance for the methylene blue (MB) solution, and the degradation rate of AgI@TCNQ (1 wt.%) composite was 1.8 times than AgI under irradiation. The reactive species trapping experiments demonstrated that ·O2-, h+, and ·OH all participated in the MB degradation process. The photocatalytic mechanism of AgI@TCNQ composites could be rationally explained by considering the Z-scheme structure, resulting in a higher redox potential and more efficient separation of charge carriers. At the same time, the unique core-shell structure provides a larger contact area, expands the charge transport channel, and increases the surface active sites, which are beneficial for improving photocatalytic performance.

Three-Dimensional Structure of PANI/CdS NRs-SiO2 Hydrogel for Photocatalytic Hydrogen Evolution with High Activity and Stability.

Three-dimensional PANI/CdSNRs-SiO2 hydrogel (CdS NRs-PANI-SiO2) was synthesized by loading polyaniline (PANI) onto the semiconductor CdS nanorods (NRs) surface and loading the binary complex on SiO2 gel. The structure, optical properties, and electrochemical properties of the composite were studied in detail. The hydrogen production amount of CdS NRs-PANI (3%)-SiO2 (20%) increased in comparison with CdS NRs and reached 43.25 mmol/g in 3 h under visible light. The three-dimensional structure of SiO2 hydrogel increased the specific surface area of the catalyst, which was conducive to exposing more active sites of the catalyst. In addition, the conductive polymer PANI coated on CdS NRs played the role of conductive charge and effectively inhibited the photo-corrosion of CdS NRs. In addition, the recovery experiment showed that the recovery rate of the composite catalyst reached 90% and hydrogen production efficiency remained unchanged after five cycles, indicating that the composite catalyst had excellent stability.

Facile Fabrication of 3D Graphene⁻Silica Hydrogel Composite for Enhanced Removal of Mercury Ions.

Adsorption is a highly promising and widely used approach to remove Hg(II) ions from contaminated water. The key to this technology is exploring the effective adsorbent. The three-dimensional (3D) graphene as reduced graphene oxide hydrogel (rGH)-encapsulated silica gel (SG-PEI/rGH) was prepared by a moderate chemical reduction strategy using ascorbic acid. This composite structure was characterized by FTIR, XRD, and SEM analysis and used as adsorbents for Hg(II) ions. Its adsorption capacity toward Hg(II) ions was 266 mg/g and increased about 32% compared with the silica gel because of reduced graphene oxide hydrogel (rGH). Mechanism study showed that the high adsorption ability was due to the formation of an N⁻Hg complex with multi-amino groups on the surface of polyethyleneimine-modified silica gel (SG-PEI) and the rapid diffusion of adsorbed ions attributed to the rGH network structure. This composite SG-PEI/rGH would be a promising material for the removal of Hg(II) ions.

The Supramolecular Organogel Formed by Self-Assembly of Ursolic Acid Appended with Aromatic Rings.

Ursolic acid (UA) as a natural ursane-triterpenoid has rich pharmacological activities. We have found that it possesses aggregation properties and could self-assemble into organogels. Based on the aggregation property of ursolic acid in suitable solvents, its derivative appended with aromatic rings by amide groups was synthesized. The property of self-assembly into organogel was studied in this paper. The results revealed that this derivative could form supramolecular gel in halogenated benzene and also gelate chloroform in the presence of toluene or p-xylene. By Fourier-transform infrared spectra (FT-IR) and variable temperature proton nuclear magnetic resonance (¹H NMR), it was proved that intermolecular hydrogen bonding and π⁻π stacking interaction were the primary driving forces for the aggregation to form organogel.

Enhanced Photocatalytic Activity toward Organic Pollutants Degradation and Mechanism Insight of Novel CQDs/Bi2O2CO3 Composite.

Novel carbon quantum dots (CQDs) modified with Bi2O2CO3 (CQDs/Bi2O2CO3) were prepared using a simple dynamic-adsorption precipitation method. X-ray diffractometry (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), and scanning electron microscopy (SEM) were used to test the material composition, structure, and band structures of the as-prepared samples. Methylene blue (MB) and colorless phenol, as target organic pollutants, were used to evaluate the photocatalytic performance of the CQDs/Bi2O2CO3 hybrid materials under visible light irradiation. Experimental investigation shows that 2⁻5 nm CQDs were uniformly decorated on the surface of Bi2O2CO3; CQDs/Bi2O2CO3 possess an efficient photocatalytic performance, and the organic matter removal rate of methylene blue and phenol can reach up to 94.45% and 61.46% respectively, within 2 h. In addition, the degradation analysis of phenol by high performance liquid chromatography (HPLC) proved that there are no other impurities in the degradation process. Photoelectrochemical testing proved that the introduction of CQDs (electron acceptor) effectively suppresses the recombination of e--h⁺, and promotes charge transfer. Quenching experiments and electron spin resonance (ESR) suggested that ·OH, h⁺, and ·O2- were involved in the photocatalytic degradation process. These results suggested that the up-conversion function of CQDs could improve the electron transfer and light absorption ability of photocatalysts and ·O2- formation. Furthermore, the up-conversion function of CQDs would help maintain photocatalytic stability. Finally, the photocatalytic degradation mechanism was proposed according to the above experimental result.

Ag3PO4@UMOFNs Core-Shell Structure: Two-Dimensional MOFs Promoted Photoinduced Charge Separation and Photocatalysis.

Metal-organic frameworks (MOFs) are a new type of functional material that is self-assembled by metal ions and organic ligands. In this paper, a bimetal-organic framework was synthesized and stripped into two-dimensional nanosheets structure via an ultrasonic method. We coated the UMOFNs (ultrathinning MOFs into two-dimensional nanosheets) on Ag3PO4 nanoparticles to obtain Ag3PO4@UMOFNs core-shell photocatalysts. Under visible-light irradiation, the degradation of phenol was 100% within 16 min, and the degradation of biphenyl A was 98.9% within 20 min via Ag3PO4@UMOFNs (5 wt %). These values were 1.6- and 1.8-times higher than Ag3PO4, respectively. The activity of the Ag3PO4@UMOFNs increased due to the synergistic effects. The π-π bonds of the organic ligands and weak interactions between UMOFNs and Ag3PO4 collectively promote charge transfer. In addition, matching energy-level structures and a sufficiently large contact area accelerate the separation of the photogenerated charges and improve the activity. This remarkably improves the photocatalytic activity.

Surface Decoration of ZnWO4 Nanorods with Cu2O Nanoparticles to Build Heterostructure with Enhanced Photocatalysis.

The surface of ZnWO4 nanorods was decorated with Cu2O nanoparticles (Cu2O/ZnWO4) prepared through a precipitation method. The Cu2O nanoparticles were tightly deposited on the ZnWO4 surface and had average diameters of 20 nm. The nanoparticles not only promoted the absorption and utilization of visible light but also facilitated the separation of photogenerated charge carriers. This brought an improvement of the photocatalytic activity. The 5 wt % Cu2O/ZnWO4 photocatalyst displayed the highest degrade efficiency for methylene blue (MB) degradation under visible light, which was 7.8 and 2 times higher than pure ZnWO4 and Cu2O, respectively. Meanwhile, the Cu2O/ZnWO4 composite photocatalyst was able to go through phenol degradation under visible light. The results of photoluminescence (PL), photocurrent, and electrochemical impedance spectra (EIS) measurements were consistent and prove the rapid separation of charge, which originated from the match level structure and the close contact with the interface. The radical and hole trapping experiments were carried out to detect the main active substances in the photodegradation process. The holes and ·O2- radicals were predicted to dominate the photocatalytic process. Based on the characterization analysis and experiment results, a possible photocatalytic mechanism for enhancing photocatalytic activity was proposed.

A separation-free 3D network ZnO/rGO-rGH hydrogel: adsorption enriched photocatalysis for environmental applications.

This study describes the encapsulation of ZnO by reduced graphene oxide to form a composite (ZnO/rGO) that can be incorporated into graphene to form hydrogels (ZnO/rGO-rGH) with three-dimensional (3D) network structures. The unique surface adsorption characteristics of graphene make ZnO/rGO-rGH materials have the ability of fast adsorption and desorption. Meanwhile, the combination of graphene and ZnO nanoparticles can promote the separation efficiency of electrons and holes and improve the photocatalytic activity. The sample showed the highest adsorption-photocatalysis synergistic activity and removed 100% of the BPA (10 mg L-1) within 20 min under UV irradiation. The purification efficiency of ZnO/rGO-rGH can reach more than 90% after 5 rounds of repeated use. We also measured the performance of ZnO/rGO-rGH in removing BPA under flow conditions, and the results showed that this approach with ZnO/rGO-rGH removed 100% of the BPA in 16 h.

Facile synthesis of an Ag@AgBr nanoparticle-decorated K4Nb6O17 photocatalyst with improved photocatalytic properties.

An Ag@AgBr nanoparticle-decorated K4Nb6O17 (Ag@AgBr/K4Nb6O17) photocatalyst was prepared via the oil-in-water self-assembly method. The Ag@AgBr nanoparticles, with average diameters of 20 nm, were uniformly deposited on the K4Nb6O17 surface. The as-prepared Ag@AgBr/K4Nb6O17 composites exhibited high visible light absorption, high photocurrent intensity, and high charge transfer efficiency, thus enhancing the photocatalytic performance for methyl-blue (MB) dye degradation. The Ag@AgBr (20 wt%)/K4Nb6O17 composite displayed the highest photocatalytic activity, degrading 96% of the MB solution under visible light irradiation for 60 min, which was 2.3-times and 8.5-times that of the bulk Ag@AgBr and K4Nb6O17, respectively. The excellent photocatalytic activity of the Ag@AgBr/K4Nb6O17 composites is due to the synergistic effect between Ag@AgBr and K4Nb6O17, where the Ag@AgBr nanoparticles not only enhanced visible light absorption efficiency due to the Ag nanoparticles' SPR, but also greatly accelerated the separation of the photogenerated electron-hole pairs. From the UV-vis spectra, the Ag@AgBr nanoparticles greatly extend the composites' visible light absorption. The data collected from photoluminescence (PL), photocurrent and electrochemical impedance spectra (EIS) were consistent and confirmed the rapid separation of charge carriers. Moreover, the composite exhibited a larger specific surface area, which was also beneficial for the photocatalytic activity. In addition, the roles of the radical species were investigated, and the holes and ·O2 - radicals were hypothesized to dominate the photocatalytic process. Based on the characterization analysis and experimental results, a possible photocatalytic mechanism for the enhancement of photocatalytic activity is proposed.

Highly ordered TiO2 nanotube arrays wrapped with g-C3N4 nanoparticles for efficient charge separation and increased photoelectrocatalytic degradation of phenol.

Novel graphitic carbon nitride nanoparticles (NPs)-wrapped TiO2 nanotube arrays (NTAs) (g-C3N4/TiO2) were fabricated by a two-step method including an electrochemical anodization technique followed by impregnation under vacuum using urea as precursor. The as-prepared photoelectrode exhibited outstanding photoelectric properties and excellent photelectrocatalytic (PEC) performance for the degradation of phenol under stimulated solar light, which was due to the enhanced light absorption property and improved charge separation efficiency. The introduction of g-C3N4 NPs strongly decreased the charge transfer resistance and boosted the charge separation efficiency of TiO2. The optimum ratio of the g-C3N4/TiO2 yielded a pronounced 4.18-fold higher photocurrent density than TiO2. Besides, the combination of g-C3N4 NPs could negatively shift for the flat band potential of TiO2, resulting in an enhanced reduction property for the photoelectrocatalytic degradation of organic pollutants. The PEC process for the degradation of phenol over g-C3N4/TiO2 was much higher than the sum of photocatalytic (PC) and electrocatalytic (EC) processes indicating that a photoelectric synergy was achieved on the as-prepared photoelectrode and resulting in an improved PEC performance for the composite photoelectrode.

Oil-in-Water Self-Assembled Synthesis of Ag@AgCl Nano-Particles on Flower-like Bi2O2CO3 with Enhanced Visible-Light-Driven Photocatalytic Activity.

In this work, a series of novel flower-like Ag@AgCl/Bi2O2CO3 were prepared by simple and feasible oil-in-water self-assembly processes. The phase structures of as-prepared samples were examined by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS), X-ray fluorescence spectrometer (XRF), etc. The characterization results indicated that the presence of Ag@AgCl did not affect the crystal structure, but exerted a great influence on the photocatalytic activity of Bi2O2CO3 and enhanced the absorption band of pure Bi2O2CO3. The photocatalytic activities of the Ag@AgCl/Bi2O2CO3 samples were determined by photocatalytic degradation of methylene blue (MB) under visible light irradiation. The Ag@AgCl (10 wt %)/Bi2O2CO3 composite showed the highest photocatalytic activity, degrading 97.9% MB after irradiation for 20 min, which is over 1.64 and 3.66 times faster than that of pure Ag@AgCl (calculated based on the equivalent Ag@AgCl content in Ag@AgCl (10 wt %)/Bi2O2CO3) and pure Bi2O2CO3, respectively. Bisphenol A (BPA) was also degraded to further prove the degradation ability of Ag@AgCl/Bi2O2CO3. Photocurrent studies indicated that the recombination of photo-generated electron-hole pairs was decreased effectively due to the formation of heterojunctions between flower-like Bi2O2CO3 and Ag@AgCl nanoparticles. Trapping experiments indicated that O2-, h⁺ and Cl° acted as the main reactive species for MB degradation in the present photocatalytic system. Furthermore, the cycling experiments revealed the good stability of Ag@AgCl/Bi2O2CO3 composites. Based on the above, a photocatalytic mechanism for the degradation of organic compounds over Ag@AgCl/Bi2O2CO3 was proposed.

Enhanced Visible Light Photocatalytic Degradation of Organic Pollutants over Flower-Like Bi2O2CO3 Dotted with Ag@AgBr.

A facile and feasible oil-in-water self-assembly approach was developed to synthesize flower-like Ag@AgBr/Bi2O2CO3 micro-composites. The photocatalytic activities of the samples were evaluated through methylene blue degradation under visible light irradiation. Compared to Bi2O2CO3, flower-like Ag@AgBr/Bi2O2CO3 micro-composites show enhanced photocatalytic activities. In addition, results indicate that both the physicochemical properties and associated photocatalytic activities of Ag@AgBr/Bi2O2CO3 composites are shown to be dependent on the loading quantity of Ag@AgBr. The highest photocatalytic performance was achieved at 7 wt % Ag@AgBr, degrading 95.18% methylene blue (MB) after 20 min of irradiation, which is over 1.52 and 3.56 times more efficient than that of pure Ag@AgBr and pure Bi2O2CO3, respectively. Bisphenol A (BPA) was also degraded to further demonstrate the degradation ability of Ag@AgBr/Bi2O2CO3. A photocatalytic mechanism for the degradation of organic compounds over Ag@AgBr/Bi2O2CO3 was proposed. Results from this study illustrate an entirely new approach to fabricate semiconductor composites containing Ag@AgX/bismuth (X = a halogen).

Novel Cu2O quantum dots coupled flower-like BiOBr for enhanced photocatalytic degradation of organic contaminant.

Here we report a highly efficient novel photocatalyst consisting of Cu2O quantum dots (QDs) incorporated into three-dimensional (3D) flower-like hierarchical BiOBr (hereafter designated QDs-Cu2O/BiOBr), which were synthesized via a simple reductive solution chemistry route and applied to decontaminate the hazardous wastewater containing phenol and organic dyes. The deposition of Cu2O QDs onto the surface of the BiOBr was confirmed by structure and composition characterizations. The QDs-Cu2O/BiOBr composites exhibited superior activity for organic contaminant degradation under visible light and 3 wt% QDs-Cu2O/BiOBr composite showed the highest degrade rate for phenol and methylene blue (MB), which was 11.8 times and 1.4 times than that of pure BiOBr, indicated the QDs-Cu2O/BiOBr composite has the great potential application in purifying hazardous organic contaminant. The incorporated Cu2O QDs played an important role in improving the photocatalytic performance, due to the enhancement of visible light absorption efficiency as well as the efficient separation of the photogenerated charge carriers originating from the intimately contacted interface and the well-aligned band-structures, which was confirmed by the results of PL, photocurrent and EIS measurements. The possible photocatalytic mechanism was proposed based on the experiments and theoretical results.

A two-phase procedure for QTL mapping with regression models.

It is typical in QTL mapping experiments that the number of markers under investigation is large. This poses a challenge to commonly used regression models since the number of feature variables is usually much larger than the sample size, especially, when epistasis effects are to be considered. The greedy nature of the conventional stepwise procedures is well known and is even more conspicuous in such cases. In this article, we propose a two-phase procedure based on penalized likelihood techniques and extended Bayes information criterion (EBIC) for QTL mapping. The procedure consists of a screening phase and a selection phase. In the screening phase, the main and interaction features are alternatively screened by a penalized likelihood mechanism. In the selection phase, a low-dimensional approach using EBIC is applied to the features retained in the screening phase to identify QTL. The two-phase procedure has the asymptotic property that its positive detection rate (PDR) and false discovery rate (FDR) converge to 1 and 0, respectively, as sample size goes to infinity. The two-phase procedure is compared with both traditional and recently developed approaches by simulation studies. A real data analysis is presented to demonstrate the application of the two-phase procedure.

Assessment of bone quality using finite element analysis based upon micro-CT images.

BACKGROUND: To evaluate the feasibility of a micro-image based finite element model to determine the efficacy of sequential treatments on the bone quality in a rat osteoporosis model. METHODS: Rat osteoporosis and treated osteoporosis models were established with the bone loss, restore and maintain concept. Thirty Sprague-Dawley rats were used in this study. A sham operation or ovariectomy was performed at 20 weeks after birth, which was followed by the respective sequential trials as follows: (1) sham-operation only, (2) ovariectomy only, (3) ovariectomized rats with parathyroid hormone maintenance, (4) ovariectomized rats treated with PTH for 5 weeks and then withdrawal, (5) ovariectomized rats treated with PTH for 5 weeks and then with 17 beta-estradiol, and (6) ovariectomized rats treated with parathyroid hormone for 5 weeks and then treated with zoledronate. The histomorphometry indices were determined using the micro-images from a micro-computed tomogram. Finite element analysis was carried out to determine the mechanical properties (Stiffness and Young's modulus) of the vertebra bodies. The differences in properties between the groups were compared using ANOVA and a Bonferroni's multiple group comparison procedure. RESULTS: The histomorphometry and mechanical properties were significantly better in groups (3) and (6) than in the groups (1) and (2) (p < 0.05). The stiffness (sigma(s)) and Young's modulus (E) was highest in group (3) following by group (6). CONCLUSIONS: Finite element analysis based on micro-images provides a useful tool that reflects the changes in micro-structural and mechanical properties of a rat vertebral body with the bone loss, restore and maintain concept.

An additional reference axis for determining rotational alignment of the femoral component in total knee arthroplasty.

No studies have examined the trochlear line connecting the most anterior projections of the lateral and medial femoral condyles in relation to the surgical epicondylar axis. To determine if the trochlear line is more consistent relative to the transepicondylar axis than the posterior condylar axis and the Whiteside's line, the angles between the surgical epicondylar axis and each of the 3 axes in 50 knees of cadavers were measured using computed tomography scans. The results showed that the variability in the trochlear line for referencing the transepicondylar axis was comparable to those of the Whiteside line and the posterior condylar axis. The trochlear line may be considered as an additional reference axis for determining the rotational alignment of the femoral component in total knee arthroplasty.